Idiopathic interstitial pulmonary fibrosis: Difference between revisions
Jump to navigation
Jump to search
Ttenbergen (talk | contribs) m 1 revision imported |
No edit summary |
||
| (26 intermediate revisions by 6 users not shown) | |||
| Line 1: | Line 1: | ||
{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =IPF| CurrentStatus = | | OldDxArticle =IPF| CurrentStatus = reconciled | ||
| InitialEditorAssigned = Lori Lovell | | InitialEditorAssigned = Lori Lovell | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | |||
| ICD10 Code=J84.1 | | ICD10 Code=J84.1 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Respiratory}} | |||
== Additional Info == | == 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(s)|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 == | == Alternate ICD10s to consider coding instead or in addition == | ||
( | |||
*[[Pulmonary hypertension, secondary (any cause)]] | |||
*[[Fibrothorax]] | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | |||
{{EndPlaceHolder}} | |||
Latest revision as of 13:04, 4 December 2025
| 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
Related Articles
| Related articles: |
Show all ICD10 Subcategories
|
ICD10 Categories: |