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Prospective Population‐Based Study of Intermittent and Continuous Convulsive Status Epilepticus in Richmond, Virginia

Purpose: Previous work suggested that there is a lower mortality for convulsive status epilepticus (SE) with intermittent seizures (intermittent SE) as opposed to SE with continuous seizure activity (continuous SE). A plausible hypothesis to explain this difference is that the shorter ictal time in...

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Published in:Epilepsia (Copenhagen) 1999-06, Vol.40 (6), p.752-758
Main Authors: Waterhouse, Elizabeth J., Garnett, Linda K., Towne, Alan R., Morton, Lawrence D., Barnes, Thomas, Ko, Daijin, DeLorenzo, Robert J.
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container_title Epilepsia (Copenhagen)
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creator Waterhouse, Elizabeth J.
Garnett, Linda K.
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Barnes, Thomas
Ko, Daijin
DeLorenzo, Robert J.
description Purpose: Previous work suggested that there is a lower mortality for convulsive status epilepticus (SE) with intermittent seizures (intermittent SE) as opposed to SE with continuous seizure activity (continuous SE). A plausible hypothesis to explain this difference is that the shorter ictal time in intermittent SE is responsible for the lower mortality in this group. This study investigates the relative contributions of total ictal time and SE duration to the differing mortalities of intermittent and continuous SE. Methods: Six hundred forty‐five cases of prospectively identified convulsive SE were examined. Nonparametric statistical methods were used to compare continuous SE and intermittent SE variables. Multivariate logistic regression analyses were used to determine which factors were most highly associated with mortality. Intermittent SE cases were analyzed to evaluate the relative contributions of ictal time versus SE duration to mortality. Results: Intermittent SE had a significantly lower mortality than continuous SE (19.6 vs. 31.4%; p < 0.001) in adults but not in children. Intermittent and continuous SE durations did not significantly differ in adult cases but did differ in pediatric cases. Ictal time was significantly shorter than SE duration for intermittent SE in both adults and children. After adjusting for age, etiology, and SE duration, SE type (continuous SE vs. intermittent SE) was shown to have an independent effect on mortality in adults. The relative risk of mortality for continuous SE was 1.79 times that of intermittent SE (p = 0.04). After controlling for SE duration, ictal time did not significantly affect mortality in adults. Conclusions: Intermittent and continuous convulsive SE were common in both pediatric and adult populations. Intermittent SE had a significantly lower mortality than did continuous SE. This difference in mortality was not completely explained by differences in SE duration, total ictal time, etiology, or age. Further research is needed to identify the factor(s) contributing to the significant difference in mortality between intermittent SE and continuous SE.
doi_str_mv 10.1111/j.1528-1157.1999.tb00774.x
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A plausible hypothesis to explain this difference is that the shorter ictal time in intermittent SE is responsible for the lower mortality in this group. This study investigates the relative contributions of total ictal time and SE duration to the differing mortalities of intermittent and continuous SE. Methods: Six hundred forty‐five cases of prospectively identified convulsive SE were examined. Nonparametric statistical methods were used to compare continuous SE and intermittent SE variables. Multivariate logistic regression analyses were used to determine which factors were most highly associated with mortality. Intermittent SE cases were analyzed to evaluate the relative contributions of ictal time versus SE duration to mortality. Results: Intermittent SE had a significantly lower mortality than continuous SE (19.6 vs. 31.4%; p &lt; 0.001) in adults but not in children. Intermittent and continuous SE durations did not significantly differ in adult cases but did differ in pediatric cases. Ictal time was significantly shorter than SE duration for intermittent SE in both adults and children. After adjusting for age, etiology, and SE duration, SE type (continuous SE vs. intermittent SE) was shown to have an independent effect on mortality in adults. The relative risk of mortality for continuous SE was 1.79 times that of intermittent SE (p = 0.04). After controlling for SE duration, ictal time did not significantly affect mortality in adults. Conclusions: Intermittent and continuous convulsive SE were common in both pediatric and adult populations. Intermittent SE had a significantly lower mortality than did continuous SE. This difference in mortality was not completely explained by differences in SE duration, total ictal time, etiology, or age. Further research is needed to identify the factor(s) contributing to the significant difference in mortality between intermittent SE and continuous SE.