Cesarone M R, De Sanctis M T, Laurora G, Ambrosoli L, Marelli C, Belcaro G
Clinica Pierangeli, Pescara, Italy.
J Cardiovasc Pharmacol. 1994;23 Suppl 4:S65-72.
The effects of trandolapril on 24-h blood pressure in mild-to-moderate hypertensive patients of both sexes were investigated by conventional (clinic) and ambulatory recording in a double-blind study at two dosages, 1 mg (n = 14) and 2 mg (n = 13) once daily for 2 weeks. Both methods of measurement showed significant end-of-treatment decreases (p < 0.01 in all cases) in diastolic and systolic pressure in the 1- and 2-mg groups. Although intergroup differences were not significant, inspection of the mean changes from baseline in the eight 3-h periods constituting the 24-h profile showed that reductions were consistently greater in the 2-mg than in the 1-mg group, by 2 mm Hg diastolic blood pressure and 6 mm Hg systolic blood pressure. Values in the last segment of the placebo washout (46-48 h after the last active dose) showed that these reductions were well maintained, notably in the 2-mg group, with a minimal tendency to drift toward pretreatment levels. No effect was observed on the normal circadian blood pressure rhythm. Both doses were well tolerated. In conclusion, trandolapril is an effective, well-tolerated antihypertensive agent for once-daily dosing at either 1 or 2 mg.
在一项双盲研究中,采用常规(诊室)和动态血压记录方法,对14例男性和14例女性轻至中度高血压患者使用两种剂量(每日1次,1毫克,n = 14;2毫克,n = 13)的群多普利进行为期2周的治疗,观察其对24小时血压的影响。两种测量方法均显示,1毫克组和2毫克组在治疗结束时舒张压和收缩压均显著下降(所有情况p < 0.01)。虽然组间差异不显著,但对构成24小时血压曲线的8个3小时时间段内基线平均变化的检查显示,2毫克组的血压降幅始终大于1毫克组,舒张压下降2毫米汞柱,收缩压下降6毫米汞柱。安慰剂洗脱期最后阶段(最后一剂活性药物后46 - 48小时)的值显示,这些降幅得到了良好维持,尤其是在2毫克组,仅有极小的向治疗前水平回升的趋势。未观察到对正常昼夜血压节律有影响。两种剂量耐受性均良好。总之,群多普利是一种有效且耐受性良好的抗高血压药物,每日服用1毫克或2毫克均可。