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Predictors of Short-Term Outcome of Kasai Portoenterostomy for Biliary Atresia in Infants: a Single-Center Study

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주제분류소아과학

초록

Purpose: The outcome predictors of Kasai portoenterostomy (KPE) for biliary atresia (BA) are controversial. This study aimed to identify possible short-term outcome predictors of KPE for BA in infants. Methods: This retrospective study included infants with BA who underwent KPE between January 2015 and December 2017 and were followed up for at least 6 months after surgery at the Pediatric Hepatology Unit, Cairo University Pediatric Hospital, Egypt. The short-term outcome was jaundice clearance within 6 months following surgery. All data were compared between the jaundice free group and those with persistent jaundice to identify the predictors of jaundice clearance. Results: The study included 75 infants. The mean age at the time of surgery was 82.43±22.77 days (range, 37–150 days), and 28 (37.3%) infants cleared their jaundice within 6 months postoperative. Age at surgery did not significantly affect the outcome (p=0.518). Infants with persistent jaundice had significantly higher pre-operative levels of aspartate aminotransferase (AST) than those who were jaundice free (p=0.041). Receiver operating characteristic curve analysis showed that preoperative AST ≤180 IU/L was predictive of a successful KPE, with sensitivity 74.5% and specificity 60.7%. Infants with bile plugs in liver biopsy had a 6-fold higher risk of persistent jaundice than those without bile plugs (95% confidence interval: 1.59–20.75, p=0.008). Conclusion: Jaundice clearance after KPE for BA can be predicted using preoperative AST and presence of bile plugs in liver biopsy.

Abstract

Purpose: The outcome predictors of Kasai portoenterostomy (KPE) for biliary atresia (BA) are controversial. This study aimed to identify possible short-term outcome predictors of KPE for BA in infants. Methods: This retrospective study included infants with BA who underwent KPE between January 2015 and December 2017 and were followed up for at least 6 months after surgery at the Pediatric Hepatology Unit, Cairo University Pediatric Hospital, Egypt. The short-term outcome was jaundice clearance within 6 months following surgery. All data were compared between the jaundice free group and those with persistent jaundice to identify the predictors of jaundice clearance. Results: The study included 75 infants. The mean age at the time of surgery was 82.43±22.77 days (range, 37–150 days), and 28 (37.3%) infants cleared their jaundice within 6 months postoperative. Age at surgery did not significantly affect the outcome (p=0.518). Infants with persistent jaundice had significantly higher pre-operative levels of aspartate aminotransferase (AST) than those who were jaundice free (p=0.041). Receiver operating characteristic curve analysis showed that preoperative AST ≤180 IU/L was predictive of a successful KPE, with sensitivity 74.5% and specificity 60.7%. Infants with bile plugs in liver biopsy had a 6-fold higher risk of persistent jaundice than those without bile plugs (95% confidence interval: 1.59–20.75, p=0.008). Conclusion: Jaundice clearance after KPE for BA can be predicted using preoperative AST and presence of bile plugs in liver biopsy.

참고문헌 (36)

