Evidence map›Paper›PMID 33421424›Full record

ArticleThe Journal of pediatrics2021

Using Clinical History Factors to Identify Bacterial Infections in Young Febrile Infants.

Jeffrey P Yaeger, Jeremiah Jones, Ashkan Ertefaie, Mary T Caserta, Edwin van Wijngaarden, Kevin Fiscella

Abstract read
In one paragraph

Article in The Journal of pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

6 authors.

Jeffrey P YaegerDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY; Department of Public Health Sciences, University of Rochester Medical Center, Rochester, NY. Electronic address: Jeffrey_Yaeger@urmc.rochester.edu.
Jeremiah JonesDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY.
Ashkan ErtefaieDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY.
Mary T CasertaDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY.
Edwin van WijngaardenDepartment of Public Health Sciences, University of Rochester Medical Center, Rochester, NY.
Kevin FiscellaDepartment of Family Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY.

Funding

Institutional Career Development CoreKL2TR001999 · NCATS · UNIVERSITY OF ROCHESTER · PI XIAO, JIN · 2016 to 2024
$5.2M
NCATS NIH HHS KL2 TR001999
6 · The paper itself

Abstract

objectiveTo develop a novel predictive model using primarily clinical history factors and compare performance to the widely used Rochester Low Risk (RLR) model. STUDY

designIn this cross-sectional study, we identified infants brought to one pediatric emergency department from January 2014 to December 2016. We included infants age 0-90 days, with temperature ≥38°C, and documented gestational age and illness duration. The primary outcome was bacterial infection. We used 10 predictors to develop regression and ensemble machine learning models, which we trained and tested using 10-fold cross-validation. We compared areas under the curve (AUCs), sensitivities, and specificities of the RLR, regression, and ensemble models.

resultsOf 877 infants, 67 had a bacterial infection (7.6%). The AUCs of the RLR, regression, and ensemble models were 0.776 (95% CI 0.746, 0.807), 0.945 (0.913, 0.977), and 0.956 (0.935, 0.975), respectively. Using a bacterial infection risk threshold of .01, the sensitivity and specificity of the regression model was 94.6% (87.4%, 100%) and 74.5% (62.4%, 85.4%), compared with 95.5% (87.5%, 99.1%) and 59.6% (56.2%, 63.0%) using the RLR model.

conclusionsCompared with the RLR model, sensitivities of the novel predictive models were similar whereas AUCs and specificities were significantly greater. If externally validated, these models, by producing an individualized bacterial infection risk estimate, may offer a targeted approach to young febrile infants that is noninvasive and inexpensive.

Indexed as

Clinical Decision RulesBacterial InfectionsCross-Sectional StudiesEmergency Service, HospitalFemaleFeverHumansInfantInfant, NewbornLinear ModelsLogistic ModelsMachine LearningMaleMedical History TakingRetrospective StudiesRisk Assessmentindividualized risk assessmentpredictive model

Identifiers

PMID33421424
PMCPMC13035059

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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.