Summary of guidelines on organ allocation and patient listing for liver transplantation.

E B Keeffe
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Abstract

In summary, a Child-Pugh class A cirrhotic patient without decompensation has a relatively long and stable natural history, but poor survival once decompensation with ascites or variceal bleeding has occurred. Thus, reasonable criteria for listing a patient for liver transplantation should be clinical decompensation of cirrhosis, particularly ascites or variceal bleeding, or combined clinical decompensation and biochemical deterioration of hepatic synthetic function that meets criteria for Child-Pugh class B or C status. On the basis of analysis of data regarding the natural history of compensated and decompensated cirrhosis, general principles of a minimal listing criteria were proposed (Table 5). These principles were used to establish non-disease-specific minimal listing criteria that are broadly applicable to all types of chronic liver diseases (Table 6). Some examples of proposed disease-specific minimal listing criteria are shown in Table 7.

肝移植器官分配和患者名单指南摘要。
总之,Child-Pugh a级无失代偿的肝硬化患者具有相对较长且稳定的自然病史,但一旦失代偿伴腹水或静脉曲张出血发生,生存率较差。因此,列入肝移植患者名单的合理标准应该是肝硬化的临床失代偿,特别是腹水或静脉曲张出血,或符合Child-Pugh B类或C类标准的临床失代偿和肝脏合成功能的生化恶化。在对代偿性肝硬化和失代偿性肝硬化的自然史数据分析的基础上,提出了最小列表标准的一般原则(表5)。这些原则被用于建立非疾病特异性最小列表标准,该标准广泛适用于所有类型的慢性肝病(表6)。表7列出了一些拟议的疾病特异性最小列表标准的示例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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