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Encyclopedia > Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis
Classification & external resources
Extensive lung fibrosis from usual interstitial pneumonitis
ICD-9 516.3
OMIM 178500
DiseasesDB 4815
MedlinePlus T378
eMedicine radio/873 
MeSH D011658

Idiopathic Pulmonary Fibrosis (IPF), also known as Cryptogenic fibrosing alveolitis, is a chronic progressive interstitial lung disease of unknown etiology. It is one of the two classic interstitial lung diseases, the other being sarcoidosis.[1] Image File history File links Size of this preview: 800 × 498 pixelsFull resolution‎ (847 × 527 pixels, file size: 385 KB, MIME type: image/png) File historyClick on a date/time to view the file as it appeared at that time. ... The International Statistical Classification of Diseases and Related Health Problems (most commonly known by the abbreviation ICD) provides codes to classify diseases and a wide variety of signs, symptoms, abnormal findings, complaints, social circumstances and external causes of injury or disease. ... The following is a list of codes for International Statistical Classification of Diseases and Related Health Problems. ... The Mendelian Inheritance in Man project is a database that catalogues all the known diseases with a genetic component, and - when possible - links them to the relevant genes in the human genome. ... The Disease Bold textDatabase is a free website that provides information about the relationships between medical conditions, symptoms, and medications. ... MedlinePlus (medlineplus. ... eMedicine is an online clinical medical knowledge base that was founded in 1996. ... Medical Subject Headings (MeSH) is a huge controlled vocabulary (or metadata system) for the purpose of indexing journal articles and books in the life sciences. ... Idiopathic means arising spontaneously or from an obscure or unknown cause. ... Interstitial lung disease (ILD), also known as diffuse parenchymal lung disease (DPLD), refers to a group of lung diseases (including idiopathic pulmonary fibrosis), affecting the alveolar epithelium, pulmonary capillary endothelium, basement membrane, perivascular and perilymphatic tissues. ...


More specifically, IPF is defined as a distinctive type of chronic fibrosing interstitial pneumonia of unknown cause associated with a histological pattern of usual interstitial pneumonia (UIP).[2] Usual Interstitial Pneumonia, commonly abbreviated UIP, is the name of a histopathological pattern seen in diffuse lung diseases. ...


Pulmonary fibrosis has often been called an autoimmune disease. However, it is perhaps better characterized as an abnormal and excessive deposition of fibrotic tissue in the pulmonary interstitium with minimal associated inflammation.[3] Autoantibodies, a hallmark of autoimmune diseases, are found in a minority of patients with truly idiopathic pulmonary fibrosis. Moreover, many autoimmune diseases associated with "pulmonary fibrosis", such as scleroderma, are more frequently associated with a related but more inflammatory disease, nonspecific interstitial pneumonitis.[4] Autoimmunity is the failure of an organism to recognize its own constituent parts (down to the sub-molecular levels) as self, which results in an immune response against its own cells and tissues. ... An autoantibody is an antibody (a type of protein) manufactured by the immune system that is directed against one or more of the individuals own proteins. ...

Contents

Classification

Idiopathic pulmonary fibrosis is a type of idiopathic interstitial pneumonia (IIP), which in turn is a type (or group) of interstitial lung diseases.[5] In medicine, idiopathic interstitial pneumonia is a term used for a type of diffuse lung disease; diffuse lung disease is also known as interstitial lung disease. ... Interstitial lung disease (ILD), also known as diffuse parenchymal lung disease (DPLD), refers to a group of lung diseases (including idiopathic pulmonary fibrosis), affecting the alveolar epithelium, pulmonary capillary endothelium, basement membrane, perivascular and perilymphatic tissues. ...


