Multi-suture craniosynostosis
ICD-10 Q75.05 is a billable code used to indicate a diagnosis of multi-suture craniosynostosis.
Multi-suture craniosynostosis is a congenital condition characterized by the premature fusion of multiple cranial sutures, which can lead to abnormal head shape and potential intracranial pressure. This condition can affect the growth and development of the skull and brain, resulting in neurological complications if not addressed. The most common types of multi-suture craniosynostosis include scaphocephaly, brachycephaly, and trigonocephaly, each presenting with distinct head shapes. Diagnosis typically involves physical examination and imaging studies such as CT scans to assess the extent of suture fusion. Treatment often requires surgical intervention to correct the skull shape and allow for normal brain growth. Early diagnosis and management are crucial for optimal outcomes, as untreated craniosynostosis can lead to cognitive impairment and other developmental delays.
Detailed growth and developmental assessments, including head circumference measurements and neurological evaluations.
Referral for surgical intervention, monitoring for developmental milestones, and management of associated conditions.
Consideration of family history and genetic counseling for syndromic cases.
Genetic testing results, family history of congenital conditions, and syndromic evaluations.
Assessment for syndromic craniosynostosis, genetic counseling for families, and management of associated genetic disorders.
Understanding the implications of genetic syndromes associated with craniosynostosis for accurate coding.
Used in surgical correction of craniosynostosis.
Operative reports detailing the procedure and indications.
Pediatric surgical documentation must include pre-operative assessments and post-operative follow-up.
Documenting associated syndromic features is crucial as it impacts the management plan, potential genetic counseling needs, and accurate coding for reimbursement. It also helps in understanding the overall health implications for the patient.
