用于体外膜氧合患者的头孢比普洛和头孢克洛:治疗药物监测的作用。

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Current drug metabolism Pub Date : 2024-09-27 DOI:10.2174/0113892002331260240919055056
Diana Morales Castro, John Granton, Eddy Fan
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引用次数: 0

摘要

简介:关于新型抗菌药物在重症患者中的治疗范围的数据有限,包括接受肾脏替代疗法或体外膜氧合(ECMO)的患者在内的药代动力学研究很少:这些干预措施可能会改变抗生素的药代动力学特征,导致治疗失败、抗菌药耐药性或毒性增加。在本报告中,我们介绍了两名接受头孢哌酮和头孢噻吩治疗的 ECMO 患者,他们在治疗药物监测(TDM)的帮助下成功治疗了严重感染。两个病例的抗生素谷浓度与之前报道的重症患者和 ECMO 患者的治疗水平一致,达到了欧洲抗菌药物敏感性检测委员会针对相应病原体推荐的最小抑菌浓度:结论:如果不根据理化特性和体外支持调整剂量,治疗可能达不到最佳效果。在病原体高度耐药的时代,这些病例凸显了及时进行实时 TDM 以优化和个性化抗菌治疗的重要性。
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Ceftobiprole and Cefiderocol for Patients on Extracorporeal Membrane Oxygenation: The Role of Therapeutic Drug Monitoring.

Introduction: Limited data exist on therapeutic ranges for newer antimicrobials in the critically ill, with few pharmacokinetic studies including patients undergoing renal replacement therapy or extracorporeal membrane oxygenation (ECMO).

Case representation: These interventions can potentially alter the pharmacokinetic profile of antibiotics, resulting in therapeutic failures, antimicrobial resistance, or increased toxicity. In this report, we present two ECMO patients treated with cefiderocol and ceftobiprole, where therapeutic drug monitoring (TDM) aided in the successful treatment of severe infections. Antibiotic trough concentrations in both cases were consistent with previously reported therapeutic levels in critically ill and ECMO patients, meeting minimal inhibitory concentrations recommended by the European Committee on Antimicrobial Susceptibility Testing for the respective pathogens.

Conclusion: Treatment might be suboptimal if doses are not adjusted based on physicochemical properties and extracorporeal support. In an era marked by highly resistant pathogens, these cases highlight the importance of timely access to real-time TDM for optimizing and individualizing antimicrobial treatment.

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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