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316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures

BACKGROUND: Fracture related infection (FRI) is a severe complication in trauma surgery but defining the full impact of these infections has been challenging with the lack of clear diagnostic criteria. This is particularly problematic for culture-negative FRI (CNFRI), which lack pathogen identificat...

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Autores principales: Weinert-Stein, Kaitlyn E, Slater, Julia C, Sagi, Henry C, Powers-Fletcher, Margaret, Palacio, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776446/
http://dx.doi.org/10.1093/ofid/ofaa439.512
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author Weinert-Stein, Kaitlyn E
Slater, Julia C
Sagi, Henry C
Powers-Fletcher, Margaret
Palacio, Federico
author_facet Weinert-Stein, Kaitlyn E
Slater, Julia C
Sagi, Henry C
Powers-Fletcher, Margaret
Palacio, Federico
author_sort Weinert-Stein, Kaitlyn E
collection PubMed
description BACKGROUND: Fracture related infection (FRI) is a severe complication in trauma surgery but defining the full impact of these infections has been challenging with the lack of clear diagnostic criteria. This is particularly problematic for culture-negative FRI (CNFRI), which lack pathogen identification to guide antimicrobial therapy. However, new consensus definition and criteria for the diagnosis of FRI (Table) may help reduce the risk of diagnostic error. The purpose of this study was to determine the proportion and clinical characteristics of CNFRI cases at a level I trauma hospital using the new diagnostic criteria. [Image: see text] METHODS: Laboratory reports were used to identify all patients with at least one specimen submitted for microbiology culture by an orthopedic surgeon at our trauma I level hospital in Cincinnati, Ohio during a three-year study period. This cohort was refined by an electronic medical record (EMR) review to select patients that met the diagnostic criteria for suspected/confirmed FRI. The specimen details and results of the cultures were recorded for the first orthopedic surgeon collection for each suspected FRI case. Clinical data, including fracture characteristics, surgical treatment, antibiotic utilization, and patient outcomes were also extracted from the EMR for each case. RESULTS: A total of 246 patients were identified with at least one culture specimen; 35.8% (n = 88) of these were deemed suspected/confirmed FRI based on consensus guidelines. The cultures for the first orthopedic surgery collection on these FRI were negative for 35% (n = 31). The most common location for CNFRI were proximal lower extremity fractures (52%), a distribution different from that of culture positive (Figure). Culture positive FRI were predominated by Staphylococcus aureus (39%) followed by gram negative rods (23%). [Image: see text] CONCLUSION: This retrospective cohort study identified a sizable proportion of CNFRI at our trauma center using the recently published consensus definition. While further analysis is necessary to determine the exact impact of these new criteria, this suggests that clearer definitions may facilitate improved recognition of CNFRI. Because of the relatively high rates of CNFRI, efforts to standardize laboratory diagnostic processes and case management will be required. DISCLOSURES: Henry C. Sagi, MD, FACS, Conexxions (Board Member)GLW trauma (Consultant)GLW trauma (Shareholder)Stryker (Consultant)
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spelling pubmed-77764462021-01-07 316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures Weinert-Stein, Kaitlyn E Slater, Julia C Sagi, Henry C Powers-Fletcher, Margaret Palacio, Federico Open Forum Infect Dis Poster Abstracts BACKGROUND: Fracture related infection (FRI) is a severe complication in trauma surgery but defining the full impact of these infections has been challenging with the lack of clear diagnostic criteria. This is particularly problematic for culture-negative FRI (CNFRI), which lack pathogen identification to guide antimicrobial therapy. However, new consensus definition and criteria for the diagnosis of FRI (Table) may help reduce the risk of diagnostic error. The purpose of this study was to determine the proportion and clinical characteristics of CNFRI cases at a level I trauma hospital using the new diagnostic criteria. [Image: see text] METHODS: Laboratory reports were used to identify all patients with at least one specimen submitted for microbiology culture by an orthopedic surgeon at our trauma I level hospital in Cincinnati, Ohio during a three-year study period. This cohort was refined by an electronic medical record (EMR) review to select patients that met the diagnostic criteria for suspected/confirmed FRI. The specimen details and results of the cultures were recorded for the first orthopedic surgeon collection for each suspected FRI case. Clinical data, including fracture characteristics, surgical treatment, antibiotic utilization, and patient outcomes were also extracted from the EMR for each case. RESULTS: A total of 246 patients were identified with at least one culture specimen; 35.8% (n = 88) of these were deemed suspected/confirmed FRI based on consensus guidelines. The cultures for the first orthopedic surgery collection on these FRI were negative for 35% (n = 31). The most common location for CNFRI were proximal lower extremity fractures (52%), a distribution different from that of culture positive (Figure). Culture positive FRI were predominated by Staphylococcus aureus (39%) followed by gram negative rods (23%). [Image: see text] CONCLUSION: This retrospective cohort study identified a sizable proportion of CNFRI at our trauma center using the recently published consensus definition. While further analysis is necessary to determine the exact impact of these new criteria, this suggests that clearer definitions may facilitate improved recognition of CNFRI. Because of the relatively high rates of CNFRI, efforts to standardize laboratory diagnostic processes and case management will be required. DISCLOSURES: Henry C. Sagi, MD, FACS, Conexxions (Board Member)GLW trauma (Consultant)GLW trauma (Shareholder)Stryker (Consultant) Oxford University Press 2020-12-31 /pmc/articles/PMC7776446/ http://dx.doi.org/10.1093/ofid/ofaa439.512 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Weinert-Stein, Kaitlyn E
Slater, Julia C
Sagi, Henry C
Powers-Fletcher, Margaret
Palacio, Federico
316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures
title 316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures
title_full 316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures
title_fullStr 316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures
title_full_unstemmed 316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures
title_short 316. Application of New Consensus Definition Identifies High Numbers of Fracture Related Infections with Negative Cultures
title_sort 316. application of new consensus definition identifies high numbers of fracture related infections with negative cultures
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776446/
http://dx.doi.org/10.1093/ofid/ofaa439.512
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