To evaluate factors associated with discontinuation of pulmonary vasodilator therapy in bronchopulmonary dysplasia-related pulmonary hypertension (BPD-PH). Retrospective study of neonatal, echocardiographic, and cardiac catheterization data in 121 infants with BPD-PH discharged on pulmonary vasodilator therapy from 2009-2020 and followed into childhood. After median 4.4 years, medications were discontinued in 58%. Those in whom medications were discontinued had fewer days of invasive support, less severe BPD, lower incidence of PDA closure or cardiac catheterization, and higher incidence of fundoplication or tracheostomy decannulation (p < 0.05). On multivariable analysis, likelihood of medication discontinuation was lower with longer period of invasive respiratory support HR 0.95 (CI:0.91-0.99), p = 0.01 and worse RV dilation on pre-discharge echocardiogram HR 0.13 (CI:0.03-0.70), p = 0.017. In those with tracheostomy, likelihood of medication discontinuation was higher with decannulation HR 10.78 (CI:1.98-58.59), p < 0.001. In BPD-PH, childhood discontinuation of pulmonary vasodilator therapy is associated with markers of disease severity.