Russian Cardiology Scientific-Industrial Complex, Moscow, Russia.
Adv Ther. 2012 Feb;29(2):134-47. doi: 10.1007/s12325-011-0095-0. Epub 2012 Jan 20.
As several international guidelines on hypertension have now recommended, single-pill/fixed-dose combination antihypertensive therapies may be particularly beneficial as first-line therapy in high-risk patients, in whom more rapid and pronounced blood pressure (BP) control is desired. Upon the single-pill combination of amlodipine and valsartan becoming available, the authors conducted this international, observational study to evaluate its efficacy and safety in a real-life practice setting.
This prospective, open-label, postmarketing surveillance study enrolled adults with arterial hypertension (systolic BP >140 mmHg and/or diastolic BP >90 mmHg) who were prescribed antihypertensive therapy with single-pill combination amlodipine/valsartan 5/80, 5/160, or 10/160 mg once daily. Patients were observed over a 3-month period (12 weeks) with approximately monthly intervals between clinic visits.
A total of 8336 patients completed all study visits and were included in the efficacy analysis. Mean age was 54.7 years and 83.4% of patients had received prior antihypertensive therapy. BP reductions were dose related. Overall, mean BP was reduced from 165.0/99.3 mmHg at baseline to 128.7/80.4 mmHg at 12 weeks (36.3/18.9 mmHg; P<0.0001). The magnitude of BP reduction rose with increasing severity of baseline BP. Control of BP (<140/90 mmHg) was achieved in 77.7% of patients. Efficacy was consistent in subgroups of patients with comorbidities and regardless of whether patients were previously treated with monotherapy or combination therapy. Adverse events were reported in 5.3% of patients. The incidence of edema declined from 10.4% at baseline to 8.5% at study end.
Single-pill combination amlodipine/valsartan safely and effectively reduced BP across all hypertension grades and allowed the vast majority of patients to achieve BP goals.
由于现在有几项国际高血压指南建议,单药/固定剂量复方降压治疗可能特别有益于高危患者的一线治疗,因为这些患者希望更快更明显地控制血压。氨氯地平-缬沙坦单片复方制剂上市后,作者进行了这项国际性、开放性、上市后监测研究,以评估其在真实临床实践中的疗效和安全性。
这项前瞻性、开放性、上市后监测研究纳入了患有高血压(收缩压>140mmHg 和/或舒张压>90mmHg)的成年人,他们接受了每日一次单药/固定剂量复方氨氯地平-缬沙坦 5/80、5/160 或 10/160mg 的降压治疗。患者在 3 个月的观察期(12 周)内,大约每月就诊一次。
共有 8336 例患者完成了所有研究访视并纳入疗效分析。平均年龄为 54.7 岁,83.4%的患者曾接受过降压治疗。血压降低与剂量相关。总体而言,平均血压从基线时的 165.0/99.3mmHg 降至 12 周时的 128.7/80.4mmHg(降低 36.3/18.9mmHg;P<0.0001)。随着基线血压严重程度的增加,血压降低幅度增大。77.7%的患者血压控制在<140/90mmHg。在有合并症的患者亚组和既往接受单药或联合治疗的患者中,疗效一致。5.3%的患者报告了不良事件。水肿的发生率从基线时的 10.4%降至研究结束时的 8.5%。
单药/固定剂量复方氨氯地平-缬沙坦安全有效地降低了所有高血压分级的血压,使绝大多数患者达到了血压目标。