Risk of Thrombolytic Therapy for Acute Ischemic Stroke in Patients With Current Malignancy
Little is known about the risk of thrombolysis in patients with malignancy, because these patients have been excluded from most clinical trials. We reviewed our acute ischemic stroke (AIS) database for clinical outcomes and complications in patients with current malignancy (CM) who received thrombol...
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Veröffentlicht in: | Journal of stroke and cerebrovascular diseases 2011-03, Vol.20 (2), p.124-130 |
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description | Little is known about the risk of thrombolysis in patients with malignancy, because these patients have been excluded from most clinical trials. We reviewed our acute ischemic stroke (AIS) database for clinical outcomes and complications in patients with current malignancy (CM) who received thrombolytic therapy. Consecutive AIS patients receiving thrombolysis between January 2003 and December 2006 were retrospectively abstracted in accordance with the American Stroke Association's Get With the Guidelines–Stroke definitions and charts were reviewed for history of malignancy. Patients with brain metastases did not receive tissue plasminogen activator (tPA). Stepwise logistic regression was used to identify independent predictors of in-hospital mortality. Of 308 AIS patients treated with thrombolytic therapy, 210 (68%) received intravenous (IV) tPA only, 41 (13%) received IV tPA plus intra-arterial therapy (IAT), and 57 (18%) received IAT only. Eighteen patients (5.8%) had a CM, and 26 patients (8.4%) had a remote history of malignancy. Patients with CM had a higher in-hospital mortality (38.9% vs 19.7 %; P = .05) and were more likely to have died due to worsening medical comorbidity (71.4% vs 9.6%; P < .001). The rate of symptomatic intracranial hemorrhage (ICH) was similar in the 2 groups (5.6% vs 2.7%; P = .47). In multivariate analysis, the only independent predictors of mortality were National Institutes of Health Stroke Scale score, history of hypertension, and smoking. CM was not independently associated with increased in-hospital mortality following thrombolysis. Mortality was attributable largely to medical comorbidities, not to symptomatic ICH. Our data suggest that thrombolysis may be a reasonable option for patients with malignancy who have acceptable medical comorbidities and performance status. Further research is warranted. |
doi_str_mv | 10.1016/j.jstrokecerebrovasdis.2009.10.010 |
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We reviewed our acute ischemic stroke (AIS) database for clinical outcomes and complications in patients with current malignancy (CM) who received thrombolytic therapy. Consecutive AIS patients receiving thrombolysis between January 2003 and December 2006 were retrospectively abstracted in accordance with the American Stroke Association's Get With the Guidelines–Stroke definitions and charts were reviewed for history of malignancy. Patients with brain metastases did not receive tissue plasminogen activator (tPA). Stepwise logistic regression was used to identify independent predictors of in-hospital mortality. Of 308 AIS patients treated with thrombolytic therapy, 210 (68%) received intravenous (IV) tPA only, 41 (13%) received IV tPA plus intra-arterial therapy (IAT), and 57 (18%) received IAT only. Eighteen patients (5.8%) had a CM, and 26 patients (8.4%) had a remote history of malignancy. Patients with CM had a higher in-hospital mortality (38.9% vs 19.7 %; P = .05) and were more likely to have died due to worsening medical comorbidity (71.4% vs 9.6%; P < .001). The rate of symptomatic intracranial hemorrhage (ICH) was similar in the 2 groups (5.6% vs 2.7%; P = .47). In multivariate analysis, the only independent predictors of mortality were National Institutes of Health Stroke Scale score, history of hypertension, and smoking. CM was not independently associated with increased in-hospital mortality following thrombolysis. Mortality was attributable largely to medical comorbidities, not to symptomatic ICH. Our data suggest that thrombolysis may be a reasonable option for patients with malignancy who have acceptable medical comorbidities and performance status. Further research is warranted.