Gerstenblith G, Schulman S P
Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Eur J Clin Pharmacol. 1990;39 Suppl 1:S25-8.
A randomized, double-blind placebo controlled trial was conducted to compare the ability of verapamil and atenolol to induce regression of left ventricular mass in elderly hypertensive patients and the effects of regression on left ventricular filling, ejection fraction, and cardiac volumes. Forty-two individuals over 60 years of age were enrolled in the protocol. Eight of 21 patients assigned to atenolol and 18 to 21 assigned to verapamil achieved blood pressure control with single-agent therapy (p less than 0.05). The addition of chlorthalidone resulted in blood pressure control in the three remaining assigned to verapamil and in ten of the remaining patients assigned to atenolol. In the verapamil group left ventricular mass index decreased from 104 +/- 5 to 85 +/- 5 g/M2, while it was unchanged in the atenolol patients (109 +/- 9 to 112 +/- 10 g/M2). In the patients in whom the left ventricular mass regressed, the peak filling rate increased from 2.42 +/- 0.2 to 3.31 +/- 0.4 EDV/s, while it did not change in the patients who did not experience regression. Furthermore, ejection fraction and cardiac output were maintained in patients who had regression, both at rest and during mild upright bicycle exercise.
进行了一项随机、双盲、安慰剂对照试验,以比较维拉帕米和阿替洛尔在老年高血压患者中诱导左心室质量消退的能力,以及消退对左心室充盈、射血分数和心脏容积的影响。42名60岁以上的个体纳入了该方案。分配到阿替洛尔组的21名患者中有8名,分配到维拉帕米组的21名患者中有18名通过单药治疗实现了血压控制(p<0.05)。加用氯噻酮后,分配到维拉帕米组的其余3名患者和分配到阿替洛尔组的其余10名患者实现了血压控制。在维拉帕米组,左心室质量指数从104±5降至85±5g/M2,而在阿替洛尔组患者中则无变化(109±9至112±10g/M2)。在左心室质量消退的患者中,峰值充盈率从2.42±0.2增至3.31±0.4EDV/s,而在未出现消退的患者中则未改变。此外,在有消退的患者中,无论是静息时还是轻度直立自行车运动时,射血分数和心输出量均得以维持。