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239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia

BACKGROUND: Stenotrophomonas maltophilia can cause nosocomial infections in immunocompromised hosts and patients with indwelling devices or broad-spectrum antibiotic exposure. Treatment of S maltophilia infections poses a challenge due to intrinsic resistance mechanisms, including inducible L1 metal...

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Autores principales: Teran, Nicholas S, Zidaru, Andrei, Phe, Kady
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677077/
http://dx.doi.org/10.1093/ofid/ofad500.312
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author Teran, Nicholas S
Zidaru, Andrei
Phe, Kady
author_facet Teran, Nicholas S
Zidaru, Andrei
Phe, Kady
author_sort Teran, Nicholas S
collection PubMed
description BACKGROUND: Stenotrophomonas maltophilia can cause nosocomial infections in immunocompromised hosts and patients with indwelling devices or broad-spectrum antibiotic exposure. Treatment of S maltophilia infections poses a challenge due to intrinsic resistance mechanisms, including inducible L1 metallo and L2 cephalosporinase beta-lactamases. Trimethoprim-sulfamethoxazole (SXT) is recognized as the agent of choice for S maltophilia infections. Outcomes with alternative antimicrobials are not well described. METHODS: We conducted a retrospective study of adults with positive blood cultures with S maltophilia who received ≥48h of directed antimicrobials at our institution between 3/2013 and 6/2022. Patients were stratified by their antimicrobial treatment, including levofloxacin, SXT, minocycline, ceftazidime, or combination therapy. The primary outcome was 30d all-cause mortality. Secondary outcomes were microbiological and clinical cure. Microbiological failure was defined as blood cultures growing S maltophilia during or within 7d of discontinuing therapy. Clinical failure was defined as a lack of resolution of signs or symptoms of infection requiring therapy adjustment. RESULTS: Of 67 patients with positive S maltophilia blood cultures, 53 patients treated with levofloxacin (n = 27), SXT (n = 10), minocycline (n = 8), combination (n = 5) or ceftazidime (n = 3) were included. The remaining 14 patients were excluded for receiving < 48h of therapy. The median Charlson comorbidity index was 4 [IQR 3-6]. The most common source of bacteremia was catheter-related (n = 27). Overall, 30d mortality was 26.4%. There was no significant difference in 30d mortality among patients treated with levofloxacin, SXT, minocycline, combination or ceftazidime (p = 0.23). Interestingly, patients with monomicrobial S maltophilia bacteremia had statistically higher 30d mortality (35.3% versus 11.8%, p < 0.05). Microbiological and clinical cure rates were similar between treatment groups (p = 0.06 and p = 0.16, respectively). CONCLUSION: Treatment options for S maltophilia bacteremia resulted in similar 30d mortality; however, findings were limited by the small sample size. Larger, prospective studies are warranted to detect differences in treatment alternatives. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106770772023-11-27 239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia Teran, Nicholas S Zidaru, Andrei Phe, Kady Open Forum Infect Dis Abstract BACKGROUND: Stenotrophomonas maltophilia can cause nosocomial infections in immunocompromised hosts and patients with indwelling devices or broad-spectrum antibiotic exposure. Treatment of S maltophilia infections poses a challenge due to intrinsic resistance mechanisms, including inducible L1 metallo and L2 cephalosporinase beta-lactamases. Trimethoprim-sulfamethoxazole (SXT) is recognized as the agent of choice for S maltophilia infections. Outcomes with alternative antimicrobials are not well described. METHODS: We conducted a retrospective study of adults with positive blood cultures with S maltophilia who received ≥48h of directed antimicrobials at our institution between 3/2013 and 6/2022. Patients were stratified by their antimicrobial treatment, including levofloxacin, SXT, minocycline, ceftazidime, or combination therapy. The primary outcome was 30d all-cause mortality. Secondary outcomes were microbiological and clinical cure. Microbiological failure was defined as blood cultures growing S maltophilia during or within 7d of discontinuing therapy. Clinical failure was defined as a lack of resolution of signs or symptoms of infection requiring therapy adjustment. RESULTS: Of 67 patients with positive S maltophilia blood cultures, 53 patients treated with levofloxacin (n = 27), SXT (n = 10), minocycline (n = 8), combination (n = 5) or ceftazidime (n = 3) were included. The remaining 14 patients were excluded for receiving < 48h of therapy. The median Charlson comorbidity index was 4 [IQR 3-6]. The most common source of bacteremia was catheter-related (n = 27). Overall, 30d mortality was 26.4%. There was no significant difference in 30d mortality among patients treated with levofloxacin, SXT, minocycline, combination or ceftazidime (p = 0.23). Interestingly, patients with monomicrobial S maltophilia bacteremia had statistically higher 30d mortality (35.3% versus 11.8%, p < 0.05). Microbiological and clinical cure rates were similar between treatment groups (p = 0.06 and p = 0.16, respectively). CONCLUSION: Treatment options for S maltophilia bacteremia resulted in similar 30d mortality; however, findings were limited by the small sample size. Larger, prospective studies are warranted to detect differences in treatment alternatives. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677077/ http://dx.doi.org/10.1093/ofid/ofad500.312 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
Teran, Nicholas S
Zidaru, Andrei
Phe, Kady
239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia
title 239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia
title_full 239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia
title_fullStr 239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia
title_full_unstemmed 239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia
title_short 239. Comparing Alternative Treatment Options for Stenotrophomonas maltophilia bacteremia
title_sort 239. comparing alternative treatment options for stenotrophomonas maltophilia bacteremia
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677077/
http://dx.doi.org/10.1093/ofid/ofad500.312
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