The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Protocol: A Randomized, Blinded, Efficacy Trial of Standard vs. Intensive Hyperglycemia Management in Acute Stroke
Rationale Patients with acute ischemic stroke and hyperglycemia have worse outcomes than those without hyperglycemia. Intensive glucose control during acute stroke is feasible and can be accomplished safely but has not been fully assessed for efficacy. Aims The Stroke Hyperglycemia Insulin Network E...
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Veröffentlicht in: | International journal of stroke 2014-02, Vol.9 (2), p.246-251 |
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creator | Bruno, Askiel Durkalski, Valerie L. Hall, Christiana E. Juneja, Rattan Barsan, William G. Janis, Scott Meurer, William J. Fansler, Amy Johnston, Karen C. |
description | Rationale
Patients with acute ischemic stroke and hyperglycemia have worse outcomes than those without hyperglycemia. Intensive glucose control during acute stroke is feasible and can be accomplished safely but has not been fully assessed for efficacy.
Aims
The Stroke Hyperglycemia Insulin Network Effort trial aims to determine the safety and efficacy of standard vs. intensive glucose control with insulin in hyperglycemic acute ischemic stroke patients.
Design
This is a randomized, blinded, multicenter, phase III trial of approximately 1400 hyperglycemic patients who receive either standard sliding scale subcutaneous insulin (blood glucose range 80–179 mg/dL, 4·44–9·93 mmol/L) or continuous intravenous insulin (target blood glucose 80–130 mg/dL, 4·44–7·21 mmol/L) for up to 72 h, starting within 12 h of stroke symptom onset. The acute treatment phase is single blind (for the patients), but the final outcome assessment is double blind. The study is powered to detect a 7% absolute difference in favorable outcome at 90 days.
Study outcomes
The primary outcome is a baseline severity adjusted 90-day modified Rankin Scale score, defined as 0, 0–1, or 0–2, if the baseline National Institutes of Health Stroke Scale score is 3–7, 8–14, or 15–22, respectively. The primary safety outcome is the rate of severe hypoglycemia ( |
doi_str_mv | 10.1111/ijs.12045 |
format | Article |
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Patients with acute ischemic stroke and hyperglycemia have worse outcomes than those without hyperglycemia. Intensive glucose control during acute stroke is feasible and can be accomplished safely but has not been fully assessed for efficacy.
Aims
The Stroke Hyperglycemia Insulin Network Effort trial aims to determine the safety and efficacy of standard vs. intensive glucose control with insulin in hyperglycemic acute ischemic stroke patients.
Design
This is a randomized, blinded, multicenter, phase III trial of approximately 1400 hyperglycemic patients who receive either standard sliding scale subcutaneous insulin (blood glucose range 80–179 mg/dL, 4·44–9·93 mmol/L) or continuous intravenous insulin (target blood glucose 80–130 mg/dL, 4·44–7·21 mmol/L) for up to 72 h, starting within 12 h of stroke symptom onset. The acute treatment phase is single blind (for the patients), but the final outcome assessment is double blind. The study is powered to detect a 7% absolute difference in favorable outcome at 90 days.
Study outcomes
The primary outcome is a baseline severity adjusted 90-day modified Rankin Scale score, defined as 0, 0–1, or 0–2, if the baseline National Institutes of Health Stroke Scale score is 3–7, 8–14, or 15–22, respectively. The primary safety outcome is the rate of severe hypoglycemia (<40 mg/dL, <2·22 mmol/L).
