Versão impressa REVISTA BRASILEIRA DE OFTALMOLOGIA vol. 73 - nº 5 - Setembro/Outubro 2014 SET/OUT 2014 VOLUME 73 NÚMERO 5 P. 253-316 100 95 75 25 RBO 5 0 DESDE 1942 CAPA REVISTA-JUL-AGO-2014 quinta-feira, 13 de novembro de 2014 11:34:53 253 ISSN 0034-7280 Revista Brasileira de (Versão impressa) ISSN 1982-8551 (Versão eletrônica) Oftalmologia PUBLICAÇÃO OFICIAL: SOCIEDADE BRASILEIRA DE OFTALMOLOGIA SOCIEDADE BRASILEIRA DE CATARATA E IMPLANTES INTRAOCULARES SOCIEDADE BRASILEIRA DE CIRURGIA REFRATIVA Sociedade Brasileira de Oftalmologia Indexada nas bases de dados: LILACS Literatura Latinoamericana em Ciências da Saúde SciELO Scientific Electronic Library OnLine WEB OF SCIENCE www.freemedicaljournals.com Disponível eletronicamente: www.sboportal.org.br Publicação bimestral Editor Chefe Newton Kara-Junior (SP) Editor Executivo Arlindo José Freire Portes (RJ) Co-editores André Luiz Land Curi (RJ) Arlindo José Freire Portes (RJ) Bruno Machado Fontes (RJ) Carlos Eduardo Leite Arieta (SP) Hamilton Moreira (PR) Liana Maria Vieira de Oliveira Ventura (PE) Marcony Rodrigues de Santhiago (RJ) Mario Martins dos Santos Motta (RJ) Maurício Maia (SP) Niro Kasahara (SP) Renato Ambrósio Jr. (RJ) Rodrigo Jorge (SP) Rodrigo Pessoa Cavalcanti Lira (PE) Silvana Artioli Schellini (SP) Walton Nosé (SP) Corpo Editorial Internacional Baruch D. Kuppermann - Califórnia - EUA Christopher Rapuano - Phyladelphia - EUA Curt Hartleben Martkin - Colina Roma - México Daniel Grigera - Olivos - Argentina Deepinder Kauer Dhaliwal - Pittsburg - EUA Felipe A. A. Medeiros - Califórnia - EUA Felix Gil Carrasco - México – México Fernando Arevalo - Riyadh - Arábia Saudita Francisco Rodríguez Alvira – Bogotá - Colombia Howard Fine - Eugene - EUA Jean Jacques De Laey - Ghent - Bélgica Kevin M. Miller - Califórnia - EUA Lawrence P. Chong - Califórnia - EUA Lihteh Wu – San José - Costa Rica Liliana Werner - Utah - EUA Miguel Burnier Jr. - Montreal - Canadá Pablo Cibils - Assunção - Paraguai Patricia Mitiko Santello Akaishi – Arábia Saudita Peter Laibson - Phyladelphia - EUA Steve Arshinoff - Toronto - Canadá Corpo Editorial Nacional A. Duarte - Rio de Janeiro - RJ Abelardo de Souza Couto - Rio de Janeiro- RJ Abrahão da Rocha Lucena - Fortaleza - CE Alexandre Augusto Cabral de Mello Ventura - Recife - PE Alexandre H. Principe de Oliveira – Salvador – BA Alexandre Seminoti Marcon – Porto Alegre - RS Ana Carolina Cabreira Vieira – Rio de Janeiro – RJ Ana Luisa Hofling de Lima - São Paulo - SP André Correa de Oliveira Romano – Americana - SP André Curi - Rio de Janeiro - RJ André Luis Freire Portes - Rio de Janeiro - RJ André Marcio Vieira Messias – Ribeirão Preto – SP Andrea Kara José Senra - São Paulo – SP Antonio Marcelo Barbante Casella - Londrina - PR Armando Stefano Crema- Rio de Janeiro- RJ Beatriz de Abreu Fiuza Gomes – Rio de Janeiro - RJ Bruna Vieira Ventura - Recife - PE Coordenação de Aperfeiçoamento de Pessoal de Nível Superior http://www.capes.gov.br Rev Bras Oftalmol, v. 73, n. 5, p. 253 - 316, Set./Out. 2014 Bruno Diniz – Goiânia - GO Carlos Augusto Moreira Jr.- Curitiba- PR Carlos Gabriel Figueiredo - São José do Rio Preto - SP Carlos Ramos de Souza Dias- São Paulo- SP Claudio do Carmo Chaves - Manaus - AM Cristiano Caixeta Umbelino - São Paulo - SP Daniel Lavinsky – Porto Alegre - RS David Leonardo Cruvinel Isaac – Goiania - GO Diego Tebaldi Q. Barbosa - São Paulo - SP Edmundo Frota De Almeida Sobrinho- Belém- PA Eduardo Buchele Rodrigues – Florianópolis - SC Eduardo Cunha de Souza – São Paulo - SP Eduardo Damasceno - Rio de Janeiro - RJ Eduardo Dib – Rio de Janeiro - RJ Eduardo Ferrari Marback- Salvador- BA Eliezer Benchimol - Rio de Janeiro - RJ Enzo Augusto Medeiros Fulco – Jundiaí - SP Eugenio Santana de Figueiredo – Juazeiro do Norte - CE Fábio Marquez Vaz – Ondina – BA Felipe Almeida - Ribeirão Preto - SP Fernando Cançado Trindade - Belo Horizonte- MG Fernando Marcondes Penha - Florianópolis - SC Fernando Oréfice- Belo Horizonte- MG Fernando Roberte Zanetti – Vitória - ES Flavio Rezende- Rio de Janeiro- RJ Francisco de Assis Cordeiro Barbosa - Recife - PE Frederico Valadares de Souza Pena – Rio de Janeiro - RJ Frederico Guerra - Niterói - RJ Giovanni N.U.I.Colombini- Rio de Janeiro- RJ Guilherme Herzog Neto- Rio de Janeiro- RJ Harley Biccas - Ribeirão Preto - SP Haroldo Vieira de Moraes Jr.- Rio de Janeiro- RJ Hélcio Bessa - Rio de Janeiro - RJ Helena Parente Solari - Niterói - RJ Heloisa Helena Abil Russ – Curitiba – PR Henderson Celestino de Almeida- Belo Horizonte- MG Hilton Arcoverde G. de Medeiros- Brasilia- DF Homero Gusmao de Almeida- Belo Horizonte- MG Italo Mundialino Marcon- Porto Alegre- RS Iuuki Takasaka – Santa Isabel - SP Ivan Maynart Tavares - São Paulo - SP Jaco Lavinsky - Porto Alegre - RS Jair Giampani Junior – Cuiabá - MT Jeffersons Augusto Santana Ribeiro - Ribeirão Preto - SP João Borges Fortes Filho- Porto Alegre- RS João Luiz Lobo Ferreira – Florianópolis – SC João Marcelo de Almeida G. 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G. Vianna - Niterói - RJ Remo Susanna Jr.- São Paulo- SP Renata Rezende - Rio de Janeiro - RJ Renato Ambrosio Jr.- Rio de Janeiro- RJ Renato Luiz Nahoum Curi- Niterói- RJ Richard Yudi Hida – São Paulo – SP Riuitiro Yamane - Niterói - RJ Roberto Lorens Marback - Salvador - BA Roberto Pinto Coelho – Ribeirão Preto – SP Rodrigo França de Espíndola – São Paulo – SP Rogerio Alves Costa- Araraquara- SP Rogerio de Almeida Torres - Curitiba - PR Rubens Belfort Neto – São Paulo – SP Rubens Camargo Siqueira- São José do Rio Preto- SP Sebastião Cronemberger So.- Belo Horizonte- MG Sérgio Henrique S. Meirelles- Rio de Janeiro- RJ Sérgio Kwitko - Porto Alegre - RS Sérgio Luis Gianotti Pimentel – São Paulo – SP Silvana Artioli Schellini - Botucatu- SP Suel Abujamra- São Paulo - SP Suzana Matayoshi - São Paulo - SP Tânia Mara Cunha Schaefer – Curitiba – PR Vitor Cerqueira - Rio de Janeiro - RJ Walter Yukihiko Takahashi – São Paulo – SP Walton Nose- São Paulo- SP Wener Passarinho Cella - Plano Piloto - DF Wesley Ribeiro Campos- Passos- MG Yoshifumi Yamane- Rio de Janeiro- RJ Redação: Rua São Salvador, 107 Laranjeiras CEP 22231-170 Rio de Janeiro - RJ Tel: (0xx21) 3235-9220 Fax: (0xx21) 2205-2240 Tiragem: 5.000 exemplares Edição:Bimestral Secretaria: Marcelo Diniz Editoração Eletrônica: Sociedade Brasileira de Oftalmologia Responsável: Marco Antonio Pinto DG 25341RJ Publicidade: Sociedade Brasileira de Oftalmologia Responsável: João Diniz [email protected] Contato publicitário: Westinghouse Carvalho Tel: (11)3726-6941 / 99274-0724 [email protected] Revisão: Eliana de Souza FENAJ-RP 15638/71/05 Normalização: Edna Terezinha Rother Assinatura Anual: R$420,00 ou US$280,00 Impressão: Gráfica Stamppa Associada a ABEC - Associação Brasileira de Editores Científicos 254 Revista Brasileira de Oftalmologia Rua São Salvador, 107 - Laranjeiras - CEP 22231-170 - Rio de Janeiro - RJ Tels: (0xx21) 3235-9220 - Fax: (0xx21) 2205-2240 - e-mail: [email protected] - www.sboportal.org.br Revista Brasileira de Oftalmologia, ISSN 0034-7280, é uma publicação bimestral da Sociedade Brasileira de Oftalmologia Diretoria da SBO 2013-2014 Presidente Marcus Vinicius Abbud Safady (RJ) Vice-presidentes Elisabeto Ribeiro Goncalves (MG) Fabíola Mansur de Carvalho (BA) João Alberto Holanda de Freitas (SP) Ricardo Lima de Almeida Neves (RJ) Tania Mara Cunha Schaefer (PR) Secretário Geral André Luis Freire Portes (RJ) 1º Secretário Sérgio Henrique S. Meirelles (RJ) 2º Secretário Giovanni N. U. I. Colombini (RJ) Tesoureiro Gilberto dos Passos (RJ) Diretor de Cursos Arlindo José Freire Portes (RJ) Diretor de Publicações Newton Kara-Junior (SP) Diretor de Biblioteca Armando Stefano Crema (RJ) Conselho Consultivo Membros eleitos Jacó Lavinsky (RS) Paulo Augusto de Arruda Mello (SP) Roberto Lorens Marback (BA) Conselho Fiscal Efetivos Francisco Eduardo Lopes Lima (GO) Leiria de Andrade Neto (CE) Roberto Pedrosa Galvão (PE) Suplentes Eduardo Henrique Morizot Leite (RJ) Jorge Alberto Soares de Oliveira (RJ) Mizael Augusto Pinto (RJ) SOCIEDADES FILIADAS À SOCIEDADE BRASILEIRA DE OFTALMOLOGIA Associação Brasileira de Banco de Olhos e Transplante de Córnea Presidente: Ari de Souza Pena Associação Maranhense de Oftalmologia Presidente: Romero Henrique Carvalho Bertand Associação Matogrossense de Oftalmologia Presidente: Maurício Donatti Associação Pan-Americana de Banco de Olhos Presidente: Luciene Barbosa de Souza Associação Paranaense de Oftalmologia Presidente: Otavio Bisneto Associação Rondoniense de Oftalmologia Presidente: Lhano Fernandes Adorno Associação Sul Matogrossense de Oftalmologia Presidente: Elson Yamasato Sociedade Alagoana de Oftalmologia Presidente: Mário Jorge Santos Sociedade Brasileira de Administração em Oftalmologia Presidente: Flávio Rezende Sociedade Brasileira de Catarata e Implantes Intraoculares Presidente: Armando Crema Sociedade Brasileira de Cirurgia Plástica Ocular Presidente: Ricardo Morschbacher Sociedade Brasileira de Cirurgia Refrativa Presidente: Renato Ambrósio Jr. Sociedade Brasileira de Ecografia em Oftalmologia Presidente: Norma Allerman Sociedade Brasileira Glaucoma Presidente: Francisco Lima Sociedade Capixaba de Oftalmologia Presidente: Cesar Ronaldo Vieira Gomes Sociedade Catarinense de Oftalmologia Presidente: Ramon Coral Ghanem Sociedade Cearense de Oftalmologia Presidente: Dácio Carvalho Costa Sociedade Goiana de Oftalmologia Presidente: Lúcia Helena Meluzzi Sociedade Norte-Nordeste de Oftalmologia Presidente: Francisco de Assis Cordeiro Barbosa Sociedade de Oftalmologia do Amazonas Presidente: Leila Suely Gouvea José Sociedade de Oftalmologia da Bahia Presidente: André Hasler Príncipe de Oliveira Sociedade de Oftalmologia do Nordeste Mineiro Presidente: Mauro César Gobira Guimarães Sociedade de Oftalmologia de Pernambuco Presidente: João Pessoa de Souza Filho Sociedade de Oftalmologia do Rio Grande do Norte Presidente: Ricardo Maia Diniz Sociedade de Oftalmologia do Rio Grande do Sul Presidente: Afonso Reichel Pereira Sociedade de Oftalmologia do Sul de Minas Presidente: Mansur Elias Ticly Junior Sociedade Paraense de Oftalmologia Presidente: Lauro José Barata de Lima Sociedade Paraibana de Oftalmologia Presidente: Saulo Zanone Lemos Neiva Sociedade Piauiense de Oftalmologia Maria de Lourdes Cristina Alcântara Paz Carvalho do Nascimento Sociedade Sergipana de Oftalmologia Presidente: Bruno Campelo 255 Revista Brasileira de ISSN 0034-7280 (Versão impressa) ISSN 1982-8551 (Versão eletrônica) Oftalmologia PUBLICAÇÃO OFICIAL: SOCIEDADE BRASILEIRA DE OFTALMOLOGIA SOCIEDADE BRASILEIRA DE CATARATA E IMPLANTES INTRAOCULARES SOCIEDADE BRASILEIRA DE CIRURGIA REFRATIVA Fundada em 01 de junho de 1942 CODEN: RBOFA9 Indexada nas bases de dados: SciELO Scientific Electronic Library OnLine WEB OF SCIENCE www.freemedicaljournals.com Disponível eletronicamente: www.sboportal.org.br LILACS Literatura Latinoamericana em Ciências da Saúde Coordenação de Aperfeiçoamento de Pessoal de Nível Superior http://www.capes.gov.br Publicação bimestral Rev Bras Oftalmol, v. 73, n. 5, p. 253 - 316, Set./Out. 2014 Contents - Sumário Editorial 257 Structure, style and writing of a scientific paper: the way in which researchers acknowledge their peers Estrutura, estilo e escrita de artigo científico: a maneira com que pesquisadores reconhecem seus pares Newton Kara-Junior 260 Social aspects of corneal transplantation in Brazil: contrast between advances in surgical technique and limiting access to the population Aspectos sociais do transplante de córnea no Brasil: contraste entre avanços na técnica cirúrgica e limitação de acesso à população Hirlana Gomes Almeida, Richard Yudi Hida Artigos originais 262 The role of Descemet’s membrane in the pathogeny of corneal edema following anterior segment surgery O papel da membrana de Descemet na patogenia do edema corneano após cirurgia de segmento anterior Karine Feitosa Ximenes, Jailton Vieira Silva, Karla Feitosa Ximenes Vasconcelos, Fernando Queiroz Monte 269 Preemptive analgesia of nepafenac 0.1% in retinal photocoagulation Analgesia preemptiva com nepafenaco 0,1% na fotocoagulação da retina Emerson Fernandes de Sousa e Castro, Erika Araki Okuda, Vinícius Balbi Amatto, Hirlana Gomes Almeida, Marina Gracia, Newton Kara-Junior 256 273 Analysis quantitative and qualitative of the tear film in patients undergoing PRK and LASIK with femtosecond Análise quantitativa e qualitativa do filme lacrimal nos pacientes submetidos a PRK e LASIK com femtossegundo Rubens Amorim Leite, Ricardo Menon Nosé , Fábio Bernardi Daga, Tatiana Adarli Fioravanti Lui, Giovana Arlene Fioravanti Lui, Adamo Lui-Netto 279 Novel spatula and dissector for safer deep anterior lamellar keratoplasty Uso de espátula e dissector para otimização da ceratoplastia lamelar anterior profunda (DALK) Gustavo Bonfadini, Eun Chul Kim, Mauro Campos, Albert S. Jun 282 Serological profile of candidates for corneal donation Perfil sorológico de candidatos a doação de córneas Adroaldo Lunardelli, Richard Beraldini Alvarenga, Maria Luiza Assmann, Dário Eduardo de Lima Brum, Mirna Adolfina Barison 287 Sealing the gap between conjunctiva and Tenon’s capsule in primary pterygium surgery Adição do selamento entre conjuntiva e cápsula de Tenon em cirurgia de pterígio primário Ricardo Alexandre Stock, Luan Felipe Lückmann, Gabriel Alexander Ken-Itchi Kondo, Elcio Luiz Bonamigo 291 Visual impairment, rehabilitation and International Classification of Functioning, Disability and Health Deficiência visual, reabilitação e Classificação Internacional de Funcionalidade, Incapacidade e Saúde Marissa Romano da Silva, Maria Inês Rubo de Souza Nobre, Keila Monteiro de Carvalho, Rita de Cássia Ietto Montilha 302 Knowledge about primary open angle glaucoma among medical students Nível de conhecimento sobre glaucoma primário de ângulo aberto entre os estudantes de medicina Saulo Costa Martins, Marcos Henrique Mendes, Ricardo Augusto Paletta Guedes, Vanessa Maria Paletta Guedes, Alfredo Chaoubah Relato de Casos 308 Central retinal artery occlusion associated with patent foramen ovale Oclusão de artéria central da retina associada a forame oval patente Patrícia Regina de Pinho Tavares, Mariana Rezende de Oliveira, Eduardo de Castro Miranda Diniz , Rafael Mourão Agostini , Daniela Vieira de Aguiar 311 Adult dacryocystocele Dacriocistocele no adulto Silvia Helena Tavares Lorena , João Amaro Ferrari Silva Instruções aos autores 314 Normas para publicação de artigos na RBO EDITORIAL 257 Structure, style and writing of a scientific paper: the way in which researchers acknowledge their peers Estrutura, estilo e escrita de artigo científico: a maneira com que pesquisadores reconhecem seus pares T he style of a scientific paper indicates to reviewers and readers whether the authors are familiar with the science. In this respect, systematically reading scientific publications is excellent training for beginning researchers. Scientific publications are documents that need to contain sufficient information for readers to understand the authors’ observations and decide whether the conclusions are justified by the data, as well as giving them the ability to repeat the experiment. All clinical research starts with a “doubt”, a question that cannot be answered based on the current knowledge found in the literature. Starting from this question, the research paper is structured as follows: 1. 2. 3. 4. Introduction – What question has been asked? Methods – How was it studied? Results – What has been found? Discussion – What do these findings mean? The Introduction should be short (three or four paragraphs) and should clearly convey the question that the authors will try to answer with the study. For the reader to understand the relevance of the authors’ question, the paper should start with a brief literature review to provide the context and justify the study, showing that it is needed to fill the current gaps in knowledge. In case the subject matter has already been approached in previous publications, the new study can be justified by showing that it can be better than the previous ones (highlighting methodological flaws, limitations in sample size, etc.). It should be noted that publishers do not want to publish, authors do not want to cite, and readers do not want to read studies that simply repeat what has already been done several times before. Thus, in the Introduction, the brief literature review should start from what is already known about the subject in order to justify the study’s objectives. Ideally, the description of existing knowledge should progressively centre on the gap that the study intends to fill. For example, if the research question is related to the existence of emotional factors that could influence cataract patients in their decision to undergo surgery, the Introduction should start by citing the importance of vision and the fear of becoming blind, followed by an explanation of the social problem of cataract blindness, and the visual benefits and risks of corrective surgery. Finally, it could point out the fact that persons with low vision may avoid cataract surgery due to emotional reasons (fear of becoming blind due to surgical complications), thus stressing the study’s importance as a way to identify such situations and to inform awareness campaigns (1). All information included in the Introduction should be backed by previous studies, and references should always be provided. Authors should avoid writing about what readers are already likely to know; instead, priority should be given to explaining what readers do not know. This requires knowing the target audience and having an idea of the type of journal the paper will be submitted to. Thus, in the previous example (1), if the readers are physicians, there is no need to explain what cataract is. Finally, the Introduction should describe the study design and clearly state the study’s objective (e.g. “a prospective, randomised, double-blind study to determine the efficacy and safety of…”). When planning a study, it can be interesting to write the Introduction before starting data collection, so that researchers remain focused on their original goals. The Methods section describes how the data were collected and how the study was conducted. The more the methods are described in a detailed and objective manner, the greater the confidence of reviewers and readers on the study results. If the methods used to answer the research question are unsound, the study results and conclusions will be limited. If the research involves a new procedure or test, it should be described in detail so that the study can be reproduced in the future. Standard measurement methods described in previous publications, unless considered unsound, should be used Rev Bras Oftalmol. 2014; 73 (5): 257-9 258 Kara-Junior N again (and the source should be mentioned) to facilitate data comparison among different papers. For example, if the study that inspired the authors to research the visual performance of a different intraocular lens model used a certain wavefront sensor, a measurement chart, and a visual satisfaction questionnaire, the new study should ideally use the same assessment methods. This helps minimise the influence of other variables in the comparison of results across studies (2,3). The Methods section should start by presenting the study design, describing the type of study, its randomisation and blinding. The place and date where the study was conducted should also be mentioned. An explanation of how the study was conducted should then follow: sample selection, inclusion criteria, approval by a research ethics committee, a precise description of materials and drug dosages, a description of the treatment, and a presentation of study variables. Finally, the statistical analysis of data should be described. Thus, while the Introduction explains “what” has been studied and “why”, the Methods section describes “how”, “when” and “where” the study was conducted. Authors should never believe that their methods are immune to criticism, as no study is flawless; instead, they are expected to avoid gross errors and to highlight the study’s limitations, so that readers can judge the validity of the results based on their own reality and needs. Ideally, the reader should first have their interest aroused by the topic presented in the Title (in response to the research question presented by the authors) and then read the Introduction in order to understand the study’s context and relevance. Next, the Methods section should be read carefully to make sure that the sample was collected and the study was conducted in a way that meets the reader’s reality and requirements. For example, a study assessing the population’s knowledge about cataract surgery in a developing country will probably not influence clinical practice in developed countries (4). A critical analysis of papers through careful assessment of the methodology allows readers to identify biases (methodological errors) that might invalidate or limit the results. Readers should not simply trust that every article published in a scientific journal is methodologically correct, even if the journal has a high impact factor (5). The Results section should present the data obtained in the study. It should not contain the authors’ interpretations or opinions. Tables should be used to group important data, and statistical analysis should be done to validate comparisons. The Results section should start by characterising the population represented by the sample and, if there is more than one study group, by determining whether they are homogeneous. Homogeneous groups indicate that the randomisation method was adequate, because if all study subjects have the same chance of being in either group, then characteristics such as gender and age should be equivalent, on average.This kind of information can be grouped into a table and will help assure readers that personal characteristics did not influence the study results. For example, in the case of a study assessing the effectiveness of two capsulorhexis techniques in intumescent cataract (6), the study sample represents the population of patients suffering from this type of cataract, so the results are only valid for this type of patient. As regards study groups (supposing each group was operated with a different capsulorhexis technique), if randomisation has been performed correctly, i.e., if all participants had the same chance of being randomly assigned to either group, then personal characteristics (sex, age, axial length, etc.) should be similar, thus indicating that individual variations probably did not influence the results. In a study, data are represented by numbers and the results represent the meaning of those numbers; thus, results should be described in writing, while data should be presented in tables. Paragraphs should start by describing the results and then refer the reader to a table, indicating what can be found in it. Tables should always be self-sufficient, presenting all the information the reader needs to understand them without the need to read the rest of the article. Whenever possible, results should be accompanied by statistical analysis, which provides credibility to comparisons (7). Qualitative, subjective terms such as “very”, “large”, “only”, and so on should be avoided; instead, the text should focus on quantitative information, such as absolute numbers and percentages. It is important to cite all the data related to the study variables and described in the Methods section, i.e. all study items listed in the Methods should appear in the Results and be mentioned in the Discussion. In the Discussion section, research findings should be correlated with data from the literature and their significance should be interpreted. The Discussion should only quote relevant studies (confirming or contradicting the present study); it is not necessary to analyse the entire literature. Data already presented in the Results should not be repeated in the Discussion. All the findings presented in the Results should be commented in the Discussion, and only the main numbers or percentages should be mentioned. The Discussion should begin with a summary of the main findings, discussing possible methodological flaws. Findings should then be compared to those of previous studies, and their clinical implications should be discussed. This is where the strengths of the study should be emphasised, and previous studies can perhaps be criticised. In the Discussion, authors should express their opinions. Even if the authors believe their study will change clinical practice, its importance should not be exaggerated, because studies in general only provide a limited contribution to any subject matter, and a subject can hardly be exhausted in a single work. The Discussion should end with a short summary of the main findings and their implications (conclusion). It is interesting to conclude with suggestions for future studies. Rev Bras Oftalmol. 2014; 73 (5): 257-9 Structure, style and writing of a scientific paper: the way in which researchers acknowledge their peers 259 Scientific writing is different from spoken scientific language. It should avoid jargon and superlatives, and words should be carefully chosen. The greatest desire of any author is to have their work read and cited by as many people as possible. Thus, the text should be pleasant to read and easy to interpret, otherwise readers can easily lose interest in the paper. In scientific writing, sentences should be simple and straightforward, stating what the reader needs to know in the shortest possible way. All abbreviations should be explained at the beginning of each section (Introduction, Methods, Tables, etc.), because readers will not necessarily read the article in the order it is presented. In the Methods section, drugs should always be referred to by their active principle, and where trade names are used, the laboratory’s name and the place of origin should always be mentioned. In the Results section, numbers should, whenever possible, be followed by a percentage, thus helping readers understand the scale of the data. In tables, calculations should be double checked, with special attention to percentages, because depending on the approximation of decimals, they may not add up to 100%. Authors should check that all tables are mentioned in the text, that the same terms are used in the table and the text, and that the header is self-sufficient. Once the paper is finished, it should be read by physicians not involved in the study before being submitted for publication; alternatively, authors should save the article for a few days and then read it again. Some authors are so familiar with the subject matter that they may write in a way that is not clear enough for readers. Newton Kara-Junior Editor-Chefe da Revista Brasileira de Oftalmologia Professor Colaborador, livre-docente e professor do Programa de Pós-graduação da Faculdade de Medicina, Universidade de São Paulo, São Paulo (SP), Brasil R EFERENCES 1. Marback, R.F.;TEMPORINI, E. R. ; Kara-Junior, N. . Emotional factors prior to cataract surgery. Clinics (USP. Paper version), v. 62, p. 433438, 2007. 2. HIDA, W. T. ; MOTTA, A. P. ; et al. Estudo comparativo do desempenho visual e análise de frente de onda entre as lentes intra-oculares multifocais difrativas Tecnis ZM900 e Acrysof Restor SN60D3. Arquivos Brasileiros de Oftalmologia (Paper version), v. 71, p. 788-792, 2008. 3. Santhiago M ; NETTO MV ; BARRETO jr J ; et al. A contralateral eye study comparing apodized difrative and full difrative lenses: wavefront analysis and distance and near uncorrected visual acuity. Clinics (USP. Paper version), v. 64, p. 953-60, 2009. 4. Kara-Junior, N. ; HOLZCHUH, N. ; KARA-JOSE, N. . Popular beliefs regarding the treatment of senile cataract. Revista de Saúde Pública, v. 36, n.3, p. 343-349, 2002. 5. CHAMON, Wallace. Plágio e condutas inadequadas em pesquisa: onde chegamos e o que podemos fazer. Arq. Bras. Oftalmol. [online]. 2013, vol.76, n.6, pp. V-VI. ISSN 0004-2749. 6. Kara-Junior, N. ; Santhiago M ; Kawakami A ; Carricondo, P., C. ; HIDA, W. T. . Mini-rhexis for white intumescent cataracts. Clinics (USP. Paper version), v. 64, p. 309-312, 2009. 7. LOPES, Bernardo et al. Biostatistics: fundamental concepts and practical applications. Rev. bras.oftalmol. [online]. 2014, vol.73, n.1, pp. 1622. ISSN 0034-7280. Rev Bras Oftalmol. 2014; 73 (5): 257-9 260 EDITORIAL Social aspects of corneal transplantation in Brazil: contrast between advances in surgical technique and limiting access to the population Aspectos sociais do transplante de córnea no Brasil: contraste entre avanços na técnica cirúrgica e limitação de acesso à população T he constant search for knowledge drives technological advances and exponentially increases the number of diagnostic and therapeutic alternatives in ophthalmology. Not infrequently, procedures that in the recent past used to be considered the gold standard are now proscribed. The development of less invasive and more effective surgical techniques increases the demand for transplants. Keratoplasty is currently a safer, more effective and successful procedure than the techniques and procedures used in the recent past, and it can be used to treat diseases once considered inoperable(1,2). Because of this, an increasing number of patients are now able to overcome obstacles such as fear and insecurity and undergo the procedure(3,4). It is known that in many cases, traditional penetrating keratoplasty can be replaced by anterior or posterior lamellar keratoplasty, in which only the damaged layers of the cornea are removed and replaced, while the healthy ones remain intact. Anterior lamellar keratoplasty is indicated for corneal opacities of the anterior or middle stroma, and it can be superficial (at the level of the stroma-stroma interface, referred to as superficial anterior lamellar keratoplasty [SALK]) or deep (at the stroma-Descemet membrane interface, referred to as deep anterior lamellar keratoplasty [DALK]). It is indicated in diseases such as keratoconus, pellucid marginal degeneration, stromal dystrophies, and ectasia after refractive surgery with healthy posterior layers(5,6,7). Even though the technique has a longer learning curve, it offers significant advantages, since it does not penetrate the anterior chamber and preserves the host endothelium, thus significantly reducing the risk of endothelial rejection(5,6,7). Posterior lamellar keratoplasty can be used to replace the damaged endothelium without the need for large incisions or corneal sutures; it can be performed by posterior lamellar keratoplasty (PLK), deep lamellar endothelial keratoplasty (DLEK), Descemet’s stripping endothelial keratoplasty (DSEK), Descemet’s stripping automated endothelial keratoplasty (DSAEK), Descemet’s membrane endothelial keratoplasty (DMEK), and Descemet’s membrane automated endothelial keratoplasty (DMAEK). It is indicated in cases of Fuchs endothelial dystrophy, pseudophakic bullous keratopathy, and endothelial failure after penetrating keratoplasty with healthy anterior layers(5,6,7). The main advantages of the procedure are minimal changes in corneal topography compared to the baseline, stable refraction, a healthy endothelium, and an eye globe less susceptible to trauma(5,6,7). Improvements in surgical techniques, however, also depend on advances in the instruments and materials available in the market, which are designed to produce less trauma and reduce the incidence of peri- and postoperative complications. Using a microkeratome or excimer laser, cuts of different thicknesses and diameters can be performed both on the host and the donor buttons(7). More recently, however, femtosecond laser, which has a greater wave length than excimer laser, has been widely used for resection of corneal tissue as well as to create the corneal flap with a shape determined by the surgeon(7). Furthermore, viscoelastic substances developed to maintain spaces (cohesive) or to protect intraocular tissues (dispersive) during surgery can now perform both functions at once(8). There have also been significant improvements in tissue processing and storage, for example by using artificial anterior chambers which allow preparation of the cornealscleral button in the same manner as with the entire eye globe(7). These advances in surgical instruments and preservation methods of the corneal button increase the quality of transplanted tissue and therefore lead to better surgical outcomes to patients and their families. Rev Bras Oftalmol. 2014; 73 (5): 260-1 Social aspects of corneal transplantation in Brazil: contrast between advances in surgical technique and limiting access to the population 261 However, it should be noted that many patients with indications for corneal transplantation do not enter the transplant waiting list and give up on visual rehabilitation. This occurs because part of the population, in particular low-income patients, even when instructed by physicians to undergo transplantation, do not receive appropriate guidance, do not understand such guidance, or cannot afford treatment costs(9). This suggests that having access to ophthalmic care and receiving an indication for corneal transplantation does not imply that patients will actually undergo definitive treatment. Therefore, improved communication is needed between the secondary and tertiary levels of care to ensure effective registration of patients in waiting lists and adequate access to corneal transplantation(9). A good example of a pioneer, effective and well-organised programme, supported by the Department of Health and the State Government, is the São Paulo State transplant programme, where the waiting list is cleared and surplus corneas are sent to other states of the Brazilian federation, helping reduce their waiting lists(10). In conclusion, there are currently less invasive surgical techniques that increase the benefits of transplantation and improve the quality of life of operated patients. However, even though technological advances in the methods and materials for corneal transplantation have contributed to increasing the safety and efficacy of the procedure, logistical obstacles and limited access to surgical treatment still prevent these advances from being evenly available to the entire population. It is thus necessary to ensure accessibility to a health system capable of diagnosing and treating the entire population. Hirlana Gomes Almeida Ph.D. Student, Medical School of the São Paulo University (USP) Richard Yudi Hida Head of the Cataract Unit and Technical Manager of the Santa Casa de Misericórdia Tissue Bank, São Paulo R EFERENCES 1. Coelho JCU, Trubian PS, Freitas ACT, Parolin MB, Schulz GJ, Martins EL. Comparação entre o custo do transplante hepático cadavérico e o intervivos. Rev Assoc Med Bras 2005;51:158-63. 