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1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children

BACKGROUND: The clinical presentation and management of acute hematogenous osteomyelitis (AHO) in children can vary significantly. Scores to predict acute complications utilize prolonged fever after antibiotics, bone abscess, suppurative arthritis, disseminated infection and delayed source control....

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Autores principales: Clemente, Adriana Sarmiento, McNeil, Jonathon C, Hulten, Kristina G, Vallejo, Jesus G, Kaplan, Sheldon L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752609/
http://dx.doi.org/10.1093/ofid/ofac492.1163
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author Clemente, Adriana Sarmiento
McNeil, Jonathon C
Hulten, Kristina G
Vallejo, Jesus G
Kaplan, Sheldon L
author_facet Clemente, Adriana Sarmiento
McNeil, Jonathon C
Hulten, Kristina G
Vallejo, Jesus G
Kaplan, Sheldon L
author_sort Clemente, Adriana Sarmiento
collection PubMed
description BACKGROUND: The clinical presentation and management of acute hematogenous osteomyelitis (AHO) in children can vary significantly. Scores to predict acute complications utilize prolonged fever after antibiotics, bone abscess, suppurative arthritis, disseminated infection and delayed source control. By contrast, elevated CRP after 48-96 hours of therapy, disseminated disease and bone debridement are predictive of chronic complications. Such scoring systems have undergone limited validation. We examined factors associated with acute and chronic AHO complications at our center to identify other variables that may enhance published scores. METHODS: A retrospective chart review was conducted of all children 6 mo-18 years with AHO and with acute symptoms of < 14 days at Texas Children’s Hospital from January 2012 through December 2020. An acute complicated course was defined as treatment failure within 6 weeks of starting antibiotics, > 2 bone debridements, prolonged admission ( >14 days) and acute avascular necrosis. Chronic complications included growth arrest or limb leg discrepancy, pathologic fracture, avascular necrosis, chronic osteomyelitis or frozen joint. Statistical analysis was completed using STATA 17. RESULTS: 418 patients met the inclusion criteria. 106 (25.4%) had an acute complicated course. 51 (13.5%) of 377 followed had a chronic complication. Clinical factors associated with acute and chronic complications were very similar. Factors associated with either an acute complicated course (Figure 1) or chronic orthopedic complications (Figure 2) included: older age, tibia involvement, infection due to S. aureus/MRSA, presence of multifocal or disseminated infection, DVT, fever > 48 hours of antibiotic therapy, admission laboratory values including higher absolute neutrophil count (ANC) and higher CRP, ICU admission, associated suppurative arthritis, bacteremia, bone abscess, surgical debridement and delayed source control. [Figure: see text] [Figure: see text] CONCLUSION: In children with AHO, risk factors for acute and chronic complications are highly similar. Older age, tibia involvement, MRSA, higher ANC and bacteremia were linked to complications in our population and will be assessed in current clinical scoring systems which may help guide management. DISCLOSURES: Jonathon C. McNeil, MD, Agency for Healthcare Research and Quality: Grant/Research Support|Allergan: Provided reagents for unrelated research|Nabriva: Site investigator for multicenter clinical trial Kristina G. Hulten, PhD, Me-med: Grant/Research Support|Pfizer: Grant/Research Support Sheldon L. Kaplan, MD, MeMed: Grant/Research Support|Pfizer: Grant/Research Support.
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spelling pubmed-97526092022-12-16 1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children Clemente, Adriana Sarmiento McNeil, Jonathon C Hulten, Kristina G Vallejo, Jesus G Kaplan, Sheldon L Open Forum Infect Dis Abstracts BACKGROUND: The clinical presentation and management of acute hematogenous osteomyelitis (AHO) in children can vary significantly. Scores to predict acute complications utilize prolonged fever after antibiotics, bone abscess, suppurative arthritis, disseminated infection and delayed source control. By contrast, elevated CRP after 48-96 hours of therapy, disseminated disease and bone debridement are predictive of chronic complications. Such scoring systems have undergone limited validation. We examined factors associated with acute and chronic AHO complications at our center to identify other variables that may enhance published scores. METHODS: A retrospective chart review was conducted of all children 6 mo-18 years with AHO and with acute symptoms of < 14 days at Texas Children’s Hospital from January 2012 through December 2020. An acute complicated course was defined as treatment failure within 6 weeks of starting antibiotics, > 2 bone debridements, prolonged admission ( >14 days) and acute avascular necrosis. Chronic complications included growth arrest or limb leg discrepancy, pathologic fracture, avascular necrosis, chronic osteomyelitis or frozen joint. Statistical analysis was completed using STATA 17. RESULTS: 418 patients met the inclusion criteria. 106 (25.4%) had an acute complicated course. 51 (13.5%) of 377 followed had a chronic complication. Clinical factors associated with acute and chronic complications were very similar. Factors associated with either an acute complicated course (Figure 1) or chronic orthopedic complications (Figure 2) included: older age, tibia involvement, infection due to S. aureus/MRSA, presence of multifocal or disseminated infection, DVT, fever > 48 hours of antibiotic therapy, admission laboratory values including higher absolute neutrophil count (ANC) and higher CRP, ICU admission, associated suppurative arthritis, bacteremia, bone abscess, surgical debridement and delayed source control. [Figure: see text] [Figure: see text] CONCLUSION: In children with AHO, risk factors for acute and chronic complications are highly similar. Older age, tibia involvement, MRSA, higher ANC and bacteremia were linked to complications in our population and will be assessed in current clinical scoring systems which may help guide management. DISCLOSURES: Jonathon C. McNeil, MD, Agency for Healthcare Research and Quality: Grant/Research Support|Allergan: Provided reagents for unrelated research|Nabriva: Site investigator for multicenter clinical trial Kristina G. Hulten, PhD, Me-med: Grant/Research Support|Pfizer: Grant/Research Support Sheldon L. Kaplan, MD, MeMed: Grant/Research Support|Pfizer: Grant/Research Support. Oxford University Press 2022-12-15 /pmc/articles/PMC9752609/ http://dx.doi.org/10.1093/ofid/ofac492.1163 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Clemente, Adriana Sarmiento
McNeil, Jonathon C
Hulten, Kristina G
Vallejo, Jesus G
Kaplan, Sheldon L
1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children
title 1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children
title_full 1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children
title_fullStr 1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children
title_full_unstemmed 1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children
title_short 1333. Prognostic Factors Associated with Complications of Acute Hematogenous Osteomyelitis in Children
title_sort 1333. prognostic factors associated with complications of acute hematogenous osteomyelitis in children
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752609/
http://dx.doi.org/10.1093/ofid/ofac492.1163
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