Agentes de abultamiento en incontinencia de orina de esfuerzo femenina: una alternativa a las mallas suburetrales / Bulking agents in female stress urinary incontinence: an alternative to suburethral mesh

OBJETIVO: Presentar una serie de casos de agentes de abultamiento (AA) de nuestro centro. MATERIAL Y MÉTODOS: Estudio retrospectivo. Se evaluaron todos los casos operados con AA entre 2017 y 2022. La inyección de AA se realizó en quirófano, bajo sedación con anestesia local periuretral o raquídea. La inyección se realizó con uretroscopia, 0,5 cc en 4 puntos periuretrales (horas 2, 5, 7 y 10). Se analizaron datos demográficos, quirúrgicos y de seguimiento. RESULTADOS: 15 casos. 13/15 presentaron incontinencia urinaria mixta. Solo dos casos tenían incontinencia de orina de esfuerzo pura. El procedimiento fue ambulatorio. La mediana del tiempo operatorio fue 15 minutos (15-20). La mediana de seguimiento fue 5 meses (1-9). El índice de severidad preoperatorio promedio fue 10,6 y en el seguimiento fue 2,79. La Escala de Mejoría Global mostró mejoría en 12/15, y 12/15 estaban satisfechas con la cirugía con mejoría en la calidad de vida. CONCLUSIÓN: Los AA son una opción quirúrgica efectiva, con una tasa de éxito del 80% en otros reportes, siendo similar con nuestra casuística. Ofrecer esta opción es posible a la hora de hablar de terapias alternativas.

OBJECTIVE: To present a case series of bulking agents (BA) from our center. MATERIAL AND METHODS: Retrospective study. All cases operated with BA between 2017 and 2022 were evaluated. A BA injection was performed in the operating room, under periurethral local anesthesia sedation or spinal anesthesia. The injection was performed with urethroscopy, 0.5 cc in 4 periurethral points (hours 2, 5, 7 and 10). Demographic, surgical, and follow-up data were analyzed. RESULTS: 15 cases were reported. 13/15 patients presented with mixed urinary incontinence. Only 2 cases had pure stress urinary incontinence. The procedure was ambulatory. Median operative time was 15 minutes (15-20). Median follow-up was 5 months (1-9). The average preoperative Sandvik Severity Index was 10.6 and in follow-up was 2.79. The PGI showed improvement in 12/15, and 12/15 were satisfied with the surgery with quality-of-life improvement. CONCLUSION: BA are an effective surgical option, with a success rate of 80%, according to other reports, being similar with our casuistry. Offer this option is possible at the moment of discussing alternative therapies.

Enhancement of cellular activity in hyperglycemic mice dermal wounds dressed with chitosan-alginate membranes

The use of specially designed wound dressings could be an important alternative to facilitate the healing process of wounds in the hyperglycemic state. Biocompatible dressings combining chitosan and alginate can speed up wound healing by modulating the inflammatory phase, stimulating fibroblast proliferation, and aiding in remodeling phases. However, this biomaterial has not yet been explored in chronic and acute lesions of diabetic patients. The aim of this study was to evaluate the effect of topical treatment with a chitosan-alginate membrane on acute skin wounds of hyperglycemic mice. Diabetes mellitus was induced by streptozotocin (60 mg · kg-1 · day-1 for 5 days, intraperitoneally) and the cutaneous wound was performed by removing the epidermis using a surgical punch. The results showed that after 10 days of treatment the chitosan and alginate membrane (CAM) group exhibited better organization of collagen fibers. High concentrations of interleukin (IL)-1α, IL-1β, granulocyte colony-stimulating factor (G-CSF), and tumor necrosis factor-alpha (TNF-α) were detected in the first and second days of treatment. G-CSF and TNF-α level decreased after 5 days, as well as the concentrations of TNF-α and IL-10 compared with the control group (CG). In this study, the inflammatory phase of cutaneous lesions of hyperglycemic mice was modulated by the use of CAM, mostly regarding the cytokines IL-1α, IL-1β, TNF-α, G-CSF, and IL-10, resulting in better collagen III deposition. However, further studies are needed to better understand the healing stages associated with CAM use.

Steroid vs. antibiotic impregnated absorbable nasal packing for wound healing after endoscopic sinus surgery: a randomized, double blind, placebo-controlled study / Tampão nasal absorvível embebido em esteroides versus antibióticos para cicatrização de feridas após cirurgia endoscópica nasossinusal: estudo randomizado, duplo cego, placebo controlado

Abstract Introduction: Endoscopic sinus surgery can lead to crusting or synechiae formation, which can affect the healing process. Objective: The aim of our study was to compare the influence of steroid versus antibiotic versus saline solution impregnated absorbable nasal spacers on postoperative wound healing and patient satisfaction. Methods: Eighty patients, 33 women and 47 men, were enrolled in this study. At the end of the surgery, two pieces of 4 cm biodegradable material were applied in each ethmoid cavity. One of them was impregnated with saline solution, while the second one with steroid, or with antibiotic. Results: We observed statistically significant differences in the Lund-Kennedy score between the control and both treatment groups: for the Antibiotic-group on days 10 and 30 (p = 0.009; p = 0.009) and for the Steroid-group on day 90 (p = 0.008). The extended endoscopic appearance of nasal mucosa indicated statistically significant differences in crust formation on day 10 comparing the steroid and control dressing (p = 0.025), in secretion type on days 10 and 30 comparing the antibiotic and control dressing (p = 0.003; p = 0.016) and additionally for steroid and control on day 90 (p = 0.046). On Day 90 we observed statistically significant differences in the absence of mucosal edema in the S-group compared to controls (p = 0.007). Conclusions: The results of this study reveal the significant positive influence of steroid- and antibiotic-impregnated biodegradable nasal packing on the postoperative healing process and patient satisfaction compared to the saline soaked dressing.

