Optimizing the management of acute ischaemic stroke: a review of the utilization of intravenous recombinant tissue plasminogen activator (tPA)
Summary What is known and Objective: Thrombolysis using intravenous tissue plasminogen activator (tPA) is the only available evidence‐based treatment for acute ischaemic stroke; however, its current utilization is very low. Therefore, the aim of this article is to review the literature regarding th...
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Veröffentlicht in: | Journal of clinical pharmacy and therapeutics 2012-12, Vol.37 (6), p.620-629 |
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description | Summary
What is known and Objective: Thrombolysis using intravenous tissue plasminogen activator (tPA) is the only available evidence‐based treatment for acute ischaemic stroke; however, its current utilization is very low. Therefore, the aim of this article is to review the literature regarding the use of intravenous tPA for the treatment of acute ischaemic stroke. The review will also compare utilization rates of thrombolysis in different centres across the world and identify key reasons for the underutilization of thrombolysis in stroke.
Methods: MEDLINE, EMBASE, International Pharmaceutical s (IPA) and Google Scholar were searched for relevant original articles, review papers and other publications over the publication period 1995–2012.
Results and Discussion: The National Institute of Neurological Disorders and Stroke (NINDS) (1995, N = 624 patients) and ECASS III (2008, N = 821 patients) are two pivotal randomized controlled trials providing evidence for the use of intravenous tPA within 3 h or 3–4·5 h from stroke onset, respectively. Both trials have shown that tPA administration decreases disability at 90 days from stroke. Furthermore, a recent pooled analysis of randomized controlled trials (2010, N = 3670 patients) supports these results, highlighting that early stroke treatment is associated with better outcomes, especially when treatment is started within 90 min of stroke onset (but suggesting that the benefit could be afforded within a 4·5‐h time window). Three major observational trials, STARS (2000, N = 389 patients), CASES (2005, N = 1135 patients) and SITS‐MOST (2007, N = 6483 patients), have reported acceptable safety and efficacy in clinical practice. However, only a small proportion of acute ischaemic stroke patients receive tPA in clinical practice, because of the limited availability of tPA‐utilizing sites and suboptimal use of tPA in sites where it is available.
What is new and Conclusion: tPA reduces disability in stroke patients. Moreover, acceptable safety has been demonstrated in routine clinical practice. However, tPA is significantly underutilized, and specific efforts are needed to encourage appropriate implementation of the stroke treatment guidelines to optimize the use of this important therapy. |
doi_str_mv | 10.1111/j.1365-2710.2012.01366.x |
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What is known and Objective: Thrombolysis using intravenous tissue plasminogen activator (tPA) is the only available evidence‐based treatment for acute ischaemic stroke; however, its current utilization is very low. Therefore, the aim of this article is to review the literature regarding the use of intravenous tPA for the treatment of acute ischaemic stroke. The review will also compare utilization rates of thrombolysis in different centres across the world and identify key reasons for the underutilization of thrombolysis in stroke.
Methods: MEDLINE, EMBASE, International Pharmaceutical s (IPA) and Google Scholar were searched for relevant original articles, review papers and other publications over the publication period 1995–2012.
Results and Discussion: The National Institute of Neurological Disorders and Stroke (NINDS) (1995, N = 624 patients) and ECASS III (2008, N = 821 patients) are two pivotal randomized controlled trials providing evidence for the use of intravenous tPA within 3 h or 3–4·5 h from stroke onset, respectively. Both trials have shown that tPA administration decreases disability at 90 days from stroke. Furthermore, a recent pooled analysis of randomized controlled trials (2010, N = 3670 patients) supports these results, highlighting that early stroke treatment is associated with better outcomes, especially when treatment is started within 90 min of stroke onset (but suggesting that the benefit could be afforded within a 4·5‐h time window). Three major observational trials, STARS (2000, N = 389 patients), CASES (2005, N = 1135 patients) and SITS‐MOST (2007, N = 6483 patients), have reported acceptable safety and efficacy in clinical practice. However, only a small proportion of acute ischaemic stroke patients receive tPA in clinical practice, because of the limited availability of tPA‐utilizing sites and suboptimal use of tPA in sites where it is available.
