Prestroke Antiplatelet Effect on Symptomatic Intracranial Hemorrhage and Functional Outcome in Intravenous Thrombolysis
- Author(s)
- Kyusik Kang; Kyung Bok Lee; Soo Joo Lee; Jae Guk Kim; Jun Lee; Man-Seok Park; Kang-Ho Choi; Joon-Tae Kim; Kyung-Ho Yu; Byung-Chul Lee; Mi-Sun Oh; Jae-Kwan Cha; Dae-Hyun Kim; Hyun-Wook Nah; Dong-Eog Kim; Wi-Sun Ryu; Beom Joon Kim; Hee-Joon Bae; Wook-Joo Kim; Dong-Ick Shin; Min-Ju Yeo; Sung Il Sohn; Jeong-Ho Hong; Juneyoung Lee; Keun-Sik Hong; Yong-Jin Cho; Jong-Moo Park; Jay Chol Choi; Ji Sung Lee; Tai Hwan Park
- Keimyung Author(s)
- Sohn, Sung Il; Hong, Jeong Ho
- Department
- Dept. of Neurology (신경과학)
- Journal Title
- Journal of Stroke
- Issued Date
- 2016
- Volume
- 18
- Issue
- 3
- Keyword
- Stroke; Thrombolytic therapy; Platelet aggregation inhibitors; Outcome assessment
- Abstract
- Background and Purpose About 30%-40% of stroke patients are taking antiplatelet at the time of their strokes, which might increase the risk of symptomatic intracranial hemorrhage (SICH) with intravenous tissue plasminogen activator (IV-TPA) therapy. We aimed to assess the effect of prestroke antiplatelet on the SICH risk and functional outcome in Koreans treated with IV-TPA.
Methods From a prospective stroke registry, we identified patients treated with IV-TPA between October 2009 and November 2014. Prestroke antiplatelet use was defined as taking antiplatelet within 7 days before the stroke onset. The primary outcome was SICH. Secondary outcomes were discharge modified Rankin Scale (mRS) score and in-hospital mortality.
Results Of 1,715 patients treated with IV-TPA, 441 (25.7%) were on prestroke antiplatelet. Prestroke antiplatelet users versus non-users were more likely to be older, to have multiple vascular risk factors. Prestroke antiplatelet use was associated with an increased risk of SICH (5.9% vs. 3.0%; adjusted odds ratio [OR] 1.79 [1.05-3.04]). However, at discharge, the two groups did not differ in mRS distribution (adjusted OR 0.90 [0.72-1.14]), mRS 0-1 outcome (34.2% vs. 33.7%; adjusted OR 1.27 [0.94-1.72), mRS 0-2 outcome (52.4% vs. 52.9%; adjusted OR 1.21 [0.90-1.63]), and in-hospital mortality (6.1% vs. 4.2%; adjusted OR 1.19 [0.71-2.01]). SimConclusions
Despite an increased risk of SICH, prestroke antiplatelet users compared to non-users had comparable functional outcomes and in-hospital mortality with IV-TPA therapy. Our results support the use of IV-TPA in eligible patients taking antiplatelet therapy before their stroke onset.
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