Resumo Introdução: A cirurgia endoscópica nasossinusal pode levar à formação de crostas e sinéquias, o que pode afetar o processo de cicatrização. Objetivo: O objetivo do nosso estudo foi comparar a influência do espaçador nasal absorvível embebido em esteroide versus antibiótico versus solução salina na cicatrização de ferida pós-operatória e na satisfação do paciente. Método: Oitenta pacientes, 33 mulheres e 47 homens, foram incluídos neste estudo. Ao final da cirurgia, dois tampões de material biodegradável de 4 cm foram aplicados em cada cavidade etmoidal. Um deles foi embebido em solução salina, enquanto no segundo foi utilizado esteroide, ou antibiótico. Resultados: Observamos diferenças estatisticamente significantes no escore de Lund-Kennedy entre os grupos controle e ambos os grupos tratamentos: para o grupo antibiótico nos dias 10 e 30 (p = 0,009; p = 0,009) e para o grupo esteroide no dia 90 (p = 0,008). O aspecto endoscópico da mucosa nasal indicou diferenças estatisticamente significantes na formação de crostas no dia 10, na comparação do esteroide com o curativo controle (p = 0,025), no tipo de secreção nos dias 10 e 30, na comparação do antibiótico com o curativo controle (p = 0,003; p = 0,016) e adicionalmente para esteroide e controle no dia 90 (p = 0,046). No dia 90, observamos diferenças estatisticamente significantes na ausência de edema da mucosa no grupo E (esteroide) em relação aos controles (p = 0,007). Conclusões: Os resultados deste estudo revelam uma influência positiva significante no uso de tampão nasal biodegradável embebido em esteroides e antibióticos no processo de cicatrização pós-operatória e satisfação do paciente em comparação com o curativo embebido em solução salina.

Influence of the geometry of nanostructured hydroxyapatite and alginate composites in the initial phase of bone repair

Abstract Purpose: To analyze, histomorphologically, the influence of the geometry of nanostructured hydroxyapatite and alginate (HAn/Alg) composites in the initial phase of the bone repair. Methods: Fifteen rats were distributed to three groups: MiHA - bone defect filled with HAn/Alg microspheres; GrHA - bone defect filled with HAn/Alg granules; and DV - empty bone defect; evaluated after 15 days postoperatively. The experimental surgical model was the critical bone defect, ≅8.5 mm, in rat calvaria. After euthanasia the specimens were embedded in paraffin and stained with hematoxylin and eosin, picrosirius and Masson-Goldner's trichrome. Results: The histomorphologic analysis showed, in the MiHA, deposition of osteoid matrix within some microspheres and circumjacent to the others, near the bone edges. In GrHA, the deposition of this matrix was scarce inside and adjacent to the granules. In these two groups, chronic granulomatous inflammation was noted, more evident in GrHA. In the DV, it was observed bone neoformation restricted to the bone edges and formation of connective tissue with reduced thickness in relation to the bone edges, throughout the defect. Conclusion: The geometry of the biomaterials was determinant in the tissue response, since the microspheres showed more favorable to the bone regeneration in relation to the granules.

Bioceramic cement in the filling of bone defects in rats

Abstract Purpose To evaluate PBS®MCIMMO cement in the filling of bone defects. Methods Thirty-six adult male Wistar rats were divided into three groups of twelve individuals each (group 1, group 2 and group 3). In all groups, a bone failure in the femur was induced, 2.0 mm wide and 7.0 mm deep. In group 1, the PBS®MCIMMO cement was applied to the bone defect produced and a titanium implant (CONNECTION®) 1.5 mm thick and 6 mm long was installed. In group 2, only the PBS® CIMMO cement was installed. In group 3, only bone failure was performed. Kruskal Wallis tests were performed to compare the mean area among the three groups. Results In all comparisons, significance was observed for group 2 (p = 0.0014-0.0026). Conclusion The PBS®CIMMO cement induced bone neoformation, and integration between the newly formed bone, cement, and implant was observed.

Changing bulking agent may require change in injection volume for endoscopic treatment of vesicoureteral reflux

ABSTRACT Introduction: Various bulking agents were utilized for endoscopic correction of VUR. A study reviewing multi-institutional data showed that the amount of injection material has increased over time with the purpose of improving success rates, which also resulted in costs. We noticed an opposite trend in our center since we started using a new bulking agent. The aim of this study was to evaluate evolution of our practice with different bulking agents. Patients and Methods: Records of VUR patients who underwent subureteric injection with polyacrylate polyalcohol copolymer (PPC) and dextronomere hyaluronic acide (DxHA) between 2005 and 2014 were reviewed. Variation of different parameters throughout the study period was evaluated along with the success rate. Success was defined as complete resolution of reflux. Results: A total of 260 patients with 384 refluxing units were included. The success rate was higher in PPC group compared to DxHA group. There was no statistically significant difference between years regarding distribution of VUR grade, body weight, patient height, and age in PPC group. Despite significant reduction in injection volume, success rate did not decrease through the years with PPC. Conclusion: Different bulking agents may require different injection volumes to achieve the same success rate in endoscopic treatment of vesicoureteral reflux. Habits gained with previous experience using other materials should be revised while using a new agent.

