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Cor pulmonale
• Cor pulmonale is right heart failure caused
  by chronic pulmonary hypertension
Causes of cor pulmonale
• Lung disease
     Asthma (severe, chronic)
     COPD
     Bronchiectasis
     Pulmonary fibrosis
     Lung resection
• Pulmonary vascular disease
     Pulmonary emboli
     Pulmonary vasculitis
     Primary pulmonary hypertension
     ARDS
     Sickle-cell disease
     Parasite infestation
• Thoracic cage abnormality
    Kyphosis
    Scoliosis
    Thoracoplasty
• Neuromuscular disease
    Myasthenia gravis
    Poliomyelitis
    Motor neurone disease
• Hypoventilation
    Sleep apnoea
    Enlarged adenoids in children
    Cerebrovascular disease
Clinical features
• Symptoms include dyspnoea, fatigue, or
  syncope. Signs: cyanosis; tachycardia;
  raised JVP with prominent a and v waves;
  RV heave; loud p2, pansystolic murmur
  (tricuspid regurgitation); early diastolic
  Graham Steell murmur; hepatomegaly
  and oedema.
Investigations
• FBC: Hb and haematocrit ↑(secondary
  polycythaemia). ABG; hypoxia, with or
  without hypercapnia. CXR; enlarged right
  atrium and ventricle, prominent pulmonary
  arteries. ECG; P pulmonale; right axis
  deviation; right ventricular hypertrophy/
  strain.
Management
• Treat underlying cause – e.g. COPD and
  pulmonary infections
• Treat respiratory failure – in the acute situation
  give 24% oxygen if PaO2 <8kPa. Monitor ABG
  and gradually increase oxygen concentration if
  Pa CO2 is stable. In COPD patients, long-term
  oxygen therapy (LTOT) for 15h/d increases
  survival. Patients with chronic hypoxia when
  clinically stable should be assessed for LTOT.
• Treat cardiac failure with diuretics such as
  frusemide (=furosemide, e.g. 40-160mg/24h
  PO). Monitor U&E and give amiloride or
  potassium supplements if necessary.
  Alternative: spironolactone.
• Consider vensection if the haematocrit is > 55%.
• Consider heart-lung transplantation in young
  patients.



Prognosis
  Poor 50% die within 5yrs.

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Cor pulmonale 1

  • 2. • Cor pulmonale is right heart failure caused by chronic pulmonary hypertension
  • 3. Causes of cor pulmonale • Lung disease Asthma (severe, chronic) COPD Bronchiectasis Pulmonary fibrosis Lung resection
  • 4. • Pulmonary vascular disease Pulmonary emboli Pulmonary vasculitis Primary pulmonary hypertension ARDS Sickle-cell disease Parasite infestation
  • 5. • Thoracic cage abnormality Kyphosis Scoliosis Thoracoplasty
  • 6. • Neuromuscular disease Myasthenia gravis Poliomyelitis Motor neurone disease
  • 7. • Hypoventilation Sleep apnoea Enlarged adenoids in children Cerebrovascular disease
  • 8. Clinical features • Symptoms include dyspnoea, fatigue, or syncope. Signs: cyanosis; tachycardia; raised JVP with prominent a and v waves; RV heave; loud p2, pansystolic murmur (tricuspid regurgitation); early diastolic Graham Steell murmur; hepatomegaly and oedema.
  • 9. Investigations • FBC: Hb and haematocrit ↑(secondary polycythaemia). ABG; hypoxia, with or without hypercapnia. CXR; enlarged right atrium and ventricle, prominent pulmonary arteries. ECG; P pulmonale; right axis deviation; right ventricular hypertrophy/ strain.
  • 10. Management • Treat underlying cause – e.g. COPD and pulmonary infections • Treat respiratory failure – in the acute situation give 24% oxygen if PaO2 <8kPa. Monitor ABG and gradually increase oxygen concentration if Pa CO2 is stable. In COPD patients, long-term oxygen therapy (LTOT) for 15h/d increases survival. Patients with chronic hypoxia when clinically stable should be assessed for LTOT.
  • 11. • Treat cardiac failure with diuretics such as frusemide (=furosemide, e.g. 40-160mg/24h PO). Monitor U&E and give amiloride or potassium supplements if necessary. Alternative: spironolactone. • Consider vensection if the haematocrit is > 55%. • Consider heart-lung transplantation in young patients. Prognosis Poor 50% die within 5yrs.