In vitro mechanical behavior and in vivo healing response of a novel thin-strut ultrahigh molecular weight poly-l-lactic acid sirolimus-eluting bioresorbable coronary scaffold in normal swine.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 21 08 2018
revised: 13 02 2019
accepted: 03 04 2019
pubmed: 11 4 2019
medline: 13 2 2020
entrez: 11 4 2019
Statut: ppublish

Résumé

New generation bioresorbable scaffolds (BRS) promise to improve the outcomes of current generation BRS technologies by decreasing wall thickness while maintaining structural strength. This study aimed to compare the biomechanical behavior and vascular healing profile of a novel thin-walled (98 μm) sirolimus-eluting ultrahigh molecular weight BRS (Magnitude, Amaranth Medical) to the Absorb everolimus-eluting bioresorbable vascular scaffold (Abbott Vascular). In vitro biomechanical testing showed lower number of fractures on accelerated cycle testing over time (at 21K cycles = 20.0 [19.0-21.0] in Absorb versus 0.0 [0.0-1.0] in Magnitude-BRS). Either Magnitude (n = 43) or Absorb (n = 22) was implanted in 65 coronary segments of 22 swine. Scaffold strut's coverage was evaluated using serial optical coherence tomography (OCT) analysis. At 14 days, Magnitude-BRS demonstrated a higher percentage of embedded struts (97.7% [95.3, 100.0] compared to Absorb (57.2% [48.0, 76.0], p = 0.003) and lower percentage of uncovered struts (0.0% [0.0, 0.0] versus Absorb 5.5% [2.6, 7.7], p = 0.02). Also, it showed a lower percent late recoil (-1.02% [-4.11, 3.21] versus 4.42% [-1.10, 8.74], p = 0.04) at 28 days. Histopathology revealed comparable neointimal proliferation and vascular healing responses between two devices up to 180 days. A new generation thin walled (98-μm) Magnitude-BRS displayed a promising biomechanical behavior and strut healing profile compared to Absorb at the experimental level. This new generation BRS platform has the potential to improve the clinical outcomes shown by the current generation BRS.

Sections du résumé

BACKGROUND
New generation bioresorbable scaffolds (BRS) promise to improve the outcomes of current generation BRS technologies by decreasing wall thickness while maintaining structural strength. This study aimed to compare the biomechanical behavior and vascular healing profile of a novel thin-walled (98 μm) sirolimus-eluting ultrahigh molecular weight BRS (Magnitude, Amaranth Medical) to the Absorb everolimus-eluting bioresorbable vascular scaffold (Abbott Vascular).
METHODS AND RESULTS
In vitro biomechanical testing showed lower number of fractures on accelerated cycle testing over time (at 21K cycles = 20.0 [19.0-21.0] in Absorb versus 0.0 [0.0-1.0] in Magnitude-BRS). Either Magnitude (n = 43) or Absorb (n = 22) was implanted in 65 coronary segments of 22 swine. Scaffold strut's coverage was evaluated using serial optical coherence tomography (OCT) analysis. At 14 days, Magnitude-BRS demonstrated a higher percentage of embedded struts (97.7% [95.3, 100.0] compared to Absorb (57.2% [48.0, 76.0], p = 0.003) and lower percentage of uncovered struts (0.0% [0.0, 0.0] versus Absorb 5.5% [2.6, 7.7], p = 0.02). Also, it showed a lower percent late recoil (-1.02% [-4.11, 3.21] versus 4.42% [-1.10, 8.74], p = 0.04) at 28 days. Histopathology revealed comparable neointimal proliferation and vascular healing responses between two devices up to 180 days.
CONCLUSION
A new generation thin walled (98-μm) Magnitude-BRS displayed a promising biomechanical behavior and strut healing profile compared to Absorb at the experimental level. This new generation BRS platform has the potential to improve the clinical outcomes shown by the current generation BRS.

Identifiants

pubmed: 30967275
pii: S0167-5273(18)35036-8
doi: 10.1016/j.ijcard.2019.04.012
pii:
doi:

Substances chimiques

Immunosuppressive Agents 0
Polyesters 0
poly(lactide) 459TN2L5F5
Sirolimus W36ZG6FT64

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

21-28

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Yanping Cheng (Y)

CRF-Skirball Center for Innovation, Orangeburg, NY, United States of America.

Pawel Gasior (P)

CRF-Skirball Center for Innovation, Orangeburg, NY, United States of America; 3rd Department of Cardiology, Medical University of Silesia, Katowice, Poland.

Kamal Ramzipoor (K)

Amaranth Medical, Inc., Mountain View, CA, United States of America.

Chang Lee (C)

Amaranth Medical, Inc., Mountain View, CA, United States of America.

Jenn C McGregor (JC)

CRF-Skirball Center for Innovation, Orangeburg, NY, United States of America.

Gerard B Conditt (GB)

CRF-Skirball Center for Innovation, Orangeburg, NY, United States of America.

Thomas McAndrew (T)

Cardiovascular Research Foundation, New York, NY, United States of America.

Grzegorz L Kaluza (GL)

CRF-Skirball Center for Innovation, Orangeburg, NY, United States of America.

Juan F Granada (JF)

CRF-Skirball Center for Innovation, Orangeburg, NY, United States of America; Cardiovascular Research Foundation, New York, NY, United States of America. Electronic address: jgranada@crf.org.

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Classifications MeSH