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The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model
Introduction. Osteomyelitis is a severe orthopaedic complication which is difficult to diagnose and treat. Previous experimental studies mainly focussed on evaluating osteomyelitis in the presence of an implant or used a sclerosing agent to promote infection onset. In contrast, we focused on the lon...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177738/ https://www.ncbi.nlm.nih.gov/pubmed/25295260 http://dx.doi.org/10.1155/2014/424652 |
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author | Odekerken, Jim C. E. Walenkamp, Geert H. I. M. Brans, Boudewijn T. Welting, Tim J. M. Arts, Jacobus J. C. |
author_facet | Odekerken, Jim C. E. Walenkamp, Geert H. I. M. Brans, Boudewijn T. Welting, Tim J. M. Arts, Jacobus J. C. |
author_sort | Odekerken, Jim C. E. |
collection | PubMed |
description | Introduction. Osteomyelitis is a severe orthopaedic complication which is difficult to diagnose and treat. Previous experimental studies mainly focussed on evaluating osteomyelitis in the presence of an implant or used a sclerosing agent to promote infection onset. In contrast, we focused on the longitudinal assessment of a nonimplant related osteomyelitis. Methods. An intramedullary tibial infection with S. aureus was established in NZW rabbits. Clinical and haematological infection status was evaluated weekly, combined with X-ray radiographs, biweekly injections of calcium binding fluorophores, and postmortem micro-CT. The development of the infection was assessed by micro-PET at consecutive time points using (18)F-FDG as an infection tracer. Results. The intramedullary contamination of the rabbit tibia resulted in an osteomyelitis. Haematological parameters confirmed infection in mainly the first postoperative weeks (CRP at the first 5 postoperative weeks, leucocyte differentiation at the second and sixth postoperative weeks, and ESR on the second postoperative week only), while micro-PET was able to detect the infection from the first post-operative week onward until the end of the study. Conclusions. This study shows that osteomyelitis in the rabbit can be induced without use of an implant or sclerosing agent. The sequential follow-up indicates that the diagnostic value of each infection parameter is time point dependant. Furthermore, from all parameters used, the diagnostic value of (18)F-FDG micro-PET is the most versatile to assess the presence of an orthopaedic infection in this model. |
format | Online Article Text |
id | pubmed-4177738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41777382014-10-07 The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model Odekerken, Jim C. E. Walenkamp, Geert H. I. M. Brans, Boudewijn T. Welting, Tim J. M. Arts, Jacobus J. C. Biomed Res Int Research Article Introduction. Osteomyelitis is a severe orthopaedic complication which is difficult to diagnose and treat. Previous experimental studies mainly focussed on evaluating osteomyelitis in the presence of an implant or used a sclerosing agent to promote infection onset. In contrast, we focused on the longitudinal assessment of a nonimplant related osteomyelitis. Methods. An intramedullary tibial infection with S. aureus was established in NZW rabbits. Clinical and haematological infection status was evaluated weekly, combined with X-ray radiographs, biweekly injections of calcium binding fluorophores, and postmortem micro-CT. The development of the infection was assessed by micro-PET at consecutive time points using (18)F-FDG as an infection tracer. Results. The intramedullary contamination of the rabbit tibia resulted in an osteomyelitis. Haematological parameters confirmed infection in mainly the first postoperative weeks (CRP at the first 5 postoperative weeks, leucocyte differentiation at the second and sixth postoperative weeks, and ESR on the second postoperative week only), while micro-PET was able to detect the infection from the first post-operative week onward until the end of the study. Conclusions. This study shows that osteomyelitis in the rabbit can be induced without use of an implant or sclerosing agent. The sequential follow-up indicates that the diagnostic value of each infection parameter is time point dependant. Furthermore, from all parameters used, the diagnostic value of (18)F-FDG micro-PET is the most versatile to assess the presence of an orthopaedic infection in this model. Hindawi Publishing Corporation 2014 2014-09-11 /pmc/articles/PMC4177738/ /pubmed/25295260 http://dx.doi.org/10.1155/2014/424652 Text en Copyright © 2014 Jim C. E. Odekerken et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Odekerken, Jim C. E. Walenkamp, Geert H. I. M. Brans, Boudewijn T. Welting, Tim J. M. Arts, Jacobus J. C. The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model |
title | The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model |
title_full | The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model |
title_fullStr | The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model |
title_full_unstemmed | The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model |
title_short | The Longitudinal Assessment of Osteomyelitis Development by Molecular Imaging in a Rabbit Model |
title_sort | longitudinal assessment of osteomyelitis development by molecular imaging in a rabbit model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177738/ https://www.ncbi.nlm.nih.gov/pubmed/25295260 http://dx.doi.org/10.1155/2014/424652 |
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