UNIVERSIDADE VEIGA DE ALMEIDA PROGRAMA DE PÓS-GRADUAÇÃO STRICTO SENSU MESTRADO PROFISSIONAL EM ODONTOLOGIA OSMAR DE AGOSTINHO NETO AVALIAÇÃO CLÍNICA E RADIOGRÁFICA DE PACIENTES SUBMETIDOS À TERAPIA IMPLANTAR COM CARREGAMENTO IMEDIATO EM MAXILA EDÊNTULA: UM ESTUDO RETROSPECTIVO COM ACOMPANHAMENTO DE ATÉ CINCO ANOS RIO DE JANEIRO 2014 OSMAR DE AGOSTINHO NETO MESTRADO PROFISSIONAL EM ODONTOLOGIA ÁREA DE CONCENTRAÇÃO: REABILITAÇÃO ORAL AVALIAÇÃO CLÍNICA E RADIOGRÁFICA DE PACIENTES SUBMETIDOS À TERAPIA IMPLANTAR COM CARREGAMENTO IMEDIATO EM MAXILA EDÊNTULA: UM ESTUDO RETROSPECTIVO COM ACOMPANHAMENTO DE ATÉ CINCO ANOS Artigo apresentado ao Programa de Pós-graduação - Stricto Sensu Mestrado Profissional em Odontologia - Universidade Veiga de Almeida, como parte dos requisitos para obtenção do título de Mestre em Odontologia. Área de concentração - Reabilitação Oral. Orientadora: Profa. Dra. Cleide Gisele Ribeiro RIO DE JANEIRO 2014 UNIVERSIDADE VEIGA DE ALMEIDA SISTEMA DE BIBLIOTECAS Rua Ibituruna, 108 – Maracanã 20271-020 – Rio de Janeiro – RJ Tel.: (21) 2574-8871 Fax.: (21) 2574-8922 FICHA CATALOGRÁFICA A275a Agostinho Neto, Osmar de. Avaliação clínica e radiográfica de pacientes submetidos à terapia implantar com carregamento imediato em maxila edêntula: um estudo retrospectivo com acompanhamento de até cinco anos. / Osmar de Agostinho Neto, 2014. 54 f.; 30 cm Dissertação (Mestrado) –Universidade Veiga de Almeida, Mestrado em Odontologia, Reabilitação Oral, Rio de Janeiro, 2014. Orientadora: Profa. Dra. Cleide Gisele Ribeiro 1. Implantes dentários. 2. Edentulismo. 3. Carga imediata I. Ribeiro, C. G. II. Universidade Veiga de Almeida, Mestrado em Odontologia, Reabilitação Oral. III. Título CDD – 617.6 DeCS Ficha Catalográfica elaborada pelo Sistema de Bibliotecas da UVA Biblioteca Maria Anunciação Almeida de Carvalho FOLHA DE APROVAÇÃO OSMAR DE AGOSTINHO NETO AVALIAÇÃO CLÍNICA E RADIOGRÁFICA DE PACIENTES SUBMETIDOS À TERAPIA IMPLANTAR COM CARREGAMENTO IMEDIATO EM MAXILA EDÊNTULA: UM ESTUDO PILOTO Artigo apresentado ao Programa de Pós-graduação - Stricto Sensu Mestrado Profissional em Odontologia - Universidade Veiga de Almeida, como parte dos requisitos para obtenção do título de Mestre em Odontologia. Área de concentração - Reabilitação Oral. Aprovado em 19 de março de 2014. BANCA EXAMINADORA __________________________________________ Profa. Dra. Cleide Gisele Ribeiro Universidade Veiga de Almeida __________________________________________ Prof. Dr. Eduardo José Veras Lourenço Universidade Veiga de Almeida __________________________________________ Prof. Dr. George Miguel Spyrides Universidade Federal do Rio de Janeiro Dedico este trabalho a minha família, especialmente a minha esposa Livia Mayer que suportou e entendeu os períodos de ausência, além da valiosa ajuda e apoio compartilhada na organização deste trabalho. AGRADECIMENTOS Ao Coordenador do Programa de Mestrado Profissional em Odontologia, Prof. Dr. Antônio Carlos Canabarro Andrade Júnior, pela dedicação e grande estrutura disponibilizada aos alunos. A minha Orientadora Profa. Dra. Cleide Gisele Ribeiro, obrigado pela dedicação, incentivo, ensinamentos, horas dedicadas à elaboração do trabalho, confiança, oferecendo todo suporte necessário por meio do conhecimento e experiência. Ao grupo de professores do Mestrado, pela paciência, ensinamentos, senso crítico e orientações. Ao professores do Departamento de Prótese e Materiais Dentários da Faculdade de Odontologia da Universidade Federal do Rio de Janeiro, em especial a Profa. Silvana Marques Miranda Spyrides, que gentilmente liberou minhas obrigações durante os horários do curso, além de toda dedicação e orientação. Aos profissionais da Faculdade de odontologia da Universidade Federal de Juiz de Fora, que ajudaram com o fornecimento de dados para a realização desse trabalho. Aos meus colegas e alunos do Curso de Mestrado, pelo compartilhamento de experiências e bons momentos durante o decorrer do curso. RESUMO A carga imediata em implantes inseridos em mandíbulas edêntulas é um método eficiente, confiável e previsível. Contudo, existem poucos trabalhos disponíveis que tenham avaliado a longevidade deste tipo de procedimento na maxila. O objetivo deste trabalho foi avaliar, retrospectivamente, as características clínicas e radiográficas de pacientes que foram submetidos a um protocolo cirúrgico para instalação de implantes dentais com carga imediata através de próteses fixas parafusadas metaloplásticas na maxila. Dez pacientes foram aleatoriamente selecionados na clínica de especialização em implantodontia da Universidade Federal de Juiz de Fora, Brasil. Foram avaliados 59 implantes através de radiografias periapicais para a avaliação da perda óssea ao redor dos implantes, e avaliação clínica, do índice de placa e da satisfação dos pacientes em relação ao tratamento. Os resultados demonstraram que a maioria dos implantes avaliados tinham ausência de perda óssea, queixa subjetiva de dor, sensação de corpo estranho ou parestesia. A taxa de sobrevivência acumulada dos implantes foi de 94,9% e a taxa de sobrevivência das próteses foi de 100%. A média de satisfação com o tratamento foi de 9,5 (escala de 0 a 10). Concluiuse que a realização de um protocolo de 5 ou 6 implantes e a instalação imediata de uma prótese fixa parafusada metaloplástica pode ser considerado um método seguro e eficaz para a reabilitação de maxilas edêntulas, com um alto nível de satisfação em relação ao tratamento, demonstrado pelos pacientes. Palavras-chave: implantes dentários, edentulismo, carga imediata. ABSTRACT Immediate loaded implants inserted in edentulous jaws is an efficient, reliable and predictable method. However, there are few studies available that have evaluated the longevity of this type of procedure in the maxilla. The aim of this study was to evaluate retrospectively the clinical and radiographic characteristics of patients who have been submitted through a surgical protocol for installation of dental implants and immediate screw-retained metaloplastic fixed prostheses in the maxilla. Ten patients were randomly selected from Implantology Specilization Clinic of Universidade Federal de Juiz de Fora, Brasil. A total of 59 implants were evaluated through periapical radiographs to assess bone loss around implants, besides clinical evaluation, plaque index and the satisfaction of patients regarding treatment. The results showed that the majority of the evaluated implants had no bone loss, subjective complaints of pain, or foreign body sensation or paresthesia. The cumulative survival rate of implants was 94.9% and denture survival rate was 100%. The mean satisfaction with treatment was 9.5 (scale from 0 to 10). It was concluded that it could be considered safe and effective to perform the protocol of 5 or 6 implants and immediate loaded placement of a metaloplastic screw-retained fixed prosthesis for the rehabilitation of edentulous maxillae, with a high satisfaction level related to treatment shown by patients. Keywords: Dental implants, edentulism, loading protocol SUMÁRIO 1- Introdução 10 2- Materiais e métodos 12 2.1- Procedimento clínico 12 2.2- Critérios avaliados 13 2.2.1- Avaliação radiográfica 13 2.2.2- Avaliação clínica 14 2.2.3- Avaliação da satisfação em relação ao tratamento 14 3- Resultados 16 4- Discussão 20 5- Conclusão 25 6- Normas da revista escolhida para publicação 26 7- Artigo – versão em inglês 33 8- Referências 50 1- INTRODUÇÃO Desde a introdução do protocolo original de Branemark para a reabilitação de pacientes edêntulos, um grande número de modificações da abordagem clínica tem sido feitas ao longo dos anos com o objetivo de atender as necessidades dos pacientes, melhorar os resultados clínicos, e reduzir o tempo total do tratamento1. De acordo com as recomendações de Branemark et al.2 (1969), o carregamento de implantes dentais deve ser realizado em um segundo estágio cirúrgico, após um período de cicatrização médio estabelecido em três meses para a mandíbula e seis meses para a maxila, ao longo do qual os implantes permanecem cobertos, tempo este considerado