Abstract

BackgroundMagnetic resonance imaging (MRI) is the medical imaging technique that benefits most from recent technological innovations, particularly the constant proposal of new MRI sequences that refine clinical information from the obtained images. However, this generates new gradient-induced potential (GIP) morphologies. These induced potentials (IPs) pollute the electrophysiological signals possibly recorded simultaneously. Several algorithms developed to eliminate this noise rely on modelling the shape of the IP. As each new sequence has a different shape of IP, it might be interesting to find a mathematical approach to building sequence-specific models. In this article, we present a preliminary study that includes wavelet decomposition of contaminated electrocardiographic (ECG) to extract IP morphologies and whose time–frequency characterization allows the elaboration of a harmonic model, using sinusoidal decomposition. MethodThe in vitro IPs are used to select analyzing wavelets. A broadband sensor (3.5Khz), placed inside a 3 T MRI scanner, is used to collect 3-lead ECGs while activating three sequences that generate very high noise levels. The in vivo IPs extracted from the polluted ECGs are characterized to verify their quasi-periodicity. Parameters of the sinusoidal model (amplitude, frequency, phase) are estimated using the Broyden-Fletcher-Goldfard-Shano optimization algorithm. ResultFour wavelets (sym7, coif3, bior2.2, bior3.3) showed efficient in vivo IP extraction results. Three evaluation criteria for the modelling algorithm, allowing the calculated models to be compared with the shapes of the extracted IPs, showed promising results. For example, for the chosen efficiency criterion Nash-Sutcliffe efficiency, the values obtained for the three leads are between 0.99980 and 1. ConclusionPromising preliminary results have been obtained for the extraction on modelling of different IPs from noisy ECG signals. Continuing this preliminary study on more MRI sequences and subjects could help build a database of IP models to initiate deep learning filtering. Since these models are sequence-specific and integrate the distribution of induced voltages on the body surface, we hope to find a generic relationship that enables the prediction of IPs by new sequences and anticipate the development of purification algorithms in a near future.

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