Pulmonary atresia
- 网络肺动脉闭锁;肺动脉瓣闭锁
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Clinical Application of Simmons Catheter for the Angiographic Diagnosis of Pulmonary Atresia
Simmons导管在肺动脉闭锁造影诊断中的临床应用
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Value of prenatal ultrasonographic diagnosis in fetal pulmonary atresia
超声在产前诊断胎儿肺动脉闭锁中的应用价值
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Research on Right Ventricular Growth after Initial Surgery for Pulmonary Atresia and Intact Ventricular Septum
室隔完整型肺动脉瓣闭锁初期术后右室发育的临床研究
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Fetal pulmonary atresia with hypoplastic right ventricle : case report
胎儿肺动脉瓣闭锁伴右室发育不全1例
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Conclusions Pulmonary atresia can be diagnosed accurately by echocardiography .
结论超声心动图可以确诊肺动脉闭锁。
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Left ventricular performance of pulmonary atresia with intact ventricular septum after right heart bypass surgery
右心行旁路手术后室间隔完整的肺动脉闭锁患者的左室功能
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X-ray Film and Cardioangiography Analyses of Pulmonary Atresia
肺动脉闭锁(室间隔完整)X线平片及心血管造影分析
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Six of the surviving patients after initial surgery for pulmonary atresia with intact ventricular septum were studied .
1982年1月至1990年6月期间,对一组室隔完整型肺动脉瓣闭锁(PA+IVS)病儿作了初期手术,近期对生存中6例来随访者作了临床研究。
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Echocardiographic analysis of pulmonary atresia
肺动脉闭锁的超声心动图分析
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Change of Blood Gas and Hemodynamic Status after Palliative Procedure in the Patients with Pulmonary Atresia and Ventricular Septal Defect
肺动脉闭锁伴室间隔缺损患者姑息手术后血气与血流动力学指标的改变
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Cardioangiographic Appearances of Pulmonary Atresia with Intact Ventricular Septum
室间隔完整肺动脉闭锁的心血管造影分析
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Objective To evaluate the indication of radical operation on tetralogy of Fallot with pulmonary atresia ( TOF PA ) .
目的探讨法乐四联症合并肺动脉闭锁(TOFPA)的外科治疗,重点讨论根治手术的适应证。
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Objective : To investigate the color doppler echocardiographic accuracy of pulmonary atresia with ventricular septal defect ( PA / VSD ) .
目的:探讨肺动脉闭锁伴室间隔缺损(PA/VSD)彩超的特点及诊断要点。
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Between 1992 and 1995,14 patients with tetralogy of Fallot with pulmonary atresia ( TOF PA ) underwent surgical treatment .
报告外科治疗法乐四联症伴肺动脉闭锁14例。
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Objective To analyze the key markers for prenatal ultrasonographic diagnosis of pulmonary atresia with intact ventricular septum ( PAIVS ) .
目的探讨室间隔完整的肺动脉闭锁的胎儿期超声诊断声像特征、检测技巧及其鉴别诊断,提高此类畸形的产前检出率。
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Five cases were diagnosed pulmonary atresia , one case was hypoplasia of right heart , and one case was mistaken for persistent truncus arteriosus .
产前超声诊断胎儿肺动脉闭锁5例,诊断右心发育不良1例,误诊永存动脉干1例。
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Excimer laser guidewire penetration of the imperforate valve and balloon valvuloplasty for pulmonary atresia with intact ventricular septum
激光打孔球囊瓣膜成形术治疗肺动脉瓣闭锁伴室间隔完整患儿的研究
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ObjectiveTo evaluate the diagnostic value of multi-slice CT ( MSCT ) and multi-dimensional reconstructions for congenital pulmonary atresia ( PA ) .
目的探讨多层螺旋CT(MSCT)多维重组技术对肺动脉闭锁(PA)的诊断价值。
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Conclusions Prenatal ultrasonographic diagnosis of tetal pulmonary atresia has great clinical value , the reverse flow of ductus arteriosus is an important clue to diagnosis .
