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增加β-内酰胺类药物剂量方案可改善因医院或呼吸机获得性肺炎首发病例而接受治疗的伴有急性肾损伤清除率增加的危重症患者的临床结局:一项前后对照研究。

Increased β-Lactams dosing regimens improve clinical outcome in critically ill patients with augmented renal clearance treated for a first episode of hospital or ventilator-acquired pneumonia: a before and after study.

机构信息

Anesthesiology and Critical Care Department, Hôpital Pellegrin, CHU Bordeaux, 33000, Bordeaux, France.

University Bordeaux Segalen, 33000, Bordeaux, France.

出版信息

Crit Care. 2019 Nov 27;23(1):379. doi: 10.1186/s13054-019-2621-4.

Abstract

BACKGROUND

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).

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ad0/6881978/59980380eddf/13054_2019_2621_Fig1_HTML.jpg

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