Valid for Submission
J84.116 is a billable diagnosis code used to specify a medical diagnosis of cryptogenic organizing pneumonia. The code J84.116 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code J84.116 might also be used to specify conditions or terms like chronic interstitial pneumonia, cryptogenic organizing pneumonia, idiopathic interstitial pneumonia, recurrent pneumonia or seasonal cryptogenic organizing pneumonia with biochemical cholestasis.
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code J84.116:
Type 1 ExcludesType 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- organizing pneumonia NOS, or due to known underlying cause J84.89
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code J84.116 are found in the index:
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Chronic interstitial pneumonia
- Cryptogenic organizing pneumonia
- Idiopathic interstitial pneumonia
- Recurrent pneumonia
- Seasonal cryptogenic organizing pneumonia with biochemical cholestasis
- CRYPTOGENIC ORGANIZING PNEUMONIA-. an interstitial lung disease of unknown etiology occurring between 21 80 years of age. it is characterized by a dramatic onset of a "pneumonia like" illness with cough fever malaise fatigue and weight loss. pathological features include prominent interstitial inflammation without collagen fibrosis diffuse fibroblastic foci and no microscopic honeycomb change. there is excessive proliferation of granulation tissue within small airways and alveolar ducts.
Diagnostic Related Groups - MS-DRG Mapping
Convert J84.116 to ICD-9 Code
Information for Patients
Interstitial Lung Diseases
Interstitial lung disease is the name for a large group of diseases that inflame or scar the lungs. The inflammation and scarring make it hard to get enough oxygen. The scarring is called pulmonary fibrosis.
Breathing in dust or other particles in the air is responsible for some types of interstitial lung diseases. Specific types include
- Black lung disease among coal miners, from inhaling coal dust
- Farmer's lung, from inhaling farm dust
- Asbestosis, from inhaling asbestos fibers
- Siderosis, from inhaling iron from mines or welding fumes
- Silicosis, from inhaling silica dust
Other causes include autoimmune diseases or occupational exposures to molds, gases, or fumes. Some types of interstitial lung disease have no known cause.
Treatment depends on the type of exposure and the stage of the disease. It may involve medicines, oxygen therapy, or a lung transplant in severe cases.
- Hypersensitivity pneumonitis (Medical Encyclopedia)
- Interstitial lung disease (Medical Encyclopedia)
- Interstitial lung disease - adults - discharge (Medical Encyclopedia)
- Pulmonary function tests (Medical Encyclopedia)
[Learn More in MedlinePlus]
Also called: Bronchopneumonia
Pneumonia is an infection in one or both of the lungs. Many germs, such as bacteria, viruses, and fungi, can cause pneumonia. You can also get pneumonia by inhaling a liquid or chemical. People most at risk are older than 65 or younger than 2 years of age, or already have health problems.
Symptoms of pneumonia vary from mild to severe. See your doctor promptly if you
- Have a high fever
- Have shaking chills
- Have a cough with phlegm that doesn't improve or gets worse
- Develop shortness of breath with normal daily activities
- Have chest pain when you breathe or cough
- Feel suddenly worse after a cold or the flu
Your doctor will use your medical history, a physical exam, and lab tests to diagnose pneumonia. Treatment depends on what kind you have. If bacteria are the cause, antibiotics should help. If you have viral pneumonia, your doctor may prescribe an antiviral medicine to treat it.
Preventing pneumonia is always better than treating it. Vaccines are available to prevent pneumococcal pneumonia and the flu. Other preventive measures include washing your hands frequently and not smoking.
NIH: National Heart, Lung, and Blood Institute
- Aspiration pneumonia (Medical Encyclopedia)
- Atypical pneumonia (Medical Encyclopedia)
- Hospital-acquired pneumonia (Medical Encyclopedia)
- Mycoplasma pneumonia (Medical Encyclopedia)
- Pneumonia (Medical Encyclopedia)
- Pneumonia - adults - discharge (Medical Encyclopedia)
- Pneumonia - children - community acquired (Medical Encyclopedia)
- Pneumonia - children - discharge (Medical Encyclopedia)
- Viral pneumonia (Medical Encyclopedia)
[Learn More in MedlinePlus]
Idiopathic pulmonary fibrosis Idiopathic pulmonary fibrosis is a chronic, progressive lung disease. This condition causes scar tissue (fibrosis) to build up in the lungs, which makes the lungs unable to transport oxygen into the bloodstream effectively. The disease usually affects people between the ages of 50 and 70. Idiopathic pulmonary fibrosis belongs to a group of conditions called interstitial lung diseases (also known as ILD), which describes lung diseases that involve inflammation or scarring in the lung.The most common signs and symptoms of idiopathic pulmonary fibrosis are shortness of breath and a persistent dry, hacking cough. Many affected individuals also experience a loss of appetite and gradual weight loss. Some people with idiopathic pulmonary fibrosis develop widened and rounded tips of the fingers and toes (clubbing) resulting from a shortage of oxygen. These features are relatively nonspecific; not everyone with these health problems has idiopathic pulmonary fibrosis. Other respiratory diseases, some of which are less serious, can cause similar signs and symptoms.In people with idiopathic pulmonary fibrosis, scarring of the lungs increases over time until the lungs can no longer provide enough oxygen to the body's organs and tissues. Some people with idiopathic pulmonary fibrosis develop other serious lung conditions, including lung cancer, blood clots in the lungs (pulmonary emboli), pneumonia, or high blood pressure in the blood vessels that supply the lungs (pulmonary hypertension). Most affected individuals survive 3 to 5 years after their diagnosis. However, the course of the disease is highly variable; some affected people become seriously ill within a few months, while others may live with the disease for a decade or longer.In most cases, idiopathic pulmonary fibrosis occurs in only one person in a family. These cases are described as sporadic. However, a small percentage of people with this disease have at least one other affected family member. When idiopathic pulmonary fibrosis occurs in multiple members of the same family, it is known as familial pulmonary fibrosis.
[Learn More in MedlinePlus]