Anesthesiology and Critical Care Department, Hôpital Pellegrin, CHU Bordeaux, 33000, Bordeaux, France.
University Bordeaux Segalen, 33000, Bordeaux, France.
Crit Care. 2019 Nov 27;23(1):379. doi: 10.1186/s13054-019-2621-4.
Augmented renal clearance (ARC) is recognized as a leading cause of β-lactam subexposure when conventional dosing regimens are used. The main objective was to compare the clinical outcome of ARC patients treated by conventional or increased β-lactam dosing regimens for a first episode of hospital or ventilator-acquired pneumonia (HAP-VAP).
In this single-center, retrospective study, every ARC patient treated by β-lactam for a first episode of HAP-VAP was included during two 15-month periods, before (Control period) and after (Treatment period) the modification of a local antibiotic therapy protocol. ARC was defined by a 24-h measured creatinine clearance ≥ 150 ml/min. The primary endpoint was defined as a therapeutic failure of the antimicrobial therapy or a HAP-VAP relapse within 28 days. Inverse probability of treatment weight (IPTW) was derived from a propensity score model. Cox proportional hazard models were used to evaluate the association between treatment period and clinical outcome.
During the study period, 177 patients were included (control period, N = 88; treatment period, N = 89). Therapeutic failure or HAP-VAP relapse was significantly lower in the treatment period (10 vs. 23%, p = 0.019). The IPTW-adjusted hazard ratio of poor clinical outcome in the treatment period was 0.35 (95% CI 0.15-0.81), p = 0.014. No antibiotic side effect was reported during the treatment period.
Higher than licensed dosing regimens of β-lactams may be safe and effective in reducing the rate of therapeutic failure and HAP-VAP recurrence in critically ill augmented renal clearance (ARC) patients.
当使用常规剂量方案时,增强的肾清除率(ARC)被认为是导致β-内酰胺类药物亚暴露的主要原因。主要目的是比较使用常规或增加β-内酰胺类药物剂量方案治疗首次发生医院或呼吸机获得性肺炎(HAP-VAP)的 ARC 患者的临床结果。
在这项单中心、回顾性研究中,在修改当地抗生素治疗方案的两个 15 个月期间,对每个接受β-内酰胺类药物治疗首次发生 HAP-VAP 的 ARC 患者进行了治疗。ARC 的定义为 24 小时内测量的肌酐清除率≥150ml/min。主要终点定义为抗菌治疗失败或 HAP-VAP 在 28 天内复发。采用逆概率治疗权重(IPTW)从倾向评分模型中得出。使用 Cox 比例风险模型评估治疗期与临床结果之间的关联。
在研究期间,共纳入 177 例患者(对照组,N=88;治疗组,N=89)。治疗期的治疗失败或 HAP-VAP 复发率明显较低(10%比 23%,p=0.019)。治疗期不良临床结局的 IPTW 校正风险比为 0.35(95%CI 0.15-0.81),p=0.014。治疗期间未报告抗生素不良反应。
对于危重症 ARC 患者,增加β-内酰胺类药物的剂量可能是安全有效的,可以降低治疗失败和 HAP-VAP 复发的发生率。