Synchronized diaphragmatic stimulation for heart failure using the VisONE system: a first-in-patient study.


Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
08 2022
Historique:
revised: 28 02 2022
received: 08 01 2022
accepted: 06 05 2022
pubmed: 28 5 2022
medline: 20 7 2022
entrez: 27 5 2022
Statut: ppublish

Résumé

Synchronized diaphragmatic stimulation (SDS) modulates intrathoracic and intra-abdominal pressures with favourable effects on cardiac function for patients with a reduced left ventricular ejection fraction (LVEF) and heart failure (HFrEF). VisONE-HF is a first-in-patient, observational study assessing the feasibility and 1 year effects of a novel, minimally invasive SDS device. The SDS system comprises a pulse generator and two laparoscopically delivered, bipolar, active-fixation leads on the inferior diaphragmatic surface. Fifteen symptomatic men with HFrEF and ischaemic heart disease receiving guideline-recommended therapy were enrolled (age 60 [56, 67] years, New York Heart Association class II [53%] /III [47%], LVEF 27 [23, 33] %, QRSd 117 [100, 125] ms, & N terminal pro brain natriuretic peptide [NT-proBNP] 1779 [911, 2,072] pg/mL). Implant success was 100%. Patients were evaluated at 3, 6, and 12 months for device-related or lead-related complications, quality of life (SF-36 QOL), 6 min hall walk distance (6MHWd), and by echocardiography. No implant procedure or SDS-related adverse event occurred, and patients were unaware of diaphragmatic stimulation. By 12 months, left ventricular end-systolic volume decreased (136 [123, 170] mL to 98 [89, 106] mL; P = 0.05), 6MHWd increased (315 [300, 330] m to 340 [315, 368] m; P = 0.004), and SF-36 QOL improved (physical scale 0 [0, 0] to 25 [0, 50], P = 0.006; emotional scale 0 [0, 33] to 33 [33, 67], P = 0.001). Although neither reached statistical significance, LVEF decreased (28 [23, 40]% vs. 34 [29, 38]%; P = ns) and NT-proBNP was lower (1784 [920, 2540] pg/mL vs. 1492 [879, 2028] pg/mL; P = ns). These data demonstrate the feasibility of laparoscopic implantation and delivery of SDS without raising safety concerns. These encouraging findings should be investigated further in adequately powered randomized trials.

Identifiants

pubmed: 35619238
doi: 10.1002/ehf2.13984
pmc: PMC9288796
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2207-2214

Informations de copyright

© 2022 VISACARDIA, INC. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Ana Jorbendaze (A)

Heart and Vascular Clinic, Tbilisi, Georgia.

Robin Young (R)

Robertson Centre for Biostatistics and Clinical Trials, University of Glasgow, University Avenue, Glasgow, G12 8QQ, UK.

Tamaz Shaburishvili (T)

Heart and Vascular Clinic, Tbilisi, Georgia.

Vitaly Demyanchuk (V)

Heart Institute, Ministry of Health of Ukraine, Kiev, Ukraine.

Roman Buriak (R)

Amosov National Institute of Cardiovascular Surgery, Kiev, Ukraine.

Borys Todurov (B)

Heart Institute, Ministry of Health of Ukraine, Kiev, Ukraine.

Kostyantyn Rudenko (K)

Amosov National Institute of Cardiovascular Surgery, Kiev, Ukraine.

Michel Zuber (M)

Heart Center, University Hospital, Zurich, Switzerland.

Simon F Stämpfli (SF)

Heart Center, University Hospital, Zurich, Switzerland.

Felix C Tanner (FC)

Heart Center, University Hospital, Zurich, Switzerland.

Paul Erne (P)

Faculty of Biomedical Sciences, University Svizzera Italiana, Lugano, Switzerland.

Michael Mirro (M)

School of Medicine, University of Indiana, Fort Wayne, IN, USA.

Marat Fudim (M)

Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Duke Clinical Research Institute, Durham, NC, USA.

Lee R Goldberg (LR)

Section of Advanced Heart Failure and Cardiac Transplant, Division of Cardiovascular Medicine, University of Pennsylvania, Philadelphia, PA, USA.

John G F Cleland (JGF)

Robertson Centre for Biostatistics and Clinical Trials, University of Glasgow, University Avenue, Glasgow, G12 8QQ, UK.

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Classifications MeSH