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Title: Successful liver transplantation across the ABO incompatibility barrier in 6 cases of biliary atresia. Author: Yamada Y, Hoshino K, Morikawa Y, Okamura J, Hotta R, Komori K, Nakao S, Obara H, Kawachi S, Fuchimoto Y, Tanabe M, Shimazu M, Kitajima M. Journal: J Pediatr Surg; 2006 Dec; 41(12):1976-9. PubMed ID: 17161185. Abstract: BACKGROUND: The problem of ABO-incompatible liver transplantation still remains unsolved in older children. In this article, we report on our experience of 6 successful ABO-incompatible liver transplantations in patients with biliary atresia. MATERIAL AND METHODS: Six patients (ABO incompatibility type A-->O:1 case, B-->O:2 cases, A-->B:3 cases) were enrolled in this study; 3 patients were aged approximately 1 year and the other 3 ranged in age from 9 to 24 years at the time of transplantation. Each patient received perioperative plasma exchange, until the anti-donor blood-type antibody titers became less than 1:16, and also systemic multidrug immunosuppressive therapy (cyclophosphamide, prednisolone, and tacrolimus). We applied the protocol of intraportal infusion therapy (local administration of prostaglandin E(1), steroid, and gabexate mesilate via a portal vein catheter), splenectomy, and rituximab administration for the older group. RESULTS: Both the patient and graft survival rates remain at 100%, with the follow-up period of the patients ranging from 12 and 123 months. Acute cellular rejection occurred in 2 cases, and both were steroid sensitive. There was no incidence of humoral rejection. Although all cases developed viral infection, all recovered uneventfully with the administration of antiviral agents. CONCLUSION: ABO-incompatible liver transplantation can be performed with a low risk of humoral rejection or late biliary complications using this combined antirejection strategy, even in older children.[Abstract] [Full Text] [Related] [New Search]