fundamental para a osseointegração e o sucesso clínico. Todavia, Chiapasco (2004)3 e Morton et al.4 (2004) ressaltaram que a espera para se submeter um implante à carga não foi baseada cientificamente e sim, clinicamente. Além disso, com a evolução da forma e do tratamento da superfície dos implantes, novas técnicas foram desenvolvidas, tornando-se possível a realização do procedimento de carga imediata. Protocolos de aplicação de carga para implantes dentais têm sido foco de discussão desde a descoberta da osseointegração e diversas conferências têm sido realizadas no intuito de divulgar recomendações para a pesquisa científica. A partir do relatório da Conferência de Consenso da ITI realizada em 2008, o termo carga imediata refere-se ao carregamento de implantes no período anterior a uma semana subsequente à instalação dos implantes dentais5. Alguns critérios devem ser seguidos para que os implantes possam ser submetidos à carga imediata, tais como a estabilidade primária do implante, o 10 uso de restaurações provisórias que promovam esplintagem e controlem a carga mecânica aplicada aos implantes, bem como a prevenção da remoção de restaurações provisórias durante o período de cicatrização recomendado5. A literatura tem considerado o procedimento de carga imediata como uma modalidade de tratamento viável e com altas taxas de sobrevivência para várias indicações, desde que boa qualidade óssea esteja presente6 e a estabilidade primária do implante seja obtida3,7,8. Em mandíbulas edêntulas, a carga imediata tem sido bem documentada e muitos estudos têm demonstrado a sua previsibilidade9,10,11 enquanto somente poucos estudos em longo prazo relacionados a carga imediata em maxilas edêntulas foram relatados na literatura 12,13,14 . Em geral, a maxila edêntula apresenta características macroscópicas e microscópicas diferentes da mandíbula. Além disso, a qualidade do tecido ósseo na região localizada entre os forames mentuais é essencialmente diferente do osso maxilar, que apresenta um tecido ósseo mais trabecular e consequentemente, uma menor densidade15. Em função disso, podemos presumir que a obtenção da estabilidade primária dos implantes inseridos na maxila se torna mais difícil16. O presente trabalho teve por objetivo avaliar, retrospectivamente, as características clínicas e radiográficas de pacientes que foram submetidos a um protocolo cirúrgico para instalação de implantes dentais com carga imediata através de próteses fixas parafusadas, a fim de se determinar a eficácia e a longevidade deste tratamento. 11 2- MATERIAIS E MÉTODOS Este projeto de pesquisa foi aprovado pelo Comitê de Ética em Pesquisa em Seres Humanos da Universidade Federal de Juiz de Fora (sob o número: 222/2010). Foram selecionados 10 pacientes de ambos os sexos, que receberam próteses híbridas em maxilas edêntulas suportadas por implantes dentais de hexágono externo (Conexão Sistemas de Prótese, São Paulo, Brasil) submetidos a carga imediata. Estes procedimentos foram realizados na Clínica de Especialização em Implantodontia da Faculdade de Odontologia da UFJF há, no mínimo dois anos e, no máximo, cinco anos. Todos os pacientes receberam informações quanto à finalidade da pesquisa e após a assinatura do Termo de Consentimento Livre e Esclarecido, foram solicitadas aos pacientes radiografias periapicais, realizadas na Clínica de Radiologia da Faculdade da mesma universidade. 2.1 - Procedimento clínico Após planejamento protético e cirúrgico detalhado, os tamanhos dos implantes foram selecionados. Foi realizada anestesia local com lidocaína a 2% com epinefrina (Alphacaine 100, DFL Indústria e Comércio S.A., Rio de Janeiro, Brasil) seguida de uma incisão no meio da crista óssea dividindo o tecido ceratinizado. Após exposição do tecido ósseo, os sítios foram preparados e implantes instalados na região inter-sinusal para cada paciente de acordo com as recomendações do fabricante (Tabela 1). Após a colocação dos implantes de hexágono externo, pilares do tipo Micro-unit (Conexão Sistema de Próteses, Arujá, São Paulo, Brasil) foram parafusados nos implantes com torque de 20 Ncm e instalados sobre eles os transferentes dos pilares. Após esse procedimento, foi realizada a sutura. Utilizando o guia 12 multifuncional confeccionado a partir da duplicação da prótese do paciente, foi realizada a moldagem do paciente com poliéter (Impregum, Penta Soft, 3M ESPE AG, Seefeld, Germany) e feito registro intermaxilar. Dentro de 48 horas após a cirurgia, uma prótese fixa parafusada metaloplástica (resina acrílica com infra-estrutura metálica) foi instalada e dado torque de 10 Ncm nos parafusos protéticos. Mínimos ajustes foram necessários para obtenção de contatos oclusais estáveis. 2.2- Critérios avaliados: 2.2.1- Avaliação radiográfica De posse das radiografias periapicais, dois examinadores especialistas em Implantodontia após calibração (análise de concordância Kappa= 0,8), avaliaram a perda óssea ao redor dos implantes, adaptando os critérios de Kwakman et al.(1998)17. A perda óssea foi classificada de acordo com a seguinte escala: Escore 0: ausência de aparente perda óssea, Escore 1: redução do nível ósseo não excedendo um terço do comprimento do implante, Escore 2: redução do nível ósseo excedendo um terço do comprimento do implante, mas não excedendo metade do seu comprimento, Escore 3: redução do nível ósseo excedendo metade do comprimento do implante, Escore 4: Ausência de osso ao redor do implante. 13 2.2.2- Avaliação Clínica Para a avaliação clínica dos implantes dentais, os pacientes tiveram suas próteses removidas. Seguindo-se os critérios de Buser et al.18(1990), foram considerados os seguintes critérios: (1) ausência de queixas subjetivas persistentes, tais como dor, sensação do corpo estranho, e/ou o parestesia, (2) ausência de infecção periimplantar recorrente com supuração e (3) ausência de mobilidade. Para o registro do depósito de placa, aqui chamado de Índice de Placa (mPi) foi utilizada uma escala de 0 a 3, apresentada por Mombelli et al.19 em 1987: Escore 0: ausência de depósitos de placa; Escore 1: placa visível apenas após correr a sonda sobre a superfície livre da gengiva marginal do implante; Escore 2: placa clinicamente visível; Escore 3: placa abundante. 2.2.3- Avaliação da satisfação em relação ao tratamento Após a avaliação clínica e radiográfica dos implantes e a reinstalação das próteses dentais, um questionário adaptado de Schropp e Isidor de 2008 foi aplicado a fim de se determinar o grau de satisfação do paciente em relação às próteses sobre implante, em termos de conforto mastigatório, aparência, estética, capacidade de limpeza, adaptação e satisfação com o tratamento de forma geral. As questões foram consideradas em uma escala visual analógica (VAS), com a expressão mais negativa no ponto zero e a mais positiva no ponto dez. 20 14 Os dados obtidos foram submetidos à análise estatística descritiva, em Software SPSS 12.0 (SPSS Inc., Chicago, USA). Figura 1: Escala visual analógica utilizada no estudo. Figura 2: Questionário aplicado aos pacientes. 