Cefoxitin versus carbapenems as definitive treatment for extended-spectrum β-lactamase-producing Klebsiella pneumoniae bacteremia in intensive care unit: a propensity-matched retrospective analysis

被引:3
作者
Dequidt, Tanguy [1 ]
Bastian, Sylvaine [2 ,3 ]
Nacher, Mathieu [4 ]
Breurec, Sebastien [2 ,3 ,5 ,6 ,7 ]
Carles, Michel [8 ]
Thiery, Guillaume [9 ]
Camous, Laurent [10 ]
Tressieres, Benoit [7 ]
Valette, Marc [10 ]
Pommier, Jean-David [10 ]
机构
[1] Univ Hosp Guadeloupe, Infect Dis Dept, Pointe A Pitre, France
[2] Univ Hosp Guadeloupe, Lab Clin Microbiol, Pointe A Pitre, France
[3] Univ Antilles, Univ Montpellier, PCCEI, INSERM,EFS, Pointe A Pitre, France
[4] Cayenne Hosp Ctr, INSERM 1424, Clin Invest Ctr Antilles French Guiana CIC, St Laurent Du Maroni, French Guiana, France
[5] Pasteur Inst Guadeloupe, Transmiss Reservoir & Divers Pathogens Unit, Pointe A Pitre, France
[6] Univ Antilles, Fac Med Hyacinthe Bastaraud, Pointe A Pitre, France
[7] INSERM, Ctr Clin Invest 1424, Pointe A Pitre Les Abymes, France
[8] Univ Hosp Nice, Infect Dis Dept, Nice, France
[9] St Etienne Univ Hosp, Med Intens Care Unit, St Priest En Jarez, France
[10] Univ Hosp Guadeloupe, Intens Care Unit, Pointe A Pitre, France
关键词
Klebsiella pneumoniae; Extended-spectrum beta-lactamase (ESBL); Cefoxitin; Carbapenem; Bloodstream infections; Intensive care unit; URINARY-TRACT-INFECTIONS; IN-VIVO SELECTION; ESCHERICHIA-COLI; ACUTE PHYSIOLOGY; FLOMOXEF; SEPSIS; SCORE; ANTIBIOTICS; RESISTANCE; THERAPY;
D O I
10.1186/s13054-023-04712-2
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background Despite cefoxitin's in vitro resistance to hydrolysis by extended-spectrum beta-lactamases (ESBL), treatment of ESBL-producing Klebsiella pneumoniae (KP) infections with cefoxitin remains controversial. The aim of our study was to compare the clinical efficacy of cefoxitin as definitive antibiotic therapy for patients with ESBL-KP bacteremia in intensive care unit, versus carbapenem therapy. Methods This retrospective study included all patients with monomicrobial bacteremia hospitalized in intensive care unit between January 2013 and January 2023 at the University Hospital of Guadeloupe. The primary outcome was the 30-day clinical success defined as a composite endpoint: 30-day survival, absence of relapse and no change of antibiotic therapy. Cox regression including a propensity score (PS) and PS-based matched analysis were performed for endpoint analysis. Results A total of 110 patients with bloodstream infections were enrolled. Sixty-three patients (57%) received definitive antibiotic therapy with cefoxitin, while forty-seven (43%) were treated with carbapenems. 30-day clinical success was not significantly different between patients treated with cefoxitin (57%) and carbapenems (53%, p = 0.823). PS-adjusted and PS-matched analysis confirmed these findings. Change of definitive antibiotic therapy was more frequent in the cefoxitin group (17% vs. 0%, p = 0.002). No significant differences were observed for the other secondary endpoints. The acquisition of carbapenem-resistant Pseudomonas aeruginosa was significantly higher in patients receiving carbapenem therapy (5% vs. 23%, p = 0.007). Conclusions Our results suggest that cefoxitin as definitive antibiotic therapy could be a therapeutic option for some ESBL-KP bacteremia, sparing carbapenems and reducing the selection of carbapenem-resistant Pseudomonas aeruginosa strains.
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