Patra Soumya, Rama Sastry Usha M K, Mahimaiha J, Subramanian Anand P, Shankarappa Ravindranath K, Nanjappa Manjunath C
1Department of Cardiology,Sri Jayadeva Institute of Cardiovascular Sciences & Research,Bangalore,Karnataka,India.
2Department of Pediatric Cardiology,Sri Jayadeva Institute of Cardiovascular Sciences & Research,Bangalore,Karnataka,India.
Cardiol Young. 2015 Jun;25(5):861-7. doi: 10.1017/S1047951114000882. Epub 2014 Jun 10.
Cyanotic CHD comprises up to 25% of cases of all causes of CHD.
There is lack of data about the present spectrum of congenital cyanotic heart disease in the paediatric age group.
The present study was undertaken to determine the spectrum of patients with congenital cyanotic heart disease in the paediatric age group in tertiary paediatric cardiac care clinic.
Prospective observational study.
Paediatric cardiac clinic of a tertiary cardiac care centre.
All children aged 0-18 years with suspected cyanotic CHD were provisionally included in this study. They underwent a thorough echocardiographic evaluation, and those patients who had definitive diagnosis of congenital cyanotic heart disease were included for final analysis.
A total of 119 children met the inclusion criteria. Tetralogy of Fallot and its variant were the most common congenital cyanotic heart disease with proportion of about 44%. Other common malformations were double outlet right ventricle (14%), pulmonary atresia with ventricular septal defect (8%), total anomalous pulmonary venous connection (7%), d-transposition of the great arteries (9%), tricuspid valve anomalies--tricuspid atresia and Ebstein's anomaly--hypoplastic left-heart syndrome, truncus arteriosus, and complex CHD such as single ventricle.
Tetralogy of Fallot and its variants were the most common cyanotic heart disease diagnosed in our patients. As there were a significant proportion of cases with complex cyanotic CHD, paediatric cardiologists should be familiar with the diagnosis and management of all these complex congenital malformations of the heart.
青紫型先天性心脏病占所有先天性心脏病病因的25%。
缺乏关于小儿年龄组先天性青紫型心脏病当前谱的资料。
本研究旨在确定三级小儿心脏保健诊所中小儿年龄组先天性青紫型心脏病患者的谱。
前瞻性观察研究。
一家三级心脏保健中心的小儿心脏诊所。
所有0至18岁疑似青紫型先天性心脏病的儿童均临时纳入本研究。他们接受了全面的超声心动图评估,最终分析纳入那些确诊为先天性青紫型心脏病的患者。
共有119名儿童符合纳入标准。法洛四联症及其变异型是最常见的先天性青紫型心脏病,比例约为44%。其他常见畸形包括右心室双出口(14%)、室间隔缺损的肺动脉闭锁(8%)、完全性肺静脉异位连接(7%)、大动脉d型转位(9%)、三尖瓣异常——三尖瓣闭锁和埃布斯坦畸形——左心发育不全综合征、动脉干、以及单心室等复杂先天性心脏病。
法洛四联症及其变异型是我们患者中最常见的青紫型心脏病。由于有相当比例的病例为复杂青紫型先天性心脏病,小儿心脏病专家应熟悉所有这些复杂先天性心脏畸形的诊断和管理。