在药剂师管理的万古霉素给药方案中实施AUC监测:一项回顾性队列研究。

Brandon L S Robinson, Blake Bennie, Mahmoud Nasiri, Kieu Nguyen, Reba Forbess, Mallory Gessner-Wharton, Cassie Robertson
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引用次数: 0

摘要

背景:2020年发布的《万古霉素治疗药物监测共识指南》认识到,与传统的波谷给药相比,使用计算的曲线下面积(AUC)来指导给药可以最大限度地提高临床疗效,并将风险降至最低。本研究的目的是确定AUC监测是否能降低在所有适应症下接受万古霉素治疗的成年患者的急性肾损伤(AKI)发生率。方法:本研究采用药学监测软件从2个时间段选取18岁及以上接受药师管理的万古霉素治疗的患者。如果患者接受少于48小时的治疗或在基线时肾功能不稳定或血液透析,则排除。测量的主要结局是每组患者AKI的发生率。结果:每组共收集数据121例。各组间使用的伴发肾毒素以及感染源相似。AUC监测未导致AKI发生率显著降低(AUC组为16.5%,槽组为14.9%;P = .61)。然而,与低谷监测组相比,接受AUC监测的患者在第一次随访时更有可能治疗(AUC组为43.2%,低谷组为33.9%;P = .03)。AUC监测也导致较低的低谷水平和总日剂量,死亡率或住院时间没有差异。结论:AUC监测未观察到AKI发生率降低。尽管如此,AUC监测方案在达到目标AUC 400-600 mg*h /L方面是有效的,并且没有增加死亡率或住院时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implementing AUC Monitoring in a Pharmacist-Managed Vancomycin Dosing Protocol: A Retrospective Cohort Study.

Background: Consensus guidelines on the therapeutic drug monitoring of vancomycin published in 2020 recognize that using the calculated area-under-the-curve (AUC) to guide dosing maximizes clinical efficacy and minimizes risk when compared to traditional trough-based dosing. The purpose of this study was to determine whether AUC monitoring results in reduced acute kidney injury (AKI) rates in adult patients receiving vancomycin for all indications.

Methods: In this study, patients 18 years or older who received pharmacist-managed vancomycin therapy were selected using pharmacy surveillance software from 2 timeframes. Patients were excluded if they received less than 48 hours of therapy or had unstable renal function or hemodialysis at baseline. The primary outcome measured was the incidence of AKI in each group of patients.

Results: Data were collected for 121 patients in each group. Concomitant nephrotoxins used in each group, as well as the sources of infection, were similar between groups. AUC monitoring did not result in a significant decrease in AKI rate (16.5% in AUC group, 14.9% in trough group; P = .61). However, patients who received AUC monitoring were more likely to be therapeutic at first follow-up compared to the trough monitoring group (43.2% in AUC group, 33.9% in trough group; P = .03). AUC monitoring also resulted in lower trough levels and total daily doses, with no difference in mortality or length of stay.

Conclusion: AUC monitoring did not result in an observed decrease in AKI rate. Despite this, the AUC monitoring protocol was effective at reaching the goal AUC of 400-600 mg*hour/L and did not increase mortality or length of stay.

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