Pulmonary HTN

Cards (12)

  • What is pulmonary arterial HTN (PAH)?

    Group of conditions characterised by progressive elevation of mean pulmonary arterial pressure to > 20 mmHg
    Not a diagnosis in itself
  • What are the different causes/classification of PAH?

    Group 1
    • Idiopathic pulmonary HTN or connective tissue disease (e.g. SLE)
    Group 2
    • LHF (most common cause)
    • usually due to MI or systemic HTN
    Group 3
    • Chronic lung disease (e.g. COPD or pulmonary fibrosis)
    Group 4
    • Pulmonary vascular disease (e.g. PE)
    Group 5
    • Miscellaneous (e.g. sarcoidosis, glycogen storage disease & haematological disorders)
  • Pathophys of PAH
    PAH occurs when there is profound vasculopathy (vasoconstriction, vascular remodelling & in situ thrombosis) → endothelial dysfunction → decreased vasodilator production → increased pro-contractile mediators, increased growth factor release, increase pro-inflammatory cytokine release → increased contractility of arteries, dysfunction of endothelium, over-proliferation of endothelial cells & vascular smooth muscle cells & increased thrombotic risk → increased pulmonary vascular resistance → increased pulmonary artery pressure
  • What are the symptoms of PAH?

    SOB (progressive & exertional)
    Chest pain
    Fatigue
    Syncope
    Cough
    Haemoptysis
    Hoarseness
  • What are the signs of PAH?

    Hypotension
    Tachycardia
    Cyanosis
    Loud pulmonary component of S2
    Third heart sound
    Pansystolic murmur (tricuspid regurgitation)
    Diastolic murmur (pulmonary regurgitation)
  • What are the signs of LATE pulmonary HTN?

    Raised JVP
    Hepatomegaly
    Peripheral oedema
    Ascites
    Parasternal heave
  • PAH causes strain of R side of heart → tries to pump blood through lungs → back pressure through R side of heart & into systemic venous system
  • What are the RFs of PAH?

    Pre-existing diseases linked to pulmonary HTN
    Obesity
    Obstructive sleep apnoea
    Altitude (prolonged exposure)
    FHx
    Female
  • What are the Inx of PAH?

    Obs
    Full Hx & examination
    ECG
    Wells score
    Bloods (FBC, U&Es, LFTs, CRP, NT-proBNP, ABG, serology (for HIV/Hep), autoimmune screen)
    CXR
    Echo (+ R heart catheterisation) -> to measure pressure in RA
    CT chest or V/Q scan
    Cardiac MRI
    Pulmonary function tests
  • What will an ECG of PAH show?
    Signs of RHF
    • P pulmonale (peaked P waves)
    • R ventricular hypertrophy (tall R waves in V1 & V2, deep S waves in V5 & V6)
    • Right axis deviation
    • RBBB
  • What is the CONSERVATIVE treatment of PAH?

    Exercise & pulmonary rehab
    Influenza & pneumococcal vaccination
    Contraceptive advice -> 30-50% increased mortality in pregnancy
    Psychosocial support
  • What is the MEDICAL/SURGICAL treatment of PAH?

    Treat underlying cause
    Diuretics
    LTOT
    Digoxin (can increase CO)
    Anticoagulation
    Endothelin receptor antagonists (macitentan)
    Phosphodiesterase-5 inhibitors (sildenafil)
    IV prostaglandins (ilioprost)
    Ca+2 channel blockers (amlodipine)
    Cardiopulmonary transplantation