Staging of pulmonary fibrosis is important to establish the optimal treatment plan and to offer the patient an accurate prognosis.
Idiopathic pulmonary fibrosis is a chronic lung disease that causes buildup of scar tissue deep inside the lungs, preventing these organs from working as they should. One of the first questions someone may have after being diagnosed with IPF is what to expect next. Find out what happens as IPF advances.
Research suggests that high levels of leptin in the plasma are associated with acute exacerbation of idiopathic pulmonary fibrosis.
Read about an analysis of active genes in individual cells from lung fibrosis patients and controls, that may offer new IPF drug targets.
The subject of the necessity of clinical trials for pulmonary fibrosis in an era where there are effective therapies is discussed.
Read about a lung disease study that identified a type of regenerative cell and a type of scar-forming cell. The discoveries could lead to new therapies.
Idiopathic pulmonary fibrosis is a chronic lung disease that causes buildup of scar tissue deep inside the lungs, preventing these organs from working as they should. One of the first questions someone may have after being diagnosed with IPF is what to expect next. Find out what happens as IPF advances.
Having surgery can come with added risks, depending on how severe your Pulmonary Fibrosis is. Here's a checklist to consider.
Assessing the severity and staging of Idiopathic Pulmonary Fibrosis utilizes pulmonary function tests. Results may be mild, moderate, severe to very severe.
A six minute walk test provides an integrated overall assessment of exercise capacity and is used to monitor Idiopathic Pulmonary Fibrosis patients.
Coughing was cited as one of the most significant symptoms of idiopathic pulmonary fibrosis and could be triggered by various factors.
Your favorite outdoor brands make better products that are only available in Japan.
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