Idiopathic interstitial pulmonary fibrosis
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| ICD10 Diagnosis | |
| Dx: | Idiopathic interstitial pulmonary fibrosis |
| ICD10 code: | J84.1 |
| Pre-ICD10 counterpart: | none assigned |
| Charlson/ALERT Scale: | none |
| APACHE Como Component: | none |
| APACHE Acute Component: | none |
| Start Date: | |
| Stop Date: | |
| Data Dependencies(Reports/Indicators/Data Elements): | No results |
| External ICD10 Documentation | |
This diagnosis is a part of ICD10 collection.
Additional Info
- This code includes a number of specific subtypes:
- IPF = idiopathic pulmonary fibrosis
- UIP = usual interstitial pneumonitis
- DIP = desquamative interstitial pneumonitis
- NSIP = nonspecific interstitial pneumonitis
- AIP = acute interstitial pneumonitis
- idiopathic fibrosing alveolitis
- Fibrosis caused by pulmonary Sarcoidosis, any organ also combine with Disorder of lung, NOS
- But it does NOT include: Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))
Alternate ICD10s to consider coding instead or in addition
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
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