24-hour blood pressure variability and treatment effect of intravenous alteplase in acute ischaemic stroke

Author:

Barow Ewgenia1ORCID,Boutitie Florent2,Cheng Bastian1,Cho Tae-Hee3,Ebinger Martin45,Endres Matthias46,Fiebach Jochen B4,Fiehler Jens7,Nickel Alina1,Puig Josep8,Roy Pascal2,Lemmens Robin91011,Thijs Vincent1213,Muir Keith W14,Nighoghossian Norbert3,Pedraza Salvador8,Simonsen Claus Z15,Gerloff Christian1,Thomalla Götz1

Affiliation:

1. Klinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

2. Hospices Civils de Lyon, Service de Biostatistique, Lyon, France

3. Hospices Civils de Lyon, Lyon, France

4. Centrum für Schlaganfallforschung Berlin (CSB), Charité – Universitätsmedizin Berlin, Berlin, Germany

5. Medical Park Berlin Humboldtmühle, Klinik für Neurologie, Berlin, Germany

6. Klinik und Hochschulambulanz für Neurologie, Charité-Universitätsmedizin Berlin, Berlin, Germany

7. Department of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

8. Department of Radiology, Institut de Diagnostic per la Image (IDI), Hospital Dr Josep Trueta, Institut d’Investigació Biomèdica de Girona (IDIBGI), Parc Hospitalari Martí i Julià de Salt - Edifici M2, Girona, Spain

9. Department of Neurology, University Hospitals Leuven, Leuven, Belgium

10. KU Leuven – University of Leuven, Department of Neurosciences, Experimental Neurology, Leuven, Belgium

11. VIB, Center for Brain & Disease Research, Laboratory of Neurobiology, Leuven, Belgium

12. Stroke Division, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Victoria, Australia

13. Austin Health, Department of Neurology, Heidelberg, Australia

14. Institute of Neuroscience & Psychology, University of Glasgow, University Avenue, Glasgow, UK

15. Department of Neurology, Aarhus University Hospital, Aarhus, Denmark

Abstract

Introduction To assess the association between 24 h blood pressure variability (BPV) on functional outcome and treatment effect of intravenous alteplase in acute ischaemic stroke. Patients and methods In all patients with acute ischaemic stroke of unknown onset randomised in the WAKE-UP (Efficacy and Safety of magnetic resonance imaging [MRI]-based Thrombolysis in Wake-Up Stroke) trial, blood pressure (BP) was measured before randomisation and after initiation of treatment at regular intervals up to 24 hours. Individual BPV was measured by coefficient of variation (CV) of all BP values. Primary outcome measure was favourable outcome defined by a modified Rankin Scale (mRS) score 0 or 1 at 90 days after stroke. Results BP measurements were available for 498 of 503 patients randomised (177 women [35.5%], mean age [SD] of 65.2 [11.5] years). Systolic BPV was not associated with the treatment effect of thrombolysis (test for interaction, p = 0.46). The adjusted odds ratio (aOR) for favourable outcome with alteplase, adjusted for age, stroke severity and baseline BP on admission, did not show an association across the quintiles of increasing systolic BPV with an aOR 1.89 (95% confidence interval [CI], 0.76–4.70) in the lowest quintile to aOR 1.05 (95% CI, 0.43–2.56) in the highest quintile. Higher mean systolic BP was associated with a smaller treatment effect of thrombolysis with a significant interaction (p = 0.033). The aOR for favourable outcome with alteplase decreased with quintiles of increasing mean systolic BP from aOR 3.16 (95% CI, 1.26–7.93) in the lowest quintile to aOR 0.84 (95% CI, 0.34–2.10) in in the highest quintile. Conclusions There was a significant interaction between mean systolic BP and treatment effect of thrombolysis with higher mean systolic BP being associated with poorer outcome. BPV was not associated with outcome after thrombolysis. ClinicalTrials.gov identifier NCT01525290.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology

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