Pulmonary Fibrosis Symptoms
What is Pulmonary Fibrosis?
Pulmonary fibrosis scars the lungs, causing intricate pulmonary passageways to thicken and harden, obstructing the free passage of oxygen through the walls of the lungs’ tiny air sacs (alveoli) into the bloodstream. The resulting lack of oxygen in the bloodstream leaves sufferers short of breath, even after periods of prolonged rest. Idiopathic pulmonary fibrosis is a form of pulmonary fibrosis with no known cause. Pulmonary fibrosis is a progressive disease that varies in the rate of degeneration from person to person.
Pulmonary fibrosis is a subset of a group of conditions referred to as interstitial lung disease.
The term interstitial lung disease refers to conditions that lead to inflammation or scarring of the lung’s delicate tissues. Some autoimmune disorders, specifically connective tissue disorders like rheumatoid arthritis can cause interstitial lung disease. Scarring of the lungs is irreversible. However,treatment options are available.
There are many causes of pulmonary fibrosis including occupational and environmental factors, reaction to medications, autoimmune disorders, infection, genetics and unknown factors. Smoking exacerbates the condition and may lead to cancer and/or other lung conditions.
Occupational and Environmental Factors:
Prolonged exposure to toxins or other pollutants can permanently damage the lungs.
- Silica dust
- Asbestos fibers
- Grain dust
- Bird and animal feces
- Burn Pits
Individuals who have received radiation therapy or have used certain medications for an extended period may be more susceptible.
- Radiation therapy
- Chemotherapeutic agents
The role of genetics in the onset of pulmonary fibrosis is still being evaluated. It is estimated that 10 to 15 percent of patients with idiopathic pulmonary fibrosis have some form of inherited pulmonary fibrosis, referred to as familial pulmonary fibrosis.
- Familial pulmonary fibrosis
- Hermansky-Pudlak syndrome
Sufferers of autoimmune diseases–specifically connective tissue disorders–can develop pulmonary fibrosis. These autoimmune disorders can lead to pulmonary fibrosis:
- Scleroderma or progressive systemic sclerosis
- Rheumatoid arthritis
- Polymyositis or dermatomyositis
Severe infections can contribute to multiple types of interstitial lung diseases, including pulmonary fibrosis.
- Viral infections
- Bacterial infections
Cellular Therapy for Pulmonary Fibrosis
In the case of pulmonary fibrosis, autologous cells are used; this means the cells come from the patient’s body. These cells are found in adult bone marrow or in blood (venous). Bone marrow or venous cells have the capacity to form many types of differentiated cells. During the procedure, cellular therapy involves isolating adult cells from bone marrow and blood tissue requiring special laboratory techniques to collect. After extraction, the cells are isolated. At this point, the cells are returned to the patient intravenously. The minimally invasive therapy can be performed as an outpatient procedure in a clinical setting under the supervision of a professional. It takes a physician that has sought specific training to perform cellular therapy adequately, safely and successfully.
If you would like to find out more about how our treatment can relieve the symptoms of pulmonary fibrosis, please contact one of our patient care coordinators today at (800) 729-3065 to schedule a free consultation.