很多类型的先天性心脏病由于发生肺动脉高压而变得更加复杂，并且肺高压的可逆性常难以预测。
Pulmonary arterial hypertension (PAH) can complicate several types of congenital heart disease, and its reversibility is often difficult to predict.
目的探讨可调式房间隔内漏术在先天性心脏病(CHD)并重度肺动脉高压(PH)术中的方法和应用价值。
Objective To investigate the method and value of adjustable interatrial fistulization in the operation of congenital heart disease (CHD) accompany with severe pulmonary arterial hypertension (PH).
目的探讨呼气末正压(PEEP)对先天性心脏病合并肺动脉高压患者术后肺呼吸功能的作用。
Objective to investigate the effects of Positive-pressure respiration (PEEP) on respiratory function after cardiac surgery in pulmonary hypertension patients with congenital heart diseases.
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