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

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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引用次数: 0

摘要

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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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
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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