Does Current Oral Antiplatelet Agent or Subtherapeutic Anticoagulation Use Have an Effect on Tissue-Plasminogen-Activator-Mediated Recanalization Rate in Patients with Acute Ischemic Stroke?

Objective: Our goal is to assess if current antiplatelet (AP) use has an effect on recanalization rate and outcome in acute stroke patients. Methods: We conducted a retrospective analysis of acute stroke patients who received intravenous (IV) recombinant tissue plasminogen activator (rt-PA) and had...

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Veröffentlicht in:Cerebrovascular diseases (Basel, Switzerland) Switzerland), 2010-10, Vol.30 (5), p.508-513
Hauptverfasser: Ibrahim, Mohamed M., Sebastian, Joseph, Hussain, Muhammad, Al-Hussain, Fawaz, Uchino, Ken, Molina, Carlos, Khan, Khurshid, Demchuk, Andrew M., Alexandrov, Andrei V., Saqqur, Maher
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container_end_page 513
container_issue 5
container_start_page 508
container_title Cerebrovascular diseases (Basel, Switzerland)
container_volume 30
creator Ibrahim, Mohamed M.
Sebastian, Joseph
Hussain, Muhammad
Al-Hussain, Fawaz
Uchino, Ken
Molina, Carlos
Khan, Khurshid
Demchuk, Andrew M.
Alexandrov, Andrei V.
Saqqur, Maher
description Objective: Our goal is to assess if current antiplatelet (AP) use has an effect on recanalization rate and outcome in acute stroke patients. Methods: We conducted a retrospective analysis of acute stroke patients who received intravenous (IV) recombinant tissue plasminogen activator (rt-PA) and had transcranial Doppler examination within 3 h of symptom onset. The TCD findings were interpreted using the Thrombolysis in Brain Ischemia flow grading system as persistent arterial occlusion, reocclusion or complete recanalization. Complete recanalization was defined as established Thrombolysis in Brain Ischemia 4 or 5 within 2 h of IV rt-PA. The patients were divided based on their current use of AP agents. Comparisons were made between the different groups based on recanalziation rate, reocclusion and good long-term outcome (mRS ≤2) using χ 2 test. Multiple regression analysis was used to identify AP use as a predictor for recanalization and outcome including symptomatic intracranial hemorrhage after controlling for age, baseline NIHSS score, time to treatment, previous vascular event, hypertension and diabetes mellitus. Results: Two hundred and eighty-four patients were included; 154 (54%) males, 130 (46%) females, with a mean age of 69.5 ± 13 years. The median baseline NIHSS score was 16 ± 5. The median time to TCD examination was 131 ± 38 min from symptom onset. The median time to IV rt-PA was 140 ± 34 min. One hundred eighty patients were not on AP prior to their stroke, 76 were on aspirin, 15 were on clopidogrel, 2 were on aspirin-dipyridamole combination, 2 were on both aspirin and clopidogrel, and 9 patients on subtherapeutic coumadin. In patients who were naïve to AP, 68/178 (38.2%) had complete recanalization, whereas in the AP group, 25/91 (28%) had complete recanalization. Patients on aspirin alone had a lower recanalization rate (16/72) as compared to those not on AP (22 vs. 39%) (p = 0.017), while those on clopidogrel had higher rates of complete recanalization (9/19, 60%). There was no difference in the rate of symptomatic intracranial hemorrhages in patients on AP agents as compared to those not on AP (9/180, 5% vs. 9/95, 9.5%) (p = 0.13). A good long-term outcome (mRS ≤2) was achieved in 85/160 (53%) of the patients naïve to AP and in 33/84 (39%) of the patients on AP (p = 0.035). In multiple regression, AP use was not a predictor of either recanalization rate (p = 0.057) or good outcome (p = 0.27). Conclusions: No correlation was found between
doi_str_mv 10.1159/000319029
