Pulmonary Arterial Hypertension: Reconfiguring the Vascular Landscape to Reverse Remodeling.

Alice G Vassiliou1, Kostas A Papavassiliou2, Nikolaos S Lotsios1

  • 1First Department of Critical Care Medicine, 'Evangelismos' Hospital, Medical School, National and Kapodistrian University of Athens, 10676 Athens, Greece.

Cells
|February 26, 2026
PubMed
Summary

Pulmonary arterial hypertension (PAH) treatments aim to improve blood flow by dilating blood vessels, easing strain on the right ventricle (RV). This approach reduces resistance, offering a therapeutic strategy for PAH patients.

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