15 3- RESULTADOS Dez pacientes (4 homens e 6 mulheres) participaram do estudo, totalizando 59 implantes avaliados (Tabela 1). A média de idade encontrada foi de 57,8 anos. Tabela 1: Número total de implantes. Distribuição dos implantes de acordo com o comprimento e diâmetro Comprimento(mm) Diâmetro (mm) 10,0 11,5 13,0 Total 19 15 25 59 3,75 A avaliação radiográfica revelou que 72,9% (frequência observada igual a 43) dos implantes não apresentaram perda óssea aparente, sendo classificados como escore 0 e 27,1% (frequência observada igual a 16) apresentaram uma redução do nível ósseo não excedendo um terço do comprimento do implante (Tabela 2). Tabela 2: Distribuição da frequência dos escores da perda óssea avaliada radiograficamente. Percentual Percentual Frequência válido acumulado Score 0 (Ausência de 43 72,9 72,9 aparente perda óssea) Perda Score 1 óssea (Redução do nível ósseo <1/3 16 27,1 100,0 do comprimento do implante) Total 59 100,0 16 A partir da avaliação clínica, observou-se que em 96,6% (frequência observada igual a 57) dos implantes não houve queixa subjetiva de dor, sensação de corpo estranho ou parestesia. Já em 3,4% (frequência observada igual a 2) houve queixa de dor (Tabela 3). Tabela 3: Distribuição de frequência dos implantes quanto à presença ou ausência de queixas subjetivas de dor, sensação de corpo estranho ou parestesia. Percentual Percentual Frequência válido acumulado Queixas Ausentes 57 96,6 96,6 Presentes 2 3,4 100,0 Total 59 100,0 Em relação à infecção periimplantar, 5,1% (frequência observada igual a 3) dos implantes apresentaram sinais deste quadro clínico e 94,9% (frequência observada igual a 56) não apresentaram infecção (Tabela 4). Tabela 4: Distribuição de frequência quanto à presença ou ausência de sinais clínicos de infecção. Percentual Percentual Frequência válido acumulado Sinais de Infecção Ausentes 56 94,9 94,9 Presentes 3 5,1 100,0 Total 59 100,0 Quanto à mobilidade, apenas 5.1% dos implantes (frequência observada igual a 3) apresentaram, levemente, esta condição, enquanto os outros 94,9% (frequência observada igual a 56) não apresentaram (Tabela 5). 17 Tabela 5: Distribuição de frequência quanto à presença ou ausência de mobilidade. Percentual Percentual Frequência válido acumulado Ausentes 56 94,9 94,9 Mobilidade Presentes 3 5,1 100,0 59 100,0 Total A avaliação do índice de placa demonstrou que 15,3% (frequência observada igual a 9) não apresentaram depósitos de placa, classificados como escore 0; 57,6% (frequência observada igual a 34) exibiram depósitos de placa apenas após correr a sonda sobre a superfície livre da gengiva marginal do implante (escore 1) e 27,1% (frequência observada igual a 16) apresentaram placa clinicamente visível, sendo classificados como escore 2. Nenhum paciente apresentou placa abundante (escore 3) (Tabela 6). Tabela 6: Distribuição de frequência dos escores de Índice de Placa (mPI). Índice de placa (mPI) Score 0 (ausência de depósitos) Score 1 (placa visível após sondagem) Score 2 (placa clinicamente visível) Total Frequência Percentual válido Percentual acumulado 9 15,3 15,3 34 57,6 72,9 16 27,1 100,0 59 100,0 18 O teste Qui-quadrado de Pearson (índice de correlação=0,8) revelou associação positiva entre o índice de placa e a perda óssea ao redor dos implantes (p = 0.016). A taxa de sobrevivência acumulada dos implantes foi de 94,9% e a taxa de sobrevivência das próteses foi de 100%. Para a avaliação subjetiva da satisfação dos pacientes em relação ao tratamento, adotou-se a média dos valores obtidos em cada amostra. Em relação ao resultado final da prótese, a média de satisfação foi de 7,4. Quanto ao tempo para adaptação ao uso da prótese, a média foi de 8,1. Para a aparência estética, o valor médio foi de 7,0. Quanto à mastigação, a média foi de 8,4. Quanto ao grau de dificuldade para a higienização da prótese, o valor médio foi de 4,1. Em relação à experiência com o tratamento, a média dos valores foi de 7,8 e quanto à possibilidade de voltar atrás e refazer o tratamento, a média encontrada foi de 9,5 (Tabela 7). Tabela 7: Média, desvio- padrão e erro- padrão dos níveis de satisfação dos pacientes em relação ao tratamento (VAS) Questão Média Desvio- padrão Erro- padrão Você ficou satisfeito com o resultado final da sua 7.4 2.119 0.670 prótese? Quando você se acostumou 8.1 1.663 0.526 com a sua prótese? De forma geral, você está satisfeito(a) com a aparência 7.0 3.127 0.989 estética da sua prótese? Como está a sua mastigação após a colocação dessa 8.4 2.119 0.670 prótese? Qual o grau de dificuldade na 4.1 3.281 1.038 higienização dessa prótese? Como foi a sua experiência, de forma geral, com o 7.8 3.393 1.073 tratamento? Se pudesse voltar atrás, você faria o tratamento 9.5 1.581 0.500 novamente? 19 4- DISCUSSÃO Devido à menor qualidade óssea do rebordo maxilar em relação ao osso mandibular, a reabilitação do arco superior edêntulo através de próteses implantossuportadas é sempre uma terapia desafiadora, principalmente em casos de edentulismo por tempo prolongado. Em determinadas situações, são necessárias alternativas terapêuticas, como a utilização de cantiléveres distais, implantes de menor comprimento, enxerto ósseo e cirurgia para a elevação do assoalho do seio maxilar, bem como a utilização de áreas anatômicas específicas para a instalação dos implantes, como a região pterigóidea e o zigoma21. Contudo, na presença de tecido ósseo suficiente para a instalação dos implantes sem a necessidade de terapias alternativas para obtenção de tecido ósseo, o protocolo de carga imediata possibilita a redução do número de procedimentos cirúrgicos e do tempo de tratamento22. Embora o osso maxilar apresente menor densidade óssea nas regiões posteriores21 e possua um padrão de reabsorção palatal que dificulta a obtenção do paralelismo entre os implantes dentais6, diversos são os relatos científicos de sucesso clínico a partir de protocolos que utilizam 4 a 6 implantes em maxila edêntula, suportando uma prótese submetida a carga imediatamente após a instalação dos mesmos6,8,14,21,23,24. Sendo a estabilidade primária do implante considerada como um dos fatores mais importantes para a osseointegração 3,6,7,8,25,26. Em nosso estudo foram encontradas taxas de sobrevivência das próteses (100%) e dos implantes dentais (96.6%) semelhantes aos relatos da literatura3,6,23,24. Atualmente, o carregamento imediato de implantes dentais é uma realidade nos consultórios de implantodontistas, principalmente pelo fato 20 de proporcionar ao paciente uma redução no tempo total do tratamento7. Diversos são os relatos de pesquisas científicas qualificando a carga imediata em pacientes totalmente edêntulos como segura e eficaz3,6,8,21,22,23,24,26,27 Testori et al.1 (2013) no entanto, não acreditam que a aplicação de carga imediata em maxilas seja sempre a melhor alternativa, a partir do momento que constataram uma significante taxa de insucesso relacionada não somente à aplicação imediata de força mastigatória, mas também à idade do paciente, ao tipo de retenção da prótese, e à razão que levou à exodontia (dentes com doença endoperiodontal levaram à maior taxa de insucesso dos implantes substitutivos). Resultados similares atingiram Andesson et al.28 (2013), com mais de 10% de insucessos em implantes com carga imediata em maxilas, no entanto atingindo 100% de aproveitamento dos implantes instalados em mandíbulas. Browaeys et al.29 (2011) por sua vez registraram perdas da ordem de 2,1%, tanto em implantes maxilares quanto mandibulares, mas ainda assim a maior perda foi registrada em maxilas. No fim de seu estudo longitudinal, a perda acumulada foi de 9%, sendo considerados como insucesso todo e qualquer implante que tenha sido perdido ou apresentado mobilidade. A principal causa para a falha de implantes dentais parece ser a micromovimentação durante o período de cicatrização, resultante de próteses provisórias desajustadas, bem como da mastigação de alimentos duros, levando a uma excessiva movimentação que compromete a osseointegração6. Para Testori et al.1 no entanto, os implantes submetidos tanto a colocação imediata em alvéolos frescos e carga imediata teve uma taxa de sobrevivência cumulativa menor e estatisticamente significativa do que outras 21 combinações. No entanto, Peñarrocha-Oltra30 et al tiveram três implantes perdidos colocados imediatamente pós-extração e imediatamente carregadas, porém estatisticamente não significativo quando foi analisada a combinação de protocolo de carga e tipo de sítio receptor. O tabagismo também foi relacionado como fator de considerável prevalência de insucesso de implantes osseointegrados31. A taxa de sucesso se mostra alta tanto em implantes instalados axialmente quanto em implantes inclinados instalados em região posterior de maxila32,33. A avaliação radiográfica do estudo relatado neste artigo revelou que 72,9% dos implantes não apresentaram perda óssea aparente e 27,1% apresentaram uma redução do nível ósseo não excedendo um terço do comprimento do implante. Li et al.,8 avaliaram as alterações ósseas de 111 pacientes submetidos a carga funcional imediata através de próteses provisórias, em maxilas e mandíbulas edêntulas e a