Pathophysiology
• Chronic airway eosinophilic inflammation, bronchial hyperresponsiveness
• Variable, reversible airflow obstruction
Common triggers
• Allergens (house dust mite, pollen, pet dander)
• Cold air
• Exercise
• NSAIDs (aspirin-sensitive asthma)
• Occupational exposures
Monitoring
• Peak expiratory flow rate (PEFR): diurnal variability >20%
• FeNO: elevated suggests eosinophilic inflammation
• O₂: maintain sats 94–98%
• Salbutamol: nebulised or high-dose via MDI + spacer
• Hydrocortisone IV or oral prednisolone
• Ipratropium bromide nebulised (severe)
• Theophylline IV (rarely, consider if poor response)
• Mg²⁺ sulfate IV (for life-threatening or non-responding severe asthma)
• Escalation: consider ICU, possible intubation
Pathophysiology
• Chronic bronchitis ("blue bloater"): productive cough ≥3 months for ≥2 years
• Emphysema ("pink puffer"): alveolar wall destruction → air trapping, hyperinflation
Key features
• Irreversible airflow limitation (post-bronchodilator FEV1/FVC <0.7)
• Hyperinflation on CXR (flattened diaphragm, increased retrosternal space)
Management
• Smoking cessation → most effective
• Bronchodilators:
o SABA or SAMA for relief
o LABA and/or LAMA for maintenance
o ICS (in combination) if frequent exacerbations or high eosinophil count
• Vaccinations: annual influenza, one-off pneumococcal
• Pulmonary rehab
• Use controlled oxygen therapy (e.g., 24–28% via Venturi mask)
• Target SpO₂ 88–92%
Features
• Early-onset panacinar emphysema, especially lower lobes
• Associated liver disease: cirrhosis, hepatocellular carcinoma
• Inheritance: autosomal recessive (PiZZ genotype most severe)
Management
• Smoking cessation critical
• IV augmentation therapy (purified A1AT) in some cases
Indications
• PaO₂ <7.3 kPa on room air
• PaO₂ <8.0 kPa with complications (e.g., polycythaemia, pulmonary hypertension, peripheral oedema)
Administration
• Minimum 15 hours per day, improves survival
• PaO₂ <8 kPa, normal/low PaCO₂
• Causes: pneumonia, pulmonary oedema, PE, ARDS, ILD
• PaO₂ <8 kPa, PaCO₂ >6.5 kPa
• Causes: COPD exacerbation, severe asthma, neuromuscular disease (e.g., Guillain–Barré), chest wall deformity
• Indicated in acute Type 2 RF with acidosis (e.g., pH <7.35, PaCO₂ >6.5)
• Common in COPD exacerbations
• First-line for obstructive sleep apnoea (OSA)
• Also used in acute pulmonary oedema
• Indications:
o Failure of NIV (worsening acidosis or consciousness)
o Respiratory arrest
o Severe hypoxaemia
Extra Revision Pearls
• Asthma: diurnal variability, reversibility clue
• COPD: no full reversibility; consider eosinophil count for ICS
• A1AT deficiency: always think if young smoker with basal emphysema + liver disease
• NIV: do not use if vomiting risk, reduced consciousness, copious secretions
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Author & Educational Disclaimer
Author:
Dr Phillip Cockrell BM FRCP DipClinEd
Dr Phillip Cockrell is a UK Consultant Physician in Internal Medicine, currently working at Queen Alexandra Hospital, Portsmouth University Hospitals NHS Trust. He has previously worked as a registrar across Intensive Care Medicine, Gastroenterology, Cardiology, Stroke Medicine, Acute Medicine, and Respiratory Medicine.
He has held senior leadership roles including Associate Clinical Director of the Acute Medical Unit, Clinical Director of Internal Medicine, and Chief of Medicine. Dr Cockrell has over 15 years’ experience in postgraduate medical education, having lectured extensively across the MRCP syllabus and contributed to MRCP revision teaching and course development.
Dr Cockrell holds a Bachelor of Medicine (BM), Fellowship of the Royal College of Physicians (FRCP), and a Diploma in Clinical Education (DipClinEd). His teaching approach is based on structured consolidation of complex medical topics to support efficient and effective revision for postgraduate examinations.
Purpose of this content:
The material on this page is intended solely for educational purposes to support revision for the MRCP (UK) Part 1 examination. It reflects examination-relevant principles of internal medicine and is designed to aid learning and pattern recognition.
Medical disclaimer:
This content is designed for postgraduate medical examination revision and does not constitute medical advice, diagnosis, or treatment guidance and must not be used as a substitute for professional clinical judgement, local guidelines, or specialist consultation. Clinical decisions should always be made in the context of individual patient circumstances and current national guidance.