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Martin J. Bishop

Publications and source records attributed to Martin J. Bishop.

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CORTET: Robust generation of simulation-ready tetrahedral meshes of the fetal cerebral cortex

Every human brain folds differently, and such natural variation confounds the search for imaging biomarkers of neurodevelopmental disorders. Physics-based simulation can help determine the causal mechanisms that underpin this variability. Yet every simulation must be initiated from a volumetric mesh of the brain's interior, tetrahedral or hexahedral, and it is the worst element in that mesh, not the average, that decides whether the simulation runs at all. Building that mesh from fetal MRI currently requires labour-intensive manual intervention. We therefore present CORTET (CORtical TETrahedral meshing): a fully automated pipeline that converts a triangulated cortical surface into a solver-ready tetrahedral mesh whose worst-element quality meets a strict quality target with no manual repair. By benchmarking against a general-purpose tetrahedral mesher on the same input surfaces, we isolate the pipeline's contribution from that of the input geometry, and we validate quality across a cohort of nearly 200 fetal subjects spanning the folding period. A mesh taken straight from the pipeline sustains a numerically stable morphoelastic folding simulation of a real fetal subject.

math-ph

An automated near-real time computational method for induction and treatment of scar-related ventricular tachycardias

Catheter ablation is currently the only curative treatment for scar-related ventricular tachycardias (VTs). However, not only are ablation procedures long, with relatively high risk, but success rates are punitively low, with frequent VT recurrence. Personalized in-silico approaches have the opportunity to address these limitations. However, state-of-the-art reaction diffusion (R-D) simulations of VT induction and subsequent circuits used for in-silico ablation target identification require long execution times, along with vast computational resources, which are incompatible with the clinical workflow. Here, we present the Virtual Induction and Treatment of Arrhythmias (VITA), a novel, rapid and fully automated computational approach that uses reaction-Eikonal methodology to induce VT and identify subsequent ablation targets. The rationale for VITA is based on finding isosurfaces associated with an activation wavefront that splits in the ventricles due to the presence of an isolated isthmus of conduction within the scar; once identified, each isthmus may be assessed for their vulnerability to sustain a reentrant circuit, and the corresponding exit site automatically identified for potential ablation targeting. VITA was tested on a virtual cohort of 7 post-infarcted porcine hearts and the results compared to R-D simulations. Using only a standard desktop machine, VITA could detect all scar-related VTs, simulating activation time maps and ECGs (for clinical comparison) as well as computing ablation targets in 48 minutes. The comparable VTs probed by the R-D simulations took 68.5 hours on 256 cores of high-performance computing infrastructure. The set of lesions computed by VITA was shown to render the ventricular model VT-free. VITA could be used in near real-time as a complementary modality aiding in clinical decision-making in the treatment of post-infarction VTs.

physics.med-ph