Skip to main content
Erschienen in: European Journal of Pediatrics 9/2003

01.09.2003 | Original Paper

A scoring system to predict the need for liver transplantation for biliary atresia after Kasai portoenterostomy

verfasst von: Chuen-Bin Jiang, Hung-Chang Lee, Chun-Yan Yeung, Jin-Cherng Sheu, Pei-Yeh Chang, Nien-Lu Wang, Ching-Yin Yeh

Erschienen in: European Journal of Pediatrics | Ausgabe 9/2003

Einloggen, um Zugang zu erhalten

Abstract

A retrospective analysis was performed of the records of 133 patients with extrahepatic biliary atresia (EHBA) who had undergone a Kasai portoenterostomy. The patients were divided into a non-transplantation group who survived but did not receive liver transplantation after the procedure and a failure group of those who died or received liver transplantation. A score was calculated that assessed nine factors, including laboratory values and complications. The data were assessed at the time complications occurred. The scores were analysed by a trend analysis to see if serial scores predicted the evolution of liver disease. A receiver operating characteristic (ROC) curve was plotted to assess the optimal cut-point for the scoring system. There were 98 patients in the non-transplantation group and 35 in the failure group. The latter group had significantly higher post-operative bilirubin (9.3±7.2 mg/dl versus 3.5±3.1 mg/dl), ALT (136±89 U/l versus 92±88 U/l), prothrombin time, and incidence of cirrhosis, ascites, oesophageal varices, portal hypertension, cholangitis and sepsis than the non-transplantation group ( P <0.05). A score of ≥8 had a high sensitivity (96.9%) and specificity (89.5%) for predicting the need for liver transplant. Conclusion:based on easily available clinical information, our scoring system can predict which patients with biliary atresia who have already undergone a Kasai procedure should be considered for liver transplantation.
Literatur
1.
Zurück zum Zitat Altman RP, Lilly JR, Greenfield J, Weinberg A, van Leeuwen K, Flanigan L (1997) A multiple risk factors analysis of the portoenterostomy (Kasai) procedure for biliary atresia. Twenty-five years of experience from two centers. Ann Surg 226: 348–355CrossRefPubMed Altman RP, Lilly JR, Greenfield J, Weinberg A, van Leeuwen K, Flanigan L (1997) A multiple risk factors analysis of the portoenterostomy (Kasai) procedure for biliary atresia. Twenty-five years of experience from two centers. Ann Surg 226: 348–355CrossRefPubMed
2.
Zurück zum Zitat Carceller A, Blanchard H, Alvarez F, St-Vil D, Bensoussan AL, Di Lorenzo M (2000) Past and future of biliary atresia. J Pediatr Surg 35: 717–720PubMed Carceller A, Blanchard H, Alvarez F, St-Vil D, Bensoussan AL, Di Lorenzo M (2000) Past and future of biliary atresia. J Pediatr Surg 35: 717–720PubMed
3.
Zurück zum Zitat Karrer FM, Price MR, Bensard DD, Sokol RJ, Narkewicz MR, Smith DJ, Lilly JR (1996) Long-term results with the Kasai operation for biliary atresia. Arch Surg 131: 493–496 Karrer FM, Price MR, Bensard DD, Sokol RJ, Narkewicz MR, Smith DJ, Lilly JR (1996) Long-term results with the Kasai operation for biliary atresia. Arch Surg 131: 493–496
4.
Zurück zum Zitat Kasai M, Mochizuki I, Ohkohchi N, Chiba T, Ohi R (1989) Surgical limitation for biliary atresia: indication for liver transplantation. J Pediatr Surg 24: 851–854 Kasai M, Mochizuki I, Ohkohchi N, Chiba T, Ohi R (1989) Surgical limitation for biliary atresia: indication for liver transplantation. J Pediatr Surg 24: 851–854
5.
Zurück zum Zitat Lipsett PA, Segev DL, Colombani PM (1997) Biliary atresia and biliary cysts. Baillieres Clin Gastroenterol 11: 619–641PubMed Lipsett PA, Segev DL, Colombani PM (1997) Biliary atresia and biliary cysts. Baillieres Clin Gastroenterol 11: 619–641PubMed
6.
Zurück zum Zitat Miyano T, Fujimoto T, Ohya T, Shimomura H (1993) Current concept of the treatment of biliary atresia. World J Surg 17: 332–336PubMed Miyano T, Fujimoto T, Ohya T, Shimomura H (1993) Current concept of the treatment of biliary atresia. World J Surg 17: 332–336PubMed
7.
Zurück zum Zitat Ohhama Y, Shinkai M, Fujita S, Nishi T, Yamamoto H (2000) Early predication of long-term survival and the timing of liver transplantation after the Kasai operation. J Pediatr Surg 35: 1031–1034CrossRefPubMed Ohhama Y, Shinkai M, Fujita S, Nishi T, Yamamoto H (2000) Early predication of long-term survival and the timing of liver transplantation after the Kasai operation. J Pediatr Surg 35: 1031–1034CrossRefPubMed
8.
Zurück zum Zitat Ohi R, Chiba T, Mochizuki I (1988) Long term follow-up of patients with biliary atresia. Conference on mechanisms and management of pediatric hepatobiliary disease, Arlington, VA, 96 Ohi R, Chiba T, Mochizuki I (1988) Long term follow-up of patients with biliary atresia. Conference on mechanisms and management of pediatric hepatobiliary disease, Arlington, VA, 96
9.
Zurück zum Zitat Okazaki T, Kobayashi H, Yamataka A, Lane GJ, Miyano T (1999) Long-term post-surgical outcome of biliary atresia. J Pediatr Surg 34: 312–315PubMed Okazaki T, Kobayashi H, Yamataka A, Lane GJ, Miyano T (1999) Long-term post-surgical outcome of biliary atresia. J Pediatr Surg 34: 312–315PubMed
10.
Zurück zum Zitat Otte JB, de Ville de Goyet J, Reding R, Hausleithner V, Sokal E, Chardot C, Debande B (1994) Sequential treatment of biliary atresia with Kasai portoenterostomy and liver transplantation: a review. Hepatology 20: 41S–48SPubMed Otte JB, de Ville de Goyet J, Reding R, Hausleithner V, Sokal E, Chardot C, Debande B (1994) Sequential treatment of biliary atresia with Kasai portoenterostomy and liver transplantation: a review. Hepatology 20: 41S–48SPubMed
11.
Zurück zum Zitat Ryckman F, Fisher R, Pedersen S, Dittrich V, Heubi J, Farrell M, Balistreri W, Ziegler M (1993) Improved survival in biliary atresia in the present era of liver transplantation. J Pediatr Surg 28: 382–386PubMed Ryckman F, Fisher R, Pedersen S, Dittrich V, Heubi J, Farrell M, Balistreri W, Ziegler M (1993) Improved survival in biliary atresia in the present era of liver transplantation. J Pediatr Surg 28: 382–386PubMed
12.
Zurück zum Zitat Ryckman FC, Alonso MH, Bucuvalas JC, Balistreri WF (1998) Biliary atresia: surgical management and treatment options as they relate to outcome. Liver Transplant Surg 4: S24–S33 Ryckman FC, Alonso MH, Bucuvalas JC, Balistreri WF (1998) Biliary atresia: surgical management and treatment options as they relate to outcome. Liver Transplant Surg 4: S24–S33
13.
Zurück zum Zitat Vacanti JP, Shamberger RC, Eraklis A, Lillehei CW (1990) The therapy of biliary combining the Kasai portoenterostomy with liver transplantation: a single center experience. J Pediatr Surg 25: 149–152PubMed Vacanti JP, Shamberger RC, Eraklis A, Lillehei CW (1990) The therapy of biliary combining the Kasai portoenterostomy with liver transplantation: a single center experience. J Pediatr Surg 25: 149–152PubMed
14.
Zurück zum Zitat Wood RP, Langnas AN, Stratta RJ, Pillen TJ, Williams L, Lindsay S, Meiergerd D, Shaw BW Jr (1990) Optimal therapy for patients with biliary atresia: portoenterostomy versus primary transplantation. J Pediatr Surg 25: 153–162PubMed Wood RP, Langnas AN, Stratta RJ, Pillen TJ, Williams L, Lindsay S, Meiergerd D, Shaw BW Jr (1990) Optimal therapy for patients with biliary atresia: portoenterostomy versus primary transplantation. J Pediatr Surg 25: 153–162PubMed
Metadaten
Titel
A scoring system to predict the need for liver transplantation for biliary atresia after Kasai portoenterostomy
verfasst von
Chuen-Bin Jiang
Hung-Chang Lee
Chun-Yan Yeung
Jin-Cherng Sheu
Pei-Yeh Chang
Nien-Lu Wang
Ching-Yin Yeh
Publikationsdatum
01.09.2003
Verlag
Springer-Verlag
Erschienen in
European Journal of Pediatrics / Ausgabe 9/2003
Print ISSN: 0340-6199
Elektronische ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-003-1268-x

