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Prospective, multicenter study of antimicrobial-coated, noncrosslinked, acellular porcine dermal matrix (XenMatrix™ AB Surgical Graft) for hernia repair in all centers for disease control and prevention wound classes: 24-month follow-up cohort

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Last modified
  • 06/25/2025
Type of Material
Authors
    Obeid N Hahi, Washington University School of Medicine in St. LouisGeorge Velmahos, Massachusetts General HospitalJeffrey E Janis, The Ohio State UniversityStephen J Kovach, University of PennsylvaniaSusan F McLean, Texas Tech University Health Sciences Center El PasoReza Askari, Brigham and Women's HospitalCourtney A Sommer, Duke University Medical CenterSuresh Agarwal, Duke University Medical CenterJahnavi Srinivasan, Emory UniversityAlex K Wong, City of Hope National Med CenterAndrea Pakula, Kern MedicalEdward P Miranda, University of California, San FranciscoKerry Breen, Massachusetts General HospitalMark Shapiro, Duke University Medical CenterCorey R Deeken, Covalent Bio, LLCCody R Stringer, Covalent Bio, LLCReed J McGraw, University of PennsylvaniaCorey Bascone, University of PennsylvaniaRobert G Martindale, Oregon Health & Science University
Language
  • English
Date
  • 2023-05-01
Publisher
  • Wolters Kluwer Health, Inc.
Publication Version
Copyright Statement
  • © 2023 the Author(s). Published by Wolters Kluwer Health, Inc
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 85
Issue
  • 5
Start Page
  • 1571
End Page
  • 1577
Grant/Funding Information
  • This project was sponsored by Davol Inc. (Warwick, RI), a subsidiary of C. R. Bard, Inc. (Franklin Lakes, NJ). Bard and Davol have joined BD (Franklin Lakes, NJ).
Abstract
  • Background: Prospective, multicenter, single-arm study of antimicrobial-coated, noncrosslinked, acellular porcine dermal matrix (AC-PDM) in a cohort involving all centers for disease control and prevention wound classes in ventral/incisional midline hernia repair (VIHR). Materials and methods: Seventy-five patients (mean age 58.6 ± 12.7 years; BMI 31.3 ± 4.9 kg/m2) underwent ventral/incisional midline hernia repair with AC-PDM. Surgical site occurrence (SSO) was assessed in the first 45 days post-implantation. Length of stay, return to work, hernia recurrence, reoperation, quality of life, and SSO were assessed at 1, 3, 6, 12, 18, and 24 months. Results: 14.7% of patients experienced SSO requiring intervention within 45 days post-implantation, and 20.0% thereafter (> 45 d post-implantation). Recurrence (5.8%), definitely device-related adverse events (4.0%), and reoperation (10.7%) were low at 24 months; all quality-of-life indicators were significantly improved compared to baseline. Conclusion: AC-PDM exhibited favourable results, including infrequent hernia recurrence and definitely device-related adverse events, with reoperation and SSO comparable to other studies, and significantly improved quality of life.
Author Notes
  • R. G. Martindale, Division of General Surgery, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd, L223A, Portland 97239, OR Tel.: (503) 494-9145; fax: (503) 494-8884. E-mail address: martindr@ohsu.edu
Keywords
Research Categories
  • Health Sciences, Medicine and Surgery

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