Circulation, Vol 51, 964-975, Copyright © 1975 by American Heart Association
EL Alderman, RO Davies, JJ Crowley, MG Lopes, JZ Brooker, JP Friedman, AF Graham, HJ Matlof and DC Harrison
Seventeen patients received placebo medication during a 12-week run-in
period, followed by four double-blind study periods of six weeks each,
during which time placebo, 80 mg, 160 mg and 320 mg propranolol dosages
were administered. Examination of the frequency of angina episodes and
nonprophylactic nitroglycerin consumption revealed significant beneficial
clinical responses for both the 160 and 320 mg dosages. Exercise testing
also demonstrated increased exercise tolerance (320 mg dose) with a shift
of the exercise end point from pain to fatigue in seven of 17 patients. The
interrelationships between propranolol daily dosage, clinical response
assessed by percent reduction in anginal episodes, beta-adrenergic blockade
measured by percent reduction in exercise heart rate and serum levels were
examined. In general, serum levels of 30 ng/ml, when drawn 90 to 180
minutes following the last oral dose, were required to achieve a 25% or
greater reduction in angina frequency. Serum levels above 30 ng/ml were
similarly correlated with a 20% or greater reduction in exercise heart rate
at equivalent levels of exercise. Detailed examination of different
patterns of clinical response with respect to beta-blockade, serum levels
and oral doses are presented.
ARTICLES
Dose response effectiveness of propranolol for the treatment of angina pectoris
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A. Flach Propranolol Withdrawal and Myocardial Infarction JAMA, January 23, 1981; 245(4): 342 - 342. [Abstract] [PDF] |
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