média de perda óssea marginal foi de 0,07 mm após um ano. Browayes et al.29 verificaram perda óssea periimplantar média da ordem de 1,2mm nos dois primeiros anos de seu estudo, não tendo avanço desta medida nos anos subsequentes. Em osso enxertado houve perda média de 0,3mm além este padrão. A avaliação do índice de placa (mPI), neste estudo, demonstrou que apenas 15,3% dos implantes não apresentaram depósitos de placa. Contudo, nenhum paciente apresentou placa abundante. Uma associação positiva foi encontrada entre o índice clínico mPI e a perda óssea avaliada em radiografias. A placa bacteriana foi, assim, considerada como um dos fatores etiológicos mais importantes para o aparecimento de uma doença periimplantar. Concordam com essa inferência Ferreira Jr. et al.34 que 22 avaliaram a correlação de três índices clínicos de inflamação gengival (índice gengival - GI, índice de sangramento sulcular, GI modificado por Mombelli) e o índice de placa modificado por Mombelli (mPI) com a real condição histológica periimplantar, concluindo que o mPI foi o único índice correlacionado estatisticamente de forma positiva com as alterações histológicas, podendo ser um bom parâmetro para se monitorar a saúde periimplantar18. Agliardi et al.33, trataram 32 pacientes com dois implantes axiais na região anterior da maxila e quatro implantes inclinados instalados posicionados nas paredes anteriores e posteriores dos seios maxilares, suportanto uma prótese total fixa com infra-estrutura metálica e foram observados por pelo menos três anos, onde o índice de placa e sangramento periimplantar reduziram significantemente durante o período de acompanhamento. A avaliação da satisfação dos pacientes em relação ao tratamento executado demonstrou que a grande maioria dos pacientes encontra-se satisfeita em relação ao resultado final da prótese. De forma semelhante, Zani et al.35 e Brennan et al.36 avaliaram o impacto da saúde bucal na qualidade de vida de pacientes tratados através de overdentures e próteses totais fixas implantossuportadas, concluindo que os pacientes tratados com próteses totais, removíveis ou fixas, estão satisfeitos com o tratamento. Em nosso estudo, apenas o grau de dificuldade para a higienização da prótese pode ser considerado como insatisfação. Marra et al.24 (2013) também reportaram satisfação elevada dos pacientes estudados, principalmente por estes terem usado anteriormente próteses totais convencionais que eram deficientes em termos de estabilidade, suporte e retenção. Agliardi et al.33 (2013) verificaram que a função mastigatória foi considerada excelente por 90,6% dos pacientes 23 de seu estudo, enquanto as funções estética e fonética foram laureadas por 87,5% dos mesmos. 24 5- CONCLUSÃO Dentro das limitações deste estudo e a partir dos achados clínicos e radiográficos, concluiu-se que a realização do protocolo cirúrgico com 5 a 6 implantes dentais e a imediata instalação de uma prótese fixa parafusada metaloplástica demonstrou ser uma terapia segura e eficaz para a reabilitação de maxilas edêntulas, o que relaciona-se a um alto nível de satisfação em relação ao tratamento, demonstrado pelos pacientes. 25 6- NORMAS DA REVISTA ESCOLHIDA PARA PUBLICAÇÃO Journal of Prosthodontics Author Guidelines Instructions to contributors Editorial office contact information David A. Felton, DDS, MS, FACP Editor-in-Chief West Virginia University School of Dentistry Robert C. Byrd Health Sciences Center PO Box 9400 Morgantown, WV 26506-9400 304-293-1000 E-mail: [email protected] Authors submitting a paper do so on the understanding that the work has not been published before, is not being considered for publication elsewhere and has been read and approved by all authors. The work shall not be published elsewhere in any language without the written consent of the publisher. The articles published in this journal are protected by copyright, which covers translation rights and the exclusive right to reproduce and distribute all of the articles printed in the journal. No material published in the journal may be stored on microfilm or videocassettes or in electronic databases and the like or reproduced photographically without the prior written permission of the publisher. Submission of Manuscripts Submission of Manuscripts Submit through our online submission and review site at http://mc.manuscriptcentral.com/jopr. Create an account, and upload the body of your manuscript. You will also be able to upload any digital figures associated with the manuscript. You will be able to track the progress of your manuscript through the peer review process. A Users Guide and online tutorial are available by clicking the “Get Help Now” link. All Journal of Prosthodontics forms and instructions are also available at the site. If you have any questions, please contact Alethea Gerding at [email protected]. Please note: the Journal of Prosthodontics will no longer review the following manuscripts: 1) Those testing groups with sample sizes less than 10 per group, unless the manuscript also includes a power calculation to determine the small group's statistical validity, or if the manuscript includes a justification for the smaller sample size (i.e., citations to similar studies also using small sample sizes). 26 2) 2D FEA studies, unless a strong case can be made that the study cannot be conducted via 3D FEA. Title page - The title page should contain the following information in the order given: 1) Full title of manuscript. 2) Authors' full names. 3) Authors' institutional affiliations including city and country. 4) A running title, not exceeding 60 letters and spaces. 5) The name and address of the author responsible for correspondence about the manuscript. If the work has previously been presented, the name, place, and date of meeting(s) must be given. If any financial support was received, the grant/contract number, sponsor name, and city, state, and country location must be supplied. Abstract page – An abstract is required for all manuscripts and must precede the body of the manuscript. Abbreviations and references should not appear in the abstract. Research manuscripts must conform to the Structured Abstract format. Structured Abstracts should not exceed 350 words and must contain the following information: (1) Purpose (2) Materials and Methods (3) Results (4) Conclusions Clinical reports and Techniques and Technology manuscripts do not need a structured abstract. Following the abstract and on the same page, there should be several words not appearing in the title of the manuscript to be titled: KEYWORDS. Text – Research manuscripts should include the following sections: Introduction, Materials and Methods, Results, Discussion, Conclusion, Acknowledgements, and References. Experimental design should be clearly described (eg, randomized clinical trial, cohort study, case-control study, case series). Other manuscripts should begin with an introductory paragraph of at least two to five sentences. The remainder of the manuscript should be divided into sections preceded by appropriate headings. The Introduction will include the following: a description of the problem that inspired the study; a brief discussion of relevant published material that addressed the same problem or that documents methodology used in the study; and the goal of the study, the purpose statement or hypothesis. The Materials and Methods section describes materials or subjects used and the methods selected to evaluate them, including information about the overall design, the nature of the sample studied, the type of interventions (or treatments) applied to the individual elements in the sample, and the principal outcome measure. Statistical methodology should be included in this section. 