Institute of Applied Health Research, University of Birmingham, United Kingdom (S.J., S.K.).
Oxford University Hospitals NHS Foundation Trust and University of Oxford, United Kingdom (G.A.F.).
Hypertension. 2022 May;79(5):1122-1131. doi: 10.1161/HYPERTENSIONAHA.121.18726. Epub 2022 Mar 10.
Deprescribing of antihypertensive medications for older patients with normal blood pressure is recommended by some clinical guidelines, where the potential harms of treatment may outweigh the benefits. This study aimed to assess the cost-effectiveness of this approach.
A Markov patient-level simulation was undertaken to model the effect of withdrawing one antihypertensive compared with usual care, over a life-time horizon. Model population characteristics were estimated using data from the OPTiMISE antihypertensive deprescribing trial, and the effects of blood pressure changes on outcomes were derived from the literature. Health-related quality of life was modeled in Quality-Adjusted Life Years (QALYs) and presented as costs per QALY gained.
In the base-case analysis, medication reduction resulted in lower costs than usual care (mean difference £185), but also lower QALYs (mean difference 0.062) per patient over a life-time horizon. Usual care was cost-effective at £2975 per QALY gained (more costly, but more effective). Medication reduction resulted more heart failure and stroke/TIA events but fewer adverse events. Medication reduction may be the preferred strategy at a willingness-to-pay of £20 000/QALY, where the baseline absolute risk of serious drug-related adverse events was ≥7.7% a year (compared with 1.7% in the base-case).
Although there was uncertainty around many of the assumptions underpinning this model, these findings suggest that antihypertensive medication reduction should not be attempted in many older patients with controlled systolic blood pressure. For populations at high risk of adverse effects, deprescribing may be beneficial, but a targeted approach would be required in routine practice.
一些临床指南建议为血压正常的老年患者停用降压药物,因为治疗的潜在危害可能超过获益。本研究旨在评估这种方法的成本效益。
采用 Markov 患者水平模拟方法,对停用一种降压药与常规治疗进行建模,以终生为时间范围。模型人群特征根据 OPTiMISE 降压药物停药试验的数据进行估计,血压变化对结果的影响来自文献。健康相关生活质量以质量调整生命年(QALY)表示,并呈现为每获得一个 QALY 的成本。
在基础分析中,药物减少的治疗成本低于常规治疗(平均差异为 185 英镑),但终生每个患者的 QALY 也较低(平均差异为 0.062)。常规治疗在每获得一个 QALY 时的成本效益为 2975 英镑(成本更高,但效果更好)。常规治疗导致更多的心衰和卒中/TIA 事件,但更少的不良反应事件。在愿意支付 20000 英镑/QALY 的情况下,药物减少可能是首选策略,此时严重药物相关不良反应的基线绝对风险≥每年 7.7%(而基础分析中为 1.7%)。
尽管该模型的许多假设存在不确定性,但这些发现表明,在血压控制良好的许多老年患者中,不应尝试减少降压药物。对于有发生不良反应高风险的人群,药物减少可能是有益的,但在常规实践中需要采取有针对性的方法。