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An experimental in-vivo canine model for adult shunt infection

BACKGROUND: Detailed human studies of the mechanisms and development of shunt infection in real time are not possible, and we have developed a canine hydrocephalus model to overcome this. The intention of this pilot study was to show that the canine hydrocephalus model could be shunted using convent...

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Autores principales: Bayston, Roger, Brant, Christine, Dombrowski, Stephen M, Hall, Geraldine, Tuohy, Marion, Procop, Gary, Luciano, Mark G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579278/
https://www.ncbi.nlm.nih.gov/pubmed/18950490
http://dx.doi.org/10.1186/1743-8454-5-17
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author Bayston, Roger
Brant, Christine
Dombrowski, Stephen M
Hall, Geraldine
Tuohy, Marion
Procop, Gary
Luciano, Mark G
author_facet Bayston, Roger
Brant, Christine
Dombrowski, Stephen M
Hall, Geraldine
Tuohy, Marion
Procop, Gary
Luciano, Mark G
author_sort Bayston, Roger
collection PubMed
description BACKGROUND: Detailed human studies of the mechanisms and development of shunt infection in real time are not possible, and we have developed a canine hydrocephalus model to overcome this. The intention of this pilot study was to show that the canine hydrocephalus model could be shunted using conventional "human" shunts, and that a shunt infection could be established so that further studies could then be planned. METHODS: Hydrocephalus was induced in seven dogs (Canis familiaris) by fourth ventricle obstruction. Four weeks later they were shunted using a Hakim Precision valve. Four of the dogs received shunts whose ventricular catheter had been inoculated with Staphylococcus epidermidis, and three were uninoculated controls. Four weeks after shunting the dogs were sacrificed and necropsy was performed. Removed shunts and tissue samples were examined microbiologically and isolates were subjected to detailed identification and genomic comparison. RESULTS: All the dogs remained well after shunting. Examination of removed shunt components revealed S. epidermidis in the brain and throughout the shunt system in the four inoculated animals, but in two of these Staphylococcus intermedius was also found. S. intermedius was also isolated from all three "negative" controls. There were slight differences between S. intermedius strains suggesting endogenous infection rather than cross- infection from a point source. CONCLUSION: Shunt infection was established in the canine model, and had the experiment been extended beyond four weeks the typical microbiological, pathological and clinical features might have appeared. The occurrence of unplanned shunt infections in control animals due to canine normal skin flora reflects human clinical experience and underlines the usual source of bacteria causing shunt infection.
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spelling pubmed-25792782008-11-05 An experimental in-vivo canine model for adult shunt infection Bayston, Roger Brant, Christine Dombrowski, Stephen M Hall, Geraldine Tuohy, Marion Procop, Gary Luciano, Mark G Cerebrospinal Fluid Res Research BACKGROUND: Detailed human studies of the mechanisms and development of shunt infection in real time are not possible, and we have developed a canine hydrocephalus model to overcome this. The intention of this pilot study was to show that the canine hydrocephalus model could be shunted using conventional "human" shunts, and that a shunt infection could be established so that further studies could then be planned. METHODS: Hydrocephalus was induced in seven dogs (Canis familiaris) by fourth ventricle obstruction. Four weeks later they were shunted using a Hakim Precision valve. Four of the dogs received shunts whose ventricular catheter had been inoculated with Staphylococcus epidermidis, and three were uninoculated controls. Four weeks after shunting the dogs were sacrificed and necropsy was performed. Removed shunts and tissue samples were examined microbiologically and isolates were subjected to detailed identification and genomic comparison. RESULTS: All the dogs remained well after shunting. Examination of removed shunt components revealed S. epidermidis in the brain and throughout the shunt system in the four inoculated animals, but in two of these Staphylococcus intermedius was also found. S. intermedius was also isolated from all three "negative" controls. There were slight differences between S. intermedius strains suggesting endogenous infection rather than cross- infection from a point source. CONCLUSION: Shunt infection was established in the canine model, and had the experiment been extended beyond four weeks the typical microbiological, pathological and clinical features might have appeared. The occurrence of unplanned shunt infections in control animals due to canine normal skin flora reflects human clinical experience and underlines the usual source of bacteria causing shunt infection. BioMed Central 2008-10-24 /pmc/articles/PMC2579278/ /pubmed/18950490 http://dx.doi.org/10.1186/1743-8454-5-17 Text en Copyright © 2008 Bayston et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Bayston, Roger
Brant, Christine
Dombrowski, Stephen M
Hall, Geraldine
Tuohy, Marion
Procop, Gary
Luciano, Mark G
An experimental in-vivo canine model for adult shunt infection
title An experimental in-vivo canine model for adult shunt infection
title_full An experimental in-vivo canine model for adult shunt infection
title_fullStr An experimental in-vivo canine model for adult shunt infection
title_full_unstemmed An experimental in-vivo canine model for adult shunt infection
title_short An experimental in-vivo canine model for adult shunt infection
title_sort experimental in-vivo canine model for adult shunt infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579278/
https://www.ncbi.nlm.nih.gov/pubmed/18950490
http://dx.doi.org/10.1186/1743-8454-5-17
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