  1. Sokol RJ, "Screening and outcomes in biliary atresia : summary of a National Institutes of Health workshop", Hepatology, 46, pp.566~581 (2007)
  2. Shneider BL, "Total serum bilirubin within 3 months of hepatoportoenterostomy predicts short-term outcomes in biliary atresia", J Pediatr, 170, pp.211~217 (2016)
  3. Hartley JL, "Biliary atresia", Lancet, 374, pp.1704~1713 (2009)
  4. Shneider BL, "A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000", J Pediatr, 148, pp.467~474 (2006)
  5. Davenport M, "Surgical outcome in biliary atresia : etiology affects the influence of age at surgery", Ann Surg, 247, pp.694~698 (2008)
  6. Davenport M, "Seamless management of biliary atresia in England and Wales(1999-2002)", Lancet, 363, pp.1354~1357 (2004)
  7. Abdel-Aziz SA, "Preoperative alkaline phosphatase is a potential predictor of short-term outcome of surgery in infants with biliary atresia", Clin Exp Hepatol, 5, pp.155~160 (2019)
  8. Davenport M, "Biliary atresia in England and Wales : results of centralization and new benchmark", J Pediatr Surg, 46, pp.1689~1694 (2011)
  9. Hadzić N, "Long-term survival following Kasai portoenterostomy : is chronic liver disease inevitable", J Pediatr Gastroenterol Nutr, 37, pp.430~433 (2003)
  10. Schreiber RA, "Biliary atresia : the Canadian experience", J Pediatr, 151, pp.659~665 (2007)
  11. Queiroz TC, "Biliary atresia : evaluation on two distinct periods at a reference pediatric service", Arq Gastroenterol, 51, pp.53~58 (2014)
  12. De Maayer T, "Outcomes of Kasai hepatoportoenterostomy in children with biliary atresia in Johannesburg, South Africa", S Afr Med J, 107, pp.12131~ (2017)
  13. Chung PH, "Predictors for failure after Kasai operation", J Pediatr Surg, 50, pp.293~296 (2015)
  14. Davenport M, "The outcome of the older(> or =100 days)infant with biliary atresia", J Pediatr Surg, 39, pp.575~581 (2004)
  15. Davenport M, "Maximizing Kasai portoenterostomy in the treatment of biliary atresia : medical and surgical options", S Afr Med J, 102(11 Pt 2), pp.865~867 (2012)
  16. Ramachandran P, "The extended Kasai portoenterostomy for biliary atresia : a preliminary report", J Indian Assoc Pediatr Surg, 21, pp.66~71 (2016)
  17. Chardot C, "Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia", J Pediatr, 138, pp.224~228 (2001)
  18. Redkar R, "Outcome of biliary atresia after Kasai's portoenterostomy : a 15-year experience", Indian Pediatr, 54, pp.291~294 (2017)
  19. Townsend MR, "Factors associated with timing and adverse outcomes in patients with biliary atresia undergoing Kasai hepatoportoenterostomy", J Pediatr, 199, pp.237~242 (2018)
  20. Neto B, "Biliary atresia-clinical series", GE Port J Gastroenterol, 25, pp.68~73 (2018)
  21. Nio M, "Impact of age at Kasai operation on short-and long-term outcomes of type III biliary atresia at a single institution", J Pediatr Surg, 45, pp.2361~2363 (2010)
  22. Cowles RA, "Pediatric surgery", pp.1321~1329 (2012), Elsevier Mosby
  23. Al-Kawaz SA, "Factors that predict mortality rate in biliary atresia", J Fac Med Baghdad, 56, pp.136~140 (2014)
  24. Carvalho E, "Biliary atresia: the Brazilian experience", J Pediatr(Rio J), 86, pp.473~479 (2010)
  25. Azarow KS, "Biliary atresia : should all patients undergo a portoenterostomy", J Pediatr Surg, 32, pp.168~172 (1997)
  26. Wong KK, "Performing Kasai portoenterostomy beyond 60 days of life is not necessarily associated with a worse outcome", J Pediatr Gastroenterol Nutr, 51, pp.631~634 (2010)
  27. Yanchar NL, "Is early response to portoenterostomy predictive of long-term outcome for patients with biliary atresia", J Pediatr Surg, 31, pp.774~778 (1996)
  28. Goda T, "The most reliable early predictors of outcome in patients with biliary atresia after Kasai's operation", J Pediatr Surg, 48, pp.2373~2377 (2013)
  29. Uchida K, "Predicting factor of quality of life in long-term jaundice-free survivors after the Kasai operation", J Pediatr Surg, 39, pp.1040~1044 (2004)
  30. Namasemayam D, "Factors influencing outcome after hepatic portoenterostomy among extrahepatic bile duct atresia patients in Hospital Sultanah Bahiyah, Alor Setar", Med J Malaysia, 72, pp.329~332 (2017)
  31. Sanghai SR, "Incidence and prognostic factors associated with biliary atresia in western India", Ann Hepatol, 8, pp.120~122 (2009)
  32. Tyraskis A, "Steroids after the Kasai procedure for biliary atresia : the effect of age at Kasai portoenterostomy", Pediatr Surg Int, 32, pp.193~200 (2016)
  33. Bezerra JA, "Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia : the START randomized clinical trial", JAMA, 311, pp.1750~1759 (2014)
  34. Dong R, "Improved outcome of biliary atresia with postoperative high-dose steroid", Gastroenterol Res Pract, 2013, pp.902431~ (2013)
  35. Kvist N, "Thirty-four years' experience with biliary atresia in Denmark : a single center study", Eur J Pediatr Surg, 21, pp.224~228 (2011)
  36. Miga D, "Survival after first esophageal variceal hemorrhage in patients with biliary atresia", J Pediatr, 139, pp.291~296 (2001)

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