What is new and Conclusion: tPA reduces disability in stroke patients. Moreover, acceptable safety has been demonstrated in routine clinical practice. However, tPA is significantly underutilized, and specific efforts are needed to encourage appropriate implementation of the stroke treatment guidelines to optimize the use of this important therapy.</description><identifier>ISSN: 0269-4727</identifier><identifier>EISSN: 1365-2710</identifier><identifier>DOI: 10.1111/j.1365-2710.2012.01366.x</identifier><identifier>PMID: 22708668</identifier><identifier>CODEN: JCPTED</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>alteplase ; Biological and medical sciences ; Brain Ischemia - drug therapy ; Brain Ischemia - pathology ; cerebrovascular accident ; Evidence-Based Medicine ; Fibrinolytic Agents - administration & dosage ; Fibrinolytic Agents - adverse effects ; Fibrinolytic Agents - therapeutic use ; Guideline Adherence ; Humans ; Medical sciences ; Neurology ; Pharmacology. Drug treatments ; Practice Guidelines as Topic ; stroke ; Stroke - drug therapy ; Stroke - pathology ; thrombolysis ; Thrombolytic Therapy - adverse effects ; Thrombolytic Therapy - methods ; Thrombolytic Therapy - utilization ; Time Factors ; tissue Plasminogen Activator (tPA) ; Tissue Plasminogen Activator - administration & dosage ; Tissue Plasminogen Activator - adverse effects ; Tissue Plasminogen Activator - therapeutic use ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Journal of clinical pharmacy and therapeutics, 2012-12, Vol.37 (6), p.620-629</ispartof><rights>2012 Blackwell Publishing Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2012 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4676-389563864f012147ac231ba091ffb0237ef060e27138a87e96c1079e926e2e343</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2710.2012.01366.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2710.2012.01366.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26585685$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22708668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eissa, A.</creatorcontrib><creatorcontrib>Krass, I.</creatorcontrib><creatorcontrib>Bajorek, B. V.</creatorcontrib><title>Optimizing the management of acute ischaemic stroke: a review of the utilization of intravenous recombinant tissue plasminogen activator (tPA)</title><title>Journal of clinical pharmacy and therapeutics</title><addtitle>J Clin Pharm Ther</addtitle><description>Summary
What is known and Objective: Thrombolysis using intravenous tissue plasminogen activator (tPA) is the only available evidence‐based treatment for acute ischaemic stroke; however, its current utilization is very low. Therefore, the aim of this article is to review the literature regarding the use of intravenous tPA for the treatment of acute ischaemic stroke. The review will also compare utilization rates of thrombolysis in different centres across the world and identify key reasons for the underutilization of thrombolysis in stroke.
Methods: MEDLINE, EMBASE, International Pharmaceutical s (IPA) and Google Scholar were searched for relevant original articles, review papers and other publications over the publication period 1995–2012.
Results and Discussion: The National Institute of Neurological Disorders and Stroke (NINDS) (1995, N = 624 patients) and ECASS III (2008, N = 821 patients) are two pivotal randomized controlled trials providing evidence for the use of intravenous tPA within 3 h or 3–4·5 h from stroke onset, respectively. Both trials have shown that tPA administration decreases disability at 90 days from stroke. Furthermore, a recent pooled analysis of randomized controlled trials (2010, N = 3670 patients) supports these results, highlighting that early stroke treatment is associated with better outcomes, especially when treatment is started within 90 min of stroke onset (but suggesting that the benefit could be afforded within a 4·5‐h time window). Three major observational trials, STARS (2000, N = 389 patients), CASES (2005, N = 1135 patients) and SITS‐MOST (2007, N = 6483 patients), have reported acceptable safety and efficacy in clinical practice. However, only a small proportion of acute ischaemic stroke patients receive tPA in clinical practice, because of the limited availability of tPA‐utilizing sites and suboptimal use of tPA in sites where it is available.
