Key result
CMR reveals unusual late anatomic sequelae in an adult after subpulmonary DORV repair.
Why the study?
Double outlet right ventricle is a heterogeneous congenital defect with varied anatomic aberrations and physiologic consequences, motivating the description of unusual cardiovascular magnetic resonance findings after complex biventricular repair.
Case Report (n=1)
May inform individualized CMR surveillance in repaired DORV; leaves open standardization for adult congenital cohorts.
Double outlet right ventricle is a heterogeneous congenital defect that encompasses a variety of anatomic aberrations and physiologic consequences. We describe the unusual cardiovascular magnetic resonance anatomic findings and sequelae of a 44-year-old man who underwent biventricular repair of double outlet right ventricle, subpulmonary type, which included tunneling of the ventricular septal defect to the pulmonary artery, right ventricular-to-pulmonary artery conduit and Damus-Kaye-Stansel procedure.
No takes yet. Share an insight, caveat, or question.
Walls et al. (2011) conducted a case report in Double outlet right ventricle, subpulmonary type (Taussig-Bing heart) (n=1). Cardiovascular magnetic resonance evaluation of biventricular repair (VSD tunneling to PA, RV-to-PA conduit, and Damus-Kaye-Stansel procedure) was evaluated on Cardiovascular magnetic resonance anatomic findings and sequelae. Cardiovascular magnetic resonance evaluated unusual anatomic findings in 1 44-year-old man following biventricular repair of subpulmonary double outlet right ventricle.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: