Skip to main content
Erschienen in: Hernia 5/2014

01.10.2014 | Original Article

Comparative analysis of histopathologic responses to implanted porcine biologic meshes

verfasst von: Y. W. Novitsky, S. B. Orenstein, D. L. Kreutzer

Erschienen in: Hernia | Ausgabe 5/2014

Einloggen, um Zugang zu erhalten

Abstract

Objectives

Biologic mesh (BM) prostheses are increasingly utilized for hernia repairs. Modern BMs are not only derived from different tissue sources, but also undergo various proprietary processing steps—factors that likely impact host tissue responses and mesh performance. We aimed to compare histopathologic responses to various BMs after implantation in a mouse model.

Materials and methods

Five-mm samples of non-crosslinked [Strattice (ST)], and intentionally crosslinked [CollaMend (CM), Permacol (PC)] porcine-derived biologic meshes were implanted subcutaneously in C57BL/6 mice. 1, 4, 8, and 12 weeks post-implantation, meshes were assessed for inflammation, foreign body reaction (FBR), neocellularization, and collagen deposition using H&E and trichrome stains.

Results

All meshes induced early polymorphonuclear cell infiltration (highest in CM; lowest in ST) that resolved by 4 weeks. ST was associated with extensive macrophage presence at 12 weeks. Foreign body response was not seen in the ST group, but was present abundantly in the CM and PC groups, highest at 8 weeks. New peripheral collagen deposition was seen only in the ST group at 12 weeks. Collagen organization was highest in the ST group as well. Both CM and PC groups were associated with fibrous encapsulation and no evidence of integration or remodeling.

