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Idiopathic Pulmonary Fibrosis - Respiratory Therapist Career Guide

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Idiopathic Pulmonary Fibrosis

Pulmonary fibrosis is a lung disease which causes deep tissue within your lungs to become stiff and thick, or scarred, over time. The development of this scar tissue is referred to as fibrosis.

As the deep tissue in the lungs thickens, your lungs cannot adequately move oxygen into your blood and carbon dioxide out. Consequently, your other organs and brain don’t get the necessary oxygen they require.

Occasionally, doctors can determine what’s causing fibrosis. But in most cases, they can’t find a cause. These cases are referred to as idiopathic pulmonary fibrosis (IPF).

Idiopathic Pulmonary Fibrosis is a serious lung disease that most often affects middle-aged adults and older adults. IPF differs from person to person. In some people, fibrosis occurs quickly. In other people, the progression is much slower. In some, the disease remains unchanged for years.

Currently, there is no known cure for IPF. Most people live only roughly 3 to approximately 5 years after receiving their diagnosis. Respiratory failure is the most familiar cause of death connected to IPF . Other roots of death include pulmonary embolism, heart failure, pulmonary hypertension, lung cancer and pneumonia.

Genetics probably play a role in the cause of IPF. The disease is called familial IPF if multiple members of your family has IPF.
Research assists physicians in learning more about IPF. Consequently, this allows them to more rapidly diagnose the IPF now than previously in the past. In addition, researchers are investigating several medications that may hinder the progress of IPF. These efforts may increase the lifespan and quality of life for people who have Idiopathic Pulmonary Fibrosis.

 
 
 
 

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