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Screening for left ventricular systolic dysfunction among patients with risk factors for heart failure

David W Baker1, Robert C Bahler, Robert S Finkelhor

  • 1Department of Medicine and the Division of General Internal Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Ill 60611, USA. dwbaker@northwestern.edu

American Heart Journal
|October 18, 2003
PubMed

Insights

Screening for left ventricular systolic dysfunction (LVSD) is feasible in high-risk patients, with a 7.9% prevalence found. Prior myocardial infarction and left ventricular hypertrophy were key predictors, suggesting value in early detection for heart failure prevention.

Area of Science:

  • Cardiology
  • Preventive Medicine
  • Diagnostic Imaging

Background:

  • Prevalence of left ventricular systolic dysfunction (LVSD) and feasibility of screening in at-risk individuals for heart failure (HF) remain undefined.
  • This study aimed to determine LVSD prevalence using limited screening echocardiography in patients with HF risk factors but no prior HF diagnosis.

Purpose of the Study:

  • To assess the prevalence of left ventricular systolic dysfunction (LVSD) in elderly patients with cardiovascular risk factors.
  • To evaluate the feasibility and yield of screening echocardiography for LVSD in this population.

Main Methods:

  • Included general medicine patients aged 60+ with hypertension, diabetes, coronary artery disease, or prior myocardial infarction (MI), excluding those with prior HF.
  • Data collected via interview, chart review, electrocardiography (ECG), and echocardiography to determine left ventricular ejection fraction (LVEF < or =45%).

Main Results:

  • Of 482 patients, 7.9% had LVEF < or =45%.
  • Prevalence was higher in patients with prior MI (15.4%) versus without (6.7%).
  • Prior MI and ECG-defined left ventricular hypertrophy were significant predictors of reduced LVEF.

Conclusions:

  • Screening for LVSD in high-risk patients is feasible and yields substantial findings, even in those without prior MI.
  • Low screening cost and available therapies for LVSD progression warrant clinical trials for high-risk subgroup screening.
Abstract

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