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ICD-10 Guide
ICD-10 CodesQ75.052

Q75.052

Billable

Pansynostosis

BILLABLE STATUSYes
IMPLEMENTATION DATEOctober 1, 2015
LAST UPDATED09/11/2025

Code Description

ICD-10 Q75.052 is a billable code used to indicate a diagnosis of pansynostosis.

Key Diagnostic Point:

Pansynostosis is a congenital condition characterized by the premature fusion of all cranial sutures, leading to abnormal head shape and potential neurological complications. This condition can result in increased intracranial pressure, developmental delays, and facial deformities due to the restricted growth of the skull. The severity of pansynostosis can vary, and it may be associated with other congenital malformations, particularly those affecting the musculoskeletal system. Children with pansynostosis may present with associated conditions such as clubfoot, hip dysplasia, or limb reduction defects, which require comprehensive evaluation and management. Early diagnosis and intervention are crucial to mitigate complications and improve outcomes. Surgical intervention is often necessary to correct the skull shape and relieve pressure on the brain, and multidisciplinary care involving pediatricians, neurosurgeons, and geneticists is essential for optimal management.

Code Complexity Analysis

Complexity Rating: Medium

Medium Complexity

Complexity Factors

  • Differentiating between types of craniosynostosis
  • Identifying associated congenital malformations
  • Understanding the implications of associated syndromes
  • Navigating documentation requirements for surgical interventions

Audit Risk Factors

  • Inadequate documentation of associated conditions
  • Failure to capture surgical interventions
  • Misclassification of craniosynostosis types
  • Lack of clarity in the relationship between pansynostosis and other congenital defects

Specialty Focus

Medical Specialties

Pediatrics

Documentation Requirements

Pediatric documentation must include growth parameters, developmental milestones, and any associated musculoskeletal conditions.

Common Clinical Scenarios

Common scenarios include referrals for developmental assessments, evaluations for surgical intervention, and management of associated conditions like clubfoot.

Billing Considerations

Accurate coding requires a thorough understanding of the child's overall health status and any additional congenital anomalies.

Genetics

Documentation Requirements

Genetic documentation should include family history, genetic testing results, and any syndromic associations.

Common Clinical Scenarios

Genetic counseling for families with a history of craniosynostosis or related syndromes.

Billing Considerations

Consideration of genetic syndromes that may present with pansynostosis is crucial for accurate coding.

Coding Guidelines

Inclusion Criteria

Use Q75.052 When
  • Follow official coding guidelines for congenital malformations, ensuring accurate documentation of all associated conditions and interventions
  • Use additional codes as necessary to capture the full clinical picture

Exclusion Criteria

Do NOT use Q75.052 When
No specific exclusions found.

Related ICD-10 Codes

Related CPT Codes

61595CPT Code

Craniectomy for craniosynostosis

Clinical Scenario

Used in surgical correction of pansynostosis.

Documentation Requirements

Document the indication for surgery, preoperative assessments, and postoperative care.

Specialty Considerations

Neurosurgical documentation must detail the surgical approach and any complications.

ICD-10 Impact

Diagnostic & Documentation Impact

Enhanced Specificity

ICD-10 Improvements

The transition to ICD-10 has allowed for more specific coding of congenital conditions like pansynostosis, improving the ability to capture associated anomalies and surgical interventions.

ICD-9 vs ICD-10

The transition to ICD-10 has allowed for more specific coding of congenital conditions like pansynostosis, improving the ability to capture associated anomalies and surgical interventions.

Reimbursement & Billing Impact

The transition to ICD-10 has allowed for more specific coding of congenital conditions like pansynostosis, improving the ability to capture associated anomalies and surgical interventions.

Resources

Clinical References

  • •
    American Academy of Pediatrics - Coding for Congenital Conditions

Coding & Billing References

  • •
    American Academy of Pediatrics - Coding for Congenital Conditions

Frequently Asked Questions

What is the primary treatment for pansynostosis?

The primary treatment for pansynostosis is surgical intervention to correct the skull shape and relieve pressure on the brain. This is typically performed in early childhood to optimize developmental outcomes.