Benfield P, Clissold S P, Brogden R N
Drugs. 1986 May;31(5):376-429. doi: 10.2165/00003495-198631050-00002.
During the intervening years since metoprolol was first reviewed in the Journal (1977), it has become widely used in the treatment of mild to moderate hypertension and angina pectoris. Although much data have accumulated, its precise mechanisms of action in these diseases remain largely uncertain. Optimum treatment of hypertension and angina pectoris with metoprolol is achieved through dose titration within the therapeutic range. It has been clearly demonstrated that metoprolol is at least as effective as other beta-blockers, diuretics and certain calcium antagonists in the majority of patients. Although a twice daily dosage regimen is normally used, satisfactory control can be maintained in many patients with single daily doses of conventional or, more frequently, slow release formulations. Addition of a diuretic may improve the overall response rate in hypertension. Several controlled trials have studied the effects of metoprolol administered during the acute phase and after myocardial infarction. In early intervention trials a reduction in total mortality was achieved in one moderately large trial of prolonged treatment, but in another, which excluded patients already being treated with beta-blockers or certain calcium antagonists and where treatment was only short term, mortality was significantly reduced only in 'high risk' patients. Overall results with metoprolol have not demonstrated that early intervention treatment in all patients produces clinically important improvement in short term mortality. Thus, the use of metoprolol during the early stages of myocardial infarction is controversial, largely because of the requirement to treat all patients to save a small number at 'high risk'. This blanket coverage approach to treatment may be more justified during the post-infarction follow-up phase since it has been shown that metoprolol slightly, but significantly, reduces the mortality rate for periods of up to 3 years. Metoprolol is generally well tolerated and its beta 1-selectivity may facilitate its administration to certain patients (e.g. asthmatics and diabetics) in whom non-selective beta-blockers are contraindicated. Temporary fatigue, dizziness and headache are among the most frequently reported side effects. After a decade of use, metoprolol is well established as a first choice drug in mild to moderate hypertension and stable angina, and is beneficial in post-infarction patients. Further study is needed in less well established areas of treatment such as cardiac arrhythmias, idiopathic dilated cardiomyopathy and hypertensive cardiomegaly.
自美托洛尔首次在本刊发表综述(1977年)后的这些年间,它已广泛用于治疗轻至中度高血压和心绞痛。尽管已积累了大量数据,但其在这些疾病中的精确作用机制仍大多不明。通过在治疗范围内进行剂量滴定可实现美托洛尔对高血压和心绞痛的最佳治疗。已明确证明,在大多数患者中,美托洛尔至少与其他β受体阻滞剂、利尿剂及某些钙拮抗剂一样有效。虽然通常采用每日两次的给药方案,但许多患者使用常规或更常用的缓释制剂每日单次给药也可维持满意的控制。加用利尿剂可能会提高高血压的总体有效率。多项对照试验研究了美托洛尔在急性期及心肌梗死后给药的效果。在早期干预试验中,一项较大规模的长期治疗试验使总死亡率有所降低,但在另一项试验中,该试验排除了已在使用β受体阻滞剂或某些钙拮抗剂治疗的患者且治疗为短期,仅“高危”患者的死亡率显著降低。美托洛尔的总体结果并未表明对所有患者进行早期干预治疗能在短期死亡率方面产生具有临床意义的改善。因此,在心肌梗死早期使用美托洛尔存在争议,主要是因为需要治疗所有患者以挽救少数“高危”患者。这种全面覆盖的治疗方法在心肌梗死后的随访阶段可能更有理由,因为已表明美托洛尔可使长达3年的死亡率略有但显著降低。美托洛尔一般耐受性良好,其β1选择性可能便于对某些非选择性β受体阻滞剂禁忌的患者(如哮喘患者和糖尿病患者)给药。暂时的疲劳、头晕和头痛是最常报告的副作用。经过十年的使用,美托洛尔已成为轻至中度高血压和稳定型心绞痛的首选药物,对心肌梗死后患者有益。在心律失常、特发性扩张型心肌病和高血压性心脏肥大等不太成熟的治疗领域还需要进一步研究。