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v1.0.0
ICD-10 Guide
ICD-10 CodesQ65.1

Q65.1

Billable

Congenital dislocation of hip, bilateral

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

Code Description

ICD-10 Q65.1 is a billable code used to indicate a diagnosis of congenital dislocation of hip, bilateral.

Key Diagnostic Point:

Congenital dislocation of the hip, also known as developmental dysplasia of the hip (DDH), is a condition where the hip joint is improperly formed, leading to dislocation. In bilateral cases, both hips are affected. This condition can occur due to genetic factors, mechanical factors during pregnancy, or a combination of both. Infants may present with limited hip abduction, asymmetrical skin folds, or a positive Ortolani or Barlow test during physical examination. Early diagnosis is crucial as untreated DDH can lead to significant complications, including osteoarthritis and impaired mobility later in life. Treatment options vary based on the age of the child and severity of the dislocation, ranging from observation and bracing to surgical intervention. The condition is often associated with other congenital malformations, including those affecting the urinary system, such as renal agenesis or bladder exstrophy, necessitating a comprehensive evaluation of the child’s overall health.

Code Complexity Analysis

Complexity Rating: Medium

Medium Complexity

Complexity Factors

  • Differentiating between unilateral and bilateral cases
  • Understanding associated congenital conditions
  • Variability in treatment approaches based on age
  • Documentation of physical examination findings

Audit Risk Factors

  • Inadequate documentation of physical exam findings
  • Failure to document associated congenital conditions
  • Incorrect coding of severity or laterality
  • Lack of follow-up documentation on treatment outcomes

Specialty Focus

Medical Specialties

Pediatrics

Documentation Requirements

Detailed physical examination notes, including hip range of motion and any imaging results.

Common Clinical Scenarios

Infants presenting with hip clicks or asymmetrical leg lengths during well-child visits.

Billing Considerations

Consideration of family history of hip dysplasia and associated congenital conditions.

Genetics

Documentation Requirements

Genetic testing results if applicable, family history of congenital conditions.

Common Clinical Scenarios

Referral for genetic counseling in cases with multiple congenital anomalies.

Billing Considerations

Understanding the genetic syndromes that may predispose to hip dislocation.

Coding Guidelines

Inclusion Criteria

Use Q65.1 When
  • Follow ICD
  • CM guidelines for coding congenital conditions, ensuring accurate documentation of laterality and associated conditions
  • Use additional codes for any related congenital anomalies

Exclusion Criteria

Do NOT use Q65.1 When
No specific exclusions found.

Related ICD-10 Codes

Related CPT Codes

27570CPT Code

Open reduction of hip dislocation

Clinical Scenario

Used in cases where non-surgical management fails.

Documentation Requirements

Operative report detailing the procedure and findings.

Specialty Considerations

Orthopedic documentation must include pre-operative assessments.

ICD-10 Impact

Diagnostic & Documentation Impact

Enhanced Specificity

ICD-10 Improvements

The transition to ICD-10 allows for more specific coding of congenital conditions, improving data accuracy and facilitating better patient management.

ICD-9 vs ICD-10

The transition to ICD-10 allows for more specific coding of congenital conditions, improving data accuracy and facilitating better patient management.

Reimbursement & Billing Impact

reimbursement.

Resources

Clinical References

  • •
    ICD-10-CM Official Guidelines for Coding and Reporting

Coding & Billing References

  • •
    ICD-10-CM Official Guidelines for Coding and Reporting

Frequently Asked Questions

What is the significance of coding bilateral congenital dislocation of the hip?

Accurate coding of bilateral congenital dislocation of the hip is crucial for treatment planning and understanding the potential for associated conditions. It ensures appropriate management and follow-up care, which can significantly impact the child's long-term outcomes.