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Pulmonary arterial hypertension (PAH)

( N = 2,151 ) as of 31 July 2024

Pulmonary arterial hypertension (PAH) is a progressive, and life-threatening disease caused by a restriction in the lungs’ arterial blood flow, leading to resistance in the pulmonary vessels, right ventricle overload, and eventually right-sided heart failure.

 

Diagram

 

 

Variables in PAH

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| Ongoing research topics

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Department of Clinical Epidemiology and Biostatistics