TY - JOUR
T1 - Multiple cArdiac seNsors for mAnaGEment of Heart Failure (MANAGE-HF) – Phase I Evaluation of the Integration and Safety of the HeartLogic Multisensor Algorithm in Patients With Heart Failure
AU - MANAGE-HF Study
AU - HERNANDEZ, ADRIAN F.
AU - ALBERT, NANCY M.
AU - ALLEN, LARRY A.
AU - AHMED, REZWAN
AU - AVERINA, VIKTORIA
AU - BOEHMER, JOHN P.
AU - COWIE, MARTIN R.
AU - CHIEN, CHRISTOPHER V.
AU - GALVAO, MARIE
AU - KLEIN, LIVIU
AU - KWAN, BRIAN
AU - LAM, CAROLYN S.P.
AU - RUBLE, STEPHEN B.
AU - STOLEN, CRAIG M.
AU - STEIN, KENNETH
N1 - Funding Information:
Funding for this research was provided by Boston Scientific. Adrian Hernandez reports research grants from American Regent, AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb, Janssen, Merck, Novartis, Pfizer, and Verily; consulting fees from AstraZeneca, Amgen, Bayer, Boston Scientific, Cytokinetics, Merck, Myokardia, Novartis, and Relypsa. Larry Allen reports research Grants from the American Heart Association, National Institutes of Health, and Patient Centered Outcomes Research Institute; and consulting fees from ACI Clinical, Amgen, Boston Scientific, Cytokinetics, and Novartis. Christopher Chien reports consulting fees from Abbott Laboratories, Astra Zeneca, and Boston Scientific. Martin Cowie reports consulting fees from Abbott, Boston Scientific, Medtronic, AstraZeenca, Novarits, Pfizer, Bayer, Boehringer Ingelheim, Roche Diagnostics, and Servier. Nancy Albert reports consulting fees from Amgen, AstraZeneca, Boston Scientific, Merck, and Novartis. Liviu Klein reports research grants from Ancora Heart, CVRx, Optima Integrated Health, Respicardia, and V-Wave Medical; and consulting fees from Abbott, Boston Scientific, and Medtronic. Carolyn Lam reports research support from Boston Scientific, Bayer, Roche Diagnostics, AstraZeneca, Medtronic, and Vifor Pharma; consultancy fees from Abbott Diagnostics, Amgen, Applied Therapeutics, AstraZeneca, Bayer, Biofourmis, Boehringer Ingelheim, Boston Scientific, Corvia Medical, Cytokinetics, Darma Inc. Us2.ai, JanaCare, Janssen Research & Development LLC, Medtronic, Menarini Group, Merck, MyoKardia, Novartis, Novo Nordisk, Radcliffe Group Ltd. Roche Diagnostics, Sanofi, Stealth BioTherapeutics, The Corpus, Vifor Pharma, and WebMD Global LLC; and is the co-founder and a nonexecutive director of Us2.ai. Rezwan Ahmed, Viktoria Averina, Brian Kwan, Stephen Ruble, Kenneth Stein, and Craig Stolen are employees and shareholders of Boston Scientific. Marie Galvao reports consulting fees from Boston Scientific. Heart Center Research, LLC, Huntsville, AL; Rex Hospital, Raleigh, NC; Cardiology Associates of Northeast Arkansas, P.A. Jonesboro, AR; Catholic Medical Center, Manchester, NH; Hopital Prive du Confluent SAS, Nantes, France; Community Heart and Vascular Hospital, Indianapolis, IN; Sacred Heart Medical Center at Riverbend, Springfield, OR; Advanced Cardiovascular Specialists, Shreveport, LA; Sentara Norfolk General Hospital, Norfolk, VA; Emory University Hospital, Atlanta, GA; Penn State Milton S Hershey Medical Center, Hershey, PA; Centracare Heart and Vascular Center, St. Cloud, MN; Sharp Memorial Hospital, San Diego, CA; Universitaetsklinikum Wuerzburg, Wuerzburg, Germany; Parkview Hospital, Inc. Fort Wayne, IN; SouthEast Texas Clinical Research Center, Beaumont, TX; Stern Cardiovascular Foundation, Inc. Memphis, TN; United Heart and Vascular Clinic, St. Paul, MN; University of Southern California Hospital, Los Angeles, CA; Bethesda North Hospital, Cincinnati, OH; Cardiology Consultants of Philadelphia, Yardley, PA; CHRU Hopital Pontchaillou, Rennes, France; Duke University Medical Center, Durham, NC; Memorial Hospital, Colorado Springs, CO; Montefiore Medical Center, Bronx, NY; University of California, San Francisco, San Francisco, CA; Cardiovascular Consultants, Concord, CA; Lindner Center for Research and Education at Christ Hosp, Cincinnati, OH; University of Colorado Hospital, Aurora, CO, DSMB Members: DSMB Chair, Inder Anand, University of Minnesota, Minneapolis, MN; Akshay Desai, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts; David DeMets, University of Wisconsin-Madison, Madison, Clinical Event Committee Members: Clinical Event Committee Chair, Brian Jaski, Sharp Memorial Hospital, San Diego, CA; Teresa De Marco, University of California, San Francisco, CA; J. Thomas Heywood, Scripps Clinic, San Diego, CA.