Saberes e práticas de biossegurança entre tatuadores: uma contribuição do enfermeiro / Biosecurity knowledge and practices among tattooists: the nurse's contribution / Conocimientos y prácticas de bioseguridad entre tatuadores: una contribución del enfermero

Introdução: o objeto de estudo trata dos conhecimentos de tatuadores acerca das medidas de proteção, na manipulação de material biológico necessárias à prática de tatuagem. Objetivos: descrever os conhecimentos do tatuador acerca da biossegurança voltada para o procedimento característico de sua profissão e analisar a aplicabilidade desses conhecimentos para a manutenção da integridade do cliente. Método: estudo descritivo, qualitativo com 10 tatuadores de dois estúdios do Rio de Janeiro. Foi utilizada entrevista semiestruturada e observação direta do procedimento, de março a maio de 2016, com aplicação da análise de conteúdo aos depoimentos. Resultados: os cuidados se restringem ao descarte e não reutilização dos perfuro cortantes; há enfoque artístico em detrimento de princípios de biossegurança. Conclusão: aponta nova área de atuação para o enfermeiro, sendo necessária padronização do processo de trabalho.

Introduction: the study object is tattooists' knowledge of the protective measures necessary to the practice of tattooing, when handling biological material. Objectives: to describe tattoo artists' knowledge of biosafety directed to the procedure characteristic of their profession and analyze the applicability of this knowledge to maintaining client health. Method: this qualitative, descriptive study of 10 tattooists from two studios in Rio de Janeiro used semi-structured interviews and direct observation of the procedure, from March to May 2016, then applying content analysis to the declarations. Results: care was restricted to disposal and non-reuse of sharps; the approach is artistic to the detriment of biosafety principles. Conclusion: this points to a new area of work for nurses, where standardization of work processes is needed.

Introdución: el objeto de estudio trata de los conocimientos de tatuadores sobre las medidas de protección en el manejo de material biológico, necesarias para la práctica del tatuaje. Objetivos: describir los conocimientos que tiene el tatuador sobre bioseguridad con vistas al procedimiento característico de su profesión y analizar la aplicabilidad de estos conocimientos en cuanto a mantener la integridad del cliente. Método: estudio descriptivo, cualitativo junto a 10 tatuadores de dos estudios en Río de Janeiro. Se utilizaron entrevistas semiestructuradas y la observación directa del procedimiento, de marzo a mayo de 2016, con aplicación del análisis de contenido para el testimonio. Resultados: los cuidados se resumen al desecho y no reutilización de los cortopunzantes; el enfoque artístico se sobrepone a los principios de bioseguridad. Conclusión: se apunta a un nuevo campo de trabajo para los enfermeros, lo que requiere la estandarización del proceso de trabajo.

A Biological Approach in Repair of Damaged Dental Pulp and Periapical Tissues using Platelet Rich Fibrin, Mineral Trioxide Aggregate and Laser Biostimulation.

This article describes about a biological approach in the repair of dental pulp and periapical tissues using biomaterials (platelet rich fibrin [PRF] and mineral trioxide aggregate [MTA]) and laser biostimulation. Case 1: Pulpotomy with PRF, MTA, and laser biostimulation. Patient follow-up was done at 1, 3, and 6 months. On 6 months follow-up, the patient was asymptomatic and tooth responded positively to pulp tests. Radiograph revealed normal periodontal ligament space and trabecular bone pattern. Case 2: Apexification procedure using PRF, MTA, and laser biostimulation in 31 and 41. Patient follow-up was done at 1, 3, and 6 months. On 6 months follow-up, radiograph revealed relative root lengthening, thickening of the canal walls in the apical one-third of root, and a healing lesion. Repair and regenerative potential of PRF, an enhanced cellular metabolism with laser biostimulation in combination with the sealing ability of MTA enhances the clinical success outcomes in pulpotomy and apexification procedures.

Estudo clínico comparativo entre diferentes sistemas de clareamento de uso em consultório / Comparative clinical trial between different in-office bleaching systems

