Predicting Recovery of Myocardial Function by Electrocardiography after Acute Infarction
Background In acute ischemic left ventricular (LV) dysfunction, distinguishing viable myocardium is clinically important. Methods Body surface potential mapping (Electrocardiography [ECG] with 123 leads), was recorded in 62 patients with acute coronary syndrome (ACS). ECG variables were computed fro...
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Published in: | Annals of noninvasive electrocardiology Vol. 18; no. 3; pp. 230 - 239 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Blackwell Publishing Ltd
01-05-2013
John Wiley & Sons, Inc John Wiley and Sons Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | Background
In acute ischemic left ventricular (LV) dysfunction, distinguishing viable myocardium is clinically important.
Methods
Body surface potential mapping (Electrocardiography [ECG] with 123 leads), was recorded in 62 patients with acute coronary syndrome (ACS). ECG variables were computed from de‐ and repolarization phases. LV segmental wall motion was assessed by echocardiography acutely and after 1 year.
Results
The number of dysfunctional segments (DFS) diminished during follow‐up in 37 patients (recovery group) and remained the same or increased in 25 patients (nonrecovery group). Acutely, DFS was 5.7 ± 2.1 versus 4.4 ± 2.4 (P = 0.02), and peak CK‐MBm 141 ± 157 versus 156 ± 167 μg/L (P = 0.78) in the recovery versus nonrecovery group. At follow‐up, DFS was 1.9 ± 1.7 versus 6.5 ± 2.6 (P < 0.001). The best ECG variable to predict decrease in DFS depended on the region of acute LV dysfunction: The best variable in the left anterior descending region was the integral of the first QRS integral (area under the curve [AUC] 0.82, P = 0.002); in the right coronary artery region, this was the integral of the ST segment (AUC 0.98, P = 0.003); and in the left circumflex region, the area including the ST segment and the T wave (AUC 0.97, P = 0.006).
Conclusions
In ACS patients, computed ECG variables predict recovery of LV function from ischemic myocardial injury, even in the presence of comparable CK‐MBm release and LV dysfunction. |
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Bibliography: | ark:/67375/WNG-FGK3LR6R-B Aarne Koskelo Foundation Instrumentarium Foundation Finnish Foundation for Cardiovascular Research, Finska Läkaresällskapet ArticleID:ANEC12015 Waldemar von Frenckell Foundation, Helsinki University Central Hospital Research Funds (EVO grant) Medicine Fund of Helsinki University, Helsinki, Finland istex:7E20290F87F1A3CD37FB070FBF3433D6AE34D441 This study was supported by grants from the Finnish Foundation for Cardiovascular Research, Finska Läkaresällskapet, the Waldemar von Frenckell Foundation, Helsinki University Central Hospital Research Funds (EVO grant), the Instrumentarium Foundation, the Aarne Koskelo Foundation; and the Medicine Fund of Helsinki University, Helsinki, Finland. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1082-720X 1542-474X |
DOI: | 10.1111/anec.12015 |