Evidence map›Paper›PMID 41201759›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Direct MALDI-TOF MS identification and EUCAST RAST from positive blood cultures: impact on turnaround time in bloodstream infections.

Bilgehan Ergan, Fatih Mehmet Akıllı, Arzu İlki

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Bilgehan ErganDepartment of Medical Microbiology, School of Medicine, Marmara University, Istanbul, Turkey.
Fatih Mehmet AkıllıDepartment of Medical Microbiology, School of Medicine, Marmara University, Istanbul, Turkey. drmehmetakilli@gmail.com.
Arzu İlkiDepartment of Medical Microbiology, School of Medicine, Marmara University, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRapid identification (ID) and antibiotic susceptibility testing are vital for the treatment of bloodstream infections (BSIs). The aim of this study was to perform direct identification and rapid antimicrobial susceptibility testing (RAST), from positive blood cultures and to compare the performance of these rapid methods with standard reference methods.

methodsBlood cultures (BC) submitted to Marmara University Pendik Training and Research Hospital Clinical Microbiology Laboratory between September 2022 - April 2023, that yielded positive signal and were determined to be monomicrobial by gram staining were selected randomly. ID was performed using MALDI-TOF MS(bioMérieux, France). Based on these results, rapid antimicrobial susceptibility testing (RAST) was applied to 103 bottles that met RAST eligibility criteria. The results of rapid ID and RAST were evaluated by comparing them with the results obtained from colony-grown isolates.

resultsRapid ID showed that out of 306 bottles, 281 (91.8%) were monomicrobial. High rates of correct identification were achieved for gram-negative bacilli (84.3%), gram-positive chain cocci (79.4%), and gram-positive cluster cocci (55.2%), while performance was lower for gram-positive bacilli (27.3%) and yeasts (37.5%). For RAST, the readability of inhibition zone diameters increased progressively with incubation time, reaching 85.2%, 94.5%, 100%, and 100% at 4, 6, 8, and 16-20 h, respectively. The categorical agreement of the test remained consistently high across all time points, measuring 98.35% at 4 h, 98.49% at 6 h, 98.38% at 8 h, and 98.84% at 16-20 h.

conclusionRapid ID of microorganisms directly from positive BC bottles, combined with RAST based on EUCAST RAST criteria, demonstrates high accuracy and reliability compared to conventional methods. These rapid approaches significantly reduce the turnaround time for both identification and susceptibility results-by approximately 16-20 h and 32-48 h, respectively thereby enabling earlier targeted antimicrobial therapy and improving clinical management of BSIs.

Indexed as

BacteremiaBacteriaBlood CultureSepsisSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAnti-Bacterial AgentsHumansMicrobial Sensitivity TestsTime FactorsAnti-Bacterial AgentsBacTALERTBloodstream infectionsDirect identificationEUCAST RASTMALDI-TOF MS

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.