What is new and Conclusion: tPA reduces disability in stroke patients. Moreover, acceptable safety has been demonstrated in routine clinical practice. However, tPA is significantly underutilized, and specific efforts are needed to encourage appropriate implementation of the stroke treatment guidelines to optimize the use of this important therapy.</description><subject>alteplase</subject><subject>Biological and medical sciences</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - pathology</subject><subject>cerebrovascular accident</subject><subject>Evidence-Based Medicine</subject><subject>Fibrinolytic Agents - administration & dosage</subject><subject>Fibrinolytic Agents - adverse effects</subject><subject>Fibrinolytic Agents - therapeutic use</subject><subject>Guideline Adherence</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Pharmacology. Drug treatments</subject><subject>Practice Guidelines as Topic</subject><subject>stroke</subject><subject>Stroke - drug therapy</subject><subject>Stroke - pathology</subject><subject>thrombolysis</subject><subject>Thrombolytic Therapy - adverse effects</subject><subject>Thrombolytic Therapy - methods</subject><subject>Thrombolytic Therapy - utilization</subject><subject>Time Factors</subject><subject>tissue Plasminogen Activator (tPA)</subject><subject>Tissue Plasminogen Activator - administration & dosage</subject><subject>Tissue Plasminogen Activator - adverse effects</subject><subject>Tissue Plasminogen Activator - therapeutic use</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0269-4727</issn><issn>1365-2710</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd9u0zAUxi0EYmXwCsgSQhoXKf6T2AkXk6aKDdDEKhji0joNJ527xCm203V7CJ4Zh5Yi4Rvb5_z8-ZzzEUI5m_K03q6mXKoiEzoFBONiytJdTbePyOSQeEwmTKgqy7XQR-RZCCvGmNJCPiVHQmhWKlVOyK-rdbSdfbBuSeMN0g4cLLFDF2nfUKiHiNSG-gawszUN0fe3-I4C9bixeDcy46sh2tY-QLS9G0PWRQ8bdP0QElj33cI6SIrRhjAgXbcQOuv6Jbr0Q7QbiL2nJ3F-9uY5edJAG_DFfj8m387fX88-ZJdXFx9nZ5dZnSutMllWhZKlypvUPM811ELyBbCKN82CCamxYYphGoMsodRYqZozXWElFAqUuTwmJzvdte9_Dhii6VKX2LbgMFVtOJeVEpwVOqGv_kNX_eBdqs7wXPJK6yJniXq5p4ZFhz_M2tsO_L35O-kEvN4DEGpoGw-utuEfp4qyUGWRuNMdd2dbvD_kOTOj82ZlRoPNaLAZnTd_nDdb82k2vx6PSSDbCdgQcXsQAH9rlJa6MN8_X5h5_qX6qs-1kfI33EewaQ</recordid><startdate>201212</startdate><enddate>201212</enddate><creator>Eissa, A.</creator><creator>Krass, I.</creator><creator>Bajorek, B. V.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Hindawi Limited</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>201212</creationdate><title>Optimizing the management of acute ischaemic stroke: a review of the utilization of intravenous recombinant tissue plasminogen activator (tPA)</title><author>Eissa, A. ; Krass, I. ; Bajorek, B. V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4676-389563864f012147ac231ba091ffb0237ef060e27138a87e96c1079e926e2e343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>alteplase</topic><topic>Biological and medical sciences</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - pathology</topic><topic>cerebrovascular accident</topic><topic>Evidence-Based Medicine</topic><topic>Fibrinolytic Agents - administration & dosage</topic><topic>Fibrinolytic Agents - adverse effects</topic><topic>Fibrinolytic Agents - therapeutic use</topic><topic>Guideline Adherence</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Neurology</topic><topic>Pharmacology. Drug treatments</topic><topic>Practice Guidelines as Topic</topic><topic>stroke</topic><topic>Stroke - drug therapy</topic><topic>Stroke - pathology</topic><topic>thrombolysis</topic><topic>Thrombolytic Therapy - adverse effects</topic><topic>Thrombolytic Therapy - methods</topic><topic>Thrombolytic Therapy - utilization</topic><topic>Time Factors</topic><topic>tissue Plasminogen Activator (tPA)</topic><topic>Tissue Plasminogen Activator - administration & dosage</topic><topic>Tissue Plasminogen Activator - adverse effects</topic><topic>Tissue Plasminogen Activator - therapeutic use</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eissa, A.</creatorcontrib><creatorcontrib>Krass, I.</creatorcontrib><creatorcontrib>Bajorek, B. V.