Ceftazidime-Avibactam for Carbapenem-Resistant Gram-Negative Bacteria Infections: A Real-World Experience in the ICU

被引:5
|
作者
Yu, Jiaxin [1 ,2 ]
Zuo, Wei [1 ,2 ]
Fan, Hongwei [1 ,3 ]
Wu, Jiayu [1 ,2 ]
Qiao, Luyao [1 ,2 ,4 ]
Yang, Benyu [1 ,2 ,5 ]
Li, Wenxi [1 ,2 ,5 ]
Yang, Yang [1 ,2 ,6 ]
Zhang, Bo [1 ,2 ,6 ]
机构
[1] Peking Union Med Coll Hosp, Dept Pharm, Beijing, Peoples R China
[2] Peking Union Med Coll Hosp, State Key Lab Complex Severe & Rare Dis, Beijing, Peoples R China
[3] Peking Union Med Coll Hosp, Dept Infect Med, Beijing, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing, Peoples R China
[5] Tianjin Univ Tradit Chinese Med, Sch Chinese Mat Med, Tianjin, Peoples R China
[6] Peking Union Med Coll Hosp, Dept Pharm, Dongdan Campus,1 Shuaifuyuan Wangfujing Dongcheng, Beijing 100730, Peoples R China
来源
关键词
ceftazidime-avibactam; renal replacement therapy; infections; intensive care unit; carbapenem-resistant gram-negative bacteria; OUTCOMES; CARE;
D O I
10.2147/IDR.S422545
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose Ceftazidime-avibactam (C-A) is a treatment option for carbapenem-resistant gram-negative bacterial (CR-GNB) infections, but little is known regarding its suitability for the intensive care unit (ICU). The current study aimed to analyze use of C-A for critically ill patients, determine independent predictors of clinical outcome and mortality and explore routine dosages for patients in continuous renal replacement therapy (CRRT).Patients and Methods A single-center, retrospective and observational study was conducted in critically ill patients receiving different C-A-based therapies for CR-GNB infections in a tertiary teaching hospital in Beijing, China. Demographic data, severity of infection, clinical outcomes and mortality were assessed. The primary and secondary outcome of this study was 90-day all-cause mortality and 14-day clinical response, respectively.Results A total of 43 patients with CR-GNB infection were enrolled, including 14 (32.6%) patients received C-A monotherapy. C-A monotherapy and combination with other agents did not affect 14-day clinical response or 90-day survival. All-cause mortality at 90-days was 39.5% (17/43). Multivariate Cox analysis showed that concomitant with bloodstream infection was independent risk factors for 90-day mortality and that the time to initiation of C-A and Acute Physiology and Chronic Health Evaluation (APACHE) score was independent predictors of 14-day clinical response. Five CRRT patients who received high-dose C-A therapy (>3.75 g/d) had prolonged survival compared with 5 who received low-dose C-A (<3.75 g/d, p = 0.03).Conclusion C-A was an effective therapy for severe CR-GNB infections and clinical response correlated with the time of C-A initiation. A dosage >3.75g/d C-A was associated with prolonged survival of CRRT patients. Randomized controlled trials or multicenter studies are needed to confirm these findings.
引用
收藏
页码:6209 / 6216
页数:8
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