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Bisoprolol/amlodipine combination therapy improves blood pressure control in patients with essential hypertension following monotherapy failure

机译:比索洛尔/氨氯地平联合治疗可改善单药治疗失败后原发性高血压患者的血压控制

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Objective: The efficacy of a bisoprolol/amlodipine fixed-dose combination (FDC) in patients with essential hypertension who had not responded to bisoprolol or amlodipine monotherapy was investigated.Research design and methods: In an 18 week, multicenter, randomized, comparative phase III study (ClinicalTrials.gov identifier: NCT01977794), patients with blood pressure uncontrolled by bisoprolol or amlodipine monotherapy (5mg OD) began treatment with bisoprolol/amlodipine FDC 5/5mg OD. Patients with controlled blood pressure (BP) at week 6/12 continued at current FDC strength, and patients with uncontrolled BP received FDC dose uptitration (maximum dose: 10/10mg). The primary efficacy endpoint was change in systolic blood pressure (SBP) at week 18 versus baseline (corresponding to SBP under monotherapy), and secondary endpoints included change from baseline in SBP after week 6/12 and percentage of BP-controlled patients at week 6, 12 and 18. Safety was assessed by number/types of adverse events (AEs).Results: Two hundred patients were randomized to treatment (100 with uncontrolled BP under bisoprolol and 100 under amlodipine monotherapy). Overall, 196 patients were eligible for analysis. The patient groups displayed similar mean SBP reductions from baseline by study end (bisoprolol monotherapy failure: 25.912.82mmHg reduction; amlodipine monotherapy failure: 24.7 +/- 11.67mmHg reduction; p<0.001 for both). Overall mean SBP decreased by 25.3 +/- 12.25mmHg (p<0.001). Mean heart rate reductions were also observed (bisoprolol monotherapy failure: 6.6 +/- 9.67 bpm reduction; amlodipine monotherapy failure: 11.5 +/- 8.65 bpm reduction; p<0.001 for both). Most patients (83.2%) displayed BP control with bisoprolol/amlodipine 5/5mg at 6 weeks. Treatment was well tolerated at all dose levels; treatment-related AEs (mostly of mild/moderate intensity) were reported by 52.5% of patients, with no severe or serious treatment-related AEs reported. As the study focused on hypertension, total cardiovascular risk was not assessed.Conclusions: Bisoprolol/amlodipine FDC therapy is associated with significant BP improvements in patients with essential hypertension following monotherapy failure.
机译:目的:研究比索洛尔/氨氯地平固定剂量联合疗法(FDC)在对比索洛尔或氨氯地平单药治疗无效的原发性高血压患者中的疗效。研究设计和方法:在18周的多中心,随机,比较III期中研究(ClinicalTrials.gov标识符:NCT01977794),比索洛尔或氨氯地平单药治疗(5mg OD)无法控制血压的患者开始用比索洛尔/氨氯地平FDC 5 / 5mg进行治疗。在第6/12周血压受控(BP)的患者继续以当前的FDC强度接受治疗,而血压未受控的患者接受FDC剂量增加(最大剂量:10 / 10mg)。主要疗效终点是第18周的收缩压(SBP)与基线相比的变化(对应于单一疗法下的SBP),次要终点包括第6/12周后的SBP与基线相比的变化以及第6周时受BP控制的患者的百分比,12和18。通过不良事件(AE)的数量/类型评估安全性。结果:200例患者被随机分配到治疗组(100例在比索洛尔下使用不受控制的BP,100例在氨氯地平单药下使用)。总共有196例患者符合分析条件。在研究结束时,患者组显示出与基线相比平均SBP降低(比索洛尔单药治疗失败:减少25.912.82mmHg;氨氯地平单药治疗失败:减少24.7 +/- 11.67mmHg;两者均p <0.001)。总体平均SBP下降25.3 +/- 12.25mmHg(p <0.001)。还观察到平均心率降低(比索洛尔单药治疗失败:降低6.6 +/- 9.67 bpm;氨氯地平单药治疗失败:降低11.5 +/- 8.65 bpm;两者均p <0.001)。大多数患者(83.2%)在6周时显示出比索洛尔/氨氯地平5 / 5mg的血压控制。在所有剂量水平上,治疗耐受性都很好; 52.5%的患者报告了与治疗相关的AE(大多数为轻度/中度),而未报告严重或严重的与治疗相关的AE。由于该研究集中于高血压,因此未评估总心血管风险。结论:比索洛尔/氨氯地平FDC治疗与单药治疗失败后的原发性高血压患者的BP显着改善有关。

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