Ann Surg Treat Res.  2025 Feb;108(2):93-97. 10.4174/astr.2025.108.2.93.

The characteristics of patients who failed initial Kasai portoenterostomy and the long-term prognosis of those who underwent redo-Kasai: a retrospective observational study

Affiliations
  • 1Division of Pediatric Surgery, Asan Medical Center Children’s Hospital, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Abstract

Purpose
The purpose of this study was to determine the characteristics of patients with failed initial Kasai portoenterostomy (KP) and to compare the long-term prognosis of redo-KP with that of liver transplantation (LT) in these patients.
Methods
The medical records of patients with biliary atresia (BA) who failed initial KP from 2010 to 2021 at a single center were retrospectively analyzed. KP failure was defined as persistent jaundice (total bilirubin concentration, ≥2.0 mg/dL) after KP or the performance of LT.
Results
During the study period, 32 patients experienced initial KP failure, with 10 undergoing redo-KP and 22 undergoing LT. Redo-KP was successful in a minority of patients with failed initial KP, but the complications, particularly cholangitis, were more frequent in the redo-KP group. The long-term prognosis of redo-KP compared to LT showed that while some patients benefited from native liver survival after redo-KP, LT remains the more definitive solution for sustained liver function and survival in patients with BA.
Conclusion
The only factor differing significantly between patients who underwent redo-KP and LT after failed initial KP was complications of cholangitis. Redo-KP was successful in 4 of 10 patients with failed initial KP, suggesting that redo-KP may be a treatment option in patients with BA and failed initial KP.

Keyword

Biliary atresia; Morbidity; Portoenterostomy

Figure

  • Fig. 1 Flowchart of patients who underwent Kasai portoenterostomy (KP) at our institution during the study period. LT, liver transplantation.

  • Fig. 2 Kaplan-Meier analysis of overall native liver survival after initial Kasai portoenterostomy of patients with biliary atresia at Asan Medical Center.


Reference

1. Davenport M, Ong E, Sharif K, Alizai N, McClean P, Hadzic N, et al. Biliary atresia in England and Wales: results of centralization and new benchmark. J Pediatr Surg. 2011; 46:1689–1694. PMID: 21929975.
Article
2. Bates MD, Bucuvalas JC, Alonso MH, Ryckman FC. Biliary atresia: pathogenesis and treatment. Semin Liver Dis. 1998; 18:281–293. PMID: 9773428.
3. Nio M. Japanese biliary atresia registry. Pediatr Surg Int. 2017; 33:1319–1325. PMID: 29039049.
4. Bondoc AJ, Taylor JA, Alonso MH, Nathan JD, Wang Y, Balistreri WF, et al. The beneficial impact of revision of Kasai portoenterostomy for biliary atresia: an institutional study. Ann Surg. 2012; 255:570–576. PMID: 22258066.
Article
5. Sugawara Y, Makuuchi M, Kaneko J, Ohkubo T, Mizuta K, Kawarasaki H. Impact of previous multiple portoenterostomies on living donor liver transplantation for biliary atresia. Hepatogastroenterology. 2004; 51:192–194. PMID: 15011862.
6. Urahashi T, Ihara Y, Sanada Y, Wakiya T, Yamada N, Okada N, et al. Effect of repeat Kasai hepatic portoenterostomy on pediatric live-donor liver graft for biliary atresia. Exp Clin Transplant. 2013; 11:259–263. PMID: 23530849.
7. Wood RP, Langnas AN, Stratta RJ, Pillen TJ, Williams L, Lindsay S, et al. Optimal therapy for patients with biliary atresia: portoenterostomy (“Kasai” procedures) versus primary transplantation. J Pediatr Surg. 1990; 25:153–162. PMID: 2299541.
8. Murase N, Uchida H, Ono Y, Tainaka T, Yokota K, Tanano A, et al. A new era of laparoscopic revision of Kasai portoenterostomy for the treatment of biliary atresia. Biomed Res Int. 2015; 2015:173014. PMID: 26266251.
Article
9. Lemoine CP, Melin-Aldana H, Brandt KA, Superina R. Identification of early clinical and histological factors predictive of Kasai portoenterostomy failure. J Clin Med. 2022; 11:6523. PMID: 36362751.
10. Qisthi SA, Saragih DS, Sutowo DW, Sirait DN, Imelda P, Kencana SM, et al. Prognostic factors for survival of patients with biliary atresia following Kasai surgery. Kobe J Med Sci. 2020; 66:E56–E60. PMID: 33024065.
11. Nakamura H, Kawano T, Yoshizawa K, Nakajima H, Suda K, Koga H, et al. Long-term follow-up for anicteric survival with native liver after redo Kasai: a first report. J Pediatr Surg. 2016; 51:2109–2112. PMID: 27680596.
12. Superina R, Magee JC, Brandt ML, Healey PJ, Tiao G, Ryckman F, et al. The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg. 2011; 254:577–585. PMID: 21869674.
Article
13. Capparelli MA, Ayarzabal VH, Halac ET, Questa HA, Minetto MJ, Cervio G, et al. Preoperative risk factors for the early failure of the Kasai portoenterostomy in patients with biliary atresia. Pediatr Surg Int. 2021; 37:1183–1189. PMID: 34057595.
14. Saito S, Tsuchida Y, Honna T. Reoperation for biliary atresia after hepatic portoenterostomy: experience in 29 cases with a report on the longest survivor in Japan. Z Kinderchir. 1984; 39:99–101. PMID: 6730726.
15. Mendoza MM, Chiang JH, Lee SY, Kao CY, Chuang JH, Tiao MM, et al. Reappraise the effect of redo-Kasai for recurrent jaundice following Kasai operation for biliary atresia in the era of liver transplantation. Pediatr Surg Int. 2012; 28:861–864. PMID: 22872304.
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