粘菌素
碳青霉烯
鲍曼不动杆菌
肺炎
美罗培南
重症监护室
医学
人口
联合疗法
呼吸机相关性肺炎
置信区间
随机对照试验
不利影响
铜绿假单胞菌
微生物学
外科
内科学
生物
抗生素
抗生素耐药性
细菌
环境卫生
遗传学
作者
Keith S. Kaye,Dror Marchaim,Visanu Thamlikitkul,Yehuda Carmeli,Cheng‐Hsun Chiu,George L. Daikos,Sorabh Dhar,Emanuele Durante‐Mangoni,Achilleas Gikas,Αναστασία Κοτανίδου,Mical Paul,Emmanuelle Roilides,Michael J. Rybak,Michael Samarkos,Matthew Sims,Dora Tancheva,Sotirios Tsiodras,Daniel H. Kett,Gopi Patel,David P. Calfee
出处
期刊:NEJM evidence
[New England Journal of Medicine]
日期:2022-12-06
卷期号:2 (1)
被引量:76
标识
DOI:10.1056/evidoa2200131
摘要
BackgroundPneumonia and bloodstream infections (BSI) due to extensively drug-resistant (XDR) Acinetobacter baumannii, XDR Pseudomonas aeruginosa, and carbapenem-resistant Enterobacterales (CRE) are associated with high mortality rates, and therapeutic options remain limited. This trial assessed whether combination therapy with colistin and meropenem was superior to colistin monotherapy for the treatment of these infections.MethodsThe OVERCOME (Colistin Monotherapy versus Combination Therapy) trial was an international, randomized, double-blind, placebo-controlled trial. We randomly assigned participants to receive colistin (5 mg/kg once followed by 1.67 mg/kg every 8 hours) in combination with either meropenem (1000 mg every 8 hours) or matching placebo for the treatment of pneumonia and/or BSI caused by XDR A. baumannii, XDR P. aeruginosa, or CRE. The primary outcome was 28-day mortality, and secondary outcomes included clinical failure and microbiologic cure.ResultsBetween 2012 and 2020, a total of 464 participants were randomly assigned to treatment, and 423 eligible patients comprised the modified intention-to-treat population. A. baumannii was the predominant trial pathogen (78%) and pneumonia the most common index infection (70%). Most patients were in the intensive care unit at the time of enrollment (69%). There was no difference in mortality (43 vs. 37%; P=0.17), clinical failure (65 vs. 58%; difference, 6.8 percentage points; 95% confidence interval [CI], −3.1 to 16.6), microbiologic cure (65 vs. 60%; difference, 4.8 percentage points; 95% CI, −5.6 to 15.2), or adverse events (acute kidney injury, 52 vs. 49% [P=0.55]; hypersensitivity reaction, 1 vs. 3% [P=0.22]; and neurotoxicity, 5 vs. 2% [P=0.29]) between patients receiving monotherapy and combination therapy, respectively.ConclusionsCombination therapy with colistin and meropenem was not superior to colistin monotherapy for the treatment of pneumonia or BSI caused by these pathogens. (Funded by the National Institute of Allergy and Infectious Diseases, Division of Microbiology and Infectious Diseases protocol 10-0065; ClinicalTrials.gov number, NCT01597973.)