2. Solar SP, Ovalle AR, Simian MEM, Escobar JH, Beca JPI. Tres factores que influyen en la actitud de las personas ante la donación de órganos. Rev. Chilena de Cirugía. 2008;60(3):262-7. 3. Temporini ER, Kara-Junior N, Kara José N, Holzchuh N. Popular beliefs regarding the treatment of senile cataract. Rev Saúde Pública. 2002;36(3):343-9. 4. Marback R, Temporinia ER, Kara-Junior N. Emotional factors prior to cataract surgery. Clinics. 2007;62(4):433-8. 5. Brito S, Cardoso A, Costa E, Rosa A, Quadrado MJ, Murta J. DSAEK: a espessura será realmente importante? Rev Sociedade Portuguesa de Oftalmologia. 2012:36(3):247-56. 6. Macedo JP, Forseto AS, Allemann N, Sousa LB. Avaliação da ceratoplastia lamelar anterior profunda em pacientes com ceratocone. Arq. Bras. Oftalmol. 2009:72(4). 7. Moreira H, Sousa LB, Sato EH, Faria MAR. Banco de olhos, transplante de córnea. In: Série Oftalmologia Brasileira. 3.ed. 2013. 8. Espíndola RF, Castro EFS, Santhiago MR, Kara-Junior N. A clinical comparison between DisCoVisc and 2% hydroxypropylmethylcellulose in phacoemulsification: a fellow eye study. Clinics. 2012;67(9):1059-62. 9. Kara-Junior N, Mourad PCA, Espíndola RF, AbilRuss HH. Expectativas e conhecimento entre pacientes com indicação de transplante de córnea. Rev Bras Oftalmol. 2011;70(4):230-4. 10. Associação Brasileira de Transplantes de Órgãos. Registro Brasileiro de Transplantes. Dimensionamento dos Transplantes no Brasil e em cada estado [online journal]. Jan/Dec 2012. Available at: http://www.abto.org.br/abtov03/Upload/file/RBT/2012/RBT-dimensionamento2012.pdf. Rev Bras Oftalmol. 2014; 73 (5): 260-1 O 262 RIGINAL ARTICLE The role of Descemet’s membrane in the pathogeny of corneal edema following anterior segment surgery O papel da membrana de Descemet na patogenia do edema corneano após cirurgia de segmento anterior Karine Feitosa Ximenes1, Jailton Vieira Silva2, Karla Feitosa Ximenes Vasconcelos3, Fernando Queiroz Monte1 A BSTRACT Objective: To find relevant factors in the pathogeny of postoperative corneal edema in post-cataract surgery and post-keratoplasty cases, through the study of histopathological findings in order to see what can be done to avoid successive keratoplasties. Methods: Retrospective descriptive study of histopathological findings in postoperative corneal edema cases. Tissues were obtained from penetrating keratoplasty in the period between september 2009 and august 2013. A medical record review was conducted primarily looking for information about previous surgeries. Results: Seventy corneal buttons were included, out of which 34 were from male patients and 36 were from female patients. The mean age was 63.1±17.20 (mean ± SD) years. Most of cases were corneal failure after keratoplasty (71.43%). The main change found in endothelium was cellular rarefaction (58 cases), and it was also the most common histopathological change. Changes in integrity predominated in Descemet’s membrane (53 cases), whether in the form of rupture, isolated detachment or detachment associated with rupture. Endothelial changes associated with the absence in Descemet’s membrane integrity were frequent. Conclusion: Descemet’s membrane detachment is a frequent histopathological finding in postoperative corneal edema cases studied, thus it should be considered an important factor in the pathogeny of such cases. This change should be carefully researched in the postoperative period in order to be diagnosed and treated early, possibly avoiding many keratoplasty indications. Keywords: Descemet membrane; Corneal edema/etiology; Corneal edema/pathology; Keratoplasty RESUMO Objetivo: Encontrar fatores importantes na patogenia do edema corneano pós-cirúrgico, em casos de pós-facectomia e pós-ceratoplastia, por meio do estudo dos achados histopatológicos, a fim de ver o que pode ser feito para evitar sucessivas ceratoplastias. Métodos: Estudo retrospectivo descritivo das alterações histopatológicas de casos de edema corneano pós-cirúrgicos. Os tecidos foram provenientes de ceratoplastia penetrante no período compreendido entre setembro de 2009 e agosto de 2013. Foi realizada revisão de prontuários em busca principalmente de informações sobre cirurgias prévias. Resultados: Foram incluídos 70 botões corneanos, sendo 34 de pacientes do sexo masculino e 36 do sexo feminino. A média das idades foi de 63,1±17,20 (média ± DP) anos. A maioria dos casos era de falência após transplante (71,43%). A rarefação celular foi a principal alteração encontrada no endotélio (58 casos), sendo também a alteração histopatológica mais frequente. Na membrana de Descemet, predominaram as alterações de integridade (53 casos), seja na forma de ruptura, de descolamento isolado ou de descolamento associado à ruptura. Foi frequente a associação de alterações endoteliais à ausência da integridade da membrana de Descemet. Conclusão: Descolamento da membrana de Descemet é um achado histopatológico frequente nos casos de edema corneano pós-cirúrgicos estudados, devendo ser considerado um fator importante na patogenia dos mesmos. Essa alteração deve ser procurada com atenção nos pós-operatórios, a fim de ser diagnosticada e tratada precocemente, vindo possivelmente a evitar muitas indicações de ceratoplastia. Descritores: Lâmina limitante posterior; Edema da córnea/etiologia; Edema da córnea/patologia; Ceratoplastia 1 Ceará State Eye Bank, Fortaleza/CE, Brazil. Federal University of Ceará, Fortaleza/CE, Brazil. 3 General Hospital of Fortaleza, Fortaleza/CE, Brazil. 2 Work conducted at the Ceará State Eye Bank, Brazil. The authors have no public and private financial support, or financial interest Received for oublication 08/04/2014 - Accepted for publication 08/06/2014 Rev Bras Oftalmol. 2014; 73 (5): 262-8 The role of Descemet’s membrane in the pathogeny of corneal edema following anterior segment surgery INTRODUCTION C orneal oedema is a clinical condition characterised by increased anteroposterior corneal thickness or diameter(1,2).It can be confined to the epithelium or part of it, and it can also affect only the stroma. Nevertheless, in most cases both the epithelium and the stroma are affected(2). Wherever oedema develops, structural elements are separated from one another. In the stroma, the keratocytes are separated from each other and from adjacent collagen fibres; these, in turn, also move apart from one another. Oedema is generally associated with loss of transparency of the affected area of the cornea(2). The two main factors in the aetiology of corneal oedema are endothelial dysfunction(2-4) and Descemet’s membrane defects. Endothelial cells form a single layer of pump cells in the posterior cornea and are responsible for constantly dehydrating the cornea. These cells decrease in number with age and are usually incapable of regeneration(5).Ophthalmologists are well aware of the limited regeneration capacity of the human corneal endothelium and of the need for extreme caution to avoid injuries to this important tissue during surgical procedures(6). Defects in Descemet’s membrane also lead to the inflow of aqueous humour into the cornea, with subsequent stromal oedema(5).Descemet’s membrane detachment can result from any factor causing a rupture in Descemet’s membrane, including surgical procedures (cataract extraction, iridectomy, cyclodialysis, penetrating keratoplasty) and tears due to congenital glaucoma, keratoconus, keratoglobus, or trauma(7).Large and extensive detachments have an exuberant presentation, with corneal oedema and marked reduction in visual acuity, and often require surgical intervention to prevent permanent corneal decompensation and the need for corneal transplantation(8). Given the above, our objective was to determine the pathogeny of postoperative corneal oedema after cataract extraction and keratoplasty by studying histopathology findings in Descemet’s membrane and the endothelium, in order to determine potential early measures that might prevent the need for repeated keratoplasties. Histopathological changes may be suggestive of what needs to be rigorously investigated during the postoperative period in patients submitted to these procedures. M ETHODS A study of corneal buttons from penetrating keratoplasties conducted between September 2009 and August 2013 and submitted to the Eye Bank for histopathological examination was conducted. Tissues were fixed in 10% neutral formaldehyde and sliced by a pathologist while lying on the endothelial side, with the cut starting from the epithelium and ending at the endothelium. Samples were embedded in paraffin, cut into 2.5ìm thick slices, and stained with haematoxylin-eosin. Following preparation, tissues were examined by the authors with an optical microscope. This was a retrospective, descriptive study of the histopathological changes found in postoperative corneal oedema. Because of the lack of studies to which our results could be compared, we simply assessed the frequency of each finding. Using this statistical method is also warranted by our interest in studying the pathogeny of the condition and examining 263 the changes found in the sample. In further studies based on these findings, statistical probabilities can also be calculated. Corneal buttons presenting stromal oedema were selected. Stromal oedema was histopathologically defined as the presence of separation between structures such as keratocytes and collagen fibres. Oedema was classified into five grades depending on the degree of separation. Epithelial oedema (cell oedema, cytoplasmic vacuoles, microcysts, and bubbles) was not considered in the classification, despite being present in almost all cases. Specimens with grade I (mild) oedema presented only a slight and sparse separation between structures (Figure 1a).Cases where the separation was more frequent and widespread were classified as grade II (mild-moderate) oedema (Figure 1b). Grade III (moderate) oedema showed generalised swelling, but with slight separation between structures (Figure 1c). In grade IV (moderate-severe) oedema, the separation was wider and very frequent (Figure 1d). Finally, specimens with grade V (severe) oedema presented greater separation with generalised swelling (Figure 1e). In some cases, a tissue sample presented oedema of varying intensity in different regions. Such cases were classified according to the predominant type of oedema or to its average intensity. The exclusion criteria were inflammatory reactions, synechiae, stromal thinning, and specimens without a medical record or with no record of prior surgery. Thus, only pure cases of postoperative corneal oedema were included, i.e. those not associated with secondary causes. The medical records of selected cases were reviewed for Figure 1a: Mild oedema (grade I) with slight, sparse separation of stromal structures. Note the thickened Descemet’s membrane. Figure 1b: Mild-moderate oedema (grade II) with more widespread separation. Rev Bras Oftalmol. 2014; 73 (5): 262-8 264 Ximenes KF, Silva JV, Vasconcelos KFX, Monte FQ During histopathological examination, samples presenting any degree of corneal and diagnosed with bullous keratopathy or graft failure were investigated for changes in Descemet’s membrane and the corneal epithelium. Changes in Descemet’s membrane included ruptures, detachment, folds, bifurcations, abnormal thickness, and distension. Endothelial changes included cell rarefaction or cell abnormalities. Since this study was focused on the pathogeny of corneal oedema, data collection was centred on its potential causal factors. Nonetheless, factors that seemed to be a consequence of the condition are also mentioned, in order to present the full array of histopathological findings. Figure 1c: Moderate oedema (grade III). The oedema is more generalised but the separation is still mild. Microcysts can be seen in the epithelium. R ESULTS Seventy corneal buttons were included in this study, of which 34 were from male patients and 36 from female patients. Mean age was 63.1 ± 17.20 years (mean ± SD). The sample included 20 cases of bullous keratopathy following cataract extraction and 50 cases of graft failure. The distribution of cases according to the five grades of oedema is shown in Table 1. The histopathological changes found in the samples are shown in Table 2. The most common changes in Descemet’s membrane were ruptures in 41 cases (58.57%) and detachment in 40 cases (57.14%), followed by folds in 25 cases (35.71%). The main change found in the endothelium was cell rarefaction, in 58 cases (82.86%). Considering all types of changes, endothelial cell rarefaction was the most common. Table 1 Figure 1d: Moderate-severe oedema (grade IV), with wider and very widespread separation. A large bubble can be seen detaching part of the epithelium. Sample distribution according to the grade of corneal oedema found in specimens submitted for examination between September 2009 and August 2013. Grade I II III IV V Total Figure 1e: Severe oedema (grade V). The oedema is generalised and the separation is much wider. Bubbles can be observed in the epithelium. information on the surgeon’s diagnosis, previous surgery, gender, and age. All cases of prior cataract extraction or corneal transplantation were recorded. Cases where the surgeon’s diagnosis indicated bullous keratopathy following cataract extraction or graft failure following a previous transplantation were considered as such. In cases where the surgeon’s diagnosis was lacking, this information was obtained in the medical record which contained a standard form for corneal transplantation. Cases of previous transplantation were considered as graft failure, and cases of previous cataract extraction were considered as bullous keratopathy. Rev Bras Oftalmol. 2014; 73 (5): 262-8 Bullous keratopathy following cataract extratction (%) 5 3 4 5 3 (25) (15) (20) (25) (15) 20 (100) Graft failure (%) 13 (26) 8 (16) 7 (14) 14 (28) 8 (16) 50 (100) Total (%) 18 11 11 19 11 (25.71) (15.71) (15.71) (27.14) (15.71) 70 (100) The distribution of histopathological changes found in cases of bullous keratopathy following cataract extraction and graft failure are shown in Table 3.Ruptures and detachment were the predominant changes in Descemet’s membrane, both for bullous keratopathy and graft failure. Cell rarefaction was the main endothelial change in both groups, as well as the most frequent histopathological change overall. The charts below show the distribution of histopathological changes along the five grades of corneal oedema following anterior segment surgery. Only those changes that can be considered as causal factors are shown, namely changes to the integrity of Descemet’s membrane (ruptures, ruptures plus detachment, and isolated detachment) and isolated endothelial changes. Chart 1 shows that changes to the integrity of Descemet’s membrane were the predominant finding, with detachment being very frequent, whether or not associated with rupture (40 cases). The role of Descemet’s membrane in the pathogeny of corneal edema following anterior segment surgery Table 2 Corneal changes found in specimens submitted for examination between September 2009 and August 2013. Changes Descemet’s membrane Endotheliun Quantidade (%) Ruptures Detachment Folds Bifurcations Thickening Thinning Distension 41 (58.57) 40 (57.14) 25 (35.71) 3 (4.29) 4 (5.71) 6 (8.57) 3 (4.29) Cell rarefaction Cellabnormalities 58 (82.86) 9 (12.86) Percentages do not add up to 100% because some specimens contained multiple changes. Table 3 Comparison of changes found in cases of bullous keratopathy following cataract extraction and graft failure in specimens submitted for examination between September 2009 and August 2013. Changes Bullous keratopathy following cataract extratction (%) Graft failure (%) Descemet’s Ruptures membrane Detachment Folds Bifurcations Thickening Thinning Distension 10 (50) 14 (70) 4 (0) 0 (0) 3 (15) 3 (15) 0 (0) 31 26 21 3 1 3 3 Endotheliun Cell rarefaction Cellabnormalities 15 (75) 1 (5) 43 (86) 8 (16) 265 associated with rupture, with 28 cases (40%). Isolated ruptures were found in 13 cases (18.57%), and isolated detachment was found in 12 cases (17.14%). Considering the distribution of changes according to the grade of oedema (Charts 3-7), it was found that changes to the integrity of Descemet’s membrane prevailed in all grades. A frequent change to the integrity of Descemet’s membrane in all grades of oedema was detachment, whether or not associated with rupture. Isolated endothelial changes were found mainly in grade IV oedema, with 9 cases (47.37%), followed by detachment, found in 8 cases (42.10%). DISCUSSION This was a descriptive study of histopathological changes found in Descemet’s membrane and the corneal endothelium of patients with corneal oedema following anterior segment surgery (keratoplasty or cataract extraction). Most cases included in the sample were graft failures, which can be attributed to the fact that most corneal buttons submitted to the Eye Bank for histopathological examination come from emergency keratoplasties, where the corneal button is routinely submitted Chart 1 Distribution of histopathological changes according to the grade of oedema. (62) (52) (42) (6) (2) (6) (6) Percentages do not add up to 100% because some specimens contained multiple changes. Table 4 Changes to the integrity of Descemet’s membrane in cases of postoperative corneal oedema. Changes Ruptures Detachment Folds N (%) Chart 2 Histopathological changes found in cases of bullous keratopathy following cataract extraction (black) and graft failure (grey). 13 (18.57) 28 (40) 12 (17.14) Percentages do not add up to 100% because this table only includes changes to Descemet’s membrane, which were not found in all specimens. Isolated endothelial changes were only found in 17 cases. The distribution of changes in both groups was relatively similar to the sample as a whole (Chart 2). The frequency of changes to the integrity of Descemet’s membrane, either in isolation or associated with other findings, are shown in Table 4.The most common change was detachment Rev Bras Oftalmol. 2014; 73 (5): 262-8 266 Ximenes KF, Silva JV, Vasconcelos KFX, Monte FQ Chart 3 Chart 6 Histopathological changes found in cases of bullous keratopathy following cataract extraction (black) and graft failure (grey) with mild (grade I) oedema. Histopathological changes found in cases of bullous keratopathy following cataract extraction (black) and graft failure (grey) with moderate-severe (grade IV) oedema. Chart 7 Chart 4 Histopathological changes found in cases of bullous keratopathy following cataract extraction (black) and graft failure (grey) with severe (grade V) oedema. Histopathological changes found in cases of bullous keratopathy following cataract extraction (black) and graft failure (grey) with mild-moderate (grade II) oedema. Chart 5 Histopathological changes found in cases of bullous keratopathy following cataract extraction (black) and graft failure (grey) with moderate (grade III) oedema. Rev Bras Oftalmol. 2014; 73 (5): 262-8 for examination, while samples from cataract extraction are only occasionally submitted. Most cases of both bullous keratopathy following cataract extraction and graft failure presented oedema grade I and IV, according to our classification.Therefore, no correlation was established between the diagnosis and the degree of oedema. The main histopathological change found both in cases of bullous keratopathy following cataract extraction and graft failure was endothelial cell rarefaction. Since isolated endothelial changes were seen in only 17 of the 70 specimens (Chart 1), endothelial changes were frequently associated with changes to the integrity of Descemet’s membrane — either isolated detachment, rupture, or both combined. We suggest that this association might not be due to chance alone — instead, changes to Descemet’s membrane could be the cause of endothelial changes. Another explanation could be related to the way the pieces were sliced, a factor we had no control over due to the retrospective nature of this study. We are also aware that endothelial cells are easily altered by fixation and staining; therefore, it is difficult to obtain a precise image of their normal and pathological structures through microscopic examination of fixed, stained slides(3).Nonetheless, we underline the reliability The role of Descemet’s membrane in the pathogeny of corneal edema following anterior segment surgery of endothelial histopathological findings based on studies such as William et al., who found a direct correlation between the number of endothelial cells in histological examination and the density of cells in specular microscopy(9).Our research, however, did not focus on the endothelium, as these changes have already been thoroughly studied. Instead, we focused mainly on Descemet’s membrane, as it was altered in 53 out of the 70 cases (Chart 1 and Table 4), and because of the potential effects of oedema on the membrane and the possibility to institute early and effective treatment against such changes. Since our main objective was to study the pathogeny of corneal oedema, we focused mainly on changes to the integrity of Descemet’s membrane (Chart 1 and Table 4), which are mentioned in literature as possible causes of the condition(5).Among these changes, detachment was a frequent finding, either associated with rupture (40% of cases) or in isolation (17.14% of cases). Detachment was thus found in 57.14% of cases, which stresses the importance of recognising it as a treatable cause. However, it is still unclear whether the rupture could have strained Descemet’s membrane to the point of detachment or whether the two events were concurrent. Among the changes unrelated to pathogeny, the most frequentwere folds, followed by thinning, thickening, distension, and bifurcations (Table 2).However, it is unclear whether these findings occurred as a consequence of oedema or by chance. Folds were roughly twice as frequent in cases of graft failure (42% of cases) than in bullous keratopathy following cataract extraction (20% of cases). This might be explained by the fact that folds tend to resolve over time on biomicroscopy, and cases of graft failure, particularly primary failure, usually undergo earlier transplantation. Most studies addressing the aetiology of bullous keratopathy or corneal oedema, however, mention endothelial cell loss or dysfunction as the main aetiological factor(1,2,10,11).Few sources in the literature mention Descemet’s membrane defects as a cause of corneal oedema(5), and they usually do not make reference to surgical trauma. Studies on changes to the integrity of Descemet’s membrane after surgery usually focus on membrane detachment following cataract extraction and its treatment. Contrary to the literature, which limits the aetiopathogenesis of bullous keratopathy and corneal oedema mostly to endothelial changes or, on a smaller scale, solely to changes to the integrity of Descemet’s membrane, our histopathological study has shown that changes to Descemet’s membrane may be associated with endothelial changes in the pathogeny of bullous keratopathy following cataract extraction. The suggestion that changes to the integrity of Descemet’s membrane are probably the main pathogenic factor in cases of bullous keratopathy following cataract extraction could also be made for cases of graft failure. Despite the improving results of penetrating keratoplasty, graft failure still remains a significant problem. Common aetiologies include primary donor failure, surgical complications, complications related to intraocular lenses, persistent epithelial defects, rejection, infection, glaucoma, trauma, and relapse of primary corneal dystrophies(12).However, changes to endothelial cells are cited in literature as one of the main factors leading to corneal graft failure, as is the case for bullous keratopathy. Bell et al.observed a low initial endothelial cell count in sequential examinations by specular microscopy and a continuous decrease in cell density over the firstfive postoperative years in patients who met the criteria for late endothelial failure and who had been subjected to repeated keratoplasties (13).Santos et al., studying corneal specimens 267 diagnosed as grafts failures, found endothelial decompensation as the most common histopathological finding (14).With the exception of studies such as Aurora et al., few papers mention Descemet’s membrane defects as part of the aetiopathogenesis of corneal graft failure(15). Considering Descemet’s membrane defects — which, in our study, involved mostly detachment associated or not with rupture — as an important factor in the pathogeny of bullous keratopathy following cataract extraction and graft failure after keratoplasty, this change should always be investigated in cases of oedema occurring in the immediate postoperative period of these procedures. Descemet’s membrane detachment is a rare but severe complication of intraocular procedures(16).It is not uncommon in cataract surgery, with a reported incidence of 0.5% and 2.6% in extracapsular surgery and phacoemulsification, respectively(17).Many approaches have been suggested for the condition, such as observation (18), injection of C3F8 (19,20) or SF6 (8,20,21) gas into the anterior chamber, injection of viscoelastic (22) , transcorneal sutures (23) , and corneal transplantation. Descemet’s membrane detachment can be classified into two types: planar, when stromal separation is under 1 mm; and non-planar, when the separation is greater than 1 mm. Both types of can be further classified as either peripheral or peripheral with central involvement(7).Vastine et al.suggest that the small planar detachments should be managed with observation, since many cases resolve spontaneously. Large planar or non-planar detachment or scrolled detachment require surgical intervention(24).Kim et al.recommend treatment with intracameral gas injection in cases of a detached yet intact Descemet’s membrane(8). In sum, as mentioned above, multiple approaches exist for treating Descemet’s membrane detachment. There are some alternative treatments to corneal transplantation that can lead to complete resolution of corneal oedema and prevent the need for transplantation. Although repositioning may take some time, the endothelium/detached Descemet’s membrane complex may remain relatively healthy in the anterior chamber, with corneal transparency eventually resuming when the repositioning takes place(21).Once again, we stress the need to thoroughly investigate the presence of this change in cases of corneal oedema in the immediate postoperative period of cataract extraction or corneal transplantation, in an attempt to avoid keratoplasty through early diagnosis and alternative therapies. We are aware that it is not always possible to visualise Descemet’s membrane with a slit lamp in cases of severe corneal oedema(16), and because more sophisticated diagnostic methods are not always easily available, we suggest considering the use of the aforementioned alternative routine methods in cases of early corneal oedema following traumatic anterior segment procedures in an attempt to treat the condition before the first or successive keratoplasties. CONCLUSION This study used histopathology findings to demonstrate that changes to the integrity of Descemet’s membrane, which in this study consisted primarily of detachment associated or not with ruptures, are frequently found in cases of corneal oedema following anterior segment surgery, in particular cataract extraction and corneal transplantation. The high frequency of this finding suggests that it plays an important role in the pathogeny of the studied cases of corneal oedema. Rev Bras Oftalmol. 2014; 73 (5): 262-8 268 Ximenes KF, Silva JV, Vasconcelos KFX, Monte FQ Endothelial cell rarefaction was also a frequent finding, although mainly associated with Descemet’s membrane defects. The acknowledgment that not only the endothelium, but also Descemet’s membrane detachment may be important in the pathogeny of corneal oedema following anterior segment surgery should prompt ophthalmologists to carefully investigate this change in the postoperative period and institute early treatment in an attempt to prevent the need for keratoplasty. As this was a retrospective descriptive study, we hope our findings will encouragefuture prospective studies that may confirm our conclusions. R EFERENCES 1. Alomar TS, Al-Aqaba M, Gray T, Lowe J, Dua HS. Histological and confocal microscopy changes in chronic corneal edema: implications for endothelial transplantation. Invest Ophthalmol Vis Sci. 2011;52(11):8193-207. 2. Goldman JN, Kuwabara T. Histopathology of corneal edema. Int Ophthalmol Clin. 1968;8(3):561-79. 3. Stocker FW. The endothelium of the cornea and its clinical implications. Trans Am Ophthalmol Soc. 1953;51:669-786. 4. Patel SP. The bull’s eye: are we off-target for corneal endothelial cell physiology? J Ophthalmic Vis Res. 2013;8(1):83-5. 5. Naumann GO, Holbach L, Kruse FE. Applied pathology for ophthalmic microsurgeons. Berlin: Springer; 2008. 6. Murphy C, Alvarado J, Juster R, Maglio M. Prenatal and postnatal cellularity of the human corneal endothelium. A quantitative histologic study. Invest Ophthalmol Vis Sci. 1984;25(3):312-22. 7. Mulhern M, Barry P, Condon P. A case of Descemet’s membrane detachment during phacoemulsification surgery. Br J Ophthalmol. 1996;80(2):185-6. 8. Kim T, Hasan SA. A new technique for repairing descemet membrane detachments using intracameral gas injection. Arch Ophthalmol. 2002;120(2):181-3. 9. Williams KK, Noe RL, Grossniklaus HE, Drews-Botsch C, Edelhauser HF. Correlation of histologic corneal endothelial cell counts with specular microscopic cell density. Arch Ophthalmol. 1992;110(8):1146-9. 10. Gonçalves ED, Campos M, Paris F, Gomes JA, Farias CC. [Bullous keratopathy: etiopathogenesis and treatment: [review]]. Arq Bras Oftalmol. 2008;71(6 suppl 0):61-4. Portuguese. 11. Yi DH, Dana MR. Corneal edema after cataract surgery: incidence and etiology. Semin Ophthalmol. 2002;17(3-4):110-4. Review. Rev Bras Oftalmol. 2014; 73 (5): 262-8 12. Wilson SE, Kaufman HE. Graft failure after penetrating keratoplasty. Surv Ophthalmol. 1990;34(5):325-56. Review. 13. Bell KD, Campbell RJ, Bourne WM. Pathology of late endothelial failure: late endothelial failure of penetrating keratoplasty: study with light and electron microscopy. Cornea. 2000;19(1):40-6. 14. Santos LN, de Moura LR, Fernandes BF, Cheema DP, Burnier MN Jr. Histopathological study of delayed regraft after corneal graft failure. Cornea. 2011;30(2):167-70. 15. Aurora AL, Khandur RC, Singh G. Pathogenesis of corneal graft failure. Indian J Ophthalmol. 1974;22(2):11-6. 16. Kothari S, Kothari K, Parikh RS. Role of anterior segment optical coherence tomogram in Descemet’s membrane detachment. Indian J Ophthalmol. 2011;59(4):303-5. 17. Anderson CJ. Gonioscopy in no-stitch cataract incisions. J Cataract Refract Surg. 1993;19(5):620-1. 18. Assia EI, Levkovich-Verbin H, Blumenthal M. Management of Descemet’s membrane detachment. J Cataract Refract Surg. 1995;21(6):714-7. 19. Lucena AR, Lucena DR, Macedo EL, Ferreira JL, Lucena AR. [C3F8 use in Descemet detachment after cataract surgery]. Arq Bras Oftalmol. 2006;69(3):339-43. Portuguese. 20. Kim T, Sorenson A. Bilateral Descemet membrane detachments. Arch Ophthalmol. 2000;118(9):1302-3. 21. Tai MC, Yieh FS, Chou PI. Repair of near total Descemet’s membrane detachment with intracameral injections of 20% sulfur hexafluoride gas. J Med Sci. 2002;22(5):231-4. 22. Sonmez K, Ozcan PY, Altintas AG. Surgical repair of scrolled descemet’s membrane detachment with intracameral injection of 1.8% sodium hyaluronate. Int Ophthalmol. 2011;31(5):421-3. 23. Pahor D, Gracner B. Surgical repair of Descemet’s membrane detachment. Coll Antropol. 2001;25 Suppl:13-6. 24. Vastine DW, Weinberg RS, Sugar J, Binder PS. Stripping of Descemet’s membrane associated with intraocular lens implantation. Arch Ophthalmol. 