is a disease that causes localized, irreversible dilatation of part of the bronchial tree
. Involved bronchi
are dilated, inflamed, and easily collapsible, resulting in airflow obstruction
and impaired clearance of secretions. Bronchiectasis is associated with a wide range of disorders, but it usually results from necrotizing
bacterial infections, such as infections caused by the Staphylococcus
species or Bordetella pertussis
Rene Theophile Hyacinthe Laënnec, the man who invented the stethoscope, used his creation to first discover bronchiectasis in 1819.. The disease was researched in greater detail by Sir William Osler in the late 1800s; in fact, it is suspected that Osler actually died of complications from undiagnosed bronchiectasis.
Dilation of the bronchial walls results in airflow obstruction and impaired clearance of secretions because the dilated areas disrupt normal air pressure in the bronchial tubes, causing sputum to pool inside the dilated areas instead of being pushed upward. The pooled sputum provides an environment conducive to the growth of infectious pathogens, and these areas of the lungs are thus very vulnerable to infection. The more infections that the lungs experience, the more damaged the lung tissue and alveoli become. When this happens, the bronchial tubes become more inelastic and dilated, creating a self-perpetuating cycle of further damage to the lungs.
There are three types of brochiectasis, varying by level of severity. Fusiform (cylindrical) bronchiectasis (the most common type) refers to mildly inflamed bronchi that fail to taper distally. In varicose bronchiectasis, the bronchial walls appear beaded, because areas of dilation are mixed with areas of constriction. Saccular (cystic) bronchiectasis is characterized by severe and irreversible ballooning of the bronchi peripherally, with or without air-fluid levels. Chronic productive cough is prominent, occurring in up to 90% of patients with bronchiectasis. Sputum is produced on a daily basis in 76% of patients.
Generally, persons suffering from bronchiectasis tend to be infected by Haemophilus influenzae early on in the disease course. Secondary infection is usually due to Staphylococcus aureus; followed by Moraxella catarrhalis and finally Pseudomonas aeruginosa.
There are both congenital
causes of bronchiectasis. Kartagener syndrome
, which affects the mobility of cilia
in the lungs, aids in the development of the disease. Another common genetic cause is cystic fibrosis
, in which a small number of patients develop severe localized bronchiectasis. Young's syndrome
, which is clinically similar to cystic fibrosis, is thought to significantly contribute to the development of bronchiectasis. This is due to the occurrence of chronic
infections. Patients with alpha 1-antitrypsin
deficiency have been found to be particularly susceptible to bronchiectasis, for unknown reasons. Other less-common congenital causes include primary immunodeficiencies
, due to the weakened or nonexistent immune system response to severe, recurrent infections that commonly affect the lung.
Acquired bronchiectasis occurs more frequently, with one of the biggest causes being tuberculosis
. Endobronchial tuberculosis
commonly leads to bronchiectasis, either from bronchial stenosis
or secondary traction
from fibrosis. An especially common cause of the disease in children is acquired immune deficiency syndrome
, stemming from the human immunodeficiency virus
. This disease predisposes patients to a variety of pulmonary ailments, such as pneumonia
and other opportunistic infection
.. Bronchiectasis can sometimes be an unusual complication of inflammatory bowel disease
, especially ulcerative colitis
. It can occur in Crohn's disease
as well, but does so less frequently. Bronchiectasis in this situation usually stems from various allergic responses to inhaled fungus spores. Recent evidence has shown an increased risk of bronchiectasis in patients with rheumatoid arthritis
who smoke. One study stated a tenfold increased prevalence
of the disease in this cohort. Still, it is unclear as to whether or not cigarette smoke is a specific primary cause of bronchiectasis.
Other acquired causes of bronchiectasis involving environmental exposures include respiratory infections, obstructions, inhalation and aspiration of ammonia and other toxic gases, pulmonary aspiration, alcoholism, heroin (drug use), and various allergies.
The diagnosis of bronchiectasis is based on the review of clinical history and characteristic patterns in high-resolution CT scan
findings. Such patterns include "tree-in-bud
" abnormalities and cysts with definable borders. In one small study, CT findings of bronchiectasis and multiple small nodules were reported to have a sensitivity
of 80%, specificity
of 87%, and accuracy
of 80% for the detection of bronchiectasis. Bronchiectasis may also be diagnosed without CT scan confirmation if clinical history clearly demonstrates frequent, respiratory infections, as well confirmation of an underlying problem via blood work
Treatment of bronchiectasis is aimed at controlling infections
and bronchial secretions, relieving airway obstruction, and preventing complications
. This includes the prolonged usage of antibiotics
to prevent detrimental infections, as well as eliminating accumulated fluid with postural drainage
and chest physiotherapy
. Surgery may also be used to treat localized bronchiectasis, removing obstructions that could cause progression of the disease.
Inhaled steroid therapy that is consistently adhered to can reduce sputum production and decrease airway constriction over a period of time, and help prevent progression of bronchiectasis. One commonly used therapy is beclometasone dipropionate, which is also used in asthma treatment. Use of inhalers such as albuterol (salbutamol), fluticasone (Flovent/Flixotide) and ipratropium (Atrovent) may help reduce likelihood of infection by clearing the airways and decreasing inflammation.
Mannitol dry inhalation powder, under the name Bronchitol, has been approved by the FDA for use in cystic fibrosis patients with or at risk for bronchiectasis. The original orphan drug indication approved in February 2005 allowed its use for the treatment of bronchiectasis. The original approval was based on the results of Phase II clinical studies showing the product to be safe, well-tolerated, and effective for stimulating mucus hydration/clearance, thereby improving quality of life in patients with chronic obstructive lung diseases like bronchiectasis. Long-term studies are underway as of 2007 to ensure the safety and effectiveness of the treatment.
Advair Diskus is also a commonly used inhaled corticosteroid which has in many cases been effective in clearing the airways, reducing sputum and reducing inflammation.
In order to prevent future development of bronchiectasis, an x-ray
of the chest should be taken after any severe attack of measles
, whooping cough
or other acute respiratory infection in childhood. While smoking
has not been found to be a direct cause of bronchiectasis, it is certainly an irritant that all patients should avoid in order to prevent the development of infections (such as bronchitis
) and further complications.
A healthy body mass index, vaccination (especially against pneumonia and influenza) and regular doctor visits may have beneficial effects on the prevention of progressing bronchiectasis. The presence of hypoxemia, hypercapnia, dyspnea level and radiographic extent can greatly affect the mortality rate from this disease.