Incidence, clinical characteristics, and risk factors associated with recurrent alcohol-associated hepatitis

Author:

Patidar Kavish R.12ORCID,Guarnizo Ortiz Maria3,Slaven James E.4ORCID,Nephew Lauren D.1ORCID,Vilar Gomez Eduardo1ORCID,Kettler Carla D.5,Ghabril Marwan S.1,Desai Archita P.1ORCID,Orman Eric S.1ORCID,Chalasani Naga6,Gawrieh Samer1ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA

2. Section of Gastroenterology and Hepatology, Department of Medicine, Baylor College of Medicine and Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas, USA

3. Department of Internal Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA

4. Department of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA

5. Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, Indiana, USA

6. Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine and Indiana University Health, Indianapolis, Indiana, USA

Abstract

Background: Alcohol relapse occurs frequently in alcohol-associated hepatitis (AH) survivors, but data on the frequency and course of recurrent alcohol-associated hepatitis (rAH) are sparse. We investigated the incidence, risk factors, and outcomes of rAH. Methods: Hospitalized patients with AH from 2010 to 2020 at a large health care system were followed until death/liver transplant, last follow-up, or end of study (December 31, 2021). AH was defined by NIAAA Alcoholic Hepatitis Consortium criteria; rAH was defined a priori as a discrete AH episode >6 months from index AH hospitalization with interim >50% improvement or normalization of total bilirubin. Multivariable competing risk analysis was performed to identify factors associated with rAH. Landmark Kaplan-Meier analysis was performed to compare survival between patients who did versus those who did not develop rAH. Results: Of 1504 hospitalized patients with AH, 1317 (87.6%) survived and were analyzed. During a 3055 person‐year follow‐up, 116 (8.8%) developed rAH at an annual incidence rate of 3.8% (95% CI: 2.8–4.8). On multivariable competing risk analysis, marital status [sub-HR 0.54 (95% CI: 0.34, 0.92), p=0.01] and medications for alcohol use disorder [sub-HR 0.56 (95% CI: 0.34, 0.91), p=0.02] were associated with a lower risk for rAH. On landmark Kaplan-Meier analysis, the cumulative proportion surviving at 1 year (75% vs. 90%) and 3 years (50% vs. 78%) was significantly lower in patients who developed rAH compared to those who did not develop rAH (log-rank p<0.001). Conclusions: rAH develops in ~1 in 10 AH survivors and is associated with lower long-term survival. Medications for alcohol use disorder lower the risk for rAH and, therefore, could be a key preventative strategy to improve outcomes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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