Key result
Right ventricular outflow tract fibrosis on CMR was strongly associated with restrictive right ventricular physiology in children after Tetralogy of Fallot repair (OR 70.0; 95% CI 5.6-882.7; P<0.001).
Why the study?
Is right ventricular outflow tract fibrosis associated with restrictive right ventricular physiology in children after Tetralogy of Fallot repair?
Population
31 children evaluated 9.2 ± 2.9 years after total correction of Tetralogy of Fallot, and 12 healthy children.
Comparison
Presence of right ventricular outflow tract… vs Absence of RVOT fibrosis on LGE-CMR
Design
Cross-sectional
Follow-up
9.2 ± 2.9 years post-repair
Authors
Loading...
Should not yet change post-TOF management; hypothesis-generating for RVOT fibrosis as driver of restrictive RV physiology.
Observational (n=31)
Is right ventricular outflow tract fibrosis associated with restrictive right ventricular physiology in children after Tetralogy of Fallot repair?
Effect estimate: OR 70.0 (95% CI 5.6-882.7)
Absolute Event Rate: 87.5% vs 9.1%
p-value: p=< 0.001
Restrictive right ventricular physiology in children after Tetralogy of Fallot repair is strongly associated with RVOT fibrosis detected by cardiac magnetic resonance imaging.
Munkhammar et al. (2013) conducted an observational in Tetralogy of Fallot (n=31). Right ventricular outflow tract fibrosis vs. No right ventricular outflow tract fibrosis was evaluated on Restrictive right ventricular physiology (OR 70.0, 95% CI 5.6-882.7, p=< 0.001). Right ventricular outflow tract fibrosis on CMR was strongly associated with restrictive right ventricular physiology in children after Tetralogy of Fallot repair (OR 70.0; 95% CI 5.6-882.7; P<0.001).