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Narrow-spectrum antibiotics for community-acquired pneumonia in Dutch adults (CAP-PACT): a cross-sectional, stepped-wedge, cluster-randomised, non-inferiority, antimicrobial stewardship intervention trial

医学 抗菌管理 整群随机对照试验 肺炎 人口 随机对照试验 社区获得性肺炎 重症监护室 感染控制 急诊医学 重症监护医学 儿科 抗生素 抗生素耐药性 内科学 环境卫生 微生物学 生物
作者
Valentijn Schweitzer,Inger van Heijl,Wim Boersma,Wouter Rozemeijer,Kees Verduin,Marco J.J.H. Grootenboers,Sanjay U. C. Sankatsing,Akke K. van der Bij,Winnie de Bruijn,Heidi S. M. Ammerlaan,Ilse Overdevest,J M Milena Roorda-van der Vegt,Elske M Engel-Dettmers,Florence E Ayuketah-Ekokobe,Michiel Haeseker,J. W. Dorigo-Zetsma,Paul D. van der Linden,C. H. E. Boel,Jan Jelrik Oosterheert,Cornelis H. van Werkhoven,Marc J. M. Bonten
出处
期刊:Lancet Infectious Diseases [Elsevier]
卷期号:22 (2): 274-283 被引量:12
标识
DOI:10.1016/s1473-3099(21)00255-3
摘要

Adults hospitalised to a non-intensive care unit (ICU) ward with moderately severe community-acquired pneumonia are frequently treated with broad-spectrum antibiotics, despite Dutch guidelines recommending narrow-spectrum antibiotics. Therefore, we investigated whether an antibiotic stewardship intervention would reduce the use of broad-spectrum antibiotics in patients with moderately severe community-acquired pneumonia without compromising their safety.In this cross-sectional, stepped-wedge, cluster-randomised, non-inferiority trial (CAP-PACT) done in 12 hospitals in the Netherlands, we enrolled immunocompetent adults (≥18 years) who were admitted to a non-ICU ward and had a working diagnosis of moderately severe community-acquired pneumonia. All participating hospitals started in a control period and every 3 months a block of two hospitals transitioned from the control to the intervention period, with all hospitals eventually ending in the intervention period. The unit of randomisation was the hospital (cluster), and electronic randomisation (by an independent data manager) decided the sequence (the time of intervention) by which hospitals would cross over from the control period to the intervention period. Blinding was not possible. The antimicrobial stewardship intervention was a bundle targeting health-care providers and comprised education, engaging opinion leaders, and prospective audit and feedback of antibiotic use. The co-primary outcomes were broad-spectrum days of therapy per patient, tested by superiority, and 90-day all-cause mortality, tested by non-inferiority with a non-inferiority margin of 3%, and were analysed in the intention-to-treat population, comprising all patients who were enrolled in the control and intervention periods. This trial was prospectively registered at ClinicalTrials.gov, NCT02604628.Between Nov 1, 2015, and Nov 1, 2017, 5683 patients were assessed for eligibility, of whom 4084 (2235 in the control period and 1849 in the intervention period) were included in the intention-to-treat analysis. The adjusted mean broad-spectrum days of therapy per patient were reduced from 6·5 days in the control period to 4·8 days in the intervention period, yielding an absolute reduction of -1·7 days (95% CI -2·4 to -1·1) and a relative reduction of 26·6% (95% CI 18·0-35·3). Crude 90-day mortality was 10·9% (242 of 2228 died) in the control period and 10·8% (199 of 1841) in the intervention period, yielding an adjusted absolute risk difference of 0·4% (90% CI -2·7 to 2·4), indicating non-inferiority.In patients hospitalised with moderately severe community-acquired pneumonia, a multifaceted antibiotic stewardship intervention might safely reduce broad-spectrum antibiotic use.None.
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