Interstitial lung disease, NOS: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Interstitial Pneumonitis| CurrentStatus = | | OldDxArticle =Interstitial Pneumonitis| CurrentStatus = reconciled | ||
| InitialEditorAssigned = Lori Lovell | | InitialEditorAssigned = Lori Lovell | ||
}} | }} |
Revision as of 13:49, 2018 April 5
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 {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
== 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
==
{sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
Candidate Combined ICD10 codes
Related CCI Codes
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