Survival Benefit From Corticosteroids in Severe Alcohol-associated Hepatitis Attributed to Clinical and Treatment Differences in a Large Multicenter Cohort.

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinical and Translational Gastroenterology Pub Date : 2025-01-01 DOI:10.14309/ctg.0000000000000791
Claire Durkin, Douglas E Schaubel, David E Kaplan, Nadim Mahmud, Therese Bittermann
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Abstract

Introduction: Corticosteroids are recommended by multiple society guidelines for the treatment of severe alcohol-associated hepatitis (AH). However, their use remains controversial due to inconsistent studies regarding their survival benefit.

Methods: This was a retrospective cohort study of first-time hospitalizations for severe AH (Maddrey discriminant function ≥ 32) admitted to the Veterans Health Administration between January 3, 2005, and December 5, 2020, (i) evaluating the effect of corticosteroid therapy on all-cause survival, (ii) characterizing the clinical and psychosocial factors associated with corticosteroid use, and (iii) determining the effect of duration of corticosteroid therapy on all-cause survival among treatment-responsive patients (Lille score < 0.45).

Results: During the study period, 2,618 patients were admitted with severe AH, of whom 1,083 (41.37%) received corticosteroids. Although corticosteroids were significantly associated with improved all-cause survival in the unadjusted model ( P = 0.022), no survival benefit was observed in the adjusted model after accounting for baseline and admission characteristics (adjusted hazard ratio [aHR] = 1.01, P = 0.818). Psychiatry consultation was the only factor evaluated that was protective against mortality (aHR = 0.67, P < 0.001). Among the 428 patients (49.7%) responsive to corticosteroids, duration of therapy was not associated with overall survival on unadjusted ( P = 0.696) or adjusted models (aHR = 1.12, P = 0.710 for a ≥28-day course compared with a ≤7-day reference).

Discussion: Despite being recommended by clinical guidelines for severe AH, corticosteroids have low utilization with no survival benefit after accounting for differences in patient characteristics and practice patterns. Among patients with treatment response per the Lille score, no difference was observed in overall survival between shorter and longer durations of corticosteroid therapy.

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在一项大型多中心队列研究中,严重酒精相关性肝炎患者使用皮质类固醇的临床和治疗差异导致生存获益。
背景:皮质类固醇被多个社会指南推荐用于治疗严重酒精相关性肝炎(AH)。然而,由于关于其生存益处的研究不一致,它们的使用仍然存在争议。方法:这是一项回顾性队列研究,对2005年3月1日至2020年12月5日期间在退伍军人健康管理局收治的首次住院的严重AH (Maddrey’s Discriminant Function≥32)患者进行研究,1)评估皮质类固醇治疗对全因生存的影响,2)描述与皮质类固醇使用相关的临床和社会心理因素。3)确定糖皮质激素治疗持续时间对治疗反应患者全因生存的影响(里尔评分)结果:在研究期间,2618例重度AH患者入院,其中1083例(41.37%)接受糖皮质激素治疗。尽管在未调整的模型中,皮质类固醇与全因生存率显著相关(p=0.022),但在考虑基线和入院特征后,调整后的模型中未观察到生存获益(调整后的风险比[aHR]=1.01, p=0.818)。结论:尽管临床指南推荐使用皮质类固醇治疗严重AH,但考虑到患者特征和实践模式的差异,皮质类固醇的使用率很低,没有生存益处。在根据里尔评分有治疗反应的患者中,在较短和较长时间的皮质类固醇治疗中,总生存期没有观察到差异。
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来源期刊
Clinical and Translational Gastroenterology
Clinical and Translational Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.00
自引率
0.00%
发文量
114
审稿时长
16 weeks
期刊介绍: Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease. Colon and small bowel Endoscopy and novel diagnostics Esophagus Functional GI disorders Immunology of the GI tract Microbiology of the GI tract Inflammatory bowel disease Pancreas and biliary tract Liver Pathology Pediatrics Preventative medicine Nutrition/obesity Stomach.
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