Köck Robin, Wüllenweber Jörg, Horn Dagmar, Lanckohr Christian, Becker Karsten, Idelevich Evgeny A
Institute of Medical Microbiology, University Hospital Münster, Domagkstr. 10, 48149 Münster, Germany ; Present address: Institute of Hospital Hygiene, University of Oldenburg, European Medical School Oldenburg-Groningen, Rahel-Straus-Str. 10, 26133 Oldenburg, Germany.
Institute of Medical Microbiology, University Hospital Münster, Domagkstr. 10, 48149 Münster, Germany.
Antimicrob Resist Infect Control. 2017 Jan 14;6:12. doi: 10.1186/s13756-017-0173-4. eCollection 2017.
Results of blood culture (BC) diagnostics should be swiftly available to guide treatment of critically ill patients. Conventional BC diagnostics usually performs species identification of microorganisms from mature solid medium colonies. Species identification might be speed up by using matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry (MS) of biomass from shortly incubated solid media.
This single-center analysis compared the applicability of MALDI-TOF-based species identification from shortly incubated cultures in laboratory routine vs. conventional diagnostics and assessed its effects of on empiric antibiotic therapy.
Median time between detection of BCs as "positive" by incubators and further processing (e.g. microscopy) was 6 h 21 min. Median time between microscopy and result reporting to the ward was 15 min. Including 193 BCs, MALDI-TOF from shortly incubated biomass resulted in significantly faster ( > 0.001) species identification. Species results became available for clinicians after a median of 188 min (231 min for Gram-positive bacteria, 151 min for Gram-negative bacteria) compared to 909 min ( = 192 BCs) when conventional diagnostics was used. For 152/179 bacteremia episodes (85%) empiric antibiotic therapy had already been started when the microscopy result was reported to the ward; microscopy led to changes of therapies in 14/179 (8%). In contrast, reporting the bacterial species (without antibiogram) resulted in therapeutic adjustments in 36/179 (20%). Evaluating these changes revealed improved therapies in 26/36 cases (72%).
Species identification by MALDI-TOF MS from shortly incubated subcultures resulted in adjustments of empiric antibiotic therapies and might improve the clinical outcome of septic patients.
血培养(BC)诊断结果应能迅速获取,以指导重症患者的治疗。传统的BC诊断通常从成熟的固体培养基菌落中对微生物进行菌种鉴定。通过对短期培养的固体培养基中的生物质进行基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱分析(MS),可以加快菌种鉴定速度。
这项单中心分析比较了在实验室常规操作中,基于MALDI-TOF从短期培养物中进行菌种鉴定与传统诊断方法的适用性,并评估了其对经验性抗生素治疗的影响。
培养箱检测到BC为“阳性”至进一步处理(如显微镜检查)的中位时间为6小时21分钟。显微镜检查至向病房报告结果的中位时间为15分钟。纳入193份BC样本,对短期培养的生物质进行MALDI-TOF分析可显著加快(>0.001)菌种鉴定速度。与使用传统诊断方法时的909分钟(=192份BC样本)相比,临床医生在中位188分钟后(革兰氏阳性菌为231分钟,革兰氏阴性菌为151分钟)即可获得菌种鉴定结果。在向病房报告显微镜检查结果时,152/179例(85%)菌血症发作的经验性抗生素治疗已经开始;显微镜检查导致14/179例(8%)治疗方案改变。相比之下,报告细菌种类(无药敏试验结果)导致36/179例(20%)治疗方案调整。评估这些改变发现,26/36例(72%)治疗方案得到改善。
通过MALDI-TOF MS对短期传代培养物进行菌种鉴定可调整经验性抗生素治疗方案,并可能改善脓毒症患者的临床结局。