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Immunotherapy for arterial ischaemic stroke in childhood: a systematic review
BackgroundThere is little evidence about either prevention or treatment of childhood arterial ischaemic stroke (AIS). However, drugs that regulate the immune and inflammatory response could theoretically prevent occurrence or recurrence of AIS. Additionally, as an acute treatment, they may limit the...
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Published in: | Archives of disease in childhood 2017-05, Vol.102 (5), p.410-415 |
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description | BackgroundThere is little evidence about either prevention or treatment of childhood arterial ischaemic stroke (AIS). However, drugs that regulate the immune and inflammatory response could theoretically prevent occurrence or recurrence of AIS. Additionally, as an acute treatment, they may limit the neurological damage caused by AIS. Here, we systematically review the evidence on the use of immunotherapy in childhood AIS.DesignA systematic review of publications in databases Embase and Medline from inception. All types of evidence were included from trials, cohorts, case–control and cross-sectional studies and case reports.Results34 reports were included: 32 observational studies and 2 trials. Immunotherapy was used in two key patient groups: arteriopathy and acute infection. The majority were cases of varicella and primary angiitis of the central nervous system. All three cohorts and 80% of the case studies were treated with steroids. Recurrence rates were low. Analytical studies weakly associated steroids with lower odds of new stroke and neurological deficits, and better cognitive outcomes in the context of Moyamoya disease and tuberculosis.ConclusionsImmunotherapies are used in children with AIS, mainly as steroids for children with arteriopathy. However, there is currently little robust evidence to either encourage or discourage this practice. There is weak evidence consistent with the hypothesis that in certain children at risk, steroids may both reduce the risk of occurrent/recurrent stroke and enhance neurological outcomes. As the potential benefit is still uncertain, this indicates that a trial of steroids in childhood AIS may be justified. |
doi_str_mv | 10.1136/archdischild-2016-311034 |
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However, drugs that regulate the immune and inflammatory response could theoretically prevent occurrence or recurrence of AIS. Additionally, as an acute treatment, they may limit the neurological damage caused by AIS. Here, we systematically review the evidence on the use of immunotherapy in childhood AIS.DesignA systematic review of publications in databases Embase and Medline from inception. All types of evidence were included from trials, cohorts, case–control and cross-sectional studies and case reports.Results34 reports were included: 32 observational studies and 2 trials. Immunotherapy was used in two key patient groups: arteriopathy and acute infection. The majority were cases of varicella and primary angiitis of the central nervous system. All three cohorts and 80% of the case studies were treated with steroids. Recurrence rates were low. Analytical studies weakly associated steroids with lower odds of new stroke and neurological deficits, and better cognitive outcomes in the context of Moyamoya disease and tuberculosis.ConclusionsImmunotherapies are used in children with AIS, mainly as steroids for children with arteriopathy. However, there is currently little robust evidence to either encourage or discourage this practice. There is weak evidence consistent with the hypothesis that in certain children at risk, steroids may both reduce the risk of occurrent/recurrent stroke and enhance neurological outcomes. As the potential benefit is still uncertain, this indicates that a trial of steroids in childhood AIS may be justified.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2016-311034</identifier><identifier>PMID: 27864289</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd</publisher><subject>Adults ; Anatomy ; Attrition (Research Studies) ; Brain Ischemia - complications ; Care and treatment ; Cell adhesion & migration ; Central nervous system ; Central Nervous System Infections - complications ; Child ; Children ; Evidence ; Evidence-Based Medicine - methods ; Glucocorticoids - therapeutic use ; Health aspects ; Humans ; Hypotheses ; Immunology ; Immunotherapy ; Immunotherapy - methods ; Infections ; Intracranial Arterial Diseases - complications ; Mortality ; Observational studies ; Patients ; Prevention ; Secondary Prevention - methods ; Steroids ; Stroke ; Stroke (Disease) ; Stroke - etiology ; Stroke - therapy ; Studies</subject><ispartof>Archives of disease in childhood, 2017-05, Vol.102 (5), p.410-415</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing</rights><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.