Social outcomes for adults with a history of childhood-onset epilepsy: A systematic review and meta-analysis
This review aimed to describe social outcomes in adulthood for people with a history of childhood-onset epilepsy and identify factors associated with these outcomes; focused on educational attainment, employment, income/financial status, independence/living arrangement, romantic relationships, paren...
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Veröffentlicht in: | Epilepsy & behavior 2019-03, Vol.92, p.297-305 |
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description | This review aimed to describe social outcomes in adulthood for people with a history of childhood-onset epilepsy and identify factors associated with these outcomes; focused on educational attainment, employment, income/financial status, independence/living arrangement, romantic relationships, parenthood, and friendships.
A comprehensive search of MEDLINE, EMBASE, and PsycINFO was conducted, as well as forward and backward citation tracking. A total of 45 articles met inclusion criteria. Random effects meta-analyses were conducted, and subgroup analyses evaluated outcomes for people with epilepsy (PWE) with good prognosis (e.g., normal intelligence, ‘epilepsy-only’) and poor prognosis (e.g., intellectual disability, Dravet syndrome), and those who underwent epilepsy surgery in childhood.
Among all PWE, 73% (95% confidence interval [CI]: 64–82%) completed secondary school education, 63% (95%CI: 56–70%) were employed; 74% (95%CI: 68–81%) did not receive governmental financial assistance; 32% (95%CI: 25–39%) were in romantic relationships; 34% (95%CI: 24–45%) lived independently; 21% (95%CI:12–33%) had children, and 79% (95%CI: 71–87%) had close friend(s). People with epilepsy often fared worse relative to healthy controls. Among PWE with a good prognosis, a comparable number of studies reported similar/better outcomes relative to controls as reported poorer outcomes. The most consistent predictor of poorer outcomes was the presence of cognitive problems; results of studies evaluating seizure control were equivocal.
People with epilepsy with a good prognosis may show similar social outcomes as controls, though robust conclusions are difficult to make given the extant literature. Seizure control does not guarantee better outcomes. There is a need for more studies evaluating prognostic factors and studies with control groups to facilitate appropriate comparisons.
•Described social outcomes of adults with childhood-onset epilepsy•Poorer outcomes were consistently associated with cognitive problems.•Seizure control did not guarantee better outcomes.•Found considerable heterogeneity in patient samples & operationalization of outcomes•The review identified gaps in knowledge that should be targets of future research. |
doi_str_mv | 10.1016/j.yebeh.2019.01.012 |
format | Article |
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A comprehensive search of MEDLINE, EMBASE, and PsycINFO was conducted, as well as forward and backward citation tracking. A total of 45 articles met inclusion criteria. Random effects meta-analyses were conducted, and subgroup analyses evaluated outcomes for people with epilepsy (PWE) with good prognosis (e.g., normal intelligence, ‘epilepsy-only’) and poor prognosis (e.g., intellectual disability, Dravet syndrome), and those who underwent epilepsy surgery in childhood.
Among all PWE, 73% (95% confidence interval [CI]: 64–82%) completed secondary school education, 63% (95%CI: 56–70%) were employed; 74% (95%CI: 68–81%) did not receive governmental financial assistance; 32% (95%CI: 25–39%) were in romantic relationships; 34% (95%CI: 24–45%) lived independently; 21% (95%CI:12–33%) had children, and 79% (95%CI: 71–87%) had close friend(s). People with epilepsy often fared worse relative to healthy controls. Among PWE with a good prognosis, a comparable number of studies reported similar/better outcomes relative to controls as reported poorer outcomes. The most consistent predictor of poorer outcomes was the presence of cognitive problems; results of studies evaluating seizure control were equivocal.
People with epilepsy with a good prognosis may show similar social outcomes as controls, though robust conclusions are difficult to make given the extant literature. Seizure control does not guarantee better outcomes. There is a need for more studies evaluating prognostic factors and studies with control groups to facilitate appropriate comparisons.
