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1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents

BACKGROUND: Spinal epidural abscess (SEA) is an uncommon but serious infection with potentially devastating sequelae. For SEA due to methicillin- susceptible S. aureus (MSSA), anti-Staphylococcal penicillins have been considered first line, however retrospective data have failed to show a difference...

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Autores principales: Fowler, Madeline, Phan, Jessica, Jaffa, Rupal K, Carlson, Travis J, Medaris, Leigh Ann, Williamson, Julie E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676831/
http://dx.doi.org/10.1093/ofid/ofad500.1161
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author Fowler, Madeline
Phan, Jessica
Jaffa, Rupal K
Carlson, Travis J
Medaris, Leigh Ann
Williamson, Julie E
author_facet Fowler, Madeline
Phan, Jessica
Jaffa, Rupal K
Carlson, Travis J
Medaris, Leigh Ann
Williamson, Julie E
author_sort Fowler, Madeline
collection PubMed
description BACKGROUND: Spinal epidural abscess (SEA) is an uncommon but serious infection with potentially devastating sequelae. For SEA due to methicillin- susceptible S. aureus (MSSA), anti-Staphylococcal penicillins have been considered first line, however retrospective data have failed to show a difference in outcomes compared to cefazolin. Comparative data in methicillin-resistant S. aureus (MRSA) SEA are sparse. METHODS: This was a multisite, retrospective cohort of adults admitted to an acute care or acute rehabilitation hospital from 1/1/2017 – 9/10/2021 with confirmed S. aureus SEA by radiology and microbiology (blood and/or surgical cultures). Recurrent or polymicrobial SEA, endocarditis, meningitis, or prosthetic joint infection cases were excluded. Therapy was grouped as lower (LCNS) or higher (HCNS) CNS penetration (Fig. 1) and was assessed as overall principal therapy (OPT) (definitive therapy for > 50% of the total course) and early principal therapy (EPT) (definitive therapy for > 50% of the first 2 weeks). Patients were also analyzed by MSSA vs MRSA. The primary outcome was composite 90-day clinical failure, (≥ 1 of the following: extension of original antibiotic course, unplanned surgical intervention related to SEA, recurrence of S. aureus bacteremia, and all-cause mortality) by OPT. Secondary outcomes included components of the primary outcome and composite 90-day clinical failure by methicillin susceptibility and EPT. [Figure: see text] RESULTS: 174 patients met inclusion: 94 (54%) in the LCNS group and 80 (46%) in the HCNS group. There was no significant difference in 90-day clinical failure of OPT between groups (Fig. 2). The composite 90-day clinical failure of OPT also did not differ between LCNS and HCNS based on methicillin susceptibility (MSSA 25.9% vs. 19.2%, p = 0.49; MRSA 30.8% vs. 31.5%, p = 0.96). Similarly, there was no difference in 90-day clinical failure based on EPT (31% vs. 24%, p = 0.28), regardless of methicillin susceptibility, (MSSA 29% vs. 17.8%, p = 0.18; MRSA 50% vs. 28.8%, p = 0.23) between the LCNS and HCNS groups, respectively (Fig. 3). [Figure: see text] Figure 2 [Figure: see text] Figure 3 [Figure: see text] CONCLUSION: There was no significant difference in the rate of 90-day composite clinical failure between OPT with LCNS and HCNS. Given the limited sample size, further study, particularly in an MSSA SEA cohort, is warranted. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106768312023-11-27 1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents Fowler, Madeline Phan, Jessica Jaffa, Rupal K Carlson, Travis J Medaris, Leigh Ann Williamson, Julie E Open Forum Infect Dis Abstract BACKGROUND: Spinal epidural abscess (SEA) is an uncommon but serious infection with potentially devastating sequelae. For SEA due to methicillin- susceptible S. aureus (MSSA), anti-Staphylococcal penicillins have been considered first line, however retrospective data have failed to show a difference in outcomes compared to cefazolin. Comparative data in methicillin-resistant S. aureus (MRSA) SEA are sparse. METHODS: This was a multisite, retrospective cohort of adults admitted to an acute care or acute rehabilitation hospital from 1/1/2017 – 9/10/2021 with confirmed S. aureus SEA by radiology and microbiology (blood and/or surgical cultures). Recurrent or polymicrobial SEA, endocarditis, meningitis, or prosthetic joint infection cases were excluded. Therapy was grouped as lower (LCNS) or higher (HCNS) CNS penetration (Fig. 1) and was assessed as overall principal therapy (OPT) (definitive therapy for > 50% of the total course) and early principal therapy (EPT) (definitive therapy for > 50% of the first 2 weeks). Patients were also analyzed by MSSA vs MRSA. The primary outcome was composite 90-day clinical failure, (≥ 1 of the following: extension of original antibiotic course, unplanned surgical intervention related to SEA, recurrence of S. aureus bacteremia, and all-cause mortality) by OPT. Secondary outcomes included components of the primary outcome and composite 90-day clinical failure by methicillin susceptibility and EPT. [Figure: see text] RESULTS: 174 patients met inclusion: 94 (54%) in the LCNS group and 80 (46%) in the HCNS group. There was no significant difference in 90-day clinical failure of OPT between groups (Fig. 2). The composite 90-day clinical failure of OPT also did not differ between LCNS and HCNS based on methicillin susceptibility (MSSA 25.9% vs. 19.2%, p = 0.49; MRSA 30.8% vs. 31.5%, p = 0.96). Similarly, there was no difference in 90-day clinical failure based on EPT (31% vs. 24%, p = 0.28), regardless of methicillin susceptibility, (MSSA 29% vs. 17.8%, p = 0.18; MRSA 50% vs. 28.8%, p = 0.23) between the LCNS and HCNS groups, respectively (Fig. 3). [Figure: see text] Figure 2 [Figure: see text] Figure 3 [Figure: see text] CONCLUSION: There was no significant difference in the rate of 90-day composite clinical failure between OPT with LCNS and HCNS. Given the limited sample size, further study, particularly in an MSSA SEA cohort, is warranted. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10676831/ http://dx.doi.org/10.1093/ofid/ofad500.1161 Text en © The Author(s) 2023. 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 Abstract
Fowler, Madeline
Phan, Jessica
Jaffa, Rupal K
Carlson, Travis J
Medaris, Leigh Ann
Williamson, Julie E
1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents
title 1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents
title_full 1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents
title_fullStr 1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents
title_full_unstemmed 1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents
title_short 1322. Outcomes Associated with Primary Antibiotic Therapy in Spinal Epidural Abscess due to Staphylococcus aureus: Comparison of First-line vs Alternative Agents
title_sort 1322. outcomes associated with primary antibiotic therapy in spinal epidural abscess due to staphylococcus aureus: comparison of first-line vs alternative agents
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676831/
http://dx.doi.org/10.1093/ofid/ofad500.1161
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