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Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation: multicentre cohort study

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Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation: multicentre cohort study. / Cromis-2 Collaboration.
In: Journal of Neurology, Neurosurgery and Psychiatry, Vol. 90, No. 3, 14.02.2019, p. 320-325.

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Cromis-2 Collaboration 2019, 'Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation: multicentre cohort study', Journal of Neurology, Neurosurgery and Psychiatry, vol. 90, no. 3, pp. 320-325. https://doi.org/10.1136/jnnp-2018-318890

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Cromis-2 Collaboration. Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation: multicentre cohort study. Journal of Neurology, Neurosurgery and Psychiatry. 2019 Feb 14;90(3):320-325. Epub 2018 Nov 19. doi: 10.1136/jnnp-2018-318890

Author

Cromis-2 Collaboration. / Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation : multicentre cohort study. In: Journal of Neurology, Neurosurgery and Psychiatry. 2019 ; Vol. 90, No. 3. pp. 320-325.

Bibtex

@article{68958960cc3d4c91a4cec9e8c5b0dbe7,
title = "Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation: multicentre cohort study",
abstract = "BACKGROUND AND PURPOSE: The optimal time to start oral anticoagulant (OAC) in patients with ischaemic stroke due to non-valvular atrial fibrillation (AF) is unknown. We reviewed OAC timing in relation to 90-day clinical outcomes as a post hoc analysis from a prospective multicentre observational study.METHODS: We included patients with data on time to initiation of OAC from CROMIS-2 (Clinical Relevence Of Microbleeds In Stroke-2), a prospective observational inception cohort study of 1490 patients with ischaemic stroke or transient ischaemic attack (TIA) and AF treated with OAC. The primary outcome was the composite outcome of TIA, stroke (ischaemic stroke or intracranial haemorrhage) or death within 90 days of the qualifying stroke or TIA. We performed adjusted logistic regression analyses to compare early (0-4 days) and later (≥5 days or never started) OAC initiation.RESULTS: We included 1355 patients, mean age 76 (SD 10), 580 (43%) women. OAC was started early in 358 (26%) patients and later (or not at all) in 997 (74%) patients. The event rate within 90 days was 48/997 (5%) in the late-OAC group (2 intracranial haemorrhages, 18 ischaemic strokes or TIAs and 31 deaths (three deaths were as a result of new ischaemic strokes)) versus 7/358 (2%) in the early-OAC group (5 ischaemic strokes or TIAs and 2 deaths). In adjusted analyses, late OAC was not associated with the composite outcome (adjusted OR 1.17, 95% CI 0.48 to 2.84, p=0.736).CONCLUSION: In adjusted analyses, early OAC after acute ischaemic stroke or TIA associated with AF was not associated with a difference in the rate of the composite outcome of stroke, TIA or death at 90 days, compared with late OAC. However, despite adjustment for important baseline factors, patients selected for early OAC and late OAC might still have differed in important respects; evaluation of OAC timing in adequately powered randomised trials is required.CLINICAL TRIAL REGISTRATION: NCT02513316.",
author = "{Cromis-2 Collaboration} and D Wilson and G Ambler and G Banerjee and C Shakeshaft and H Cohen and TA Yousry and Al-Shahi, {Salman R} and GYH Lip and H Houlden and MM Brown and KW Muir and HR J{\"a}ger and DJ Werring and Hedley Emsley",
note = "{\textcopyright} Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.",
year = "2019",
month = feb,
day = "14",
doi = "10.1136/jnnp-2018-318890",
language = "English",
volume = "90",
pages = "320--325",
journal = "Journal of Neurology, Neurosurgery and Psychiatry",
issn = "0022-3050",
publisher = "BMJ Publishing Group",
number = "3",

}

RIS

TY - JOUR

T1 - Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation

T2 - multicentre cohort study

AU - Cromis-2 Collaboration

AU - Wilson, D

AU - Ambler, G

AU - Banerjee, G

AU - Shakeshaft, C

AU - Cohen, H

AU - Yousry, TA

AU - Al-Shahi, Salman R

AU - Lip, GYH

AU - Houlden, H

AU - Brown, MM

AU - Muir, KW

AU - Jäger, HR

AU - Werring, DJ

AU - Emsley, Hedley

N1 - © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.

