Armstrong Eric, Kulikova Maria, Yee Noelle, Rishu Asgar, Muscedere John, Sibley Stephanie, Maslove David, Boyd J Gordon, Evans Gerald, Detsky Michael, Marshall John, Taggart Linda R, Friedrich Jan O, Tsang Jennifer L Y, Duan Erick, Ali Firdous Karim, McCullagh David, Findlater Aidan, Fowler Rob, Daneman Nick, Coburn Bryan
Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada.
Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Open Forum Infect Dis. 2025 Mar 14;12(3):ofaf137. doi: 10.1093/ofid/ofaf137. eCollection 2025 Mar.
Maintaining a diverse gut microbiome and minimizing antimicrobial resistance gene (ARG) carriage through reduced antibiotic utilization may decrease antimicrobial resistance. We compared gut microbiome disruption and ARG carriage following 7 or 14 days of antibiotics for treatment of bacteremia in a substudy of the BALANCE randomized controlled trial.
The BALANCE randomized controlled trial enrolled 3631 participants with bacteremia, who were randomized 1:1 to receive 7 or 14 days of antibiotics. Rectal swabs were collected from 131 participants and analyzed with metagenomic sequencing to characterize the gut microbiome and ARGs. The primary outcome was change in gut microbiome diversity at day 7 vs 14.
Forty-one participants (n = 28 in the 14-day group, n = 13 in the 7-day group) had samples available for the primary analysis, with an imbalance in piperacillin-tazobactam exposure between groups. Change in gut microbiome diversity at day 7 vs 14 was comparable between the 14-day group (median, 0.07; IQR, -0.46 to +0.51) and 7-day group (median, 0.19; IQR, -0.77 to +0.22; = .49). Change in ARG abundance at day 7 vs 14 did not differ by treatment duration, nor did the abundance of individual ARGs. We did not observe any change in gut microbiome diversity or ARG carriage at enrollment vs day 7.
In this subset of patients from the BALANCE randomized controlled trial, we did not detect greater gut microbiome disruption or ARG carriage among participants who received 14 vs 7 days of antibiotics, but we were limited by small sample size and imbalances between groups.
维持多样化的肠道微生物群,并通过减少抗生素使用来降低抗菌药物耐药基因(ARG)携带,可能会降低抗菌药物耐药性。在BALANCE随机对照试验的一项子研究中,我们比较了使用7天或14天抗生素治疗菌血症后肠道微生物群的破坏情况和ARG携带情况。
BALANCE随机对照试验纳入了3631例菌血症患者,他们被1:1随机分配接受7天或14天的抗生素治疗。从131例参与者中采集直肠拭子,并通过宏基因组测序进行分析,以表征肠道微生物群和ARGs。主要结局是第7天与第14天肠道微生物群多样性的变化。
41例参与者(14天组28例,7天组13例)有样本可用于主要分析,两组之间哌拉西林-他唑巴坦暴露情况不均衡。第7天与第14天肠道微生物群多样性的变化在14天组(中位数为0.07;IQR为-0.46至+0.51)和7天组(中位数为0.19;IQR为-0.77至+0.22;P = 0.49)之间具有可比性。第7天与第14天ARG丰度的变化在治疗持续时间方面没有差异,单个ARG的丰度也没有差异。我们未观察到入组时与第7天肠道微生物群多样性或ARG携带情况有任何变化。
在BALANCE随机对照试验的这部分患者中,我们未检测到接受14天抗生素治疗的参与者比接受7天抗生素治疗的参与者有更严重的肠道微生物群破坏或ARG携带情况,但我们受到样本量小和组间不均衡的限制。