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血管紧张素受体阻滞剂(ARB)/钙通道阻滞剂与 HCTZ 的联合用药与 HCTZ 最大推荐剂量的 ARB 相比在 2 期高血压患者中的应用:依福地平与缬沙坦治疗 2 期收缩期高血压(EXALT)研究。

Combination angiotensin-receptor blocker (ARB)/calcium channel blocker with HCTZ vs the maximal recommended dose of an ARB with HCTZ in patients with stage 2 hypertension: the exforge as compared to losartan treatment in stage 2 systolic hypertension (EXALT) study.

机构信息

Pacific Heart Institute, Santa Monica, CA 90404, USA.

出版信息

J Clin Hypertens (Greenwich). 2011 Aug;13(8):588-97. doi: 10.1111/j.1751-7176.2011.00492.x. Epub 2011 Jul 14.

Abstract

This study compared the efficacy and safety of combination angiotensin-receptor blocker (ARB)/calcium-channel blocker (CCB) with hydrochlorothiazide (valsartan/amlodipine/HCTZ 160/5/2mg) vs maximal available combination doses of an ARB with HCTZ (losartan/HCTZ 100/25 mg) in the management of stage 2 hypertension. After 1 to 2 weeks of antihypertensive drug washout, patients with a mean sitting systolic blood pressure (MSSBP) of ≥ 160 mm Hg and <200 mm Hg were randomized to valsartan/amlodipine 160/5 mg (n = 241) or losartan 100 mg (n = 247). At week 3, HCTZ 25 mg was added to both treatments. The primary end point, reduction in MSSBP from baseline to week 6, was significantly greater in the valsartan/amlodipine group than in the losartan group (least-squares [LS] mean change, -31.8 mm Hg vs -26.4 mm Hg; P<.001). Additional reductions occurred after titrating to 320/10/25 mg at week 6 in the valsartan/amlodipine group and switching from losartan/HCTZ to valsartan/amlodipine/HCTZ (week 6, 160/5/25 mg; week 9, 320/10/25 mg) in the losartan group. Achievement of blood pressure <140/90 mm Hg also favored the valsartan/amlodipine group. Dizziness was the only adverse event reported in >5% of patients (5.4% valsartan/amlodipine group, 3.6% losartan group). Moderate doses of an ARB/CCB combination with HCTZ reduced blood pressure more effectively than the maximal dose of an ARB with HCTZ.

摘要

这项研究比较了血管紧张素受体阻滞剂(ARB)/钙通道阻滞剂(CCB)联合氢氯噻嗪(缬沙坦/氨氯地平/HCTZ 160/5/2mg)与 ARB 联合 HCTZ 的最大可用剂量(氯沙坦/HCTZ 100/25mg)在 2 级高血压治疗中的疗效和安全性。在 1 至 2 周的降压药物洗脱期后,平均坐位收缩压(MSSBP)≥160mmHg 且<200mmHg 的患者被随机分为缬沙坦/氨氯地平 160/5mg 组(n=241)或氯沙坦 100mg 组(n=247)。第 3 周时,两组均加用氢氯噻嗪 25mg。缬沙坦/氨氯地平组的主要终点(从基线到第 6 周 MSSBP 的降低)显著大于氯沙坦组(最小二乘[LS]平均变化,-31.8mmHg 与-26.4mmHg;P<.001)。在缬沙坦/氨氯地平组第 6 周时将剂量滴定至 320/10/25mg,以及在氯沙坦组从氯沙坦/HCTZ 转换为缬沙坦/氨氯地平/HCTZ(第 6 周,160/5/25mg;第 9 周,320/10/25mg)后,血压进一步下降。血压<140/90mmHg 的达标率也有利于缬沙坦/氨氯地平组。头晕是唯一报告发生率超过 5%的不良事件(缬沙坦/氨氯地平组 5.4%,氯沙坦组 3.6%)。ARB/CCB 联合 HCTZ 的中等剂量比 ARB 联合 HCTZ 的最大剂量更有效地降低血压。

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