27 Please note: All human subject research (including surveys) must include a statement of ethical or institutional review board approval. Please note: For research reports, we require a minimum of ten (10) specimens per experimental group UNLESS a power calculation has been performed by a statistician to demonstrate that the sample size is capable of providing statistical significance. Or UNLESS the manuscript includes a justification for the smaller sample size (i.e., citations to similar studies also using small sample sizes). The Results section will be a clear statement of the findings and an evaluation of their validity based on the outcome of statistical tests. The Discussion section presents the research in its broader context, describes its clinical implications, identifies limitations or problems that emerged during the course of the study, characterizes the larger significance of the findings, and articulates any further questions remaining to be answered on the subject. The Conclusion section includes only a brief and succinct summary of the findings. References - Number references consecutively in the order in which they are first mentioned in the text. Identify references in texts, tables, and legends by superscript Arabic numerals. Use the style of the examples below, which are based on the format used by the US National Library of Medicine in Index Medicus. For abbreviations of journals, consult the 'List of the Journals Indexed' printed annually in the January issue of Index Medicus. For standard journal articles list all authors when three or fewer; when three or more, list first three authors and add et al. Example: Raghoebar GM, Brouwer TJ, Reintesma H, et al: Augmentation of the maxillary sinus floor of autogenous bone for the placement of endosseous implants: A preliminary report. J Oral Maxillofac Surg 1993;51:1198-1203 Chapter in book Phoenix, RD: Denture base resins: Technical considerations and processing techniques, in Anusavice KJ (ed): Phillips’ Science of Dental Materials, vol 1 (ed 10). Philadelphia, PA, Saunders, 1996, pp 237-271 Tables – Tables should be positioned following the references, not in the body of the manuscript. The tables should be numbered consecutively with Arabic numerals. Each table should be typed on a separate sheet. Include any necessary legends on the same page with the associated table. Illustrations – All graphs, drawings, and photographs are considered figures and should be numbered in sequence with Arabic numerals. Each figure 28 should have a legend and all legends should be typed together on a separate sheet and numbered correspondingly. The inclusion of color illustrations is at the discretion of the editor. Details must be large enough to retain their clarity after reduction in size. Micrographs should be designed to be reproduced without reduction, and they should be dressed directly on the micrograph with a linear size scale, arrows, and other designators as needed. Figures submitted to the Journal of Prosthodontics Photographs of People The Journal of Prosthodontics follows current HIPAA guidelines for the protection of patient/subject privacy. If an individual pictured in a digital image or photograph can be identified, his or her permission is required to publish the image. The corresponding author may submit a letter signed by the patient authorizing the Journal of Prosthodontics to publish the image/photo. Or, a form provided by the Journal of Prosthodontics (available by clicking the “Instructions and Forms” link in ScholaOne Manuscripts) may be downloaded for your use. This approval must be received by the Editorial Office prior to final acceptance of the manuscript for publication. Otherwise, the image/photo must be altered such that the individual cannot be identified (black bars over eyes, etc). Manipulation of Digital Photos Authors should be aware that the Journal considers digital images to be data. Hence, digital images submitted should contain the same data as the original image captured. Any manipulation using graphical software should be identified in either the Methods section or the caption of the photo itself. Identification of manipulation should include both the name of the software and the techniques used to enhance or change the graphic in any way. Such a disclaimer ensures that the methods are repeatable and ensures the scientific integrity of the work. No specific feature within an image may be enhanced, obscured, moved, removed, or introduced. The grouping of images from different SEMS, different teeth, or the mouths of different patients must be made explicit by the arrangement of the figure (i.e., by using dividing lines) and in the text of the figure legend. Adjustments of brightness, contrast, or color balance are acceptable if they are applied to the whole image and as long as they do not obscure, eliminate, or misrepresent any information present in the original, including backgrounds. The removal of artifacts or any non-integral data held in the image is not allowed. For instance, removal of papillae or “cleaning up” of saliva bubbles is not allowed. 29 Cases of deliberate misrepresentation of data will result in rejection of a manuscript, or if the misrepresentation is discovered after a manuscript’s acceptance, revocation of acceptance, and the incident will be reported to the corresponding author's home institution or funding agency. Letters to the Editor - Letters to the editor of the Journal of Prosthodontics are welcomed. You may submit through our online submission site (http://mc.manuscriptcentral.com/jopr) or email directly to the editor-in-chief at [email protected]. While we will read and respond to all letters, we will only publish a select few. We are most likely to publish letters that deal with a controversial topic or that take issue with research published in the Journal of Prosthodontics. While a letter may be critical, in order to be considered for publication, it must not be insulting. Criticism should be constructive, and arguments made should be appropriately referenced to previously published work. Upon approval for publication, we will publish the letter in the next available print issue of the Journal of Prosthodontics. When written in response to an article published in the Journal, we will also give the author of the original article the opportunity to respond. If they choose to do so, we will attempt to publish the letter and response in the same issue. Abbreviations, symbols and nomenclature – Authors are to use current prosthodontic nomenclature and are referred to the Glossary of Prosthodontic Terms (8th Edition) for accepted terminology. Generic names should be used for all drugs and equipment. When a trade name must be used, cite parenthetically the trade name and the name, city, state, and country of the manufacturer. Measurements should be in the metric system. Permissions – Any illustrations or tables that have been published previously must be accompanied by a letter of permission from the copyright holder (usually the publisher). Illustrations or tables that have been adapted or modified must also be accompanied by letters of permission. Copyright – Authors will be required to fill out a copyright assignment form prior to their articles being published. The form can be found here. 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The Journal of Prosthodontics defines major plagiarism as any case involving: • • • unattributed copying of another person's data/findings, or resubmission of an entire publication under another author's name (either in the original language or in translation), or verbatim copying of >100 words of original material in the absence of any citation to the source material, or unattributed use of original, published, academic work, such as the structure, argument or hypothesis/idea of another person or group where this is a major part of the new publication and there is evidence that it was not developed independently. Minor plagiarism is defined as: • • verbatim copying of <100 words without indicating that these are a direct quotation from an original work (whether or not the source is cited), unless the text is accepted as widely used or standardized (eg the description of a standard technique) close copying (not quite verbatim, but changed only slightly from the original) of significant sections (eg >100 words) from another work (whether or not that work is cited). 