方法：利用野百合碱诱发大鼠肺动脉高压模型。
Methods: The model of pulmonary hypertension induced by monocrotaline was established in rats.
供给肺脏的动脉的血压增高称之为肺动脉高压。
High blood pressure in the arteries that supply the lungs is called pulmonary hypertension (PHT).
目的：寻找抑制肺动脉高压肺血管重建的药物。
Objective: to find a therapeutic inhibitor of vascular remodelling in pulmonary hypertension.
目的：研究缺氧性肺动脉高压大鼠右心室重构情况。
Objective: To study the pattern of right ventricle remodeling in hypoxic pulmonary hypertension rats.
如果此过程累及许多肺动脉，就可能导致肺动脉高压。
If many pulmonary arteries are involved by this process, pulmonary hypertension could result.
目的：观察肺心汤对慢性缺氧性肺动脉高压大鼠的作用。
Objective: To observe effects of Feixin Tang (FXT) on the chronic hypoxia pulmonary hypertension rats.
手术死亡的主要原因为肺动脉高压危象和严重心律失常。
The main causes of death were pulmonary hypertensive crisis and arrhythmia.
术后主要并发症为肺部感染、肺动脉高压危象和心律失常。
The leading complications were pulmonary infection, pulmonary hypertensive crisis and heart arrhythmia.
结局是否证实首个口服治疗策略可用于肺动脉高压的管理？
Does the Outcome Justify an Oral-First Treatment Strategy for Management of Pulmonary Arterial Hypertension?
戏剧性的功能改善下列减肥手术患者肺动脉高压和病态肥胖。
Dramatic functional improvement following bariatric surgery in a patient with pulmonary arterial hypertension and morbid obesity.
结论：缺氧性肺动脉高压大鼠右心室早期表现为离心性肥大。
Conclusion : Eccentric hypertrophy accounts for the early change of right ventricle in hypoxic pulmonary hypertension rats.
目的探讨左肺反向循环(LLIC)逆转肺动脉高压的机制。
Objective To study left lung inverse circulation (LLIC) reversing pulmonary hypertension (PH) in canines.
目的：观察布瑞宁注射液对慢性肺心病患者肺动脉高压的影响。
Objective: to observe the influence of Puerarine injection to the chronic cardiopulmonary disease with pulmonary arterial hypertension.
肾功能不全与血液动力学和肺动脉高压病死率相关性目前并不清楚。
How renal dysfunction relates to hemodynamics and mortality in pulmonary arterial hypertension (PAH) remains unclear.
结论：肺心合剂能部分逆转肺血管结构重建，有效降低肺动脉高压。
CONCLUSION: Feixin mixture reverses partially the remodeling of pulmonary vascular structure and reduces effectively pulmonary hypertension.
ES病人与那些未经治疗的特发性肺动脉高压病人比较，生存率更佳。
Patients with ES show significantly more favorable survival rates, as compared with those with untreated idiopathic pulmonary hypertension.
目的应用声学定量(AQ)技术，研究肺动脉高压患者右房功能改变。
Objective: To evaluate the Right atrial (RA) function in patients with pulmonary hypertension using acoustic quantification (AQ) technique.
目的：探讨彩色多普勒超声诊断胎儿伴肺动脉高压型房间隔缺损的方法。
Objective: To study the diagnosis of fetal atrial septal defect with pulmonary hypertension by color Doppler.
目的探讨吸入一氧化氮(NO)治疗不同类型的肺动脉高压的适应证及疗效。
Objective To study the indication and effectiveness of NO inhalation in acute all types of pulmonary hypertension.
结果表明，本制剂有明显的降肺动脉高压、右心室压和逆转右心肥大的作用。
The results indicated that GLXBBXD had the function of reducing the pulmonary hypertension and reversing the hypertrophy of right heart obviously.
结论在常规治疗的基础上联合使用PGE1可以明显降低继发性肺动脉高压。
Conclusion Combined use of PGE1 with conventional therapy has much stronger efficacy in the treatment of secondary pulmonary hypertension.
目的研究经导管肺动脉局部溶栓加抗凝治疗在急性肺栓塞性肺动脉高压的作用。
Objective To investigate local thrombolysis and anticoagulation by catheter in the treatment of acute thromboembolic pulmonary hypertension.
我们的研究显示18.5%的病人在超声心动图上有提高的收缩期肺动脉高压。
Our study showed an 18.5% prevalence of patients with elevated systolic pulmonary artery pressure at echocardiography.
目的：探讨波生坦治疗肺动脉高压的药理机制，并评价其临床疗效和用药安全性。
OBJECTIVE: To study pharmacological mechanism of bosentan for treatment of pulmonary artery hypertension (PAH) and evaluate its clinical efficacy and the safety.
目的探讨肺动脉局部肾素-血管紧张素系统对缺氧性肺动脉高压(PAH)的影响。
Objective To study the effect of local pulmonary arterial renin angiotensin system on hypoxic pulmonary hypertension (PAH).
该项研究通过调查以下市场：孤儿疾病，高歇病和欧洲的肺动脉高压（PAH）市场。
This study thoroughly examines the following markets: orphan diseases, Gaucher's Disease and Pulmonary Arterial Hypertension (PAH) markets in Europe.
结果与结论：肺动脉高压的特点是肺血管阻力进行性增加，最终导致右心衰竭和死亡。
RESULTS & CONCLUSION: The feature of PAH is that pulmonary vascular resistance progressively increases, and finally leads to right heart failure and death.
结果与结论：肺动脉高压的特点是肺血管阻力进行性增加，最终导致右心衰竭和死亡。
RESULTS & CONCLUSION: The feature of PAH is that pulmonary vascular resistance progressively increases, and finally leads to right heart failure and death.
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