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Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder

BACKGROUND: Superior capsule reconstruction addresses massive rotator cuff tears using allografts and aims to restore the natural superior constraint of the shoulder and therefore shoulder biomechanics and function. There is no evidence relating to the histological incorporation of these grafts. MET...

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Autores principales: Ravenscroft, Matthew J., Riley, James A., Morgan, Barnes W., Sandher, Dilraj S., Odak, Saurabh S., Joseph, Preethi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535153/
https://www.ncbi.nlm.nih.gov/pubmed/31129749
http://dx.doi.org/10.1186/s40634-019-0189-1
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author Ravenscroft, Matthew J.
Riley, James A.
Morgan, Barnes W.
Sandher, Dilraj S.
Odak, Saurabh S.
Joseph, Preethi
author_facet Ravenscroft, Matthew J.
Riley, James A.
Morgan, Barnes W.
Sandher, Dilraj S.
Odak, Saurabh S.
Joseph, Preethi
author_sort Ravenscroft, Matthew J.
collection PubMed
description BACKGROUND: Superior capsule reconstruction addresses massive rotator cuff tears using allografts and aims to restore the natural superior constraint of the shoulder and therefore shoulder biomechanics and function. There is no evidence relating to the histological incorporation of these grafts. METHODS: 27 superior capsule reconstructions were performed between June 2016 and November 2017. Follow-up was with clinical assessment and Magnetic Resonance Imaging, to identify graft failure. Reverse total shoulder replacement was offered for ruptured grafts and the graft was sent for histological analysis along with the footprint of graft attachment where possible. RESULTS: Five patients (18.5%) had evidence of graft failure, three of whom (11.1%) underwent revision procedures. Of the five ruptures, four failed at the glenoid insertion, and one was an intra-substance tear. Histological analysis showed extensive fibroblastic infiltration. The intra-substance tear showed some vascularity at the medial and lateral ends, and one of the glenoid pull-outs demonstrated micro-calcification and osteoid formation. There was no evidence of in-growth into the bone. DISCUSSION: An inflammatory response to the grafts was seen, with neo-vascularisation, and micro-calcification observed. These findings are from ruptured grafts, so may not represent the characteristics of those which have not ruptured. Further evidence from explanted intact grafts could be gained to improve our understanding of its incorporation. LEVEL OF EVIDENCE: Level IV evidence
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spelling pubmed-65351532019-05-28 Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder Ravenscroft, Matthew J. Riley, James A. Morgan, Barnes W. Sandher, Dilraj S. Odak, Saurabh S. Joseph, Preethi J Exp Orthop Research BACKGROUND: Superior capsule reconstruction addresses massive rotator cuff tears using allografts and aims to restore the natural superior constraint of the shoulder and therefore shoulder biomechanics and function. There is no evidence relating to the histological incorporation of these grafts. METHODS: 27 superior capsule reconstructions were performed between June 2016 and November 2017. Follow-up was with clinical assessment and Magnetic Resonance Imaging, to identify graft failure. Reverse total shoulder replacement was offered for ruptured grafts and the graft was sent for histological analysis along with the footprint of graft attachment where possible. RESULTS: Five patients (18.5%) had evidence of graft failure, three of whom (11.1%) underwent revision procedures. Of the five ruptures, four failed at the glenoid insertion, and one was an intra-substance tear. Histological analysis showed extensive fibroblastic infiltration. The intra-substance tear showed some vascularity at the medial and lateral ends, and one of the glenoid pull-outs demonstrated micro-calcification and osteoid formation. There was no evidence of in-growth into the bone. DISCUSSION: An inflammatory response to the grafts was seen, with neo-vascularisation, and micro-calcification observed. These findings are from ruptured grafts, so may not represent the characteristics of those which have not ruptured. Further evidence from explanted intact grafts could be gained to improve our understanding of its incorporation. LEVEL OF EVIDENCE: Level IV evidence Springer Berlin Heidelberg 2019-05-25 /pmc/articles/PMC6535153/ /pubmed/31129749 http://dx.doi.org/10.1186/s40634-019-0189-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Ravenscroft, Matthew J.
Riley, James A.
Morgan, Barnes W.
Sandher, Dilraj S.
Odak, Saurabh S.
Joseph, Preethi
Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
title Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
title_full Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
title_fullStr Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
title_full_unstemmed Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
title_short Histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
title_sort histological incorporation of acellular dermal matrix in the failed superior capsule reconstruction of the shoulder
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535153/
https://www.ncbi.nlm.nih.gov/pubmed/31129749
http://dx.doi.org/10.1186/s40634-019-0189-1
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