Respiratory Flashcards
Describe/draw the flow volume curves of normal, restrictive and obstructive lung disease

What is restrictive lung disease?
Pulmonary fibrosis that decreases lung volume and increases work of breathing with inadequate ventilation
- Low FEV1
- Low FVC
- Normal FEV1/FVC ratio
Name some causes of restrictive lung disease
- Pneumoconiosis
- Pulmonary fibrosis
- TB
- Chest wall disease (kyphoscoliosis)
- Weak respiratory muscles
- Sarcoidosis
- RA
What is obstructive lung disease?
Narrowing of airways due to excessive smooth muscle contraction
- Normal FVC
- Low FEV1
- Low FEV1/FVC ratio (<0.7)
Name some causes of obstructive lung disease
- Chronic bronchitis
- COPD
- Asthma
- Bronchiectasis
- CF
Describe/draw the spirometry curve of normal, obstructive and restrictive lung disease

What is respiratory failure?
When gas exchange in the lungs is inadequate which results in hypoxia. It is defined as pO2 < 8kPa. Divided into:
- Type 1 - normal or low pCO2
- Type 2 - high pCO2
Name some causes of Type 1 respiratory failure
Mainly ventilation perfusion mismatch
- Pneumonia
- Pulmonary oedema
- PE
- Asthma
- Pneumothorax
- Fibrosing alveolitis
- ARDS
Name some causes of Type 2 respiratory failure
Alveolar hypoventilation
- Pulmonary disease - COPD, fibrosis,
- Reduced respiratory drive - Opiates, CNS tumour, trauma
- Neuromuscular disease - Cervical cord lesion, diaphragmatic paralysis, myasthenia gravis
- Thoracic wall disease - flail chest, kyphoscoliosis
Describe the effects of hypoxia (Type 1 and 2 respiratory failure)
- Impaired CNS function
- Confusion
- Agitation
- Dyspnoea
- Restlessness
- Central cyanosis
- Pulmonary hypertension
- Cardiac arrhythmia
Describe the effects of hypercapnia (Type 2 respiratory failure)
- Headache
- Peripheral vasodilation
- Tachycardia
- Bounding pulse
- Tremor/flap
- Papilloedema
- Confusion
- Drowsiness
- Coma
How is respiratory failure investigated?
- Bloods
- FBC
- U&E
- CRP
- ABG
- CXR
- Sputum culture (if febrile)
- Spirometry
How is respiratory failure managed?
- Treat underlying cause
- Airway maintenance
- Clearance of secretions
- Oxygen by face mask
- Assisted ventilation (CPAP/BIPAP) if pO2 < 8 kPa
- Intubation
What is asthma?
A chronic inflammatory disorder characterised by increased responsiveness of the bronchi to various stimuli, causing reversible airway obstruction
- Airway hyperresponsiveness
- Increased mucosal inflammation
- Hypersecretion of mucus
Describe the symptoms of asthma
- Intermittent dyspnoea
- Wheeze
- Cough (often nocturnal)
- Sputum production
- Exercise intolerance
Name some asthma precipitants
- Allergens (pollen, house dust mites, animals)
- Smoke
- Stress
- Exercise
- VIral infections
- Drugs - NSAIDs, aspirin, beta blockers
Name the clinical signs of asthma
- Tachypnoea
- Audible polyphonic wheeze
- Hyper-inflated chest
- Hyper-resonant percussion
- Diminished air entry
How is asthma investigated?
- Peak expiratory flow monitoring
- Obstructive spirometry result
- Improvement of FEV1 by 12% with beta agonist
- CXR
- Skin prick test - identify triggers
- Fractionated exhlaed FeNO test (>40)
- Bronchial provocation - inhalation of increase dose of histamine until FEV1 declines by 20%
Describe the guidelines to treating chronic asthma
- Short acting inhaled B2 agonist
- Add inhaled low dose steroid (beclometasone 100-400microg/12hrs)
- Add leukotriene receptor antagonist (montelukast)
- Add long acting B2 agonist (salmeterol 50microg/12hrs)
- Increase dose of steroids (up to 1000) / oral theophylline / oral B2 agonist / oral leukotriene receptor antagonist
Continue until no daytime symptoms, no limitations on activity, no exacerbations, no night-time awakening and normal lung function
