Roberto Badagliacca1, Michele D'Alto2, Stefano Ghio3, Paola Argiento2, Vincenzo Bellomo4, Natale Daniele Brunetti5, Gavino Casu6, Marco Confalonieri7, Marco Corda8, Michele Correale9, Carlo D'Agostino10, Lucrezia De Michele10, Giuseppe Galgano4, Alessandra Greco3, Carlo Lombardi11, Giovanna Manzi1, Valentina Mercurio12, Massimiliano Mulè13, Giuseppe Paciocco14, Silvia Papa1, Emanuele Romeo2, Laura Scelsi3, Davide Stolfo15, Patrizio Vitulo16, Robert Naeije17, Carmine Dario Vizza1. 1. Department of Cardiovascular and Respiratory Sciences, Sapienza University of Rome, Rome, Italy. 2. Department of Cardiology, Monaldi Hospital, University L. Vanvitelli, Naples, Italy. 3. Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Policlinico S Matteo, Pavia, Italy. 4. Department of Cardiology, F.Miulli Hospital, Acquaviva delle Fonti, Bari, Italy. 5. Department of Medical and Surgical Sciences, University of Foggia, Foggia, Italy. 6. Azienda per la Tutela della Salute Sardegna-Area Socio Sanitaria Locale Nuoro, San Francesco Hospital, Nuoro, Italy. 7. Pulmonology Unit, Heart-Thorax-Vessels Department, University Hospital of Cattinara, Trieste, Italy. 8. Azienda Ospedaliera G. Brotzu San Michele, Cagliari, Italy. 9. Cardiology Department, Ospedali Riuniti University Hospital, Foggia, Italy. 10. Cardiology Department, University Hospital Policlinico Consorziale Bari, Italy. 11. Cardiologia, Università degli studi di Brescia, Brescia, Italy. 12. Department of Translational Medical Sciences, Federico II University of Naples, Naples, Italy. 13. Ferrarotto Hospital, Catania, Italy. 14. Dipartimento Cardio-Toraco-Vascolare, Clinica Pneumologica, Azienda Ospedaliera San Gerardo, Monza, Italy. 15. Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy. 16. Pulmonology Unit, Istituti di Ricovero e Cura a Carattere Scientifico, Istituto Mediterraneo Trapianti e Terapie ad Alta Specializzazione, Palermo, Italy; and. 17. Department of Pathophysiology, Free University of Brussels, Brussels, Belgium.
Abstract
Rationale: An initial oral combination of drugs is being recommended in pulmonary arterial hypertension (PAH), but the effects of this approach on risk reduction and pulmonary vascular resistance (PVR) are not known. Objectives: To test the hypothesis that a low-risk status would be determined by the reduction of PVR in patients with PAH treated upfront with a combination of oral drugs. Methods: The study enrolled 181 treatment-naive patients with PAH (81% idiopathic) with a follow-up right heart catheterization at 6 months (interquartile range, 144-363 d) after the initial combination of endothelin receptor antagonist + phosphodiesterase-5 inhibitor drugs and clinical evaluation and risk assessments by European guidelines and Registry to Evaluate Early and Long-Term PAH Disease Management scores.Measurements and Main Results: Initial combination therapy improved functional class and 6-minute-walk distance and decreased PVR by an average of 35% (median, 40%). One-third of the patients had a decrease in PVR <25%. This poor hemodynamic response was independently predicted by age, male sex, pulmonary artery pressure and cardiac index, and at echocardiography, a right/left ventricular surface area ratio of greater than 1 associated with low tricuspid annular plane systolic excursion of less than 18 mm. A low-risk status at 6 months was achieved or maintained in only 34.8% (Registry to Evaluate Early and Long-Term PAH Disease Management score) to 43.1% (European score) of the patients. Adding criteria of poor hemodynamic response improved prediction of a low-risk status.Conclusions: A majority of patients with PAH still insufficiently improved after 6 months of initial combinations of oral drugs is identifiable at initial evaluation by hemodynamic response criteria added to risk scores.
Rationale: An initial oral combination of drugs is being recommended in pulmonary arterial hypertension (PAH), but the effects of this approach on risk reduction and pulmonary vascular resistance (PVR) are not known. Objectives: To test the hypothesis that a low-risk status would be determined by the reduction of PVR in patients with PAH treated upfront with a combination of oral drugs. Methods: The study enrolled 181 treatment-naive patients with PAH (81% idiopathic) with a follow-up right heart catheterization at 6 months (interquartile range, 144-363 d) after the initial combination of endothelin receptor antagonist + phosphodiesterase-5 inhibitor drugs and clinical evaluation and risk assessments by European guidelines and Registry to Evaluate Early and Long-Term PAH Disease Management scores.Measurements and Main Results: Initial combination therapy improved functional class and 6-minute-walk distance and decreased PVR by an average of 35% (median, 40%). One-third of the patients had a decrease in PVR <25%. This poor hemodynamic response was independently predicted by age, male sex, pulmonary artery pressure and cardiac index, and at echocardiography, a right/left ventricular surface area ratio of greater than 1 associated with low tricuspid annular plane systolic excursion of less than 18 mm. A low-risk status at 6 months was achieved or maintained in only 34.8% (Registry to Evaluate Early and Long-Term PAH Disease Management score) to 43.1% (European score) of the patients. Adding criteria of poor hemodynamic response improved prediction of a low-risk status.Conclusions: A majority of patients with PAH still insufficiently improved after 6 months of initial combinations of oral drugs is identifiable at initial evaluation by hemodynamic response criteria added to risk scores.
Authors: Rebecca R Vanderpool; Kendall S Hunter; Michael Insel; Joe G N Garcia; Edward J Bedrick; Ryan J Tedford; Franz P Rischard Journal: Chest Date: 2021-10-09 Impact factor: 10.262
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