Literature DB >> 7789292

Isradipine. An update of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in the treatment of mild to moderate hypertension.

R N Brogden1, E M Sorkin.   

Abstract

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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Year:  1995        PMID: 7789292     DOI: 10.2165/00003495-199549040-00009

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  185 in total

1.  Long-term (2-year) isradipine data in the treatment of mild-to-moderate hypertension.

Authors:  G D'Hont; J P Meurant; D L Clement; G Rorive; L Hermans; P De Keyser; K J Westelinck
Journal:  J Cardiovasc Pharmacol       Date:  1992       Impact factor: 3.105

Review 2.  Pathophysiology of cyclosporin A nephrotoxicity: experimental and clinical observations.

Authors:  P G McNally; J Feehally
Journal:  Nephrol Dial Transplant       Date:  1992       Impact factor: 5.992

3.  Double-blind multicentre isradipine dose-confirmation study in Pakistan.

Authors:  S M Rab; M A Mirza; M H Khan; A Samad; M Ahmed
Journal:  Drugs       Date:  1990       Impact factor: 9.546

4.  Acute hemodynamic effects of intravenous isradipine.

Authors:  E K van den Berg; G J Dehmer
Journal:  Am J Cardiol       Date:  1988-05-01       Impact factor: 2.778

5.  Efficacy and tolerability of isradipine and metoprolol in treatment of hypertension: the Finnish Isradipine Study in Hypertension (FISH).

Authors:  K Luomanmäki; J Inkovaara; M Hartikainen; M Helin; J Viikari; M Kataja; K Ekman; K Harjula
Journal:  J Cardiovasc Pharmacol       Date:  1992-08       Impact factor: 3.105

6.  [Comparison of the cardiodepressive effects of nifedipine, isradipine, nisoldipine and felodipine in patients with coronary heart disease].

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Journal:  Z Kardiol       Date:  1993-01

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Authors:  F Rocha-Gonçalves; B Moura; J M Pereira-Miguel; A Correa-Nunes; G Mariano-Pego
Journal:  Am J Hypertens       Date:  1994-07       Impact factor: 2.689

8.  Hypertension following myocardial revascularization: its prevalence and etiology.

Authors:  R W Landymore; D A Murphy; C E Kinley
Journal:  Can J Surg       Date:  1980-09       Impact factor: 2.089

9.  Pharmacokinetics and metabolism of nifedipine.

Authors:  K D Raemsch; J Sommer
Journal:  Hypertension       Date:  1983 Jul-Aug       Impact factor: 10.190

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Authors:  P C Rüegg; U Karmann; H Keller
Journal:  Am J Hypertens       Date:  1991-02       Impact factor: 2.689

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Authors:  C J Ferro; D J Webb
Journal:  Drugs       Date:  1997       Impact factor: 9.546

2.  Deletion of the distal C terminus of CaV1.2 channels leads to loss of beta-adrenergic regulation and heart failure in vivo.

Authors:  Ying Fu; Ruth E Westenbroek; Frank H Yu; John P Clark; Misty R Marshall; Todd Scheuer; William A Catterall
Journal:  J Biol Chem       Date:  2011-01-07       Impact factor: 5.157

Review 3.  Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions.

Authors:  R J Bertz; G R Granneman
Journal:  Clin Pharmacokinet       Date:  1997-03       Impact factor: 6.447

Review 4.  A review of calcium channel antagonists in the treatment of pediatric hypertension.

Authors:  Shobha Sahney
Journal:  Paediatr Drugs       Date:  2006       Impact factor: 3.022

  4 in total

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