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A protocol for the management of pediatric type I open fractures

BACKGROUND: The management of pediatric type I open fractures remains controversial. There has been no consistent protocol established in the literature for the non-operative management of these injuries. METHODS: A protocol was developed at our institution for the non-operative management of pediat...

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Autores principales: Iobst, Christopher A., Spurdle, Craig, Baitner, Avi C., King, Wesley F., Tidwell, Michael, Swirsky, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935019/
https://www.ncbi.nlm.nih.gov/pubmed/24488846
http://dx.doi.org/10.1007/s11832-014-0554-7
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author Iobst, Christopher A.
Spurdle, Craig
Baitner, Avi C.
King, Wesley F.
Tidwell, Michael
Swirsky, Stephen
author_facet Iobst, Christopher A.
Spurdle, Craig
Baitner, Avi C.
King, Wesley F.
Tidwell, Michael
Swirsky, Stephen
author_sort Iobst, Christopher A.
collection PubMed
description BACKGROUND: The management of pediatric type I open fractures remains controversial. There has been no consistent protocol established in the literature for the non-operative management of these injuries. METHODS: A protocol was developed at our institution for the non-operative management of pediatric type I open forearm fractures. Each patient was given a dose of intravenous antibiotics at the time of the initial evaluation in the emergency department. The wound was then irrigated and a closed reduction performed in the emergency department. The patient was admitted for three doses of intravenous antibiotics (over approximately a 24-h period) and then discharged home without oral antibiotics. RESULTS: In total, 45 consecutive patients were managed with this protocol at our hospital between 2004 and 2008. The average age was 10 (range 4–17) years. The average number of doses of intravenous antibiotics was 4.06 per patient. Thirty patients (67 %) received cefazolin (Ancef®) as the treating medication and 15 patients received clindamycin (33 %). There were no infections in any of the 45 patients. CONCLUSION: In this study we outline a consistent management protocol for type I open pediatric forearm fractures that has not previously been documented in the literature. Our results corroborate the those reported in the literature that pediatric type I open fractures may be managed safely in a non-operative manner. There were no infections in our prospective series of 45 consecutive type I open pediatric forearm fractures using our protocol. Using a protocol of only four doses of intravenous antibiotics (one in the emergency department and three additional doses during a 24-h hospital admission) is a safe and efficient method for managing routine pediatric type I open fractures non-operatively.
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spelling pubmed-39350192014-03-04 A protocol for the management of pediatric type I open fractures Iobst, Christopher A. Spurdle, Craig Baitner, Avi C. King, Wesley F. Tidwell, Michael Swirsky, Stephen J Child Orthop Original Clinical Article BACKGROUND: The management of pediatric type I open fractures remains controversial. There has been no consistent protocol established in the literature for the non-operative management of these injuries. METHODS: A protocol was developed at our institution for the non-operative management of pediatric type I open forearm fractures. Each patient was given a dose of intravenous antibiotics at the time of the initial evaluation in the emergency department. The wound was then irrigated and a closed reduction performed in the emergency department. The patient was admitted for three doses of intravenous antibiotics (over approximately a 24-h period) and then discharged home without oral antibiotics. RESULTS: In total, 45 consecutive patients were managed with this protocol at our hospital between 2004 and 2008. The average age was 10 (range 4–17) years. The average number of doses of intravenous antibiotics was 4.06 per patient. Thirty patients (67 %) received cefazolin (Ancef®) as the treating medication and 15 patients received clindamycin (33 %). There were no infections in any of the 45 patients. CONCLUSION: In this study we outline a consistent management protocol for type I open pediatric forearm fractures that has not previously been documented in the literature. Our results corroborate the those reported in the literature that pediatric type I open fractures may be managed safely in a non-operative manner. There were no infections in our prospective series of 45 consecutive type I open pediatric forearm fractures using our protocol. Using a protocol of only four doses of intravenous antibiotics (one in the emergency department and three additional doses during a 24-h hospital admission) is a safe and efficient method for managing routine pediatric type I open fractures non-operatively. Springer Berlin Heidelberg 2014-01-25 2014-02 /pmc/articles/PMC3935019/ /pubmed/24488846 http://dx.doi.org/10.1007/s11832-014-0554-7 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Clinical Article
Iobst, Christopher A.
Spurdle, Craig
Baitner, Avi C.
King, Wesley F.
Tidwell, Michael
Swirsky, Stephen
A protocol for the management of pediatric type I open fractures
title A protocol for the management of pediatric type I open fractures
title_full A protocol for the management of pediatric type I open fractures
title_fullStr A protocol for the management of pediatric type I open fractures
title_full_unstemmed A protocol for the management of pediatric type I open fractures
title_short A protocol for the management of pediatric type I open fractures
title_sort protocol for the management of pediatric type i open fractures
topic Original Clinical Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935019/
https://www.ncbi.nlm.nih.gov/pubmed/24488846
http://dx.doi.org/10.1007/s11832-014-0554-7
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