</description><identifier>ISSN: 1052-3057</identifier><identifier>EISSN: 1532-8511</identifier><identifier>DOI: 10.1016/j.jstrokecerebrovasdis.2009.10.010</identifier><identifier>PMID: 20598579</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Boston ; Brain Ischemia - complications ; Brain Ischemia - drug therapy ; Brain Ischemia - mortality ; Cardiovascular ; Chi-Square Distribution ; Comorbidity ; Female ; Fibrinolytic Agents - administration & dosage ; Fibrinolytic Agents - adverse effects ; Hospital Mortality ; Humans ; ICH ; in-hospital mortality ; Intracranial Hemorrhages - chemically induced ; Intracranial Hemorrhages - mortality ; Logistic Models ; Male ; Neoplasms - complications ; Neoplasms - mortality ; Neurology ; Odds Ratio ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Stroke - drug therapy ; Stroke - etiology ; Stroke - mortality ; thrombolysis ; Thrombolytic Therapy - adverse effects ; Thrombolytic Therapy - mortality ; Tissue Plasminogen Activator - administration & dosage ; Tissue Plasminogen Activator - adverse effects ; tPA ; Treatment Outcome</subject><ispartof>Journal of stroke and cerebrovascular diseases, 2011-03, Vol.20 (2), p.124-130</ispartof><rights>National Stroke Association</rights><rights>2011 National Stroke Association</rights><rights>Copyright © 2011 National Stroke Association. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-353b8bda37c4ce9dfe6ea4a4957455cec73628c15b9bcf0bfcaf809facb22ea03</citedby><cites>FETCH-LOGICAL-c458t-353b8bda37c4ce9dfe6ea4a4957455cec73628c15b9bcf0bfcaf809facb22ea03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2009.10.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20598579$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masrur, Shihab, MD</creatorcontrib><creatorcontrib>Abdullah, Abdul R., MD</creatorcontrib><creatorcontrib>Smith, Eric E., MD, MPH</creatorcontrib><creatorcontrib>Hidalgo, Renzo, MD</creatorcontrib><creatorcontrib>El-Ghandour, Ahmed, MD</creatorcontrib><creatorcontrib>Rordorf, Guy, MD</creatorcontrib><creatorcontrib>Schwamm, Lee H., MD</creatorcontrib><title>Risk of Thrombolytic Therapy for Acute Ischemic Stroke in Patients With Current Malignancy</title><title>Journal of stroke and cerebrovascular diseases</title><addtitle>J Stroke Cerebrovasc Dis</addtitle><description>Little is known about the risk of thrombolysis in patients with malignancy, because these patients have been excluded from most clinical trials. We reviewed our acute ischemic stroke (AIS) database for clinical outcomes and complications in patients with current malignancy (CM) who received thrombolytic therapy. Consecutive AIS patients receiving thrombolysis between January 2003 and December 2006 were retrospectively abstracted in accordance with the American Stroke Association's Get With the Guidelines–Stroke definitions and charts were reviewed for history of malignancy. Patients with brain metastases did not receive tissue plasminogen activator (tPA). Stepwise logistic regression was used to identify independent predictors of in-hospital mortality. Of 308 AIS patients treated with thrombolytic therapy, 210 (68%) received intravenous (IV) tPA only, 41 (13%) received IV tPA plus intra-arterial therapy (IAT), and 57 (18%) received IAT only. Eighteen patients (5.8%) had a CM, and 26 patients (8.4%) had a remote history of malignancy. Patients with CM had a higher in-hospital mortality (38.9% vs 19.7 %; P = .05) and were more likely to have died due to worsening medical comorbidity (71.4% vs 9.6%; P < .001). The rate of symptomatic intracranial hemorrhage (ICH) was similar in the 2 groups (5.6% vs 2.7%; P = .47). In multivariate analysis, the only independent predictors of mortality were National Institutes of Health Stroke Scale score, history of hypertension, and smoking. CM was not independently associated with increased in-hospital mortality following thrombolysis. Mortality was attributable largely to medical comorbidities, not to symptomatic ICH. Our data suggest that thrombolysis may be a reasonable option for patients with malignancy who have acceptable medical comorbidities and performance status. Further research is warranted.