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Copyright of Arquivos Brasileiros de Oftalmologia is the property of Arquivos Brasileiros de Oftalmologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The objective of this study is to present a clinical case of oral rehabilitation using digital workflow, encompassing the entire process from planning to treatment completion. The evolution of implantation techniques, incorporating intraorais scanners, tomographies, and digital planning software, has led to guided surgeries. These surgeries offer greater precision, reduced surgical time, and less discomfort for patients. The report describes surgical procedures performed on the maxilla and mandible. The use of surgical guides was crucial in guiding implant drilling, following a defined protocol of drills and guide sleeves. The fabrication of prostheses was based on intraoral scans, allowing for precise planning. The digital workflow provides a high level of predictability in the outcome of both surgical and prosthetic phases. Efficient and aesthetic outcomes, reduced surgical time, increased post-operative patient comfort, and shorter prosthetic fabrication time are distinct advantages of this technique. [ABSTRACT FROM AUTHOR]

Este trabalho relata atividades síncronas e assíncronas do Ensino Remoto Emergencial desenvolvidas no projeto de extensão “Restaurações Indiretas Dento e Implantossuportadas” utilizando a Plataforma Microsoft Teams. Esse projeto de extensão executa o tratamento clínico restaurador em dentes naturais e sobre implantes dentários em pacientes que buscam atendimento na Universidade Federal de Minas Gerais (UFMG). A prestação de serviço é realizada por alunos de graduação, monitores de pós-graduação e professores das áreas de Dentística e Prótese Dentária do Departamento de Odontologia Restauradora, que compreendem que o tratamento odontológico utilizando implantes dentários proporcionou aos indivíduos com ausência parcial ou total dos dentes o restabelecimento da saúde bucal, restaurando a função mastigatória e estética, oferecendo, assim, maior conforto e qualidade de vida. As atividades clínicas eram presenciais até 2019, entretanto, devido à pandemia de COVID-19, as atividades foram reestruturadas. Foram elaborados doze e-books com os temas relacionados à prótese, todos publicados na Câmara Brasileira do Livro. As atividades realizadas proporcionaram a divulgação de novas informações sobre saúde bucal para alunos e pacientes da Faculdade de Odontologia da UFMG, englobando o conceito da interação dialógica junto à sociedade.

O Autor, neste trabalho, salienta os problemas inerentes à confecção de uma prótese facial, destacando aqueles referentes ao seu uso durante o período "noturno". Propõe método de confecção de prótese nasal de recobrimento em PVC resiliente, utilizando aparelho Omnivac IV, usado em prótese dental na construção de vários aparelhos. Após a descrição do método, conclui que este ofereceu uma série de vantagens. Os portadores destas próteses mostraram-se satisfeitos, e sob o ponto de vista do autor o único inconveniente é ser o material incolor.

RESUMO Objetivo: Analisar retrospectivamente as alterações na ceratometria e no astigmatismo corneano obtidas após cirurgia de implante de anel intraestromal, comparando o uso de um segmento de arco longo versus o implante de dois segmentos de comprimento de arco tradicional. Métodos: A partir de um estudo transversal, obtivemos os dados de 94 olhos de pacientes diagnosticados com ceratocone, que foram submetidos ao implante de anel corneano. Eles foram divididos em dois grupos, dependendo do tipo de implante recebido: Grupo A, um segmento de arco longo; Grupo B, dois segmentos tradicionais. Todos os segmentos implantados possuíam 250µ de espessura. Os dados do pré-operatório dos dois grupos foram comparados, para garantir que as amostras eram similares (as diferenças encontradas entre os dois grupos não eram estatisticamente significativas). As variáveis analisadas no pré e no pós-operatório foram acuidade visual com correção, ceratometria, astigmatismo corneano e refração. Resultados: A amostra que recebeu apenas um segmento de arco longo (Grupo A) obteve redução da ceratometria média de 4,42D (8,7%) e do astigmatismo corneano de 2,43D (40,4%). Já na amostra dos olhos que receberam dois segmentos de arco tradicional (Grupo B), houve redução média de 2,66D (5,1%) em relação à ceratometria média e redução média de 2,11D (34,8%) em relação ao astigmatismo corneano. A redução obtida na ceratometria média no Grupo A foi maior que a obtida no Grupo B (diferença estatisticamente significativa). A redução obtida no astigmatismo do Grupo A não foi estatisticamente significante, se comparada com o resultado obtido no Grupo B (considerando p≤0,05). Conclusão: Foi demonstrado que o uso de um segmento de arco longo possui maior capacidade de aplanação corneana, se comparado com o uso de dois segmentos com comprimento de arco tradicional. Em relação à redução do astigmatismo, os dois grupos mostraram resultados equivalentes.

