Risk factor and prediction modeling for sudden cardiac death in women with coronary artery disease

Rajat Deo1, Eric Vittinghoff, Feng Lin

  • 1Section of Electrophysiology, Division of Cardiovascular Medicine, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104, USA. Rajat.Deo@uphs.upenn.edu

Insights

Sudden cardiac death (SCD) is a major concern for women with coronary artery disease (CAD). Key risk factors like heart failure and diabetes significantly increase SCD risk, improving prediction when combined with LVEF.

Area of Science:

  • Cardiology
  • Women's Health
  • Public Health

Background:

  • Sudden cardiac death (SCD) risk and prediction models are understudied in women with coronary artery disease (CAD).
  • This study addresses the incidence of SCD and its risk factors in this population.

Purpose of the Study:

  • To evaluate the incidence of SCD in postmenopausal women with CAD.
  • To identify independent risk factors for SCD.
  • To assess the predictive accuracy of these risk factors, alone and with left ventricular ejection fraction (LVEF).

Main Methods:

  • Analysis of 2763 postmenopausal women with CAD from the Heart and Estrogen/progestin Replacement Study.
  • Cox proportional hazards models to identify SCD predictors.
  • C-index and net reclassification improvement to compare predictive models.

Main Results:

  • SCD accounted for 136 of 254 cardiac deaths, with an annual incidence of 0.79%.
  • Independent predictors of SCD included myocardial infarction, heart failure, low estimated glomerular filtration rate, atrial fibrillation, physical inactivity, and diabetes.
  • Combining clinical risk factors with LVEF improved SCD prediction (C-index 0.681) compared to LVEF alone (C-index 0.600).

Conclusions:

  • SCD is the predominant cause of cardiac death in postmenopausal women with CAD.
  • Identified risk factors significantly enhance SCD prediction beyond LVEF alone.
  • These findings are crucial for risk stratification and targeted interventions in women with CAD.
Abstract

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