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ICD-10 Coding for Sickle Cell Trait(D57.3)

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

Also known as:

SCTSickle Cell Carrier

Related ICD-10 Code Ranges

Complete code families applicable to Sickle Cell Trait

D57.3Primary Range

Sickle-cell trait

This code is used to identify individuals who carry the sickle cell trait but do not have sickle cell disease.

Key Information: ICD-10 code for sickle cell trait

Essential facts and insights about Sickle Cell Trait

The ICD-10 code for sickle cell trait is D57.3, used for individuals carrying the trait without symptoms of sickle cell disease.

Primary ICD-10-CM Code for sickle cell trait

Sickle-cell trait
Billable Code

Decision Criteria

clinical Criteria

  • Patient has HbAS genotype confirmed by lab tests.

documentation Criteria

  • Documentation must specify 'sickle cell trait' and include lab results.

Applicable To

  • Glomerular disorder due to sickle cell trait

Excludes

Clinical Validation Requirements

  • Hemoglobin electrophoresis showing HbAS
  • Positive solubility test with normal CBC

Code-Specific Risks

  • Misclassification as sickle cell disease
  • Incorrect DRG assignment

Coding Notes

  • Ensure documentation specifies 'trait' and confirmatory testing results.

Ancillary Codes

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

Other specified abnormal findings of blood chemistry

R79.89
Use when abnormal hemoglobin is noted but SCT status is unclear.

Differential Codes

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

Sickle-cell anemia

D57.0
Presence of anemia and recurrent pain crises.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Sickle Cell Trait to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code D57.3.

Impact

Clinical: May lead to inappropriate treatment decisions., Regulatory: Could result in audit findings and penalties., Financial: Affects reimbursement due to incorrect DRG assignment.

Mitigation Strategy

Educate clinicians on the importance of specificity., Implement documentation audits.

Impact

Reimbursement: Incorrect coding can lead to improper DRG assignment and reimbursement loss., Compliance: Misclassification can result in compliance issues during audits., Data Quality: Impacts the accuracy of patient records and data analytics.

Mitigation Strategy

Verify lab results and ensure documentation specifies 'trait'.

Impact

Lack of specificity in documentation can lead to audit issues.

Mitigation Strategy

Ensure all documentation specifies 'sickle cell trait' and includes lab results.

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 Sickle Cell Trait, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Sickle Cell Trait

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

Routine physical with SCT noted

Specialty: Family Medicine

Required Elements

  • Patient history
  • Lab results
  • Family history

Example Documentation

Patient is a carrier of sickle cell trait (HbAS) confirmed by electrophoresis. No symptoms of sickle cell disease.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Positive sickle cell.
Good Documentation Example
Sickle cell trait confirmed by hemoglobin electrophoresis.
Explanation
The good example specifies the trait and includes confirmatory test results.

Need help with ICD-10 coding for Sickle Cell Trait? Ask your questions below.

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