Dipyridamole stress echocardiography for risk stratification in hypertensive patients with chest pain

L Cortigiani1, E A Paolini, E Nannini

  • 1Cardiovascular Unit, Hospital of Lucca, Italy.

Circulation
|December 22, 1998
PubMed

Insights

Dipyridamole stress echocardiography effectively stratifies risk in hypertensive patients with chest pain and unknown coronary artery disease (CAD). This safe and feasible test predicts cardiac events, aiding prognostic assessment.

Area of Science:

  • Cardiology
  • Diagnostic Imaging
  • Hypertension Management

Background:

  • Assessing coronary artery disease (CAD) noninvasively in hypertensive patients remains challenging.
  • Hypertension is a significant risk factor for CAD, necessitating reliable prognostic tools.

Purpose of the Study:

  • To evaluate the utility of dipyridamole stress echocardiography for risk stratification.
  • To assess its prognostic value in hypertensive patients presenting with chest pain and undiagnosed CAD.

Main Methods:

  • Conducted dipyridamole stress echocardiography on 257 hypertensive patients with chest pain and no prior CAD diagnosis.
  • Monitored for cardiac events (death, myocardial infarction, unstable angina) and revascularization during follow-up.
  • Utilized multivariate analysis to identify predictors of cardiac events.

Main Results:

  • The test demonstrated high feasibility (98.4%) with minimal complications.
  • A positive echocardiographic response predicted hard cardiac events (OR 5.5) and spontaneous cardiac events (OR 4.2).
  • Three-year survival rates differed significantly between patients with negative (97%) and positive (87%) echocardiographic results for hard cardiac events.

Conclusions:

  • Dipyridamole stress echocardiography is a safe, feasible, and effective tool for risk stratification in this patient group.
  • It offers valuable prognostic information for hypertensive patients with chest pain and unknown CAD.
  • The procedure is a recommended option for assessing the prognosis of this specific clinical population.
Abstract

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