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Boston</subject><subject>Brain Ischemia - complications</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - mortality</subject><subject>Cardiovascular</subject><subject>Chi-Square Distribution</subject><subject>Comorbidity</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration & dosage</subject><subject>Fibrinolytic Agents - adverse effects</subject><subject>Hospital Mortality</subject><subject>Humans</subject><subject>ICH</subject><subject>in-hospital mortality</subject><subject>Intracranial Hemorrhages - chemically induced</subject><subject>Intracranial Hemorrhages - mortality</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Neoplasms - complications</subject><subject>Neoplasms - mortality</subject><subject>Neurology</subject><subject>Odds Ratio</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Stroke - drug therapy</subject><subject>Stroke - etiology</subject><subject>Stroke - mortality</subject><subject>thrombolysis</subject><subject>Thrombolytic Therapy - adverse effects</subject><subject>Thrombolytic Therapy - mortality</subject><subject>Tissue Plasminogen Activator - administration & dosage</subject><subject>Tissue Plasminogen Activator - adverse effects</subject><subject>tPA</subject><subject>Treatment Outcome</subject><issn>1052-3057</issn><issn>1532-8511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkU1v1DAQhi0EoqXwF5BvSEhZxkm8SS5IZcVHpa2KaBESF8uZjFlnk3hrJ5Xy73HY0gPi0pM98qN3xs8w9lbASoBYv2tXbRi92xOSp9q7Ox0aG1YpQBWBFQh4wk6FzNKklEI8jXeQaZKBLE7YixBaACFkKZ-zkxRkVcqiOmU_v9mw587wm513fe26ebQYC_L6MHPjPD_HaSR-EXBHfXy6_jMBtwP_qkdLwxj4Dzvu-GbyPlb8Unf216AHnF-yZ0Z3gV7dn2fs-6ePN5svyfbq88XmfJtgLssxyWRWl3WjswJzpKoxtCad67ySRS4lEhbZOi1RyLqq0UBtUJsSKqOxTlPSkJ2xN8fcg3e3E4VR9TYgdZ0eyE1BlTLLCxCFjOSHI4neheDJqIO3vfazEqAWxapV_1OsFsULExXHkNf37aa6p-Yh4q_TCGyPAMVP31nyKmAUhdRYTziqxtnH9Xv_Txx2drCouz3NFFo3-SHqVUKFVIG6Xpa-7BwqgFTKKvsNGHWyaQ</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Masrur, Shihab, MD</creator><creator>Abdullah, Abdul R., MD</creator><creator>Smith, Eric E., MD, MPH</creator><creator>Hidalgo, Renzo, MD</creator><creator>El-Ghandour, Ahmed, MD</creator><creator>Rordorf, Guy, MD</creator><creator>Schwamm, Lee H., MD</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20110301</creationdate><title>Risk of Thrombolytic Therapy for Acute Ischemic Stroke in Patients With Current Malignancy</title><author>Masrur, Shihab, MD ; Abdullah, Abdul R., MD ; Smith, Eric E., MD, MPH ; Hidalgo, Renzo, MD ; El-Ghandour, Ahmed, MD ; Rordorf, Guy, MD ; Schwamm, Lee H., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-353b8bda37c4ce9dfe6ea4a4957455cec73628c15b9bcf0bfcaf809facb22ea03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Boston</topic><topic>Brain Ischemia - complications</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - mortality</topic><topic>Cardiovascular</topic><topic>Chi-Square Distribution</topic><topic>Comorbidity</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration & dosage</topic><topic>Fibrinolytic Agents - adverse effects</topic><topic>Hospital Mortality</topic><topic>Humans</topic><topic>ICH</topic><topic>in-hospital mortality</topic><topic>Intracranial Hemorrhages - chemically induced</topic><topic>Intracranial Hemorrhages - mortality</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Neoplasms - complications</topic><topic>Neoplasms - mortality</topic><topic>Neurology</topic><topic>Odds Ratio</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Stroke - drug therapy</topic><topic>Stroke - etiology</topic><topic>Stroke - mortality</topic><topic>thrombolysis</topic><topic>Thrombolytic Therapy - adverse effects</topic><topic>Thrombolytic Therapy - mortality</topic><topic>Tissue Plasminogen Activator - administration & dosage</topic><topic>Tissue Plasminogen Activator - adverse