Eldridge J E, Burdick D C, Jones R H, Hossack K F
Department of Medicine, University of Colorado, Denver.
J Cardiovasc Pharmacol. 1987 Sep;10(3):315-9. doi: 10.1097/00005344-198709000-00010.
Fifteen patients with stable angina participated in a 12-week crossover study to evaluate the efficacy of nifedipine and nitroglycerin patches. There was an initial 2-week drug washout period followed by a 2-week control period when patients received no other antianginal treatment other than sublingual nitroglycerin for relief of angina episodes. At the end of the 2-week control period, exercise performance was assessed with treadmill exercise testing and measurement of oxygen consumption during the final third of the dosing interval. Myocardial perfusion was assessed using thallium scintigraphy with the injection of thallium at 85% of the maximum oxygen consumption. Patients were then randomized to nifedipine or nitroglycerin patches, and the dosage was titrated at weekly intervals according to symptomatic response. The final dose was received for at least 2 weeks. After 4 weeks, patients received the alternate medication. Maximal exercise testing and thallium scintigraphy were repeated after each drug period. Both nifedipine (mean dose, 70 mg/day) and nitroglycerin patches (mean dose, 16 cm/day) significantly reduced the frequency of angina and the consumption of sublingual nitroglycerin. Nifedipine decreased the reversible thallium defect score (49 +/- 29 vs. 28 +/- 26 U, p less than 0.01). Both drugs reduced electrocardiographic evidence of myocardial ischemia at submaximal exercise. Maximal oxygen consumption was not significantly increased by either drug when the test was done during the latter part of the dosing interval. The clinical implications of this study are that the dosage of nifedipine and nitrate patches, based on symptomatic criteria of angina frequency reduction, may not result in objective improvement in exercise performance.
15名稳定型心绞痛患者参与了一项为期12周的交叉研究,以评估硝苯地平和硝酸甘油贴片的疗效。最初有2周的药物洗脱期,随后是2周的对照期,在此期间,患者除了舌下含服硝酸甘油以缓解心绞痛发作外,未接受其他抗心绞痛治疗。在2周对照期结束时,通过跑步机运动试验和在给药间隔最后三分之一时间内测量耗氧量来评估运动能力。使用铊闪烁显像评估心肌灌注,在最大耗氧量的85%时注射铊。然后将患者随机分为硝苯地平组或硝酸甘油贴片组,并根据症状反应每周调整剂量。最终剂量至少服用2周。4周后,患者换用另一种药物。每个药物治疗期后重复进行最大运动试验和铊闪烁显像。硝苯地平(平均剂量,70毫克/天)和硝酸甘油贴片(平均剂量,16厘米/天)均显著降低了心绞痛发作频率和舌下硝酸甘油的使用量。硝苯地平降低了可逆性铊缺损评分(49±29对28±26单位,p<0.01)。两种药物均减少了次极量运动时心肌缺血的心电图证据。当在给药间隔后期进行试验时,两种药物均未显著增加最大耗氧量。本研究的临床意义在于,基于心绞痛发作频率降低的症状标准来确定硝苯地平和硝酸盐贴片的剂量,可能无法使运动能力得到客观改善。