CHARACTERISTICS OF WAVE-FRONTS DURING VENTRICULAR-FIBRILLATION IN HUMAN HEARTS WITH DILATED CARDIOMYOPATHY - ROLE OF INCREASED FIBROSIS IN THE GENERATION OF REENTRY
Tj. Wu et al., CHARACTERISTICS OF WAVE-FRONTS DURING VENTRICULAR-FIBRILLATION IN HUMAN HEARTS WITH DILATED CARDIOMYOPATHY - ROLE OF INCREASED FIBROSIS IN THE GENERATION OF REENTRY, Journal of the American College of Cardiology, 32(1), 1998, pp. 187-196
Objectives. We sought to evaluate the characteristics of wave fronts d
uring ventricular fibrillation (VF) in human hearts with dilated cardi
omyopathy (DCM) and to determine the role of increased fibrosis in the
generation of reentry during VF. Background. The role of increased fi
brosis in reentry formation during human VF is unclear. Methods. Five
hearts from transplant recipients with DCM were supported by Langendor
ff perfusion and were mapped during VF. A plaque electrode array,vith
477 bipolar electrodes (1.6-mm resolution) was used for epicardial map
ping. In heart no. 5, we also used 440 transmural bipolar recordings.
Each mapped area was analyzed histologically. Results. Fifteen runs of
VF (8 s/run) recorded from the epicardium were analyzed, and 55 episo
des of reentry were observed. The life span of reentry was short (one
to four cycles), and the mean cycle length was 172 +/- 24 ms. In heart
no. 5, transmural scroll waves were demonstrated. The most common mod
e of initiation of reentry was epicardial breakthrough, followed by a
line of conduction block parallel to the epicardial fiber orientation
(34 [62%] of 55 episodes). In the areas with lines of block, histologi
c examination showed significant fibrosis separating the epicardial mu
scle fibers and bundles along the longitudinal axis of fiber orientati
on. The mean percent fibrous tissue in these areas (n = 20) was signif
icantly higher than that in the areas without block (n = 28) (24 +/- 7
.5% vs. 10 +/- 3.8%, p < 0.0001). Conclusions. In human hearts with DC
M, epicardial reentrant wave fronts and transmural scroll waves were p
resent during VF. Increased fibrosis provides; a site for conduction b
lock, leading to the continuous generation of reentry.