Department of Neurology and Cerebrovascular Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio.
Duke Clinical Research Institute, Duke University, Durham, North Carolina.
JAMA. 2020 Jun 2;323(21):2170-2184. doi: 10.1001/jama.2020.5697.
Earlier administration of intravenous tissue plasminogen activator (tPA) in acute ischemic stroke is associated with reduced mortality by the time of hospital discharge and better functional outcomes at 3 months. However, it remains unclear whether shorter door-to-needle times translate into better long-term outcomes.
To examine whether shorter door-to-needle times with intravenous tPA for acute ischemic stroke are associated with improved long-term outcomes.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study included Medicare beneficiaries aged 65 years or older who were treated for acute ischemic stroke with intravenous tPA within 4.5 hours from the time they were last known to be well at Get With The Guidelines-Stroke participating hospitals between January 1, 2006, and December 31, 2016, with 1-year follow-up through December 31, 2017.
Door-to-needle times for intravenous tPA.
The primary outcomes were 1-year all-cause mortality, all-cause readmission, and the composite of all-cause mortality or readmission.
Among the 61 426 patients treated with tPA within 4.5 hours, the median age was 80 years and 43.5% were male. The median door-to-needle time was 65 minutes (interquartile range, 49-88 minutes). The 48 666 patients (79.2%) who were treated with tPA and had door-to-needle times of longer than 45 minutes, compared with those treated within 45 minutes, had significantly higher all-cause mortality (35.0% vs 30.8%, respectively; adjusted HR, 1.13 [95% CI, 1.09-1.18]), higher all-cause readmission (40.8% vs 38.4%; adjusted HR, 1.08 [95% CI, 1.05-1.12]), and higher all-cause mortality or readmission (56.0% vs 52.1%; adjusted HR, 1.09 [95% CI, 1.06-1.12]). The 34 367 patients (55.9%) who were treated with tPA and had door-to-needle times of longer than 60 minutes, compared with those treated within 60 minutes, had significantly higher all-cause mortality (35.8% vs 32.1%, respectively; adjusted hazard ratio [HR], 1.11 [95% CI, 1.07-1.14]), higher all-cause readmission (41.3% vs 39.1%; adjusted HR, 1.07 [95% CI, 1.04-1.10]), and higher all-cause mortality or readmission (56.8% vs 53.1%; adjusted HR, 1.08 [95% CI, 1.05-1.10]). Every 15-minute increase in door-to-needle times was significantly associated with higher all-cause mortality (adjusted HR, 1.04 [95% CI, 1.02-1.05]) within 90 minutes after hospital arrival, but not after 90 minutes (adjusted HR, 1.01 [95% CI, 0.99-1.03]), higher all-cause readmission (adjusted HR, 1.02; 95% CI, 1.01-1.03), and higher all-cause mortality or readmission (adjusted HR, 1.02 [95% CI, 1.01-1.03]).
Among patients aged 65 years or older with acute ischemic stroke who were treated with tissue plasminogen activator, shorter door-to-needle times were associated with lower all-cause mortality and lower all-cause readmission at 1 year. These findings support efforts to shorten time to thrombolytic therapy.
急性缺血性脑卒中患者早期给予静脉注射组织型纤溶酶原激活剂(tPA)治疗,与出院时死亡率降低和 3 个月时功能结局更好有关。然而,目前尚不清楚更短的门到针时间是否能转化为更好的长期结局。
检查急性缺血性脑卒中患者接受静脉 tPA 治疗时,门到针时间较短是否与长期预后改善相关。
设计、地点和参与者:这项回顾性队列研究纳入了年龄在 65 岁或以上的 Medicare 受益人群,他们在 Get With The Guidelines-Stroke 参与医院发病后 4.5 小时内接受静脉 tPA 治疗,随访时间为 1 年,截至 2017 年 12 月 31 日。
静脉注射 tPA 的门到针时间。
主要结局是 1 年全因死亡率、全因再入院率以及全因死亡率或再入院的复合结局。
在 61426 例在 4.5 小时内接受 tPA 治疗的患者中,中位年龄为 80 岁,43.5%为男性。中位门到针时间为 65 分钟(四分位距,49-88 分钟)。与接受 tPA 治疗且门到针时间超过 45 分钟的 48666 例患者(79.2%)相比,接受 tPA 治疗且门到针时间在 45 分钟以内的患者的全因死亡率明显更高(分别为 35.0%和 30.8%;校正后 HR,1.13[95%CI,1.09-1.18]),全因再入院率也更高(分别为 40.8%和 38.4%;校正后 HR,1.08[95%CI,1.05-1.12]),全因死亡率或再入院率也更高(分别为 56.0%和 52.1%;校正后 HR,1.09[95%CI,1.06-1.12])。与接受 tPA 治疗且门到针时间超过 60 分钟的 34367 例患者(55.9%)相比,接受 tPA 治疗且门到针时间在 60 分钟以内的患者的全因死亡率明显更高(分别为 35.8%和 32.1%;校正后 HR,1.11[95%CI,1.07-1.14]),全因再入院率也更高(分别为 41.3%和 39.1%;校正后 HR,1.07[95%CI,1.04-1.10]),全因死亡率或再入院率也更高(分别为 56.8%和 53.1%;校正后 HR,1.08[95%CI,1.05-1.10])。门到针时间每增加 15 分钟,与入院后 90 分钟内全因死亡率增加显著相关(校正后 HR,1.04[95%CI,1.02-1.05]),但在入院 90 分钟后没有显著相关性(校正后 HR,1.01[95%CI,0.99-1.03]),全因再入院率(校正后 HR,1.02;95%CI,1.01-1.03)和全因死亡率或再入院率(校正后 HR,1.02[95%CI,1.01-1.03])也更高。
在接受组织型纤溶酶原激活剂治疗的年龄在 65 岁或以上的急性缺血性脑卒中患者中,较短的门到针时间与 1 年内全因死亡率和全因再入院率降低相关。这些发现支持缩短溶栓治疗时间的努力。