Brogden R N, Sorkin E M
Adis International Limited, Auckland, New Zealand.
Drugs. 1995 Apr;49(4):618-49. doi: 10.2165/00003495-199549040-00009.
Since the earlier review in Drugs substantial additional data have accumulated regarding the antihypertensive efficacy of isradipine in various clinical situations, as well as data on its clinical effects in atherosclerosis. Recent therapeutic trials confirm that the efficacy of isradipine in the treatment of patients with mainly mild to moderate hypertension, when administered orally as a conventional or modified release preparation, is similar to that of titrated dosages of amlodipine, felodipine, nifedipine, diltiazem, captopril, methyldopa, metoprolol, prazosin and hydrochlorothiazide. A further decrease in blood pressure can be expected when isradipine is combined with another antihypertensive drug in patients who have not responded adequately to monotherapy. Initial studies have shown that intravenous isradipine is effective in controlling hypertension following coronary artery bypass graft surgery and that it appears useful in the treatment of intraoperative hypertension and hypertensive crisis, and in hypertensive disorders in pregnancy, when administered orally or intravenously. A large study, the Multicentre Isradipine Diuretic Atherosclerosis Study (MIDAS), was designed to compare the efficacy of isradipine and hydrochlorothiazide in reducing the rate of progression of carotid artery wall thickness, measured by B-mode ultrasound, as a surrogate for early atherosclerosis. Results indicated that wall thickness increased significantly less with isradipine than hydrochlorothiazide after 6 months of therapy. Thereafter the rate of progression remained parallel for the remainder of the 3-year trial. The confirmation of its antihypertensive efficacy, along with its favourable haemodynamic profile and reversal of left ventricular hypertrophy, minimal effect on glucose and lipid metabolism, preservation of quality of life and good tolerability, makes isradipine a suitable drug for the treatment of most patients with mild to moderate hypertension.
自《药物》杂志上较早的综述发表以来,已积累了大量关于伊拉地平在各种临床情况下的降压疗效的数据,以及其在动脉粥样硬化方面的临床效应的数据。近期的治疗试验证实,当以常规或缓释制剂口服给药时,伊拉地平在治疗主要为轻至中度高血压患者方面的疗效,与滴定剂量的氨氯地平、非洛地平、硝苯地平、地尔硫䓬、卡托普利、甲基多巴、美托洛尔、哌唑嗪和氢氯噻嗪相似。在对单一疗法反应不佳的患者中,伊拉地平与另一种降压药联合使用时,有望进一步降低血压。初步研究表明,静脉注射伊拉地平在冠状动脉搭桥手术后控制高血压有效,且在口服或静脉给药时,它似乎对治疗术中高血压和高血压危象以及妊娠高血压疾病有用。一项大型研究,即多中心伊拉地平利尿剂动脉粥样硬化研究(MIDAS),旨在比较伊拉地平和氢氯噻嗪在降低通过B型超声测量的颈动脉壁厚度进展速率方面的疗效,以此作为早期动脉粥样硬化的替代指标。结果表明,治疗6个月后,伊拉地平组的壁厚度增加明显少于氢氯噻嗪组。此后,在为期3年的试验剩余时间里,进展速率保持平行。伊拉地平降压疗效的确证,连同其良好的血流动力学特征、左心室肥厚的逆转、对葡萄糖和脂质代谢的最小影响、生活质量的维持以及良好的耐受性,使伊拉地平成为治疗大多数轻至中度高血压患者的合适药物。