Heart Rhythm
Volume 5, Issue 7 , Pages 1029-1035, July 2008

Electrogram fractionation in murine HL-1 atrial monolayer model

  • Karthikeyan Umapathy, PhD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Stephane Masse, MASc

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Karolina Kolodziejska, PhD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • George D. Veenhuyzen, MD

      Affiliations

    • Libin Cardiovascular Institute of Alberta, University of Calgary, Division of Cardiovascular Sciences, Calgary, Alberta, Canada.
  • ,
  • Vijay S. Chauhan, MD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Mansoor Husain, MD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Talha Farid, MD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Eugene Downar, MD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Elias Sevaptsidis, DCS

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
  • ,
  • Kumaraswamy Nanthakumar, MD

      Affiliations

    • Division of Cardiology, Toronto General Hospital, Toronto, Canada
    • Corresponding Author InformationAddress reprint requests and correspondence: Dr. Kumaraswamy Nanthakumar, Division of Cardiology, University Health Network, The Toby Hull Cardiac Fibrillation Management Laboratory, Toronto General Hospital, 150 Gerrard Street West, GW 3-522, Toronto, Ontario, Canada M5G 2C4.

published online 25 March 2008.

Background

Complex fractionated atrial electrograms have been suggested as important targets for catheter ablation of atrial fibrillation. The etiology and the mechanism of these signals have not been completely elucidated because of limitations of interpretation of these signals in relation to simultaneously acquired signals in the neighboring atrial tissue.

Objective

This study sought to study the origin of electrogram fractionation under the conditions of rotor formation and wave fragmentation, using atrial monolayer preparations.

Methods

We performed optical mapping of 45 atrial monolayer preparations using a complementary metal oxide semiconductor (CMOS) Brainvision Ultima camera system (SciMedia-Brainvision, Tokyo, Japan).

Results

We observed stable rotors in 32 of the 45 recordings. The derived bipolar electrograms did not show complex fractionation at the core of the rotor in any of the 32 recordings. We were also able to show that 2 bipolar electrodes placed adjacent to the core of a stable rotor in a zone where there is no wave break will record electrical activity for the majority of the rotor's cycle length. In 13 of the 45 recordings, wave break or wave collision events were present. Of these, 8 of 13 recordings showed complex fractionation. In 19 of the 27, simulation of meandering rotors also showed complex fractionation.

Conclusion

Complex fractionated electrograms can be recorded at sites of migrating rotors and wave break. No fractionation occurs at the core of a stable rotor. Electrograms that span the rotor cycle length and alternate between 2 bipoles that straddle the core can identify site of a stable rotor.

Keywords: Fractionated electrograms, Atrial fibrillation, Atrial monolayer model, Rotors, Ablation

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 This study was supported by the Canadian Institutes of Health Research Grant NA 777687 to Dr. Nanthakumar.

PII: S1547-5271(08)00325-1

doi:10.1016/j.hrthm.2008.03.022

Heart Rhythm
Volume 5, Issue 7 , Pages 1029-1035, July 2008