Effect of Prophylactic Antibiotics on Mortality in Severe Alcohol-Related Hepatitis

医学 内科学 泼尼松龙 安慰剂 入射(几何) 随机对照试验 阿莫西林 肝炎 外科 酒精性肝炎 抗生素 肝硬化 酒精性肝病 病理 替代医学 物理 光学 微生物学 生物
作者
Alexandre Louvet,Julien Labreuche,Thông Dao,Thierry Thévenot,F. Oberti,Christophe Bureau,Thierry Paupard,Eric Nguyen‐Khac,Anne Minello,Brigitte Bernard‐Chabert,Rodolphe Anty,F. Wartel,Nicolas Carbonell,Georges‐Philippe Pageaux,Marie‐Noëlle Hilleret,Romain Moirand,Pierre Nahon,Camille Potey,Alain Duhamel,Philippe Mathurin
出处
期刊:JAMA [American Medical Association]
卷期号:329 (18): 1558-1558 被引量:45
标识
DOI:10.1001/jama.2023.4902
摘要

The benefits of prophylactic antibiotics for hospitalized patients with severe alcohol-related hepatitis are unclear.To determine the efficacy of amoxicillin-clavulanate, compared with placebo, on mortality in patients hospitalized with severe alcohol-related hepatitis and treated with prednisolone.Multicenter, randomized, double-blind clinical trial among patients with biopsy-proven severe alcohol-related hepatitis (Maddrey function score ≥32 and Model for End-stage Liver Disease [MELD] score ≥21) from June 13, 2015, to May 24, 2019, in 25 centers in France and Belgium. All patients were followed up for 180 days. Final follow-up occurred on November 19, 2019.Patients were randomly assigned (1:1 allocation) to receive prednisolone combined with amoxicillin-clavulanate (n = 145) or prednisolone combined with placebo (n = 147).The primary outcome was all-cause mortality at 60 days. Secondary outcomes were all-cause mortality at 90 and 180 days; incidence of infection, incidence of hepatorenal syndrome, and proportion of participants with a MELD score less than 17 at 60 days; and proportion of patients with a Lille score less than 0.45 at 7 days.Among 292 randomized patients (mean age, 52.8 [SD, 9.2] years; 80 [27.4%] women) 284 (97%) were analyzed. There was no significant difference in 60-day mortality between participants randomized to amoxicillin-clavulanate and those randomized to placebo (17.3% in the amoxicillin-clavulanate group and 21.3% in the placebo group [P = .33]; between-group difference, -4.7% [95% CI, -14.0% to 4.7%]; hazard ratio, 0.77 [95% CI, 0.45-1.31]). Infection rates at 60 days were significantly lower in the amoxicillin-clavulanate group (29.7% vs 41.5%; mean difference, -11.8% [95% CI, -23.0% to -0.7%]; subhazard ratio, 0.62; [95% CI, 0.41-0.91]; P = .02). There were no significant differences in any of the remaining 3 secondary outcomes. The most common serious adverse events were related to liver failure (25 in the amoxicillin-clavulanate group and 20 in the placebo group), infections (23 in the amoxicillin-clavulanate group and 46 in the placebo group), and gastrointestinal disorders (15 in the amoxicillin-clavulanate group and 21 in the placebo group).In patients hospitalized with severe alcohol-related hepatitis, amoxicillin-clavulanate combined with prednisolone did not improve 2-month survival compared with prednisolone alone. These results do not support prophylactic antibiotics to improve survival in patients hospitalized with severe alcohol-related hepatitis.ClinicalTrials.gov Identifier: NCT02281929.
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