© Copyright 2025 American Medical Association. All rights reserved.
Craniosynostosis is a congenital condition characterized by the premature fusion of one or more cranial sutures in infants. This early closure can lead to increased intracranial pressure, which may hinder normal brain development and result in distinct head shape abnormalities. The condition can manifest independently or as part of various syndromes, including Crouzon, Apert, Carpenter, Chotzen, or Pfeiffer syndrome, which are associated with additional physical anomalies. Craniosynostosis is categorized into two types: simple, where only a single cranial suture is affected, and complex, where multiple sutures are involved. The surgical intervention for this condition, specifically a craniectomy for a single cranial suture, involves the excision of bone segments from the skull to alleviate pressure and allow for proper brain growth. The procedure is performed through a skin incision over the affected suture, followed by the elevation of a scalp flap to access the skull. This intervention is critical for preventing potential developmental issues and ensuring the infant's head shape can normalize as they grow.
© Copyright 2025 Coding Ahead. All rights reserved.
The procedure is indicated for the treatment of craniosynostosis, specifically when a single cranial suture has fused prematurely. The following conditions warrant the performance of a craniectomy for craniosynostosis:
The craniectomy for craniosynostosis involves several detailed procedural steps to ensure effective treatment. The following outlines the key steps involved in the procedure:
Post-procedure care is essential for ensuring proper recovery and optimal outcomes. After the craniectomy, the infant will be monitored for any signs of complications, such as infection or excessive bleeding. The custom-made helmet will be worn to guide the reshaping of the skull as the child grows. Follow-up appointments will be necessary to assess the healing process and the effectiveness of the helmet in achieving the desired head shape. Parents or caregivers will receive specific instructions regarding care at home, including how to manage any discomfort and when to seek medical attention if concerns arise.
Short Descr | RELEASE OF SKULL SEAMS | Medium Descr | CRANIECTOMY CRANIOSYNOSTOSIS 1 CRANIAL SUTURE | Long Descr | Craniectomy for craniosynostosis; single cranial suture | Status Code | Active Code | Global Days | 090 - Major Surgery | PC/TC Indicator (26, TC) | 0 - Physician Service Code | Multiple Procedures (51) | 2 - Standard payment adjustment rules for multiple procedures apply. | Bilateral Surgery (50) | 0 - 150% payment adjustment for bilateral procedures does NOT apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 2 - Payment restriction for assistants at surgery does not apply to this procedure... | Co-Surgeons (62) | 1 - Co-surgeons could be paid, though supporting documentation is required... | Team Surgery (66) | 0 - Team surgeons not permitted for this procedure. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | APC Status Indicator | Inpatient Procedures, not paid under OPPS | Type of Service (TOS) | 2 - Surgery | Berenson-Eggers TOS (BETOS) | P1G - Major procedure - Other | MUE | 1 | CCS Clinical Classification | 9 - Other OR therapeutic nervous system procedures |
This is a primary code that can be used with these additional add-on codes.
69990 | Addon Code MPFS Status: Restricted APC N ASC N1 PUB 100 CPT Assistant Article 1Microsurgical techniques, requiring use of operating microscope (List separately in addition to code for primary procedure) |
Date
|
Action
|
Notes
|
---|---|---|
Pre-1990 | Added | Code added. |