Literature DB >> 7774515

Ramipril. An updated review of its therapeutic use in essential hypertension and heart failure.

J E Frampton1, D H Peters.   

Abstract

Ramipril is a second generation angiotensin converting enzyme (ACE) inhibitor. Like enalapril, it is a prodrug and is hydrolysed in vivo to release the active metabolite, ramiprilat, which has a long elimination half-life, permitting once-daily administration. The antihypertensive efficacy of ramipril has been confirmed in large-scale noncomparative studies conducted in general practice as well as in more rigorously controlled clinical trials. In the former, approximately 85% of patients with mild to moderate essential hypertension have responded successfully to treatment with ramipril 2.5 or 5 mg/day, while comparative trials indicate that the antihypertensive efficacy of the drug is equivalent to that of other established ACE inhibitors and the beta-adrenoceptor antagonist atenolol. As expected, the response rate to ramipril monotherapy is lower in patients with severe hypertension (around 40%), although the blood pressure lowering effect can be enhanced with the addition of a diuretic such as hydrochlorothiazide or piretanide. The antihypertensive efficacy of ramipril is maintained in patients with diabetes mellitus and preliminary data indicate that the drug has the beneficial effect of decreasing urinary albumin excretion in diabetic patients with nephropathy. Ramipril is superior to atenolol in causing regression of left ventricular hypertrophy, although the clinical significance of this effect per se remains to be established. The large-scale Acute Infarction Ramipril Efficacy (AIRE) study demonstrated that ramipril 5 or 10 mg/day significantly decreased the risk of all-cause mortality by 27% in patients with clinical evidence of heart failure after acute myocardial infarction, even if transient. The beneficial effect of ramipril was apparent by 30 days of treatment and appeared to be greatest in patients with more severe ventricular damage after infarction. Ramipril is well tolerated in general practice, with 5% or fewer patients discontinuing therapy because of drug intolerance. The data available suggest that ramipril shares a similar tolerability profile to that of other established ACE inhibitors. Thus, clinical data confirm ramipril as a useful alternative ACE inhibitor for the treatment of patients with mild to moderate hypertension, and indicate a beneficial effect of the drug in patients with clinical evidence of heart failure after acute myocardial infarction. It is also reasonable to assume that ramipril will be of value in the treatment of patients with more established heart failure or asymptomatic left ventricular dysfunction.

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Year:  1995        PMID: 7774515     DOI: 10.2165/00003495-199549030-00008

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


  120 in total

1.  ACE inhibition improves insulin-sensitivity in aged insulin-resistant hypertensive patients.

Authors:  G Paolisso; A Gambardella; M Verza; A D'Amore; S Sgambato; M Varricchio
Journal:  J Hum Hypertens       Date:  1992-06       Impact factor: 3.012

2.  Assessment of the efficacy, tolerance, and safety of ramipril in diabetic patients with mild-to-moderate hypertension: a retrospective analysis.

Authors:  W Erhard; U Lindner; H Krall; A Breitstadt; C Pfeiffer
Journal:  J Cardiovasc Pharmacol       Date:  1991       Impact factor: 3.105

3.  Comparison of response rates to the angiotensin-converting enzyme inhibitor ramipril in mild-to-moderate hypertension in a double-blind, parallel-group study and an open single-blind study.

Authors:  D Vasmant; P Lendresse; J C Lemarie; M Gallet
Journal:  J Cardiovasc Pharmacol       Date:  1991       Impact factor: 3.105

4.  Antihypertensive efficacy, tolerance, and safety of ramipril in young vs. old patients: a retrospective study.

Authors:  R Saalbach; G Wochnik; H Mauersberger; V Cairns; A Breitstadt; B Rangoonwala
Journal:  J Cardiovasc Pharmacol       Date:  1991       Impact factor: 3.105

5.  Clinical pharmacology of ramipril.

Authors:  S G Ball; J I Robertson
Journal:  Am J Cardiol       Date:  1987-04-24       Impact factor: 2.778

Review 6.  Lisinopril. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension and congestive heart failure.

Authors:  S G Lancaster; P A Todd
Journal:  Drugs       Date:  1988-06       Impact factor: 9.546

7.  The neurohormonal hypothesis: a theory to explain the mechanism of disease progression in heart failure.

Authors:  M Packer
Journal:  J Am Coll Cardiol       Date:  1992-07       Impact factor: 24.094

Review 8.  Differences in structure of angiotensin-converting enzyme inhibitors might predict differences in action.

Authors:  A G Herman
Journal:  Am J Cardiol       Date:  1992-10-08       Impact factor: 2.778

9.  Ramipril and captopril in patients with heart failure: effects on hemodynamics and vasoconstrictor systems.

Authors:  J Manthey; K J Osterziel; N Röhrig; R Dietz; E Hackenthal; H Schmidt-Gayk; W Kübler
Journal:  Am J Cardiol       Date:  1987-04-24       Impact factor: 2.778

10.  Cough and ACE inhibitors.

Authors:  S R Simon; H R Black; M Moser; W E Berland
Journal:  Arch Intern Med       Date:  1992-08
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  5 in total

Review 1.  Ramipril/felodipine extended-release fixed-dose combination: a review of its use in the management of essential hypertension.

Authors:  Risto S Cvetković; Greg L Plosker
Journal:  Drugs       Date:  2005       Impact factor: 9.546

2.  Catalytic Divergent [3+3]- and [3+2]-Cycloaddition by Discrimination Between Diazo Compounds.

Authors:  Yongming Deng; Lynée A Massey; Yeray A Rodriguez Núñez; Hadi Arman; Michael P Doyle
Journal:  Angew Chem Int Ed Engl       Date:  2017-08-24       Impact factor: 15.336

Review 3.  Formulary management of ACE inhibitors.

Authors:  K R Gerbrandt; K C Yedinak
Journal:  Pharmacoeconomics       Date:  1996-12       Impact factor: 4.981

Review 4.  Ramipril: a review of its use in the prevention of cardiovascular outcomes.

Authors:  Gregory T Warner; Caroline M Perry
Journal:  Drugs       Date:  2002       Impact factor: 9.546

5.  First-line antihypertensive treatment in patients with pre-diabetes: rationale, design and baseline results of the ADaPT investigation.

Authors:  Walter Zidek; Joachim Schrader; Stephan Lüders; Stephan Matthaei; Christoph Hasslacher; Joachim Hoyer; Peter Bramlage; Claus-Dieter Sturm; W Dieter Paar
Journal:  Cardiovasc Diabetol       Date:  2008-07-24       Impact factor: 9.951

  5 in total

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