Long‐Term Outcomes and Risk Factors for Mortality After Single Ventricle Palliation for Asplenia Syndrome

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Authors: Yasuyuki Kobayashi, Shunji Sano, Yuhei Tokuda, Ayari Kimura, Steven J. Staffa, David Zurakowski, Shingo Kasahara, Yasuhiro Kotani
Cited by: 0
References: 19

Abstract

Background This study evaluated the long‐term outcomes of asplenia syndrome with single ventricle palliation, hypothesizing that total anomalous pulmonary vein connection (TAPVC), pulmonary atresia (PA), and greater than or equal to moderate atrioventricular valve regurgitation increase mortality risk. Methods This retrospective review analyzed 151 patients with asplenia syndrome who underwent single ventricle palliation between 1990 and 2024. The primary end point was mortality, with risk factors assessed by Cox regression analysis over a mean follow‐up of 9.3 years. Results The median age at initial operation was 35 days, including 70 neonates (46%). Overall, 62 (41%) patients died, whereas 66 (44%) patients are alive post‐Fontan completion. Survival probabilities at 1 and 20 years were 75.7% (95% CI, 67.9–81.8) and 53.7% (95% CI, 44.5–62.0), respectively. TAPVC ( P =0.014), PA ( P =0.007), and greater than or equal to moderate atrioventricular valve regurgitation ( P =0.040) emerged as independent risk factors for mortality in the overall cohort. In the TAPVC cohort, independent risk factors for mortality included PA ( P =0.019), infracardiac TAPVC ( P =0.045), and neonatal TAPVC repair ( P =0.018). When stratified by the risk factors of TAPVC, PA, or greater than or equal to moderate atrioventricular valve regurgitation, survival probabilities did not differ between patients with none or 1 of these conditions ( P =0.181) but were significantly lower in those with ≥2 risk factors ( P

Fields of Study & Subjects

Congenital Heart Disease Studies Congenital heart defects research Cardiac Arrhythmias and Treatments

Publication details

Journal / source
Journal of the American Heart Association
Volume
15
Issue
3
Pages
e044756–e044756
Publication date
30 January 2026
Language
EN