Clinical efficacy of ceftazidime/avibactam combination therapy for severe hospital-acquired pulmonary infections caused by carbapenem-resistant and difficult-to-treat Pseudomonas aeruginosa

被引:8
|
作者
Xu, Chenfeng [1 ,2 ]
Zeng, Fang [1 ,2 ]
Huang, Yifei [1 ,2 ]
Xu, Qiling [1 ,2 ]
Yang, Yu [1 ,2 ]
Gong, Weijing [1 ,2 ]
Shi, Chen [1 ,2 ,3 ]
Zhang, Yu [1 ,2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pharm, Wuhan, Peoples R China
[2] Hubei Prov Clin Res Ctr Precis Med Crit Illness, Wuhan, Peoples R China
[3] Huazhong Univ Sci & Technol, Dept Pharm, Union Hosp, Tongji Med Coll, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
Ceftazidime/avibactam; Severe hospital-acquired pulmonary infections; Carbapenem-resistant; Difficult-to-treat Pseudomonas aeruginosa; ANTIMICROBIAL THERAPY; INFUSION;
D O I
10.1016/j.ijantimicag.2023.107021
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: This retrospective study aimed to identify the effectiveness of ceftazidime/avibactam (CAZ/AVI) and its optimisation programs for severe hospital-acquired pulmonary infections (sHAPi) caused by carbapenem-resistant and difficult-to-treat Pseudomonas aeruginosa (CRPA and DTR -P. aeruginosa).Methods: We retrospectively analysed observational data on treatment and outcomes of CAZ/AVI for sHAPi caused by CRPA or DTR-P. aeruginosa. The primary study outcomes were to evaluate the clinical and microbiology efficacy of CAZ/AVI.Results: The cohort consisted of 84 in-patients with sHAPi caused by CRPA (n = 39) and DTR-P. aeruginosa (n = 45) who received at least 72 h of CAZ/AVI therapy. The clinical cure rate was 63.1% in total. There was no significant difference in study outcomes between patients treated with CAZ/AVI monotherapy and those managed with combination regimens. CAZ/AVI as first-line therapy possessed prominent clinical benefits regarding infections caused by DTR-P. aeruginosa. The clinical cure rate was positively relevant with loading dose for CAZ/AVI (odds ratio [OR] 0.03; 95% confidence interval [CI] 0.004-0.19; P < 0.001) and with CAZ/AVI administration by prolonged infusion (odds ratio 0.15; 95% confidence interval 0.03- 0.77; P = 0.002). APACHE II score > 15 ( P = 0.013), septic shock at infection onset ( P = 0.001), and CAZ/AVI dose adjustment for renal dysfunction ( P = 0.003) were negative predictors of clinical cure.Conclusion: CAZ/AVI is a valid alternative for sHAPi caused by CPRA and DTR-P. aeruginosa, even when used alone. Optimisations of the treatment with CAZ/AVI in critically ill patients, including loading dose, adequate maintenance dose and prolonged infusion, were positively associated with potential clinical benefits.(c) 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.
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页数:6
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