Evidence map›Paper›PMID 41995094›Full record

Observational studyActa anaesthesiologica Scandinavica2026

Early Prediction of Neurological Outcome After Cardiac Arrest-Rationale and Design of the Prospective International Observational EARLY-NEURO, a STEPCARE Substudy.

Marion Moseby-Knappe, Erik Westhall, Marjolein Admiraal, Margareta Lang, Helena Levin, Johanna Hästbacka, Marjaana Tiainen, Markus Skrifvars, Gisela Lilja, Janus C Jacobsen and 39 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Acta anaesthesiologica Scandinavica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

49 authors.

Marion Moseby-KnappeDepartment of Neurological Rehabilitation, Skåne University Hospital, Lund, Sweden.ORCID 0000-0001-8160-5957
Erik WesthallDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Marjolein AdmiraalDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Margareta LangDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Helena LevinDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Johanna HästbackaFaculty of Medicine and Health Technology, Tampere University Hospital, Wellbeing Services County of Pirkanmaa and Tampere University, Tampere, Finland.
Marjaana TiainenDepartment of Neurology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.ORCID 0000-0001-5107-1990
Markus SkrifvarsDepartment of Anesthesia and Intensive Care, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.ORCID 0000-0002-0341-0262
Gisela LiljaDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0003-1860-1456
Janus C JacobsenCopenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.
Alice LagebrantDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Matt WiseAdult Critical Care, University Hospital of Wales, Cardiff, UK.
Matti ReinikainenInstitute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
Paul YoungIntensive Care Unit, Wellington Hospital, Wellington, New Zealand.
Manoj SaxenaCritical Care Division and Department of Intensive Care Medicine, the George Institute for Global Health and St George Hospital Clinical School, University of New South Wales, Sydney, Australia.
Simon SchmidbauerDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Naomi HammondCritical Care Program, the George Institute for Global Health, UNSW Sydney, Randwick, New South Wales, Australia.
Frances BassThe George Institute for Global Health, Sydney, Australia.
Ameldina CericDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Caroline KampCopenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0002-7756-4694
Christina SillassenCopenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.ORCID 0009-0004-9247-5245
Christoph LeithnerCharité-Universitätsmedizin Berlin, Department of Neurology, Freie Universität and Humboldt-Universität Zu Berlin, Berlin, Germany.
Pascal StammetDepartment of Anesthesia and Intensive Care Medicine, Centre Hospitalier de Luxembourg, Luxembourg, Luxembourg.
Matthias P HiltyInstitute of Intensive Care Medicine University Hospital Zurich, Zurich, Switzerland.
Pedro D Wendel-GarciaInstitute of Intensive Care Medicine University Hospital Zurich, Zurich, Switzerland.
Georg RoylDepartment of Neurology, University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.
Tobias GrafUniversity Heart Center Lübeck, University Hospital Schleswig-Holstein, Schleswig-Holstein, Germany.
Matt ThomasIntensive Care Unit, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.
Katie SweetIntensive Care Unit, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.ORCID 0009-0000-3635-7480
Stepani BendelDepartment of Intensive Care, Kuopio University Hospital, Kuopio, Finland.ORCID 0000-0002-1209-8397
Joonas TirkkonenIntensive Care Unit, Tampere University Hospital, Tampere, Finland.
Annerose MengelDepartment of Neurology and Stroke, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Maria-Ioanna StefanouDepartment of Neurology and Stroke, University Medicine Tübingen, Germany.
Luis Georg RomundstadDepartment of Anesthesia and Intensive Care Medicine, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Philipp SeidelDepartment of Intensive Care Medicine, Stavanger University Hospital, Stavanger, Norway.
Jessica KåhlinPerioperative Medicine and Intensive Care, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0001-5266-5272
Jonathan GripPerioperative Medicine and Intensive Care, Karolinska University Hospital, Stockholm, Sweden.
Jonna HeinonenDepartment of Anesthesia and Intensive Care, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Rakesh H JadavDepartment of Neurophysiology, University Hospital of Wales, Cardiff, UK.
Jens NeeDepartment of Nephrology and Intensive Care Medicine Charité-Universitätsmedizin Berlin, Berlin, Germany.
Daniela NowakInstitute of Intensive Care Medicine University Hospital Zurich, Zurich, Switzerland.
Matthias HänggiInstitute of Intensive Care Medicine University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-5845-031X
Johan UndénDepartment of Operation and Intensive Care, Hallands Hospital, Halmstad, Sweden.
Anna LybeckDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0001-7574-3958
Joachim DüringDepartment of Clinical Sciences, Helsingborg, Lund University, Helsingborg, Sweden.
Martin KendaDepartment of Neurology, University Hospital LMU Munich, Munich, Germany.
Jesper JohnssonDepartment of Anesthesia and Intensive Care, Skane University Hospital, Lund, Sweden.
Niklas NielsenDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Tobias CronbergDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.

Funding

Vetenskapsrådet
6 · The paper itself

Abstract

backgroundGuidelines discourage prediction of neurological outcome in comatose patients within the first 72 h after cardiac arrest. Increasing evidence suggests that patients with the most severe brain injury and those with no or minimal brain injury may be identified before 72 h using novel methods. We present a protocol for the EARLY-NEURO study, which aims to evaluate whether good and poor outcomes can be reliably predicted already from 24 h after cardiac arrest using the most commonly available methods.

methodsProtocol for a prospective international multicenter substudy within the Sedation, TEmperature and Pressure after Cardiac Arrest and REsuscitation (STEPCARE) trial where adults post-arrest are randomized to minimal or deep sedation, fever treatment with or without a temperature management device and to two different targets of mean arterial blood pressure. Patients sedated or still unconscious at 24 h are examined with head computed tomography (CT) and electroencephalogram (EEG). Blood samples are collected at 24 h after randomization, and stored for analysis of the brain injury marker neurofilament light. CT and EEG examinations will be centrally evaluated for signs of a likely poor or good outcome applying standardized criteria by raters blinded to treatment allocations and patient outcomes. Intensive care treatment, neurological prognostication, and criteria for withdrawal of care will be according to the STEPCARE protocol. Timepoint and reasons for withdrawal of life-sustaining therapy (WLST) will be recorded. WLST prior to 72 h after randomization based on a presumed futile neurological prognosis is strongly discouraged. Primary outcome will be good or poor functional outcome, assessed by the modified Rankin Scale (dichotomized as 0-3 versus 4-6) at 6 months. Results will be reported in accordance with the Standards for Reporting Diagnostic Accuracy (STARD).

conclusionsEarlier prognostication aims to balance the avoidance of premature treatment withdrawal in patients with favorable potential against the prevention of unnecessary intervention in patients with a definitely poor prognosis.

Indexed as

Brain InjuriesHeart ArrestNervous System DiseasesAdultComaElectroencephalographyHumansHypothermia, InducedPrognosisProspective StudiesResearch DesignTomography, X-Ray ComputedTreatment Outcomebrain injury markerscardiac arrestCTEEGoutcomeprognostication

Identifiers

PMID41995094
PMCPMC13088753

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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.