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Idiopathic Pulmonary Fibrosis

By

Joyce Lee

, MD, MAS, University of Colorado Denver

Last full review/revision Jun 2021| Content last modified Jun 2021
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Idiopathic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial pneumonia, causes progressive pulmonary fibrosis. Symptoms and signs develop over months to years and include exertional dyspnea, cough, and fine (Velcro) crackles. Diagnosis is based on history, physical examination, high-resolution CT, and/or lung biopsy, if necessary. Treatment may include antifibrotic drugs and oxygen therapy. Most patients deteriorate; median survival is about 3 years from diagnosis.

Idiopathic pulmonary fibrosis, identified histologically as usual interstitial pneumonia, accounts for most cases of idiopathic interstitial pneumonia Overview of Idiopathic Interstitial Pneumonias Idiopathic interstitial pneumonias (IIPs) are interstitial lung diseases of unknown etiology that share similar clinical and radiologic features and are distinguished primarily by the histopathologic... read more . IPF affects men and women > 50 in a ratio of 2:1, with a markedly increased incidence with each decade of age. Current or former cigarette smoking is most strongly associated with the disorder. There is some genetic predisposition; familial clustering occurs in up to 20% of cases.

Etiology of Idiopathic Pulmonary Fibrosis

A combination of environmental, genetic, and other unknown factors probably contribute to alveolar epithelial cell dysfunction or reprogramming, which leads to abnormal fibroproliferation in the lung. There is ongoing research into the contributions of genetics, environmental stimuli, inflammatory cells, the alveolar epithelium, mesenchyme, and matrix.

Pathology of Idiopathic Pulmonary Fibrosis

The key histologic findings of idiopathic pulmonary fibrosis are subpleural fibrosis with sites of fibroblast proliferation (fibroblast foci) and dense scarring, alternating with areas of normal lung tissue (heterogeneity). Scattered interstitial inflammation occurs with lymphocyte, plasma cell, and histiocyte infiltration. Cystic abnormality (honeycombing) occurs in all patients and increases with advanced disease. A similar histologic pattern uncommonly occurs in cases of interstitial lung diseases of known etiology (see table Key Features of Idiopathic Interstitial Pneumonias Key Features of Idiopathic Interstitial Pneumonias* Idiopathic interstitial pneumonias (IIPs) are interstitial lung diseases of unknown etiology that share similar clinical and radiologic features and are distinguished primarily by the histopathologic... read more ).

Symptoms and Signs of Idiopathic Pulmonary Fibrosis

Symptoms and signs of idiopathic pulmonary fibrosis typically develop over 6 months to several years and include dyspnea on exertion and nonproductive cough. Constitutional symptoms, such as low-grade fever and myalgias, are uncommon. The classic sign of IPF is fine, dry, inspiratory crackles (Velcro crackles) at both bases. Clubbing is present in about 50% of cases. The remainder of the examination is normal until disease is advanced, at which time signs of pulmonary hypertension Pulmonary Hypertension Pulmonary hypertension is increased pressure in the pulmonary circulation. It has many secondary causes; some cases are idiopathic. In pulmonary hypertension, pulmonary vessels become constricted... read more and right ventricular systolic dysfunction Cor Pulmonale Cor pulmonale is right ventricular enlargement secondary to a lung disorder that causes pulmonary artery hypertension. Right ventricular failure follows. Findings include peripheral edema, neck... read more Cor Pulmonale may develop.

Diagnosis of Idiopathic Pulmonary Fibrosis

  • High-resolution CT (HRCT)

  • Sometimes surgical lung biopsy

Diagnosis requires HRCT and in some cases surgical lung biopsy.

Chest x-ray typically shows diffuse reticular opacities in the lower and peripheral lung zones. Small cystic lesions (honeycombing) and dilated airways due to traction bronchiectasis are additional findings.

HRCT shows diffuse, patchy, subpleural, reticular opacities with irregularly thickened interlobular septa and intralobular lines; subpleural honeycombing; and traction bronchiectasis. This is referred to as the usual interstitial pneumonia (UIP) pattern. Ground-glass opacities affecting > 30% of the lung suggest an alternative diagnosis.

Laboratory testing plays little role in diagnosis.

Prognosis for Idiopathic Pulmonary Fibrosis

Most patients have moderate to advanced clinical disease at the time of diagnosis and deteriorate despite treatment. Median survival is about 3 years from time of diagnosis. Several prognostic models have been proposed. Among the factors that portend a worse prognosis are older age, male sex, lower forced vital capacity, and lower diffusing capacity for carbon monoxide (DLCO).

Treatment of Idiopathic Pulmonary Fibrosis

  • Pirfenidone or nintedanib

  • Oxygen and pulmonary rehabilitation

  • Sometimes lung transplantation

Many novel therapies for IPF are under development or being tested as treatments for IPF, and patients should be encouraged to participate in clinical trials when appropriate.

Treatment references

Key Points

  • Idiopathic pulmonary fibrosis accounts for most idiopathic interstitial pneumonia and tends to affect older people.

  • Symptoms and signs (eg, subacute dyspnea, nonproductive cough, and Velcro crackles) are nonspecific and usually caused by other, more common disorders.

  • High-resolution CT can help in diagnosis by showing findings such as diffuse, patchy, subpleural, reticular opacities with irregularly thickened interlobular septa and intralobular lines; subpleural honeycombing; and traction bronchiectasis.

  • Treat supportively and, if available, use pirfenidone or nintedanib.

  • Encourage participation in clinical trials and, if patients are < 65 years and otherwise healthy, consider lung transplantation at the time of diagnosis.

Drugs Mentioned In This Article

Drug Name Select Trade
ESBRIET
OFEV
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