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v1.0.0
ICD-10 Guide
ICD-10 CodesD57.432

D57.432

Billable

Sickle-cell thalassemia beta zero with splenic sequestration

BILLABLE STATUSYes
IMPLEMENTATION DATEOctober 1, 2015
LAST UPDATED09/05/2025

Code Description

ICD-10 D57.432 is a billable code used to indicate a diagnosis of sickle-cell thalassemia beta zero with splenic sequestration.

Key Diagnostic Point:

Sickle-cell thalassemia beta zero with splenic sequestration is a complex hemolytic anemia resulting from the combination of sickle cell disease and beta-thalassemia. This condition arises due to mutations in the HBB gene, leading to the production of abnormal hemoglobin (HbS) and reduced beta-globin chains. Patients with this condition experience episodes of splenic sequestration, where sickled red blood cells become trapped in the spleen, causing acute splenic enlargement and potentially severe anemia. Symptoms may include pain crises, fatigue, jaundice, and splenomegaly. The management of this condition often requires a multidisciplinary approach, including regular blood transfusions, hydroxyurea therapy, and monitoring for complications such as infections and acute chest syndrome. Genetic counseling is also essential for affected families, as this condition is inherited in an autosomal recessive pattern. Understanding the interplay between sickle cell disease and thalassemia is crucial for effective treatment and management.

Code Complexity Analysis

Complexity Rating: High

High Complexity

Complexity Factors

  • Combination of two genetic disorders (sickle cell disease and beta-thalassemia)
  • Variability in clinical presentation and severity among patients
  • Need for detailed documentation of splenic sequestration episodes
  • Potential for multiple comorbidities and complications

Audit Risk Factors

  • Inadequate documentation of splenic sequestration episodes
  • Failure to document genetic testing results
  • Misclassification of the type of thalassemia
  • Lack of evidence for ongoing management and treatment plans

Specialty Focus

Medical Specialties

Hematology

Documentation Requirements

Detailed history of hemolytic episodes, laboratory results, and treatment plans.

Common Clinical Scenarios

Management of pain crises, blood transfusions, and monitoring for splenic sequestration.

Billing Considerations

Ensure accurate documentation of genetic testing and family history.

Genetics

Documentation Requirements

Genetic testing results, family pedigree, and counseling notes.

Common Clinical Scenarios

Counseling families about inheritance patterns and risks for future offspring.

Billing Considerations

Document the implications of genetic findings on treatment and management.

Coding Guidelines

Inclusion Criteria

Use D57.432 When
  • Follow ICD
  • CM guidelines for coding hemolytic anemias and ensure accurate documentation of the condition's complexity
  • Include details about splenic sequestration and any related complications

Exclusion Criteria

Do NOT use D57.432 When
No specific exclusions found.

Related ICD-10 Codes

Related CPT Codes

36430CPT Code

Transfusion, blood or blood components

Clinical Scenario

Used during acute splenic sequestration episodes requiring transfusion.

Documentation Requirements

Document the reason for transfusion and patient response.

Specialty Considerations

Hematology specialists should ensure accurate coding of transfusion episodes.

ICD-10 Impact

Diagnostic & Documentation Impact

Enhanced Specificity

ICD-10 Improvements

The transition to ICD-10 has allowed for more specific coding of complex conditions like sickle-cell thalassemia beta zero, improving the accuracy of patient records and reimbursement processes.

ICD-9 vs ICD-10

The transition to ICD-10 has allowed for more specific coding of complex conditions like sickle-cell thalassemia beta zero, improving the accuracy of patient records and reimbursement processes.

Reimbursement & Billing Impact

reimbursement processes.

Resources

Clinical References

  • •
    Sickle Cell Disease Association of America

Coding & Billing References

  • •
    Sickle Cell Disease Association of America

Frequently Asked Questions

What is the significance of splenic sequestration in sickle-cell thalassemia beta zero?

Splenic sequestration is a critical complication that can lead to acute anemia and requires immediate medical attention. It is essential to document these episodes accurately for proper management and coding.