[急性肝衰竭]。

Axel Holstege
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引用次数: 0

摘要

急性肝衰竭是一种严重的危及生命的事件,与急性心力衰竭合并心源性休克或急性肾衰竭相当。导致肝功能衰竭的潜在急性肝病在不同的地理区域和发病率之间存在差异。在欧洲,病毒、药物和毒素等病原比其他更罕见的原因占主导地位。不同的有毒物质导致肝细胞坏死和/或凋亡,并导致肝细胞特异性功能的丧失,随后肝细胞功能下降到临界数量以下。该综合征的临床特点是在首次表现为肝病(暴发性肝病)后7天内迅速发作肝性脑病。既往存在慢性肝病患者的肝功能衰竭在很大程度上由黄疸和脑病(超急性、急性、亚急性肝功能衰竭)发生之间的时间来定义。肝脏特异性功能的急性丧失伴随着一些严重的危及生命的并发症,如脑水肿、循环衰竭、感染、肾功能衰竭和凝血缺陷。暴发性肝病患者的管理需要肝病学和重症监护医学的深厚知识。与肝移植单位的密切合作是成功治疗的绝对先决条件。用健康的人类肝脏进行永久或暂时的辅助肝脏替代,可使接受此类移植手术的患者的存活率达到60%至70%。在暂时替代特定肝细胞功能方面取得了进展,弥合了肝功能衰竭和肝细胞功能恢复或供体肝脏可用性之间的时间间隔。不同的人工肝脏已被设计并引入临床试验。然而,迫切需要进一步的评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Acute liver failure].

Acute liver failure represents a serious life-threatening event comparable to acute heart failure with cardiogenic shock or acute renal failure. Underlying acute liver diseases leading to hepatic failure differ between different geographic regions and in their incidence rates. In Europe etiological agents like viruses, drugs and toxins predominate over other much rarer causes. The different noxious agents lead to hepatocellular necrosis and/or apoptosis with loss of liver cell specific functions subsequent to a fall of functioning hepatocytes below a critical number. The syndrome is clinically characterized by the rapid onset of hepatic encephalopathy within 7 days after a first manifestation of liver disease (fulminant liver disease). Liver failure in patients with preexisting chronic liver disease is largely defined by the time which elapses between the occurrence of jaundice and encephalopathy (hyperacute, acute, subacute liver failure). The acute loss of liver specific functions is accompanied by a number of severe life-threatening complications like cerebral edema, circulatory failure, infections, renal failure and defective coagulation. Management of patients with fulminant liver disease requires a profound knowledge of hepatology and intensive care medicine. A close cooperation with a liver transplant unit is an absolute prerequisite for successful therapy. Permanent or temporary auxiliary liver replacement by a healthy human liver allows for a survival of 60 to 70% of patients selected for such a transplant procedure. Progress has been made in the temporary substitution of specific liver cell functions bridging the time period between liver failure and resumption of hepatocellular functions or availability of a donor liver. Different artificial livers have been designed and introduced into clinical trials. However, further evaluation is urgently needed.

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