Cardiac activation mapping by MRI

Radionuclide angiography (RNA) permits analysis of contractility and conduction abnormalities. We determined the parameters of normal ventricular synchronization, assessed the reproducibility of the technique, and compared first harmonic (1H) and third harmonic (3H) analysis. Forty-four normal subjects (28 men and 16 women) were studied. RNA was performed in left anterior oblique (LAO) and left lateral (LL) projections. The onset (To), mean time (Tm), total contraction time (Tt) for right ventricle (RV) and left ventricle (LV), interventricular time (T(RV-LV) = Tm(LV - Tm(RV)) in LAO, and the apex-to-base time (T(a-b)) in LL were measured on the histograms of the time-activity curve. Reproducibility (R) was tested by studying 26 consecutive patients with two successive RNAs. RV starts contracting 25 ms before LV (To(RV) = 29 +/- 37 ms; To(LV) = 54 +/- 39 ms; mean +/- SD) with a 37 ms longer total contraction time. T(RV-LV) is 3 +/- 16 ms. In LL projection, apex and base contract synchronously: T(a-b) = 2 +/- 16 ms. 3H analysis enlarges all duration parameters (To, Tm and Tt), but does not alter synchronization (deltaT(a-b) and deltaT(RV-LV) between 1H and 3H <1%, p = NS). Reproducibility of the duration (T(tLV) and T(tRv)) and synchronization parameters (T(a-b) and T(RV-LV)) is high (R < or = 2.2%). In conclusion, the simultaneous contraction of right and left ventricles and of apex and base can be quantified by RNA phase analysis with high reproducibility. These results, consistent with published electrophysiological data, provide the basis for further non-invasive investigations of ventricular resynchronization in patients with basal electrical or mechanical asynchrony.

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Toussaint

Peix

Lavergne

et al. 2002

The International Journal of Cardiac Imaging

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Fourier Phase Mapping of the Human Heart

Knollmann

Mäurer

Wlodarczyk

et al. 1996

Investigative Radiology

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Using the unsegmented SPAMM two-dimensional FISP sequence, a more consistent tag-to-myocardium contrast and a higher number of cardiac phases was achieved than by using the segmented version of this sequence. The typical tag displacement reflected complex intramyocardial dynamics, including rotation. Phase mapping displayed a pattern of contraction consistent with electrophysiologic concepts of cardiac activation. In contrast, the segmented sequence did not reflect any differences in the onset of cardiac contraction, although tag displacement was apparent with this sequence as well. CONCLUSIONS. Fourier phase mapping of cardiac MR imaging tagging studies allows for noninvasive analysis of intramyocardial activation patterns. A temporal resolution of 50 mseconds per image at a heart rate of 75 beats per minute allows for an assessment of spatial differences in the onset of myocardial activation.

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Mapping propagation of mechanical activation in the paced heart with MRI tagging

Wyman

Hunter

Prinzen

et al. 1999

American Journal of Physiology-Heart and Circulatory Physiology

197

179

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The temporal evolution of three-dimensional (3-D) strain maps derived from magnetic resonance imaging (MRI) tagging were used to noninvasively evaluate mechanical activation in the left ventricle (LV) while seven canine hearts were paced in situ from three different sites: the base of the LV free wall (LVb), the right ventricular apex (RVa), and the right atrium (RA). Strain maps plotted against time showed the evolution of shortening over the entire LV midwall and were used to generate mechanical activation maps showing the onset of circumferential shortening. RA pacing showed rapid synchronous shortening; LVb pacing showed a wave front of mechanical activation propagating slowly and steadily from the pacing site, whereas RVa pacing showed regions of rapid and slower propagation. The mechanical (M) activation times correlated linearly with the electrical (E) activation (M = 1.06E + 8.4 ms, R = 0.95). The time for 90% activation of the LV was 63.1 ± 24.3 ms for RA pacing, 130.2 ± 9.8 ms for LVb pacing, and 121.3 ± 17.9 ms for RVa pacing. The velocity of mechanical activation was calculated for LVb and RVa pacing and was similar to values reported for electrical conduction in myocardium. The propagation of mechanical activation for RVa pacing showed regional variations, whereas LVb pacing did not.

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Cardiac activation mapping by MRI

Cited by 3 publications

References 18 publications

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Fourier Phase Mapping of the Human Heart

Mapping propagation of mechanical activation in the paced heart with MRI tagging

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