Evidence map›Paper›PMID 38917034›Full record

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

Characterization of Gram-negative Bloodstream Infections in Hospitalized Australian Children and Their Clinical Outcomes.

Sophie C H Wen, Patrick N A Harris, Brian Forde, Budi Permana, Mark D Chatfield, Colleen L Lau, Geoffrey Spurling, Michelle J Bauer, Ross Balch, Henry Chambers and 11 more

Abstract read
In one paragraph

Article 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Empirical Antibiotic Activity and Outcomes in Pediatric Gram-negative Bloodstream Infections: A Rank-based Composite Outcome Analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  2. Review
  3. Comparative evaluation of BacT/ALERT PF Plus and PF pediatric blood culture bottles: A dual in vitro and clinical retrospective study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  4. Article
  5. Molecular determinants ofFrontiers in cellular and infection microbiology · 2026
    Article
  6. Review
  7. Review
  8. Observational
  9. 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

21 authors.

Sophie C H WenThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0002-7727-4443
Patrick N A HarrisThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Brian FordeThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0002-2264-4785
Budi PermanaThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Mark D ChatfieldThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.ORCID 0000-0002-0004-6274
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.
Michelle J BauerThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Ross BalchThe University of Queensland, Centre for Clinical Research, Brisbane, Queensland, Australia.
Henry ChambersSchool of Medicine, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0001-5317-4491
Luregn J SchlapbachThe University of Queensland, Child Health Research Centre, Brisbane, Queensland, Australia.
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 Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, Western Australia, Australia.
Philip N BrittonDepartment of Infectious Diseases and Microbiology, The Children's Hospital Westmead, Sydney, New South Wales, Australia.
Vanessa CliffordInfectious Diseases Unit, Royal Children's Hospital, Melbourne, Victoria, Australia.
Gabrielle M HaeuslerInfectious Diseases Unit, Royal Children's Hospital, Melbourne, Victoria, Australia.
Brendan McMullanInfectious Diseases and Microbiology, Sydney Children's Hospital, Sydney, New South Wales, Australia.
Ushma WadiaWesfarmer Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, Western Australia, Australia.
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.

Funding

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

Abstract

backgroundGram-negative bloodstream infections (GNBSIs) more commonly occur in children with comorbidities and are increasingly associated with antimicrobial resistance. There are few large studies of GNBSIs in children that relate the clinical presentation, pathogen characteristics, and outcomes.

methodsA 3-year prospective study of GNBSIs in children aged <18 years was conducted in 5 Australian children's hospitals between 2019 and 2021. The clinical characteristics, disease severity, and outcomes were recorded. Causative pathogens underwent antibiotic susceptibility testing and whole genome sequencing.

resultsThere were 931 GNBSI episodes involving 818 children. Median age was 3 years (interquartile range, 0.6-8.5). A total of 576/931 episodes (62%) were community onset, though 661/931 (71%) occurred in children with comorbidities and a central venous catheter was present in 558/931 (60%). Central venous catheter (145/931) and urinary tract (149/931) were the most common sources (16% each). One hundred of 931 (11%) children required intensive care unit admission and a further 11% (105/931) developed GNBSIs in intensive care unit. A total of 659/927 (71%) isolates were Enterobacterales, of which 22% (138/630) were third-generation cephalosporin resistant (3GCR). Extended spectrum beta-lactamase genes were confirmed in 65/138 (47%) 3GCR Enterobacterales. Most common extended spectrum beta-lactamase genes were blaCTX-M-15 (34/94, 36%) and blaSHV-12 (10/94, 11%). There were 48 deaths overall and 30-day in-hospital mortality was 3% (32/931). Infections with 3GCR Enterobacterales were independently associated with higher mortality (adjusted odds ratio, 3.2; 95% confidence interval, 1.6-6.4).

conclusionsGNBSIs in children are frequently healthcare associated and affect children younger than age 5 years. Infections with 3GCR Enterobacterales were associated with worse outcomes. These findings will inform optimal management guidelines and help prioritize future antimicrobial clinical trials.

Indexed as

Anti-Bacterial AgentsBacteremiaGram-Negative BacteriaGram-Negative Bacterial InfectionsAdolescentAustraliaChildChild, HospitalizedChild, PreschoolFemaleHospitalizationHumansInfantMaleMicrobial Sensitivity TestsProspective StudiesAnti-Bacterial Agentsantimicrobial resistancebloodstream infectionsGram-negativeoutcomepediatric

Identifiers

PMID38917034
PMCPMC11426278

What OpenQuestion holds

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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.