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Effects of dipyridamole on cardiac and systemic haemodynamics: real-time three-dimensional stress echo beyond regional wall motion. | LitMetric

Effects of dipyridamole on cardiac and systemic haemodynamics: real-time three-dimensional stress echo beyond regional wall motion.

J Cardiovasc Med (Hagerstown)

Noninvasive Cardiology, Department of Heart and Vessels, A.O.U. Careggi, Florence, Italy.

Published: July 2011

AI Article Synopsis

  • The study explores the effects of dipyridamole on heart function and blood flow in patients with low risk for coronary artery disease during non-invasive stress testing.
  • It involved 132 subjects who had normal heart health and showed no issues after dipyridamole stress echocardiography, allowing for a thorough analysis of heart mechanics and blood volume changes.
  • Findings indicated that dipyridamole improves heart efficiency and synchronization of heart muscle contractions, but the relationship between heart rate and blood pressure changes is complex, suggesting traditional metrics may not fully capture how the body responds.

Article Abstract

Aims: Coronary vasodilation and coronary steal are the basis for routine use of dipyridamole in stress echocardiography for non-invasive assessment of coronary artery disease (CAD). This study investigates dipyridamole effects on cardiac (regional function, synchronicity and contractility) and systemic (ventricular arterial coupling) haemodynamics during real-time three-dimensional (RT3D) stress echocardiography in very low CAD risk patients.

Methods: From our RT3D stress echocardiography database, we identified 132 subjects (75 men, aged 68 ± 10 years) referred to stress echocardiography because of risk factors and/or atypical chest pain, who had normal baseline echocardiography, negative dipyridamole stress echocardiography and uneventful 2-year follow-up. All participants had good-quality RT3D datasets acquired during dipyridamole stress echocardiography (0.84 mg/kg in 10 min). From full volume datasets, ventricular volumes, regional subvolume curves and dyssynchrony index (SDI) were obtained; ventricular arterial coupling was calculated as stroke volume/end-systolic volume.

Results: In all participants, ventricular arterial coupling increased, whereas SDI decreased. End-systolic volume decreased and stroke index increased independently of pressure drop; the relationship between heart rate and arterial pressure changes was non-linear (quadratic regression, r = 0.368, P < 0.0001). The decrease in systemic resistance showed a curvilinear behaviour with respect to the ventricular arterial coupling increase.

Conclusion: In a large population of normal individuals, dipyridamole administration improved ventricular energetics and better synchronization of regional contraction may be one of the mechanisms. The relationship between blood pressure and heart rate response suggests that heart rate response is of little help in identifying the systemic haemodynamic response to dipyridamole.

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Source
http://dx.doi.org/10.2459/JCM.0b013e328343c2b8DOI Listing

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