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  • 标题:Long-term outcomes of emergency ABO-incompatible living donor liver transplantation using a modified desensitization protocol for highly sensitized patients with acute liver failure: A case report
  • 本地全文:下载
  • 作者:Boram Lee ; Jai Young Cho ; Ho-Seong Han
  • 期刊名称:Korean Journal of Hepato-Biliary-Pancreatic Surgery
  • 印刷版ISSN:1738-6349
  • 出版年度:2021
  • 卷号:25
  • 期号:4
  • 页码:571-574
  • DOI:10.14701/ahbps.2021.25.4.571
  • 语种:English
  • 出版社:by The Korean Association of Hepato-Biliary-Pancreatic Surgery
  • 摘要:Although there is no established desensitization protocol for liver transplantation (LT), desensitization usually entails treatment with rituximab, plasmapheresis, splenectomy, and intravenous immunoglobulin (IVIG) infusion together with a local graft. The desensitization protocol is usually initiated 2 to 3 weeks before transplantation. Therefore, patients with acute liver failure warranting urgent LT are usually ineligible for ABO-incompatible (ABOi) LT. For these reasons, several attempts have been made to abridge the desensitization protocol and extend the indication for ABOi living donor LT (LDLT). Here we report a 40-year-old female diagnosed with chronic hepatitis B and acute-on-chronic liver failure (model for end-stage liver disease score, 31). In the absence of a suitable compatible liver donor, emergency ABOi LT was planned using a modified desensitization protocol. The preoperative isoagglutinin (IA) titer was 1 : 1,024 and the preoperative T- and B-cell cross-matches were positive. The patient received a single dose of rituximab (375 mg/m2) and IVIG (0.8 g/kg) was administered from the anhepatic phase until three days after transplantation. Although the patient developed acute cellular rejection in the early stages after LT, she has maintained a stable graft function, even after 5 years. In summary, a modified desensitization protocol consisting of rituximab and IVIG is a feasible strategy for highly sensitized patients with elevated IA titers indicated for urgent LDLT.
  • 关键词:Liver transplantation;Graft rejection;Immunoglobulins;intravenous;Liver failure;acute
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