1974
DOI: 10.1016/s0022-3468(74)80288-5
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Hepatic portoenterostomy—Is it indicated in the treatment of biliary atresia?

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Cited by 26 publications
(4 citation statements)
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“…The disappointing results of surgical intervention, including portoenterostomy, in this series are similar to those recently reported by Campbell et al (1974a). Ineffective surgery in this series did not cause increased morbidity or significantly earlier death.…”
Section: Discussionsupporting
confidence: 88%
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“…The disappointing results of surgical intervention, including portoenterostomy, in this series are similar to those recently reported by Campbell et al (1974a). Ineffective surgery in this series did not cause increased morbidity or significantly earlier death.…”
Section: Discussionsupporting
confidence: 88%
“…Only 5 % of cases have distal obstructions with patent bile-containing proximal bile ducts which allow bile drainage by standard surgical techniques (Arima, Fonkalsrud, and Neerhout, 1974). Many of these will have developed cirrhosis by early childhood, though occasional cases survive to adulthood (Berenson, Garde, and Moody, 1974).The remaining 95 % usually die by the age of 2 years (Campbell et al, 1974a), though the operation of hepatic portoenterostomy introduced in Japan 15 years ago by Kasai and co-workers has given …”
mentioning
confidence: 99%
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“…Without surgical repair, the prognosis of both groups is grave with a 99% chance of death by 2 years of age (23). In the first portoenterostomy series, Campbell et al reported 100% mortality at an average time of 15.3 months after the operation (24). Very similar results were reported in the early reports from the United Kingdom and United States (7,25).…”
Section: Extrahepatic Biliary Atresiamentioning
confidence: 63%