Yu Chen-Huan, Tsai Mao-Song, Liao Chun-Hsing, Yang Chia-Jui
Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City, Taiwan.
Division of Infectious Disease, Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City, Taiwan.
Infect Drug Resist. 2024 Dec 5;17:5363-5374. doi: 10.2147/IDR.S475679. eCollection 2024.
Ceftazidime-avibactam (CZA), a novel beta-lactam/beta-lactamase inhibitor, plays an important role in the threat of emerging carbapenem-resistant Enterobacterales (CRE) infection. The study aims to analyze the clinical effectiveness and factors influencing treatment response to CZA for carbapenem-resistant (CRKP) infections.
From February 2020 to December 2021, patients with CRKP infection treated with CZA were enrolled in this retrospective, single-center cohort study in northern Taiwan. The primary outcome was 28-day survival rate. The secondary outcomes were clinical success, and microbiological cure. Multivariate regression analysis was used to evaluate factors associated with 28-day survival.
A total of 142 patients treated with CZA alone (n=82) or in combination therapy (n=60) were included. We found 28-day survival rate, microbiological cure, and clinical success rate were 78% (111/142), 86% (87/101), and 48% (63/132), respectively. In multivariate analysis, there were no significant differences in 28-day survival between monotherapy group and combination therapy group (P=0.424). A relative lower microbiological cure rate can be observed in lower respiratory tract infection from univariate analysis (P=0.07). In addition, significantly better survival was observed in patients with creatinine clearance rate (CCr) ≥50 mL/min than CCr <50 mL/min (P=0.005).
CZA is an effective and important treatment option for CRKP infection even when it is treated as monotherapy. In patients with impaired renal function, a potential impact of CZA dose adjustments on poor survival outcomes has been observed, indicating the need for further research to determine optimal renal dose adjustment strategies.
头孢他啶-阿维巴坦(CZA)是一种新型β-内酰胺/β-内酰胺酶抑制剂,在应对新出现的耐碳青霉烯类肠杆菌科细菌(CRE)感染威胁方面发挥着重要作用。本研究旨在分析CZA治疗耐碳青霉烯类肺炎克雷伯菌(CRKP)感染的临床疗效及影响治疗反应的因素。
2020年2月至2021年12月,在台湾北部进行的这项回顾性单中心队列研究中,纳入了接受CZA治疗的CRKP感染患者。主要结局为28天生存率。次要结局为临床成功和微生物学清除。采用多因素回归分析评估与28天生存相关的因素。
共纳入142例单独接受CZA治疗(n = 82)或联合治疗(n = 60)的患者。我们发现28天生存率、微生物学清除率和临床成功率分别为78%(111/142)、86%(87/101)和48%(63/132)。多因素分析显示,单药治疗组和联合治疗组的28天生存率无显著差异(P = 0.424)。单因素分析显示,下呼吸道感染的微生物学清除率相对较低(P = 0.07)。此外,肌酐清除率(CCr)≥50 mL/min的患者生存率显著高于CCr < 50 mL/min的患者(P = 0.005)。
即使作为单药治疗,CZA也是治疗CRKP感染的一种有效且重要的治疗选择。在肾功能受损的患者中,已观察到CZA剂量调整对不良生存结局的潜在影响,这表明需要进一步研究以确定最佳的肾脏剂量调整策略。