Evidence map›Paper›PMID 38767234›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2024

Distinct Clinical Endpoints of Staphylococcus aureus Bacteraemia Complicate Assessment of Outcome.

Clark D Russell, Karla Berry, George Cooper, Wynne Sim, Rui Shian Lee, Tze Yi Gan, William Donlon, Antonia Besu, Emily Heppenstall, Luke Tysall and 4 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Impact of Methicillin Resistance on Outcomes ofOpen forum infectious diseases · 2026
    Article
  5. Reproducible Identification of Staphylococcus aureus Bacteremia Clinical Subphenotypes.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Observational
  6. Article
  7. Emergence of a methicillin-susceptibleFrontiers in cellular and infection microbiology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Clinical Subphenotypes of Staphylococcus aureus Bacteremia.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Observational
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.

Clark D RussellCentre for Inflammation Research, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, United Kingdom.
Karla BerryClinical Infection Research Group, Western General Hospital, Edinburgh, United Kingdom.
George CooperCentre for Inflammation Research, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, United Kingdom.
Wynne SimEdinburgh Medical School, The University of Edinburgh, Edinburgh, United Kingdom.
Rui Shian LeeEdinburgh Medical School, The University of Edinburgh, Edinburgh, United Kingdom.
Tze Yi GanEdinburgh Medical School, The University of Edinburgh, Edinburgh, United Kingdom.
William DonlonEdinburgh Medical School, The University of Edinburgh, Edinburgh, United Kingdom.
Antonia BesuEdinburgh Medical School, The University of Edinburgh, Edinburgh, United Kingdom.
Emily HeppenstallMedical Microbiology, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Luke TysallMedical Microbiology, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Andrew RobbScottish Microbiology Reference Laboratory, New Lister Building, Glasgow, United Kingdom.
Simon DewarMedical Microbiology, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Andrew SmithScottish Microbiology Reference Laboratory, New Lister Building, Glasgow, United Kingdom.ORCID 0000-0003-0580-4078
Vance G FowlerDivision of Infectious Diseases and International Health, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.

Funding

HLA Fine Mapping to Elucidate S. aureus SusceptibilityR01AI165671 · NIAID · DUKE UNIVERSITY · PI FOWLER, VANCE G., SCOTT, WILLIAM K · 2021 to 2025
$3.8M
Edinburgh Clinical Academic TrackNIAID NIH HHS R01 AI165671NIH HHSWellcome TrustWellcome Trust 214178/Z/18/Z
6 · The paper itself

Abstract

backgroundWe aimed to test the hypothesis that development of metastatic infection represents a distinct clinical endpoint from death due to Staphylococcus aureus bacteremia (SAB).

methodsWe conducted a retrospective observational study of adults with SAB between 20 December 2019 and 23 August st2022 (n = 464). Simple logistic regression, odds ratios, and z-scores were used to compare host, clinical, and microbiologic features.

resultsCo-occurrence of attributable mortality and metastatic infection was infrequent. Charlson Comorbidity Index and age were strongly associated with attributable mortality, but not metastatic infection. We compared patients with fatal SAB (without clinically-apparent metastatic complications, 14.4% of cohort), metastatic SAB (without attributable mortality, 22.2%), neither complication (56.7%), and overlapping fatal/metastatic SAB (6.7%). Compared to SAB without complications, fatal SAB was specifically associated with older age and multi-morbidity. Metastatic SAB was specifically associated with community acquisition, persistent fever, persistent bacteremia, and recurrence. Endocarditis was over-represented in the fatal/metastatic SAB overlap group, which shared patient characteristics with fatal SAB. In contrast to other (predominantly musculoskeletal) metastatic complications, endocarditis was associated with increased mortality, with death occurring in older multi-morbid patients later after SAB onset.

conclusionsPatients with SAB experience distinct clinical endpoints: (i) early death, associated with multi-morbidity and age; (ii) metastatic (predominantly musculoskeletal) SAB; (iii) endocarditis, associated with late death occurring in older people with multi-morbidity, and (iv) bacteraemia without complications. These distinctions could be important for selecting appropriate outcomes in clinical trials: different interventions might be required to reduce mortality versus improve clinical response in patients with metastatic SAB.

Indexed as

BacteremiaStaphylococcal InfectionsStaphylococcus aureusAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective Studiesbacteraemiaclinical outcomesclinical trialsmortalityStaphylococcus aureus

Identifiers

PMID38767234
PMCPMC11426269

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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.