Pulmonary Fibrosis ~ Wikipedia

Pulmonary fibrosis is the formation or development of excess fibrous connective tissue(fibrosis) in the lungs. It is also described as "scarring of the lung".^[1]

Contents   [hide]  1 Symptoms 2 Cause 3 Pathogenesis 4 Diagnosis 5 Treatment and prevention 6 Prognosis 7 Epidemiology 8 References

Symptoms[edit]

Symptoms of pulmonary fibrosis are mainly:

• Shortness of breath, particularly with exertion^[1]
• Chronic dry, hacking coughing^[1]
• Fatigue and weakness^[1]
• Chest discomfort^[1]
• Loss of appetite and rapid weight loss^[1]

Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion.^[2] Sometimes fine inspiratorycrackles can be heard at the lung bases on auscultation.^[2] A chest x-ray may or may not be abnormal, but high Resolution CT will frequently demonstrate abnormalities.^[2]

Cause[edit]

Further information: Interstitial lung disease

Pulmonary fibrosis may be a secondary effect of other diseases. Most of these are classified as interstitial lung diseases. Examples include autoimmune disorders, viral infections or other microscopic injuries to the lung.^[1] However, pulmonary fibrosis can also appear without any known cause. In this case, it is termed "idiopathic".^[3] Most idiopathic cases are diagnosed as idiopathic pulmonary fibrosis. This is a diagnosis of exclusion of a characteristic set of histologic/pathologic features known as usual interstitial pneumonia (UIP). In either case, there is a growing body of evidence which points to a genetic predisposition in a subset of patients. For example, a mutation in Surfactant protein C (SP-C) has been found to exist in some families with a history of pulmonary fibrosis.^[1]

Diseases and conditions that may cause pulmonary fibrosis as a secondary effect include:

• Inhalation of environmental and occupational pollutants,^[1] such as in asbestosis,^[2] silicosis^[2] and exposure to certain gases.^[2] Coal miners, ship workers and sand blasters among others are at higher risk.^[3]
  • Hypersensitivity pneumonitis, most often resulting from inhaling dust contaminated with bacterial, fungal, or animal products.^[2]
• Cigarette smoking^[1] can increase the risk or make the illness worse.^[3]
• Some typical connective tissue diseases^[3] such as rheumatoid arthritis,^[1][2] SLE^[1][2] and scleroderma^[1]
• Other diseases that involve connective tissue, such as sarcoidosis^[1][2] and Wegener's granulomatosis.^[2]
• Infections^[2]
• Certain medications, e.g. amiodarone, bleomycin (pingyangmycin), busulfan, methotrexate, and ^[1][3] nitrofurantoin^[4]
• Radiation therapy to the chest^[1][2]

A helpful mnemonic for medical students and healthcare professionals to remember the causes of apical or basal fibrosis are as follows:

Apical - BREAST CLAP

• Berylliosis
• Radiation
• Extrinsic Allergic Alveolitis
• Allergic Bronchopulmonary Aspergillosis
• Sarcoidosis
• Tuberculosis

• Coal worker's Pneumoconiosis
• Langerhans cell histiocytosis
• Ankylosing Spondylitis
• Psoriasis

Basal - DR CIA

• Drugs
• Rheumatoid Arthritis
• Connective Tissue Disease
• Idiopathic Pulmonary Fibrosis
• Asbestosis

Pathogenesis[edit]

Further information: Fibrosis

Pulmonary fibrosis involves gradual exchange of normal lung parenchyma with fibrotic tissue. The replacement of normal lung with scar tissue causes irreversible decrease in oxygen diffusion capacity.^[1] In addition, decreased compliance makes pulmonary fibrosis arestrictive lung disease. It is the main cause of restrictive lung disease that is intrinsic to the lung parenchyma. In contrast, quadriplegia^[5]and kyphosis^[6] are examples of causes of restrictive lung disease that do not necessarily involve pulmonary fibrosis

Diagnosis[edit]

HRCT of lung showing extensive fibrosis possibly from usual interstitial pneumonitis. There is also a large emphysematous bulla.

