Ali S K
Department of Paediatric Cardiology, Sudan Heart Centre, Khartoum Erkaweit, Sudan.
Cardiovasc J Afr. 2009 Mar-Apr;20(2):112-5.
Congential heart disease (CHD) is an important cause of morbidity and mortality in patients with Down's syndrome (DS).
All patients with DS seen at the Sudan Heart Centre from July 2004 to November 2007 were included in the study. All patients were examined clinically and echocardiographically, and cardiac catheterisation was carried out in selected patients. All patients were prospectively followed up.
In the study period, 1 566 patients were evaluated for heart disease. Of these, 80 patients with DS were identified (5%). Their ages ranged from 15 days to 18 years. Cardiac abnormalities included atrioventricular septal defect (AVSD) in 38 patients (48%), with the complete form in 25, a partial form in seven, AVSD with intact atrial septum in one, and complex AVSD in four patients. In one patient there was AVSD with right atrioventricular valve malformation with severe valve regurgitation and functional pulmonary atresia. The other main lesions were ventricular septal defect (VSD) in 19 patients (23%) and tetralogy of Fallot (TOF) in five (6%). Cardiac catheterisation was done in four patients with AVSD to measure pulmonary pressures and resistance, and in one patient with patent ductus arteriosus for device closure. Ten percent of the patients had Eisenmenger's syndrome at the time of presentation. Only 15% of patients who were in need of surgery were operated on; all had an uneventful postoperative course and a good outcome at a mean follow-up period of one year.
The pattern of CHD in Sudanese patients with DS was comparable with that in the literature, including the rare occurrence of AVSD with intact atrial septum. In addition, we described an unreported association with right atrioventricular valve malformation. Although there was a significant delay in diagnosis and surgery, surgical results and short-term follow up were good.
先天性心脏病(CHD)是唐氏综合征(DS)患者发病和死亡的重要原因。
纳入2004年7月至2007年11月在苏丹心脏中心就诊的所有DS患者。所有患者均接受临床和超声心动图检查,部分患者进行了心导管检查。所有患者均进行前瞻性随访。
在研究期间,对1566例患者进行了心脏病评估。其中,确诊80例DS患者(5%)。年龄范围为15天至18岁。心脏异常包括38例(48%)房室间隔缺损(AVSD),其中完全型25例,部分型7例,房间隔完整的AVSD 1例,复杂AVSD 4例。1例患者为AVSD合并右房室瓣畸形,伴有严重瓣膜反流和功能性肺动脉闭锁。其他主要病变为19例(23%)室间隔缺损(VSD)和5例(6%)法洛四联症(TOF)。4例AVSD患者进行了心导管检查以测量肺动脉压力和阻力,1例动脉导管未闭患者进行了封堵器械治疗。10%的患者在就诊时患有艾森曼格综合征。仅15%需要手术的患者接受了手术;所有患者术后过程顺利,平均随访1年时预后良好。
苏丹DS患者的CHD模式与文献报道相似,包括房间隔完整的AVSD罕见情况。此外,我们描述了一种未报道的与右房室瓣畸形的关联。尽管诊断和手术存在显著延迟,但手术结果和短期随访良好。