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ICD-10 Coding for Thalassemia(D56.1, D56.3)

Complete ICD-10-CM coding and documentation guide for Thalassemia. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

Cooley's AnemiaMediterranean Anemia

Related ICD-10 Code Ranges

Complete code families applicable to Thalassemia

D56.0-D56.9Primary Range

Thalassemia

This range covers all types of thalassemia, including alpha, beta, and other specified and unspecified forms.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
D56.1Beta thalassemiaUse for patients with symptomatic beta thalassemia requiring regular transfusions.
  • Hb <7 g/dL
  • β⁰/β⁺ mutation
  • Elevated HbF (>10%)
D56.3Thalassemia minorUse for asymptomatic carriers confirmed via genetic testing.
  • Normal Hb (12-16 g/dL)
  • MCV <80 fL
  • β-globin heterozygosity

Clinical Decision Support

Always review the patient's clinical documentation thoroughly. When in doubt, choose the more specific code and ensure documentation supports it.

Key Information: ICD-10 code for beta thalassemia

Essential facts and insights about Thalassemia

The ICD-10 code for beta thalassemia major and intermedia is D56.1.

Primary ICD-10-CM Codes for thalassemia

Beta thalassemia
Billable Code

Decision Criteria

clinical Criteria

  • Patient requires regular blood transfusions.

Applicable To

  • Beta thalassemia major
  • Beta thalassemia intermedia

Excludes

  • Beta thalassemia minor (D56.3)

Clinical Validation Requirements

  • Hb <7 g/dL
  • β⁰/β⁺ mutation
  • Elevated HbF (>10%)

Code-Specific Risks

  • Confusing with beta thalassemia minor
  • Incorrect sequencing with complications

Coding Notes

  • Ensure documentation specifies 'beta thalassemia major' or 'intermedia'.

Ancillary Codes

Additional codes that should be used in conjunction with the main diagnosis codes when applicable.

Hepatomegaly

R18.1
Use when hepatomegaly is present as a complication.

Differential Codes

Alternative codes to consider when ruling out similar conditions to the primary diagnosis.

Thalassemia minor

D56.3
Use for asymptomatic carriers with normal Hb levels.

Beta thalassemia

D56.1
Use for symptomatic cases requiring transfusions.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Thalassemia to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code D56.1.

Impact

Clinical: Inaccurate patient management., Regulatory: Non-compliance with coding standards., Financial: Potential claim denials.

Mitigation Strategy

Verify transfusion history before coding., Ensure documentation includes transfusion frequency.

Impact

Reimbursement: May lead to denied claims or reduced reimbursement., Compliance: Non-compliance with coding guidelines., Data Quality: Poor data quality affecting patient records.

Mitigation Strategy

Always use the most specific code available based on clinical documentation.

Impact

Inadequate documentation of transfusion dependency.

Mitigation Strategy

Implement regular audits of patient records for transfusion documentation.

Documentation errors, coding pitfalls, and audit risks are interconnected aspects of medical coding and billing. Addressing all three areas helps ensure accurate coding, optimal reimbursement, and regulatory compliance.

Frequently Asked Questions

Common questions about ICD-10 coding for Thalassemia, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Thalassemia

Use these documentation templates to ensure complete and accurate documentation for Thalassemia. These templates include all required elements for proper coding and billing.

Beta Thalassemia Major

Specialty: Hematology

Required Elements

  • Genetic test results
  • Transfusion history
  • Hb levels

Example Documentation

Patient diagnosed with β-thalassemia major, confirmed via genetic testing (HBB: c.118C>T). Requires biweekly PRBC transfusions. Hb 6.8 g/dL, MCV 68 fL.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Thalassemia, anemia present.
Good Documentation Example
β-thalassemia major confirmed via DNA analysis, requiring biweekly transfusions.
Explanation
The good example provides specific genetic confirmation and treatment details.

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