Pivotal Clinical Study to Evaluate the Safety and Effectiveness of the MANTA Percutaneous Vascular Closure Device.


Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
07 2019
Historique:
entrez: 13 7 2019
pubmed: 13 7 2019
medline: 27 5 2020
Statut: ppublish

Résumé

Open surgical closure and small-bore suture-based preclosure devices have limitations when used for transcatheter aortic valve replacement, percutaneous endovascular abdominal aortic aneurysm repair, or percutaneous thoracic endovascular aortic aneurysm repair. The MANTA vascular closure device is a novel collagen-based technology designed to close large bore arteriotomies created by devices with an outer diameter ranging from 12F to 25F. In this study, we determined the safety and effectiveness of the MANTA vascular closure device. A prospective, single arm, multicenter investigation in patients undergoing transcatheter aortic valve replacement, percutaneous endovascular abdominal aortic aneurysm repair, or thoracic endovascular aortic aneurysm repair at 20 sites in North America. The primary outcome was time to hemostasis. The primary safety outcomes were accessed site-related vascular injury or bleeding complications. A total of 341 patients, 78 roll-in, and 263 in the primary analysis cohort, were entered in the study between November 2016 and September 2017. For the primary analysis cohort, transcatheter aortic valve replacement was performed in 210 (79.8%), and percutaneous endovascular abdominal aortic aneurysm repair or thoracic endovascular aortic aneurysm repair was performed in 53 (20.2%). The 14F MANTA was used in 42 cases (16%), and the 18F was used in 221 cases(84%). The mean effective sheath outer diameter was 22F (7.3 mm). The mean time to hemostasis was 65±157 seconds with a median time to hemostasis of 24 seconds. Technical success was achieved in 257 (97.7%) patients, and a single device was deployed in 262 (99.6%) of cases. Valve Academic Research Consortium-2 major vascular complications occurred in 11 (4.2%) cases: 4 received a covered stent (1.5%), 3 had access site bleeding (1.1%), 2 underwent surgical repair (0.8%), and 2 underwent balloon inflation (0.8%). In a selected population, this study demonstrated that the MANTA percutaneous vascular closure device can safely and effectively close large bore arteriotomies created by current generation transcatheter aortic valve replacement, percutaneous endovascular abdominal aortic aneurysm repair, and thoracic endovascular aortic aneurysm repair devices. URL: https://www.clinicaltrials.gov . Unique identifier: NCT02908880.

Sections du résumé

BACKGROUND
Open surgical closure and small-bore suture-based preclosure devices have limitations when used for transcatheter aortic valve replacement, percutaneous endovascular abdominal aortic aneurysm repair, or percutaneous thoracic endovascular aortic aneurysm repair. The MANTA vascular closure device is a novel collagen-based technology designed to close large bore arteriotomies created by devices with an outer diameter ranging from 12F to 25F. In this study, we determined the safety and effectiveness of the MANTA vascular closure device.
METHODS AND RESULTS
A prospective, single arm, multicenter investigation in patients undergoing transcatheter aortic valve replacement, percutaneous endovascular abdominal aortic aneurysm repair, or thoracic endovascular aortic aneurysm repair at 20 sites in North America. The primary outcome was time to hemostasis. The primary safety outcomes were accessed site-related vascular injury or bleeding complications. A total of 341 patients, 78 roll-in, and 263 in the primary analysis cohort, were entered in the study between November 2016 and September 2017. For the primary analysis cohort, transcatheter aortic valve replacement was performed in 210 (79.8%), and percutaneous endovascular abdominal aortic aneurysm repair or thoracic endovascular aortic aneurysm repair was performed in 53 (20.2%). The 14F MANTA was used in 42 cases (16%), and the 18F was used in 221 cases(84%). The mean effective sheath outer diameter was 22F (7.3 mm). The mean time to hemostasis was 65±157 seconds with a median time to hemostasis of 24 seconds. Technical success was achieved in 257 (97.7%) patients, and a single device was deployed in 262 (99.6%) of cases. Valve Academic Research Consortium-2 major vascular complications occurred in 11 (4.2%) cases: 4 received a covered stent (1.5%), 3 had access site bleeding (1.1%), 2 underwent surgical repair (0.8%), and 2 underwent balloon inflation (0.8%).
CONCLUSIONS
In a selected population, this study demonstrated that the MANTA percutaneous vascular closure device can safely and effectively close large bore arteriotomies created by current generation transcatheter aortic valve replacement, percutaneous endovascular abdominal aortic aneurysm repair, and thoracic endovascular aortic aneurysm repair devices.
CLINICAL TRIAL REGISTRATION
URL: https://www.clinicaltrials.gov . Unique identifier: NCT02908880.

Identifiants

pubmed: 31296082
doi: 10.1161/CIRCINTERVENTIONS.119.007258
doi:

Banques de données

ClinicalTrials.gov
['NCT02908880']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e007258

Commentaires et corrections

Type : CommentIn

Auteurs

David A Wood (DA)

Center for Heart Valve Innovation, St Paul's and Vancouver General Hospital, University of British Columbia, Vancouver, Canada (D.A.W., J.S., S.L., J.G.W.).

