Evidence map›Paper›PMID 41965115›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2026

Empirical Antibiotic Activity and Outcomes in Pediatric Gram-negative Bloodstream Infections: A Rank-based Composite Outcome Analysis.

Sophie C H Wen, Melissa J Hardy, Abdullah T Aslan, Patrick N A Harris, Mark D Chatfield, Colleen L Lau, Geoffrey Spurling, Julia E Clark, Sonia Dougherty, Christopher C Blyth and 10 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 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

20 authors.

Sophie C H WenThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0002-7727-4443
Melissa J HardyThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0002-2427-6082
Abdullah T AslanThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Patrick N A HarrisThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0002-2895-0345
Mark D ChatfieldThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Colleen L LauThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Geoffrey SpurlingThe University of Queensland, General Practice Clinical Unit, Brisbane, Queensland, Australia.ORCID 0000-0002-3525-4663
Julia E ClarkInfection Management Prevention Service, Children's Health Queensland, Brisbane, Queensland, Australia.
Sonia DoughertyInfection Management Prevention Service, Children's Health Queensland, Brisbane, Queensland, Australia.
Christopher C BlythWesfarmer's Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, Western Australia, Australia.ORCID 0000-0003-2017-0683
Philip N BrittonDepartment of Infectious Diseases and Microbiology, The Children's Hospital Westmead, Sydney, New South Wales, Australia.ORCID 0000-0002-2993-6000
Vanessa CliffordInfectious Diseases Department, Royal Children's Hospital, Melbourne, Victoria, Australia.
Gabrielle M HaeuslerInfectious Diseases Department, Royal Children's Hospital, Melbourne, Victoria, Australia.
Brendan McMullanInfectious Diseases and Microbiology, Sydney Children's Hospital, Sydney, New South Wales, Australia.
Ushma WadiaWesfarmer's Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, Western Australia, Australia.
Luregn SchlapbachDepartment of Intensive Care and Neonatology, and Children's Research Center, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0003-2281-2598
Henry ChambersUniversity of California SanFrancisco, San Francisco, USA.
David L PatersonADVANCE-ID, Saw Swee Hock School of Public Health, National University of Singapore, Singapore.
Adam D IrwinThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0001-8974-6789
PAEDS Network

Funding

Children's Hospital Foundation Accelerator 50314National Health and Medical Research Council 1197743NHMRC Early Career Fellowship APP1145817NHMRC Emerging Leader Fellowship APP1173857NHMRC Investigator 1193826NOMIS FoundationQueensland Health Advancing Clinical ResearchThomas and Doris Ammann Foundation
6 · The paper itself

Abstract

backgroundTimely active empirical therapy (AET) may improve outcomes following bloodstream infection. In high-income settings, low pediatric mortality following gram-negative bloodstream infection (GNBSI) limits its value as a sole endpoint. Composite measures that incorporate multiple clinically relevant outcomes may detect differences more readily. We assessed the effect of AET on clinical outcomes in pediatric GNBSI.

methodsWe analyzed data from a prospective surveillance study of hospitalized Australian children with GNBSI. A ranked composite endpoint included 30-day all-cause mortality (30D ACM), time to death, intensive care unit (ICU) admission, relapse, and hospitalization duration. Baseline differences were adjusted using inverse probability of treatment weighting. Generalized pairwise comparison (GPC) generated win statistics. Analyses were stratified by comorbidity, acquisition setting, and organism.

resultsActive empirical therapy occurred in 597 episodes and inactive empirical therapy (IET) in 62. Median treatment duration was similar (AET 10 vs IET 11 days, P = .44). Generalized pairwise comparison analysis showed an adjusted win ratio of 1.04 (95% CI .72-1.52, P = .83), indicating no significant difference. Contributions from each composite component (AET vs IET) were the following: 30D ACM (2.2% vs 1.3%), time to death (0.02% vs 0.01%), ICU admission (7.5% vs 9.1%), relapse (2.6% vs 1.4%), and hospitalization duration (37.3% vs 36.0%). Stratified estimates were similar for comorbidity and acquisition.

conclusionsIn this large multicenter pediatric GNBSI cohort, AET was not associated with improved outcomes. In high-resource settings, the impact of initial antibiotic activity may be smaller than traditionally assumed, though timely effective therapy remains essential for severe illness and low-resource settings.

Indexed as

Anti-Bacterial AgentsBacteremiaGram-Negative Bacterial InfectionsAdolescentAustraliaChildChild, PreschoolFemaleGram-Negative BacteriaHospitalizationHumansInfantMaleProspective StudiesTreatment OutcomeAnti-Bacterial Agentsantimicrobial therapybloodstream infectionsGram-negativeoutcomepediatric

Identifiers

PMID41965115
PMCPMC13537164

What OpenQuestion holds

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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.