Internal Medicine (Theory) · MU Sofia

2. Chronic obstructive pulmonary disease (COPD);

Covers COPD as a progressive, largely irreversible airflow limitation and its two components, emphysema and chronic obstructive bronchitis. For each, it sets out definition, causes, symptoms, examination findings, laboratory and instrumental tests, and complications. It ends with a side-by-side comparison table contrasting the two conditions, including the pink puffer and blue bloater pictures.

Inside: 4 sections · 7 labelled pictures · 2 tables · 12 flashcards · 6 min

Topic 2 of 58 in the MU Sofia syllabus for Internal Medicine (Theory) (Medicine, Year 3). The free AceMed note covers it in 4 sections, about 637 words (6 min of reading), with 12 flashcards.

In this note

  1. Chronic Obstructive Pulmonary Disease (COPD)
  2. Definition
  3. Pulmonary Emphysema
  4. Chronic Obstructive Bronchitis

Definition

Chronic obstructive pulmonary disease is a progressive, irreversible, obstructive lung disease characterized by persistent respiratory symptoms and airflow limitation, which is not fully reversible even after bronchodilator use. It includes:

  • Pulmonary emphysema: alveolar wall destruction and distal airspace enlargement
  • Chronic obstructive bronchitis: chronic productive cough due to mucus hypersecretion and inflammation

Both conditions often coexist, and patients usually present with overlapping features.

Pulmonary Emphysema

Definition

Emphysema is defined as the abnormal, permanent enlargement of airspaces distal to terminal bronchioles, accompanied by destruction of alveolar walls and capillaries, without significant fibrosis. This leads to air trapping, reduced surface area for gas exchange, and hyperinflated lungs.

Etiology

  • Smoking – chronic exposure leads to neutrophil activation and protease release, damaging alveolar walls
  • α1-antitrypsin deficiency – inherited condition causing lack of protection from elastase → early-onset emphysema
  • Can also occur as a complication of chronic bronchitis, bronchiectasis, or asthma due to long-standing airway inflammation

Symptoms

  • Progressive dyspnea, first on exertion and later at rest – due to loss of elastic recoil and ventilation-perfusion mismatch
  • Mild cough, with minimal sputum – not a major feature
  • Fatigue, decreased exercise tolerance (from poor oxygenation and increased work of breathing)
  • Dyspnea is not relieved in sitting position (distinguishes it from cardiac dyspnea)

Physical Examination

  • Barrel chest – caused by chronic air trapping and hyperinflation
  • Short neck, sometimes prominent neck veins due to accessory muscle use
  • Use of accessory respiratory muscles, often seen during even mild activity
  • Decreased vocal fremitus, hyperresonant percussion – due to overinflated lungs
  • Decreased vesicular breath sounds, prolonged expiration, often with snoring or whistling wheezes
  • In advanced disease: central cyanosis and polycythemia from chronic hypoxia.
  • Pink Puffer

Lab Tests

  • Decreased Hemoglobin, RBC, and hematocrit – from secondary polycythemia due to long-standing hypoxia
  • Decreased ESR – thickened blood from polycythemia slows sedimentation
  • Sputum testing only if infection is suspected

Instrumental Tests

  • Chest X-ray:
  • Hyperinflated lungs
  • Flattened diaphragm
  • Widened intercostal spaces
  • ↑ Retrosternal air space
  • May show ↑ lung markings if coexisting bronchitis is present
  • Spirometry:
  • Obstructive pattern: ↓ FEV1, ↓ FEV1/FVC (<70%)
  • Not significantly reversible with bronchodilators
  • Shows difficulty in exhalation due to alveolar collapse
  • Blood gases:
  • Hypoxemia (↓ pO₂) and hypercapnia (↑ pCO₂) due to poor gas exchange
  • ↓ O₂ saturation especially in advanced cases

Complications

  • Right-sided heart failure (cor pulmonale) – from chronic hypoxic vasoconstriction causing pulmonary hypertension
  • Pneumothorax – may occur if alveolar bullae rupture
  • Frequent respiratory infections – due to poor airway clearance

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