Jt. Jacobson et al., Effect of underlying heart disease on the frequency content of ventricularfibrillation in the dog heart, PACE, 23(2), 2000, pp. 243-252
Citations number
20
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Although prior studies have examined the frequency content of local electro
gram characteristics during fibrillation, little is know about the effects
of underlying heart disease on these parameters. This study was designed to
compare the frequency content of local electrograms during VF in canine mo
dels of acute ischemia, subacute infarction, and chronic myocardial infarct
ion (MI) to those in control animals to test the hypothesis that underlying
heart disease can alter the basic characteristics of VF. VF was induced us
ing burst pacing in three groups of mongrel dogs. Five dogs were evaluated
8 weeks after LAD occlusion MI, five were evaluated 5 days after experiment
al MI, and 5 had VF induced before (control) and immediately after LAD occl
usion (ischemia). During SIF, unipolar electrograms were recorded from 122
sites on the anterior LV and electrograms were evaluated 15 and 30 seconds
after VF initiation in each group. Electrograms were analyzed by fast Fouri
er transform. No significant time dependent changes in VF characteristics w
ere noted. The peak frequency was highest in control animals and 8-week MI,
intermediate in 5-day MI, and lowest in acute ischemia (P < 0.01 for pairw
ise comparisons). In contrast, the fractional of energy within a bandwidth
of 25% peak amplitude Mas highest in acute ischemia, (P < 0.001) and simila
r in the other three groups. Infarction decreased total energy by approxima
tely 50%. In conclusion, the pressure of ischemia or infarction alters the
frequency content of VF in a complex fashion. In addition to decreasing the
peak frequency the shape of the power spectral curve is altered in models
of structural heart disease. These results suggest that the electrophysiolo
gical changes produced by infarction or ischemia alter the structural organ
ization of ventricular fibrillation.