Intensive versus guideline-recommended blood pressure reduction in acute lacunar stroke with intravenous thrombolysis therapy: The ENCHANTED trial.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
03 2021
Historique:
received: 13 08 2020
accepted: 14 10 2020
pubmed: 18 10 2020
medline: 13 8 2021
entrez: 17 10 2020
Statut: ppublish

Résumé

This was an investigation of the differential effects of early intensive versus guideline-recommended blood pressure (BP) lowering between lacunar and non-lacunar acute ischaemic stroke (AIS) in the BP arm of the Enhanced Control of Hypertension and Thrombolysis Stroke Study (ENCHANTED). In 1,632 participants classified as having definite or probable lacunar (n = 454 [27.8%]) or non-lacunar AIS according to pre-specified definitions based upon clinical and adjudicated imaging findings, mean BP changes over days 0-7 were plotted, and systolic BP differences by treatment between subgroups were estimated in generalized linear models. Logistic regression models were used to estimate the BP treatment effects on 90-day outcomes (primary, an ordinal shift of modified Rankin scale scores) across lacunar and non-lacunar AIS after adjustment for baseline covariables. Most baseline characteristics, acute BP and other management differed between lacunar and non-lacunar AIS, but mean systolic BP differences by treatment were comparable at each time point (all p There were no differences in the treatment effect of early intensive versus guideline-recommended BP lowering across lacunar and non-lacunar AIS.

Sections du résumé

BACKGROUND AND PURPOSE
This was an investigation of the differential effects of early intensive versus guideline-recommended blood pressure (BP) lowering between lacunar and non-lacunar acute ischaemic stroke (AIS) in the BP arm of the Enhanced Control of Hypertension and Thrombolysis Stroke Study (ENCHANTED).
METHODS
In 1,632 participants classified as having definite or probable lacunar (n = 454 [27.8%]) or non-lacunar AIS according to pre-specified definitions based upon clinical and adjudicated imaging findings, mean BP changes over days 0-7 were plotted, and systolic BP differences by treatment between subgroups were estimated in generalized linear models. Logistic regression models were used to estimate the BP treatment effects on 90-day outcomes (primary, an ordinal shift of modified Rankin scale scores) across lacunar and non-lacunar AIS after adjustment for baseline covariables.
RESULTS
Most baseline characteristics, acute BP and other management differed between lacunar and non-lacunar AIS, but mean systolic BP differences by treatment were comparable at each time point (all p
CONCLUSIONS
There were no differences in the treatment effect of early intensive versus guideline-recommended BP lowering across lacunar and non-lacunar AIS.

Identifiants

pubmed: 33069172
doi: 10.1111/ene.14598
doi:

Substances chimiques

Fibrinolytic Agents 0
Tissue Plasminogen Activator EC 3.4.21.68

Banques de données

ClinicalTrials.gov
['NCT01422616']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

783-793

Informations de copyright

© 2020 European Academy of Neurology.

Références

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Auteurs

Zien Zhou (Z)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Department of Radiology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Chao Xia (C)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, China.

Cheryl Carcel (C)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Department of Neurology, Royal Prince Alfred Hospital, Sydney Health Partners, Sydney, NSW, Australia.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Sohei Yoshimura (S)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.

Xia Wang (X)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.

Candice Delcourt (C)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Department of Neurology, Royal Prince Alfred Hospital, Sydney Health Partners, Sydney, NSW, Australia.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Alejandra Malavera (A)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.

Xiaoying Chen (X)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.

Grant Mair (G)

Division of Neuroimaging Sciences, Edinburgh Imaging and Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

Mark Woodward (M)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
The George Institute for Global Health, School of Public Health, Imperial College London, London, UK.

John Chalmers (J)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.

Andrew M Demchuk (AM)

Departments of Clinical Neurosciences and Radiology, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Richard I Lindley (RI)

The George Institute for Global Health and University of Sydney, Sydney, NSW, Australia.

Thompson G Robinson (TG)

Department of Cardiovascular Sciences and NIHR Leicester Biomedical Research Center, University of Leicester, Leicester, UK.

Mark W Parsons (MW)

South Western Clinical School, University of New South Wales, Sydney, NSW, Australia.
Department of Medicine, Melbourne Brain Centre, Royal Melbourne Hospital, University of Melbourne, Parkville, Vic, Australia.

Joanna M Wardlaw (JM)

Division of Neuroimaging Sciences, Edinburgh Imaging and Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
UK Dementia Research Institute, University of Edinburgh, Edinburgh, UK.

Craig S Anderson (CS)

The George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Department of Neurology, Royal Prince Alfred Hospital, Sydney Health Partners, Sydney, NSW, Australia.
The George Institute China at Peking University Health Science Center, Beijing, China.

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