Conclusions

Inflammation appears to be a common component of integration of all biologic meshes studied. Pronounced inflammatory responses as well as profound FBR likely lead to observed encapsulation and poor host integration of the crosslinked BMs. Overall, ST was associated with the lowest foreign body response and the highest degree of new collagen deposition and organization. These features may be key predictors for improved mesh performance during hernia repair.
Literatur
3.
Zurück zum Zitat Rutkow IM (2003) Demographic and socioeconomic aspects of hernia repair in the United States in 2003. Surg Clin North Am 83(5):1045–1051 (v–vi)PubMedCrossRef Rutkow IM (2003) Demographic and socioeconomic aspects of hernia repair in the United States in 2003. Surg Clin North Am 83(5):1045–1051 (v–vi)PubMedCrossRef
6.
Zurück zum Zitat Milburn ML, Holton LH, Chung TL, Li EN, Bochicchio GV, Goldberg NH, Silverman RP (2008) Acellular dermal matrix compared with synthetic implant material for repair of ventral hernia in the setting of peri-operative Staphylococcus aureus implant contamination: a rabbit model. Surg Infect (Larchmt) 9(4):433–442. doi:10.1089/sur.2007.044 CrossRef Milburn ML, Holton LH, Chung TL, Li EN, Bochicchio GV, Goldberg NH, Silverman RP (2008) Acellular dermal matrix compared with synthetic implant material for repair of ventral hernia in the setting of peri-operative Staphylococcus aureus implant contamination: a rabbit model. Surg Infect (Larchmt) 9(4):433–442. doi:10.​1089/​sur.​2007.​044 CrossRef
7.
Zurück zum Zitat Saettele TM, Bachman SL, Costello CR, Grant SA, Cleveland DS, Loy TS, Kolder DG, Ramshaw BJ (2007) Use of porcine dermal collagen as a prosthetic mesh in a contaminated field for ventral hernia repair: a case report. Hernia 11(3):279–285. doi:10.1007/s10029-006-0186-z PubMedCrossRef Saettele TM, Bachman SL, Costello CR, Grant SA, Cleveland DS, Loy TS, Kolder DG, Ramshaw BJ (2007) Use of porcine dermal collagen as a prosthetic mesh in a contaminated field for ventral hernia repair: a case report. Hernia 11(3):279–285. doi:10.​1007/​s10029-006-0186-z PubMedCrossRef
15.
Zurück zum Zitat Rosen MJ (2010) Biologic mesh for abdominal wall reconstruction: a critical appraisal. Am Surg 76(1):1–6PubMed Rosen MJ (2010) Biologic mesh for abdominal wall reconstruction: a critical appraisal. Am Surg 76(1):1–6PubMed
20.
Zurück zum Zitat Sandor M, Xu H, Connor J, Lombardi J, Harper JR, Silverman RP, McQuillan DJ (2008) Host response to implanted porcine-derived biologic materials in a primate model of abdominal wall repair. Tissue Eng Part A 14(12):2021–2031. doi:10.1089/ten.tea.2007.0317 PubMedCrossRef Sandor M, Xu H, Connor J, Lombardi J, Harper JR, Silverman RP, McQuillan DJ (2008) Host response to implanted porcine-derived biologic materials in a primate model of abdominal wall repair. Tissue Eng Part A 14(12):2021–2031. doi:10.​1089/​ten.​tea.​2007.​0317 PubMedCrossRef
21.
Zurück zum Zitat Khor E (1997) Methods for the treatment of collagenous tissues for bioprostheses. Biomaterials 18(2):95–105PubMedCrossRef Khor E (1997) Methods for the treatment of collagenous tissues for bioprostheses. Biomaterials 18(2):95–105PubMedCrossRef
22.
Zurück zum Zitat Schmidt CE, Baier JM (2000) Acellular vascular tissues: natural biomaterials for tissue repair and tissue engineering. Biomaterials 21(22):2215–2231PubMedCrossRef Schmidt CE, Baier JM (2000) Acellular vascular tissues: natural biomaterials for tissue repair and tissue engineering. Biomaterials 21(22):2215–2231PubMedCrossRef
23.
Zurück zum Zitat Chaplin JM, Costantino PD, Wolpoe ME, Bederson JB, Griffey ES, Zhang WX (1999) Use of an acellular dermal allograft for dural replacement: an experimental study. Neurosurgery 45(2):320–327PubMedCrossRef Chaplin JM, Costantino PD, Wolpoe ME, Bederson JB, Griffey ES, Zhang WX (1999) Use of an acellular dermal allograft for dural replacement: an experimental study. Neurosurgery 45(2):320–327PubMedCrossRef
25.
Zurück zum Zitat Xu H, Wan H, Sandor M, Qi S, Ervin F, Harper JR, Silverman RP, McQuillan DJ (2008) Host response to human acellular dermal matrix transplantation in a primate model of abdominal wall repair. Tissue Eng Part A 14(12):2009–2019. doi:10.1089/ten.tea.2007.0316 PubMedCrossRef Xu H, Wan H, Sandor M, Qi S, Ervin F, Harper JR, Silverman RP, McQuillan DJ (2008) Host response to human acellular dermal matrix transplantation in a primate model of abdominal wall repair. Tissue Eng Part A 14(12):2009–2019. doi:10.​1089/​ten.​tea.​2007.​0316 PubMedCrossRef
26.
Zurück zum Zitat Gouk SS, Lim TM, Teoh SH, Sun WQ (2008) Alterations of human acellular tissue matrix by gamma irradiation: histology, biomechanical property, stability, in vitro cell repopulation, and remodeling. J Biomed Mater Res B Appl Biomater 84(1):205–217. doi:10.1002/jbm.b.30862 PubMedCrossRef Gouk SS, Lim TM, Teoh SH, Sun WQ (2008) Alterations of human acellular tissue matrix by gamma irradiation: histology, biomechanical property, stability, in vitro cell repopulation, and remodeling. J Biomed Mater Res B Appl Biomater 84(1):205–217. doi:10.​1002/​jbm.​b.​30862 PubMedCrossRef
27.
Zurück zum Zitat Orenstein SB, Qiao Y, Klueh U, Kreutzer DL, Novitsky YW (2010) Activation of human mononuclear cells by porcine biologic meshes in vitro. Hernia. doi:10.1007/s10029-010-0634-7 Orenstein SB, Qiao Y, Klueh U, Kreutzer DL, Novitsky YW (2010) Activation of human mononuclear cells by porcine biologic meshes in vitro. Hernia. doi:10.​1007/​s10029-010-0634-7
29.
Zurück zum Zitat Xu H, Wan H, Sandor M, Qi S, Ervin F, Harper JR, Silverman RP, McQuillan DJ (2008) Host response to human acellular dermal matrix transplantation in a primate model of abdominal wall repair. Tissue Eng Part A 14(12):2009–2019. doi:10.1089/ten.tea.2007.0316 PubMedCrossRef Xu H, Wan H, Sandor M, Qi S, Ervin F, Harper JR, Silverman RP, McQuillan DJ (2008) Host response to human acellular dermal matrix transplantation in a primate model of abdominal wall repair. Tissue Eng Part A 14(12):2009–2019. doi:10.​1089/​ten.​tea.​2007.​0316 PubMedCrossRef
32.
Zurück zum Zitat Melman L, Jenkins ED, Hamilton NA, Bender LC, Brodt MD, Deeken CR, Greco SC, Frisella MM, Matthews BD (2011) Early biocompatibility of crosslinked and non-crosslinked biologic meshes in a porcine model of ventral hernia repair. Hernia 15(2):157–164. doi:10.1007/s10029-010-0770-0 PubMedCrossRefPubMedCentral Melman L, Jenkins ED, Hamilton NA, Bender LC, Brodt MD, Deeken CR, Greco SC, Frisella MM, Matthews BD (2011) Early biocompatibility of crosslinked and non-crosslinked biologic meshes in a porcine model of ventral hernia repair. Hernia 15(2):157–164. doi:10.​1007/​s10029-010-0770-0 PubMedCrossRefPubMedCentral
Metadaten
Titel
Comparative analysis of histopathologic responses to implanted porcine biologic meshes
verfasst von
Y. W. Novitsky
S. B. Orenstein
D. L. Kreutzer
Publikationsdatum
01.10.2014
Verlag
Springer Paris
Erschienen in
Hernia / Ausgabe 5/2014
Print ISSN: 1265-4906
Elektronische ISSN: 1248-9204
DOI
https://doi.org/10.1007/s10029-013-1203-7

Weitere Artikel der Ausgabe 5/2014

Hernia 5/2014 Zur Ausgabe

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

Karpaltunnelsyndrom BDC Leitlinien Webinare
CME: 2 Punkte

Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

Radiusfraktur BDC Leitlinien Webinare
CME: 2 Punkte

Das Webinar beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

Appendizitis BDC Leitlinien Webinare
CME: 2 Punkte

Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.