Strathclyde Institute of Pharmacy and Biomedical Science, University of Strathclyde, Glasgow, UK.
Department of Pharmacology, College of Pharmacy, Hawler Medical University, Erbil, Iraq.
J Hypertens. 2019 Jun;37(6):1285-1293. doi: 10.1097/HJH.0000000000002009.
To evaluate the clinical and cost impact of switching angiotensin receptor blockers (ARBs) to angiotensin-converting enzyme inhibitors (ACEIs) in patients with hypertension.
This study used the UK Clinical Practice Research Datalink, linking with the Hospital Episode Statistics (April 2006 to March 2012). Adults with hypertension (n = 470) were followed from the first ARB prescription date to the switching date (preswitching period); then from the switching date to the date when study ended, patient left the dataset or died (postswitching period). Patients were divided into ACEIs-combined (n = 369) and ACEIs-monotherapy (n = 101) groups by whether additional antihypertensive drugs were prescribed with ACEIs in the postswitching period. Proportion of days covered (PDC), clinical outcomes and costs were compared between the preswitching and postswitching periods using a multilevel regression.
Overall, in the postswitching period, there was a significant increase in the proportion of nonadherence (PDC < 80%) (OR: 2.4; 95% CI: 1.6-3.7), but a significant reduction in mean SBP (mean difference: -2.3; 95 CI: -3.4 to 1.2 mmHg) and mean DBP (mean difference: -1.9; 95% CI: -2.6 to -1.2 mmHg). However, these results were only observed in the ACEIs-combined group. There was no postswitching significant difference in either the incidence of individual or composite hypertension-related complications (OR: 0.9; 95% CI: 0.4-2.0). There was a significant reduction in the overall annual medical cost per patient by £329 (95% CI: -534 to -205).
Switching of ARBs to ACEIs monotherapy appeared to be clinically effective and a cost-saving strategy. The observed changes in the ACEIs-combined group are assumed to be related to factors other than the ARBs switching.
评估高血压患者将血管紧张素受体阻滞剂(ARB)转换为血管紧张素转换酶抑制剂(ACEI)的临床和成本影响。
本研究使用了英国临床实践研究数据链接,并与医院病例统计数据(2006 年 4 月至 2012 年 3 月)进行了链接。470 名高血压成年患者从首次 ARB 处方日期到转换日期(转换前时期)开始接受随访;然后从转换日期到研究结束、患者离开数据集或死亡的日期(转换后时期)。根据 ACEI 转换后是否开具了其他降压药物,将患者分为 ACEI 联合治疗组(n=369)和 ACEI 单药治疗组(n=101)。使用多层回归比较转换前和转换后的天数覆盖率(PDC)、临床结局和成本。
总体而言,在转换后时期,不依从率(PDC<80%)显著增加(OR:2.4;95%CI:1.6-3.7),但平均 SBP(平均差值:-2.3;95%CI:-3.4 至 1.2mmHg)和平均 DBP(平均差值:-1.9;95%CI:-2.6 至 -1.2mmHg)显著降低。然而,这些结果仅在 ACEI 联合治疗组中观察到。ACEI 联合治疗组患者的单个或复合高血压相关并发症的发生率在转换后时期没有显著差异(OR:0.9;95%CI:0.4-2.0)。每位患者的年度医疗总费用降低了 329 英镑(95%CI:-534 至-205)。
将 ARB 转换为 ACEI 单药治疗似乎具有临床疗效,并且是一种节省成本的策略。在 ACEI 联合治疗组中观察到的变化被认为与 ARB 转换以外的因素有关。