结论产前超声检出动脉导管反向血流是诊断胎儿肺动脉闭锁的重要依据,具有重要的临床意义。
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The associated deformities are observed and discussed with clinical significance : VSD in 7 cases , straddling of atrio-ventricular valve in 4 cases and pulmonary atresia in 1 case .
其伴随畸形有室间隔缺损(7例),房室瓣骑跨(3例)和肺动脉闭锁(1例)等,并对其临床意义略加讨论。
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Objective To evaluate the echocardiographic features and diagnostic accuracy in patients with pulmonary atresia with intact ventricular septum ( PA + IVS ), and to assess it 's clinical prognosis .
目的探讨室间隔完整型肺动脉闭锁(PA+IVS)的超声表现及探测要点,并依据结果作初步临床评估。
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Objective To evaluate the initial experience of using Excimer laser guidewire penetration of the imperforate valve and balloon valvuloplasty for infants with pulmonary atresia and intact ventricular septum .
目的探讨激光打孔球囊瓣膜成形术治疗婴儿及新生儿肺动脉瓣闭锁伴室间隔完整的方法的可行性。
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The associated cardiac anomalies included pulmonary atresia in 3 cases , patent foramen ovale or atrial septal defect in 12 cases , and left superior vena cava in 6 cases .
合并卵圆孔未闭或继发孔房缺12例;左上腔静脉6例。
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There were six patients with hypoplastic right ventricle including tricuspid atresia (ⅰ a type ), tricuspid stenosis , pulmonary atresia with intact ventricular septum , pulmonary stenosis and ventricular septum defect .
其中包括三尖瓣闭锁(a型)、三尖瓣狭窄、室间隔完整型肺动脉闭锁、肺动脉狭窄和室间隔缺损等合并右心发育不良6例;
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Objective To evaluate the surgical approach of right ventricular outflow tract construction ( RVOT ) for pulmonary atresia ( PA ) with ventricular septal defect ( VSD ) in infant and younger children .
目的探讨和评价小儿肺动脉闭锁(PA)伴室间隔缺损(VSD)右室流出道重建方法的应用。
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The diagnosis included : 8 cases of tetralogy of Fallot ( TOF ) ( 3 cases of TOF with pulmonary atresia , 1 case of TOF with anomaly of coronary artery , 2 cases of TOF with left pulmonary atresia , 2 cases of TOF with severe pulmonary hypoplasia );
诊断为法乐氏四联症(TOF)8例,其中伴肺动脉瓣闭锁3例;冠状动脉畸形1例;
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Both qualitative and quantitative pulsatile studies were employed on models of normal pulmonary and pulmonary artery atresia with RVOT reconstruction using various extracardiac conduits .
对正常肺动脉及肺动脉闭锁并各种心外管道重建RVOT模型的脉动流场进行定性和定量研究。
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Conclusion Artery fistula as source of pulmonary circulation in pulmonary atresia with ventricular septal defect is a rare complex anomaly , cardioangiography is the gold standard of preoperative diagnosis .
结论以冠状动脉肺动脉瘘为肺循环主要供血来源的肺动脉闭锁合并室间隔缺损是一种罕见畸形,术前确诊的金标准仍是心血管造影。
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Objective To investigate the outcome of hybrid approaches of balloon valvuloplasty via pulmonary valve without cardiopulmonary bypass for pulmonary atresia with intact ventricular septum in neonates .
目的总结室间隔完整型肺动脉闭锁患儿在开胸非体外循环下肺动脉瓣穿刺球囊扩张的镶嵌治疗经验。
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The diagnosis included ventricular septal defect with pulmonary hypertension , tetralogy of Fallot , pulmonary atresia , transposition of the great artery , and single ventricle .
病种为室间隔缺损伴肺动脉高压、法洛四联症、肺动脉闭锁、大动脉错位和单心室等。