Steven Thomas

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Establishing minimally important differences for cardiac MRI end-points in pulmonary arterial hypertension

Aug 3, 2023 | erj.ersjournals.com | Ahmed Maiter |Catherine Hill |Steven Thomas |Rebecca Gossling

IntroductionIn patients with pulmonary arterial hypertension (PAH), symptoms and survival are determined primarily by right ventricular (RV) function. In PAH, a progressive pulmonary vasculopathy results in elevation of mean pulmonary arterial pressure (mPAP) and an increase in RV afterload [1].

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