</rights><rights>Copyright: 2016 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b508t-803edbd2a98523013720a36756eae585771ac15f9f8485666ee1814e148bdd223</citedby><cites>FETCH-LOGICAL-b508t-803edbd2a98523013720a36756eae585771ac15f9f8485666ee1814e148bdd223</cites><orcidid>0000-0002-1885-4771</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1894678777/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1894678777?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,21357,21373,27901,27902,33588,33589,33854,33855,43709,43856,73964,74140</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27864289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Edwards, Hannah B</creatorcontrib><creatorcontrib>Mallick, Andrew A</creatorcontrib><creatorcontrib>O'Callaghan, Finbar J K</creatorcontrib><title>Immunotherapy for arterial ischaemic stroke in childhood: a systematic review</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><description>BackgroundThere is little evidence about either prevention or treatment of childhood arterial ischaemic stroke (AIS). However, drugs that regulate the immune and inflammatory response could theoretically prevent occurrence or recurrence of AIS. Additionally, as an acute treatment, they may limit the neurological damage caused by AIS. Here, we systematically review the evidence on the use of immunotherapy in childhood AIS.DesignA systematic review of publications in databases Embase and Medline from inception. All types of evidence were included from trials, cohorts, case–control and cross-sectional studies and case reports.Results34 reports were included: 32 observational studies and 2 trials. Immunotherapy was used in two key patient groups: arteriopathy and acute infection. The majority were cases of varicella and primary angiitis of the central nervous system. All three cohorts and 80% of the case studies were treated with steroids. Recurrence rates were low. Analytical studies weakly associated steroids with lower odds of new stroke and neurological deficits, and better cognitive outcomes in the context of Moyamoya disease and tuberculosis.ConclusionsImmunotherapies are used in children with AIS, mainly as steroids for children with arteriopathy. However, there is currently little robust evidence to either encourage or discourage this practice. There is weak evidence consistent with the hypothesis that in certain children at risk, steroids may both reduce the risk of occurrent/recurrent stroke and enhance neurological outcomes. As the potential benefit is still uncertain, this indicates that a trial of steroids in childhood AIS may be justified.</description><subject>Adults</subject><subject>Anatomy</subject><subject>Attrition (Research Studies)</subject><subject>Brain Ischemia - complications</subject><subject>Care and treatment</subject><subject>Cell adhesion & migration</subject><subject>Central nervous system</subject><subject>Central Nervous System Infections - complications</subject><subject>Child</subject><subject>Children</subject><subject>Evidence</subject><subject>Evidence-Based Medicine - methods</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Immunology</subject><subject>Immunotherapy</subject><subject>Immunotherapy - methods</subject><subject>Infections</subject><subject>Intracranial Arterial Diseases - complications</subject><subject>Mortality</subject><subject>Observational studies</subject><subject>Patients</subject><subject>Prevention</subject><subject>Secondary Prevention - methods</subject><subject>Steroids</subject><subject>Stroke</subject><subject>Stroke (Disease)</subject><subject>Stroke - etiology</subject><subject>Stroke - therapy</subject><subject>Studies</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>CJNVE</sourceid><sourceid>M0P</sourceid><recordid>eNqNkU1v1DAQhi0EokvhLyBLXLgE_O0xt2oFpVJRL3C2nGTSzZLEi50U9t_XSwpCnHoaafTMOzN6CKGcveNcmvchNbu2z82uH9pKMG4qyTmT6gnZcGWgtJR6SjaMMVk5ADgjL3LeM8YFgHxOzoQFowS4DflyNY7LFOcdpnA40i4mGtKMqQ8DPS0IOPYNzXOK35H2E_29chdj-4EGmo95xjHMhUh41-PPl-RZF4aMrx7qOfn26ePX7efq-ubyantxXdWawVwBk9jWrQgOtJCMSytYkMZqgwE1aGt5aLjuXAcKtDEGkQNXyBXUbSuEPCdv19xDij8WzLMfy7E4DGHCuGTPwVnpuHbuEaji1jlnTUHf_Ifu45Km8sgpUBkL1tpCVSt1Gwb0_dTEacZfcxOHAW_Rlz-3N_5COStAM8MKDyvfpJhzws4fUj-GdPSc-ZNN_69Nf7LpV5tl9PXDQUs9Yvt38I--AsgVqMf942PvAYFErQA</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Edwards, Hannah B</creator><creator>Mallick, Andrew A</creator><creator>O'Callaghan, Finbar J K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group 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>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope><orcidid>https://orcid.org/0000-0002-1885-4771</orcidid></search><sort><creationdate>20170501</creationdate><title>Immunotherapy