Presentation
Start/End Time:
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Friday,
May 11, 2007, 11:15 AM -11:29 AM
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Author
Block:
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Daniel
P. Morin, MD, MPH, Eran S. Zacks, MD, Andreas C. Mauer, MD, Shaun Ageno, MD,
Matthew Janik, MD, Steven M. Markowitz, MD, Sei Iwai, MD, Bindi K. Shah, MD,
Bruce B. Lerman, MD and Kenneth M. Stein, MD. Cornell University Medical
Center, New York, NY
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Introduction:
T-wave alternans (TWA) and electrophysiology study (EPS) are used for risk
stratification for sudden death. We hypothesized that TWA and EPS yield
additive information. Methods: 386 pts (311 M, LVEF 29±8%) with CAD, NSVT,
and LVEF < 40% underwent both TWA and EPS. TWA was determined with
atrial pacing, and positive and indeterminate TWA were grouped together as
nonnegative ("+"). Positive EPS was defined as monomorphic VT
induced with up to triple ventricular extrastimuli (VES) or polymorphic VT or
VF induced with up to double VES. Follow-up for the combined endpoint of VT,
VF, or death was conducted via chart review, device interrogation, and query
of the Social Security Death Index. Results: TWA was nonnegative in 259
(67%), and EPS was positive in 197 (51%). 144 (37%) had positive results in
both TWA and EPS, while only 74 (19%) pts had negative results in both tests.
168 (44%) pts had incongruent results (115 TWA+/EPS- and 53 TWA-/EPS+). In
univariate analysis, both TWA and EPS predicted events (HR 1.52, p=0.035 and
HR 1.75, p=0.002). In multivariate analysis, both tests remained predictive
(TWA: HR=2.20, p=0.02; EPS: HR=2.92, p<0.01) with a trend toward a
multiplicative interaction between the two tests (p=0.07). Thus, the only
lower-risk group consisted of those pts with negative results of both tests.
Two-year event rates: TWA-/EPS- 11%, TWA+/EPS- 22%, TWA-/EPS+ 30%, TWA+/EPS+
30%. Conclusions: In pts referred for EP testing due to ischemic
cardiomyopathy and NSVT, both TWA and EPS stratify patients by risk for VT,
VF, or death. The only lower-risk group consists of pts with negative results
of both tests, while the other 3 groups had relatively high event rates. A
screening strategy using both TWA and EPS in this population would be limited
by the small number who screen negative in both tests, and by the nontrivial
2-year event rate in those pts.

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