effects</topic><topic>tPA</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masrur, Shihab, MD</creatorcontrib><creatorcontrib>Abdullah, Abdul R., MD</creatorcontrib><creatorcontrib>Smith, Eric E., MD, MPH</creatorcontrib><creatorcontrib>Hidalgo, Renzo, MD</creatorcontrib><creatorcontrib>El-Ghandour, Ahmed, MD</creatorcontrib><creatorcontrib>Rordorf, Guy, MD</creatorcontrib><creatorcontrib>Schwamm, Lee H., MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of stroke and cerebrovascular diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masrur, Shihab, MD</au><au>Abdullah, Abdul R., MD</au><au>Smith, Eric E., MD, MPH</au><au>Hidalgo, Renzo, MD</au><au>El-Ghandour, Ahmed, MD</au><au>Rordorf, Guy, MD</au><au>Schwamm, Lee H., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of Thrombolytic Therapy for Acute Ischemic Stroke in Patients With Current Malignancy</atitle><jtitle>Journal of stroke and cerebrovascular diseases</jtitle><addtitle>J Stroke Cerebrovasc Dis</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>20</volume><issue>2</issue><spage>124</spage><epage>130</epage><pages>124-130</pages><issn>1052-3057</issn><eissn>1532-8511</eissn><abstract>Little is known about the risk of thrombolysis in patients with malignancy, because these patients have been excluded from most clinical trials. We reviewed our acute ischemic stroke (AIS) database for clinical outcomes and complications in patients with current malignancy (CM) who received thrombolytic therapy. Consecutive AIS patients receiving thrombolysis between January 2003 and December 2006 were retrospectively abstracted in accordance with the American Stroke Association's Get With the Guidelines–Stroke definitions and charts were reviewed for history of malignancy. Patients with brain metastases did not receive tissue plasminogen activator (tPA). Stepwise logistic regression was used to identify independent predictors of in-hospital mortality. Of 308 AIS patients treated with thrombolytic therapy, 210 (68%) received intravenous (IV) tPA only, 41 (13%) received IV tPA plus intra-arterial therapy (IAT), and 57 (18%) received IAT only. Eighteen patients (5.8%) had a CM, and 26 patients (8.4%) had a remote history of malignancy. Patients with CM had a higher in-hospital mortality (38.9% vs 19.7 %; P = .05) and were more likely to have died due to worsening medical comorbidity (71.4% vs 9.6%; P < .001). The rate of symptomatic intracranial hemorrhage (ICH) was similar in the 2 groups (5.6% vs 2.7%; P = .47). In multivariate analysis, the only independent predictors of mortality were National Institutes of Health Stroke Scale score, history of hypertension, and smoking. CM was not independently associated with increased in-hospital mortality following thrombolysis. Mortality was attributable largely to medical comorbidities, not to symptomatic ICH. Our data suggest that thrombolysis may be a reasonable option for patients with malignancy who have acceptable medical comorbidities and performance status. Further research is warranted.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20598579</pmid><doi>10.1016/j.jstrokecerebrovasdis.2009.10.010</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Boston Brain Ischemia - complications Brain Ischemia - drug therapy Brain Ischemia - mortality Cardiovascular Chi-Square Distribution Comorbidity Female Fibrinolytic Agents - administration & dosage Fibrinolytic Agents - adverse effects Hospital Mortality Humans ICH in-hospital mortality Intracranial Hemorrhages - chemically induced Intracranial Hemorrhages - mortality Logistic Models Male Neoplasms - complications Neoplasms - mortality Neurology Odds Ratio Retrospective Studies Risk Assessment Risk Factors Stroke - drug therapy Stroke - etiology Stroke - mortality thrombolysis Thrombolytic Therapy - adverse effects Thrombolytic Therapy - mortality Tissue Plasminogen Activator - administration & dosage Tissue Plasminogen Activator - adverse effects tPA Treatment Outcome |
title | Risk of Thrombolytic Therapy for Acute Ischemic Stroke in Patients With Current Malignancy |
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