31 If the editorial board of the Journal of Prosthodontics suspects a case of plagiarism, we will first contact the authors for clarification. If the authors are unable to sufficiently explain the potential plagiarism, we reserve the right to inform the authors' institutions and funding agencies. If a published article is suspected of plagiarism, we will take the further step of informing our readers. 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The information will be disclosed in the published article. Proofreading – The designated corresponding author is provided with proofs and is asked to proofread them for typesetting errors. Important changes in the data are allowed, but authors will be charged for excessive alterations in proof. Offprints – Free access to the final PDF offprint of your article will be available via Author Services. Please sign up for Author Services if you would like to access your article PDF offprint upon publication of your paper, and enjoy the many other benefits the service offers. Visit http://authorservices.wiley.com/bauthor/ to sign up for Author Services. If you wish to order hardcopy offprints from this journal please visit: https://caesar.sheridan.com/reprints/redir.php?pub=10089&acro=JOPR NEW: Online production tracking is now available for your article through Wiley-Blackwell Author Services. Author Services enables authors to track their article – once it has been accepted – through the production process to publication online and in print. Authors can check the status of their articles online and choose to receive automated e-mails at key stages of production. The author will receive an email with a unique link that enables them to register and have their article automatically added to the system. Please ensure that a complete e-mail address is provided when submitting the manuscript. Visit http://authorservices.wiley.com/ for more details on online production tracking and for a wealth of resources including FAQs and tips on article preparation, submission and more. 32 7- ARTIGO – VERSÃO EM INGLÊS Formatado para o periódico: Journal of Prosthodontics Clinical and radiographic evaluation of patients submitted to immediate loading of implants placed in the edentulous maxilla: retrospective study with a follow up to five years. Osmar de Agostinho Neto, DDS, MS student, University Veiga de Almeida, Rio de Janeiro, Brazil Cleide Gisele Ribeiro, DDS, MS, PhD Professor, Federal University of Juiz de Fora, Juiz de Fora, Brazil Corresponding author: Profª. Drª Cleide Gisele Ribeiro Faculdade de Odontologia da Universidade Federal de Juiz de Fora -FO/UFJF Departamento de Clínica Odontológica Rua José Lourenço Kelmer, Campus Universitário Bairro São Pedro, Juiz de Fora, Minas Gerais, Brasil CEP: 36036-900 Telephone: +55-32-2102-3882 E-mail: [email protected] Disclosure The authors of the manuscript entitled “Clinical and radiographic evaluation of patients submitted to immediate loading of implants placed in the edentulous maxilla: a pilot study” claim to have no conflict of interest in personal, commercial, academic, political or financial orders in the manuscript, in any company or any of the products mentioned in this article. 33 Abstract Immediate loaded implants inserted in edentulous jaws is an efficient, reliable and predictable method. However, there are few studies available that have evaluated the longevity of this type of procedure in the maxilla. The aim of this study was to evaluate retrospectively the clinical and radiographic characteristics of patients who have been submitted through a surgical protocol for installation of dental implants and immediate screw-retained metaloplastic fixed prostheses in the maxilla. Ten patients were randomly selected from Implantology Specilization Clinic of Universidade Federal de Juiz de Fora, Brasil. A total of 59 implants were evaluated through periapical radiographs to assess bone loss around implants, besides clinical evaluation, plaque index and the satisfaction of patients regarding treatment. The results showed that the majority of the evaluated implants had no bone loss, subjective complaints of pain, or foreign body sensation or paresthesia. The cumulative survival rate of implants was 94.9% and denture survival rate was 100%. The mean satisfaction with treatment was 9.5 (scale from 0 to 10). It was concluded that it could be considered safe and effective to perform the protocol of 5 or 6 implants and immediate loaded placement of a metaloplastic screw-retained fixed prosthesis for the rehabilitation of edentulous maxillae, with a high satisfaction level related to treatment shown by patients. Keywords: Dental implants, edentulism, loading protocol 34 Introduction Since the introduction of Branemark’s original protocol to edentulous patients rehabilitation, a major number of clinical approach modifications have taken place throughout time aiming to reach patients’ needs, improve clinical results, and reduce total treatment time.1 According to the recommendations of Branemark et al.2 in 1969, dental implant loading should be performed in a second surgical stage, after a mean healing period established as being three months for the mandible and six months for the maxilla, throughout which the implants remained covered, this time being considered fundamental for osseointegration and clinical success to occur. Nevertheless, Chiapasco (2004) 3 and Morton et al. (2004) 4 pointed out that waiting to load an implant was not scientifically but clinically based, justifying the increasing number of researches that evaluated certain situations in which this period could be reduced without causing harm in the long term. Furthermore, with the advancement in the shape and surface treatment implants, new techniques have been developed, making it possible to perform the immediate loading procedure. Loading protocols for dental implants have been the focus of discussion since the discovery of osseointegration, and various conferences have been held with the purpose of divulging recommendations for scientific research. From the report of the ITI Conference of Consensus held in 2008, immediate loading refers to implant loading in the period before one week after dental implant placement5. Some criteria must be followed in order to submit implants to immediate loading, such as primary stability of the implant, the use of provisional 35 restorations that promote splinting and control the mechanical load applied on implants, as well as preventing the removal of temporary restorations during the recommended healing period5. The literature has considered the immediate loading protocol a feasible treatment modality with high survival rates for various indications, provided that there is good bone quality present6, and primary stability of the implant is obtained 3,7,8. When it comes to mandibles, immediate loading have been documented and many studies have shown its predictability9, 10, 11 while only a few long term studies have been related to immediate loading in edentulous maxilla in the literature12, 13, 14 . Usually, edentulous maxilla presents different macroscopic and microscopic features from the mandibles. Besides, bone quality in the region between mentual foramen is essentially different from maxillar bone, which shows a more trabecular bone tissue and, therefore lower density15. On that basis, we can presume that the obtention of primary stability of implants in the maxilla is more difficult.16 The aim of the present study was to evaluate the clinical and radiographic characteristics of patients who were submitted to a surgical protocol for the placement and immediate loading of implants in the maxillary arch using a screw-retained prosthesis, in order to determine the efficacy and longevity of this treatment. 