COMPETENCE Trial: The EVAHEART 2 continuous flow left ventricular assist device.


Journal

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
ISSN: 1557-3117
Titre abrégé: J Heart Lung Transplant
Pays: United States
ID NLM: 9102703

Informations de publication

Date de publication:
01 2023
Historique:
received: 09 05 2022
revised: 19 09 2022
accepted: 09 10 2022
pubmed: 9 11 2022
medline: 24 12 2022
entrez: 8 11 2022
Statut: ppublish

Résumé

Continuous flow left ventricular assist devices have improved outcomes in patients with end-stage heart failure that require mechanical circulatory support. Current devices have an adverse event profile that has hindered widespread application. The EVAHEART®2 left ventricular assist device (EVA2) has design features such as large blood gaps, lower pump speeds and an inflow cannula that does not protrude into the left ventricle that may mitigate the adverse events currently seen with other continuous flow devices. A prospective, multi-center randomized non-inferiority study, COMPETENCE Trial, is underway to assess non-inferiority of the EVA2 to the HeartMate 3 LVAS when used for the treatment of refractory advanced heart failure. The primary end-point is a composite of the individual primary outcomes: Survival to cardiac transplant or device explant for recovery; Free from disabling stroke; Free from severe Right Heart Failure after implantation of original device. Randomization is in a 2:1 (EVA2:HM3) ratio. The first patient was enrolled into the COMPETENCE Trial in December of 2020, and 25 subjects (16 EVA2 and 9 HM3) are currently enrolled. Enrollment of a safety cohort is projected to be completed by third quarter of 2022 at which time an interim analysis will be performed. Short-term cohort (92 EVA2 subjects) and long-term cohort is expected to be completed by the end of 2023 and 2024, respectively. The design features of the EVA2 such as a novel inflow cannula and large blood gaps may improve clinical outcomes but require further study. The ongoing COMPETENCE trial is designed to determine if the EVA2 is non-inferior to the HM3.

Sections du résumé

BACKGROUND
Continuous flow left ventricular assist devices have improved outcomes in patients with end-stage heart failure that require mechanical circulatory support. Current devices have an adverse event profile that has hindered widespread application. The EVAHEART®2 left ventricular assist device (EVA2) has design features such as large blood gaps, lower pump speeds and an inflow cannula that does not protrude into the left ventricle that may mitigate the adverse events currently seen with other continuous flow devices.
METHODS
A prospective, multi-center randomized non-inferiority study, COMPETENCE Trial, is underway to assess non-inferiority of the EVA2 to the HeartMate 3 LVAS when used for the treatment of refractory advanced heart failure. The primary end-point is a composite of the individual primary outcomes: Survival to cardiac transplant or device explant for recovery; Free from disabling stroke; Free from severe Right Heart Failure after implantation of original device. Randomization is in a 2:1 (EVA2:HM3) ratio.
RESULTS
The first patient was enrolled into the COMPETENCE Trial in December of 2020, and 25 subjects (16 EVA2 and 9 HM3) are currently enrolled. Enrollment of a safety cohort is projected to be completed by third quarter of 2022 at which time an interim analysis will be performed. Short-term cohort (92 EVA2 subjects) and long-term cohort is expected to be completed by the end of 2023 and 2024, respectively.
CONCLUSIONS
The design features of the EVA2 such as a novel inflow cannula and large blood gaps may improve clinical outcomes but require further study. The ongoing COMPETENCE trial is designed to determine if the EVA2 is non-inferior to the HM3.

Identifiants

pubmed: 36347767
pii: S1053-2498(22)02180-5
doi: 10.1016/j.healun.2022.10.011
pii:
doi:

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

33-39

Informations de copyright

Copyright © 2022 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

Auteurs

Steven R Allen (SR)

Penn State Health, Milton S. Hershey Medical Center, Hershey, Pennsylvania. Electronic address: sallen4@pennstatehealth.psu.edu.

Mark S Slaughter (MS)

University of Louisville, Louisville, Kentucky.

Mustafa M Ahmed (MM)

University of Florida, Gainesville, Florida.

Carlo R Bartoli (CR)

Geisinger Medical Center, Danville, Pennsylvania.

Ravi Dhingra (R)

University of Wisconsin Hospitals and Clinics, Madison, Wisconsin.

Gregory F Egnaczyk (GF)

The Christ Hospital, Cincinnati, Ohio.

Sanjeev K Gulati (SK)

Atrium Health Sanger Heart and Vascular Institute, Charlotte, North Carolina.

Michael S Kiernan (MS)

Tufts Medical Center, Boston, Massachusetts.

Claudius Mahr (C)

University of Washington, Seattle, Washington.

Dan M Meyer (DM)

Baylor Scott and White, Dallas, Texas.

Tadashi Motomura (T)

Evaheart, Inc, Houston, Texas.

Masahiro Ono (M)

Methodist Healthcare, San Antonio, Texas.

Ashwin Ravichandran (A)

Saint Vincent Health, Indianapolis, Indiana.

Alexis Shafii (A)

Baylor College of Medicine St. Luke's Medical Center, Houston, Texas.

Jason Smith (J)

University of Wisconsin Hospitals and Clinics, Madison, Wisconsin.

Behzad Soleimani (B)

Penn State Health, Milton S. Hershey Medical Center, Hershey, Pennsylvania.

Yoshiya Toyoda (Y)

Temple University Medical Center, Philadelphia, Pennsylvania.

Leora T Yarboro (LT)

University of Virginia, Charlottesville, Virginia.

Robert D Dowling (RD)

The Christ Hospital, Cincinnati, Ohio.

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