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  3. Does Antiplatelet Therapy during Bridging Thrombolysis Increase Rates of Intracerebral Hemorrhage in Stroke Patients?

Does Antiplatelet Therapy during Bridging Thrombolysis Increase Rates of Intracerebral Hemorrhage in Stroke Patients?

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DOI
10.7892/boris.94166
Publisher DOI
10.1371/journal.pone.0170045
PubMed ID
28095449
Abstract
BACKGROUND

Symptomatic intracerebral hemorrhage (sICH) after bridging thrombolysis for acute ischemic stroke is a devastating complication. We aimed to assess whether the additional administration of aspirin during endovascular intervention increases bleeding rates.

METHODS

We retrospectively compared bleeding complications and outcome in stroke patients who received bridging thrombolysis with (tPA+ASA) and without (tPA-ASA) aspirin during endovascular intervention between November 2008 and March 2014. Furthermore, we analyzed bleeding complications and outcome in antiplatelet naïve patients with those with prior or acute antiplatelet therapy.

RESULTS

Baseline characteristics, previous medication, and dosage of rtPA did not differ between 50 tPA+ASA (39 aspirin naïve, 11 preloaded) and 181 tPA-ASA patients (p>0.05). tPA+ASA patients had more often internal carotid artery (ICA) occlusion (p<0.001), large artery disease (p<0.001) and received more often acute stenting of the ICA (p<0.001). 10/180 (5.6%) tPA-ASA patients and 3/49 (6.1%) tPA+ASA patients suffered a sICH (p = 1.0). Rates of asymptomatic intracerebral hemorrhage, systemic bleeding complications and outcome did not differ between both groups (p>0.1). There were no differences in bleeding complications and mortality among 112 bridging patients with antiplatelet therapy (62 preloaded, 39 acute administration, 11 both) and 117 antiplatelet naïve patients. In a logistic regression analysis, aspirin administration during endovascular procedure was not a predictor of sICH.

CONCLUSION

Antiplatelet therapy before or during bridging thrombolysis in patients with acute ischemic stroke did not increase the risk of bleeding complications and had no impact on outcome. This finding has to be confirmed in larger studies.
Date Issued
2017
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
en
Author(s)
Broeg-Morvay, Anne  
Universitätsklinik für Neurologie  
Mordasini, Pasquale Renato  
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie  
Slezak, Agnieszka Anna  
Universitätsklinik für Neurologie  
Liesirova, Kai Timo  
Universitätsklinik für Neurologie  
Meisterernst, Julia Anne  
Universitätsklinik für Neurologie  
Schroth, Gerhard
Arnold, Marcel  
Universitätsklinik für Neurologie  
Departement Klinische Forschung, Forschungsgruppe Neurologie  
Jung, Simon  
Departement Klinische Forschung, Forschungsgruppe Neurologie  
Universitätsklinik für Neurologie  
Mattle, Heinrich  
Universitätsklinik für Neurologie  
Departement Klinische Forschung, Forschungsgruppe Neurologie  
Gralla, Jan  
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie  
Fischer, Urs Martin  
Universitätsklinik für Neurologie  
Departement Klinische Forschung, Forschungsgruppe Neurologie  
Additional Credits
Universitätsklinik für Neurologie  
Departement Klinische Forschung, Forschungsgruppe Neurologie  
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie  
Journal
PLoS ONE
Publisher
Public Library of Science
ISSN
1932-6203
Access(Rights)
open.access
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