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Building evidence on safety of endovascular thrombectomy for patients under anticoagulation with vitamin K antagonists

A recent study by Brian Mac Grory and colleagues investigated the safety of endovascular thrombectomy (EVT) among patients under vitamin K antagonists (VKAs) use within 7 days prior to hospital admission. Through this retrospective, observational cohort study, they found prior VKA use did not increa...

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Published in:CNS neuroscience & therapeutics 2024-07, Vol.30 (7), p.e14777-n/a
Main Authors: Gao, Li, Sun, Xiaowei, Li, Peiying
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description A recent study by Brian Mac Grory and colleagues investigated the safety of endovascular thrombectomy (EVT) among patients under vitamin K antagonists (VKAs) use within 7 days prior to hospital admission. Through this retrospective, observational cohort study, they found prior VKA use did not increase the risk of symptomatic intracranial hemorrhage (sICH) overall. However, recent VKA use with a presenting international normalized ratio (INR) > 1.7 was associated with a significantly increased risk of sICH. Future large‐scale randomized controlled trials should be conducted to further clarify the effects and feasibility of EVT therapy in ischemic stroke patients under anticoagulation. In this study, a total of 32,715 patients with acute ischemic stroke undergoing endovascular thrombectomy (EVT) were included. In total, 29,628 patients (90.6%) were not taking a vitamin K antagonist (VKA) prior to stroke, and 3087 patients (9.4%) were taking a VKA. The incidence of symptomatic intracranial hemorrhage (sICH) among the VKA group is 6.8%, which is comparable to those non‐VKA users with an incidence of 6.4%. Then, the international normalized ratio (INR) was dichotomized as ≤1.7 and >1.7 to assess the risk of sICH in each subgroup. Among 830 patients taking a VKA with an INR greater than 1.7, the incidence of sICH was 8.3%, which is significantly higher than those not taking a VKA (6.4%). Meanwhile, those with an INR of 1.7 or lower (n = 1585) had no significant difference of the risk of sICH (6.7%).
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Through this retrospective, observational cohort study, they found prior VKA use did not increase the risk of symptomatic intracranial hemorrhage (sICH) overall. However, recent VKA use with a presenting international normalized ratio (INR) &gt; 1.7 was associated with a significantly increased risk of sICH. Future large‐scale randomized controlled trials should be conducted to further clarify the effects and feasibility of EVT therapy in ischemic stroke patients under anticoagulation. In this study, a total of 32,715 patients with acute ischemic stroke undergoing endovascular thrombectomy (EVT) were included. In total, 29,628 patients (90.6%) were not taking a vitamin K antagonist (VKA) prior to stroke, and 3087 patients (9.4%) were taking a VKA. The incidence of symptomatic intracranial hemorrhage (sICH) among the VKA group is 6.8%, which is comparable to those non‐VKA users with an incidence of 6.4%. Then, the international normalized ratio (INR) was dichotomized as ≤1.7 and &gt;1.7 to assess the risk of sICH in each subgroup. Among 830 patients taking a VKA with an INR greater than 1.7, the incidence of sICH was 8.3%, which is significantly higher than those not taking a VKA (6.4%). 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Through this retrospective, observational cohort study, they found prior VKA use did not increase the risk of symptomatic intracranial hemorrhage (sICH) overall. However, recent VKA use with a presenting international normalized ratio (INR) &gt; 1.7 was associated with a significantly increased risk of sICH. Future large‐scale randomized controlled trials should be conducted to further clarify the effects and feasibility of EVT therapy in ischemic stroke patients under anticoagulation. In this study, a total of 32,715 patients with acute ischemic stroke undergoing endovascular thrombectomy (EVT) were included. In total, 29,628 patients (90.6%) were not taking a vitamin K antagonist (VKA) prior to stroke, and 3087 patients (9.4%) were taking a VKA. The incidence of symptomatic intracranial hemorrhage (sICH) among the VKA group is 6.8%, which is comparable to those non‐VKA users with an incidence of 6.4%. Then, the international normalized ratio (INR) was dichotomized as ≤1.7 and &gt;1.7 to assess the risk of sICH in each subgroup. Among 830 patients taking a VKA with an INR greater than 1.7, the incidence of sICH was 8.3%, which is significantly higher than those not taking a VKA (6.4%). 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Then, the international normalized ratio (INR) was dichotomized as ≤1.7 and &gt;1.7 to assess the risk of sICH in each subgroup. Among 830 patients taking a VKA with an INR greater than 1.7, the incidence of sICH was 8.3%, which is significantly higher than those not taking a VKA (6.4%). Meanwhile, those with an INR of 1.7 or lower (n = 1585) had no significant difference of the risk of sICH (6.7%).</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38958388</pmid><doi>10.1111/cns.14777</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0002-5721-9914</orcidid><orcidid>https://orcid.org/0000-0002-3606-4837</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antagonists
Antibiotics
Anticoagulants
Anticoagulants - adverse effects
Anticoagulants - therapeutic use
anticoagulation
Cardiovascular system
Clinical trials
Conflicts of interest
Contraindications
Endovascular Procedures - adverse effects
Endovascular Procedures - methods
endovascular thrombectomy
Hemorrhage
Humans
Ischemia
ischemic stroke
Ischemic Stroke - surgery
Observational studies
Retrospective Studies
Stroke
symptomatic intracranial hemorrhage
Thrombectomy - adverse effects
Thrombectomy - methods
Vitamin K
Vitamin K - antagonists & inhibitors
vitamin K antagonists
title Building evidence on safety of endovascular thrombectomy for patients under anticoagulation with vitamin K antagonists
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