Chest
Clinical InvestigationsCARDIOLOGYIncidence, Predictive Factors, and Prognostic Significance of Supraventricular Tachyarrhythmias in Congestive Heart Failure
Section snippets
Eligibility and Randomization
Details of rationale, design, baseline characteristics, and mainoutcome of the DIG study have been publishedpreviously.56 The DIG study was a large, simpledouble-blind, placebo-controlled clinical trial on the effect of digoxin on mortality and hospitalization in heart failure. Briefly, patients with CHF who were in sinus rhythm at baseline were eligiblefor enrollment. Patients with CHF and a left ventricular ejectionfraction of ≤ 0.45 (n = 6,800) were enrolled into the main trial;patients with
Results
Table 1summarizes the baseline characteristics of the total DIG study cohortand compares these characteristics in the subset that experienced SVTwith those of the remaining patients (sample sizes for the currentanalysis were slightly lower because of missing values, but thebaseline percentages were unchanged). Patients who had SVT were olderand had a longer duration of CHF. A greater proportion of patients whoexperienced SVT had a cardiothoracic ratio > 0.50 and were in NYHAfunctional class
Incidence and Risk Factors for SVT
To our knowledge, no previous studies have prospectivelydetermined the incidence and risk factors for developing SVT in a largecohort of CHF patients who were in sinus rhythm at baseline. In thecurrent study, the incidence of SVT in a large heterogeneous populationof patients with CHF during a 3-year period was 11%. Older age, malesex, longer duration of CHF, and an enlarged heart predicted asignificantly increased risk of this complication in patients with CHF. These results parallel in part
Conclusion
In a large, heterogeneous population of patients with CHF andsinus rhythm, older age, male sex, longer duration of CHF, andincreased cardiothoracic ratio are significant risk factors for thedevelopment of SVT. Development of SVT in patients with CHF is a strongand independent predictor of death, stroke, and hospitalization forworsening CHF. Treatment with digoxin does not reduce the risk of development of SVT in patients with CHF. Further studies to determinethe effect of interventions to
ACKNOWLEDGMENT
The authors thank Ruby N. Stubbs-Stamps, Shari L. Berry, Michael Wold, Stephanie E. Pritchett, and Shanti M. Mathew forassistance in preparation of the manuscript. A complete list of the DIGinvestigators and institutional affiliations has been publishedpreviously.6
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Presented in part at the 47th Annual Scientific Sessions of the American College of Cardiology, Atlanta, GA, March 31, 1998.