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  2. Ambrisentan - Wikipedia

    en.wikipedia.org/wiki/Ambrisentan

    Ambrisentan, sold under the brand name Letairis among others, is a drug used for the treatment of pulmonary hypertension. [3] [5] It is an endothelin receptor antagonist. [3] The peptide endothelin constricts muscles in blood vessels, increasing blood pressure.

  3. Pulmonary hypertension - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_hypertension

    Medications specifically used to treat pulmonary hypertension include epoprostenol, treprostinil, iloprost, bosentan, ambrisentan, macitentan, and sildenafil, tadalafil, selexipag, riociguat. [4] Lung transplantation may be an option in severe cases. [6] The frequency of occurrence is estimated at 1,000 new cases per year in the United States.

  4. Balloon pulmonary angioplasty - Wikipedia

    en.wikipedia.org/wiki/Balloon_pulmonary_angioplasty

    Balloon pulmonary angioplasty (BPA) is an emerging minimally invasive procedure to treat chronic thromboembolic pulmonary hypertension (CTEPH) in people who are not suitable for pulmonary thromboendarterectomy (PTE) or still have residual pulmonary hypertension and areas of narrowing in the pulmonary arterial tree following previous PTE.

  5. 'I Was Diagnosed With Pulmonary Arterial Hypertension ... - AOL

    www.aol.com/diagnosed-pulmonary-arterial...

    Katrina Berry was 24 years old when she first started experiencing symptoms of pulmonary arterial hypertension (PAH), a progressive health condition that leads to reduced cardiac output and right ...

  6. Can hormone replacement therapy help treat pulmonary ... - AOL

    www.aol.com/hormone-replacement-therapy-help...

    Additionally, those in the pulmonary hypertension Group 1 had lower mean pulmonary artery pressure, pulmonary vascular resistance, and higher right ventricular ejection fraction if exposed to HRT.

  7. Actelion - Wikipedia

    en.wikipedia.org/wiki/Actelion

    Veletri (epoprostenol for injection): is approved by the U.S. Food and Drug Administration (FDA) for the long-term intravenous treatment of primary pulmonary hypertension and pulmonary hypertension associated with the scleroderma spectrum of disease in NYHA Class III and Class IV patients who do not respond adequately to conventional therapy. [20]

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