ISRADIPINE - AN UPDATE OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC EFFICACY IN THE TREATMENT OF MILD-TO-MODERATE HYPERTENSION
Rn. Brogden et Em. Sorkin, ISRADIPINE - AN UPDATE OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC EFFICACY IN THE TREATMENT OF MILD-TO-MODERATE HYPERTENSION, Drugs, 49(4), 1995, pp. 618-649
Since the earlier review in Drugs substantial additional data have acc
umulated regarding the antihypertensive efficacy of isradipine in vari
ous clinical situations, as well as data on its clinical effects in at
herosclerosis. Recent therapeutic trials confirm that the efficacy of
isradipine in the treatment of patients with mainly mild to moderate h
ypertension, when administered orally as a conventional or modified re
lease preparation, is similar to that of titrated dosages of amlodipin
e, felodipine, nifedipine, diltiazem, captopril, methyldopa, metoprolo
l, prazosin and hydrochlorothiazide. A further decrease in blood press
ure can be expected when isradipine is combined with another antihyper
tensive drug in patients who have not responded adequately to monother
apy. Initial studies have shown that intravenous isradipine is effecti
ve 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 hydrochlorothiazid
e in reducing the rate of progression of carotid artery wall thickness
, measured by B-mode ultrasound, as a surrogate for early atherosclero
sis. Results indicated that wall thickness increased significantly les
s 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 efficac
y along with its favourable haemodynamic profile and reversal of left
ventricular hypertrophy, minimal effect on glucose and lipid metabolis
m, preservation of quality of life and good tolerability makes isradip
ine a suitable drug for the treatment of most patients with mild to mo
derate hypertension.