1983;101(7):1042-5. Corresponding author: Karine Feitosa Ximenes Rua Andrade Furtado, 150, apto 1501, Cocó Fortaleza, CE, Brazil – CEP: 60192-070 Tel: +5585 3262 6781; +5585 9673 3132 E-mail: [email protected] ORIGINAL ARTICLE 269 Preemptive analgesia of nepafenac 0.1% in retinal photocoagulation Analgesia preemptiva com nepafenaco 0,1% na fotocoagulação da retina Emerson Fernandes de Sousa e Castro1,2, Erika Araki Okuda2, Vinícius Balbi Amatto2, Hirlana Gomes Almeida1, Marina Gracia1, Newton Kara-Junior1 A BSTRACT Objective: To evaluate the preemptive effect of nepafenac 0,1% in patients undergoing retinal photocoagulation for the treatment of proliferative diabetic retinopathy. Methods: Thirty patients underwent argon laser photocoagulation in both eyes. The contralateral eye of each patient was the control. The nepafenac and placebo were used 30 minutes before the application of the laser. Both eyes were photocoagulated in the same day. Pain intensity was assessed by visual analog scale and descriptive pain scale. Results: The analysis of the interaction instillation versus nepafenac showed that patients in the placebo group had similar levels of pain in both eyes, and the nepafenac group had significant reduction in pain in the eye that was instilled suspension of 0,1% when compared to the contralateral eye which received placebo (p = 0.023). Conclusion: This study suggests that a suspension of 0,1% nepafenac helpful for preemptive analgesia in patients undergoing retinal photocoagulation compared to placebo. Keywords: Pain/prevent & control; Analgesia; Anti-inflammatory agents, non-steroidal/administration & dosage; Anti-inflammatory agents, non-steroidal/therapeutic use; Light coagulation; Diabetic retinopathy/drug therapy RESUMO Objetivo: Avaliar o efeito preemptivo com nepafenaco 0,1% em pacientes submetidos à fotocoagulação da retina para tratamento da retinopatia diabética proliferativa. Métodos: Trinta pacientes foram submetidos à fotocoagulação com laser de argônio em ambos os olhos. O olho contralateral de cada paciente foi o controle. O nepafenaco e o placebo foram utilizados 30 minutos antes da aplicação do laser. Ambos os olhos foram fotocoagulados no mesmo dia. A intensidade da dor foi avaliada por meio da escala analógica visual e da escala descritiva de dor. Resultados: A análise da interação instilação versus nepafenaco mostrou que os pacientes do grupo placebo apresentaram níveis de dor semelhantes em ambos os olhos, e os do grupo nepafenaco apresentaram redução importante do nível de dor no olho em que foi instilado a suspensão de 0,1% quando comparado ao olho contralateral que recebeu placebo (p=0,023). Conclusão: Este estudo sugere que a suspensão de 0,1% de nepafenaco foi útil na analgesia preemptiva de pacientes submetidos à fotocoagulação de retina quando comparada ao placebo. Descritores: Dor/prevenção & controle; Analgesia; Anti-inflamatórios não esteroides/administração & dosagem; Anti-inflamatórios não esteroides/uso terapêutico; Fotocoagulação; Retinopatia diabética/quimioterapia 1 2 Medical School, São Paulo University, São Paulo/SP, Brazil. São Paulo State Civil Servants Hospital “Francisco Morato de Oliveira”, São Paulo/SP, Brazil. This study received no financial support. The authors declare no conflict of interest. Received for publication 13/06/2014 - Acceped for publication 11/07/2014 Rev Bras Oftalmol. 2014; 73 (5): 269-72 270 Castro EFS, Okuda EA, Amatto VB, Almeida HG, Gracia M, Kara-Junior N INTRODUCTION P reemptive analgesia aims to reduce the intensity and duration of pain, both during and after procedures, by preventing reflex hyperexcitability in the spinal cord(1). Analgesic agents are not generally used during argon laser retinal photocoagulation, yet most patients complain of pain during and after the procedure, despite the use of anaesthetic eye drops. General anaesthesia or local anaesthetic block, indicated in cases of intolerable pain, increase the morbidity and mortality of the procedure(2). Non-steroidal anti-inflammatory drugs (NSAIDs) with local or systemic effect have analgesic and antipyretic properties(3). The only NSAID suitable for topical application is nepafenac 0.1% ophthalmic suspension, which non-selectively inhibits the cyclooxygenase enzyme and presents superior anti-inflammatory properties compared to conventional NSAIDs(3). Nepafenac 0.1% has only been approved for the treatment of pain and inflammation associated with cataract surgery(3). The aim of this study was to determine whether using an analgesic agent in addition to the anaesthetics commonly used in retinal photocoagulation provides any additional benefit. METHODS A prospective, randomised, double-blind case-control study was conducted on 30 consecutive patients diagnosed with proliferative diabetic retinopathy presenting clear ocular media who underwent argon laser photocoagulation in both eyes between June 2011 and May 2012. The project was approved by the Research Ethics Committee of the São Paulo State Civil Servants Hospital under number 094/10 and was authorised by the hospital manager. All patients provided their free and informed consent. Exclusion criteria were: presence of retinal abnormalities associated with other systemic diseases, uncooperative patients, pregnancy, use of systemic analgesic or anti-inflammatory agents, and refusal to participate in the study. The study variables were divided into dependent (pain level) and independent (age, gender, use of placebo or nepafenac 0.1%). Data were collected through a questionnaire using the Visual Analogue Scale (VAS) and the Descriptive Pain Scale (DPS), both frequently used in other studies in the literature(4,5). Patients were divided into two groups of 15 patients each, who used either nepafenac 0.1% or placebo. The two groups were matched for age and gender. A single drop of anaesthetic eye drops was administered to each patient 5 minutes before laser application. The study medication was administered 30 minutes before laser application. The contralateral eye was used as a control, undergoing photocoagulation the same day. Fifteen minutes after laser application, subjects responded to the VAS and DPS questionnaire. For all subjects, photocoagulation was carried out using a Visulas 532s Zeiss device set to spot size 100 µm, power setting 0.20 mW, time 0.10 seconds, and approximately 200 burns. The pain response of patients was analysed using mixedmodel ANOVA for multiple factors. This model was chosen due to the study design which combines paired and unpaired samples. The pain level was assessed in relation to three variables: 1) anaesthetic eye drops administered to one eye versus non- Rev Bras Oftalmol. 2014; 73 (5): 269-72 administration to the contralateral eye (paired samples); 2) nepafenac 0.1% administered to one group versus placebo given to the other group (unpaired samples); and 3) gender. Patient age was included as a covariate and its potential influence was controlled for by the model. The three factors above were assessed both in isolation and combined. A p-value <0.05 was adopted for rejection of the null hypothesis. RESULTS As illustrated in Table 1, the results from the DPS show that the effects of age, gender, nepafenac 0.1%, and anaesthetic eye drops were not statistically significant in isolation, nor were the interactions between anaesthetic eye drops and age, gender and nepafenac 0.1%, or anaesthetic eye drops and gender and nepafenac 0.1%. However, the interactions between anaesthetic eye drops and gender, and anaesthetic eye drops and nepafenac 0.1% produced statistically-significant results. Table 1 Isolated and combined effects of the study variables on patients submitted to photocoagulation. Isolated effects F Age Genre Nepafenac 0,1% Anaesthetic eye drop 2.09 0.37 2.02 0.40 0.1602 0.5470 0.1673 0.5304 F p-value 0.11 6.97 5.85 0.85 3.59 0.7474 0.0141 0.0232 0.3657 0.0697 Interações Anaesthetic eye drop x Age Anaesthetic eye drop x Genre Anaesthetic eye drop x Nepafenac Genre x Nepafenac Anaesthetic eye drop x Genre x Nepafenac p-value Figure 1 shows that administering nepafenac 0.1% or a placebo to men does not alter the level of pain, whereas in women nepafenac significantly reduces pain perception. Figure 1: Comparison of anaesthetic eye drops and gender in patients submitted to photocoagulation between June 2011 and May 2012. Preemptive analgesia of nepafenac 0.1% in retinal photocoagulation Figure 2 shows that patients in the placebo group had similar pain levels in both eyes. However, patients in the nepafenac group presented a significant reduction of pain perception in the eye that received nepafenac 0.1% compared to the contralateral eye, which received no eye drops 271 nepafenac 0.1%, or anaesthetic eye drops and gender and nepafenac 0.1%. However, the interactions between anaesthetic eye drops and gender, and anaesthetic eye drops and nepafenac 0.1% produced statistically-significant results. Figure 1 shows that administering nepafenac 0.1% or a placebo to men does not alter the level of pain, whereas in women nepafenac significantly reduces pain perception. Figure 2 shows that patients in the placebo group had similar pain levels in both eyes. However, patients in the nepafenac group presented a significant reduction of pain perception in the eye that received nepafenac 0.1% compared to the contralateral eye, which received no eye drops. CONCLUSION This study shows that nepafenac 0.1% ophthalmic suspension was effective for the preemptive analgesia of patients submitted to retinal photocoagulation compared to placebo, particularly in women. R EFERENCES Figure 2: Comparison of anaesthetic eye drops and nepafenac 0.1% in patients submitted to photocoagulation between June 2011 and May 2012. DISCUSSION Pain perception varies between individuals and is dependent on many factors, including cultural and gender differences, past experience and anxiety levels(2). Diabetic retinopathy is the most common cause of blindness among the economically active population in the United Kingdom(7). Argon laser retinal photocoagulation is an effective treatment to reduce severe visual loss in proliferative diabetic retinopathy(8). As many patients report some degree of pain both during and after laser treatment(9), several studies have attempted to identify the best form of analgesia for this procedure(10). Invasive procedures such as retrobulbar, peribulbar and subtenon anaesthesia have been suggested, but they can cause serious complications which limit their use(11). A study carried out on 60 eyes of 30 patients with proliferative diabetic retinopathy concluded that topical ketorolac tromethamine 0.5% is no more effective than artificial tears for relieving pain during photocoagulation(12). Preemptive analgesia involves the administration of analgesics before the painful stimulus, thus preventing or reducing the hypersensitivity response and pain memory in the nervous system; this produces long-term benefits for the patient’s quality of life and helps reduce expenses on further treatments(13). Another alternative suggested in the literature is to reduce the retina’s time of exposure to laser, which significantly reduces the level of pain(14). As shown in Table 1, the results from the DPS show that the effects of age, gender, nepafenac 0.1%, and anaesthetic eye drops were not statistically significant in isolation, nor were the interactions between anaesthetic eye drops and age, gender and 1. Alves AS, Campello RA, Mazzanti A, Alievi MM, Faria RX, Stedile R, Braga FA. Emprego do antiinflamatório não esteróide ketoprofeno na analgesia preemptiva em cães. Cienc Rural (Santa Maria). 2001;31(3):439-44. 2. Vaideanu D, Taylor P, McAndrew P, Hildreth A, Deady JP, Steel DH. Double masked randomised controlled trial to assess the effectiveness of paracetamol in reducing pain in panretinal photocoagulation. Br J Ophthalmol. 2006;90(6):713-7. 3. Weinberger D, Ron Y, Lichter H, Rosenblat I, Axer-Siegel R, Yassur Y. Analgesic effect of topical sodium diclofenac 0.1% drops during retinal laser photocoagulation. Br J Ophthalmol. 2000;84(2):135-7. 4. Fortes AC, Martinelli EJ, Ribeiro LG, Corpa JH, Tarcha FA, Rehder JR. Ação do anestésico tópico diluído e da mitomicina sobre a sintomatologia e re-epitelização corneana no pós-operatório da ceratectomia fotorrefrativa. Rev Bras Oftalmol. 2013;72(4):237-43. 5. Lucena CR, Ramos Filho JA, Messias AM, Silva JÁ, Almeida FP, Scott IU, et al. Panretinal photocoagulation versus intravitreal injection retreatment pain in high-risk proliferative diabetic retinopathy. Arq Bras Oftalmol. 2013;76(1):18-20. 6 . Gaynes BI, Onyekwuluje A. Topical ophthalmic NSAIDs: a discussion with focus on nepafenac ophthalmic suspension. Clin Ophthalmol. 2008;2(2):355-68. 7 . British Diabetic Association, Department of Health. St Vincent Joint Task Force for Diabetes: report of the Visual Impairment Subgroup. London: British Diabetic Association, Department of Health; 1994. 8 . Tonello M, Costa RA, Almeida FP, Barbosa JC, Scott IU, Jorge R. Panretinal photocoagulation versus PRP plus intravitreal bevacizumab for high-risk proliferative diabetic retinopathy (IBeHi study). Acta Ophthalmol. 2008;86(4):385-9. 9 . Zakrzewski PA, O’Donnell HL, Lam WC. Oral versus topical diclofenac for pain prevention during panretinal photocoagulation. Ophthalmology. 2009;116:1168-1744. 10. Tamai M, Mizuno K. Distribution of intra- and extraocular pain induced by argon laser photocoagulation. Tahoku J Exp Med. 1984;142(4):427-35. 11. Wu WC, Hsu KH, Chen TL, Hwang YS, Lin KK, Li ML, Shih CP, La i CC. Interventions for relieving pain associated with panretinal photocoagulation: a prospective randomized trial. Eye (Lond). 2009;20(6):712-9. Rev Bras Oftalmol. 2014; 73 (5): 269-72 272 Castro EFS, Okuda EA, Amatto VB, Almeida HG, Gracia M, Kara-Junior N 12. Esgin H, Samut HS. Topical ketorolac 0.5% for ocular pain relief during scatter laser photocoagulation with 532 nm green laser. J Ocul Pharmacol Ther .2006;22(6):460-4. 13. Grass JA, editor. Problems in anesthesia. vol. 10. Management of acute pain. Philadelphia:Lippincott-Raven; 1998. p.107-21. 14. Al-Hussainy S, Dodson PM, Gibson JM. Pain response and follow-up of patients undergoing panretinal laser photocoagulation with reduced exposure times. Eye (Lond). 2008;22(1):96-9. Rev Bras Oftalmol. 2014; 73 (5): 269-72 Corresponding Author: Hirlana Gomes Almeida Rua dos Médicis, 30, apto. 903 CEP: 50070-290 – Recife (PE), Brazil Tel: +5581 3049 1907 E-mail: [email protected] ORIGINAL ARTICLE 273 Analysis quantitative and qualitative of the tear film in patients undergoing PRK and LASIK with femtosecond Análise quantitativa e qualitativa do filme lacrimal nos pacientes submetidos a PRK e LASIK com femtossegundo Rubens Amorim Leite1, Ricardo Menon Nosé 1, Fábio Bernardi Daga 1, Tatiana Adarli Fioravanti Lui1, Giovana Arlene Fioravanti Lui2, Adamo Lui-Netto2 A BSTRACT Purpose: To evaluate tear film stability, ocular surface staining and tear secretion in patients undergoing PRK and femtosecond laser LASIK. Methods: Twenty eyes of 10 patients submitted to femtosecond laser LASIK and 11 eyes of the 6 patients submitted do PRK underwent tear film break-up time (TBUT), Schirmer’s basal and lissamine green staining measurements pre and postoperatively on days 15 (PO 15) and 30 (PO 30). Results: When grouping all eyes TBUT was reduced on PO 15 (p=0.025) and on PO 30 (p=0.001) compared to preoperative values. No difference was found between PO 15 and PO 30 (p=0.219). Compared to preoperative measurements, lissamine green test demonstrated a significant increase in score on PO 15 (p=0.021) and a significant reduction on PO 30 (p=0.010), when both groups were analyzed together (all 42 eyes). No changes in Schirmer’s basal test were detected in all 3 time periods (p=0.107). TBUT, lissamine green and Schirmer’s basal measurements were no different in all 3 time periods when both groups (PRK and femtosecond laser LASIK) were compared. Conclusion: TBUT and lissamine green measurements were altered after refractive surgery regardless the technique (PRK or femtosecond laser LASIK). When comparing one technique to the other, no difference was found in all measurements. Keywards: Dry eye syndromes; Tears; Refractive surgical procedures; Keratomileusis, laser in situ; Corneal surgery, laser; Photorefractive keratectomies RESUMO Objetivo: Analisar a secreção lacrimal, coloração da superfície ocular e estabilidade do filme lacrimal em indivíduos submetidos à cirurgia de PRK e LASIK com laser de femtossegundo (femto LASIK). Métodos: Vinte olhos de 10 pacientes submetidos à técnica de Femto LASIK e 11 olhos de 6 pacientes submetidos à técnica de PRK foram estudados de forma prospectiva, longitudinal e intervencionista. Tempo de rotura do filme lacrimal (TRFL), teste de Schirmer basal e coloração da superfície ocular com lissamina verde foram analisados no pré-operatório (pré), no 15º e no 30º dia pós-operatório (15º pós e 30º pós, respectivamente). Resultados: Agrupando todos os olhos, observou-se que o TRFL reduziu-se de forma estatisticamente significante no 15º pós em relação ao valor pré-operatório (p=0,025), mantendo-se reduzido no 30º pós (p= 0,001); não houve diferença estatisticamente significativa entre o 15º pós e o 30º pós (p=0,219). No teste da lissamina verde, houve aumento significativo desse escore, no 15º pós em relação ao período pré-operatório (p=0,021), havendo, posteriormente, redução no 30º pós (p=0,010). No teste de Schirmer basal, não foi detectada mudança estatisticamente significante ao longo dos três momentos (p=0,107). Comparando-se os testes TRFL, lissamina verde ou Schirmer basal, nos dois grupos estudados (PRK e LASIK), não houve diferença estatisticamente significante em nenhum dos três momentos (pré, 15º pós e 30º pós). Conclusão: Evidenciou-se alteração do filme lacrimal nos pacientes submetidos à cirurgia refrativa, quando foram utilizados os testes de TRFL e lissamina verde. Nas duas técnicas empregadas, não houve diferença estatisticamente significante de alteração do filme lacrimal, quando comparadas entre si (PRK e LASIK). Descritores: Síndrome do olho seco; Lágrimas; Procedimentos cirúrgicos refrativos; Ceratomileuse assistida por excimer laser in situ; Cirurgia da córnea a laser; Ceratectomia fotorrefrativa 1 2 Santa Casa de Misericórdia Hospital, São Paulo/SP, Brazil. Refractive Surgery Unit, Santa Casa de Misericórdia Hospital, São Paulo/SP, Brazil. The authors declare no conflict of interest. Received for publication 24/06/2014 - Accepted for publication 02/07/2014 Rev Bras Oftalmol. 2014; 73 (5): 273-8 274 Leite RA, Nosé RM1, Daga FB, Lui TAF, Lui GAF, Lui-Netto A INTRODUCTION METHODS efractive surgery techniques have been continually evolving, with photorefractive keratectomy (PRK) and laser-assisted in situ keratomileusis (LASIK) being the two most commonly used techniques.Both procedures are considered safe and produce photoablation of corneal tissue, thus changing its refractive power.(1,2) Studies show that LASIK is the most common refractive procedure for mild to moderate myopia, and there are different devices for creating the corneal flap. (2,3) Mechanical microkeratomes are the most used, promoting rapid visual recovery with minimal discomfort..An alternative is femtosecond laser, an automated device for creating a corneal flap; it is safer, more reliable and predictable, and may reduce the risk of epithelial defects and striae on the corneal flap.(4,5) In clinical practice, many patients complain of dry eye sensation after refractive surgery.(1,2)Attention should be given to this matter, because dry eye syndrome can severely affect a patient’s quality of life.For example, patients with moderate to severe dry eye report quantitative quality of life scores similar to patients with moderate to severe angina or patients undergoing dialysis.Furthermore, dry eye is the main cause for dissatisfaction after refractive surgery.(2,5,6) Several studies based on quantitative tests have demonstrated an increased incidence of dry eye in the first monthsafter refractive surgery.(1,2,5-8) Several theories attempt to explain the onset of the syndrome after refractive surgery.There is a complex interaction between afferent sensory nerves of the ocular surface and autonomic efferent nerves of the lacrimal gland which modulate tear secretion.Any factor interfering with that relationship can cause dry eye.(1,5) Sensory nerves of the corneaarisingfrom the ophthalmic and maxillary branches of the trigeminal nerve penetrate through the limbus, forming a thick nerve bundle in the anterior third of the cornea; those nerves then penetrate Bowman’s layer and form the epithelial-subepithelial plexus between the basal epithelial cells and Bowman’s layer.When these nerves are cut while creating the corneal flap in LASIK and during photoablation in PRK, this harmony is affected, which can cause dry eye. (1,2,5-8) In addition, postoperative inflammation near the nerve endings could stimulate the production of cytokines, thus exacerbating the condition.Furthermore, both refractive surgery techniques alter the corneal curvature, changing the relationship betweenthe tear surface and the eyelids during blinking and affecting tear distribution. (5) Another proposed pathophysiological mechanism is based on the observation that the number of goblet cells can be decreasedin patients submitted to LASIK, probably due to direct damage by the suction deviceduring the creation of the corneal flap (using either a microkeratome or femtosecond laser).(4,5) The aim of this study was to determine whether patients undergoing PRK and LASIK with femtosecond laser exhibit postoperativequantitative changes in tear production or changes in tear film stability and whether any of the two techniques is associated with a higher incidence of such changes, using the following tests:tear film breakup time (TFBU), the basal Schirmer test, and the lissamine green test. A prospective, longitudinal intervention study was performed on 31 eyes (16 patients), of which 20 eyes (10 patients) were submitted to LASIK with femtosecond laser and 11 eyes (6 patients) underwent PRK.Patients were seen at the Refractive Surgery Unit of Santa Casa de Misericórdia Hospital, São Paulo, between August 2012 and May 2013; all procedures were performed on June 27, 2013 at the Eye Clinic Day Hospital, a private eye clinic, free of any charge.Patients with contact lensesdiscontinued their useone month before surgery. The study was approved by the Research Ethics Committee of Santa Casa de Misericórdia under number 261728. Inclusion criteria weresubjects over 21 years of age with refractive errorsthat had been stable for at least one year, with a spherical equivalent between -1.50 and - 6.00 dioptres and less than 2.00 cylindrical dioptres, normal corneal topography, and without other eye diseases. Exclusion criteria werepatientsunable to attend follow-up visits, previous eye surgery, systemic diseases and/or eye diseases that could alter the tear film, and patients using drugs that could interfere with tear production. The decision to use PRK or LASIK was based on each patient’s corneal thickness and refractive error. Patients underwent the following tests a week before surgery (Pre), on the 15th postoperative day (15 PO), and on the 30 thPO day (30 PO): TFBU,the basal Schirmer test, and the lissamine green test.All tests were performed in the same environment, in a closed room. TFBU was performed instilling one drop of fluorescein on the conjunctival sac.The patient was instructed to blink several times to distribute the fluorescein evenly, being then submitted to slit lamp examination with a cobalt blue filter.A digital stopwatch was used to count the time (in seconds) between the last blink and the appearance of the first dry spot. Lissamine green staining was then performed by placing the lissamine tape in contact with the lacrimal meniscus of the lower conjunctival sac, with analysis 2 minutes laterusing the van Bijsterveld classification.The palpebral fissure was divided into 3 areas:lateral bulbar conjunctiva, cornea, and medial bulbar conjunctiva.In each area, the following classification was used:0, no staining; 1, isolated thin spots; 2, grouped coarse spots; 3,plaque.The sum for each of these areas was then calculated, producing the final score (range, 0-9). After 10 minutes the basal Schirmer test was performed.A drop of anaesthetic was instilled in the inferior fornix.A strip of Whatman filter paper No.41, 5-mm wide and 35-mm long, was then placed between the middle and lateral thirds of the lower eyelid.After 5 minutes, the strip was removed and the moist part of the filter paper was measured. R Rev Bras Oftalmol. 2014; 73 (5): 273-8 Surgical technique WaveLight EX500™ (Alcon) excimer laser was used for PRK.Bandage contact lenses were applied after the procedure for seven days.Patients were prescribed moxifloxacin 0.5% (Vigamox™ Alcon) eye drops every 6 hours for 7 days, ketorolac tromethamine (Acular™, Alcon) eye drops every 6 hours for 3 days, and prednisolone acetate0.12% (Ster MD™, Genom), which was phased out over six weeks. Analysis quantitative and qualitative of the tear film in patients undergoing PRK and LASIK with femtosecond In patients submitted to LASIK, the corneal flap was created using the LDV Z6™ (Ziemer) femtosecond laser with a 110-µm thickness, and photoablation was done using the WaveLight EX500™ (Alcon) excimer laser.Patients were prescribed combined eye drops of moxifloxacin 0.5% + dexamethasone 0.1% (Vigadexa™, Alcon) for seven days. 275 Chart 1 Distribution of patients submitted to PRK and LASIK according to gender. R ESULTS The following tests were used for statistical analysis: • Fisher’s exact test for comparing the gender distribution of patients between the two groups (PRK and LASIK); • Student’s t-test for independent samples for comparing the age (years) of patients between the two groups; • ANOVA with blocks for comparing the results of TFBU (seconds), lissamine green (score), and basal Schirmer test (millimetres) at the different time points (Pre, 15 PO and 30 PO), as well as the LSD method for multiple comparisons when necessary; • ANOVA with repeated measures for comparing the results of TRFL, lissamine green and basal Schirmer test at the different time points (Pre, Post 15 and Post 30)between the two groups (PRK vs. LASIK). Chart 2 One-dimensional scatter plot for the age (years) of patients submitted to PRK and LASIK. In all conclusions reached through inferential analysis a significance level of p = 5% was adopted. Table 1 Distribution of patients submitted to PRK and LASIK according to gender and age. Genre (n%) Female Male Total Age (years) 0 N Mean Median Minimum Maximum Standarddeviation a PRK LASIK Total p-value 5 83.3 1 16.7 6 100.0 7 70.0 3 30.0 10 100.0 12 75.0 4 25.0 16 100.0 >0.999a 6 10 16 33.7 33.5 26.0 45.0 32.1 32.0 22.0 52.0 32.7 32.0 22.0 52.0 7.6 9.0 8.3 0.728b Fisher’s exact test, bStudent’s t-test for independent samples. In the PRK group 83.3% of patients were female, compared to 70% in the LASIK group.There were no statistically-significant differences between groups regarding gender (p >0.999).Mean age was 33.7 ± 7.6 in the PRK group and 32.1 ± 9.0 in the LASIK group, and the difference was not significant (p = 0.728). (Table 1, Charts 1 and 2). The TFBU results for all patients combined were13.2 ± 3.3 preoperatively, 11.3 ± 4.4 at 15 PO, and 10.4 ± 3.2 at 30 PO.Statistically-significant differences were found between Pre and 15 PO (p = 0.025) and between Pre and 30 PO (p = 0.001), but not between 15 PO and 30 PO(p = 0.219).The results of the lissamine green test were1.0 ± 0.9 preoperatively, 1.3 ± 1.0 at 15 PO, and 1.0 ± 1.0 at 30 PO.Statistically-significant differences were found between Pre and 15 PO (p = 0.021) and between 15 PO and 30 PO (p = 0.010), but not between Pre and 30 PO(p = 0.768).Finally, the results of the Schirmer testwere17.6 ± 10.6 preoperatively, 14.5 ± 10.8 at 15 PO, and 16.2 ± 11.0 at 30 PO; there were no statistically-significant differences between the three time points (p = 0.107) (Table 2). Rev Bras Oftalmol. 2014; 73 (5): 273-8 276 Leite RA, Nosé RM1, Daga FB, Lui TAF, Lui GAF, Lui-Netto A Table 2 Mean values and standard deviation of the results ofTFBU (seconds), lissamine green (score) and basal Schirmer test (millimetres). p - Valuec p-Valued Time Mean ± Standard deviation Range pre 15 PO 30 PO 13.2 ± 3.3 11.3 ± 4.4 10.4 ± 3.2 8,0 – 18.0 4,0 – 20.0 6,0 – 16.0 Lissamine pre 15 PO 30 PO 1.0 ± 0.9 1.3 ± 1.0 1.0 ± 1.0 0,0 – 3.0 0,0 – 3.0 0,0 – 3.0 0.019 0.021* 0.010** 0.768*** Schirmer pre 15 PO 30 PO 17.6 ± 10.6 14.5 ± 10.8 16.2 ± 11.0 0,0 – 35.0 0,0 – 35.0 0,0 – 35.0 0.107 - TRFL 0.003 0.025* 0.219** 0.001*** c ANOVA with blocks, dMultiple comparisons using the LSD method *Comparison between Pre and 15 PO; **Comparison between 15 PO and 30 PO; ***Comparison between Pre and 30 PO. Table 3 Means and standard deviationsfor the results of TFBU (seconds), lissamine green (score) and basal Schirmertest (millimetres). Test Teme PRK LASIK p-Value TRFL pre 15 PO 30 PO 12.7 ± 2.8 10.5 ± 3.1 10.8 ± 3.0 13.4 ± 3.5 11.8 ± 5.1 10.2 ± 3.4 0.744c Lissamine pre 15 PO 30 PO 1.5 ± 0.9 1.7 ± 0.9 1.4 ± 1.1 0.8 ± 0.9 1.1 ± 1.0 0.8 ± 0.9 0.093c Schirmer pre 15º PO 30 PO 15.9 ± 10.4 11.9 ± 7.1 13.8 ± 6.9 18.6 ± 10.9 16.1 ± 12.5 17.7 ± 12.9 0.394c c p-value for the comparison between PRK and LASIK using ANOVA with repeated measures. Chart 3 Chart 4 Mean individual profiles for the results of TFBU (seconds)in patients submitted to PRK and LASIK. Mean individual profiles for the results of the lissamine green test (score) in patients submitted to PRK and LASIK. Rev Bras Oftalmol. 2014; 73 (5): 273-8 Analysis quantitative and qualitative of the tear film in patients undergoing PRK and LASIK with femtosecond Chart 5 Mean individual profiles for the results of the basal Schirmer test (millimetres) in patients submitted to PRK and LASIK. When the two groups (PRK and LASIK) were analysed separately, the following results were found:in the TFBU test, the values at Pre, 15 PO and 30 PO, respectively, were12.7 ± 2.8, 10.5 ± 3.1, and 10.8 ± 3.0 for the PRK group, and13.4 ± 3.5, 11.8 ± 5.1, and 10.2 ± 3.4 for the LASIK group. There were no statistically-significant differences between groups (p = 0.744).In the lissamine green test, the values at Pre, 15 PO, and 30 PO were1.5 ± 0.9; 1.7 ± 0.9 1.4 ± 1.1 for the PRK group, and0.8 ± 0.9, 1.1 ± 1.0, and 0.8 ± 0.9 for the LASIK group.Again, there were no significant differencesbetween groups (p = 0.093).In the basal Schirmer test, the values at Pre, 15 PO and 30 PO were15.9 ± 10.4, 11.9 ± 7.1, and 13.8 ± 6.9 for the PRK group, and18.6 ± 10.9, 16.1 ± 12.5, and 17.7 ± 12.9 for the LASIK group.Once again, there were no statistically-significant differences between groups (p = 0.394) (Table 3). DISCUSSION Regarding the sample population of this study, it is important to stress that there were no statistically-significant differences between groups (PRK and LASIK)regarding age or gender (Table 1, Charts 1 and 2) which could influence the incidence of dry eye in each group.Older patients and women are more likely to develop dry eye.(6) When all patients were grouped together, there was a statistically-significant reduction inTFBU values at 15 POin relation to preoperative values, and at 30 PO the values had decreased a little more (but with no significant difference compared to 15 PO) (Table 2, Chart 3).This is consistent with some studies in the literature which found a decrease in TFBU.(7,8) TFBU is an important test to assess the stability of the tear film, and together with the evaluation of symptoms, it is considered the most reliable test for dry eye syndrome because it is more reproducible, i.e. it shows less variation between two tests.(9)Thus, this study confirms that patients undergoing refractive surgery have a tendency to develop dry eye. 277 In the lissamine green test, a significant increase was found at 15 POcompared to the preoperative period, followed by a significant decrease at 30 PO, reaching a score statistically similar to preoperative values (Table 2, Chart 4).Lissamine green is an important dye thatstains damagedcells in the conjunctival and corneal epithelium, which can be found in patients with lacrimal film deficiency.Its action is similar to rose bengaldye, but it causes less irritation.The lissamine green test is moderately reproducible. (9)Itshowed that epithelial cells were actually damaged in the first two postoperativeweeks regardless of the surgical technique, with scores returning to normal within a month after surgery.Such damage may have been caused by the procedure itself or may be a consequence of dry eye. In the basal Schirmer test, no statistically-significant differenceswere found between the three time points (Pre, 15 PO, and 30 PO) (Table 3, Chart 5), in contrast with several other studies.(1,7,8)As can be seen in the chart, Schirmer test values tended to decrease postoperatively, but the reduction was not statistically significant.It should be noted that most previous studies used the type 1Schirmer test (without instillation of anaesthetic eye drops) following refractive surgery instead of the basal Schirmer test used in ourstudy (where anaesthetic eye drops were instilled in conjunctival sac before placing the Schirmer strip).The type 1 Schirmer test is probably more affected after refractive surgery, as it assesses both basal and reflex tear secretion, while the basal Schirmer test assesses basal secretion only.However, Nichols et al.(9)showed that the type 1 Schirmer test has poor reproducibility in patients with mild to moderate dry eye, being more reliable only in patients with severe dry eye.This is why we elected to use the basal Schirmer test in this study.Moreover, the preoperativeevaluation of patients included an assessment of static refraction with anaesthetic, cycloplegic, and tropicamide eye drops on the same day as the dry eye tests were conducted;therefore, the basal Schirmer test was also preferred to avoid any bias that could have been caused by the residual influence of those drugs. It should also be noted that even though all tests were conducted in the same environment in a closed room, there were variations in temperature and humidity in the city of São Paulo, where the experiment was conducted, which could certainly have influenced results. Some studies show that patients submitted LASIK have a higher incidence and a longer duration of dry eye than those undergoing PRK(7,8).In our study, however, neither technique was superior to the other in the three time points (Pre, 15 PO and 30 PO) (Table 3).This may be related to the fact that other studies used a microkeratome, instead of femtosecond laser, to create the corneal flap.The introduction of femtosecond laser in LASIK has created the prospect to reduce the incidence of dry eye, as it is a safer and more accurate method than the microkeratome. (4,5) Salomão et al. (10) found that patients submitted to LASIK whose corneal flap had been created using the femtosecond laser showed less dry eye than those whose flap had beencreated with a manual microkeratome.In contrast, Golas et al.