Describe the emergency treatment of acute severe asthma
- Oxygen via non-rebreathe bag (15L)
- Aim for 94-98% sats
- Salbutamol 5mg delivered with oxygen
- Hydrocortisone 100mg IV or prednisolone 30mg PO
- Continue for 5 days
- Add ipatropium bromide 0.5mg nebuliser
- CXR to exclude pneumothorax
- If life-threatening: add magnesium sulphate 1.2-2mg IV over 20 min
- Salbutamol nebulisers every 15 min
Name some ADRs of B2 agonists
- Muscle tremor
- Tachycardia
- Palpitations
- Arrhythmias
- Hypokalaemia
- Headache
What is chronic bronchitis?
Chronic mucosal inflammation, mucus gland hypertrophy and mucus hypersecretion
What is emphysema?
Progressive destruction of the alveolar septa and capillaries producing enlarged spaces (bullae) with decreased compliance and increased collapsibility
What is COPD?
An irreversible expiratory airflow obstruction. hyperinflation, mucus hypersecretion and increased work of breathing. Includes chronic bronchitis and emphysema.
What signs differentiate COPD with asthma?
- Age of onset > 35
- Smoking related
- Chronic dyspnoea
- Sputum production
- No diurnal variation
What are pink puffers and blue bloaters?
Pink puffers:
- Purse lipped breathing
- Normal PO2 and normal/low CO2
- Barrel chest
- Dyspnoea
Blue bloater:
- Dec alveolar ventilation
- Low PO2 and high PCO2
- Cyanosed but not breathless
- Rely on hypoxic drive
Name some symptoms of COPD
- Cough
- Sputum production
- Dyspnoea
- wheeze
Name some signs of COPD
- Use of accessory muscles
- Hyperinflation
- Dec. expansion
- Resonant on percussion
- Cyanosis
- Cor pulmonale
What are the risk factors for developing COPD?
- Male
- Age > 50
- Smoking
- Asthma
- Childhood chest infections
- Low SES
- A1 anti trypsin deficiency
- Heavy metal exposure
Describe some investigations into COPD
- CXR
- Hyperinflation (>6 ant. ribs seen above diaphragm in mid-clavicular line)
- Flat hemidiaphragm
- Large pulmonary arteries
- ECG - cor pulmonale (hypertrophy)
- ABG - low PO2 +/- high PCO2
- Spirometry - irreversible airway obstruction (FEV1/FVC < 0.7)
Name some complications of COPD
- Acute exacerbations
- Infection
- H influenzae most common in COPD
- Polycythaemia
- Cor pulmonale
- Respiratory failure
- Lung cancer
- Pneumothorax
How is the severity of COPD assessed?
- Mild = FEV1 60-80% predicted
- Moderate = FEV1 40-59% predicted
- Severe = FEV1 < 40% predicted
Describe the guidelines to treating chronic COPD
- Non pharmacological - smoking cessation, regular exercise, diet, flu vaccine
- Pulmonary rehabilitation
- Oxygen therapy
- Long acting inhaled B2 agonists (salmeterol)
- Inhaled steroid if FEV1 < 50%
- Inhaled ipatromium (LAMA)
- Surgery
- Lung volume reduction
- Transplant
Name some side effects of steroids
CUSHINGOID
- Cataracts
- Ulcers
- Skin: striae, bruising, thinning
- Hypertension / hirsutism / hyperglycaemia
- Infections
- Necrosis (avascular necrosis of the femoral head)
- Glycosuria
- Osteoporosis / obesity
- Immunosuppression
- Diabetes
What is cor pulmonale?
Right heart failure caused by chronic pulmonary hypertension
How is pulmonary hypertension investigated?
- Bloods - Hb, ABG, LFTs, autoantibodies, HIV
- CXR
- Enlarged right atrium and ventricle
- Prominent pulmonary artieries
- Parenchymal disease?
- ECG
- RIght axis deviation
- Right ventricular hypertrophy
- Echo
What is sarcoidosis?
Multi system immune deposits characterised by non-caseating granulomas and an abnormal, antigen-triggered CD4 T cell response.
Unknown aetiology.
Name some clinical features of sarcoidosis
- Acute = erythema nodosum, arthralgia, fever, bihilar lymphadenopathy
- Constitutional = fatigue, malaise, weight loss
