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Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor?
BACKGROUND AND PURPOSE: Aseptic loosening is a major cause of failure in total ankle arthroplasty (TAA). In contrast to other total joint replacements, large periarticular cysts (ballooning osteolysis) have frequently been observed in this context. We investigated periprosthetic tissue responses in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967284/ https://www.ncbi.nlm.nih.gov/pubmed/27196532 http://dx.doi.org/10.1080/17453674.2016.1188346 |
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author | Singh, Gurpal Reichard, Theresa Hameister, Rita Awiszus, Friedemann Schenk, Katja Feuerstein, Bernd Roessner, Albert Lohmann, Christoph |
author_facet | Singh, Gurpal Reichard, Theresa Hameister, Rita Awiszus, Friedemann Schenk, Katja Feuerstein, Bernd Roessner, Albert Lohmann, Christoph |
author_sort | Singh, Gurpal |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Aseptic loosening is a major cause of failure in total ankle arthroplasty (TAA). In contrast to other total joint replacements, large periarticular cysts (ballooning osteolysis) have frequently been observed in this context. We investigated periprosthetic tissue responses in failed TAA, and performed an element analysis of retrieved tissues in failed TAA. PATIENTS AND METHODS: The study cohort consisted of 71 patients undergoing revision surgery for failed TAA, all with hydroxyapatite-coated implants. In addition, 5 patients undergoing primary TAA served as a control group. Radiologically, patients were classified into those with ballooning osteolysis and those without, according to defined criteria. Histomorphometric, immunohistochemical, and elemental analysis of tissues was performed. Von Kossa staining and digital microscopy was performed on all tissue samples. RESULTS: Patients without ballooning osteolysis showed a generally higher expression of lymphocytes, and CD3+, CD11c+, CD20+, and CD68+ cells in a perivascular distribution, compared to diffuse expression. The odds of having ballooning osteolysis was 300 times higher in patients with calcium content >0.5 mg/g in periprosthetic tissue than in patients with calcium content ≤0.5 mg/g (p < 0.001). INTERPRETATION: There have been very few studies investigating the pathomechanisms of failed TAA and the cause-effect nature of ballooning osteolysis in this context. Our data suggest that the hydroxyapatite coating of the implant may be a contributory factor. |
format | Online Article Text |
id | pubmed-4967284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49672842017-01-11 Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? Singh, Gurpal Reichard, Theresa Hameister, Rita Awiszus, Friedemann Schenk, Katja Feuerstein, Bernd Roessner, Albert Lohmann, Christoph Acta Orthop Articles BACKGROUND AND PURPOSE: Aseptic loosening is a major cause of failure in total ankle arthroplasty (TAA). In contrast to other total joint replacements, large periarticular cysts (ballooning osteolysis) have frequently been observed in this context. We investigated periprosthetic tissue responses in failed TAA, and performed an element analysis of retrieved tissues in failed TAA. PATIENTS AND METHODS: The study cohort consisted of 71 patients undergoing revision surgery for failed TAA, all with hydroxyapatite-coated implants. In addition, 5 patients undergoing primary TAA served as a control group. Radiologically, patients were classified into those with ballooning osteolysis and those without, according to defined criteria. Histomorphometric, immunohistochemical, and elemental analysis of tissues was performed. Von Kossa staining and digital microscopy was performed on all tissue samples. RESULTS: Patients without ballooning osteolysis showed a generally higher expression of lymphocytes, and CD3+, CD11c+, CD20+, and CD68+ cells in a perivascular distribution, compared to diffuse expression. The odds of having ballooning osteolysis was 300 times higher in patients with calcium content >0.5 mg/g in periprosthetic tissue than in patients with calcium content ≤0.5 mg/g (p < 0.001). INTERPRETATION: There have been very few studies investigating the pathomechanisms of failed TAA and the cause-effect nature of ballooning osteolysis in this context. Our data suggest that the hydroxyapatite coating of the implant may be a contributory factor. Taylor & Francis 2016-08 2016-05-19 /pmc/articles/PMC4967284/ /pubmed/27196532 http://dx.doi.org/10.1080/17453674.2016.1188346 Text en © 2016 The Author(s). Published by Taylor & Francis on behalf of the Nordic Orthopedic Federation. https://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (https://creativecommons.org/licenses/by-nc/3.0) |
spellingShingle | Articles Singh, Gurpal Reichard, Theresa Hameister, Rita Awiszus, Friedemann Schenk, Katja Feuerstein, Bernd Roessner, Albert Lohmann, Christoph Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? |
title | Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? |
title_full | Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? |
title_fullStr | Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? |
title_full_unstemmed | Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? |
title_short | Ballooning osteolysis in 71 failed total ankle arthroplasties: Is hydroxyapatite a risk factor? |
title_sort | ballooning osteolysis in 71 failed total ankle arthroplasties: is hydroxyapatite a risk factor? |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967284/ https://www.ncbi.nlm.nih.gov/pubmed/27196532 http://dx.doi.org/10.1080/17453674.2016.1188346 |
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