Objective: to present the radiographic clinical follow-up of the prosthetic rehabilitation of a patient with an atrophic mandible, with the installation of short implants associated with an implant of regular length. Method: case report of a completely edentulous patient with an atrophic mandible and a 6-year radiographic clinical follow-up conducted at the dental clinic of the Federal University of Piauí, Teresina, from February 2011 to January 2020. After collecting sociodemographic data, health records, clinical radiographic examinations, and prosthetic surgical planning, four dental implants were installed between the mental foramina. After three months, mini-conical abutments and a fixed prosthesis screwed onto the implants were installed and monitored every six months for a period of six years. Results: the clinical evaluation revealed tissue stability without significant peri-implant changes after the follow-up period. Radiographically, bone resorption was not observed around the implant. Stability of the prosthesis and absence of prosthetic complications were observed during the follow-up period. Conclusion: short implants associated with regular-length implants can be placed in the anterior region of an atrophic mandible for rehabilitation with fixed complete dentures. [ABSTRACT FROM AUTHOR]

Purpose: To retrospectively analyze the changes in corneal keratometry and astigmatism after intrastromal ring surgery, comparing the use of one long arch segment versus two traditional arc length segments. Methods: A cross-sectional study obtained data from 94 eyes of patients diagnosed with keratoconus that underwent surgical treatment with corneal ring implant. They were divided into two groups according to the type of implant received: one long-arch segment (Group A) or two traditional segments (Group B), both 250 microns thick. Preoperative data from the two groups were compared to ensure that the samples were similar (the differences between the two groups were not statistically significant). The variables (pre and post-operatively) analyzed were: best corrected visual acuity, keratometry, corneal astigmatism and refraction. Results: Group A, which received one long arch segment, showed a Km decrease of 4.42D (8.7%) and a corneal astigmatism reduction of 2.43D (40.4%). Group B, where the eyes acquired two traditional arch segments, showed an average Km decrease of 2.66D (5.1%) and corneal astigmatism reduction of 2.11D (34.8%). The mean keratometry (Km) reduction obtained was statistically significant (p≤0.05) when comparing both groups (A and B). The mean corneal astigmatism reduction was not statistically significant (p≤0.05) when comparing both groups (A and B). Conclusions: One long-arch segment has been demonstrated to have a greater capacity to reduce corneal curvature when compared to the use of two traditional-sized arch segments. No significant differences were found regarding the reduction of corneal astigmatism after comparing the results obtained in both groups. [ABSTRACT FROM AUTHOR]

Copyright of Acta Paulista de Enfermagem is the property of Universidade Federal de Sao Paulo, Escola Paulista de Enfermagem and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Brazilian Dental Science is the property of Brazilian Dental Science Journal-ICT-UNESP and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objetivo: O objetivo deste estudo é fornecer ao cirurgião-dentista conhecimento sobre aspectos gerais da zircônia e abordar a introdução das diferentes gerações. Materiais e métodos: Foi realizada uma pesquisa eletrônica da literatura atual em inglês, incluindo artigos científicos publicados até 2019. Resultados: De acordo com os artigos selecionados, diferenças importantes foram encontradas em relação as novas composições da zircônia, sua microestrutura, diferenças no conteúdo da fase cúbica, e de ítria na fase tetragonal, levando a diferentes propriedades ópticas, mecânicas e de resistência ao envelhecimento. Conclusão: A zircônia é o material mais resistente disponível entre as cerâmicas, com diferenças mecânicas e ópticas entre os materiais disponíveis. A introdução das coroas monolíticas resolveu o problema de lascamento da porcelana de cobertura, mas foram necessárias modificações estruturais para fornecer adequada translucidez.