Objetivos: Estudos clínicos longitudinais que acompanham os pacientes por longos períodos não são muito comuns na literatura, ainda mais quando associados a grandes amostras (veio do fim do resumo). Por isso, o objetivo do trabalho foi determinar a eficiência, estabilidade de cor e sensibilidade dental, trans e pós operatória, dentro de um período de 365 dias, de quatro protocolos de clareamento em consultório. Material e Métodos: Foi realizado um estudo clínico randomizado, cego (para os pacientes), composto por 120 sujeitos (n=30). A amostra foi formada por pacientes adultos, sem distinção de gênero e etnia, e idade superior a 18 anos que foram selecionados por meio de avaliação clínica na qual foi verificada a cor dos dentes, a condição de higiene oral e a presença de restaurações e/ou próteses nas regiões em que os procedimentos seriam realizados. Todos os sujeitos foram submetidos a uma sessão de clareamento de acordo com as instruções do fabricante e obedecendo a aplicação ou não da luz, para os clareadores baseados no sistema Foto-Fenton (havia faltado citar nos métodos do resumo), e qual o seu tipo: Zoom Advanced Power, peróxido de hidrogênio (PH) 25% - Zoom! + luz UVA (Phillips Oral Healthcare); Zoom Whitespeed, PH 25% - Zoom! + luz Whitespeed (Phillips Oral Healthcare); Zoom sem luz, PH 25% - Zoom! (Phillips Oral Healthcare). Boost, PH 38% - Opalescence Xtra Boost (Ultradent). As alterações de cor foram avaliadas utilizando as escalas Vita Classical e Vita Bleachedguide 3D Master e o Espectrofotômetro Vita-Easyshade. As medições foram feitas em incisivos centrais e caninos uperiores antes, imediatamente e 7, 14, 30, 180 e 365 dias após o tratamento. Os dados foram analisados estatisticamente por meio do software Statistica 8.0 (StatSoft - Tulsa, OK) através da análise de variância (ANOVA) para medidas repetidas na avaliação das médias e as comparações foram realizadas através de contrastes (Tukey). Resultados: Para a escala Vita Classical, Zoom AP e WS foram semelhantes entre si porém diferentes de Opalescence e Zoom sem luz, exceto para a avaliação de 30 dias (caninos) e 365 dias (incisivos) onde o Zoom WS demonstrou dados semelhantes ao Opalescence e Zoom sem luz Já para a escala Vita Bleached, Zoom AP e WS foram semelhantes entre si, porém diferentes de Opalescence e Zoom sem luz, exceto para as avaliações de 30 e 180 dias onde o Zoom WS demonstrou dados semelhantes ao Opalescence e Zoom sem luz (caninos). Para dentes incisivos, os achados foram semelhantes, exceto que houve diferença entre o Zoom AP e WS e as semelhanças entre Zoom WS, Opalescence e Zoom sem luz foram encontradas nas avaliações de 180 e 365 dias. Na avalição com o espectrofotômetro Vita Easyshade Zoom AP e WS foram semelhantes entre si e diferentes do Opalescence que, por sua vez, foi diferente do Zoom sem luz, exceto para as avaliações de 7, 14 e 30 dias (caninos). Para incisivos, Zoom AP e WS foram semelhantes entre si e diferentes de Opalescence e Zoom sem luz, exceto para a avaliação de 14 dias onde o Zoom AP foi diferente do Zoom WS. Por fim, a sensibilidade apresentou um aumento nos seus valores na avaliação imediatamente após o clareamento, com uma redução na avalição de 7 dias, para todos os grupos que ainda apresentaram valores de sensibilidade semelhantes em todos os períodos de avaliação. Conclusão: O acompanhamento até 365 dias demonstrou a eficiência dos protocolos de clareamento analisados uma vez que nenhum deles recidivou para os tons iniciais, demonstrando a durabilidade dos procedimentos. Os dois grupos com os clareadores Foto-Fenton obtiveram maior efeito clareador (substituiu desempenho, tinha ficado vago), exceto nas seguintes avaliações: Vita Classical, 30 dias (caninos) e 365 dias (incisivos) e Vita Bleached, 30 e 180 dias (caninos) e 180 e 365 dias (incisivos). Observou-se uma estabilização da cor após sete dias em todos os grupos. A sensibilidade...

Objectives: Longitudinal clinical studies that follow patients for long periods are not very common in the literature, especially when associated with large samples. The objective of this study was to determinate the efficacy, color stability and sensitivity within a 365 day period of four in-office bleaching protocols. Methods: A randomized clinical trial, blinded (for patients), composed of 120 subjects (n=30) was conducted. The sample consisted of adult patients, without gender and ethnic distinction, with age superior than 18 years old that were selected through clinical evaluation in which was verified the color of teeth, the condition of oral hygiene and the presence of restorations and/or prostheses in the areas where the procedures would be carried out. All subjects were submitted to a session of bleaching according to the manufacturer's instructions: Zoom Advanced Power, 25% hydrogen peroxide (HP) - Zoom! + UVA light (Phillips Oral Healthcare); Zoom Whitespeed, 25% HP - Zoom! + Whitespeed light (Phillips Oral Healthcare); Zoom without light, 25% HP - Zoom! (Phillips Oral Healthcare). Boost, 38% HP - Opalescence Xtra Boost (Ultradent). Color changes were evaluated using Vita Classical and Vita Bleachedguide 3D Master shade guides and Vita-Easyshade spectrophotometer. Measurements were made on the superior central incisive and canines before, immediately and 7, 14, 30, 180 and 365 days after the treatment. Statistical analysis of the data were made with the software Statistica 8.0 (StatSoft - Tulsa, OK) through the analysis of variance (ANOVA) for repeated measures in the mean evaluation and comparisons were made by using contrasts (Tukey). Results: For the Vita Classical shade guide, Zoom AP and WS were similar but different from Opalescence and Zoom without light except for the 30 day (canines) and 365 days evaluations (incisives) where the Zoom WS showed similar data to Opalescence and Zoom without light...

Estudo clínico comparativo entre diferentes sistemas de clareamento de uso em consultório / Comparative clinical trial between different in-office bleaching systems

