Exhaustive Notes on Respiratory Medicine: Anatomy, Physiology, and Disease

Clinical Examination of the Respiratory System

  • General Observation:

    • Hands: Check for digital clubbing, tar staining (nicotine), peripheral cyanosis, and signs of occupation. Look for a CO2CO_2 retention flap and assess the radial pulse for rate and rhythm.

    • Blood Pressure: Monitor for arterial paradox.

    • Neck: Assess the Jugular Venous Pulse (JVP) for elevation or pulsatile nature.

    • Face, Mouth, and Eyes: Look for pursed-lip breathing, central cyanosis, anaemia (conjunctival pallor), and Horner syndrome.

    • Trachea: Ensure the trachea is central; measure the cricosternal distance (< 3 finger breadths suggests hyperinflation).

    • Legs: Check for leg oedema (suggests salt/water retention, cor pulmonale, or venous thrombosis).

    • General State: Note respiratory rate, cachexia (weight loss), fever, rash, sputum characteristics, and fetor (breath odour).

  • Thoracic Examination (Palpation, Percussion, and Auscultation):

    • Inspection: Look for deformity (e.g., pectus excavatum, kyphoscoliosis), scars, intercostal indrawing, symmetry of expansion, hyperinflation, and paradoxical rib movement (indicates a low, flat diaphragm).

    • Palpation: Assess for cardiac apex displacement, cervical lymphadenopathy, and expansion symmetry (from both front and back).

    • Percussion: Differentiate between resonant, dull (consolidation), and "stony dull" (pleural effusion).

    • Auscultation:

      • Breath sounds: Identify normal, bronchial, louder, or softer sounds.

      • Added sounds: Wheezes (obstruction), crackles (fluid/fibrosis), and rubs (pleurisy).

      • Vocal resonance: Absent in effusion; increased in consolidation.

      • Whispering pectoriloquy: Whispered voice heard clearly through a stethoscope over consolidation.

  • Sputum Types:

    • Serous/Frothy/Pink: Indicates pulmonary oedema.

    • Mucopurulent: Indicates bronchial or pneumonic infection.

    • Purulent: Indicates established bronchial or pneumonic infection.

    • Blood-stained: Potential cancer, tuberculosis, bronchiectasis, or pulmonary embolism.

Functional Anatomy and Physiology

  • Anatomy:

    • Diaphragm: Innervated by the phrenic nerves (C3C3, C4C4, and C5C5).

    • Pleura: Parietal and visceral layers facilitate sliding contact; negative pressure in the pleural space balances elastic recoil.

    • Conducting Airways: Total cross-section is smallest at the glottis and trachea, making them vulnerable to obstruction. Air is filtered, heated, and saturated with water vapour in the nose.

    • Gas-Exchange Unit: The acinus comprises branching respiratory bronchioles and clusters of alveoli. The gas-to-blood distance is < 0.4\,’…m.

    • Alveolar Cells: Type I pneumocytes (flattened epithelial) and Type II pneumocytes (cuboidal; produce surfactant to reduce surface tension and prevent collapse).

  • Control of Breathing:

    • Originates in the respiratory motor neurons of the posterior medulla oblongata.

    • Central Chemoreceptors: Located in the ventrolateral medulla; sense cerebrospinal fluid (CSF) pHpH and are stimulated by arterial PCO2PCO_2 rise.

    • Carotid Bodies: Sense hypoxaemia; primarily activated when arterial PO_2 < 8\,kPa (60mmHg60\,mmHg).

  • Ventilation and Perfusion (V/QV/Q):

    • Hypoxia constricts pulmonary arterioles to match perfusion to ventilation; airway CO2CO_2 dilates bronchi.

    • Pulmonary Circulation: Operates at low pressure (approx. 24/9mmHg24/9\,mmHg). Hypertension occurs if vessels are destroyed (emphysema) or obstructed (thrombus).

Investigation of Respiratory Disease

  • Imaging:

    • Chest X-ray (CXR): Standard is Posteroanterior (PA). Count ribs to check for hyperinflation (> 10 ribs visible posteriorly). Look for consolidation (shadowing with air bronchogram) or collapse (mediastinal shift toward the side of volume loss).

    • Computed Tomography (CT): High-resolution thin-section scans assess parenchymal disease, bronchiectasis, and emphysema. CT Pulmonary Angiography (CTPA) is the gold standard for pulmonary thromboembolism.

    • Positron Emission Tomography (PET): Uses radiotracer 18F-fluorodeoxyglucose (FDG)^{18}F\text{-fluorodeoxyglucose (FDG)} to quantify glucose metabolism. Assessment uses the Standardised Uptake Value (SUV).

    • Ultrasound: Distinguishes fluid from thickening; guides pleural asipiration or biopsy.