Copyright of RGO: Revista Gaúcha de Odontologia is the property of RGO: Revista Gaucha de Odontologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Acta Odontologica Latinoamericana: AOL is the property of Acta Odontologica Latinoamericana and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Fisioterapia e Pesquisa is the property of Universidade de Sao Paulo, Faculdade de Medicina and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Introdução: As próteses são definidas como dispositivos destinados a suprir a funcionalidade completa ou parcial de um membro ausente, de forma a prover independência ao indivíduo amputado, além de melhorar aspectos psicológicos e sociais. Portanto, a escolha da prótese adequada tem um papel fundamental no processo de reabilitação desses pacientes. Nesse contexto, a tecnologia de impressão tridimensional (3D) aplicada na área da saúde tem agregado novas possibilidades na fabricação de próteses. Objetivo: Analisar as evidências da utilização de próteses fabricadas utilizando a tecnologia de impressão 3D em amputados. Métodos: Trata-se de uma revisão de literatura de artigos científicos indexados nas bases de dados MEDLINE, SciELO e LILACS. A pesquisa foi realizada sem restrição de data ou idioma, com base na combinação das palavras-chave: amputação, próteses, impressão tridimensional e membros artificiais. Resultados: A análise foi desenvolvida utilizando 13 artigos que apresentaram como principais vantagens das próteses fabricadas em impressão 3D o baixo custo e menor tempo de fabricação, personalização, manutenção barata, próteses mais leves, modelos digitais de próteses disponíveis gratuitamente e possibilidade de agregar outros sistemas como polias e sistemas mioelétricos. As desvantagens incluem próteses com materiais menos duráveis, menos rígidos, com pouca estabilidade térmica, além de apresentarem baixa força de preensão manual e necessidade de mais profissionais qualificados para o processo de fabricação. Conclusão: As próteses desenvolvidas utilizando a tecnologia de impressão 3D melhoram a qualidade de vida em indivíduos com deficiência física, permitindo-os executar ações perdidas pela ausência do membro. Embora exista alguns obstáculos e desvantagens, a tecnologia de impressão 3D tem emergido como potencial ferramenta para construção de próteses personalizadas e mais acessíveis.

Introdução: O carcinoma adenoide cístico (CAC) é um tumor raro e apresenta alto potencial de metástase. Em situações na qual o tumor possui localização crítica, como no caso do palato, a remoção cirúrgica pode ser extremamente invasiva e mutilante, gerando sequelas que resultam em prejuízos funcionais e estéticos ao paciente. Objetivo: Relatar o caso clínico de confecção de prótese obturadora de palato implantossuportada para o tratamento de um paciente com comunicação buco-nasal decorrente da cirurgia de remoção de CAC. Relato de Caso: Paciente de 33 anos, sexo feminino, procurou atendimento odontológico 6 meses após a remoção cirúrgica de um CAC em região nasopalatal, para reabilitação de comunicação buco-nasal. Para correção desta comunicação, foi realizada a confecção de uma prótese obturadora imediata, implantossuportada, com o sistema Barra-Clip. Para isso, houve a instalação de implantes osseointegrados, convencional e zigomático, além de confecção de uma barra de metal para fixação da prótese. Com a prótese palatina confeccionada, realizou-se a captura de dois Clips com resina acrílica autopolimerizável. Após a confecção e instalação da prótese, a paciente foi acompanhada mensalmente durante seis meses. Conclusão: As próteses bucomaxilofaciais são eficazes na reabilitação das sequelas advindas do tratamento cirúrgico em pacientes oncológicos. A utilização de implantes osseointegrados e sistema Barra-Clip se mostram como boas alternativas para a confecção de pilares de sustentação desses dispositivos, conferindo estabilidade e retenção.

