Stone P H
Am J Cardiol. 1987 Jan 30;59(3):101B-115B. doi: 10.1016/0002-9149(87)90089-0.
The calcium antagonists provide a unique tool to reduce myocardial oxygen demand and prevent increases in coronary vasomotor tone. For patients with Prinzmetal's variant angina, diltiazem, nifedipine and verapamil are extremely effective in preventing episodes of coronary vasospasm and symptoms of ischemia. Unstable angina pectoris is a more complex pathophysiologic syndrome with episodes of ischemia due to increases in coronary vasomotor tone, intermittent platelet aggregation or alterations in the underlying atherosclerotic plaque. Each of the calcium antagonists is effective as monotherapy in decreasing the frequency of angina at rest. Nifedipine is the only calcium antagonist that has been studied in a combination regimen with beta blockers and nitrates for patients with unstable angina, and control of angina is better with the combination regimen than with either form of therapy alone. Although symptoms of myocardial ischemia in unstable angina are reduced by calcium antagonists, these agents do not seem to decrease the incidence of adverse outcomes. Antiplatelet therapy appears to improve morbidity and mortality in patients with unstable angina, suggesting that thrombus formation may play a central role in that disorder. Episodes of silent or asymptomatic myocardial ischemia, identified by ST-segment monitoring, occur in a variety of disorders of coronary disease. Among patients with Prinzmetal's variant angina and unstable angina, episodes of silent ischemia appear to be as frequent as episodes of angina and the calcium antagonists are effective in decreasing episodes of ischemia regardless of the presence or absence of symptoms. Persisting episodes of silent ischemia among patients with unstable angina despite maximal medical therapy identify patients at high risk for an early unfavorable outcome. Among patients with stable exertional angina, episodes of silent ischemia may be up to 5 times as frequent as episodes of angina, and may be due to increases in coronary vasomotor tone, transient platelet aggregation or increases in myocardial oxygen demand. Preliminary experience suggests that calcium antagonists and beta blockers are effective in decreasing episodes of silent ischemia in patients with stable exertional angina and that a combination regimen may be more effective than either form of therapy alone.
钙拮抗剂为降低心肌需氧量和预防冠状动脉血管张力增加提供了一种独特的手段。对于变异型心绞痛患者,地尔硫䓬、硝苯地平和维拉帕米在预防冠状动脉痉挛发作和缺血症状方面极为有效。不稳定型心绞痛是一种更为复杂的病理生理综合征,其缺血发作是由于冠状动脉血管张力增加、间歇性血小板聚集或潜在动脉粥样硬化斑块改变所致。每种钙拮抗剂作为单一疗法在降低静息性心绞痛发作频率方面均有效。硝苯地平是唯一一种针对不稳定型心绞痛患者与β受体阻滞剂和硝酸盐联合使用进行研究的钙拮抗剂,联合治疗方案对心绞痛的控制效果优于单独使用任何一种治疗方法。尽管钙拮抗剂可减轻不稳定型心绞痛患者的心肌缺血症状,但这些药物似乎并未降低不良结局的发生率。抗血小板治疗似乎可改善不稳定型心绞痛患者的发病率和死亡率,这表明血栓形成可能在该疾病中起核心作用。通过ST段监测发现的无症状心肌缺血发作见于多种冠心病。在变异型心绞痛和不稳定型心绞痛患者中,无症状缺血发作似乎与心绞痛发作一样频繁,且无论有无症状,钙拮抗剂均可有效减少缺血发作。尽管进行了最大程度的药物治疗,不稳定型心绞痛患者仍持续出现无症状缺血发作,这表明这些患者早期出现不良结局的风险较高。在稳定型劳力性心绞痛患者中,无症状缺血发作的频率可能是心绞痛发作的5倍,可能是由于冠状动脉血管张力增加、短暂性血小板聚集或心肌需氧量增加所致。初步经验表明,钙拮抗剂和β受体阻滞剂可有效减少稳定型劳力性心绞痛患者的无症状缺血发作,联合治疗方案可能比单独使用任何一种治疗方法更有效。