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首页> 外文期刊>Drugs and aging >Antihypertensive treatment in elderly patients aged 75 years or over: a 24-week study of the tolerability of candesartan cilexetil in relation to hydrochlorothiazide.
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Antihypertensive treatment in elderly patients aged 75 years or over: a 24-week study of the tolerability of candesartan cilexetil in relation to hydrochlorothiazide.

机译:75岁或75岁以上老年患者的降压治疗:坎地沙坦酯对氢氯噻嗪的耐受性为期24周的研究。

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OBJECTIVE: To assess the safety and tolerability of the AT1-receptor blocker candesartan cilexetil in relation to the diuretic hydrochlorothiazide (HCTZ) in elderly patients. DESIGN AND SETTING: A multicentre, double-blind, randomised, parallel group study. 32 general practice centres and 3 hospital centres in Denmark and Finland participated in this study. Patients: 185 patients aged > or =75 years with mean sitting diastolic blood pressure (DBP) of 95 to 114mm Hg. INTERVENTIONS: After a placebo run-in period of 4 to 8 weeks, patients were randomised to once daily treatment with candesartan cilexetil 8mg or HCTZ 12.5mg for 24 weeks. In both treatment groups the dosage could be doubled after > or =2 weeks [according to blood pressure (BP) response] and, if necessary, subsequently decreased if the higher dosage was poorly tolerated. MAIN OUTCOME MEASURES: Proportion of patients with at least 1 adverse event; changes in laboratory values, electrocardiogram and BP during the double-blind treatment period. RESULTS: Once daily candesartan cilexetil 8 to 16mg was very well tolerated. The most common adverse events in both treatment groups were dizziness or vertigo and headache. Although the profile of adverse events was generally similar in the 2 treatment groups, it was notable that hypokalaemia and hyperuricaemia were not found in patients treated with candesartan cilexetil but occurred in 8.1 and 6.5%, respectively, of patients treated with HCTZ. At week 24, the adjusted mean changes in sitting DBP (24 hours postdose) from baseline were -12.0mm Hg [95% confidence interval (CI) -1 0.4 to -13.6] in patients treated with candesartan cilexetil and -11.4mm Hg (95% CI -9.3 to -13.6) in patients treated with HCTZ. The difference between treatments in favour of candesartan cilexetil was not statistically significant. CONCLUSIONS: This study shows that antihypertensive treatment with candesartan cilexetil in elderly patients (aged > or =75 years) is well tolerated with a good safety profile and avoids the metabolic adverse effects of diuretic therapy.
机译:目的:评估AT1受体阻滞剂坎地沙坦西酯与利尿剂氢氯噻嗪(HCTZ)在老年患者中的安全性和耐受性。设计与设置:一项多中心,双盲,随机,平行分组研究。丹麦和芬兰的32个普通科中心和3个医院中心参加了这项研究。患者:185岁以上或= 75岁的患者平均舒张压(DBP)为95至114mm Hg。干预措施:安慰剂磨合期4到8周后,患者被随机分配至每天一次接受8 mg坎地沙坦cilexetil或12.5 mg HCTZ的治疗,持续24周。在两个或以上的治疗组中,在≥2周后(根据血压(BP)反应),剂量可以加倍;如果需要,如果耐受性较差,则随后降低剂量。主要观察指标:至少发生1次不良事件的患者所占比例;双盲治疗期间实验室值,心电图和血压的变化。结果:每天一次坎地沙坦酯8至16mg的耐受性非常好。两个治疗组中最常见的不良事件是头晕或眩晕和头痛。尽管在2个治疗组中不良事件的概况通常相似,但值得注意的是,坎地沙坦酯治疗的患者未发现低血钾和高尿酸血症,而HCTZ治疗的患者分别发生了8.1和6.5%。在第24周时,接受坎地沙坦cilexetil和-11.4mm Hg治疗的患者坐姿DBP(给药后24小时)相对于基线的校正后平均变化为-12.0mm Hg [95%置信区间(CI)-1 0.4至-13.6]( HCTZ治疗的患者中95%CI -9.3至-13.6)。支持坎地沙坦酯治疗的治疗之间的差异无统计学意义。结论:这项研究表明,坎地沙坦西拉克汀对老年患者(年龄≥75岁)的抗高血压治疗耐受性良好,安全性良好,并且避免了利尿剂治疗对代谢的不良影响。

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