(6)found no statistically-significant differences between these two groups as regards dry eye symptoms. It is therefore important to stress the need to observe patients closely for the development of dry eye after surgery.Furthermore, according to our results, there were no significant differences between both surgical techniques as regards changes in the tear film. Rev Bras Oftalmol. 2014; 73 (5): 273-8 278 Leite RA, Nosé RM1, Daga FB, Lui TAF, Lui GAF, Lui-Netto A CONCLUSION The present study foundchanges in the tear film of patients submitted to PRK and LASIK with femtosecond laser; in particular, changes were observed in the TFBU and lissamine green tests, with the latter returning to preoperative values within a month after surgery.No significant changes were found in the Schirmer test within the first postoperative month.PRK and LASIK with femtosecond laser produced similar changes to the tear film. R EFERENCES 1. 2. 3. 4. Credie MG, Nishiwaki-Dantas MC, Felberg S, Amorim F, Dantas PE. Alterações quantitativas do filme lacrimal após cirurgia refrativa: estudo comparativo entre PRK e LASIK. Arq Bras Oftalmol. 2007;70(1):23-30. Murakami Y, Manche EE. Prospective, randomized comparison of self-reported postoperative dry eye and visual fluctuation in LASIK and photorefractive keratectomy. Ophthalmology. 2012;119(11):2220–4. Netto MV, Espíndola RF, Nogueira RG, Campos M, Ambrósio Jr. R, Andrade NL. Censo Brasileiro de Cirurgia Refrativa. Arq Bras Oftalmol. 2013;76(1):29-32. Rodriguez AE, Rodriguez-Prats JL, Hamdi IM, Galal A, Awadalla M, Alio JL. Comparison of Goblet cell density after femtosecond laser and mechanical microkeratome in LASIK. Invest Ophthalmol Vis Sci. 2007; 48(6): 2570–5. Rev Bras Oftalmol. 2014; 73 (5): 273-8 5. Shtein RM. Post-LASIK dry eye. Expert Rev Ophthalmol. 2011; 6(5):575–82. 6. Golas L, Manche EE. Dry eye after laser in situ keratomileusis with femtosecond laser and mechanical keratome. J Cataract Refract Surg. 2011; 37(8):1476-80. 7. Lee JB, Ryu CH, Kim J, Kim EK, Kim HB. Comparison of tear secretion and tear film instability after photorefractive keratectomy and laser in situ keratomileusis. J Cataract Refract Surg. 2000; 26(9):1326–31. 8. Nejima R, Miyata K, Tanabe T, Okamoto F, Hiraoka T, Kiuchi T, Oshika T Corneal barrier function, tear film stability, and corneal sensation after photorefractive keratectomy and laser in situ keratomileusis. Am J Ophthalmol. 2005; 139(1):64-71. 9. Nichols KK, Mitchell GL, Zadnik K. The repeatability of clinical measurements of dry eye. Cornea. 2004;23 3):272–85. 10. Salomão MQ, Ambrósio R Jr, Wilson SE. Dry eye associated with laser in situ Keratomileusis: Mechanical microkeratome versus femtosecond laser. J Cataract Refract Surg. 2009; 35(10):1756-60. Correspondência com o autor: Rubens Amorim Leite Rua Doutor Diogo de Faria, no85, apto 72, Vila Clementino, São Paulo, Brazil. Phone: (11) 98568-5500 E-mail: [email protected] ORIGINAL ARTICLE 279 Novel spatula and dissector for safer deep anterior lamellar keratoplasty Uso de espátula e dissector para otimização da ceratoplastia lamelar anterior profunda (DALK) Gustavo Bonfadini1,2,3, Eun Chul Kim1,4, Mauro Campos3, Albert S. Jun1 A BSTRACT Objective: We describe a novel spatula and dissector to facilitate the big-bubble technique in deep anterior lamellar keratoplasty (DALK). Methods: A 29-year-old man who was diagnosed with bilateral keratoconus underwent deep anterior lamellar keratoplasty (DALK). After 350µm partial thickness incision of the recipient cornea, the Bonfadini dissector was inserted at the deepest point in the peripheral incision and could be advanced to the center of the cornea safely because of its “semi-sharp” tip. After achieving the big-bubble (BB) separation of Descemet membrane (DM) from the overlying stroma, the anterior stromal disc was removed. Viscoelastic material was placed on the stromal bed to prevent uncontrolled collapse and perforation of DM during the paracentesis blade incision into the BB. We could detect the safe opening of the BB using the Bonfadini dissector by the leakage of air bubbles into the viscoelastic material. After injecting viscoelastic material into the BB space, we inserted the Bonfadini spatula into the bigbubble safely because of its curved profile and blunt edges. The groove along the length of the Bonfadini spatula enables safe and efficient incision or the residual stromal tissue using the pointed end of a sharp blade while protecting the underlying DM. After removal of posterior stroma, the donor button was sutured with 16 interrupted 10-0 nylon sutures. Results: This technique and the use of the Bonfadini spatula and dissector facilitate exposure of Descemet membrane. Conclusion: The smooth Bonfadini DALK spatula and dissector facilitate safe and efficient completion of DALK surgery. Keywords: Deep anterior lamellar keratoplasty; Corneal transplantation/methods; Keratoplasty; Bonfadini dissector; Bonfadini spatula RESUMO Objetivo: Descrevemos o uso de novos instrumentais cirúrgicos para facilitar a técnica de “big-bubble” na ceratoplastia lamelar anterior profunda (DALK). Métodos: Paciente masculino, 29 anos, foi diagnosticado com ceratocone bilateral e submetido à ceratoplastia lamelar anterior profunda (DALK). Após incisão da córnea receptora numa profundidade de 350µm de espessura parcial, o dissector Bonfadini foi inserido no ponto mais profundo da incisão periférica e pode avançar para o centro da córnea com segurança devido à sua ponta semiafiada. Depois de realizar a “big-bubble” (BB) e atingir a separação da Membrana de Descemet (MD) do estroma sobrejacente, o disco corneano de estroma anterior foi removido. Um viscoelástico foi colocado sobre o leito do estroma remanescente para impedir o colapso não-controlado e perfuração da MD durante a incisão na BB com lâmina de paracentese. Verificamos segurança no rompimento do estroma remanescente com o auxílio do dissector Bonfadini, para liberação da bolha de ar da BB através do viscoelástico. Depois de injetar o viscoelástico no espaço da BB, inserimos a espátula Bonfadini neste espaço, o que demonstrou-se seguro devido ao formato curvo e das bordas arredondadas do instrumental. A chanfradura ao longo do comprimento da espátula Bonfadini permite a incisão pela ponta de uma lâmina afiada, protegendo assim a MD subjacente. Após a remoção do estroma posterior, o botão doador foi suturado com 16 pontos interrompidos de fio nylon 10.0. Resultados: Esta técnica e o uso da espátula Bonfadini e dissector facilitam a exposição de membrana de Descemet. Conclusão: A superfície lisa da espátula Bonfadini e dissector, facilitam a realização segura e eficiente da ceratoplastia lamelar anterior profunda (DALK). Descritores: Ceratoplastia lamelar anterior profunda; Transplante de córnea/métodos; Ceratoplastia; Dissector Bonfadini; Espátula Bonfadini 1 Cornea & Anterior Segment Service, Wilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, Maryland, USA; Rio de Janeiro Eye Bank, Rio de Janeiro, RJ, Brazil; 3 Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil; 4 College of Medicine, Catholic University of Korea, Seoul, Korea. 2 The authors have no public and private financial support, or financial interest Received for publication 25/02/2014 - Accepted for publication 26/04/2014 Rev Bras Oftalmol. 2014; 73 (5): 279-81 280 Bonfadini G, Kim EC, Campos M, Jun AS INTRODUCTION D eep anterior lamellar keratoplasty (DALK) has been proposed as an alternative to penetrating keratoplasty (PK) for the treatment of various corneal diseases not affecting the endothelium. DALK surgery removes the anterior layers of the cornea, cleaving the deep stroma from Descemet membrane (DM). The advantages of the DALK technique for corneal stromal diseases include absence of endothelial rejection, avoidance of potential open-sky intra-operative complications of PK, faster visual rehabilitation due to earlier suture removal, and a predicted longer graft survival because of the lower rate of endothelial cell loss (1). DALK is a time-consuming and technically demanding procedure. The most frequent intraoperative complication is perforation of DM while attempting to separate it from the overlying stroma during creation of the big-bubble (BB) (2). Sarnicola et al.(3) reported that a smooth spatula and cannula can facilitate a high percentage of successful DALK and make the procedure more reliable than compared to air injection with a needle. In this report, we describe a novel Bonfadini dissector and spatula for safely manipulating the big-bubble and removing posterior stroma. Surgical technique A 29-year-old man diagnosed with bilateral keratoconus 6 years ago, visited our service complaining of ocular pain and decreased vision in the right eye. He had worn rigid gas permeable (RGP) contact lenses for 16 years. His best spectacle corrected visual acuity OD was 20/80 and OS was 20/25. Slitlamp examination revealed marked corneal stromal scarring and epithelial punctuate erosions on the right central cornea. Hence, deep anterior lamellar keratoplasty (DALK) was completed uneventfully in the right eye. The operation was performed under sub-Tenon anesthesia by A.S.J; The technique described by Anwar et al.(4) was followed with the described modifications. A surgical marking pen was used to mark the center of the host cornea. An 8.5mm diameter trephine was used to lightly score the epithelium of the host cornea to outline the recipient bed. An astigmatic keratotomy blade was used to incise the recipient cornea to a depth of 350µm along the 8.5mm trephine mark. Through a small peripheral clear cornea paracentesis, the anterior chamber (AC) was filled with air, and approximately physiologic intraocular pressure confirmed. The Bonfadini dissector (Katena Products, USA; Figure 1A) was inserted at the deepest point in the peripheral groove and was advanced toward the center of the cornea. Once the Bonfadini dissector was approximately 1-2mm from the apex of the cone (Figure 1B), it was removed and the Fogla 27 gauge air injection cannula (Bausch & Lomb Storz Ophthalmic, USA), attached to a 5mL syringe filled with air was introduced into the corneal tunnel. Air was then injected into the stroma to achieve the formation of a big-bubble (figure 1C). The central anterior stromal disc was removed with an angled crescent knife, and then air was evacuated through the previously placed paracentesis. To enter into the big-bubble, we used the Ophthalmic Viscosurgical Device–Assisted Incision technique (5). A cohesive viscoelastic (Healon, Abbott Medical Optics) was placed on the stromal bed and a 1.0mm incision was then created with a paracentesis blade using only the tip of the blade with a “lifting” motion to prevent rapid collapse of the bubble which could result in Descemet membrane perforation. Entry into the big-bubble was confirmed by the appearance of a small bubble within the overlying viscoelastic material, which also served to prevent rapid egress of air from the big-bubble and rapid collapse leading to a higher probability of perforating the Descemet membrane (figure 1D). Rev Bras Oftalmol. 2014; 73 (5): 279-81 Entry into the big-bubble was confirmed by the appearance of a small bubble within the overlying viscoelastic material, which also served to prevent rapid egress of air from the big-bubble and rapid collapse leading to a higher probability of perforating the Descemet membrane (figure 1D). Viscoelastic material was injected into the pre-Descemet space to expand the potential space and separate the Descemet membrane from the overlying stromal tissue. The Bonfadini spatula (Katena Products, USA; figure 2A) was introduced into the pre-Descemet space. This instrument has blunt edges and a curved profile to minimize inadvertent damage to Descemet membrane. The groove along the length of the Bonfadini spatula serves as a guide to allow for rapid incision of the posterior stromal tissue using the sharp point of a Figure 1: The Bonfadini dissector has a fine, rounded tip to enable stromal dissection while preventing inadvertent perforation of Descemet membrane (A); use of the Bonfadini dissector to create a deep tunnel toward the center of the cornea from a peripheral partial thickness groove incision (B); big-bubble formation by deep, intrastromal air injection with accompanying stromal opacification (C); opening of the big-bubble with a sharp blade was detected by air leaking into viscoelastic material placed on the posterior stromal bed (D) paracentesis blade (figure 2B). The spatula serves to protect the DM from inadvertent perforation while incising the posterior stromal tissue. Once sufficient radial incisions in the posterior stroma were completed, we removed stroma with cornealscleral scissors along the peripheral partial thickness groove incision. The full-thickness donor graft was punched at 8.75mm diameter from the endothelial side, and the endothelium was stripped from the posterior surface using surgical spears. The donor button was then sutured into position with 16 interrupted 10-0 nylon sutures (figure 2C). The patient achieved uncorrected visual acuity of 20/125 and 20/60 with pinhole on day 1 postoperatively with a wellattached graft. At 3 months after DALK, his uncorrected visual acuity was 20/60 and best spectacle corrected visual acuity (-1.25 + 1.5 x 30 degrees) was 20/25 OD. DISCUSSION Corneal transplantation is singular because it is habitually performed on persons with visual deficiency but with preserved life expectancy, mobility and social life. A graft not well succeeded may cause real blindness and permanent misery due to pain and discomfort (6). To obtain a satisfactory surgical result, there is a need of an appropriate patient selection and guidance about their eye problem, the proposed surgery, care and risk per and post operative as well as the visual rehabilitation perspective (7). Novel spatula and dissector for safer deep anterior lamellar keratoplasty 281 In the technique described here, viscoelastic material is placed on the stromal bed before opening the big-bubble (5). We can detect entry into the big-bubble (BB) by air leaking into the viscoelastic material. This sign allows a very controlled entry into the BB as it is readily and immediately visible and prevents rapid egress of air and collapse of the BB. Once the BB is accessed and further expanded by injection of viscoelastic into the BB, the design of the Bonfadini spatula allows it to be manipulated within the BB space with minimal chance of inadvertent trauma to DM. The groove along the length of the Bonfadini spatula also serves as a convenient guide to facilitate rapid incision of the posterior stroma into wedges, which can be excised at the periphery using standard corneal scissors. Thus, we present the novel Bonfadini dissector and spatula as aids for the successful completion of DALK surgery. In summary, the benefits of our proposed technique could be shown more conclusively in a case–control or prospective study with a larger number of patients to validate our findings. Figure 2: The groove along the Bonfadini spatula serves as a guide to protect Descemet membrane (DM) from inadvertent perforation when incising the posterior stroma with a blade (A); creation of wedgeshaped incisions of posterior stroma, using a blade guided along the groove of the Bonfadini spatula. The spatula serves to protect inadvertent perforation of DM (B); donor button was sutured into position with 16 interrupted 10-0 nylon sutures (C) Keratoconus is one of the main indications of keratoplasty in Brazil (8), and DALK is more cost-effective than penetrating keratoplasty (PK) (9). Prevention of immune-mediated graft rejection can be achieved through meticulous surgical technique such as lamellar surgery (10). DALK aims to remove and replace total or near-total corneal stroma while preserving host healthy endothelium. The advantages of DALK include reducing the risk of endothelial graft rejection, preservation of host endothelium with minimal surgical trauma, efficient visual rehabilitation relative to penetrating keratoplasty (PK), and also fewer intraoperative and postoperative complications including expulsive hemorrhage, anterior synechia, postoperative endophthalmitis, and glaucoma in comparison to PK. This procedure also requires less rigid criteria for donor corneal tissue selection that is often weighted toward donor endothelium in PK (11). Major disadvantages of anterior lamellar keratoplasty as compared to penetrating keratoplasty are the irregularity and sub-optimal optics of the corneal stromal bed which occur following manual lamellar dissection techniques (12). These issues are avoided in DALK. However, the challenge with DALK continues to be the learning curve for novice surgeons when trying to expose DM (descemetic DALK [dDALK]) versus dissection in a pre-Descemetic stromal plane (pre-Descemetic DALK [pdDALK]) (3). The dDALK procedure allows faster visual recovery than pdDALK(13). Thus, the goal of DALK is to expose the DM without damage and to achieve dDALK. Lamellar dissection of the stroma can be performed by a manual technique using a variety of instruments, including lamellar knives and dissectors (14). Using the Bonfadini dissector, we could create a deep tunnel near the corneal center prior to air injection. The Bonfadini dissector has a fine, rounded tip, which can dissect stromal tissue relatively easily while reducing the likelihood of penetrating Descemet membrane. Accessing the deep stroma for air injection may improve the success of achieving the big-bubble. The most serious complication during big-bubble DALK surgery is intraoperative perforation of Descemet membrane, which may require subsequent conversion to full-thickness penetrating keratoplasty (15). Perforation of Descemet membrane is more likely to occur as a result of direct needle trauma during initial air injection and dissection of the corneal stroma (16). As well, perforation of DM can occur while opening the big-bubble and dissecting remaining stroma over Descemet membrane. R EFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. Shimmura S, Tsubota K. Deep anterior lamellar keratoplasty. Curr Opin Ophthalmol. 2006;17(4):349-55. Review. Michieletto P, Balestrazzi A, Balestrazzi A, Mazzotta C, Occhipinti I, Rossi T. Factors predicting unsuccessful big bubble deep lamellar anterior keratoplasty. Ophthalmologica. 2006;220(6):379-82. Sarnicola V, Toro P. Blunt cannula for descemetic deep anterior lamellar keratoplasty. Cornea. 2011;30(8):895-8. Anwar M, Teichmann KD. Big-bubble technique to bare Descemet’s membrane in anterior lamellar keratoplasty. J Cataract Refract Surg. 2002;28(3):398-403. Goshe J, Terry MA, Shamie N, Li J. Ophthalmic viscosurgical deviceassisted incision modification for the big-bubble technique in deep anterior lamellar keratoplasty. J Cataract Refract Surg. 2011;37(11):1923-7. Marcomini LA, Sobral RM, Seixas GO, Sousa SJ. [Corneal selection for transplants]. Rev Bras Oftalmol. 2011;70(6):430-6. Portuguese. Kara-Junior N, Mourad PC, Espíndola RF, AbilRuss HH. [Expectation and knowledge among patients with keratoplasty indication]. Rev Bras Oftalmol. 2011;70(4):230-4. Portuguese. Zeschau A, Balestrin IG, Stock RA, Bonamigo EL. [Indications of keratoplasty: a retrospective study in a University Hospital]. Rev Bras Oftalmol. 2013;72(5):316-20. Portuguese. Koo TS, Finkelstein E, Tan D, Mehta JS. Incremental cost-utility analysis of deep anterior lamellar keratoplasty compared with penetrating keratoplasty for the treatment of keratoconus. Am J Ophthalmol. 2011;152(1):40-47.e2. Costa DC, Kara-Joseì N. [Corneal transplant rejection]. Rev Bras Oftalmol. 2008; 67(5):255-63. Portuguese. Espandar L, Carlson AN. Lamellar Keratoplasty: A Literature Review. J Ophthalmol. 2013;2013:894319. Review. Parthasarathy A, Por YM, Tan DT. Use of a “small-bubble technique” to increase the success of Anwar’s “big-bubble technique” for deep lamellar keratoplasty with complete baring of Descemet’s membrane. Br J Ophthalmol. 2007;91(10):1369-73. Sarnicola V, Toro P, Gentile D, Hannush SB. Descemetic DALK and predescemetic DALK: outcomes in 236 cases of keratoconus. Cornea. 2010;29(1):53-9. Bonfadini G, Moreira H, Jun AS, Campos M, Kim EC, Arana E, et al. Modified femtosecond laser-assisted sutureless anterior lamellar keratoplasty. Cornea. 2013;32(4):533-7. Jhanji V, Sharma N, Vajpayee RB. Intraoperative perforation of Descemet’s membrane during “big bubble” deep anterior lamellar keratoplasty. Int Ophthalmol. 2010;30(3):291-5. Leccisotti A. Descemet’s membrane perforation during deep anterior lamellar keratoplasty: prognosis. J Cataract Refract Surg. 2007;33(5):825-9. Address reprint requests to: Albert S. Jun Cornea and External Disease Service Wilmer Smith Building 5011, The Johns Hopkins Medical Institutions 400 N. Wolfe Street, Baltimore, MD 21231 Rev Bras Oftalmol. 2014; 73 (5): 279-81 O 282 RIGINAL ARTICLE Serological profile of candidates for corneal donation Perfil sorológico de candidatos a doação de córneas Adroaldo Lunardelli1, Richard Beraldini Alvarenga1, Maria Luiza Assmann1, Dário Eduardo de Lima Brum1, Mirna Adolfina Barison1 A BSTRACT Objective: The purpose of this study is to map the serological profile of candidates to corneal donation at Irmandade Santa Casa de Misericórdia de Porto Alegre, identifying the percentage of disposal by serology and the marker involved. Methods: There have been analised – retrospectively – the results of serology of all corneal donors, made between the period of 1st january 2006 and 31st december 2012. Data analised were related to age, gender and the results of serology pertinent to viral markers (HBsAg, anti-HBc, anti-HCV and anti-HIV), these, determined by immunosorbent tests (ELISA). Results: In the period of the study, there were 2476 corneal donors at the institution, with a major incidence on the male gender, on an average of 58.7 years old. 23% of retention because of serological unfitness was also identified, that is, 570 samples were non-negative to any of the used tests. The marker antiHBc was the most prevalent on the studied population, followed by the Hepatitis C virus (HCV) and by the Human Immunodeficiency Virus (HIV). Conclusion: From the data found through this study, it is essential to have the participation of an efficient service on the serological evaluation of the candidates to corneal donation, once the security of the receptor must be taken into consideration in a population of donors with 23% of unfitness prevalence, in which the most prevalent marker is the one of Hepatits B. Keywords: Serology; Córnea/immunology; Corneal transplantation RESUMO Objetivo: O intento deste desígnio é mapear o perfil sorológico dos candidatos a doação de córneas na Irmandade Santa Casa de Misericórdia de Porto Alegre, identificando o percentual de descarte por sorologia e o marcador envolvido. Métodos: Foram analisados – retrospectivamente – os resultados da sorologia de todos os doadores de córneas compreendidos entre 01 de janeiro de 2006 a 31 de dezembro de 2012. Foram avaliados os dados de idade, sexo e os resultados da sorologia pertinentes aos marcadores virais (HBsAg, anti-HBc, anti-HCV e anti-HIV) determinados por testes imunoenzimáticos (ELISA). Resultados: No período coberto pelo estudo, houve 2476 doadores de córneas na instituição, com maior ocorrência do sexo masculino e média de 58,7 anos de idade. Foram verificados 23,0% de retenção por inaptidão sorológica, ou seja, 570 amostras mostraram-se não-negativas para qualquer dos testes empregados. O marcador anti-HBc foi o mais prevalente na população aferida, seguido pelo vírus da hepatite C (HCV) e pelo vírus da imunodeficiência humana (HIV). Conclusão: Diante dos dados encontrados por este estudo, torna-se decisiva a participação de um serviço eficaz no tangente à avaliação sorológica dos candidatos à doação de córnea, uma vez que a segurança do receptor deve ser considerada numa população de doadores com prevalência de retenção por inaptidão sorológica de 23,0%, donde o marcador mais prevalente é o de hepatite B. Descritores: Sorologia; Córnea/imunologia; Transplante de córnea; 1 Serviço de Hemoterapia, Irmandade Santa Casa de Misericórdia de Porto Alegre, Porto Alegre (RS), Brazil. Study carried out at Serviço de Hemoterapia, Irmandade Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil The authors have no public and private financial support, or financial interest Received for publication 15/5/2013 - Accepted for publication 14/10/2013 Rev Bras Oftalmol. 2014; 73 (5): 282-6 Serological profile of candidates for corneal donation INTRODUCTION C orneal diseases are the second cause of reversible blindness around the world and affects a young and active population, leading to an important economic and social problem (1). The corneal transplant (keratoplasty) has developed fast through the last 10 years (2), and it is considered the most successful procedure among the human tissue transplants (3). Corneal transplantation is indicated to a huge variety of diseases and it provides visual recovering, in an efficient form and low cost, to patients with corneal opacities and irregularities. The success of this surgical procedure has been set due to the fact that the cornea is avascular and there are immunological privileges on this structure. Advances on the surgical technique (4) , equipment, materials, methods to preserve the donated cornea and postoperative handling have also contributed to the success of the corneal transplants (5). The intervention of the eye banks is essential in the search for donors, in the interview with the families, in the quality of processing and distribution of the donated tissues. The quality control of the whole process and distribution of donor cornea begins with the selection of the donors, careful processing using proper techniques of ocular globe enucleation, preservation of the cornea and evaluation of parameters, such as donor serology and endothelial cells counting and the slit lamp evaluation of the donor cornea by an experienced ophthalmologist (6). Because of the increase in the number of corneas donated and kept for longer periods, the careful evaluation becomes an indispensable procedure and of high responsibility by the ocular tissue banks (7). Positive serologic testing results are one of the major reasons for discarding donor corneas (8). Despite being rare, the potential for the transmission of diseases through organ and tissue grafts exists; even with avascular tissues, as the cornea, have already demonstrated being a way of contamination and transmition. There are reports of infections caused by bacteria, fungi, viruses and even prions acquired by corneal transplant (9). The Brazilian Law does not allow the use of tissues to transplant whose donor present positive serology to hepatitis B, hepatitis C or human immunodeficiency virus (HIV) (9) (according to Resolução da Diretoria Colegiada – RDC – number 67). The intention of this study is to map the serological profile of the candidates of corneal donation at Irmandade Santa Casa de Misericórdia de Porto Alegre (ISCMPA), and identify the percentage of disposal by serology and the marker involved. 283 Genescreen HIV 1/2 version 2 Bio-Rad). To Hepatitis C, the research of anti-HCV antibodies was made with the kit HCV 3.0 Ortho improved by SAVe. To Hepatitis B, anti HBc and HBsAg were measured through the kits anti-HBc Plus Bio-Rad and HBsAg Ultra Bio-Rad, respectively. The results of each serology were classified as fit (negative, according to manufacturer’s criteria) or unfit (inconclusive or positive, according to manufacturer’s criteria). The data is shown in absolute numbers or percentages. No statistical analysis was applied because it is exposed descriptive data. R ESULTS This study shows that, on average, Irmandade de Santa Casa de Misericórdia de Porto Alegre receives 353 corneas donations a year. During the period of the study, there were 2476 corneal donors at the institution (figure 1), mostly from the male gender (56% male, figure 2) and average of 58,7 years old (±15,5, standard deviation) and median and mode of 61 and 62, respectively. Table 1 shows the age distribution of 2182 donors, from whom there had been access to the referred parameter. Twenty-three per cent of retention because of serological unfitness was also identified, that is, 570 samples were nonnegative to any of the used tests (figure 3). The marker anti-HBc was the most prevalent on the studied population, followed by the hepatitis C virus (HCV) and by the human immunodeficiency virus (HIV), as shown on table 2. Figure 1: Distribution of the number of candidates to corneal donation stratified per year M ETHODS There have been analysed – retrospectively – the results of serology of all corneal donors at ISCMPA between the period of 1st january 2006 and 31st december 2012. Data was obtained through the analisys of the electronic data bank of the institution, Irmandade Santa Casa de Misericórdia de Porto Alegre. All corneas which were captured, evaluated and kept are there in this data bank. There have been evaluated data related to age, gender and the results of serology pertaining to viral markers (HBsAg, anti-HBc, anti-HCV and anti-HIV). The blood samples were obtained according to conditions of accessibility. The blood was kept in a dry and non-preservative tube, centrifuged to 3000 rpm for five minutes and the supernatant serum was used to dosages of immunoenzymatic tests (ELISA). Two tests to detect HIV were used: Genescreen Ultra HIV AgAb Bio-Rad and Figure 2: Distribution of corneal donors, showing the percentage of individuals from the male (M) and female (F) gender Rev Bras Oftalmol. 2014; 73 (5): 282-6 284 Lunardelli A, Alvarenga RB, Assmann ML, Brum DEL, Barison MA DISCUSSION Figure 3: Distribution of the percentual of individuals according to serological fitness Table 1 Distribution of the percentual of corneal donors according to age range Age range (%) ≤ 20 21 to 30 31 to 40 41 to 50 51 to 60 61 to 70 71 to 80 ≥ 81 3.16 4.17 4.95 10.72 25.44 26.49 24.66 0.41 Total 100.0 Table 2 Distribution of corneal donors stratified by serology Test Frequency Percentage on the total of donors Percentage on the total of restraints 1.58 55.26 19.82 7.89 4.74 6.67 2.11 1.40 0.35 0.18 HBsAg A-HBc HCV HIV A-HBc + HBsAg A-HBc + HCV A-HBc + HIV A-HBc + HCV + HIV A-HBc + HBsAg + HIV HCV + HIV 9 315 113 45 27 38 12 8 2 1 0.36 12.72 4.56 1.82 1.09 1.53 0.48 0.32 0.08 0.04 Total 570 23.0 Rev Bras Oftalmol. 