First human safety and effectiveness study of defibrillation with a novel patch wearable cardioverter-defibrillator.


Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
02 Jul 2024
Historique:
received: 16 05 2024
accepted: 30 06 2024
medline: 31 7 2024
pubmed: 31 7 2024
entrez: 31 7 2024
Statut: ppublish

Résumé

Wearable cardioverter-defibrillators (WCDs) are indicated in patients at risk of sudden cardiac arrest who are not immediate candidates for implantable defibrillator therapy. Limitations of existing WCDs include poor compliance and high false alarm rates. The Jewel is a novel patch-WCD (P-WCD) that addresses these limitations with an adhesive-based design for near-continuous wear and a machine learning algorithm designed to minimize inappropriate detections. This was a first-in-human study of the Jewel P-WCD conducted in an electrophysiology (EP) lab to determine the safety and effectiveness of the device in terminating ventricular tachycardia/ventricular fibrillation (VT/VF) with a single shock. The aim was to evaluate the safety and effectiveness of terminating VT/VF with a single shock using the Jewel P-WCD. This was a first-in-human, prospective, single-arm, single-centre study in patients scheduled for an EP procedure in which VT/VF was expected to either spontaneously occur or be induced. The Jewel P-WCD was placed on consented patients; upon confirmation of VT/VF, a single shock (150 J) was delivered via the device. A group sequential design and Pocock alpha spending function was used to measure the observed proportion of successful VT/VF single-shock terminations. The endpoint was achieved if the lower confidence limit exceeded the performance goal of 62%, using a one-sided lower 97.4% exact confidence bound. Of 18 eligible subjects, 16 (88.9%, 97.4% confidence bound: 65.4%) were successfully defibrillated with a single shock, exceeding the primary endpoint performance goal with no adverse events. This first-in-human evaluation of the Jewel P-WCD demonstrated the safety and effectiveness of terminating VT/VF. URL: https://clinicaltrials.gov/; Unique identifier: NCT05490459.

Identifiants

pubmed: 39082728
pii: 7723837
doi: 10.1093/europace/euae189
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT05490459']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Element Science, Inc

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Milan Chovanec (M)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.

Jan Petrů (J)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.

Pavel Hála (P)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.

Stepan Kralovec (S)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.

Anjali B Thakkar (AB)

Division of Cardiology, Department of Medicine, University of California San Francisco, 505 Parnassus Avenue, San Francisco, CA 94143, USA.

Kiran Mathews (K)

Element Science, Inc., Redwood City, CA, USA.

Maarten Dinger (M)

Element Science, Inc., Redwood City, CA, USA.

Steven Ullery (S)

North American Science Associates, Walnut Creek, CA, USA.

Zubin J Eapen (ZJ)

Element Science, Inc., Redwood City, CA, USA.

Uday N Kumar (UN)

Element Science, Inc., Redwood City, CA, USA.

Petr Neužil (P)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.

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Classifications MeSH