Both bronchitis and bronchiectasis are respiratory disorders whose pathogenesis is significantly contributed by chronic smoking. The inflammation of the bronchial walls is known as bronchitis. Bronchiectasis is a pathological condition of the respiratory system characterized by the presence of abnormally and permanently dilated airways. As mentioned in the definitions, the dilation of the bronchi happens only in bronchiectasis and not in bronchitis. This is the key difference between bronchitis and bronchiectasis, which helps to distinguish these two conditions.
CONTENTS
1. Overview and Key Difference
2. What is Bronchitis
3. What is Bronchiectasis
4. Similarities Between Bronchitis and Bronchiectasis
5. Side by Side Comparison – Bronchitis vs Bronchiectasis in Tabular Form
6. Summary
What is Bronchitis?
The inflammation of the bronchial walls is known as bronchitis. There are main two forms of bronchitis, depending on the duration of the symptoms.
Acute Bronchitis
Acute bronchitis in previously healthy subjects is most often due to viral infections. In chronic smokers, bronchitis of acute duration usually occurs due to superimposed bacterial infections. Initially, there is a discomfort behind the sternum along with a non- productive cough. This is a self-limiting condition that is spontaneously resolved within 4-8 days.
Chronic Bronchitis
When there is a persistent cough with mucus production for at least three months in a minimum of two successive years when all the other possible causes have been excluded, that is diagnosed as chronic bronchitis.
Complications of Chronic Bronchitis
- Progression to COPD
- Cor pulmonale and heart failure
- Squamous metaplasia of the respiratory epithelium of airways that can act as precursor lesions of the pulmonary carcinomas.
Pathogenesis
Various inhaled irritants can trigger inflammation of the walls of the bronchi giving rise to numerous pathological changes. These irritants include tobacco smoke, SO2, NO2 and different other environmental pollutants.
Inflammation of the bronchial walls
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Hypertrophy and hyperplasia of the submucosal glands along with the proliferation of goblet cells in the respiratory epithelium
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Mucus production increases due to the resultant hypersecretion
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Accumulation of mucus in the airway and the formation of mucus plugs
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Partial or complete occlusion of the airways
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Repeated infections of the respiratory tract
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Acute exacerbations and gradual progression of the disease
Clinical Features
Chronic productive cough is the only manifestation during the initial phase of the disease.
Typically, patients with chronic bronchitis have a relatively low capacity to overventilate and compensate for hypoxemia. Therefore, these patients are hypoxaemic and hypercapnic – blue bloaters.
Pulmonary hypertension, cor pulmonale, and heart failure are the subsequent complications of this disease. In the advanced stages, the patient is more likely to have emphysema as a comorbidity.
Diagnosis
- Chest X-ray
- Examination and culture of sputum
- Pulmonary function tests
Management
- As previously mentioned, acute bronchitis is a self-limiting condition that does not require any treatments.
- The medical interventions undertaken depend on the stage of disease progression.
- Antibiotics may be required to control the superimposed bacterial infections.
- Bronchodilators, corticosteroids, and phosphodiesterase 4 inhibitors are the drugs that are usually prescribed.
What is Bronchiectasis?
Bronchiectasis is a pathological condition of the respiratory system characterized by the presence of abnormally and permanently dilated airways. As a result of chronic inflammation, bronchial walls get thickened and irreversibly damaged. The impairment of the mucociliary transport mechanism increases the risk superimposed infections.
Aetiology
- Congenital defects such as deficiency of bronchial wall elements and pulmonary sequestration
- Obstruction of the bronchial wall due to mechanical causes such as tumors
- Postinfective bronchial damage
- Granuloma formation in conditions such as tuberculosis and sarcoidosis
- Diffuse diseases of the lung parenchyma such as pulmonary fibrosis
- Immunological overresponse in conditions such as post lung transplant
- Immune deficiencies
- Mucociliary clearance defects in diseases such as cystic fibrosis
Clinical Features
- The production of green or yellow color sputum is the only clinical manifestation in mild bronchiectasis
- With the disease progression, the patient can get other serious symptoms such as persistent halitosis, recurrent febrile episodes with malaise and recurrent bouts of pneumonia.
- Clubbing of the fingernails
- During the auscultation, coarse crackles can be heard over the infected regions
- Breathlessness
- Hemoptysis
Investigations
- Chest X-ray – this usually shows the presence of dilated bronchi with thickened walls. Occasionally multiple cysts filled with fluids can also be observed.
- High-resolution CT scanning
- Examination and culture of sputum are essential for the identification of the etiological agent as well as for the determination of the suitable antibiotics that have to be prescribed in the management of the superimposed infections.