Discussion
This trial will provide important novel information about preferred management of acute ischemic stroke patients with hyperglycemia. It will determine the potential benefits and risks of intensive glucose control during acute stroke.</description><identifier>ISSN: 1747-4930</identifier><identifier>ISSN: 1747-4949</identifier><identifier>EISSN: 1747-4949</identifier><identifier>DOI: 10.1111/ijs.12045</identifier><identifier>PMID: 23506245</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>acute ischemic stroke ; Adult ; Blood ; Blood Glucose - drug effects ; cerebral infarction ; clinical trial ; Double-Blind Method ; Female ; Humans ; hyperglycemia ; Hyperglycemia - etiology ; Hyperglycemia - therapy ; Hypoglycemic Agents - therapeutic use ; Insulin - therapeutic use ; Male ; Middle Aged ; protocols ; Stroke - complications ; Time Factors ; Treatment Outcome ; United States ; Young Adult</subject><ispartof>International journal of stroke, 2014-02, Vol.9 (2), p.246-251</ispartof><rights>2013 The Authors</rights><rights>2013 The Authors. International Journal of Stroke © 2013 World Stroke Organization</rights><rights>2013 The Authors. International Journal of Stroke © 2013 World Stroke Organization.</rights><rights>International Journal of Stroke © 2014 World Stroke Organization</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4525-56b2a05692455458259528a8b1a3c2b0935b09b5f4227f5cfed7cb3eed2d03f53</citedby><cites>FETCH-LOGICAL-c4525-56b2a05692455458259528a8b1a3c2b0935b09b5f4227f5cfed7cb3eed2d03f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1111/ijs.12045$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1111/ijs.12045$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,777,781,1412,21800,27905,27906,43602,43603,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23506245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bruno, Askiel</creatorcontrib><creatorcontrib>Durkalski, Valerie L.</creatorcontrib><creatorcontrib>Hall, Christiana E.</creatorcontrib><creatorcontrib>Juneja, Rattan</creatorcontrib><creatorcontrib>Barsan, William G.</creatorcontrib><creatorcontrib>Janis, Scott</creatorcontrib><creatorcontrib>Meurer, William J.</creatorcontrib><creatorcontrib>Fansler, Amy</creatorcontrib><creatorcontrib>Johnston, Karen C.</creatorcontrib><creatorcontrib>SHINE investigators</creatorcontrib><title>The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Protocol: A Randomized, Blinded, Efficacy Trial of Standard vs. Intensive Hyperglycemia Management in Acute Stroke</title><title>International journal of stroke</title><addtitle>Int J Stroke</addtitle><description>Rationale
Patients with acute ischemic stroke and hyperglycemia have worse outcomes than those without hyperglycemia. Intensive glucose control during acute stroke is feasible and can be accomplished safely but has not been fully assessed for efficacy.
Aims
The Stroke Hyperglycemia Insulin Network Effort trial aims to determine the safety and efficacy of standard vs. intensive glucose control with insulin in hyperglycemic acute ischemic stroke patients.
Design
This is a randomized, blinded, multicenter, phase III trial of approximately 1400 hyperglycemic patients who receive either standard sliding scale subcutaneous insulin (blood glucose range 80–179 mg/dL, 4·44–9·93 mmol/L) or continuous intravenous insulin (target blood glucose 80–130 mg/dL, 4·44–7·21 mmol/L) for up to 72 h, starting within 12 h of stroke symptom onset. The acute treatment phase is single blind (for the patients), but the final outcome assessment is double blind. The study is powered to detect a 7% absolute difference in favorable outcome at 90 days.
Study outcomes
The primary outcome is a baseline severity adjusted 90-day modified Rankin Scale score, defined as 0, 0–1, or 0–2, if the baseline National Institutes of Health Stroke Scale score is 3–7, 8–14, or 15–22, respectively. The primary safety outcome is the rate of severe hypoglycemia (<40 mg/dL, <2·22 mmol/L).
Discussion
This trial will provide important novel information about preferred management of acute ischemic stroke patients with hyperglycemia. It will determine the potential benefits and risks of intensive glucose control during acute stroke.</description><subject>acute ischemic stroke</subject><subject>Adult</subject><subject>Blood</subject><subject>Blood Glucose - drug effects</subject><subject>cerebral infarction</subject><subject>clinical trial</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Humans</subject><subject>hyperglycemia</subject><subject>Hyperglycemia - etiology</subject><subject>Hyperglycemia - therapy</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>protocols</subject><subject>Stroke - complications</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>United States</subject><subject>Young Adult</subject><issn>1747-4930</issn><issn>1747-4949</issn><issn>1747-4949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkd1uEzEQhS0Eoj9wwQsgS0iolUjq390sd6EKTapSEAnXK693XJzuroO922r7VDxinSapUBESvhjPxTfnzOgg9IaSIY3vxC7DkDIi5DO0T1ORDkQmsuePPSd76CCEJYlEypOXaI9xSRIm5D76vfgJeN56dw142q_AX1W9htoqPGtCV9kGX0J76_w1nhjjfIuP5tPZ5eQYL7xVFf7mXeu0qz7iMf6umtLV9g7KD_hTnCzXTZyyWul-yzsTzSKnfIlvwjCatNAEe_PU_Itq1BXU0LQ4rjDWXbvb8hV6YVQV4PX2P0Q_Pk8Wp9PBxdez2en4YqCFZHIgk4IpIpMsXimFHDGZSTZSo4IqrllBMi5jKaQRjKVGagNlqgsOULKScCP5ITra6K68-9VBaPPaBg1VpRpwXcipyJJRJhLxXygliWApj-i7J-jSdb6Jh6wpIlORSRqp4w2lvQvBg8lX3tbK9zkl-TrxPCaePyQe2bdbxa6ooXwkdxFH4GQD3NoK-n8r5bPz-U7y_WYixAz-WPAv73tKI8Cs</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Bruno, Askiel</creator><creator>Durkalski, Valerie L.