肝移植治疗急性肝衰竭。

Philippe Ichai, Didier Samuel
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引用次数: 0

摘要

abo兼容原位肝移植(OLT)是急性肝衰竭(ALF)患者符合预后不良标准的标准治疗方法。肝移植禁忌症可能与存在严重的医学或精神合并症有关,或与移植不相容的不稳定临床状态有关。早期死亡率预测评分和因素已经被开发出来,以识别加剧器官短缺的无效移植。然而,这些评分不够可靠,不能作为移植的禁忌症。辅助肝移植、两期移植(全肝切除门静脉吻合后延迟原位肝移植)、abo不相容肝移植、活体供体移植和活体辅助肝供体移植是OLT的替代方案。适当技术的选择必须满足特定的标准。abo血型不相容移植仍然是一个例外,尽管免疫抑制策略改善了预后。ALF肝移植后1年和5年的总生存率和移植物生存率在欧洲分别为79%和72%,在美国分别为84%和73%。近年来生存率显著提高。
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Liver transplantation in acute liver failure.

ABO-compatible Orthotopic Liver Transplantation (OLT) is the standard treatment for patients with acute liver failure (ALF) who meet the criteria for poor prognosis. Contraindications to liver transplantation may be related to the presence of severe medical or psychiatric comorbidities, or to an unstable clinical state incompatible with transplantation. Early mortality predictive scores and factors have been developed to identify futile transplantations that exacerbate organ shortage. However, these scores are not sufficiently reliable to contraindicate transplantation. Auxiliary liver transplantation, two-stage transplantation (total hepatectomy with portal-caval anastomosis followed by delayed orthotopic liver transplantation), ABO-incompatible liver transplantation, living-donor transplantation, and living-auxiliary liver donor transplantation are alternatives to OLT. The selection of appropriate techniques must fulfill specific criteria. ABO-incompatible transplantation remains an exception, even though immunosuppressive strategies have improved prognosis. The overall survival and graft survival rates at 1 and 5 years after liver transplantation for ALF are 79 % and 72 % in Europe, and 84 % and 73 % in the United States, respectively. The survival rate has significantly improved in recent years.

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Advanced strategies for intensive care management of acute liver failure. Basic concepts in the management of Acute Liver Failure. Coagulopathy in acute liver failure. Definitions, etiopathogenesis and epidemiology of ALF. Evaluation and management of neurological complications in acute liver failure.
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