An Open-Label, Randomized Trial Comparing Fidaxomicin With Oral Vancomycin for the Treatment of Clostridioides difficile Infection in Hospitalized Patients Receiving Concomitant Antibiotics for Concurrent Infections

非达霉素 医学 相伴的 万古霉素 腹泻 内科学 梭菌纲 随机对照试验 抗生素 临床试验 随机化 外科 胃肠病学 微生物学 细菌 金黄色葡萄球菌 生物 遗传学
作者
Krishna Rao,Qianzi Zhao,J.N.B. Bell,Jay Krishnan,Oryan Henig,Jolene Daniel,Kara L. Sawaya,Owen Albin,John Mills,Lindsay A Petty,Kevin Gregg,Daniel Kaul,Anurag N. Malani,Jason M. Pogue,Keith S. Kaye
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:78 (2): 277-282 被引量:5
标识
DOI:10.1093/cid/ciad606
摘要

Abstract Background Recurrent Clostridioides difficile infection (rCDI) occurs frequently, and concomitant antibiotic (CA) during the initial episode for treatment of non-CDI is a major risk factor. We sought to address the comparative efficacy of fidaxomicin versus vancomycin in the setting of CA during the initial CDI episode. Methods We conducted a randomized, controlled, open-label trial at 2 hospitals in Ann Arbor, Michigan. We consecutively consented and enrolled hospitalized patients ≥18 years old with diarrhea, a positive test for C. difficile, and ≥1 qualifying CA. Complicated CDI, CDI treatment for >24 hours prior to enrollment, and planned long-term (>12 weeks) CA use were notable exclusions. Clinical cure was defined as resolution of diarrhea for 2 consecutive days maintained until 2 days after therapy, and rCDI as recurrent diarrhea with positive testing ≤30 days after initial treatment. Patients were randomized to fidaxomicin or vancomycin. Results Baseline characteristics were similar in the 2 groups of 144 patients. Rates of clinical cure (73% vs 62.9%, P = .195) and rCDI (3.3% vs 4.0%; P > .99) were similar for fidaxomicin and vancomycin in the intention-to-treat and per-protocol cohorts, respectively. Only 4 patients developed rCDI. Conclusions In this study of patients with CDI receiving CA, a numerically higher proportion were cured with fidaxomicin versus vancomycin, but this result did not reach statistical significance. Overall recurrence was lower than anticipated in both arms compared with previous studies that did not extend duration of CDI treatment during CA. Clinical Trials Registration www.clinicaltrials.gov (NCT02692651).
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