Idiopathic Pulmonary Fibrosis
Alternate Names : CFA, Cryptogenic Fibrosing Alveolitis, Fibrosing Alveolitis, Idiopathic Diffuse Interstitial Pulmonary Fibrosis, IPF, Pulmonary Fibrosis, UIP, Usual Interstitial Pneumonitis
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Prognosis (Expectations)
Some patients may improve on treatment with corticosteroids or cytotoxic drugs, but most patients suffer from progressive disease despite treatment. Pulmonary hypertension (high blood pressures in the vessels of the lungs) and respiratory failure is the eventual outcome. Average survival time is 5-6 years, but this varies greatly between patients.
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