The occurrence of cardiovascular side effects is sometimes associated
with the utilization of beta-adrenoceptor agonists, The most important
causes of these undesirable pharmacologic actions are as follows: (1)
direct stimulation of cardiac beta-adrenoceptors; (2) reflex activati
on of adrenergic mechanisms due to peripheral vasodilation; (3) hypoka
lemia; and (4) hypoxemia. The aim of this study was to evaluate the po
tential short-term, cardiovascular side effects of salmeterol, a long-
acting and highly selective beta(2)-adrenoceptor agonist, Eight volunt
eer healthy subjects and eight patients with reversible airway obstruc
tion and without cardiovascular alterations were treated with 50 mu g
of salmeterol mice a day for 3 days and then with 100 mu g of salmeter
ol twice a day for a further 3-day period. The 24-h ECG (Molter) monit
oring and measurement of arterial BP, performed on the admission day a
nd on the third and the sixth day of pharmacologic treatment, showed t
hat salmeterol did not produce any significant change in mean heart ra
te, number of supraventricular and ventricular premature complexes, an
d BP, Furthermore, no ECG abnormality related to myocardial ischemia w
as recorded during 24-h Holter monitoring. These data suggest that sal
meterol, administered in regular and high doses for a short period, do
es not cause significant cardiovascular effects in both normal subject
s and patients with reversible airway obstruction.