Evidence map›Paper›PMID 42622709›Full record

ArticleEuropean journal of pediatrics2026

Interleukin-6 as a sepsis biomarker in neonatal and pediatric care: A retrospective real world cohort study.

Seán Olann Whelan, Grainne Kelleher, Sharon Campbell, Aisling Walsh, Naomi McCallion, Frank Moriarty, Mohamed Elsammak, Richard John Drew

Abstract readMulticenter Study
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In one paragraph

Article in European journal of pediatrics, 2026. 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. Review
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

8 authors.

Seán Olann WhelanDepartment of Clinical Microbiology, Children's Health Ireland at Temple Street, Dublin, Ireland. sean.whelan@childrenshealthireland.ie.ORCID http://orcid.org/0000-0002-0272-2889
Grainne KelleherDepartment of Chemical Pathology, Rotunda Hospital, Dublin, Ireland.
Sharon CampbellDepartment of Chemical Pathology, Rotunda Hospital, Dublin, Ireland.
Aisling WalshDepartment of Paediatric Critical Care, Children's Health Ireland at Temple Street, Dublin, Ireland.
Naomi McCallionDepartment of Neonatology, Rotunda Hospital, Dublin, Ireland.
Frank MoriartySchool of Pharmacy and Biomolecular Sciences, RCSI University of Medicine and Health Sciences, Dublin, Ireland.
Mohamed ElsammakDepartment of Chemical Pathology, Rotunda Hospital, Dublin, Ireland.
Richard John DrewIrish Meningitis and Sepsis Reference Laboratory, Children's Health Ireland at Temple Street, Dublin, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to assess the diagnostic performance of Interleukin-6 (IL-6) in comparison to other biomarkers (C-reactive protein [CRP], procalcitonin [PCT], neutrophil-lymphocyte ratio [NLR]) in a pediatric and neonatal setting. This retrospective cohort study in 2 Dublin hospitals (one pediatric and one maternity/neonatal) included all pediatric and neonatal patients who had IL-6 testing for clinically suspected sepsis in a one-year period. Cases were categorized according to clinical, microbiological and radiological criteria. Paediatric cases were described along two axes -physiological (from normal to septic shock) and etiological (bacterial, viral or no infection), while neonatal sepsis was defined from a composite of bacteremia, septic shock and clinical sepsis. Biomarker performance was assessed by area under the receiver operating characteristic curves (AUROC) and measures of diagnostic accuracy at optimal cut-offs. Overall, 180 cases were included (111 pediatric cases and 69 neonates). Amongst pediatric cases 34.2% were classified as sepsis or septic shock, and 55.8% had bacterial infections. Among neonates, 49.3% met sepsis criteria. In the pediatric analysis all biomarkers had statistically significant differences between physiological and etiological categories, although only IL-6 and PCT showed stepwise progression along both axes. IL-6 had statistically higher AUROC values than all other biomarkers for the primary physiological and etiological axes outcomes (0.85 [Interquartile range 0.78, 0.93] and 0.91 [IQR 0.85, 0.96], with higher sensitivity than other biomarkers. Over time, IL-6 showed significantly greater negative rates of change. In neonates, all biomarkers other than CRP showed statistically significant differences between categories, although IL-6 alone showed clinically significant differences. For neonatal sepsis the IL-6 AUROC was 0.86 (IQR 0.77, 0.95), statistically higher than CRP and NLR. However, sensitivity was lower than other analyses (67.6%), although this increased to 81.2% when the sepsis category was restricted to culture positive or shock cases only.

conclusionIL-6 had superior diagnostic performance to most other sepsis biomarkers across axes, with high sensitivities and AUROC, in a broad general pediatric and neonatal population. Combined with favorable biomarker kinetics over serial sampling, these findings encourage further prospective evaluation and evaluation of the impact on patient outcomes. WHAT IS KNOWN: • Interleukin-6 (IL-6) is a promising sepsis diagnostic biomarker, due to its kinetics it more closely temporally mirrors infectious or inflammatory insults. • Evaluation of IL-6 in pediatric sepsis has been limited to specific populations, with limited evaluation in a broad general pediatric population of children with suspected sepsis. WHAT IS NEW: • IL-6 is a discerning biomarker, categorizing children into physiological and etiological categories with higher diagnostic accuracy than other biomarkers in common use. • Sensitivity for both bacterial infection and physiological compromise was high for pediatric cases, but lower in neonates.

Indexed as

Interleukin-6Neonatal SepsisSepsisBiomarkersChildChild, PreschoolC-Reactive ProteinFemaleHumansInfantInfant, NewbornMaleProcalcitoninRetrospective StudiesROC CurveSensitivity and SpecificityBiomarkersC-Reactive ProteinIL6 protein, humanInterleukin-6ProcalcitoninBiomarkersInterleukin-6Neonatal sepsisPediatric sepsisSepsis

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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.