在败血症和血流感染中引入快速识别细菌和早期抗生素敏感性试验后的临床和经济改进。现象研究的结果。

GMS infectious diseases Pub Date : 2020-12-15 eCollection Date: 2020-01-01 DOI:10.3205/id000069
Michael Wilke, Wolfgang Heinlein, Luis Stiefenhofer, Klaus-Friedrich Bodmann
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引用次数: 0

摘要

背景:脓毒症和血液感染是重症监护的严峻挑战。早期可靠的诊断是治疗成功的关键。本研究的目的是研究新型PhenoTM BC检测的临床和经济效果,该检测可在血培养呈阳性(BC+)后约7小时内进行细菌鉴定(ID)和抗菌药敏试验(AST)。方法:历史对照介入研究。人群:BC+及ICU入院患者。不适当的初始抗菌治疗(IAT)需要根据结果改变治疗。展望新试验的应用前景。主要终点:以小时为单位的到结果的时间。计算贡献利润率(CM),即收入-成本。所有患者均为意向治疗人群(ITT)。费用资料完整的患者组成改良ITT组(mITT)。CM结果计算了mITT和PP。进一步分析:住院时间(LOS)和死亡率。结果:纳入223例历史患者和200例预期患者。结果时间(ITT)缩短了51.1小时(83小时vs. 31.9小时;结论:新的PhenoTM ID+AST检测可更快获得有临床意义的结果,并通过缩短ICU的LOS节省资金。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical and economical improvements after introducing rapid identification of bacteria and early antibiotic susceptibility testing in sepsis and bloodstream infections. Results of the PHENOMENON study.

Clinical and economical improvements after introducing rapid identification of bacteria and early antibiotic susceptibility testing in sepsis and bloodstream infections. Results of the PHENOMENON study.

Clinical and economical improvements after introducing rapid identification of bacteria and early antibiotic susceptibility testing in sepsis and bloodstream infections. Results of the PHENOMENON study.

Clinical and economical improvements after introducing rapid identification of bacteria and early antibiotic susceptibility testing in sepsis and bloodstream infections. Results of the PHENOMENON study.

Background: Sepsis and bloodstream infections pose severe challenges in intensive care. Early reliable diagnosis is the key to successful therapy. The objective of the study presented here was to investigate the clinical and economical effects of the new PhenoTM BC test, which allows bacteria identification (ID) and antimicrobial susceptibility testing (AST) in approximately 7 hours after a blood culture becomes positive (BC+). Methods: Historically controlled interventional study. Population: patients with BC+ and ICU admission. Inadequate initial antimicrobial therapy (IAT) is need of therapy change based on result. Prospectively the new test was used in addition. Primary endpoint: time-to-result in hours. Contribution margin (CM) i.e. revenue - costs was computed. All patients formed the intention-to-treat population (ITT). Patients with complete cost data formed the modified ITT group (mITT). CM results were calculated for mITT and PP. Further analyses: length-of-stay (LOS) and mortality. Results: 223 historical and 200 prospective patients were included. Time to result (ITT) was shortened by 51.1 hours (83 vs. 31.9; p<0.001). Overall savings (mITT) were 257,100 € (-301,264 € vs. -44,164 €). 143 of 181 (79%) patients had a test performed, 126 of 143 (88%) having a clinically useable result. 40 (32%) had IAT vs. 65 (29%) in the historic cohort. Median time to AST in PP was shortened by 61.7 hours (89.5 vs. 27.8; p<0.001). LOS was shortened 7 days (28 vs. 19; p=0.226) and mortality was 8% (40.5% vs. 32.5%; p=0.440) lower. Median CM +3,074.80 € per case (-2,350.50 € vs. +724.70 €; p=0.040). Conclusion: The new PhenoTM ID+AST test leads to faster and clinically meaningful results and saves money by shortening LOS on the ICU.

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