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Methods: We conducted a retrospective analysis of acute stroke patients who received intravenous (IV) recombinant tissue plasminogen activator (rt-PA) and had transcranial Doppler examination within 3 h of symptom onset. The TCD findings were interpreted using the Thrombolysis in Brain Ischemia flow grading system as persistent arterial occlusion, reocclusion or complete recanalization. Complete recanalization was defined as established Thrombolysis in Brain Ischemia 4 or 5 within 2 h of IV rt-PA. The patients were divided based on their current use of AP agents. Comparisons were made between the different groups based on recanalziation rate, reocclusion and good long-term outcome (mRS ≤2) using χ 2 test. Multiple regression analysis was used to identify AP use as a predictor for recanalization and outcome including symptomatic intracranial hemorrhage after controlling for age, baseline NIHSS score, time to treatment, previous vascular event, hypertension and diabetes mellitus. Results: Two hundred and eighty-four patients were included; 154 (54%) males, 130 (46%) females, with a mean age of 69.5 ± 13 years. The median baseline NIHSS score was 16 ± 5. The median time to TCD examination was 131 ± 38 min from symptom onset. The median time to IV rt-PA was 140 ± 34 min. One hundred eighty patients were not on AP prior to their stroke, 76 were on aspirin, 15 were on clopidogrel, 2 were on aspirin-dipyridamole combination, 2 were on both aspirin and clopidogrel, and 9 patients on subtherapeutic coumadin. In patients who were naïve to AP, 68/178 (38.2%) had complete recanalization, whereas in the AP group, 25/91 (28%) had complete recanalization. Patients on aspirin alone had a lower recanalization rate (16/72) as compared to those not on AP (22 vs. 39%) (p = 0.017), while those on clopidogrel had higher rates of complete recanalization (9/19, 60%). There was no difference in the rate of symptomatic intracranial hemorrhages in patients on AP agents as compared to those not on AP (9/180, 5% vs. 9/95, 9.5%) (p = 0.13). A good long-term outcome (mRS ≤2) was achieved in 85/160 (53%) of the patients naïve to AP and in 33/84 (39%) of the patients on AP (p = 0.035). In multiple regression, AP use was not a predictor of either recanalization rate (p = 0.057) or good outcome (p = 0.27). Conclusions: No correlation was found between AP use and recanalization rate and good outcome in patients with acute stroke who received IV rt-PA treatment. Prior AP use should not defer patients from receiving IV rt-PA treatment in an acute stroke setting.</description><identifier>ISSN: 1015-9770</identifier><identifier>EISSN: 1421-9786</identifier><identifier>DOI: 10.1159/000319029</identifier><identifier>PMID: 20861622</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject><![CDATA[Administration, Oral ; Aged ; Aged, 80 and over ; Anticoagulants - administration & dosage ; Anticoagulants - therapeutic use ; Aspirin - administration & dosage ; Aspirin - therapeutic use ; Drug Therapy, Combination ; Female ; Fibrinolytic Agents - administration & dosage ; Fibrinolytic Agents - adverse effects ; Fibrinolytic Agents - therapeutic use ; Humans ; Injections, Intravenous ; Male ; Middle Aged ; Original Paper ; Platelet Aggregation Inhibitors - administration & dosage ; Platelet Aggregation Inhibitors - therapeutic use ; Prospective Studies ; Retrospective Studies ; Stroke - drug therapy ; Thrombolytic Therapy - methods ; Ticlopidine - administration & dosage ; Ticlopidine - analogs & derivatives ; Ticlopidine - therapeutic use ; Tissue Plasminogen Activator - administration & dosage ; Tissue Plasminogen Activator - adverse effects ; Tissue Plasminogen Activator - therapeutic use ; Treatment Outcome ; Warfarin - administration & dosage ; Warfarin - therapeutic use]]></subject><ispartof>Cerebrovascular diseases (Basel, Switzerland), 2010-10, Vol.30 (5), p.508-513</ispartof><rights>2010 S. Karger AG, Basel</rights><rights>Copyright © 2010 S. Karger AG, Basel.