Real-world efficacy of fimasartan vs. other angiotensin receptor blockers in combination with calcium channel blockers: a nationwide cohort study.

IF 2.6 Q2 PERIPHERAL VASCULAR DISEASE
Huijin Lee, Chan Soon Park, Bongseong Kim, Tae-Min Rhee, Heesun Lee, Yong-Jin Kim, Kyungdo Han, Hyung-Kwan Kim
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Abstract

Background: The antihypertensive efficacy of fimasartan was assessed based on the transition rate from a combination of calcium channel blockers (CCB) and angiotensin receptor blockers (ARB) to three-drug combination therapy, as compared to other ARBs.

Methods: This nationwide cohort study used data obtained from the Korean National Health Insurance Service database. Patients who had received national health checkups within 2 years prior to January 1, 2017, and were concurrently prescribed ARBs and CCBs for > 30 days during the 6 months from January 1, 2017, to June 30, 2017 were included in the study. Patients were categorized into the 'fimasartan group' (those prescribed fimasartan) and the 'non-fimasartan group' (those prescribed ARBs other than fimasartan). The index date was set as the last day of a 30-day prescription period for ARBs and CCBs, with a subsequent 2.5-year follow-up to observe the potential addition of a third drug, such as beta-blockers or diuretics.

Results: The study included 34,422 patients with a mean age of 60.3 years and 58.3% being male. The fimasartan group constituted 2.7% (n = 928) of the total, and the non-fimasartan group, 97.3% (n = 33,494). During the follow-up period, 38 patients in the fimasartan group (14.3 per 1,000 person-years) and 3,557 patients in the non-fimasartan group (42.8 per 1,000 person-years) required additional antihypertensive medications. After multivariate adjustment for age, sex, diabetes mellitus, dyslipidemia, cancer, heart failure, systolic blood pressure, and diastolic blood pressure, the fimasartan group showed a significantly lower rate of adding a third medication (hazard ratio 2.68, 95% confidence interval 1.95-3.69) compared to that of the non-fimasartan group.

Conclusions: Fimasartan is associated with a lower need for additional antihypertensive drugs compared to other ARBs. This implies its greater effectiveness in hypertension management, potentially enhancing cardiovascular outcomes, and minimizing polypharmacy.

菲马沙坦与其他血管紧张素受体阻滞剂联合钙通道阻滞剂的实际疗效:一项全国性队列研究。
背景:根据从钙通道阻滞剂(CCB)和血管紧张素受体阻滞剂(ARB)联合疗法到三药联合疗法的转换率,评估了非马沙坦与其他 ARB 相比的降压疗效:这项全国性队列研究使用的数据来自韩国国民健康保险服务数据库。在 2017 年 1 月 1 日至 2017 年 6 月 30 日的 6 个月期间,接受过国民健康检查且同时服用 ARB 和 CCBs 超过 30 天的患者被纳入研究。患者被分为 "非马沙坦组"(处方为非马沙坦的患者)和 "非马沙坦组"(处方为非马沙坦以外的 ARBs 的患者)。指标日期设定为 ARB 和 CCB 30 天处方期的最后一天,随后进行 2.5 年的随访,以观察是否可能增加第三种药物,如β-受体阻滞剂或利尿剂:研究共纳入 34422 名患者,平均年龄为 60.3 岁,58.3% 为男性。菲马沙坦组占总数的 2.7%(n = 928),非菲马沙坦组占 97.3%(n = 33 494)。在随访期间,菲马沙坦组有38名患者(每千人年14.3人)和非菲马沙坦组有3557名患者(每千人年42.8人)需要额外服用降压药。在对年龄、性别、糖尿病、血脂异常、癌症、心力衰竭、收缩压和舒张压进行多变量调整后,与非非马沙坦组相比,非马沙坦组患者增加第三种药物的比例显著降低(危险比为2.68,95%置信区间为1.95-3.69):结论:与其他抗高血压药物相比,菲马沙坦需要额外服用的抗高血压药物更少。结论:与其他抗高血压药物相比,菲马沙坦需要额外服用的抗高血压药物更少,这意味着菲马沙坦在高血压管理方面更有效,有可能改善心血管预后,并最大限度地减少多重用药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Hypertension
Clinical Hypertension PERIPHERAL VASCULAR DISEASE-
CiteScore
5.40
自引率
4.80%
发文量
34
审稿时长
6 weeks
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