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.
方法：选取合并重度肺动脉高压左向右分流型先天性心脏病患儿38例，于矫治手术中取肺活检。
Methods: Lung biopsies were taken in the corrective operations in 38 young children suffered from left to right shunt congenital heart defects associated with severe pulmonary hypertension.
目的探讨先天性心脏病(先心病)伴重度肺动脉高压(肺高压)患儿手术指征的判定标准。
Objective To determine the standard for operative indication of severe pulmonary hypertension (PH) in children with congenital heart defect (CHD).
绝大多数先天性动脉导管未闭症可做常规闭合术，但对少部分合并重度肺动脉高压者将冒极大风险。
Majority of the cases with congenital PDA can be operated on with routine technique, but it will be very dangerous for some patients complicated with severe pulmonary hypertension.
目的探讨先天性心脏病患儿血浆降钙素基因相关肽(CGRP)水平与肺动脉高压的关系和基因序列检测的临床意义。
Objective To investigate the clinical significance of CGRP level and gene sequence in congenital heart disease (CHD) with pulmonary hypertension.
先天性心脏病合并肺动脉高压是严重影响儿童身心健康的主要病症之一，在全世界范围内呈上升趋势。
Congenital heart disease with pulmonary hypertension is a major disease affecting the physical and mental health of children.
结论血浆CGRP水平失衡在先天性心脏病肺动脉高压的发生机制中起重要作用。
Conclusion the CGRP might be involved in the pathophysiologic process of pulmonary hypertension in CHD.
目的评估应用单向活瓣补片治疗合并重度肺动脉高压双向分流的先天性房室间隔缺损患者的术后效果。
Objective to discuss the surgical effect with one-way-valved patch to treat cardiac septal defects with severe pulmonary hypertension with bi-directional shunt.
先天性心脏病也能引起肺动脉高压。
新指南也讨论了患各种先天性心脏病和肺动脉高压儿童及婴儿的复苏抢救。
The new guidelines also discuss resuscitation of infants and children with various congenital heart diseases and 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.
小选今年18岁了，从出生就发现患病，一直无钱接受治疗，今年被县医院确诊为先天性心脏病肺动脉高压。
This year Little Xuan is 18 years old. They knew she had a heart defect from birth, but all the while they didn't have money to get treatment.
小选今年18岁了，从出生就发现患病，一直无钱接受治疗，今年被县医院确诊为先天性心脏病肺动脉高压。
This year Little Xuan is 18 years old. They knew she had a heart defect from birth, but all the while they didn't have money to get treatment.
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