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 = needs review | |||
| InitialEditorAssigned = Lori Lovell | | InitialEditorAssigned = Lori Lovell | ||
}} | }} | ||
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== Additional Info == | == Additional Info == | ||
incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis | incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis | ||
== Alternate ICD10s to consider coding instead or in addition | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Interstitial lung disease, drug-induced (acute or chronic)]] | *[[Interstitial lung disease, drug-induced (acute or chronic)]] | ||
*[[Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)]] | *[[Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)]] | ||
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*[[Pulmonary emphysema or bullous disease without COPD]] | *[[Pulmonary emphysema or bullous disease without COPD]] | ||
*[[Fibrothorax]] | *[[Fibrothorax]] | ||
{sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic} | {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic} | ||
{{discussion}} the SC diagnoses need to be replaced by links to the relevant ICD10 pages | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
{{ICD10 infection}} | {{ICD10 infection}} | ||
== Related CCI Codes == | == Related CCI Codes == |
Revision as of 13:59, 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
{sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
Template:Discussion the SC diagnoses need to be replaced by links to the relevant ICD10 pages
Candidate Combined ICD10 codes
Related CCI Codes
Related Articles
Show all ICD10 Subcategories