© 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, which can lead to significant complications. This early closure restricts the normal growth of the skull, resulting in increased intracranial pressure that can adversely affect brain development. Additionally, it can cause noticeable deformities in the shape of the head. The condition may present as an isolated issue or as part of a broader syndrome, such as Crouzon, Apert, Carpenter, Chotzen, or Pfeiffer syndrome, which are associated with various other physical abnormalities. Craniosynostosis is categorized into two types: simple, where only a single suture is involved, and complex, where multiple sutures are fused. The procedure described by CPT® Code 61557 involves a craniotomy specifically for craniosynostosis, utilizing a bifrontal bone flap. This surgical intervention aims to correct the abnormal skull shape and alleviate pressure on the brain, thereby facilitating normal brain growth and development. The technique involves creating a bone flap from the frontal bone, which is then elevated to allow access to the underlying structures, ensuring that the skull can be reshaped appropriately to support healthy cranial development.
© Copyright 2025 Coding Ahead. All rights reserved.
The procedure described by CPT® Code 61557 is indicated for the treatment of craniosynostosis, particularly when a bifrontal bone flap is required. The following conditions may warrant this surgical intervention:
The procedure for CPT® Code 61557 involves several critical steps to effectively address craniosynostosis through the creation and elevation of a bifrontal bone flap:
Post-procedure care following the craniotomy for craniosynostosis involves monitoring the infant for any signs of complications, such as infection or excessive swelling. The infant will typically be placed in a custom-made helmet that aids in the reshaping of the skull as it heals and grows. Regular follow-up appointments are essential to assess the healing process and ensure that the skull is developing correctly. Parents or caregivers will receive instructions on how to care for the surgical site and what signs to watch for that may indicate complications. Overall, the expected recovery involves gradual improvement in head shape and brain function as the infant grows.
Short Descr | INCISE SKULL/SUTURES | Medium Descr | CRANIECTOMY CRANIOSYNOSTOSIS BIFRONTAL BONE FLAP | Long Descr | Craniotomy for craniosynostosis; bifrontal bone flap | 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 | 1 - Incision and excision of CNS |
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
|
---|---|---|
1991-01-01 | Added | First appearance in code book in 1991. |
Get instant expert-level medical coding assistance.