J84.10 ICD 10 Code is a billable and specific code that can be used to indicate a diagnosis of Pulmonary fibrosis, unspecified for reimbursement purposes. The 2023 edition of the American ICD-10-CM code became effective on October 1, 2022.
Possible back-references that may be applicable or related to J84.10 ICD10 Code:
- J00-J99 Diseases of the respiratory system
- J80-J84 Other respiratory diseases principally affecting the interstitium
- J84 Other interstitial pulmonary diseases
- J84.0 Alveolar and parieto-alveolar conditions
- J84.1 Other interstitial pulmonary diseases with fibrosis
- J84.8 Other specified interstitial pulmonary diseases
Present On Admission (POA Exempt)
J84.10 ICD 10 code is considered exempt from POA reporting
Clinical information about J84.10 ICD 10 code
Pulmonary fibrosis is a condition in which the tissue deep in your lungs becomes scarred over time. This tissue gets thick and stiff. That makes it hard for you to catch your breath, and your blood may not get enough oxygen.
Causes of pulmonary fibrosis include environmental pollutants, some medicines, some connective tissue diseases, and interstitial lung disease. Interstitial lung disease is the name for a large group of diseases that inflame or scar the lungs. In most cases, the cause cannot be found. This is called idiopathic pulmonary fibrosis.
Symptoms include:
- Shortness of breath
- A dry, hacking cough that doesn't get better
- Fatigue
- Weight loss for no known reason
- Aching muscles and joints
- Clubbing, which is the widening and rounding of the tips of the fingers or toes
Your doctor may use your medical history, imaging tests, a biopsy, and lung function tests to diagnose pulmonary fibrosis. There is no cure. Treatments can help with symptoms and improve your quality of life. They include medicines, oxygen therapy, pulmonary rehabilitation, or a lung transplant.
NIH: National Heart, Lung, and Blood Institute
The information in this box was provided by MedlinePlus.gov