Urinary Bladder Matrix Scaffolds Promote Pericardium Repair in a Porcine Model.


Journal

The Journal of surgical research
ISSN: 1095-8673
Titre abrégé: J Surg Res
Pays: United States
ID NLM: 0376340

Informations de publication

Date de publication:
05 2020
Historique:
received: 11 09 2019
revised: 14 11 2019
accepted: 27 12 2019
pubmed: 1 2 2020
medline: 1 8 2020
entrez: 1 2 2020
Statut: ppublish

Résumé

Pericardium closure after cardiac surgery is recommended to prevent postoperative adhesions to the sternum. Synthetic materials have been used as substitutes, with limited results because of impaired remodeling and fibrotic tissue formation. Urinary bladder matrix (UBM) scaffolds promote constructive remodeling that more closely resemble the native tissue. The aim of the study is to evaluate the host response to UBM scaffolds in a porcine model of partial pericardial resection. Twelve Landrace pigs were subjected to a median sternotomy. A 5 × 7 cm pericardial defect was created and then closed with a 5 × 7 cm multilayer UBM patch (UBM group) or left as an open defect (control group). Animals were survived for 8 wk. End points included gross morphology, biomechanical testing, histology with semiquantitative score, and cardiac function. The UBM group showed mild adhesions, whereas the control group showed fibrosis at the repair site, with robust adhesions and injury to the coronary bed. Load at failure (gr) and stiffness (gr/mm) were lower in the UBM group compared with the native pericardium (199.9 ± 59.2 versus 405.3 ± 99.89 g, P = 0.0536 and 44.23 ± 15.01 versus 146.5 ± 24.38 g/mm, P = 0.0025, respectively). In the UBM group, the histology resembled native pericardial tissue, with neovascularization, neofibroblasts, and little inflammatory signs. In contrast, control group showed fibrotic tissue with mononuclear infiltrates and a lack of organized collagen fibers validated with a histologic score. Both groups had normal ultrasonography results without cardiac motility disorders. In this setting, UBM scaffolds showed appropriate features for pericardial repair, restoring tissue properties that could help reduce postsurgical adhesions and prevent its associated complications.

Identifiants

pubmed: 32001387
pii: S0022-4804(20)30011-1
doi: 10.1016/j.jss.2019.12.033
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

216-224

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Natalia Amigo (N)

Instituto de Medicina Traslacional, Trasplante y Bioingeniería (IMeTTyB), Universidad Favaloro-CONICET, Buenos Aires, Argentina.

Juan Martin Riganti (JM)

Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina.

Mauricio Ramirez (M)

Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina.

Lorenzi Andrea (L)

Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina.

Pedro Renda (P)

Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina.

Romina Lovera (R)

Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina.

Ariel Pascaner (A)

Instituto de Medicina Traslacional, Trasplante y Bioingeniería (IMeTTyB), Universidad Favaloro-CONICET, Buenos Aires, Argentina.

Carlos Vigliano (C)

Instituto de Medicina Traslacional, Trasplante y Bioingeniería (IMeTTyB), Universidad Favaloro-CONICET, Buenos Aires, Argentina; Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina.

Damián Craiem (D)

Instituto de Medicina Traslacional, Trasplante y Bioingeniería (IMeTTyB), Universidad Favaloro-CONICET, Buenos Aires, Argentina.

Thomas W Gilbert (TW)

Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania; ACell, Inc, Columbia, Maryland.

Nathaniel T Remlinger (NT)

Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania; ACell, Inc, Columbia, Maryland.

Alejandro Nieponice (A)

Instituto de Medicina Traslacional, Trasplante y Bioingeniería (IMeTTyB), Universidad Favaloro-CONICET, Buenos Aires, Argentina; Esophageal Unit, Hospital Universitario Fundación Favaloro, Buenos Aires, Argentina; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pensilvania. Electronic address: anieponi@ffavaloro.org.

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Classifications MeSH