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ICD-10 Coding for Chronic Interstitial Lung Disease(J84.112, J84.89, J84.10)

Complete ICD-10-CM coding and documentation guide for Chronic Interstitial Lung Disease. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

Chronic ILDPulmonary FibrosisInterstitial Pulmonary Disease

Related ICD-10 Code Ranges

Complete code families applicable to Chronic Interstitial Lung Disease

J84.1-J84.9Primary Range

Other interstitial pulmonary diseases

This range includes various forms of interstitial lung diseases, including idiopathic pulmonary fibrosis and other specified interstitial diseases.

Respiratory conditions due to external agents

Used for ILD caused by exposure to external agents such as chemicals or dust.

Respiratory disorders in diseases classified elsewhere

Used for ILD secondary to systemic diseases like sarcoidosis.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
J84.112Idiopathic pulmonary fibrosisUse when idiopathic pulmonary fibrosis is confirmed by HRCT and multidisciplinary discussion.
  • HRCT showing usual interstitial pneumonia pattern
  • Multidisciplinary discussion confirming diagnosis
J84.89Other specified interstitial pulmonary diseasesUse when ILD is associated with a known connective tissue disease.
  • Specific connective tissue disease diagnosis
  • Radiologic correlation with CTD
J84.10Pulmonary fibrosis, unspecifiedUse when fibrosis is present but no specific cause is identified.
  • Exclusion of known causes after full workup

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 idiopathic pulmonary fibrosis

Essential facts and insights about Chronic Interstitial Lung Disease

The ICD-10 code for idiopathic pulmonary fibrosis is J84.112, confirmed by HRCT and multidisciplinary discussion.

Primary ICD-10-CM Codes for chronic interstitial lung disease

Idiopathic pulmonary fibrosis
Billable Code

Decision Criteria

clinical Criteria

  • HRCT shows honeycombing and traction bronchiectasis.

documentation Criteria

  • Multidisciplinary discussion confirms diagnosis.

Applicable To

  • Usual interstitial pneumonia

Excludes

  • Pulmonary fibrosis due to external agents (J70.9)

Clinical Validation Requirements

  • HRCT showing usual interstitial pneumonia pattern
  • Multidisciplinary discussion confirming diagnosis

Code-Specific Risks

  • Misclassification if not confirmed by HRCT and MDD

Coding Notes

  • Ensure documentation includes HRCT findings and multidisciplinary discussion notes.

Ancillary Codes

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

Secondary pulmonary hypertension

I27.21
Use when pulmonary hypertension is secondary to ILD.

Rheumatoid lung disease

M05.1-
Use when ILD is due to rheumatoid arthritis.

Differential Codes

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

Other specified interstitial pulmonary diseases

J84.89
Use J84.89 for interstitial lung diseases associated with connective tissue diseases.

Idiopathic pulmonary fibrosis

J84.112
Use J84.112 when no connective tissue disease is present.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Chronic Interstitial Lung Disease to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code J84.112.

Impact

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

Mitigation Strategy

Ensure MDD is documented in the patient's chart., Include detailed findings and conclusions.

Impact

Clinical: Reduces specificity of patient records., Regulatory: Non-compliance with coding guidelines., Financial: May affect reimbursement rates.

Mitigation Strategy

Review documentation for specific diagnosis details., Use the most specific code available.

Impact

Reimbursement: May lead to incorrect DRG assignment and reimbursement issues., Compliance: Non-compliance with coding guidelines., Data Quality: Decreases accuracy of clinical data.

Mitigation Strategy

Use specific codes like J84.112 or J84.89 when documentation supports them.

Impact

Reimbursement: Potential for claim denials., Compliance: Violates coding standards., Data Quality: Compromises data integrity.

Mitigation Strategy

Ensure physician documentation explicitly states the diagnosis.

Impact

High risk of audit if unspecified codes are used without justification.

Mitigation Strategy

Ensure documentation supports the use of specific codes.

Impact

Audits may target cases of IPF without documented MDD.

Mitigation Strategy

Ensure MDD is documented for all IPF diagnoses.

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 Chronic Interstitial Lung Disease, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Chronic Interstitial Lung Disease

Use these documentation templates to ensure complete and accurate documentation for Chronic Interstitial Lung Disease. These templates include all required elements for proper coding and billing.

Idiopathic Pulmonary Fibrosis Diagnosis

Specialty: Pulmonology

Required Elements

  • Patient history
  • HRCT findings
  • Multidisciplinary discussion
  • Exclusion of other causes

Example Documentation

Patient presents with progressive dyspnea and cough. HRCT shows usual interstitial pneumonia pattern. MDD confirms idiopathic pulmonary fibrosis. No evidence of connective tissue disease.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient has lung fibrosis.
Good Documentation Example
Patient diagnosed with idiopathic pulmonary fibrosis confirmed by HRCT and MDD.
Explanation
The good example provides specific diagnosis and supporting evidence.

Connective Tissue Disease-Associated ILD

Specialty: Rheumatology

Required Elements

  • Connective tissue disease diagnosis
  • Temporal relationship
  • Radiologic correlation

Example Documentation

Patient with known rheumatoid arthritis presents with ILD. HRCT shows NSIP pattern. ILD onset 2 years after RA diagnosis.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient has ILD.
Good Documentation Example
Patient with RA presents with ILD. HRCT shows NSIP pattern. ILD onset 2 years after RA diagnosis.
Explanation
The good example links ILD to RA and provides radiologic findings.

Need help with ICD-10 coding for Chronic Interstitial Lung Disease? Ask your questions below.

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