BiMAP-AF Version 1.0

  • Research type

    Research Study

  • Full title

    Biatrial global high-density electroanatomical mapping of atrial fibrillation – a prospective mechanistic registry study

  • IRAS ID

    245096

  • Contact name

    Tim Betts

  • Contact email

    tim.betts@ouh.nhs.uk

  • Sponsor organisation

    Oxford University Hospitals NHS Foundation Trust

  • Duration of Study in the UK

    1 years, 5 months, 29 days

  • Research summary

    Atrial fibrillation (AFib) is the most common sustained arrhythmia with increasing prevalence and significant morbidity and mortality. Current therapy is based around either control of heart rate or maintaining a normal rhythm. Medications to control heart rhythm are often ineffective and poorly tolerated. Understanding of the role of rapid extra beats originating from the pulmonary veins in initiating AFib led to the development of catheter ablation procedures to electrically isolate the pulmonary veins through radio-frequency ablation. Although this procedure is increasingly performed, success rates can be limited, especially in patients with more persistent AFib, and the electrophysiological mechanisms are incompletely understood. Non-pulmonary vein triggers are poorly characterised and further mechanisms involved in propagating and sustaining the arrhythmia are thought to exist but vary significantly between individuals. Furthermore, focus has traditionally been on the left atrium in maintaining AFib, but the importance of the right atrium is increasingly recognised.
    This study aims to use two linked novel electroanatomical mapping systems developed by ACUTUS Medical that will allow simultaneous visualisation of whole chamber activation of both the left and right atria during AFib, normal rhythm and when pacing the heart from different regions and at different rates. This will be combined with standard 3-dimensional mapping systems to identify mechanisms involved with AFib propagation such as focal impulses, rotational activity or re-entry circuits, correlate these regions with voltage and conduction properties during normal rhythm and pacing, and explore how both atria interact to perpetuate the arrhythmia.

  • REC name

    South Central - Hampshire A Research Ethics Committee

  • REC reference

    18/SC/0409

  • Date of REC Opinion

    30 Aug 2018

  • REC opinion

    Further Information Favourable Opinion