Valsartan/hydrochlorothiazide is effective in hypertensive patients inadequately controlled by valsartan monotherapy.

Jean-Michel Mallion, Renzo Carretta, Peter Trenkwalder, Jean-Felipe Martinez, Andrzej Tykarski, Ivor Teitelbaum, Pascale Oddou, Timothy Fagan
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引用次数: 60

Abstract

Objective: This double-blind parallel-group randomized trial compared the efficacy and safety of fixed combination valsartan 160 mg/hydrochlorothiazide 12.5 mg (Val 160/HCTZ 12.5) once daily (o.d.) and Val 160/hydrochlorothiazide 25 mg (Val 160/HCTZ 25) o.d. vs Val 160 o.d. monotherapy in patients with mild-to-moderate essential hypertension not adequately controlled with valsartan monotherapy.

Method: A total of 2002 patients whose BP was inadequately controlled with 4 weeks of Val 160 mg o.d. monotherapy were randomized to treatment for 8 weeks with Val 160 (n = 666), Val 160/HCTZ 12.5 (n = 670) or Val 160/HCTZ 25 (n = 666).

Results: Active treatment significantly reduced BP in all groups over the 12 weeks of the study (p < 0.001). The greatest reductions were achieved with Val 160/HCTZ 25. Reductions were 10.8, 12.8 and 14.2 mmHg (sitting diastolic blood pressure) and 15.7, 19.4 and 21.8 mmHg (sitting systolic blood pressure), for the Val 160, Val 160/HCTZ 12.5 and Val 160/HCTZ 25 groups, respectively. Responder rates were high in all groups (49%, 62% and 68%). In elderly patients (> or = 65 years) responder rates of 70% were achieved with Val 160/HCTZ 25. All treatments were well tolerated, in all patient groups.

Conclusions: The combination of Val 160 plus HCTZ 12.5 or HCTZ 25 provides effective and well-tolerated treatment in patients inadequately controlled after 4 weeks of monotherapy. In elderly patients a responder rate of 70% was achieved with Val 160/HCTZ 25.

缬沙坦/氢氯噻嗪对缬沙坦单药治疗控制不充分的高血压患者有效。
目的:本双盲平行组随机试验比较缬沙坦160 mg/氢氯噻嗪12.5 mg (Val 160/HCTZ 12.5)每日1次和缬沙坦160/氢氯噻嗪25 mg (Val 160/HCTZ 25)每日1次与缬沙坦160 o.d.单药治疗未充分控制的轻中度原发性高血压患者的疗效和安全性。方法:将2002例接受缬氨酸160 mg单药治疗4周后血压控制不充分的患者随机分为缬氨酸160 (n = 666)、缬氨酸160/HCTZ 12.5 (n = 670)或缬氨酸160/HCTZ 25 (n = 666)治疗8周的患者。结果:在12周的研究中,积极治疗显著降低了所有组的血压(p < 0.001)。在Val 160/HCTZ 25时实现了最大的减少。Val 160、Val 160/HCTZ 12.5和Val 160/HCTZ 25组分别降低10.8、12.8和14.2 mmHg(坐位舒张压)和15.7、19.4和21.8 mmHg(坐位收缩压)。所有组的应答率都很高(49%,62%和68%)。在老年患者(>或= 65岁)中,Val 160/HCTZ 25的应答率达到70%。在所有患者组中,所有治疗均具有良好的耐受性。结论:Val 160联合HCTZ 12.5或HCTZ 25对单药治疗4周后控制不充分的患者提供了有效且耐受性良好的治疗。在老年患者中,Val 160/HCTZ 25的应答率达到70%。
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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