School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
School of Pharmacy, Chapman University, Irvine, CA, USA; Department of Pediatrics, The Lundquist Institute, Torrance, CA, USA; Harbor-UCLA Medical Center, Torrance, CA, USA.
Clin Microbiol Infect. 2021 Sep;27(9):1346.e1-1346.e7. doi: 10.1016/j.cmi.2020.11.008. Epub 2020 Nov 19.
Area under the time-concentration curve (AUC) -guided dosing provides better estimates of exposure than vancomycin trough concentrations. Though clinical benefits have been reported, the costs of AUC-guided dosing are uncertain. The objective of this study was to quantify the costs of single-sample Bayesian or two-sample AUC strategies versus trough-guided dosing.
A cost-benefit analysis from the institutional perspective was conducted using a decision tree to model the probabilities and costs of acute kidney injury (AKI) associated with vancomycin administered over 48 hours up to 21+ days. Costs included vancomycin concentrations, Bayesian software and AKI hospitalization costs, and probabilities were obtained from primary literature. Robustness was assessed via both one-way and probabilistic sensitivity analyses.
In the base-case model, two-sample AUC versus trough dosing saved an average of US$ 846 per patient encounter, and single-sample Bayesian AUC versus trough dosing saved an average of US$ 2065 per patient encounter. This translates into annual cost-savings of US$ 846 810 and US$ 2 065 720 for two-sample and single-sample Bayesian methods versus trough dosing, respectively, assuming 1000 vancomycin-treated patients per year. Assuming a budget of US$ 100 000 per year for Bayesian software, an institution would need to treat ≥41 patients with vancomycin for at least 48 hours to break even.
There are significant institutional cost benefits using two-sample AUC or single-sample Bayesian methods over trough dosing, even after accounting for the annual costs of Bayesian programs. The potential to decrease rates of AKI, improve clinical outcomes and reduce costs to the institution strongly warrants consideration of improved dosing methods for vancomycin.
与万古霉素谷浓度相比,时间-浓度曲线下面积(AUC)指导的给药方案能更好地估计暴露量。虽然已经报道了临床获益,但 AUC 指导给药方案的成本尚不确定。本研究的目的是量化单次样本贝叶斯或双样本 AUC 策略与谷浓度指导给药相比的成本。
采用决策树从机构角度进行成本效益分析,以建立模型,计算 48 小时至 21 天以上万古霉素给药相关急性肾损伤(AKI)的概率和成本。成本包括万古霉素浓度、贝叶斯软件和 AKI 住院费用,概率来自原始文献。通过单向和概率敏感性分析评估稳健性。
在基本模型中,与谷浓度相比,双样本 AUC 给药方案平均为每位患者节省 846 美元,与谷浓度相比,单样本贝叶斯 AUC 给药方案平均为每位患者节省 2065 美元。这意味着每年与谷浓度相比,双样本和单样本贝叶斯方法分别节省 846810 美元和 2065720 美元,假设每年有 1000 例万古霉素治疗患者。假设每年用于贝叶斯软件的预算为 10 万美元,机构需要治疗至少 48 小时的 41 名以上万古霉素患者才能收支平衡。
与谷浓度相比,即使考虑到贝叶斯方案的年度成本,使用双样本 AUC 或单样本贝叶斯方法也具有显著的机构成本效益。降低 AKI 发生率、改善临床结局和降低机构成本的潜力强烈表明,需要考虑改进万古霉素的给药方法。