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Therapeutic drug monitoring-guided piperacillin dosing in critically ill patients undergoing continuous renal replacement therapy: a systematic review

哌拉西林 加药 医学 治疗药物监测 肾脏替代疗法 重症监护医学 哌拉西林/他唑巴坦 药代动力学 内科学 遗传学 细菌 铜绿假单胞菌 生物
作者
Nazatul Adhwa Mohd Rozi,Nor Asyikin Mohd Tahir,Shamin Mohd Saffian,Mohd Makmor‐Bakry,Aliza Mohamad Yusof,Ruslinda Mustafar,Muhammad Nordin M Saud
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
标识
DOI:10.1093/jac/dkae332
摘要

Abstract Background Continuous renal replacement therapy (CRRT) complicates antibiotic dosing in critically ill patients due to altered pharmacokinetics. The optimal dosing of piperacillin remains unclear. Therapeutic drug monitoring (TDM) can personalize piperacillin therapy and improve outcomes. Objectives This review investigates the effects of TDM-guided piperacillin dosing on pharmacokinetic target attainment and clinical outcomes in CRRT patients, analyses correlations with clinical outcomes, provides optimal dosing strategies for piperacillin and identifies future research areas. Methods A systematic search of PubMed, Scopus and Web of Science was conducted until December 2023, identifying studies on piperacillin pharmacokinetics and clinical outcomes in adult CRRT patients. Data on study characteristics, piperacillin exposures, TDM use, target attainment rates, mortality and length of stay were extracted. The risk of bias was assessed using the Newcastle–Ottawa Scale. Results Eleven observational studies were included. High pharmacokinetic variability was evident, with piperacillin target non-attainment in up to 74% of cases without TDM. Two studies with routine TDM showed increased target attainment rates of 80%–100%. Mortality ranged from 17% to 56%, with supratherapeutic concentrations (≥100 mg/L) associated with higher mortality. The impact of optimized piperacillin exposures on outcomes was inconclusive. Most studies demonstrated a low risk of bias. Conclusions TDM-guided piperacillin dosing in CRRT patients improved target attainment rates (≥80%). Mortality rates ranged from 17% to 56%, with inconsistent correlations between drug exposures and survival. Supratherapeutic concentrations were linked to higher mortality. Standardized TDM protocols are needed. Future research should establish clear exposure–response relationships and the impact of TDM on clinical outcomes.

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