</creator><creator>Hall, Christiana E.</creator><creator>Juneja, Rattan</creator><creator>Barsan, William G.</creator><creator>Janis, Scott</creator><creator>Meurer, William J.</creator><creator>Fansler, Amy</creator><creator>Johnston, Karen C.</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201402</creationdate><title>The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Protocol: A Randomized, Blinded, Efficacy Trial of Standard vs. Intensive Hyperglycemia Management in Acute Stroke</title><author>Bruno, Askiel ; Durkalski, Valerie L. ; Hall, Christiana E. ; Juneja, Rattan ; Barsan, William G. ; Janis, Scott ; Meurer, William J. ; Fansler, Amy ; Johnston, Karen C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4525-56b2a05692455458259528a8b1a3c2b0935b09b5f4227f5cfed7cb3eed2d03f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>acute ischemic stroke</topic><topic>Adult</topic><topic>Blood</topic><topic>Blood Glucose - drug effects</topic><topic>cerebral infarction</topic><topic>clinical trial</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Humans</topic><topic>hyperglycemia</topic><topic>Hyperglycemia - etiology</topic><topic>Hyperglycemia - therapy</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>protocols</topic><topic>Stroke - complications</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>United States</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bruno, Askiel</creatorcontrib><creatorcontrib>Durkalski, Valerie L.</creatorcontrib><creatorcontrib>Hall, Christiana E.</creatorcontrib><creatorcontrib>Juneja, Rattan</creatorcontrib><creatorcontrib>Barsan, William G.</creatorcontrib><creatorcontrib>Janis, Scott</creatorcontrib><creatorcontrib>Meurer, William J.</creatorcontrib><creatorcontrib>Fansler, Amy</creatorcontrib><creatorcontrib>Johnston, Karen C.</creatorcontrib><creatorcontrib>SHINE 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>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of stroke</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bruno, Askiel</au><au>Durkalski, Valerie L.</au><au>Hall, Christiana E.</au><au>Juneja, Rattan</au><au>Barsan, William G.</au><au>Janis, Scott</au><au>Meurer, William J.</au><au>Fansler, Amy</au><au>Johnston, Karen C.</au><aucorp>SHINE investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Protocol: A Randomized, Blinded, Efficacy Trial of Standard vs. Intensive Hyperglycemia Management in Acute Stroke</atitle><jtitle>International journal of stroke</jtitle><addtitle>Int J Stroke</addtitle><date>2014-02</date><risdate>2014</risdate><volume>9</volume><issue>2</issue><spage>246</spage><epage>251</epage><pages>246-251</pages><issn>1747-4930</issn><issn>1747-4949</issn><eissn>1747-4949</eissn><abstract>Rationale
Patients with acute ischemic stroke and hyperglycemia have worse outcomes than those without hyperglycemia. Intensive glucose control during acute stroke is feasible and can be accomplished safely but has not been fully assessed for efficacy.
Aims
The Stroke Hyperglycemia Insulin Network Effort trial aims to determine the safety and efficacy of standard vs. intensive glucose control with insulin in hyperglycemic acute ischemic stroke patients.
Design
This is a randomized, blinded, multicenter, phase III trial of approximately 1400 hyperglycemic patients who receive either standard sliding scale subcutaneous insulin (blood glucose range 80–179 mg/dL, 4·44–9·93 mmol/L) or continuous intravenous insulin (target blood glucose 80–130 mg/dL, 4·44–7·21 mmol/L) for up to 72 h, starting within 12 h of stroke symptom onset. The acute treatment phase is single blind (for the patients), but the final outcome assessment is double blind. The study is powered to detect a 7% absolute difference in favorable outcome at 90 days.
Study outcomes
The primary outcome is a baseline severity adjusted 90-day modified Rankin Scale score, defined as 0, 0–1, or 0–2, if the baseline National Institutes of Health Stroke Scale score is 3–7, 8–14, or 15–22, respectively. The primary safety outcome is the rate of severe hypoglycemia (<40 mg/dL, <2·22 mmol/L).
Discussion
This trial will provide important novel information about preferred management of acute ischemic stroke patients with hyperglycemia. It will determine the potential benefits and risks of intensive glucose control during acute stroke.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>23506245</pmid><doi>10.1111/ijs.12045</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete; SAGE Complete A-Z List |
subjects | acute ischemic stroke Adult Blood Blood Glucose - drug effects cerebral infarction clinical trial Double-Blind Method Female Humans hyperglycemia Hyperglycemia - etiology Hyperglycemia - therapy Hypoglycemic Agents - therapeutic use Insulin - therapeutic use Male Middle Aged protocols Stroke - complications Time Factors Treatment Outcome United States Young Adult |
title | The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Protocol: A Randomized, Blinded, Efficacy Trial of Standard vs. Intensive Hyperglycemia Management in Acute Stroke |
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