28 research outputs found

    Recognizing and treating HFpEF: the biggest pulmonary arterial hypertension imitator!

    No full text

    Portopulmonary rhapsody: everything you need to know about portopulmonary hypertension

    No full text

    Grace Under Pressure.

    No full text

    Assessing hemodynamic response to submaximal exercise in pulmonary arterial hypertension patients using an implantable hemodynamic monitor.

    No full text
    Pulmonary arterial hypertension (PAH) is a chronic, progressive disease that is incurable, even with effective therapy. Long-term outcome in PAH is best preserved by targeting hemodynamic improvements to reduce risk of subsequent right ventricular (RV) failure. Methods that can assess RV adaptation to stress have important implications to better understand an individual\u27s physiology and may play a pivotal role in guiding therapy in PAH. In this novel pilot study, we evaluate the feasibility of monitoring hemodynamic response to 6-minute walk distance in patients with PAH using the CardioMEMS HF System
    corecore