Pre‐emptive treatment of heart failure exacerbations in patients managed with the HeartLogic™ algorithm

Author:

Garcia Rodrigue12ORCID,Gras Daniel3,Mansourati Jacques4,Defaye Pascal5,Bisson Arnaud67,Boveda Serge89,Gandjbakhch Estelle10,Gras Matthieu1,Gueffet Jean‐Pierre3,Himbert Caroline10,Jacon Peggy5,Khattar Pierre11,Lequeux Benoit1,Li Anthony12,Mansourati Vincent4,Minois Damien13,Marijon Eloi1415,Pierre Bertrand6,Probst Vincent13,Degand Bruno1,

Affiliation:

1. Department of Cardiology University Hospital of Poitiers Poitiers France

2. Centre d'investigation clinique 1402 University Hospital of Poitiers Poitiers France

3. Department of Cardiology Hôpital privé du Confluent Nantes France

4. Department of Cardiology University Hospital of Brest Brest France

5. Department of Cardiology University Hospital Grenoble Alpes Grenoble France

6. Department of Cardiology University Hospital of Tours Chambray‐lès‐Tours France

7. Department of Cardiology University Hospital of Orléans Orléans France

8. Department of Cardiology Clinique Pasteur Toulouse France

9. Universiteit Ziekenhuis, Vrije Universiteit Brussel (VUB) Jette Belgium

10. Department of Cardiology Hôpital la Pitié Salpétrière Paris France

11. Department of Cardiology Hospital of Lorient Lorient France

12. Department of Cardiology St. George's University of London, Cranmer Terrace London UK

13. Department of Cardiology University Hospital of Nantes Nantes Cedex 1 France

14. Department of Cardiology Hôpital Européen Georges Pomipdou Paris France

15. Paris‐Sudden Death Expertise Center (Paris‐SDEC) Paris France

Abstract

AbstractAimsHeart failure (HF) is a chronic disease affecting 64 million people worldwide and places a severe burden on society because of its mortality, numerous re‐hospitalizations and associated costs. HeartLogic™ is an algorithm programmed into implanted devices incorporating several biometric parameters which aims to predict HF episodes. It provides an index which can be monitored remotely, allowing pre‐emptive treatment of congestion to prevent acute decompensation. We aim to assess the impact and security of pre‐emptive HF management, guided by the HeartLogic™ index.Methods and resultsThe HeartLogic™ France Cohort Study is an investigator‐initiated, prospective, multi‐centre, non‐randomized study. Three hundred ten patients with a history of HF (left ventricular ejection fraction ≤40%; or at least one episode of clinical HF with elevated NT‐proBNP ≥450 ng/L) and implanted with a cardioverter defibrillator enabling HeartLogic™ index calculation will be included across 10 French centres. The HeartLogic™ index will be monitored remotely for 12 months and in the event of a HeartLogic™ index ≥16, the local investigator will contact the patient for assessment and adjust HF treatment as necessary. The primary endpoint is unscheduled hospitalization for HF. Secondary endpoints are all‐cause mortality, cardiovascular death, HF‐related death, unscheduled hospitalizations for ventricular or atrial arrhythmia and HeartLogic™ index evolution over time. Blood samples will be collected for biobanking, and quality of life will be assessed. Finally, the safety of a HeartLogic™‐triggered strategy for initiating or increasing diuretic therapy will be assessed. A blind and independent committee will adjudicate the events.ConclusionsThe HeartLogic™ France Cohort Study will provide robust real‐world data in a cohort of HF patients managed with the HeartLogic™ algorithm allowing pre‐emptive treatment of heart failure exacerbations.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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