36 Materials and Methods After approval of this research Project by the Ethics Committee on Research in Human Beings, of the Federal University of Juiz de Fora, Protocol No. 222/2010, 10 patients of both genders, who were submitted to surgical therapy for the placement and immediate loading of external hexagon dental implants (Conexão Sistemas de Prótese, São Paulo, Brazil) in the maxilla using screw-retained prostheses, at the Specialization Clinic in Implant Dentistry of the UFJF School of Dentistry, a minimum of two years and a maximum of five years ago, were randomly selected. They were contacted by telephone, and invited to have their dental implants evaluated. Immediately, during the first contact, all patients were provided with information as regards the purpose of the research and after signing the Term of Free and Informed Consent, they were asked to have periapical radiographs taken at the Radiology Clinic of the UFJF School of Dentistry. Clinical Procedure After surgical and prosthetic detailed planning, implant sizes were selected. Local anesthesia was administered with 2% lidocaine with epinephrine (Alphacaine 100, DFL Indústria e Comércio S.A., Rio de Janeiro, Brazil) followed by an incision in the middle of the bone crest to divide the keratinized. After exposure of the bone tissue, the sites were prepared and implants were placed in each patient’s inter-sinus region in accordance with the implant manufacturers’ recommendations (Table 1). After placement of the external hexagon implants, screws were tightened onto the Microunit abutments (Conexão Sistema de Próteses, Arujá, São Paulo, Brasil) with a torque of 20 Ncm and the transfers were placed on them. After this procedure, 37 suturing was performed. Using the multifuntional guide fabricated from a duplication of the patient’s denture, the patient’s impression was taken with polyether material (Impregum, Penta Soft, 3M ESPE AG, Seefeld, Germany) and the intermaxillary record was made. Within 48 hours after surgery, a metaloplastic screwed fixed prosthesis (acrylic resin with metal infrastructure) was put into place and the prosthetic screws were tightened with a torque of 10. Minimal adjustments were necessary to obtain bilateral stable occlusal contacts. Radiographic Evaluation Two examiners, specialists in implant dentistry, after calibration (analysis of concordance of Kappa = 0,8), examined the periapical radiographs to evaluate bone loss around the implants, comparing the radiographic images of the present follow-up period with those taken at the time of implant placement, adapting the Kwakman et al. (1998) criteria 17 . Bone loss was classified according to the following scale: Score 0: absence of apparent bone loss, Score 1: reduction in bone level not exceeding one third of implant length, Score 2: reduction in bone level exceeding one third of implant length, but not exceeding half its length, Score 3: reduction in bone level exceeding half of implant length, Score 4: absence of bone around the implant. Clinical Evaluation For clinical evaluation of the dental implants, the patient’s dentures were unscrewed. According to the criteria of Buser et al. (1990) 18 , the 38 following factors were considered: (1) absence of persistent subjective complaints, such as pain, foreign body sensation, and/or paresthesia, (2) absence of recurrent peri-implant infection with suppuration and (3) absence of mobility. To Record plaque deposits, here referred to as the Plaque index (mPi) a scale from 0 to 3, presented by Mombelli et al.19 in 1987, was used: Score 0: absence of plaque deposits, Score 1: visible plaque only after running the probe over the free marginal gingiva surface of the implant. Implants with surfaces treated with titanium spray in this area, Score 2: clinically visible plaque, Score 3: abundant plaque. Evaluation of satisfaction with treatment After clinical and radiographic evaluation of the implants and reinsertion of the dental prostheses, an adapted questionnaire from Schropp ans Isidor, 2008 was applied in order to determine the degree of patient satisfaction with the implant supported denture, in terms of masticatory comfort, esthetic appearance, cleaning capacity, fit and satisfaction with treatment in a general manner. The questions were considered on a visual analog scale (VAS), with the most negative expression on point zero and the most positive on point ten.20 The data obtained were submitted to descriptive statistical analysis using SPSS 12.0 Software (SPSS Inc., Chicago, USA). 39 Figure 1: Visual Analog Scale used at work. Figure 2: Questionnaire applied to patients. 40 Results Ten patients (4 men and 6 women) participated in the study, totaling 59 implants evaluated (Table 1). The mean age was 57.8 years. Radiographic evaluation revealed that 72.9% (frequency observed equal to 43) of the implants presented no apparent bone loss, being classified as Score 0 and 27.1% (frequency observed equal to 16) presented a reduction in bone level not exceeding one third of the implant length (Table 2). Table 1: Total number of implants. Distribution of implants according to the length and diameter Length (mm) Diameter 3,75 10,0 11,5 13,0 Total 19 15 25 59 (mm) Table 2: Frequency distribution of scores of bone loss assessed radiographically. Frequency Bone score 0 (Absence of apparent bone loss) Loss Score 1 Percent Cumulative Percent 43 72,9 72,9 (Reduction of bone level less than 1/3 of implant length) 16 27,1 100,0 Total 59 100,0 From the clinical evaluation it was observed that in 96.6% (frequency observed equal to 57) of the implants there was no subjective complaint of 41 pain, foreign body sensation or paresthesia. Where as in 3.4% (frequency observed equal to 2) there was complaint of pain (Table 3). Table 3: Frequency distribution of the implants for the presence or absence of subjective complaints of pain, foreign body sensation or paresthesia. Frequency Complaints Percent Cumulative Percent Absent 57 96,6 96,6 Present 2 3,4 100,0 Total 59 100,0 With regard to peri-implant infection, 5.1% (frequency observed equal to 3) of the implants presented signs of this clinical condition, and 94,9% (frequency observed equal to 56) presented no infection (Table 4). Table 4: Frequency distribution for the presence or absence of clinical signs of infection. Frequency Percent Cumulative Percent Absent 56 94,9 94,9 Signs of infection Present 3 5,1 100,0 59 100,0 Total As regards mobility, only 5.1% of the implants (frequency observed equal to 3) slightly presented this condition, while the other 94.9% (frequency observed equal to 56) showed no mobility (Table 5). 42 Table 5: Frequency distribution for the presence or absence of mobility. Mobility Frequency Percent Cumulative Percent Absent 56 94,9 94,9 Present 3 5,1 100,0 Total 59 100,0 The plaque index evaluation demonstrated that 15.3% (frequency observed equal to 9) presented no plaque deposits, classified as Score 0; 57.6% (frequency observed equal to 34) plaque deposits only after running the prove over the free marginal gingiva surface of the implant (Score 1) and 27.1% (frequency observed equal to 16) presented clinically visible plaque, being classified with Score 2. No patient presented abundant plaque (Score 3) (Table 6). Table 6: Frequency distribution of scores for Plaque Index (MPI). Frequency Percent Cumulative Percent 9 15,3 15,3 Score 1 (visible plaque after probing) 34 57,6 72,9 Score 2 (plaque clinically visible) 16 27,1 100,0 Total 59 100,0 Score 0 (absence of deposits) Plaque Index (mPI) Pearson’s Chi-Square test (correlation index = 0,8) showed positive association between the plaque index and bone loss around implants (p = 43 0.016). The cumulative survival rate of implants was 94.9% and the denture survival rate was 100%. For subjective evaluation of patient satisfaction with treatment, the mean of values obtained from each sample was adopted as the measure representative of the sample. As regards the end result of the denture, the mean satisfaction was 7.4. With reference to time taken to adapt to the use of the denture, the mean was 8.1. For esthetic appearance the mean value was 7.0, and for mastication it was 8.4. As regards the degree of difficulty of cleaning the denture, the mean value was 4.1. With regard to experience with treatment, the mean of values was 7.8 and for the possibility of going back and re-doing treatment, the mean found was 9.5 (Table 7). Table 7: Mean, standard deviation and standard error of the levels of patient satisfaction in relation to treatment (VAS) Question Mean Standard Deviation Standard Error Were you satisfied with the end result of your dentures? 