Idiopathic interstitial pneumonias include:

  • idiopathic pulmonary fibrosis (IPF) (the most common)
  • nonspecific interstitial pneumonia
  • cryptogenic organizing pneumonia
  • acute interstitial pneumonia
  • respiratory bronchiolitis-associated interstitial lung disease
  • desquamative interstitial pneumonia
  • lymphoid interstitial pneumonia

Cryptogenic Organising Pneumonitis (COP) or Bronchiolitis Obliterans Organizing Pneumonia (BOOP) is a rapidly developing pneumonia-like illness characterised by lung inflammation and scarring that obstruct the small airways and air sacs of the lungs (alveoli). ... Hamman-Rich syndrome (also known as acute interstitial pneumonia) is a rare, severe lung disease which usually affects otherwise healthy individuals. ...

Clinical features

Idiopathic Pulmonary Fibrosis is slightly more common in males and usually presents in patients greater than 50 years of age. Average survival from time of diagnosis varies between 2.5 and 3.5 years.[5]


Symptoms are gradual in onset. The most common are dyspnea, but also include nonproductive cough, clubbing, and crackles.[5] It should be noted that these features are non-specific and can occur in a spectrum of other pulmonary disorders. Dyspnea (R06. ... Clubbing is also used to refer to the activity of gathering socially at nightclubs. ... Rales, crackles or crepitations, are the clicking, rattling, or crackling noises heard on auscultation of the lungs with a stethoscope during inhalation. ...


The key issue facing clinicians is whether the presenting history, symptoms/signs, radiology, and pulmonary function testing are collectively in keeping with the diagnosis of IPF (which carries the relatively poor prognosis described above) or whether the findings are due to another process. It has long been recognized that patients with interstitial lung disease related to asbestos exposure, drugs (particularly chemotherapeutic agents), a connective tissue disease, or other diseases may have features that are difficult to distinguish from IPF. Important differential diagnostic considerations include asbestosis; interstitial lung disease related to scleroderma, mixed connective tissue disease, or rheumatoid arthritis; advanced sarcoidosis, hypersensitivity pneumonitis, or Langerhans' cell histiocytosis; chronic aspiration; radiation-induced fibrosis; as well as previous therapy with cyclophosphamide, nitrofurantoin, methotrexate, and other drugs.


When diagnostic uncertainty remains, a surgical lung biopsy may be required to establish the diagnosis. Generally, lung biopsy is only undertaken when it is deemed that its risks are outweighed by the potential benefits of identifying a disease process that may be amenable to a treatment that the patient would likely be able to tolerate.


The 2002 American Thoracic Society/European Respiratory Society Consensus Guidelines on the Idiopathic Interstitial Pneumonias have formalized criteria for situations in which it is possible to establish the diagnosis of IPF without a lung biopsy.[5]


Radiology

Plain chest x-rays reveal decreased lung volumes, typically with prominent reticular interstitial markings near the lung bases and posteriorly. Honeycombing, a pattern of dense fibrosis characterized by multiple tiny air-filled spaces located at the bases of the lungs, is frequently seen in advanced cases. In less severe cases, these changes may not be evident on a plain chest film. Frontal chest X-ray. ...


High-resolution CT scans of the chest demonstrate a symmetrical pattern of bibasilar, peripheral, and subpleural intralobular septal thickening, fibrotic changes, honeycombing, and traction bronchiectasis and bronchiolectasis. There may be associated ground glass opacity of the lungs but these changes are relatively minor in comparison with the fibrotic changes.[6] CAT apparatus in a hospital Computed axial tomography (CAT), computer-assisted tomography, computed tomography, CT, or body section roentgenography is the process of using digital processing to generate a three-dimensional image of the internals of an object from a large series of two-dimensional X-ray images taken around...


Pulmonary function tests

Spirometry classically reveals a reduction in the vital capacity with either a proportionate reduction in airflows, or increased airflows for the observed vital capacity. The latter finding reflects the increased lung stiffness (reduced lung compliance) associated with pulmonary fibrosis, which leads to increased lung elastic recoil.[7] Flow-Volume loop showing successful FVC maneuver. ...


