Congenital occlusion of ureter, unspecified
ICD-10 Q62.10 is a billable code used to indicate a diagnosis of congenital occlusion of ureter, unspecified.
Congenital occlusion of the ureter refers to a blockage that occurs in the ureter, which is the tube that carries urine from the kidney to the bladder. This condition can lead to significant complications, including hydronephrosis, urinary tract infections, and impaired renal function. The occlusion may be due to various factors, including developmental anomalies during fetal growth, such as ureteral atresia or stenosis. In pediatric patients, this condition is often diagnosed through imaging studies such as ultrasound or voiding cystourethrogram. Treatment typically involves surgical intervention to relieve the obstruction and restore normal urinary flow. Early diagnosis and management are crucial to prevent long-term renal damage. Congenital malformations of the urinary system, such as renal agenesis, polycystic kidney disease, bladder exstrophy, and posterior urethral valves, may coexist with ureteral occlusion, complicating the clinical picture and necessitating a comprehensive approach to care.
Pediatric documentation should include detailed clinical history, imaging results, and treatment plans. It is essential to document any associated congenital anomalies and the patient's growth and development.
Common scenarios include a newborn presenting with hydronephrosis, a child with recurrent urinary tract infections, or a patient undergoing evaluation for renal function impairment.
Coders should be aware of the developmental milestones and potential long-term impacts of urinary tract anomalies on pediatric patients.
Genetic documentation should include family history, genetic testing results, and any syndromic associations with congenital urinary tract anomalies.
Scenarios may involve genetic counseling for families with a history of congenital anomalies or syndromes associated with urinary tract malformations.
Consideration of chromosomal abnormalities that may be linked to urinary tract malformations is crucial for accurate coding.
Used in cases of ureteral obstruction to facilitate urine flow.
Document the indication for stent placement and any imaging studies performed.
Urology specialists should provide detailed operative notes.
Common congenital anomalies include renal agenesis, bladder exstrophy, and posterior urethral valves. These conditions can complicate the clinical management of patients with ureteral occlusion and require careful documentation and coding.
