Interstitial lung disease, NOS: Difference between revisions

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{{ICD10 transition status
{{ICD10 transition status
| OldDxArticle =Interstitial Pneumonitis| CurrentStatus = reconciled
| 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 {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
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.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • J84.9
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories

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


{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

Template:ICD10 infection

Related CCI Codes

Related Articles

Related articles:


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