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Research Article| Volume 58, P34-38, March 2023

Expert provider survey of longitudinal assessment in patients with pulmonary arterial hypertension

Published:November 10, 2022DOI:https://doi.org/10.1016/j.hrtlng.2022.10.016

      Highlights

      • 40 PH providers answered focused questions of longitudinal patient assessment.
      • Patients with advanced disease are generally followed more frequently in clinic.
      • Providers trend toward more frequent objective testing in sicker patients.
      • Heterogenous longitudinal assessment patterns prevail among PH providers.

      Abstract

      Background

      Patients suffering from pulmonary arterial hypertension (PAH) demand frequent assessment to keep pace with a dynamic and sometimes rapidly progressive disease course. To improve our understanding of patient monitoring, we conducted a survey of pulmonary hypertension (PH) providers to establish real-world practice patterns.

      Objective

      To evaluate the type and frequency of patient assessment methods employed by expert PH providers following PAH diagnosis

      Methods

      A descriptive cross-sectional survey of PH providers across the United States was utilized to assess provider practices. Between September 14, 2017 to October 17, 2017, a survey was distributed electronically to PH experts assessing follow-up frequency and testing evaluation of patients with PAH.

      Results

      40 (11.4%) providers completed the survey, representing cardiologists, pulmonologists, and advanced practice providers at centers who cared for an average of 95 patients per year with PAH. Follow-up testing and clinic evaluation was influenced by severity of patient illness. Frequency of re-assessment of clinic follow-up, six-minute walk test, echocardiogram, brain natriuretic peptide, and right heart catheterization in various clinical scenarios all reflected disparate practice.

      Conclusions

      Current clinical practice patterns in the monitoring of patients with PAH are variable and do not necessarily reflect guideline-based practices, suggesting the need for further research and improved guidelines on the frequency of follow up and repeat testing.

      Keywords

      Abbreviations:

      PAH (Pulmonary Arterial Hypertension), PH (Pulmonary Hypertension), SQ (Subcutaneous), IV (Intravenous), TTE (Transthoracic Echocardiogram), RHC (Right Heart Catheterization), CPET (cardiopulmonary exercise test)
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      References

