Related to: J. Rio J. I PhD. Hospital A. Seis pacientes apresentaram mais de uma anomalia.
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Related to: J. Rio J. I PhD. Hospital A. Seis pacientes apresentaram mais de uma anomalia. O encaminhamento tardio dos pacientes com AB continua sendo um problema em todo o Brasil.
Biliary atresia: current concepts and research directions. Summary of a symposium. Five- and year survival rates after surgery for biliary atresia: a report from the Japanese Biliary Atresia Registry. J Pediatr Surg. Epidemiology of biliary atresia: a population-based study.
The frequency and outcome of biliary atresia in the UK and Ireland. Biliary atresia: the Canadian experience. J Pediatr. Extrahepatic biliary atresia: current concepts and future directions. J Pediatr Rio J. Advances in biliary atresia: from patient care to research. Braz J Med Biol Res. Late referral for biliary atresia--missed opportunities for effective surgery. Nio M, Ohi R. Biliary atresia. Semin Pediatr Surg. Prognosis of biliary atresia in the era of liver transplantation: French national study from to Kelly DA, Davenport M.
Current management of biliary atresia. Arch Dis Child. A multicenter study of the outcome of biliary atresia in the United States, to Management of patients with biliary atresia in France: results of a decentralized policy Seamless management of biliary atresia in England and Wales Biliary atresia: Swiss national study, J Pediatr Gastroenterol Nutr.
Long-term prognosis and factors affecting biliary atresia from experience over a 25 year period. Chang Gung Med J. Epidemiological features of biliary atresia in Taiwan, a national study J Gastroenterol Hepatol.
Biliary atresia: we still operate too late. Narkewicz MR. Biliary atresia: an update on our understanding of the disorder. Curr Opin Pediatr.
Pathogenesis and outcome of biliary atresia: current concepts. Short-term results of Kasai operation for biliary atresia: experience from one institution.
Asian J Surg. Management of biliary atresia in Nigeria: the ongoing challenge. Ann Trop Paediatr. Outcome of biliary atresia in Malaysia: a single-centre study. J Paediatr Child Health. Incidence and prognostic factors associated with biliary atresia in western India. Ann Hepatol. Biliary atresia registry, to Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop.
Initial response to portoenterostomy determines long-term outcome in patients with biliary atresia. Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia? Kasai operation in the age of liver transplantation. Healing or merely palliative technique?
Cir Pediatr. Outcome in adulthood of biliary atresia: a study of 63 patients who survived over 20 years with their native liver. British paediatric surveillance unit study of biliary atresia: outcome at 13 years. Chardot C, Serinet MO.
Prognosis of biliary atresia: what can be further improved? Earlier identification of biliary atresia and hepatobiliary disease: selective screening in the third week of life. Matsui A, Dodoriki M. Screening for biliary atresia. Screening for biliary atresia by infant stool color card in Taiwan. Universal screening for biliary atresia using an infant stool color card in Taiwan. Biliary atresia: the Brazilian experience.
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Carlos Gomes, cj. How to cite this article.
Biliary Atresia - Clinical Series
Introduction: Biliary atresia is the main cause of death by hepatic failure and the main indication for liver transplant in children. Material and methods: Descriptive, observational, and retrospective study, including the patients with biliary atresia, diagnosed and treated between January 1, and December 31, We analyzed epidemiologic, clinical, biochemical, and image data, as well as registered complications and present status. Results: Eighteen patients were evaluated. The median age at time of Kasai portoenterostomy was 63 days of life, with better prognosis for those patients who had surgery before 72 days. There was a significant association between recurrent cholangitis and survival.
Atresia das vias biliares
Colestasis neonatal e infantil. Universidad de Los Andes. Universidad Nacional de Colombia. La incidencia de colestasis neonatal es de aproximadamente 1 de cada 2. En la tabla 2 se resume el comportamiento HNI.
Atresia biliar: continuamos operando tarde. Carlos O. Kieling I ; Jorge L. Lorentz IV ; Themis R.
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