Objetivos: Estudos clínicos longitudinais que acompanham os pacientes por longos períodos não são muito comuns na literatura, ainda mais quando associados a grandes amostras (veio do fim do resumo). Por isso, o objetivo do trabalho foi determinar a eficiência, estabilidade de cor e sensibilidade dental, trans e pós operatória, dentro de um período de 365 dias, de quatro protocolos de clareamento em consultório. Material e Métodos: Foi realizado um estudo clínico randomizado, cego (para os pacientes), composto por 120 sujeitos (n=30). A amostra foi formada por pacientes adultos, sem distinção de gênero e etnia, e idade superior a 18 anos que foram selecionados por meio de avaliação clínica na qual foi verificada a cor dos dentes, a condição de higiene oral e a presença de restaurações e/ou próteses nas regiões em que os procedimentos seriam realizados. Todos os sujeitos foram submetidos a uma sessão de clareamento de acordo com as instruções do fabricante e obedecendo a aplicação ou não da luz, para os clareadores baseados no sistema Foto-Fenton (havia faltado citar nos métodos do resumo), e qual o seu tipo: Zoom Advanced Power, peróxido de hidrogênio (PH) 25% - Zoom! + luz UVA (Phillips Oral Healthcare); Zoom Whitespeed, PH 25% - Zoom! + luz Whitespeed (Phillips Oral Healthcare); Zoom sem luz, PH 25% - Zoom! (Phillips Oral Healthcare). Boost, PH 38% - Opalescence Xtra Boost (Ultradent). As alterações de cor foram avaliadas utilizando as escalas Vita Classical e Vita Bleachedguide 3D Master e o Espectrofotômetro Vita-Easyshade. As medições foram feitas em incisivos centrais e caninos uperiores antes, imediatamente e 7, 14, 30, 180 e 365 dias após o tratamento. Os dados foram analisados estatisticamente por meio do software Statistica 8.0 (StatSoft - Tulsa, OK) através da análise de variância (ANOVA) para medidas repetidas na avaliação das médias e as comparações foram realizadas através de contrastes (Tukey). Resultados:

Para a escala Vita Classical, Zoom AP e WS foram semelhantes entre si porém diferentes de Opalescence e Zoom sem luz, exceto para a avaliação de 30 dias (caninos) e 365 dias (incisivos) onde o Zoom WS demonstrou dados semelhantes ao Opalescence e Zoom sem luz Já para a escala Vita Bleached, Zoom AP e WS foram semelhantes entre si, porém diferentes de Opalescence e Zoom sem luz, exceto para as avaliações de 30 e 180 dias onde o Zoom WS demonstrou dados semelhantes ao Opalescence e Zoom sem luz (caninos). Para dentes incisivos, os achados foram semelhantes, exceto que houve diferença entre o Zoom AP e WS e as semelhanças entre Zoom WS, Opalescence e Zoom sem luz foram encontradas nas avaliações de 180 e 365 dias. Na avalição com o espectrofotômetro Vita Easyshade Zoom AP e WS foram semelhantes entre si e diferentes do Opalescence que, por sua vez, foi diferente do Zoom sem luz, exceto para as avaliações de 7, 14 e 30 dias (caninos). Para incisivos, Zoom AP e WS foram semelhantes entre si e diferentes de Opalescence e Zoom sem luz, exceto para a avaliação de 14 dias onde o Zoom AP foi diferente do Zoom WS. Por fim, a sensibilidade apresentou um aumento nos seus valores na avaliação imediatamente após o clareamento, com uma redução na avalição de 7 dias, para todos os grupos que ainda apresentaram valores de sensibilidade semelhantes em todos os períodos de avaliação. Conclusão: O acompanhamento até 365 dias demonstrou a eficiência dos protocolos de clareamento analisados uma vez que nenhum deles recidivou para os tons iniciais, demonstrando a durabilidade dos procedimentos. Os dois grupos com os clareadores Foto-Fenton obtiveram maior efeito clareador (substituiu desempenho, tinha ficado vago), exceto nas seguintes avaliações: Vita Classical, 30 dias (caninos) e 365 dias (incisivos) e Vita Bleached, 30 e 180 dias (caninos) e 180 e 365 dias (incisivos). Observou-se uma estabilização da cor após sete dias em todos os grupos. A sensibilidade...

Objectives: Longitudinal clinical studies that follow patients for long periods are not very common in the literature, especially when associated with large samples. The objective of this study was to determinate the efficacy, color stability and sensitivity within a 365 day period of four in-office bleaching protocols. Methods: A randomized clinical trial, blinded (for patients), composed of 120 subjects (n=30) was conducted. The sample consisted of adult patients, without gender and ethnic distinction, with age superior than 18 years old that were selected through clinical evaluation in which was verified the color of teeth, the condition of oral hygiene and the presence of restorations and/or prostheses in the areas where the procedures would be carried out. All subjects were submitted to a session of bleaching according to the manufacturer's instructions: Zoom Advanced Power, 25% hydrogen peroxide (HP) - Zoom! + UVA light (Phillips Oral Healthcare); Zoom Whitespeed, 25% HP - Zoom! + Whitespeed light (Phillips Oral Healthcare); Zoom without light, 25% HP - Zoom! (Phillips Oral Healthcare). Boost, 38% HP - Opalescence Xtra Boost (Ultradent). Color changes were evaluated using Vita Classical and Vita Bleachedguide 3D Master shade guides and Vita-Easyshade spectrophotometer. Measurements were made on the superior central incisive and canines before, immediately and 7, 14, 30, 180 and 365 days after the treatment. Statistical analysis of the data were made with the software Statistica 8.0 (StatSoft - Tulsa, OK) through the analysis of variance (ANOVA) for repeated measures in the mean evaluation and comparisons were made by using contrasts (Tukey). Results:

For the Vita Classical shade guide, Zoom AP and WS were similar but different from Opalescence and Zoom without light except for the 30 day (canines) and 365 days evaluations (incisives) where the Zoom WS showed similar data to Opalescence and Zoom without light...

