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应用中断时间序列分析评价万古霉素精准剂量咨询服务对目标暴露量达成的效果。

Evaluation of a Pilot Vancomycin Precision Dosing Advisory Service on Target Exposure Attainment Using an Interrupted Time Series Analysis.

机构信息

Department of Clinical Pharmacology & Toxicology, St Vincent's Hospital, Sydney, New South Wales, Australia.

St Vincent's Clinical School, Faculty of Medicine, The University of New South Wales, Sydney, New South Wales, Australia.

出版信息

Clin Pharmacol Ther. 2021 Jan;109(1):212-221. doi: 10.1002/cpt.2113. Epub 2020 Dec 5.

Abstract

This study evaluated the ability of a pilot therapeutic drug monitoring (TDM) Advisory Service to facilitate vancomycin therapeutic target attainment within a real-world clinical setting. The Service provided area under the concentration-time curve (AUC)-guided vancomycin dose recommendations, using Bayesian forecasting software and clinical expertise, to prescribers at an Australian hospital. A retrospective audit of intravenous vancomycin therapy (> 48 hours) in adults (≥ 18 years old) was undertaken over a 54-month period to evaluate attainment of established vancomycin pharmacokinetic/pharmacodynamic targets (AUC over 24 hours / minimum inhibitory concentration: 400-600) before (36-month period) and after (18-month period) Service implementation. Interrupted time series analysis was employed to evaluate monthly measures of the median proportion of therapy spent within the target range. Indices of time to target attainment were also assessed before and after Service implementation. The final cohort comprised 1,142 courses of vancomycin (816 patients); 835 courses (596 patients) and 307 courses (220 patients) administered before and after Service implementation, respectively. Prior to piloting the Service, the median proportion of time in the target range was 40.1% (95% CI, 34.3-46.0%); this increased by 10.4% (95% CI, 1.2-19.6%, P = 0.03) after the Service, and was sustained throughout the post-Service evaluation period. Post-Service target attainment at 48-72 hours after initiation of therapy was increased (7.8%, 95% CI, 1.3-14.3%, P = 0.02). The findings of this study provide evidence that a consultative TDM Service can facilitate attainment of vancomycin therapeutic targets; however, optimization of the Service may further improve the use of vancomycin.

摘要

本研究评估了一个试点治疗药物监测(TDM)咨询服务在真实临床环境中促进万古霉素治疗目标达成的能力。该服务使用贝叶斯预测软件和临床专业知识,为澳大利亚一家医院的开处方者提供 AUC 指导的万古霉素剂量建议。在实施该服务之前(36 个月期间)和之后(18 个月期间),对成年人(≥18 岁)静脉万古霉素治疗(>48 小时)进行了回顾性审计,以评估达到既定万古霉素药代动力学/药效学目标(24 小时 AUC/最低抑菌浓度:400-600)的情况。采用中断时间序列分析评估实施服务前后每月目标范围内治疗时间中位数的比例。还评估了实施服务前后达到目标的时间指数。最终队列包括 1142 例万古霉素疗程(816 例患者);分别在实施服务之前和之后管理 835 例(596 例患者)和 307 例(220 例患者)。在试行该服务之前,目标范围内的时间中位数比例为 40.1%(95%CI,34.3-46.0%);实施服务后增加了 10.4%(95%CI,1.2-19.6%,P=0.03),并在整个服务后评估期间保持稳定。治疗开始后 48-72 小时达到目标的比例增加(7.8%,95%CI,1.3-14.3%,P=0.02)。本研究的结果提供了证据,表明咨询 TDM 服务可以促进万古霉素治疗目标的达成;然而,对该服务的优化可能会进一步改善万古霉素的使用。

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