Idiopathic interstitial pulmonary fibrosis: Difference between revisions
No edit summary |
No edit summary |
||
| (11 intermediate revisions by 5 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 | ||
}} | }} | ||
| Line 14: | Line 14: | ||
**IPF = idiopathic pulmonary fibrosis | **IPF = idiopathic pulmonary fibrosis | ||
**UIP = usual interstitial pneumonitis | **UIP = usual interstitial pneumonitis | ||
**DIP = desquamative | **DIP = desquamative interstitial pneumonitis | ||
**NSIP = nonspecific interstitial pneumonitis | **NSIP = nonspecific interstitial pneumonitis | ||
**AIP = acute interstitial | **AIP = acute interstitial pneumonitis | ||
*But it does NOT include: | **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 == | == 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 == | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||