Recombinant Tissue-Type Plasminogen Activator Plus Eptifibatide Versus Recombinant Tissue-Type Plasminogen Activator Alone in Acute Ischemic Stroke
Author(s) -
Opeolu Adeoye,
Heidi Sucharew,
Jane Khoury,
Thomas A. Tomsick,
Pooja Khatri,
Yuko Y. Palesch,
Pamela Schmit,
Arthur Pancioli,
Joseph P. Broderick
Publication year - 2014
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.114.006743
Subject(s) - medicine , eptifibatide , stroke (engine) , tissue plasminogen activator , fibrinolytic agent , modified rankin scale , plasminogen activator , randomized controlled trial , t plasminogen activator , thrombolysis , surgery , gastroenterology , ischemic stroke , ischemia , percutaneous coronary intervention , myocardial infarction , mechanical engineering , engineering
The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke-Enhanced Regimen (CLEAR-ER) trial demonstrated safety of recombinant tissue-type plasminogen activator (r-tPA) plus eptifibatide in acute ischemic stroke (AIS). CLEAR-ER randomized AIS patients (5:1) to 0.6 mg/kg r-tPA plus eptifibatide versus standard r-tPA (0.9 mg/kg). Interventional Management of Stroke III randomized AIS patients to r-tPA plus endovascular therapy versus standard r-tPA. Albumin in Acute Stroke Part 2 randomized patients to albumin±r-tPA versus saline±r-tPA. Our aim was to compare outcomes in CLEAR-ER combination arm patients to propensity score-matched r-tPA only subjects in Albumin in Acute Stroke Part 2 and Interventional Management of Stroke III.
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