Evidence map›Paper›PMID 41877237›Full record

ArticlePediatric rheumatology online journal2026

Predicting recalcitrant hyperinflammatory disease course in children with Kawasaki disease and MIS-C.

Özlem Satirer, Fehime Kara Eroglu, Johannes Nordmeyer, Matthias Kumpf, Felix Neunhoeffer, Vanya Icheva, Christiane Reiser, Oana Buzoianu, Susanne M Benseler, Jasmin B Kuemmerle-Deschner

Abstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Özlem Satirer *Paediatric Rheumatology, Department of Paediatrics and Autoinflammation Reference Center Tuebingen (arcT), University Hospital Tuebingen, Tuebingen, Germany.
Fehime Kara Eroglu *Paediatric Rheumatology, Department of Paediatrics and Autoinflammation Reference Center Tuebingen (arcT), University Hospital Tuebingen, Tuebingen, Germany.
Johannes NordmeyerDepartment of Pediatric Cardiology, University Children's Hospital, University of Tübingen, Tübingen, Germany.
Matthias KumpfDepartment of Pediatric Cardiology, University Children's Hospital, University of Tübingen, Tübingen, Germany.
Felix NeunhoefferDepartment of Pediatric Cardiology, University Children's Hospital, University of Tübingen, Tübingen, Germany.
Vanya IchevaDepartment of Pediatric Cardiology, University Children's Hospital, University of Tübingen, Tübingen, Germany.
Christiane ReiserPaediatric Rheumatology, Department of Paediatrics and Autoinflammation Reference Center Tuebingen (arcT), University Hospital Tuebingen, Tuebingen, Germany.
Oana BuzoianuPaediatric Rheumatology, Department of Paediatrics and Autoinflammation Reference Center Tuebingen (arcT), University Hospital Tuebingen, Tuebingen, Germany.
Susanne M Benseler *Department of Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Jasmin B Kuemmerle-Deschner *Paediatric Rheumatology, Department of Paediatrics and Autoinflammation Reference Center Tuebingen (arcT), University Hospital Tuebingen, Tuebingen, Germany. kuemmerle.deschner@uni-tuebingen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHyperinflammation ranges from monophasic to rapidly progressive, life-threatening courses. Early biomarkers to identify high-risk children are needed.

methodsThis single-center cohort included consecutive children with hyperinflammation between 01/2021 and 01/2024. Demographic, clinical, laboratory, cardiac imaging, and treatment data were analysed.

resultsOf 80 patients, 56 (70%) had a recalcitrant course. Fever was universal. Rash, mucosal involvement, and conjunctivitis were more common in the monophasic group, while abdominal pain, neurological signs, pleural effusion, lymphopenia, thrombocytopenia, hypoalbuminemia, and elevated ferritin characterised the recalcitrant group (p < 0.01). Myocarditis and reduced ejection fraction occurred only in the recalcitrant cohort; coronary artery changes were more frequent in monophasic cases (21% vs. 5%). All survived. All received IVIG; steroids and anakinra were used only in recalcitrant cases, who also had longer hospital stays, ICU admissions (21% vs. 0%, p < 0.01), and required inotropes/ventilation. Baseline SAA, IL-2R, and NT-proBNP were significantly higher in the recalcitrant cohort. In ROC analyses, NT-proBNP showed the highest diagnostic accuracy (AUC 0.912), followed by IL-2R (AUC 0.873) and SAA (AUC 0.793) (all p < 0.001).

conclusionsNT-proBNP, IL-2R, and SAA were strongly associated with a recalcitrant hyperinflammatory course and may aid early prognostication and monitoring.

Indexed as

Mucocutaneous Lymph Node SyndromeSystemic Inflammatory Response SyndromeBiomarkersChildChild, PreschoolCOVID-19Disease ProgressionFemaleHumansImmunoglobulins, IntravenousInfantInterleukin 1 Receptor Antagonist ProteinMaleMyocarditisNatriuretic Peptide, BrainPeptide FragmentsBiomarkersImmunoglobulins, IntravenousInterleukin 1 Receptor Antagonist ProteinNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Receptors, Interleukin-2Serum Amyloid A ProteinBiomarkersdisease courseHyperinflammationIL-2RNT-proBNPSAA

Identifiers

PMID41877237
PMCPMC13063582

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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.