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Risk of Sudden Cardiac Arrest in Children With Epilepsy and Sleep Apnea
Po-Ming Wu1,2, Chi-Wu Chiang3,4, Yen-Hsien Wu5
1Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Insights
Pediatric patients with epilepsy and sleep apnea (SA) face a higher risk of sudden cardiac arrest (SCA) and cardiac dysrhythmia. Adenotonsillectomy may lower this risk, while long-term CPAP use might increase it.
Area of Science:
- Pediatric Cardiology
- Neurology
- Sleep Medicine
Background:
- Pediatric epilepsy patients are susceptible to sudden cardiac arrest (SCA).
- Sleep apnea (SA) may worsen cardiac risks in children with epilepsy.
Purpose of the Study:
- To investigate the incidence and risk of SCA and cardiac dysrhythmia in pediatric patients with epilepsy and SA.
- To compare risks between epilepsy patients with and without SA.
Main Methods:
- Utilized the TriNetX global research network for patient identification (epilepsy diagnosis: 2000-2025).
- Identified SA using ICD-10-CM codes and polysomnography.
- Matched epilepsy cohorts (with/without SA) using propensity scores for 5- and 10-year follow-ups.
Main Results:
- SCA incidence was highest in epilepsy + SA patients (50.5/10,000 person-years).
- Epilepsy and SA significantly increased SCA risk (5-year HR: 1.99; 10-year HR: 1.74) and cardiac dysrhythmia (10-year HR: 2.06).
- Refractory epilepsy, long-term CPAP use (OR: 3.41), and adenotonsillectomy (OR: 0.40) impacted SCA risk.
Conclusions:
- Pediatric patients with epilepsy and SA have a substantially elevated risk of SCA and cardiac dysrhythmia.
- Adenotonsillectomy may reduce this risk, while prolonged CPAP therapy might increase it.
- Individualized treatment is crucial for managing SCA risk in pediatric epilepsy patients with comorbid SA.
Objective:
Pediatric patients with epilepsy are at risk for sudden cardiac arrest (SCA), and sleep apnea (SA) may exacerbate this risk. This study investigates the incidence and risk of SCA and cardiac dysrhythmia in pediatric patients with epilepsy and SA.
Methods:
Using the TriNetX global research network, we identified pediatric patients (aged younger than 18 years) who were diagnosed with epilepsy between January 2000 and March 2025. SA was identified using International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes and polysomnography records. Two cohorts, ie, patients with epilepsy with and without SA, were matched using propensity scores. SCA and cardiac dysrhythmia were assessed over 5- and 10-year follow-up periods.
Results:
The incidence of SCA was highest in patients with both epilepsy and SA (50.5 per 10 000 person-years) compared with those with epilepsy alone (20.0 per 10 000) or SA alone (9.0 per 10 000). Patients with epilepsy and SA had an increased risk of SCA (5-year hazard ratio [HR]: 1.99; 10-year HR: 1.74; both P < .001) and cardiac dysrhythmia (10-year HR: 2.06; P < .001). Refractory epilepsy increased the risk of SCA (odds ratio [OR]: 1.74; 95% CI: 1.25-2.42). Additionally, long-term continuous positive airway pressure (CPAP) therapy was associated with increased SCA risk (OR: 3.41; 95% CI: 2.27-5.11), whereas adenotonsillectomy reduced it (OR: 0.40; 95% CI: 0.27-0.60).
Conclusions:
Pediatric patients with epilepsy and SA are at significantly increased risk for SCA and cardiac dysrhythmia. Adenotonsillectomy may mitigate this risk, whereas long-term CPAP use may increase it. These findings highlight the importance of individualized treatment strategies in pediatric patients with epilepsy and comorbid SA to reduce the risk of SCA.
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