Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan, USA; email:
Gastroenterology Section, Ann Arbor Veterans Affairs Healthcare System, Ann Arbor, Michigan, USA.
Annu Rev Med. 2024 Jan 29;75:233-245. doi: 10.1146/annurev-med-051322-122539. Epub 2023 Sep 26.
The MELD (model for end-stage liver disease) 3.0 score was developed to replace the MELD-Na score that is currently used to prioritize liver allocation for cirrhotic patients awaiting liver transplantation in the United States. The MELD 3.0 calculator includes new inputs from patient sex and serum albumin levels and has new weights for serum sodium, bilirubin, international normalized ratio, and creatinine levels. It is expected that use of MELD 3.0 scores will reduce overall waitlist mortality modestly and improve access for female liver transplant candidates. The utility of MELD 3.0 and PELD (pediatric end-stage liver disease, creatinine) scores for risk stratification in cirrhotic patients undergoing major abdominal surgery, placement of a transjugular intrahepatic portosystemic shunt, and other interventions requires further study. This article reviews the background of the MELD score and the rationale to create MELD 3.0 as well as potential implications of using this newer risk stratification tool in clinical practice.
MELD(终末期肝病模型)3.0 评分系统旨在取代目前用于美国等待肝移植的肝硬化患者肝脏分配的 MELD-Na 评分。MELD 3.0 计算器包含了患者性别和血清白蛋白水平的新指标,并对血清钠、胆红素、国际标准化比值和肌酐水平赋予了新的权重。预计使用 MELD 3.0 评分将适度降低整个候补名单死亡率,并改善女性肝移植候选人的获得机会。MELD 3.0 和 PELD(儿童终末期肝病,肌酐)评分在接受重大腹部手术、经颈静脉肝内门体分流术和其他干预措施的肝硬化患者中的风险分层的实用性需要进一步研究。本文回顾了 MELD 评分的背景以及创建 MELD 3.0 的基本原理,以及在临床实践中使用这种新的风险分层工具的潜在影响。