Trimethoprim-sulfamethoxazole versus levofloxacin for the treatment of Stenotrophomonas maltophilia infections: A multicenter cohort study.

Levofloxacin Stenotrophomonas maltophilia Trimethoprim-sulfamethoxazole

Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
29 May 2024
Historique:
received: 30 10 2023
revised: 05 04 2024
accepted: 20 05 2024
medline: 1 6 2024
pubmed: 1 6 2024
entrez: 31 5 2024
Statut: aheadofprint

Résumé

Trimethoprim-sulfamethoxazole (TMP-SMX) has long been considered the treatment of choice for infections caused by Stenotrophomonas maltophilia. Levofloxacin has emerged as a potential option for treating these infections. This study aimed to evaluate the clinical outcomes in patients who received TMP-SMX versus levofloxacin for treating S. maltophilia infections. A retrospective, cohort study was conducted in 4 tertiary centers and included patients who were treated with either TMP-SMX or levofloxacin for infections caused by S. maltophilia. The main study outcomes were overall in-hospital mortality, 30-day mortality, and clinical cure. Safety outcomes were also evaluated. Multivariate analysis using logistic regression was used to control for the effect of the covariables. We included 371 patients in this study, 316 received TMP-SMX and 55 patients received levofloxacin. A total of 70% were in the intensive care unit and 21% presented with bacteremia. No statistically significant differences were observed in overall in-hospital mortality (52% vs 40%; p = 0.113; OR, 1.59; 95% CI, 0.89-2.86), 30-day mortality (28% vs 25%; p = 0.712; OR, 1.13; 95% CI, 0.59-2.18), or clinical cure (55% vs 64%; p = 0.237; OR, 0.70; 95% CI, 0.37-1.31). Rates of acute kidney injury were comparable between the two groups (11% vs 7%; p = 0.413). Patients receiving levofloxacin for the treatment of infections caused by S. maltophilia demonstrated clinical outcomes similar to those receiving TMP-SMX. Our study suggests that levofloxacin can be a reasonable alternative to TMP-SMX to treat these infections.

Sections du résumé

BACKGROUND BACKGROUND
Trimethoprim-sulfamethoxazole (TMP-SMX) has long been considered the treatment of choice for infections caused by Stenotrophomonas maltophilia. Levofloxacin has emerged as a potential option for treating these infections. This study aimed to evaluate the clinical outcomes in patients who received TMP-SMX versus levofloxacin for treating S. maltophilia infections.
METHOD METHODS
A retrospective, cohort study was conducted in 4 tertiary centers and included patients who were treated with either TMP-SMX or levofloxacin for infections caused by S. maltophilia. The main study outcomes were overall in-hospital mortality, 30-day mortality, and clinical cure. Safety outcomes were also evaluated. Multivariate analysis using logistic regression was used to control for the effect of the covariables.
RESULTS RESULTS
We included 371 patients in this study, 316 received TMP-SMX and 55 patients received levofloxacin. A total of 70% were in the intensive care unit and 21% presented with bacteremia. No statistically significant differences were observed in overall in-hospital mortality (52% vs 40%; p = 0.113; OR, 1.59; 95% CI, 0.89-2.86), 30-day mortality (28% vs 25%; p = 0.712; OR, 1.13; 95% CI, 0.59-2.18), or clinical cure (55% vs 64%; p = 0.237; OR, 0.70; 95% CI, 0.37-1.31). Rates of acute kidney injury were comparable between the two groups (11% vs 7%; p = 0.413).
CONCLUSION CONCLUSIONS
Patients receiving levofloxacin for the treatment of infections caused by S. maltophilia demonstrated clinical outcomes similar to those receiving TMP-SMX. Our study suggests that levofloxacin can be a reasonable alternative to TMP-SMX to treat these infections.

Identifiants

pubmed: 38821443
pii: S2213-7165(24)00105-X
doi: 10.1016/j.jgar.2024.05.016
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflicts of interest to disclose.

Auteurs

Thamer A Almangour (TA)

Department of Clinical Pharmacy College of Pharmacy, King Saud University, P.O. Box 2457 Riyadh 11451, Saudi Arabia. Electronic address: talmangour@ksu.edu.sa.com.

Zakiyah Alkherb (Z)

Clinical Pharmacy Services, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.

Shatha Alruwaite (S)

Department of Clinical Pharmacy College of Pharmacy, King Saud University, P.O. Box 2457 Riyadh 11451, Saudi Arabia.

Renad Alsahli (R)

Department of Clinical Pharmacy College of Pharmacy, King Saud University, P.O. Box 2457 Riyadh 11451, Saudi Arabia.

Hussain Alali (H)

Clinical Pharmacy Services, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.

Abdullah Almohaizeie (A)

Pharmaceutical Care Division, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia; College of Pharmacy, Alfaisal University, Riyadh, Saudi Arabia.

Sara Almuhisen (S)

Pharmacy services administration, King Fahad Medical City, Riyadh, Saudi Arabia.

Shuroug A Alowais (SA)

Department of Pharmacy Practice, College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia; Pharmaceutical Care Department, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, Saudi Arabia.

Khalid Bin Saleh (KB)

Department of Pharmacy Practice, College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia; Pharmaceutical Care Department, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, Saudi Arabia.

Lolwa Fetyani (L)

Department of Pharmacy Practice, College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia; Pharmaceutical Care Department, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, Saudi Arabia.

Fai Alnashmi (F)

Department of Pharmacy Practice, College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia; Pharmaceutical Care Department, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, Saudi Arabia.

Alnajla Alghofaily (A)

Pharmaceutical Care Division, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

Noran Ibrahim Abouobaid (NI)

Pharmaceutical Care Division, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

Khalifa M Binkhamis (KM)

Department of Pathology, College of Medicine, King Saud University, Riyadh, Saudi Arabia; King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.

Essam A Tawfik (EA)

Advanced Diagnostics and Therapeutics Institute, Health Sector, King Abdulaziz City for Science and Technology (KACST), Riyadh 11442, Saudi Arabia.

Yazed Saleh Alsowaida (YS)

Department of Clinical Pharmacy, College of Pharmacy, Hail University, P.O. Box 6166, Hail 81442, Saudi Arabia.

Classifications MeSH