Two year fesults of PROACTIVE-HF trial stratified by LVEF

Authors

Jason L. Guichard, Department of Medicine, Division of Cardiology, Section for Advanced Heart Failure, Pulmonary Hypertension, and Mechanical Circulatory Support, Prisma Health-Upstate, Greenville, South Carolina, United States. Electronic address: jason.guichard@prismahealth.org.
Eric L. Bonno, Department of Medicine, Division of Cardiology, Section for Advanced Heart Failure, Pulmonary Hypertension, and Mechanical Circulatory Support, Prisma Health-Upstate, Greenville, South Carolina, United States.
Michael E. Nassif, Saint Luke's Mid-American Heart Institute, Kansas City, Missouri, United States.
Taiyeb M. Khumri, Saint Luke's Mid-American Heart Institute, Kansas City, Missouri, United States.
David Miranda, Department of Cardiology, Minneapolis Heart Institute, Minneapolis, Minnesota, United States.
Orvar Jonsson, Department of Cardiology, Sanford Heart Hospital, Sioux Falls, South Dakota, United States.
Hirak Shah, Department of Cardiology, University of Kanas Medical Center, Kansas City, Kansas, United States.
Tamas Alexy, Department of Cardiology, University of Minnesota Medical Center, Minneapolis, Minnesota, United States.
Gregory P. Macaluso, Advocate Health - MidwestFollow
Gavin Hickey, Department of Cardiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States.
Patrick McCann, Department of Cardiology, Prisma Health, Columbia, South Carolina, United States.
Jennifer A. Cowger, Division of Cardiovascular Medicine, Henry Ford Hospital, Detroit, Michigan, United States.
Amit Badiye, Department of Cardiology, Sentara Healthcare, Norfolk, Virginia, United States.
Yasmin Raza, Department of Cardiology, Northwestern, Chicago, Illinois, United States.
Luke Masha, Department of Cardiology, Oregon Health & Science University, Portland, Oregon, United States.
Chandra Kunavarapu, Department of Cardiology, Methodist Healthcare, San Antonio, Texas, United States.
Mosi Bennett, Department of Cardiology, Minneapolis Heart Institute, Minneapolis, Minnesota, United States.
Faisal Sharif, Department of Cardiology, Galway University Hospital, Saolta Group, CURAM and University of Galway; Galway, Ireland.
Michael Kiernan, Cardiovascular Center, Division of Cardiology, Tufts Medical Center, Boston, Massachusetts, United States.
Wilfried Mullens, Department of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium and Hasselt University, Hasselt, Belgium.
Sandra V. Chaparro, Miami Cardiac and Vascular Institute, Division of Cardiology, Baptist Health South Florida, Miami, Florida, United States.
Claudius Mahr, Institute for Advanced Cardiac Care, Medical City Heart Hospital, Dallas, Texas, United States.
Rohit R. Amin, Department of Cardiology, Ascension Sacred Heart Hospital, Pensacola, Florida, United States.
Lynne Warner Stevenson, Division of Cardiology, Section of Heart Failure and Cardiac Transplantation, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Liviu Klein, Advanced Heart Failure Comprehensive Care Center and Division of Cardiology, University of California San Francisco, San Francisco, California, United States.

Affiliations

Advocate Christ Medical Center

Abstract

Background: In the PROACTIVE-HF trial, remote heart failure (HF) management using comprehensive vital signs and seated mean pulmonary artery pressure (mPAP) was safe and resulted in a low reported rate of HF hospitalization (HFH) and all-cause mortality (HFH/D) through 12 months. In this report, we extend the results from the PROACTIVE-HF study through 2 years, stratified by ejection fraction (EF).

Methods and results: PROACTIVE-HF was a prospective, multi-center, open-label, single-arm trial evaluating the safety and efficacy of patient management using the CordellaTM PA pressure sensor system in patients with New York Heart Association (NYHA) class III symptoms, regardless of EF. In the first 24 months, the incidence of HF events (HFE)/D was 0.89 [95% CI: 0.81, 0.99] events per patient, driven by HFH. Patients with HF with reduced EF (HFrEF) had higher HFE/D rates than those with HF with preserved EF (HFpEF) (1.0 vs 0.8 events per patient, p=0.048).

Conclusions: For HF patients experiencing moderate-severe symptoms, management using the Cordella PA sensor system was associated with low event rates and improved health status at 2 years, regardless of EF. Comprehensive remote monitoring of vital signs, seated PAP, and patient-reported symptoms via a digital platform supports sustained benefit for high-risk patients with HF.

Type

Article

PubMed ID

41833749


 

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