Idiopathic interstitial pulmonary fibrosis: Difference between revisions
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*[[Interstitial Pneumonitis]] | *[[Interstitial Pneumonitis]] | ||
*[[Pneumonitis NYD]] | *[[Pneumonitis NYD]] | ||
*[[Pulmonary hypertension, secondary (any cause)]]= | |||
*[[Fibrothorax]] | *[[Fibrothorax]] |
Revision as of 13:52, 5 April 2018
ICD10 Diagnosis | |
Dx: | Idiopathic interstitial pulmonary fibrosis |
ICD10 code: | J84.1 |
Pre-ICD10 counterpart: | Idiopathic Pulmonary Fibrosis |
Charlson/ALERT Scale: | none |
APACHE Como Component: | Respiratory |
APACHE Acute Component: | none |
Start Date: | |
Stop Date: | |
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 interstitital pneumonitis
- NSIP = nonspecific interstitial pneumonitis
- AIP = acute interstitial pnemonitis
- 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
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