2025 AMA Research Challenge – Member Premier Access

October 22, 2025

Virtual only, United States

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Background

There is limited data on sleep-related breathing disorders (SRBDs) in pediatric patients with single ventricle congenital heart disease (SVCHD) who have undergone surgical correction, but available studies indicate it is commonly present. The impact of SRBDs in these patients remains poorly understood. This study investigates the prevalence of SRBDs in patients who have undergone the Fontan procedure.

Methods

We conducted a retrospective chart review of 62 pediatric patients with SVCHD who had undergone the Fontan procedure and had a polysomnographic study (PSG) before or after the Fontan procedure between 2000 and 2024. Data was abstracted from patients’ most recent PSGs and included demographic characteristics, apnea-hypopnea indices (oAHI and CAI), end-tidal CO2 (ETCO2) and oxygen saturation metrics.

Results

The cohort’s mean age at the time of their first PSG was 9.1 ± 5.1 years. The cohort’s mean age at the time of the Fontan procedure was 3.6 ± 0.8 years. 66% of the cohort were male (41/62). 37/62 patients (60%) had OSA. 14 subjects exclusively had PSGs performed only before Fontan; 42 subjects exclusively had PSGs only after Fontan. 10% of patients (6/62) had PSGs both before and after Fontan. The pre-Fontan cohort had 4 mild OSA, 2 moderate OSA and 1 severe OSA. The post-Fontan cohort had 19 mild OSA, 6 moderate OSA and 4 severe OSA. There was improvement in AHI in 2/6 patients who had pre and post Fontan PSG. 6/62 patients had CSA (CAI ≥ 5/hr.) and none met criteria for hypoventilation (ETCO2 >50 mmHg for >25% of total sleep time).

The average oAHI pre-Fontan was 3.27 ± 5.1 and the average oAHI post-Fontan was 4.7 ± 8.4. The average oxygen saturation (SpO2) pre-Fontan was 83% and the average SpO2 post-Fontan was 92%. The average SpO2 nadir pre-Fontan was 73% and the average SpO2 nadir post-Fontan was 84%. SpO2 nadir of < 90% was seen in 19 patients prior to the Fontan procedure and in 38 patients after the Fontan procedure.

Conclusion

There was a high prevalence of SRBDs in pediatric patients with SVCHD patients’ post-surgical correction. Most patients demonstrated mild OSA. Our data suggest that early screening for SRBDs in this population is essential.

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