Key result
Nonspecific intraventricular conduction delay (NIVCD) and prolonged QRS duration significantly increased the risk of sudden cardiac death in acute coronary syndrome patients (HR 3.00 and 1.80, respectively).
Why the study?
Prolonged QRS duration and coronary artery disease are risk factors for sudden cardiac death, but the risk associated with specific intraventricular conduction disorders in ACS patients warranted exploration.
Do intraventricular conduction disorders (prolonged QRS, RBBB, LBBB, NIVCD) predict sudden cardiac death in invasively treated acute coronary syndrome patients?
Cohort (n=9,700)
No
Do intraventricular conduction disorders (prolonged QRS, RBBB, LBBB, NIVCD) predict sudden cardiac death in invasively treated acute coronary syndrome patients?
Hazard Ratio: 3 (95% CI 2.06–4.35)
Absolute Event Rate: 14.5% vs 4%
p-value: p=<0.001
Nonspecific intraventricular conduction delay (NIVCD) and prolonged QRS duration (110-119 ms) are strong, independent predictors of sudden cardiac death in post-ACS patients, identifying a high-risk group that may benefit from improved primary prevention strategies.
Backround and aims Prolonged QRS duration (≥ 110 ms) and coronary artery disease are risk factors for sudden cardiac death (SCD). We explored the SCD risk associated with intraventricular conduction disorders – a prolonged QRS duration of 110–119 ms, right bundle branch block (RBBB), left bundle branch block (LBBB), and a nonspecific intraventricular conduction delay (NIVCD) – in patients with acute coronary syndrome (ACS). Methods This is a retrospective study of 9,700 consecutive, invasively treated ACS patients with ECGs available for analysis (2007–2018). SCD definition was based on an in-depth review of written medical records and death certificates describing the circumstances leading to the events. Endpoint data were available until December 31, 2021 (no losses to follow-up). The risk associated with conduction disorders was analyzed by calculating subdistribution hazard estimates (deaths due to other causes being considered competing events). Results The median follow-up time was 6.8 years (IQR 4.0–10.2), during which 3,420 (35.3%) patients died. SCDs were overrepresented as a cause of death among patients with NIVCD (16.4%) or with a prolonged QRS duration (15.3%) when compared to patients with LBBB (5.3%), RBBB (7.1%), or with a normal QRS duration (10.5%). In an analysis adjusted for age, sex, and cardiac comorbities, NIVCD and a prolonged QRS were significant predictors of SCD (HR 3.00, 2.06– 4.35, P < 0.001; and HR 1.80, 1.37–2.35, P < 0.001, respectively). After adjusting the analysis with left ventricular ejection fraction, NIVCD and a prolonged QRS duration remained as significant risk factors for SCD. LBBB and RBBB did not predict SCD. Conclusion The incidence of SCD is significantly higher in patients with NIVCD and a prolonged QRS duration. Approximately 23% of all SCDs occur among these patients.
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Lahti et al. (2023) conducted a cohort in Acute coronary syndrome (n=9,700). Nonspecific intraventricular conduction delay (NIVCD) vs. Normal QRS duration (< 110 ms) was evaluated on Sudden cardiac death (HR 3.00, 95% CI 2.06-4.35, p=<0.001). Nonspecific intraventricular conduction delay (NIVCD) and prolonged QRS duration significantly increased the risk of sudden cardiac death in acute coronary syndrome patients (HR 3.00 and 1.80, respectively).
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