Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/44803
Title: Seated Pulmonary Artery Pressure Monitoring in Patients With Heart Failure Results of the PROACTIVE-HF Trial
Authors: Guichard, Jason L.
Bonno, Eric L.
Nassif, Michael E.
Khumri, Taiyeb M.
Miranda, David
Jonsson, Orvar
Shah, Hirak
Alexy, Tamas
Macaluso, Gregory P.
Sur, James
Hickey, Gavin
Mccann, Patrick
Cowger, Jennifer A.
Badiye, Amit
Old, Wayne D.
Raza, Yasmin
Masha, Luke
Kunavarapu, Chandra R.
Bennett, Mosi
Sharif, Faisal
Kiernan, Michael
MULLENS, Wilfried 
Chaparro, Sandra V.
Mahr, Claudius
Amin, Rohit R.
Stevenson, Lynne Warner
Hiivala, Nicholas J.
Owens, Max M.
Sauerland, Andrea
Forouzan, Omid
Klein, Liviu
Issue Date: 2024
Publisher: ELSEVIER SCI LTD
Source: Jacc-heart Failure, 12 (11) , p. 1879 -1893
Abstract: BACKGROUND Monitoring supine pulmonary artery pressures to guide heart failure (HF) management has reduced HF hospitalizations in select patients. OBJECTIVES The purpose of this study was to evaluate the effect of managing seated mean pulmonary artery pressure (mPAP) with the Cordella Pulmonary Artery sensor on outcomes in patients with HF. METHODS Following GUIDE-HF (Hemodynamic-GUIDEd Management of Heart Failure Trial), with U.S. Food and Drug Administration input, PROACTIVE-HF (A Prospective, Multi-Center, Open Label, Single Arm Clinical Trial Evaluating the Safety and Efficacy of the Cordella Pulmonary Artery Sensor System in NYHA Class III Heart Failure Patients trial) was changed from a randomized to a single-arm, open label trial, conducted at 75 centers in the USA and Europe. Eligible patients had chronic HF with NYHA functional class III symptoms, irrespective of the ejection fraction, and recent HF hospitalization and/or elevated natriuretic peptides. The primary effectiveness endpoint at 6 months required the HF hospitalization or all-cause mortality rate to be lower than a performance goal of 0.43 events/patient, established from previous hemodynamic monitoring trials. Primary safety endpoints at 6 months were freedom from device- or system- related complications or pressure sensor failure. RESULTS Between February 7, 2020, and March 31, 2023, 456 patients were successfully implanted in modified intent-to-treat cohort. The 6-month event rate was 0.15 (95% CI: 0.12-0.20) which was significantly lower than performance goal (0.15 vs 0.43; P < 0.0001). Freedom from device- or system-related complications was 99.2% and freedom from sensor failure was 99.8% through 6 months. CONCLUSIONS Remote management of seated mPAP is safe and results in a low rate of HF hospitalizations and mortality. These results support the use of seated mPAP monitoring and extend the growing body of evidence that pulmonary artery pressure-guided management improves outcomes in heart failure.
Notes: Klein, L (corresponding author), Univ Calif San Francisco, M-1178B,Box 0124,505 Parnassus Ave, San Francisco, CA 94143 USA.
Liviu.Klein@ucsf.edu
Keywords: GDMT;heart failure;pulmonary artery pressure;remote monitoring
Document URI: http://hdl.handle.net/1942/44803
ISSN: 2213-1779
e-ISSN: 2213-1787
DOI: 10.1016/j.jchf.2024.05.017
ISI #: 001362415600001
Rights: 2024 THE AUTHORS. PUBLISHED BY ELSEVIER ON BEHALF OF THE AMERICAN COLLEGE OF CARDIOLOGY FO UNDATION. THIS IS AN OPEN ACCESS ARTICLE UNDER THE CC BY LICENSE ( http://creativecommons.org/licenses/by/4.0/ ) .
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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