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B型利钠肽在先天性心脏病患儿中的诊断价值
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作者 koch a. Zink S. +2 位作者 Singer H. 黄浙勇(译) 任付先(校) 《世界核心医学期刊文摘(心脏病学分册)》 2006年第8期31-32,共2页
Aims: To examine the diagnostic value of B-type natriuretic peptide(BNP) plasma concentration in congenital heart disease. Methods and results: BNP was measured in 288 consecutive patients(mean age 6.0± 6.4 years... Aims: To examine the diagnostic value of B-type natriuretic peptide(BNP) plasma concentration in congenital heart disease. Methods and results: BNP was measured in 288 consecutive patients(mean age 6.0± 6.4 years) with left-to-right shunt, left or right heart obstruction, tetralogy of Fallot, functionally univentricular heart, or impaired left ventricular function and compared with age- and gender-specific normal values, and to haemodynamic and echocardiographic data. BNP increased with decreasing left ventricular shortening fraction(r=-0.80; P< 0.001). In patients with left-to-right shunt, BNP was increased(mean SDS + 1.64; P< 0.001) and positively correlated(P< 0.001) to shunt volume(r=0.66), systolic right ventricular pressure(r=0.69), mean pressure of the pulmonary artery(r=0.66), and pulmonary resistance(r=0.59). There was no correlation between BNP and invasive pressure gradient or extent of ventricular hypertrophy in patients with left or right heart obstruction. In patients with tetralogy of Fallot, BNP was not significantly increased. Patients with functionally univentricular heart had elevated BNP plasma levels(mean SDS + 1.39; P< 0.001)without decrease after volume unloading by cavopulmonary connection. Conclusion: In children with congenital heart defects, plasma BNP correlates closely to ventricular function. BNP plasma levels do not reflect directly the extent of ventricular pressure or volume work, but mirror the impairment of the loaded ventricles. Normal BNP cannot exclude pathology, but reflects a compensated status of the heart. 展开更多
关键词 先天性心脏病 B型利钠肽 诊断价值 患儿 全腔静脉-肺动脉连接术 功能性单心室 梗阻性病变 血浆水平 左向右分流 法洛四联症
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主动脉弓偏移和锁骨下动脉畸形是否为22q11.2缺失综合征的可靠标志
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作者 RauchR. Rauch a. +3 位作者 koch a. M. Hofbeck M.Hofbeck 郭战宏 《世界核心医学期刊文摘(儿科学分册)》 2005年第4期35-36,共2页
多种心脏先天性畸形包括永存交通动脉干、Fallot四联征、肺动脉闭锁伴室间隔缺损及主动脉弓间断等常被总称为锥干性心脏畸形。在有这些心脏先天性畸形的患者中,常发现其22号染色体上有一常见的微小缺失,即所谓的22q11.2单体。本研究的... 多种心脏先天性畸形包括永存交通动脉干、Fallot四联征、肺动脉闭锁伴室间隔缺损及主动脉弓间断等常被总称为锥干性心脏畸形。在有这些心脏先天性畸形的患者中,常发现其22号染色体上有一常见的微小缺失,即所谓的22q11.2单体。本研究的目的是确定这些患者其主动脉弓偏移或存在锁骨下动脉畸形(SAA)是否是22q11.2单体的标志。 展开更多
关键词 q11.2 锁骨下动脉 动脉干 室间隔缺损 肺动脉闭锁 单体的 干性 ATRESIA tetralogy aorta
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