The diagnosis can be confirmed by lung biopsy.^[2] A videoscopic assisted thoracoscopic wedge biopsy (VATS) under general anesthesia may be necessary to obtain enough tissue to make an accurate diagnosis. This kind of biopsy involves placement of several tubes through the chest wall, one of which is used to cut off a piece of lung to send for evaluation .^[2] The removed tissue is examined histopathologically by microscopy to confirm the presence and pattern of fibrosis as well as presence of other features that may indicate a specific cause e.g. specific types of mineral dust or possible response to therapy e.g. a pattern of so-called non-specific interstitial fibrosis.^[2]

Misdiagnosis is common because, while overall pulmonary fibrosis is not rare, each individual type of pulmonary fibrosis is uncommon and the evaluation of patients with these diseases is complex and requires a multidisciplinary approach.^[1] Terminology has been standardized but difficulties still exist in their application.^[1] Even experts may disagree with the classification of some cases.

On spirometry, as a restrictive lung disease, both the FEV1 (Forced Expiratory Volume in 1 Second) and FVC (Forced Vital Capacity) are reduced so the FEV1/FVC ratio is normal or even increased in contrast to obstructive lung disease where this ratio is reduced. The values for residual volume and total lung capacity are generally decreased in restrictive lung disease.^[7]

Treatment and prevention[edit]

Pulmonary fibrosis creates scar tissue. The scarring is permanent once it has developed.^[2] Slowing the progression and prevention depends on the underlying cause:

• Treatment options for idiopathic pulmonary fibrosis are very limited.^[2] Though research trials are ongoing, there is no evidence that any medications can significantly help this condition. Lung transplantation is the only therapeutic option available in severe cases. Since some types of lung fibrosis can respond to corticosteroids (such as Prednisone) and/or other medications that suppress the body's immune system, these types of drugs are sometimes prescribed in an attempt to slow the processes that lead to fibrosis.

The immune system is felt to play a central role in the development of many forms of pulmonary fibrosis. The goal of treatment with immune suppressive agents such as corticosteroids is to decrease lung inflammation and subsequent scarring. Responses to treatment are variable. Those whose conditions improve with immune suppressive treatment probably do not have idiopathic pulmonary fibrosis, for idiopathic pulmonary fibrosis has no significant treatment or cure.^[2] There are pharmacological agents in the experimental phase intended to prevent scarring.^[1] Anti-inflammatory agents have only limited success in reducing the fibrotic progress.^[1]

• Some of the other types of fibrosis, such as nonspecific interstitial pneumonitis (NSIP), may respond to immunosuppressive therapy such as corticosteroids.^[2] However, only a minority of patients respond to corticosteroids alone, so additional immunosuppressants, such as cyclophosphamide, azathioprine, methotrexate, penicillamine, and cyclosporine may be used.^[2] Colchicine has also been used with limited success.^[2] There are ongoing trials with newer drugs such as IFN-γ, mycophenolate mofetil, and pirfenidone.
• Hypersensitivity pneumonitis, a less severe form of pulmonary fibrosis, is prevented from becoming aggravated by avoiding contact with the causative material.

Oxygen supplementation improves the quality of life and exercise capacity.^[1] Lung transplantation may be considered for some patients.^[1]

Prognosis[edit]

Lung with end-stage pulmonary fibrosis at autopsy

Hypoxia caused by pulmonary fibrosis can lead to pulmonary hypertension, which, in turn, can lead to heart failure of the right ventricle. This can be prevented with oxygen supplementation.^[2]

Pulmonary fibrosis may also cause increased risk for pulmonary emboli, which can be prevented by anticoagulants.^[2]

Epidemiology[edit]

Five million people worldwide are affected by pulmonary fibrosis.^[1] A wide range of incidence and prevalence rates have been reported for pulmonary fibrosis. The rates below are per 100,000 persons, and the ranges reflect narrow and broad inclusion criteria, respectively.

Study authors		Incidence rate	Prevalence rate	Population	Years covered
Raghu et al. [8]	--	6.8-16.3	14.0-42.7	U.S. health care claims processing system	1996–2000
Fernandez Perezet al. [9]	--	8.8-17.4	27.9-63.0	Olmstead County, MN	1997–2005
Coultas et al. [10]	Male	27.5	30.3	Bernalillo County, NM	1988–1990
	Female	11.5	14.5

Based on these rates, pulmonary fibrosis prevalence in the United States could range from more than 29,000 to almost 132,000, based on the population in 2000 that was 18 years or older. The actual numbers may be significantly higher due to misdiagnosis.^[1] Typically, patients are in their forties and fifties when diagnosed while the incidence of idiopathic pulmonary fibrosis increases dramatically after the age of fifty. However, loss of pulmonary function is commonly ascribed to old age, heart disease or to more common lung diseases. Fibrosis is best known for killing Peter Benchley in 2006.^[1]