OUP user menu

Fourier analysis of ventricular fibrillation of varied aetiology

E. J. F. CARLISLE , J. D. ALLEN , W. G. KERNOHAN , J. ANDERSON , A. A. J. ADGEY
DOI: http://dx.doi.org/ 173-181 First published online: 2 February 1990

Abstract

Fast Fourier Transform analysis was used to study ventricular fibrillation induced by several different methods in 43 greyhounds anaesthetized with sodium pentobarbitone. The dominant frequency at the body surface of ventricular fibrillation induced electrically in non-ischaemic hearts was initially 9–9 ±0–7 Hz, remained above 9 Hz for 70 s and then rapidly fell to 5 Hz. The dominant frequency of ventricular fibrillation induced by acute occlusion (initially 12–3 ± 0–2 Hz), or by reperfusion (12–2 + 0–4 Hz) of the anterior descending branch of the left coronary artery, showed a similar time-course. However, ventricular fibrillation induced by administration of potassium (4–8±0–8 Hz) or ouabain (7–1 ± 11 Hz) was significantly slower. Fibrillation recordedfrom the endocardium of the heart initially showed a similar dominant frequency to that recorded at the body surface, but there was no significant fall in frequency over 3–3 mins. There was little difference in the time-course of fibrillation in the non-ischaemic heart recorded directly from the epicardium or from a surface lead. These findings may be of relevance to the poor response to DC countershock after prolonged ventricular fibrillation, hyperkalaemia or cardiac glycosides

  • Ventricular fibrillation
  • myocardial ischaemia
  • reperfusion
  • cardiac glycosides
  • potassium

Footnotes

    • Received November 7, 1988.
    • Revision received June 1, 1989.

Sign In

ESC members Follow the 'ESC Member and Congress Delegate Sign In' link below for free online access if your subscription to this journal is via the European Society of Cardiology, either as a member or an ESC Congress delegate. Discover if you are an ESC member here.

Otherwise, if your subscription is via OUP, enter your OUP username and password, or select an alternative sign in option below.
 

Log in through your institution