Key result
Random survival forests using remote monitoring data predict 6-month VT/VF after NSVT with ~0.79 C-index.
Why the study?
It is unknown when ICD patients will need therapy or how to action remote monitoring NSVT alerts, and whether remote monitoring data improves risk assessment over clinical information alone.
Do machine learning models using remote monitoring data improve the prediction of sustained VT/VF within six months after an NSVT alert in ICD patients compared to clinical data alone or classical survival models?
Cohort (n=744)
No
Do machine learning models using remote monitoring data improve the prediction of sustained VT/VF within six months after an NSVT alert in ICD patients compared to clinical data alone or classical survival models?
Effect estimate: C-index 0.790 (95% CI 0.765-0.807)
Machine learning applied to ICD remote monitoring data significantly improves the prediction of sustained VT/VF following an NSVT alert compared to traditional clinical data and classical survival models.
May enhance NSVT risk stratification via remote monitoring in ICD patients; hypothesis-generating pending prospective validation.
Introduction We do not know when patients with an implantable cardioverter-defibrillator (ICD) will require therapy or how to action alerts for non-sustained ventricular tachycardia (NSVT). Accurate prediction could enable preventive interventions for shock therapies, improving quality of life and morbidity [1-3]. Machine learning models (ML) using remote monitoring (RM) may provide accurate short-term risk prediction of malignant arrhythmias [3,4], but we do not know how to integrate risk assessment into clinical care, nor if RM is more useful than clinical information alone. Purpose (1) Evaluate ML-based and classical survival models in predicting sustained VT/VF following a common RM alert (NSVT). (2) Compare model performance using RM versus baseline clinical and demographic data. Methods Retrospective study of 744 patients with 13717 NSVT episodes at a tertiary hospital (Figure 1). To avoid oversampling NSVT clusters, episodes were capped at the mean per patient (20) and one per day, leaving 5908 episodes. The primary outcome was VT/VF >160bpm with guideline-based programming within six months after NSVT. Clinical and demographic data were collected at implant and RM data including electrogram features, in the 30 days before NSVT. Feature selection was performed via LASSO-penalised Cox proportional hazard (CPH) regression. An 80/20% split of the patient cohort was used for training and independent test set. Harrell’s C-index and time-dependent area under the curve (AUC) [5,6] were evaluated for CPH, random survival forest (RSF) and deep learning survival models (DL-COX). Model performance was evaluated when trained on RM-only data, clinical characteristics, or both. Results VT/VF occurred in 2382 (40%) of NSVT episodes within six months (median survival: 25 days, interquartile range: 4-77). There was good overall predictive performance for RSF (0.790 [95% CI: 0.765-0.807]), outperforming CPH and DL-COX models (0.760 [0.727-0.774] and 0.765 [0.742-0.788], respectively). RSF demonstrated good short- and long-term prediction (mean AUC: 0.865 [95% CI: 0.845-0.885]), with a modest decline over time (1-, 7-, and 180-day AUC: 0.911, 0.889, 0.799). High- vs low-risk patient stratification showed imminent (<24 hours) and late Kaplan-Meier curve separation (Figure 2). RSFs trained using RM data outperformed baseline-only models (C-index: 0.790 vs 0.782 vs 0.550; mean AUC: 0.865 vs 0.862 vs 0.579 for all data, only RM and only baseline data, respectively). Highly predictive features were similar across models, including time since previous VT/VF and number of ventricular arrhythmia events in previous 30 days. Conclusions Machine learning using remote monitoring data effectively predicts imminent and six-month VT/VF risk, more than clinical data alone or classical survival models. This work proposes a pathway to integrate ML assessment into remote monitoring, enabling proactive rather than reactive anti-arrhythmia intervention.
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Campbell et al. (2025) conducted a cohort in Implantable cardioverter-defibrillator with non-sustained ventricular tachycardia (n=744). Random survival forest model using remote monitoring data vs. Baseline clinical data alone or classical survival models was evaluated on VT/VF >160bpm with guideline-based programming within six months after NSVT (C-index 0.790, 95% CI 0.765-0.807). A random survival forest model using remote monitoring and clinical data predicted sustained VT/VF within six months of an NSVT alert better than baseline data alone (C-index 0.790 vs 0.550).
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