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亚胺培南在机械通气相关性肺炎重症患者中的药效学

Pharmacodynamics of imipenem in critically ill patients with ventilator-associated pneumonia.

作者信息

Jaruratanasirikul Sutep, Aeinlang Nanchanit, Jullangkoon Monchana, Wongpoowarak Wibul

机构信息

Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.

出版信息

J Med Assoc Thai. 2013 May;96(5):551-7.

Abstract

BACKGROUND

Drug dispositions are altered in critically ill patients, including ventilator-associated pneumonia (VAP) when compared with healthy subjects leading to fluctuations of plasma concentrations.

OBJECTIVE

To compare the probability of target attainment (PTA) and cumulative fraction of response (CFR) for imipenem between administration by 0.5-hour and 2-hour infusions.

MATERIAL AND METHOD

The present study was a randomized three-way crossover in nine patients with VAP Each patient received imipenem in three regimens consecutively: (i) a 0.5-hour infusion of 0.5 g every six hours for 24 hours; (ii) a 2-hour infusion of 0.5 g every six hours for 24 hours; and (iii) a 2-hour infusion of 1 g every six hours for 24 hours. Monte Carlo simulation was performed to determine the PTA at various regimens and the study used susceptibility patterns obtained from EUCAST and MYSTIC for assessment of CFR.

RESULTS

For an MIC of 2 microg/ml, the PTAs achieving 40% T > MIC following a 0.5-hour infusion of 0.5 g, a 2-hour infusion of 0.5 g, and a 2-hour infusion of 1 g were 90.93%, 98.97%, and 100%, respectively. Only a 2-hour infusion of 1 g achieved 98.75% of the PTA of 40% T > MGC for an MIC of 4 microg/ml. All regimens were predicted to achieve CFR > 99% against E. coli and Klebsiella spp.

CONCLUSION

A 2-hour infusion of 1 g regimen was predicted to have the highest PTA rates. All regimens achieved a high CFR against E. coli and Klebsiella spp.

摘要

背景

与健康受试者相比,重症患者(包括呼吸机相关性肺炎患者)的药物处置发生改变,导致血浆浓度波动。

目的

比较亚胺培南0.5小时输注和2小时输注给药时的达标概率(PTA)和反应累积分数(CFR)。

材料与方法

本研究为9例呼吸机相关性肺炎患者的随机三交叉试验。每位患者连续接受三种亚胺培南给药方案:(i)每6小时0.5小时输注0.5g,共24小时;(ii)每6小时2小时输注0.5g,共24小时;(iii)每6小时2小时输注1g,共24小时。进行蒙特卡罗模拟以确定不同给药方案的PTA,并使用从欧洲抗菌药物敏感性试验委员会(EUCAST)和微生物监测与药敏试验综合数据库(MYSTIC)获得的药敏模式评估CFR。

结果

对于最低抑菌浓度(MIC)为2μg/ml,0.5小时输注0.5g、2小时输注0.5g和2小时输注1g后达到40%T>MIC的PTA分别为90.93%、98.97%和100%。对于MIC为4μg/ml,仅2小时输注1g达到40%T>MIC的PTA的98.75%。所有给药方案预计对大肠杆菌和克雷伯菌属的CFR>99%。

结论

预计2小时输注1g方案的PTA率最高。所有给药方案对大肠杆菌和克雷伯菌属均具有较高的CFR。

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