The efficacy of surgical shunts to treat severe portal hypertension after a Kasai procedure for biliary atresia

Florent Guérin, Lionel Charre, Stéphanie Jasienski, Mathieu Duché, Stéphanie Franchiabella, Olivier Bernard, Emmanuel Jacquemin, Hélène Agostini, Frédéric Gauthier, Sophie Branchereau

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

5 Citations (Scopus)

Résumé

Background: To assess the outcome of patients with biliary atresia (BA) who underwent a surgical shunt (SS) for severe portal hypertension (PH) following a Kasai procedure. Methods: We collected and analyzed the data and outcomes of patients with BA who underwent SS for severe PH following a Kasai procedure between 1974 and 2014, focusing on complications related to the procedure, overall survival (OS), and transplant-free survival (TFS). Results: SS was performed at a median age of 5.5 years [2–13.5] in 38 patients. Conjugated bilirubin level (cBL) was ≤ 20 μmol/l in 24 patients at time of SS. Median follow-up was 15 years [1–32]. OS at 5 and 10 years was 91% and 87% respectively. TFS at 5 and 10 years was 84% and 70% respectively. Long-term complications included hepatic encephalopathy in 9 patients, and hepatopulmonary syndrome in 3. At last follow-up, 10/14 patients without LT and 18/ 24 who had a delayed LT at a median delay of 11 years [1.5–22] were alive. Conclusion: Surgical shunt for severe portal hypertension in biliary atresia may delay the need for liver transplantation. However complications are indications for transplantation. Level of evidence: Type of study: Therapeutic. Level of evidence III.

langue originaleAnglais
Pages (de - à)531-536
Nombre de pages6
journalJournal of Pediatric Surgery
Volume54
Numéro de publication3
Les DOIs
étatPublié - 1 mars 2019
Modification externeOui

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