Zvonimir Krajcer (Z)

Baylor St Luke Hospital, Houston, TX (Z.K., N.S.).

Janarthanan Sathananthan (J)

Center for Heart Valve Innovation, St Paul's and Vancouver General Hospital, University of British Columbia, Vancouver, Canada (D.A.W., J.S., S.L., J.G.W.).

Neil Strickman (N)

Baylor St Luke Hospital, Houston, TX (Z.K., N.S.).

Chris Metzger (C)

Wellmont CVA Heart Institution, TN (C.M.).

William Fearon (W)

Stanford University Medical Center, CA (W.F., J.T.L., M.D.).

Mark Aziz (M)

Holston Valley Medical Center, TN (M.A.).

Lowell F Satler (LF)

MedStar Washington Hospital Center, Washington DC (L.F.S., R.W., I.B.-D., N.B.).

Ron Waksman (R)

MedStar Washington Hospital Center, Washington DC (L.F.S., R.W., I.B.-D., N.B.).

Marvin Eng (M)

Henry Ford Hospital, MI (M.E., W.W.O.).

Samir Kapadia (S)

Cleveland Clinic Foundation, OH (S. Kapadia, A.K.).

Adam Greenbaum (A)

Emory University Hospital, GA (A.G.).

Molly Szerlip (M)

The Heart Hospital Baylor Plano, TX (M.S., S.P., D.B.).

David Heimansohn (D)

St Vincent Heart Center, IN (D.H., A.S., S.M.).

Andrew Sampson (A)

St Vincent Heart Center, IN (D.H., A.S., S.M.).

Paul Coady (P)

Lankenau Medical Center, PA (P.C., R.R.).

Roberto Rodriguez (R)

Lankenau Medical Center, PA (P.C., R.R.).

Amar Krishnaswamy (A)

Cleveland Clinic Foundation, OH (S. Kapadia, A.K.).

Jason T Lee (JT)

Stanford University Medical Center, CA (W.F., J.T.L., M.D.).

Itsik Ben-Dor (I)

MedStar Washington Hospital Center, Washington DC (L.F.S., R.W., I.B.-D., N.B.).

Sina Moainie (S)

St Vincent Heart Center, IN (D.H., A.S., S.M.).

Susheel Kodali (S)

Columbia-Presbyterian Hospital, NY (S. Kodali).

Adnan K Chhatriwalla (AK)

Saint Luke's Mid America Heart Institute, Kansas City (A.K.C., D.J.C.).

Pradeep Yadav (P)

Penn State Health/Hershey Medical Center, PA (P.Y., M.K.).

Brian O'Neill (B)

Temple University Hospital, PA (B.O.).

Mark Kozak (M)

Penn State Health/Hershey Medical Center, PA (P.Y., M.K.).

John M Bacharach (JM)

North Central Heart, SD (J.M.B.).

Ted Feldman (T)

Evanston Hospital, IL (T.F.).

Mayra Guerrero (M)

Mayo Clinic, MN (M.G.).

Aravinda Nanjundappa (A)

CAMC Health Education and Research, WV (A.N., J.C.).

Robert Bersin (R)

Swedish Heart and Vascular, WA (R.B., M.Z.).

Ming Zhang (M)

Swedish Heart and Vascular, WA (R.B., M.Z.).

Srinivasa Potluri (S)

The Heart Hospital Baylor Plano, TX (M.S., S.P., D.B.).

Colin Barker (C)

DeBakey Heart and Vascular Center, TX (C.B.).

Nelson Bernardo (N)

MedStar Washington Hospital Center, Washington DC (L.F.S., R.W., I.B.-D., N.B.).

Alan Lumsden (A)

The Houston Methodist Hospital, TX (A.L.).

Andrew Barleben (A)

University of California San Diego, CA (A.B.).

John Campbell (J)

CAMC Health Education and Research, WV (A.N., J.C.).

David J Cohen (DJ)

Saint Luke's Mid America Heart Institute, Kansas City (A.K.C., D.J.C.).

Michael Dake (M)

Stanford University Medical Center, CA (W.F., J.T.L., M.D.).

David Brown (D)

The Heart Hospital Baylor Plano, TX (M.S., S.P., D.B.).

Nathaniel Maor (N)

Essential Medical Inc, PA (N.M., S.N.).

Samuel Nardone (S)

Essential Medical Inc, PA (N.M., S.N.).

Sandra Lauck (S)

Center for Heart Valve Innovation, St Paul's and Vancouver General Hospital, University of British Columbia, Vancouver, Canada (D.A.W., J.S., S.L., J.G.W.).

William W O'Neill (WW)

Henry Ford Hospital, MI (M.E., W.W.O.).

John G Webb (JG)

Center for Heart Valve Innovation, St Paul's and Vancouver General Hospital, University of British Columbia, Vancouver, Canada (D.A.W., J.S., S.L., J.G.W.).

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