Safety, usability, and performance of a wireless left atrial pressure monitoring system in patients with heart failure: the VECTOR‐HF trial

Author:

D'Amario Domenico123,Meerkin David4,Restivo Attilio2,Ince Hüseyin56,Sievert Horst7,Wiese Andrea8,Schaefer Ulrich9,Trani Carlo12,Bayes‐Genis Antoni10,Leyva Francisco11,Whinnett Zachary I.12,Di Mario Carlo13,Jonas Michael14,Manhal Habib15,Amat‐Santos Ignacio J.16,Del Trigo Maria17,Gal Tuvia Ben1819,Avraham Binyamin Ben1819,Hasin Tal4,Feickert Sebastian56,D'Ancona Giuseppe56,Altisent Omar Abdul‐Jawad1020,Koren Oran19,Caspi Oren15,Abraham William T.21,Crea Filippo12,Anker Stefan D.22,Kornowski Ran18,Perl Leor1819,

Affiliation:

1. Department of Cardiovascular Sciences Fondazione Policlinico Universitario A. Gemelli IRCCS Rome Italy

2. Department of Cardiovascular and Thoracic Sciences Catholic University of the Sacred Heart Rome Italy

3. Department of Translational Medicine Maggiore della Carità Hospital, University of Eastern Piedmont Novara Italy

4. Jesselson Integrated Heart Center, Shaare Zedek Medical Center, Hebrew University Jerusalem Israel

5. Department of Cardiology Vivantes Klinikum im Friedrichshain and Am Urban Berlin Germany

6. Department of Cardiology Rostock University, Medical Center Rostock Germany

7. CardioVascular Center Frankfurt Frankfurt Germany

8. Department of Cardiology Angiology and Intensive Care Medicine, Marienhospital Hamburg Germany

9. Innovative Interventional Cardiology, Cardiovascular Center Bad Bevensen Germany

10. Department of Cardiology Germans Trias University Hospital Badalona Spain

11. Department of Cardiovascular Medicine Queen Elizabeth Hospital Birmingham UK

12. National Heart and Lung Institute, Imperial College London, Hammersmith Hospital London UK

13. Structural Interventional Cardiology Division, Department of Experimental and Clinical Medicine, Careggi University Hospital Florence Italy

14. Heart Institute, Kaplan Medical Center, Hebrew University School of Medicine Rehovot Israel

15. Departments of Cardiology Rambam Medical Centre and B Rappaport Faculty of Medicine, Technion Medical School Haifa Haifa Israel

16. CIBERCV, Cardiology Department, Hospital Clínico Universitario de Valladolid Valladolid Spain

17. Interventional Cardiology, Hospital Puerta de Hierro Majadahonda Madrid Spain

18. Cardiology Department, Rabin Medical Center, Tel‐Aviv University Petach Tikva Israel

19. School of Medicine, Tel‐Aviv University Tel‐Aviv Israel

20. Interventional Cardiologist, ICCV Hospital Clínic de Barcelona Barcelona Spain

21. Division of Cardiovascular Medicine The Ohio State University Columbus OH USA

22. Department of Cardiology (CVK) of German Heart Center Charité Institute of Health Center for Regenerative Therapies (BCRT); German Centre for Cardiovascular Research (DZHK), partner site Berlin, Charité Universitätsmedizin Berlin Germany

Abstract

AbstractAimsIn heart failure (HF), implantable haemodynamic monitoring devices have been shown to optimize therapy, anticipating clinical decompensation and preventing hospitalization. Direct left‐sided haemodynamic sensors offer theoretical benefits beyond pulmonary artery pressure monitoring systems. We evaluated the safety, usability, and performance of a novel left atrial pressure (LAP) monitoring system in HF patients.Methods and resultsThe VECTOR‐HF study (NCT03775161) was a first‐in‐human, prospective, multicentre, single‐arm, clinical trial enrolling 30 patients with HF. The device consisted of an interatrial positioned leadless sensor, able to transmit LAP data wirelessly. After 3 months, a right heart catheterization was performed to correlate mean pulmonary capillary wedge pressure (PCWP) with simultaneous mean LAP obtained from the device. Remote LAP measurements were then used to guide patient management. The miniaturized device was successfully implanted in all 30 patients, without acute major adverse cardiac and neurological events (MACNE). At 3 months, freedom from short‐term MACNE was 97%. Agreement between sensor‐calculated LAP and PCWP was consistent, with a mean difference of −0.22 ± 4.92 mmHg, the correlation coefficient and the Lin's concordance correlation coefficient values were equal to 0.79 (p < 0.0001) and 0.776 (95% confidence interval 0.582–0.886), respectively. Preliminary experience with V‐LAP‐based HF management was associated with significant improvements in New York Heart Association (NYHA) functional class (32% of patients reached NYHA class II at 6 months, p < 0.005; 60% of patients at 12 months, p < 0.005) and 6‐min walk test distance (from 244.59 ± 119.59 m at baseline to 311.78 ± 129.88 m after 6 months, p < 0.05, and 343.95 ± 146.15 m after 12 months, p < 0.05).ConclusionThe V‐LAP™ monitoring system proved to be generally safe and provided a good correlation with invasive PCWP. Initial evidence also suggests possible improvement in HF clinical symptoms.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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