Division of Infectious Diseases, Department of Internal Medicine, Seoul National University Hospital and College of Medicine, Seoul, Republic of Korea.
Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Int J Antimicrob Agents. 2022 Jul;60(1):106604. doi: 10.1016/j.ijantimicag.2022.106604. Epub 2022 May 17.
A randomised controlled trial showed that rapid phenotypic antibiotic susceptibility testing (AST) with antimicrobial stewardship programme (ASP) increases the proportion of haematological patients with bacteraemia receiving optimal targeted therapy within 72 h of blood culture collection. This post-hoc analysis aimed to evaluate the effects of rapid phenotypic AST intervention in haematological patients at high risk of a poor outcome from bacteraemia. Haematological patients with bacteraemia (n = 116) were assigned randomly to a conventional AST group or a rapid AST group. The two outcome measures were the proportion of patients receiving optimal targeted therapy at 72 h post blood culture collection and the time to optimal targeted therapy; subgroup analysis was conducted based on baseline demographics (age, sex) and prognostic (Charlson comorbidity index, haematological treatment intensity, Pitt bacteraemia score, appropriateness of empirical antibiotic therapy and multidrug-resistant organism) indicators. The interaction effect between the intervention and subgroup factors was examined using regression model analysis. Age, sex, Charlson comorbidity index, haematological treatment intensity, Pitt bacteraemia score and appropriateness of empirical antibiotic therapy had no significant interaction effects on the proportion of patients receiving optimal targeted therapy (P = 0.129-0.826). However, infection by a multidrug-resistant organism did have a significant interaction effect (P = 0.042). Regarding time to optimal targeted therapy, there were no significant interaction effects between the intervention and subgroup factors (P = 0.156-0.848). In conclusion, rapid phenotypic AST with ASP intervention may accelerate early optimal targeted antimicrobial treatment of haematological patients, even those in high-risk subgroups with bacteraemia.
一项随机对照试验表明,快速表型抗生素药敏试验(AST)联合抗菌药物管理计划(ASP)可提高血培养采集后 72 小时内接受最佳靶向治疗的血液患者比例。本事后分析旨在评估快速表型 AST 干预对血液感染患者的影响,这些患者存在因菌血症而导致不良结局的高风险。将血培养阳性的血液患者(n=116)随机分为常规 AST 组或快速 AST 组。两个主要结局指标为血培养采集后 72 小时内接受最佳靶向治疗的患者比例和达到最佳靶向治疗的时间;基于基线人口统计学(年龄、性别)和预后(Charlson 合并症指数、血液治疗强度、Pitt 菌血症评分、经验性抗生素治疗的适当性和多重耐药菌)指标进行亚组分析。采用回归模型分析检验干预和亚组因素之间的交互效应。年龄、性别、Charlson 合并症指数、血液治疗强度、Pitt 菌血症评分和经验性抗生素治疗的适当性对接受最佳靶向治疗的患者比例无显著交互效应(P=0.129-0.826)。然而,多重耐药菌感染有显著的交互效应(P=0.042)。关于达到最佳靶向治疗的时间,干预和亚组因素之间没有显著的交互效应(P=0.156-0.848)。总之,快速表型 AST 联合 ASP 干预可能会加速血液感染患者的早期最佳靶向抗菌治疗,即使是处于菌血症高风险亚组的患者也是如此。