Congenital heart disease and Down syndrome: various aspects of a confirmed association
Autor: | Sanaa Benhaourech, Ayoub El Hammiri, Abdenasser Drighil |
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Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Adult Heart Defects Congenital Male Pediatrics medicine.medical_specialty Down syndrome Time Factors Heart disease Adolescent Population 030204 cardiovascular system & hematology Hospitals University 03 medical and health sciences Young Adult 0302 clinical medicine medicine Humans Atrioventricular Septal Defect cardiovascular diseases Young adult Cardiac Surgical Procedures education Child Cause of death Retrospective Studies education.field_of_study business.industry Mortality rate Cardiovascular Topics Infant Newborn Infant Retrospective cohort study General Medicine Middle Aged medicine.disease Prognosis congenital heart disease therapeutic Morocco 030104 developmental biology Child Preschool epidemiology Female Cardiology and Cardiovascular Medicine business Maternal Age |
Zdroj: | Cardiovascular Journal of Africa |
ISSN: | 1680-0745 1995-1892 |
Popis: | Background Congenital heart disease (CHD) is frequently described in patients with Down syndrome (DS) and is the main cause of death in this population during the first two years of life. The spectrum of CHD patterns in DS varies widely worldwide; this variation could be due to sociodemographic, genetic and geographic factors. Methods A six-year retrospective, descriptive study was carried out from December 2008 to October 2014, based on the Paediatric Unit CHD registry of Ibn Rochd University Hospital. Clinical, echocardiographic and outcomes data were collected and sorted according to confirmation of the syndrome. Results Among 2 156 patients with CHD, 128 were identified with Down syndrome. The genders were equally represented (gender ratio 1) and the median age at diagnosis was 9.5 months (2 days to 16 years). The median age of mothers at delivery was 39 years (16-47). Of the 186 CHD lesions reported, the most common was atrioventricular septal defect (AVSD, 29%), followed by ventricular septal defect (VSD, 21.5%) and atrial septal defect (ASD, 19.9%). The most common associations of CHD were AVSD + ASD (10%) and VSD + ASD (7.8%). Surgery was the most common modality of treatment (54.3%). The overall mortality rate was 14.1%. Conclusion Our study confirmed that the profile and type of CHD in DS in the Moroccan setting exhibited slight differences in the distribution of these CHDs compared with European neighbours and other Western countries. Further studies are needed to determine which variables have an impact on these differences. |
Databáze: | OpenAIRE |
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