Hydrogel of polysaccharide of sugarcane molasses as carrier of bone morphogenetic protein in the reconstruction of critical bone defects in rats

PURPOSE: To evaluate the benefit of using carriers such as the biopolymer gel (hidrogel of polysaccharide of sugarcane molasses) associated with the bone morphogenetic proteins (BMP's) in the repair of critical bone defects in calvaria of Wistar rats. METHODS: Forty-two rats were submitted to a surgical calvaria bone defects. These animals were divided into two experimental groups, positive control group and negative control group. The Group I the calvaria defect was filled up with biopolymer gel, biological membrane, BMP and lyophilized graft. The Group II was treated with biopolymer gel, BMP and lyophilized graft. And the group III (positive control group) was treated with BMP, lyophilized graft and biological membrane. In the negative control group (Group IV) a defect was made in the rat calvaria and the animals were sacrificed immediately after the surgery. The animals of experimental groups and positive control group were slaughtered after subsequent periods of 90 and 180 days. In these periods, the histological analysis and image assessment by cone bean tomographic imaging were obtained. RESULTS: There was highest bone tissue formation with statistically significant results in the groups that associated biopolymer gel and membrane (Group I), followed by the group III (BMP, lyophilized graft and biological membrane). The lower bone formation occurred in the group not using the sugarcane biopolymer gel (Group II). The radiolucent areas of the analyzes of 180 days among the groups studied were respectively, 14.98 mm², 26.65 mm² and 35.81 mm². CONCLUSION: The biopolymer gel showed to be an excellent bone morphogenetic protein carrier, probably by facilitating the controlled release of these proteins in the process of bone repair.

A new proposal to evaluate the healing of open skin wounds: volumetry / Nova proposta para avaliar cicatrização de ferida cutânea aberta: volumetria

PURPOSE: To present a new proposal to evaluate the healing of an open subcutaneous and skin wound, which we termed "volumetry". METHODS: A total of 32 circular wounds were performed in the subcutaneous tissues and skin of four feet of pigs (8 each). Each wound had about 1 cm in diameter and was 0.2 cm deep. Volume was calculated from the wound filled with saline and mass Xantopren. With the aid of a magnifying glass and local lighting, the liquid was dripped with a micropipette inside the wound until complete fullness. Volume repletion was calculated in microliters, corresponding to the volume of the wound. The mass of Xantopren was placed inside the wound to obtain a mold of the lesion. Mold volume was calculated using the formula of the volume of a cylinder closest resembling a geometric figure with mold. RESULTS: The calculation of wound volume was possible with both Xantopren and mold techniques. Volume as calculated by micropipette was 119.37 ± 30.87 microliters while the volume calculated by mold was 122.41 ± 33.90 mm3 (p=0.79). CONCLUSIONS: Volumetry in pig feet is simple and reproducible. Volumetry perfomed with saline did not differ from the volumetry with mass Xantopren. This method may be a useful tool to help evaluate the healing of open skin wounds in experimental and clinical research.

OBJETIVO: Apresentar nova proposta para avaliar a cicatrização de uma ferida cutânea aberta, denominada "volumetria." MÉTODOS: Foram provocadas 32 feridas circulares cutâneas, com cerca de 1 cm de diâmetro e 0.2 cm de profundidade, em quatro patas de suíno. O volume da ferida foi calculado com solução salina e massa de xantopren. O líquido foi gotejado com uma micropipeta no interior da ferida até sua completa repleção, o que foi auxiliado com uma lupa de aumento e iluminação local. O volume de repleção foi calculado em microlitros e correspondeu ao volume da ferida. A massa de xantopren foi colocada no interior da ferida para se obter um molde da lesão. O volume do molde foi calculado utilizando-se a fórmula do volume de um cilindro que foi a figura geométrica mais parecida com o molde. RESULTADOS: O cálculo do volume da ferida foi possível com as duas técnicas propostas. O volume calculado pela micropipeta foi 119.37 ± 30.8693 microlitros e o volume calculado pelo molde foi 122.4088 ± 33.8997 mm³ (p=0.79). CONCLUSÕES: A volumetria realizada em patas de suíno é um método simples, reprodutível. A volumetria realizada com líquido não diferiu da volumetria realizada com massa de Xantopren. Esse método poderá ser útil para auxiliar na análise da cicatrização da ferida cutânea aberta em trabalhos clínicos e experimentais.

Grafting Using Injectable Calcium Sulfate in Bone Tumor Surgery: Comparison with Demineralized Bone Matrix-based Grafting

BACKGROUND: Injectable calcium sulfate is a clinically proven osteoconductive biomaterial, and it is an injectable, resorbable and semi-structural bone graft material. The purpose of this study was to validate the clinical outcomes of injectable calcium sulfate (ICS) grafts as compared with those of a demineralized bone matrix (DBM)-based graft for filling in contained bony defects created by tumor surgery. METHODS: Fifty-six patients (41 males and 15 females) with various bone tumors and who were surgically treated between September 2003 and October 2007 were included for this study. The patients were randomly allocated into two groups, and either an ICS graft (28 patients) or a DBM-based graft (28 patients) was implanted into each contained defect that was developed by the surgery. The radiographic outcomes were compared between the two groups and various clinical factors were included for the statistical analysis. RESULTS: When one case with early postoperative pathologic fracture in the DBM group was excluded, the overall success rates of the ICS and DBM grafting were 85.7% (24/28) and 88.9% (24/27) (p > 0.05), respectively. The average time to complete healing was 17.3 weeks in the ICS group and 14.9 weeks in the DBM group (p > 0.05). Additionally, the ICS was completely resorbed within 3 months, except for one case. CONCLUSIONS: Although the rate of resorption of ICS is a concern, the injectable calcium sulfate appears to be a comparable bone graft substitute for a DBM-based graft, with a lower cost, for the treatment of the bone defects created during surgery for various bone tumors.