2014; 73 (5): 282-6 100.0 The cornea is the most commonly transplanted tissue in the world (2); however, one of the major restrictions for the increase of transplants is due to the number of donations (10). In many states of Brazil, the lack of ocular tissues and eye banks which are able to provide corneas in adequate number and quantity to be transplanted is, unfortunately, real (11). However, efforts have been made to change this reality (12). This study shows, according to other authors, that there is a high percentage of donors of the male gender (9,13). The minimum and maximum ages of a donor for the usage of the tissue vary according to medical regulations of each eye bank (1) . In this study, the minimum and maximum ages found were of 3 and 84, respectively. The age average found in this study (58.6 years old) supports other studies, which show an age average of 60 (1,9), despite other works refer to minimum ages even lower (3,13,14). Scientific literature shows that there is no restriction of age to corneas donated and age is not issue to low survival of the graft; what’s more, quality in the biomicroscopic and specular microscopic evaluation of the endothelium have to be taken into consideration when using corneas (7). However, old age is taken as a limiting factor, once most surgeons prefer not to use corneas from patients over 75 years old. This age is arbitrary, once the age of the donor does not seem to be related to the survival of the graft (1), though, factors as advanced age range and presence of debilitating diseases tend to coexist and increase the chances of finding a worse evaluation of quality when compared to corneas of young donors and/or trauma deaths (7). Studies show that corneas of donors in advanced ages can be perfectly acceptable for transplants, showing that these tissues when coming from older donors (over 80 years old) present a lower chance of failure or post transplant rejection than younger corneas (15). There are eye banks that stipulate a minimum age for donation, and it can reach 10 years old (1,11). Because of this, scientific literature is conflicting and inconclusive about the effect of the age of donors related to the survival of the transplanted cornea (16,17). Viral infections transmitted through transplants have already been reported, once the viruses remain in the tissue after the collection; because of this, the serological screening is an important precondition to the tissue banks (8) and the clinic screening does not exclude the undertaking of serological tests. In this study, the corneas to be used in donation, 23% (570) were retained for being considered serologically inappropriate. This percentage is lower than the ones found in other studies, for instance, an eye bank in São Paulo, Brazil, registered a disposal of 33.4% in 2006-2007 (9) or the eye bank in Cascavel, a city in the state of Paraná, also in Brazil, reported a serological disposal of 51.8% (11); however, the percentage found in this study is higher than the one found in a study in Minas Gerais, Brazil, where 9% of 1668 corneas were discarded because of positive serology (18). It is important to mention that the commercial tests are not recommended to serum of corpses; however, there are not specific tests to this end. The corpse sample is usually of low quality. In many cases, the serological tests can show false-positive results in samples post-mortem, which can lead to an unnecessary disposal of the cornea. The time of collection after death and the immediate separation of the serum (centrifugation) are two steps that can affect the quality of the sample (8). It is crucial that the multidisciplined team – militant in the procedures of collection and Serological profile of candidates for corneal donation storage of ocular tissues – is shrewd to proceed to the blood collection as soon as possible after the death of the donor and make the centrifugation of the collected material right after that. These measures increase serological tests in quality. What’s more, it is clear that the combination between the lower period of time from death to the preservation of the material generates better quality of the cornea. Among the explanations of the influence from the time of death and enucleation and/or preservation of the corneal tissue quality are the possible metabolical alterations or even anatomical alterations in the cornea during this process (15). The Brazilian Law (RDC 67 from 30th september 2008) demands two serological tests to the detection of hepatitis B (HBsAg and anti-HBc), which exclude donors in case of positivity. In this study, the major part (55.26%) of retentions is due to anti-HBc (table 2) individually, which represents 12.72% from the total of donations. A study made with corneal donors in the region of Cascavel (state of Paraná) revealed disposal because of isolated positivity of anti-HBc of 47.4% on the total of donors. It has already been reported that, in this city, positivity to antiHBc in donors of blood is significantly higher than in other regions of the same state; however, when the presence of the DNA of hepatitis B virus was detected (a more sensitive and specific test to determine the potential of infectivity of the virus) in donors of blood with positive serology to anti-HBc and negative to HBsAg, there had reached to the result of inexistence of the DNA of the hepatitis B virus in the samples (11). Experts question the adoption of serology anti-HBc to screening corneas (18) due to its high sensitivity but low specificity (11). The Eye Bank Association of America forebodes only the undertaking of HBsAg as a screening method to hepatitis B, not including in its routine the anti-HBc (11). This idea does not seem reasonable, for most tests used to the serological diagnosis being very sensitive and specific; they cannot detect all cases of hepatitis B. Several studies show that, after undertaking the conventional screening (HBsAg and anti-HBc), when making the research of anti-HBs in the individuals non-reagent to HBsAg, but reagent to antiHBc, 10 to 34% will be also non-reagent to anti-HBs, being classified as anti-HBc isolated (19). The presence of this profile is consistent with (a) old infection with low levels of anti-HBs, (b) period of immunological window, (c) false positive reaction and (d) HBsAg chronic carrier non-detectable. Through tests of amplification of nucleic acids, it was proved the presence of the DNA of the hepatitis B virus in 1.34% of donors HBsAg negative with anti-HBc positive (19). The detection of cases with anti-HBc isolated can be avoiding not only the transmission of wild strain (not detected due to the low viral load present in individuals with non-detectable levels of HBsAg) but also the transmission of mutant strains (19). Nowadays, the non-detection of HBsAg marker due to the appearance of these mutant strains has been cause of concern. The analytic sensitivity of tests to the detection of HBsAg may rely on the genotype or subtype of the hepatitis B virus (19). In this study, the presence of anti-HBc together with HBsAg was found in 4.74% of unable donors, reaching 1.09% of the total of donations. This rate is similar to the one in the region of Cascavel, which shows 1.5% of retention to this association of markers (11). This profile is consistent with the acute phase or the chronic carry of hepatitis B (20). Also, in this study there is a report on table 2 about the prevalence of 4.56% to HCV and 1.82% to HIV. These levels are 285 superior to the ones found in eye banks of São Paulo (9) and Cascavel (11). The presence of anti-HBc together with HCV was found in 38 candidates to donation, prevailing 1.53% (6.67% among the retained ones). This situation is common, and it can represent several other situations, among them, hidden hepatitis B in patients with chronic hepatitis C (21,22). The usage of nucleic acid tests to confirm (or not) positive results is foreboded once these tests would really detect the existence of infection, for antibodies detected through traditional serological methods could persist for longer time after active infection has stopped; however, one of the limiting factors to serological screening with acid nucleic tests are the costs (9). Tissue Banks must evaluate the usage of this kind of test because they reduce the risk of viral infections caused by grafts (8). This ideal situation is still not tangible to our reality, because of the excessive burden of the process. The plurality of professionals involved in a transplant of cornea is imperative facing the extensive work done in this process. It is essential, though, that the teams are aligned with the development of the work. It is essential to have the participation of an efficient service on the serological evaluation of the candidates to corneal donation, once the security of the receptor must be taken into consideration in a population of donors with high unfitness prevalence. In this context, the adoption of nucleic acid tests will enhance quality to the process in a near future. Works like this one are of elementary importance because they bring – to the scientific community – the profile of the corneal tissues donated, and from these data, they enable institutions to take measures in relation to implementing services of eye banks based on the knowledge they have about the target public. In our study, we show retention of 23% for serological unfitness. This index is considered high if compared to serological retention of blood donation, for instance. This fact occurs because there is no clinic retention to candidates of corneal donation, once the personal interview is impossible to be made, as the donors are corpses. The most prevalent marker was referent to Hepatitis B, followed by HCV and HIV. This study confirms the validity and the importance of serological tests so to exclude positive serological corneas to prevent infections, which could be transmitted to eventual cornea receptors Aknowlodgements The authors thank Marcela Migliavacca Alvarenga for their translation support. R EFERENCES 1. 2. 3. 4. Adán CB, Diniz AR, Perlatto D, Hirai FE, Sato EH. [Ten years of corneal donation to the Hospital São Paulo Eye Bank: characteristics of cornea donors from 1996 to 2005]. Arq Bras Oftalmol. 2008;71(2):176-81. Portuguese. Tan DT, Dart JK, Holland EJ, Kinoshita S. Corneal transplantation. Lancet. 2012;379(9827):1749-61. Review. Chalita MR, Diazgranados EB, Sato EH, Branco BC, Freitas D. [Corneal graft rejection after penetrating keratoplasty: analysis of the Eye Bank of the Hospital São Paulo - Escola Paulista de Medicina]. Arq Bras Oftalmol. 2000;63(1):55-8. Portuguese. Kara-Junior N, Mourad PC, Espíndola RF, AbilRuss HH. [Expectation and knowledge among patients with keratoplasty indication]. Rev Bras Oftalmol. 2011;70(4):230-4. Portuguese. Rev Bras Oftalmol. 2014; 73 (5): 282-6 286 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. Lunardelli A, Alvarenga RB, Assmann ML, Brum DEL, Barison MA Fabris C, Corrêa ZM, Marcon AS, Castro TN, Marcon IM, Pawlowski C. [Retrospective study of penetrating keratoplasty at the Santa Casa of Porto Alegre]. Arq Bras Oftalmol. 2001;64(5):449-53. Portuguese. Marcomini LA, Sobral RM, Seixas GO, Sousa SJ. [Corneal selection for transplants]. Rev Bras Oftalmol. 2011;70(6):430-6. Portuguese. Pantaleão GR, Zapparolli M, Guedes GB, Dimartini Junior WM, Vidal CC, Wasilewski D, et al. [Evaluation of the quality of donor corneas in relation to the age of donor and cause of death]. Arq Bras Oftalmol. 2009;72(5):631-5. Portuguese. Bensoussan D, Jeulin H, Decot V, Agrinier N, Venard V. Analyses of the effects of collection and processing time on the results of serology testing of cadaveric cornea donors. Diagn Microbiol Infect Dis. 2010;68(1):40-5. Viegas MT, Pessanha LC, Sato EH, Hirai FE, Adán CB. [Discarded corneas due to positive donor’s serologic test in the Hospital São Paulo Eye Bank: a two-year study]. Arq Bras Oftalmol. 2009;72(2):180-4. Portuguese. Mello GH, Massanares TM, Guedes GB, Wasilewski D, Moreira H. [Study of cornea potential donors at the Clinical Hospital of UFPR]. Rev Bras Oftalmol. 2010;69(5):290-3. Portuguese. Shiratori CN, Hirai FE, Sato EH. [Characteristics of corneal donors in the Cascavel Eye Bank: impact of the anti-HBc test for hepatitis B]. Arq Bras Oftalmol. 2011;74(1):17-20. Portuguese. Almeida Sobrinho EF, Negrão BC, Almeida HG. [Epidemiological profile of patients waiting for penetrating keratoplasty in state of Pará, Brazil]. Rev Bras Oftalmol. 2011;70(6):384-90. Portuguese. Calix Netto MJ, Giustina ED, Ramos GZ, Peccini RF, Sobrinho M, de Souza LB. [Major indications for corneal penetrating keratoplasty at a reference service in São Paulo state (Sorocaba - SP, Brazil)]. Arq Bras Oftalmol. 2006;69(5):661-4. Portuguese. Cattani S, Kwitko S, Kroeff MA, Marinho D, Rymer S, Bocaccio FL. [Indications for corneal graft surgery at the Hospital de Clínicas of Porto Alegre]. Arq Bras Oftalmol. 2002;65(1):95-98. Portuguese. Rev Bras Oftalmol. 2014; 73 (5): 282-6 15. Hirai FE, Adán CB, Sato EH. [Factors associated with quality of donated corneas in the Hospital São Paulo Eye Bank]. Arq Bras Oftalmol. 2009;72(1):57-61. Portuguese. 16. Cornea Donor Study Investigator Group, gal RL, Dontchev M, Beck RW, Mannis MJ, Holland EJ, Kollman C, Dunn SP, Heck EL, Lass JH, Montoya MM, Schultze RL, Stulting RD, Sugar A, Sugar J, Tennant B, Verdier DD. The effect of donor age on corneal transplantation outcome results of the cornea donor study. Ophthalmology. 2008;115(4):620-626.e6. 17. Al-Muammar A, Hodge WG. Donor age as a predictor of cornea transplant success. Can J Ophthalmol. 2005;40(4):460-6. 18. Saldanha BO, Oliveira RE Jr, Araújo PL, Pereira WA, Simão Filho C. Causes of nonuse of corneas donated in 2007 in Minas Gerais. Transplant Proc. 2009;41(3):802-3. 19. Caetano MM, Beck ST. [Importance of anti-HBC antibodies determination in blood transfusion centers to prevent the posttransfusional hepatitis B virus (HBV)]. RBAC. 2006;38(4):235-7. Portuguese. 20. Ferreira WA, Ávila SL. Diagnóstico laboratorial: das principais doenças infecciosas e auto-imunes. 2a ed. Rio de Janeiro: Guanabara Koogan; 2001. 21. Khattab E, Chemin I, Vuillermoz I, Vieux C, Mrani S, Guillaud O, et al. Analysis of HCV co-infection with occult hepatitis B virus in patients undergoing IFN therapy. J Clin Virol. 2005;33(2):150-7. 22. Helmy A, Al-Sebayel MI. Isolated antibody to hepatitis B core antigen in patients with chronic hepatitis C virus infection. World J Gastroenterol. 2006;12(27):4406-10. Corresponding author: Dário Eduardo de Lima Brum Serviço de Hemoterapia, Irmandade Santa Casa de Misericórdia de Porto Alegre Rua Professor Annes Dias, nº 295- CEP 90020-09 - Porto Alegre (RS), Brazil - Phone: 55 (51) 3214-8263 E-mail: [email protected] ORIGINAL ARTICLE 287 Sealing the gap between conjunctiva and Tenon’s capsule in primary pterygium surgery Adição do selamento entre conjuntiva e cápsula de Tenon em cirurgia de pterígio primário Ricardo Alexandre Stock1, Luan Felipe Lückmann2, Gabriel Alexander Ken-Itchi Kondo2, Elcio Luiz Bonamigo1 A BSTRACT Objective: To assess the results of an alternative surgical approach in the excision of primary pterygium by analyzing the rates of recurrence and of intraoperative and postoperative complications. Methods: Retrospective cross-sectional study based reviewing the clinical records of individuals subjected to surgery for pterygium, with conjunctival autograft transplantation, fibrin glue and intraoperative application of mitomycin C. In addition, sealing was performed by suturing the gap between the conjunctiva and Tenon’s capsule. A total of 36 eyes from 35 individuals were subjected to the assessed techniques. The study variables were complications of surgery and recurrence rates during a minimun follow-up period of 6 months. Results: No recurrence occurred during the follow-up period. One graft (2.8%) exhibited partial retraction, but pterygium did not recur. The intraocular pressure increased in one eye (2.8%) and was controlled by clinical methods. Conclusion: Eyes in which a barrier was established between the conjunctiva and Tenon’s capsule by sealing the gap between them showed an absence of recurrence in the sample studied. However, there is the need of a random prospective study with a control group for a more accurate conclusion on the efficacy of the technique. Keywords: Pterygium/surgery; Autografts; Transplantation, autologous; Mitomycin/therapeutic use; Fibrin tissue adhesive; Recurrence RESUMO Objetivo: Avaliar os resultados de uma abordagem cirúrgica alternativa na excisão de pterígio primário por meio da observação das taxas de recidiva e de complicações intraoperatórias e pós-operatórias. Métodos: Estudo retrospectivo e transversal realizado a partir da revisão de prontuários de pacientes submetidos à cirurgia de pterígio com transplante autólogo de conjuntiva, cola de fibrina e aplicação intraoperatória de mitomicina C. Além disso, foi realizado através de sutura, o selamento da lacuna entre a conjuntiva e cápsula de Tenon. No total, 36 olhos de 35 pacientes foram submetidos à técnica. As variáveis do estudo foram complicações da cirurgia e taxas de recidiva durante um período mínimo de 6 meses de seguimento. Resultados: Não foram constatadas recidivas durante o tempo de seguimento. Um enxerto (2,8%) desenvolveu retração parcial, sem posterior recorrência do pterígio, e um olho (2,8%) apresentou aumento da pressão intraocular, que foi controlada clinicamente. Conclusão: A criação de uma barreira entre a conjuntiva e cápsula de Tenon, por meio do selamento da lacuna, mostrou ausência de recidiva na amostra estudada. Necessita-se, no entanto, de um estudo prospectivo randomizado com grupo controle para uma conclusão mais precisa da eficácia da técnica. Descritores: Pterígio/cirurgia; Autoenxerto; Transplante autólogo; Mitomicina/uso terapêutico; Adesivo tecidual de fibrina; Recidiva 1 2 Department of Ophthalmology, Universidade do Oeste do Estado de Santa Catarina, Campus de Joaçaba (SC), Brazil; Student, Medical School, Universidade do Oeste do Estado de Santa Catarina, Campus de Joaçaba (SC), Brazil. Study conducted at the Department of Ophthalmology, Universidade do Oeste de Santa Catarina - Campus de Joaçaba, SC, Brazil The authors have no public and private financial support, or financial interest Received for publication 01/07/2014 - Accepted for publication 11/07/2014 Rev Bras Oftalmol. 2014; 73 (5): 287-90 288 Stock RA, Lückmann LF, Kondo GAKI, Bonamigo EL INTRODUCTION P terygium, from the Greek, “pterygos”, small wing, is a triangle- or trapezoid-shaped fibrovascular growth of the conjunctiva, usually located in the nasal side of the sclera and extending towards the cornea (1,2). Its growth over time can cause visual and esthetic problems, impairing the quality of life of the patients and consequently requiring surgical removal. Although it is a common eye problem, its standard surgical treatment has not yet been established. The high rates of postoperative recurrence, which exhibit remarkable variation among studies, are the main challenge patients and surgeons must address. Simple excision with bare sclera was widely performed in the past; however, the associated recurrence rates were unacceptable, as they could reach as high as 50% (²). In addition to other factors that influence the treatment outcomes, such as the pterygium morphological characteristics, some demographic variables and the postoperative regimen, surgical parameters not yet fully elucidated lead to divergent results (3). In this regard, some authors observed that a gap is inevitably created between the conjunctiva and Tenon’s capsule after the excision of pterygium and Tenon’s resection, through which fibrovascular tissue remnants can pass to cause recurrence. By closing this gap during surgery, the recurrence rate achieved in one study was only 3.1% in all the groups, thus pointing to the potential utility of this technique (3). Therefore, the aim of this study was to assess the response to surgical treatment of primary pterygium including sealing of the gap between the conjunctiva and Tenon’s capsule, combined with conjunctival autograft transplantation using fibrin glue and the application of mitomycin C (MMC). METHODS The clinical records of individuals subjected to excision of primary pterygium using intraoperative MMC, nonpedunculated conjunctival autograft transplantation fixated with fibrin glue and the sealing of the gap by means of a suture between the conjunctiva and Tenon’s capsule, from february 2011 to august 2012, were retrospectively reviewed. The records were available at the database of BellotoStock Ophthalmology Center (Centro Oftalmológico BellotoStock), where the patients were assisted before and after surgery. During this period, this technique was applied to all of the patients who underwent pterygium surgery. Only individuals who were followed up for at least six months after surgery were included in the study. Cases of recurrent pterygium and cases that did not complete the minimum follow up period were excluded from analysis. The total sample comprised 36 eyes from 35 individuals. The following data were collected before surgery: age, gender and pterygium localization. The same surgeon (R.A.S.) performed all the surgical procedures at Santa Terezinha University Hospital (Hospital Universitário Santa Terezinha - HUST), Joaçaba (SC), Brazil, always using the same surgical and antiseptic techniques. The surgical technique was based on the one described by Liuet al. (3) The procedure started with peribulbar anesthesia using 2% lidocaine and 0.75% bupivacaine in 1:1 ratio. Asepsis was performed using 5% povidone-iodine followed by the placement of sterile surgical drapes and the eye speculum. Using conjunctival scissors, the pterygium body and underlying Tenon’s capsule were dissected. The underlying Tenon’s capsule was minimally resected 1mm below the conjunctival edge, and cauterization was kept to a minimum. A Rev Bras Oftalmol. 2014; 73 (5): 287-90 surgical sponge was soaked in 0.02% MMC (Ophtalmos, São Paulo, Brazil) and placed on the bare sclera for two minutes. The sponge was then removed, and the eye was copiously irrigated with a balanced salt solution (BSS – Alcon, Fort Worth, USA). Finally, the pterygium head was resected. The gap invariably created between the conjunctiva and the underlying Tenon’s capsule following pterygium excision was first identified using two 0.12-mm forceps, one to grab the conjunctiva and the other to grab the Tenon’s capsule. The gap was then sealed by means of continuous suture with Vicryl 8.0 (Ethicon, Johnson & Johnson, São Paulo, Brazil) of both tissues, which blocked the emanation of fibrovascular tissue and restored the normal morphological features of the caruncle (Figure 1)(4). The surgeon trained for the procedure by attending the course “Surgical Strategies for Recurrent Pterygium With or Without Motility Restriction” promoted by the American Academy of Ophthalmology (AAO) and taught by Scheffer C. G. Tseng MD PhD. Figure 1: Concept of sealing of the gap; fibrovascular tissue sandwiched between the conjunctiva (pink) and the Tenon capsule (green) flattens the caruncle (A, solid arrow) and anteriorly displaces the semilunar fold (A, broken arrow), causing recurrent pterygium (D); this gap is invariably created when the pterygium head and body is removed (B); the gap is best demonstrated by two 0.12-mm forceps grabbing each tissue edge (E); when the gap is sealed, the dome-shaped caruncle is recreated by pulling the Tenon capsule when it naturally retracts posteriorly (C, arrow), and the surrounding conjunctival edge is also bent and rounded (F) Source: Liu et al., JAMA, 2012. The techniques to elaborate and fixate the conjunctival autograft were based on the techniques described by Kenyon et al. (4) and Koranyi et al. (5), respectively. The ipsilateral inferior conjunctival graft was marked horizontally and vertically and dissected without the Tenon’s capsule and with a margin of 2 mm larger than the excised conjunctiva measurements. The free conjunctival graft was then transplanted to the receiving bed while complying with the limbus to limbus origin. The graft was fixed to the receiving site using fibrin glue Evicel® (Omrx Biopharmaceuticals, Ramat Gan, Israel). First, one drop of fibrinogen solution was applied to the scleral bed; then,the graft was placed on the bed, and one drop of thrombin and calcium chloride solution was applied on top. The excess glue was removed, and the graft was trimmed wherever necessary. Finally, moxifloxacin (Vigamox®, Alcon, São Paulo, Brazil) was administered, followed by a single subconjunctival application of betamethasone (Celestone®, Mantecorp, São Paulo, Brazil). An dressing was applied, which was removed 24 hours later. During the postoperative period, the following was prescribed: one drop of moxifloxacin eyedrops (Vigamox®, Alcon, São Paulo, Brazil) every four hours over 15 days; one drop of prednisolone acetate (PredFort®, Allergan, São Paulo, Sealing the gap between conjunctiva and Tenon’s capsule in primary pterygium surgery Brazil) every two hours over 15 days, tapered along two months; and one drop of eye lubricant (Optive®, Allergan, São Paulo, Brazil) every three hours as needed. The patients were assessed on days 1, 15, 30, 60, 120 and 180 and then every three months as to occurrence of relapse, which was defined as any growth of fibrovascular tissue that reached the corneal surface and extended beyond the limbus in the area corresponding to the excised pterygium. The Vicryl suture was removed two weeks after surgery with scissors under a slit lamp following the instillation of anesthetic eye drops. In the follow-up visits, the participants were subjected to slit lamp biomicroscopic examination, assessment of visual acuity and degree of conjunctival hyperemia and measurement of the intraocular pressure (IOP), and external photographs of all the eyes were acquired. To construct tables and graphics, the data were entered in a Microsoft Excel 2007 (Microsoft Corporation, Redmond, USA) spreadsheet. The study started after approval by the Research Ethics Committee of the University of West Santa Catarina on july 25 2012, ruling nº 66686. 289 Figure 2: A) Clinical appearance of partial graft retraction two weeks after surgery; B) Appearance three months after surgery; C) Appearance six months after surgery R ESULTS The sample comprised 35 volunteers, 18 males (51.4%) and 17 females (48.6%). Twenty-one participants (60%) had pterygium in the right eye (RE), 13 (37.1%) in the left eye (LE) and one (2.9%) in both eyes. All the lesions were primary and located on the nasal side of the sclera (table 1). Table 1 Demographic and clinical data of individuals with primary pterygium treated by gap sealing Average age in years Age in years (minimum and maximum) Gender (n) Male Female Pterygium side (n) Right eye Left eye Both eyes 44.37 (±10.72) 29 – 71 18 (51.4%) 17 (48.6%) 21 (60%) 14 (37.1%) 1 (2.9%) The average age of the participants on the date of surgery was 44.37 years old, standard deviation (SD) ± 10.87, varying from 29 to 74 years old. Fourteen participants (40%) were 20 to 39 years old, 17 (48.5%) were 40 to 59 years old, and four (11.5%) were 60 years old or older. The duration of follow-up lasted 6 to 22 months, mean= 9 months, SD= ±3.69, and all of the patients completed the minimum follow-up period adopted. None of the 36 eyes exhibited pterygium recurrence during the follow-up period. No intraoperative complications occurred. One eye (2.8%) exhibited partial graft retraction, which did not require additional intervention and was not classified as recurrence due to later occurrence of conjunctivalization, which was complete by day 30 after surgery (figure 2). Another eye (2.8%) exhibited a moderate increase in the IOP, which was successfully handled by discontinuing the corticoid eye drops and introducing antiglaucoma eye drops. The esthetic results of the grafts were satisfactory, and the donor sites exhibited full recovery in all cases, while no instance of symblepharon, graft loss or excessive bleeding occurred during or after surgery (figure 3) Figure 3: A) Clinical appearance before surgery; B) Clinical appearance six months after surgery DISCUSSION Although many attempts have been made at improving the surgical treatment of pterygium, there is not yet a consensus on the ideal technique, and the recurrence rates after surgical excision exhibit remarkable variation among studies. Recently, quite complex approaches have been developed to reduce such variation and the rates of recurrence. The technique selected in this study was the surgical excision of the pterygium, with minimal resection of Tenon’s capsule combined with conjunctival autograft transplantation using fibrin glue and intraoperative application of MMC, which are usual techniques, in addition to an alternative procedure: the sealing of the gap between the conjunctiva and Tenon’s capsule by means of suture. The proponents of this technique (3) recommend the resection of Tenon’s capsule to be minimal and its suture with the conjuntiva to be continuous. The aim of surgical sealing is to hinder the propagation of residues of the fibrovascular tissue across the gap created between the conjunctiva and Tenon’s capsule after the pterygium excision, thus preventing its recurrence (3). Although the study that first demonstrated the efficacy of this procedure was conducted with individuals exhibiting multiple pterygium recurrence, the authors suggested the possibility of applying it to the treatment of primary pterygium (3). That comment motivated the performance of this study, which included a sample exclusively composed of individuals with primary pterygium. The sealing of the gap by continuous sutures was successful in all the treated eyes, and the continuous sutures proved to be effective to restore a normal caruncle compared to the use of anchored sutures or anchored sutures combined with fibrin glue (3). The procedure was brief, and the gaps were easily identified in all cases. Rev Bras Oftalmol. 2014; 73 (5): 287-90 290 Stock RA, Lückmann LF, Kondo GAKI, Bonamigo EL In contrast to other authors (3) who used cryopreserved amniotic membrane grafts, conjunctival autografts were preferred in this study. This choice was based on the results of a randomized study (6) and an official AAO report (7) describing significantly lower recurrence rates in the cases in which conjunctival autografts were used versus amniotic membrane grafts. One further peculiarity of the conjunctival grafts in the present study was the donor site. As a rule, grafts are taken from the ipsilateral upper conjunctiva; however, in this study, they were taken from the ipsilateral inferior conjunctiva to preserve the upper conjunctiva in case the patients might require antiglaucoma surgery in the future. In addition, one study failed to find a significant difference in the recurrence rates when the upper or inferior conjunctival quadrants were used as donor sites for primary pterygium surgery (8). In this study, conjunctival autograft transplantation and the intraoperative application of MMC as an adjuvant treatment were added to gap sealing. The combination of those two procedures for the treatment of primary pterygium, involving fixation of the conjunctival graft to the sclera by means of suture, has been successfully employed in comparative studies (9,10).With regard to recurrent pterygium, two recent studies reported excellent results using a modification of that technique, which consisted of fixing the conjunctival graft with fibrin glue instead of sutures (11,12). The use of fibrin glue helps to reduce the rate of recurrence, postoperative discomfort and the duration of surgery. For those reasons, it was used in this study (5,13) .Those results are lent further support by an official report published by the AAO, according to which the combination of conjunctival autograft transplantation and MMC results in lower rates of recurrence following the excision of pterygium, compared to each procedure alone (7).In addition, the combination of the two procedures allows reduction of the dose and the intraoperative exposure of MMC, which makes the technique safer (14). Using these technical improvement (i.e., gap sealing, conjunctival autograft transplantation fixated with fibrin glue and intraoperative MMC), the recurrence rate was ideal, i.e., 0%, during the follow-up period. Among the studies that applied a similar technique, only one achieved 0% recurrence (10), while the other studies reported low recurrence rates, to wit, 2% (9), 3.5% (11) and 9.2% (14). In one study that performed conjunctival autograft transplantation only with fibrin glue, but did not include gap sealing, the recurrence rate was higher, at 11.3% (15).In the study most similar to this one, which also performed gap sealing in all the treated eyes, the adjusted recurrence rate was 3.1% in all the groups (3). The average duration of follow-up after surgery was 9 months; a period of 6 months is considered sufficient to detect 50% to 86% of the instances of relapse (16), while 93% of such cases are detected when follow-up is extended to 9 months (17). Moderate inflammation might occur during the first two weeks after surgery due to the presence of the Vicryl suture, which fully disappears following its removal. For that reason, topical corticoids should be used more intensively during that period, and the dose should be reduced after suture removal. No intraoperative complications occurred in this series. In one eye (2.8%), the graft exhibited partial retraction during the first days after surgery, but no intervention was required, and pterygium did not recur. The retraction was possibly due to excessive Tenon’s capsule remnants identified on slit lamp examination. That complication also occurred in one of the 28 eyes treated in another study (11). One eye (2.8%) exhibited a moderate increase in IOP, which was attributed to the topical corticoid used after surgery. That condition was fully controlled following discontinuance of the corticoid eye drops and the institution of clinical treatment. Rev Bras Oftalmol. 2014; 73 (5): 287-90 CONCLUSION The pterygium recurrence rate was 0% in the studied sample, and the two post-operative complications receded spontaneously or with the aid of a clinical treatment. Although the result was promising, a prospective randomized trial comparing groups treated with and without sealing of the gap between the conjunctiva and Tenon’s capsule is needed to establish more precise conclusions regarding the efficacy of that technique in the treatment of primary pterygium. R EFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. Duke-Elder S. System of ophthalmology: disease of the outer eye. Vol. VIII. Parte I. London: Henry Kimpton, 1977. Hirst L. The treatment of pterygium. Surv Ophthalmol. 2003; 48(2): 145-80. Liu J, Fu Y, Xu Y, Tseng SG. New grading system to improve the surgical outcome of multirecurrent pterygia. Arch Ophthalmol. 2012;130(1):39-49. Kenyon KR, Wagoner MD, Hettinger ME. Conjunctival autograft transplantation for advanced and recurrent pterygium. Ophthalmology. 1985;92(11):1461-70. Koranyi G, Seregard S, Kopp ED. Cut and paste: a no suture, small incision approach to pterygium surgery. Br J Ophthalmol. 2004;88(7):911-4. Luanratanakorn P, Ratanapakorn T, Suwan-Apichon O, Chuck RS. Randomised controlled study of conjunctival autograft versus amniotic membrane graft in pterygium excision. Br J Ophthalmol. 2006;90(12):1476-80. Kaufman SC, Jacobs DS, Lee WB, Deng SX, Rosenblatt MI, Shtein RM. Options and adjuvants in surgery for pterygium: a report by the American Academy of Ophthalmology. Ophthalmology. 2013;120(1):201-8. Shrestha A, Shrestha A, Bhandari S, Maharjan N, Khadka D, Pant SR. Inferior conjunctival autografting for pterygium surgery: an alternative way of preserving the glaucoma filtration site in far western Nepal. Clin Ophthalmol. 2012;6:315-9. Segev F, Jaeger-Roshu S, Gefen-Carmi N, Assia EI. Combined mitomycin C application and free flap conjunctival autograft in pterygium surgery. Cornea. 2003;22(7):598-603. Frucht-Pery J, Raiskup F, Ilsar M, Landau D, Orucov F, Solomon A. Conjunctival autografting combined with low-dose mitomycin C for prevention of primary pterygium recurrence. Am J Ophthalmol. 2006;141(6):1044-50. Shehadeh-Mashor R, Srinivasan S, Boimer C, Lee K, Tomkins O, Slomovic AR. Management of recurrent pterygium with intraoperative mitomycin C and conjunctival autograft with fibrin glue. Am J Ophthalmol. 2011;152(5):730-2. Bakshi R, Gupta H, Khurana C, Sachdev MS. Conjunctival limbal autograft with fibrin glue with mitomycin-C in managing recurrent pterygium. Cornea. 