Idiopathic interstitial pulmonary fibrosis: Difference between revisions
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{{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 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}} | {{ICD10 footer}} | ||
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