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Therapeutic hypothermia for acute ischaemic stroke. Results of a European multicentre, randomised, phase III clinical trial

van der Worp, H Bart; Macleod, Malcolm R; Bath, Philip MW; Bathula, Raj; Christensen, Hanne; Colam, Bridget; Cordonnier, Charlotte; Demotes-Mainard, Jacques; Durand-Zaleski, Isabelle; Gluud, Christian; Jakobsen, Janus Christian; Kallmünzer, Bernd; Kollmar, Rainer; Krieger, Derk W; Lees, Kennedy R; Michalski, Dominik; Molina, Carlos; Montaner, Joan; Roine, Risto O; Petersson, Jesper; Perry, Richard; Sprigg, Nikola; Staykov, Dimitre; Szabo, Istvan; Vanhooren, Geert; Wardlaw, Joanna M; Winkel, Per; Schwab, Stefan; the EuroHYP-1 investigators

Therapeutic hypothermia for acute ischaemic stroke. Results of a European multicentre, randomised, phase III clinical trial Thumbnail


Authors

H Bart van der Worp

Malcolm R Macleod

Philip MW Bath

Raj Bathula

Hanne Christensen

Bridget Colam

Charlotte Cordonnier

Jacques Demotes-Mainard

Isabelle Durand-Zaleski

Christian Gluud

Janus Christian Jakobsen

Bernd Kallmünzer

Rainer Kollmar

Derk W Krieger

Kennedy R Lees

Dominik Michalski

Carlos Molina

Joan Montaner

Risto O Roine

Jesper Petersson

Richard Perry

NIKOLA SPRIGG nikola.sprigg@nottingham.ac.uk
Professor of Stroke Medicine

Dimitre Staykov

Istvan Szabo

Geert Vanhooren

Joanna M Wardlaw

Per Winkel

Stefan Schwab

the EuroHYP-1 investigators



Abstract

© European Stroke Organisation 2019. Introduction: We assessed whether modest systemic cooling started within 6 hours of symptom onset improves functional outcome at three months in awake patients with acute ischaemic stroke. Patients and methods: In this European randomised open-label clinical trial with blinded outcome assessment, adult patients with acute ischaemic stroke were randomised to cooling to a target body temperature of 34.0–35.0°C, started within 6 h after stroke onset and maintained for 12 or 24 h, versus standard treatment. The primary outcome was the score on the modified Rankin Scale at 91 days, as analysed with ordinal logistic regression. Results: The trial was stopped after inclusion of 98 of the originally intended 1500 patients because of slow recruitment and cessation of funding. Forty-nine patients were randomised to hypothermia versus 49 to standard treatment. Four patients were lost to follow-up. Of patients randomised to hypothermia, 15 (31%) achieved the predefined cooling targets. The primary outcome did not differ between the groups (odds ratio for good outcome, 1.01; 95% confidence interval, 0.48–2.13; p = 0.97). The number of patients with one or more serious adverse events did not differ between groups (relative risk, 1.22; 95% confidence interval, 0.65–1.94; p = 0.52). Discussion: In this trial, cooling to a target of 34.0–35.0°C and maintaining this for 12 or 24 h was not feasible in the majority of patients. The final sample was underpowered to detect clinically relevant differences in outcomes. Conclusion: Before new trials are launched, the feasibility of cooling needs to be improved.

Journal Article Type Article
Acceptance Date Feb 27, 2019
Online Publication Date Apr 20, 2019
Publication Date 2019-09
Deposit Date May 30, 2019
Publicly Available Date May 30, 2019
Journal European Stroke Journal
Electronic ISSN 2396-9881
Publisher SAGE Publications
Peer Reviewed Peer Reviewed
Volume 4
Issue 3
Pages 254-262
DOI https://doi.org/10.1177/2396987319844690
Public URL https://nottingham-repository.worktribe.com/output/2109943
Publisher URL https://journals.sagepub.com/doi/10.1177/2396987319844690

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