What question did this study set out to answer?

To highlight a rare case of heart failure attributable to a major aortopulmonary collateral artery in a neonate with transposition of the great arteries.

May 16, 2026Open Access

Major Aortopulmonary Collateral Artery as a Rare Cause of Heart Failure in a Neonate with Transposition of the Great Arteries: An Unexpected Turn in an Otherwise Routine Case

Puntos clave

To highlight a rare case of heart failure attributable to a major aortopulmonary collateral artery in a neonate with transposition of the great arteries.
Describes a neonate with heart failure and pulmonary overcirculation post-arterial switch operation.
Utilized transcatheter occlusion of MAPCA with a vascular coil to relieve symptoms.
Monitored hemodynamic status and patient recovery.
Patient achieved rapid hemodynamic stabilization post-obstruction of MAPCA.
Successful extubation following intervention indicated improved respiratory status.

Resumen

The association of a major aortopulmonary collateral artery (MAPCA) with simple transposition of the great arteries (TGA) is uncommon. Such high-flow lesions in the postoperative period following arterial switch operation (ASO) may lead to pulmonary hypertension, pulmonary hemorrhage, heart failure (HF), failure to thrive and prolonged mechanical ventilation. We report a neonate who developed pulmonary overcirculation and HF in the early postoperative period due to a hemodynamically significant MAPCA. Although the association of MAPCA with simple TGA is infrequent, such lesions should be considered in cases of unexplained cardiovascular compromise following ASO. Following transcatheter occlusion of the MAPCA with a vascular coil, rapid hemodynamic stabilization and subsequent extubation of the patient were achieved.

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