Why the study?
Do tissue Doppler imaging and velocity vector imaging detect subclinical left ventricular dysfunction in asymptomatic patients with severe aortic regurgitation and normal ejection fraction compared to controls?
Do tissue Doppler imaging and velocity vector imaging detect subclinical left ventricular dysfunction in asymptomatic patients with severe aortic regurgitation and normal ejection fraction compared to controls?
VVI-derived strain imaging and TDI-derived IVA can reliably detect subclinical left ventricular dysfunction in asymptomatic patients with severe aortic regurgitation and normal ejection fraction, potentially aiding in optimal surgical timing.
Impaired TDI IVA and VVI strain in severe AR with preserved EF may indicate subclinical LV dysfunction; leaves open whether these markers should guide timing of intervention.
OBJECTIVES: Our aim was to evaluate subclinical left ventricular (LV) dysfunction, by two novel echocardiographic techniques, velocity vector imaging (VVI)-derived strain imaging and tissue Doppler imaging (TDI), in patients with asymptomatic, severe aortic regurgitation (AR). METHODS: Forty patients with severe AR with normal ejection fraction and 30 controls were included to the study. All patients underwent a standard echocardiography extended with TDI and VVI analyses. To evaluate the LV longitudinal and circumferential deformation, segmental systolic peak strain and strain rate (SRs) data were acquired from parasternal short axis, apical four-chamber, two-chamber, and long axis views, and additionally LV myocardial velocities, isovolumic myocardial acceleration (IVA), peak systolic velocity (Sa) and peak myocardial velocity during isovolumic contraction (IVV) assessed by TDI. RESULTS: IVA was the only TDI-derived parameter which was significantly impaired in AR patients (P = 0.0001). Both longitudinal and circumferential strain and SRs of the LV were significantly decreased in patients with severe AR (P = 0.0001). Longitudinal and circumferential strain/SRs and TDI-derived LV IVA were inversely correlated with LV end-diastolic diameter (P = 0.0001) and end-systolic diameter (P = 0.0001). TDI-derived IVA was also very well correlated with longitudinal deformation parameters (P = 0.0001). CONCLUSIONS: VVI- derived strain imaging and TDI-derived IVA may be used as adjunctive, reliable, noninvasive parameters for evaluating subclinical ventricular dysfunction in patients with chronic, severe AR. This may help to identify patients for closer follow-up and to determine the need for surgery before developing irreversible, severe heart failure.
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Tayyareci et al. (2010) studied this question.
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