头孢吡肟在成人体外膜氧合患者中的药代动力学。

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Lily Zheng , Mohammad H. Alshaer , Charles Peloquin , Veena Venugopalan , Hassan M. Alnuaimat , Maureen Converse
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引用次数: 0

摘要

背景:体外膜氧合(ECMO)对β -内酰胺类抗生素药代动力学/动力学(PK/PD)的影响总体上尚未得到很好的研究,但头孢吡肟的相关数据最少。我们的目的是研究ECMO是否会改变成人重症监护病房(ICU)患者头孢吡肟的PK。方法:本单中心、回顾性病例对照研究评估ECMO患者的头孢吡肟治疗性药物监测(TDM)结果与非ECMO患者的TDM结果在药物方案和肾功能方面的1:1匹配。主要终点是ECMO与非ECMO ICU患者头孢吡肟的PK/PD差异。次要结局包括住院时间、治疗失败、重复感染、细菌耐药性和存活至出院。结果:纳入82例患者,每组44例匹配头孢吡肟浓度。ECMO患者游离最大浓度(fCmax)较高(p = 0.003),游离最小浓度(fCmin)/1 ×最小抑制浓度(MIC)比值较低(p = 0.040),游离Cmin/4 × MIC达到率较低(p = 0.010)。两组间游离Cmin、超过1xMIC或4xmic的时间、药代动力学参数(ke、半衰期和Vd)均无差异。在存活至出院的患者中,ECMO组的住院时间更长(p )。结论:这些数据表明,ECMO患者可能需要更积极的经验剂量。治疗药物监测和未来的前瞻性研究将为指导剂量调整的决策提供更多的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cefepime pharmacokinetics in adult extracorporeal membrane oxygenation patients

Background

The impact of extracorporeal membrane oxygenation (ECMO) on the pharmacokinetics/dynamics (PK/PD) of beta-lactam antibiotics have not been well studied in general, but cefepime specifically has the least amount of data. We aimed to investigate whether ECMO alters the PK of cefepime in adult intensive care unit (ICU) patients.

Methods

This single-center, retrospective case-control study evaluated cefepime therapeutic drug monitoring (TDM) results from ECMO patients that were matched 1:1 with TDM results in non-ECMO patients for drug regimen and renal function. The primary outcome was the difference in PK/PD of cefepime in ECMO compared with non-ECMO ICU patients. Secondary outcomes included hospital length of stay, treatment failure, superinfection, bacterial resistance, and survival to discharge.

Results

Eighty-two patients were included with 44 matched cefepime concentrations in each group. ECMO patients had higher free maximum concentrations (fCmax) (p = 0.003), lower free minimum concentration (fCmin)/1x minimum inhibitory concentration (MIC) ratios (p = 0.040), and lower attainment of free Cmin/4x MIC (p = 0.010). There were no differences between the groups for free Cmin, time above 1xMIC or 4x MIC, and pharmacokinetic parameters (ke, half-life, and Vd). Of those who survived to discharge, hospital length of stay was longer in the ECMO group (p < 0.001). Patients on ECMO were more likely to experience treatment failure (p = 0.036). The incidence of bacterial resistance, superinfection, or survival were similar among the groups.

Conclusion

These data suggest that more aggressive empiric dosing may be warranted in patients on ECMO. Therapeutic drug monitoring and future prospective studies would provide more evidence to guide decision making regarding dose adjustments.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
41
审稿时长
42 days
期刊介绍: Pulmonary Pharmacology and Therapeutics (formerly Pulmonary Pharmacology) is concerned with lung pharmacology from molecular to clinical aspects. The subject matter encompasses the major diseases of the lung including asthma, cystic fibrosis, pulmonary circulation, ARDS, carcinoma, bronchitis, emphysema and drug delivery. Laboratory and clinical research on man and animals will be considered including studies related to chemotherapy of cancer, tuberculosis and infection. In addition to original research papers the journal will include review articles and book reviews. Research Areas Include: • All major diseases of the lung • Physiology • Pathology • Drug delivery • Metabolism • Pulmonary Toxicology.
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