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Comparative study of the efficacy of olmesartan/amlodipine vs. perindopril/amlodipine in peripheral blood pressure after missed dose in type 2 diabetes

机译:奥美沙坦/氨氯地平与培哚普利/氨氯地平在2型糖尿病患者错过剂量后对外周血压的疗效比较研究

摘要

Introduction: Combination therapy is needed to control blood pressure (BP) in a large number of hypertensive patients with diabetes mellitus. Adherence to treatment is a major clinical problem; therefore, the time duration of the antihypertensive action of a drug determines BP control when a dose is skipped. Objectives: The aim was to determine whether the fixed-dose combination of olmesartan/amlodipine provides equal efficacy and safety as the perindopril/amlodipine combination when a drug dose is missed. Methods: In this noninferiority trial with a randomized, double-blind, double-dummy parallel group, controlled design, 260 patients received either olmesartan 20-40 mg/amlodipine 5-10 mg or perindopril 4-8 mg/amlodipine 5-10 mg for 24 weeks. The main outcome was the sitting office DBP after 24 weeks of treatment at 48 h from last administration. Results: The olmesartan/amlodipine combination reached noninferiority criteria in reduction of office DBP after 24 weeks of treatment and after the missed dose, compared with the perindopril/amlodipine combination (-11.7 and -10.5 mmHg, respectively). Office SBP and pulse pressure were significantly lower in both groups after 24 weeks of treatment and 48 h after the missed dose, observing a trend to greater SBP reduction in the olmesartan/amlodipine group. Conclusions: The combination olmesartan/amlodipine is safe, well tolerated, and as effective as the combination of perindopril/amlodipine in the control of essential hypertension in patients with diabetes mellitus. A missed dose does not leave the patients unprotected in both treatments; however, a faster control with less dose increment is observed with olmesartan/amlodipine.
机译:简介:在许多高血压糖尿病患者中,需要联合治疗来控制血压(BP)。坚持治疗是一个主要的临床问题。因此,药物的降压作用持续时间决定了跳过剂量时的BP控制。目的:目的是确定当错过药物剂量时,奥美沙坦/氨氯地平的固定剂量组合是否与培哚普利/氨氯地平组合提供相同的疗效和安全性。方法:在这项非劣效性试验中,采用随机,双盲,双假平行组,对照设计,有260名患者接受了奥美沙坦20-40 mg /氨氯地平5-10 mg或培哚普利4-8 mg /氨氯地平5-10 mg持续24周。主要结局是上次给药后48小时治疗24周后的就座办公室DBP。结果:与培哚普利/氨氯地平联合治疗(分别为-11.7和-10.5 mmHg)相比,奥美沙坦/氨氯地平联合治疗24周和漏服后达到降低办公室DBP的非劣效标准。在治疗24周后和错过剂量后48小时,两组的办公室SBP和脉压均显着降低,这表明奥美沙坦/氨氯地平组的SBP降低趋势更大。结论:奥美沙坦/氨氯地平联合用药与培哚普利/氨氯地平联合用药在控制糖尿病原发性高血压中安全,有效。错过剂量并不能使患者在两种治疗中均不受保护;但是,使用奥美沙坦/氨氯地平观察到更快的控制且剂量增加较少。

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