2003;22:598-603. Koranyi G, Seregard S, Kopp ED. The cut-and-paste method for primary pterygium surgery: long-term follow-up. Acta Ophthalmol Scand. 2005;83(3):298-301. Wong VA, Law FCH. Use of mitomycin C with conjunctival autograft in pterygium surgery in Asian-Canadians. Ophthalmology. 1999;106(8):1512-5. Coral-Ghanem R, Oliveira RF, Furlanetto E, Ghanem MA, Ghanem VC. Transplante autólogo de conjuntiva com uso de cola de fibrina em pterígios primários. Arq Bras Oftalmol. 2010;73(4):350-3. Avisar R, Arnon A, Avisar E, Weinberger D. Primary pterygium recurrence time. Isr Med Assoc J. 2001;3(11):836-7. Ti S, Chee S, Dear K, Tan D. Analysis of variation in success rates in conjunctival autografting for primary and recurrent pterygium. Br J Ophthalmol. 2000;84(4):385-9. Corresponding author: Ricardo Alexandre Stock Rua Rio Branco, 589 – Joaçaba (SC), Brazil Telephone: +55 (49) 3522-0788 - Fax:+55 (49) 3522-5059 E-mail: [email protected] ORIGINAL ARTICLE 291 Visual impairment, rehabilitation and International Classification of Functioning, Disability and Health Deficiência visual, reabilitação e Classificação Internacional de Funcionalidade, Incapacidade e Saúde Marissa Romano da Silva1, Maria Inês Rubo de Souza Nobre2, Keila Monteiro de Carvalho3, Rita de Cássia Ietto Montilha2 A BSTRACT Objective: To describe the characteristics of people with visual impairment who participated in the Visual Rehabilitation Groups, according to the ICD-10 and the International Classification of Functioning, Disability and Health (ICF). Methods: Quantitative, cross-sectional survey, developed in a university rehabilitation research center between october and december 2012. The users from the Visual Rehabilitation Groups were invited; 13 of them agreed to participate. We performed an occupational therapy evaluation – with anamnesis, performance evaluation and functional vision assessment – an analysis of medical charts and patient description with the use of the ICF. Results: The major causes of visual impairment were diabetic retinopathy, glaucoma, optical neuritis and keratoconus. Some functions and structures of the body, performance and capabilities in activities and participation, environmental factors facilitators or limiters were highlighted in this study, allowing the description of the characteristics of each participant through the functionality and the improvement of the therapeutic planning. Assistive technologies, optical and nonoptical aids used and their everyday benefits were presented. Conclusion: Visual loss, at any level, led to functional impairments, limiting and restricting the participation and performance in everyday activities, interfering with the individuals’ independence, autonomy and quality of life. However, the use of optical aids, non-optical aids and environmental adaptations proved to be beneficial for increasing the functionality, showing the influence of external factors on the performance. Knowing and recognizing the existence of diversities within the visual impairment universe allows us to understand who the treated individual is, avoiding the generalization by the visual condition. The ICF showed to have a fundamental role in this context. Keywords: International Classification of Functioning Disability and Health; International Classification of Diseases; Rehabilitation; Blindness; Low vision; Activities of daily living 1 Masters in Health, Interdisciplinary and Rehabilitation Program, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas (SP), Brazil; 2 Centro de Estudos e Pesquisas em Reabilitação “Prof. Dr. Gabriel O.S. Porto”, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas (SP), Brazil; 3 Department of Ophtmalogy, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas (SP), Brazil. The authors have no public and private financial support, or financial interest Received for publication 17/06/2014 - Accepted for publication 13/07/2014 Rev Bras Oftalmol. 2014; 73 (5): 291-301 292 Silva MR, Nobre MIRS, Carvalho KM, Montilha RCL RESUMO Objetivo: Descrever as características das pessoas com deficiência visual participantes de Grupos de Reabilitação Visual, segundo a CID-10 e a Classificação Internacional de Funcionalidade, Incapacidade e Saúde (CIF). Métodos: Pesquisa quantitativa de corte transversal, desenvolvida em um centro universitário de pesquisas em reabilitação entre outubro e dezembro de 2012. Usuários de Grupos de Reabilitação Visual foram convidados, sendo 13 os que aceitaram participar. Foi realizada avaliação de terapia ocupacional – com anamnese, avaliação de desempenho e avaliação funcional da visão – consulta aos prontuários e a classificação dos participantes utilizando a CIF. Resultados: As principais causas de deficiência visual foram retinopatia diabética, glaucoma, neurite óptica e ceratocone. Algumas funções e estruturas do corpo, desempenho e capacidades em atividades e participação, fatores ambientais facilitadores ou limitadores foram destacados neste estudo, possibilitando descrever as características de cada participante por meio de sua funcionalidade e auxiliando no planejamento terapêutico. Tecnologias assistivas, auxílios ópticos e não ópticos utilizados e seus benefícios cotidianos foram apresentados. Conclusão: A perda visual, em qualquer nível, levou a prejuízos funcionais, limitando e restringindo a participação e o desempenho em atividades cotidianas, interferindo na independência, autonomia e qualidade de vida dos sujeitos. Entretanto, o uso de recursos ópticos, não ópticos, auxílios e adaptações ambientais mostraram-se benéficos para a ampliação da funcionalidade, evidenciando a influência de fatores externos no desempenho do indivíduo. Conhecer e reconhecer a existência da diversidade dentro do universo da deficiência visual possibilita entender quem é o sujeito atendido, evitando a generalização pela condição visual, tendo a CIF papel fundamental nesse contexto. Descritores: Classificação Internacional de Funcionalidade, Incapacidade e Saúde; Classificação Internacional de Doenças; Reabilitação; Cegueira; Baixa visão; Atividades cotidianas INTRODUCTION C urrent estimates of the World Health Organization reveal that there are 314 million visually impaired people in the world – 269 million of these have subnormal vision and 45 million are blind (1-3), including uncorrected refractive errors. Etiologies are related to biological and contextual factors, mostly preventable, treatable and curable (2,4-5), associated to nutritional and infectious factors, lack of available technology, tobacco use, ultraviolet radiation exposure, vitamin A deficiency, high body mass index and metabolic disorders (1-2,5). The main causes of visual impairment in the world are uncorrected refractive error, cataracts, age-related macular degeneration, diabetic retinopathy, trachoma and corneal opacity (1-3,5-6). Vision is an afferent which is able to promote integration with other sensory information. It is a continuous stimulus that enables self-directed and intentional motor conducts, critical to locate and identify distant objects that cannot be captured by other senses, understand spatial relations, the position of the body in relation to space, capture effectively and quickly the environment in safe and confident manner, maintaining proper body posture, among other functions (7-9). Visual loss causes a sensory imbalance, to which the human body itself is not prepared to face, requiring adaptation and support (7). Thus, any visual impairment affects the individual’s health in all its aspects and brings it to functional impairments, generating interference in quality of life (9-11). Activities ranging from independent mobility inside and outside the house, carrying out basic and instrumental daily actions such as bathing, dressing, going to the grocery store or the bank, as well as to social activities, leisure and work, all of them may represent impairment in the daily life of the visually impaired (11-13). Along with the individual limitations there are the physical and social environmental factors that may constitute, respectively, architectural and attitudinal barriers. Rehabilitation is inserted in this context which can be defined as a process that is built according to the individuals´ constant identification of needs and demands, involving their current health condition, interests, context and expectations. Actions in rehabilitation should include the assistance of a Rev Bras Oftalmol. 2014; 73 (5): 291-301 multispecialty team in order to provide timely and complete support to individuals with disabilities (2,11,14-15). According to the experiences of Lamoureux et al. (12), Aciem e Mazzotta (13) e Bittencourt et al. (16), the rehabilitation of the visual impairment has shown to be effective in the improvement of the users´ quality life in the services studied. To assist in this process, the International Classification of Functioning, Disability and Health (ICF) is to establish tasks as a standardized language on health and its conditions, enabling scientific basis for understanding health and its correlated states , comparing health actions on the same subject, helping in the decision making for the individualized rehabilitation process (17). The ICF puts functioning and disability under new perspectives, recognizes disability as a condition not of a minority but as an inherent human experience. Considering the strong influence of the context, it comprehends the relationship of health and environment as dynamic, which may give rise to changes in the health status of the subject. Moreover, it changes the focus in the disease classification since it favors the classification of the impacts of this disease on the individuals’ lives (17). The ICF is a milestone in legitimizing the Social Model in health and human rights, enabling communication between the Biomedical and Social Models. The university research center in rehabilitation involved in this research works on the rehabilitation of the visually impaired. One of the modalities of assistance which are practiced concerns the Visual Rehabilitation Groups, which are proposed to discuss immediate issues related to disability and rehabilitation, enabling participants to share their difficulties and strategies in solving them. This research was conducted with the aim of describing the characteristics of people with visual impairments, participants in the Visual Rehabilitation Groups, according to the International Classification of Diseases, Tenth Revision (ICD10) and the ICF. METHODS This is a quantitative cross-sectional research, developed in a university research center in rehabilitation. To participate in the study, the subjects should have the ICD-10 corresponding to visual impairment (18), aged over 18 Visual impairment, rehabilitation and International Classification Of Functioning, Disability And Health years and attending the Visual Rehabilitation Group of a university research center. As exclusion criteria is the non acceptance and not signing the consent form. The users inserted in the Visual Rehabilitation Groups (total = 19), from october to december 2012 were invited, with the elucidated objectives and procedures of the research. Thirteen people agreed to participate in this study. After the acceptance of those who attended, it was asked on a date and time for signing the consent form and the evaluation of the occupational therapy. At this time, the medical records of each participant were consulted as source of data on the cause of the visual loss, visual acuity and other information related to the eye health. Evaluation of the occupational therapy comprising history, performance evaluation and functional vision assessment was performed. Such procedures which lasted about 40 minutes were videotaped and analyzed by two examiners, and described using the International Classification of Functioning, Disability and Health (ICF). The ICF belongs to the family of international classifications developed by the WHO which encompasses aspects of human health and components related to welfare. It describes them in terms of health domains (such as seeing, hearing, and walking) and health-related fields (such as transportation, social interaction). It is proposed to describe situations related to the human functioning and restrictions, as an organizing structure of information in a model that can be “significant, integrated and accessible” (17). This classification is divided into two sections, part 1 refers to the functionality and disability and part 2 concerns contextual factors. Each one of the parts is subdivided into two components, which receive specific alphanumeric codes in order to be differentiated: part 1 includes the functions of the body (letter b for body), Body Structures (letter s for structure) and activities and participation (letter d for domain), while part 2 covers the environmental factors (letter e for environment) and personal factors (17). The functions and structures of the body relate to physiological functions and anatomical parts of the body, respectively. Problems in the functions and/or structures of the body are considered impairments. Activities and participation include, in this order, the execution of a task by the individual 293 and his involvement in everyday situations. Difficulties in implementing the activities are called limitations while problems in performing these activities are called participation restrictions. Finally, environmental factors include the physical, social and attitudinal environment in which individuals are placed. For the ICF, all these components interact dynamically, considering functioning, disability and health as an interactive and evolutional process (17). The components of the classification are followed by numerical codes, the first is representative of the number of the chapter (one digit), followed by the second level (two digits) and the third and fourth levels (one digit each). The codes are only complete when adding the qualifier, which indicates the magnitude of the issue. The qualifiers are present after the period (or delimiter). Without the qualifier number, the codes of the ICF have no meaning. The components of part 1 (Body Functions and Structures, Activities and Participation) are qualified by the same general range of numbers (0-4). For the Functions and Structures of the body the qualifier is the magnitude of the impairment. The Structures of the body receive three different levels of qualifiers, the first qualifier for the degree of the commitment generated (0-4), the second corresponds to the nature of structural change (0-7) and finally brings the third location of this change (0-7) (table 1). For the component Activities and Participation are the constructs of this Performance and Capacity. The Performance (first qualifier) is what the subject does in his usual environment, while capacity (second qualifier) is what the subject is able to do in his likely maximum level of functionality without assistance. The third qualifier refers to the level of the subject’s ability to perform that activity with assistance. Finally, for the Environmental Factors, qualifiers can be called barriers or facilitators, depending on the effects of that factor in the subject’s life. Any barriers as facilitators have the same numerical scale (0-4), but the separation between the code and the domain qualifier takes place by means of a period (.) for barriers and a plus sign (+) for facilitators. After classification, the results of the participants were described in tables and charts with frequencies of ophthalmic diagnoses, limitations, restrictions, physical and attitudinal environmental barriers (17). The study was approved by the Ethics Committee on Research by the ruling nº 143.693/2012. Table 1 Structures of the body First qualifier xxx.0 xxx.1 xxx.2 xxx.3 xxx.4 NO Impairment LIGHT Impairment MODERATE Impairment SEVERE Impairment COMPLETE Impairment Second qualifier Third qualifier 0 No change in the structure 1 Total absence 2 Partial absence 3 Additional part 4 Abnormal dimensions 5 Discontinuity 6 Deflected position 7 Qualitative changes in the structure, including accumulation of fluid 0 More than one region 1 Right 2 Left 3 Both sides 4 Front part 5 Back part 6 Proximal 7 Distal Source: WHO, 2003 Rev Bras Oftalmol. 2014; 73 (5): 291-301 294 Silva MR, Nobre MIRS, Carvalho KM, Montilha RCL Table 3 R ESULTS The sample consisted of 13 participants, 54% were female, mean age of 44 years (± 18.42), and a large share of it in relation to the employment condition is off work (62%). The main causes of visual impairment which were presented were diabetic retinopathy, glaucoma, keratoconus and optic neuritis (15% each). With regard to the type of visual impairment, 77%, presented low vision, most of them were acquired (92%) (table 2). Number of participants by gender, according to visual impairment Gender H54.0a ƒ % H54.1b ƒ % H54.2 ƒ % n=13 Total ƒ % Female Male Total 1 2 3 3 2 5 3 2 5 7 6 13 8 15 23 23 15,5 38,5 23 15,5 38,5 54 46 100 a H54.0: Blindness in both eyes; bH54.1: Blindness, one eye, low vision in the other; c H54.2: Subnormal vision in both eyes Table 2 Sample characterization n=13 ƒ Gender Female Male Average age Marital status Married Single Divorced Widow/Widower Work Conditions On sick leave Employed Retired Unemployed Ophthalmic Diagnosiss Diabetic retinopathy Glaucoma Optic neuritis Keratoconus Retinitis pigmentosa Macular chorioretinitis Age-related macular degeneration Central serous maculopathy Cortical Visual Impairment Acquired Congenital Ophthalmologic diagnosis and body structure changes, according to the ICF 7 54 6 46 44 (±18,42) 6 46 5 38 1 8 1 8 8 2 2 1 62 15 15 8 2 2 2 2 1 1 1 1 1 15 15 15 15 8 8 8 8 8 12 1 92 8 Visual Condition (CID-10) H54.0 Blindness in both eyes 3 H54.1 Blindness, one eye, low vision in the other 5 H54.2 Subnormal vision in both eyes 5 23 38,5 38,5 According to the ICD-10, 23% attendees are blind in both eyes (H54.0), 38.5% are blind in one eye and low vision in the other (H54.1) and 38.5% with low vision in both eyes (H54.2) (table 3). According to the causes of visual impairment, the most affected structures of the eyeball (s220) were: retina (s2203), structure of the cranial nerves (optic nerve, optic tract) (s1106) and cornea (s2201) (table 4). Rev Bras Oftalmol. 2014; 73 (5): 291-301 Table 4 % n=13 Ophtalmologic Diagnosis Body structure ICF Diabetic Retinopathy Retina s2203 Retinitis Pigmentosa Retina 1 Macular Chorioretinitis Retina 1 Age-related macular degeneration Retina 1 Central serous maculopathy Retina 1 Cortical Optic tract s1106 Optic neuritis Optic nerve 2 Keratoconus Cornea s2201 Glaucoma Eyeball s220 ƒ % 2 46 1 23 2 2 15,5 15,5 With regard to body functions by the ICF classification, the monocular acuity of farsighted vision (b21001) for the right eye (RE) presented 1 subject with moderate disability (.2), 5 individuals with severe disabilities (.3) and other 7 people with complete deficiency (.4), while for the left eye (LE) 7 participants were classified with moderate disability (.2), 3 with severe disabilities (.3) and 3 with complete deficiency (.4) for this domain. For binocular acuity of short-sighted vision (b21002), 1 participant presented no difficulty (.0), another subject presented mild disability (.1), 6 subjects showed moderate disability (.2) and 5 presented complete deficiency (.4). Other body functions related to vision are described in table 5 as functions of the visual field (b2101), light sensitivity (b21020), color vision (b21021), contrast sensitivity (b21022) and quality of the visual image (b21023). The analysis of the data related to the component activities and participation, the tasks that are highlighted in this study showed higher difficulty within the repertoire of activities of the participants or significant change in the distribution of subjects compared to the performance and the ability to perform each task, with and without assistance. These activities include the areas of Reading (d166) and the accomplishment of the daily chores (d640), and the categories of walking on different surfaces (d4502) and socialization (d9205). In fields that refer to environmental factors, 4 participants considered the immediate family (e310), extended family (e315) and friends (e320) and their attitudes (e410, e415, e420), as complete facilitators (+4) of process of acceptance of disability, inclusion in the Visual Rehabilitation service and resumption of the daily activities. However, the strangers’ individual attitudes (e445) to 9 participants are deemed social barriers such as light Visual impairment, rehabilitation and International Classification Of Functioning, Disability And Health (.1) to moderate (.2). For a participant (S12), the strangers’ attitudes represent complete barriers (.4), preventing her from leaving her residence to perform certain activities in the community. Products and assistive technology for mobility and personal transportation in internal and external environments (e1201) are often used by 5 people and are considered complete facilitators (e1201 +4) for 4 participants. In the case of visual impairment, this device is the white cane. The cane was presented to 8 other participants and they were trained in groups of visual rehabilitation of a university research center, concerning its correct and safe use since they do not use it daily. Products and assistive technology for communication (e1251), representing specialized writing devices, hardware and software, glasses or contact lenses are used by all the participants to assist in transmitting and receiving information. In addition, all participants reported that they benefit from products and technology used in designing, building and construction (e150), mainly in the categories of entering and exiting public buildings (e1500), such as ramps and level thresholds, and direction, guidance course and designation of places (e1502), using written signs or in Braille signs and embossed surface of the floors. The intensity of light (e2400) is identified by 8 participants as a barrier such as from moderate (.2) to complete (.4) limiting the involvement and performance in the daily activities. As for the quality of light (e2401), 11 participants reported as a facilitator from moderate (+2) to complete (+4), enabling them to fulfill their activities accurately and safely. Regarding non-optical devices, all participants reported using them in everyday life, the most cited: light control, use of contrast, aid to writing and electronic magnification, for carrying out the activities, especially reading. Three participants who are blind use a writing guide for signing their names. As for optical devices, 6 participants use these aids. Out of these, 4 participants use the aid for near and 5 use it for far sight. It is possible to illustrate the CIF rankings in visual impairment through S1 (table 5). With this example there is an attempt to guide the understanding and comprehension of the ICF domains and their practical applicability. The first participant, JVC, 67, is married, 3 daughters and, on sick leave, presents the ophthalmic glaucoma diagnosis and ICD-10 of blindness in both eyes (H54.0). According to the ICF, J. presents complete deficiency in all the Functions of the body (.4), since it is a case of blindness. The structure of the body is most affected, according to the diagnosis of glaucoma, the eyeball (s220.473) completely affected (.4) with a qualitative change in the structure, including accumulation of fluid (7), in both eyes (3). Regarding the activities and participation for the activity of reading (d166) J. presents complete constraint (.4 ) and total participation restrictions (. 4).Without the aid of assistive technology, however, when added to the task of using external resources, the participant begins to perform the activities with less limitations (d166.443). In the activity walking on different surfaces (d4502), the participant has considerable limitation (.3) and restriction (.3), but when there is the use of an aid for wandering the performance comes to moderate difficulty (d4502.332). For the activity accomplishing the daily chores (d640) she shows complete limitation (.4), severe restriction (.3), but with the use of aids she shall perform such activities with slight difficulty (d640.431). Lastly, for the activity of socialization (d9205), J. shows severe difficulty (.3), with little restriction (.1), and after the use of resources, her limitation ceases to exist 295 (d9205.310). For the domains related to environmental factors, S1 is aided by the white cane daily and benefits from this feature completely (e1201+4), while products and assistive technology for communication are used by her (as specialized writing devices, hardware and software), but they facilitate her daily activities moderately (e1251+2). Products and technology used in designing, building and construction for entering and exiting public buildings (e1500), such as ramps and level thresholds are considerable facilitators (e1500+3), enabling her to transit in public buildings with higher security, independence and autonomy. Products and technology used in design, architecture and construction for direction indication, route guidance and designation of places (e1502), using cards in Braille represent for this person, at the time of the evaluation a moderate facilitator (e1502+2) since she has not mastered Braille yet. The intensity of light (e2400) and Quality of light (e2401) for S1 are not considered barriers or facilitators due to their visual condition: blindness in both eyes. J. considers the immediate family (e310), extended family (e315), Friends (e320) and their attitudes as complete facilitators in her everyday life. However, she identifies the strangers’ Individual attitudes (e445) as moderate barriers, discouraging both engagement and conducting social activities. DISCUSSION This research was conducted with the aim of describing the characteristics of people with visual impairment, rehabilitation group participants, according to the ICD-10 and the ICF. After assessing thirteen participants, and following the ICF´s classification, it was possible to identify the causes of visual impairment, the functions and structures of the body with disabilities, the main limitations and constraints faced by these people, the type of disability according to the ICD-10 the frequency of gender, average age, among other characteristics of this population. It was found that the prevalence of low vision in relation to blindness is compatible with national and international findings (1-3,5-6,19-22) . Two major eye diseases found in this study (glaucoma and diabetic retinopathy) are the causes of visual impairment highlighted in Brazilian and global studies with several populations (3,6,19-21,23-26). While glaucoma and age-related macular degeneration are the major causes of visual impairment in subjects from 50 years old on, brazilian studies highlight these diseases in this age group (4,20,23). According to the WHO (6), the number of individuals over 50 years old exceeds the visually impaired other age groups. However, there is the small number of people over this age inserted the Visual Rehabilitation Groups (n = 3) and that may be the cause of such low demand for health services. The group of people, mostly elderly, with high predisposition to acquire diseases and high need for the access to the health services, is not being assisted due to low demand, either by distance from places of care, poor financial conditions or inadequate and little stimulating support from the family (4,27-28). The architectural and attitudinal barriers found in cities as they can be seen in the social nucleus may discourage the subject to seek services. The search for rehabilitation is delayed if the network does not encourage support, if the barriers are limiting and if there is not easy access to the health care services, to all of these there is the visual impairment itself, which is limiting and imposes restrictions as identified in this study (28). In a study by Rev Bras Oftalmol. 2014; 73 (5): 291-301 296 Silva MR, Nobre MIRS, Carvalho KM, Montilha RCL Table 5 Characteristics of the subjects according to ophthalmologic diagnosis, ICD-10 and ICF Diagnosis S1 S1 S3 S4 Glaucoma Glaucoma Optic Neuritis Diabetic retinopathy ICD-10 H54.0 H54.0 H54.0 H54.1 Body functions b21001.4 (RE*) b21001.4 (LE**) b21002.4 b2101.4 b21020.4 b21021.4 b21022.4 b21023.4 b21001.4 (RE) b21001.4 (LE) b21002.4 b2101.4 b21020.4 b21021.4 b21022.4 b21023.4 b21001.4 (RE) b21001.4 (LE) b21002.4 b2101.3 b21020.3 b21021.3 b21022.3 b21023.3 b21001.4 (RE) b21001.2 (LE) b21002.2 b2101.1 b21020.1 b21021.0 b21022.0 b21023.2 Rev Bras Oftalmol. 2014; 73 (5): 291-301 Body structures s1106.423 s 220.473 s1106.423 s220.473 s1106.423 s2203.273 ICF Activities and participation d166.443 d4502.332 d640.431 d9205.310 d166.443 d4502.321 d640.221 d9205.220 d166.432 d4502.320 d640.221 d9205.332 d166.221 d4502.110 d640.310 d9205.100 Environment factors e1201+4 e1251+2 e1500+3 e1502+2 e2400.0 e2401+0 e310+4 e315+4 e320+4 e410+4 e415+4 e420+4 e445.2 e1201+4 e1251+1 e1500+2 e1502+1 e2400.0 e2401+0 e310+4 e315+4 e320+4 e410+4 e415+4 e420+4 e445.0 e1201+4 e1251+2 e1500+3 e1502+4 e2400.3 e2401+3 e310+3 e315+3 e320+2 e410.1 e415+3 e420+2 e445.2 e1201+3 e1251+4 e1500+3 e1502+4 e2400.2 e2401+4 e310+4 e315+4 e320+3 e410+4 e415+4 e420+3 e445.0 J.V.C., female, 67 years old, married, 3 daughters, on sick leave A.M.S., male, 74 years old, widower, 7 children, retired V.V.S., male, 47 years old, divorced, 3 daughters, on sick leave J.M.R., male, 31 years old, single, 1 son, on sick leave Visual impairment, rehabilitation and International Classification Of Functioning, Disability And Health Diagnosis S5 S6 S7 S8 Diabetic retinopathy Retinitis pigmentosa AMD Optic neuritis ICD-10 H54.1 H54.1 H54.1 H54.2 Body functions b21001.4 (RE) b21001.2 (LE) b21002.2 b2101.0 b21020.0 b21021.0 b21022.0 b21023.2 b21001.4 (RE) b21001.2 (LE) b21002.2 b2101.2 b21020.0 b21021.2 b21022.3 b21023.1 b21001.4 (RE) b21001.2 (LE) b21002.2 b2101.2 b21020.0 b21021.0 b21022.1 b21023.2 b21001.3 (RE) b21001.3 (LE) b21002.4 b2101.2 b21020.3 b21021.0 b21022.2 b21023.3 Body structures s2203.273 s2203.411(RE) s2203.222(LE) s2203.223 s1106.323 ICF Activities and participation d166.210 d4502.210 d640.110 d9205.310 d166.221 d4502.320 d640.110 d9205.300 d166.311 d4502.221 d640.110 d9205.200 d166.331 d4502.321 d640.211 d9205.332 297 Environment factors e1201+1 e1251+4 e1500+1 e1502+3 e2400.2 e2401+4 e310+4 e315+4 e320+4 e410+4 e415+4 e420+4 e445.1 e1201+1 e1251+2 e1500+1 e1502+3 e2400.2 e2401+3 e310+4 e315+3 e320+2 e410+4 e415+3 e420+2 e445.2 e1201+0 e1251+3 e1500+3 e1502+3 e2400.1 e2401+3 e310+4 e315+3 e320+2 e410+4 e415+4 e420+2 e445.0 e1201+4 e1251+2 e1500+4 e1502+4 e2400.4 e2401+3 e310+4 e315+4 e320+3 e410+4 e415+4 e420+3 e445.1 R.C.G., female, 29 years old, single, pedagogue E.A.A., female, 34 years old, single, 1 son, cleaner B.P., female, 83 years old, single, retired. H.M.V., male, 33 years old, married, 1 daughter, on sick leave Rev Bras Oftalmol. 2014; 73 (5): 291-301 298 Silva MR, Nobre MIRS, Carvalho KM, Montilha RCL Diagnosis S9 S11 S12 Body functions b21001.2(RE) b21001.2 (LE) b21002.0 b2101.2 b21020.0 b21021.0 b21022.0 b21023.1 Macular C chorioretinitis AO S10 ICD-10 Central serous maculo pathysequel Keratoconus Keratoconus H54.2 H54.2 H54.2 H54.2 b21001.3 (RE) b21001.3 (LE) b21002.4 b2101.3 b21020.2 b21021.0 b21022.2 b21023.3 b21001.3 (RE) b21001.2 (LE) b21002.2 b2101.0 b21020.2 b21021.0 b21022.1 b21023.2 b21001.3 (RE) b21001.2 (LE) b21002.1 b2101.0 b21020.1 b21021.0 b21022.1 b21023.3 Rev Bras Oftalmol. 