Impact of reporting rapid susceptibility results in Gram negative bloodstream infections: a real world prospective study.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Anne-Sophie Messiaen, Stien Vandendriessche, Emilie De Muynck, Gregory Strubbe, Liesbet De Bus, Petra Schelstraete, Kristen Decommer, Sanne De Smet, Alexander Soetens, Leslie Naesens, Katrien Timmermans, Jan J De Waele, Diana Huis In 't Veld, Jerina Boelens
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引用次数: 0

Abstract

Purpose: Mortality and morbidity of patients with bloodstream infection (BSI) remain high despite advances in diagnostic methods and efforts to speed up reporting. This study investigated the impact of reporting rapid Minimum Inhibitory Concentration (MIC)-results in Gram negative BSIs with the ASTar system (Q-linea, Uppsala, Sweden) on the adaptation of empirically started antimicrobial therapy. We performed a real-world study during which antimicrobial susceptibility testing (AST) results were instantly reported to the treating physician in an established multidisciplinary antimicrobial stewardship setting.

Methods: Consecutive patients with Gram negative bacteremia were included in the study (monomicrobial Gram stain, life expectancy of at least 48 h and flagging positive before 2 PM). Rapid AST (RAST) reporting with ASTar was added on top of the standard workflow. Technical performance of the system was evaluated as well as the impact on antimicrobial treatment and timelines of achieving effective and optimal antimicrobial therapy.

Results: A total of 79 analyses were performed in 77 patients, of which 68 episodes were eligible for analysis. A categorical agreement was observed in 97,5% of 1160 MIC results without false susceptible results. All patients on ineffective empirical therapy (12/68) were switched after a median time of approximately one hour (5 min - 15 h) after communication of the result. Furthermore, 20/55 non-optimal therapies were adapted within a median period of 3 h after communication.

Conclusion: The implementation of rapid MICs, measured by the ASTar system, in our low antimicrobial resistance setting with elaborate antimicrobial guidelines, was easy and led to early adaptation of empirical treatment in 32/55 instances (12 ineffective and 20 non-optimal therapy).

Trial registration number: NCT06218277 (date of registration: 18-12-2023).

报告快速敏感性结果对革兰氏阴性血流感染的影响:一项真实世界的前瞻性研究。
目的:尽管诊断方法的进步和加快报告的努力,血液感染(BSI)患者的死亡率和发病率仍然很高。本研究调查了ASTar系统(Q-linea, Uppsala, Sweden)报告革兰氏阴性bsi的快速最低抑制浓度(MIC)结果对经验开始的抗菌治疗适应性的影响。我们进行了一项真实世界的研究,在此期间,抗菌药物敏感性试验(AST)结果立即报告给治疗医生,建立了多学科抗菌药物管理设置。方法:连续纳入革兰氏阴性菌血症患者(单菌革兰氏染色,预期寿命至少48 h,下午2点前呈阳性)。快速AST (RAST)报告与ASTar被添加到标准工作流程之上。评估了该系统的技术性能以及对抗菌治疗的影响和实现有效和最佳抗菌治疗的时间表。结果:共对77例患者进行了79次分析,其中68次符合分析条件。1160例MIC结果中97.5%的结果完全一致,无假敏感结果。所有接受无效经验治疗的患者(12/68)在告知结果后中位时间约1小时(5分钟- 15小时)后切换。此外,20/55的非最佳疗法在沟通后的中位3小时内适应。结论:通过ASTar系统测量的快速mic在我们的低耐药性环境中实施容易,并导致32/55例患者(12例无效,20例非最佳治疗)早期适应经验治疗。试验注册号:NCT06218277(注册日期:18-12-2023)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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