Antimicrobial Resistance Rates and Treatment Options in Bloodstream Infections: A Prospective Observational Study

Emerging antibacterial resistance is a constant threat. Broad-spectrum antibiotics are preferred in empirical treatment for bloodstream infections (BSI) due to increasing resistance rates. A prospective observational study was conducted in three tertiary hospitals in Türkiye. Microbiologically docum...

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Veröffentlicht in:Journal of global antimicrobial resistance. 2024-12, Vol.39, p.28-29
Hauptverfasser: Gücer, Lal Sude, Pınarlık, Fatihan, Farzana, Refath, Ataç, Nazlı, GENÇ, ZELİHA, Madran, Bahar, BULBUL, IREM SENA, Şahin, Feyza, SENGEL, Buket ERTURK, Tigen, Elif Tukenmez, Ilki, Arzu, SARI, NURAN, Azap, Özlem Kurt, can, Fusun, Walsh, Timothy R., Ergönül, Önder
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Sprache:eng
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Zusammenfassung:Emerging antibacterial resistance is a constant threat. Broad-spectrum antibiotics are preferred in empirical treatment for bloodstream infections (BSI) due to increasing resistance rates. A prospective observational study was conducted in three tertiary hospitals in Türkiye. Microbiologically documented BSIs were collected between 1 November 2023 and 1 June 2024. Demographics, clinical information, and antimicrobial susceptibility tests for each BSI case were collected. A total of 618 BSI patients were included in the study and 55 (8.9%) of these BSIs were polymicrobial. Among 563 monomicrobial BSIs, the causative agent was gram-negative in 278 (49.4%), gram-positive in 247 (43.9%), and Candida spp. in 38 (6.7%) patients. Gram-positive and gram-negative species distribution is depicted in Figure 1 and 2, respectively. Methicillin-resistant S. aureus (MRSA) rate was 37%. Carbapenem resistance rate for K. pneumoniae was 62%. 30-day mortality was 48% in gram-negative BSI, and it was 66% if the causative agent is carbapenem resistant. BSI caused by MRSA had a 30-day mortality of 36%. The two most common empirical treatment choices were meropenem and piperacillin-tazobactam. Of patients receiving ineffective empirical treatment, 35% failed escalation in 24 hours after susceptibility results. More than 24-hour delay in de-escalation of meropenem was observed in 82% of gram-negative BSIs. Escalation in 24 hours was achieved in MRSA BSIs. Mean delay of 3.9 days were observed in de-escalation of vancomycin or teicoplanin in methicillin-susceptible S. aureus BSIs. Timely transition to targeted therapies is critical for antimicrobial stewardship especially when broad-spectrum antibiotics are preferred in empirical therapy.
ISSN:2213-7165
DOI:10.1016/j.jgar.2024.10.088