TY - JOUR
T1 - Effect of diltiazem on cardiac rate and rhythm after myocardial infarction
AU - Bigger, J. Thomas
AU - Coromilas, James
AU - Rolnitzky, Linda M.
AU - Fleiss, Joseph L.
AU - Kleiger, Robert E.
N1 - Funding Information:
From the Division of Cardiology, Department of Medicine, and Division of Biostatistics, School of Public Health, Columbia University, New York, New York, and the Department of Medicine, Washington University School of Medicine, St. Louis, Missouri. This study was supported in part by a consortium grant from Dodecke Aktiengesell-schaft, Germany, Laboratorios Dr Ssteve, SA, Spain, Marion Laboratories, Inc., United States, Nordic Laboratories, Inc., Canada, Lars Synthelabo, France, Tanabe Seiyaku Co., Ltd., Japan, and Wamer-Lambert International, United States. The study was supported in part by National Institutes of Health grant HG70204 from the National Heart, Lung, and Blood Institute, Bethesda, Maryland, by grant RR-00645 from the Research Resources Administration, Bethesda; and by funds from The Mibtein Family Foundation, The Dover Foundation, George and Abby O’Neill, Robert Winthrop, and the Shilee and Henry Benach Foundation, New York, New York. Manuscript received September 5.1989; revised manuscript received October 27,1989, and accepted October 28. Address for reprints: J.T. Bigger, Jr., MD, Arrhythmia Control Unit, Columbia-Presbyterian Medical Center, 630 West 168th Street, New York, New York 10032. * See Appendix.
PY - 1990/3/1
Y1 - 1990/3/1
N2 - The a priori hypothesis that diltiazem would reduce the frequency and repetitiveness off ventricular arrhythmias was tested 3 months after myocardial infarction in patients participating in the Multi-center Diltiazem Postinfarction Trial. After 3 months of follow-up, 1,546 of the 2,466 patients enrolled had a 24-hour continuous electrocardiographic recording that contained ≥ 12 hours of analyzable data. They were similar to the patients who survived 3 months but chose not to have a 24-hour ehctrocardiographic recording (i.e., they were representative of the entire group that survived 3 months). After 3 months of follow-up, there were no significant differences between the diltiazem and placebo groups in the prevalence of atrioventricular block, the frequency of atrial arrhythmias or the frequency or repetitiveness of ventricular arrhythmias. Heart rate was significantly lower (67 ± 12 vs 71 ± 12 beats/min) and there was a significantly greater proportion of patients with sinus pauses ≥ 2 seconds in duration in the diltiazem group (6%) than in the placebo group (3%). Comparison with placebo revealed no evidence either for an anti- or proarrhythmic effect of diltiazem. There was no reduction in sudden or arrhythmic death attributable to diltiazem treatment; the fraction of total deaths that were arrhythmic by the Hinkle classification was 41% in the placebo group and 42% in the diltiazent group. It may be that the lack of effect of diltiazem on ventricular arrhythmias is partially responsible for its lack off effect on mortality after myocardial infarction.
AB - The a priori hypothesis that diltiazem would reduce the frequency and repetitiveness off ventricular arrhythmias was tested 3 months after myocardial infarction in patients participating in the Multi-center Diltiazem Postinfarction Trial. After 3 months of follow-up, 1,546 of the 2,466 patients enrolled had a 24-hour continuous electrocardiographic recording that contained ≥ 12 hours of analyzable data. They were similar to the patients who survived 3 months but chose not to have a 24-hour ehctrocardiographic recording (i.e., they were representative of the entire group that survived 3 months). After 3 months of follow-up, there were no significant differences between the diltiazem and placebo groups in the prevalence of atrioventricular block, the frequency of atrial arrhythmias or the frequency or repetitiveness of ventricular arrhythmias. Heart rate was significantly lower (67 ± 12 vs 71 ± 12 beats/min) and there was a significantly greater proportion of patients with sinus pauses ≥ 2 seconds in duration in the diltiazem group (6%) than in the placebo group (3%). Comparison with placebo revealed no evidence either for an anti- or proarrhythmic effect of diltiazem. There was no reduction in sudden or arrhythmic death attributable to diltiazem treatment; the fraction of total deaths that were arrhythmic by the Hinkle classification was 41% in the placebo group and 42% in the diltiazent group. It may be that the lack of effect of diltiazem on ventricular arrhythmias is partially responsible for its lack off effect on mortality after myocardial infarction.
UR - http://www.scopus.com/inward/record.url?scp=0025343743&partnerID=8YFLogxK
U2 - 10.1016/0002-9149(90)91028-5
DO - 10.1016/0002-9149(90)91028-5
M3 - Article
C2 - 2178379
AN - SCOPUS:0025343743
SN - 0002-9149
VL - 65
SP - 539
EP - 546
JO - The American journal of cardiology
JF - The American journal of cardiology
IS - 9
ER -