</description><identifier>ISSN: 0013-9580</identifier><identifier>EISSN: 1528-1167</identifier><identifier>DOI: 10.1111/j.1528-1157.1999.tb00774.x</identifier><identifier>PMID: 10368074</identifier><identifier>CODEN: EPILAK</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Age Distribution ; Age Factors ; Biological and medical sciences ; Child ; Child, Preschool ; Continuous seizures ; Duration ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; Ictal time ; Infant ; Intermittent seizures ; Medical sciences ; Multivariate Analysis ; Nervous system (semeiology, syndromes) ; Neurology ; Odds Ratio ; Prospective Studies ; Risk Factors ; Severity of Illness Index ; Status epilepticus ; Status Epilepticus - classification ; Status Epilepticus - epidemiology ; Status Epilepticus - mortality ; Virginia - epidemiology</subject><ispartof>Epilepsia (Copenhagen), 1999-06, Vol.40 (6), p.752-758</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4942-2d50ea6ac174f53eac76dae0ce24e45c8b4d73f36a9539712a7d3c2ca54498d33</citedby><cites>FETCH-LOGICAL-c4942-2d50ea6ac174f53eac76dae0ce24e45c8b4d73f36a9539712a7d3c2ca54498d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1807270$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10368074$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Waterhouse, Elizabeth J.</creatorcontrib><creatorcontrib>Garnett, Linda K.</creatorcontrib><creatorcontrib>Towne, Alan R.</creatorcontrib><creatorcontrib>Morton, Lawrence D.</creatorcontrib><creatorcontrib>Barnes, Thomas</creatorcontrib><creatorcontrib>Ko, Daijin</creatorcontrib><creatorcontrib>DeLorenzo, Robert J.</creatorcontrib><title>Prospective Population‐Based Study of Intermittent and Continuous Convulsive Status Epilepticus in Richmond, Virginia</title><title>Epilepsia (Copenhagen)</title><addtitle>Epilepsia</addtitle><description>Purpose: Previous work suggested that there is a lower mortality for convulsive status epilepticus (SE) with intermittent seizures (intermittent SE) as opposed to SE with continuous seizure activity (continuous SE). A plausible hypothesis to explain this difference is that the shorter ictal time in intermittent SE is responsible for the lower mortality in this group. This study investigates the relative contributions of total ictal time and SE duration to the differing mortalities of intermittent and continuous SE. Methods: Six hundred forty‐five cases of prospectively identified convulsive SE were examined. Nonparametric statistical methods were used to compare continuous SE and intermittent SE variables. Multivariate logistic regression analyses were used to determine which factors were most highly associated with mortality. Intermittent SE cases were analyzed to evaluate the relative contributions of ictal time versus SE duration to mortality. Results: Intermittent SE had a significantly lower mortality than continuous SE (19.6 vs. 31.4%; p &lt; 0.001) in adults but not in children. Intermittent and continuous SE durations did not significantly differ in adult cases but did differ in pediatric cases. Ictal time was significantly shorter than SE duration for intermittent SE in both adults and children. After adjusting for age, etiology, and SE duration, SE type (continuous SE vs. intermittent SE) was shown to have an independent effect on mortality in adults. The relative risk of mortality for continuous SE was 1.79 times that of intermittent SE (p = 0.04). After controlling for SE duration, ictal time did not significantly affect mortality in adults. Conclusions: Intermittent and continuous convulsive SE were common in both pediatric and adult populations. Intermittent SE had a significantly lower mortality than did continuous SE. This difference in mortality was not completely explained by differences in SE duration, total ictal time, etiology, or age. Further research is needed to identify the factor(s) contributing to the significant difference in mortality between intermittent SE and continuous SE.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Distribution</subject><subject>Age Factors</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Continuous seizures</subject><subject>Duration</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>Ictal time</subject><subject>Infant</subject><subject>Intermittent seizures</subject><subject>Medical sciences</subject><subject>Multivariate Analysis</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Odds Ratio</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Severity of Illness Index</subject><subject>Status epilepticus</subject><subject>Status Epilepticus - classification</subject><subject>Status Epilepticus - epidemiology</subject><subject>Status Epilepticus - mortality</subject><subject>Virginia - epidemiology</subject><issn>0013-9580</issn><issn>1528-1167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqVkN2K1DAUgIMo7uzqK0gR8Wpb85_GC0GHUQcWHFz1NmSSVDO0abdJd3fufASf0ScxZQp6a25yOOc7P3wAPEewQvm9OlSI4bpEiIkKSSmrtIdQCFrdPwCrpcTFQ7CCEJFSshqegfMYDzBTXJDH4AxBwmso6Arc7cY-Ds4kf-uKXT9MrU6-D79__nqno7PFdZrsseibYhuSGzufkgup0MEW6z4kH6Z-inN4O7VxHnGddMqZzeBbNyRvcuxD8dmbH10f7GXxzY_fffD6CXjU6Da6p8t_Ab6-33xZfyyvPn3Yrt9elYZKiktsGXSaa4MEbRhx2ghutYPGYeooM_WeWkEawrVkRAqEtbDEYKMZpbK2hFyAl6e5w9jfTC4m1floXNvq4PLpissacwZ5Bl-fQJOFxNE1ahh9p8ejQlDN2tVBzW7VrF3N2tWiXd3n5mfLlmnfOftP68lzBl4sgI5Gt82og_HxL5chLGDG3pywu6zv-B8XqM1uKxgmfwBysqLi</recordid><startdate>199906</startdate><enddate>199906</enddate><creator>Waterhouse, Elizabeth J.</creator><creator>Garnett, Linda K.</creator><creator>Towne, Alan R.</creator><creator>Morton, Lawrence D.</creator><creator>Barnes, Thomas</creator><creator>Ko, Daijin</creator><creator>DeLorenzo, Robert J.