Meropenem for the Pharmacological Treatment of Severe Infections in Critically Ill Pediatric Patients: Breakthrough Standard Treatment Strategies Based on PK/PD.

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xin He, Yaoyan Liu, Xiaodan Gong, Li Wang, Feng Chen
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Abstract

Meropenem, as a carbapenem antibiotic, is commonly used in critically ill pediatric patients with severe infection because of its broad antimicrobial spectrum, high penetration into tissues, and favorable safety profile. Due to pathophysiological changes in critically ill children, the available evidence has demonstrated that the standard dosage regimens of meropenem could not meet an appropriate pharmacodynamic (PD) target attainment in severely infected children. Therefore, we reviewed the pharmacokinetic (PK) profile of meropenem in critically ill children, therapeutic drug monitoring (TDM), and dose optimization based on PK/PD. Meropenem kills bacteria in a timedependent manner and its efficacy is positively correlated with the percentage of the time of dosing interval during which the free serum concentration of meropenem remains above the minimum inhibitory concentration (MIC) of the pathogen (%fT>MIC), which is related to PK/PD targets. For critically ill children, TDM-based dosage optimization and setting even higher PK/PD targets seem necessary to be considered. The currently available studies have revealed that increasing the dose and the application of the extended or continuous infusion of meropenem were able to achieve better PK/PD targets. According to limited clinical data on efficacy and safety, these treatment measures cannot yet be adopted as routine regimens only when serious infections caused by drug-resistant bacteria or strains with high values of MIC are suspected. Further high-quality randomized controlled trials (RCTs) or observational studies with sufficient sample sizes are required to confirm the efficacy and safety of these modes of administration.

美罗培南治疗小儿危重患者重症感染:基于PK/PD的突破性标准治疗策略
美罗培南作为一种碳青霉烯类抗生素,因其抗菌谱广、对组织渗透性高、安全性好等优点,常用于小儿重症感染的重症患者。由于重症儿童的病理生理变化,现有证据表明,美罗培南的标准剂量方案不能满足严重感染儿童适当的药效学(PD)目标的实现。因此,我们对美罗培南在危重儿童中的药代动力学(PK)、治疗药物监测(TDM)和基于PK/PD的剂量优化进行了综述。美罗培南杀灭细菌呈时间依赖性,其效果与给药间隔时间美罗培南游离血清浓度保持在病原体最低抑制浓度(MIC)以上的时间百分比(%fT>MIC)呈正相关,这与PK/PD靶点有关。对于危重患儿,有必要考虑以tdm为基础的剂量优化和设定更高的PK/PD目标。目前已有的研究表明,增加剂量和延长或持续输注美罗培南能够达到更好的PK/PD目标。根据有限的疗效和安全性临床数据,只有当怀疑耐药菌或MIC值高的菌株引起严重感染时,这些治疗措施才不能作为常规方案采用。需要进一步的高质量随机对照试验(rct)或足够样本量的观察性研究来证实这些给药方式的有效性和安全性。
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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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