Cox J P, O'Boyle C A, Mee F, Kelly J, Atkins N, Coakley D, O'Brien E T, O'Malley K
Blood Pressure Clinic, Charitable Infirmary, Dublin 1, Ireland.
J Hum Hypertens. 1988 Jun;2(1):41-7.
To assess the efficacy, tolerability and pharmacokinetics of verapamil in the elderly, ten patients with blood pressure greater than 160/90 mmHg were studied in a randomized double-blind placebo-controlled cross-over trial. Nine patients aged 75 (+/- 4.9) years completed the study. After titration, doses of verapamil varying from 40 to 120 mg (40 mg in four, 80 mg in one and 120 mg in four patients) twice daily for six weeks were taken. Mean (+/- SEM) clinic lying blood pressure was reduced on verapamil from 187 +/- 6.8/100 +/- 4.1 to 167 +/- 4.6/86 +/- 3.1 mmHg, [P less than 0.001). Mean ambulatory blood pressure was reduced from 174 +/- 1.4/95 +/- 1.0 to 169 +/- 1.3/90 +/- 0.8 mmHg, (P less than 0.01). Lying heart rate was significantly reduced but glomerular filtration rate, renal blood flow and mental function, were not altered by treatment. The mean plasma half-life of verapamil was 6.9 +/- 1.1 hours. Side effects were minimal. We conclude that verapamil is an effective blood pressure lowering agent in the elderly.
为评估维拉帕米在老年人中的疗效、耐受性和药代动力学,在一项随机双盲安慰剂对照交叉试验中对10例血压高于160/90 mmHg的患者进行了研究。9例年龄为75(±4.9)岁的患者完成了研究。滴定后,患者每日两次服用剂量为40至120 mg的维拉帕米(4例患者服用40 mg,1例患者服用80 mg,4例患者服用120 mg),持续六周。服用维拉帕米时,平均(±标准误)诊室卧位血压从187±6.8/100±4.1 mmHg降至167±4.6/86±3.1 mmHg,[P<0.001]。平均动态血压从174±1.4/95±1.0 mmHg降至169±1.3/90±0.8 mmHg,(P<0.01)。卧位心率显著降低,但肾小球滤过率、肾血流量和精神功能未因治疗而改变。维拉帕米的平均血浆半衰期为6.9±1.1小时。副作用极小。我们得出结论,维拉帕米是一种有效的老年降压药。