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1.
Artículo en Portugués | LILACS | ID: biblio-1087729

RESUMEN

Introdução: a pandemia provocada pelo 2019 Novel Coronavírus (COVID-19) provocou um desafio global de saúde pública, com repercussões em diversos setores da sociedade. As práticas médicas necessitaram adaptar-se no atendimento ao doente portador do COVID-19 ou suspeito. Métodos: realizou-se pesquisa bibliográfica de publicações e de diretrizes de sociedades médicas em relação às abordagens cirúrgicas de emergência nesta atual pandemia. Resultados: o material bibliográfico ainda é escasso, indefinido e de baixa evidência, mas são adequados neste momento inicial de enfrentamento do COVID-19 no Brasil. Conclusão: para reduzir o risco de contaminação dos profissionais de saúde, as técnicas e decisões cirúrgicas precisam adaptar-se ao cenário de pandemia do COVID-19.(AU)


Introduction: the pandemic caused by the 2019 Novel Coronavirus (COVID-19) has caused a global public health challenge, with repercussions in several sectors of society. Medical practices needed to adapt in the care of patients with or suspected of having COVID-19. Methods: Bibliographic research of publications and guidelines of medical societies regarding emergency surgical approaches in this current pandemic was carried out. Results: the bibliographic material is still scarce, undefined and of low evidence, but which are adequate in this initial moment of coping with COVID-19 in Brazil. Conclusion: to reduce the risk of contamination of health professionals, surgical techniques and decisions need to adapt to the pandemic scenario of COVID-19.(AU)


Asunto(s)
Humanos , Centros Quirúrgicos/normas , Personal de Salud/normas , Infecciones por Coronavirus/prevención & control , Infecciones por Coronavirus/transmisión , Contaminación Biológica/prevención & control , Pandemias , Brasil
2.
Arq Gastroenterol ; 56(3): 300-303, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31633729

RESUMEN

BACKGROUND: Bile duct injury is a life-threatening complication that requires proper management to prevent the onset of negative outcomes. Patients may experience repeated episodes of cholangitis, secondary biliary cirrhosis, end-stage liver disease and death. OBJECTIVE: To report a single center experience in iatrogenic secondary liver transplantation after cholecystectomy and review the literature. METHODS: This was a retrospective single center study. Of the 1662 liver transplantation realized, 10 (0.60 %) were secondary to iatrogenic bile ducts injuries due cholecystectomies. Medical records of these patients were reviewed in this study. RESULTS: Nine of 10 patients were women; the median time in waiting list and between cholecystectomy and inclusion in waiting list was of 222 days and of 139.9 months, respectively. Cholecystectomy was performed by open approach in eight (80%) cases and by laparoscopic approach in two (20%) cases. The patients underwent an average of 3.5 surgeries and procedures before liver transplantation. Biliary reconstruction was realized with a Roux-en-Y hepaticojejunostomy in nine (90%) cases. Mean operative time was 447.2 minutes and the median red blood cell transfusion was 3.4 units per patient. Mortality in the first month was of 30%. CONCLUSION: Although the liver transplantation is an extreme treatment for an initially benign disease, it has its well-defined indications in treatment of bile duct injuries after cholecystectomy, either in acute or chronic scenario.


Asunto(s)
Conductos Biliares/lesiones , Colecistectomía Laparoscópica/efectos adversos , Cirrosis Hepática Biliar/cirugía , Trasplante de Hígado , Adulto , Anciano , Conductos Biliares/cirugía , Femenino , Humanos , Enfermedad Iatrogénica , Cirrosis Hepática Biliar/etiología , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
3.
Arq. gastroenterol ; 56(3): 300-303, July-Sept. 2019. tab
Artículo en Inglés | LILACS | ID: biblio-1038721

RESUMEN

ABSTRACT BACKGROUND: Bile duct injury is a life-threatening complication that requires proper management to prevent the onset of negative outcomes. Patients may experience repeated episodes of cholangitis, secondary biliary cirrhosis, end-stage liver disease and death. OBJECTIVE: To report a single center experience in iatrogenic secondary liver transplantation after cholecystectomy and review the literature. METHODS: This was a retrospective single center study. Of the 1662 liver transplantation realized, 10 (0.60 %) were secondary to iatrogenic bile ducts injuries due cholecystectomies. Medical records of these patients were reviewed in this study. RESULTS: Nine of 10 patients were women; the median time in waiting list and between cholecystectomy and inclusion in waiting list was of 222 days and of 139.9 months, respectively. Cholecystectomy was performed by open approach in eight (80%) cases and by laparoscopic approach in two (20%) cases. The patients underwent an average of 3.5 surgeries and procedures before liver transplantation. Biliary reconstruction was realized with a Roux-en-Y hepaticojejunostomy in nine (90%) cases. Mean operative time was 447.2 minutes and the median red blood cell transfusion was 3.4 units per patient. Mortality in the first month was of 30%. CONCLUSION: Although the liver transplantation is an extreme treatment for an initially benign disease, it has its well-defined indications in treatment of bile duct injuries after cholecystectomy, either in acute or chronic scenario.


