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Clinical outcomes of two revision strategies for failed total disc replacements
PURPOSE: To compare mid-term clinical outcomes of two revision strategies for patients with failed SB Charité III total disc replacements (TDRs). METHODS: Eighteen patients with a failed TDR underwent posterolateral instrumented fusion (fusion group); in 21 patients, the TDR was removed and the inte...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3508220/ https://www.ncbi.nlm.nih.gov/pubmed/22576159 http://dx.doi.org/10.1007/s00586-012-2354-4 |
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author | Punt, Ilona Willems, Paul Kurtz, Steven van Rhijn, Lodewijk van Ooij, André |
author_facet | Punt, Ilona Willems, Paul Kurtz, Steven van Rhijn, Lodewijk van Ooij, André |
author_sort | Punt, Ilona |
collection | PubMed |
description | PURPOSE: To compare mid-term clinical outcomes of two revision strategies for patients with failed SB Charité III total disc replacements (TDRs). METHODS: Eighteen patients with a failed TDR underwent posterolateral instrumented fusion (fusion group); in 21 patients, the TDR was removed and the intervertebral defect was filled with a bone strut graft, followed by an instrumented posterolateral fusion (removal group). Visual analogue scale (VAS) for pain and Oswestry Disability Index (ODI) were completed pre- and post-revision surgery. Intra- and post-operative complications of both revision strategies were assessed. RESULTS: Mean follow-up was 3.7 years (range 1.0–6.4) in the removal group and 4.4 years (range 0.7–11.0) in the fusion group. Although the removal group showed a significantly lower VAS and ODI score post-revision surgery as compared to preoperative (P < 0.01 and P = 0.01, respectively), no significant differences were found between the removal and fusion groups before and after revision surgery in VAS and ODI. A clinical relevant improvement in VAS and ODI was found in 47 and 21 % respectively in the removal group, and in 22 and 27 % respectively in the fusion group. Substantial complications were observed only in the removal group. CONCLUSIONS: Both procedures showed improvement clinically. There were no significant additional benefits of removing the TDR as compared to fusion alone at mid-term follow-up. The clinical decision to remove the TDR should be carefully weighed up against potential risks and complications of this procedure. |
format | Online Article Text |
id | pubmed-3508220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-35082202012-11-28 Clinical outcomes of two revision strategies for failed total disc replacements Punt, Ilona Willems, Paul Kurtz, Steven van Rhijn, Lodewijk van Ooij, André Eur Spine J Original Article PURPOSE: To compare mid-term clinical outcomes of two revision strategies for patients with failed SB Charité III total disc replacements (TDRs). METHODS: Eighteen patients with a failed TDR underwent posterolateral instrumented fusion (fusion group); in 21 patients, the TDR was removed and the intervertebral defect was filled with a bone strut graft, followed by an instrumented posterolateral fusion (removal group). Visual analogue scale (VAS) for pain and Oswestry Disability Index (ODI) were completed pre- and post-revision surgery. Intra- and post-operative complications of both revision strategies were assessed. RESULTS: Mean follow-up was 3.7 years (range 1.0–6.4) in the removal group and 4.4 years (range 0.7–11.0) in the fusion group. Although the removal group showed a significantly lower VAS and ODI score post-revision surgery as compared to preoperative (P < 0.01 and P = 0.01, respectively), no significant differences were found between the removal and fusion groups before and after revision surgery in VAS and ODI. A clinical relevant improvement in VAS and ODI was found in 47 and 21 % respectively in the removal group, and in 22 and 27 % respectively in the fusion group. Substantial complications were observed only in the removal group. CONCLUSIONS: Both procedures showed improvement clinically. There were no significant additional benefits of removing the TDR as compared to fusion alone at mid-term follow-up. The clinical decision to remove the TDR should be carefully weighed up against potential risks and complications of this procedure. Springer-Verlag 2012-05-11 2012-12 /pmc/articles/PMC3508220/ /pubmed/22576159 http://dx.doi.org/10.1007/s00586-012-2354-4 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Punt, Ilona Willems, Paul Kurtz, Steven van Rhijn, Lodewijk van Ooij, André Clinical outcomes of two revision strategies for failed total disc replacements |
title | Clinical outcomes of two revision strategies for failed total disc replacements |
title_full | Clinical outcomes of two revision strategies for failed total disc replacements |
title_fullStr | Clinical outcomes of two revision strategies for failed total disc replacements |
title_full_unstemmed | Clinical outcomes of two revision strategies for failed total disc replacements |
title_short | Clinical outcomes of two revision strategies for failed total disc replacements |
title_sort | clinical outcomes of two revision strategies for failed total disc replacements |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3508220/ https://www.ncbi.nlm.nih.gov/pubmed/22576159 http://dx.doi.org/10.1007/s00586-012-2354-4 |
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