Weitere Artikel der Ausgabe 9/2003

European Journal of Pediatrics 9/2003 Zur Ausgabe

Neuer Typ-1-Diabetes bei Kindern am Wochenende eher übersehen

23.04.2024 Typ-1-Diabetes Nachrichten

Wenn Kinder an Werktagen zum Arzt gehen, werden neu auftretender Typ-1-Diabetes und diabetische Ketoazidosen häufiger erkannt als bei Arztbesuchen an Wochenenden oder Feiertagen.

Neue Studienergebnisse zur Myopiekontrolle mit Atropin

22.04.2024 Fehlsichtigkeit Nachrichten

Augentropfen mit niedrig dosiertem Atropin können helfen, das Fortschreiten einer Kurzsichtigkeit bei Kindern zumindest zu verlangsamen, wie die Ergebnisse einer aktuellen Studie mit verschiedenen Dosierungen zeigen.

Spinale Muskelatrophie: Neugeborenen-Screening lohnt sich

18.04.2024 Spinale Muskelatrophien Nachrichten

Seit 2021 ist die Untersuchung auf spinale Muskelatrophie Teil des Neugeborenen-Screenings in Deutschland. Eine Studie liefert weitere Evidenz für den Nutzen der Maßnahme.

Fünf Dinge, die im Kindernotfall besser zu unterlassen sind

18.04.2024 Pädiatrische Notfallmedizin Nachrichten

Im Choosing-Wisely-Programm, das für die deutsche Initiative „Klug entscheiden“ Pate gestanden hat, sind erstmals Empfehlungen zum Umgang mit Notfällen von Kindern erschienen. Fünf Dinge gilt es demnach zu vermeiden.

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.