Other congenital malformations of pulmonary valve
ICD-10 Q22.3 is a billable code used to indicate a diagnosis of other congenital malformations of pulmonary valve.
Congenital malformations of the pulmonary valve can manifest in various forms, including pulmonary valve stenosis, atresia, or other structural anomalies that affect the normal flow of blood from the right ventricle to the pulmonary artery. These malformations can lead to significant hemodynamic changes, resulting in right ventricular hypertrophy, increased pressure in the right heart, and potential heart failure if not addressed. The severity of the condition often dictates the clinical management approach, which may include surgical intervention or catheter-based procedures. Accurate diagnosis typically involves echocardiography, which provides detailed imaging of the heart's structure and function. In some cases, additional imaging modalities such as MRI or CT scans may be utilized to assess the anatomy and associated anomalies. The presence of other congenital heart defects, such as septal defects or coarctation of the aorta, may complicate the clinical picture, necessitating a comprehensive evaluation and multidisciplinary management plan.
Detailed pediatric history and physical examination findings, including growth and development assessments.
Infants presenting with cyanosis, failure to thrive, or heart murmurs; routine follow-up for known congenital heart defects.
Consideration of age-related anatomical changes and the impact of growth on congenital heart defects.
Family history of congenital heart defects, genetic testing results, and syndromic associations.
Genetic counseling for families with a history of congenital heart disease; evaluation of syndromic conditions such as DiGeorge syndrome.
Understanding the genetic basis of congenital heart defects and the implications for family planning.
Used for initial evaluation and follow-up of congenital heart defects.
Echocardiographic findings must be documented clearly.
Pediatric cardiology may require specific echocardiographic views.
Common associated conditions include other congenital heart defects such as atrial septal defects, ventricular septal defects, and coarctation of the aorta. Accurate coding requires documentation of all associated anomalies.