Measurement of static lung volumes using body plethysmography or other techniques typically reveals reduced lung volumes (restriction). This reflects the difficulty encountered in inflating the fibrotic lungs. Body Plethysmographs-To do a body plethysomograph, the person is enclosed in an airtight chamber often referred to as a body box. ...


The diffusing capacity for carbon monoxide (DLCO) is invariably reduced in IPF and may be the only abnormality in mild or early disease. Its impairment underlies the propensity of patients with IPF to exhibit oxygen desaturation with exercise.


Histology

Histologic specimens for the diagnosis of IPF must be large enough that the pathologist can comment on the underlying lung architecture. Small biopsies, such as those obtained via transbronchial lung biopsy (performed during bronchoscopy) are generally not sufficient for this purpose. Hence, larger biopsies obtained surgically via a thoracotomy or thoracoscopy are usually necessary.[5] This drawing shows a bronchoscope inserted through the mouth, trachea, and bronchus into the lung; lymph nodes along trachea and bronchi; and cancer in one lung. ...


The histological pattern of fibrosis associated with IPF is referred to as usual interstitial pneumonia (UIP). Although UIP is required for the diagnosis of IPF, it can be seen in other diseases as well.[8] Key features of UIP include fibroblast foci, a pattern of temporal heterogeneity, dense interstitial fibrosis in a paraseptal and subpleural distribution, and a relatively mild or minor component of interstitial chronic inflammation.[5] To help narrow the differential diagnosis, an absence of significant granulomatous inflammation, microorganisms, eosinophils, and asbestos bodies is required. Usual Interstitial Pneumonia, commonly abbreviated UIP, is the name of a histopathological pattern seen in diffuse lung diseases. ...


Diagnosis

The diagnosis of IPF can be made by demonstrating UIP pattern on lung biopsy in a patient without clinical features suggesting an alternate diagnosis (see clinical features, above). Establishing the diagnosis of IPF without a lung biopsy has been shown to be reliable when expert clinicians and radiologists concur that the presenting features are typical of IPF.[9] Based on this evidence, the 2002 ATS/ERS Multidisciplinary Consensus Statement on the Idiopathic Interstitial Pneumonias proposes the following criteria for establishing the diagnosis of IPF without a lung biopsy:[5]


MAJOR CRITERIA (all 4 required):

  • Exclusion of other known causes of interstitial lung disease (drugs, exposures, connective tissue diseases)
  • Abnormal pulmonary function tests with evidence of restriction (reduced FVC) and impaired gas exchange (pO2, p(A-a)O2, DLCO)
  • Bibasilar reticular abnormalities with minimal ground glass on high-resolution CT scans
  • Transbronchial lung biopsy or bronchoalveolar lavage (BAL) showing no features to support an alternative diagnosis

MINOR CRITERIA (3 of 4 required): Spirometry, also known as Pulmonary Function Testing (PFT), is the measurement of lung function, specifically by measuring the volume and speed of air that can be inhaled and exhaled. ... CAT apparatus in a hospital Computed axial tomography (CAT), computer-assisted tomography, computed tomography, CT, or body section roentgenography is the process of using digital processing to generate a three-dimensional image of the internals of an object from a large series of two-dimensional X-ray images taken around...

  • Age > 50
  • Insidious onset of otherwise unexplained exertional dyspnea
  • Duration of illness > 3 months
  • Bibasilar inspiratory crackles

Treatment

There is currently no consensus on the treatment of IPF. Hence, none of what follows should be taken as specific advice regarding therapy, as the latter is a decision that must be made on a case-by-case basis in individual patients.


There is a lack of large, randomized placebo-controlled trials of therapy for IPF. Moreover, many of the earlier studies were based on the hypothesis that IPF is an inflammatory disorder, and hence studied anti-inflammatory agents such as corticosteroids. Another problem has been that studies conducted prior to the more recent classification of idiopathic interstitial pneumonias failed to distinguish IPF/UIP from NSIP in particular. Hence, many patients with arguably more steroid-responsive diseases were included in earlier studies, confounding the interpretation of their results.[10] In physiology, corticosteroids are a class of steroid hormones that are produced in the adrenal cortex. ...


