Prominent ear
ICD-10 Q17.5 is a billable code used to indicate a diagnosis of prominent ear.
Prominent ear, also known as protruding ear, is a congenital malformation characterized by an abnormal shape or position of the ear, leading to a noticeable protrusion from the side of the head. This condition can occur as an isolated anomaly or as part of a syndrome involving other congenital malformations. The prominence of the ear is typically due to an underdeveloped antihelix or an excessive conchal bowl, which can be assessed through physical examination. While prominent ears are not associated with hearing loss, they can lead to psychological distress or social stigma, particularly in children. Surgical correction, often performed in early childhood, can improve both the aesthetic appearance and the psychosocial well-being of affected individuals. Accurate coding of prominent ear is essential for proper documentation and management of the condition, especially in pediatric populations where early intervention may be beneficial.
Pediatric documentation should include detailed descriptions of the ear's morphology, any associated conditions, and the psychosocial impact on the child.
Common scenarios include routine pediatric examinations where prominent ears are noted, referrals for surgical evaluation, and follow-up visits post-correction.
Consideration should be given to the child's age and developmental milestones when planning interventions.
Genetic documentation should include family history, potential syndromic associations, and any genetic testing results.
Scenarios may involve genetic counseling for families with a history of congenital ear anomalies or syndromes that include prominent ears.
Geneticists should assess for syndromic features that may require additional coding and management.
Used for surgical correction of prominent ears in children.
Pre-operative assessment, surgical consent, and post-operative follow-up notes.
Pediatric surgeons should document the rationale for surgery and any associated conditions.
Accurate coding of prominent ear is crucial for proper management, surgical planning, and understanding the psychosocial impact on affected individuals. It also aids in tracking congenital anomalies for public health purposes.
