首页> 外文期刊>American journal of cardiovascular drugs: drugs, devices, and other interventions >Clinical experience with perindopril in elderly hypertensive patients : a subgroup analysis of a large community trial.
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Clinical experience with perindopril in elderly hypertensive patients : a subgroup analysis of a large community trial.

机译:培哚普利在老年高血压患者中的临床经验:一项大型社区试验的亚组分析。

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摘要

OBJECTIVE: To evaluate the effectiveness and safety of perindopril in a subgroup of 3010 elderly (>/=65 years) hypertensive patients, who participated in a large US general practice-based community trial. METHODS: All patients received open-label perindopril 4mg once a day for 6 weeks. After 6 weeks the dosage was either maintained (group I) or increased to 8 mg/day (group II) based on the physician's assessment of blood pressure (BP) response. Patients were then followed for another 6 weeks for a total study duration of 12 weeks. RESULTS: Demographic and baseline clinical characteristics revealed a higher proportion of women, longer duration of hypertension and higher baseline systolic BP (SBP) among elderly than young (<65 years, n = 7332) hypertensive patients. A clinically relevant BP reduction of similar magnitude was obtained in elderly and young patients with perindopril monotherapy. At week 12, the mean reduction in BP from baseline was 18.4/8.7mm Hg in the elderly and 17.5/11.3mm Hg in the young. Elderly patients with hypertension not responding adequately to the 4 mg/day dosage at week 6 had a BP reduction of 6.3/3.6mm Hg (group II). Up-titration to an 8 mg/day dosage for another 6 weeks gave an additional 8.9/3.5mm Hg reduction resulting in a total reduction of 15.2/7.1mm Hg from baseline. A similar magnitude of increase in response to up-titration of perindopril was seen in young patients. BP control (<140/90mm Hg) on perindopril monotherapy was achieved in 41.4% of elderly and 51.9% of young patients. In both age groups, up-titration to an 8.0 mg/day dosage in group II patients increased BP control by approximately 5-fold at week 12 (28.2% in the elderly and 36.4% in the young). A similar increased response on BP reduction and BP control (<140/90mm Hg) with up-titration was seen in elderly subgroups of African American and diabetic patients. The 7th Report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure recommended target goal of <130/80mm Hg was achieved with perindopril monotherapy in 15.6% of hypertensive diabetic patients. Perindopril reduced BP effectively and safely in very elderly (>/=75 years) hypertensive patients. Perindopril was well tolerated in elderly patients including high-risk groups. The incidence of cough (7-10%), the most common symptom, was similar in all age groups. The low incidence of postural hypotension (
机译:目的:评估培哚普利在3010例老年(> / = 65岁)高血压患者亚组中的有效性和安全性,这些患者参加了一项基于美国一般实践的大型社区试验。方法:所有患者均接受每天一次开放标签培哚普利4mg治疗,持续6周。 6周后,根据医师对血压(BP)反应的评估,维持剂量(组I)或增加至8 mg /天(组II)。然后,对患者再随访6周,总研究时间为12周。结果:人口统计学和基线临床特征显示,与年轻(<65岁,n = 7332)高血压患者相比,老年人中女性比例更高,高血压持续时间更长,基线收缩压更高(SBP)。培哚普利单药治疗的老年和青年患者的临床相关血压降低幅度相似。在第12周,老年人的BP与基线相比平均下降为18.4 / 8.7mm Hg,年轻人为17.5 / 11.3mm Hg。在第6周对4 mg /天剂量没有充分反应的老年高血压患者的BP降低了6.3 / 3.6mm Hg(第二组)。再滴定至8 mg /天的剂量再持续6周,则可进一步降低8.9 / 3.5mm Hg,从而比基线降低了15.2 / 7.1mm Hg。在年轻患者中,观察到对培哚普利升高反应的增加幅度相似。培哚普利单药治疗的血压控制(<140 / 90mm Hg)在老年患者中占41.4%,在年轻患者中占51.9%。在这两个年龄组中,第二组患者中调高剂量至8.0 mg / day的剂量在第12周时都将BP控制提高了约5倍(老年人为28.2%,年轻人为36.4%)。在非洲裔美国人和糖尿病患者的老年亚组中,随着滴定,对血压降低和血压控制(<140 / 90mm Hg)的响应增加相似。全国预防,检测,评估和治疗高血压联合委员会的第七次报告建议在15.6%的高血压糖尿病患者中使用培哚普利单一疗法可达到<130 / 80mm Hg的目标。培哚普利可有效,安全地降低老年(> / = 75岁)高血压患者的血压。培哚普利对包括高危人群在内的老年患者耐受良好。在所有年龄组中,最常见的症状是咳嗽的发生率(7-10%)相似。在老年人和非常老年人中观察到的姿势性低血压的发生率较低(

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