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坎地沙坦酯32毫克与氢氯噻嗪25毫克联合治疗可产生各成分的完全相加降压效果:一项在初级保健机构开展的随机、双盲、平行组研究。

Combination therapy with candesartan cilexetil 32 mg and hydrochlorothiazide 25 mg provides the full additive antihypertensive effect of the components: A randomized, double-blind, parallel-group study in primary care.

作者信息

Edes Istvan

机构信息

DEOEC Institute of Cardiology, Debrecen, Hungary.

出版信息

Clin Drug Investig. 2009;29(5):293-304. doi: 10.2165/00044011-200929050-00002.

Abstract

BACKGROUND AND OBJECTIVE

Fixed-combination tablets of candesartan (orally administered as the pro-drug candesartan cilexetil and hereafter referred to as candesartan) and hydrochlorothiazide (HCTZ) 8/12.5 mg and 16/12.5 mg are effective and well tolerated. However, some patients require higher doses to attain target blood pressure, and combination tablets containing candesartan and HCTZ at the upper end of their respective dose ranges are now being developed. This study aimed to assess the antihypertensive effect and tolerability of the combination of candesartan 32 mg and HCTZ 25 mg versus candesartan 32 mg monotherapy, HCTZ 25 mg monotherapy, and placebo.

METHODS

This was a randomized, double-blind, parallel-group study, with 8 weeks of follow-up, carried out in primary-care outpatients. 1524 men or women (age 20-80 years) with mild to moderate primary hypertension and sitting diastolic blood pressure (DBP) 90-114 mmHg after 4 weeks' single-blind placebo treatment were included in the study. Candesartan/HCTZ 32/25 mg combination therapy, candesartan 32 mg monotherapy, HCTZ 25 mg monotherapy, and placebo, allocated in a 5 : 5 : 5 : 1 ratio, were administered once daily. The main outcome measure was adjusted (analysis of covariance) mean reductions in systolic blood pressure (SBP) and DBP.

RESULTS

Mean reductions in SBP and DBP were significantly greater with candesartan/HCTZ 32/25 mg (21/14 mmHg) than with candesartan 32 mg (13/9 mmHg), HCTZ 25 mg (12/8 mmHg) or placebo (4/3 mmHg) [p < 0.001 for all comparisons]. The proportion of patients with controlled blood pressure (SBP <140 mmHg and DBP <90 mmHg) at the end of the study was also significantly greater in the candesartan/HCTZ 32/25 mg group (63%) than in the other treatment groups (p < 0.001 for all comparisons). All study treatments were generally well tolerated.

CONCLUSION

The antihypertensive effect of candesartan/HCTZ 32/25 mg represents fully additive contributions from each of its components, and is generally well tolerated in patients with mild to moderate primary hypertension. This combination adds to the treatment options for improving blood pressure control in patients with hypertension.

摘要

背景与目的

坎地沙坦(以其前体药物坎地沙坦酯口服给药,以下简称坎地沙坦)与氢氯噻嗪(HCTZ)的固定复方片剂8/12.5毫克和16/12.5毫克有效且耐受性良好。然而,一些患者需要更高剂量才能达到目标血压,目前正在研发坎地沙坦和HCTZ在各自剂量范围上限的复方片剂。本研究旨在评估坎地沙坦32毫克与HCTZ 25毫克联合用药相对于坎地沙坦32毫克单药治疗、HCTZ 25毫克单药治疗及安慰剂的降压效果和耐受性。

方法

这是一项在基层医疗门诊患者中进行的随机、双盲、平行组研究,随访8周。纳入1524名年龄20 - 80岁、患有轻度至中度原发性高血压且在4周单盲安慰剂治疗后坐位舒张压(DBP)为90 - 114 mmHg的男性或女性。坎地沙坦/HCTZ 32/25毫克联合治疗、坎地沙坦32毫克单药治疗、HCTZ 25毫克单药治疗及安慰剂按5 : 5 : 5 : 1的比例分配,每日给药一次。主要观察指标为经调整(协方差分析)的收缩压(SBP)和DBP的平均降低值。

结果

坎地沙坦/HCTZ 32/25毫克组SBP和DBP的平均降低值(21/14 mmHg)显著大于坎地沙坦32毫克组(13/9 mmHg)、HCTZ 25毫克组(12/8 mmHg)或安慰剂组(4/3 mmHg)[所有比较p < 0.001]。研究结束时血压得到控制(SBP < 140 mmHg且DBP < 90 mmHg)的患者比例在坎地沙坦/HCTZ 32/25毫克组(63%)也显著高于其他治疗组(所有比较p < 0.001)。所有研究治疗一般耐受性良好。

结论

坎地沙坦/HCTZ 32/25毫克的降压效果代表了其各成分的完全相加作用,在轻度至中度原发性高血压患者中一般耐受性良好。这种联合用药增加了改善高血压患者血压控制的治疗选择。

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