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical pharmacy and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eissa, A.</au><au>Krass, I.</au><au>Bajorek, B. V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimizing the management of acute ischaemic stroke: a review of the utilization of intravenous recombinant tissue plasminogen activator (tPA)</atitle><jtitle>Journal of clinical pharmacy and therapeutics</jtitle><addtitle>J Clin Pharm Ther</addtitle><date>2012-12</date><risdate>2012</risdate><volume>37</volume><issue>6</issue><spage>620</spage><epage>629</epage><pages>620-629</pages><issn>0269-4727</issn><eissn>1365-2710</eissn><coden>JCPTED</coden><abstract>Summary
What is known and Objective: Thrombolysis using intravenous tissue plasminogen activator (tPA) is the only available evidence‐based treatment for acute ischaemic stroke; however, its current utilization is very low. Therefore, the aim of this article is to review the literature regarding the use of intravenous tPA for the treatment of acute ischaemic stroke. The review will also compare utilization rates of thrombolysis in different centres across the world and identify key reasons for the underutilization of thrombolysis in stroke.
Methods: MEDLINE, EMBASE, International Pharmaceutical s (IPA) and Google Scholar were searched for relevant original articles, review papers and other publications over the publication period 1995–2012.
Results and Discussion: The National Institute of Neurological Disorders and Stroke (NINDS) (1995, N = 624 patients) and ECASS III (2008, N = 821 patients) are two pivotal randomized controlled trials providing evidence for the use of intravenous tPA within 3 h or 3–4·5 h from stroke onset, respectively. Both trials have shown that tPA administration decreases disability at 90 days from stroke. Furthermore, a recent pooled analysis of randomized controlled trials (2010, N = 3670 patients) supports these results, highlighting that early stroke treatment is associated with better outcomes, especially when treatment is started within 90 min of stroke onset (but suggesting that the benefit could be afforded within a 4·5‐h time window). Three major observational trials, STARS (2000, N = 389 patients), CASES (2005, N = 1135 patients) and SITS‐MOST (2007, N = 6483 patients), have reported acceptable safety and efficacy in clinical practice. However, only a small proportion of acute ischaemic stroke patients receive tPA in clinical practice, because of the limited availability of tPA‐utilizing sites and suboptimal use of tPA in sites where it is available.
What is new and Conclusion: tPA reduces disability in stroke patients. Moreover, acceptable safety has been demonstrated in routine clinical practice. However, tPA is significantly underutilized, and specific efforts are needed to encourage appropriate implementation of the stroke treatment guidelines to optimize the use of this important therapy.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22708668</pmid><doi>10.1111/j.1365-2710.2012.01366.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alteplase Biological and medical sciences Brain Ischemia - drug therapy Brain Ischemia - pathology cerebrovascular accident Evidence-Based Medicine Fibrinolytic Agents - administration & dosage Fibrinolytic Agents - adverse effects Fibrinolytic Agents - therapeutic use Guideline Adherence Humans Medical sciences Neurology Pharmacology. Drug treatments Practice Guidelines as Topic stroke Stroke - drug therapy Stroke - pathology thrombolysis Thrombolytic Therapy - adverse effects Thrombolytic Therapy - methods Thrombolytic Therapy - utilization Time Factors tissue Plasminogen Activator (tPA) Tissue Plasminogen Activator - administration & dosage Tissue Plasminogen Activator - adverse effects Tissue Plasminogen Activator - therapeutic use Vascular diseases and vascular malformations of the nervous system |
title | Optimizing the management of acute ischaemic stroke: a review of the utilization of intravenous recombinant tissue plasminogen activator (tPA) |
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