- Resp = Non productive cough, dyspnoea, pain, decrease exercise tolerance
- Eye = uveitis, conjunctivitis
- Neuro = neuropathy, meningitis
- Cardiac = arrhythmia, heart failure
- Gastro = hepato/splenomegaly
- Renal impairment
How is sarcoidosis diagnosed?
- CXR - bihilar lymphadenopathy, upper lobe fibrosis, pulmonary infiltrates
- Tissue biopsy - non-caseating granuloma
- Bloods - FBC, biochemistry, Ca, LFT, SACE
- Lung function test - normal or restrictive
- Mantoux - exclude TB
- Slit lamp examination
- Bronchoalveolar lavage - Inc lymphocytes
How is sarcoidosis managed?
- Acute - bed rest, NSAIDs
- Steroids (4-6 weeks) if:
- Parenchymal lung disease
- Uveitis
- Hypercalcaemia
- Neuro or cardio involvement
- Immunosuppression (methotrexate, azathioprine, cyclosporin)
- Transplant
Name some differentials for granulomatous diseases
- TB
- Sarcoidosis
- Vasculitis (Wegeners)
- Crohns
- Extrinsic allergic alveolitis
- Syphilis
How can PEs be prevented?
- Compression stockings
- Heparin to all immobile patients
- Stop HRT / OCP
- Investigations for thrombophilia
- Encourage mobilisation
What is interstital lung disease?
Inflammation and/or fibrosis of the pulmonary intersitium caused by inhalation of allergens which provokes a hypersensitivity reaction or is idiopathic.
With chronic exposure, granulomas and obliterative bronchiolitis occur
How is interstital lung disease classified?
- Idiopathic Interstital Pneumonias
- Usual Interstital Pneumonias / Idiopathic Pulmonary Fibrosis = minimal inflammation with fibrosis
- Non-Usual Interstital Pneumonias = more diffuse pulmonary involvement with less fibrosis
- Non-idopathic causes
- Drug-induced = nitrofurantoin, bleomycin, amiodarone
- Hypersensitivity (extrinsic allergic alveolitis)
- Connective Tissue Disease = RA/vasculitis
- Occupational lung disease = pneumoconiosis/asbestosis
- Granulomatosis (sarcoidosis)
- Other causes
- Infiltrative (amyloidosis)
- Malignant
- Post-infective (HIV)
What are the clinical features of ILD?
- Dyspnoea
- Dry cough
- Weight loss
- Type 1 respiratory failure
- Clubbing
- RHF and hypoxaemia if advanced
How is ILD diagnosed?
- History - drugs, occupation, CTD, sarcoidosis
- Bloods - rheumatoid factor, Inc ESR, neutrophilia
- Serology - positive precipitans
- Pulmonary function tests - Restrictive deficit with dec TLC, dec FRC and dec RV
- CXR - mid-zone mottling/consolidation, hilar lymphadenopathy, upper-zone fibrosis, honeycomb lung
- Decreased gas transfer
- Broncholaveolar Lavage - inc lymphocytes and mast cells
- Biopsy (non-IUP)
How is ILD treated?
- Oxygen therapy
- Pulmonary rehab
- Smoking cessation
- Avoid allergens
- Pharmacological
- Steroids (non-IUP)
- Immunosuppressants (azathioprine / methotrexate)
- Lung transplant
NB: non-IUP = low dose prednisolone, azathioprine, N-acetylcysteine
Name some causes of hypersensitivity pneumonitis / EAA
- Mouldy hay (thermophilic actinomycetes) - Farmers Lung
- Compost - Mushroom Workers Lung
- Feathers / excreta - Pigeon Fanciers Lung
- Contaminated water (klebseilla) - Humidifiers Fever
Describe Coal Worker’s Pneumoconiosis
Inflammatory reaction to the presence of coal dust in the lungs
- Weakens bronchiolar walls to cause emphysema
- Irreversible airflow limitation
- Dec TLC
- Dec compliance
- Dec gas transfer
- Limited treatment
Describe asbestosis
Fibrosing lung disease caused by inhalation of asbestos particles
- Presents with progressive dyspnoea, inspiratory basal crackles and clubbing
- Restrictive deficit with dec gas transfer
- Predisposes to mesothelioma
- No treatment available
Describe the x-ray appearance of asbestosis
- Diffuse streaky shadows
- Thickened visceral pleura
- Honeycombing in lower lobes