2014; 73 (5): 291-301 Body structures s2203.223 s2203.373 s2201.263 s2201.263 ICF Activities and participation d166.110 d4502.110 d640.100 d9205.000 d166.331 d4502.320 d640.221 d9205.332 d166.110 d4502.220 d640.321 d9205.320 d166.110 d4502.221 d640.211 d9205.310 Environment factors e1201+0 e1251+4 e1500+2 e1502+3 e2400.0 e2401+4 e310+4 e315+4 e320+4 e410+4 e415+4 e420+4 e445.2 F.S.A., female, 29 years old, married 1 son, unemployed e1201+0 e1251+4 e1500+1 e1502+3 e2400.4 e2401+3 e310+4 e315+4 e320+4 e410+4 e415+3 e420+3 e445.2 D.C.F., male, 43 years old, married, 2 daughters, on sick leave e1201+1 e1251+4 e1500+2 e1502+4 e2400.3 e2401+4 e310+4 e315+4 e320+3 e410+4 e415+4 e420+3 e445.2 R.D.A.A., male, 48 years old, single, on sick leave e1201+2 e1251+4 e1500+3 e1502+4 e2400.2 e2401+4 e310+4 e315+4 e320+3 e410+4 e415+4 e420+3 e445.4 Visual impairment, rehabilitation and International Classification Of Functioning, Disability And Health Diagnosis S13 Cortical ICD-10 H54.2 Body functions b21001.3(RE) b21001.3(LE) b21002.2 b2101.2 b21020.0 b21021.0 b21022.0 b21023.3 Body structures s1106.452 ICF Activities and participation d166.220 d4502.220 d640.110 d9205.221 299 Environment factors e1201+0 e1251+4 e1500+3 e1502+3 e2400.1 e2401+2 e310+4 e315+4 e320+4 e410+4 e415+4 e420+3 e445.2 M.V.C.B., female, 33 years old, married, pregnant, on sick leave (*) RE: right eye; (**) LE: left eye Douglas et al. (29), the social and individual barriers found in the sample population prevented considerably the frequent outing of these people from their homes, the public transport was identified during the study as a major barrier in the subjects’ daily basis activities, besides the challenge to create awareness among the visual impaired population who sees the restraints of mobility as inherent to their condition, thus failing to access the health services. The visual functions with disabilities which were here presented implicated, at various levels, the activities and participation of the users, either under limiting or even disabling forms, these implications were also identified in studies of Marback, Temporini & Kara-Júnior (11) and Aciem & Mazzotta (13) . However, from the analysis of the obtained results it can be seen that the use of optical and non-optical devices were shown to be an effective aid for increasing the functionality with improved performance and participation in the daily activities and they can lead to increased self-esteem and social participation, as evidenced in other national and international researches (13,24,3032) . In the research conducted by Carvalho et al. (23), the optical devices prescribed for the visually impaired old people, after the assessment and knowledge of the visual category of each individual, their individual needs and aspects of their daily life, they helped in improving the functional performance and were recognized by the elderly as valid resources for managing their everyday activities. The findings of this study allow us to highlight the Basic Activities of Daily Life (ADLs), such as functional communication (d166), functional mobility (d4502) and socialization (d9205), were more implicated in this group of participants, than the Instrumental Activities of Daily Living such as household chores (d640). Although ADLs are less complex activities – in relation to required skills, the participants at the time of the survey are in the beginning of the rehabilitation process. Owsley et al. (33) , during the tracking of the vision rehabilitation services in the United States and the characteristics of the population assisted, found that reading is a performing task that is more compromised, about 85.9% of assisted subjects presented difficulty in reading, so as in this study, in which 76.92% presented impairment in the reading performance from moderate (.2) to complete (.4). When it comes to mobility (41.2%) and household chores (39.1%), these activities are shown as difficult to implement, though less prominently (33). The performance data of socialization, in which 7 people reported severe difficulty and 1 person complete difficulty in social performance (d9205), meets Cunha’s and Enumo’s speech (8) , which argues that deficiency leads to social losses. For other participants evaluated and ranked, social environmental factors are not barriers to their acceptance and engagement in activities, but facilitators. On the other hand, there are physical environments that are not prepared to receive the visually impaired, causing limitations and restrictions on the participation of people in public and private environments, creating real barriers, interfering with the right to come and go, and as mentioned previously, discouraging the access to and search for health services (4,27-29). The context of the health network, which is highlighted here, refers to the rehabilitation of the visual impaired. The rehabilitation goes beyond empowering, training or presenting resources, techniques and strategies to the individuals in dealing with their environment. It aims to take actions to facilitate and promote their social inclusion and integration, enabling the individuals to perform daily with autonomy, independence and quality of life. Visual rehabilitation groups stand for sources of experience for the participants, legitimizing capabilities, the possibilities for action, assisting in the reconstruction of their personal and social identities (13). It is important to highlight that the family members participate actively in some meetings, so they are constantly guided and kept close. The rapprochement of the family during the rehabilitation process is essential for the engagement, attendance and stimulation of the visually impaired. The visual loss at any level, studied in this research, was the cause of the functional impairment, regarding the independence of the activities in the daily living and, consequently, the quality of life of the individuals. In order to enable the participants to reach their maximum functionality and their well-being it is crucial in the habilitation and rehabilitation care process to count on a multi-skilled team and knowledge in order to encompass the individual as a whole being and rehabilitate him effectively (2,1115,33) . This wide and global approach is carried out at the research center as well as in the approach of the Visual Rehabilitation Group from the assessment until the discharge process. This Rev Bras Oftalmol. 2014; 73 (5): 291-301 300 Silva MR, Nobre MIRS, Carvalho KM, Montilha RCL approach leads the therapeutic goals to be plotted according to the user’s individual needs in all aspects and his rehabilitation is closely monitored and is planned properly. The archaic concept of disability as irreversible condition and applied to small groups that should be medicalized and rehabilitated to bring the individual to the maximum of the expected standard of functionality, brings forth - and still does discrimination and segregation. In order to educate society that disability is inherent to the human diversity, constant actions are required and performed. Another significant struggle within the universe of disability refers to the different forms of limitations and the constraints that are usually faced. Impaired people experience their disabilities in different ways; they perform and participate in their daily activities on their own terms due to their personal factor, preferences, settings, facilitators, barriers, different history and culture. The lack of understanding that the same deficiency leads to various restrictions and limitations for each person who experiences it may lead to misconceptions, myths and prejudices in several areas, whether educational, legislative, financial, technological. It is precisely the importance of researching on the diversity within human diversity, i.e., within the peculiarities of the visual impairment, which are based on the rehabilitation process. It is this diversity that is the source of action in health. To research the diversity is to seek forms of intervention based on the needs and individualized demands. An example of diversity within the universe of visual impairment can be seen in Table 5. The S3 individual, considered blind in both eyes (H54.0), compared to S1 and S2, both with blindness in both eyes by the ICD-10, has less limiting and restrictive functional responses related to the visual impairment. When the same individual (S 3) is compared to S 8 and S 10, considered visually impaired with low vision in both eyes (H54.2), his performance and ability to perform daily activities is similar or slightly lower. These different responses within this universe allow the understanding about the individual who is assisted by the clinic such as his singularities. It is extremely important to plan the rehabilitation conduct preventing the generalization by the visual condition. The ICF has an essential role in this context, since it comes to discuss, extend and articulate the concepts about disability. Used as a tool in this study, the ICF proved to be a suitable tool for classifying visual disabilities that should be incorporated into the professional practice in the health field in order to guide actions centered on the needs of the individual with low vision or blindness, to turn the rehabilitation process individualized and effective. It is suggested that the ICF does not guide actions alone, but combined with other standardized structured and semi-structured assessment and mainly with the observation and approach to the subject assisted to improve strategic interventions that may be conducted. CONCLUSION The visual loss, at any level, led to functional impairments, limiting and restricting the individuals’ participation and performance in the daily activities interfering with their independence, autonomy and their quality of life. However, the use of optical resources, non optical, aids and environmental adaptations proved to be beneficial for increasing the Rev Bras Oftalmol. 2014; 73 (5): 291-301 functionality, showing the influence of external factors on the individual’s performance. Knowing and recognizing the existence of diversity within the universe of visual impairment allows the understanding who the assisted subject is, avoiding the generalization by the visual condition. From this research it was possible to describe the characteristics of each individual diagnosed with visual impairment according to the ICD-10, and classify him according to the ICF. This process showed that the classification in the ICF favors the rehabilitation conduct since it covers the individual in his particularities and context, reaching his individual sphere that is embedded in a socio-cultural context historiography, based in unique and complex needs. R EFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. World Health Organization. Vision 2020 – The Right to Sight: Global initiative for the elimination of avoidable blindness – Action plan 2006-2011 [Internet]. 2007 [cited 2012 Oct 13]. Available from: http://www.who.int/blindness/Vision2020_report.pdf. World Health Organization. Action Plan for the Prevention of Avoidable Blindness and Visual Impairment - 2009-2013 [Internet]. 2010. [cited 2012 Oct 10]. 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Perfis de utilização de serviços de saúde no Brasil. Ciênc Saúde Coletiva. 2002;7(4):757-76. Temporini ER, Kara-Júnior N, Kara-José N, Holzchuh N. Popular beliefs regarding the treatment of senile cataract. Revista de Saúde Pública. 2002; 36(3):343-9. Douglas G, Pavey S, Corcoran C, Clements B. Evaluating the use of the ICF as a framework for the interviewing people with a visual impairment about their mobility and travel. Br J Visual Impairment. 2012;30(1):6-21. Lucas MB, Leal DB, Tavares SS, Barros EA, Aranha ST. Condutas reabilitacionais em pacientes com baixa visão. Arq Bras Oftalmol. 2003; 66(1):77-82. Montilha RC, Temporini ER, Nobre MI, Gasparetto ME, KaraJose N. Utilização de recursos ópticos e equipamentos por escolares com deficiência visual. Arq Bras Oftalmol. 2006;69(2):207-11. Haddad MA, Sampaio MW, Haddad M, et al. Auxílios para baixa visão. In: Sampaio MW, Haddad MA, Costa Filho HA, Siaulys MO. Baixa visão e cegueira: os caminhos para a reabilitação, a educação e a inclusão. Rio de Janeiro: Cultura Médica; Guanabara Koogan; 2010. p.113-39. Owsley C, McGwin Jr G, Lee PP, Wasserman N, Searcey K. Characteristics of low-vision rehabilitation services in the United States. Arch Ophthalmol. 2009;127(5):681-9. Corresponding of author: Rua Primo Chiorlin, nº 80 CEP: 13105-556 – Campinas (SP), Brazil E-mail: [email protected] Rev Bras Oftalmol. 2014; 73 (5): 291-301 ORIGINAL ARTICLE 302 Knowledge about primary open angle glaucoma among medical students Nível de conhecimento sobre glaucoma primário de ângulo aberto entre os estudantes de medicina Saulo Costa Martins1, Marcos Henrique Mendes1, Ricardo Augusto Paletta Guedes2, Vanessa Maria Paletta Guedes3, Alfredo Chaoubah 4 A BSTRACT Objective: To assess the knowledge of primary open-angle glaucoma among medical students from Federal University of Juiz de Fora. Methods: In this cross sectional study, we conducted a survey among students attending the last two years of Medical School. The questionnaire consisted in 11 questions about epidemiology, risk factors, symptoms, diagnosis, treatment and primary openangle glaucoma (POAG) consequences. The students were also asked if they considered their knowledge about POAG sufficient. Students’ characteristics (age, sex and intended area of specialization) were identified. Results: Women comprised 52.9% of the students. Only 22.5% identified POAG as having a genetic origin. Almost half of them (46.1%) did not know that POAG is asymptomatic and 1 out of 3 students did not know that glaucoma blindness is irreversible. The great majority (91.2%) correctly identified tonometry as an important tool for diagnosis and that glaucoma can be treated through medications (70.6%) or surgery (71.6%). However, few students identified fundoscopy (35.3%) and perimetry (28.7%) as important tools for glaucoma assessment. Almost everyone (95.1%) considered their knowledge insufficient. Conclusion: The majority of the participants believe that their knowledge of POAG is insufficient. This gap can lead to some serious consequences from both individual (blindness) and collective (negative impact in health system and society) perspectives. Keywords: Glaucoma, open-angle/diagnosis; Glaucoma, open-angle/prevention & control; Ophthalmology/education; Medical, students; Education, medical RESUMO Objetivo: Avaliar o conhecimento dos alunos de graduação do curso de Medicina da Universidade Federal de Juiz de Fora em relação ao glaucoma primário de ângulo aberto. Métodos: Neste estudo transversal, aplicou-se aos alunos dos 5º e 6º ano um questionário contendo 11 questões referentes a epidemiologia, fatores de risco, sintomas, diagnóstico, tratamento, consequências do glaucoma e por último se consideram os conhecimentos adquiridos na universidade como suficientes. Características dos alunos (idade, sexo, especialidade pretendida) foram identificadas. Resultados: Entre os estudantes, 52,9% eram mulheres. A origem genética da doença foi identificada por 22,5%. Quase a metade (46,1%) não sabia que o glaucoma na maioria das vezes é assintomático. Aproximadamente 1 em cada 3 alunos não sabia que a cegueira do glaucoma era irreversível. A grande maioria (91,2%) identificou corretamente que a tonometria era um exame importante na avaliação do glaucoma e que o tratamento poderia ser clínico (70,6%) ou cirúrgico (71,6%). Porém, poucos alunos deram a real importância para os exames de fundoscopia (35,3%) e campimetria (28,7%). Quase a totalidade (95,1%) dos entrevistados considerou o próprio conhecimento como insuficiente. Conclusão: A maioria dos entrevistados acha que o conhecimento sobre glaucoma primário de ângulo aberto adquirido na graduação é insuficiente. Tal desconhecimento pode levar a oportunidades de diagnóstico perdidas e gerar consequências graves tanto do ponto de vista individual (cegueira) quanto do ponto de vista coletivo (impacto para o sistema de saúde e sociedade). Descritores: Glaucoma de ângulo aberto/diagnóstico; Glaucoma de ângulo aberto/prevenção & controle; Oftalmologia/educação; Estudantes de Medicina; Educação em graduação de Medicina 1 Medical Student, Medical School of the Federal University of Juiz de Fora (UFJF), Juiz de Fora/MG, Brazil. Ophthalmologist, Researcher at the Federal University of Juiz de Fora (UFJF), Juiz de Fora/MG, Brazil. 3 Ophthalmologist, Head of the Ophthalmology Department, Santa Casa de Misericórdia Hospital, Juiz de Fora; Researcher at the Federal University of Juiz de Fora (UFJF), Juiz de Fora/MG, Brazil. 4 Professor and Researcher at the Department of Statistics, Federal University of Juiz de Fora (UFJF), Juiz de Fora/MG, Brazil 2 Work conducted at the Federal University of Juiz de Fora (UFJF), Juiz de Fora/MG, Brazil. The authors declare no conflict of interest. Received for publication 25/09/2012 - Accepted for publication 29/8/2014 Rev Bras Oftalmol. 2014; 73 (5): 302-7 Knowledge about primary open angle glaucoma among medical students INTRODUCTION G laucoma is a chronic optic neuropathy with marked changes in the optic disc and the retinal nerve fibre layer, leading to significant visual field changes(1-3). The disease is classified according to the mechanisms of obstruction of aqueous humour drainage as primary open angle glaucoma (POAG), primary angle closure glaucoma (PACG), and secondary glaucoma(4). According to the World Health Organization, glaucoma is the second leading cause of blindness in the world (12.3%) after cataract (47.8%). Studies in Brazil have found a prevalence of 3,4% for glaucoma, with POAG being the most prevalent type (2.4%)(1). It is important to note that cataract blindness can be reversed with surgical treatment, while glaucoma blindness is irreversible(5). Several predictive and prognostic risk factors have been described for POAG, such as increased intraocular pressure (IOP), family and genetic history, ethnic origin, myopia, and diabetes mellitus(1,2). Of these, IOP is more consistently associated with glaucoma and is the most important factor, as it is the only one that can be acted upon effectively(1-3). The disease is asymptomatic in its early stages, and its insidious onset often leads to late diagnosis(1-3). Thus, it is estimated that over half of glaucoma cases remain undiagnosed and untreated(6,7). Given that ophthalmic consultations represent 9% of all medical visits and that ophthalmologists are unevenly distributed throughout the country, it is clear that general practitioners have an important role in the prevention of blindness(8,9). In this context, medical education should train medical students to diagnose, refer patients appropriately, and even treat some of the most prevalent and disabling eye diseases, including glaucoma(5,10,11). For POAG in particular, students should learn to identify its key risk factors, refer patients for glaucoma testing, and stress the importance of prevention, especially in higherrisk cases. Medical education should also stress the need to promote adhesion to continuous treatment, which contributes to reducing disease progression(5). However, studies have shown that the basic knowledge of ophthalmology among undergraduate students is insufficient, suggesting the need to reassess the way ophthalmology is taught in medical school(8,10). It is thus important to study the knowledge of POAG among students who will soon become general practitioners, offer them appropriate training, and contribute to discussions on curriculum reform. The aim of this study was to assess the level of knowledge of POAG among students in the last two years of Medical School in the Federal University of Juiz de Fora, Brazil. M ETHODS A cross-sectional observational study was conducted from August to September 2012. The sample included medical students of the Federal University of Juiz de Fora (UFJF), and a sampling error of ±4.5% was considered. The study subjects were approached while in the university, being randomly selected and invited to answer the questionnaire voluntarily, free of any charge. 303 Inclusion criteria were: medical students over 18 years of age attending the 9th, 10th, 11th or 12th semesters and immediately available to answer the questionnaire. Students in other semesters, who were not immediately available to answer the questionnaire, who refused to participate, who did not answer the questionnaire in full, or who did not provide their Free and Informed Consent were excluded from the study. Participants were approached in a standardised manner by a trained researcher, having previously provided their free and informed consent to answer the questionnaire individually and voluntarily. Two medical students were responsible for data collection. Training on data collection was done during a pilot study conducted on 16 subjects in order to test the instrument, identify difficulties in understanding the questions, make appropriate changes to the questionnaire, and organise the field work. The data collection instrument was a structured questionnaire (Appendix 1) including 11 questions on the risk factors, symptoms, diagnosis, treatment, and consequences of glaucoma, aimed at testing the knowledge of subjects about the condition. Student characteristics (age, sex, and the medical specialty they intended to pursue) were collected. SPSS software (SPSS Inc., Chicago, USA) was used to prepare the database and for statistical analysis. Results were analysed using a confidence interval of 95% and a p-value under 0.05. The study followed the guidelines on human research provided for in Resolution 196/96 of the Brazilian National Health Council/Ministry of Health. The study was submitted to the Research Ethics Committee of Santa Casa de Misericórdia Hospital in Juiz de Fora, having been approved under Opinion 73374/2012. R ESULTS In total, 102 students were invited and agreed to participate in the study. They were distributed as follows: 25 in the 9th semester, 27 in the 10th semester, 25 in the 11th semester, and 25 in the 12th semester. The mean age (± standard deviation) of respondents was 24.9 (±2.2) years. Most respondents (52.9%) were female. Only 2.9% of respondents intended to specialise in ophthalmology, while 80.4% intended to pursue another medical specialty and 16.7% had not yet chosen a specialty. A family history of glaucoma was found in 15.7% of respondents. Approximately 7% were unaware of glaucoma cases in their family, while most respondents (76.5%) stated there were no cases of the disease in their family. Figure 1 shows the responses of students when asked about the leading cause of irreversible blindness worldwide. Most students (59.8%) gave the correct answer, glaucoma. However, 25.5% of respondents chose diabetic retinopathy. All students intending to specialise in ophthalmology answered correctly, but among the other students (those intending to pursue another specialisation, or still undecided), 26.3% thought the correct answer was diabetic retinopathy. Glaucoma blindness was classified as irreversible by 64.7% of respondents, but 17.6% thought it was reversible with some treatment, and a similar number did not know the answer, i.e. 35.3% of students (approximately 1 in 3) did not know that Rev Bras Oftalmol. 2014; 73 (5): 302-7 304 Martins SC, Mendes MH, Guedes RAP, Guedes VMP, Chaoubah A glaucoma blindness is irreversible. There were no significant differences between answers when respondents were grouped based on their intended medical speciality (p = 0.964, chi-squared test), study semester (p = 0.076, chi-squared test), or a family history of glaucoma (p = 0.122, chi-squared test). POAG was identified as the most common type of glaucoma by 58.8%, but 19.6% (1 in 5) did not know what the answer. Again, no differences were found between groups based on intended medical speciality (p = 0.387, chi-squared test), study semester (p = 0.045, chi-squared test), or a family history of glaucoma (p = 0.782, chi-squared test). Most students (67.6%) wrongly thought IOP was a causal factor of POAG. Only 22.5% correctly identified genetic factors as a cause of POAG, and 16.7% did not know the answer. There were no differences between groups based on intended medical speciality, study semester, or a family history of glaucoma. and symptoms were mentioned by respondents as part of the clinical picture of POAG: sudden loss of central vision (24.5%); eye pain (33.3%); red eye (9.8%); tearing (11.8%); periocular headache (24.5%); frontal headache (5.9%); photophobia (11.8%). There were no differences between groups based on intended medical speciality, study semester, or a family history of glaucoma. The vast majority of respondents (91.2%) correctly replied that tonometry (IOP measurement) is an important test in the assessment of glaucoma. However, only 35.3% considered fundus examination and 28.7% considered perimetry as important tests for glaucoma. There were no differences between groups based on intended medical speciality, study semester, or a family history of glaucoma. Figura 3: Possibilidades de tratamento do glaucoma primário de ângulo aberto segundo os entrevistados Figure 1: Leading cause of irreversible blindness, according to respondents. Figure 2 shows the variables identified by the respondents as risk factors for POAG. High IOP was mentioned by 88.2% of students, but many other important factors were missed by most students, including: hypertension (49%); diabetes mellitus (26.5%); myopia (4.9%); ocular trauma (15.7%); corticosteroids (43.1%); and black race (15.7%). A family history of glaucoma was correctly identified as a risk factor by 72.5% of respondents. There were no differences between groups based on intended medical speciality, study semester, or a family history of glaucoma. Figure 3 shows the distribution of answers regarding the treatment of glaucoma. Most respondents correctly replied that glaucoma can be treated medically (70.6%) and surgically (71.6%). Laser therapy, however, was only mentioned as a treatment alternative by 23.5% of respondents. There were no differences between groups based on intended medical speciality, study semester, or a family history of glaucoma. Figura 4: Proportion of respondents who thought they had acquired sufficient knowledge on primary open-angle glaucoma during medical school. Figure 2: Risk factors of primary open-angle glaucoma, according to respondents. In total, 15.7% of respondents stated they did not know what the signs and symptoms of POAG were. Only 53.9% correctly replied that POAG was asymptomatic. Several signs Rev Bras Oftalmol. 2014; 73 (5): 302-7 Figure 4 shows the proportion of respondents who considered they had learned enough about POAG during their medical studies. DISCUSSION This study found that students in the last two years of medical school at the Federal University of Juiz de Fora feel Knowledge about primary open angle glaucoma among medical students unable to identify the main epidemiological and clinical characteristics and the therapeutic possibilities for POAG. This was confirmed by their responses to the standardised questionnaire used in this study. General clinical knowledge is key to increasing the number of early POAG diagnoses and therefore the number of patients who receive treatment. Furthermore, misconceptions and knowledge gaps are important barriers to preventive eye health actions(5,12). Assessing the knowledge of medical students in the last years of medical school is a tool that can be used to prompt reflections on the knowledge of physicians, as many of those students will soon be managing patients(5). This assessment is particularly relevant because an increase in the prevalence of glaucoma is expected worldwide as a result of population ageing and insufficient ophthalmic resources for effective intervention against the condition(5). In our sample, most respondents correctly ranked glaucoma as the most prevalent cause of irreversible blindness worldwide, although approximately one quarter of them thought the correct answer was diabetic retinopathy. This could suggest that preventive campaigns led by organisations such as the American Diabetes Association and the Brazilian Diabetes Society raise more awareness than glaucoma campaigns. This is evidenced by the continuous, broad-scope nature of programmes like the Hiperdia (Hypertension and Diabetes) campaign and the National Diabetic Retinopathy Campaign(13,14) and the lack of investment and programme continuity in actions such as the Glaucoma Campaign by the Brazilian Ministry of Health(5,14). Furthermore, there is a greater focus on diabetes during medical education because it involves more subjects in the medical curriculum, while glaucoma is only studied during the ophthalmology course. As regards the classification of glaucoma, most students correctly identified POAG as the most common type of glaucoma, but it is noteworthy that 1 in 5 respondents did not know what the most common type of glaucoma was. One of the most common sources of error in the assessment of glaucoma is to consider elevated intraocular pressure as a causal factor. High IOP is only a risk factor(1), and there are cases of ocular hypertension that never progress to glaucoma. Likewise, there are cases of glaucoma with normal IOP levels(1). When asked about the causal factor of POAG, most respondents incorrectly answered that an elevated IOP was a causal factor. Only 22.5% correctly mentioned genetic factors as the cause of POAG. On the other hand, and contradictorily (a causal factor cannot be a risk factor at the same time!), most respondents correctly identified elevated IOP as an important risk factor for glaucoma. A family history of glaucoma was correctly identified as a risk factor by 72.5% of respondents. POAG is a multifactorial disease, and it is essential that physicians know its risk factors(1). The subjects of this study were medical students who will soon become medical doctors, a large part of which will probably work in Primary Health Care. Since primary care is the gateway to a network of services providing universal access, it is responsible for coordinating care in the network in all of its dimensions(5). The results of this study, however, indicate a gap in the functions of primary care with regard to eye health, i.e. the need to recognise risk factors in order to prevent and control certain causes of preventable blindness and visual impairment(5). 305 Recognising the clinical presentation of glaucoma is key to preventing and controlling the condition (5). Glaucoma is a neurodegenerative disorder characterised by insidious and progressive retinal ganglion cell degeneration (3), and it is asymptomatic in its early stages(1,2,5). Thus, physicians should know that patients with suspected or confirmed glaucoma will not present with exuberant symptoms or directly complaining of ocular involvement. This assessment of the knowledge of the clinical features of POAG among medical students found that 15.7% did not know the signs and symptoms of POAG, and just over half of respondents (53.9%) correctly stated that POAG is most often asymptomatic. When asked about the key tests for diagnosing POAG, the vast majority of respondents correctly identified tonometry as an important test. However, important tests such as fundus examination and perimetry and were only mentioned by a few respondents. This study indicates a serious deficiency in medical education, as glaucoma is a disease of the optic nerve (optic neuropathy) whose evaluation (diagnosis and management) can only be done through adequate and reliable fundus examination and perimetry(1). Current recommendations for the treatment of POAG include lowering the IOP, which remains the only demonstrated treatable risk factor for the disease(3). This can be done through medical, surgical and laser treatment. In our study, most respondents correctly stated that glaucoma can be treated medically and surgically. Laser treatment is also an alternative, but it was only mentioned by 23.5% of participants. In all questions there were no differences between groups based on intended medical speciality, study semester, or a family history of glaucoma. This shows that misconceptions regarding important factors related to glaucoma are not limited to a particular class in medical school. It also suggests that patients with glaucoma and their families do not receive proper guidance and have insufficient knowledge about the condition. In this study, almost all participants felt their knowledge of glaucoma was insufficient. A similar study conducted with students in the last semesters of medical schools in the state of São Paulo found significant gaps in the knowledge of ophthalmology of future general practitioners(15), while a study conducted at the Federal University of Piauí in 2011 found that 99.1% of students felt insecure about treating eye disorders(10). The results of our work are thus in line with those of studies conducted in other medical schools, showing that students recognise the gaps in their ophthalmology training and consequently feel unprepared to manage patients with eye complaints. This suggests the need to change how the subject is taught — ophthalmology courses should be targeted at primary care(16), with a stronger focus on prevention and early diagnosis. CONCLUSION The results of this study show that most respondents think the knowledge of glaucoma they acquired during medical school was insufficient. This gap creates major misconceptions about key issues such as the aetiology, risk factors, clinical picture, and treatment of glaucoma, which can lead to missed diagnoses with serious individual (blindness) and collective (impact on the healthcare system and society) consequences. Rev Bras Oftalmol. 2014; 73 (5): 302-7 306 Martins SC, Mendes MH, Guedes RAP, Guedes VMP, Chaoubah A Appendix 1 Questionnaire applied to medical students. Age: ___________________ Sex: _______________________ Semester: _____________________________________________ Intended specialization :____________________________________________________________________________________ Do you have any family members with glaucoma? Yes No I don’t know The most prevalent cause of irreversible blindness worldwide is: Catarat Glaucoma Age-related macular degeneration Diabetic retinopathy I don’t know Glaucoma can lead to blindless. Glaucoma blindless is: Reversible with any tyoe of treatment (medical or surgical) Reversible only through surgical treatment Irreversible I don’t know The most common yype of glaucoma is: Primary open angle glaucoma Primary narrow angle glaucoma Congenital glaucoma Secondary glaucoma I don’t know The causes of primary angle glaucoma include : Genetic factors Elevated intraocular pressure Infection I don’t know Please mark the main risk factors for primary open angle glaucoma (one or more): Elevated intraocular pressure High blood pressure Diabetes Neurological disease Young age Hiperopia Myopia Family history of glaucoma Eye trauma Corticosteroids Black race R EFERENCES 1. 2. Sociedade Brasileira de Glaucoma. 3º Consenso Brasileiro. glaucoma primário de ângulo aberto. São Paulo: BestPoint; 2009. Disponível em: http://www.sbglaucoma.com.br/pdf/consenso03.pdf National Health and Medical Research Council (NHMRC). A guide to glaucoma for primary care providers. A companion document to NHMRC Guidelines for the screening, prognosis, diagnosis, management and prevention of glaucoma. Camberra, Australia: NHMRC; 2011. Disponível em: http://www.nhmrc.gov.au/ _files_nhmrc/publications/attachments/cp113_b_glaucoma_ guide_healthcare_workers.pdf Rev Bras Oftalmol. 