Early Versus Delayed Anticoagulation in Acute Ischaemic Stroke with Atrial Fibrillation According to Infarct Volume and Location: a Prespecified Subgroup Analysis of the OPTIMAS Randomised Controlled Trial.
Authors
Affiliations (12)
Affiliations (12)
- Stroke Research Centre, Department of Translational Neuroscience and Stroke, UCL Queen Square Institute of Neurology, London, UK.
- High Dimensional Neurology Group, Department of Translational Neuroscience and Stroke, UCL Queen Square Institute of Neurology, London, UK.
- High Dimensional Neurology Group, Department of Translational Neuroscience and Stroke, UCL Queen Square Institute of Neurology, London, UK; and Groupe d'Imagerie Neurofonctionnelle (GIN), Institut des Maladies Neurodegeneratives-UMR 5293, CNRS, Bordeaux, France.
- Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.
- Department of Haematology, Cancer Institute, UCL, UK; and University College London Hospitals NHS Foundation Trust, London, UK.
- Neurology and Neurorehabilitation, University Department of Geriatric Medicine FELIX PLATTER; University of Basel, Switzerland.
- Medical Sciences Division, University of Oxford, Oxford, UK.
- Royal Devon & Exeter Hospital, and University of Exeter Medical School, Exeter, UK.
- Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK; and Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
- MRC Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.
- Department of Clinical Sciences, Department of Neurology, Sk氓ne University Hospital, Lund University, Lund, Sweden.
- Stroke Trials Unit, Division of Mental Health and Clinical Neuroscience, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, UK.
Abstract
BackgroundRandomised trials have demonstrated that early anticoagulation after acute atrial fibrillation-associated ischaemic stroke is safe and non-inferior to delayed initiation. Whether anticoagulation should be delayed in people with larger infarcts is uncertain.AimsTo investigate whether ischaemic stroke infarct volume, measured precisely by segmentation, modifies the treatment effect of early anticoagulation with a direct oral anticoagulant (DOAC).MethodsWe did a prespecified secondary analysis of OPTIMAS (NCT: 03759938), a randomised, parallel group, open-label trial with blinded outcome assessment which randomised people with acute ischaemic stroke and atrial fibrillation to early initiation of any licensed DOAC, within four days of onset, or delayed initiation 7-14 days from onset. The primary outcome was a composite of recurrent ischaemic stroke, symptomatic intracranial haemorrhage (ICH) and systemic arterial embolism within 90 days. A central neuroimaging laboratory determined infarct volume using diffusion-weighted MRI using a validated deep learning segmentation model; on CT, infarcts were segmented manually. We modelled infarct volume as a continuous variable using restricted cubic splines, and tested for an interaction with treatment allocation in mixed effects logistic regression.ResultsWe included 3572 participants (mean age 78卤10 years, 45% female), 98路6% of the main trial population. The effect of early versus delayed anticoagulation did not vary with infarct volume (pinteraction=0.18). Rates of the primary outcome were 17/568 (3.0%) and 12/599 (2.0%) for early vs. delayed initiation with infarcts of 0-5mls; 6/220 (2.7%) and 11/229 (4.8%) with infarcts of 5-10mls; 13/258 (4.6%) and 10/283 (3.5%) with infarcts of 10-25mls; 6/145 (4.1%) and 8/145 (5.5%) with infarcts of 25-50mls; 1/93 (1.1%) and 7/94 (7.4%) with infarcts of >50mls; and 14/481 (2.9%) and 10/430 (2.2%) in participants with no infarct visible on clinically-acquired brain imaging. Corresponding odds ratios and 95% confidence intervals were 1路52 (0路71-3.20), 0路55 (0路20-1路51), 1路29 (0路55-3路00), 0路74 (0路25-2路21), 0.13 (0路02-1路11), and 1.25 (0.55-2.86) respectively. There were no increased rates of symptomatic ICH with respect to anticoagulation timing for those with very large infarcts (>25mls); there were 3/238 (1.3%) events in the early group and 5/239 (2.1%) in the delayed group.ConclusionsThe treatment effect of early anticoagulation with a DOAC in acute ischaemic stroke associated with atrial fibrillation was not modified by infarct volume. Adverse outcomes were not increased with early anticoagulation in people with larger infarcts. Our results provide no evidence that anticoagulation initiation should be delayed beyond four days on the basis of infarct size.