Late-onset pulmonary arterial hypertension (PAH) is a rare but fatal complication in patients with childhood surgical repair of dextro-transposition of great arteries (D-TGA), especially with the Mustard and Senning procedures. The pathogenic mechanisms of PAH in patients with repaired D-TGA are not well understood and treatment is not standardized. In this manuscript, we present a case of late-onset PAH in an adult D-TGA patient after Mustard repair and discuss the pathogenic mechanisms, diagnosis, and treatment of pulmonary hypertension in repaired D-TGA.
|Original language||English (US)|
|Number of pages||4|
|State||Published - Jun 2017|
Bibliographical noteFunding Information:
TT was funded by an AHA Scientist Development Grant 15SDG25560048 and a Lillehei Heart Institute High Risk and High Reward Grant.
© The Author(s) 2017.
- Right ventricle