Evidence map›Paper›PMID 39862301›Full record

Trial reportEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2025

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

Anne-Sophie Messiaen, Stien Vandendriessche, Emilie De Muynck, Gregory Strubbe, Liesbet De Bus, Petra Schelstraete, Kristen Decommer, Sanne De Smet, Alexander Soetens, Leslie Naesens and 4 more

Registry-linked trialAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06218277 (Rapid Antimicrobial Susceptibility Testing with MIC Directly from Positive Blood Cultures with ASTar), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06218277 nacompletednot on this map

Rapid Antimicrobial Susceptibility Testing with MIC Directly from Positive Blood Cultures with ASTar

TypeinterventionalSponsorUniversity Hospital, GhentRan2024 to 2024Enrolled80ConditionsBacteremiaArmsASTAR
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Direct MALDI-TOF MS identification and EUCAST RAST from positive blood cultures: impact on turnaround time in bloodstream infections.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Anne-Sophie MessiaenLaboratory of Medical Microbiology, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0002-3501-0140
Stien VandendriesscheLaboratory of Medical Microbiology, Ghent University Hospital, Ghent, Belgium.
Emilie De MuynckLaboratory of Medical Microbiology, Ghent University Hospital, Ghent, Belgium.
Gregory StrubbeLaboratory of Medical Microbiology, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0001-6104-9340
Liesbet De BusDepartment of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0003-1456-5857
Petra SchelstraeteDepartment of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University Ghent, Ghent, Belgium.ORCID http://orcid.org/0000-0002-9560-8275
Kristen DecommerDepartment of Internal Medicine and Infectious Diseases, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0001-7518-3524
Sanne De SmetDepartment of Internal Medicine and Infectious Diseases, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0009-0003-1550-9782
Alexander SoetensDepartment of Internal Medicine and Infectious Diseases, Ghent University Hospital, Ghent, Belgium.
Leslie NaesensDepartment of Internal Medicine and Infectious Diseases, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0003-1715-0665
Katrien TimmermansDepartment of Internal Medicine and Infectious Diseases, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0009-0002-3360-9878
Jan J De WaeleDepartment of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0003-1017-9748
Diana Huis In 't VeldDepartment of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University Ghent, Ghent, Belgium.ORCID http://orcid.org/0000-0002-5806-4352
Jerina BoelensLaboratory of Medical Microbiology, Ghent University Hospital, Ghent, Belgium. jerina.boelens@uzgent.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMortality 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.

methodsConsecutive 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.

resultsA 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.

conclusionThe 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).

Indexed as

Anti-Bacterial AgentsBacteremiaGram-Negative BacteriaGram-Negative Bacterial InfectionsAdultAgedAged, 80 and overAntimicrobial StewardshipFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedProspective StudiesSwedenAnti-Bacterial AgentsAntimicrobial stewardshipEUCASTGram negative bacteremiaMICRAST

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Registered trials

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.