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Computational Identification of Ventricular Arrhythmia Risk in Pediatric Myocarditis
Mark J Cartoski1, Plamen P Nikolov2, Adityo Prakosa2
1Divison of Pediatric Cardiology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. mark.cartoski@nemours.org.
Insights
This study shows personalized cardiac models can predict ventricular tachycardia (VT) risk in children with myocarditis. This non-invasive approach may help identify at-risk patients, improving myocarditis management.
Area of Science:
- Cardiology
- Biomedical Engineering
- Medical Imaging
Background:
- Children with myocarditis face a higher risk of ventricular tachycardia (VT) due to heart muscle inflammation and remodeling.
- Current methods for stratifying VT risk in pediatric myocarditis patients are lacking.
Purpose of the Study:
- To investigate the potential of personalized computational cardiac models, derived from late gadolinium-enhanced magnetic resonance imaging (LGE-MRI), for determining VT risk in children with myocarditis.
Main Methods:
- Reconstructed personalized 3D computational cardiac models from LGE-MRI scans of 12 pediatric myocarditis patients (4 with VT, 8 without).
- Incorporated patient-specific fibrosis distribution and myocardial fiber orientations into models.
- Assessed VT inducibility via rapid pacing simulations from 26 ventricular sites.
Main Results:
- Sustained reentrant VT was successfully induced in all patients with a history of clinical VT.
- No sustained reentry was induced in patients without clinical VT during simulations.
Conclusions:
- Personalized computational cardiac models utilizing LGE-MRI data can effectively differentiate VT risk in pediatric myocarditis.
- This non-invasive simulation approach shows promise for identifying children at risk of developing VT, aiding clinical decision-making.
Abstract:
Children with myocarditis have increased risk of ventricular tachycardia (VT) due to myocardial inflammation and remodeling. There is currently no accepted method for VT risk stratification in this population. We hypothesized that personalized models developed from cardiac late gadolinium enhancement magnetic resonance imaging (LGE-MRI) could determine VT risk in patients with myocarditis using a previously-validated protocol. Personalized three-dimensional computational cardiac models were reconstructed from LGE-MRI scans of 12 patients diagnosed with myocarditis. Four patients with clinical VT and eight patients without VT were included in this retrospective analysis. In each model, we incorporated a personalized spatial distribution of fibrosis and myocardial fiber orientations. Then, VT inducibility was assessed in each model by pacing rapidly from 26 sites distributed throughout both ventricles. Sustained reentrant VT was induced from multiple pacing sites in all patients with clinical VT. In the eight patients without clinical VT, we were unable to induce sustained reentry in our simulations using rapid ventricular pacing. Application of our non-invasive approach in children with myocarditis has the potential to correctly identify those at risk for developing VT.
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