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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)

 
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URL:
https://doi.org/10.1136/heartjnl-2019-315437

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.
BMJ
15.11.2019

Holkeri A, Eranti A, Haukilahti MAE, et al. Heart, 2020;106:427–433, https://doi.org/10.1136/heartjnl-2019-315437

https://rightsstatements.org/vocab/InC/1.0/
© 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.
https://rightsstatements.org/vocab/InC/1.0/
doi:https://doi.org/10.1136/heartjnl-2019-315437
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Julkaisun pysyvä osoite on
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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