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ICD-10 Coding for Scleroderma(M34.0, M34.1, M34.81, L94.1)

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

Also known as:

Systemic sclerosisCREST syndromeDiffuse sclerodermaLimited scleroderma

Related ICD-10 Code Ranges

Complete code families applicable to Scleroderma

M34Primary Range

Systemic sclerosis (scleroderma)

This range includes codes for different types of systemic sclerosis, including diffuse and limited forms, as well as complications.

Localized scleroderma (morphea)

This code is used for localized forms of scleroderma without systemic involvement.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
M34.0Progressive systemic sclerosisUse when there is diffuse skin involvement and rapid organ involvement.
  • Skin thickening extending proximal to MCP/MTP joints
  • Anti-Scl-70 antibodies
  • HRCT showing lung fibrosis
M34.1CR(E)ST syndromeUse for limited cutaneous disease with CREST features.
  • Presence of CREST features
  • Anti-centromere antibodies
M34.81Systemic sclerosis with lung involvementUse when interstitial lung disease is confirmed in a patient with systemic sclerosis.
  • HRCT showing lung fibrosis
  • Reduced FVC and DLCO
L94.1Localized scleroderma (morphea)Use for localized skin involvement without systemic features.
  • Localized skin lesions without systemic involvement

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 diffuse scleroderma

Essential facts and insights about Scleroderma

The ICD-10 code for diffuse scleroderma is M34.0, indicating progressive systemic sclerosis.

Primary ICD-10-CM Codes for scleroderma

Progressive systemic sclerosis
Billable Code

Decision Criteria

clinical Criteria

  • Presence of diffuse skin thickening and organ involvement.

Applicable To

  • Diffuse scleroderma

Excludes

  • Localized scleroderma (L94.1)

Clinical Validation Requirements

  • Skin thickening extending proximal to MCP/MTP joints
  • Anti-Scl-70 antibodies
  • HRCT showing lung fibrosis

Code-Specific Risks

  • Misclassification if skin involvement is not documented properly.

Coding Notes

  • Ensure documentation specifies the extent of skin involvement and any organ complications.

Ancillary Codes

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

Systemic sclerosis with lung involvement

M34.81
Use alongside M34.0 when interstitial lung disease is present.

Esophageal obstruction

K22.2
Use when esophageal involvement is documented.

Differential Codes

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

CR(E)ST syndrome

M34.1
Use M34.1 for limited cutaneous involvement with CREST features.

Progressive systemic sclerosis

M34.0
Use M34.0 for diffuse skin involvement.

Pulmonary fibrosis, unspecified

J84.10
Use J84.10 for pulmonary fibrosis without systemic sclerosis.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Scleroderma to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code M34.0.

Impact

Clinical: Leads to misdiagnosis or inappropriate treatment., Regulatory: Non-compliance with documentation standards., Financial: Potential claim denials or reduced reimbursement.

Mitigation Strategy

Train clinicians on specific documentation requirements., Use templates to ensure comprehensive notes.

Impact

Reimbursement: Incorrect coding may lead to denied claims., Compliance: Non-compliance with coding guidelines., Data Quality: Inaccurate clinical data representation.

Mitigation Strategy

Confirm absence of visceral involvement; use M34 codes if present.

Impact

Reimbursement: Potential loss of additional reimbursement for complications., Compliance: Failure to meet coding standards., Data Quality: Incomplete clinical picture.

Mitigation Strategy

Require explicit HRCT findings and PFTs in documentation.

Impact

Failure to document all affected organ systems can lead to audit findings.

Mitigation Strategy

Implement comprehensive documentation templates and regular audits.

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 Scleroderma, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Scleroderma

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

Rheumatology Progress Note

Specialty: Rheumatology

Required Elements

  • Skin involvement details
  • Organ systems affected
  • Lab results
  • Treatment responses

Example Documentation

**Skin Exam**: Thickening extends to [elbows/knees/other]; modified Rodnan score __/51. **Organ Involvement**: - Pulmonary: FVC __%, DLCO __%, HRCT findings: [texture] - GI: [Dysphagia/Reflux] confirmed by [manometry/endoscopy] **Labs**: Anti-Scl-70 [positive/negative], ACA [titer], ESR __. **Treatment Plan**: [Drug] for [organ system]; monitoring every [interval].

Examples: Poor vs. Good Documentation

Poor Documentation Example
Scleroderma with lung issues.
Good Documentation Example
Diffuse systemic sclerosis (M34.0) with ILD (M34.81): FVC 68%, DLCO 55%, HRCT bibasilar fibrosis. Current treatment: mycophenolate 1500 mg BID.
Explanation
The good example provides specific details on skin involvement, lung function tests, and treatment, supporting the chosen codes.

Need help with ICD-10 coding for Scleroderma? Ask your questions below.

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