Papers

Peer-reviewed International journal
Apr, 2016

Thrombolysis with Low-Dose Tissue Plasminogen Activator 3-4.5 h After Acute Ischemic Stroke in Five Hospital Groups in Japan.

Translational stroke research
  • Ryuta Morihara
  • Syoichiro Kono
  • Kota Sato
  • Nozomi Hishikawa
  • Yasuyuki Ohta
  • Toru Yamashita
  • Kentaro Deguchi
  • Yasuhiro Manabe
  • Yoshiki Takao
  • Kenichi Kashihara
  • Satoshi Inoue
  • Hideki Kiriyama
  • Koji Abe
  • Display all

Volume
7
Number
2
First page
111
Last page
9
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1007/s12975-016-0448-8

Clinical data from Japan on the safety and real-world outcomes of alteplase (tPA) thrombolysis in the extended therapeutic window are lacking. The aim of this study was to assess the safety and real-world outcomes of tPA administered within 3-4.5 h of stroke onset. The study comprised consecutive acute ischemic stroke patients (n = 177) admitted across five hospitals between September 2012 and August 2014. Patients received intravenous tPA within <3 or 3-4.5 h of stroke onset. Endovascular therapy was used for tPA-refractory patients. In the 3-4.5 h subgroup (31.6 % of patients), tPA was started 85 min later than the <3 h group (220 vs. 135 min, respectively). However, outcome measures were not significantly different between the <3 and 3-4.5 h subgroups for recanalization rate (67.8 vs. 57.1 %), symptomatic intracerebral hemorrhage (2.5 vs. 3.6 %), modified Rankin Scale score of 0-1 at 3 months (36.0 vs. 23.4 %), and mortality (6.9 vs. 8.3 %). We present data from 2005 to 2012 using a therapeutic window <3 h showing comparable results. tPA following endovascular therapy with recanalization might be superior to tPA only with recanalization (81.0 vs. 59.1 %). Compared with administration within 3 h of ischemic stroke onset, tPA administration within 3-4.5 h of ischemic stroke onset in real-world stroke emergency settings at multiple sites in Japan is as safe and has the same outcomes.

Link information
DOI
https://doi.org/10.1007/s12975-016-0448-8
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26815291
ID information
  • DOI : 10.1007/s12975-016-0448-8
  • Pubmed ID : 26815291

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