• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

评价在成熟腹侧切口疝修补的猪模型中使用开窗和非开窗生物移植物。

Evaluation of fenestrated and non-fenestrated biologic grafts in a porcine model of mature ventral incisional hernia repair.

机构信息

Section of Minimally Invasive Surgery, Department of Surgery, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box #8109, St. Louis, MO 63110, USA.

出版信息

Hernia. 2010 Dec;14(6):599-610. doi: 10.1007/s10029-010-0684-x. Epub 2010 Jun 12.

DOI:10.1007/s10029-010-0684-x
PMID:20549274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3826826/
Abstract

INTRODUCTION

The purpose of this study is to compare the tissue incorporation of a novel fenestrated and non-fenestrated crosslinked porcine dermal matrix (CPDM) (CollaMend™, Davol Inc., Warwick, RI) in a porcine model of ventral hernia repair.

METHODS

Bilateral abdominal wall defects were created in 12 Yucatan minipigs and repaired with a preperitoneal or intraperitoneal technique 21 days after hernia creation. Animals were randomized to fenestrated or non-fenestrated CPDM for n = 6 pieces of each graft in the preperitoneal or intraperitoneal location. All animals were sacrificed at 1 month. Adhesion characteristics and graft contraction/growth were measured by the Garrard adhesion grading scale and transparent grid overlay. Histological analysis of hematoxylin and eosin (H&E)-stained slides was performed to assess graft incorporation. Tissue incorporation strength was measured by a T-peel tensile test. The strength of explanted CPDM alone and de novo CPDM was measured by a uniaxial tensile test using a tensiometer (Instron, Norwood, MA) at a displacement rate of 0.42 mm/s. Statistical significance (P < 0.05) was determined for histological analysis using a Kruskal-Wallis non-parametric test with a Bonferroni correction, and for all other analyses using a two-way analysis of variance (ANOVA) with a Bonferroni post-test or a Kruskal-Wallis non-parametric test with a Dunn's post-test.

RESULTS

Intraperitoneal placement of fenestrated CPDM resulted in a significantly higher area of adhesions and adhesion score compared to the preperitoneal placement of fenestrated CPDM (P < 0.05). For both preperitoneal and intraperitoneal placement, histological findings demonstrated greater incorporation of the graft due to the fenestrations. No significant differences were detected in the uniaxial tensile strengths of the graft materials alone, either due to the graft type (non-fenestrated vs. fenestrated) or due to the placement location (preperitoneal vs. intraperitoneal). The incorporation strength (T-peel force) was significantly greater for fenestrated compared to non-fenestrated CPDM when placed in the preperitoneal location (P < 0.01). The incorporation strength was also significantly greater for fenestrated CPDM placed in the preperitoneal location compared to fenestrated CPDM placed in the intraperitoneal location (P < 0.05).

CONCLUSIONS

Fenestrations in CPDM result in greater tissue incorporation strength and lower adhesion area and score when placed in the preperitoneal location. Fenestrations in CPDM allow for greater tissue incorporation without accelerating graft degradation. Fenestrations may be placed in CPDM while still allowing adequate graft strength for intraperitoneal and preperitoneal hernia repairs at 1 month in a porcine model.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/cace51186c13/nihms-513411-f0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/2ddfb1c975b5/nihms-513411-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/e5b01e8b7c7c/nihms-513411-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/08fe3f885089/nihms-513411-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/7596821ab50e/nihms-513411-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/6d35689a66c7/nihms-513411-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/b3b08f3c4b02/nihms-513411-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/73f216973789/nihms-513411-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/d9252c2d5408/nihms-513411-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/2aea57fe45c6/nihms-513411-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/f0b10531cb95/nihms-513411-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/cace51186c13/nihms-513411-f0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/2ddfb1c975b5/nihms-513411-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/e5b01e8b7c7c/nihms-513411-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/08fe3f885089/nihms-513411-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/7596821ab50e/nihms-513411-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/6d35689a66c7/nihms-513411-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/b3b08f3c4b02/nihms-513411-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/73f216973789/nihms-513411-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/d9252c2d5408/nihms-513411-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/2aea57fe45c6/nihms-513411-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/f0b10531cb95/nihms-513411-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a0/3826826/cace51186c13/nihms-513411-f0011.jpg
摘要

