TY - JOUR
T1 - Clinical use of oral verapamil in chronic and paroxysmal atrial fibrillation
AU - Stern, E. H.
AU - Pitchon, R.
AU - King, B. D.
AU - Guerrero, J.
AU - Schneider, R. R.
AU - Wiener, I.
N1 - Funding Information:
Supported in part by a grant from Knoll Pharmaceutical Company, Whippany, New Jersey
PY - 1982
Y1 - 1982
N2 - We evaluated the effectiveness of oral verapamil therapy for control of ventricular rate in digitalized patients with atrial fibrillation (AF) with three clinical problems: chronic AF with rapid rate at rest (four patients), chronic AF with accelerated rate during modest exercise (five patients), and rapid rates during paroxysmal AF (four patients). Patients in the first two categories were evaluated both by open-label dosage titration and by a randomized, double-blind, cross-over protocol. In chronic AF with rapid rate of rest, there was a significant reduction in resting heart rate (from 125 ± 7 to 87 ± 14, P<0.01) and in peak exercise heart rate (from 162 ± 33 to 126 ± 25, P<0.01). In chronic AF with rapid rate during exercise, there was also a significant decrease in resting heart rate (from 90 ± 7 to 66 ± 4, P<0.01) and in peak exercise heart rate (from 126 ± 19 to 101 ± 15, P<0.01). These effects continued during longterm follow-up of one to 12 months (mean seven months). In patients with paroxysmal AF, verapamil slowed the ventricular response from 160 ± 24 to 72 ± 4, P<0.01) with only some amelioration of symptoms. Therapy was well tolerated despite a high prevalence (seven of 13 patients) of radiographic cardiomegaly (cardiothoracic ratio > 0.55). We conclude that verapamil is a safe and useful drug for control of ventricular rate in digitalized patients with chronic and paroxysmal AF.
AB - We evaluated the effectiveness of oral verapamil therapy for control of ventricular rate in digitalized patients with atrial fibrillation (AF) with three clinical problems: chronic AF with rapid rate at rest (four patients), chronic AF with accelerated rate during modest exercise (five patients), and rapid rates during paroxysmal AF (four patients). Patients in the first two categories were evaluated both by open-label dosage titration and by a randomized, double-blind, cross-over protocol. In chronic AF with rapid rate of rest, there was a significant reduction in resting heart rate (from 125 ± 7 to 87 ± 14, P<0.01) and in peak exercise heart rate (from 162 ± 33 to 126 ± 25, P<0.01). In chronic AF with rapid rate during exercise, there was also a significant decrease in resting heart rate (from 90 ± 7 to 66 ± 4, P<0.01) and in peak exercise heart rate (from 126 ± 19 to 101 ± 15, P<0.01). These effects continued during longterm follow-up of one to 12 months (mean seven months). In patients with paroxysmal AF, verapamil slowed the ventricular response from 160 ± 24 to 72 ± 4, P<0.01) with only some amelioration of symptoms. Therapy was well tolerated despite a high prevalence (seven of 13 patients) of radiographic cardiomegaly (cardiothoracic ratio > 0.55). We conclude that verapamil is a safe and useful drug for control of ventricular rate in digitalized patients with chronic and paroxysmal AF.
UR - http://www.scopus.com/inward/record.url?scp=0020056979&partnerID=8YFLogxK
U2 - 10.1378/chest.81.3.308
DO - 10.1378/chest.81.3.308
M3 - Article
C2 - 7056105
AN - SCOPUS:0020056979
VL - 81
SP - 308
EP - 311
JO - Unknown Journal
JF - Unknown Journal
IS - 3
ER -