Standard pre‑examination protocol – must be demonstrated:
Action: Introduce yourself, explain examination, obtain verbal consent.
Key observations – “Bronchiectasis” clues:
Inspection findings in bronchiectasis:
Palpation findings in bronchiectasis:
Percussion findings in bronchiectasis:
Auscultation findings in bronchiectasis:
Systematic GPE – identify aetiology & complications:
Assess developmental regression and associated features:
📋 Case Presentation – (fill in during exam)
I have examined _____, _____ years old who is conscious and cooperative, having _____ built and a cannula in his _____ arm. He is _____ (pink / cyanosed) in room air with _____ (no / signs of) respiratory distress or dysmorphism.
His respiration is _____ (abdominothoracic / thoracic) with a rate of _____ per minute.
Inspection: Chest is _____ (normal in shape / barrel‑shaped). There are no scars, prominent veins or Harrison sulcus. He has _____ (no mediastinal shifting / mediastinal shift) as evident by _____ (central trachea / tracheal shift). Apex beat is in _____ ICS about _____ cms lateral to midclavicular line.
Palpation: Superficial palpation reveals no tenderness. My findings are bilateral in the form of slightly reduced chest expansion and normal vocal fremitus.
Percussion: Normal / Hyperresonant percussion note bilaterally.
Auscultation: Vesicular breathing with coarse crackles bilaterally (more prominent in dependent areas) and normal vocal resonance.
Back: Back is normal in shape with no visible deformity and similar findings are found in the infrascapular areas.
He is _____ (afebrile / febrile), Pulse is _____ beats/min, regular in rhythm and normal in volume and character, BCG scar mark is _____ (present / absent), throat is normal.
There is no evidence of cyanosis, clubbing, lymphadenopathy, rash and oral ulcers.
I would like to know his height and weight.
I want to see his chest X-ray.
• Bronchiectasis – cystic fibrosis, PCD, post‑infective
• Cystic fibrosis – sweat chloride, pancreatic insufficiency
• Primary ciliary dyskinesia (Kartagener's) – situs inversus, sinusitis
• Immunodeficiency – recurrent infections
• Foreign body aspiration – focal bronchiectasis
• Tuberculosis – post‑TB bronchiectasis
• Allergic bronchopulmonary aspergillosis – asthma, eosinophilia
• Alpha‑1 antitrypsin deficiency – emphysema + bronchiectasis
• Connective tissue disorders – rheumatoid, SLE
• Chest X-ray – tram‑tracking, crowding, cystic spaces
• High‑resolution CT (HRCT) – gold standard; shows bronchial dilatation
• Sputum culture & sensitivity – identify organisms
• Complete blood count, CRP, ESR – infection / inflammation
• Pulmonary function tests – obstructive pattern
• Bronchoscopy – if foreign body / localized disease
• Sweat chloride test – cystic fibrosis
• Immunoglobulin levels (IgG, IgA, IgM, IgE) – immunodeficiency
• Ciliary biopsy / saccharin test – PCD
• Mantoux test / gastric aspirate – TB
• Alpha‑1 antitrypsin levels – deficiency
• Autoantibodies (ANA, RF) – collagen vascular
• Aspergillus precipitins / IgE – ABPA
• Pulmonary function tests (VC, MIP) – respiratory failure
• Autonomic function – BP/HR monitoring
• Swallow study – aspiration risk
• DVT prophylaxis – Doppler if immobile
• ECG / echocardiography – cor pulmonale
🔹 Management – Across Organ Systems
Chest physiotherapy (postural drainage, percussion), bronchodilators, mucolytics. Oxygen if hypoxic.
Antibiotics for exacerbations (culture‑guided), prophylactic antibiotics (if recurrent).
Immunoglobulins (if deficiency), anti‑inflammatory (if ABPA / CF).
Lobectomy (if localized disease), lung transplantation (if end‑stage).
High‑calorie feeds (chronic illness), pancreatic enzymes (if CF).
Respiratory therapy, dietitian, physiotherapy, social work.
📈 Prognosis
📋 Follow‑up Schedule