Descrbe the x-ray appearance of extrinsic allergic alveolitis / hypersensitivity pneumonitis
- Fluffy nodular shadowing
- Ground glass opacity
- Honeycomb lung

Name some indications for mechanical ventilation
Prevent type 2 respiratory failure:
- Surgery
- Respiratory centre depression (PCO2 > 7-9kPa)
- Head injury
- Opiate overdose
- Raised intracranial pressure
- Lung disease
- Pneumonia
- ARDS
- Severe asthma
- Exacerbation of COPD
- Cervical cord damage above C4
- Neuromuscular disorders
- Chest wall disorders
- Cardiac arrest
Describe the different types of mechanical ventilation
- Intermittent Positive Pressure Ventilation = air is driven into lungs by raising airway pressure via a tracheostomy tube
- Expiration = pressure falls to 0
- Positive End-Expiratory Pressure = IPPV but positive airway pressure is maintained during expiration
- Continuous Positive Airway Pressure = standing pressure applied to a facemask during spontaneous breathing
- Biphasic Positive Airway Pressure = maintains pressure during inspiration and expiration
- Non-Invasive Intermittent Positive Pressure Ventilation - IPPV delivered by face/nasal mask
Name some complications of using mechanical ventilation
- During intubation
- Aspiration of gastric contents
- Laryngospasm
- Of intubation
- Intubation of oeseophagus / bronchus
- Laryngeal / tracheal damage or stenosis
- Sedation
- Cardiac depression
- Respiratory depression
- Mechanical ventilation
- Barotrauma
- Pneumothorax
Name some indications for the use of oxygen therapy
- Cardiac / respiratory arrest
- Hypoxia (pO2 < 8kPa)
- Hypotension (systolic BP < 100mmHg)
- Low cardiac output
- Metabolic acidosis (bicarp < 18mmol/L)
- Respiratory distress (RR > 24)
What blood concentration of oxygen is aimed for?
- Normal patients = SaO2 of 94-98%
- Risk of type 2 respiratory failure = SaO2 of 88-92%
- COPD
- If increased, risk of CO2 retention, dec ventilation and acidosis
Describe the different delivery methods of oxygen and which groups of patients they are appropriate for
- High dose (>60%) by non-rebreathe, resvoir mask at 10-15 L/min
- Cardiac arrest
- Shock
- Sepsis
- CO poisoning
- Moderate dose (40-60%) by nasal cannulae at 2-6 L/min
- Pneumonia
- Low dose (24-28%) by Venturi mask
- CO2 retention
- COPD
- Neuromuscular disease
- Cystic fibrosis
What are the risks of using oxygen therapy?
- CO2 retention
- COPD patients
- Rebound hypoxaemia (if suddenly withdrawn)
- Absorption collapse / atelectasis
- Toxicity
- ARDS
- Coronary / cerebro vasospasm
- Burns (in smokers)
- Cerebral vasoconstriction and epileptic fits (Paul-Bert effect)
What are the classifications of pneumonia?
- Community acquired - within 48 hours of hospital admission in patients that had not been hospitalised for 14 days
- Hospital acquired - > 2 days after admission
- Aspiration (stroke, myasthenia gravis, dec. consciousness, oesophageal disease)
- Opportunistic - immunosuppressed patients
- Recurrent - CF, bronchiectasis
Name some risk factors for contracting pneumonia
- Age > 65
- Chronic disease
- Diabetes
- COPD
- Immunosuppression/compromised
- Steroids
- Alcohol dependency
- Malnutrition
- Mechanical ventilation
- Post-operative
- IVDU
Name the commin causative agents of CAP
- Strep pneumoniae
- Haemophilus influenza
- Klebsiella pneumoniae
- Influenza
- Mycoplasma
- Aspergillus
What are the clinical features of pneumonia?
- General - fever, malaise, rigors, myalgia
- Chest - dyspnoea, pleurisy, cough, haemoptysis
- Cyanosis
- Tachypnoea
- Tachycardia
- Confusion
- Auscultation - focal dullness, crepitations, bronchial breathing, pleuritic rub
- Hypotension
What investigations are needed for pneumia?
- Bloods - FBC, CRP, LFTs, ABG, U&Es, cultures
- CXR - lobar infiltrates, cavitations, pleural effusion
- O2 sats
- Other cultures - sputum, pleural fluid, bronchoalveolar lavage
- Serology (virus/atypical organism)
How is the severity of pneumonia assessed?
CURB 65 score
- Confusion (mental test < 8)
- Urea > 7 mmol/L
- RR > 30/min
- Systolic BP <90 or diastolic BP < 60
- Age > 65
Score > 1 indicates severe pneumonia
What is the general management of pneumonia?
- Antibiotics
- Oxygen (keep pO2 > 8kPa and sats > 92%)
- IV fluids
- Paracetemol if pleurisy
- Sputum clearance
- Ventilatory support (CPAP)
- ITU if severe or failure to imrpove, shock or hypercapnic
Describe the antibiotic treatment regimes for the different types of pneumonia
- CAP - amoxicllin 500mg/8hr or erythromycin 500mg/6hr
- Severe - IV Co-amoxiclav or cephalosporin AND erythromycin
- Legionella - clarithromycin 500mg/12hr
- Chlamydia - tetracycline
- Gram negative - IV aminoglycoside
Name some complications of pneumonia
- Respiratory failure
