Division of Gastroenterology and Hepatology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama.
Division of Gastroenterology and Hepatology, University of Florida College of Medicine.
Eur J Gastroenterol Hepatol. 2024 Mar 1;36(3):318-325. doi: 10.1097/MEG.0000000000002701. Epub 2023 Dec 27.
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.
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.
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].
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.
患有酒精使用障碍(AUD)的患者可能会发展为酒精相关脂肪性肝病(AFLD)。然而,AFLD 对结局的影响尚不清楚。我们研究了 AFLD 对因 AUD 住院患者的再入院、30 天死亡率和总死亡率的影响。
回顾性评估了 2011 年至 2019 年期间在一家三级医疗中心因 AUD 住院的患者。我们的研究人群包括患有 AUD 合并 AFLD 的患者:AST 和 ALT 升高和血清胆红素<3mg/dl。没有肝脏疾病证据的 AUD 患者作为对照,被标记为无 ALD。患有酒精性肝硬化(AC)和酒精性肝炎(AH)的患者也包括在内进行比较。进行 Kaplan-Meier 生存分析和多变量回归分析以预测死亡率和生存情况。
共有 7522 名患者,其中 32.44%为女性,平均年龄为 51.86±14.41 岁。患者分布包括无 ALD(n=3775)、AFLD(n=2192)、AC(n=1017)和 AH(n=538)组。与无 ALD 组相比,AFLD 组的 30 天死亡率明显更高[4.43%比 1.56%,风险比(HR):2.84;P<0.001]、总死亡率[15.97%比 12.69%,HR 1.40,P<0.001]和 30 天再入院率[21.85%比 18.49%,比值比:1.21;P<0.01]。
我们证明了 AFLD 不是良性实体,并且会带来显著的死亡风险。我们的研究结果表明,AFLD 可能被低估了,这突显了在出院后需要对其进行有针对性的管理和密切随访。