Pulmonary Arterial Hypertension

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Transforming PAH Management Through Innovation and Strategic Care

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Blood pressure graphic | Image Credit: © Dzianis Vasilyeu-stock.adobe.com

The findings from this single-center retrospective study compare outcomes between 2 groups of patients living with connective tissue disease–associated pulmonary arterial hypertension (CTD-PAH) stratified by their Heart Failure Association–preserved ejection fraction (HFA-PEFF) algorithm score.

Pulmonary hypertension | Image Credit: © Uladzislau-stock.adobe.com

Pulmonary hypertension is a common consequence of interstitial lung disease (PH-ILD), with the highest rate seen among individuals who have idiopathic pulmonary fibrosis. Overall, most cases of PH in the setting of ILD are mild.

Measuring BP in pregnancy | Image Credit: ©Mediteraneo-stock.adobe.com

Pulmonary arterial hypertension (PAH) can be a challenging complication to manage during pregnancy; women with PAH who are pregnant are considered a high-risk population, and they face higher rates of maternal and fetal complications.

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