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Home/Diagnosis/ICD-10 Coding for Idiopathic Pulmonary Fibrosis

ICD-10 Coding for Idiopathic Pulmonary Fibrosis

J84.112

Complete ICD-10-CM coding and documentation guide for icd-10 coding for idiopathic pulmonary fibrosis includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
IPF
Cryptogenic Fibrosing Alveolitis
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Key Information: ICD-10 Coding for Idiopathic Pulmonary Fibrosis

Essential facts and insights about ICD-10 Coding for Idiopathic Pulmonary Fibrosis

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 with honeycombing
documentation:
  • • Exclusion of other interstitial lung diseases

Applicable To

  • • Usual interstitial pneumonia (UIP) pattern

Important Notes

  • • Ensure HRCT findings and exclusion of other causes are documented.
Ancillary Codes

Additional codes that may be used with this diagnosis

R06.00

Dyspnea

Use when dyspnea is documented as a symptom.

I27.23

Pulmonary hypertension

Use when pulmonary hypertension is a documented comorbidity.

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 confirms a UIP pattern and other causes are excluded.

How is idiopathic pulmonary fibrosis diagnosed?

Idiopathic pulmonary fibrosis is diagnosed through HRCT showing a UIP pattern and exclusion of other interstitial lung diseases.

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