Molars extraction for bone graft study in rabbits / Extração de molares para estudos de enxertos ósseos em coelhos

PURPOSE: The aim of this study was to describe an experimental surgical technique to be used in the evaluation of bone grafts in rabbits. METHODS: The operative technique was performed in jaws, with external approach from the labial commissure to the last molar tooth. An incision about 1cm extended forward to the alveolar ridge, followed by a exposing the cervical region of the alveolar bone and dental elements was done. Thus, after extraction of first molar with forceps, the tooth socket left was filled with hydroxyapatite. The bone gain was analyzed by histopathological studies. RESULTS: The histological analyses indicated formed bone surrounding the biomaterial. CONCLUSION: The experimental model using the tooth socket of the rabbit molar is a feasible procedure for studies of bone grafts.

OBJETIVO: Descrever uma técnica cirúrgica em coelhos para avaliação de enxertos ósseos. MÉTODOS: A técnica operatória consiste numa incisão na topografia da comissura labial até o ultimo molar. Uma incisão de 1cm no rebordo para expor o osso alveolar e a região cervical dos molares. Realizou-se a exodontia com fórceps e o alvéolo é preenchido com hidroxiapatita. Após o tempo de cicatrização é realizada a avaliação histológica. RESULTADOS: A análise histológica mostrou o novo osso formado rodeando biomaterial. CONCLUSÃO: O modelo cirúrgico para avaliação de enxertos ósseos utilizando molares de coelhos se mostrou factível.

Uso de carbonos pirolíticos (Durasphere) no tratamento da insuficiência glótica: estudo experimental em cães / Use of pyrolytic carbon coated beads (Durasphere) to treat glottic failure: an experimental study in dogs

Nenhum tecido ou substância ideal foi encontrado para a injeção em pregas vocais. O objetivo deste estudo prospectivo foi avaliar o uso do Durasphere como substância de injeção na prega vocal canina. Materiais e métodos: Em seis cães adultos foram injetados 0,3mL de Durasphere no terço médio da prega vocal direita no músculo tireoaritenoideo e 0,3mL de soro fisiológico na prega contralateral. Os animais foram sacrificados após 7 dias (três cães) e 90 dias (três cães). Analisamos os processos inflamatórios no músculo vocal e na lâmina própria das pregas vocais. Resultados: No músculo vocal com Durasphere havia uma inflamação significativamente maior que no músculo controle, formouse um infiltrado linfomononuclear moderado após 7 dias e leve após 90 dias. Não observamos formação de corpos estranhos ou granulomas. Já na lâmina própria houve um processo inflamatório leve nos dois grupos, sem diferença entre eles. Conclusão: Trata-se de uma substância com biocompatibilidade comprovada em humanos, com resultados preliminares e inéditos de sua injeção em pregas vocais caninas que causou um processo inflamatório moderado no músculo vocal após 7 dias e leve após 90 dias, sem formação de corpos estranhos ou granulomas.

There is no ideal tissue or substance to be injected in the vocal folds. The objective of the present study was to assess the use of Durasphere in canine vocal fold injection. Materials and methods: in six adult dogs we injected 0.3 mL of Durasphere in the middle third of the thyroarytenoid muscle and 0.3 mL of saline solution in the contralateral vocal fold. The animals were slaughtered after seven days (three dogs) and after 90 days (three dogs). We analyzed the inflammatory process in the vocal fold and in the lamina propria of the vocal folds. Results: in the vocal muscle which received Durasphere there was a significantly more intense inflammation when compared to the control muscle - there was a moderate lymphomodular infiltrate after seven days and mild after 90 days. We did not observe foreign bodies nor granulomas. On the lamina propria there was a mild inflammatory process in the two groups, without difference between them. Conclusion: this is a substance of proven biocompatibility in humans, with preliminary and unprecedented results and its injection in canine vocal folds caused a moderate inflammatory process after seven days and mild after 90 days, without foreign bodies or granuloma formation.

Comparison of the biocompatibility of different root canal irrigants

The purpose of this study was to compare the reaction of rat subcutaneous connective tissue to 0.9 percent sterile saline, 2.5 percent sodium hypochlorite (NaOCl), 5.25 percent NaOCl and 2 percent chlorhexidine gluconate solution or gel. Six circles were demarcated on the dorsal skin of 24 male Wistar rats, leaving 2 cm between each circle. Using a syringe, 0.1 mL of each root canal irrigant was injected subcutaneously into 5 circles. In the 6th circle, the needle of an empty syringe was introduced into the skin, but no irrigant was injected (control group). Evaluations were undertaken at 2 h, 48 h, 14 days and 30 days post-procedure. Tissue samples were excised, embedded in paraffin blocks and 3-µm-thick sections were obtained and stained with hematoxylin and eosin. The areas of inflammatory reaction were evaluated and analyzed statistically by ANOVA and Tukey's test. The control group showed few or no inflammatory reaction areas in the subcutaneous tissue. 0.9 percent saline solution, 2.0 percent chlorhexidine solution and 2.5 percent NaOCl showed a good biocompatibility, as very mild inflammatory reaction was detected at 14 days and tissue repair occurred at 30 days. 5.25 percent NaOCl was the most toxic irrigant, as the number of inflammatory cells remained elevated at 14 and 30 days. The group treated with 2.0 percent chlorhexidine gluconate gel presented a moderate inflammatory response at 14 days, which decreased at 30 days, being considered similar to that of the control group, 0.9 percent saline solution, 2.0 percent chlorhexidine solution and 2.5 percent NaOCl at this experimental period.

