Other atresia of aorta
ICD-10 Q25.29 is a billable code used to indicate a diagnosis of other atresia of aorta.
Other atresia of the aorta refers to congenital malformations where there is a complete or partial obstruction of the aorta, which can lead to significant hemodynamic changes and complications in the circulatory system. This condition may manifest as a result of various developmental anomalies during fetal life, leading to inadequate blood flow to the body. Patients may present with symptoms such as cyanosis, heart failure, and poor growth. Diagnosis typically involves imaging studies such as echocardiography, MRI, or CT scans to assess the anatomy and blood flow. Management often requires surgical intervention to restore normal blood flow and may involve complex procedures depending on the severity and associated anomalies. Other congenital heart defects, such as septal defects, tetralogy of Fallot, and coarctation of the aorta, may coexist, complicating the clinical picture and management strategies.
Thorough documentation of clinical findings, imaging results, and treatment plans is essential. Pediatric cardiology consultations may be necessary.
Infants presenting with cyanosis, failure to thrive, or heart murmurs requiring echocardiographic evaluation.
Consideration of growth and developmental milestones in the context of congenital heart disease.
Genetic testing results, family history of congenital conditions, and any syndromic associations should be documented.
Cases where congenital heart defects are part of a genetic syndrome, requiring genetic counseling and testing.
Awareness of chromosomal abnormalities that may be associated with congenital heart defects, such as Down syndrome.
Used in surgical management of aortic atresia.
Operative reports detailing the procedure and indications.
Pediatric cardiothoracic surgery documentation standards.
Common associated conditions include other congenital heart defects such as ventricular septal defects, atrial septal defects, and coarctation of the aorta. Genetic syndromes may also be present, necessitating thorough evaluation.
