Evidence map›Paper›PMID 36917566›Full record

ArticlePloS one2023

Defibrillation effectiveness and safety of the shock waveform used in a contemporary wearable cardioverter defibrillator: Results from animal and human studies.

Marye J Gleva, Joseph Sullivan, Thomas C Crawford, Greg Walcott, Ulrika Birgersdotter-Green, Kelley R Branch, Rahul N Doshi, Kaisa Kivilaid, Kelly Brennan, Ron K Rowbotham and 2 more

Registry-linked trialOpen access · goldFull text read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04132466 (ASSURE WCD Clinical Evaluation - Conversion Efficacy Study), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04132466 nacompletednot on this map

ASSURE WCD Clinical Evaluation - Conversion Efficacy Study (ACE-CONVERT)

TypeinterventionalSponsorKestra Medical Technologies, Inc.Ran2019 to 2020Enrolled13ConditionsDeath, Sudden, CardiacArmsDefibrillation using the ASSURE wearable cardioverter defibrillator therapy delivered via a waveform delivery test system
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. First human safety and effectiveness study of defibrillation with a novel patch wearable cardioverter-defibrillator.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 · 2024
    Trial
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Marye J GlevaDivision of Cardiology, Department of Medicine, Washington University in Saint Louis School of Medicine in Saint Louis, St. Louis, Missouri, United States of America.ORCID 0000-0002-0755-6437
Joseph SullivanKestra Medical Technologies, Inc., Redmond, Washington, United States of America.
Thomas C CrawfordDivision of Cardiology, Department of Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
Greg WalcottDivision of Cardiovascular Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Ulrika Birgersdotter-GreenUniversity of California San Diego, San Diego, CA, United States of America.
Kelley R BranchDivision of Cardiology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, United States of America.
Rahul N DoshiHonor Health, Scottsdale, AZ, United States of America.
Kaisa KivilaidLabcorp Inc., Minneapolis, MN, United States of America.
Kelly BrennanKestra Medical Technologies, Inc., Redmond, Washington, United States of America.ORCID 0000-0002-7698-7353
Ron K RowbothamKestra Medical Technologies, Inc., Redmond, Washington, United States of America.
Laura M GustavsonKestra Medical Technologies, Inc., Redmond, Washington, United States of America.ORCID 0000-0002-8212-3762
Jeanne E PooleDivision of Cardiology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, United States of America.
University of Washington · USHonorHealth · USUniversity of Alabama at Birmingham · USUniversity of California San Diego · USUniversity of Michigan · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe wearable cardioverter defibrillator (WCD) is used to protect patients at risk for sudden cardiac arrest. We examined defibrillation efficacy and safety of a biphasic truncated exponential waveform designed for use in a contemporary WCD in three animal studies and a human study.

methodsAnimal (swine) studies: #1: Efficacy comparison of a 170J BTE waveform (SHOCK A) to a 150J BTE waveform (SHOCK B) that approximates another commercially available waveform. Primary endpoint first shock success rate. #2: Efficacy comparison of the two waveforms at attenuated charge voltages in swine at three prespecified impedances. Primary endpoint first shock success rate. #3: Safety comparison of SHOCK A and SHOCK B in swine. Primary endpoint cardiac biomarker level changes baseline to 6 and 24 hours post-shock. Human Study: Efficacy comparison of SHOCK A to prespecified goal and safety evaluation. Primary endpoint cumulative first and second shock success rate. Safety endpoint adverse events.

resultsAnimal Studies #1: 120 VF episodes in six swine. First shock success rates for SHOCK A and SHOCK B were 100%; SHOCK A non-inferior to SHOCK B (entire 95% CI of rate difference above -10% margin, p < .001). #2: 2,160 VF episodes in thirty-six swine. Attenuated SHOCK A was non-inferior to attenuated SHOCK B at each impedance (entire 95% CI of rate difference above -10% margin, p < .001). #3: Ten swine, five shocked five times each with SHOCK A, five shocked five times each with SHOCK B. No significant difference in troponin I (p = 0.658) or creatine phosphokinase (p = 0.855) changes from baseline between SHOCK A and SHOCK B. Human Study: Thirteen patients, 100% VF conversion rate. Mild skin irritation from adhesive defibrillation pads in three patients.

conclusionsThe BTE waveform effectively and safely terminated induced VF in swine and a small sample in humans.

trial registrationHuman study clinical trial registration: URL: https://clinicaltrials.gov; Unique identifier: NCT04132466.

Indexed as

Ventricular FibrillationWearable Electronic DevicesAnimalsDefibrillatorsElectric CountershockHumansSwineTreatment Outcome

Identifiers

PMID36917566
PMCPMC10013906
OpenAlexW4324129684

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read120
identifiers read23
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.