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Cardiac abnormalities of Sudanese patients with Down's syndrome and their short-term outcome
1Department of Paediatric Cardiology, Sudan Heart Centre, Khartoum Erkaweit, Sudan. sulafakhalid2000@yahoo.com
Insights
Congenital heart disease (CHD) in Down's syndrome (DS) patients is common. Atrioventricular septal defect was the most frequent anomaly, and surgical outcomes were positive despite diagnostic delays.
Area of Science:
- Cardiology
- Genetics
- Pediatrics
Background:
- Congenital heart disease (CHD) is a significant cause of mortality in individuals with Down's syndrome (DS).
- Understanding the spectrum of CHD in DS is crucial for timely intervention and improved patient outcomes.
Purpose of the Study:
- To investigate the prevalence and patterns of congenital heart disease (CHD) in patients with Down's syndrome (DS).
- To describe the clinical characteristics, diagnostic methods, and surgical outcomes of CHD in DS patients.
Main Methods:
- A prospective study of patients with DS evaluated at the Sudan Heart Centre between July 2004 and November 2007.
- Clinical examination, echocardiography, and cardiac catheterization were utilized for diagnosis.
- Patients were followed up post-intervention.
Main Results:
- Eighty patients with DS were identified, with CHD present in all.
- Atrioventricular septal defect (AVSD) was the most common anomaly (48%), followed by ventricular septal defect (VSD) (23%) and tetralogy of Fallot (TOF) (6%).
- Despite delays in diagnosis and surgery, 15% of indicated surgical cases had an uneventful postoperative course and good short-term outcomes.
Conclusions:
- The pattern of CHD in Sudanese DS patients aligns with international findings, including rare presentations like AVSD with an intact atrial septum.
- An unreported association between AVSD and right atrioventricular valve malformation was observed.
- Prompt diagnosis and surgical intervention are vital, as surgical results in this cohort were favorable.
Background:
Congential heart disease (CHD) is an important cause of morbidity and mortality in patients with Down's syndrome (DS).
Methods:
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.
Results:
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.
Conclusion:
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.
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