首页> 外文期刊>Current medical research and opinion >Effect of eprosartan and enalapril in the treatment of black hypertensive patients: subgroup analysis of a 26-week, double-blind, multicentre study. Eprosartan Multinational Study Group.
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Effect of eprosartan and enalapril in the treatment of black hypertensive patients: subgroup analysis of a 26-week, double-blind, multicentre study. Eprosartan Multinational Study Group.

机译:依普罗沙坦和依那普利在治疗黑人高血压患者中的作用:一项为期26周,双盲,多中心研究的亚组分析。依普罗沙坦跨国研究组。

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A double-blind comparator study was performed in 528 hypertensive patients [baseline sitting diastolic blood pressure (SitDBP) 95-114 mmHg]. The primary objective was to compare the incidence of drug-related cough in patients treated with enalapril and eprosartan. The secondary objective was to compare antihypertensive efficacy between treatments. This paper reports the results of a prespecified subgroup analysis performed in the 40 black patients recruited into the study. Eprosartan was titrated from 200 mg b.i.d. to 300 mg b.i.d. and enalapril from 5 mg o.d. to 20 mg o.d. over 12 weeks. Hydrochlorothiazide (HCTZ) 12.5-25 mg o.d. could be added where required to the treatment for the final six weeks of the titration phase if SitDBP > or = 90 mmHg. Patients received the maximum titrated dosage during the maintenance phase. In the study overall, the incidence of cough at monotherapy endpoint was significantly higher in the enalapril-treated group than in the eprosartan-treated group (p = 0.018). This trend was reflected in the black subgroup but the numbers were too small to confirm significance. At study endpoint the mean change in SitDBP was -10.5 +/- 1.9 mmHg and -9.6 +/- 2.4 mmHg for eprosartan-treated and enalapril-treated patients, respectively. The mean change in SitSBP for eprosartan-treated black patients was -18.8 +/- 3.5 mmHg and for enalapril-treated patients was -10.5 +/- 3.7 mmHg. The black subpopulation mirrored the response of the study as a whole. Both treatments lowered BP with a further reduction evident following the addition of HCTZ at week 18. In conclusion, eprosartan is effective and appears to be safe in black hypertensive patients. The combination of eprosartan and HCTZ was also well tolerated and provided additional efficacy in those patients not responding to eprosartan alone. The incidence of treatment-associated cough in the black subgroup was low, but there were no apparent differences between treatment groups.
机译:在528名高血压患者中进行了双盲比较研究[基线坐位舒张压(SitDBP)95-114 mmHg]。主要目的是比较依那普利和依普罗沙坦治疗的患者中与药物有关的咳嗽发生率。次要目标是比较治疗之间的抗高血压功效。本文报告了对纳入研究的40名黑人患者进行的预先指定的亚组分析的结果。依普罗沙坦从200 mg b.i.d.滴定。至300 mg b.i.d.和依那普利5毫克/天至20 mg o.d.超过12周。氢氯噻嗪(HCTZ)12.5-25 mg o.d.如果SitDBP>或= 90 mmHg,则可以在滴定阶段最后六周的治疗中添加所需的溶液。患者在维持阶段接受最大滴定剂量。在整个研究中,依那普利治疗组的单药治疗终点咳嗽发生率显着高于依普罗沙坦治疗组(p = 0.018)。这种趋势反映在黑色亚组中,但数量太少,无法确定其重要性。在研究终点,依普罗沙坦治疗组和依那普利治疗组的SitDBP平均变化分别为-10.5 +/- 1.9 mmHg和-9.6 +/- 2.4 mmHg。依普罗沙坦治疗的黑人患者的SitSBP平均变化为-18.8 +/- 3.5 mmHg,依那普利治疗的患者为-10.5 +/- 3.7 mmHg。黑色亚群反映了整个研究的反应。两种疗法均在第18周添加HCTZ后降低了BP,并进一步降低了血压。总之,依普罗沙坦有效,对黑人高血压患者似乎是安全的。依普罗沙坦和HCTZ的组合也被很好地耐受,并且在那些对依普罗沙坦单独无反应的患者中提供了额外的疗效。黑色亚组中与治疗相关的咳嗽的发生率较低,但各治疗组之间无明显差异。

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