» Articles » PMID: 39487308

Multicenter Evaluation of Ceftazidime-avibactam Use in Carbapenem-resistant Klebsiella Pneumoniae Bloodstream Infections in OXA-48 Endemic Regions

Abstract

Data in the literature on the use of ceftazidime-avibactam (CAZ-AVI) in carbapenem-resistant Klebsiella pneumoniae bloodstream infections (CRKP-BSIs) are limited especially in OXA-48 (Oxacillinase-48) predominant regions. Our study aimed to evaluate the effect of CAZ-AVI use on outcomes in CRKP-BSIs in Turkey, where OXA-48 is endemic. A multicenter retrospective observational study was conducted between January 2017 and September 2021. The effects of clinical and treatment characteristics on 30-day mortality and relapse in CRKP-BSIs were analyzed. Predictors of outcomes were detected using a Cox regression model. The study enrolled 106 adults with CAZ-AVI-sensitive CRKP-BSIs who received CAZ-AVI for at least 72 h. Patients who received CAZ-AVI as initial therapy had lower mortality rates when compared to those who switched from last resort regimens [14.3% (n = 3/21) vs. 37.7% (n = 32/85), p = 0.04]. In multivariate analysis, older age and severe neutropenia were detected to be associated with higher mortality, significantly. Initiation of CAZ-AVI on the day of blood culture was obtained, was found to be significantly associated with lower mortality (HR: 0.25, CI: 0.07-0.84, p = 0.025). CAZ-AVI monotherapy is an important treatment option for CRKP-BSIs in OXA-48 endemic areas. Early initiation of CAZ-AVI should be preferred rather than switching from a last-resort regimen as it profoundly improves the survival rates.

References
1.
Menekse S, Cag Y, Isik M, Sahin S, Haciseyitoglu D, Can F . The effect of colistin resistance and other predictors on fatality among patients with bloodstream infections due to Klebsiella pneumoniae in an OXA-48 dominant region. Int J Infect Dis. 2019; 86:208-211. DOI: 10.1016/j.ijid.2019.06.008. View

2.
Medeiros G, Rigatto M, Falci D, Zavascki A . Combination therapy with polymyxin B for carbapenemase-producing Klebsiella pneumoniae bloodstream infection. Int J Antimicrob Agents. 2019; 53(2):152-157. DOI: 10.1016/j.ijantimicag.2018.10.010. View

3.
Isler B, Ozer B, Cinar G, Aslan A, Vatansever C, Falconer C . Characteristics and outcomes of carbapenemase harbouring carbapenem-resistant Klebsiella spp. bloodstream infections: a multicentre prospective cohort study in an OXA-48 endemic setting. Eur J Clin Microbiol Infect Dis. 2022; 41(5):841-847. DOI: 10.1007/s10096-022-04425-4. View

4.
Falcone M, Bassetti M, Tiseo G, Giordano C, Nencini E, Russo A . Time to appropriate antibiotic therapy is a predictor of outcome in patients with bloodstream infection caused by KPC-producing Klebsiella pneumoniae. Crit Care. 2020; 24(1):29. PMC: 6993311. DOI: 10.1186/s13054-020-2742-9. View

5.
Genc S, Kolayli F, Ozcelik E . Molecular characterization of carbapenemase producing Klebsiella pneumoniae strains by multiplex PCR and PFGE methods: The first K.pneumoniae isolates co-producing OXA-48/KPC and KPC/NDM in Turkey. J Infect Chemother. 2021; 28(2):192-198. DOI: 10.1016/j.jiac.2021.10.009. View