Common symptoms of idiopathic pulmonary fibrosis are fatigue, a dry cough and a drop in body weight, according to Cleveland Clinic. Patients may also feel short of breath during or after exercise or other physical exertion. These symptoms usually develop incrementally and often go unnoticed in the e
The end stage of pulmonary fibrosis is respiratory failure, states Mayo Clinic. The damage from pulmonary fibrosis renders the lungs extremely stiff, much like an old sponge. This makes it progressively impossible to breathe, adding to the patient's loss of appetite and fatigue.
Patients with end-stage pulmonary fibrosis can expect their respiratory symptoms to worsen, according to the Coalition for Pulmonary Fibrosis. They may find it difficult to perform certain activities, including climbing stairs and walking.
The final stages of pulmonary fibrosis involve pulmonary hypertension, respiratory failure and heart failure, explains the American Lung Association. Patients may need supplemental oxygen to breathe.
According to WebMD, pulmonary fibrosis is described as scarring that occurs in the lungs. The resulting thickened lung tissue makes it hard for lungs to properly function. According to Mayo Clinic, the lung damage incurred cannot be fixed; however, some treatments and therapies may be effective at c
Symptoms of pulmonary fibrosis include shortness of breath, dry cough, fatigue, unexplained weight loss and aching muscles and joints, according to the Mayo Clinic. However, symptoms and progression of the disease vary from person to person.
As of 2015, doctors have not found a cure for pulmonary fibrosis, states WebMD. In the majority of cases, doctors cannot determine the cause of the disease, and treatment is focused on slowing the spread of lung damage and helping patients maintain comfortable breathing.
End-stage pulmonary disease is a medical term that refers to the most severe stage of chronic obstructive pulmonary disease, states Healthline. People who live with this level of disease typically have severe issues with breathlessness and exercise intolerance, frequent symptom flare-ups and a dimin
Interstitial pulmonary fibrosis describes a disease where tissue surrounding the air sacs of the lungs becomes inflamed and damaged, according to the National Library of Medicine. As the tissue stiffens and scars, the alveoli are prevented from fully expanding, and less oxygen is breathed into the b
People with pulmonary fibrosis live an average of three years after diagnosis, according to Merck Manual. The condition causes progressive lung scarring and gradually decreases oxygen levels in blood, triggering symptoms such as difficulty breathing, coughing, tiredness and shortness of breath durin