4.2 Article

Comparison of outcome of patients with acute minor ischaemic stroke treated with intravenous t-PA, DAPT or aspirin

Journal

STROKE AND VASCULAR NEUROLOGY
Volume 6, Issue 2, Pages 187-193

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/svn-2019-000319

Keywords

stroke; thrombolysis

Funding

  1. National Natural Science Foundation of China [81825007]
  2. Beijing Outstanding Young Scientist Program [BJJWZYJH01201910025030]
  3. 'Thirteenth-Five' Key Development and Research Plan by the Ministry of Science and Technology of the People's Republic of China [2017YFC1307900]
  4. Beijing Science and Technology Plan by Beijing Municipal Science and Technology Commission [D171100003017001]
  5. Beijing Excellent Talents Training and Supporting-Top Youth Team by Beijing Municipal Science and Technology Commission [2016000021223TD03]
  6. Beijing Talent Project-Class A: Innovation and Development [2018A12]

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Based on the study findings, there was no significant advantage of intravenous t-PA over DAPT or aspirin in patients with minor stroke.
Background Whether to treat minor stroke with intravenous tissue plasminogen activator (t-PA) treatment or antiplatelet therapy is a dilemma. Our study aimed to explore whether intravenous t-PA treatment, dual antiplatelet therapy (DAPT) and aspirin have different efficacies on outcomes in patients with minor stroke. Methods A post hoc analysis of patients with acute minor stroke treated with intravenous t-PA within 4.5 hours from a nationwide multicentric electronic medical record and patients with acute minor stroke treated with DAPT and aspirin from the Clopidogrel with Aspirin in Acute Minor Stroke or Transient Ischemic Attack Database. Minor stroke was defined by a score of 0-3 on the National Institutes of Health Stroke Scale at randomisation. Favourable functional outcome (defined as modified Rankin Scale (mRS) score of 0-1 or 0-2 at 3 months). Results Compared with those treated with intravenous t-PA, no significant association with 3-month favourable functional outcome (defined as mRS score of 0-1) was found neither in patients treated with aspirin (87.8% vs 89.4%; OR, 0.83; 95% CI, 0.46 to 1.50; p=0.53) nor those treated with DAPT (87.4% vs 89.4%; OR, 0.84; 95% CI, 0.46 to 1.52; p=0.56). Similar results were observed for the favourable functional outcome defined as mRS score of 0-2 at 3 months. Conclusions In our study, no significant advantage of intravenous t-PA over DAPT or aspirin was found. Due to insufficient sample size, our study is probably unable to draw such a conclusion that that intravenous t-PA was superior or non-superior to DAPT.

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