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In recent years,research has involved percutaneous aortic valve replacement,percutaneous mitral valve reconstruction and even percutaneous pulmonary valve replacement after successful application of percutaneous mitral commissurotomy in clinical practice.

除经皮二尖瓣分离术外,近年来还涉及经皮主动脉瓣替换、经皮二尖瓣修复以及经皮肺动脉瓣替换等领域,并取得了一定的成果,文章对此作一概述。

To confirm the utility of continuous wave Doppler echocardiography in assessing pulmonary artery wedge pressure in patients with mitral regurgitation.

目的探讨连续波多普勒超声在评估二尖瓣返流患者的肺动脉楔压中的作用。

Contractile response of PARs to PE varied with the different doses of ONOO〓.

3ONOO〓孵育对肺动脉的收缩反应因剂量不同而有差异。

The exclusion criteria were the following: Patients with an sign of infection or any conditions that would contraindicate glucocorticoids; systolic blood pressure lower than 80 mm Hg or higher than 140 mm Hg; cardiogenic shock; volume depletion; mechanical ventilation; hypertrophic or restrictive cardiomyopathy; constrictive pericarditis, pulmonary arterial hypertension, or active myocarditis.

排除标准包括:有感染症状或有糖皮质激素禁忌症的;收缩压低于80 mmHg或高于140 mmHg的心源性休克;血容量不足;机械通气;肥厚型或限制型心肌病;缩窄性心包炎;肺动脉高压;活动性心肌炎。

Background: Hyperkinetic pulmonary hypertension is a common complication of congenital heart disease with left to right shunt, which has an important effect on achievement ratio of surgical correction and long term survival of patients with CHD.

研究背景:高动力性肺动脉高压是左向右分流型先天性心脏病常见的合并症,严重影响先天性心脏病外科矫治手术的时机、成功率以及患者术后长期生存质量。

The degree of cyanosis is related to the presence of other defects that allow blood to mix, including a patent ductus arteriosus - a fetal connection between the aorta and the pulmonary artery present in the newborn, which usually closes in the first few days after birth.

紫绀的程度取决于伴随的可以使血液混合的其它心脏畸形,包括动脉导管未闭-新生儿存在的在胎儿期主动脉和肺动脉之间的连接,一般在生后头几天里闭合。

Characterization of the enzymic capacity for cysteine desulphhydration in liver and kidney of the rat .

气体信号一氧化氮与硫化氢在肺动脉舒张反应中的相互作用。

The murmur is usually high-pitched and blowing in quality with a decrescendo configuration.

肺动脉瓣和主动脉瓣反流的分辨很难,需通过插管才能确诊。

Types of the combination were as follows: ASD and VSD, 2 cases; ASD and PS, 2 cases; ASD and MS, 1 case; ASD and coronary artery stenosis, which needed interventional treatment, 1 case; VSD and PDA, 3 cases; ASD and anomalous inferior vein cava drainage, 1 case; PDA and B-preexcitation syndrome, 1 case; PDA and dextrocardia, anomalous inferior vein cava drainage, 1 case.

复合类型为:房间隔缺损合并室间隔缺损2例,ASD合并肺动脉瓣狭窄2例,ASD合并二尖瓣狭窄1例,ASD合并冠脉狭窄需介入治疗1例,ASD合并右位心1例,VSD合并动脉导管未闭3例,PDA合并B型预激综合征1例,PDA右位心、下腔静脉肝段缺如1例,VSD合并下腔静脉肝段缺如1例。

Results Of total 11 patients, 10 cases were mirror-image dextrocardia, 1 case was dextroversion. Among 10 patients were diagnosed as mirror-image dextrocardia, 5 patients were found to have concomitant cardiovascular malformations, the major anomalies were VSD,TOF, DORV. 1 case of dextroversion with complex cardiac anomalies: CECD+SA+DORV+PS. Conclusion Congenital dextrocardia may present with complex anomalies.

结果:11例先天性右位心患者中,镜像右位心10例,右旋心1例。10例镜像右位心中5例合并心内畸形,主要畸形为:室间隔缺损2例,法洛四联症2例,右室双出口1例;超声漏诊2例合并双上腔静脉。1例右旋心合并复杂畸形:完全型心内膜垫缺损、单心房、右室双出口、肺动脉瓣重度狭窄。

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