Prognostic significance of beat-to-beat variability of spatial heterogeneity of repolarization analyzed from a 5-minute resting electrocardiogram in coronary artery disease
Rahola, Janne T; Mattila, Severi M; Kiviniemi, Antti M; Ukkola, Olavi H; Tulppo, Mikko P; Junttila, M Juhani; Huikuri, Heikki V; Kenttä, Tuomas V; Perkiömäki, Juha S (2024-04-10)
Rahola, Janne T
Mattila, Severi M
Kiviniemi, Antti M
Ukkola, Olavi H
Tulppo, Mikko P
Junttila, M Juhani
Huikuri, Heikki V
Kenttä, Tuomas V
Perkiömäki, Juha S
Elsevier
10.04.2024
Rahola, J. T., Mattila, S. M., Kiviniemi, A. M., Ukkola, O. H., Tulppo, M. P., Junttila, M. J., Huikuri, H. V., Kenttä, T. V., & Perkiömäki, J. S. (2024). Prognostic significance of beat-to-beat variability of spatial heterogeneity of repolarization analyzed from a 5-minute resting electrocardiogram in coronary artery disease. Heart Rhythm, 21(7), 1093–1099. https://doi.org/10.1016/j.hrthm.2024.02.052
https://creativecommons.org/licenses/by/4.0/
© 2024 Heart Rhythm Society. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
© 2024 Heart Rhythm Society. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202405273979
https://urn.fi/URN:NBN:fi:oulu-202405273979
Tiivistelmä
Abstract
Background:
Data on the prognostic significance of temporal variability of spatial heterogeneity of electrocardiographic repolarization in coronary artery disease (CAD) are limited.
Objective:
The purpose of this study was to evaluate the prognostic value of temporal variability of T-wave morphology analyzed from a 5-minute resting electrocardiogram in CAD.
Methods:
The standard deviation (SD) of T-wave morphology dispersion (TMD-SD) and the SD of total cosine R-to-T were analyzed on a beat-to-beat basis from a 5-minute period of the standard resting 12-lead electrocardiogram obtained before the clinical stress test in 1702 patients with angiographically verified CAD and well-preserved left ventricular function.
Results:
During an average of 8.7 ± 2.2 years of follow-up, 60 patients experienced sudden cardiac death/arrest (SCD/SCA) (3.5%), 69 patients nonsudden cardiac death (NSCD) (4.1%), and 161 patients noncardiac death (9.5%). TMD-SD was significantly higher in patients who experienced SCD/SCA than in other patients (1.72 ± 2.00 vs 1.12 ± 1.75; P = .01) and higher in patients who succumbed to NSCD than in other patients (1.57 ± 1.74 vs 1.12 ± 1.76; P = .04), but it did not differ significantly between patients who experienced noncardiac death and those without such an event (1.16 ± 1.42 vs 1.14 ± 1.79; P = .86). In the Cox multivariable hazards model, TMD-SD retained its significant association with the risk of SCD/SCA (hazard ratio 1.119; 95% confidence interval 1.015–1.233; P = .024) but not with the risk of NSCD (hazard ratio 1.089; 95% confidence interval 0.983–1.206; P = .103).
Conclusion:
TMD-SD is independently associated with the long-term risk of SCD/SCA in patients with CAD.
Background:
Data on the prognostic significance of temporal variability of spatial heterogeneity of electrocardiographic repolarization in coronary artery disease (CAD) are limited.
Objective:
The purpose of this study was to evaluate the prognostic value of temporal variability of T-wave morphology analyzed from a 5-minute resting electrocardiogram in CAD.
Methods:
The standard deviation (SD) of T-wave morphology dispersion (TMD-SD) and the SD of total cosine R-to-T were analyzed on a beat-to-beat basis from a 5-minute period of the standard resting 12-lead electrocardiogram obtained before the clinical stress test in 1702 patients with angiographically verified CAD and well-preserved left ventricular function.
Results:
During an average of 8.7 ± 2.2 years of follow-up, 60 patients experienced sudden cardiac death/arrest (SCD/SCA) (3.5%), 69 patients nonsudden cardiac death (NSCD) (4.1%), and 161 patients noncardiac death (9.5%). TMD-SD was significantly higher in patients who experienced SCD/SCA than in other patients (1.72 ± 2.00 vs 1.12 ± 1.75; P = .01) and higher in patients who succumbed to NSCD than in other patients (1.57 ± 1.74 vs 1.12 ± 1.76; P = .04), but it did not differ significantly between patients who experienced noncardiac death and those without such an event (1.16 ± 1.42 vs 1.14 ± 1.79; P = .86). In the Cox multivariable hazards model, TMD-SD retained its significant association with the risk of SCD/SCA (hazard ratio 1.119; 95% confidence interval 1.015–1.233; P = .024) but not with the risk of NSCD (hazard ratio 1.089; 95% confidence interval 0.983–1.206; P = .103).
Conclusion:
TMD-SD is independently associated with the long-term risk of SCD/SCA in patients with CAD.
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