        • Humbert M.
        • Sitbon O.
        • Yaïci A.
        • Montani D.
        • O'Callaghan D.S.
        • Jaïs X.
        • et al.
        Survival in incident and prevalent cohorts of patients with pulmonary arterial hypertension.
        Eur Respir J. 2010; 36: 549-555https://doi.org/10.1183/09031936.00057010
        • Benza R.L.
        • Miller D.P.
        • Gomberg-Maitland M.
        • Frantz R.P.
        • Foreman A.J.
        • Coffey C.S.
        • et al.
        Predicting survival in pulmonary arterial hypertension: Insights from the registry to evaluate early and long-term pulmonary arterial hypertension disease management (REVEAL).
        Circulation. 2010; 122: 164-172https://doi.org/10.1161/CIRCULATIONAHA.109.898122
        • Galiè N.
        • Humbert M.
        • Vachiery J.L.
        • Gibbs S.
        • Lang I.
        • Torbicki A.
        • et al.
        2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension.
        Eur Respir J. 2015; 46: 903-975https://doi.org/10.1183/13993003.01032-2015
        • Benza R.L.
        • Miller D.P.
        • Foreman A.J.
        • Frost A.E.
        • Badesch D.B.
        • Benton W.W.
        • et al.
        Prognostic implications of serial risk score assessments in patients with pulmonary arterial hypertension: A Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL) analysis.
        J Hear Lung Transplant. 2015; 34: 356-361https://doi.org/10.1016/j.healun.2014.09.016
        • McLaughlin V.V.
        • Archer S.L.
        • Badesch D.B.
        • Barst R.J.
        • Farber H.W.
        • Lindner J.R.
        • et al.
        ACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension: A Report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association.
        Circulation. 2009; 119: 2250-2294https://doi.org/10.1161/CIRCULATIONAHA.109.192230
        • Nickel N.
        • Golpon H.
        • Greer M.
        • Knudsen L.
        • Olsson K.
        • Westerkamp V.
        • et al.
        The prognostic impact of follow-up assessments in patients with idiopathic pulmonary arterial hypertension.
        Eur Respir J. 2012; 39: 589-596https://doi.org/10.1183/09031936.00092311
        • Frost A.E.
        • Badesch D.B.
        • Miller D.P.
        • Benza R.L.
        • Meltzer L.A.
        • McGoon M.D.
        Evaluation of the predictive value of a clinical worsening definition using 2-year outcomes in patients with pulmonary arterial hypertension: A REVEAL registry analysis.
        Chest. 2013; 144: 1521-1529https://doi.org/10.1378/chest.12-3023
        • Tonelli A.R.
        • Conci D.
        • Tamarappoo B.K.
        • Newman J.
        • Dweik R.A.
        Prognostic value of echocardiographic changes in patients with pulmonary arterial hypertension receiving parenteral prostacyclin therapy.
        J Am Soc Echocardiogr. 2014; 27 (e2.): 733-741https://doi.org/10.1016/j.echo.2014.03.012
        • Sahay S.
        • Tonelli A.R.
        • Selej M.
        • Watson Z.
        • Benza R.L.
        Risk assessment in patients with functional class II pulmonary arterial hypertension: Comparison of physician gestalt with ESC/ERS and the REVEAL 2.0 risk score.
        PLoS One. 2020; 15: 1-12https://doi.org/10.1371/journal.pone.0241504
        • Hoeper M.M.
        • Kramer T.
        • Pan Z.
        • Eichstaedt C.A.
        • Spiesshoefer J.
        • Benjamin N.
        • et al.
        Mortality in pulmonary arterial hypertension: Prediction by the 2015 European pulmonary hypertension guidelines risk stratification model.
        Eur Respir J. 2017; 50: 1-10https://doi.org/10.1183/13993003.00740-2017
        • Boucly A.
        • Weatherald J.
        • Savale L.
        • Jaïs X.
        • Cottin V.
        • Prevot G.
        • et al.
        Risk assessment, prognosis and guideline implementation in pulmonary arterial hypertension.
        Eur Respir J. 2017; 50: 1-10https://doi.org/10.1183/13993003.00889-2017
        • Benza R.L.
        • Gomberg-Maitland M.
        • Elliott C.G.
        • Farber H.W.
        • Foreman A.J.
        • Frost A.E.
        • et al.
        Predicting Survival in Patients With Pulmonary Arterial Hypertension: The REVEAL Risk Score Calculator 2.0 and Comparison With ESC/ERS-Based Risk Assessment Strategies.
        Chest. 2019; 156: 323-337https://doi.org/10.1016/j.chest.2019.02.004
        • Galiè N.
        • Channick R.N.
        • Frantz R.P.
        • Grünig E.
        • Jing Z.C.
        • Moiseeva O.
        • et al.
        Risk stratification and medical therapy of pulmonary arterial hypertension.
        Eur Respir J. 2019; 53https://doi.org/10.1183/13993003.01889-2018
        • Kylhammar D.
        • Kjellström B.
        • Hjalmarsson C.
        • Jansson K.
        • Nisell M.
        • Söderberg S.
        • et al.
        A comprehensive risk stratification at early follow-up determines prognosis in pulmonary arterial hypertension.
        Eur Heart J. 2018; 39: 4175-4181https://doi.org/10.1093/eurheartj/ehx257
        • Humbert M.
        • Weatherald J
        Right heart catheterisation is still a fundamental part of the follow-up assessment of pulmonary arterial hypertension.
        Eur Respir J. 2018; 52: 6-8https://doi.org/10.1183/13993003.00738-2018
        • Howard L.S.
        Is right heart catheterisation still a fundamental part of the follow-up assessment of pulmonary arterial hypertension? The argument against.
        Eur Respir J. 2018; 52: 6-8https://doi.org/10.1183/13993003.00996-2018
        • Boucly A.
        • Weatherald J.
        • Savale L.
        • Jaïs X.
        • Cottin V.
        • Prevot G.
        • et al.
        Risk assessment, prognosis and guideline implementation in pulmonary arterial hypertension [CE: This is duplicate referene with reference 11.].
        Eur Respir J. 2017; 50: 1-10https://doi.org/10.1183/13993003.00889-2017
        • Benza R.L.
        • Kanwar M.K.
        • Raina A.
        • Scott J.V.
        • Zhao C.L.
        • Selej M.
        • et al.
        Development and Validation of an Abridged Version of the REVEAL 2.0 Risk Score Calculator, REVEAL Lite 2, for Use in Patients With Pulmonary Arterial Hypertension.
        Chest. 2021; 159: 337-346https://doi.org/10.1016/j.chest.2020.08.2069
        • Benza R.
        • Biederman R.
        • Murali S.
        • Gupta H.
        Role of Cardiac Magnetic Resonance Imaging in the Management of Patients With Pulmonary Arterial Hypertension.
        J Am Coll Cardiol. 2008; 52: 1683-1692https://doi.org/10.1016/j.jacc.2008.08.033
        • Laffon E.
        • Vallet C.
        • Bernard V.
        • Montaudon M.
        • Ducassou D.
        • Laurent F.
        • et al.
        A computed method for noninvasive MRI assessment of pulmonary arterial hypertension.
        J Appl Physiol. 2004; 96: 463-468https://doi.org/10.1152/japplphysiol.00225.2004
        • Pi H.
        • Kosanovich C.M.
        • Handen A.
        • Tao M.
        • Visina J.
        • Vanspeybroeck G.
        • et al.
        Outcomes of Pulmonary Arterial Hypertension Are Improved in a Specialty Care Center.
        Chest. 2020; 158: 330-340https://doi.org/10.1016/j.chest.2020.01.046