Evidence map›Paper›PMID 40062924›Full record

SynthesisCardiology journal2025

The utility of brain biomarkers in predicting survival and neurological outcomes in pediatric patients after cardiac arrest: A systematic review and meta-analysis.

Halla Kamińska, Krzysztof Kurek, Michał Zembala, Sagar Galwankar, Monika Tomaszewska, Shraddha Singh, Nicola Luigi Bragazzi, Michał Pruc, Basar Cander, Francesco Chirico and 8 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Cardiology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

18 authors.

Halla KamińskaDepartment of Pediatrics and Children's Diabetology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Poland.ORCID 0000-0003-0960-8365
Krzysztof KurekDepartment of Clinical Research and Development, LUXMED Group, Warsaw, Poland.ORCID 0009-0005-8904-9947
Michał ZembalaInstitute of Medical Science, Collegium Medicum, The John Paul II Catholic University of Lublin, Lublin, Poland.ORCID 0000-0001-6043-3762
Sagar GalwankarThe World Academic Council of Emergency Medicine (WACEM), Sarasota, FL, United States.ORCID 0009-0007-4530-9107
Monika TomaszewskaDepartment of Clinical Research and Development, LUXMED Group, Warsaw, Poland.ORCID 0000-0003-3641-323X
Shraddha Singh1st Department of Cardiology, Medical University of Gdansk, Gdansk, Poland.ORCID 0009-0000-5855-1487
Nicola Luigi BragazziLaboratory for Industrial and Applied Mathematics (LIAM), Department of Mathematics and Statistics, York University, Toronto, Ontario, Canada.ORCID 0000-0001-8409-868X
Michał PrucDepartment of Clinical Research and Development, LUXMED Group, Warsaw, Poland.ORCID 0000-0002-2140-9732
Basar CanderThe World Academic Council of Emergency Medicine (WACEM), Sarasota, FL, United States.ORCID 0000-0002-3308-5843
Francesco ChiricoPost-Graduate School of Occupational Health, Catholic University of the Sacred Heart, Rome, Italy.ORCID 0000-0002-8737-4368
Amelia RizzoDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy.ORCID 0000-0002-6229-6463
Jacek KubicaDepartment of Cardiology and Internal Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.ORCID 0000-0001-8250-754X
Ayman El-MenyarThe World Academic Council of Emergency Medicine (WACEM), Sarasota, FL, United States.ORCID 0000-0003-2584-953X
Anne LepetitThe World Academic Council of Emergency Medicine (WACEM), Sarasota, FL, United States.ORCID 0009-0007-2942-9045
Pawel PatrzylasDepartment of Molecular Biology, The John Paul II Catholic University of Lublin, Lublin, Poland.ORCID 0000-0003-2968-3995
Zubaid RafiqueHenry JN Taub Department of Emergency Medicine, Baylor College of Medicine, Houston, Texas, United States.ORCID 0000-0002-4176-5988
W Frank PeacockHenry JN Taub Department of Emergency Medicine, Baylor College of Medicine, Houston, Texas, United States.ORCID 0000-0002-2730-6742
Łukasz SzarpakDepartment of Clinical Research and Development, LUXMED Group, Warsaw, Poland. lukasz.szarpak@gmail.com.ORCID 0000-0002-0973-5455

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiac arrest in children is associated with high morbidity and mortality, primarily due to neurological injury. Biomarkers linked to brain injury, released into circulation from compromised elements of the neurovascular unit, act as significant prognostic indicators in patients suffering from hypoxic-ischemic brain injury (HIBI) subsequent to the restoration of spontaneous circulation (ROSC) after pediatric cardiac arrest. The aim of this systematic review and meta-analysis is to evaluate the prognostic utility of brain injury biomarkers in predicting neurological outcomes and survival in patients following cardiac arrest in the pediatric population.

methodsBibliographic databases (PubMed, the Cochrane Library, and Embase) were searched from their inception to November 2024. A random-effect model was used for all analyses.

resultsOur meta-analysis demonstrates significant associations between various biomarkers and survival or neurological outcomes after cardiac arrest. Neuron-specific enolase (NSE) levels were consistently elevated in non-survivors and patients with unfavorable neurological outcomes, with pronounced differences observed on Days 2 and 3 (e.g., Day 3 mean difference: -88.48, 95%CI: -146.77 to -30.19, P = 0.003). Emerging biomarkers, including UCH-L1 and GFAP, showed striking differences, such as elevated UCH-L1 levels on Day 1 (mean difference: -415.41, 95%CI: -474.41 to -356.61, P < 0.001) and GFAP levels exceeding 4000 ng/mL in non-survivors on Day 2 (P < 0.001).

conclusionsOur findings underscore the significant prognostic value of biomarkers in predicting survival and neurological outcomes following cardiac arrest. Neuron-specific enolase (NSE) consistently demonstrated its reliability across multiple time points, while emerging biomarkers like UCH-L1 and GFAP showed promising potential for early outcome stratification.

Indexed as

BrainHeart ArrestHypoxia-Ischemia, BrainPhosphopyruvate HydrataseBiomarkersCardiopulmonary ResuscitationChildGlial Fibrillary Acidic ProteinHumansPredictive Value of TestsPrognosisSurvival RateUbiquitin ThiolesteraseBiomarkersENO2 protein, humanGFAP protein, humanGlial Fibrillary Acidic ProteinPhosphopyruvate HydrataseUbiquitin ThiolesteraseUCHL1 protein, humanbrain markerscardiac arrestmeta-analysisneuron-specific enolaseS100β proteinsurvival

Identifiers

PMID40062924
PMCPMC12068238

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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.