简介

本研究旨在比较新型有孔和无孔交联猪真皮基质(CPDM)(CollaMend™,Davol Inc.,Warwick,RI)在猪腹疝修补模型中的组织整合。

方法

在 12 只 Yucatan 小型猪中创建双侧腹壁缺损,并在疝形成后 21 天通过腹膜前或腹腔内技术进行修复。动物随机分为有孔或无孔 CPDM,每组 n = 6 块,分别放置在腹膜前或腹腔内。所有动物均在 1 个月时处死。通过 Garra rd 粘连分级量表和透明网格叠加测量粘连特征和移植物收缩/生长。通过苏木精和伊红(H&E)染色载玻片的组织学分析评估移植物整合。通过 T 剥离拉伸试验测量组织整合强度。通过张力计(Instron,Norwood,MA)以 0.42mm/s 的位移率对单独植入的 CPDM 和新形成的 CPDM 进行单轴拉伸试验,测量 CPDM 的强度。使用 Kruskal-Wallis 非参数检验和 Bonferroni 校正进行组织学分析的统计学意义(P < 0.05),使用双向方差分析(ANOVA)和 Bonferroni 后检验或 Kruskal-Wallis 非参数检验和 Dunn 后检验进行所有其他分析。

结果

与腹膜前放置有孔 CPDM 相比,腹膜内放置有孔 CPDM 导致粘连面积和粘连评分显著升高(P < 0.05)。对于腹膜前和腹腔内放置,组织学发现由于有孔导致移植物的整合度更高。单独的移植物材料的单轴拉伸强度没有因移植物类型(无孔与有孔)或放置位置(腹膜前与腹腔内)而有显著差异。与无孔 CPDM 相比,当放置在腹膜前位置时,有孔 CPDM 的整合强度(T 剥离力)显著更高(P < 0.01)。与腹腔内放置的有孔 CPDM 相比,当放置在腹膜前位置时,有孔 CPDM 的整合强度也显著更高(P < 0.05)。

结论

CPDM 中的孔可在腹膜前位置提供更高的组织整合强度、更低的粘连面积和评分。CPDM 中的孔可在不加速移植物降解的情况下促进组织整合。在猪模型中,CPDM 中的孔可以放置在 1 个月时的腹膜内和腹膜前疝修补术中,同时保持足够的移植物强度。

相似文献

1
Evaluation of fenestrated and non-fenestrated biologic grafts in a porcine model of mature ventral incisional hernia repair.评价在成熟腹侧切口疝修补的猪模型中使用开窗和非开窗生物移植物。
Hernia. 2010 Dec;14(6):599-610. doi: 10.1007/s10029-010-0684-x. Epub 2010 Jun 12.
2
Biomechanical and histologic evaluation of fenestrated and nonfenestrated biologic mesh in a porcine model of ventral hernia repair.生物力学和组织学评价多孔和非多孔生物补片在猪腹疝修补模型中的应用。
J Am Coll Surg. 2011 Mar;212(3):327-39. doi: 10.1016/j.jamcollsurg.2010.12.006.
3
Histologic and biomechanical evaluation of a novel macroporous polytetrafluoroethylene knit mesh compared to lightweight and heavyweight polypropylene mesh in a porcine model of ventral incisional hernia repair.新型多孔聚四氟乙烯编织网与轻质和重质聚丙烯网在猪腹侧切口疝修补模型中的组织学和生物力学评价。
Hernia. 2011 Aug;15(4):423-31. doi: 10.1007/s10029-011-0787-z. Epub 2011 Jan 30.
4
Remodeling characteristics and biomechanical properties of a crosslinked versus a non-crosslinked porcine dermis scaffolds in a porcine model of ventral hernia repair.在猪腹疝修补模型中,交联与非交联猪真皮支架的重塑特征和生物力学特性
Hernia. 2015 Apr;19(2):207-18. doi: 10.1007/s10029-013-1070-2. Epub 2013 Mar 13.
5
Histologic and biomechanical evaluation of crosslinked and non-crosslinked biologic meshes in a porcine model of ventral incisional hernia repair.交联和非交联生物补片在猪腹侧切口疝修补模型中的组织学和生物力学评价。
J Am Coll Surg. 2011 May;212(5):880-8. doi: 10.1016/j.jamcollsurg.2011.01.006. Epub 2011 Mar 23.
6
Evaluation of intraperitoneal placement of absorbable and nonabsorbable barrier coated mesh secured with fibrin sealant in a New Zealand white rabbit model.评价可吸收和不可吸收的涂有防粘连膜的屏障网在新西兰大白兔模型中的腹腔内放置情况,并用纤维蛋白胶固定。
Surg Endosc. 2011 Feb;25(2):604-12. doi: 10.1007/s00464-010-1230-8. Epub 2010 Jul 22.
7
Pore size and pore shape--but not mesh density--alter the mechanical strength of tissue ingrowth and host tissue response to synthetic mesh materials in a porcine model of ventral hernia repair.孔径和孔隙形状——而非网孔密度——会改变猪腹疝修补模型中组织向内生长的机械强度以及宿主组织对合成网片材料的反应。
J Mech Behav Biomed Mater. 2015 Feb;42:186-97. doi: 10.1016/j.jmbbm.2014.11.011. Epub 2014 Nov 26.
8
Early biocompatibility of crosslinked and non-crosslinked biologic meshes in a porcine model of ventral hernia repair.交联与非交联生物补片在猪腹疝修补模型中的早期生物相容性。
Hernia. 2011 Apr;15(2):157-64. doi: 10.1007/s10029-010-0770-0. Epub 2011 Jan 8.
9
Non-cross-linked porcine acellular dermal matrices for abdominal wall reconstruction.用于腹壁重建的非交联猪脱细胞真皮基质。
Plast Reconstr Surg. 2010 Jan;125(1):167-176. doi: 10.1097/PRS.0b013e3181c2a6ed.
10
Sublay repair results in superior mesh incorporation and histological fibrogenesis in comparison to onlay and primary suture in an experimental rat model.在实验性大鼠模型中,与覆盖法和一期缝合相比,衬层修补术可实现更好的补片植入和组织纤维生成。
Hernia. 2018 Dec;22(6):1089-1100. doi: 10.1007/s10029-018-1808-y. Epub 2018 Aug 27.

引用本文的文献

1
Safety and tissue remodeling assay of small intestinal submucosa meshes using a modified porcine surgical hernia model.使用改良猪手术疝模型评估小肠黏膜下层网片的安全性和组织重塑。
Sci Rep. 2024 Jan 3;13(1):23108. doi: 10.1038/s41598-023-50425-5.
2
Evaluation of a Novel Hybrid Viable Bioprosthetic Mesh in a Model of Mesh Infection.在网状物感染模型中对一种新型混合活性生物假体网状物的评估。
Plast Reconstr Surg Glob Open. 2017 Aug 10;5(8):e1418. doi: 10.1097/GOX.0000000000001418. eCollection 2017 Aug.
3
Combined in vivo and ex vivo analysis of mesh mechanics in a porcine hernia model.

本文引用的文献

1
Multi-institutional experience using human acellular dermal matrix for ventral hernia repair in a compromised surgical field.在手术条件不佳的情况下使用人脱细胞真皮基质进行腹疝修补的多机构经验。
Arch Surg. 2009 Mar;144(3):209-15. doi: 10.1001/archsurg.2009.12.
2
Are biologic grafts effective for hernia repair?: a systematic review of the literature.生物移植物对疝修补有效吗?:文献系统评价
Surg Innov. 2009 Mar;16(1):26-37. doi: 10.1177/1553350609331397. Epub 2009 Feb 17.
3
The use of porcine acellular dermal material for TRAM flap donor-site closure.
体内与体外联合分析猪疝模型中补片力学。
Surg Endosc. 2018 Feb;32(2):820-830. doi: 10.1007/s00464-017-5749-9. Epub 2017 Jul 21.
4
Bone Marrow-Derived Mesenchymal Stem Cells Enhance Bacterial Clearance and Preserve Bioprosthetic Integrity in a Model of Mesh Infection.骨髓间充质干细胞在网片感染模型中增强细菌清除并维持生物假体完整性。
Plast Reconstr Surg Glob Open. 2016 Jun 17;4(6):e751. doi: 10.1097/GOX.0000000000000765. eCollection 2016 Jun.
5
Cell-coating affects tissue integration of synthetic and biologic meshes: comparative analysis of the onlay and underlay mesh positioning in rats.细胞包被影响合成材料和生物补片的组织整合:大鼠体内外置片和内置片补片定位的比较分析
Surg Endosc. 2016 Oct;30(10):4445-53. doi: 10.1007/s00464-016-4764-6. Epub 2016 Feb 19.
6
Blood vessel matrix seeded with cells: a better alternative for abdominal wall reconstruction-a long-term study.接种细胞的血管基质:腹壁重建的更佳选择——一项长期研究
Biomed Res Int. 2015;2015:890613. doi: 10.1155/2015/890613. Epub 2015 Feb 5.
7
Remodeling characteristics and collagen distribution in biological scaffold materials explanted from human subjects after abdominal soft tissue reconstruction: an analysis of scaffold remodeling characteristics by patient risk factors and surgical site classifications.腹部软组织重建后从人体取出的生物支架材料的重塑特征及胶原分布:按患者风险因素和手术部位分类对支架重塑特征的分析
Ann Surg. 2015 Feb;261(2):405-15. doi: 10.1097/SLA.0000000000000471.
8
Biomechanical evaluation of fixation properties of fibrin glue for ventral incisional hernia repair.生物力学评估纤维蛋白胶在修复腹侧切口疝中的固定性能。
Hernia. 2015 Feb;19(1):161-6. doi: 10.1007/s10029-013-1163-y. Epub 2013 Sep 24.
9
Comparison of contracture, adhesion, tissue ingrowth, and histologic response characteristics of permanent and absorbable barrier meshes in a porcine model of laparoscopic ventral hernia repair.在猪腹腔镜腹疝修补模型中比较永久性和可吸收性屏障网片的挛缩、粘连、组织内生长和组织学反应特征。
Hernia. 2012 Feb;16(1):69-76. doi: 10.1007/s10029-011-0854-5. Epub 2011 Jul 12.
10
Laparoscopic fixation of biologic mesh at the hiatus with fibrin or polyethylene glycol sealant in a porcine model.腹腔镜下在猪模型中使用纤维蛋白或聚乙二醇密封剂在裂孔处固定生物网。
Surg Endosc. 2011 Oct;25(10):3405-13. doi: 10.1007/s00464-011-1741-y. Epub 2011 May 19.
猪脱细胞真皮材料用于横行腹直肌肌皮瓣供区闭合。
Plast Reconstr Surg. 2009 Feb;123(2):74e-76e. doi: 10.1097/PRS.0b013e31819597d4.
4
Host response to implanted porcine-derived biologic materials in a primate model of abdominal wall repair.在灵长类动物腹壁修复模型中宿主对植入猪源生物材料的反应。
Tissue Eng Part A. 2008 Dec;14(12):2021-31. doi: 10.1089/ten.tea.2007.0317.
5
Results of AlloDerm use in abdominal hernia repair.脱细胞异体真皮基质在腹部疝修补术中的应用结果。
Hernia. 2008 Jun;12(3):247-50. doi: 10.1007/s10029-007-0319-z. Epub 2008 Jan 22.
6
Xenograft use in reconstructive pelvic surgery: a review of the literature.异种移植在骨盆重建手术中的应用:文献综述
Int Urogynecol J Pelvic Floor Dysfunct. 2007 May;18(5):555-63. doi: 10.1007/s00192-006-0288-2. Epub 2007 Jan 17.
7
Extracellular matrix bioscaffolds for orthopaedic applications. A comparative histologic study.用于骨科应用的细胞外基质生物支架。一项比较组织学研究。
J Bone Joint Surg Am. 2006 Dec;88(12):2673-86. doi: 10.2106/JBJS.E.01008.
8
Porcine dermal collagen (Permacol) for abdominal wall reconstruction.用于腹壁重建的猪真皮胶原蛋白(Permacol)
Curr Surg. 2006 Jul-Aug;63(4):255-8. doi: 10.1016/j.cursur.2006.05.003.
9
Cross-linked acellular porcine dermal collagen implant in laparoscopic ventral hernia repair: case-controlled study of operative variables and early complications.交联脱细胞猪真皮胶原蛋白植入物在腹腔镜腹疝修补术中的应用:手术变量及早期并发症的病例对照研究
Int Surg. 2005 Jul-Aug;90(3 Suppl):S24-9.
10
Histopathologic changes of porcine dermis xenografts for transvaginal suburethral slings.经阴道尿道下吊带术所用猪真皮异种移植物的组织病理学变化
Am J Obstet Gynecol. 2005 May;192(5):1643-8. doi: 10.1016/j.ajog.2004.11.044.