首页> 外文期刊>Advances in therapy. >Effective and safe reduction of blood pressure with the combination of amlodipine 5 mg and valsartan 160 mg in hypertensive patients not controlled by calcium channel blocker monotherapy.
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Effective and safe reduction of blood pressure with the combination of amlodipine 5 mg and valsartan 160 mg in hypertensive patients not controlled by calcium channel blocker monotherapy.

机译:在不受钙通道阻滞剂单一疗法控制的高血压患者中,氨氯地平5 mg和缬沙坦160 mg的组合可安全有效地降低血压。

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INTRODUCTION: The addition of an angiotensin II receptor blocker to calcium channel blocker-based antihypertensive therapy may be associated with enhanced efficacy and reduced risk of adverse events. METHODS: This 8-week, open-label, single-arm trial evaluated the efficacy and tolerability of the combination of amlodipine and valsartan in patients not responding adequately to treatment with amlodipine or felodipine alone. Patients aged >/=18 years with moderate essential hypertension (defined as mean sitting systolic blood pressure [MSSBP] >/=160 and <180 mmHg) were treated for 4 weeks with once-daily amlodipine 5 mg or felodipine 5 mg. At week 4, patients not adequately responding were treated for an additional 4 weeks with once-daily amlodipine 5 mg plus valsartan 160 mg. Of 214 patients treated for 4 weeks with amlodipine 5 mg or felodipine 5 mg, 181 failed to achieve MSSBP <140 mmHg. These non-responders were treated for an additional 4 weeks with amlodipine 5 mg and valsartan 160 mg. RESULTS: A clinically and statistically significant additional reduction in MSSBP of 13.1 mmHg (95% confidence interval [CI]: 11.4, 14.7; P<0.0001) and a mean sitting diastolic blood pressure of 5.3 mmHg (95% CI: 4.3, 6.3; P<0.0001) were observed. Of patients treated with amlodipine 5 mg and valsartan 160 mg, 51.1% achieved target blood pressure levels (<140/90 mmHg) after 4 weeks. Adverse event rates were low in both treatment phases, and most were mild or moderate in severity. CONCLUSION: The combination of amlodipine/valsartan was effective and well tolerated.
机译:简介:在基于钙通道阻滞剂的抗高血压治疗中添加血管紧张素II受体阻滞剂可能与提高疗效和减少不良事件的风险有关。方法:这项为期8周的开放性单臂试验评估了氨氯地平和缬沙坦联合治疗对单独使用氨氯地平或非洛地平治疗无效的患者的疗效和耐受性。年龄> / = 18岁的中度原发性高血压(定义为平均坐位收缩压[MSSBP]> / = 160且<180 mmHg),每天用氨氯地平5 mg或非洛地平5 mg治疗4周。在第4周,每天反应不佳的患者再用氨氯地平5 mg加缬沙坦160 mg再次治疗4周。用氨氯地平5 mg或非洛地平5 mg治疗4周的214名患者中,有181名未能达到MSSBP <140 mmHg。用氨氯地平5 mg和缬沙坦160 mg将这些无反应者再治疗4周。结果:在临床和统计学上,MSSBP进一步降低了13.1 mmHg(95%置信区间[CI]:11.4,14.7; P <0.0001),平均舒张压坐位血压为5.3 mmHg(95%CI:4.3、6.3; P <0.0001)。用氨氯地平5 mg和缬沙坦160 mg治疗的患者在4周后达到了目标血压水平(<140/90 mmHg)。在两个治疗阶段,不良事件发生率均较低,严重程度大多为轻度或中度。结论:氨氯地平/缬沙坦联合使用有效且耐受性好。

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