Phillips Morgan, Rose Jeremy, Hamel Ashlee, Ingemi Amanda
Sentara RMH Medical Center, Harrisonburg, Virginia, USA.
Sentara Norfolk General Hospital, Norfolk, Virginia, USA.
Microbiol Spectr. 2023 Feb 22;11(2):e0331322. doi: 10.1128/spectrum.03313-22.
Vancomycin is used for Gram-positive infections, including methicillin-resistant Staphylococcus aureus. The 2020 vancomycin guidelines described by M. J. Rybak, J. Le, T. P. Lodise, D. P. Levine, et al. (Am J Health Syst Pharm 77:835-864, 2020, https://doi.org/10.1093/ajhp/zxaa036) provided an update on vancomycin dosing, which recommended an optimal area under the concentration-time curve over 24 h to MIC (AUC/MIC) target of 400 to 600. In 2021, a pharmacy-driven AUC/MIC vancomycin dosing protocol was implemented across 12 Sentara Health System hospitals. The primary objective of this study was to assess if the pharmacy-driven AUC/MIC vancomycin dosing protocol led to fewer acute kidney injury (AKI) events than trough-based dosing. Secondary objectives included vancomycin duration, hospital length of stay, administered vancomycin dose during admission, vancomycin labs drawn during standard lab times, and cost. AKI was assessed in two separate ways: (i) modified AKIN (Acute Kidney Injury Network) criteria and (ii) a modified version from the vancomycin guidelines. Inferential statistics were used to analyze the results of this retrospective study. Per the AKIN definition, the rates of AKI were 13.9% (349/2,507) in the trough-based group and 14.9% (369/2,471) in the AUC/MIC-based group ( = 0.309). Per the definition of the vancomycin guidelines, the rates of AKI were 6.7% (169/2,507) in the trough-based group and 7.6% (187/2,471) in the AUC/MIC-based group ( = 0.258). A total of 52% (2,679/5,151) of vancomycin labs were obtained during standard lab times in the AUC group and 24% (1,144/4,766) in the trough group ( < 0.05). There was no difference in AKI events between AUC and trough dosing. Use of contrast dye may confound these results. AUC/MIC dosing was associated with more lab draws during standard times, a larger number of labs drawn per person, and less total use of vancomycin. In this article, we report that there were no differences in rates of acute kidney injury between trough-based vancomycin dosing and AUC/MIC-based vancomycin dosing across 12 hospitals. AUC/MIC dosing resulted in more vancomycin lab draws during standard lab draw times compared to trough dosing, thus making it more convenient for health care personnel. This study includes all uses for vancomycin, including empirical use, and all patient severity levels. Therefore, this research reflects real-world use of vancomycin in hospitals. AUC/MIC dosing is supported by various infectious disease societies. However, the feasibility of incorporating AUC/MIC dosing in hospitals is undetermined. This study is unique in that it includes hospitals of various sizes (small community hospitals and an academic teaching hospital), and it includes a feasibility component. Therefore, this study has broad applicability to other hospitals across the United States. This original research includes the clinical application of vancomycin in a multicenter health system.
万古霉素用于革兰氏阳性菌感染,包括耐甲氧西林金黄色葡萄球菌感染。M. J. 里巴克、J. 勒、T. P. 洛迪斯、D. P. 莱文等人(《美国卫生系统药学杂志》77:835 - 864, 2020, https://doi.org/10.1093/ajhp/zxaa036)描述的2020年万古霉素指南提供了万古霉素给药方案的更新内容,建议24小时浓度 - 时间曲线下面积与最低抑菌浓度之比(AUC/MIC)的最佳目标值为400至600。2021年,一项由药房主导的AUC/MIC万古霉素给药方案在森塔拉医疗系统的12家医院实施。本研究的主要目的是评估由药房主导的AUC/MIC万古霉素给药方案是否比基于谷浓度的给药方案导致更少的急性肾损伤(AKI)事件。次要目标包括万古霉素使用时长、住院时间、住院期间给予的万古霉素剂量、在标准实验室检测时间抽取的万古霉素检测样本,以及成本。AKI通过两种不同方式进行评估:(i)改良的AKIN(急性肾损伤网络)标准,以及(ii)万古霉素指南的改良版本。使用推断统计学方法分析这项回顾性研究的结果。根据AKIN定义,基于谷浓度给药组的AKI发生率为13.9%(349/2,507),基于AUC/MIC给药组为14.9%(369/2,471)(P = 0.309)。根据万古霉素指南的定义,基于谷浓度给药组的AKI发生率为6.7%(169/2,507),基于AUC/MIC给药组为7.6%(187/2,471)(P = 0.258)。在AUC组中,52%(2,679/5,151)的万古霉素检测样本是在标准实验室检测时间抽取的,而在谷浓度组中这一比例为24%(1,144/4,766)(P < 0.05)。AUC给药和谷浓度给药之间的AKI事件发生率没有差异。使用对比剂可能会混淆这些结果。AUC/MIC给药与在标准时间抽取更多检测样本、每人抽取的检测样本数量更多以及万古霉素的总使用量更少相关。在本文中,我们报告在12家医院中,基于谷浓度的万古霉素给药和基于AUC/MIC的万古霉素给药在急性肾损伤发生率方面没有差异。与谷浓度给药相比,AUC/MIC给药在标准实验室检测时间导致抽取更多万古霉素检测样本,因此对医护人员来说更方便。本研究涵盖了万古霉素的所有使用情况,包括经验性使用,以及所有患者严重程度级别。因此,这项研究反映了医院中万古霉素的实际使用情况。AUC/MIC给药得到了多个传染病学会的支持。然而,在医院采用AUC/MIC给药的可行性尚未确定。本研究的独特之处在于它包括了各种规模的医院(小型社区医院和一所学术教学医院),并且包含了可行性部分。因此, 这项研究对美国其他医院具有广泛的适用性。这项原创性研究包括了万古霉素在多中心医疗系统中的临床应用。