Other specified congenital malformations of kidney
ICD-10 Q63.8 is a billable code used to indicate a diagnosis of other specified congenital malformations of kidney.
Congenital malformations of the kidney encompass a variety of structural abnormalities that can significantly impact renal function and overall health. This code specifically refers to conditions that do not fall into the more commonly classified categories of renal agenesis, polycystic kidney disease, or other well-defined malformations. Renal agenesis, characterized by the absence of one or both kidneys, can lead to severe complications, including oligohydramnios and pulmonary hypoplasia. Polycystic kidney disease, a genetic disorder, results in the formation of numerous cysts in the kidneys, leading to renal failure over time. Bladder exstrophy is a rare condition where the bladder is exposed outside the body, often associated with other urinary tract anomalies. Posterior urethral valves, a condition where abnormal folds of tissue obstruct the urethra, can lead to hydronephrosis and renal damage. Accurate coding of these conditions is crucial for appropriate management and treatment planning.
Pediatric documentation should include detailed birth history, prenatal imaging findings, and any surgical interventions performed.
Common scenarios include newborns presenting with renal agenesis or polycystic kidney disease, requiring immediate intervention and long-term follow-up.
Consideration must be given to the age of the patient and the developmental implications of the congenital malformation.
Genetic documentation should include family history, genetic testing results, and any syndromic associations with the congenital malformation.
Scenarios may involve genetic counseling for families with a history of congenital kidney malformations or syndromic presentations.
Genetic implications of congenital malformations should be documented to guide future family planning and management.
Used in cases of renal agenesis or severe malformations requiring surgical intervention.
Operative reports detailing the procedure and indication for surgery.
Pediatric surgical documentation must include growth and developmental assessments.
Documentation must include a clear diagnosis of the specific congenital malformation, any imaging studies performed, and details of associated conditions or complications. It is essential to provide a comprehensive clinical narrative to support the coding.
