Patients with early-stage alcohol-associated liver disease are at increased risk of hospital readmission and death

Author:

Aryan Mahmoud1,Qian Steve2,Chen Zhiguo3,Louissaint Jeremy4,Qian Xia2,Rosenblatt Russell5,Verna Elizabeth4,Brown Robert5,Wong Robert6,Clark Virginia2,Zhang Wei27

Affiliation:

1. Division of Gastroenterology and Hepatology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama

2. Division of Gastroenterology and Hepatology, University of Florida College of Medicine

3. Department of Biostatistics, University of Florida, Gainesville, Florida

4. Center for Liver Disease and Liver Transplantation, Columbia University Vagelos College of Physicians and Surgeons

5. Division of Gastroenterology and Hepatology, Weill Cornell Medicine, New York, New York

6. Division of Gastroenterology and Hepatology, Stanford University School of Medicine and Veterans Affairs Palo Alto Healthcare System, Palo Alto, California

7. Liver Center, Gastrointestinal Division, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

Abstract

Background and aims Patients with alcohol use disorder (AUD) can develop alcohol-associated fatty liver disease (AFLD). However, the impact of AFLD on outcomes remains unclear. We studied the impact of AFLD on readmission, 30-day mortality, and overall mortality in patients admitted with AUD. Methods Hospitalized patients with AUD between 2011 and 2019 at a tertiary medical center were retrospectively evaluated. Our population included patients with AUD with AFLD: AST and ALT elevation and serum bilirubin <3 mg/dl. Patients with AUD without evidence of liver disease served as control and were labeled as no ALD. Patients with alcohol-associated cirrhosis (AC) and alcohol-associated hepatitis (AH) were included for comparison. Kaplan–Meier survival analysis and multivariable regression for predictors of mortality and survival were performed. Results There were 7522 patients of which 32.44% were female with mean age of 51.86 ± 14.41 years. Patient distribution included no ALD (n = 3775), AFLD (n = 2192), AC (n = 1017) and AH (n = 538) groups. Compared to no ALD group, AFLD group was associated with significantly higher 30-day mortality [4.43% vs. 1.56%, hazard ratio (HR): 2.84; P < 0.001], overall mortality [15.97% vs. 12.69%, HR 1.40, P < 0.001], and 30-day readmission [21.85% vs. 18.49%, odds ratio: 1.21; P < 0.01]. Conclusion We demonstrated that AFLD is not a benign entity and poses significant mortality risk. Our results suggest that AFLD may be under-recognized and highlight the need for focused management and close follow-up after discharge.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference32 articles.

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5. Alcohol-related liver disease is rarely detected at early stages compared with liver diseases of other etiologies worldwide.;Shah;Clin Gastroenterol Hepatol,2019

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