Pulmonary Vascular Disease Flashcards

1
Q

Pulmonary embolism

A
  • Thrombus forms in the venous system, usually in deep veins of the legs and embolises to the pulmonary arteries.
  • Massive PE can be fatal, although minor PE treated with anticoagulation has a very good prognosis.
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2
Q

Venous thromboembolism - Major risk factors

A
  • Recent major trauma
  • Recent surgery
  • Cancer
  • Significant cardiopulmonary disease e.g. MI
  • Pregnancy
  • Inherited thrombophilia e.g Factor V Leiden, Protein C or S deficiency
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3
Q

Symptoms of pulmonary embolism

A
  1. Pleuritic chest pain, cough and haemoptysis
  2. Isolated acute dyspnoea
  3. Syncope or cardiac arrest (massive PE)
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4
Q

Signs of pulmonary embolism

A
  1. Pyrexia, pleural rub, stony dullness to percussion at base (pleural effusion)
  2. Tachycardia, tachypnoea, hypoxia
  3. Tachycardia, hypotension, tachypnoea, hypoxia
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5
Q

Pre-test probability of pulmonary embolism

A
  • Wells Score
    • Includes symptoms and signs of VTE, previous VTE and risk factors
  • Revised Geneva Score
    • Based on risk factors, symptoms and signs (heart rate)
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6
Q

Investigations for pulmonary embolism

A
  • Full blood count, biochemistry, TnI, blood gases
  • Chest X-Ray
  • ECG
  • D-dimer
  • CT Pulmonary Angiogram (CTPA)
  • V/Q scan
  • Echocardiography
  • Consider CT abdomen and mammography
  • Consider thrombophilia testing
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7
Q

Treatment for pulmonary embolism

A
  • Oxygen
  • Low molecular weight heparin e.g. dalteparin
  • Warfarin
  • Direct Oral Anticoagulants (DOAC)
    • rivaroxaban, apixaban
  • Thrombolysis
    • Alteplase (rt-PA)
  • Pulmonary Embolectomy
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8
Q

Duration of treatment for pulmonary embolism

A
  • Provoked PE – 3 months anticoagulation
  • Unprovoked PE – Haematology to assess annual risk of recurrence and consider lifelong anticoagulation.
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9
Q

Prognosis of pulmonary embolism

A
  • Mortality at 30 days varies from 0 to 25%
  • PESI Score
    • Based on age, sex, comorbidity and physiological parameters
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10
Q

Pulmonary hypertension

A
  • Elevated blood pressure in the pulmonary arterial tree.
  • Defined as a mean pulmonary artery pressure of > 20 mmHg.
  • Either idiopathic or secondary to other conditions.
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11
Q

Epidemiology of pulmonary hypertension

A
  • Idiopathic pulmonary arterial hypertension is rare and has an incidence of 1-2 per million population.
  • Untreated it is a rapidly progressive condition that leads to premature death.
  • Pulmonary hypertension secondary to other medical conditions is more common and tends to occur in an older age group.
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12
Q

Causes of pulmonary hypertension

A
  • Idiopathic (group 1)
    • idiopathic
    • collagen vascular disease
    • portal hypertension
    • congenital heart disease (L to R shunt)
    • HIV infection
  • Secondary to left heart disease (group 2)
  • Secondary to chronic respiratory disease (group 3)
  • Chronic Thromboembolic PH (CTEPH) ( group 4)
  • Miscellaneous (group 5)
    • Sarcoidosis
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13
Q

Symptoms of pulmonary hypertension

A
  • Exertional dyspnoea
  • Chest tightness
  • Exertional presyncope or syncope
  • Haemoptysis
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14
Q

Signs of pulmonary hypertension

A
  • Elevated JVP
  • Right ventricular heave
  • Loud pulmonary second heart sound
  • Hepatomegaly (enlarged liver)
  • Ankle oedema
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15
Q

Investigations for pulmonary hypertension

A
  • ECG
  • Lung function tests (reduced gas transfer)
  • Chest X-Ray
  • Echocardiography
  • V/Q scan
  • CTPA
  • Right heart catheterisation
    • allows direct measure of pulmonary artery pressure
    • measurement of wedge pressure
    • measurement of cardiac output
    • vasodilator trial with nitric oxide
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16
Q

General treatment of pulmonary hypertension

A
  • Treat underlying condition
  • Oxygen
  • Anticoagulation (for IPAH only)
  • Diuretics
17
Q

Specific treatment of pulmonary hypertension

A
  • Calcium channel antagonists (if positive vasodilator trial)
  • Prostaglandins e.g. iloprost
  • Prostacyclin agonist (selexipag)
  • Phosphodiesterase inhibitors
    • sildenafil
    • tadalafil
  • Endothelin receptor antagonists
    • bosentan
    • ambrisentan
  • Riociguat (for CTEPH)
18
Q

Other treatments of pulmonary hypertension

A
  • Thromboendarterectomy (CTEPH)
  • Lung or heart lung transplant