Evidence map›Paper›PMID 42377271›Full record

ReviewThe Journal of infectious diseases2026

Rationalizing Heterogeneity in Staphylococcus aureus Bacteremia: Current Progress and Future Goals.

Clark D Russell, Sofía De La Villa, Maaike C Swets, Annette C Westgeest, Giulia Zumbo, Patricia Muñoz, David H Dockrell, Vance G Fowler, Belén Gutiérrez-Gutiérrez

Abstract readReview
In one paragraph

Review in The Journal of infectious diseases, 2026. 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

9 authors.

Clark D RussellCentre for Inflammation Research, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0002-9873-8243
Sofía De La VillaClinical Microbiology and Infectious Diseases Department, Hospital General Universitario Gregorio Marañón, Madrid/Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.ORCID 0000-0002-1371-6417
Maaike C SwetsDepartment of Internal Medicine, Haaglanden Medical Center, The Hague, The Netherlands.ORCID 0000-0003-0901-9560
Annette C WestgeestLeiden University Center for Infectious Diseases, Leiden University Medical Center, Leiden University, Leiden, The Netherlands.ORCID 0000-0002-0648-3555
Giulia ZumboDivision of Infectious Diseases and Microbiology, Virgen Macarena University Hospital, Seville, Spain.
Patricia MuñozClinical Microbiology and Infectious Diseases Department, Hospital General Universitario Gregorio Marañón, Madrid/Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.ORCID 0000-0001-5706-5583
David H DockrellCentre for Inflammation Research, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0002-2718-4861
Vance G FowlerDivision of Infectious Diseases and International Health, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Belén Gutiérrez-GutiérrezBiomedical Research Networking Centre for Infectious Diseases (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0002-9668-0770

Funding

HLA Fine Mapping to Elucidate S. aureus SusceptibilityR01AI165671 · NIAID · DUKE UNIVERSITY · PI FOWLER, VANCE G., SCOTT, WILLIAM K · 2021 to 2025
$3.8M
Chief Scientist Office (CSO) Scotland MR/W028506/1Chief Scientist Office (CSO) Scotland MR/Y013131/1Chief Scientist Office (CSO) Scotland PCL/25/21CIBERINFEC 21/13/00012CIBERINFEC PI21/01801European UnionInstituto de Salud Carlos III (ISCIII)MRCNIAID NIH HHS R01 AI165671NIH HHSSHIELD consortium "Optimising Innate Host Defence to Combat Antimicrobial Resistance" MR/NO2995X/1SHIELD consortium "Optimising Innate Host Defence to Combat Antimicrobial Resistance" R01-AI165671
6 · The paper itself

Abstract

Clinical and biological heterogeneity in Staphylococcus aureus bacteremia (SAB) continue to pose significant challenges for the clinical management of individual patients and for research efforts. We contend that investigating SAB as a single disease is impeding the identification of beneficial therapeutic approaches. Recently, three data-driven approaches for patient stratification in SAB have been reported, using routinely available data to identify clinically distinct subphenotypes with differences in mortality, microbiologic outcomes, and response to adjunctive antimicrobial therapies (the Swets et al, FEN-AUREUS, and MRSA-GEIRAS-SEIMC studies). In this review, we compare the methodologies and findings from these studies, discuss their limitations, and identify goals for future research in this space. We expect that transformative advances in SAB management will only be achieved by addressing clinical and biological heterogeneity, enabling progress from observable clinical subphenotypes to mechanism-based endotypes defined by treatable traits.

Indexed as

BacteremiaStaphylococcal InfectionsStaphylococcus aureusAnti-Bacterial AgentsHumansPhenotypeAnti-Bacterial Agentsendotypespatient stratificationpersonalized medicineStaphylococcus aureus bacteremiasubphenotypes

Identifiers

PMID42377271
PMCPMC13600396

What OpenQuestion holds

Textmetadata
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.