Complete ICD-10-CM coding and documentation guide for icd-10 coding for interstitial pulmonary fibrosis includes clinical validation requirements, medical necessity guidelines, and coding policies.
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Essential facts and insights about ICD-10 Coding for Interstitial Pulmonary Fibrosis
Use ICD-10 code J84.112 for idiopathic pulmonary fibrosis, ensuring proper documentation in clinical notes.
Additional codes that may be used with this diagnosis
Interstitial lung disease with progressive fibrotic phenotype
Use when there is documented progression in fibrosis and an underlying condition.
The ICD-10 code for idiopathic pulmonary fibrosis is J84.112, used when HRCT confirms a UIP pattern and other causes are excluded.
Use J84.170 for progressive fibrotic phenotype when there is documented fibrosis progression and an underlying condition.