固定剂量厄贝沙坦/氢氯噻嗪早期与晚期滴定的有效性和安全性:ACTUAL研究。

Xavier Girerd, David Rosenbaum, Joseph Aoun
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引用次数: 2

摘要

高血压管理指南建议每4-6周逐步滴定降压药。我们比较了厄贝沙坦/氢氯噻嗪治疗10周后早期和晚期滴定的疗效和安全性。单药治疗未控制的高血压患者随机分为两组。早期滴药组(E),患者接受厄贝沙坦/氢氯噻嗪150/12.5 mg,持续2周;未控制的患者在第2周和第6周时将剂量增加到300/25 mg。晚期滴注组(L),患者接受150/12.5 mg,持续6周;未控制的患者在第6周(W6)将剂量增加到300/25 mg。采用协方差分析模型研究各组患者基线至第10周平均收缩压(SBP)和舒张压(DBP)的变化。使用Fisher精确检验比较W10组间对照患者的百分比。在来自14个国家的833例患者中,意向治疗人群包括795例(平均年龄58 +/- 12岁,女性60%,肥胖38%,糖尿病22%)。在w6时,平均收缩压下降为:E - 28.8 mmHg vs L - 26.3 mmHg (p = 0.02)。在W10时,有相似的平均收缩压下降:E - 29.5 mmHg vs L- 31.0 mmHg (p = 0.14)。W10控制率分别为58% (E)和64% (L), p = 0.06。E组严重不良事件发生率更高(2.5% vs 0.7%, p= 0.044)。早期和晚期滴药方案的降压和控制率相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of early versus late titration of fixed-dose irbesartan/hydrochlorothiazide: ACTUAL study.

Hypertension management guidelines recommend titrating antihypertensive drugs stepwise every 4-6 weeks.We compared efficacy and safety of early versus late titration after 10 weeks' treatment with irbesartan/hydrochlorothiazide. Hypertensive patients uncontrolled on monotherapy were randomized into two groups. In the early titration group (E), patients received irbesartan/hydrochlorothiazide 150/12.5 mg for 2 weeks; uncontrolled patients were up-titrated to 300/25 mg at weeks 2 and 6. In the late titration group (L), patients received 150/12.5 mg for 6 weeks; uncontrolled patients were up-titrated to 300/25 mg at week 6 (W6). The change of mean systolic (SBP) and diastolic blood pressure (DBP) from baseline to week 10 (W10) were studied using a covariance analysis model. The percentage of controlled patients at W10 was compared between groups using Fisher's exact test. Of 833 patients enrolled from 14 countries, the intent-to-treat (ITT) population included 795 (mean age 58 +/- 12 years, female 60%, obesity 38%, diabetes 22%). AtW6, mean SBP decrease was: E - 28.8 mmHg vs L - 26.3 mmHg (p = 0.02). At W10, there was similar mean SBP decrease: E - 29.5 mmHg vs L- 31.0 mmHg (p = 0.14). The control rate at W10 was 58% (E) and 64% (L), p = 0.06. Serious adverse events were more frequent in E (2.5% vs 0.7%, p= 0.044). Both early and late titration regimens provide similar BP decrease and control rate.

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