AI-Enabled Sensor Technologies for Remote Arrhythmic Monitoring in High-Risk Cardiomyopathy Genotypes

Nardi Tetaj1,2, Andrea Segreti1,2, Francesco Piccirillo1,2

  • 1Cardiology Unit, Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.

Insights

Artificial intelligence (AI) sensor technology offers remote arrhythmic monitoring for inherited cardiomyopathies. This approach promises proactive prevention of sudden cardiac death by analyzing continuous data, but requires genotype-specific validation.

Area of Science:

  • Cardiology
  • Biomedical Engineering
  • Artificial Intelligence

Background:

  • Inherited cardiomyopathies carry high risk for malignant ventricular arrhythmias and sudden cardiac death, often unrelated to traditional markers.
  • Current surveillance methods are inadequate for detecting silent electrical instability in these high-risk patients.
  • Genotype-specific risk stratification is crucial for understanding disease progression.

Purpose of the Study:

  • To review the role of artificial intelligence (AI)-enabled sensor technologies in remote arrhythmic monitoring for inherited cardiomyopathy patients.
  • To evaluate the potential of continuous electrophysiological and hemodynamic data acquisition for early detection of arrhythmic vulnerability.
  • To identify challenges and future directions for implementing AI-driven sensing in genotype-specific cohorts.

Main Methods:

  • Narrative review of emerging AI-enabled sensor technologies, including wearable ECGs, implantable monitors, and multisensor devices.
  • Analysis of how AI enhances signal processing, automated event detection, and remote data triage.
  • Examination of digital biomarkers derived from continuous data streams for early detection of arrhythmias and decompensation.

Main Results:

  • AI-enabled sensors provide continuous electrophysiological and hemodynamic data, generating digital biomarkers for early arrhythmic risk.
  • AI analytics can improve signal processing and automated event detection, potentially reducing clinical workload.
  • Current evidence is limited, with most studies in general heart failure or arrhythmia populations, necessitating genotype-specific validation.

Conclusions:

  • AI-enabled sensing combined with genotype information offers a promising shift towards proactive, precision-guided arrhythmic prevention in inherited cardiomyopathies.
  • Further research, including genotype-focused studies and standardized digital endpoints, is essential for safe and effective clinical implementation.
  • Addressing challenges like algorithm generalizability and data integration is key to realizing the full potential of these technologies.

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