Introduction: Quality of life is an important measure for health-outcome evaluation. Although otitis media is one of the most common childhood diseases, its impact on Portuguese children’s quality of life is unknown. The aim of this study is to determine the quality of life of Portuguese children with chronic otitis media with effusion and/or recurrent acute otitis media and the short-term impact of transtympanic ventilation tubes, using the Portuguese version of the OM-6 questionnaire, a valid, reliable and sensitive instrument to evaluate the health-related quality of life in children with otitis media. Material and Methods: This study was conducted in a tertiary referral center, to where children are referred from primary care and hospital pediatric consultations. The Portuguese version of the OM-6 questionnaire was applied to children with chronic otitis media with effusion and/or recurrent acute otitis media. The instrument was re-administered at two months postoperatively to a group of children who underwent tympanostomy tube placement, to evaluate the change in quality of life with the surgical procedure. Results: The study involved a sample of 169 children, aged between 6 months and 12 years (mean: 4.20 ± 2.05 years). The average score in the survey was 3.3 ± 1.47, of a maximum of 7 (worst quality of life). The domains ‘caregiver concerns’, ‘hearing loss’ and ‘physical suffering’ had the highest scores. The domain ‘hearing loss’ was correlated with the domain ‘speech impairment’ (rs = 0.41; p < 0.001) and the domain ‘physical suffering’ correlated with the domain ‘activity limitation’ (rs = 0.47; p < 0.001). There was a correlation between the score on ‘hearing loss’ and the presence of conduction hearing loss (χ2 (6) = 24.662; p = 0.022). Children with chronic otitis media with effusion had lower scores on the domain ‘physical suffering’, while children with recurrent acute otitis media had lower scores in the domain ‘hearing loss’ and higher scores in the domain ‘emotional distress’. There was an improvement in the quality of life in all the dimensions studied by the questionnaire after surgery. The improvement was large in 55%, moderate in 15% and small in 10% of the cases. The presence of otorrhea postoperatively did not decrease the quality of life improvement achieved with surgery. Conclusion: Otitis media has a negative impact on Portuguese children quality of life. Tympanostomy tubes improve quality of life related to the middle ear in most children. The application of validated disease-specific questionnaires allows an enhanced understanding of the impact of otitis media on Portuguese children quality of life and of the success of therapeutic measures.

Local anesthetics are commonly used in medicine and dentistry and have a low cost, but their action as a microbicidal agent is still controversial. This study aimed to evaluate the antimicrobial effects of lidocaine against bacteria that most commonly infect surgical wounds. We evaluated Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Proteus mirabilis and Enterococcus faecalis. The solutions tested were saline, chlorhexidine, lidocaine (solution and pure) and an antibiotic solution. The agar diffusion test was performed using Petri dishes. The agar plates were made in duplicate and incubated in an oven at 37°C for 48 h. Subsequently, the inhibition halos were measured. The plates tested with lidocaine (pure or solution) presented no inhibition halo. The antibiotic solution presented the largest inhibition halos for all the bacteria (p<0.05). Chlorhexidine formed an inhibition halo similar to that of the antibiotic solution for Escherichia coli (p>0.05). Lidocaine did not present an antimicrobial effect for any of the tested bacteria. However, the antibiotic solution and the chlorhexidine inhibited the growth of all bacteria. [ABSTRACT FROM AUTHOR]

Copyright of Arquivos Brasileiros de Oftalmologia is the property of Arquivos Brasileiros de Oftalmologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of RGO: Revista Gaúcha de Odontologia is the property of RGO: Revista Gaucha de Odontologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Fisioterapia Brasil is the property of Atlantica Editora and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

ABSTRACT Proximal femoral nails with a helical blade are a new generation of implants used for treating transtrochanteric fractures. The blade design provides rotational and angular stability for the fracture. Despite greater biomechanical resistance, they sometimes present complications. In the literature, there are some reports of cases of perforation of the femoral head caused by helical blades. Here, a clinical case of medial migration of the helical blade through the femoral head and acetabulum into the pelvic cavity is presented.

RESUMO Objetivo: Avaliar a biocompatibilidade da Nanoskin para reposição de volume em cavidades enucleadas ou evisceradas de coelhos. Métodos: Estudo experimental, utilizando implantes de Nanoskin (Innovatecs®, São Carlos, Brasil), celulose bacteriana produzida pela bactéria Acetobacter xylinum tendo como substrato o chá-verde. Implantes de 10mm de diâmetro/5mm de espessura foram colocados em cavidades enucleadas (G1) ou evisceradas (G2) de 21 coelhos, avaliados clinicamente todos os dias, sacrificados aos 7, 30 e 90 dias após a cirurgia. O material foi removido e preparado para exame de microscopia óptica. Resultados: Sinais flogísticos discretos no pósoperatório imediato, não tendo sido evidenciados sinais infecciosos ou extrusão de nenhum implante. Houve aparente redução do volume ao longo do período experimental. Histologicamente ambos os grupos foram muito semelhantes, apresentando aos 7 dias células inflamatórias (predominantemente monócitos e neutrófilos), rede de fibrina e hemácias. A Nanoskin apresentava-se como pequenas esferas, de cor rósea, com pequenos espaços entre elas, permeados por escassas células inflamatórias. As células inflamatórias se modificaram ao longo de período experimental, sendo possível observar aos 30 dias células gigantes multinucleadas e fibroblastos maduros permeando o implante. Aos 90 dias, a estrutura do implante apresentava-se desorganizada, amorfa, com restos necróticos e com áreas ovoides, revestidas por fina membrana rósea, que pareciam se agrupar, vazias ou preenchidas por material acelular, róseo ou acinzentado. Conclusão: A Nanoskin provocou reação inflamatória que levou à reabsorção e redução do volume do implante. Novas formulações devem ser estudadas a fim de ter um produto que seja permanente para reparo da cavidade anoftálmica.