PY - 2019/2/14

Y1 - 2019/2/14

N2 - BACKGROUND AND PURPOSE: The optimal time to start oral anticoagulant (OAC) in patients with ischaemic stroke due to non-valvular atrial fibrillation (AF) is unknown. We reviewed OAC timing in relation to 90-day clinical outcomes as a post hoc analysis from a prospective multicentre observational study.METHODS: We included patients with data on time to initiation of OAC from CROMIS-2 (Clinical Relevence Of Microbleeds In Stroke-2), a prospective observational inception cohort study of 1490 patients with ischaemic stroke or transient ischaemic attack (TIA) and AF treated with OAC. The primary outcome was the composite outcome of TIA, stroke (ischaemic stroke or intracranial haemorrhage) or death within 90 days of the qualifying stroke or TIA. We performed adjusted logistic regression analyses to compare early (0-4 days) and later (≥5 days or never started) OAC initiation.RESULTS: We included 1355 patients, mean age 76 (SD 10), 580 (43%) women. OAC was started early in 358 (26%) patients and later (or not at all) in 997 (74%) patients. The event rate within 90 days was 48/997 (5%) in the late-OAC group (2 intracranial haemorrhages, 18 ischaemic strokes or TIAs and 31 deaths (three deaths were as a result of new ischaemic strokes)) versus 7/358 (2%) in the early-OAC group (5 ischaemic strokes or TIAs and 2 deaths). In adjusted analyses, late OAC was not associated with the composite outcome (adjusted OR 1.17, 95% CI 0.48 to 2.84, p=0.736).CONCLUSION: In adjusted analyses, early OAC after acute ischaemic stroke or TIA associated with AF was not associated with a difference in the rate of the composite outcome of stroke, TIA or death at 90 days, compared with late OAC. However, despite adjustment for important baseline factors, patients selected for early OAC and late OAC might still have differed in important respects; evaluation of OAC timing in adequately powered randomised trials is required.CLINICAL TRIAL REGISTRATION: NCT02513316.

AB - BACKGROUND AND PURPOSE: The optimal time to start oral anticoagulant (OAC) in patients with ischaemic stroke due to non-valvular atrial fibrillation (AF) is unknown. We reviewed OAC timing in relation to 90-day clinical outcomes as a post hoc analysis from a prospective multicentre observational study.METHODS: We included patients with data on time to initiation of OAC from CROMIS-2 (Clinical Relevence Of Microbleeds In Stroke-2), a prospective observational inception cohort study of 1490 patients with ischaemic stroke or transient ischaemic attack (TIA) and AF treated with OAC. The primary outcome was the composite outcome of TIA, stroke (ischaemic stroke or intracranial haemorrhage) or death within 90 days of the qualifying stroke or TIA. We performed adjusted logistic regression analyses to compare early (0-4 days) and later (≥5 days or never started) OAC initiation.RESULTS: We included 1355 patients, mean age 76 (SD 10), 580 (43%) women. OAC was started early in 358 (26%) patients and later (or not at all) in 997 (74%) patients. The event rate within 90 days was 48/997 (5%) in the late-OAC group (2 intracranial haemorrhages, 18 ischaemic strokes or TIAs and 31 deaths (three deaths were as a result of new ischaemic strokes)) versus 7/358 (2%) in the early-OAC group (5 ischaemic strokes or TIAs and 2 deaths). In adjusted analyses, late OAC was not associated with the composite outcome (adjusted OR 1.17, 95% CI 0.48 to 2.84, p=0.736).CONCLUSION: In adjusted analyses, early OAC after acute ischaemic stroke or TIA associated with AF was not associated with a difference in the rate of the composite outcome of stroke, TIA or death at 90 days, compared with late OAC. However, despite adjustment for important baseline factors, patients selected for early OAC and late OAC might still have differed in important respects; evaluation of OAC timing in adequately powered randomised trials is required.CLINICAL TRIAL REGISTRATION: NCT02513316.

UR - http://europepmc.org/abstract/med/30455404

U2 - 10.1136/jnnp-2018-318890

DO - 10.1136/jnnp-2018-318890

M3 - Journal article

C2 - 30455404

VL - 90

SP - 320

EP - 325

JO - Journal of Neurology, Neurosurgery and Psychiatry

JF - Journal of Neurology, Neurosurgery and Psychiatry

SN - 0022-3050

IS - 3

ER -