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SLE PAH — RACP Adult Medicine MCQ

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HardRheumatologySLE PAHRACP Adult Medicine

A woman with systemic lupus erythematosus has progressive exertional dyspnoea, reduced DLCO and estimated pulmonary artery systolic pressure 55 mmHg. CTPA excludes chronic thromboembolism. What test is required before pulmonary arterial hypertension-specific treatment?

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Correct answer: ERight-heart catheterisation to confirm haemodynamics and classify pulmonary hypertension

The best answer is “Right-heart catheterisation to confirm haemodynamics and classify pulmonary hypertension”. Echocardiography estimates probability but cannot definitively classify pulmonary hypertension. Right-heart catheterisation measures mean pulmonary artery pressure, wedge pressure, cardiac output and pulmonary vascular resistance, distinguishing precapillary PAH from left-heart or mixed disease before targeted therapy. CTPA exclusion of emboli does not complete that classification.

Reference: Lung Foundation Australia: Pulmonary arterial hypertension: https://lungfoundation.com.au/support-resources/resource-hub/pulmonary-arterial-hypertension-fact-sheet/