The Development and Appraisal of MELD 3.0 in Liver Diseases: Good Things Never Come Easy.

IF 3.1 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Gaoyue Guo, Wanting Yang, Jia Li, Ziyi Yang, Jing Liang, Chao Sun
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Abstract

Since its proposal, the Model for End-Stage Liver Disease (MELD) score has been employed to predict short-term mortality among patients with chronic liver disease and those awaiting liver transplantation, serving as the primary criterion for organ allocation. However, as the demographic and epidemiological characteristics of chronic liver disease and liver transplantation have evolved, a range of MELD-related scores has emerged, including MELD-Na, iMELD, delta MELD, MELD XI, MELD-LA, and pediatric end-stage liver disease, culminating in the recently proposed MELD 3.0, which builds upon MELD-Na. This study aimed to comprehensively review and summarize relevant studies on MELD 3.0 in various scenarios, assessing its effectiveness in organ allocation, post-transplantation outcomes, and mortality prediction for patients with end-stage liver disease. Our preliminary findings indicate superior predictive performance of MELD 3.0, warranting further in-depth investigations to broaden its clinical implications.

MELD 3.0在肝脏疾病中的发展与评价:好事来之不易。
终末期肝病模型(Model for End-Stage Liver Disease, MELD)评分自提出以来,已被用于预测慢性肝病患者和等待肝移植患者的短期死亡率,作为器官分配的主要标准。然而,随着慢性肝病和肝移植的人口统计学和流行病学特征的演变,一系列MELD相关评分出现了,包括MELD- na、iMELD、delta MELD、MELD XI、MELD- la和儿科终末期肝病,最终在MELD- na的基础上提出了MELD 3.0。本研究旨在全面回顾和总结MELD 3.0在各种情况下的相关研究,评估其在终末期肝病患者器官分配、移植后预后和死亡率预测方面的有效性。我们的初步研究结果表明,MELD 3.0具有优越的预测性能,值得进一步深入研究以扩大其临床应用。
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来源期刊
Journal of Clinical and Translational Hepatology
Journal of Clinical and Translational Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.40
自引率
2.80%
发文量
496
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