Eisenmenger Syndrome.
Think about it this way. The pulmonary circulation is supposed to be low pressure. Given extensive volume overload (Aorta-to-LPA), there will be intimal proliferation and medial hypertrophy with fibrosis. As a result, you get increased pulmonary vascular resistance. If the resistance is so high that you have right-to-left shunting, then that's a heck of a lot of resistance. Acutely loading the right ventricle like that will lead to decompensation and death. I'm not sure if the pulmonary hypertension would be amenable to the typical stuff for pulmonary hypertension: nifedipine, sildenafil, bosentan, IV epoprostenol, etc. I think it might be since congenital heart disease leading to PH is in Group I of the Dana Point update to the Evian Classification of pulmonary hypertension.