Eljaaly Khalid, Enani Mushira A, Al-Tawfiq Jaffar A
Department of Clinical Pharmacy, College of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Infectious Diseases, King Abdulaziz University Hospital, Jeddah, Saudi Arabia; College of Pharmacy, University of Arizona, Tucson, AZ, USA.
Medical Specialties Department, Section of Infectious Diseases, King Fahad Medical City, Riyadh, Saudi Arabia.
J Infect Chemother. 2018 Nov;24(11):915-920. doi: 10.1016/j.jiac.2018.08.004. Epub 2018 Sep 6.
Imipenem and meropenem are the recommended antipseudomonal carbapenems for nosocomial pneumonia per clinical practice guidelines. However, these agents have a relatively broader spectrum of activity than other antibiotics and need to be reserved. Carbapenems might cause higher rate of superinfection. The aim of this study was to compare the rate of superinfection between patients who received imipenem or meropenem versus those who received non-carbapenem treatment. PubMed, EMBASE, Cochrane Library databases and two trial registries were searched for relevant randomized controlled trials of hospitalized adults with pneumonia through February 24, 2017 without date or language restrictions. Risk ratios (RRs) with 95% confidence intervals (CIs) were estimated using random-effects models. The primary outcome was based on the intention-to-treat analysis while clinically evaluable patients were analyzed as secondary outcome. Eight RCTs were included in this meta-analysis. A statistically higher risk of superinfection with low heterogeneity (RR = 1.690, 95% CI 1.247-2.291, p = 0.001, I = 0%) was associated with the two carbapenems compared to non-carbapenems. However, in comparison with non-carbapenems, superinfection with imipenem was significantly higher (RR = 1.694, 95% CI 1.234-2.325, p = 0.001, I = 0%), while it was non-significant with meropenem (RR = 1.647, 95% CI 0.552-4.919, p = 0.371, I = 0%). Superinfection was statistically higher in both double-blind and open-label studies and when carbapenems were compared to other antipseudomonal beta-lactams. This meta-analysis identified significantly higher superinfection with imipenem compared to non-carbapenems. The findings confirm the theory of higher superinfections with broader spectrum agents and provide additional support for reserving carbapenems for the treatment of infections caused by multidrug-resistant organisms.
根据临床实践指南,亚胺培南和美罗培南是医院获得性肺炎推荐使用的抗假单胞菌碳青霉烯类药物。然而,这些药物的抗菌谱相对比其他抗生素更广,需要谨慎使用。碳青霉烯类药物可能导致更高的二重感染发生率。本研究的目的是比较接受亚胺培南或美罗培南治疗的患者与接受非碳青霉烯类药物治疗的患者之间的二重感染发生率。检索了PubMed、EMBASE、Cochrane图书馆数据库以及两个试验注册库,以查找截至2017年2月24日的有关住院成人肺炎的相关随机对照试验,无日期或语言限制。使用随机效应模型估计风险比(RR)及其95%置信区间(CI)。主要结局基于意向性分析,而将临床可评估的患者作为次要结局进行分析。本荟萃分析纳入了8项随机对照试验。与非碳青霉烯类药物相比,两种碳青霉烯类药物导致二重感染的风险在统计学上显著更高,异质性较低(RR = 1.690,95% CI 1.247 - 2.291,p = 0.001,I² = 0%)。然而,与非碳青霉烯类药物相比,亚胺培南导致的二重感染显著更高(RR = 1.694,95% CI 1.234 - 2.325,p = 0.001,I² = 0%),而美罗培南则无显著差异(RR = 1.647,95% CI 0.552 - 4.919,p = 0.371,I² = 0%)。在双盲和开放标签研究中,以及将碳青霉烯类药物与其他抗假单胞菌β - 内酰胺类药物进行比较时,二重感染在统计学上均更高。本荟萃分析确定,与非碳青霉烯类药物相比,亚胺培南导致的二重感染显著更高。这些发现证实了抗菌谱更广的药物导致更高二重感染发生率的理论,并为将碳青霉烯类药物保留用于治疗多重耐药菌引起的感染提供了额外支持。