Early versus delayed anticoagulation in acute ischemic stroke with atrial fibrillation according to infarct volume and location : A prespecified subgroup analysis of the OPTIMAS randomized controlled trial
(2026) In International Journal of Stroke- Abstract
Background: Randomized trials have demonstrated that early anticoagulation after acute atrial fibrillation-associated ischemic stroke is safe and non-inferior to delayed initiation. Whether anticoagulation should be delayed in people with larger infarcts is uncertain. Aims: To investigate whether ischemic stroke infarct volume, measured precisely by segmentation, modifies the treatment effect of early anticoagulation with a direct oral anticoagulant (DOAC). Methods: We did a prespecified secondary analysis of OPTIMAS (NCT: 03759938), a randomized, parallel-group, open-label trial with blinded outcome assessment which randomized people with acute ischemic stroke and atrial fibrillation to early initiation of any licensed DOAC, within 4... (More)
Background: Randomized trials have demonstrated that early anticoagulation after acute atrial fibrillation-associated ischemic stroke is safe and non-inferior to delayed initiation. Whether anticoagulation should be delayed in people with larger infarcts is uncertain. Aims: To investigate whether ischemic stroke infarct volume, measured precisely by segmentation, modifies the treatment effect of early anticoagulation with a direct oral anticoagulant (DOAC). Methods: We did a prespecified secondary analysis of OPTIMAS (NCT: 03759938), a randomized, parallel-group, open-label trial with blinded outcome assessment which randomized people with acute ischemic stroke and atrial fibrillation to early initiation of any licensed DOAC, within 4 days of onset, or delayed initiation 7-14 days from onset. The primary outcome was a composite of recurrent ischemic stroke, symptomatic intracranial hemorrhage (ICH), and systemic arterial embolism within 90 days. A central neuroimaging laboratory determined infarct volume using diffusion-weighted magnetic resonance imaging (MRI) using a validated deep learning segmentation model; on computed tomography (CT), infarcts were segmented manually. We modeled infarct volume as a continuous variable using restricted cubic splines and tested for an interaction with treatment allocation in mixed effects logistic regression. Results: We included 3572 participants (mean age = 78 ± 10 years, 45% female), 98.6% 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 versus delayed initiation with infarcts of 0-5 mL; 6/220 (2.7%) and 11/229 (4.8%) with infarcts of 5-10 mL; 13/258 (4.6%) and 10/283 (3.5%) with infarcts of 10-25 mL; 6/145 (4.1%) and 8/145 (5.5%) with infarcts of 25-50 mL; 1/93 (1.1%) and 7/94 (7.4%) with infarcts of >50 mL; 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 1.52 (0.71-3.20), 0.55 (0.20-1.51), 1.29 (0.55-3.00), 0.74 (0.25-2.21), 0.13 (0.02-1.11), and 1.25 (0.55-2.86), respectively. There were no increased rates of symptomatic ICH with respect to anticoagulation timing for those with large infarcts (>25 mL); there were 3/238 (1.3%) events in the early group and 5/239 (2.1%) in the delayed group. Conclusion: The treatment effect of early anticoagulation with a DOAC in acute ischemic 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 4 days on the basis of infarct size.
(Less)
- author
- author collaboration
- organization
- publishing date
- 2026
- type
- Contribution to journal
- publication status
- epub
- subject
- keywords
- anticoagulation, Atrial fibrillation, infarct volume, intracranial hemorrhage, ischemic stroke, timing
- in
- International Journal of Stroke
- publisher
- Wiley-Blackwell
- external identifiers
-
- pmid:41906919
- scopus:105036681519
- ISSN
- 1747-4930
- DOI
- 10.1177/17474930261441297
- language
- English
- LU publication?
