Congenital tricuspid stenosis
ICD-10 Q22.4 is a billable code used to indicate a diagnosis of congenital tricuspid stenosis.
Congenital tricuspid stenosis is a rare heart defect characterized by the narrowing of the tricuspid valve, which impedes blood flow from the right atrium to the right ventricle. This condition can lead to increased pressure in the right atrium and may result in right heart failure if not addressed. Patients may present with symptoms such as cyanosis, fatigue, and signs of heart failure. The stenosis can be isolated or associated with other congenital heart defects, such as atrial septal defects or ventricular septal defects. Diagnosis is typically made through echocardiography, which can visualize the structure and function of the heart valves. Treatment often involves surgical intervention to repair or replace the tricuspid valve, especially in symptomatic patients. Early detection and management are crucial to improving outcomes and preventing complications associated with this congenital malformation.
Documentation should include detailed clinical findings, echocardiographic results, and any surgical interventions performed.
Pediatric patients presenting with heart murmurs, failure to thrive, or cyanosis may require evaluation for congenital tricuspid stenosis.
Consideration of growth and development impacts on management and follow-up care is essential.
Genetic counseling documentation should include family history, potential syndromic associations, and genetic testing results if applicable.
Patients with congenital tricuspid stenosis may be evaluated for genetic syndromes, especially if associated with other anomalies.
Awareness of chromosomal abnormalities that may co-occur with congenital heart defects is crucial for accurate coding.
Used during surgical intervention for congenital tricuspid stenosis.
Document the indication for surgery, findings during the procedure, and post-operative care.
Pediatric cardiology may require additional documentation regarding the patient's growth and development post-surgery.
Common associated conditions include atrial septal defects, ventricular septal defects, and other congenital heart defects. Genetic syndromes may also be present, necessitating thorough evaluation.
