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Home/Diagnosis/ICD-10 Coding for Interstitial Lung Disease

ICD-10 Coding for Interstitial Lung Disease

J84.112
J70.4

Complete ICD-10-CM coding and documentation guide for icd-10 coding for interstitial lung disease includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
Diffuse Parenchymal Lung Disease
Pulmonary Fibrosis
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Key Information: ICD-10 Coding for Interstitial Lung Disease

Essential facts and insights about ICD-10 Coding for Interstitial Lung Disease

Use ICD-10 code J84.112 for idiopathic pulmonary fibrosis, ensuring proper documentation in clinical notes.

Primary ICD-10-CM Codes

Idiopathic pulmonary fibrosis

Billable Code
J84.112
Billable

Diagnostic Criteria

clinical:
  • • HRCT shows UIP pattern
documentation:
  • • Exclusion of other known causes

Applicable To

  • • Usual interstitial pneumonia (UIP)

Important Notes

  • • Ensure documentation of exclusion criteria for idiopathic classification.

Drug-induced interstitial lung disorders

Billable Code
J70.4
Billable

Diagnostic Criteria

clinical:
  • • Temporal relationship with drug exposure
  • • Improvement upon drug cessation

Applicable To

  • • Interstitial lung disease due to medications

Important Notes

  • • Ensure documentation of drug exposure and response to cessation.
Ancillary Codes

Additional codes that may be used with this diagnosis

Z87.010

Personal history of tobacco use

Use to document smoking history when relevant.

T45.1X5A

Adverse effect of antineoplastic and immunosuppressive drugs

Use to specify the drug causing the ILD.

Frequently Asked Questions

What is the ICD-10 code for idiopathic pulmonary fibrosis?

The ICD-10 code for idiopathic pulmonary fibrosis is J84.112. It is used when HRCT shows a UIP pattern and other causes are excluded.

How do you code drug-induced interstitial lung disease?

Use J70.4 for drug-induced ILD, ensuring documentation of the specific drug and temporal relationship. Additional codes may be required to specify the drug.

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