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首页> 外文期刊>Blood Pressure Monitoring >Use of 24-h ambulatory blood pressure monitoring to assess blood pressure control: a comparison of olmesartan medoxomil and amlodipine besylate.
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Use of 24-h ambulatory blood pressure monitoring to assess blood pressure control: a comparison of olmesartan medoxomil and amlodipine besylate.

机译:使用24小时动态血压监测来评估血压控制:奥美沙坦medoxomil与苯磺酸氨氯地平的比较。

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OBJECTIVE: Olmesartan medoxomil is an angiotensin II receptor blocker with similar antihypertensive efficacy as the calcium channel blocker amlodipine besylate in patients with mild-to-moderate hypertension. In addition to a drug's ability to lower blood pressure, the effectiveness of the agent in enabling patients to achieve specific blood pressure targets is an important clinical consideration. This secondary analysis of a randomized, double-blind study compared the efficacy of olmesartan medoxomil with that of amlodipine besylate in achieving ambulatory blood pressure goals among patients with mild-to-moderate hypertension. METHODS: Following a 4-week placebo run-in, 440 study participants aged >or=18 years were randomized to olmesartan medoxomil (20 mg/day), amlodipine besylate (5 mg/day), or placebo for 8 weeks. The proportion of participants achieving specific systolic and diastolic ambulatory blood pressure goal levels was calculated by dividing the number of participants who had achieved a particular blood pressure goal by the total number of patients in the intent-to-treat population. RESULTS: After 8 weeks of treatment, a mean 24-h ambulatory blood pressure of <130/80 or <130/85 mmHg was achieved by significantly more participants in the olmesartan medoxomil group (18.1 and 30.4%, respectively) than in the amlodipine besylate (7.0 and 14.0%, respectively) or placebo (1.9% for both) groups. The target daytime ambulatory blood pressure of <135/85 mmHg was achieved by more participants in the olmesartan medoxomil group than in the amlodipine besylate group (15.8 vs. 5.8%, respectively; P<0.01). CONCLUSION: In a previous publication of the same study, we demonstrated that starting doses of olmesartan medoxomil and amlodipine besylate produced similar mean reductions in blood pressure. In this subanalysis of the blood pressure data from that primary publication, however, olmesartan medoxomil therapy was shown to result in a greater proportion of patients achieving specific ambulatory blood pressure goals than therapy with amlodipine besylate. As blood pressure goal attainment may be of more direct clinical relevance than numerical blood pressure lowering, the achievement of blood pressure goals should be a key efficacy parameter assessed in clinical trials of antihypertensive medications.
机译:目的:奥美沙坦medoxomil是一种血管紧张素II受体阻滞剂,在轻度至中度高血压患者中具有与钙通道阻滞剂氨氯地平苯磺酸盐相似的降压功效。除了药物降低血压的能力外,该药物在使患者能够达到特定血压目标方面的有效性是重要的临床考虑因素。这项对一项随机,双盲研究的二级分析比较了奥美沙坦美多西莫和苯磺酸氨氯地平在轻度至中度高血压患者中实现动态血压目标的功效。方法:在进行了4周的安慰剂磨合后,将440名年龄≥18岁的研究参与者随机分为奥美沙坦medoxomil(20 mg /天),苯磺酸氨氯地平(5 mg /天)或安慰剂8周。通过将达到特定血压目标的参与者人数除以意向治疗人群中的患者总数,即可计算出达到特定的收缩压和舒张性非门诊血压目标水平的参与者比例。结果:治疗8周后,奥美沙坦美多西米组的参与者(分别为18.1和30.4%)比氨氯地平的参与者多得多(分别为<130/80或<130/85 mmHg)苯磺酸盐组(分别为7.0%和14.0%)或安慰剂(两组均为1.9%)。 olmesartan medoxomil组的参与者比苯磺酸氨氯地平组的白天白天目标门诊血压<135/85 mmHg多(分别为15.8和5.8%; P <0.01)。结论:在同一项研究的先前出版物中,我们证明了奥美沙坦美多西米和苯磺酸氨氯地平的起始剂量可产生相似的平均血压降低。但是,在该主要出版物的血压数据的亚分析中,与苯磺酸氨氯地平治疗相比,奥美沙坦美多西莫疗法可导致更大的患者达到特定的门诊血压目标。由于达到血压目标可能比降低数字血压更直接的临床相关性,因此,达到血压目标应该是抗高血压药物临床试验中评估的关键功效参数。

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