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Electrocardiographic estimates of regional action potential durations and repolarization time subintervals reveal ischemia-induced abnormalities in acute coronary syndrome not evident from global QT.
- Source :
- Journal of Electrocardiology; Nov2011, Vol. 44 Issue 6, p718-724, 7p
- Publication Year :
- 2011
-
Abstract
- Abstract: We evaluated electrocardiogram estimates of repolarization times (RTs) and action potential durations (APD) separately for initial and terminal repolarization periods in a reference group of 5376 healthy men and women and in 125 acute coronary syndrome patients with and 657 without diagnostic ST elevation (ST-elevation myocardial infarction [STEMI] and non-STEMI [NSTEMI], respectively). Two key covariates in the model are the rate-adjusted QT peak interval (QT<subscript>pa</subscript>), assigned to earliest epicardial RT (RT<subscript>epi</subscript>), and (T<subscript>p</subscript>-T<subscript>xd</subscript>), the rate-invariant interval from T<subscript>p</subscript> to the inflection point (T<subscript>xd</subscript>) at T wave downstroke. (T<subscript>p</subscript>-T<subscript>xd</subscript>) defines the crossmural RT gradient (XMRT<subscript>grad</subscript>). Transmural RT<subscript>grad</subscript> (TMRT<subscript>grad</subscript>) is obtained as CosΘ(R<subscript>max</subscript>|T<subscript>max</subscript>)*XMRT<subscript>grad</subscript>, where Θ is the spatial angle between the maximal QRS and T vectors. Derived endocardial variables are the XMRT<subscript>endo</subscript>, equal to QT<subscript>pa</subscript> + XMRT<subscript>grad</subscript> and TMRT<subscript>endo</subscript>, equal to QT<subscript>pa</subscript> + TMRT<subscript>grad</subscript>. Noting that excitation time (ET) and RT define APD, APD<subscript>epi</subscript> = RT<subscript>epi</subscript> - QR<subscript>p</subscript> in V6 and TMAPD<subscript>endo</subscript> = TMRT<subscript>endo</subscript> - 10 milliseconds. Compared to the reference group, the estimates for APD<subscript>epi</subscript> and TMAPD<subscript>endo</subscript> were shortened in STEMI by 20 and 31 milliseconds, respectively, (p <0.001 for both) signifying transmural ischemia. In contrast, in NSTEMI, TMAPD<subscript>endo</subscript> was shortened by 28 milliseconds (P <0.001) with a lesser, 5 millisecond shortening of APD<subscript>epi</subscript>, signifying subendocardial ischemia. QT was prolonged by 6 milliseconds in STEMI (P <0.05) and by 8 milliseconds in NSTEMI (P <0.001). Prolonged QT with shortened APD<subscript>epi</subscript> suggests that prolonged repolarization in terminal possibly non-ischemic regions accounts for QT prolongation in both myocardial infarction groups. These substantial differences in ischemia-induced regional manifestations of repolarization abnormalities revealed by the repolarization model were not evident from evaluation of the global QT. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 00220736
- Volume :
- 44
- Issue :
- 6
- Database :
- Supplemental Index
- Journal :
- Journal of Electrocardiology
- Publication Type :
- Academic Journal
- Accession number :
- 66763992
- Full Text :
- https://doi.org/10.1016/j.jelectrocard.2011.08.007