- Hypotension due to dehydration / septic vasodilation
- Atrial fibrillation
- Pleural effusion
- Empyema
- Lung abscess (cavitating area of infection)
- Sepsis
- Pericarditis
What are the risks of developing hospital acquired pneumonia?
Oropharyngeal colonisation with enteric gram negative bacteria due to:
- Immobilisation
- Impaired consciousness
- Instrumentation
- Poor hygiene
- Inhibition of gastric acid (aspiration)
Name some common organisms for HAP
- Staph aureus
- CAP organisms
- MRSA
- Gram negative bacilli
Name some causes of pneumothorax
- Primary (idiopathic) mainly in young men
- Secondary
- COPD
- Asthma
- TB
- Pneumonia
- HCTD
- Carcinoma
- Fibrosis
- Traumatic
What are the clinical features of pneumothorax?
- Sudden breathlessness
- Sharp pleuritic pain
- Reduced air entry
- Hyperresonant percussion
- Cyanosis
- Tachycardia
- Respiratory failure
- Hypertension
How is pneumothorax investigated?
- CXR (if tension not suspected) = area devoid of lung markings
- ABG = respiratory failure
How is pneumothorax managed?
- Oxygen
- Analgesia
- If >2cm and/or breathless = aspirate in 2nd intercostal space mid-clavicular with 16-28G cannula
- If unsuccessful - chest drain in 5th intercostal space in axilla
Describe the pathogenesis of TB
- Primary = inital infection by inhaling acid-fast bacill (mycobacterium tuberculosis) affecting the upper lobes
- Granuloma (Ghon focus) and enlarged hilar lymph nodes = Ghon complex
- Post-primary = if Ghon focus fails to heal due to poor defences or following immunocompromised reactivation (HIV, malignancy, diabetes, steroids)
- Lung lesions fibrose
- Local dissemination
- Bloodborne spread
What are the clinical features of pulmonary TB?
- Primary
- Fever
- Erythema nodosum
- Small pleural effusions
- Lymphadenopathy
- Wheeze
- Post-primary
- Malaise
- Weight loss
- Night sweats
- Productive cough
- Dyspnoea
- Chest pain
- Haemoptysis
- Pneumonia
How is TB diagnosed?
- Sputum sample for MC+S (acid fast bacillus / Ziehl-Neilson stain)
- Other relevant samples for culture - pleural fluid, urine, pus, ascites etc
- Histology - caseating granuloma
- CXR - consolidation, cavitation, fibrosis, calcification
- Immunological tests
- Mantoux (>10mm)
- Tuberculin skin test - cell-mediated response to intradermal TB antigen
- Heaf (screening)
- Bloods - anaemia, dec Na+, inc Ca2+
How is TB managed?
- Isolation
- Notify communicable diseases practitioner
- Inital antiobiotics (RIPE) for 2 months
- Rifampicin
- Isoniazid (+ pyridoxine / vit B6)
- Pyrazinamide
- Ethambutol
- Continuation antibiotics (4 months)
- Rifampicin
- Isoniazid (+ pyridoxine / vit B6)
Name some side effects of the antibiotics treatment of TB. How are these monitored?
- Rifampicin - hepatitis, orange discolouration of urine and tears (contact lens staining), inactivation of OCP
- LFTs
- Isoniazid - hepatitis, neuropathy, vit B6 deficiency
- Ethambutol - optic neuritis
- Ishihara (colour) chart
- Pyrazinamide - hepatitis, arthralgia
Name some complications of TB
- Reactivation when immunocompromised
- Bronchiectasis
- Lung cavities
- Cranial nerve lesions
- Renal tract obstruction
- Multi-drug resistance
How do you present a chest x-ray?
DRSABCDE
- Details - Patient details, type of film (AP) date and time
- RIE (image quality) - rotation, inspiration (5-6 ant. ribs) exposure
- Soft tissues and bones
- Airway
- Breathing
- Circulation
- Diaphragm
- Extras
What is looked for in ‘soft tissue and bones’ of CXR?
- Ribs, sternum, spine, clavicles – symmetry, fractures, dislocations, lytic lesions, density
- Soft tissues – looking for symmetry, swelling, loss of tissue planes, subcutaneous air, masses
- Breast shadows
- Calcification – great vessels, carotids
What is looked for in ‘airway’ of CXR?
- Trachea – central?
- Carina & RMB/LMB
- Mediastinal width <8cm on PA film
- Aortic knob
- Hilum – T6-7 IV disc level, left hilum is usually higher (2cm) and squarer than the V-shaped right hilum.
- Check vessels, calcification.
What is looked for in ‘breathing’ of CXR?
Lung fields:
- Vascularity – to ~2cm of pleural surface (~3cm in apices), vessels in bases > apices
- Pneumothorax – don’t forget apices
- Lung field outlines – abnormal opacity/lucency, atelectasis, collapse, consolidation, bullae
- Pulmonary infiltrates – interstitial vs alveolar pattern
- Coin lesions
- Cavitary lesions
Pleura
- Pleural reflections
- Pleural thickening
What is looked for in ‘circulation’ of CXR?
- Heart position –⅔ to left, ⅓ to right
- Heart size – measure cardiothoracic ratio on PA film (normal <0.5)
- Heart borders – R) border is R) atrium, L) border is L) ventricle & atrium
- Heart shape
- Aortic stripe
Describe this x-ray