- yes
- id
- bf2c5783-7103-45b9-85f6-0045141d7019
- date added to LUP
- 2026-05-19 15:37:35
- date last changed
- 2026-07-02 00:40:22
@article{bf2c5783-7103-45b9-85f6-0045141d7019,
abstract = {{<p>Background: Randomized trials have demonstrated that early anticoagulation after acute atrial fibrillation-associated ischemic stroke is safe and non-inferior to delayed initiation. Whether anticoagulation should be delayed in people with larger infarcts is uncertain. Aims: To investigate whether ischemic stroke infarct volume, measured precisely by segmentation, modifies the treatment effect of early anticoagulation with a direct oral anticoagulant (DOAC). Methods: We did a prespecified secondary analysis of OPTIMAS (NCT: 03759938), a randomized, parallel-group, open-label trial with blinded outcome assessment which randomized people with acute ischemic stroke and atrial fibrillation to early initiation of any licensed DOAC, within 4 days of onset, or delayed initiation 7-14 days from onset. The primary outcome was a composite of recurrent ischemic stroke, symptomatic intracranial hemorrhage (ICH), and systemic arterial embolism within 90 days. A central neuroimaging laboratory determined infarct volume using diffusion-weighted magnetic resonance imaging (MRI) using a validated deep learning segmentation model; on computed tomography (CT), infarcts were segmented manually. We modeled infarct volume as a continuous variable using restricted cubic splines and tested for an interaction with treatment allocation in mixed effects logistic regression. Results: We included 3572 participants (mean age = 78 ± 10 years, 45% female), 98.6% of the main trial population. The effect of early versus delayed anticoagulation did not vary with infarct volume (p<sub>interaction</sub> = 0.18). Rates of the primary outcome were 17/568 (3.0%) and 12/599 (2.0%) for early versus delayed initiation with infarcts of 0-5 mL; 6/220 (2.7%) and 11/229 (4.8%) with infarcts of 5-10 mL; 13/258 (4.6%) and 10/283 (3.5%) with infarcts of 10-25 mL; 6/145 (4.1%) and 8/145 (5.5%) with infarcts of 25-50 mL; 1/93 (1.1%) and 7/94 (7.4%) with infarcts of >50 mL; 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 1.52 (0.71-3.20), 0.55 (0.20-1.51), 1.29 (0.55-3.00), 0.74 (0.25-2.21), 0.13 (0.02-1.11), and 1.25 (0.55-2.86), respectively. There were no increased rates of symptomatic ICH with respect to anticoagulation timing for those with large infarcts (>25 mL); there were 3/238 (1.3%) events in the early group and 5/239 (2.1%) in the delayed group. Conclusion: The treatment effect of early anticoagulation with a DOAC in acute ischemic 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 4 days on the basis of infarct size.</p>}},
author = {{Nash, Philip S. and Best, Jonathan G. and Lyon, James and Ruffle, James K. and Amornpojnimman, Thanyalak and Mendel, Rom and Foulon, Chris and Dehbi, Hakim Moulay and Ahmed, Norin and Arram, Liz and Balogun, Maryam and Bennett, Kate and Bordea, Ekaterina and Caverly, Emilia and Chau, Marisa and Cohen, Hannah and Cullen, Mairead and Doré, Caroline J. and Engelter, Stefan T. and Fenner, Robert and Ford, Gary A. and Gill, Aneet and Hunter, Rachael and James, Martin and Jayanthi, Archana and Lip, Gregory Y.H. and Massingham, Sue and Murray, Macey L. and Mazurczak, Iwona and Ndoutoumou, Amalia and Norrving, Bo and Philip, Jenny and Sims, Hannah and Sprigg, Nikola and Vanniyasingam, Tishok and Nachev, Parashkev and Freemantle, Nick and Doig, David and Werring, David J.}},
issn = {{1747-4930}},
keywords = {{anticoagulation; Atrial fibrillation; infarct volume; intracranial hemorrhage; ischemic stroke; timing}},
language = {{eng}},
publisher = {{Wiley-Blackwell}},
series = {{International Journal of Stroke}},
title = {{Early versus delayed anticoagulation in acute ischemic stroke with atrial fibrillation according to infarct volume and location : A prespecified subgroup analysis of the OPTIMAS randomized controlled trial}},
url = {{http://dx.doi.org/10.1177/17474930261441297}},
doi = {{10.1177/17474930261441297}},
year = {{2026}},
}