•Described social outcomes of adults with childhood-onset epilepsy•Poorer outcomes were consistently associated with cognitive problems.•Seizure control did not guarantee better outcomes.•Found considerable heterogeneity in patient samples & operationalization of outcomes•The review identified gaps in knowledge that should be targets of future research.</description><identifier>ISSN: 1525-5050</identifier><identifier>EISSN: 1525-5069</identifier><identifier>DOI: 10.1016/j.yebeh.2019.01.012</identifier><identifier>PMID: 30731296</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Education ; Employment ; Income ; Marital status ; Pediatric ; Psychosocial</subject><ispartof>Epilepsy & behavior, 2019-03, Vol.92, p.297-305</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-a18a9e33bdb69e3903f69bb24f8020621ee7c319ef23b37b1edf1661d263cc3c3</citedby><cites>FETCH-LOGICAL-c359t-a18a9e33bdb69e3903f69bb24f8020621ee7c319ef23b37b1edf1661d263cc3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1525505018308850$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30731296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Puka, Klajdi</creatorcontrib><creatorcontrib>Tavares, Tamara P.</creatorcontrib><creatorcontrib>Speechley, Kathy N.</creatorcontrib><title>Social outcomes for adults with a history of childhood-onset epilepsy: A systematic review and meta-analysis</title><title>Epilepsy & behavior</title><addtitle>Epilepsy Behav</addtitle><description>This review aimed to describe social outcomes in adulthood for people with a history of childhood-onset epilepsy and identify factors associated with these outcomes; focused on educational attainment, employment, income/financial status, independence/living arrangement, romantic relationships, parenthood, and friendships.
A comprehensive search of MEDLINE, EMBASE, and PsycINFO was conducted, as well as forward and backward citation tracking. A total of 45 articles met inclusion criteria. Random effects meta-analyses were conducted, and subgroup analyses evaluated outcomes for people with epilepsy (PWE) with good prognosis (e.g., normal intelligence, ‘epilepsy-only’) and poor prognosis (e.g., intellectual disability, Dravet syndrome), and those who underwent epilepsy surgery in childhood.
Among all PWE, 73% (95% confidence interval [CI]: 64–82%) completed secondary school education, 63% (95%CI: 56–70%) were employed; 74% (95%CI: 68–81%) did not receive governmental financial assistance; 32% (95%CI: 25–39%) were in romantic relationships; 34% (95%CI: 24–45%) lived independently; 21% (95%CI:12–33%) had children, and 79% (95%CI: 71–87%) had close friend(s). People with epilepsy often fared worse relative to healthy controls. Among PWE with a good prognosis, a comparable number of studies reported similar/better outcomes relative to controls as reported poorer outcomes. The most consistent predictor of poorer outcomes was the presence of cognitive problems; results of studies evaluating seizure control were equivocal.
People with epilepsy with a good prognosis may show similar social outcomes as controls, though robust conclusions are difficult to make given the extant literature. Seizure control does not guarantee better outcomes. There is a need for more studies evaluating prognostic factors and studies with control groups to facilitate appropriate comparisons.
