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氨氯地平和阿替洛尔治疗轻至中度高血压的多中心安慰剂对照比较

Multicenter placebo-controlled comparison of amlodipine and atenolol in mild to moderate hypertension.

作者信息

de Bruijn B, Cocco G, Tyler H M

机构信息

Ziekenhuis de Stadsmaten, Enschede, The Netherlands.

出版信息

J Cardiovasc Pharmacol. 1988;12 Suppl 7:S107-9. doi: 10.1097/00005344-198812007-00024.

Abstract

Once-daily administration of amlodipine, a long-acting dihydropyridine calcium-channel blocker, and atenolol, a cardioselective beta-adrenoceptor blocking agent, were compared in patients with mild to moderate hypertension in a multicenter placebo-controlled trial. The starting dose of amlodipine was 2.5 mg, with upward adjustment to 5.0 mg and 10.0 mg at 2-weekly intervals; atenolol was started at 50 mg and titrated to 100 mg after 4 weeks. After 8 weeks of treatment, amlodipine and atenolol both reduced blood pressure to a statistically and clinically significant extent at 24 h postdose, and with a small trough-peak (i.e., 24 h to 8 h postdose) difference. Unlike atenolol, amlodipine had no effects on heart rate. The incidence of side effects was low. There were no clinically significant changes in serum lipids with either drug. It is concluded that once-daily dosing with either amlodipine or atenolol significantly reduces blood pressures. Both amlodipine and atenolol were well tolerated.

摘要

在一项多中心安慰剂对照试验中,对长效二氢吡啶类钙通道阻滞剂氨氯地平和心脏选择性β肾上腺素受体阻滞剂阿替洛尔在轻至中度高血压患者中的每日一次给药情况进行了比较。氨氯地平的起始剂量为2.5毫克,每两周向上调整至5.0毫克和10.0毫克;阿替洛尔起始剂量为50毫克,4周后滴定至100毫克。治疗8周后,氨氯地平和阿替洛尔在给药后24小时均使血压降低至具有统计学意义和临床意义的程度,且谷峰(即给药后24小时至8小时)差异较小。与阿替洛尔不同,氨氯地平对心率无影响。副作用发生率较低。两种药物对血脂均无临床显著影响。结论是,每日一次服用氨氯地平或阿替洛尔均可显著降低血压。氨氯地平和阿替洛尔耐受性均良好。

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