- Sinus X –rays – a majority of the patients can have rhinosinusitis too
- Serum immunoglobulins – this test to performed to identify any immunodeficiencies
- Sweat electrolytes are measured if cystic fibrosis is suspected
Treatment
- Postural drainage
- Antibiotics – the type of antibiotic used depends on the causative agent
- It is necessary to use bronchodilators sometimes to avoid the limitations to the airflow
- Anti-inflammatory drugs such as oral or nasal corticosteroids can arrest the disease progression
Complications
- Pneumonia
- Pneumothorax
- Empyema
- Metastatic cerebral abscesses
What is the Similarity Between Bronchitis and Bronchiectasis?
- Both diseases predominantly affect the bronchial walls.
What is the Difference Between Bronchitis and Bronchiectasis?
Bronchitis vs Bronchiectasis
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The inflammation of the bronchial walls is known as bronchitis. | Bronchiectasis is a pathological condition of the respiratory system characterized by the presence of abnormally and permanently dilated airways. |
Airways | |
Airways are not dilated. | Airways are dilated. |
Etiology | |
Chronic smoking is the most common etiology. | Etiological factors include
· Congenital defects such as deficiency of bronchial wall elements and pulmonary sequestration · Obstruction of the bronchial wall due to mechanical causes such as tumors · Postinfective bronchial damage · Granuloma formation in conditions such as tuberculosis and sarcoidosis · Diffuse diseases of the lung parenchyma such as pulmonary fibrosis · Immunological overresponse in conditions such as post lung transplant · Immune deficiencies · Mucociliary clearance defects in diseases such as cystic fibrosis |
Clinical Features | |
Chronic productive cough is the only manifestation during the initial phase of the disease.
Typically the patients with chronic bronchitis have a relatively low capacity to overventilate and compensate for hypoxemia. Therefore, these patients are hypoxemic and hypercapnic – blue bloaters. In the advanced stages, the patient is more likely to have emphysema also as a comorbidity. |
· The production of green or yellow color sputum is the only clinical manifestation in mild bronchiectasis
· With the disease progression, the patient can get other serious symptoms such as persistent halitosis, recurrent febrile episodes with malaise and recurrent bouts of pneumonia. · Clubbing of the fingernails · During the auscultation, coarse crackles can be heard over the infected regions · Breathlessness · Hemoptysis |
Complications | |
Pulmonary hypertension, cor pulmonale, and heart failure are the usual complications of this disease. | Complications of bronchiectasis include
· Pneumonia · Pneumothorax · Empyema · Metastatic cerebral abscesses |
Diagnosis | |
Diagnosis is through chest X-ray, examination, and culture of sputum and pulmonary function tests | Chest X-ray, high-resolution CT scanning, examination and culture of sputum, sinus X –rays and serum immunoglobulins are the investigations that are performed to diagnose the disease.
Sweat electrolytes are measured if cystic fibrosis is suspected. |
Treatment | |
Antibiotics may be required to control the superimposed bacterial infections.
Bronchodilators, corticosteroids, and phosphodiesterase 4 inhibitors are the drugs that are usually prescribed. Acute bronchitis is self -limiting and therefore does not require any treatments. |
The following drugs and procedures are used in the treatment of bronchiectasis
· Postural drainage · Antibiotics – the type of antibiotic used depends on the causative agent · It is necessary to use bronchodilators sometimes to avoid the limitations to the airflow · Anti-inflammatory drugs such as oral or nasal corticosteroids can arrest the disease progression |
Summary – Bronchitis vs Bronchiectasis
Bronchiectasis is a pathological condition of the respiratory system characterized by the presence of abnormally and permanently dilated airways. The inflammation of the bronchial walls is known as bronchitis. The most outstanding morphological difference between bronchitis and bronchiectasis is that dilation of the bronchi happens only in bronchiectasis and not in bronchitis.
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References:
1. Kumar, Parveen J., and Michael L. Clark. Kumar & Clark clinical medicine. Edinburgh: W.B. Saunders, 2009.
2. Kumar, Vinay, Stanley Leonard Robbins, Ramzi S. Cotran, Abul K. Abbas, and Nelson Fausto. Robbins and Cotran pathologic basis of disease. 9th ed. Philadelphia, Pa: Elsevier Saunders, 2010. Print.
Image Courtesy:
1. “Bronchitis” By National Heart Lung and Blood Institute – National Heart Lung and Blood Institute (Public Domain) via Commons Wikimedia
2. “Bronchiectasis” By BruceBlaus – Own work (CC BY-SA 4.0) via Commons Wikimedia