Interstitial lung disease, NOS
| 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)
- To code pulmonary fibrosis post-COVID19, combine this code with Post COVID-19 condition
Alternate ICD10s to consider coding instead or in addition
- Interstitial lung disease, drug-induced (acute or chronic)
- Hypersensitivity pneumonitis (extrinsic allergic alveoliltis), NOS
- Malignancy (clonal disorder) of blood or lymphoid tissue, 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
Infections
Infections in ICD10 have combined coding requirements for some of their pathogens. Any that have antibiotic resistances would store those as Combined ICD10 codes as well. If the infection is acquired in the hospital, see Nosocomial infection, NOS. See Lab and culture reports for confirmation and details about tests. See Infections in ICD10 for more general info.
Attribution of infections
Related CCI Codes
Data Integrity Checks (automatic list)
| App | Status | |
|---|---|---|
| Query check ICD10 Inf Potential Infection must have pathogen or alt | CCMDB.accdb | declined |
| Query Check Inf Pathogens must have Infection requiring pathogen or Potential Infection | CCMDB.accdb | implemented |
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