IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2025-02-17 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S489603
Yaru Peng, Yalan Liu, Zeneng Cheng, Qiang Zhang, Feifan Xie, Sucui Zhu, Sanwang Li
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引用次数: 0

摘要

目的:为提高重症患者的临床疗效,越来越多地采用延长美罗培南输注时间的方法。然而,在接受持续肾脏替代疗法(CRRT)的肾功能受损患者中,有关此类给药方案的研究却很少。本研究旨在对重症 CRRT 患者长期输注美罗培南的群体药代动力学(PK)进行分析,为最佳给药方案提供依据:方法:利用21名中国重症CRRT患者每8-12小时输注1克美罗培南2-3小时的94个浓度构建群体PK模型。采用蒙特卡洛模拟评估了基于PK/PD目标(100% fT>MIC或100% fT>4×MIC)的疗效和延长美罗培南给药方案(每6-12小时输注3小时,每次0.5-2克)的肾毒性风险(谷浓度≥45毫克/升):结果:美罗培南的浓度数据可以用线性消除的单室模型充分描述,肌酐清除率(CLCR)对美罗培南的内源性清除率有显著影响。0.5 克 q6h 和 1 克 q8h 可以达到理想的 100% fT>MIC 目标,MIC≤4 毫克/升,CRRT 患者的毒性风险在 10-50 毫升/分钟的 CLCR 范围内可以忽略不计。患者需要 2 g q6h 和 2 g q8h 才能达到 100% fT>4×MIC 的目标,但相关的毒性风险非常高(>20%):结论:建立了中国CRRT患者延长美罗培南输注时间的人群PK模型,0.5克 q6h和1克 q8h可能是延长输注时间的最佳方案。
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Population Pharmacokinetics of Prolonged Infusion for Meropenem: Tailoring Dosing Recommendations for Chinese Critically Ill Patients on Continuous Renal Replacement Therapy with Consideration for Renal Function.

Objective: Extended meropenem infusion is increasingly employed to enhance clinical outcomes in critically ill patients. Nonetheless, investigations into such dosing regimens in renal-impaired patients undergoing continuous renal replacement therapy (CRRT) are scarce. This study aims to perform a population pharmacokinetic (PK) analysis of prolonged meropenem infusion in critically ill CRRT patients to inform optimal dosing regimens.

Methods: Ninety-four concentrations from 21 Chinese critically ill CRRT patients receiving 1 g meropenem every 8-12 hours infused over 2-3 hours were utilized to construct the population PK model. Monte Carlo simulations were employed to assess the efficacy based on PK/PD targets (100% fT>MIC or 100% fT>4×MIC) and the risk of nephrotoxicity (trough concentration ≥45 mg/L) for extended meropenem dosing regimens (0.5-2 g with a 3-hour infusion administered every 6-12 hours).

Results: Meropenem concentration data was adequately described by a one-compartment model with linear elimination, and creatinine clearance (CLCR) significantly influenced meropenem's endogenous clearance. 0.5 g q6h and 1 g q8h could achieve desirable attainment of 100% fT>MIC target against an MIC≤4 mg/L, with negligible risk of toxicity for CRRT patients across a CLCR range of 10-50 mL/min. 2 g q6h and 2 g q8h is required for targeting 100% fT>4×MIC for the patients, but the associated risk of toxicity is very high (>20%).

Conclusion: A population PK model was developed for prolonged meropenem infusion in Chinese CRRT patients, and 0.5 g q6h and 1 g q8h may be the optimal regimen for prolonged infusion.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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