Safety and Efficacy of Intravenous Thrombolysis in the 3- to 4.5-hour Window in Acute Ischemic Stroke Patients Who Have Both Diabetes Mellitus and History of Prior Stroke

Boyoung Kim, J. S. Lee, Hong‐Kyun Park, Youngbok Yung, Ki Chang Oh, Jeong Joo Park, Yong‐Jin Cho, K. Kang, Soo‐Joo Lee, J. Kim, J. Cha, Dae-Hyun Kim, H. Bae, T. Park, Sang-Soon Park, K. Lee, Jun Lee, Byung‐Chul Lee, M. Lee, Joon-Tae Kim, K. Choi, Dong-Eog Kim, J. Choi, Dong-Ick Shin, J. Kwon, Wook-Joo Kim, S. Sohn, Jeong‐Ho Hong, Hyungjong Park, S. Jang, Kwang-Yeol Park, Sang-Hwa Lee, Jong-Moo Park, K. Hong
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Abstract

Background: For acute ischemic stroke (AIS) patients with history of prior stroke (PS) and diabetes mellitus (DM), intravenous recombinant tissue plasminogen activator (IV-tPA) therapy in the 3- to 4.5-hour window is off-label in Korea. This study aimed to assess the safety and efficacy of IV-tPA in these patients.Methods: Using data from a prospective multicenter stroke registry between January 2009 and March 2021, we identified AIS patients who received IV-tPA in the 3- to 4.5-hour window, and compared the outcomes of symptomatic intracranial hemorrhage (SICH), 3-month mortality, 3-month modified Rankin Scale (mRS) score 0-1 and 3-month mRS distribution between patients with both PS and DM (PS/DM, n=56) versus those with neither PS nor DM, or with only one (non-PS/DM, n=927).Results: The PS/DM group versus the non-PS/DM group was more likely to have a prior disability, hypertension, hyperlipidemia, coronary heart disease and less likely to have atrial fibrillation. The PS/DM and the non-PS/DM groups had comparable rates of SICH (0% vs. 1.7%; p>0.999) and 3-month mortality (10.7% vs. 10.2%; p=0.9112). The rate of 3-month mRS 0-1 was non-significantly lower in the PS/DM group than in the non-PS/DM group (30.4% vs. 40.7%; adjusted odds ratio [95% confidence interval], 0.81 [0.41-1.59]).Conclusions: In the 3- to 4.5-hour window, AIS patients with PS/DM, as compared to those with non-PS/DM, might benefit less from IV-tPA. However, given the similar risks of SICH and mortality, IV-tPA in the late time window could be considered in patients with both PS and DM.
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静脉溶栓治疗合并糖尿病和卒中史的急性缺血性卒中患者3- 4.5小时内的安全性和有效性
背景:在韩国,对于有卒中(PS)和糖尿病(DM)病史的急性缺血性卒中(AIS)患者,在3- 4.5小时内静脉注射重组组织型纤溶酶原激活剂(IV-tPA)治疗属于标签外治疗。本研究旨在评估IV-tPA在这些患者中的安全性和有效性。方法:利用2009年1月至2021年3月期间的前瞻性多中心卒中登记数据,我们确定了在3- 4.5小时窗口内接受IV-tPA治疗的AIS患者,并比较了症状性颅内出血(SICH)、3个月死亡率、3个月修正兰金量表(mRS)评分0-1的结局,以及PS和DM患者(PS/DM, n=56)与既没有PS也没有DM或只有一种(非PS/DM, n=927)之间的3个月mRS分布。结果:与非PS/DM组相比,PS/DM组有残疾、高血压、高脂血症、冠心病的可能性更大,房颤的可能性更小。PS/DM组和非PS/DM组的SICH发生率相当(0% vs. 1.7%;P >0.999)和3个月死亡率(10.7% vs. 10.2%;p = 0.9112)。PS/DM组3个月mRS 0-1发生率低于非PS/DM组(30.4% vs 40.7%;校正优势比[95%可信区间],0.81[0.41-1.59])。结论:在3- 4.5小时内,与非PS/DM患者相比,伴有PS/DM的AIS患者可能从IV-tPA中获益较少。然而,考虑到SICH和死亡率相似的风险,对于PS和DM患者,可以考虑在晚时间窗使用IV-tPA。
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