Evidence map›Paper›PMID 40693492›Full record

ArticleThe Journal of antimicrobial chemotherapy2025

Impact of vancomycin resistance on attributable mortality among Enterococcus faecium bloodstream infections: propensity score analysis of a large, multicentre retrospective study.

M Del Monte, S Kaleci, J Chester, V Zerbato, M Remitti, A Tili, A Dessilani, I Baldisserotto, S Esperti, M D Di Trapani and 13 more

Abstract readMulticenter Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Temporal Trends and Mortality of Vancomycin-ResistantPathogens (Basel, Switzerland) · 2026
    Observational
  4. Article
  5. Article
  6. Article
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

23 authors.

M Del MonteInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0009-0000-8679-7863
S KaleciDermatology Unit, Department of Surgical, Medical, Dental and Morphological Science with Interest Transplant, Oncological and Regenerative Medicine, University of Modena and Reggio Emilia, Modena, Italy.
J ChesterDermatology Unit, Department of Surgical, Medical, Dental and Morphological Science with Interest Transplant, Oncological and Regenerative Medicine, University of Modena and Reggio Emilia, Modena, Italy.
V ZerbatoClinical Department of Medical, Surgical and Health Sciences, Trieste University, Trieste, Italy.ORCID 0000-0002-9204-032X
M RemittiInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
A TiliInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
A DessilaniInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
I BaldisserottoInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
S EspertiInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
M D Di TrapaniInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
G OrlandoInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
S CasolariInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0003-2494-464X
A CataniaInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
A BediniInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-4041-1459
E FranceschiniInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0001-6922-5759
M SartiClinical Microbiology Laboratory, University of Modena and Reggio Emilia, Modena, Italy.
C VenturelliClinical Microbiology Laboratory, University of Modena and Reggio Emilia, Modena, Italy.
I VenturelliClinical Microbiology Laboratory, University of Modena and Reggio Emilia, Modena, Italy.
L RofranoClinical Microbiology Laboratory, University of Modena and Reggio Emilia, Modena, Italy.
E RicchizziAgenzia Sanitaria e sociale Regionale, Regione Emilia-Romagna, Bologna, Italy.
S Di BellaClinical Department of Medical, Surgical and Health Sciences, Trieste University, Trieste, Italy.
C MussiniInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.
M MeschiariInfectious Diseases Unit, Policlinico di Modena, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-1254-9995

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConflicting results exist about mortality risk of infections caused by vancomycin-susceptible Enterococcus faecium (VSEfm) and vancomycin-resistant Enterococcus faecium (VREfm). Our aim was to compare risk factors and clinical outcomes among patients with VSEfm and VREfm bloodstream infections (BSIs).

methodsA retrospective, multicentre, cohort study enrolled consecutive adult patients with VSEfm and VREfm BSI diagnosis between 2018-2022. Primary outcomes were 30-day-attributable and 30-day-overall mortality. Multivariable analysis propensity-weighted adjusted for timing to active therapy, Pitt Bacteremia Score (PBS) and Charlson Comorbidity Index (CCI) were performed to identify variables independently associated with 30-day mortality.

resultsOverall, 446 patients were enrolled: 140 (31.4%) VREfm and 306 (68.6%) VSEfm. Comparatively, VREfm patients more frequently received inappropriate antibiotic therapy, had higher sequential organ failure assessment, PBS and BSI relapses. 30-day-attributable and 30-day-overall mortality did not differ significantly between the two groups. Independent risk factors for 30-day attributable mortality were age (HR 1.04, CI95%, 1.00-1.08, P = 0.022), corticosteroid therapy (HR 3.05, CI95%, 1.24-7.47, P = 0.014) and septic shock (HR 9.10, CI95%, 3.80-21.79, P≤0.001), and overall mortality were age (HR 1.04, CI95%, 1.02-1.05, P≤0.001.), chronic liver failure (HR 1.67, CI95%, 1.02-2.75, P = 0.04) and haematological disease (HR 2.25, CI95%, 1.28-3.94, P = 0.005). Vancomycin resistance is not an independent risk factor for mortality when data are adjusted for confounding factors.

conclusionsAdjusted analyses for time to active antibiotic therapy suggest that vancomycin resistance is not an independent risk factor for overall or attributable mortality among patients with Enterococcus faecium BSI. Independent risk factors identified in this study were exclusively comorbidities, severity and corticosteroids use.

Indexed as

Anti-Bacterial AgentsBacteremiaEnterococcus faeciumGram-Positive Bacterial InfectionsVancomycin ResistanceVancomycin-Resistant EnterococciAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPropensity ScoreRetrospective StudiesRisk FactorsAnti-Bacterial AgentsVancomycin

Identifiers

PMID40693492
PMCPMC12404782

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Registered trials

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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.