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Zofenopril or irbesartan plus hydrochlorothiazide in elderly patients with isolated systolic hypertension untreated or uncontrolled by previous treatment: a double-blind, randomized study

机译:未经治疗或先前治疗无法控制的老年单纯收缩期高血压患者中的佐非诺普利或厄贝沙坦加氢氯噻嗪:一项双盲,随机研究

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Objective:To compare zofenopril+hydrochlorothiazide (Z+H) vs. irbesartan+hydrochlorothiazide (I+H) efficacy on daytime SBP in elderly (>65 years) patients with isolated systolic hypertension (ISH), untreated or uncontrolled by a previous monotherapy.Methods:After a 1-week run-in, 230 ISH patients (office SBP140mmHg and DBP<90mmHg+daytime SBP135mmHg and daytime DBP<85mmHg) were randomized double-blind to 18-week treatment with Z+H (30+12.5mg) or I+H (150+12.5mg) once daily, in an international, multicenter study. Z and I doses could be doubled after 6 and 12 weeks, and nitrendipine 20mg added at 12 weeks in nonnormalized patients.Results:In the full analysis set (n=216) baseline-adjusted average (95% confidence interval) daytime SBP reductions after 6 weeks (primary study end point) were similar (P=0.888) with Z+H [7.7 (10.7, 4.6)mmHg, n=107] and I+H [7.9 (10.7, 5.0)mmHg, n=109]. Daytime SBP reductions were sustained during the study, and larger (P=0.028) with low-dose Z+H at study end [16.2 (20.0, 12.5)mmHg vs. 11.2 (14.4, 7.9)mmHg I+H]. Daytime SBP normalization (<135mmHg) rate was similar under Z+H and I+H at 6 and 12 weeks, but more common under Z+H at 18 weeks (68.2 vs. 56.0%, P=0.031). Both drugs equally reduced SBP in the last 6h of the dosing interval and homogeneously reduced SBP throughout the 24h. The proportion of patients reporting drug-related adverse events was low (Z+H: 4.4% vs. I+H: 6.0%; P=0.574).Conclusion:Elderly patients with ISH respond well to both low and high-dose Z or I combined with H.
机译:目的:比较未经治疗或未经单一疗法控制的老年(> 65岁)单纯收缩期高血压(ISH)患者的佐芬普利+氢氯噻嗪(Z + H)与厄贝沙坦+氢氯噻嗪(I + H)在白天SBP的疗效。方法:经过1周的磨合后,将230例ISH患者(办公室SBP140mmHg和DBP <90mmHg +白天SBP135mmHg +白天DBP <85mmHg)随机双盲至18周接受Z + H(30 + 12.5mg)治疗在一项国际多中心研究中,每天一次或一次I + H(150 + 12.5mg)。在非正常化的患者中,第6周和第12周的Z和I剂量可加倍,第12周时可加用尼群地平20mg。结果:在整个分析集中(n = 216),基线校正后平均基线(95%置信区间)白天的SBP降低6周(主要研究终点)与Z + H [7.7(10.7,4.6)mmHg,n = 107]和I + H [7.9(10.7,5.0)mmHg,n = 109]相似(P = 0.888)。在研究期间,白天的SBP降低持续,并且在研究结束时以低剂量Z + H较大(P = 0.028)[16.2(20.0,12.5)mmHg对11.2(14.4,7.9)mmHg I + H]。 Z + H和I + H在6周和12周时的白天SBP正常化率(<135mmHg)相似,但18周在Z + H下的白天SBP归一化率更高(68.2 vs. 56.0%,P = 0.031)。两种药物在给药间隔的最后6小时均能降低SBP,并在整个24小时内均等降低SBP。报告药物相关不良事件的患者比例较低(Z + H:4.4%vs. I + H:6.0%; P = 0.574)。结论:ISH的老年患者对低剂量和高剂量Z或我结合了H。

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