Standard guidelines for the use of dermal fillers.

Currently used fillers vary greatly in their sources, efficacy duration and site of deposition; detailed knowledge of these properties is essential for administering them. Indications for fillers include facial lines (wrinkles, folds), lip enhancement, facial deformities, depressed scars, periocular melanoses, sunken eyes, dermatological diseases-angular cheilitis, scleroderma, AIDS lipoatrophy, earlobe plumping, earring ptosis, hand, neck, décolleté rejuvenation. PHYSICIANS' QUALIFICATIONS: Any qualified dermatologist may use fillers after receiving adequate training in the field. This may be obtained either during postgraduation or at any workshop dedicated to the subject of fillers. The physicians should have a thorough knowledge of the anatomy of the area designated to receive an injection of fillers and the aesthetic principles involved. They should also have a thorough knowledge of the chemical nature of the material of the filler, its longevity, injection techniques, and any possible side effects. FACILITY: Fillers can be administered in the dermatologist's minor procedure room. PREOPERATIVE COUNSELING AND INFORMED CONSENT: Detailed counseling with respect to the treatment, desired effects, and longevity of the filler should be discussed with the patient. Patients should be given brochures to study and adequate opportunity to seek information. Detailed consent forms need to be completed by the patients. A consent form should include the type of filler, longevity expected and possible postoperative complications. Preoperative photography should be carried out. Choice of the filler depends on the site, type of defect, results needed, and the physician's experience. Injection technique and volume depend on the filler and the physician's preference, as outlined in these guidelines.

Inyección submucosa uretral con agente Vantris® en el manejo de la incontinencia urinaria femenina, seguimiento a un año / Submucosal ureteral inyection with vantris® bulking agent for the management of urinary incontinence, one year follow-up

El objetivo del tratamiento de la incontinencia de orina (IOE) por disfunción esfinteriana es aumentarla resistencia uretral al escape de orina. Analizamos la eficacia y seguridad del agente inyectable VANTRIS® en IOE femenina prospectivamente en 23 pacientes. Estudio urodinámico pre-operatorio y uroflujometría tres meses después del procedimiento, se aplicó cuestionario ICIQ-SF antes de lacirugía, a los 3, 6, 9 y 12 meses. Se observó una disminución del ICIQ-SF promedio de 18,0 a 8,65 puntos y el Qmáx promedio a los 3 meses fue de 22,56 ml/s. El 56,52 por ciento permanecieron secas, el 8,69 por ciento mejoraron y el 8,69 por ciento no experimentaron cambios. El uso de VANTRIS® es mínimamente invasivo y seguro, pero requiere seguimiento a largo plazo para evaluar sus resultados.

The Urinary incontinence treatment caused by sphincteric dysfuntion is focused to increase urethral outflow resistance. We made a 23 patients prospective analysis to observe the efficacy and safety of a urethral bulking agent VANTRIS®. Preoperative Urodynamic study and uroflujometry three months later from the inyection, ICIQ-SF cuestionary preoperative, 3, 6, 9 and 12 months later. Outcomes were an increase of ICIQ-SF average from 18 to 8.65 points, the Q max average at 3 month analysis was 22.56 ml/s; 56.52 percent of patients were dry; 8.69 percent healthy and a 8.69 percent without changes. VANTRIS® treatment is a safety and minimally invasive procedure, but we need more follow up for a better evaluation of it’s results.

Adhesivos titulares en cirugía / Tissue adhesives in surgery

Los adhesivos tisulares son utilizados con frecuencia como adyuvantes en la práctica quirúrgica. Entre ellos, los más utilizados mundialmente son los sellantes de fibrina, si bien en Cuba se han obtenido excelentes resultados con los adhesivos de cianoacrilato a partir de la introducción en la práctica médica del Tisuacryl®, desarrollado en el Centro de Biomateriales de la Universidad de La Habana. Mientras se desarrollan técnicas cada vez menos invasivas en la cirugía, los adhesivos, entre otros usos en el área clínica, pueden ser de gran utilidad en el cierre de las heridas quirúrgicas o como sellantes en las líneas de sutura y para prevenir o disminuir las dehiscencias y fístulas. En este trabajo se resumen los resultados de una revisión bibliográfica realizada con el objetivo conocer las aplicaciones actuales de los adhesivos tisulares, especialmente los derivados cianoacrílicos, los cuales se han introducido paulatinamente en la práctica médica cubana. De ahí la importancia del conocimiento de este tipo de productos(AU)

The adhesive tisulares is frequently used as adyuvantes in the surgical practice. Among them, those more used worldwide they are the fibrina sellantes, although in Cuba excellent results have been obtained with the cianoacrilato adhesives starting from the introduction in the medical practice of the Tisuacryl®, developed in the Center of Biomateriales of the University of Havana. While they are developed technical less and less invasivas in the surgery, the adhesives, among other uses in the clinical area, they can be of great utility in the closing of the surgical wounds or I eat sellantes in the suture lines and to prevent or to diminish the dehiscencias and water-pipes. In this work summary the results of a bibliographical revision carried out with the objective to know the current applications of the adhesive tisulares, especially the derived cianoacrílicos, which have been introduced gradually in the Cuban medical practice. Of there the importance of the knowledge of this type of products(AU)