Evidence map›Paper›PMID 30097020›Full record

ArticleBMC infectious diseases2018

Infection characteristics and treatment of Staphylococcus aureus bacteraemia at a tertiary children's hospital.

Alasdair P S Munro, Christopher C Blyth, Anita J Campbell, Asha C Bowen

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 38% of its field
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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Observational
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  4. Quantifying patient- and hospital-level antimicrobial resistance dynamics inmedRxiv : the preprint server for health sciences · 2023
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  5. Article
  6. Intravenous versus Oral Step-Down for the Treatment ofPharmacy (Basel, Switzerland) · 2022
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  7. 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

4 authors at 4 institutions in 1 country.

Alasdair P S MunroDepartment of Infectious Diseases, Perth Children's Hospital, Hospital Ave, Nedlands, WA, 6009, Australia. a.munro@doctors.org.uk.
Christopher C BlythDepartment of Infectious Diseases, Perth Children's Hospital, Hospital Ave, Nedlands, WA, 6009, Australia.
Anita J CampbellDepartment of Infectious Diseases, Perth Children's Hospital, Hospital Ave, Nedlands, WA, 6009, Australia.
Asha C BowenDepartment of Infectious Diseases, Perth Children's Hospital, Hospital Ave, Nedlands, WA, 6009, Australia. Asha.bowen@health.wa.gov.au.
Pathwest Laboratory Medicine · AUPerth Children's HospitalPrincess Margaret Hospital for Children · AUUniversity of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStaphylococcus aureus bacteraemia (SAB) causes considerable morbidity and mortality in children. Despite this, its epidemiology and risk factors are poorly understood, with minimal paediatric clinical trial data available to guide clinicians in management. We conducted a pilot study to characterise SAB and validate a severity classification for use in future clinical trials.

methodsPatients with SAB were prospectively identified at Princess Margaret Hospital for Children (Perth, Western Australia) from May 2011 to December 2013. Retrospective data were collected from clinical and laboratory records. Cases were classified based on a priori defined criteria as simple (single or contiguous, peripheral site focus) or complex (multi-site, deep tissue, no focus or sepsis) and tested against risk factors and markers of severity of infection.

resultsThere were 49 cases of SAB (median age 7.7 years), with classification as simple (n = 30, 61%) and complex (n = 19, 39%) respectively. There were no deaths or relapses in our cohort. Only 10% of isolates were methicillin resistant S. aureus (MRSA), and none of these were healthcare-associated. Age, gender, Indigenous status, MRSA and healthcare-associated infections were not predictive of complex infection. Pre-existing malignancy was a risk factor for complex infection (p = 0.02). Complex infections were associated with a higher median maximum C reactive protein (216 mg/L vs 50 mg/L, p = < 0.001), longer median length of stay (42 vs 10 days, p = < 0.001) and longer duration of antibiotic therapy (43 vs 34 days, p = 0.03). DISCUSSION: This is the first attempt to categorise paediatric SAB as simple versus complex, to guide clinicians in decision making.

conclusionsThere is a wide spectrum of disease severity in paediatric SAB, with maximum CRP, length of stay, and duration of therapy greater in those with complex disease. Distinct cohorts with simple and complex courses which may be a target for future clinical trials have been described.

Indexed as

BacteremiaStaphylococcal InfectionsAnti-Bacterial AgentsChildChild, PreschoolCohort StudiesCross InfectionFemaleHospitals, PediatricHumansMaleMethicillin-Resistant Staphylococcus aureusMorbidityPilot ProjectsRetrospective StudiesStaphylococcus aureusAnti-Bacterial AgentsBacteraemiaPaediatricSepsisStaphylococcus aureus

Identifiers

PMID30097020
PMCPMC6086073
OpenAlexW2885936139

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.