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Clinical Experience with Ceftazidime-Avibactam for the Treatment of Infections due to Multidrug-Resistant Gram-Negative Bacteria Other than Carbapenem-Resistant Enterobacterales

头孢他啶/阿维巴坦 头孢他啶 阿维巴坦 医学 菌血症 内科学 碳青霉烯 铜绿假单胞菌 抗生素 外科 微生物学 生物 细菌 遗传学
作者
Antonio Vena,Daniele Roberto Giacobbe,Nadia Castaldo,Anna Maria Cattelan,Cristina Mussini,Roberto Luzzati,Francesco Giuseppe De Rosa,Filippo Del Puente,Claudio Maria Mastroianni,Antonio Cascio,Sergio Carbonara,Alessandro Capone,Silvia Boni,Chiara Sepulcri,Marianna Meschiari,Francesca Raumer,Alessandra Oliva,Silvia Corcione,Matteo Bassetti
出处
期刊:Antibiotics [Multidisciplinary Digital Publishing Institute]
卷期号:9 (2): 71-71 被引量:85
标识
DOI:10.3390/antibiotics9020071
摘要

Background: Experience in real clinical practice with ceftazidime-avibactam for the treatment of serious infections due to gram−negative bacteria (GNB) other than carbapenem-resistant Enterobacterales (CRE) is very limited. Methods: We carried out a retrospective multicenter study of patients hospitalized in 13 Italian hospitals who received ≥72 h of ceftazidime-avibactam for GNB other than CRE to assess the rates of clinical success, resistance development, and occurrence of adverse events. Results: Ceftazidime-avibactam was used to treat 41 patients with GNB infections other than CRE. Median age was 62 years and 68% of them were male. The main causative agents were P. aeruginosa (33/41; 80.5%) and extended spectrum beta lactamase (ESBL)-producing Enterobacterales (4/41, 9.8%). Four patients had polymicrobial infections. All strains were susceptible to ceftazidime-avibactam. The most common primary infection was nosocomial pneumonia (n = 20; 48.8%), primary bacteremia (n = 7; 17.1%), intra-abdominal infection (n = 4; 9.8%), and bone infection (n = 4; 9.8%). Ceftazidime-avibactam was mainly administered as a combination treatment (n = 33; 80.5%) and the median length of therapy was 13 days. Clinical success at the end of the follow-up period was 90.5%, and the only risk factor for treatment failure at multivariate analysis was receiving continuous renal replacement therapy during ceftazidime-avibactam. There was no association between clinical failures and type of primary infection, microbiological isolates, and monotherapy with ceftazidime-avibactam. Only one patient experienced recurrent infection 5 days after the end of treatment. Development of resistance to ceftazidime-avibactam was not detected in any case during the whole follow-up period. No adverse events related to ceftazidime-avibactam were observed in the study population. Conclusions: Ceftazidime-avibactam may be a valuable therapeutic option for serious infections due to GNB other than CRE.

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