Other hypospadias
ICD-10 Q54.8 is a billable code used to indicate a diagnosis of other hypospadias.
Hypospadias is a congenital malformation of the male urethra characterized by an abnormal opening of the urethra on the ventral surface of the penis, rather than at the tip. The severity of hypospadias can vary, with the location of the urethral opening ranging from the glans to the scrotum. 'Other hypospadias' encompasses cases that do not fit into the more common classifications of distal or proximal hypospadias. This condition can be associated with other genital anomalies, such as cryptorchidism (undescended testicles) and ambiguous genitalia. The etiology of hypospadias is multifactorial, involving genetic, hormonal, and environmental factors. Diagnosis is typically made at birth during a physical examination, and management may involve surgical correction to reposition the urethral opening and ensure normal urinary function and cosmetic appearance. Early intervention is crucial to prevent complications such as urinary obstruction, recurrent urinary tract infections, and psychological distress related to genital appearance.
Detailed physical examination findings, including the location of the urethral opening and any associated anomalies.
Newborns presenting with hypospadias, cases requiring surgical intervention, and follow-up visits post-surgery.
Consideration of the psychological impact on the child and family, as well as the need for potential referral to urology.
Family history of congenital anomalies, genetic testing results if applicable, and any syndromic associations.
Cases where hypospadias is part of a genetic syndrome, such as Turner syndrome or Klinefelter syndrome.
Understanding the genetic implications and counseling families about recurrence risks.
Used in cases of surgical correction of hypospadias.
Document the type of hypospadias and details of the surgical procedure.
Urology specialists typically perform this procedure.
Hypospadias is characterized by the urethral opening being located on the underside of the penis, while epispadias involves the urethral opening being located on the upper side. Both are congenital conditions but require different coding and management approaches.
