Evidence map›Paper›PMID 40782300›Full record

Observational studyEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2025

Gram-negative bloodstream infections: where can we do better? A retrospective cohort study.

Manouc Guit, Konstantin Tanida, Nicole Degel-Brossmann, Martin Christner, Martin Aepfelbacher, Holger Rohde, Flaminia Olearo

Abstract readObservational Study
In one paragraph

Observational study 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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Manouc GuitCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Konstantin TanidaCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Nicole Degel-BrossmannCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Martin ChristnerCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Martin AepfelbacherCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Holger RohdeCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Flaminia OlearoCenter for Diagnostics, Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. f.olearo@uke.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGram-negative bloodstream infections (GN-BSI) significantly impact hospital admissions, presenting major health challenges. Despite guidelines advocating de-escalation, oralization, and appropriate treatment durations, real-world clinical management remains unclear.

methodsThis retrospective observational study assessed GN-BSI management at a tertiary care hospital, comparing uncomplicated (uGN-BSI) and complicated (cGN-BSI) cases from January to December 2022. It focused on identifying risk factors for suboptimal therapy, defined as failure to adopt the narrowest effective spectrum suggested by susceptibility reports within 24 h of result availability.

resultsAmong 194 patients studied, 52.1% had uGN-BSI which were predominantly caused by Escherichia coli (54.6%) with a urinary tract source, while cGN-BSI showed higher rates of AmpC producers (22.6%) and Pseudomonas aeruginosa (8.6%). Treatment durations deviated by a median of + 2 days (interquartile 0-5) for cGN-BSI. Missed opportunities for oralization were higher in uGN-BSI (76.2%) than in cGN-BSI (55.9%). Average time to oralization was 5.5 days in uGN-BSI versus 6.5 days in cGN-BSI. Rates of optimal treatment initiation within 24 h post-antibiogram were low (uGN-BSI: 22.8%, cGN-BSI: 26.9%). Third-generation cephalosporine resistant isolates (OR 0.3, CI95% 0.1-0.9) and AmpC-producers (OR 0.3, CI95% 0.1-0.8) were least associated with suboptimal therapy, while urinary tract sources in uGN-BSI trended to pose higher risk. cGN-BSI patients had fewer missed oralization opportunities than uGN-BSI patients, with a protective trend in the multivariate (OR 0.5, CI95% 0.2-1).

conclusionGN-BSI management frequently does not meet guideline standards, especially in de-escalation and oralization. uGN-BSI could benefit from antibiotic stewardship interventions, whereas cGN-BSI requires tailored strategies, including individualized ID consultations.

Indexed as

Anti-Bacterial AgentsBacteremiaGram-Negative BacteriaGram-Negative Bacterial InfectionsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsTertiary Care CentersAnti-Bacterial AgentsAntibiotic de-escalation (ADE)Antimicrobial stewardship (AMS)Gram-negative bloodstream infection (GN-BSI)OralizationUncomplicated GN-BSI

Identifiers

PMID40782300
PMCPMC12619705

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.