- Visible pleural edge
- Lung markings not visible beyond this point
- Rib fracture
Diagnosis = left pneumothorax due secondary to rib fracture
Tracheal and mediastinal structures are not deviated so no ‘tension’

Describe this x-ray

- The left lower zone is uniformly white
- At the top of this white area there is a concave surface - meniscus sign
- The left heart border, costophrenic angle and hemidiaphragm are obscured
- Slight blunting of the right costophrenic angle indicates a small pleural effusion on that side
Diagnosis - large left pleural effusion

Describe this x-ray

- The right heart border (right atrial edge) is obscured
- Consolidation (asterisk) is limited above by a crisp line, formed by the horizontal fissure
- The pathology must therefore involve the right middle lobe
- More extensive shadowing also involves the right and left peri-hilar regions
Diagnosis = pneumonia involving the right middle lobe

Describe the x-ray

- The horizontal fissure (white line) has been displaced upwards from its original position (red line)
- Dense opacification (asterisk) of the medial part of the right upper zone
- Enlarged right hilum
Diagnosis = right upper lobe collapse

Describe the x-ray

- Large, round, thick-walled lung cavity
- The cavity is in the left middle zone, close to the hilum
Diagnosis = Left lower lobe lung cavity, possible due to a squamous cell carcinoma

Describe this x-ray

- Both costophrenic angles are blunt due to lung hyper-expansion
- The hemidiaphragms are flattened indicating hyperexpansion
- The lung markings are distorted bilaterally
Diagnosis = COPD

Describe this x-ray

- The lungs are normal
- The diaphragm is crisply defined on both sides (arrowheads)
- Air under the diaphragm (asterisks) is seen as crescents of relatively low density (black)
- Black air can be seen on both sides of the bowel wall (blue line) – this is known as the double-wall sign or Rigler’s sign (usually only seen on abdominal X-rays)
Diagnosis = perforated duodenal ulcer (pneumoperitoneum)

