Relationship between updated MELD and prognosis in alcohol-associated hepatitis: Opportunities for more efficient trial design.

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY ACS Applied Materials & Interfaces Pub Date : 2024-07-31 eCollection Date: 2024-08-01 DOI:10.1097/HC9.0000000000000495
Mustafa Al-Karaghouli, Meritxell Ventura-Cots, Yu Jun Wong, Joan Genesca, Francisco Bosques, Robert S Brown, Philippe Mathurin, Alexandre Louvet, Debbie Shawcross, Victor Vargas, Elizabeth C Verna, Bernd Schnabl, Joan Caballeria, Vijay J Shah, Patrick S Kamath, Michael R Lucey, Guadalupe Garcia-Tsao, Ramon Bataller, Juan G Abraldes
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Abstract

Background: Alcohol-associated hepatitis (AH) is associated with significant mortality. Model for End-Stage Liver Disease (MELD) score is used to predict short-term mortality and aid in treatment decisions. MELD is frequently updated in the course of AH. However, once the most updated MELD is known, it is uncertain if previous ones still have prognostic value, which might be relevant for transplant allocation and trial design. We aimed to investigate the predictive performance of updated MELDs in a prospectively collected cohort of patients with AH by the InTeam consortium.

Methods: Three hundred seven patients (with 859 MELD values within 60 d of admission) fulfilled the inclusion criteria. The main endpoint was time to death or transplant up to 90 days. We used a joint model approach to assess the predictive value of updated MELDs.

Results: Updated MELD measurements had a strong prognostic value for death/transplant (HR: 1.20, 95% CI: 1.14-1.27) (p < 0.0001). Previous MELD values did not add predictive value to the most current MELD. We also showed that MELD at day 28 (MELD28) had a significant predictive value for subsequent mortality/transplant in a landmark analysis (HR: 1.18, 95% CI: 1.12-1.23). We show that the use of an ordinal scale including death, transplant, and MELD28 as a trial outcome could substantially reduce the sample size required to demonstrate short-term benefit of an intervention.

Conclusion: We show that updated MELDs during the trajectory of AH predict subsequent mortality or the need for transplant. MELD28 inclusion in an ordinal outcome (together with death or transplant) could increase the efficiency of randomized controlled trials.

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酒精相关性肝炎的最新 MELD 与预后之间的关系:提高试验设计效率的机会。
背景:酒精相关性肝炎(AH)与严重的死亡率有关。终末期肝病模型(MELD)评分用于预测短期死亡率并帮助做出治疗决定。在 AH 的治疗过程中,MELD 会经常更新。然而,一旦知道了最新的 MELD,就不能确定以前的 MELD 是否仍有预后价值,这可能与移植分配和试验设计有关。我们的目的是在 InTeam 联盟前瞻性收集的 AH 患者队列中调查更新的 MELD 的预测性能:符合纳入标准的患者有 37 名(入院 60 天内有 859 个 MELD 值)。主要终点是90天内死亡或移植的时间。我们采用联合模型法评估更新后的 MELD 的预测价值:最新的MELD测量值对死亡/移植有很强的预后价值(HR:1.20,95% CI:1.14-1.27)(P < 0.0001)。之前的 MELD 值并没有增加最新 MELD 的预测价值。我们还发现,在一项标志性分析中,第 28 天的 MELD 值(MELD28)对随后的死亡率/移植具有显著的预测价值(HR:1.18,95% CI:1.12-1.23)。我们的研究表明,使用包括死亡、移植和 MELD28 作为试验结果的序数量表可以大大减少证明干预措施短期获益所需的样本量:结论:我们的研究表明,在 AH 跟踪期间更新的 MELD 可预测随后的死亡率或移植需求。将 MELD28(与死亡或移植一起)列为序贯结果可提高随机对照试验的效率。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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