Sirijatuphat Rujipas, Thawornkaew Supawas, Ruangkriengsin Darat, Thamlikitkul Visanu
Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Antibiotics (Basel). 2022 Nov 26;11(12):1707. doi: 10.3390/antibiotics11121707.
The in vitro study of sitafloxacin against carbapenem-resistant (CR) demonstrated activity against most strains of CR , and the combination of colistin and sitafloxacin showed an in vitro synergistic effect against CR . This study aimed to compare efficacy and safety between colistin plus sitafloxacin with colistin alone for therapy for CR infection. This randomized controlled trial enrolled 56 patients with CR infection (28/group) during 2018-2021, and the treatment duration was 7-14 days. The study outcomes were 28-day mortality, clinical and microbiological responses, and adverse events. There was no significant difference in 28-day mortality between groups (32.1% combination vs. 32.1% monotherapy, = 1.000). Favorable clinical response at the end of treatment was comparable between groups (81.5% combination vs. 77.8% monotherapy, = 0.788). Microbiological response at the end of treatment was also comparable between groups (73.1% combination vs. 74.1% monotherapy, = 0.934). Acute kidney injury was found in 53.8% of the combination group, and in 45.8% of the monotherapy group ( = 0.571). In conclusion, there was no significant difference in 28-day mortality between the colistin monotherapy and the colistin plus sitafloxacin groups. There was also no significant difference in adverse events between groups.
西他沙星对耐碳青霉烯类(CR)的体外研究表明其对大多数CR菌株具有活性,并且黏菌素与西他沙星联合使用对CR显示出体外协同作用。本研究旨在比较黏菌素联合西他沙星与单用黏菌素治疗CR感染的疗效和安全性。这项随机对照试验在2018年至2021年期间纳入了56例CR感染患者(每组28例),治疗持续时间为7至14天。研究结果包括28天死亡率、临床和微生物学反应以及不良事件。两组之间的28天死亡率无显著差异(联合治疗组为32.1%,单药治疗组为32.1%,P = 1.000)。治疗结束时的良好临床反应在两组之间相当(联合治疗组为81.5%,单药治疗组为77.8%,P = 0.788)。治疗结束时的微生物学反应在两组之间也相当(联合治疗组为73.1%,单药治疗组为74.1%,P = 0.934)。联合治疗组53.8%的患者出现急性肾损伤,单药治疗组为45.8%(P = 0.571)。总之,黏菌素单药治疗组与黏菌素联合西他沙星组之间的28天死亡率无显著差异。两组之间的不良事件也无显著差异。