Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1785150044980117504 |
---|---|
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 |
format | Online Article Text |
id | pubmed-10677077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT terannicholass 239comparingalternativetreatmentoptionsforstenotrophomonasmaltophiliabacteremia AT zidaruandrei 239comparingalternativetreatmentoptionsforstenotrophomonasmaltophiliabacteremia AT phekady 239comparingalternativetreatmentoptionsforstenotrophomonasmaltophiliabacteremia |