Evidence map›Paper›PMID 37105710›Full record

ArticleArchives of disease in childhood2023

Diagnosing early-onset neonatal sepsis in low-resource settings: development of a multivariable prediction model.

Samuel R Neal, Felicity Fitzgerald, Simba Chimhuya, Michelle Heys, Mario Cortina-Borja, Gwendoline Chimhini

Open access · hybridAbstract read
In one paragraph

Article in Archives of disease in childhood, 2023. 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
4.1field-weighted citation impact, top 6% 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, 15 citations in OpenAlex.

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  5. A practical predictive model to predict 30-day mortality in neonatal sepsis.Revista da Associacao Medica Brasileira (1992) · 2024
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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 at 2 institutions in 2 countries.

Samuel R NealPopulation, Policy and Practice, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0001-6832-9839
Felicity FitzgeraldInfection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0001-9594-3228
Simba ChimhuyaChild and Adolescent Health Unit, University of Zimbabwe, Harare, Zimbabwe.
Michelle HeysPopulation, Policy and Practice, UCL Great Ormond Street Institute of Child Health, London, UK m.heys@ucl.ac.uk.
Mario Cortina-Borja *Population, Policy and Practice, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0003-0627-2624
Gwendoline Chimhini *Child and Adolescent Health Unit, University of Zimbabwe, Harare, Zimbabwe.
Great Ormond Street Hospital · GBUniversity of Zimbabwe · ZW

Funding

Department of HealthWellcome Trust
6 · The paper itself

Abstract

objectiveTo develop a clinical prediction model to diagnose neonatal sepsis in low-resource settings.

designSecondary analysis of data collected by the Neotree digital health system from 1 February 2019 to 31 March 2020. We used multivariable logistic regression with candidate predictors identified from expert opinion and literature review. Missing data were imputed using multivariate imputation and model performance was evaluated in the derivation cohort.

settingA tertiary neonatal unit at Sally Mugabe Central Hospital, Zimbabwe. PATIENTS: We included 2628 neonates aged <72 hours, gestation ≥32

interventionsParticipants received standard care as no specific interventions were dictated by the study protocol.

main outcome measuresClinical early-onset neonatal sepsis (within the first 72 hours of life), defined by the treating consultant neonatologist.

resultsClinical early-onset sepsis was diagnosed in 297 neonates (11%). The optimal model included eight predictors: maternal fever, offensive liquor, prolonged rupture of membranes, neonatal temperature, respiratory rate, activity, chest retractions and grunting. Receiver operating characteristic analysis gave an area under the curve of 0.74 (95% CI 0.70-0.77). For a sensitivity of 95% (92%-97%), corresponding specificity was 11% (10%-13%), positive predictive value 12% (11%-13%), negative predictive value 95% (92%-97%), positive likelihood ratio 1.1 (95% CI 1.0-1.1) and negative likelihood ratio 0.4 (95% CI 0.3-0.6).

conclusionsOur clinical prediction model achieved high sensitivity with low specificity, suggesting it may be suited to excluding early-onset sepsis. Future work will validate and update this model before considering implementation within the Neotree.

Indexed as

Neonatal SepsisSepsisHumansInfant, NewbornModels, StatisticalPrognosisROC CurveGlobal HealthInfectious Disease MedicineIntensive Care Units, NeonatalNeonatologySepsis

Identifiers

PMID37105710
PMCPMC10423484
OpenAlexW4367175933

What OpenQuestion holds

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LicenceCC BY
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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.