Ceftazidime-Avibactam Use for Klebsiella pneumoniae Carbapenemase–Producing K. pneumoniae Infections: A Retrospective Observational Multicenter Study

医学 头孢他啶/阿维巴坦 内科学 倾向得分匹配 菌血症 回顾性队列研究 观察研究 胃肠病学 抗生素 肺炎克雷伯菌 微生物学 生物 大肠杆菌 生物化学 基因
作者
Mario Tumbarello,Francesca Raffaelli,Maddalena Giannella,Elisabetta Mantengoli,Alessandra Mularoni,Mario Venditti,Francesco Giuseppe De Rosa,Loredana Sarmati,Matteo Bassetti,Gaetano Brindicci,Marianna Rossi,Roberto Luzzati,Paolo Grossi,Alberto Corona,Alessandro Capone,Marco Falcone,Cristina Mussini,Enrico Maria Trecarichi,Antonio Cascio,Elena Guffanti
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:73 (9): 1664-1676 被引量:204
标识
DOI:10.1093/cid/ciab176
摘要

Abstract Background A growing body of observational evidence supports the value of ceftazidime-avibactam (CAZ-AVI) in managing infections caused by carbapenem-resistant Enterobacteriaceae. Methods We retrospectively analyzed observational data on use and outcomes of CAZ-AVI therapy for infections caused by Klebsiella pneumoniae carbapenemase–producing K. pneumoniae (KPC-Kp) strains. Multivariate regression analysis was used to identify variables independently associated with 30-day mortality. Results were adjusted for propensity score for receipt of CAZ-AVI combination regimens versus CAZ-AVI monotherapy. Results The cohort comprised 577 adults with bloodstream infections (n = 391) or nonbacteremic infections involving mainly the urinary tract, lower respiratory tract, and intra-abdominal structures. All received treatment with CAZ-AVI alone (n = 165) or with ≥1 other active antimicrobials (n = 412). The all-cause mortality rate 30 days after infection onset was 25% (146/577). There was no significant difference in mortality between patients managed with CAZ-AVI alone and those treated with combination regimens (26.1% vs 25.0%, P = .79). In multivariate analysis, mortality was positively associated with presence at infection onset of septic shock (P = .002), neutropenia (P < .001), or an INCREMENT score ≥8 (P = .01); with lower respiratory tract infection (LRTI) (P = .04); and with CAZ-AVI dose adjustment for renal function (P = .01). Mortality was negatively associated with CAZ-AVI administration by prolonged infusion (P = .006). All associations remained significant after propensity score adjustment. Conclusions CAZ-AVI is an important option for treating serious KPC-Kp infections, even when used alone. Further study is needed to explore the drug’s seemingly more limited efficacy in LRTIs and potential survival benefits of prolonging CAZ-AVI infusions to ≥3 hours.
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