7.4 2.119 0.670 When you get used to your dentures? 8.1 1.663 0.526 Overall, are you satisfied with the aesthetic appearance of your dentures? 7.0 3.127 0.989 How is your mastication after the placement of this prosthesis? 8.4 2.119 0.670 What degree of difficulty in cleaning of dentures? 4.1 3.281 1.038 How was your experience in general, with the treatment? 7.8 3.393 1.073 If you could go back, would you do the treatment again? 9.5 1.581 0.500 44 Discussion Due to the lower bone quality of the maxillary in comparison with the mandibular ridge, rehabilitation of the edentulous maxillary arch by means of implant supported prosthesis is always a challenging therapy, particularly in cases of edentulism in which the teeth have been missing for many years. So that in certain situations, alternative therapeutic modalities are required, such as the use of distal cantilevers, shorter implants, bone grafts and maxillary sinus lift surgery may be required, as well as the use of specific anatomic areas for implant placement, such as the pterygoid and zygomatic regions21. However, in the presence of sufficient bone tissue for implant placement without the need for alternative therapies to obtain bone issue, the immediate loading protocol makes it possible to reduce the number of surgical procedures and treatment time22. Although maxillary bone is less dense in the posterior regions21 and has a palatal resorption pattern that makes it difficult to obtain parallelism between dental implants6, with the advancement in implant loading protocols, there have been various scientific reports of clinical success with protocols that use 4 to 6 implants in the edentulous maxilla, supporting a denture immediately after their placement 6, 8,14,21,23,24 . Primary stability of the implant is considered one of the most important factors for osseointegration3, 6,7,8,25,26. In the present study denture and dental implant survival rates were found similar to those mentioned in the literature 3, 6, 23, 24 (100% and 96,6% respectively). At present, immediate loading of dental implants is a reality in implant dentistry offices, particularly due to the fact of providing the patient with a result in the short term and avoiding a second surgical intervention7. 45 There are various reports of scientific researches qualifying immediate loading as safe and efficient 3, 6, 8, 21, 22, 23, 24, 26, 27. Testori et al, 1(2013) nevertheless, didn’t believe that maxilla immediate loading was the best alternative, from the moment that found significant failure rate related not only to immediate chewing strength, but also to patient’s age, denture’s retention type, and the reason that led to extraction (endoperiodontal disease led to a major failure rate of following implants). Similar results have been found by Anderson et al. 28 (2013), with more than 10% of failure on maxilla immediate loaded implants, although reaching 100% success on mandibles implants. Browaeys et al. 29 (2011) on the other hand registered 2,1% loss, both in maxilla and mandible implants, but still bigger loss was registered in maxilla. In the end of their long term study, the accumulated loss was 9%, and it was considered failure every implant that had been lost or had presented mobility. The main cause of dental implant failure appears to have been micromovement during the healing period, resulting from maladjustment of the provisional dentures, and chewing hard food, leading to excessive movement that compromised osseointegration6. To Testori et al.1, nonetheless, implants submitted to immediate placement into fresh sockets or immediate loading had a lower cumulative survival rate and significant statistically than other combinations. Although, Peñarrocha-Oltra et al. 30 had three lost implants, these placed right after extraction and immediately loaded, but not statistically significant when analized the combination protocol / reception site type. Smoking habit was also related as a high prevalence factor of failure on osseointegrated 46 implants31. The success rate is shown high for both implants placed axially inclined as for implants placed in the posterior maxilla32, 33. The radiographic evaluation of the study reported in this article revealed that 72.9% of the implants presented no apparent bone loss, being classified as Score 0 and 27.1% presented a reduction in bone level not exceeding one third of implant length. Li et al.8 in 2009, evaluated the bone alterations in 111 patients submitted to immediate functional loading through provisional dentures in edentulous maxillae and mandibles, and mean marginal bone loss was 0.07 mm after one year. Browayes et al 29 found peri-implant bone loss of 1,2mm on the first two years of their study this measure didn’t grow on the following years though. On grafted bone there was loss of 0,3mm besides this pattern. The plaque index (mPI) evaluation in this study demonstrated that 15.3% of the implants presented no plaque deposits and were classified as Score 0. No patient presented abundant plaque. A positive association (p = 0.016) was found between the clinical plaque index mPI and bone loss evaluated in radiographs. Bacterial plaque was therefore considered one of the most important etiological factors for the appearance of peri-implant disease. In agreement with this inference were Ferreira Jr. et al. (2009) 34 who evaluated the correlation of three clinical indices of gingival inflammation (gingival index - GI, sulcus bleeding index, GI modified by Mombelli) and plaque index modified by Mombelli (mPI) with the real histological peri-implant condition, and concluded that the mPI was the only index statistically correlated in a positive manner with the histological alterations, and could be a good parameter for monitoring per-implant health. Agliardi et al.33 (2013) treated 32 patients with two axial implants in the anterior maxilla and four tilted 47 implants positioned at the anterior and posterior walls of the maxillary sinuses, supporting a total prosthesis fixed with metal infrastructure and were observed for at least three years, where the plaque index and peri-implant bleeding decreased significantly during the follow-up period. Assessment of patient satisfaction in relation to the treatment performed showed that the vast majority of patients is satisfied in relation to the final outcome of the prosthesis. Similarly, Zani et al.35 and Brennan et al.36 assessed the impact of oral health on quality of life of patients treated by total overdentures and fixed prostheses implant supported, concluding that patients treated with total, removable or fixed prostheses, are satisfied with the treatment. In our study, only the degree of difficulty for the cleaning of the prosthesis can be considered as dissatisfaction. Marra et al.24 (2013) also reported high satisfaction of patients, mainly because they have previously used conventional total prostheses that were deficient in terms of support, stability and retention. Agliardi et al.33 (2013) found that masticatory function was considered excellent by 90.6% of patients in their study, while the aesthetic and phonetic functions were honored by 87.5% of them. 48 Conclusion Within the limitations of this study, and from the clinical and radiographic findings, it was concluded that at the Implant Dentistry Clinic of the UFJF School of Dentistry, performing the protocol composed of 5 to 6 dental implants and the immediate insertion of a metaloplastic screw-retained fixed prosthesis was demonstrated to a safe and effective therapy for the rehabilitation of edentulous maxillae, which was related to a high level of satisfaction with treatment demonstrated by the patients. 49 8- REFERÊNCIAS 1- Testori T, Zuffetti F, Capelli M, et al. 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