Department of Internal Medicine, University of Iowa-Des Moines Campus, Des Moines, IA, USA.
Department of Pharmacy, UnityPoint Health-Des Moines, Des Moines, IA, USA.
J Appl Lab Med. 2022 May 4;7(3):776-781. doi: 10.1093/jalm/jfab170.
Rapid initiation of optimal antimicrobial therapy is crucial for the management of Gram-negative (GN) bacteremia. We aimed to evaluate the impact of Accelerate PhenoTM (AxDx) system on change in therapy and length of stay among patients with GN bacteremia.
We conducted a retrospective cohort study of adult patients hospitalized who had at least 1 blood culture with presence of Enterobacterales. We compared clinical outcomes among patients who had their blood cultures processed through standard methods alone vs AxDx.
We identified 255 bacteremia episodes among 243 unique patients. In the AxDx group, 31.1% of patients had deescalation of antibiotics within 48 h from blood culture collection compared to 20.0% of patients in the control group (P = 0.09). We found no impact of AxDx on the odds of deescalation at 48 h from blood culture collection [odds ratio (OR) 1.80 (95% CI 0.91-3.56), P = 0.09] or Gram stain report [OR 1.61 (95% CI 0.86-3.01), P = 0.14]. Escalation in therapy at 48 h from blood culture collection occurred in 16.8% and 16.9% of patients in the AxDx and control groups, respectively (P = 0.99). There was no impact on the odds of escalation at 48 h from blood culture collection [OR 0.99 (95% CI 0.47-2.11), P = 0.99] or Gram stain report [OR 1.26 (95% CI 0.57-2.80), P = 0.57]. No differences were seen in length of stay and mortality between the 2 groups.
The impact of rapid identification and susceptibility technologies may differ according to the setting in which they are implemented.
快速启动最佳抗菌治疗对于革兰氏阴性(GN)菌血症的治疗至关重要。我们旨在评估 Accelerate PhenoTM(AxDx)系统对 GN 菌血症患者治疗改变和住院时间的影响。
我们对至少有 1 份血培养物中存在肠杆菌科的住院成人患者进行了回顾性队列研究。我们比较了仅通过标准方法处理血培养物的患者与 AxDx 组的临床结果。
我们确定了 243 名患者中的 255 例菌血症发作。在 AxDx 组中,与对照组(20.0%)相比,31.1%的患者在血培养采集后 48 小时内抗生素降级,(P=0.09)。我们发现 AxDx 对血培养采集后 48 小时降级的可能性没有影响[比值比(OR)1.80(95%置信区间 0.91-3.56),P=0.09]或革兰氏染色报告[OR 1.61(95%置信区间 0.86-3.01),P=0.14]。在血培养采集后 48 小时,治疗升级的患者分别为 AxDx 组和对照组的 16.8%和 16.9%,(P=0.99)。在血培养采集后 48 小时升级的可能性没有影响[OR 0.99(95%置信区间 0.47-2.11),P=0.99]或革兰氏染色报告[OR 1.26(95%置信区间 0.57-2.80),P=0.57]。两组患者的住院时间和死亡率无差异。
快速鉴定和药敏技术的影响可能因实施环境而异。