Literature DB >> 2861738

Efficacy of carvedilol (BM 14,190), a new beta-blocking drug with vasodilating properties, in exercise-induced ischemia.

J C Kaski, L Rodriguez-Plaza, J Brown, A Maseri.   

Abstract

The exercise response to a single oral dose (25 mg) of a new beta-blocking agent that also has potent vasodilating properties, carvedilol (BM 14,190), was assessed in 15 patients with stable exertional angina, positive exercise test responses (greater than or equal to 1 mm of ST depression) and coronary artery disease. A single-blind, placebo-controlled, randomized, crossover design was used. Compared with placebo, 25 mg of carvedilol significantly reduced both heart rate (HR) and blood pressure (BP) at rest (p less than 0.01). After administration of carvedilol, 10 of 15 patients did not have angina at peak exercise (p less than 0.01) and 5 had ST shifts of less than 1 mm (p less than 0.05). Total exercise time and time to 1 mm of ST depression were prolonged and ST-segment depression at peak exercise was significantly reduced (p less than 0.01). Systolic BP was reduced both at peak exercise and at 1 mm of ST depression (p less than 0.05), whereas mean HR at peak exercise did not change significantly compared with placebo. Overall, mean HR-BP product at peak exercise was significantly reduced by carvedilol compared with placebo (p less than 0.05). However, 4 patients actually achieved a higher HR-BP product but did not have angina and had less ST depression (or no ST-segment shifts) at peak exercise. This indicates an increase in their coronary flow reserve. These results suggest that carvedilol is effective therapy for effort-induced angina, and this may be related to its combined beta-blocking and potent vasodilatory properties.

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Year:  1985        PMID: 2861738     DOI: 10.1016/0002-9149(85)90562-4

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  10 in total

1.  Analysis of the mechanism underlying the vasodilator action of carvedilol in pithed spontaneously hypertensive rats.

Authors:  H Hashimoto; M Tanaka; A Kanda; A Akashi
Journal:  Drugs       Date:  1988       Impact factor: 9.546

2.  Vasodilating mechanism and response to physiological pressor stimuli of acute doses of carvedilol compared with labetalol, propranolol and hydralazine.

Authors:  B Tomlinson; F Bompart; B R Graham; J B Liu; B N Prichard
Journal:  Drugs       Date:  1988       Impact factor: 9.546

Review 3.  Combined action drugs in the treatment of hypertension.

Authors:  L Hansson
Journal:  Drugs       Date:  1988       Impact factor: 9.546

4.  Treatment of angina and microvascular coronary dysfunction.

Authors:  Arang Samim; Lynn Nugent; Puja K Mehta; Chrisandra Shufelt; C Noel Bairey Merz
Journal:  Curr Treat Options Cardiovasc Med       Date:  2010-08

Review 5.  Cardiac Syndrome X: update 2014.

Authors:  Shilpa Agrawal; Puja K Mehta; C Noel Bairey Merz
Journal:  Cardiol Clin       Date:  2014-06-02       Impact factor: 2.213

Review 6.  Carvedilol. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy.

Authors:  D McTavish; D Campoli-Richards; E M Sorkin
Journal:  Drugs       Date:  1993-02       Impact factor: 9.546

Review 7.  Antihypertensive profile of carvedilol.

Authors:  W Meyer-Sabellek; B Agrawal
Journal:  Clin Investig       Date:  1992

8.  Single and repeated doses of the vasodilator/beta-adrenergic antagonist, carvedilol, block cirazoline- and isoproterenol-mediated hemodynamic responses in the conscious rat.

Authors:  E F Smith; M J Slivjak; R Gagnon
Journal:  Cardiovasc Drugs Ther       Date:  1992-10       Impact factor: 3.727

9.  Beta-blockers in hypertension: truths and half-truths.

Authors:  C Venkata S Ram
Journal:  J Clin Hypertens (Greenwich)       Date:  2008-07       Impact factor: 3.738

10.  Comprehensive treatment of microvascular angina in overweight women - a randomized controlled pilot trial.

Authors:  Kira Bang Bove; Malin Nilsson; Lene Rørholm Pedersen; Nicolai Mikkelsen; Hannah Elena Suhrs; Arne Astrup; Eva Prescott
Journal:  PLoS One       Date:  2020-11-05       Impact factor: 3.240

  10 in total

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