Other congenital malformations of aorta
ICD-10 Q25.49 is a billable code used to indicate a diagnosis of other congenital malformations of aorta.
Congenital malformations of the aorta encompass a variety of structural abnormalities that can significantly impact cardiovascular function. These malformations may include conditions such as aortic coarctation, which is characterized by a narrowing of the aorta, leading to increased blood pressure proximal to the defect and decreased blood flow distal to it. Other anomalies may involve abnormal branching patterns or the presence of additional vessels that can complicate normal hemodynamics. Congenital heart defects (CHDs) often coexist with aortic malformations, including septal defects, where there is an abnormal opening between the heart chambers, and tetralogy of Fallot, a complex condition involving four heart defects that can lead to cyanosis and heart failure. Accurate diagnosis typically involves echocardiography, MRI, or CT imaging to visualize the aorta and associated structures. Management may require surgical intervention, particularly in severe cases, to correct the anatomical defects and restore normal blood flow. Early detection and intervention are crucial for improving outcomes in affected pediatric patients.
Detailed clinical notes including physical examination findings, imaging results, and treatment plans are essential for accurate coding.
Pediatric patients presenting with symptoms of heart failure, failure to thrive, or cyanosis due to congenital heart defects.
Consideration of growth and development milestones in pediatric patients with congenital conditions is crucial for comprehensive care.
Genetic testing results, family history, and any syndromic associations should be documented to support the diagnosis of congenital malformations.
Patients with known genetic syndromes presenting with congenital heart defects, requiring genetic counseling and testing.
Understanding the genetic basis of congenital malformations can aid in risk assessment and management of affected families.
Used in cases where surgical intervention is required for aortic coarctation.
Operative reports detailing the procedure and indication for surgery.
Pediatric cardiology may have specific protocols for documenting congenital heart surgeries.
Common congenital malformations of the aorta include coarctation of the aorta, aortic stenosis, and aortic arch anomalies. These conditions can lead to significant cardiovascular complications and often require surgical intervention.
