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Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip
INTRODUCTION: A devastating complication after total hip arthroplasty (THA) is chronic periprosthetic joint infection (PJI). Most frequently spacers (Sp) with or without antibiotics are implanted in a two-stage procedure even though not always indicated due to unknown pathogen, femoral and acetabul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030410/ https://www.ncbi.nlm.nih.gov/pubmed/35534712 http://dx.doi.org/10.1007/s00402-022-04463-9 |
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author | Adl Amini, Dominik Wu, Chia H. Perka, Carsten Bäcker, Henrik C. |
author_facet | Adl Amini, Dominik Wu, Chia H. Perka, Carsten Bäcker, Henrik C. |
author_sort | Adl Amini, Dominik |
collection | PubMed |
description | INTRODUCTION: A devastating complication after total hip arthroplasty (THA) is chronic periprosthetic joint infection (PJI). Most frequently spacers (Sp) with or without antibiotics are implanted in a two-stage procedure even though not always indicated due to unknown pathogen, femoral and acetabular defects or muscular insufficiency. MATERIALS AND METHODS: A retrospective analysis of a prospectively collected database was conducted, analyzing the treatment of 44 consecutive cases with chronic PJI undergoing two-stage revision using a Girdlestone situation (GS) in the interim period between 01/2015 and 12/2018. Diagnostics included intraoperative microbiological cultures, histological analysis, sonication of the initial implant, analysis of hip aspiration, as well as laboratory diagnostics and blood cultures. We analyzed the general and age-group-specific success rate of treatment using GS. Furthermore, we compared our data with the current literature on spacer implantation regarding common complications. RESULTS: In total, 21 female and 23 male patients at a mean age of 59.3 ± 9.6 years were included. Age groups were divided into young, mid-age, and elderly. In most patients, microbiology revealed Staphylococcus epidermidis in 39.1% of cases, following Staphylococcus lugdunensis and Staphylococcus aureus in 10.9% after THA explantation. For histology, Krenn and Morawietz type 2 (infectious type) was diagnosed in 40.9%, type 3 (infectious and abrade-induced type) in 25.0%. With GS, the total cure rate was 84.1% compared to 90.1% (range 61–100%) using Sp as described in the literature. Among age-groups, cure rate varied between 77.8 and 100%. Other complications, which only occurred in the mid-age and elderly group, included the necessity of transfusion in 31.1%, and in total, one periprosthetic fracture was identified (2.3%). CONCLUSION: GS shows an acceptable cure rate at a minimum of 2 years when compared to the cure rate reported in the literature for Sp without major complications. For patients with increased risks for treatment failure using spacer, GS seems to be an alternative for chronic PJI when looking at the success rate of treatment. LEVEL OF EVIDENCE: III, Retrospective trial. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00402-022-04463-9. |
format | Online Article Text |
id | pubmed-10030410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100304102023-03-23 Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip Adl Amini, Dominik Wu, Chia H. Perka, Carsten Bäcker, Henrik C. Arch Orthop Trauma Surg Hip Arthroplasty INTRODUCTION: A devastating complication after total hip arthroplasty (THA) is chronic periprosthetic joint infection (PJI). Most frequently spacers (Sp) with or without antibiotics are implanted in a two-stage procedure even though not always indicated due to unknown pathogen, femoral and acetabular defects or muscular insufficiency. MATERIALS AND METHODS: A retrospective analysis of a prospectively collected database was conducted, analyzing the treatment of 44 consecutive cases with chronic PJI undergoing two-stage revision using a Girdlestone situation (GS) in the interim period between 01/2015 and 12/2018. Diagnostics included intraoperative microbiological cultures, histological analysis, sonication of the initial implant, analysis of hip aspiration, as well as laboratory diagnostics and blood cultures. We analyzed the general and age-group-specific success rate of treatment using GS. Furthermore, we compared our data with the current literature on spacer implantation regarding common complications. RESULTS: In total, 21 female and 23 male patients at a mean age of 59.3 ± 9.6 years were included. Age groups were divided into young, mid-age, and elderly. In most patients, microbiology revealed Staphylococcus epidermidis in 39.1% of cases, following Staphylococcus lugdunensis and Staphylococcus aureus in 10.9% after THA explantation. For histology, Krenn and Morawietz type 2 (infectious type) was diagnosed in 40.9%, type 3 (infectious and abrade-induced type) in 25.0%. With GS, the total cure rate was 84.1% compared to 90.1% (range 61–100%) using Sp as described in the literature. Among age-groups, cure rate varied between 77.8 and 100%. Other complications, which only occurred in the mid-age and elderly group, included the necessity of transfusion in 31.1%, and in total, one periprosthetic fracture was identified (2.3%). CONCLUSION: GS shows an acceptable cure rate at a minimum of 2 years when compared to the cure rate reported in the literature for Sp without major complications. For patients with increased risks for treatment failure using spacer, GS seems to be an alternative for chronic PJI when looking at the success rate of treatment. LEVEL OF EVIDENCE: III, Retrospective trial. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00402-022-04463-9. Springer Berlin Heidelberg 2022-05-09 2023 /pmc/articles/PMC10030410/ /pubmed/35534712 http://dx.doi.org/10.1007/s00402-022-04463-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Hip Arthroplasty Adl Amini, Dominik Wu, Chia H. Perka, Carsten Bäcker, Henrik C. Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
title | Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
title_full | Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
title_fullStr | Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
title_full_unstemmed | Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
title_short | Cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
title_sort | cure rate of infections is not an argument for spacer in two-stage revision arthroplasty of the hip |
topic | Hip Arthroplasty |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030410/ https://www.ncbi.nlm.nih.gov/pubmed/35534712 http://dx.doi.org/10.1007/s00402-022-04463-9 |
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