Sluiter H E
Department of Medicine, Sint Radboud University Hospital, Nijmegen, The Netherlands.
Drugs. 1987;34 Suppl 3:97-106. doi: 10.2165/00003495-198700343-00023.
In a double-blind study, 128 patients with essential hypertension, refractory to beta-blocker monotherapy, were randomised to 1 of 4 treatment groups. Felodipine 2.5 mg twice daily, 5mg twice daily, 10mg twice daily or matched placebo twice daily were administered in addition to the beta-blocker for 4 weeks. Mean supine blood pressure before randomisation to treatment was 167/104 +/- 20/7mm Hg. After 4 weeks of treatment, supine blood pressures 2 hours after dose were 161/98 +/- 20/10mm Hg (P), 152/92 +/- 23/8mm Hg (felodipine 2.5mg), 142/87 +/- 18/7mm Hg (felodipine 5mg) and 142/86 +/- 17/7mm Hg (felodipine 10mg). The falls in systolic and diastolic blood pressures were significantly greater for all 3 felodipine groups than for placebo. Blood pressure reductions were less marked 14 hours after dosage: 161/100 +/- 20/9mm Hg (P), 160/97 +/- 24/9mm Hg (felodipine 2.5mg), 153/97 +/- 21/11mm Hg (felodipine 5mg), and 157/94 +/- 19/9mm Hg (felodipine 10mg); but the two higher doses of felodipine produced a significantly greater sustained fall in blood pressure than placebo. There was a correlation between the dose of felodipine and its antihypertensive effect. Standing blood pressures were reduced to the same extent as supine measurements. Heart rate was not significantly affected. Bodyweight did not increase during the study. Side effects of felodipine therapy were minor, and mostly attributable to the vasodilatory properties of the drug. Only 4 patients withdrew because of side effects. It is concluded that felodipine is an effective and well tolerated antihypertensive drug, and that 5mg twice daily is a suitable starting dose in hypertensive patients refractory to beta-blocker monotherapy. It may be necessary to increase this dose to 10mg twice daily in selected patients.
在一项双盲研究中,128例对β受体阻滞剂单一疗法无效的原发性高血压患者被随机分为4个治疗组中的1组。除β受体阻滞剂外,分别给予患者每日两次服用非洛地平2.5毫克、5毫克、10毫克或匹配的安慰剂,为期4周。随机分组接受治疗前的平均仰卧血压为167/104±20/7毫米汞柱。治疗4周后,服药后2小时的仰卧血压分别为161/98±20/10毫米汞柱(安慰剂)、152/92±23/8毫米汞柱(非洛地平2.5毫克)、142/87±18/7毫米汞柱(非洛地平5毫克)和142/86±17/7毫米汞柱(非洛地平10毫克)。所有3个非洛地平组的收缩压和舒张压下降幅度均显著大于安慰剂组。服药14小时后血压降低不太明显:161/100±20/9毫米汞柱(安慰剂)、160/97±24/9毫米汞柱(非洛地平2.5毫克)、153/97±21/11毫米汞柱(非洛地平5毫克)和157/94±19/9毫米汞柱(非洛地平10毫克);但两个较高剂量的非洛地平产生的血压持续下降幅度显著大于安慰剂。非洛地平剂量与其降压效果之间存在相关性。站立血压降低程度与仰卧测量相同。心率未受到显著影响。研究期间体重未增加。非洛地平治疗的副作用较小,主要归因于该药物的血管舒张特性。只有4例患者因副作用退出。结论是非洛地平是一种有效且耐受性良好的降压药物,对于对β受体阻滞剂单一疗法无效的高血压患者,每日两次服用5毫克是合适的起始剂量。在部分患者中可能有必要将此剂量增加至每日两次10毫克。