(Circulation. 1996;93:1845-1859.)
© 1996 American Heart Association, Inc.
Articles |
From the Research Centre, Hôpital du Sacré-Coeur de Montréal, the Departments of Pharmacology and Surgery, and the Institut de Génie Biomédical, Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada.
Correspondence to René Cardinal, PhD, Centre de Recherche, Hôpital du Sacré-Coeur de Montréal, 5400 Gouin Blvd W, Montréal, Québec, Canada H4J 1C5.
Background The aim of this study was to determine whether cycle length (CL) variations at the onset of monomorphic ventricular tachycardias follow distinctive patterns.
Methods and Results We retrospectively analyzed 59
monomorphic ventricular tachycardias induced in 40
patients in whom intraoperative mapping was performed with 63
epicardial and 64 endocardial electrograms recorded
simultaneously. Activation times and CL were determined at
each electrode site over several beats (36±10 beats, mean±SD)
starting with the first after programmed stimulation. In the majority
of the tachycardias, CL variations were accounted for by
fitting to an exponential function:
CL=CLs+Ae-b/
,
where CLs is the stable CL, b is beat number,
is the
time constant (in beat number), and A is the magnitude of CL
relaxation. A decelerating trend (with reference to rate) (negative A)
accounted for 21 tachycardias, an accelerating trend in rate
(positive A) accounted for 12 tachycardias, and 4 others
displayed a double dynamic behavior, with an initial acceleration
followed by a decelerating trend in rate. Among the
ventricular tachycardias that were not fitted to
exponential models, 12 showed a constant trend and 10 others showed
irregular CL fluctuations. The monomorphic character of the
tachycardias was established by principal-component
analysis, which also indicated that CL dynamics associated with
the accelerating and decelerating trends may be related to shortening
or prolongation of activation times, respectively, occurring in equal
proportion at all recording sites. In canine preparations in
which reentry circuits could be mapped with high resolution, CL showed
an accelerating trend in rate when circus movement of excitation
occurred around a transmural scar in muscle generating unipolar
electrograms with relatively high
-dV/dtmax, and a decelerating trend in
rate occurred when functional reentry occurred in muscle generating
unipolar electrograms with depressed
-dV/dtmax.
Conclusions Beat-to-beat CL variations may occur at the onset of sustained monomorphic ventricular tachycardia as a result of uniform acceleration or deceleration of activation times while the overall activation pattern remains constant. The associated initial trends in the rate of sustained monomorphic ventricular tachycardia follow typical patterns that might provide "signatures" corresponding to reentry substrates with distinctive functional properties.
Key Words: tachycardia reentry myocardial infarction
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