Small early studies demonstrated that the combination of prednisone with either cyclophosphamide or azathioprine over many months had very modest, if any, beneficial effect in IPF, and were associated with substantial adverse effects (predominantly myelotoxicity). Other treatments studied have included interferon gamma-1b and the antifibrotic agent pirfenidone. While neither drug has been shown to have substantial benefits over time, both are currently being studied in patients with IPF. Finally, the addition of the antioxidant N-acetylcysteine to prednisone and azathioprine produced a slight benefit in terms of FVC and DLCO over 12 months of follow up. However, the major benefit appeared to be prevention of the myelotoxicity associated with azathioprine.[11] Prednisone is a synthetic corticosteroid drug which is usually taken orally but can be delivered by intramuscular injection and can be used for a great number of different conditions. ... Interferon-gamma or IFN-g is a dimerized soluble cytokine which is a Type II Interferon. ... Space-filling model of the antioxidant metabolite glutathione. ... Prednisone is a synthetic corticosteroid drug which is usually taken orally but can be delivered by intramuscular injection and can be used for a great number of different conditions. ...


References

  1. ^ The Washington Manual of Medical Therapeutics, 32nd Ed., p. 276.
  2. ^ Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment, Am. J. Respir. Crit. Care Med., Volume 161, Number 2, February 2000, 646-664.
  3. ^ Selman M., King TE. Jr., Pardo A. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann Intern Med 2001;134:136-51.
  4. ^ King, TE. Jr. Centennial review: clinical advances in the diagnosis and therapy of the interstitial lung diseases. Am. J. Respir. Crit. Care Med. 2005:172;268-79.
  5. ^ a b c d e f g American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias , Am. J. Respir. Crit. Care Med., Volume 165, Number 2, January 2002, 277-304.
  6. ^ Webb, W.R., Muller, N.L., Naidich, D.P. High-resolution CT of the lung. Lippincott Williams & Wilkins, Philadelphia (2001), p.196.
  7. ^ Pellegrino R., Viegi G., Brusasco V., Crapo RO., et al. ATS/ERS Task Force: Standardisation of Lung Function Testing. Interpretative strategies for lung function tests. Eur. Respir. J. 2005:26;948-68.
  8. ^ Robbins and Cotran's Pathological Basis of Disease, 7th edition (2005), p.729.
  9. ^ Flaherty KR., King TE. Jr., Raghu G., Lynch JP. III., et al. Idiopathic interstitial pneumonia: what is the effect of a multidisciplinary approach to diagnosis? Am. J. Respir. Crit. Care Med., 2004:170;904-10.
  10. ^ Selman M., King TE. Jr., Pardo A. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann Intern Med 2001;134:136-51.
  11. ^ Demedts, M., Behr, J., Buhl, R., et al. High-dose acetylcysteine in idiopathic pulmonary fibrosis. The IFIGENIA Study. N. Engl. J. Med. 2005:353;2229-42.

External links


  Results from FactBites:
 
MedlinePlus Medical Encyclopedia: Idiopathic pulmonary fibrosis (578 words)
Idiopathic pulmonary fibrosis involves scarring or thickening of tissues deep in the lung without a known cause.
Idiopathic pulmonary fibrosis is a disease of the lower respiratory tract that damages the air sacs (alveoli) and leads to reduced transfer of oxygen to the blood.
Pulmonary hypertension (high blood pressures in the vessels of the lungs) and respiratory failure is the eventual outcome.
Idiopathic pulmonary fibrosis (536 words)
In addition to a physical examination, your health care provider will take a careful history in order to exlude other similar diseases.
Patients with advanced disease may have cyanosis (blueness around the mouth or in the fingernails due to low oxygen).
The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition.
  More results at FactBites »

 
 

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