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Comparison of nifedipine and isosorbide dinitrate when added to maximal propranolol therapy in stable angina pectoris
Authors:R W Nesto  H D White  J Wynne  B L Holman  E M Antman
Affiliation:1. Keele Cardiovascular Research Group, Keele University, Stoke-on-Trent, UK;2. St. Helens & Knowsley Teaching Hospital (NHS) Trust, Whiston Hospital, Prescot, UK;3. Manchester Heart Centre, Manchester Royal Infirmary, UK;4. University Hospital of North Midlands, Stoke-on-Trent, UK;5. Farr Institute, Institute of Population Health, University of Manchester, Manchester, UK;1. University of Texas Medical Branch, Department of Preventive Medicine and Community Health, Galveston, TX, 77555-1150, United States;2. University of Texas Medical Branch, Departments of Internal Medicine, Galveston, TX, 77555-1167, United States;3. University of Texas Medical Branch, Department of Clinics Administration & Support, League City, TX 77573-1210, United States;4. University of Texas Medical Branch, Pathology, Galveston, TX 77555-0652, United States
Abstract:A study was performed to compare isosorbide dinitrate and nifedipine as adjunctive therapy in 14 patients with coronary artery disease and stable angina pectoris taking maximal beta-blocking drugs. Drug titration phases ensured maximal therapy of propranolol, isosorbide or nifedipine. The combination of nifedipine and propranolol was more effective than the combination of isosorbide and propranolol in reducing angina and increasing exercise capacity (323 vs 416 seconds, p less than 0.005) during exercise treadmill testing. Nifedipine produced a greater reduction in systolic blood pressure at submaximal exercise than isosorbide. Global and regional ejection fraction at rest and exercise was assessed with radionuclide ventriculography. The substitution of nifedipine for isosorbide depressed the global ejection fraction at rest (0.61 to 0.56 p less than 0.05) and produced a slight improvement in exercise ejection fraction (0.47 to 0.51, difference not significant). The decrease in ejection fraction from rest to exercise was 0.14 to 0.04 with nifedipine (p less than 0.005). The benefit of nifedipine compared with isosorbide occurred in regions with marked exercise-induced ischemia. In patients treated with maximal beta-blocking therapy, nifedipine is an effective alternative to isosorbide as a combination agent with propranolol. The salutary effects of nifedipine included afterload reduction with exercise and possible improvements in coronary blood supply.
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