Right aortic arch
ICD-10 Q25.47 is a billable code used to indicate a diagnosis of right aortic arch.
Right aortic arch is a congenital malformation characterized by the aorta arching to the right side of the body instead of the left. This condition can occur in isolation or in conjunction with other congenital heart defects, such as ventricular septal defects, atrial septal defects, or tetralogy of Fallot. The right aortic arch may lead to compression of the trachea and esophagus, resulting in respiratory and feeding difficulties in infants. Diagnosis is typically made via echocardiography, MRI, or CT imaging, which can visualize the aortic arch's position and any associated anomalies. Management may involve surgical intervention, especially if the right aortic arch is causing significant symptoms or is associated with other critical congenital heart defects. Understanding the implications of this condition is crucial for pediatric care, as it can significantly impact the child's growth and development.
Detailed clinical notes on symptoms, imaging results, and management plans are essential.
Infants presenting with respiratory distress or feeding difficulties due to a right aortic arch.
Consideration of growth and developmental milestones in children with congenital heart defects.
Genetic testing results and family history documentation are critical for understanding potential syndromic associations.
Cases where right aortic arch is part of a genetic syndrome, requiring genetic counseling.
Awareness of chromosomal abnormalities that may co-occur with congenital heart defects.
Used for initial diagnosis and monitoring of right aortic arch.
Detailed report of echocardiographic findings.
Pediatric cardiology may require specific imaging protocols.
Common symptoms include respiratory distress, feeding difficulties, and failure to thrive in infants. Symptoms may vary based on associated congenital heart defects.
