ECG-I mapping of AF

  • Research type

    Research Study

  • Full title

    ECG-I Mapping of Atrial Fibrillation to Optimise Patient Selection and Targeting of Ablation Therapy.

  • IRAS ID

    218367

  • Contact name

    Gurpreet Dhillon

  • Contact email

    guppydhillon@gmail.com

  • Sponsor organisation

    Barts Health Centre, Queen Mary University of London

  • Duration of Study in the UK

    3 years, 0 months, 1 days

  • Research summary

    Atrial Fibrillation (AF) is an irregular heart rhythm associated with significant mortality and morbidity. Catheter ablation (CA) is an established treatment using catheters that are passed into the heart to isolate and disrupt heart tissue causing and maintaining AF. Success rates of CA of persistent AF are approximately 30-60%. It is thought that AF is maintained by multiple re-entry circuits in the atria of the heart.

    The ECG-I is an electrical mapping system that involves wearing a jacket consisting of ECG electrodes. A CT scan localises the electrodes relative to the heart, and computer modelling is used to reconstruct the movements of electricity on the surface of the heart and suggest location of tissue that can cause and maintain (drivers of AF) AF.

    We aim to study the efficacy of the ECG-I in identifying the drivers of AF and investigate the properties of these drivers to better understand the mechanisms of AF.

    There are 2 arms to this study. The ‘Combined approach’ study arm will involve mapping to look for evidence of drivers at locations predicted by ECG-I followed by targeted ablation of these areas and then standard ablation therapy for AF. These patients will then be followed up for one year. This will provide insight into whether targeted ablation of drivers of AF lead to higher rates of freedom from AF. This is standard treatment.

    The ‘staged approach’ study arm will involve 2 phases. Phase 1 will involve ECG-I analysis followed by standard ablation targeting the pulmonary veins to see if activation patterns can predict who will respond to standard ablation. Those patients with recurrent AF after phase 1 will progress to phase 2 where they will undergo ablation targeting the drivers of AF directly based on ECG-I analysis and will be followed up to evaluate their response.

  • REC name

    East Midlands - Leicester South Research Ethics Committee

  • REC reference

    17/EM/0333

  • Date of REC Opinion

    10 Oct 2017

  • REC opinion

    Further Information Favourable Opinion