ISRADIPINE - AN UPDATE OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC EFFICACY IN THE TREATMENT OF MILD-TO-MODERATE HYPERTENSION

被引:29
作者
BROGDEN, RN
SORKIN, EM
机构
[1] Adis International Limited, Auckland, 41 Centorian Drive, Private Bag 65901, Mairangi Bay
关键词
D O I
10.2165/00003495-199549040-00009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
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页码:618 / 649
页数:32
相关论文
共 211 条
[1]   ACUTE HEMODYNAMIC-EFFECTS OF ISRADIPINE IN HYPERTENSIVE HEART-TRANSPLANT RECIPIENTS [J].
AASS, H ;
SIMONSEN, S .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 45 (02) :187-189
[2]   ISRADIPINE DOSE-CONFIRMATION STUDY IN FILIPINO PATIENTS WITH MILD TO MODERATE HYPERTENSION [J].
ABARQUEZ, RF ;
CABRAL, EI ;
NAMIN, EP ;
CALLEJA, HB ;
PORCIUNCULA, CI ;
DIVINAGRACIA, RA ;
ANASTACIO, RV ;
CASTILLO, RR .
DRUGS, 1990, 40 :33-37
[3]  
AMIR M, 1994, BLOOD PRESSURE, V3, P40
[4]   BLOOD-PRESSURE CONTROL AND HEMODYNAMIC ADAPTATION WITH THE DIHYDROPYRIDINE CALCIUM-ANTAGONIST ISRADIPINE - A CONTROLLED-STUDY IN MIDDLE-AGED HYPERTENSIVE MEN [J].
ANDERSSON, OK ;
PERSSON, B ;
HEDNER, T ;
AURELL, M ;
WYSOCKI, M .
JOURNAL OF HYPERTENSION, 1989, 7 (06) :465-469
[5]  
ANDERSSON OK, 1990, J CARDIOVASC PHARM, V15, pS87
[6]   NITRENDIPINE KINETICS IN NORMAL AND IMPAIRED RENAL-FUNCTION [J].
ARONOFF, GR ;
SLOAN, RS .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1985, 38 (02) :212-218
[7]  
AROSIO E, 1993, CLIN THER, V15, P705
[8]   ANTIHYPERTENSIVE EFFECT OF ONCE DAILY SUSTAINED-RELEASE ISRADIPINE - A PLACEBO CONTROLLED CROSS-OVER STUDY [J].
ARZILLI, F ;
GANDOLFI, E ;
DELPRATO, C ;
INNOCENTI, P ;
PONZANELLI, F ;
CAIAZZA, A ;
GHISONI, F ;
SABA, P ;
GIUNTOLI, F ;
BORGNINO, C ;
SALVETTI, A .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 44 (01) :23-25
[9]   EFFECTS OF ISRADIPINE ON RENAL-FUNCTION IN CYCLOSPORINE-TREATED RENAL TRANSPLANTED PATIENTS [J].
BERG, KJ ;
HOLDAAS, H ;
ENDRESEN, L ;
FAUCHALD, P ;
HARTMANN, A ;
PRAN, T ;
SOLBU, D .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1991, 6 (10) :725-730
[10]   COMPARISON OF THE EFFECTS OF ISRADIPINE AND LISINOPRIL ON LEFT-VENTRICULAR STRUCTURE AND FUNCTION IN ESSENTIAL-HYPERTENSION [J].
BIELEN, EC ;
FAGARD, RH ;
LIJNEN, PJ ;
TJANDRAMAGA, TB ;
VERBESSELT, R ;
AMERY, AK .
AMERICAN JOURNAL OF CARDIOLOGY, 1992, 69 (14) :1200-1206