Heart Rhythm
Volume 4, Issue 8 , Pages 1057-1068, August 2007

Spatially discordant voltage alternans cause wavebreaks in ventricular fibrillation

  • Bum-Rak Choi, PhD

      Affiliations

    • Department of Cell Biology and Physiology, University of Pittsburgh, Pittsburgh, Pennsylvania
    • Dr. Choi’s current addresses is Cardiovascular Research Center, Rhode Island Hospital & Brown Medical School, Providence, Rhode Island 02903.
    • Corresponding Author InformationAddress reprint requests and correspondence: Dr. Bum-Rak Choi, Cardiovascular Research Center, Rhode Island Hospital & Brown Medical School, One Hoppin Street, Providence, Rhode Island 02903.
  • ,
  • Woncheol Jang, PhD

      Affiliations

    • Department of Statistics, Carnegie Mellon University, Pittsburgh, Pennsylvania
  • ,
  • Guy Salama, PhD

      Affiliations

    • Department of Cell Biology and Physiology, University of Pittsburgh, Pittsburgh, Pennsylvania
    • Corresponding Author InformationDr. Guy Salama, University of Pittsburgh, School of Medicine, Department of Cell Biology and Physiology, 200 Lothrop Street, Pittsburgh, Pennsylvania 15261.

Received 11 August 2006; accepted 28 March 2007. published online 14 June 2007.

Background

Ventricular fibrillation (VF) is characterized by complex ECG patterns emanating from multiple, short-lived, reentrant electrical waves. The incessant breakup and creation of new daughter waves (wavebreaks) perpetuate VF. Dispersion of refractoriness (static or dynamic) has been implicated as a mechanism underlying wavebreaks.

Objective

The purpose of this study was to investigate the mechanisms underlying wavefront instability in VF by localizing wave fractionation sites (the appearance of multiple waves) and their relationship to local spatial dispersion of voltage (Vm) oscillations.

Methods

Wave fractionations were identified by tracking Vm oscillations optically at unprecedented spatial (100 × 100 pixels) and temporal (2,000 frames per second) resolution using a CMOS camera viewing the surface (1 × 1 cm2) of perfused guinea pig hearts (n = 6). VF was induced by burst stimulation, and wavefront dynamics were highlighted using region-based image analysis to automatically detect wavebreaks. Direct detection of wavebreak locations by image analysis was more reliable than the phase reconstruction method because baseline noise obstructed the correct identification of phase singularities by detecting false-positives.

Results

Wave fractionations (34 ± 4 splits/s·cm2) fell into three categories: decremental conduction (49% ± 7%), wave collisions (32% ± 8%), and wavebreaks (17 ± 2%). Wavebreaks occurred at a frequency of 5.8 ± 1 splits/s·cm2 and did not preferentially occur at anatomic obstacles (i.e., coronary vessels) but coincided with discordant alternans where Vm amplitudes and durations shifted from high to low to from low to high on opposite sides of wavebreak sites.

Conclusion

Spatial discordant alternans cause wavebreaks most likely because they are sites of abrupt dispersion of refractoriness.

Keywords: Wavebreaks, Ventricular fibrillation, Optical mapping, Image analysis

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 This work was supported by a Beginning Grant-in-Aid from the Western Pennsylvania Affiliate of the American Heart Association to Dr. Choi and by National Institutes of Health Grants HL057929, HL70722, and HL69097 to Dr. Salama.

PII: S1547-5271(07)00370-0

doi:10.1016/j.hrthm.2007.03.037

Heart Rhythm
Volume 4, Issue 8 , Pages 1057-1068, August 2007