  • Respiratory Function Testing:

    • Spirometry: Measures Forced Expired Volume in 1 second (FEV1FEV_1) and Forced Vital Capacity (FVCFVC). Obstructive defect is defined as an FEV1/FVCFEV_1/FVC ratio < 70\%.

    • Reversibility: Defined as an increase of > 12\% and > 200\,mL in FEV1FEV_1 or FVCFVC after bronchodilators.

    • Lung Volumes: Helium dilution (measures gas mixing with tidal breaths) or body plethysmography (measures total intrathoracic gas).

    • Diffusion Capacity: Measured as Carbon Monoxide Transfer Factor (TLCOTLCO) or KCOKCO (transfer factor per unit lung volume).

Presenting Problems

  • Cough:

    • Acute: Viral infection, aspiration, or post-nasal drip.

    • Chronic: COPD, asthma, GORD, ACE inhibitor usage, or lung cancer.

    • Bovine Cough: Prolonged, low-pitched, inefficient cough caused by vocal cord palsy (recurrent laryngeal nerve involvement).

  • Breathlessness (Dyspnoea):

    • Pathophysiology: Stimulated by sensory nerves (pneumothorax), mechanical load (fibrosis/obstruction), or metabolic triggers (CO2CO_2, acidosis, hypoxia).

    • Nijmegen Questionnaire: Used to assess breathing pattern disorders (psychogenic hyperventilation; score > 26 is significant).

  • Finger Clubbing: Symmetrical painless swelling. Common causes include lung cancer, bronchiectasis, cystic fibrosis, and idiopathic pulmonary fibrosis (IPF).

  • Haemoptysis: Major causes include bronchial cancer, bronchiectasis, tuberculosis, and pulmonary infarction. Massive haemoptysis may require bronchial artery embolisation.

  • Pleural Effusion: Accumulation of fluid in the pleural space.

    • Light's Criteria (Exudate vs. Transudate): Exudate if Protein ratio > 0.5, LDH ratio > 0.6, or pleural LDH > 2/3 of upper limit of normal serum LDH.

    • Common Causes: Transudates (Heart/liver/renal failure); Exudates (Pneumonia, TB, malignancy, pulmonary infarction).

    • Empyema: Collection of pus; diagnosed by pH < 7.2, glucose < 3.3\,mmol/L, and high LDH.

Obstructive Pulmonary Diseases

  • Asthma:

    • Chronic inflammatory disorder with airway hyper-responsiveness (AHR).

    • Immediate Assessment of Severe Asthma: PEF 3350%33--50\% predicted, Heart Rate 110 bpm\ge 110\text{ bpm}, Respiratory Rate 25 breaths/min\ge 25\text{ breaths/min}.

    • Management: Stepwise approach from Step 1 (Low-dose inhaled glucocorticoid (ICS)) to Step 5 (Biologics like Omalizumab or Mepolizumab).

  • Chronic Obstructive Pulmonary Disease (COPD):

    • Spectrum of Chronic Bronchitis (cough/sputum for 33 months in 22 years) and Emphysema (alveolar destruction).

    • BODE Index: Predicts mortality based on BMI (BB), Obstruction (OO), Dyspnoea (DD), and Exercise capacity (EE).

    • Oxygen Therapy (LTOT): Indicated if PaO_2 < 7.3\,kPa or 7.38kPa7.3--8\,kPa with cor pulmonale symptoms, polycythaemia, or hypertension.

  • Cystic Fibrosis (CF):

    • Autosomal recessive; Chromosome 7; mutation in CFTRCFTR gene (most common: ΔF508\Delta F508). Causes thick secretions, bronchiectasis, malabsorption, and male infertility.

Infections of the Respiratory System

  • Pneumonia:

    • CURB-65 Score: Confusion, Urea > 7\,mmol/L, Respiratory Rate 30/min\ge 30/min, Blood Pressure (sBP < 90 or dBP60dBP \le 60), Age 65\ge 65. Score 3+3+ indicates severe pneumonia.

    • Hospital-Acquired Pneumonia (HAP): Presents 48hours\ge 48\,hours after admission.

  • Tuberculosis (TB):

    • Caused by Mycobacterium tuberculosis. Primary infection forms a "Ghon focus" which spreads to hilar nodes (Ranke complex).

    • Treatment: 6-month regimen (2 months of HRZE: Isoniazid, Rifampicin, Pyrazinamide, Ethambutol; followed by 4 months of HR).

Pulmonary Vascular Disease

  • Pulmonary Embolism (PE):

    • Wells Score: Used to estimate clinical probability. Likelihood > 4\text{ points} warrants immediate CTPA.

    • Management: Anticoagulation (LMWH, DOACs). Thrombolysis is reserved for massive/haemodynamically unstable PE.

  • Pulmonary Hypertension (PH):

    • Defined as mean pulmonary artery pressure > 25\,mmHg at rest. Classifications: Type I (Arterial), Type II (Left Heart), Type III (Lung Disease), Type IV (CTEPH).