2014; 73 (5): 302-7 Please mark the most common signs and symptons of primary open angle glaucoma: Sudden loss of central vision Eye pain Red eye Tearing Periocular headache Frontal headache Photofobia The condition is mostly asynptomatic I don’t know The main diagnostic tests for glaucoma include: Visual acuity Fundus examination Measuring intraocular pressure (tonometry) Perimetry Magnetic resonance imaging I don’t know Glaucoma can be treated using (one or more): Eye drops Surgery Laser No treatment exists for the condition I don’t know Successful glaucoma treatment promotes: Cure Disease control, preventing blindness Symptomatic releief, although the condition inevitably leads to blindness No treatment exists for the condition I don’t know Do you think the knowledge of glaucoma you acquired during medical school is sufficient to recognise a possible case of primary open angle glaucoma? Yes No 3. 4. 5. 6. Weinreb RN, Khaw PT. Primary open-angle glaucoma. Lancet. 2004;363(9422):1711-20. Review. Shields MB, Ritch R, Krupin T. Classifications of the glaucomas. Ritch R, Shields MB, Krupin T, editors. The glaucomas. 2nd ed. St. Louis: Mosby; 1996. vol. 2. Guedes RA. As estratégias de prevenção em saúde ocular no âmbito da saúde coletiva e da Atenção Primária à Saúde - APS. Revista APS. 2007;10(1): 66-73. Guedes RA, Guedes VM. Custo crescente em glaucoma: atualidades e seu impacto na saúde coletiva. Revista APS. 2008;11(4):444-50. Knowledge about primary open angle glaucoma among medical students 7. 8. 9. 10. 11. 12. 13. Póvoa CA, Nicolela MT, Valle AL, Gomes LE, Neustein I. Prevalência de glaucoma identificada em campanha de detecção em São Paulo. Arq Bras Oftalmol. 2001;64(4): 303-7. Manica MB, Corrêa ZM, Marcon IM, Telichevesky N, Loch LF. O que os pediatras conhecem sobre afecções oculares na criança? Arq Bras Oftalmol. 2003;66(4):489-92. Silva MR. O Ensino da Oftalmologia. Rev Bras Oftalmol. 2009; 68(3):127-8. Lopes Filho JB, Leite RA, Leite DA, Castro AR, Andrade LS. Avaliação dos conhecimentos oftalmológicos básicos em estudantes de Medicina da Universidade Federal do Piauí. Rev Bras Oftalmol. 2011;70(1):27-31. Temporini ER, Kara-José N, Gondim EL, Dantas FJ. Conhecimentos sobre saúde ocular entre profissionais de um hospital universitário. Medicina (Ribeirão Preto). 2002;35(1):53-61. Espíndola RF, Rodrigues BA, Penteado LT, Tan-Ho G, Gozzan JO, Freitas JA. Conhecimento de estudantes de medicina sobre o processo de doação de córneas. Arq Bras Oftalmol. 2007;70(4):581-4. Brasil. Ministério da Saúde. Portal da Saúde. Campanha: Dia Mundial do Diabetes. 2012. Disponível em: http:// portalsaude.saude.gov.br/portalsaude/ 307 14. Brasil. Ministério da Saúde. Secretaria Executiva. Departamento de Apoio à Descentralização. Coordenação-Geral de Apoio à Gestão Descentralizada. Diretrizes operacionais dos Pactos pela Vida, em Defesa do SUS e de Gestão. 2a. ed. Brasília: Ministério da Saúde, 2006. 76p. 15. Ginguerra MA, Ungaro AB, Villela FF, Kara-José AC, Kara-José N. Aspectos do ensino de graduação em oftalmologia. Arq Bras Oftalmol. 1998;61(5):546-50. 16. Kara-José AC, Passos LB, Kara-José FC, Kara-José, N. Ensino extracurricular em Oftalmologia: grupos de estudos/ligas de alunos de graduação. Rev Bras Educ Med. 2007;31(2):166-72. Corresponding author: Saulo Costa Martins Rua Doutor Constantino Paletta 10/401 - Centro CEP: 36015-450, Juiz de Fora (MG), Brazil E-mail: [email protected] Rev Bras Oftalmol. 2014; 73 (5): 302-7 308 CASE REPORT Central retinal artery occlusion associated with patent foramen ovale Oclusão de artéria central da retina associada ao forame oval patente Patrícia Regina de Pinho Tavares 1, Mariana Rezende de Oliveira 2, Eduardo de Castro Miranda Diniz3 , Rafael Mourão Agostini4 , Daniela Vieira de Aguiar5 A BSTRACT Central retinal artery occlusion it’s a disease most encountered in older patients, however it can be seen in children and young persons. In this situation the principal causes are cardiac abnormalities, and the patent foramen ovale is the most observed. The purpose of this study is to report a case of central retinal artery occlusion in a young patient with patent foramen ovale and, also, describe the importance of a detailed management in cases of retinal vascular occlusions. Keywords: Central retinal artery/pathology; Cardiac abnormalities; Foramen ovale, patent; Retinal artery occlusion; Young adult; Case reports RESUMO Oclusão da artéria central da retina é uma doença comumente encontrada em pacientes idosos, mas pode também ser vista em crianças e adultos jovens. Nestes, as principais causas são anomalias cardíacas, sendo o forame oval patente o mais observado. O objetivo do trabalho é relatar o caso de um paciente jovem com oclusão da artéria central da retina apresentando persistência de forame oval e, também, salientar a importância de uma propedêutica detalhada nos casos de oclusões vasculares da retina. Descritores: Artéria central da retina/patologia; Anomalias cardíacas; Forame oval patente; Oclusão da artéria retiniana; Adulto jovem; Relatos de casos. 1 Oculoplastic Surgery Department, Ophthalmic Centre of Minas Gerais, Belo Horizonte/MG, Brazil. Oculoplastic Surgery Department, Eye Clinic of Santa Casa de Belo Horizonte, Belo Horizonte/MG, Brazil. 3 Glaucoma Department, Ophthalmic Centre of Minas Gerais, Belo Horizonte/MG, Brazil. 4 Retina Department, Eye Clinic of Santa Casa de Belo Horizonte, Belo Horizonte/MG, Brazil. 5 Retina Department, Eye Clinic of Santa Casa de Belo Horizonte, Belo Horizonte/MG, Brazil. 2 The authors declare no conflict of interest. Received for publication 20/10/2011 - Accepted for publication 27/3/2012 Rev Bras Oftalmol. 2014; 73 (5): 308-10 Central retinal artery occlusion associated with patent foramen ovale Table 1 INTRODUCTION C entral retinal artery occlusion (CRAO) is characterised by a sudden, painless and severe loss of vision. It generally affects adults around the age of 60, and rarely below the age of 30. Men are more likely to be affected than women. In the large majority of cases, vision is worse than 20/400, but some patients present a cilioretinal artery which preserves a central vision of about 20/40 or better. Its most common cause is thrombosis due to atherosclerosis at the level of the lamina cribrosa(1). However, in young patients it is most frequently associated with cardiac disorders, trauma, haemoglobinopathies and ocular abnormalities such as optic disc drusen and peripapillary arterial loop(2). This paper describes a case of CRAO in a young patient with patent foramen ovale. To the best of our knowledge, this is the first such case report in the Brazilian literature. CASE REPORT RVS, a 19-year-old male student, was referred to the Santa Casa de Belo Horizonte Eye Clinic (MG) with a sudden and painless loss of visual acuity in the left eye (LE) occurring approximately 20 days earlier. He had no history of any disease, trauma, or use of medications or illegal drugs, including cigarettes. Ophthalmic examination found a visual acuity of 20/20 in the right eye (RE) and hand motion in the LE, showing no improvement with use of a pinhole. Biomicroscopy found an afferent pupillary defect in the LE and no changes in the RE. Intraocular pressure was 10 mmHg. Fundus examination showed optic disc and retinal pallor, arteriolar narrowing, flame-shaped haemorrhages and sequelae of oedema in the macular region, accumulation of hard exudates in the fovea, and mild macular star formation. Due to suspected retinal vascular disease, the patient was referred for thromboembolism screening (Table 1), retinal fluorescein angiography, optical coherence tomography (OCT), and cardiac and haematological evaluation. In the assessment of thromboembolic events, only the transthoracic echocardiogram was abnormal, showing an interatrial septum with a small right-to-left shunt suggestive of patent foramen ovale. Retinal fluorescein angiography (Figure 1) found hypofluorescent spots corresponding to the retinal haemorrhages and increased foveal hypofluorescence suggesting ischemia. OCT (Figure 2) found increased thickness and reflectivity of the internal layers of the retina corresponding to intracellular oedema and ischemia, attenuating the optical signals from the external retinal layers (RPE/Bruch membrane/ choriocapillaris complex). The patient is currently taking acetylsalicylic acid 100 mg/day as prescribed by his cardiologist. 309 Protocol for retinal thrombosis and vasculitis of the Retina and Vitreous Unit, Santa Casa de Misericórdia, Belo Horizonte. · SimpleRetinography · Angiography · Coagulation testing · Homocysteine · Protein electrophoresis · Complete blood count: factors VII, IX, XI, fibrinogen anemia – Hb, electrophoresis, search for sickle cells, bilirubin, Serun Fe, transderrin, ferritin, WBC/platelet count – mieloproliferative/ disorders / neoplasms · Fasting serum glucose · Erytrocyte sedimentatiom rate · ANF · Lupus anticoagulant · Anticardiolipin IgG/IgM · Antiphospholipid · Antithrombin B · Protein C and S · Factor V Leiden · Prothrombin gene · C3 – CH50 · Urea e creatinine · Urinalysis (sediments analysis) · VDRL – FTA-Abs · PPD · Toxoplasmosis IgM/IgG · Anti-HIV · CMV · Herpes virus · Hepatitis B, A e C mutation Figure 1A a 1D: Retinography and fluorescein angiography showing signs of central retinal arteryocclusion. DISCUSSION According to the RECO (Retinal Emboli of Cardiac Origin) study, 45% of patients under 45 years of age with CRAO also present cardiac abnormalities, of whom 27% need to take anticoagulants or undergo cardiac surgery(3). Patent foramen ovale is the most common congenital cardiac abnormality, and it can cause cerebral and systemic emboli Figure 2: Optical coherence tomography of patient with central retinal artery occlusion Rev Bras Oftalmol. 2014; 73 (5): 308-10 310 Tavares PRP, Oliveira MR, Diniz ECM , Agostini RM , Aguiar DV before the age of 55 years(4). In cases of large patent foramen ovale with spontaneous right-to-left shunt, surgical treatment is recommended(5). In the case presented here, the patient had a small patent foramen ovale without spontaneous shunt, being therefore eligible for medical treatment with an anticoagulant. The occurrence of CRAO stresses the importance of a detailed systemic evaluation to identify its exact aetiology, with careful follow-up to prevent further thromboembolic events. For this reason, specialist services should have a screening protocol for cases of retinal vascular occlusion. 4. 5. Ho IV, Spaide R. Central retinal artery occlusion associated with a patent foramen ovale. Retina. 2007;27(2):259-60. Kramer M, Goldenberg-Cohen N, Shapira Y, Axer-Siegel R, Shmuely H, Adler Y, et al. Role of transesophageal echocardiography in the evaluation of patients with retinal artery occlusion. Ophtalmology. 2001;108(8):1461-4. Comment in Ophthalmology. 2002;109(5):829; author reply 829. R EFERENCES 1. 2. 3. Liesegng TJ, Skuta GL, Cantor LB, editors. Basic and Clinical Science Course. Section 12: Retina and vitreous. San Francisco:American Academy of Ophthalmology; 2005. p.54-79. Sharma S, Brown GC. Retinal artery obstruction. In: Ryan SJ. Retina, 3rd ed. St. Louis: Mosby; 2001. Vol. 1, p.1350-67. Clifford L, Sievers R, Salmon A, Newson RS. Central retinal artery occlusion: association with patent foramen ovale. Eye (Lond). 2006;20(6):736-8. Rev Bras Oftalmol. 2014; 73 (5): 308-10 Corresponding author: Patrícia Regina de Pinho Tavares R. Alvarenga Peixoto, 580-401 CEP 30180120, Belo Horizonte (MG), Brazil. Telephone: +5531 3657 3583 or +5531 8891 8537 E-mail: [email protected] CASE REPORT 311 Adult dacryocystocele Dacriocistocele no adulto Silvia Helena Tavares Lorena 1 , João Amaro Ferrari Silva 2 ABSTRACT The dacryocystocele represents a dilated lacrimal sac and is often considered as having a congenital etiology. However, dacryocystocele is a rare disease in adults. The clinical feature is characterized by a painless bulge in the medial region of the orbit, below the medial canthal ligament. The lacrimal excretion test, endoscopy, computerized tomography and magnetic resonance image are used to make the diagnosis of dacryocystocele. Similar to pediatric patients, endoscopic marsupialization of the cyst with nasal stenting seems to be the appropriate therapy. In some cases the treatment consists of external dacryocystorhinostomy. Keywords: Orbit; Nasolacrimal duct obstruction; Dacryocystocele; Dacryocystorhinostomy RESUMO A dacriocistocele representa um saco lacrimal dilatado e é frequentemente considerada como tendo uma etiologia congênita. No entanto, dacriocistocele é uma doença rara em adultos. A característica clínica se caracteriza por um abaulamento indolor na região medial da órbita, inferior ao ligamento cantal medial. O teste de excreção lacrimal, endoscopia, tomografia computadorizada e ressonância magnética são utilizados para fazer o diagnóstico de dacriocistocele. Semelhante a pacientes pediátricos, marsupialização endoscópica do cisto nasal e a colocação de stent parece ser a terapêutica adequada. Em alguns casos o tratamento consiste na dacriocistorrinostomia externa. Descritores: Órbita; Obstrução do ducto lacrimal; Dacriocistocele; Dacriocistorrinostomia 1 2 Post-Graduation (Ph.D.) Programme at the Lacrimal Pathways Unit, Federal University of São Paulo (UNIFESP), São Paulo/SP, Brazil. Lacrimal Pathways Unit, Federal University of São Paulo (UNIFESP), São Paulo/SP, Brazil. Work conducted at the Lacrimal Pathways Unit, Federal University of São Paulo (UNIFESP), São Paulo/SP, Brazil. The authors declare no conflict of interest. Received for publication 11/11/2011 - Accepted for publication em 3/9/2012 Rev Bras Oftalmol. 2014; 73 (5): 311-13 312 Lorena SHT , Silva JAF INTRODUCTION D acryocystocele is characterised by a dilated lacrimal sac and is often regarded as a congenital condition. However, it is a rare disease in adults. It presents as a painless bulge in the medial region of the orbit below the medial ligament. Its mechanism involves an acquired obstruction at the level of Krause’s valve and obstruction proximal to the common canaliculus, at the level of Rosenmuller’s valve.(1-3) In a patient with nasal obstruction, the differential diagnosis includes masses such as haemangioma, glioma, encephalocele, and dermoid cyst, as well as congenital bone anomalies such as choanal atresia.(4,5) The tear secretion test, endoscopy, computed tomography, and magnetic resonance imaging can be used to diagnose the condition. Dacryocystocele in adults should be considered as an obstruction of the nasolacrimal duct, and intranasal examination should be performed before external dacryocystorhinostomy.(68) Similar to paediatric patients, endoscopic marsupialization of the nasal cyst with stent placement seems to be the appropriate therapeutic approach. Some cases can be treated with external dacryocystorhinostomy.(9-11) CASE REPORT A white, 42-year-old woman presented with epiphora in the right eye and progressive ipsilateral nasal congestion starting 4 months earlier. She had no history of epistaxis, facial fracture, or sinus and nasal disorders. Ophthalmic examination found a soft mass in the medial region of the right orbit (Figure 1). Biomicroscopy showed no hyperaemia in the bulbar conjunctiva and no anterior chamber reaction. The Milder test was intensely positive. Catheterisation found a soft stop after introducing the Bowman probe 9 mm into the canaliculus. The Jones 1 test was negative. Examination of the left eye was normal, including eyelid position. Right anterior rhinoscopy found no mass below the inferior turbinate. The patient was prescribed prophylactic antibiotic therapy and cold packs, and the dacryocystocele resolved after 2 weeks, progressing to chronic dacryocystitis. The patient will undergo external dacryocystorhinostomy. DISCUSSION Dacryocystocele in the medial orbital region is a relatively rare condition, but congenital dacryocystocele has been recognised as an individual disease since 1933(12). Congenital dacryocystocele is found almost exclusively in paediatric patients(13), and it has a specific natural history, clinical features, disease mechanism, and treatment. Lacrimal sac dilation occurs because of distal nasolacrimal duct obstruction and functional obstruction of the common canaliculus. In cases of nasolacrimal duct obstruction, secretions can accumulate in the lacrimal sac, culminating in its dilation and obstructing the common canaliculus. Another mechanism proposed for dacryocystocele involves folds in the common canaliculus due to a dilated lacrimal sac and Rosenmuller’s valve malfunction secondary to oedema and inflammation.(13) Children with dacryocystocele are treated with antibiotics, massage, and cold compresses, and if medical treatment is ineffective, probing and irrigation of the lacrimal pathway associated with intranasal endoscopic marsupialisation of the cyst are then indicated.(14) There are a few reports of dacryocystocele in adults(15). Its clinical picture includes painless bulging of the medial region of the orbit below the medial ligament. The lacrimal secretion test, endoscopy, computed tomography, and magnetic resonance imaging can be used to diagnose the condition.(16) The disease mechanism of dacryocystocele is similar in adults and children, but the nasolacrimal duct obstruction in adults is acquired. A complication of dacryocystocele is chronic dacryocystitis.(17) Treatment involves placement of a nasolacrimal stent or dacryocystorhinostomy.(18,19) It may be necessary to differentiate dacryocystocele from a tumour of the lacrimal sac.(20,21) Adult dacryocystocele can be adequately diagnosed through studies such as ultrasound imaging, computed tomography, and magnetic resonance imaging. Computed tomography has become the most important method for locating and characterising an orbital mass. CT can determine the correct anatomical diagnosis by showing the dacryocystocele in the lacrimal sac and is also helpful in differentiating dacryocystocele from other masses that can affect the medial canthus in adults. An orbital tumour in the medial orbital region such as haemangioma, neurofibroma, lymphangioma, or rhabdomyosarcoma can be seen on CT as a solid mass. R EFERENCES 1. 2. 3. 4. 5. Figure 1. Frontal and lateral images of right dacryocystocele. Rev Bras Oftalmol. 2014; 73 (5): 311-13 6. Lai PC, Wang JK, Liao SL. A case of dacryocystocele in an adult. Jpn J Ophthalmol. 2004;48(4):419-21. Xiao MY, Tang LS, Zhu H, Li YJ, Li HL, Wu XR. Adult nasolacrimal sac mucocele. Ophthalmologica. 2008;222(1):21-6. Ansari SA, Pak J, Shields M. Pathology and imaging of the lacrimal drainage system. Neuroimaging Clin N Am. 2005;15(1):221-37. Lelli GJ, Levy RL. Epidermoid cyst masquerading as dacryocystocele: case report and review. Orbit. 2011;30(2):114-5. Debnam JM, Esmaeli B, Ginsberg LE. Imaging characteristics of dacryocystocele diagnosed after surgery for sinonasal cancer. AJNR Am J Neuroradiol. 2007;28(10):1872-5. Weber AL, Rodriguez-DeVelasquez A, Lucarelli MJ, Cheng HM. Normal anatomy and lesions of the lacrimal sac and duct: evalu- Adult dacryocystocele 7. 8. 9. 10. 11. 12. 13. 14. 15. ated by dacryocystography, computed tomography, and MR imaging. Neuroimaging Clin N Am. 1996;6(1):199-217. Berlucchi M, Tomenzoli D, Trimarchi M, Lombardi D, Battaglia G, Nicolai P.[Dacryocystocele in the adult: etiology, diagnosis and treatment]. ActaOtorhinolaryngol Ital. 2001;21(2):100-4. Day S, Hwang TN, Pletcher SD, Bhatki A, McCulley TJ. Interactive image- guided endoscopic dacryocystorhinostomy. Ophthal Plast Reconstr Surg. 2008;24(4):338-40. Plaza G, Nogueira A, González R, Ferrando J, Toledano N. Surgical treatment of familial dacryocystocele and lacrimal puncta agenesis. Ophthal Plast Reconstr Surg. 2009;25(1):52-3. Song HY, Lee DH, Ahn H, Kim JH, Kang SG, Yoon HK, et al. Lacrimal system obstruction treated with lacrimal polyurethane stents: outcome of removal of occluded stents. Radiology. 1998;208(3):689-94. Yazici B, Yazici Z, Parlak M. Treatment of nasolacrimal duct obstruction in adults with polyurethane stent. Am J Ophthalmol. 2001;131(1): 37-43. Duke-Elder SS, editor. System of ophthalmology: normal and abnormal development: congenital deformities. St Louis: Mosby; 1964. Vol. 3, Pt 2. p. 934-41. Rand PK, Ball WS Jr, Kulwin DR. Congenital nasolacrimal mucoceles: CT evaluation. Radiology. 1989;173(3):691-4. Shashy RG, Durairaj V, Holmes JM, Hohberger GG, Thompson DM, Kasperbauer JL. Congenital dacryocystocele associated with intranasal cysts: diagnosis and management. Laryngoscope. 2003;113(1):37-40. Erratum in Laryngoscope. 2005;115(4):759. Durairaj, Vikram [corrected to Durairaj, Vikram D]. Yip CC, McCulley TJ, Kersten RC, Bowen AT, Alam S, Kulwin DR. Adult nasolacrimal duct mucocele. Arch Ophthalmol. 313 2003;121(7):1065-6. 16. PerryLJ, Jakobiec FA, Zakka FR, Rubin PA. Giant dacryocystomucopyoce in na adult a review of lacrimal sac enlargements with clinical and histopathologic differencial diagnoses. Sury Ophthalmol. 2012;57(5):474-85. 17. Meyer JR, Quint DJ, Holmes JM, Wiatrak BJ. Infected congenital mucocele of the nasolacrimal duct. AJNR Am J Neuroradiol. 1993;14(4):1008-10. 18. Perena MF, Castillo J, Medrano J, De Gregorio MA, Loras E, Cristobal JA. Nasolacrimal polyurethane stent placement: preliminary results. Eur J Ophthalmol. 2001;11(1):25-30. 19. Eloy P, Martinez A, Leruth E, Levecq L, Bertrand B. Endonasal endoscopic dacryocystorhinostomy for a primary dacryocystocele in an adult. B-ENT. 2009;5(3):179-82. 20. Fliss DM, Freeman JL, Hurwitz JJ, Heathcote JG. Mucoepidermoid carcinoma of the lacrimal sac: a report of two cases, with observations on the histogenesis. Can J Ophthalmol. 1993;28(5):228-35. 21. Sabet SJ, Tarbet KJ, Lemke BN, Smith ME, Albert DM. Granular cell tumor of the lacrimal sac and nasolacrimal duct: no invasive behavior with incomplete resection. Ophthalmology. 2000;107(11):1992-4. Corresponding author: Silvia Helena Tavares Lorena Rua Flórida 1404, Brooklin CEP: 04561-030, São Paulo/SP, Brazil E-mail: [email protected] Rev Bras Oftalmol. 2014; 73 (5): 311-13 314 Instruções aos autores A Revista Brasileira de Oftalmologia (Rev Bras Oftalmol.) - ISSN 0034-7280, publicação científica da Sociedade Brasileira de Oftalmologia, se propõe a divulgar artigos que contribuam para o aperfeiçoamento e o desenvolvimento da prática, da pesquisa e do ensino da Oftalmologia e de especialidades afins. Todos os manuscritos, após aprovação pelos Editores, serão avaliados por dois ou três revisores qualificados (peer review), sendo o anonimato garantido em todo o processo de julgamento. Os comentários dos revisores serão devolvidos aos autores para modificações no texto ou justificativa de sua conservação. Somente após aprovações finais dos revisores e editores, os manuscritos serão encaminhados para publicação. 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A Revista Brasileira de Oftalmologia não endossa a opinião dos autores, eximindo-se de qualquer responsabilidade em relação a matérias assinadas. Os artigos podem ser escritos em português, espanhol, inglês ou francês. A versão “on-line” da revista poderá ter artigos apenas em inglês. A Revista Brasileira de Oftalmologia recebe para publicação: Artigos Originais de pesquisa básica, experimentação clínica ou cirúrgica; Divulgação e condutas em casos clínicos de relevante importância; Revisões de temas específicos, Atualizações; Cartas ao editor. Os Editoriais serão escritos a convite, apresentando comentários de trabalhos relevantes da própria revista, pesquisas importantes publicadas ou comunicações dos editores de interesse para a especialidade. Artigos com objetivos comerciais ou propagandísticos serão recusados. Os manuscritos deverão obedecer as seguintes estruturas: Artigo Original: Descreve pesquisa experimental ou investigação clínica - prospectiva ou retrospectiva, randomizada ou duplo cego. Deve ter: Título em português e inglês, Resumo estruturado, Descritores; Abstract, Keywords, Introdução, Métodos, Resultados, Discussão, Conclusão e Referências. Rev Bras Oftalmol. 2014; 73 (5): 316-17 B) Segunda folha Resumo e Descritores: Resumo, em português e inglês, com no máximo 250 palavras. Para os artigos originais, deverá ser estruturado (Objetivo, Métodos, Resultados, Conclusão), ressaltando os dados mais significativos do trabalho. Para Relatos de Caso, Revisões ou Atualizações, o resumo não deverá ser estruturado. Abaixo do resumo, especificar no mínimo cinco e no máximo dez descritores (Keywords) que definam o assunto do trabalho. Os descritores deverão ser baseados no DeCS Descritores em Ciências da Saúde - disponível no endereço eletrônico http://decs.bvs.br/ Abaixo do Resumo, indicar, para os Ensaios Clínicos, o número de registro na base de Ensaios Clínicos (http://clinicaltrials.gov)* C) Texto Deverá obedecer rigorosamente a estrutura para cada categoria de manuscrito. Em todas as categorias de manuscrito, a citação dos autores no texto deverá ser numérica e sequencial, utilizando algarismos arábicos entre parênteses e sobrescritos. As citações no texto deverão ser numeradas sequencialmente em números arábicos sobrepostos, devendo evitar a citação nominal dos autores. Introdução: Deve ser breve, conter e explicar os objetivos e o motivo do trabalho. 315 Métodos: Deve conter informação suficiente para saber-se o que foi feito e como foi feito. A descrição deve ser clara e suficiente para que outro pesquisador possa reproduzir ou dar continuidade ao estudo. Descrever a metodologia estatística empregada com detalhes suficientes para permitir que qualquer leitor com razoável conhecimento sobre o tema e o acesso aos dados originais possa verificar os resultados apresentados. Evitar o uso de termos imprecisos tais como: aleatório, normal, significativo, importante, aceitável, sem defini-los. Os resultados da pesquisa devem ser relatados neste capítulo em seqüência lógica e de maneira concisa. Informação sobre o manejo da dor pós-operatório, tanto em humanos como em animais, deve ser relatada no texto (Resolução nº 196/96, do Ministério da Saúde e Normas Internacionais de Proteção aos Animais). Resultados: Sempre que possível devem ser apresentados em Tabelas, Gráficos ou Figuras. Discussão: Todos os resultados do trabalho devem ser discutidos e comparados com a literatura pertinente. Conclusão: Devem ser baseadas nos resultados obtidos. Agradecimentos: Devem ser incluídos colaborações de pessoas, instituições ou agradecimento por apoio financeiro, auxílios técnicos, que mereçam reconhecimento, mas não justificam a inclusão como autor. Referências: Devem ser atualizadas contendo, preferencialmente, os trabalhos mais relevantes publicados, nos últimos cinco anos, sobre o tema. Não deve conter trabalhos não referidos no texto. Quando pertinente, é recomendável incluir trabalhos publicados na RBO. As referências deverão ser numeradas consecutivamente, na ordem em que são mencionadas no texto e identificadas com algarismos arábicos. A apresentação deverá seguir o formato denominado “Vancouver Style”, conforme modelos abaixo. Os títulos dos periódicos deverão ser abreviados de acordo com o estilo apresentado pela National Library of Medicine, disponível, na “List of Journal Indexed in Index medicus” no endereço eletrônico: http://www.ncbi.nlm.nih.gov/ entrez/query.fcgi?db=journals. Para todas as referências, citar todos os autores até seis. Quando em número maior, citar os seis primeiros autores seguidos da expressão et al. Artigos de Periódicos: Dahle N, Werner L, Fry L, Mamalis N. Localized, central optic snowflake degeneration of a polymethyl methacrylate intraocular lens: clinical report with pathological correlation. Arch Ophthalmol. 2006;124(9):1350-3. Arnarsson A, Sverrisson T, Stefansson E, Sigurdsson H, Sasaki H, Sasaki K, et al. Risk factors for five-year incident age-related macular degeneration: the Reykjavik Eye Study. Am J Ophthalmol. 2006;142(3):419-28. Livros: Yamane R. Semiologia ocular. 2a ed. Rio de Janeiro: Cultura Médica; 2003. Capítulos de Livro: Oréfice F, Boratto LM. Biomicroscopia. In: Yamane R. Semiologia ocular. 2ª ed. Rio de Janeiro: Cultura Médica; 2003. Dissertações e Teses: Cronemberger S. Contribuição para o estudo de alguns aspectos da aniridia [tese]. São Paulo: Universidade Federal de São Paulo; 1990. Publicações eletrônicas: Herzog Neto G, Curi RLN. Características anatômicas das vias lacrimais excretoras nos bloqueios funcionais ou síndrome de Milder. Rev Bras Oftalmol [periódico na Internet]. 2003 [citado 2006 jul 22];62(1):[cerca de 5p.]. Disponível em: www.sboportal.org.br Tabelas e Figuras: A apresentação desse material deve ser em preto e branco, em folhas separadas, com legendas e respectivas numerações impressas ao pé de cada ilustração. No verso de cada figura e tabela deve estar anotado o nome do manuscrito e dos autores. Todas as tabelas e figuras também devem ser enviadas em arquivo digital, as primeiras preferencialmente em arquivos Microsoft Word (r) e as demais em arquivos Microsoft Excel (r), Tiff ou JPG. As grandezas, unidades e símbolos utilizados nas tabelas devem obedecer a nomenclatura nacional. Fotografias de cirurgia e de biópsias onde foram utilizadas colorações e técnicas especiais serão consideradas para impressão colorida, sendo o custo adicional de responsabilidade dos autores. Legendas: Imprimir as legendas usando espaço duplo, acompanhando as respectivas figuras (gráficos, fotografias e ilustrações) e tabelas. Cada legenda deve ser numerada em algarismos arábicos, correspondendo as suas citações no texto. Abreviaturas e Siglas: Devem ser precedidas do nome completo quando citadas pela primeira vez no texto ou nas legendas das tabelas e figuras. Se as ilustrações já tiverem sido publicadas, deverão vir acompanhadas de autorização por escrito do autor ou editor, constando a fonte de referência onde foi publicada. O texto deve ser impresso em computador, em espaço duplo, papel branco, no formato 210mm x 297mm ou A4, em páginas separadas e numeradas, com margens de 3cm e com letras de tamanho que facilite a leitura (recomendamos as de nº 14). O original deve ser encaminhado em uma via, acompanhado de CD, com versão do manuscrito, com respectivas ilustrações, digitado no programa “Word for Windows 6.0. A Revista Brasileira de Oftalmologia reserva o direito de não aceitar para avaliação os artigos que não preencham os critérios acima formulados. Versão português-inglês: Seguindo os padrões dos principais periódicos mundiais, a Revista Brasileira de Oftalmologia contará com uma versão eletrônica em inglês de todas as edições. Desta forma a revista impressa continuará a ser em português e a versão eletrônica será em inglês. A Sociedade Brasileira de Oftalmologia, Sociedade Brasileira de Catarata e Implantes Intraoculares e Sociedade Brasileira de Cirurgia Refrativa, se comprometem a custear a tradução dos artigos para língua inglesa, porém seus autores uma vez que tenham aprovado seus artigos se disponham a traduzir a versão final para o inglês, está será publicada na versão eletrônica antecipadamente a publicação impressa (ahead of print). * Nota importante: A “Revista Brasileira de Oftalmologia” em apoio às políticas para registro de ensaios clínicos da Organização Mundial de Saúde (OMS) e do Intemational Committee of Medical Joumal Editors (ICMJE), reconhecendo a importância dessas iniciativas para o registro e divulgação internacional de informação sobre estudos clínicos, em acesso somente aceitará para publicação, a partir de 2008, os artigos de pesquisas clínicas que tenham recebido um número de identificação em um dos Registros de Ensaios Clínicos validados pelos critérios estabelecidos pela OMS e ICMJE, disponível no endereço: http://clinicaltrials.gov ou no site do Pubmed, no item <ClinicalTrials.gov>. O número de identificação deverá ser registrado abaixo do resumo. Os trabalhos poderão ser submetidos pela Internet, pelo site rbo.emnuvens.com.br Rev Bras Oftalmol. 2014; 73 (5): 316-17 316 Revista Brasileira de Oftalmologia Declaração dos Autores (é necessária a assinatura de todos os autores) Em consideração ao fato de que a Sociedade Brasileira de Oftalmologia está interessada em editar o manuscrito a ela encaminhado pelo(s) o(s) autor(es) abaixo subscrito(s), transfere(m) a partir da presente data todos os direitos autorais para a Sociedade Brasileira de Oftalmologia em caso de publicação pela Revista Brasileira de Oftalmologia do manuscrito............................................................. . Os direitos autorais compreendem qualquer e todas as formas de publicação, tais como na mídia eletrônica, por exemplo. O(s) autor (es) declara (m) que o manuscrito não contém, até onde é de conhecimento do(s) mesmo(s), nenhum material difamatório ou ilegal, que infrinja a legislação brasileira de direitos autorais. Certificam que, dentro da área de especialidade, participaram cientemente deste estudo para assumir a responsabilidade por ele e aceitar suas conclusões. Certificam que, com a presente carta, descartam qualquer possível conflito financeiro ou de interesse que possa ter com o assunto tratado nesse manuscrito. Título do Manuscrito___________________________________________________________________________ Nome dos Autores_______________________________________________________________________________ _____________________________________________________________________________________________ Minha assinatura abaixo indica minha total concordância com as três declarações acima. Data____________Assinatura do Autor____________________________________________________________ Data____________Assinatura do Autor____________________________________________________________ Data____________Assinatura do Autor_____________________________________________________________ Data____________Assinatura do Autor_____________________________________________________________ Data____________Assinatura do Autor____________________________________________________________ Data____________Assinatura do Autor_____________________________________________________________ Rev Bras Oftalmol. 2014; 73 (5): 318