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Diffuse interstitial pulmonary fibrosis
Alternative Names: Diffuse parenchymal lung disease; Alveolitis; Idiopathic pulmonary fibrosis (IPF); Cryptogenic Fibrosing Alveolitis (CFA); Idiopathic pulmonary pneumonitis (IPP) Treatment: The treatment depends upon the underlying cause of the disease. Most often, anti-inflammatory drugs, such as corticosteroids or immunosuppressing drugs, are given. If there is no specific treatment for an underlying disorder, supportive therapy is indicated. Supplemental oxygen is prescribed for people with low blood oxygen levels. Pulmonary rehabilitation can help people combat the debilitation that accompanies advanced ILD. Text Continues Below Exposure to agents known to cause lung disease (certain dusts, gases, fumes, vapors, medications, and radiation) should be restricted. Quitting cigarettes can slow the progression of existing ILD. Lung transplantation may be indicated in some patients with advanced ILD. Support Groups: The stress of the illness can often be helped by joining a support group where members share common experiences and problems. See lung disease - support group. Expectations (prognosis): Chances for recovery or progression of the disease depend on the underlying cause. Complications: hypoxemia pulmonary hypertension right sided heart failure (cor pulmonale) respiratory failure Calling your health care provider: Page:  1 | 2 | Next >>