Tracking psychosocial health in adults with epilepsy—Estimates from the 2010 National Health Interview Survey
Abstract Objective This study provides population-based estimates of psychosocial health among U.S. adults with epilepsy from the 2010 National Health Interview Survey. Methods Multinomial logistic regression was used to estimate the prevalence of the following measures of psychosocial health among...
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| Veröffentlicht in: | Epilepsy & behavior 2014-12, Vol.41, p.66-73 |
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| creator | Kobau, R Cui, W Kadima, N Zack, M.M Sajatovic, M Kaiboriboon, K Jobst, B |
| description | Abstract Objective This study provides population-based estimates of psychosocial health among U.S. adults with epilepsy from the 2010 National Health Interview Survey. Methods Multinomial logistic regression was used to estimate the prevalence of the following measures of psychosocial health among adults with epilepsy and those without epilepsy: 1) the Kessler-6 scale of serious psychological distress; 2) cognitive limitation, the extent of impairments associated with psychological problems, and work limitation; 3) social participation; and 4) the Patient-Reported Outcome Measurement Information System Global Health Scale. Results Compared with adults without epilepsy, adults with epilepsy, especially those with active epilepsy, reported significantly worse psychological health, more cognitive impairment, difficulty in participating in some social activities, and reduced health-related quality of life (HRQOL). Conclusions These disparities in psychosocial health in U.S. adults with epilepsy serve as baseline national estimates of their HRQOL, consistent with Healthy People 2020 national objectives on HRQOL. |
| doi_str_mv | 10.1016/j.yebeh.2014.08.002 |
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Methods Multinomial logistic regression was used to estimate the prevalence of the following measures of psychosocial health among adults with epilepsy and those without epilepsy: 1) the Kessler-6 scale of serious psychological distress; 2) cognitive limitation, the extent of impairments associated with psychological problems, and work limitation; 3) social participation; and 4) the Patient-Reported Outcome Measurement Information System Global Health Scale. Results Compared with adults without epilepsy, adults with epilepsy, especially those with active epilepsy, reported significantly worse psychological health, more cognitive impairment, difficulty in participating in some social activities, and reduced health-related quality of life (HRQOL). Conclusions These disparities in psychosocial health in U.S. adults with epilepsy serve as baseline national estimates of their HRQOL, consistent with Healthy People 2020 national objectives on HRQOL.</description><identifier>ISSN: 1525-5050</identifier><identifier>EISSN: 1525-5069</identifier><identifier>DOI: 10.1016/j.yebeh.2014.08.002</identifier><identifier>PMID: 25305435</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Cognition ; Cognition Disorders - epidemiology ; Cognition Disorders - etiology ; Cognition Disorders - psychology ; Epilepsy ; Epilepsy - complications ; Epilepsy - epidemiology ; Epilepsy - psychology ; Female ; Health Surveys - statistics & numerical data ; Humans ; Limitations ; Male ; Middle Aged ; Neurology ; Pain ; Psychological distress ; Quality of life ; Quality of Life - psychology ; Social participation ; Social Participation - psychology ; United States - epidemiology ; Young Adult</subject><ispartof>Epilepsy & behavior, 2014-12, Vol.41, p.66-73</ispartof><rights>2014</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c547t-f8cb95605a9f2ecda8071c35811dc58ab86ac171da0bcdb612169858c8738f723</citedby><cites>FETCH-LOGICAL-c547t-f8cb95605a9f2ecda8071c35811dc58ab86ac171da0bcdb612169858c8738f723</cites><orcidid>0000-0001-9754-3180 ; 0000-0002-0746-2318</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1525505014002807$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25305435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobau, R</creatorcontrib><creatorcontrib>Cui, W</creatorcontrib><creatorcontrib>Kadima, N</creatorcontrib><creatorcontrib>Zack, M.M</creatorcontrib><creatorcontrib>Sajatovic, M</creatorcontrib><creatorcontrib>Kaiboriboon, K</creatorcontrib><creatorcontrib>Jobst, B</creatorcontrib><title>Tracking psychosocial health in adults with epilepsy—Estimates from the 2010 National Health Interview Survey</title><title>Epilepsy & behavior</title><addtitle>Epilepsy Behav</addtitle><description>Abstract Objective This study provides population-based estimates of psychosocial health among U.S. adults with epilepsy from the 2010 National Health Interview Survey. Methods Multinomial logistic regression was used to estimate the prevalence of the following measures of psychosocial health among adults with epilepsy and those without epilepsy: 1) the Kessler-6 scale of serious psychological distress; 2) cognitive limitation, the extent of impairments associated with psychological problems, and work limitation; 3) social participation; and 4) the Patient-Reported Outcome Measurement Information System Global Health Scale. Results Compared with adults without epilepsy, adults with epilepsy, especially those with active epilepsy, reported significantly worse psychological health, more cognitive impairment, difficulty in participating in some social activities, and reduced health-related quality of life (HRQOL). Conclusions These disparities in psychosocial health in U.S. adults with epilepsy serve as baseline national estimates of their HRQOL, consistent with Healthy People 2020 national objectives on HRQOL.