Department of Pharmacy Practice, Albany College of Pharmacy and Health Sciences, Albany, NY, USA.
Global Health Economics and Outcomes Research, Allergan plc, Madison, NJ, USA.
BMC Infect Dis. 2018 Dec 5;18(1):625. doi: 10.1186/s12879-018-3524-8.
Temporal relationships between the time to appropriate antibiotic therapy and outcomes are not well described.
A systematic literature review and meta-analysis was performed to examine this relationship in patients hospitalized with Klebsiella pneumoniae or Escherichia coli infections.
Twenty identified studies contained data for patients who received delayed appropriate therapy (DAT) versus appropriate antibiotic therapy for these pathogens. Of the 20 included studies, the majority (19/20) focused on patients with bloodstream infections, and only 1 study evaluated patients with pneumonia. When all DAT results were combined (any delay > 24 h from culture collection or any delay after culture and susceptibility reporting [C& SR]), there was an increased risk of mortality (odds ratio [OR], 1.60 [95% CI, 1.25-2.50]). The risk of mortality was greater when DAT > 48 h from culture collection or DAT > C&SR results were combined (OR, 1.76 [95% CI, 1.27-2.44]).
Our findings suggest there is a need to shift current treatment practices away from antibiotic escalation strategies that contribute to delayed appropriate therapy and toward early, relatively aggressive and comprehensive, antibiotic therapy, especially among patients with bloodstream infections due to K. pneumoniae or E. coli.
抗生素治疗时机与结局之间的时间关系尚未得到充分描述。
进行了系统的文献回顾和荟萃分析,以研究住院感染肺炎克雷伯菌或大肠埃希菌患者的这种关系。
20 项已确定的研究包含了接受延迟适当治疗(DAT)与这些病原体适当抗生素治疗的患者的数据。在 20 项纳入的研究中,大多数(19/20)侧重于血流感染患者,只有 1 项研究评估了肺炎患者。当综合所有 DAT 结果(从培养物采集后任何延迟>24 小时或在培养物和药敏报告后任何延迟[C&SR])时,死亡率风险增加(优势比[OR],1.60 [95%CI,1.25-2.50])。从培养物采集后 DAT > 48 小时或 DAT > C&SR 结果的死亡率风险更高(OR,1.76 [95%CI,1.27-2.44])。
我们的研究结果表明,需要改变当前的治疗实践,避免导致延迟适当治疗的抗生素升级策略,转而采用早期、相对积极和全面的抗生素治疗,尤其是针对由肺炎克雷伯菌或大肠埃希菌引起的血流感染患者。