Neuroprognostication after cardiac arrest in patients without withdrawal of life-sustaining therapy: a prospective observational multicenter study.

Danae Goetze, Jan Rémi, Christoph Leithner, Victoria Diethei, Vincent Fleischhauer, Bastian Pauli, Bernadette Einhaeupl, Tina Luther, Martin Rosenfelder, Alex Lopez-Rolon, Stefan Czermak, Matthias W A Angstwurm, Suzette Heck, Bernhard Zwissler, Hanns Lohner, Ana-Lioara Arva, Thomas Pfefferkorn, Andreas Blüthgen, Markus Naumann, Philip Raake, Hauke Schneider, Rüdiger Ilg, Friedemann Müller, Jürgen Herzog, Katrin Rauen, Ralf Strobl, Daniela Koller, Eva Grill, Andreas Straube, Andreas Bender

Journal: Critical care (London, England) 2026;30(1):

PMID: 42509572

Abstract

BACKGROUND

Neuroprognostication after cardiac arrest (CA) is critical for guiding treatment decisions. However, concerns about self-fulfilling prophecy related to withdrawal of life-sustaining therapy (WLST) complicate outcome prediction. This study evaluated the accuracy of guideline-recommended prognostic markers within 14 days after CA for predicting poor 12-month outcomes in patients without WLST during the first four weeks after CA.

METHODS

This prospective multicenter observational study enrolled adults who remained comatose 72 h after CA across eight German hospitals between 2014 and 2017. Patients with WLST during the first four weeks, stroke, pre-existing disorders of consciousness, or terminal malignancy were excluded, leaving 101 patients for analysis. Prognostic markers assessed included pupillary light and corneal reflexes (PLR + CR), EEG, somatosensory evoked potentials (SEP), neuron-specific enolase (NSE) concentration, and the best Coma Recovery Scale-Revised (CRS-R) score. Poor outcome was defined as a modified Rankin Scale score of 4-6 at 12 months.

RESULTS

Poor outcomes occurred in 67.3% of patients. Individual markers demonstrated high specificity but limited sensitivity, with variable false-positive rates (FPRs). Repeated assessments and the combination of two or more unfavorable markers markedly reduced FPRs. Within 14 days, the presence of two or more unfavorable markers yielded no false positives and was strongly associated with poor outcome (adjusted OR 34.7). Adding the best CRS-R score to established markers significantly improved prognostic discrimination (AUC 0.925 vs. 0.888).

CONCLUSIONS

In patients who remained comatose three days after CA and in whom multimodal prognosis becomes clinically relevant, guideline-recommended assessment identified poor-outcome patients with high specificity and consistency with prior multimodal prognostication cohorts. Although self-fulfilling-prophecy bias cannot be fully excluded in any observational prognostication cohort, the marker profiles of WLST-excluded patients within the first four weeks matched or exceeded those of patients with documented poor outcomes and did not resemble those of recoverable patients, which reduces - though it does not completely rule it out - the likelihood that such bias is the primary reason for the observed associations. The best CRS-R score provided additional prognostic value, particularly in cases of uncertain prognosis, supporting its integration into multimodal assessment frameworks.

TRIAL REGISTRATION

ClinicalTrials.gov: NCT02231060. Registered: August 2014. First patient enrolled: October 2014.

© 2026. The Author(s).

Address: Neurorehabilitation, Faculty of Medicine, University of Augsburg, Augsburg, Germany. [email protected].; Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), LMU Medizin, Ludwig-Maximilians-Universität München, Pettenkofer School of Public Health, Munich, Germany. [email protected].; Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.; Department of Neurology and Experimental Neurology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.; Neurorehabilitation, Faculty of Medicine, University of Augsburg, Augsburg, Germany.; Therapiezentrum Burgau, Hospital for Neurological Rehabilitation, Burgau, Germany.; Neurorehabilitation, Faculty of Medicine, University of Augsburg, Augsburg, Germany.; Therapiezentrum Burgau, Hospital for Neurological Rehabilitation, Burgau, Germany.; Klinik für Neurologie, München Klinik Harlaching, Munich, Germany.; Department of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.; Klinik für Anästhesiologie, Klinikum der Universität München, LMU München, Munich, Deutschland.; Neurologische Klinik, RoMed Klinikum Rosenheim, Rosenheim, Germany.; Department of Neurology, Klinikum Ingolstadt, Ingolstadt, Germany.; Department of Internal Medicine I, University Hospital Augsburg, University of Augsburg, Augsburg, Germany.; Department of Neurology and Clinical Neurophysiology, University Hospital Augsburg, Augsburg, Germany.; Department of Neurology, University Hospital Augsburg, Augsburg, Germany.; Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.; Asklepios Stadtklinik, Bad Tölz, Germany.; Schön Klinik Bad Aibling, Bad Aibling, Germany.; Schön Klinik Munich- Schwabing, Munich, Germany.; Schön Klinik Bad Aibling, Bad Aibling, Germany.; Psychiatric University Hospital Zurich & Neuroscience Center Zurich (ZNZ), Zurich, Switzerland.; Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.; Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.; Department of Orthopaedics and Trauma Surgery, Musculoskeletal University Center Munich (MUM), University Hospital, LMU Munich, Munich, Germany.; Neurorehabilitation, Faculty of Medicine, University of Augsburg, Augsburg, Germany.; Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.; Therapiezentrum Burgau, Hospital for Neurological Rehabilitation, Burgau, Germany.

Link outs

Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.