Idiopathic interstitial pulmonary fibrosis: Difference between revisions

Revision as of 14:52, 5 April 2018

ICD10 Diagnosis
Dx:	Idiopathic interstitial pulmonary fibrosis
ICD10 code:	J84.1
Pre-ICD10 counterpart:	none assigned
Charlson/ALERT Scale:	none
APACHE Como Component:	none
APACHE Acute Component:	none
Start Date:
Stop Date:
Data Dependencies(Reports/Indicators/Data Elements):	No results
External ICD10 Documentation	ICD-10 CM Wikipedia ICD-10 Wikipedia WHO ICD10 documentation ICD10data.com

This diagnosis is a part of ICD10 collection.

This code includes a number of specific subtypes:
- IPF = idiopathic pulmonary fibrosis
- UIP = usual interstitial pneumonitis
- DIP = desquamative interstitital pneumonitis
- NSIP = nonspecific interstitial pneumonitis
- AIP = acute interstitial pnemonitis
But it does NOT include: Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))

== Alternate ICD10s to consider coding instead or in addition

@@ Line 22: / Line 22: @@
 *[[Interstitial Pneumonitis]]
 *[[Pneumonitis NYD]]
-==
+*[[Pulmonary hypertension, secondary (any cause)]]=
 *[[Fibrothorax]]

Skin	Trauma	Renal/urinary	Infectious disease
ENT	Testing	Cardiovascular	Hereditary/congenital
Eye	Mechanism	Neoplastic	Heme/immunology
Misc	Reproductive	Gastrointestinal	Musculoskeletal/soft tissue
Psych	Respiratory	Poisoning
Neuro	Symptom/Sign	Endocrine disorder