Describe this x-ray

- Cardiomegaly CTR = 18/30 (>50%)
- Upper zone vessel enlargement (1) – a sign of pulmonary venous hypertension
- Septal (Kerley B) lines (2) – a sign of interstitial oedema – see next picture
- Airspace shadowing (3) – due to alveolar oedema – acutely in a peri-hilar (bat’s wing) distribution
- Blunt costophrenic angles (4) – due to pleural effusions
Diagnosis = left ventricular failure with pulmonary oedema

Describe this x-ray

- Dense airspace shadowing is due to alveolar oedema caused by fluid filling the alveoli and small airways
- In the acute setting this airspace shadowing radiates from the hilar regions in a ‘bat’s wing’ distribution and then becomes more generalised
Diagnosis = alveolar pulmonary oedema

Describe this x-ray

- Sternal wires and aortic valve prosthesis (arrowhead)
- Massive aortic knuckle (red line)
- Displaced trachea (arrow)
- Widened, tortuous descending aorta (blue lines)
Diagnosis = chronic thoracic aortic aneurysm (treated with surgical repair of the aortic root)

Describe this x-ray

- No patient rotation - the spinous processes (red line) are central between the medial clavicles (blue lines)
- Trachea (asterisk) shifted to the left of the midline
- Soft tissue mass mainly to the right of the trachea

What is Acute Respiratory Distress Syndrome?
An acute, diffuse inflammatory lung injury in response to a variety of direct (inhaled) or indirect (bloodborne) insults.
Name some causes of ARDS
Direct:
- Infection
- Trauma
- Near-drowning
- Gas inhalation
Indirect:
- Sepsis
- Burns
- Haemorrhage
- Post-arrest
What are the clinical features of ARDS?
- Dyspnoea and tachypnoea
- Central cyanosis
- Hypoxic confusion
- Bilateral fine inspiratory crepitations
- Peripheral vasodilations
*
What is the diagnostic criteria for ARDS?
- Acute onset
- Bilateral infiltrates on CXR
- Pulmonary capillary wedge pressure (PCWP) < 19mmHg
- Hypoxaemia
How is ARDS managed?
- Treat underlying cause
- Respiratory support
- CPAP / PEEP with 40-60% O2
- Circulatory support
- Inotropes
- Vasodilators
- Blood transfusion
- Sepsis - empirical broad spectrum
- Nutritional support
What is bronchiectasis?
Chronic infection (staph aureus, h influenzae, strep pneumoniae, pseudomonas aeruginosa) of the bronchi and bronchioles leading to permenant dilation of these airways
Name some causes of bronchiectasis
- Congenital - cystic fibrosis
- Post-infection - measles, pertussis, pneumonia, TB, HIV
- Bronchial obstruction - tumour, foreign body
- RA
- UC
- Idiopathic
What are the clinical features of bronchiectasis?
- Persistent cough
- Copious purulent sputum
- Intermittent haemoptysis
- Clubbing
- Coarse inspiratory crepitations
- Wheeze
How is bronchiectasis investigated?
- Sputum culture
- CXR
- Cystic shadows
- Thickened bronchial walls
- High-resolution CT
- SPirometry - obstructive
How is bronchiectasis managed?
- Postural drainage twice a day
- Chest physiotherapy
- Antibiotics
- Bronchodilators (nebulised salbutamol)
- Surgery
Name the different types of lung tumour
- Non-small cell
- Squamous
- Adenocarcinoma
- Large cell (poorly differentiated)
- Small cell - neuroendocrine tumour with poorer prognosis
- Mesothelioma
Name the guidelines for urgent CXR guidelines in suspected lung cancer
Aged over 40 if 2 or more OR ever smoked with 1:
- Cough
- Fatigue
- Shortness of breath
- Chest pain
- Weight loss
- Appetite loss
Describe the guidelines for prescribing LTOT in a COPD patient
- pO2 < 7.3 kPa
- pO2 7.3-8.0 kPa if:
- Secondary polycythaemia
- Nocturnal hypoxaemia
- Peripheral oedema
- Pulmonary hypertension