检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王琦光[1] 朱鲜阳[1] 韩秀敏[1] 张端珍[1] 崔春生[1] 陈火元[1] 肖家旺[1]
机构地区:[1]沈阳军区总医院先心病内科,辽宁沈阳110016
出 处:《心脏杂志》2014年第1期43-45,55,共4页Chinese Heart Journal
摘 要:目的:总结分析Down综合征(Down’s syndrome)并发的先天性心脏病畸形及血流动力学资料。方法:2008年7月-2012年10月,采用经胸二维超声心动图并彩色多普勒显像及右心导管/心血管造影检查方法,诊断36例并发先心病的Down综合征患者,本文通过36例临床资料分析,探讨Down综合征并发的先心病畸形及其血流动力学。结果:36例患者中室间隔缺损(VSD)10例,房室间隔缺损(AVSD)6例,动脉导管未闭(PDA)6例,房间隔缺损(ASD)2例,ASD+PDA2例,ASD+VSD1例,ASD+PDA+VSD1例,VSD+PDA4例,PDA十二叶主动脉瓣(BAV)1例,法洛四联症(TOF)2例,TOF+ASD1例,18例有肺动脉高压者,其中5例为阻力型肺动脉高压。结论:①Down综合征并发的心血管畸形中,以VSD、AVSD和PDA最为常见,并常并发ASD、TOF。②在无肺动脉狭窄的患者中,约50%并发有肺动脉高压。AIM: To analyze congenital heart deformity and hemodynamic data of Down syndrome. METHODS : Clinical data of Down' s syndrome with congenital heart disease and its hemodynamics were analyzed in 36 patients diagnosed with congenital heart disease patients with Down syndrome by transtho- racic two-dimensional echoeardiography, color Doppler flow imaging and right heart catheterization or angiocardiography from July 2008 to October 2012. RESULTS: Among the 36 cases, there were ten patients with VSD, six patients with AVSD, six patients with PDA, two patients with ASD, two cases with ASD + PDA, one case with ASD + VSD, one patient with ASD + PDA + VSD, four patients with VSD + PDA, one patient with PDA + BAV, two patients with TOF 2, and once patient with TOF + ASD. Eighteen patients had pulmonary hypertension including five cases of resistant pulmonary arterial hyper- tension. CONCLUSION: In cardiovascular malformations with Down syndrome, VSD (28%), AVSD ( 17% ) and PDA ( 17% ) are most common and are often associated with ASD or TOF. In patients with- out pulmonary artery stenosis, about half are complicated with pulmonary artery hypertension.
关 键 词:DOWN综合征 先天性心脏病 心脏畸形 心导管检查 肺动脉高压
分 类 号:R541.1[医药卫生—心血管疾病]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.7