Copyright of Brazilian Journal of Occupational Therapy / Cadernos Brasileiros de Terapia Ocupacional is the property of Cadernos de Terapia Ocupacional da UFSCar and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Implant Dentistry is the property of Lippincott Williams & Wilkins and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Arquivos Brasileiros de Oftalmologia is the property of Arquivos Brasileiros de Oftalmologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Implant Dentistry is the property of Lippincott Williams & Wilkins and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The authors report a succinct update of the main deep vein thrombosis prevention methods after total knee arthroplasty, divided into mechanical and pharmacological. They relate the main drugs used, their dosage and comparative risks and benefits. [ABSTRACT FROM AUTHOR]

Objective:this study aimed to evaluate the fixation of the trabecular metal wedge in patients undergoing revision of total hip arthroplasty.Methods:twenty-three cases with minimum grading of Paprosky II-B that were operated between July 2008 and February 2013 were evaluated. These cases were evaluated based on radiographs before the operation, immediately after the operation and later on after the operation. Loss of fixation was defined as a change in the abduction angle of the component greater than 10° or any mobilization greater than 6 mm.Results:it was found that there was 100% fixation of the acetabula after a mean of 29.5 months. One case underwent removal of the implanted components due to infection.Conclusions:there is still no consensus regarding the best option for reconstructing hips with bone loss. However, revision using a trabecular metal wedge has presented excellent short-and medium-term results. This qualifies it as an important tool for achieving a fixed and stable acetabular component.

OBJECTIVE: to present a retrospective analysis on the clinical-functional results and complications among patients with rotator cuff arthropathy (RCA) who underwent reverse arthroplasty of the shoulder.METHODS: patients with a diagnosis of RCA associated with pseudoparalysis of anterior elevation who underwent reverse arthroplasty of the shoulder with a minimum follow-up of one year were selected.RESULTS: preoperative information was gathered from our shoulder and elbow arthroplasty register, comprising age, sex, laterality, history of previous procedures, Constant's functional scores and the preoperative range of motion as described in the protocol of the American Academy of Shoulder and Elbow Surgery (ASES). After a mean follow-up of 44 months, 17 patients (94%) were satisfied with the result from the procedure.CONCLUSION: reverse arthroplasty for treating RCA in patients with pseudoparalysis of the shoulder was shown to be effective in achieving a statistically significant improvement in range of motion regarding anterior flexion and abduction. However, in this series, there was no improvement in range of motion regarding external and internal rotation. Reverse arthroplasty is a procedure that reestablishes shoulder joint function in patients who previously did not present any therapeutic possibilities.

OBJECTIVES: the aim of this study was to evaluate the surgical technique and determine the initial results, with a minimum follow-up of two years, from total knee arthroplasty revisions in which trabecular metal cones made of tantalum were used at the Knee Surgery Center of the National Institute of Traumatology and Orthopedics (INTO) or at the authors' private clinic between July 2008 and December 2010.METHODS: ten patients were included in the study prospectively, through clinical and radiographic evaluations.RESULTS: seven patients presented evolution without complications relating to the tantalum cones used. Five of these patients said that they did not have any pain and all of them were able to walk without needing crutches. In all the cases, we observed that osseointegration of the tantalum cones had occurred. No migration or loosening of the implants was observed, nor was osteolysis.CONCLUSION: use of trabecular metal cones made of tantalum for treating AORI type II or II bone defects was capable of providing efficient structural support to the prosthetic revision implants, in evaluations with a short follow-up.

