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248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia

BACKGROUND: Anti-Staphylococcal penicillins (ASPCN) are first-line agents in the treatment of methicillin-susceptible Staphylococcus aureus bacteremia (MSSA-B), and continuous infusion (CI) of oxacillin was associated with higher rates of 30-day microbiological cure versus intermittent (II) in infec...

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Autores principales: Williamson, Julie E, Wood, Sarah, Carlson, Travis J, Jaffa, Rupal K, Boger, Michael S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678796/
http://dx.doi.org/10.1093/ofid/ofad500.321
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author Williamson, Julie E
Wood, Sarah
Carlson, Travis J
Jaffa, Rupal K
Boger, Michael S
Boger, Michael S
author_facet Williamson, Julie E
Wood, Sarah
Carlson, Travis J
Jaffa, Rupal K
Boger, Michael S
Boger, Michael S
author_sort Williamson, Julie E
collection PubMed
description BACKGROUND: Anti-Staphylococcal penicillins (ASPCN) are first-line agents in the treatment of methicillin-susceptible Staphylococcus aureus bacteremia (MSSA-B), and continuous infusion (CI) of oxacillin was associated with higher rates of 30-day microbiological cure versus intermittent (II) in infective endocarditis. Nafcillin (NAF) is the formulary ASPCN at Atrium Health (AH) and is variably ordered as CI or II. The purpose of this study is to compare NAF infusion strategies and related outcomes in the treatment of MSSA-B. METHODS: This was a retrospective, observational, multisite study at 15 sites in the Greater Charlotte, NC Region of AH. Hospitalized adults with MSSA-B who received NAF from 1/1/2020 – 3/31/2022 were included. The primary outcome was receipt of CI vs II NAF. Secondary outcomes included time to microbiological cure (TTMIC), in-hospital 30-day all-cause mortality, hospital length of stay (LOS), and rates of adverse drug events (ADE) - acute kidney injury (serum creatinine increase at least 1.5 times baseline), transaminitis (aspartate aminotransferase / alanine transaminase ≥ 5 times the upper limit of normal), hypokalemia (potassium of ≤ 2.9 mmol/L), and allergic reaction. TTMIC, in-hospital mortality, LOS, and ADEs were also evaluated in a cohort of patients in the ICU within 48 hours of NAF start. RESULTS: A total of 166 patients were included: 99 (59.6%) in the CI group and 67 (40.4%) in the II group. Thirteen patients in the II group were eventually changed to CI, but their results were analyzed in the II group. TTMIC was not significantly different between the CI and II group (5 vs 4 days, respectively p = 0.56), with similar time to receipt of NAF in both groups (Figure 1). In-hospital mortality, hospital LOS, and rates of ADE also did not differ between groups (Figure 1). Forty-seven patients were included in the ICU cohort: 29 in the CI group and 18 in the II group. Trends observed in the ICU cohort were similar to those observed in the larger population (Figure 2). [Figure: see text] Figure 1 [Figure: see text] Figure 2 [Figure: see text] CONCLUSION: In a small, unmatched, observational cohort of patients with MSSA-B, outcomes were not different based on NAF administration route. This suggests that administration strategy should be determined based on patient specific factors, such as available lines and patient convenience. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106787962023-11-27 248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia Williamson, Julie E Wood, Sarah Carlson, Travis J Jaffa, Rupal K Boger, Michael S Boger, Michael S Open Forum Infect Dis Abstract BACKGROUND: Anti-Staphylococcal penicillins (ASPCN) are first-line agents in the treatment of methicillin-susceptible Staphylococcus aureus bacteremia (MSSA-B), and continuous infusion (CI) of oxacillin was associated with higher rates of 30-day microbiological cure versus intermittent (II) in infective endocarditis. Nafcillin (NAF) is the formulary ASPCN at Atrium Health (AH) and is variably ordered as CI or II. The purpose of this study is to compare NAF infusion strategies and related outcomes in the treatment of MSSA-B. METHODS: This was a retrospective, observational, multisite study at 15 sites in the Greater Charlotte, NC Region of AH. Hospitalized adults with MSSA-B who received NAF from 1/1/2020 – 3/31/2022 were included. The primary outcome was receipt of CI vs II NAF. Secondary outcomes included time to microbiological cure (TTMIC), in-hospital 30-day all-cause mortality, hospital length of stay (LOS), and rates of adverse drug events (ADE) - acute kidney injury (serum creatinine increase at least 1.5 times baseline), transaminitis (aspartate aminotransferase / alanine transaminase ≥ 5 times the upper limit of normal), hypokalemia (potassium of ≤ 2.9 mmol/L), and allergic reaction. TTMIC, in-hospital mortality, LOS, and ADEs were also evaluated in a cohort of patients in the ICU within 48 hours of NAF start. RESULTS: A total of 166 patients were included: 99 (59.6%) in the CI group and 67 (40.4%) in the II group. Thirteen patients in the II group were eventually changed to CI, but their results were analyzed in the II group. TTMIC was not significantly different between the CI and II group (5 vs 4 days, respectively p = 0.56), with similar time to receipt of NAF in both groups (Figure 1). In-hospital mortality, hospital LOS, and rates of ADE also did not differ between groups (Figure 1). Forty-seven patients were included in the ICU cohort: 29 in the CI group and 18 in the II group. Trends observed in the ICU cohort were similar to those observed in the larger population (Figure 2). [Figure: see text] Figure 1 [Figure: see text] Figure 2 [Figure: see text] CONCLUSION: In a small, unmatched, observational cohort of patients with MSSA-B, outcomes were not different based on NAF administration route. This suggests that administration strategy should be determined based on patient specific factors, such as available lines and patient convenience. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678796/ http://dx.doi.org/10.1093/ofid/ofad500.321 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
Williamson, Julie E
Wood, Sarah
Carlson, Travis J
Jaffa, Rupal K
Boger, Michael S
Boger, Michael S
248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia
title 248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia
title_full 248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia
title_fullStr 248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia
title_full_unstemmed 248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia
title_short 248. Evaluation of Continuous versus Intermittent Infusion of Nafcillin in the Treatment of Methicillin-Susceptible Staphylococcus aureus Bacteremia
title_sort 248. evaluation of continuous versus intermittent infusion of nafcillin in the treatment of methicillin-susceptible staphylococcus aureus bacteremia
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678796/
http://dx.doi.org/10.1093/ofid/ofad500.321
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