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.
低氧性肺动脉高压(HPH)是高原适应生理的重要环节，也是各型高原病的发病机理。
Hypoxic pulmonary hypertension (HPH) is a key link of the adaptation physiology in high altitude area and the pathogenesis of all types of high altitude diseases.
应用漂浮导管监测前列腺素E1（PGE1）对11例以二尖瓣狭窄为主的风湿性心脏病合并肺动脉高压患者的体循环和肺循环的血液动力学作用。
The hemodynamic effects of prostaglandin E1(PGE1)on pulmonary and systemic circulations were studied in 11 patients with rheumatic mitral disease complicated by pulmonary hypertension.
目的探讨先天性心脏病(简称先心病)合并重度肺动脉高压患儿器质性肺动脉高压(简称肺高压)的诊断标准。
Objective to determine the diagnostic standard for organic pulmonary hypertension (PH). Methods the patients with congenital heart defects and severe PH were divided into two groups.
目的探讨先天性心脏病(简称先心病)合并重度肺动脉高压患儿器质性肺动脉高压(简称肺高压)的诊断标准。
Objective to determine the diagnostic standard for organic pulmonary hypertension (PH). Methods the patients with congenital heart defects and severe PH were divided into two groups.
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