Sever P
Imperial College School of Medicine at St Mary's Hospital, London, UK.
J Hum Hypertens. 1997 Sep;11 Suppl 2:S91-5.
Candesartan is a potent and selective angiotensin II type 1 receptor blocker which binds tightly to and dissociates slowly from the AT1 receptor. It is administered orally as the prodrug candesartan cilexetil, which is rapidly and completely converted to the active compound, candesartan, during gastrointestinal absorption. In hypertensive patients, candesartan cilexetil dose-dependently lowers diastolic and systolic blood pressure (BP) over the 24-h dose interval and it maintains its antihypertensive effects in the long term. Clinical trials indicate that a once-daily dose of 4-16 mg provides a clinically relevant reduction in BP. The usual maintenance doses of candesartan cilexetil are expected to be 8 mg and 16 mg once-daily and dosage adjustment does not appear to be necessary in elderly patients or those with mild to moderate renal or hepatic impairment. Adverse events during treatment with candesartan cilexetil occur at a similar low incidence as with placebo and no dose-dependent events or adverse metabolic effects have been noted. As once-daily monotherapy, candesartan cilexetil 8 mg is as effective as enalapril 10-20 mg, amlodipine 5 mg or hydrochlorothiazide 25 mg, and candesartan cilexetil 16 mg is more effective than losartan 50 mg. The trough to peak ratio for the reduction in BP with candesartan cilexetil has been shown to be in the order of 80-100%, confirming the smooth 24-h BP-lowering profile of the drug. Combined treatment with candesartan cilexetil and hydrochlorothiazide or amlodipine provides an enhanced BP-lowering effect that is useful in patients with inadequate response to initial treatment after step-up titration. Candesartan cilexetil is similarly well tolerated as placebo, both when given as monotherapy, and in combination for example with hydrochlorothiazide. Candesartan cilexetil with its flexible dosage regimen therefore appears to offer an effective and well-tolerated alternative to other established agents in the treatment of a wide range of hypertensive patients.
坎地沙坦是一种强效且具有选择性的血管紧张素II 1型受体阻滞剂,它与AT1受体紧密结合且从该受体上解离缓慢。它作为前体药物坎地沙坦酯口服给药,在胃肠道吸收过程中迅速且完全转化为活性化合物坎地沙坦。在高血压患者中,坎地沙坦酯在24小时给药间隔内剂量依赖性地降低舒张压和收缩压,并且能长期维持其降压效果。临床试验表明,每日一次服用4 - 16毫克可使血压得到临床上有意义的降低。坎地沙坦酯的常用维持剂量预计为每日一次8毫克和16毫克,老年患者或轻度至中度肾或肝功能损害患者似乎无需调整剂量。坎地沙坦酯治疗期间的不良事件发生率与安慰剂相似,未观察到剂量依赖性事件或不良代谢效应。作为每日一次的单一疗法,8毫克坎地沙坦酯与10 - 20毫克依那普利、5毫克氨氯地平或25毫克氢氯噻嗪效果相当,16毫克坎地沙坦酯比50毫克氯沙坦更有效。已证明坎地沙坦酯降低血压的谷峰比约为80 - 100%,证实了该药物平稳的24小时降压曲线。坎地沙坦酯与氢氯噻嗪或氨氯地平联合治疗可增强降压效果,这对逐步滴定初始治疗反应不佳的患者有用。坎地沙坦酯无论是作为单一疗法还是例如与氢氯噻嗪联合使用时,耐受性都与安慰剂相似。因此,坎地沙坦酯灵活的给药方案似乎为治疗广泛的高血压患者提供了一种有效且耐受性良好的替代其他已确立药物的选择。