Congenital dilation of aorta
ICD-10 Q25.44 is a billable code used to indicate a diagnosis of congenital dilation of aorta.
Congenital dilation of the aorta refers to an abnormal widening of the aorta, which can occur at any segment of the vessel. This condition is often associated with other congenital heart defects and can lead to significant cardiovascular complications if not diagnosed and managed appropriately. The dilation may be isolated or part of a syndrome involving other vascular or cardiac anomalies. Patients may present with symptoms such as heart murmurs, chest pain, or signs of heart failure, depending on the severity of the dilation and associated defects. Diagnosis typically involves imaging studies such as echocardiography, MRI, or CT scans to assess the extent of the dilation and any coexisting anomalies. Treatment may include surgical intervention, especially in cases where the dilation poses a risk of rupture or significant hemodynamic compromise. Regular follow-up is essential to monitor the condition and manage any associated complications.
Detailed pediatric history, including prenatal factors and family history of congenital heart disease.
Infants presenting with heart murmurs or failure to thrive due to undiagnosed congenital heart defects.
Consideration of growth and development milestones in relation to cardiac function.
Genetic testing results, family history of genetic syndromes, and any chromosomal abnormalities.
Patients with syndromic presentations such as Turner syndrome or Marfan syndrome, which may include aortic dilation.
Importance of genetic counseling for families with a history of congenital heart defects.
Used for initial diagnosis and monitoring of congenital heart defects.
Complete echocardiographic report detailing findings.
Pediatric cardiology may require additional imaging studies.
Accurate coding of congenital dilation of the aorta is crucial for appropriate management, treatment planning, and reimbursement. It helps in tracking the prevalence of congenital heart defects and ensuring that patients receive the necessary follow-up care.