</rights><rights>Copyright (c) 2010 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c364t-f2c38ab2e88d7802d6eda4276d7478081057c722283074e7db108dc44c8e98273</citedby><cites>FETCH-LOGICAL-c364t-f2c38ab2e88d7802d6eda4276d7478081057c722283074e7db108dc44c8e98273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2430,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20861622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ibrahim, Mohamed M.</creatorcontrib><creatorcontrib>Sebastian, Joseph</creatorcontrib><creatorcontrib>Hussain, Muhammad</creatorcontrib><creatorcontrib>Al-Hussain, Fawaz</creatorcontrib><creatorcontrib>Uchino, Ken</creatorcontrib><creatorcontrib>Molina, Carlos</creatorcontrib><creatorcontrib>Khan, Khurshid</creatorcontrib><creatorcontrib>Demchuk, Andrew M.</creatorcontrib><creatorcontrib>Alexandrov, Andrei V.</creatorcontrib><creatorcontrib>Saqqur, Maher</creatorcontrib><creatorcontrib>CLOTBUST Investigators</creatorcontrib><creatorcontrib>for the CLOTBUST Investigators</creatorcontrib><title>Does Current Oral Antiplatelet Agent or Subtherapeutic Anticoagulation Use Have an Effect on Tissue-Plasminogen-Activator-Mediated Recanalization Rate in Patients with Acute Ischemic Stroke?</title><title>Cerebrovascular diseases (Basel, Switzerland)</title><addtitle>Cerebrovasc Dis</addtitle><description>Objective: Our goal is to assess if current antiplatelet (AP) use has an effect on recanalization rate and outcome in acute stroke patients. Methods: We conducted a retrospective analysis of acute stroke patients who received intravenous (IV) recombinant tissue plasminogen activator (rt-PA) and had transcranial Doppler examination within 3 h of symptom onset. The TCD findings were interpreted using the Thrombolysis in Brain Ischemia flow grading system as persistent arterial occlusion, reocclusion or complete recanalization. Complete recanalization was defined as established Thrombolysis in Brain Ischemia 4 or 5 within 2 h of IV rt-PA. The patients were divided based on their current use of AP agents. Comparisons were made between the different groups based on recanalziation rate, reocclusion and good long-term outcome (mRS ≤2) using χ 2 test. Multiple regression analysis was used to identify AP use as a predictor for recanalization and outcome including symptomatic intracranial hemorrhage after controlling for age, baseline NIHSS score, time to treatment, previous vascular event, hypertension and diabetes mellitus. Results: Two hundred and eighty-four patients were included; 154 (54%) males, 130 (46%) females, with a mean age of 69.5 ± 13 years. The median baseline NIHSS score was 16 ± 5. The median time to TCD examination was 131 ± 38 min from symptom onset. The median time to IV rt-PA was 140 ± 34 min. One hundred eighty patients were not on AP prior to their stroke, 76 were on aspirin, 15 were on clopidogrel, 2 were on aspirin-dipyridamole combination, 2 were on both aspirin and clopidogrel, and 9 patients on subtherapeutic coumadin. In patients who were naïve to AP, 68/178 (38.2%) had complete recanalization, whereas in the AP group, 25/91 (28%) had complete recanalization. Patients on aspirin alone had a lower recanalization rate (16/72) as compared to those not on AP (22 vs. 39%) (p = 0.017), while those on clopidogrel had higher rates of complete recanalization (9/19, 60%). There was no difference in the rate of symptomatic intracranial hemorrhages in patients on AP agents as compared to those not on AP (9/180, 5% vs. 9/95, 9.5%) (p = 0.13). A good long-term outcome (mRS ≤2) was achieved in 85/160 (53%) of the patients naïve to AP and in 33/84 (39%) of the patients on AP (p = 0.035). In multiple regression, AP use was not a predictor of either recanalization rate (p = 0.057) or good outcome (p = 0.27). Conclusions: No correlation was found between AP use and recanalization rate and good outcome in patients with acute stroke who received IV rt-PA treatment. Prior AP use should not defer patients from receiving IV rt-PA treatment in an acute stroke setting.