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Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model

BACKGROUND: Osteomyelitis is a serious disease which can be difficult to treat despite properly instituted antibiotic therapy. This appears to be related at least partly to degraded vascularisation in the osteomyelitic (OM) lesions. Studies of perfusion in OM bones are, however, few and not quantita...

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Autores principales: Jødal, Lars, Nielsen, Ole L., Afzelius, Pia, Alstrup, Aage K. O., Hansen, Søren B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237436/
https://www.ncbi.nlm.nih.gov/pubmed/28091979
http://dx.doi.org/10.1186/s13550-016-0251-2
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author Jødal, Lars
Nielsen, Ole L.
Afzelius, Pia
Alstrup, Aage K. O.
Hansen, Søren B.
author_facet Jødal, Lars
Nielsen, Ole L.
Afzelius, Pia
Alstrup, Aage K. O.
Hansen, Søren B.
author_sort Jødal, Lars
collection PubMed
description BACKGROUND: Osteomyelitis is a serious disease which can be difficult to treat despite properly instituted antibiotic therapy. This appears to be related at least partly to degraded vascularisation in the osteomyelitic (OM) lesions. Studies of perfusion in OM bones are, however, few and not quantitative. Quantitative assessment of perfusion could aid in the selection of therapy. A non-invasive, quantitative way to study perfusion is dynamic [(15)O]water positron emission tomography (PET). We aim to demonstrate that the method can be used for measuring perfusion in OM lesions and hypothesize that perfusion will be less elevated in OM lesions than in soft tissue (ST) infection. The study comprised 11 juvenile pigs with haematogenous osteomyelitis induced by injection of Staphylococcus aureus into the right femoral artery 1 week before scanning (in one pig, 2 weeks). The pigs were dynamically PET scanned with [(15)O]water to quantify blood perfusion. OM lesions (N = 17) in long bones were studied, using the left limb as reference. ST lesions (N = 8) were studied similarly. RESULTS: Perfusion was quantitatively determined. Perfusion was elevated by a factor 1.5 in OM lesions and by a factor 6 in ST lesions. CONCLUSIONS: Blood perfusion was successfully determined in pathological subacute OM lesions; average perfusion was increased compared to that in a healthy bone, but as hypothesized, the increase was less than in ST lesions, indicating that the infected bone has less perfusion reserve than the infected soft tissue. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13550-016-0251-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-52374362017-01-27 Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model Jødal, Lars Nielsen, Ole L. Afzelius, Pia Alstrup, Aage K. O. Hansen, Søren B. EJNMMI Res Original Research BACKGROUND: Osteomyelitis is a serious disease which can be difficult to treat despite properly instituted antibiotic therapy. This appears to be related at least partly to degraded vascularisation in the osteomyelitic (OM) lesions. Studies of perfusion in OM bones are, however, few and not quantitative. Quantitative assessment of perfusion could aid in the selection of therapy. A non-invasive, quantitative way to study perfusion is dynamic [(15)O]water positron emission tomography (PET). We aim to demonstrate that the method can be used for measuring perfusion in OM lesions and hypothesize that perfusion will be less elevated in OM lesions than in soft tissue (ST) infection. The study comprised 11 juvenile pigs with haematogenous osteomyelitis induced by injection of Staphylococcus aureus into the right femoral artery 1 week before scanning (in one pig, 2 weeks). The pigs were dynamically PET scanned with [(15)O]water to quantify blood perfusion. OM lesions (N = 17) in long bones were studied, using the left limb as reference. ST lesions (N = 8) were studied similarly. RESULTS: Perfusion was quantitatively determined. Perfusion was elevated by a factor 1.5 in OM lesions and by a factor 6 in ST lesions. CONCLUSIONS: Blood perfusion was successfully determined in pathological subacute OM lesions; average perfusion was increased compared to that in a healthy bone, but as hypothesized, the increase was less than in ST lesions, indicating that the infected bone has less perfusion reserve than the infected soft tissue. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13550-016-0251-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-01-14 /pmc/articles/PMC5237436/ /pubmed/28091979 http://dx.doi.org/10.1186/s13550-016-0251-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Jødal, Lars
Nielsen, Ole L.
Afzelius, Pia
Alstrup, Aage K. O.
Hansen, Søren B.
Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model
title Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model
title_full Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model
title_fullStr Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model
title_full_unstemmed Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model
title_short Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model
title_sort blood perfusion in osteomyelitis studied with [(15)o]water pet in a juvenile porcine model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237436/
https://www.ncbi.nlm.nih.gov/pubmed/28091979
http://dx.doi.org/10.1186/s13550-016-0251-2
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