TY - JOUR
T1 - Beat-to-beat electrocardiographic morphology variation in healed myocardial infarction
AU - Ben-Haim, Shlomo A.
AU - Becker, Bruno
AU - Edoute, Yeouda
AU - Kochanovski, Mira
AU - Azaria, Orly
AU - Kaplinsky, Elieser
AU - Palti, Yoram
N1 - Funding Information:
From the Cardiovascular ResearchG roup, Rappaport Family Institute for Researchi n the Medical Sciences,a nd the Department of Physiolc-gy and Biophysics, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, the Department of Cardiology, Meir Hospital, Kfar Saba, and the Heart Institute, Chaim Sheba Medical Center, Tel Ha-shomer, Tel Aviv, Israel. This study was supported in part by Grant 12321f rom the Basic ResearchF und administeredb y the Israel Academy of Sciences and Humanities and from the Technion V.P.R. Fund-W. and S. Wein Research Fund. Manuscript received February 19,199l; revised manuscript received and acceptedM ay 16,199l.
PY - 1991/9/15
Y1 - 1991/9/15
N2 - Using high-fidelity electrocardiographic (ECG) amplifiers, we measured subtle beat-to-beat ECG morphologic variations at different phases of the ECG complex. The electrocardiograms were recorded from 49 men with a documented Q-wave myocardial infarction and from 30 age-matched normal men. Forty consecutive beats were averaged to achieve an average ECG signal from which variance could be calculated. The relative variance, defined as the ratio between the integrated variance of the examined window and the integrated variance of the ECG signal that was close to full cycle length, was calculated at QRS onset and at offset in 2 frequency bands (4 to 40 and 60 to 120 Hz). Patients with healed infarction had a relative variance of 2.1 ± 0.5 (mean ± standard deviation [SD]) at QRS offset (a window of 40 ms), which was significantly lower than that of the healthy volunteers: 2.5 ± 0.33 (mean ± SD; p < 0.02) at the low-frequency band. At the high-frequency band, patients with healed infarction had a significantly higher relative variance than the control subjects at QRS onset: 1.95 ± 0.58 vs 1.55 ± 0.35 (mean ± SD; p < 0.005). A model based on the numerous minor conduction abnormalities that exist in the chronically ischemic myocardium is presented to explain the changes in variance at the onset and offset of the QRS. The variance changes described can eventually serve as quantitative indexes of myocardial injury and electrical stability in patients with ischemic heart disease.
AB - Using high-fidelity electrocardiographic (ECG) amplifiers, we measured subtle beat-to-beat ECG morphologic variations at different phases of the ECG complex. The electrocardiograms were recorded from 49 men with a documented Q-wave myocardial infarction and from 30 age-matched normal men. Forty consecutive beats were averaged to achieve an average ECG signal from which variance could be calculated. The relative variance, defined as the ratio between the integrated variance of the examined window and the integrated variance of the ECG signal that was close to full cycle length, was calculated at QRS onset and at offset in 2 frequency bands (4 to 40 and 60 to 120 Hz). Patients with healed infarction had a relative variance of 2.1 ± 0.5 (mean ± standard deviation [SD]) at QRS offset (a window of 40 ms), which was significantly lower than that of the healthy volunteers: 2.5 ± 0.33 (mean ± SD; p < 0.02) at the low-frequency band. At the high-frequency band, patients with healed infarction had a significantly higher relative variance than the control subjects at QRS onset: 1.95 ± 0.58 vs 1.55 ± 0.35 (mean ± SD; p < 0.005). A model based on the numerous minor conduction abnormalities that exist in the chronically ischemic myocardium is presented to explain the changes in variance at the onset and offset of the QRS. The variance changes described can eventually serve as quantitative indexes of myocardial injury and electrical stability in patients with ischemic heart disease.
UR - http://www.scopus.com/inward/record.url?scp=0025999427&partnerID=8YFLogxK
U2 - 10.1016/0002-9149(91)90643-Y
DO - 10.1016/0002-9149(91)90643-Y
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AN - SCOPUS:0025999427
VL - 68
SP - 725
EP - 728
JO - American Journal of Cardiology
JF - American Journal of Cardiology
SN - 0002-9149
IS - 8
ER -