</description><subject>Administration, Oral</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anticoagulants - administration &amp; dosage</subject><subject>Anticoagulants - therapeutic use</subject><subject>Aspirin - administration &amp; dosage</subject><subject>Aspirin - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration &amp; dosage</subject><subject>Fibrinolytic Agents - adverse effects</subject><subject>Fibrinolytic Agents - therapeutic use</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original Paper</subject><subject>Platelet Aggregation Inhibitors - administration &amp; dosage</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Prospective Studies</subject><subject>Retrospective Studies</subject><subject>Stroke - drug therapy</subject><subject>Thrombolytic Therapy - methods</subject><subject>Ticlopidine - administration &amp; dosage</subject><subject>Ticlopidine - analogs &amp; derivatives</subject><subject>Ticlopidine - therapeutic use</subject><subject>Tissue Plasminogen Activator - administration &amp; dosage</subject><subject>Tissue Plasminogen Activator - adverse effects</subject><subject>Tissue Plasminogen Activator - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Warfarin - administration &amp; dosage</subject><subject>Warfarin - therapeutic use</subject><issn>1015-9770</issn><issn>1421-9786</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqF0Utv1DAQAOAIUdFSOHBHyOKCOKTYjhM7JxQthVYqatXHOfI6k123Sbz40ar8OH4bs93tHrhw8szomxnJk2XvGD1irKy_UEoLVlNev8gOmOAsr6WqXmJMWYmxpPvZ6xBukVVMsVfZPqeqYhXnB9mfbw4CmSXvYYrk3OuBNFO0q0FHGCCSZrGuO0-u0jwuwesVpGjNEzJOLxJC6yZyE4Cc6HsgeiLHfQ8GmyZybUNIkF8MOox2cjgrb0y09zo6n_-EzuKWjlyC0ZMe7O_NqEssEjuRC0xxeSAPNi5JYxKWT4NZwoj7r6J3d_D1TbbX6yHA2-17mN18P76eneRn5z9OZ81ZbopKxLznplB6zkGpTirKuwo6LbisOikwV4yW0kjOuSqoFCC7OaOqM0IYBbXisjjMPm3mrrz7lSDEdrTBwDDoCVwKbV2KUlWyLv8rZSlljVig_PiPvHXJ40eskVKCirpA9HmDjHcheOjblbej9o8to-36-O3u-Gg_bAem-QjdTj5fG8H7DbjTfgF-B7b9fwEjybQN</recordid><startdate>201010</startdate><enddate>201010</enddate><creator>Ibrahim, Mohamed M.</creator><creator>Sebastian, Joseph</creator><creator>Hussain, Muhammad</creator><creator>Al-Hussain, Fawaz</creator><creator>Uchino, Ken</creator><creator>Molina, Carlos</creator><creator>Khan, Khurshid</creator><creator>Demchuk, Andrew M.</creator><creator>Alexandrov, Andrei V.</creator><creator>Saqqur, Maher</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>201010</creationdate><title>Does Current Oral Antiplatelet Agent or Subtherapeutic Anticoagulation Use Have an Effect on Tissue-Plasminogen-Activator-Mediated Recanalization Rate in Patients with Acute Ischemic Stroke?</title><author>Ibrahim, Mohamed M. ; Sebastian, Joseph ; Hussain, Muhammad ; Al-Hussain, Fawaz ; Uchino, Ken ; Molina, Carlos ; Khan, Khurshid ; Demchuk, Andrew M. ; Alexandrov, Andrei V. ; Saqqur, Maher</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c364t-f2c38ab2e88d7802d6eda4276d7478081057c722283074e7db108dc44c8e98273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Administration, Oral</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anticoagulants - administration &amp; dosage</topic><topic>Anticoagulants - therapeutic use</topic><topic>Aspirin - administration &amp; dosage</topic><topic>Aspirin - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration &amp; dosage</topic><topic>Fibrinolytic Agents - adverse