Interstitial lung disease, NOS: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Interstitial Pneumonitis | | OldDxArticle =Interstitial Pneumonitis | ||
| CurrentStatus = | | CurrentStatus = reconciled | ||
| InitialEditorAssigned = Lori Lovell | | InitialEditorAssigned = Lori Lovell | ||
}} | }} | ||
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*[[Fibrothorax]] | *[[Fibrothorax]] | ||
*[[Idiopathic interstitial pulmonary fibrosis]] | |||
*[[Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))]] | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == |
Revision as of 14:01, 2018 April 10
ICD10 Diagnosis | |
Dx: | Interstitial lung disease, NOS |
ICD10 code: | J84.9 |
Pre-ICD10 counterpart: | Pneumonitis NYD, Other respiratory problems |
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
incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis
Alternate ICD10s to consider coding instead or in addition
- Interstitial lung disease, drug-induced (acute or chronic)
- Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)
- Hypersensitivity pneumonitis (extrinsic allergic alveoliltis), NOS
- Pulmonary emphysema or bullous disease without COPD
- Fibrothorax
- Idiopathic interstitial pulmonary fibrosis
- Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))
Candidate Combined ICD10 codes
Related CCI Codes
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Show all ICD10 Subcategories