for arterial ischaemic stroke in childhood: a systematic review</title><author>Edwards, Hannah B ; Mallick, Andrew A ; O'Callaghan, Finbar J K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b508t-803edbd2a98523013720a36756eae585771ac15f9f8485666ee1814e148bdd223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adults</topic><topic>Anatomy</topic><topic>Attrition (Research Studies)</topic><topic>Brain Ischemia - complications</topic><topic>Care and treatment</topic><topic>Cell adhesion & migration</topic><topic>Central nervous system</topic><topic>Central Nervous System Infections - complications</topic><topic>Child</topic><topic>Children</topic><topic>Evidence</topic><topic>Evidence-Based Medicine - methods</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Immunology</topic><topic>Immunotherapy</topic><topic>Immunotherapy - methods</topic><topic>Infections</topic><topic>Intracranial Arterial Diseases - complications</topic><topic>Mortality</topic><topic>Observational studies</topic><topic>Patients</topic><topic>Prevention</topic><topic>Secondary Prevention - methods</topic><topic>Steroids</topic><topic>Stroke</topic><topic>Stroke (Disease)</topic><topic>Stroke - etiology</topic><topic>Stroke - therapy</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Edwards, Hannah B</creatorcontrib><creatorcontrib>Mallick, Andrew A</creatorcontrib><creatorcontrib>O'Callaghan, Finbar J K</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 Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Education</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Edwards, Hannah B</au><au>Mallick, Andrew A</au><au>O'Callaghan, Finbar J K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunotherapy for arterial ischaemic stroke in childhood: a systematic review</atitle><jtitle>Archives of disease in childhood</jtitle><addtitle>Arch Dis Child</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>102</volume><issue>5</issue><spage>410</spage><epage>415</epage><pages>410-415</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><coden>ADCHAK</coden><abstract>BackgroundThere is little evidence about either prevention or treatment of childhood arterial ischaemic stroke (AIS). However, drugs that regulate the immune and inflammatory response could theoretically prevent occurrence or recurrence of AIS. Additionally, as an acute treatment, they may limit the neurological damage caused by AIS. Here, we systematically review the evidence on the use of immunotherapy in childhood AIS.DesignA systematic review of publications in databases Embase and Medline from inception. All types of evidence were included from trials, cohorts, case–control and cross-sectional studies and case reports.Results34 reports were included: 32 observational studies and 2 trials. Immunotherapy was used in two key patient groups: arteriopathy and acute infection. The majority were cases of varicella and primary angiitis of the central nervous system. All three cohorts and 80% of the case studies were treated with steroids. Recurrence rates were low. Analytical studies weakly associated steroids with lower odds of new stroke and neurological deficits, and better cognitive outcomes in the context of Moyamoya disease and tuberculosis.ConclusionsImmunotherapies are used in children with AIS, mainly as steroids for children with arteriopathy. However, there is currently little robust evidence to either encourage or discourage this practice. There is weak evidence consistent with the hypothesis that in certain children at risk, steroids may both reduce the risk of occurrent/recurrent stroke and enhance neurological outcomes. As the potential benefit is still uncertain, this indicates that a trial of steroids in childhood AIS may be justified.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd</pub><pmid>27864289</pmid><doi>10.1136/archdischild-2016-311034</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-1885-4771</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adults Anatomy Attrition (Research Studies) Brain Ischemia - complications Care and treatment Cell adhesion & migration Central nervous system Central Nervous System Infections - complications Child Children Evidence Evidence-Based Medicine - methods Glucocorticoids - therapeutic use Health aspects Humans Hypotheses Immunology Immunotherapy Immunotherapy - methods Infections Intracranial Arterial Diseases - complications Mortality Observational studies Patients Prevention Secondary Prevention - methods Steroids Stroke Stroke (Disease) Stroke - etiology Stroke - therapy Studies |
title | Immunotherapy for arterial ischaemic stroke in childhood: a systematic review |
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