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阿利吉仑与缬沙坦联合治疗高血压患者的长期安全性、耐受性及疗效:6个月中期分析

Long-term safety, tolerability and efficacy of aliskiren in combination with valsartan in patients with hypertension: a 6-month interim analysis.

作者信息

Chrysant Steven G, Murray Alexander V, Hoppe Uta C, Dattani Dan, Patel Samir, Hsu Huang, Zhang Jack

机构信息

University of Oklahoma, Oklahoma City, OK 73132, USA.

出版信息

Curr Med Res Opin. 2008 Apr;24(4):1039-47. doi: 10.1185/030079908x280581. Epub 2008 Feb 27.

Abstract

BACKGROUND

Renin-angiotensin system (RAS) blockade with ACE inhibitor and/or angiotensin receptor blocker therapy can lead to increased potassium levels, hence the need to assess dual blockade involving a direct renin inhibitor. Here we report the results of a pre-planned 6-month interim analysis of a long-term, open-label study examining the safety, tolerability and efficacy of the aliskiren/valsartan 300/320-mg combination in patients with hypertension.

METHODS

A total of 601 patients with hypertension (msDBP > or = 90 and < 110 mmHg) received a combination of aliskiren/valsartan 150/160 mg for 2 weeks followed by forced titration to aliskiren/valsartan 300/320 mg once daily for a targeted duration of 52 weeks. Optional hydrochlorothiazide (HCTZ) addition was allowed from week 8 for inadequate BP control (> or = 140/90 mmHg). The primary objective was to assess the safety of combination therapy; potassium elevations were a predefined safety outcome. BP was measured at regular intervals during the study.

RESULTS

At the 6-month cut-off date, 512 patients (85.2%) were still ongoing with study treatment, and 192 patients had received at least one dose of HCTZ add-on during this period. Combination therapy was generally well-tolerated; the most commonly reported adverse events were headache (7.5%), dizziness (7.3%) and nasopharyngitis (7.2%). Ten patients (2.5%) receiving aliskiren/valsartan and two patients (1.0%) receiving aliskiren/valsartan/HCTZ had serum potassium elevations > 5.5 mmol/L. Only one patient (0.2%) exhibited potassium levels > or = 6.0 mmol/L during this period and the patient was treated with aliskiren/valsartan. Mean msSBP/DBP reductions of 22.3/14.4 mmHg were observed at 6-month endpoint (LOCF analysis) and 73.4% of patients achieved BP control (< 140/90 mmHg; LOCF).

CONCLUSIONS

Although lack of an active comparator group is a limitation of the study, our findings show that long-term treatment with the aliskiren/valsartan 300/320-mg combination provided clinically significant BP lowering, was well-tolerated and was associated with a very low rate of potassium elevations in patients with hypertension.

摘要

背景

使用血管紧张素转换酶抑制剂和/或血管紧张素受体阻滞剂进行肾素-血管紧张素系统(RAS)阻断治疗可导致血钾水平升高,因此有必要评估涉及直接肾素抑制剂的双重阻断治疗。在此,我们报告一项长期开放标签研究的预先计划的6个月中期分析结果,该研究旨在考察阿利吉仑/缬沙坦300/320毫克联合用药在高血压患者中的安全性、耐受性和疗效。

方法

总共601例高血压患者(平均坐位舒张压≥90且<110 mmHg)接受阿利吉仑/缬沙坦150/160毫克联合用药治疗2周,随后强制滴定至阿利吉仑/缬沙坦300/320毫克,每日一次,目标疗程为52周。从第8周起,若血压控制不佳(≥140/90 mmHg),可选择加用氢氯噻嗪(HCTZ)。主要目标是评估联合治疗的安全性;血钾升高是一项预先定义的安全结果。在研究期间定期测量血压。

结果

在6个月的截止日期时,512例患者(85.2%)仍在继续接受研究治疗,在此期间有192例患者接受了至少一剂加用的HCTZ。联合治疗总体耐受性良好;最常报告的不良事件为头痛(7.5%)、头晕(7.3%)和鼻咽炎(7.2%)。接受阿利吉仑/缬沙坦治疗的10例患者(2.5%)和接受阿利吉仑/缬沙坦/HCTZ治疗的2例患者(1.0%)血清钾升高>5.5 mmol/L。在此期间,仅有1例患者(0.2%)血钾水平≥6.0 mmol/L,该患者接受的是阿利吉仑/缬沙坦治疗。在6个月终点(末次观察结转分析)时,平均坐位收缩压/舒张压降低了22.3/14.4 mmHg,73.4%的患者实现了血压控制(<140/90 mmHg;末次观察结转)。

结论

尽管缺乏活性对照组是本研究的一项局限性,但我们的研究结果表明,阿利吉仑/缬沙坦300/320毫克联合用药长期治疗可使血压显著降低,耐受性良好,且高血压患者血钾升高率极低。

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