ArticleThe Eurasian journal of medicine2026
Spectrum of Congenital Heart Diseases in Iraqi Patients.
Article in The Eurasian journal of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundEarly detection and risk stratification of congenital heart disease (CHD) are of utmost importance for timely management. This study aimed to report on CHD among patients in Baghdad, Iraq.
methodsThis prospective study was conducted from September 1, 2022 to September 1, 2023 among 2221 patients of all age groups diagnosed with CHD.
resultsThis study analyzed 2221 patients with CHD, of whom 76.7% had acyanotic CHD and 23.3% had cyanotic CHD. The mean age was higher for acyanotic cases (81.3 months) than for cyanotic cases (25.6 months). Almost half (47.5%) of the diagnoses were made in infancy, and 10.9% were made in the neonatal period. Only 13.2% of the diagnoses were made in adulthood. Ventricular septal defect (VSD) was the most frequent lesion, mainly diagnosed in infancy, whereas atrial septal defect (ASD) was often recognized in adulthood (42%). Critical conditions such as D-transposition of great arteries and hypoplastic left heart syndrome were mostly neonatal diagnoses. Gender distribution was balanced overall, though ASD and patent ductus arteriosus were significantly more common in females, while aortic stenosis, D-transposition of the great arteries, and coarctation predominated in males. Ventricular septal defect (30.2%) was the leading acyanotic lesion, while Tetralogy of Fallot (9.4%) was the most common cyanotic CHD.
conclusionsThis research indicates that acyanotic CHD prevails in Iraq, with VSD being the most common. More than half of the sample was diagnosed by the age of 2. A male predominance was observed throughout indicating a need for early screening with gender consideration. Cite this article as: Al-Hamash SM, Amer AN, Maerozy KAM, Khalid KA. Spectrum of congenital heart diseases in Iraqi patients. Eurasian J Med. 2026, 58(1), 1236, doi: 10.5152/eurasianjmed.2026.251236.
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