Objective: To analyze the quality and quantity of data in the questionnaires and in request forms for magnetic resonance imaging. Methods: This retrospective study was conducted with data from 300 medical records. The research used the following data from the questionnaires: patient age, reason for the magnetic resonance imaging, reason for placing the breast implant, report of any signs or symptoms, time elapsed since surgery to place the current breast implant, replacement implant surgery, chemotherapy, and/or radiation therapy treatments. From the magnetic resonance imaging request forms, information about the breast implant, the implant placement surgery, patient clinical information and ordering physician specialty were verified. Results: The mean age of patients was 48.8 years, and the mean time elapsed since breast implant surgery was 5 years. A total of 60% of women in the sample were submitted to aesthetic surgery, while 23.7% were submitted to chemotherapy and/or radiation therapy. In the request forms, 23.7% of physicians added some piece of information about the patient, whereas 2.3% of them informed the type of implant and 5.2% informed about the surgery. Conclusion: The amount of information in the magnetic resonance imaging request forms is very limited, and this may hinder quality of radiological reports. Institutional and technological measures should be implemented to encourage the requesting physicians and radiologists to share information. [ABSTRACT FROM AUTHOR]

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Otosclerose é uma doença que provoca fixação do estribo, levando à perda auditiva tipicamente condutiva, corrigida com aparelhos auditivos ou cirurgia de estapedotomia, substituindo o estribo doente por uma prótese. O material mais recentemente utilizado é o titânio e no Brasil há apenas duas próteses comercialmente disponíveis. A prótese de pistão tipo Fisch, da Storz, não possui resultados relatados na literatura. OBJETIVO: Estudo retrospectivo avaliando resultado auditivo após estapedotomia com uso desta prótese. MÉTODO: Usando critérios da Academia Americana de Otorrinolaringologia, comparou-se o gap nas audiometrias pré e pós-operatórias, avaliando-se melhora auditiva. RESULTADOS: O gap pós-operatório em baixas frequências teve média de 12,9 dB, em altas frequências de 5,2 dB (média 9,1 dB), mediana 8,8 dB, mínimo 1,3 dB e máximo 21,6 dB, desvio padrão 5,7 e p < 0,001. Dividindo o resultado conforme o gap pós-operatório a cada 10 dB, em 25 pacientes (75,8%) foi < ou igual a 10 dB, em 32 pacientes (96,9%) foi < ou igual a 20 dB, em 100% dos casos foi < ou igual a 30 dB. CONCLUSÃO: Prótese de pistão tipo Fisch apresenta resultados compatíveis com a literatura, podendo ser usada com segurança como mais uma boa opção para estapedotomia.Otosclerosis causes the fixation of the stapes and conductive hearing loss, usually corrected with the use of hearing aids or through stapedotomy and the replacement of the involved stapes with a prosthesis. Titanium has been the most recently used material of choice in stapedotomy prostheses. Only two prostheses are commercially available in Brazil. There are no reports in the literature on the Fisch-type Storz titanium stapes piston prosthesis. OBJECTIVE: This retrospective study aims to look into the auditory outcomes of patients submitted to stapedotomy and titanium stapes piston prosthesis implantation. METHOD: The criteria described by the American Academy of Otolaryngology were used to compare pre and postoperative air-bone gaps seen in audiometry tests. RESULTS: The mean low-frequency postoperative air-bone gap was 12.9 dB; the mean high-frequency air-bone gap was 5.2 dB (mean 9.1 dB); median gap was 8.8 dB, with a minimum of 1.3 dB and a maximum of 21.6 dB; standard deviation was 5.7 dB, and p < 0.001. Twenty-five (75.8%) patients had air-bone gaps of 10 dB and under; 32 (96.9%) patients had gaps of 20 dB and under; and all patients had gaps of 30 dB and under. CONCLUSION: The Fisch-type titanium stapes piston prosthesis presented outcomes consistent with the literature and can be used safely in stapedotomy procedures.

OBJECTIVE: to compare the laboratorial results of opening suction drainage 6 hours and 12 hours after total knee arthroplasty surgery. METHODS: prospective and randomized study in 88 patients undergoing with total knee arthroplasty in two groups: in one group the opening suction drainage was performed 6 hours (n = 45) after the surgery and in the other 12 hours (n = 43) after the surgery. RESULTS : the outcome was a significant fall in the three laboratorial variables (hemoglobin, red blood cells and hematocrit) between the pre and post-operative in the total sample and in the six and 12 hour opening suction drainage groups. In the group with opening suction drainage after 12 hours, the drainage volume was significantly lower than in the group with opening suction drainage after 6 hours (p = 0.0003). However, no significant difference was observed in the absolute delta of the laboratorial variables between the two groups. CONCLUSION: the opening suction drainage in six and 12 hours did not show significant difference from the laboratorial values although the volume of the blood drained was higher in the opening suction drainage in six hours.

