arXiv subjects

Mark L. Trew

Publications and source records attributed to Mark L. Trew.

3 recordsLinked to original sources

arXiv2026

Multicentre Bi-atrial Segmentation from LGE-MRI for Atrial Fibrillation with a 2D and 3D Framework

Accurate delineation of bi-atrial structures from late gadolinium enhancement MRI (LGE-MRI) is an important prerequisite for structural analysis and future fibrosis-quantification workflows in atrial fibrillation (AF). However, automated segmentation is challenging due to thin-walled anatomy, domain shifts across imaging centres, and limited benchmarking of existing methods. This study presents a two-stage segmentation framework and benchmarking platform for evaluating how ROI localisation, encoder design, 2D/3D dimensionality, and ensemble fusion affect bi-atrial wall and cavity segmentation across multicentre LGE-MRI datasets. The framework integrates 3D localisation and fine segmentation using 2D and 3D U-Net variants with ResNeXt encoders and compares them with convolutional, transformer-based, and state-space architectures. { Evaluation across three independent cohorts assessed accuracy and cross-domain transfer without target-domain fine-tuning. Cavity segmentation transferred more consistently across centres than atrial wall segmentation, while wall performance remained sensitive to domain shift, particularly in the Kobe cohort.} By quantifying how 2D, 3D, and ensemble architectures behave across centres and between walls and cavities, this work provides a reproducible benchmark for future methodological development and clinical validation.

eess.IV↗

arXiv2021

Impulse data models for the inverse problem of electrocardiography

The proposed method re-frames traditional inverse problems of electrocardiography into regression problems, constraining the solution space by decomposing signals with multidimensional Gaussian impulse basis functions. Impulse HSPs were generated with single Gaussian basis functions at discrete heart surface locations and projected to corresponding BSPs using a volume conductor torso model. Both BSP (inputs) and HSP (outputs) were mapped to regular 2D surface meshes and used to train a neural network. Predictive capabilities of the network were tested with unseen synthetic and experimental data. A dense full connected single hidden layer neural network was trained to map body surface impulses to heart surface Gaussian basis functions for reconstructing HSP. Synthetic pulses moving across the heart surface were predicted from the neural network with root mean squared error of $9.1\pm1.4$%. Predicted signals were robust to noise up to 20 dB and errors due to displacement and rotation of the heart within the torso were bounded and predictable. A shift of the heart 40 mm toward the spine resulted in a 4\% increase in signal feature localization error. The set of training impulse function data could be reduced and prediction error remained bounded. Recorded HSPs from in-vitro pig hearts were reliably decomposed using space-time Gaussian basis functions. Predicted HSPs for left-ventricular pacing had a mean absolute error of $10.4\pm11.4$ ms. Other pacing scenarios were analyzed with similar success. Conclusion: Impulses from Gaussian basis functions are potentially an effective and robust way to train simple neural network data models for reconstructing HSPs from decomposed BSPs. The HSPs predicted by the neural network can be used to generate activation maps that non-invasively identify features of cardiac electrical dysfunction and can guide subsequent treatment options.

q-bio.QM↗

arXiv2017

An intracardiac electrogram model to bridge virtual hearts and implantable cardiac devices

Virtual heart models have been proposed to enhance the safety of implantable cardiac devices through closed loop validation. To communicate with a virtual heart, devices have been driven by cardiac signals at specific sites. As a result, only the action potentials of these sites are sensed. However, the real device implanted in the heart will sense a complex combination of near and far-field extracellular potential signals. Therefore many device functions, such as blanking periods and refractory periods, are designed to handle these unexpected signals. To represent these signals, we develop an intracardiac electrogram (IEGM) model as an interface between the virtual heart and the device. The model can capture not only the local excitation but also far-field signals and pacing afterpotentials. Moreover, the sensing controller can specify unipolar or bipolar electrogram (EGM) sensing configurations and introduce various oversensing and undersensing modes. The simulation results show that the model is able to reproduce clinically observed sensing problems, which significantly extends the capabilities of the virtual heart model in the context of device validation.

eess.SY↗