Emergency Department, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Chiayi, Taiwan.
School of Medicine, Tzu Chi University, Hualien, Taiwan.
JAMA Intern Med. 2024 Jan 1;184(1):37-45. doi: 10.1001/jamainternmed.2023.6160.
Current guidelines advise against intravenous alteplase therapy for treatment of acute ischemic stroke in patients previously treated with non-vitamin K antagonist oral anticoagulants (NOACs).
To evaluate the risk of bleeding and mortality after alteplase treatment for acute ischemic stroke among patients treated with NOACs compared to those not treated with NOACs.
DESIGN, SETTING, AND PARTICIPANTS: This nationwide, population-based cohort study was conducted in Taiwan using data from Taiwan's National Health Insurance Research Database from January 2011 through November 2020 and included 7483 patients treated with alteplase for acute ischemic stroke. A meta-analysis incorporating the results of the study with those of previous studies was performed, and the review protocol was prospectively registered with PROSPERO.
NOAC treatment within 2 days prior to stroke, compared to either no anticoagulant treatment or warfarin treatment.
The primary outcome was intracranial hemorrhage after intravenous alteplase during the index hospitalization (the hospitalization subsequent to alteplase administration). Secondary outcomes were major bleeding events and mortality during the index hospitalization. Propensity score matching was used to control potential confounders. Logistic regression was used to estimate the odds ratio (OR) of outcome events. Meta-analysis was performed using a random-effects model.
Of the 7483 included patients (mean [SD] age, 67.4 [12.7] years; 2908 [38.9%] female individuals and 4575 [61.1%] male individuals), 91 (1.2%), 182 (2.4%), and 7210 (96.4%) received NOACs, warfarin, and no anticoagulants prior to their stroke, respectively. Compared to patients who were not treated with anticoagulants, those treated with NOACs did not have significantly higher risks of intracranial hemorrhage (risk difference [RD], 2.47% [95% CI, -4.23% to 9.17%]; OR, 1.37 [95% CI, 0.62-3.03]), major bleeding (RD, 4.95% [95% CI, -2.56% to 12.45%]; OR, 1.69 [95% CI, 0.83-3.45]), or in-hospital mortality (RD, -4.95% [95% CI, -10.11% to 0.22%]; OR, 0.45 [95% CI, 0.15-1.29]) in the propensity score-matched analyses. Furthermore, the risks of bleeding and mortality were not significantly different between patients treated with NOACs and those treated with warfarin. Similar results were obtained in the meta-analysis.
In this cohort study with meta-analysis, compared to no treatment with anticoagulants, treatment with NOACs prior to stroke was not associated with a higher risk of intracranial hemorrhage, major bleeding, or mortality in patients receiving intravenous alteplase for acute ischemic stroke.
目前的指南建议避免在先前使用非维生素 K 拮抗剂口服抗凝剂 (NOAC) 的患者中使用阿替普酶进行急性缺血性卒中的静脉治疗。
评估与未使用 NOAC 治疗的患者相比,NOAC 治疗的患者接受阿替普酶治疗急性缺血性卒中的出血和死亡率风险。
设计、地点和参与者:这项全国性、基于人群的队列研究在台湾进行,使用了台湾全民健康保险研究数据库 2011 年 1 月至 2020 年 11 月的数据,纳入了 7483 例接受阿替普酶治疗急性缺血性卒中的患者。进行了荟萃分析,纳入了该研究和先前研究的结果,该研究方案已在 PROSPERO 前瞻性注册。
卒中前 2 天内使用 NOAC 治疗,与未接受抗凝治疗或华法林治疗相比。
主要结局是指数住院期间(阿替普酶给药后的住院期间)静脉内阿替普酶治疗后的颅内出血。次要结局是指数住院期间的主要出血事件和死亡率。采用倾向评分匹配控制潜在混杂因素。采用 logistic 回归估计结局事件的优势比 (OR)。采用随机效应模型进行荟萃分析。
在纳入的 7483 例患者中(平均[SD]年龄,67.4[12.7]岁;2908[38.9%]女性和 4575[61.1%]男性),分别有 91(1.2%)、182(2.4%)和 7210(96.4%)例患者在卒中前接受了 NOAC、华法林和未接受抗凝治疗。与未接受抗凝治疗的患者相比,接受 NOAC 治疗的患者颅内出血风险无显著升高(风险差异[RD],2.47%[95%CI,-4.23%至 9.17%];OR,1.37[95%CI,0.62-3.03])、主要出血(RD,4.95%[95%CI,-2.56%至 12.45%];OR,1.69[95%CI,0.83-3.45])或院内死亡率(RD,-4.95%[95%CI,-10.11%至 0.22%];OR,0.45[95%CI,0.15-1.29])在倾向评分匹配分析中。此外,NOAC 治疗与华法林治疗的患者之间出血和死亡率的风险无显著差异。荟萃分析也得到了类似的结果。
在这项具有荟萃分析的队列研究中,与未抗凝治疗相比,卒中前使用 NOAC 治疗与接受阿替普酶治疗急性缺血性卒中的患者颅内出血、主要出血或死亡率增加无关。