Efficacy and safety of cefmetazole for bacteremia caused by extended-spectrum β-lactamase-producing Enterobacterales compared with carbapenems: A retrospective study

医学 头孢美唑 菌血症 内科学 碳青霉烯 头孢菌素 回顾性队列研究 抗生素 外科 微生物学 生物
作者
Eriko Kashihara,Ryuichi Sada,Yukio Tsugihashi,H. Obayashi,Akihiro Nakamura,Noriyuki Abe,Hirofumi Miyake,Hiroyuki Akebo
出处
期刊:Open Forum Infectious Diseases [Oxford University Press]
卷期号:10 (10)
标识
DOI:10.1093/ofid/ofad502
摘要

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.
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