Predicting sudden cardiac death in a general population using an electrocardiographic risk score
Holkeri, Arttu; Eranti, Antti; Haukilahti, M. Anette E.; Kerola, Tuomas; Kenttä, Tuomas V.; Tikkanen, Jani T.; Anttonen, Olli; Noponen, Kai; Seppänen, Tapio; Rissanen, Harri; Heliövaara, Markku; Knekt, Paul; Junttila, M. Juhani; Huikuri, Heikki V.; Aro, Aapo L. (2019-11-15)
Holkeri A, Eranti A, Haukilahti MAE, et al. Heart, 2020;106:427–433, https://doi.org/10.1136/heartjnl-2019-315437
© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ. This is the Author's Accepted Manuscript Version of the published article. The Definitive Version of Record can be found online at: https://doi.org/10.1136/heartjnl-2019-315437.
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https://urn.fi/URN:NBN:fi-fe2020042922927
Tiivistelmä
Abstract
Objective: We investigated whether combining several ECG abnormalities would identify general population subjects with a high sudden cardiac death (SCD) risk.
Methods: In a sample of 6830 participants (mean age 51.2±13.9 years; 45.5% male) in the Mini-Finland Health Survey, a general population cohort representative of the Finnish adults aged ≥30 years conducted in 1978—1980, we examined their ECGs, following subjects for 24.3±10.4 years. We analysed the association between individual ECG abnormalities and 10-year SCD risk and developed a risk score using five ECG abnormalities independently associated with SCD risk: heart rate >80 beats per minute, PR duration >220 ms, QRS duration >110 ms, left ventricular hypertrophy and T-wave inversion. We validated the score using an external general population cohort of 10 617 subjects (mean age 44.0±8.5 years; 52.7% male).
Results No ECG abnormalities were present in 4563 subjects (66.8%), while 96 subjects (1.4%) had ≥3 ECG abnormalities. After adjusting for clinical factors, the SCD risk increased progressively with each additional ECG abnormality. Subjects with ≥3 ECG abnormalities had an HR of 10.23 (95% CI 5.29 to 19.80) for SCD compared with those without abnormalities. The risk score similarly predicted SCD risk in the validation cohort, in which subjects with ≥3 ECG abnormalities had HR 10.82 (95% CI 3.23 to 36.25) for SCD compared with those without abnormalities.
Conclusion: The ECG risk score successfully identified general population subjects with a high SCD risk. Combining ECG risk markers may improve the risk stratification for SCD.
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