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Cognition</subject><subject>Cognition Disorders - epidemiology</subject><subject>Cognition Disorders - etiology</subject><subject>Cognition Disorders - psychology</subject><subject>Epilepsy</subject><subject>Epilepsy - complications</subject><subject>Epilepsy - epidemiology</subject><subject>Epilepsy - psychology</subject><subject>Female</subject><subject>Health Surveys - statistics & numerical data</subject><subject>Humans</subject><subject>Limitations</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Pain</subject><subject>Psychological distress</subject><subject>Quality of life</subject><subject>Quality of Life - psychology</subject><subject>Social participation</subject><subject>Social Participation - psychology</subject><subject>United States - epidemiology</subject><subject>Young Adult</subject><issn>1525-5050</issn><issn>1525-5069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNksFu1DAQhiMEoqXwBEjIRy4bxnGcOAcqoarQShUcWs6W40wab73xYjtb5cZD8IQ8CV5SVsAFTrbl__89M5-z7CWFnAKt3qzzGVsc8gJomYPIAYpH2THlBV9xqJrHhz2Ho-xZCGsASjmjT7OjgjPgJePHmbvxSt-Z8ZZsw6wHF5w2ypIBlY0DMSNR3WRjIPcmHXFrLCbd96_fzkM0GxUxkN67DYkDklQHkI8qGjemhIsl4XKM6HcG78n15Hc4P8-e9MoGfPGwnmSf35_fnF2srj59uDx7d7XSvKzjqhe6bXgFXDV9gbpTAmqqGReUdpoL1YpKaVrTTkGru7aiBa0awYUWNRN9XbCT7HTJ3U7tBjuNY_TKyq1PVftZOmXknzejGeSt28mSVyVwngJePwR492XCEOXGBI3WqhHdFCStKmANByH-Q8rqpqkTnyRli1R7F4LH_lARBbmnKtfyJ1W5pypByMX16vdmDp5fGJPg7SLANNI0bS-DNjhq7IxHHWXnzD8eOP3Lr60ZjVb2DmcMazf5xDR1IkMhQV7vP9b-X9EyuRMa9gNOx8uv</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Kobau, R</creator><creator>Cui, W</creator><creator>Kadima, N</creator><creator>Zack, M.M</creator><creator>Sajatovic, M</creator><creator>Kaiboriboon, K</creator><creator>Jobst, B</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><scope>7T2</scope><scope>7TK</scope><scope>7U2</scope><scope>C1K</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9754-3180</orcidid><orcidid>https://orcid.org/0000-0002-0746-2318</orcidid></search><sort><creationdate>20141201</creationdate><title>Tracking psychosocial health in adults with epilepsy—Estimates from the 2010 National Health Interview Survey</title><author>Kobau, R ; Cui, W ; Kadima, N ; Zack, M.M ; Sajatovic, M ; Kaiboriboon, K ; Jobst, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c547t-f8cb95605a9f2ecda8071c35811dc58ab86ac171da0bcdb612169858c8738f723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Cognition</topic><topic>Cognition Disorders - epidemiology</topic><topic>Cognition Disorders - etiology</topic><topic>Cognition Disorders - psychology</topic><topic>Epilepsy</topic><topic>Epilepsy - complications</topic><topic>Epilepsy - epidemiology</topic><topic>Epilepsy - psychology</topic><topic>Female</topic><topic>Health Surveys - statistics & numerical data</topic><topic>Humans</topic><topic>Limitations</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Pain</topic><topic>Psychological distress</topic><topic>Quality of life</topic><topic>Quality of Life - psychology</topic><topic>Social participation</topic><topic>Social Participation - psychology</topic><topic>United States - epidemiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobau, R</creatorcontrib><creatorcontrib>Cui, W</creatorcontrib><creatorcontrib>Kadima, N</creatorcontrib><creatorcontrib>Zack, M.M</creatorcontrib><creatorcontrib>Sajatovic, M</creatorcontrib><creatorcontrib>Kaiboriboon, K</creatorcontrib><creatorcontrib>Jobst, B</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><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Epilepsy & behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobau, R</au><au>Cui, W</au><au>Kadima, N</au><au>Zack, M.M</au><au>Sajatovic, M</au><au>Kaiboriboon, K</au><au>Jobst, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tracking psychosocial health in adults with epilepsy—Estimates from the 2010 National Health Interview Survey</atitle><jtitle>Epilepsy & behavior</jtitle><addtitle>Epilepsy Behav</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>41</volume><spage>66</spage><epage>73</epage><pages>66-73</pages><issn>1525-5050</issn><eissn>1525-5069</eissn><abstract>Abstract Objective This study provides population-based estimates of psychosocial health among U.S. adults with epilepsy from the 2010 National Health Interview Survey. Methods Multinomial logistic regression was used to estimate the prevalence of the following measures of psychosocial health among adults with epilepsy and those without epilepsy: 1) the Kessler-6 scale of serious psychological distress; 2) cognitive limitation, the extent of impairments associated with psychological problems, and work limitation; 3) social participation; and 4) the Patient-Reported Outcome Measurement Information System Global Health Scale. Results Compared with adults without epilepsy, adults with epilepsy, especially those with active epilepsy, reported significantly worse psychological health, more cognitive impairment, difficulty in participating in some social activities, and reduced health-related quality of life (HRQOL). Conclusions These disparities in psychosocial health in U.S. adults with epilepsy serve as baseline national estimates of their HRQOL, consistent with Healthy People 2020 national objectives on HRQOL.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25305435</pmid><doi>10.1016/j.yebeh.2014.08.002</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-9754-3180</orcidid><orcidid>https://orcid.org/0000-0002-0746-2318</orcidid><oa>free_for_read</oa></addata></record> |
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| subjects | Adolescent Adult Aged Cognition Cognition Disorders - epidemiology Cognition Disorders - etiology Cognition Disorders - psychology Epilepsy Epilepsy - complications Epilepsy - epidemiology Epilepsy - psychology Female Health Surveys - statistics & numerical data Humans Limitations Male Middle Aged Neurology Pain Psychological distress Quality of life Quality of Life - psychology Social participation Social Participation - psychology United States - epidemiology Young Adult |
| title | Tracking psychosocial health in adults with epilepsy—Estimates from the 2010 National Health Interview Survey |
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