effects</topic><topic>Fibrinolytic Agents - therapeutic use</topic><topic>Humans</topic><topic>Injections, Intravenous</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original Paper</topic><topic>Platelet Aggregation Inhibitors - administration &amp; dosage</topic><topic>Platelet Aggregation Inhibitors - therapeutic use</topic><topic>Prospective Studies</topic><topic>Retrospective Studies</topic><topic>Stroke - drug therapy</topic><topic>Thrombolytic Therapy - methods</topic><topic>Ticlopidine - administration &amp; dosage</topic><topic>Ticlopidine - analogs &amp; derivatives</topic><topic>Ticlopidine - therapeutic use</topic><topic>Tissue Plasminogen Activator - administration &amp; dosage</topic><topic>Tissue Plasminogen Activator - adverse effects</topic><topic>Tissue Plasminogen Activator - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Warfarin - administration &amp; dosage</topic><topic>Warfarin - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ibrahim, Mohamed M.</creatorcontrib><creatorcontrib>Sebastian, Joseph</creatorcontrib><creatorcontrib>Hussain, Muhammad</creatorcontrib><creatorcontrib>Al-Hussain, Fawaz</creatorcontrib><creatorcontrib>Uchino, Ken</creatorcontrib><creatorcontrib>Molina, Carlos</creatorcontrib><creatorcontrib>Khan, Khurshid</creatorcontrib><creatorcontrib>Demchuk, Andrew M.</creatorcontrib><creatorcontrib>Alexandrov, Andrei V.</creatorcontrib><creatorcontrib>Saqqur, Maher</creatorcontrib><creatorcontrib>CLOTBUST Investigators</creatorcontrib><creatorcontrib>for the CLOTBUST Investigators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Cerebrovascular diseases (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ibrahim, Mohamed M.</au><au>Sebastian, Joseph</au><au>Hussain, Muhammad</au><au>Al-Hussain, Fawaz</au><au>Uchino, Ken</au><au>Molina, Carlos</au><au>Khan, Khurshid</au><au>Demchuk, Andrew M.</au><au>Alexandrov, Andrei V.</au><au>Saqqur, Maher</au><aucorp>CLOTBUST Investigators</aucorp><aucorp>for the CLOTBUST Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does Current Oral Antiplatelet Agent or Subtherapeutic Anticoagulation Use Have an Effect on Tissue-Plasminogen-Activator-Mediated Recanalization Rate in Patients with Acute Ischemic Stroke?</atitle><jtitle>Cerebrovascular diseases (Basel, Switzerland)</jtitle><addtitle>Cerebrovasc Dis</addtitle><date>2010-10</date><risdate>2010</risdate><volume>30</volume><issue>5</issue><spage>508</spage><epage>513</epage><pages>508-513</pages><issn>1015-9770</issn><eissn>1421-9786</eissn><abstract>Objective: Our goal is to assess if current antiplatelet (AP) use has an effect on recanalization rate and outcome in acute stroke patients. Methods: We conducted a retrospective analysis of acute stroke patients who received intravenous (IV) recombinant tissue plasminogen activator (rt-PA) and had transcranial Doppler examination within 3 h of symptom onset. The TCD findings were interpreted using the Thrombolysis in Brain Ischemia flow grading system as persistent arterial occlusion, reocclusion or complete recanalization. Complete recanalization was defined as established Thrombolysis in Brain Ischemia 4 or 5 within 2 h of IV rt-PA. The patients were divided based on their current use of AP agents. Comparisons were made between the different groups based on recanalziation rate, reocclusion and good long-term outcome (mRS ≤2) using χ 2 test. Multiple regression analysis was used to identify AP use as a predictor for recanalization and outcome including symptomatic intracranial hemorrhage after controlling for age, baseline NIHSS score, time to treatment, previous vascular event, hypertension and diabetes mellitus. Results: Two hundred and eighty-four patients were included; 154 (54%) males, 130 (46%) females, with a mean age of 69.5 ± 13 years. The median baseline