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><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></search><sort><creationdate>199906</creationdate><title>Prospective Population‐Based Study of Intermittent and Continuous Convulsive Status Epilepticus in Richmond, Virginia</title><author>Waterhouse, Elizabeth J. ; Garnett, Linda K. ; Towne, Alan R. ; Morton, Lawrence D. ; Barnes, Thomas ; Ko, Daijin ; DeLorenzo, Robert J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4942-2d50ea6ac174f53eac76dae0ce24e45c8b4d73f36a9539712a7d3c2ca54498d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Distribution</topic><topic>Age Factors</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Continuous seizures</topic><topic>Duration</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>Ictal time</topic><topic>Infant</topic><topic>Intermittent seizures</topic><topic>Medical sciences</topic><topic>Multivariate Analysis</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Odds Ratio</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Severity of Illness Index</topic><topic>Status epilepticus</topic><topic>Status Epilepticus - classification</topic><topic>Status Epilepticus - epidemiology</topic><topic>Status Epilepticus - mortality</topic><topic>Virginia - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waterhouse, Elizabeth J.</creatorcontrib><creatorcontrib>Garnett, Linda K.</creatorcontrib><creatorcontrib>Towne, Alan R.</creatorcontrib><creatorcontrib>Morton, Lawrence D.</creatorcontrib><creatorcontrib>Barnes, Thomas</creatorcontrib><creatorcontrib>Ko, Daijin</creatorcontrib><creatorcontrib>DeLorenzo, Robert J.</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Epilepsia (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waterhouse, Elizabeth J.</au><au>Garnett, Linda K.</au><au>Towne, Alan R.</au><au>Morton, Lawrence D.</au><au>Barnes, Thomas</au><au>Ko, Daijin</au><au>DeLorenzo, Robert J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prospective Population‐Based Study of Intermittent and Continuous Convulsive Status Epilepticus in Richmond, Virginia</atitle><jtitle>Epilepsia (Copenhagen)</jtitle><addtitle>Epilepsia</addtitle><date>1999-06</date><risdate>1999</risdate><volume>40</volume><issue>6</issue><spage>752</spage><epage>758</epage><pages>752-758</pages><issn>0013-9580</issn><eissn>1528-1167</eissn><coden>EPILAK</coden><abstract>Purpose: Previous work suggested that there is a lower mortality for convulsive status epilepticus (SE) with intermittent seizures (intermittent SE) as opposed to SE with continuous seizure activity (continuous SE). A plausible hypothesis to explain this difference is that the shorter ictal time in intermittent SE is responsible for the lower mortality in this group. This study investigates the relative contributions of total ictal time and SE duration to the differing mortalities of intermittent and continuous SE. Methods: Six hundred forty‐five cases of prospectively identified convulsive SE were examined. Nonparametric statistical methods were used to compare continuous SE and intermittent SE variables. Multivariate logistic regression analyses were used to determine which factors were most highly associated with mortality. Intermittent SE cases were analyzed to evaluate the relative contributions of ictal time versus SE duration to mortality. Results: Intermittent SE had a significantly lower mortality than continuous SE (19.6 vs. 31.4%; p &lt; 0.001) in adults but not in children. Intermittent and continuous SE durations did not significantly differ in adult cases but did differ in pediatric cases. Ictal time was significantly shorter than SE duration for intermittent SE in both adults and children. After adjusting for age, etiology, and SE duration, SE type (continuous SE vs. intermittent SE) was shown to have an independent effect on mortality in adults. The relative risk of mortality for continuous SE was 1.79 times that of intermittent SE (p = 0.04). After controlling for SE duration, ictal time did not significantly affect mortality in adults. Conclusions: Intermittent and continuous convulsive SE were common in both pediatric and adult populations. Intermittent SE had a significantly lower mortality than did continuous SE. This difference in mortality was not completely explained by differences in SE duration, total ictal time, etiology, or age. Further research is needed to identify the factor(s) contributing to the significant difference in mortality between intermittent SE and continuous SE.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10368074</pmid><doi>10.1111/j.1528-1157.1999.tb00774.x</doi><tpages>7</tpages></addata></record>
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ispartof Epilepsia (Copenhagen), 1999-06, Vol.40 (6), p.752-758
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subjects Adolescent
Adult
Age Distribution
Age Factors
Biological and medical sciences
Child
Child, Preschool
Continuous seizures
Duration
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
Ictal time
Infant
Intermittent seizures
Medical sciences
Multivariate Analysis
Nervous system (semeiology, syndromes)
Neurology
Odds Ratio
Prospective Studies
Risk Factors
Severity of Illness Index
Status epilepticus
Status Epilepticus - classification
Status Epilepticus - epidemiology
Status Epilepticus - mortality
Virginia - epidemiology
title Prospective Population‐Based Study of Intermittent and Continuous Convulsive Status Epilepticus in Richmond, Virginia
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