Optimal timing of anticoagulation after acute ischemic stroke with atrial fibrillation (OPTIMAS): Protocol for a randomized controlled trial.


Journal

International journal of stroke : official journal of the International Stroke Society
ISSN: 1747-4949
Titre abrégé: Int J Stroke
Pays: United States
ID NLM: 101274068

Informations de publication

Date de publication:
06 2022
Historique:
pubmed: 13 1 2022
medline: 3 6 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

Atrial fibrillation causes one-fifth of ischemic strokes, with a high risk of early recurrence. Although long-term anticoagulation is highly effective for stroke prevention in atrial fibrillation, initiation after stroke is usually delayed by concerns over intracranial hemorrhage risk. Direct oral anticoagulants offer a significantly lower risk of intracranial hemorrhage than other anticoagulants, potentially allowing earlier anticoagulation and prevention of recurrence, but the safety and efficacy of this approach has not been established. Optimal timing of anticoagulation after acute ischemic stroke with atrial fibrillation (OPTIMAS) will investigate whether early treatment with a direct oral anticoagulant, within four days of stroke onset, is as effective or better than delayed initiation, 7 to 14 days from onset, in atrial fibrillation patients with acute ischemic stroke. OPTIMAS is a multicenter randomized controlled trial with blinded outcome adjudication. Participants with acute ischemic stroke and atrial fibrillation eligible for anticoagulation with a direct oral anticoagulant are randomized 1:1 to early or delayed initiation. As of December 2021, 88 centers in the United Kingdom have opened. The primary outcome is a composite of recurrent stroke (ischemic stroke or symptomatic intracranial hemorrhage) and systemic arterial embolism within 90 days. Secondary outcomes include major bleeding, functional status, anticoagulant adherence, quality of life, health and social care resource use, and length of hospital stay. A total of 3478 participants assuming event rates of 11.5% in the control arm and 8% in the intervention arm, 90% power and 5% alpha. We will follow a non-inferiority gatekeeper analysis approach with a non-inferiority margin of 2 percentage points. OPTIMAS aims to provide high-quality evidence on the safety and efficacy of early direct oral anticoagulant initiation after atrial fibrillation-associated ischemic stroke.

Identifiants

pubmed: 35018878
doi: 10.1177/17474930211057722
doi:

Substances chimiques

Anticoagulants 0

Banques de données

ClinicalTrials.gov
['NCT03759938']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

583-589

Subventions

Organisme : British Heart Foundation
ID : CS/17/6/33361
Pays : United Kingdom

Auteurs

Jonathan G Best (JG)

Stroke Research Centre, Department of Brain Repair and Rehabilitation, UCL Queen Square Institute of Neurology, London, UK.

Liz Arram (L)

Stroke Research Centre, Department of Brain Repair and Rehabilitation, UCL Queen Square Institute of Neurology, London, UK.

Norin Ahmed (N)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Maryam Balogun (M)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Kate Bennett (K)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Ekaterina Bordea (E)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Marta G Campos (MG)

MRC Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Emilia Caverly (E)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Marisa Chau (M)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Hannah Cohen (H)

Haemostasis Research Unit, Department of Haematology, UCL, London, UK.

Hakim-Moulay Dehbi (HM)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Caroline J Doré (CJ)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Stefan T Engelter (ST)

Neurology and Neurorehabilitation, University Department of Geriatric Medicine FELIX PLATTER, University of Basel, Basel, Switzerland.

Robert Fenner (R)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Nick Freemantle (N)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Rachael Hunter (R)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Martin James (M)

Royal Devon & Exeter Hospital, University of Exeter Medical School, Exeter, UK.

Gregory Yh Lip (GY)

Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Heart & Chest Hospital, Liverpool, UK.
Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Macey L Murray (ML)

MRC Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

Bo Norrving (B)

Department of Clinical Sciences, Department of Neurology, Skåne University Hospital, Lund University, Lund, Sweden.

Nikola Sprigg (N)

Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, UK.

Roland Veltkamp (R)

Department of Brain Sciences, Imperial College London, London, UK.
Department of Neurology, Alfried Krupp Krankenhaus, Essen, Germany.

Iwona Zaczyk (I)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

David J Werring (DJ)

Stroke Research Centre, Department of Brain Repair and Rehabilitation, UCL Queen Square Institute of Neurology, London, UK.

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Classifications MeSH