阿利克伦/氢氯噻嗪单片联合治疗阿利克伦无应答者的疗效。

Georg Nickenig, Vladimir Simanenkov, Giuseppe Lembo, Pablo Rodriguez, Thomas Salko, Shannon Ritter, Jack Zhang
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引用次数: 27

摘要

目的:评估直接肾素抑制剂阿利克伦和氢氯噻嗪(HCT)单片联合治疗高血压和阿利克伦单药治疗血压反应不足(阿利克伦300mg 4周后平均坐位舒张压[msDBP] > 90和<或= 110 mmHg)的患者的疗效、安全性和耐受性。方法:在这项研究中,880例高血压患者对阿利克伦单药治疗血压反应不足,随机分为每日1次,双盲治疗,阿利克伦/HCT 300/ 25mg或300/12.5 mg单药联合治疗,或阿利克伦300 mg单药治疗。在第8周终点,对意向治疗人群的平均坐位收缩压/舒张压(msSBP/DBP)从基线的最小二乘平均变化进行分析。结果:Aliskiren/HCT 300/ 25mg和300/12.5 mg比单独使用Aliskiren 300 mg (8.0/7.4 mmHg;结论:在对阿利克伦300 mg单药治疗无反应的患者中,阿利克伦/HCT单药联合治疗可提供临床显著的额外血压降低和改善的血压控制率。
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Efficacy of aliskiren/hydrochlorothiazide single-pill combinations in aliskiren non-responders.

Objectives: To evaluate the efficacy, safety and tolerability of a single-pill combination of the direct renin inhibitor aliskiren and hydrochlorothiazide (HCT) in patients with hypertension and an inadequate BP response to aliskiren monotherapy (mean sitting diastolic BP [msDBP] > 90 and < or = 110 mmHg following 4 weeks of aliskiren 300 mg).

Methods: In this study, 880 patients with hypertension and an inadequate BP response to aliskiren monotherapy were randomized to once-daily, double-blind treatment with a single-pill combination of aliskiren/HCT 300/25 mg or 300/12.5 mg, or aliskiren 300 mg monotherapy. At the week 8 endpoint, least-squares mean changes in mean sitting systolic/diastolic BP (msSBP/DBP) from baseline were analyzed for the intent-to-treat population.

Results: Aliskiren/HCT 300/25 mg and 300/12.5 mg provided significantly greater msSBP/DBP reductions from baseline (15.9/11.0 mmHg and 13.5/10.5 mmHg, respectively) than aliskiren 300 mg alone (8.0/7.4 mmHg; both p<0.001). Rates of BP control (<140/90 mmHg) were significantly higher with aliskiren/HCT 300/25 mg (60.2%) and 300/12.5 mg (57.9%) than with aliskiren 300 mg alone (40.9%; both p<0.001). Aliskiren/HCT single-pill combination treatment showed similar tolerability to aliskiren monotherapy.

Conclusions: Aliskiren/HCT single-pill combinations provide clinically significant additional BP reductions and improved BP control rates over aliskiren alone in patients who are non-responsive to aliskiren 300 mg monotherapy.

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