Evidence map›Paper›PMID 40181355›Full record

ArticleBMC pediatrics2025

Scoping review of clinical decision aids in the assessment and management of febrile infants under 90 days of age.

Etimbuk Umana, Hannah Norman-Bruce, Thomas Waterfield

Abstract readScoping Review
In one paragraph

Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Etimbuk UmanaWellcome Wolfson Institute of Experimental Medicine, Queen's University Belfast, 97 Lisburn Rd, Belfast, BT9 7BL, UK. eumana01@qub.ac.uk.
Hannah Norman-BruceWellcome Wolfson Institute of Experimental Medicine, Queen's University Belfast, 97 Lisburn Rd, Belfast, BT9 7BL, UK.
Thomas WaterfieldWellcome Wolfson Institute of Experimental Medicine, Queen's University Belfast, 97 Lisburn Rd, Belfast, BT9 7BL, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical decision aids (CDA) play an important role in the management of young febrile infants (under 90 days of age) who are at risk of serious or invasive bacterial infections (SBI/IBI). Since 2010, a number of tailored CDAs have been developed that allow for lower-risk infants to be managed safely while undergoing fewer investigations and not receiving parenteral antibiotics. We aimed to map the CDAs developed since 2010, their derivation methodology, and their variable components.

methodsA scoping review based on the Joana Briggs Institute framework was conducted for studies published between 2010 and 2025. A database search was conducted using Medline, Embase, Scopus, Web of Science, Google Scholar, and the Cochrane library. Studies evaluating the derivation, validation, and application of CDAs for the assessment of febrile infants were eligible for inclusion. Two reviewers independently screened, analysed, and extracted data from the literature.

resultsA total of 32 studies met the inclusion criteria. The majority of studies were conducted in North America and Canada (56%), followed by Europe (28%), and Asia (16%). Of the 32 studies, 14 were retrospective, 9 prospective and 9 secondary analysis of an available dataset. There were 32 CDAs that were either derived or validated across 32 studies. The derivation methodology was classified into four themes: (i) expert consensus and evidence synthesis; (ii) regression analysis; (iii) recursive partitioning; and (iv) machine learning. CDAs typically either identified a low-risk cohort through sequential assessment (n = 12) or predicted the risk of IBI/SBI using prediction models (n = 20). CDA sensitivity and specificity ranged from 46 - 100% and 9 - 95% respectively for SBI/IBI. The majority (n = 18) of the more complex CDA prediction models have been published in the last five years. The most common variables included within the CDAs were age, urinalysis, height of fever, C-reactive protein, and absolute neutrophil count.

conclusionThis scoping review highlights a wide range of CDAs with a trend towards prediction modelling rather than sequential assessment in the last five years. There is still variability in CDA properties, applicability, and diagnostic performance, necessitating further validation of common CDA and prediction models.

Indexed as

Bacterial InfectionsDecision Support TechniquesFeverHumansInfantInfant, NewbornBacterial infectionClinical decision aidFebrile infant

Identifiers

PMID40181355
PMCPMC11969967

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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.