Search Results - "MCGOON, Michael D"

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  1. 1

    An Evaluation of Long-term Survival From Time of Diagnosis in Pulmonary Arterial Hypertension From the REVEAL Registry by Benza, Raymond L., MD, Miller, Dave P., MS, Barst, Robyn J., MD, FCCP, Badesch, David B., MD, FCCP, Frost, Adaani E., MD, FCCP, McGoon, Michael D., MD, FCCP

    Published in Chest (01-08-2012)
    “…Background The Registry to Evaluate Early and Long-term Pulmonary Arterial Hypertension Disease Management (REVEAL Registry) was established to characterize…”
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    Journal Article
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    Five-Year Outcomes of Patients Enrolled in the REVEAL Registry by Farber, Harrison W., MD, FCCP, Miller, Dave P., MS, Poms, Abby D., BS, RRT, Badesch, David B., MD, FCCP, Frost, Adaani E., MD, Rouzic, Erwan Muros-Le, MPH, Romero, Alain J., PharmD, PhD, Benton, Wade W., PharmD, Elliott, C. Gregory, MD, McGoon, Michael D., MD, FCCP, Benza, Raymond L., MD

    Published in Chest (01-10-2015)
    “…BACKGROUND Pulmonary arterial hypertension (PAH) is a rare, severe disease characterized by worsening right-sided heart failure, decreasing functional status,…”
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    Journal Article
  3. 3

    The importance of patient perspectives in pulmonary hypertension by McGoon, Michael D, Ferrari, Pisana, Armstrong, Iain, Denis, Migdalia, Howard, Luke S, Lowe, Gabi, Mehta, Sanjay, Murakami, Noriko, Wong, Brad A

    Published in The European respiratory journal (01-01-2019)
    “…The assessment of objective measurement of cardiopulmonary status has helped us achieve better clinical outcomes for patients and develop new therapies through…”
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    Journal Article
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    Updated Treatment Algorithm of Pulmonary Arterial Hypertension by Galiè, Nazzareno, MD, Corris, Paul A., MD, Frost, Adaani, MD, Girgis, Reda E., MD, Granton, John, MD, Jing, Zhi Cheng, MD, Klepetko, Walter, MD, McGoon, Michael D., MD, McLaughlin, Vallerie V., MD, Preston, Ioana R., MD, Rubin, Lewis J., MD, Sandoval, Julio, MD, Seeger, Werner, MD, Keogh, Anne, MD

    “…The demands on a pulmonary arterial hypertension (PAH) treatment algorithm are multiple and in some ways conflicting. The treatment algorithm usually includes…”
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    Journal Article Conference Proceeding
  5. 5

    Predicting outcomes in pulmonary arterial hypertension based on the 6-minute walk distance by Farber, Harrison W., MD, Miller, Dave P., MS, McGoon, Michael D., MD, Frost, Adaani E., MD, Benton, Wade W., PharmD, Benza, Raymond L., MD

    “…Background Clinical studies of pulmonary arterial hypertension have used the change in the 6-minute walk distance (6MWD) as a clinical end point; however, its…”
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    Journal Article
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    The 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: a practical chronicle of progress by Lau, Edmund M T, Tamura, Yuichi, McGoon, Michael D, Sitbon, Olivier

    Published in The European respiratory journal (01-10-2015)
    “…The first World Health Organization (WHO) Symposium on Pulmonary Hypertension was held in 1973 in response to the sudden increase in the number of patients…”
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    Journal Article
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    The REVEAL Registry Risk Score Calculator in Patients Newly Diagnosed With Pulmonary Arterial Hypertension by Benza, Raymond L., MD, Gomberg-Maitland, Mardi, MD, FCCP, Miller, Dave P., MS, Frost, Adaani, MD, FCCP, Frantz, Robert P., MD, Foreman, Aimee J., MA, Badesch, David B., MD, FCCP, McGoon, Michael D., MD, FCCP

    Published in Chest (01-02-2012)
    “…Background In pulmonary arterial hypertension (PAH), survival predictions can be important for optimization of therapeutic strategies. The present study aimed…”
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    Journal Article
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    Four- and Seven-Year Outcomes of Patients With Congenital Heart Disease–Associated Pulmonary Arterial Hypertension (from the REVEAL Registry) by Barst, Robyn J., MD, Ivy, D. Dunbar, MD, Foreman, Aimee J., MA, McGoon, Michael D., MD, Rosenzweig, Erika B., MD

    “…Uncorrected congenital heart disease (CHD) frequently leads to pulmonary arterial hypertension (PAH), the most severe form of which is Eisenmenger syndrome…”
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    Journal Article
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    Functional Class Improvement and 3-Year Survival Outcomes in Patients With Pulmonary Arterial Hypertension in the REVEAL Registry by Barst, Robyn J., MD, Chung, Lorinda, MD, Zamanian, Roham T., MD, Turner, Michelle, MS, McGoon, Michael D., MD

    Published in Chest (01-07-2013)
    “…Objective New York Heart Association/World Health Organization functional class (FC) is associated with outcomes in pulmonary arterial hypertension (PAH). We…”
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    Journal Article
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    Portopulmonary hypertension: Results from a 10‐year screening algorithm by Krowka, Michael J., Swanson, Karen L., Frantz, Robert P., McGoon, Michael D., Wiesner, Russell H.

    Published in Hepatology (Baltimore, Md.) (01-12-2006)
    “…Portopulmonary hypertension (POPH) is the elevation of pulmonary artery pressure due to increased resistance to pulmonary blood flow in the setting of portal…”
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    Journal Article
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    Relationship of Pulmonary Arterial Capacitance and Mortality in Idiopathic Pulmonary Arterial Hypertension by Mahapatra, Srijoy, Nishimura, Rick A., Sorajja, Paul, Cha, Stephen, McGoon, Michael D.

    “…Relationship of Pulmonary Arterial Capacitance and Mortality in Idiopathic Pulmonary Arterial Hypertension Srijoy Mahapatra, Rick A. Nishimura, Paul Sorajja,…”
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    Journal Article
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    Characterization of First-Time Hospitalizations in Patients With Newly Diagnosed Pulmonary Arterial Hypertension in the REVEAL Registry by Burger, Charles D, MD, Long, Pamela K, RN, Shah, Monarch R, MS, McGoon, Michael D, MD, Miller, Dave P, MS, Romero, Alain J, PharmD, PhD, Benton, Wade W, PharmD, Safford, Robert E, MD, PhD

    Published in Chest (01-11-2014)
    “…BACKGROUND Hospitalization is an important outcome in pulmonary arterial hypertension (PAH), shown previously to correlate with survival. Using the Registry to…”
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    Journal Article
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    Treatment of patients with pulmonary arterial hypertension at the time of death or deterioration to functional class IV: Insights from the REVEAL Registry by Farber, Harrison W., MD, Miller, Dave P., MS, Meltzer, Leslie A., PhD, McGoon, Michael D., MD

    “…Background Current guidelines recommend intravenous prostacyclin as first-line therapy for patients with pulmonary arterial hypertension (PAH) in New York…”
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    Journal Article
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    Pulmonary Hypertension in Hereditary Hemorrhagic Telangiectasia by Lyle, Melissa A., MD, Fenstad, Eric R., MD, McGoon, Michael D., MD, Frantz, Robert P., MD, Krowka, Michael J., MD, Kane, Garvan C., MD, PhD, Swanson, Karen L., DO

    Published in Chest (01-02-2016)
    “…Background A subset of patients with hereditary hemorrhagic telangiectasia (HHT) develops pulmonary hypertension (PH) by mechanisms including pulmonary…”
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    Journal Article