RESUMO CONTEXTO: A lesão da via biliar é uma complicação que pode ameaçar a vida e que requer manejo adequado para prevenir o aparecimento de desfechos negativos. Os pacientes podem apresentar episódios repetidos de colangite, cirrose biliar secundária, doença hepática terminal e até mesmo morte. OBJETIVO: Avaliar a experiência de um único centro em transplante hepático secundário a lesão iatrogênica de via biliar pós-colecistectomia e fazer uma revisão de literatura. MÉTODOS: Este foi um estudo retrospectivo de um único centro. Dos 1662 transplantes de fígado, 10 (0,60%) foram secundários a lesões iatrogênicas das vias biliares devido à colecistectomias. Os prontuários médicos desses pacientes foram revisados neste estudo. RESULTADOS: Nove dos dez pacientes eram mulheres; o tempo médio em lista de espera de transplante e entre colecistectomia e inclusão na lista de espera foi de 222 dias e de 139,9 meses, respectivamente. A colecistectomia foi realizada por abordagem aberta em oito (80%) casos e por abordagem laparoscópica em dois (20%) casos. Os pacientes foram submetidos a uma média de 3,5 cirurgias e procedimentos antes do transplante de fígado e a reconstrução biliar foi realizada com hepaticojejunostomia em Y-de-Roux em nove (90%) casos. O tempo operatório médio foi de 447,2 minutos e a média de transfusão de concentrados de hemácias foi de 3,4 unidades por paciente. Mortalidade no primeiro mês foi de 30%. CONCLUSÃO: Embora o transplante de fígado seja um tratamento extremo para uma doença inicialmente benigna, ele tem suas indicações bem definidas no tratamento de lesões biliares após colecistectomia, seja em um cenário agudo ou crônico.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Conductos Biliares/lesiones , Trasplante de Hígado , Colecistectomía Laparoscópica/efectos adversos , Cirrosis Hepática Biliar/cirugía , Conductos Biliares/cirugía , Estudios Retrospectivos , Enfermedad Iatrogénica , Cirrosis Hepática Biliar/etiología , Persona de Mediana Edad
4.
Acta Cir Bras ; 30(1): 24-33, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25627268

RESUMEN

PURPOSE: To evaluate the effect of propranolol on capsular architecture around silicone implants by measuring the inflammation, capsular thickness, and collagen fiber density, using a guinea pig experimental model. METHODS: Thirty six adult male guinea pigs randomly divided into two groups (n=18) were used. Each one received a silicone implant with textured-surface. The capsular tissue around implants from untreated or treated animals with the beta-adrenoceptor antagonist propranolol (10 mg/kg, dissolved in daily water) were analyzed for inflammation by histological scoring, capsular thickness by computerized histometry, and collagen fibers type I and Type III density by picrosirius polarization at different time points (7, 14 or 21 days after silicone implantation). RESULTS: Propranolol treatment reduced inflammation and impaired capsular thickness and delayed collagen maturation around the textured implant. CONCLUSION: Propranolol reduces the risk of developing capsular contracture around silicone implants with textured surface.


Asunto(s)
Antagonistas Adrenérgicos beta/farmacología , Contractura Capsular en Implantes/prevención & control , Propranolol/farmacología , Geles de Silicona/efectos adversos , Antagonistas Adrenérgicos beta/uso terapéutico , Animales , Implantes de Mama/efectos adversos , Colágeno Tipo I/análisis , Colágeno Tipo I/efectos de los fármacos , Colágeno Tipo III/análisis , Colágeno Tipo III/efectos de los fármacos , Modelos Animales de Enfermedad , Cobayas , Humanos , Contractura Capsular en Implantes/patología , Implantes Experimentales/efectos adversos , Masculino , Propranolol/uso terapéutico , Distribución Aleatoria , Reproducibilidad de los Resultados , Tejido Subcutáneo/efectos de los fármacos , Tejido Subcutáneo/patología , Factores de Tiempo , Resultado del Tratamiento
5.
Acta cir. bras ; 30(1): 24-33, 01/2015. tab, graf
Artículo en Inglés | LILACS | ID: lil-735711

RESUMEN

PURPOSE: To evaluate the effect of propranolol on capsular architecture around silicone implants by measuring the inflammation, capsular thickness, and collagen fiber density, using a guinea pig experimental model. METHODS: Thirty six adult male guinea pigs randomly divided into two groups (n=18) were used. Each one received a silicone implant with textured-surface. The capsular tissue around implants from untreated or treated animals with the beta-adrenoceptor antagonist propranolol (10 mg/kg, dissolved in daily water) were analyzed for inflammation by histological scoring, capsular thickness by computerized histometry, and collagen fibers type I and Type III density by picrosirius polarization at different time points (7, 14 or 21 days after silicone implantation). RESULTS: Propranolol treatment reduced inflammation and impaired capsular thickness and delayed collagen maturation around the textured implant. CONCLUSION: Propranolol reduces the risk of developing capsular contracture around silicone implants with textured surface. .


Asunto(s)
Animales , Cobayas , Humanos , Masculino , Antagonistas Adrenérgicos beta/farmacología , Contractura Capsular en Implantes/prevención & control , Propranolol/farmacología , Geles de Silicona/efectos adversos , Antagonistas Adrenérgicos beta/uso terapéutico , Implantes de Mama/efectos adversos , Colágeno Tipo I/análisis , Colágeno Tipo I/efectos de los fármacos , Colágeno Tipo III/análisis , Colágeno Tipo III/efectos de los fármacos , Modelos Animales de Enfermedad , Contractura Capsular en Implantes/patología , Implantes Experimentales/efectos adversos , Propranolol/uso terapéutico , Distribución Aleatoria , Reproducibilidad de los Resultados , Tejido Subcutáneo/efectos de los fármacos , Tejido Subcutáneo/patología , Factores de Tiempo , Resultado del Tratamiento
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