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A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis

Background: Conflicting results from previous studies have led to dissent over whether surgical mesh is safe and effective in ventral hernia repair. A newer class of mesh known as a reinforced tissue matrix, combining a biologic scaffold and minimal polymer reinforcement, offers promise in reducing...

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Detalles Bibliográficos
Autores principales: DeNoto, George, Ceppa, Eugene P., Pacella, Salvatore J., Sawyer, Michael, Slayden, Geoffrey, Takata, Mark, Tuma, Gary, Yunis, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584945/
https://www.ncbi.nlm.nih.gov/pubmed/34768516
http://dx.doi.org/10.3390/jcm10214998
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author DeNoto, George
Ceppa, Eugene P.
Pacella, Salvatore J.
Sawyer, Michael
Slayden, Geoffrey
Takata, Mark
Tuma, Gary
Yunis, Jonathan
author_facet DeNoto, George
Ceppa, Eugene P.
Pacella, Salvatore J.
Sawyer, Michael
Slayden, Geoffrey
Takata, Mark
Tuma, Gary
Yunis, Jonathan
author_sort DeNoto, George
collection PubMed
description Background: Conflicting results from previous studies have led to dissent over whether surgical mesh is safe and effective in ventral hernia repair. A newer class of mesh known as a reinforced tissue matrix, combining a biologic scaffold and minimal polymer reinforcement, offers promise in reducing inflammatory response and increasing abdominal wall support. This study sought to assess the clinical utility of a reinforced tissue matrix (OviTex) in ventral hernia repair 12 months after implantation. Methods: This is a prospective, single-arm, multi-center study to evaluate the clinical performance of OviTex(®) 1S Permanent (OviTex) in the repair of primary or recurrent ventral hernias (VH) in consecutive patients (ClinicalTrials.gov/NCT03074474). The rate of surgical site occurrences (SSOs) was evaluated 90 days post-surgery as the primary endpoint. Hernia recurrence and the incidence of postoperative events were evaluated between three and 12 months as secondary endpoints. The incidence of other complications and patient-reported outcomes were also recorded. Results: Ninety-two (92) patients were enrolled in the study, of whom seventy-six (76) reached the 12-month follow-up. All patients were at least 18 years of age with a BMI of <40 kg/m(2). Hernia defects were <20 × 20 cm, classified as class I–III according to the CDC wound classification system. Of the 76 patients who reached 12-month follow-up, twenty-six (34%) had previous VH repairs and thirteen (17%) had previous surgical infection. Sixty (79%) had factors known to increase the risk of recurrence. Twenty patients (26%) experienced SSOs, with ten (13%) requiring procedural intervention. Two of the 75 patients (2.7%) experienced a recurrence. Conclusions: The low rate of hernia recurrence and SSOs requiring intervention illustrates the potential that reinforced tissue matrices, and OviTex 1S, in particular, have to improve outcomes in VH repairs. Follow-up to 24 months is ongoing.
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spelling pubmed-85849452021-11-12 A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis DeNoto, George Ceppa, Eugene P. Pacella, Salvatore J. Sawyer, Michael Slayden, Geoffrey Takata, Mark Tuma, Gary Yunis, Jonathan J Clin Med Article Background: Conflicting results from previous studies have led to dissent over whether surgical mesh is safe and effective in ventral hernia repair. A newer class of mesh known as a reinforced tissue matrix, combining a biologic scaffold and minimal polymer reinforcement, offers promise in reducing inflammatory response and increasing abdominal wall support. This study sought to assess the clinical utility of a reinforced tissue matrix (OviTex) in ventral hernia repair 12 months after implantation. Methods: This is a prospective, single-arm, multi-center study to evaluate the clinical performance of OviTex(®) 1S Permanent (OviTex) in the repair of primary or recurrent ventral hernias (VH) in consecutive patients (ClinicalTrials.gov/NCT03074474). The rate of surgical site occurrences (SSOs) was evaluated 90 days post-surgery as the primary endpoint. Hernia recurrence and the incidence of postoperative events were evaluated between three and 12 months as secondary endpoints. The incidence of other complications and patient-reported outcomes were also recorded. Results: Ninety-two (92) patients were enrolled in the study, of whom seventy-six (76) reached the 12-month follow-up. All patients were at least 18 years of age with a BMI of <40 kg/m(2). Hernia defects were <20 × 20 cm, classified as class I–III according to the CDC wound classification system. Of the 76 patients who reached 12-month follow-up, twenty-six (34%) had previous VH repairs and thirteen (17%) had previous surgical infection. Sixty (79%) had factors known to increase the risk of recurrence. Twenty patients (26%) experienced SSOs, with ten (13%) requiring procedural intervention. Two of the 75 patients (2.7%) experienced a recurrence. Conclusions: The low rate of hernia recurrence and SSOs requiring intervention illustrates the potential that reinforced tissue matrices, and OviTex 1S, in particular, have to improve outcomes in VH repairs. Follow-up to 24 months is ongoing. MDPI 2021-10-27 /pmc/articles/PMC8584945/ /pubmed/34768516 http://dx.doi.org/10.3390/jcm10214998 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
DeNoto, George
Ceppa, Eugene P.
Pacella, Salvatore J.
Sawyer, Michael
Slayden, Geoffrey
Takata, Mark
Tuma, Gary
Yunis, Jonathan
A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis
title A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis
title_full A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis
title_fullStr A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis
title_full_unstemmed A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis
title_short A Prospective, Single Arm, Multi-Center Study Evaluating the Clinical Outcomes of Ventral Hernias Treated with OviTex(®) 1S Permanent Reinforced Tissue Matrix: The BRAVO Study 12-Month Analysis
title_sort prospective, single arm, multi-center study evaluating the clinical outcomes of ventral hernias treated with ovitex(®) 1s permanent reinforced tissue matrix: the bravo study 12-month analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584945/
https://www.ncbi.nlm.nih.gov/pubmed/34768516
http://dx.doi.org/10.3390/jcm10214998
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