Department of Neurology, Duke University School of Medicine, Durham, North Carolina.
Duke Clinical Research Institute, Durham, North Carolina.
JAMA. 2023 Jun 20;329(23):2038-2049. doi: 10.1001/jama.2023.8073.
Use of oral vitamin K antagonists (VKAs) may place patients undergoing endovascular thrombectomy (EVT) for acute ischemic stroke caused by large vessel occlusion at increased risk of complications.
To determine the association between recent use of a VKA and outcomes among patients selected to undergo EVT in clinical practice.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective, observational cohort study based on the American Heart Association's Get With the Guidelines-Stroke Program between October 2015 and March 2020. From 594 participating hospitals in the US, 32 715 patients with acute ischemic stroke selected to undergo EVT within 6 hours of time last known to be well were included.
VKA use within the 7 days prior to hospital arrival.
The primary end point was symptomatic intracranial hemorrhage (sICH). Secondary end points included life-threatening systemic hemorrhage, another serious complication, any complications of reperfusion therapy, in-hospital mortality, and in-hospital mortality or discharge to hospice.
Of 32 715 patients (median age, 72 years; 50.7% female), 3087 (9.4%) had used a VKA (median international normalized ratio [INR], 1.5 [IQR, 1.2-1.9]) and 29 628 had not used a VKA prior to hospital presentation. Overall, prior VKA use was not significantly associated with an increased risk of sICH (211/3087 patients [6.8%] taking a VKA compared with 1904/29 628 patients [6.4%] not taking a VKA; adjusted odds ratio [OR], 1.12 [95% CI, 0.94-1.35]; adjusted risk difference, 0.69% [95% CI, -0.39% to 1.77%]). Among 830 patients taking a VKA with an INR greater than 1.7, sICH risk was significantly higher than in those not taking a VKA (8.3% vs 6.4%; adjusted OR, 1.88 [95% CI, 1.33-2.65]; adjusted risk difference, 4.03% [95% CI, 1.53%-6.53%]), while those with an INR of 1.7 or lower (n = 1585) had no significant difference in the risk of sICH (6.7% vs 6.4%; adjusted OR, 1.24 [95% CI, 0.87-1.76]; adjusted risk difference, 1.13% [95% CI, -0.79% to 3.04%]). Of 5 prespecified secondary end points, none showed a significant difference across VKA-exposed vs VKA-unexposed groups.
Among patients with acute ischemic stroke selected to receive EVT, VKA use within the preceding 7 days was not associated with a significantly increased risk of sICH overall. However, recent VKA use with a presenting INR greater than 1.7 was associated with a significantly increased risk of sICH compared with no use of anticoagulants.
使用口服维生素 K 拮抗剂 (VKA) 可能会使接受血管内血栓切除术 (EVT) 治疗由大血管闭塞引起的急性缺血性中风的患者发生并发症的风险增加。
确定在临床实践中选择接受 EVT 的患者中,近期使用 VKA 与结局之间的关系。
设计、地点和参与者:基于美国心脏协会的 Get With the Guidelines-Stroke 计划的回顾性、观察性队列研究,研究时间为 2015 年 10 月至 2020 年 3 月。从美国 594 家参与医院中,纳入了 32715 名在发病后 6 小时内接受 EVT 的急性缺血性中风患者。
在入院前 7 天内使用 VKA。
主要终点是症状性颅内出血 (sICH)。次要终点包括危及生命的全身性出血、另一种严重并发症、再灌注治疗的任何并发症、住院死亡率以及住院死亡率或出院至临终关怀。
在 32715 名患者(中位年龄 72 岁;50.7%为女性)中,3087 名(9.4%)使用了 VKA(中位国际标准化比值 [INR],1.5 [IQR,1.2-1.9]),29628 名患者在入院前未使用 VKA。总体而言,先前使用 VKA 与 sICH 风险增加无关(211/3087 名服用 VKA 的患者[6.8%]与 1904/29628 名未服用 VKA 的患者[6.4%]相比;调整后的优势比 [OR],1.12 [95% CI,0.94-1.35];调整后的风险差异,0.69% [95% CI,-0.39%至 1.77%])。在 830 名服用 INR 大于 1.7 的 VKA 的患者中,sICH 风险明显高于未服用 VKA 的患者(8.3%比 6.4%;调整后的 OR,1.88 [95% CI,1.33-2.65];调整后的风险差异,4.03% [95% CI,1.53%-6.53%]),而 INR 为 1.7 或更低的患者(n=1585)在 sICH 风险方面无显著差异(6.7%比 6.4%;调整后的 OR,1.24 [95% CI,0.87-1.76];调整后的风险差异,1.13% [95% CI,-0.79%至 3.04%])。在 5 个预设次要终点中,没有一个在 VKA 暴露组和 VKA 未暴露组之间显示出显著差异。
在选择接受 EVT 的急性缺血性中风患者中,在发病前 7 天内使用 VKA 与总体 sICH 风险增加无关。然而,与不使用抗凝剂相比,近期使用 INR 大于 1.7 的 VKA 与 sICH 风险显著增加相关。