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Clinical Trial
. 2024 Jul 2;26(7):euae189.
doi: 10.1093/europace/euae189.

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

Affiliations
Clinical Trial

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

Milan Chovanec et al. Europace. .

Abstract

Aims: 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.

Methods and results: 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.

Conclusion: This first-in-human evaluation of the Jewel P-WCD demonstrated the safety and effectiveness of terminating VT/VF.

Clinical trial registration: URL: https://clinicaltrials.gov/; Unique identifier: NCT05490459.

Keywords: Sudden cardiac arrest; Ventricular arrhythmia; Wearable cardioverter-defibrillator.

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Figures

Graphical Abstract
Graphical Abstract
Figure 1
Figure 1
Schematic diagrams of the Jewel P-WCD and Jewel EP lab device. (A) Schematic diagram of the commercial-use Jewel P-WCD components and photo of the Jewel P-WCD applied to a patient’s body. (B) Schematic diagram of the manually operated Jewel P-WCD components (used in this study) including operator shock control and photo of the modified Jewel P-WCD applied to a patient’s body.

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