Deanfield John E, Detry Jean-Marie, Sellier Philippe, Lichtlen Paul R, Thaulow Eric, Bultas Jan, Brennan Claudia, Young Sarah T, Beckerman Bruce
Vascular Physiology Unit, Great Ormond Street Hospital for Children, London, United Kingdom.
J Am Coll Cardiol. 2002 Sep 4;40(5):917-25. doi: 10.1016/s0735-1097(02)02050-8.
The Circadian Anti-ischemia Program in Europe (CAPE II) compared the efficacy of amlodipine and diltiazem (Adizem XL) and the combination of amlodipine/atenolol and diltiazem (Adizem XL)/isosorbide 5-mononitrate on exercise and ambulatory myocardial ischemia during regular therapy and after omission of medication.
The optimal medical therapy for ischemia suppression and the impact of irregular dosing using agents with different pharmacologic properties has not been established in patients with coronary disease.
Patients with > or = 4 ischemic episodes or > or = 20 min of ST segment depression on 72-h electrocardiogram were randomized to amlodipine 10 mg once daily or diltiazem (Adizem XL) 300 mg once daily in a 14-week double-blind randomized multicountry study. In the second phase, atenolol 100 mg was added to amlodipine and isosorbide 5-mononitrate 100 mg to diltiazem (Adizem XL). Ambulatory monitoring (72 h) and exercise testing were repeated after both phases, on treatment and after a 24-h drug-free interval.
Both monotherapy with amlodipine and diltiazem (Adizem XL) were effective on symptoms and ambulatory and exercise ischemia. Combination therapy reduced ischemia further, with amlodipine/atenolol superior to diltiazem (Adizem XL)/isosorbide 5-mononitrate. Amlodipine/atenolol was significantly superior during the drug-free interval with maintenance of ischemia reduction.
Amlodipine, with its intrinsically long half-life alone or together with beta-blocker, is likely to produce superior ischemia reduction in clinical practice when patients frequently forget to take medication or dose irregularly.
欧洲昼夜抗缺血计划(CAPE II)比较了氨氯地平和地尔硫䓬(Adizem XL)以及氨氯地平/阿替洛尔与地尔硫䓬(Adizem XL)/5-单硝酸异山梨酯联合用药在常规治疗期间及停药后对运动及动态心肌缺血的疗效。
对于冠心病患者,尚未确定抑制缺血的最佳药物治疗方案以及使用具有不同药理特性的药物进行不规则给药的影响。
在一项为期14周的双盲随机多国研究中,将72小时心电图显示有≥4次缺血发作或ST段压低≥20分钟的患者随机分为每日一次服用10毫克氨氯地平或每日一次服用300毫克地尔硫䓬(Adizem XL)。在第二阶段,氨氯地平组加用100毫克阿替洛尔,地尔硫䓬(Adizem XL)组加用100毫克5-单硝酸异山梨酯。在两个阶段的治疗后以及停药24小时后,重复进行动态监测(72小时)和运动试验。
氨氯地平和地尔硫䓬(Adizem XL)单药治疗对症状、动态及运动性缺血均有效。联合治疗进一步减少了缺血,氨氯地平/阿替洛尔优于地尔硫䓬(Adizem XL)/5-单硝酸异山梨酯。在停药期间,氨氯地平/阿替洛尔在维持缺血减轻方面明显更优。
氨氯地平本身半衰期长,单独使用或与β受体阻滞剂联合使用时,在临床实践中,当患者经常忘记服药或给药不规律时,可能会更有效地减少缺血。