1) severe pulmonary hypertension
重度肺动脉高压
1.
Surgical management of congenital heart disease with severe pulmonary hypertension;
先天性心脏病合并重度肺动脉高压的外科治疗体会
2.
Surgical management of rheumatic heart disease with severe pulmonary hypertension
风湿性心脏病合并重度肺动脉高压的手术治疗
3.
Methods Preoperatively PGE1,15～20 ng/(kg·min) was administrated intra-centralvenous in 30 patients with severe pulmonary hypertension(mPAP≥61 mmHg),and the changes of pulmonary artery pressure,PaO2,SaO2,arotic blood pressure were measured after the drugs were given for 7 to 10 days.
目的:观察前列腺素E1在合并重度肺动脉高压的先天性心脏病围手术期的应用效果。
2) ASD associated severe pulmonary hypertension
房间隔缺损并重度肺动脉高压
3) Pulmonary arterial hypertension
肺动脉高压
1.
NO and pulmonary arterial hypertension;
一氧化氮与肺动脉高压的关系研究进展
2.
Pharmacology and clinical study of ambrisentan for treatment of pulmonary arterial hypertension;
治疗肺动脉高压新药安贝生坦的药理与临床研究
3.
Clinic Study on Shenfu Injection to Treat Pulmonary Arterial Hypertension of Chronic Cardiopulmonary Disease;
参附针治疗慢性肺心病肺动脉高压症的临床研究
4) Pulmonary artery hypertension
肺动脉高压
1.
Effects of Enalapril or Metoprolol on plasm brain natriuretice peptide in congenital heart disease combined with pulmonary artery hypertension after transcatheter closure;
经导管封堵对先天性心脏病伴肺动脉高压患者血浆脑钠素的影响及其药物干预研究
2.
Preparation and identification of animal model with hypoxia-induced pulmonary artery hypertension;
急性缺氧型肺动脉高压动物模型制备
3.
Clinical observation on the left ventricular myocardial remodel and dysfunction in children with congenital heart disease and hypoxia-induced pulmonary artery hypertension.;
先天性心脏病肺动脉高压患儿左室心肌重塑和舒张功能的临床观察
5) pulmonary hypertension
肺动脉高压
1.
Effects of fasudil on hypoxia-induced pulmonary hypertension and vascular remodeling in rats;
法舒地尔对大鼠低氧性肺动脉高压及其肺血管结构重建的影响
2.
Role of endogenous hydrogen sulfide in pulmonary hypertension induced by lipopolysaccharide;
内源性硫化氢在脂多糖引起的肺动脉高压中的作用
3.
Treatment of patent ductus arteriosus accompanied with severe pulmonary hypertension with transcatheter occlusion;
经导管封堵治疗动脉导管未闭伴重度肺动脉高压
6) PAH
[英][pɑ:] [美][pɑ]
肺动脉高压
1.
The Association of Polymorphism of Endothelial Nitric Oxide Synthase Gene in Patients with PAH of Chronic Obstructive Pulmonary Disease;
COPD肺动脉高压与内皮型一氧化氮合酶第4内含子VNTR多态相关性研究
2.
On Correlation between Syndrome of Sinking of Pectoral Qi and PAH;
大气下陷证与肺动脉高压相关性机理探讨
3.
The Research of the Applying Value of PG in the Diagnosis and Therapy of PAH by PHD;
三尖瓣返流压力差在肺心病肺动脉高压诊断和治疗中应用价值的研究
补充资料：肺动脉高压
| 肺动脉高压 pulmonary hypertension 肺循环压力高于正常的病理状态。多并发于心肺疾病 ，也可由肺血管病本身引起。临床上不少见。肺动脉高压可致右心室肥厚或肺源性心脏病。 静息状态下肺动脉平均压＞ 2.67千帕（kPa）（20毫米汞高）或收缩压＞4.00kPa（30毫米汞高）。为肺动脉高压。 病理生理 肺毛细血管和／或左房压力升高、肺血管床总截断面积下降、肺动脉血流量增加、缺氧等是引起肺动脉压力升高的重要因素。当上述因素持续存在并达到一定程度时，肺血管发生形态学改变。肺动脉和静脉中层肥厚，内膜增生，管径变小，增加了肺血管阻力，产生肺动脉高压。 病因及分类 ①原发性肺动脉高压，病因不清。可能与先天性肺小动脉病变、肺小动脉痉挛或自身免疫等因素有关。②继发性肺动脉高压，由已知病因引起，如肺气肿、肺纤维化及肺血栓栓塞；左向右分流的先天性心脏病、二尖瓣病变、心包积液等。 临床表现和体征 易疲乏，有劳力性呼吸困难、晕厥 、咯血等；颈静脉搏动增强，肺动脉瓣区收缩期搏动，肺动脉第二音增强或分裂，有收缩期喷射音和喷射性杂音；右心衰竭后出现相应症状。 心电图可出现电轴右倾、肺型 P 波、右室肥厚和右束支传导阻滞，胸部 X 射线检查显示肺动脉段突出、右下肺动脉增宽等，超声心动图示右房右室增大及肺动脉高压征象。 治疗 处理原发病及有关影响因素，选用血管扩张药降低肺动脉压力。 |
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参考词条