NIHSS score was 16 ± 5. The median time to TCD examination was 131 ± 38 min from symptom onset. The median time to IV rt-PA was 140 ± 34 min. One hundred eighty patients were not on AP prior to their stroke, 76 were on aspirin, 15 were on clopidogrel, 2 were on aspirin-dipyridamole combination, 2 were on both aspirin and clopidogrel, and 9 patients on subtherapeutic coumadin. In patients who were naïve to AP, 68/178 (38.2%) had complete recanalization, whereas in the AP group, 25/91 (28%) had complete recanalization. Patients on aspirin alone had a lower recanalization rate (16/72) as compared to those not on AP (22 vs. 39%) (p = 0.017), while those on clopidogrel had higher rates of complete recanalization (9/19, 60%). There was no difference in the rate of symptomatic intracranial hemorrhages in patients on AP agents as compared to those not on AP (9/180, 5% vs. 9/95, 9.5%) (p = 0.13). A good long-term outcome (mRS ≤2) was achieved in 85/160 (53%) of the patients naïve to AP and in 33/84 (39%) of the patients on AP (p = 0.035). In multiple regression, AP use was not a predictor of either recanalization rate (p = 0.057) or good outcome (p = 0.27). Conclusions: No correlation was found between AP use and recanalization rate and good outcome in patients with acute stroke who received IV rt-PA treatment. Prior AP use should not defer patients from receiving IV rt-PA treatment in an acute stroke setting.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>20861622</pmid><doi>10.1159/000319029</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1015-9770
ispartof Cerebrovascular diseases (Basel, Switzerland), 2010-10, Vol.30 (5), p.508-513
issn 1015-9770
1421-9786
language eng
recordid cdi_proquest_miscellaneous_954586795
source MEDLINE; Karger Journals Complete; Alma/SFX Local Collection
subjects Administration, Oral
Aged
Aged, 80 and over
Anticoagulants - administration & dosage
Anticoagulants - therapeutic use
Aspirin - administration & dosage
Aspirin - therapeutic use
Drug Therapy, Combination
Female
Fibrinolytic Agents - administration & dosage
Fibrinolytic Agents - adverse effects
Fibrinolytic Agents - therapeutic use
Humans
Injections, Intravenous
Male
Middle Aged
Original Paper
Platelet Aggregation Inhibitors - administration & dosage
Platelet Aggregation Inhibitors - therapeutic use
Prospective Studies
Retrospective Studies
Stroke - drug therapy
Thrombolytic Therapy - methods
Ticlopidine - administration & dosage
Ticlopidine - analogs & derivatives
Ticlopidine - therapeutic use
Tissue Plasminogen Activator - administration & dosage
Tissue Plasminogen Activator - adverse effects
Tissue Plasminogen Activator - therapeutic use
Treatment Outcome
Warfarin - administration & dosage
Warfarin - therapeutic use
title Does Current Oral Antiplatelet Agent or Subtherapeutic Anticoagulation Use Have an Effect on Tissue-Plasminogen-Activator-Mediated Recanalization Rate in Patients with Acute Ischemic Stroke?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T04%3A11%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_karge&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Does%20Current%20Oral%20Antiplatelet%20Agent%20or%20Subtherapeutic%20Anticoagulation%20Use%20Have%20an%20Effect%20on%20Tissue-Plasminogen-Activator-Mediated%20Recanalization%20Rate%20in%20Patients%20with%20Acute%20Ischemic%20Stroke?&rft.jtitle=Cerebrovascular%20diseases%20(Basel,%20Switzerland)&rft.au=Ibrahim,%20Mohamed%20M.&rft.aucorp=CLOTBUST%20Investigators&rft.date=2010-10&rft.volume=30&rft.issue=5&rft.spage=508&rft.epage=513&rft.pages=508-513&rft.issn=1015-9770&rft.eissn=1421-9786&rft_id=info:doi/10.1159/000319029&rft_dat=%3Cproquest_karge%3E2165103031%3C/proquest_karge%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=758840493&rft_id=info:pmid/20861622&rfr_iscdi=true