•Described social outcomes of adults with childhood-onset epilepsy•Poorer outcomes were consistently associated with cognitive problems.•Seizure control did not guarantee better outcomes.•Found considerable heterogeneity in patient samples & operationalization of outcomes•The review identified gaps in knowledge that should be targets of future research.</description><subject>Education</subject><subject>Employment</subject><subject>Income</subject><subject>Marital status</subject><subject>Pediatric</subject><subject>Psychosocial</subject><issn>1525-5050</issn><issn>1525-5069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kEFv1DAQhS0EoqXwC5CQj1yyeGzijZE4VBXQSpU4AGfLsSeKV068eByq_PumbOkR6UlvDu_NaD7G3oLYgQD94bBbscdxJwWYnYBN8hk7h1a2TSu0ef40t-KMvSI6CAHQKnjJzpTYK5BGn7P0I_voEs9L9XlC4kMu3IUlVeJ3sY7c8TFSzWXleeB-jCmMOYcmz4SV4zEmPNL6iV9yWqni5Gr0vOCfiHfczYFPWF3jZpdWivSavRhcInzz6Bfs19cvP6-um9vv326uLm8br1pTGwedM6hUH3q9uRFq0Kbv5cehE1JoCYh7r8DgIFWv9j1gGEBrCFIr75VXF-z9ae-x5N8LUrVTJI8puRnzQlZCp6Azpu22qDpFfclEBQd7LHFyZbUg7ANme7B_MdsHzFbAJrm13j0eWPoJw1PnH9ct8PkUwO3NDUax5CPOHkMs6KsNOf73wD1YJpCh</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Puka, Klajdi</creator><creator>Tavares, Tamara P.</creator><creator>Speechley, Kathy N.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201903</creationdate><title>Social outcomes for adults with a history of childhood-onset epilepsy: A systematic review and meta-analysis</title><author>Puka, Klajdi ; Tavares, Tamara P. ; Speechley, Kathy N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-a18a9e33bdb69e3903f69bb24f8020621ee7c319ef23b37b1edf1661d263cc3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Education</topic><topic>Employment</topic><topic>Income</topic><topic>Marital status</topic><topic>Pediatric</topic><topic>Psychosocial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Puka, Klajdi</creatorcontrib><creatorcontrib>Tavares, Tamara P.</creatorcontrib><creatorcontrib>Speechley, Kathy N.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Epilepsy & behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Puka, Klajdi</au><au>Tavares, Tamara P.</au><au>Speechley, Kathy N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Social outcomes for adults with a history of childhood-onset epilepsy: A systematic review and meta-analysis</atitle><jtitle>Epilepsy & behavior</jtitle><addtitle>Epilepsy Behav</addtitle><date>2019-03</date><risdate>2019</risdate><volume>92</volume><spage>297</spage><epage>305</epage><pages>297-305</pages><issn>1525-5050</issn><eissn>1525-5069</eissn><abstract>This review aimed to describe social outcomes in adulthood for people with a history of childhood-onset epilepsy and identify factors associated with these outcomes; focused on educational attainment, employment, income/financial status, independence/living arrangement, romantic relationships, parenthood, and friendships.
A comprehensive search of MEDLINE, EMBASE, and PsycINFO was conducted, as well as forward and backward citation tracking. A total of 45 articles met inclusion criteria. Random effects meta-analyses were conducted, and subgroup analyses evaluated outcomes for people with epilepsy (PWE) with good prognosis (e.g., normal intelligence, ‘epilepsy-only’) and poor prognosis (e.g., intellectual disability, Dravet syndrome), and those who underwent epilepsy surgery in childhood.
Among all PWE, 73% (95% confidence interval [CI]: 64–82%) completed secondary school education, 63% (95%CI: 56–70%) were employed; 74% (95%CI: 68–81%) did not receive governmental financial assistance; 32% (95%CI: 25–39%) were in romantic relationships; 34% (95%CI: 24–45%) lived independently; 21% (95%CI:12–33%) had children, and 79% (95%CI: 71–87%) had close friend(s). People with epilepsy often fared worse relative to healthy controls. Among PWE with a good prognosis, a comparable number of studies reported similar/better outcomes relative to controls as reported poorer outcomes. The most consistent predictor of poorer outcomes was the presence of cognitive problems; results of studies evaluating seizure control were equivocal.
People with epilepsy with a good prognosis may show similar social outcomes as controls, though robust conclusions are difficult to make given the extant literature. Seizure control does not guarantee better outcomes. There is a need for more studies evaluating prognostic factors and studies with control groups to facilitate appropriate comparisons.
•Described social outcomes of adults with childhood-onset epilepsy•Poorer outcomes were consistently associated with cognitive problems.•Seizure control did not guarantee better outcomes.•Found considerable heterogeneity in patient samples & operationalization of outcomes•The review identified gaps in knowledge that should be targets of future research.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30731296</pmid><doi>10.1016/j.yebeh.2019.01.012</doi><tpages>9</tpages></addata></record> |
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subjects | Education Employment Income Marital status Pediatric Psychosocial |
title | Social outcomes for adults with a history of childhood-onset epilepsy: A systematic review and meta-analysis |
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