Improved left ventricular performance during exercise with verapamil or nifedipine in patients with chronic stable angina (original) (raw)

1987, American Heart Journal

ov exercige with v6br with chronic st To examine the effects of chronic oral therapy with verapamii, 120 mg three times a day, and nifedipine, 20 mg four times daiiy, on left ventricular ejection fraction and regional wail motion at rest and exercise, 10 patients with chronic stable angina pectoris underwent serial rest and exercise radionuctide angiography. Pre drug control study reveaied a resting left ventricular ejection fraction (LVEF) of 0.62 ? 0.08, faiiing to 0.54 + 0.12 at peak exercise (p < 0.05). Wail motion score deteriorated from a resting vatue of 13.8-t 2.3 to 10.8 + 1.8 (p < 0.01) with exercise. Patients were subsequently randomized to verapamii or nifediptne for 4 weeks each in an open-labeled crossover design. Rest and exercise radionuciide angtography were repeated at the end of each 4-week period. Neither verspamii nor nifedtpine had a significant effect on resting LVEF (verapamii LVEF = 0.81 + 0.10, nifedipine LVEF = 0.84 f 0.02). Likewise, they had no significant effect on resting wail motion score (verapamii = 14.2-+ 2.2, nifedipine = 14.4 f 1.8). Both verapamii and nifedipine signpicantiy increased LVEF at peak exercise (verapamii = 0.63 + 0.09, nifedipine = 0.65 + 0.08, p < 0.05 vs pre drug control) and improved peak exercise wail motion score (verapamii = 13 ? 1.9, nifedipine = 13.8 f 1.6, p < 0.05 vs pre drug control). Both drugs significantly reduced maximal ST depression at peak exercise and prolonged exercise duration. Episodes of angina and nitroglycerin use were also significantly reduced. in summary, verapamii and nifedipine improved left ventricular performance at exercise in patients with angina pectoris. (AM HEART J 1987; 113:700.

Effect of nifedipine on exercise-induced left ventricular dysfunction and myocardial hypoperfusion in stable angina

The American Journal of Cardiology, 1982

To assess the effects of nifedipine on left ventricular function and regional myocardial perfusion, exercise radionuclide ventriculography was performed in 15 men (median age 59 years) and exercise thallium-201 scintigraphy was done in 11 of them, before and 90 minutes after the oral administration of 20 mg of nifedipine. All patients had stable angina and angiographically proved coronary artery disease without evidence of spasm. Exercise tolerance after administration of nifedipine increased from 343 f 42 seconds to 471 150 seconds (p <0 .01), whereas the peak exercise double product remained essentially unchanged (difference not significant). Ejection traction improved significantly at rest (from 49 f 3 .6% to 52 f 3 .3%, p <0 .05) and at peak Nifedipine is a calcium antagonist with potent vasodilating properties.)-1 It has been used successfully in the treatment of stable angina pectoris and other ischemic syndromes 5-10 and has also been noted to have a negative inotropic effect in the isolated cardiac muscle preparation. 11 However, reports on its effects on myocardial function in patients with cardiac disease have been conflicting. 12-14 In particular, its possible influence on the acute left ventricular dysfunction resulting from stress-induced ischemia has not been sufficiently investigated. The present study was designed to assess the effects of nifedipine on left ventricular function at rest and during exercise in patients with coronary artery

Randomized double-blind comparison of verapamil and nifedipine in chronic stable angina

The American Journal of Cardiology, 1982

A randomized double-blind crossover trial was performed in 32 patients with chronic stable angina to compare the antianginal actions of verapamil (120 mg 3 times daily) and nifedipine (20 mg 3 times daily). Efficacy was assessed using objective end points obtained by computer-assisted exercise testing and 24 hour ambulatory monitoring for S-T segment shift. Twenty-eight patients completed the trial. The mean exercise time to produce angina improved from 5.7 f 0.3 minutes (mean f standard error of the mean) in patients on placebo, to 7.9 f 0.5 minutes in those on nifedipine and 10.0 f 0.7 minutes in those on verapamil. Similar improvement was seen in all other objective variables. Generally, verapamil produced mild bradycardia and nifedipine mild tachycardia. Four patients complained of palpitations and angina after ingestion of nifedipine and were identified by ambulatory monitoring to have tachycardia and persistent S-T depression. These opposite effects on heart rate may explain the differences in efficacy between these 2 potent calcium ion antagonists.

Calcium antagonist drugs in chronic stable angina. Comparison of verapamil and nifedipine

Heart, 1981

The relative efficacy of two calcium antagonist drugs, verapamil, 120 mg three times a day and nifedipine, 20 mg three times a day, was examined in a double-blind randomised trial. Patients were assessed at the end of four week periods by a maximal treadmill exercise test, the frequency of anginal attacks, glyceryl trinitrate consumption, and side effects. Sixteen point praecordial maps were recorded at rest, immediately after exercise, and at minute intervals for 10 minutes. Total ST segment depression (. ST) was used as a measure of myocardial ischaemia. Both verapamil and nifedipine increased maximal work capacity but i ST at the termination of the test remained constant. Both drugs reduced the frequency of anginal attacks and glyceryl trinitrate consumption. Systolic blood pressure at rest and on exercise was reduced by both drugs. Verapamil and nifedipine were equally effective in treating angina, but side effects were more common with nifedipine.

Effects of nifedipine on coronary hemodynamic findings during exercise in patients with stable exertional angina

Circulation, 1983

To investigate the mechanism by which nifedipine improves exercise tolerance in patients with coronary artery disease, we studied 14 patients with stable exertional angina and left anterior descending artery disease by measuring great cardiac vein flow (GCVF) and calculating anterior regional coronary resistance (ARCR) during exercise before and after sublingual administration of 20 mg of nifedipine. After nifedipine seven patients (group I) had no increase in exercise capacity and showed a similar magnitude of ST segment depression at peak exercise, while another seven patients (group II) had prolonged exercise duration (p less than .001) with less ST segment depression at peak exercise (p less than .01). Such effects were achieved despite a significant increase in double product, an indirect index of myocardial oxygen consumption. In group I patients no significant change was induced by nifedipine in GCVF or in ARCR either at rest or at peak exercise. In contrast, in group II pati...

Improved exercise tolerance after propranolol, diltiazem or nifedipine in angina pectoris: Comparison at 1, 3 and 8 hours and correlation with plasma drug concentration

The American Journal of Cardiology, 1984

Exercise tolerance 1, 3 and 8 hours after 80 mg of propranolol, 120 mg of diltiazem and 20 mg of nifedipine, and after 20 minutes of 0.6 mg of sublingual nitroglycerin were compared with placebo in 15 men who had chronic stable angina pectoris. Three hours after drug ingestion, the exercise time was prolonged by 72 f 26,162 f 27 and 161 f 30 seconds (p <0.05) for propranolol, diltiazem and nifedipine, respectively, and by 123 f 35 seconds (p <O.OOl) 20 minutes after sublingual nitroglycerin compared with placebo. The onset of ST-segment depression 20.1 mV was delayed by 120 f 34,203 f 29 and 189 f 35 seconds (p <O.OS) and by 79 f 23 seconds (p <0.05), respectively. Afler propranolol, the peak rate-pressure product decreased compared with placebo (15.1 f 1.1 U [10B3] vs 20.0 f 1.5 U, p <O.Ol). In contrast, the peak rate-pressure product was greater after diltiazem and nifedipine than after placebo (22.2 f 1.3 U [p <O.OSl and 23.8

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