Interstitial lung disease, NOS: Difference between revisions
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== Additional Info == | == Additional Info == | ||
*This code includes: | |||
**Alveolar proteinosis | |||
**Idiopathic pulmonary hemosiderosis | |||
**Lipoid interstitial pneumonitis -- sometimes incorrectly called or Lipoid interstitial pneumonia | |||
**Lymphangioleiomyomatosis (LAM) | |||
**Histiocytosis X | |||
**Langerhans cell histiocytosis | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == |
Revision as of 10:21, 2018 April 11
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
- This code includes:
- Alveolar proteinosis
- Idiopathic pulmonary hemosiderosis
- Lipoid interstitial pneumonitis -- sometimes incorrectly called or Lipoid interstitial pneumonia
- Lymphangioleiomyomatosis (LAM)
- 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