Efficacy and Safety of Cefmetazole for Bacteremia Caused by Extended-Spectrum β-Lactamase–Producing Enterobacterales vs Carbapenems: A Retrospective Study

Author:

Kashihara Eriko1,Sada Ryuichi Minoda123ORCID,Tsugihashi Yukio4,Obayashi Hitoshi5,Nakamura Akihiro6,Abe Noriyuki7,Miyake Hirofumi1,Akebo Hiroyuki1

Affiliation:

1. Department of General Internal Medicine, Tenri Hospital , Nara , Japan

2. Department of Infection Control, Graduate School of Medicine, Osaka University , Osaka , Japan

3. Department of Transformative Protection to Infectious Disease, Graduate School of Medicine, Osaka University , Osaka , Japan

4. Medical Home Care Center, Tenri Hospital Shirakawa Branch , Nara , Japan

5. Tenri Institute of Medical Research , Nara , Japan

6. Department of Clinical Laboratory Science, Faculty of Health Care, Tenri University , Tenri , Japan

7. Department of Clinical Microbiology, Clinical Laboratory Medicine, Tenri Hospital , Tenri , Japan

Abstract

Abstract Background Extended-spectrum β-lactamase (ESBL)–producing Enterobacterales have become a global concern owing to increased infections, high mortality, and limited antibiotic treatment options. Carbapenems (CPMs) are effective against ESBL-producing Enterobacterales, but their overuse leads to the emergence of multidrug-resistant bacteria. Cefmetazole (CMZ) is effective in vitro; however, its clinical efficacy remains unclear. Methods We retrospectively reviewed patients who were treated with CMZ or CPMs for bacteremia caused by ESBL-producing Enterobacterales between 1 April 2014 and 31 September 2022 at Tenri Hospital. The primary outcome measure was 90-day mortality. We also evaluated resistance genes and sequence types of ESBL-producing Enterobacterales. Results In total, 156 patients were enrolled in this study. Ninety patients (58%) received CMZ therapy. Patients in the CMZ group were significantly older than those in the CPM group (median [IQR], 79 years [71–86] vs 74 years [64–83]; P = .001). The severity of the Pitt bacteremia score of the CMZ group was lower than that in the CPM group (0 [0–2] vs 2 [0–2], P = .042). Six patients (7%) in the CMZ group and 10 (15%) in the CPM group died by day 90 (P = .110). Charlson Comorbidity Index and prevalence of sequence 131 between the groups were statistically insignificant. Conclusions Our findings suggest that CMZ is a well-tolerated alternative to CPM for treating bacteremia caused by ESBL-producing Enterobacterales.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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