Evidence map›Paper›PMID 41360904›Full record

ArticleScientific reports2025

Impact of meningoencephalitis and sepsis on delirium and subsequent neurological impairment in pediatric patients: a prospective proof-of-concept biomarker and EEG study.

Felix Klawitter, Johanna Hackenberg, Lena Danckert, Astrid Bertsche, Axel Petzold, Heidi A B Smith, Eugene Wesley Ely, Christian Spang, Rika Bajorat, Dagmar-Christiane Fischer and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 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

17 authors.

Felix KlawitterDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Johanna HackenbergDepartment of Paediatrics, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Lena DanckertDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Astrid BertscheDepartment of Paediatrics, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Axel PetzoldThe National Hospital for Neurology and Neurosurgery, University College London & Moorfields Eye Hospital, London, UK.
Heidi A B SmithDepartment of Paediatrics, Children's Hospital, Vanderbilt University Medical Centre, Monroe Carell Jr, Nashville, USA.
Eugene Wesley ElyCritical Illness, Brain Dysfunction, Survivorship (CIBS) Centre, Department of Medicine, Vanderbilt University Medical Centre, Nashville, USA.
Christian SpangDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Rika BajoratDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Dagmar-Christiane FischerDepartment of Paediatrics, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Gerd KlinkmannDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Anne Körmann-GüntherDepartment of Paediatrics, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany.
Robert FleischmannDepartment of Neurology, University Medicine Greifswald, Greifswald, Germany.
Amanda HeslegraveUK Dementia Research Institute at University College London, Fluid Biomarker Laboratory, London, WC1E 6BT, UK.
Henrik ZetterbergUK Dementia Research Institute at University College London, Fluid Biomarker Laboratory, London, WC1E 6BT, UK.
Hessel Peters-SengersCenter for Infection and Molecular Medicine, Location AMC, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands.
Johannes EhlerDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Interdisciplinary Paediatric Intensive Care Medicine, University Medical Centre Rostock, Rostock, Germany. johannes.ehler@med.uni-jena.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To assess the incidence and severity of delirium and subsequent neurological impairment in pediatric intensive care unit (PICU) patients with meningoencephalitis (ME) and sepsis. Prospective study enrolling PICU patients with sepsis or meningoencephalitis (ME) and healthy controls. Daily delirium assessment, repeated electroencephalography, blood sampling at days 1, 3, 5 and lumbar puncture, if clinically indicated, for cerebrospinal fluid (CSF) sampling were performed. Biomarkers of inflammation (CRP, PCT, IL-6), endothelial activation (NT-proCNP), neurodegeneration (NSE, tau), neuroaxonal damage (NfL, NfH, UCHL-1) and glial injury (GFAP, S100B) were measured. Neurological status was assessed using the Functional Status Scale (FSS), the pediatric overall performance category (POPC) and the pediatric cerebral performance scale (PCPC) before admission and after three months. Twenty-four PICU patients (ME n = 9, sepsis n = 15) and eleven controls were enrolled. The delirium incidence was not statistically higher in patients with sepsis (60%, n = 9/15) compared to ME (33%, n = 3/9, p = 0.105). Children with delirium (n = 12) had a higher FSS (10.0 [9.8, 12.0] vs. 7.5 [7.0, 9.0], p = 0.009) at day 1 than children without delirium (n = 12), without significant differences in blood and CSF biomarker levels. Patients with ME presented higher levels of blood NfL compared to sepsis patients at day 3 (16.8 [12.9, 77.5] vs. 10.7 [8.6, 12.2] pg/ml, p = 0.011) and day 5 (16.2 [6.8, 170.4] vs. 12.0 [7.9, 14.3] pg/ml, p = 0.005). Routine EEG results did not differ between the groups, but quantitative EEG parameters representing encephalopathy correlated with biomarkers of brain injury. FSS, POPC and PCPC after three months were identical between in all patients. Independent from the origin of inflammatory stimulation by sepsis or ME delirium is associated with transient neurological dysfunction in PICU patients, without neurological impairment after three months, as confirmed by biomarker levels.

Indexed as

DeliriumMeningoencephalitisSepsisAdolescentBiomarkersChildChild, PreschoolElectroencephalographyFemaleHumansInfantIntensive Care Units, PediatricMaleProof of Concept StudyProspective StudiesBiomarkersBody fluid biomarkersBrain injuryChildrenDeliriumEncephalopathyIntensive care unit

Identifiers

PMID41360904
PMCPMC12695873

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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.