O objetivo deste trabalho foi avaliar o resultado da osseointegração de implantes extraorais lemento de suporte e retenção de próteses nas reabilitações de deformidades faciais. MÉTODO: Estudo retrospectivo de prontuários de 59 indivíduos operados de câncer, submetidos a 164 implantes para retenção de prótese facial. RESULTADOS: Dos 59 indivíduos, 14 foram previamente irradiados e receberam 42 implantes. Quarenta e cinco indivíduos não foram irradiados e receberam 122 implantes. Do total de 164 implantes, oito não osseointegraram, dos quais dois foram instalados em osso previamente irradiados. O resultado representou o sucesso de 116 (95,1%) implantes osseointegrados nos indivíduos não irradiados. E sucesso de 40 (95,3%) implantes osseointegrados em ossos irradiados. CONCLUSÃO: Concluiu-se que o uso de implantes extraorais é uma técnica segura e eficaz como suporte e retenção para próteses faciais em indivíduos com deformidades nessa região. A radioterapia não impede a osseointegração.The aim of this study is to analyze the success of extraoral osseointegrated implants used to support designed to rehabilitate craniofacial deformities. METHOD: This study was based on the retrospective assessment of charts from 59 patients submitted to cancer surgery and who received 164 extraoral implants to contain facial prosthesis. RESULTS: Among 164 implants, 42 were fixed in previously irradiated regions. Eight of the implants did not have osseointegration; and from these, two were fixed in irradiated bone. The result show 116 (95.1%) successfully osseointegrated implants in non-irradiated sites. The success rate among 42 implants fixed in previously irradiated bones was 40 (95.3%) osseointegrated implants. CONCLUSION: The use of extraoral craniofacial implants represents a safe and effective approach to treat facial deformities as a support for the rehabilitation prosthesis. Radiotherapy treatment does not prevent osseointegration.

O implante coclear para pacientes com disacusia grave/profunda revolucionou o modo com que estes interagem com o meio ambiente. A Neurelec desenvolveu um sistema que permite fixação com uso de dois simples parafusos de titânio, sem necessidade de broqueamento do osso do crânio do paciente. Este artigo teve o objetivo de descrever uma casuística de pacientes submetidos a implante coclear com o Digisonic® SP, para mostrar os resultados cirúrgicos e detalhes do procedimento. MÉTODO: Estudo retrospectivo que avaliou os pacientes, no período de 18 meses, submetidos a implante coclear com o Digisonic® SP. Todos os pacientes eram pós-linguais. Coleta dos dados realizada por meio da análise dos prontuários dos pacientes, além de questionário padronizado aplicado nos cirurgiões que realizaram o procedimento. RESULTADOS: Os seis casos implantados com o Digisonic® SP foram realizados por cirurgiões experientes e o tempo cirúrgico variou de 95 a 203 minutos (média de 135 minutos), que é menor do que o descrito com outras formas de fixação. Não houve nenhum tipo de complicação e o ganho auditivo foi satisfatório. CONCLUSÃO: O implante Digisonic® SP desenvolvido pela Neurelec apresentou bons resultados audiológicos em adultos, tempo de cirurgia menor e não ocorreram complicações cirúrgicas ou pós-operatórias.Cochlear implants have revolutionized the way patients affected by severe hearing loss experience the world. Neurelec developed a fixation system with two titanium screws that requires no skull bone drilling. OBJECTIVE: To describe the outcomes and procedure-related details of a series of patients implanted with the Digisonic® SP cochlear implant. METHOD: This retrospective study analyzed patients submitted to cochlear implant placement within a period of 18 months. All patients had postlingual hearing impairment. Data was collected from patient charts and standard questionnaires answered by the surgeons in charge of carrying out the procedures. RESULTS: The six patients offered the Digisonic® SP cochlear implants were operated by experienced surgeons. The procedures took 95 to 203 minutes (mean = 135') to be completed, which is less time than what has been described for other fixation approaches. No complications were recorded and hearing improvement was satisfactory. CONCLUSION: The Digisonic® SP cochlear implant developed by Neurelec offered good audiological results for adult patients, shorter surgery time, and no surgical or postoperative complications.

