chronic obstructive pulmonary disease

Chest X-ray

of an 81 year old man with chronic obstructive pulmonary disease (COPD), presenting with acute COPD exacerbation, mainly productive cough. It shows an opacity in the inferior parts of the right upper lobe. A nasopharyngeal swab detected Haemophilus influenzae.

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Chest X-ray

of an 81 year old man with chronic obstructive pulmonary disease (COPD), presenting with acute COPD exacerbation, mainly productive cough. It shows an opacity in the inferior parts of the right upper lobe. A nasopharyngeal swab detected Haemophilus influenzae.

Wikipedia • CC0

COPD und

CTEPH. Deutlich abgeflachte Zwerchfellkuppen beidseits. Prominente zentrale Pulmonalarterien mit Kalibersprung.

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Radiopaedia • CC-by-nc-sa 3.0 • de

Chronic obstructive pulmonary disease (COPD) represents a spectrum of obstructive airway diseases. It includes two key components which are chronic bronchitis-small airways disease and emphysema.

Epidemiology

The most common cause has historically been, and unfortunately continues to be, smoking. It takes many years of smoking to develop COPD and as such typically patients are older adults. There are however a number of other less common risk factors/etiologies, each with their own demographics. They include:

cigarette smoking
industrial exposure (e.g. mining)
cystic fibrosis
alpha-1 antitrypsin deficiency
intravenous drug use
immune deficiency syndromes
vasculitides and connective tissue disorders

Clinical presentation

Symptoms of COPD include dyspnea on exertion, wheezing, productive cough, pursed-lip breathing, and use of accessory muscles. Patients with chronic bronchitis are classically "blue bloaters," while those with emphysema are known as "pink puffers". In advanced cases, muscle wasting, asterixis, and peripheral edema may be seen.

ECG

poor R wave progression
- requires an R wave in V3 <3 mm
clockwise rotation of the heart secondary to hyperinflation results in a delayed precordial transition zone
- the lead in which the R/S ratio becomes >1, usually occurring in V3 or V4, shifts laterally (to V5 or V6)
- deep S waves in the lateral leads (I, aVL, V5, V6)
low QRS voltage
- amplitude of QRS complexes <5 mm in the limb leads or <10 mm in the precordial leads
right ventricular hypertrophy
- right axis deviation
- dominant R wave in V1 with an amplitude >7 mm
- often associated with "P pulmonale" (right atrial enlargement)
multifocal atrial tachycardia

Pathology

In contrast to asthma, the histologic changes of COPD are irreversible and gradually progress over time. In chronic bronchitis, there is diffuse hyperplasia of mucous glands with associated hypersecretion and bronchial wall inflammation.

Emphysema involves the destruction of alveolar septa and pulmonary capillaries, leading to decreased elastic recoil and resultant air trapping. The morphological subtypes of emphysema include:

centrilobular (centriacinar): associated with smoking and spreads peripherally from bronchioles
panacinar: homozygous AAT1 deficiency and uniformly destroys alveoli
paraseptal (distal acinar): involves the distal airways

Pulmonary function testing (PFT) reveals airflow obstruction, as evidenced by a decreased forced expiratory volume in 1 second to forced vital capacity (FEV1/FVC) ratio. Administration of bronchodilators has no effect, unlike the reversible obstruction seen in asthma.

Severity classification

The global initiative for chronic obstructive lung disease (GOLD) staging system is a commonly used severity staging system based on airflow limitation. According to this, there are 4 key stages with latest revision at time of writing being in 2019 :

stage I: mild, FEV1 > 80% of normal
stage II: moderate, FEV1 = 50-79% of normal
stage III: severe, FEV1 = 30-49% of normal
stage IV: very severe, FEV1 <30% of normal or <50% of normal with presence of chronic respiratory failure present

The FEV1:FVC ratio should be <0.70 for all stages.

The GOLD staging system may be insensitive in early stages .

Quantitative analysis of low attenuation areas can aid in classifying the severity of the disease .

Clinical phenotypes

Several distinct clinical phenotypes have been described :

emphysema predominant
airways predominant
- small airways predominant
- large airways predominant
mixed

Radiographic features

Plain radiograph

Findings of chronic bronchitis on chest radiography are non-specific and include increased bronchovascular markings and cardiomegaly. Emphysema manifests as lung hyperinflation with flattened hemidiaphragms, a small heart, and possible bullous changes. On the lateral radiograph, a "barrel chest" with widened anterior-posterior diameter may be visualized. The "saber-sheath trachea" sign refers to marked coronal narrowing of the intrathoracic trachea (frontal view) with concomitant sagittal widening (lateral view).

CT

Findings of COPD may be seen in a variety of CT chest studies, e.g. contrast-enhanced CT, CT pulmonary angiography, staging CT chest, HRCT chest, etc.

Chronic bronchitis

In chronic bronchitis, bronchial wall thickening may be seen in addition to enlarged vessels. Repeated inflammation can lead to scarring with bronchovascular irregularity and fibrosis.

Emphysema

Emphysema is diagnosed by alveolar septal destruction and airspace enlargement, which may occur in a variety of distributions. Centrilobular emphysema is predominantly seen in the upper lobes with panacinar emphysema predominating in the lower lobes. Paraseptal emphysema tends to occur near lung fissures and pleura. Formation of giant bullae may lead to compression of mediastinal structures, while rupture of pleural blebs may produce spontaneous pneumothorax/pneumomediastinum.

Complications

Exacerbations

exacerbation of COPD
- infective exacerbation of COPD
- non-infective exacerbation of COPD

Treatment and prognosis

Barring whole-lung transplantation, there is currently no cure for COPD, but it is highly preventable and treatable.

Lifestyle measures

Risk factor reduction via smoking cessation, occupational health, and air pollution reduction should be instituted. Patients should also have all available vaccinations.

Pharmacology

Pharmacological management is generally first-line. It involves the use of bronchodilators, corticosteroids, and other medications (e.g. methylxanthines, leukotriene receptor antagonists, phosphodiesterase type-4 inhibitors, omalizumab), as well as supplemental oxygen and pulmonary rehabilitation. Long-acting β2-agonist (LABA) and long-acting muscarinic antagonist (LAMA) combination therapies are currently considered the most effective strategy .

Acute exacerbations are treated with high-dose corticosteroids, short-acting bronchodilators, supplemental oxygen, and antibiotics if indicated.

Surgery

Surgical therapy is usually reserved for COPD refractory to pharmacological management. In addition to the aforementioned whole-lung lung transplant, other surgical procedures include: