Literature DB >> 23651550

Characterisation of clinical and newly fabricated meshes for pelvic organ prolapse repair.

Sharon L Edwards1, Jerome A Werkmeister, Anna Rosamilia, John A M Ramshaw, Jacinta F White, Caroline E Gargett.   

Abstract

Clinical meshes used in pelvic organ prolapse (POP) repair are predominantly manufactured from monofilament polypropylene (PP). Complications from the use of these meshes in transvaginal kits, including mesh exposure and pain, have prompted two public health notifications by the FDA. The aim of this study was to compare several clinical PP POP meshes to new fabricated POP meshes, knitted from alternative polymers, for their mechanical properties using standard and clinically relevant multi-axial testing methods. Five new meshes were warp knitted to different architectures and weights from polyamide and polyetheretherketone monofilaments. A composite mesh of a polyamide mesh incorporating a gelatin layer was also fabricated to enable the potential delivery of cells on these meshes. Meshes were assessed for their structural characteristics and mechanical properties, using uniaxial stiffness, permanent strain, bending rigidity and multi-axial burst strength methods. Results were compared to three clinical urogynaecological polypropylene meshes: Polyform®, Gynemesh(TM)PS, and IntePro®. New fabricated meshes were uniaxially less stiff (less than 0.24 N/mm and 1.20 N/mm in toe and linear regions, respectively) than the Gynemesh (0.48 N/mm and 2.08 N/mm in toe and linear regions, respectively) and IntePro (0.57 N/mm in toe region) clinical meshes, with the gelatin coated PA mesh exhibiting lower permanent strain than Polyform clinical mesh (8.1% vs. 23.5%). New meshes had lower burst stiffness than Polyform (less than 16.9 N/mm for new meshes and 26.6N/mm for Polyform). Within the new mesh prototypes, the PA meshes, either uncoated (4.7-5.7 μN m) or with gelatin coating (16.7 μN m) possessed lower bending rigidity than both Polyform and Gynemesh (46.2 μN m and 36.4 μN m, respectively). The new fabricated mesh designs were of similar architecture, but with some improved mechanical properties, compared to clinical POP meshes. Multi-axial analysis of new and clinical mesh designs provides greater discriminatory power in analysing mesh mechanical properties for clinical applications.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23651550     DOI: 10.1016/j.jmbbm.2013.04.002

Source DB:  PubMed          Journal:  J Mech Behav Biomed Mater        ISSN: 1878-0180


  10 in total

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Review 3.  Endometrial mesenchymal stem cells as a cell based therapy for pelvic organ prolapse.

Authors:  Stuart J Emmerson; Caroline E Gargett
Journal:  World J Stem Cells       Date:  2016-05-26       Impact factor: 5.326

4.  Human endometrial mesenchymal stem cells modulate the tissue response and mechanical behavior of polyamide mesh implants for pelvic organ prolapse repair.

Authors:  Daniela Ulrich; Sharon Lee Edwards; Kai Su; Ker Sin Tan; Jacinta F White; John A M Ramshaw; Camden Lo; Anna Rosamilia; Jerome A Werkmeister; Caroline E Gargett
Journal:  Tissue Eng Part A       Date:  2013-11-21       Impact factor: 3.845

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6.  Endometrial Mesenchymal Stem/Stromal Cells Modulate the Macrophage Response to Implanted Polyamide/Gelatin Composite Mesh in Immunocompromised and Immunocompetent Mice.

Authors:  S Darzi; J A Deane; C A Nold; S E Edwards; D J Gough; S Mukherjee; S Gurung; K S Tan; A V Vashi; J A Werkmeister; C E Gargett
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7.  Development of 3D Printed Biodegradable Mesh with Antimicrobial Properties for Pelvic Organ Prolapse.

Authors:  Jiongyu Ren; Rebecca Murray; Cynthia S Wong; Jilong Qin; Michael Chen; Makrina Totsika; Andrew D Riddell; Andrea Warwick; Nicholas Rukin; Maria A Woodruff
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Authors:  Caroline E Gargett; Kjiana E Schwab; James A Deane
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  10 in total

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