PURPOSES: To evaluate whether polyurethane foam leads more intense foreign-body reaction than silicone foam. To compare the vascularization of the capsules surrounding the foam implants. To investigate if the capsule of polyurethane foam implanted has greater amount of collagen than that of silicone foam. METHODS: Sixty-four young male Wistar rats were allocated into two groups: polyurethane foam and silicone foam. Subcutaneous discs were implanted into the dorsum of the animals in both groups. The capsules were assessed 28 days, two months, three months and six months postoperatively. Microscopic analysis with H&E stain was performed to evaluate the acute and chronic inflammatory process, foreign-body reaction and neovascularization. The analysis with picrosirius red was performed using the ImageProPlus software, to measure the number of vessels and collagen types I and III. RESULTS: There were no statistical differences between the two groups regarding the acute and chronic inflammatory processes. All rats from the polyurethane group, in all times, exhibited moderate or intense foreign-body reaction, with statistic significant difference (p=0.046) when compared with the silicone group, in which the reaction was either mild or nonexistent at two months. Vascular proliferation was significantly different between the groups at 28 days (p=0.0002), with the polyurethane group displaying greater neovascularization with H&E stain. Similar results were obtained with picrosirius red, which revealed in the polyurethane group a much greater number of vessels than in the silicone group (p=0.001). The collagen area was larger in the polyurethane group, significantly at 28 days (p=0.001) and at two months (p=0.030). CONCLUSIONS: Polyurethane foam elicited more intense foreign-body reaction when compared with silicone foam. The number of vessels was higher in the capsules of the polyurethane foam implants 28 days after the operation. The capsule of the polyurethane foam implants showed a greater amount of collagen than that of the silicone foam implants.OBJETIVOS: Avaliar, em relação ao uso de próteses, se a espuma de poliuretano apresenta maior reação de corpo estranho no organismo ao ser comparada com a espuma de silicone. Se há diferenças na vascularização das cápsulas formada ao redor das duas espumas implantadas. Se as cápsulas dos implantes de espuma de poliuretano apresentam quantidade maior de fibras colágenas ao serem comparadas com as da espuma de silicone. MÉTODOS: Utilizou-se 64 ratos albinos da linhagem Wistar, distribuídos em dois grupos de 34, grupo espuma de poliuretano e grupo espuma de silicone e receberam implantes discóides subcutâneos em seu dorso. Foram analisadas as cápsulas peri-implante com 28 dias, dois, três e seis meses após a introdução. A análise microscópica com H&E considerou as variáveis: inflamação aguda, inflamação crônica, reação de corpo estranho e neoformação vascular. A análise da coloração com picrosirius-red usando ImageProPlus considerou o número de vasos e colágeno tipo I e tipo III. RESULTADOS: Em relação à inflamação aguda e crônica, não foram encontradas diferenças estatísticas nos dois grupos. Todos os animais do grupo poliuretano, em todos os momentos, apresentaram reação de corpo estranho moderada ou intensa e foi encontrada diferença estatística significativa (p=0,046) ao serem comparados com o grupo silicone, cuja reação era ausente ou discreta aos dois meses. A neoformação vascular apresentou diferenças significativas nos dois grupos, aos 28 dias (p=0,0002); o grupo poliuretano com H&E apresentava quantidade maior de vasos neoformados e o mesmo ocorrendo com o picrosirius, cujo número de vasos era maior que no grupo silicone (p=0,001). A área de colágeno em todos os momentos foi maior no grupo poliuretano, sendo significativa com 28 dias (p=0,001) e com dois meses (p=0,030). CONCLUSÕES: A espuma de poliuretano apresentou maior reação de corpo estranho no organismo do que a espuma de silicone. A quantidade de vasos foi maior na cápsula da espuma de poliuretano com 28 dias após o implante. Aos 28 dias as cápsulas dos implantes de espuma de poliuretano apresentaram quantidade significativamente maior de colágeno do que as de espuma de silicone.

Uma breve revisão de resultados e complicações da ceratoprótese (KPro) de Dohlman-Doane tipo 1. A KProDohlman-Doane é atualmente uma boa opção em casos graves de cegueira corneana, para os quais o transplante penetrante de córnea não apresenta bom prognóstico. As evoluções no design da KPro e as melhorias no procedimento cirúrgico, aliados a obtenção de condições favoráveis da superfície ocular pré-operatórias, garantem bons resultados da KPro em doenças não autoimunes. As principais complicações da KPro são membrana inflamatória retroprotética de fibrina, glaucoma, necrose corneana, vitreíte e infecção (ceratite e endoftalmite). Acompanhamento constante com exames pós-operatórios periódicos é necessário para monitorar e prevenir complicações sérias.