Funding Information:
Funding for this research was provided by Boston Scientific.
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/8
Y1 - 2022/8
N2 - Background: Patients with heart failure (HF) and reduced ejection fraction suffer from a relapsing and remitting disease course, where early treatment changes may improve outcomes. We assessed the clinical integration and safety of the HeartLogic multisensor index and alerts in HF care. Methods: The Multiple cArdiac seNsors for mAnaGEment of Heart Failure (MANAGE-HF) study enrolled 200 patients with HF and reduced ejection fraction (<35%), New York Heart Association functional class II–III symptoms, implanted with a cardiac resynchronization therapy-defibrillator or and implantable cardioverter defibrillator, who had either a hospitalization for HF within 12 months or unscheduled visit for HF exacerbation within 90 days or an elevated natriuretic peptide concentration (brain natriuretic peptide [BNP] of ≥150 pg/mL or N-terminal pro-BNP [NT-proBNP] of ≥600 pg/mL). This phase included the development of an alert management guide and evaluated changes in medical treatment, natriuretic peptide levels, and safety. Results: The mean age of participants was 67 years, 68% were men, 81% were White, and 61% had a HF hospitalization in prior 12 months. During follow-up, there were 585 alert cases with an average of 1.76 alert cases per patient-year. HF medications were augmented during 74% of the alert cases. HF treatment augmentation within 2 weeks from an initial alert was associated with more rapid recovery of the HeartLogic Index. Five serious adverse events (0.015 per patient-year) occurred in relation to alert-prompted medication change. NTproBNP levels decreased from median of 1316 pg/mL at baseline to 743 pg/mL at 12 months (P <.001). Conclusions: HeartLogic alert management was safely implemented in HF care and may optimize HF management. This phase supports further evaluation in larger studies. Trial Registration: ClinicalTrials.gov
AB - Background: Patients with heart failure (HF) and reduced ejection fraction suffer from a relapsing and remitting disease course, where early treatment changes may improve outcomes. We assessed the clinical integration and safety of the HeartLogic multisensor index and alerts in HF care. Methods: The Multiple cArdiac seNsors for mAnaGEment of Heart Failure (MANAGE-HF) study enrolled 200 patients with HF and reduced ejection fraction (<35%), New York Heart Association functional class II–III symptoms, implanted with a cardiac resynchronization therapy-defibrillator or and implantable cardioverter defibrillator, who had either a hospitalization for HF within 12 months or unscheduled visit for HF exacerbation within 90 days or an elevated natriuretic peptide concentration (brain natriuretic peptide [BNP] of ≥150 pg/mL or N-terminal pro-BNP [NT-proBNP] of ≥600 pg/mL). This phase included the development of an alert management guide and evaluated changes in medical treatment, natriuretic peptide levels, and safety. Results: The mean age of participants was 67 years, 68% were men, 81% were White, and 61% had a HF hospitalization in prior 12 months. During follow-up, there were 585 alert cases with an average of 1.76 alert cases per patient-year. HF medications were augmented during 74% of the alert cases. HF treatment augmentation within 2 weeks from an initial alert was associated with more rapid recovery of the HeartLogic Index. Five serious adverse events (0.015 per patient-year) occurred in relation to alert-prompted medication change. NTproBNP levels decreased from median of 1316 pg/mL at baseline to 743 pg/mL at 12 months (P <.001). Conclusions: HeartLogic alert management was safely implemented in HF care and may optimize HF management. This phase supports further evaluation in larger studies. Trial Registration: ClinicalTrials.gov
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U2 - 10.1016/j.cardfail.2022.03.349
DO - 10.1016/j.cardfail.2022.03.349
M3 - Article
C2 - 35460884
AN - SCOPUS:85131130942
SN - 1071-9164
VL - 28
SP - 1245
EP - 1254
JO - Journal of Cardiac Failure
JF - Journal of Cardiac Failure
IS - 8
ER -