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    NASHVILLE, Tenn. — Initiation of oral selexipag within 12 months of pulmonary arterial hypertension diagnosis may reduce all-cause hospitalizations and overall medical costs, according to a new analysis.“One of the key take-home findings is that earlier initiation of PAH combination therapy can deliver improvement in outcomes, particularly reduction in all-cause

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    • Presented at #CHEST2022: Initiation of #selexipag within 12 months of pulmonary artery hypertension diagnosis may reduce #hospitalizations and medical costs, according to a new analysis @Journal_CHEST #PAH https://t.co/MMbDg4onYX

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    SAN FRANCISCO — New real-world data demonstrate treatment with selexipag improved outcomes in patients with pulmonary arterial hypertension associated with connective tissue disease.At the American Thoracic Society International Conference, Sean Gaine, MD, with the National Pulmonary Hypertension Unit at Mater Misericordiae Hospital in Dublin, Ireland, and colleagues reported patient

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    • #ICYMI: Presented at #ATS2022: #Selexipag initiation improved outcomes in patients with #PAH associated with connective tissue disease. @CardiologyToday https://t.co/spvneMVsEk

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    SAN FRANCISCO — New real-world data demonstrate treatment with selexipag improved outcomes in patients with pulmonary arterial hypertension associated with connective tissue disease.At the American Thoracic Society International Conference, Sean Gaine, MD, with the National Pulmonary Hypertension Unit at Mater Misericordiae Hospital in Dublin, Ireland, and colleagues reported patient

    Tweet Tweets with this article
    • New real-world data demonstrate #selexipag initiation improved outcomes in patients with pulmonary arterial hypertension associated with connective tissue disease. Read more below #ATS2022 #PAH @CardiologyToday https://t.co/tClOzpNQt9

    • New real-world data demonstrate #selexipag initiation improved outcomes in patients with pulmonary arterial hypertension associated with connective tissue disease. Read more below #ATS2022 #PAH @CardiologyToday https://t.co/3FOmk4Lb6l

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    The FDA has approved selexipag for IV use in adults with WHO functional class II to III pulmonary arterial hypertension who are temporarily unable to take oral therapy. Selexipag (Uptravi, Janssen) for IV use will allow patients to avoid short-term interruptions and stay on their therapy, as uninterrupted treatment is important for patients with PAH, according to a company press release.

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    • #FDA approves #selexipag for intravenous use in adults with #pulmonaryhypertension @CardiologyToday #PAH https://t.co/sMYbBnw7CZ

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    The FDA has approved selexipag for IV use in adults with WHO functional class II to III pulmonary arterial hypertension who are temporarily unable to take oral therapy. Selexipag (Uptravi, Janssen) for IV use will allow patients to avoid short-term interruptions and stay on their therapy, as uninterrupted treatment is important for patients with PAH, according to a company press release.

    Tweet Tweets with this article
    • #FDA approves #selexipag for intravenous use in adults with #pulmonaryhypertension @CardiologyToday #PAH https://t.co/sMYbBnw7CZ

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    The FDA has approved selexipag for IV use in adults with WHO functional class II to III pulmonary arterial hypertension who are temporarily unable to take oral therapy. Selexipag (Uptravi, Janssen) for IV use will allow patients to avoid short-term interruptions and stay on their therapy, as uninterrupted treatment is important for patients with PAH, according to a company press release.

    Tweet Tweets with this article
    • #FDA approves #selexipag for intravenous use in adults with #pulmonaryhypertension @CardiologyToday #PAH https://t.co/SQhor5L7N3

    • #FDA approves #selexipag for intravenous use in adults with #pulmonaryhypertension @CardiologyToday #PAH https://t.co/QtaUdi5COG