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Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects?
BACKGROUND: Evidence suggests a growing incidence of revision total hip arthroplasty (THA) including a subset with large acetabular defects. Revision THA for severe acetabular bone loss is associated with a relatively high rate of mechanical failure. QUESTIONS/PURPOSES: We questioned whether cementi...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018232/ https://www.ncbi.nlm.nih.gov/pubmed/20857251 http://dx.doi.org/10.1007/s11999-010-1546-7 |
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author | Hansen, Erik Shearer, David Ries, Michael D. |
author_facet | Hansen, Erik Shearer, David Ries, Michael D. |
author_sort | Hansen, Erik |
collection | PubMed |
description | BACKGROUND: Evidence suggests a growing incidence of revision total hip arthroplasty (THA) including a subset with large acetabular defects. Revision THA for severe acetabular bone loss is associated with a relatively high rate of mechanical failure. QUESTIONS/PURPOSES: We questioned whether cementing a cage to the reconstructed acetabular defect and pelvis would improve the rate of mechanical failure for patients with Type 3 defects (Paprosky et al.) with and without pelvic discontinuity in comparison to historical controls. METHODS: We retrospectively collected data on 33 patients who underwent 35 revision THAs using an acetabular reconstruction cage cemented to morselized allograft and either structural allograft or trabecular metal augmentation for Type 3 defects in the presence (n = 13) and absence (n = 22) of pelvic discontinuity at a mean followup of 59 months (range, 24–92 months). The primary outcome was mechanical failure, defined as revision of the acetabular reconstruction for aseptic loosening. RESULTS: Revision surgery for mechanical failure occurred in four of the 13 patients with pelvic discontinuity and two of the 22 patients without discontinuity. Radiographic loosening occurred in one patient with and one patient without pelvic discontinuity. Seven of the 35 revisions were subsequently revised for deep infection all in patients who were immunocompromised. CONCLUSIONS: Cementing the cage to the pelvis can offer an advantage for treating severe acetabular defects. Trabecular metal augmentation appears to provide better initial mechanical stability than a structural allograft, but successful allograft reconstruction may restore bone stock. LEVEL OF EVIDENCE: Level IV, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence. |
format | Text |
id | pubmed-3018232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-30182322011-02-04 Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? Hansen, Erik Shearer, David Ries, Michael D. Clin Orthop Relat Res Symposium: Papers Presented at the Hip Society Meetings 2010 BACKGROUND: Evidence suggests a growing incidence of revision total hip arthroplasty (THA) including a subset with large acetabular defects. Revision THA for severe acetabular bone loss is associated with a relatively high rate of mechanical failure. QUESTIONS/PURPOSES: We questioned whether cementing a cage to the reconstructed acetabular defect and pelvis would improve the rate of mechanical failure for patients with Type 3 defects (Paprosky et al.) with and without pelvic discontinuity in comparison to historical controls. METHODS: We retrospectively collected data on 33 patients who underwent 35 revision THAs using an acetabular reconstruction cage cemented to morselized allograft and either structural allograft or trabecular metal augmentation for Type 3 defects in the presence (n = 13) and absence (n = 22) of pelvic discontinuity at a mean followup of 59 months (range, 24–92 months). The primary outcome was mechanical failure, defined as revision of the acetabular reconstruction for aseptic loosening. RESULTS: Revision surgery for mechanical failure occurred in four of the 13 patients with pelvic discontinuity and two of the 22 patients without discontinuity. Radiographic loosening occurred in one patient with and one patient without pelvic discontinuity. Seven of the 35 revisions were subsequently revised for deep infection all in patients who were immunocompromised. CONCLUSIONS: Cementing the cage to the pelvis can offer an advantage for treating severe acetabular defects. Trabecular metal augmentation appears to provide better initial mechanical stability than a structural allograft, but successful allograft reconstruction may restore bone stock. LEVEL OF EVIDENCE: Level IV, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence. Springer-Verlag 2010-09-21 2011-02 /pmc/articles/PMC3018232/ /pubmed/20857251 http://dx.doi.org/10.1007/s11999-010-1546-7 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Symposium: Papers Presented at the Hip Society Meetings 2010 Hansen, Erik Shearer, David Ries, Michael D. Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? |
title | Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? |
title_full | Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? |
title_fullStr | Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? |
title_full_unstemmed | Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? |
title_short | Does a Cemented Cage Improve Revision THA for Severe Acetabular Defects? |
title_sort | does a cemented cage improve revision tha for severe acetabular defects? |
topic | Symposium: Papers Presented at the Hip Society Meetings 2010 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018232/ https://www.ncbi.nlm.nih.gov/pubmed/20857251 http://dx.doi.org/10.1007/s11999-010-1546-7 |
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