TY - JOUR
T1 - Prenatally vs. Postnatally Diagnosed Congenitally Corrected Transposition of the Great Arteries is Associated with Higher Rates of Conduction Disease, Intervention and Earlier Mortality
AU - DISCO study group
AU - Nield, Lynne E.
AU - Grasswill, Mélanie
AU - Romefort, Bénédicte
AU - Prigent, Solène
AU - Belli, Emre
AU - Babu-Narayan, Sonya V.
AU - Elder, Robert W.
AU - Ladouceur, Magalie
AU - Khairy, Paul
AU - Kowalik, Ewa
AU - Kalfa, David M.
AU - Conway, Miriam
AU - Werner, Oscar
AU - Sellal, Jean Marc
AU - Monier, Astrid
AU - Buratto, Edward
AU - Padovani, Paul
AU - Barron, David J.
AU - Bacha, Emile A.
AU - Gatzoulis, Michael A.
AU - McLeod, Christopher J.
AU - Karakachoff, Matilde
AU - Baruteau, Alban Elouen
AU - Van Hare, George F.
AU - Fraisse, Alain
AU - Vaksmann, Guy
AU - Thambo, Jean Benoit
AU - Temple, Joel
AU - Sanatani, Shubhayan
AU - Pass, Robert H.
AU - Ovaert, Caroline
AU - Mussa, Shafi
AU - Maury, Philippe
AU - Martin-Bonnet, Caroline
AU - Liberman, Leonardo
AU - Gloan, Laurianne Le
AU - Bloa, Mathieu Le
AU - Lachaud, Matthias
AU - Karsenty, Clément
AU - Houeijeh, Ali
AU - Hiippala, Anita
AU - Hiel, Bérengère
AU - Happonen, Juha Matti
AU - Benbrik, Nadir
AU - Grunenwald, Céline
AU - Fournier, Emmanuelle
AU - Erickson, Christopher C.
AU - Duthoit, Guillaume
AU - Combes, Nicolas
AU - Charbonneau, Anne
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2026.
PY - 2026/3/4
Y1 - 2026/3/4
N2 - Congenitally corrected transposition of the great arteries (ccTGA) with biventricular physiology is presumed to carry a favorable outcome. We aimed to explore the differences in associated diagnoses (including conduction disease), management and outcomes among prenatally vs. postnatally diagnosed ccTGA cases. Secondary objective was to examine outcomes in isolated ccTGA. An international, multicenter, retrospective cohort study was conducted in 29 tertiary hospitals (6 countries) from 1990 to 2018. Patients with a single ventricle, heterotaxy syndrome, or valvar atresia were excluded. Of 331 ccTGA patients with a median follow-up of 8.6 years [IQR: 3.5–14.1], 128 (38.7%) were diagnosed prenatally at a median gestational age of 22 weeks. As compared to the postnatal group, prenatally diagnosed patients experienced earlier cardiac conduction disorders (median age at diagnosis of conduction disorders: 0.3 versus 2.7 years, p = 0.010), earlier pacemaker implantation (median age at pacing: 6.5 years [2.5–11.6] versus 0.9 year [0.1-3.0], p < 0.001) and earlier surgical intervention (intervention-free survival rate at 3 years: 50.3% versus 34.7%, p < 0.001). The 3-year survival rate was significantly lower in patients diagnosed prenatally (91.1% versus 98.4%, p = 0.002) and the median age at death was significantly younger among patients diagnosed prenatally (0.2 versus 7.0 years, p < 0.001). In both groups, isolated ccTGA (n = 63, 19%) was associated with superior outcomes with no intervention in 46.8% and only one death. Prenatally diagnosed patients with ccTGA had earlier conduction disorders and interventions than postnatally diagnosed patients and died at a younger age. Outcomes were best in patients with isolated ccTGA.
AB - Congenitally corrected transposition of the great arteries (ccTGA) with biventricular physiology is presumed to carry a favorable outcome. We aimed to explore the differences in associated diagnoses (including conduction disease), management and outcomes among prenatally vs. postnatally diagnosed ccTGA cases. Secondary objective was to examine outcomes in isolated ccTGA. An international, multicenter, retrospective cohort study was conducted in 29 tertiary hospitals (6 countries) from 1990 to 2018. Patients with a single ventricle, heterotaxy syndrome, or valvar atresia were excluded. Of 331 ccTGA patients with a median follow-up of 8.6 years [IQR: 3.5–14.1], 128 (38.7%) were diagnosed prenatally at a median gestational age of 22 weeks. As compared to the postnatal group, prenatally diagnosed patients experienced earlier cardiac conduction disorders (median age at diagnosis of conduction disorders: 0.3 versus 2.7 years, p = 0.010), earlier pacemaker implantation (median age at pacing: 6.5 years [2.5–11.6] versus 0.9 year [0.1-3.0], p < 0.001) and earlier surgical intervention (intervention-free survival rate at 3 years: 50.3% versus 34.7%, p < 0.001). The 3-year survival rate was significantly lower in patients diagnosed prenatally (91.1% versus 98.4%, p = 0.002) and the median age at death was significantly younger among patients diagnosed prenatally (0.2 versus 7.0 years, p < 0.001). In both groups, isolated ccTGA (n = 63, 19%) was associated with superior outcomes with no intervention in 46.8% and only one death. Prenatally diagnosed patients with ccTGA had earlier conduction disorders and interventions than postnatally diagnosed patients and died at a younger age. Outcomes were best in patients with isolated ccTGA.
KW - Congenital heart disease
KW - Congenitally corrected transposition of the great arteries
KW - Heart block
KW - Prenatal diagnosis
KW - Ventricular discordance
UR - https://www.scopus.com/pages/publications/105032159395
U2 - 10.1007/s00246-026-04198-z
DO - 10.1007/s00246-026-04198-z
M3 - Article
C2 - 41779175
AN - SCOPUS:105032159395
SN - 0172-0643
JO - Pediatric Cardiology
JF - Pediatric Cardiology
ER -