van der Wall E E, Kerkkamp H J, Simoons M L, van Rijk P P, Reiber J H, Bom N, Lubsen J C, Lie K I
Eur J Nucl Med. 1986;11(11):428-33. doi: 10.1007/BF00261004.
In 1981, a large, double-blind, randomized trial was started in The Netherlands to evaluate the therapeutic effects of nifedipine and/or metoprolol in patients with unstable angina. This study has been called the Holland Interuniversity Nifedipine/metoprolol Trial (HINT) and required several hundred patients to establish potential therapeutic effects. From December 1982 to January 1984 the effects of nifedipine on left ventricular (LV) performance in a subgroup of 52 HINT patients were studied using radionuclide techniques. All patients (23 on nifedipine, 29 controls) underwent thallium-201 scintigraphy or radionuclide angiography just before and 48 h after the start of experimental medication. The radionuclide angiographic studies were also performed at 1 and 4 h after treatment. Nifedipine did not influence the incidence or disappearance of perfusion defects on the 48-h thallium images. No significant differences in overall LV ejection fraction (EF) were seen at any time between nifedipine-treated patients and controls. However, paired observations in 37 patients showed improvement of LVEF after 48 h in 8 patients on nifedipine and in only 1 control patient. Scintigraphic measurements on admission were not related to clinical outcome after 48 h. Concomitant administration of metoprolol did not influence LVEF in either group. It is concluded that nifedipine improves LVEF after 48 h in a subset of patients with unstable angina without affecting myocardial perfusion. This finding indicates that nifedipine has a predominant effect on afterload reduction in patients with unstable angina. However, early scintigraphic measurements had no significant predictive value for subsequent cardiac events.
1981年,荷兰启动了一项大型双盲随机试验,以评估硝苯地平及/或美托洛尔对不稳定型心绞痛患者的治疗效果。这项研究被称为荷兰大学间硝苯地平/美托洛尔试验(HINT),需要数百名患者来确定潜在的治疗效果。1982年12月至1984年1月,使用放射性核素技术研究了硝苯地平对52名HINT患者亚组左心室(LV)功能的影响。所有患者(23名服用硝苯地平,29名作为对照)在开始试验用药前及用药后48小时接受了铊-201闪烁显像或放射性核素血管造影检查。治疗后1小时和4小时也进行了放射性核素血管造影研究。硝苯地平对48小时铊图像上灌注缺损的发生率或消失情况没有影响。硝苯地平治疗组患者和对照组在任何时间的总体左心室射血分数(EF)均无显著差异。然而,对37名患者的配对观察显示,服用硝苯地平的8名患者在48小时后左心室射血分数有所改善,而对照组只有1名患者。入院时的闪烁显像测量结果与48小时后的临床结果无关。两组中同时服用美托洛尔均不影响左心室射血分数。得出的结论是,硝苯地平可使一部分不稳定型心绞痛患者在48小时后左心室射血分数得到改善,而不影响心肌灌注。这一发现表明,硝苯地平对不稳定型心绞痛患者的后负荷降低有显著作用。然而,早期闪烁显像测量对随后的心脏事件没有显著的预测价值。