Gillett Eric, Aleissa Muneerah M, Pearson Jeffrey C, Solomon Daniel A, Kubiak David W, Dionne Brandon, Edrees Heba H, Okenla Adetoun, Chan Brian T
Department of Pharmacy, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Division of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Open Forum Infect Dis. 2024 Oct 18;11(11):ofae600. doi: 10.1093/ofid/ofae600. eCollection 2024 Nov.
Current vancomycin monitoring guidelines recommend monitoring 24-hour area under the concentration-time curve (AUC) to minimum inhibitory concentration ratios for patients with serious methicillin-resistant infections. However, there are sparse data on the safety, feasibility, and efficacy of vancomycin AUC monitoring for outpatients. Traditional AUC pharmacokinetic calculations require 2 concentrations, while bayesian software allows for single-concentration AUC estimations.
We conducted a single-center, quasi-experimental, interrupted time series study of patients enrolled in the outpatient parenteral antimicrobial therapy program at our institution for vancomycin management. Our institution implemented a pharmacist-driven vancomycin AUC monitoring program from September 2019 to February 2020, and again from September 2022 to March 2023. Patients enrolled underwent vancomycin monitoring using an AUC goal of 400-600 mg⋅h/L, estimated through bayesian modeling. Patients enrolled in the outpatient parenteral antimicrobial therapy program from July 2021 through August 2022 for trough-based monitoring were used for comparison. The primary outcome was nephrotoxicity incidence, defined as a serum creatinine increase by ≥0.5 mg/dL or ≥50% during outpatient vancomycin therapy.
We enrolled 63 patients in the AUC group and 60 patients in the trough-based group. Nephrotoxicity was significantly lower in the AUC cohort (6.3% vs 23.3%; = .01). The number of unusable vancomycin concentrations was also significantly lower in the AUC cohort (0% vs 6%; < .01). There was no difference in composite 90-day all-cause mortality or readmission (33.3% vs 38.3%; = .56).
Following implementation of a pharmacist-driven AUC monitoring program, patients were less likely to develop nephrotoxicity during outpatient vancomycin therapy.
当前的万古霉素监测指南建议,对于患有严重耐甲氧西林感染的患者,监测24小时浓度-时间曲线下面积(AUC)与最低抑菌浓度的比值。然而,关于门诊患者万古霉素AUC监测的安全性、可行性和有效性的数据较少。传统的AUC药代动力学计算需要两个浓度,而贝叶斯软件允许进行单浓度AUC估计。
我们对在本机构参加门诊肠外抗菌治疗计划进行万古霉素管理的患者进行了一项单中心、准实验性、中断时间序列研究。我们机构在2019年9月至2020年2月以及2022年9月至2023年3月实施了由药剂师驱动的万古霉素AUC监测计划。纳入的患者通过贝叶斯建模估计,使用400 - 600mg·h/L的AUC目标进行万古霉素监测。将2021年7月至2022年8月参加门诊肠外抗菌治疗计划进行谷浓度监测的患者作为对照。主要结局是肾毒性发生率,定义为门诊万古霉素治疗期间血清肌酐升高≥0.5mg/dL或≥50%。
我们在AUC组纳入了63例患者,在谷浓度组纳入了60例患者。AUC队列中的肾毒性显著更低(6.3%对23.3%;P = 0.01)。AUC队列中不可用的万古霉素浓度数量也显著更低(0%对6%;P < 0.01)。90天综合全因死亡率或再入院率无差异(33.3%对38.3%;P = 0.56)。
在实施由药剂师驱动的AUC监测计划后,门诊万古霉素治疗期间患者发生肾毒性的可能性降低。