Antibody-Mediated Status Epilepticus: A Retrospective Multicenter Survey
Background: In recent years, an increasing number of auto-antibodies (AB) have been detected in the CSF and serum of patients with new onset epilepsy. Some of these patients develop convulsive or nonconvulsive status epilepticus (AB-SE), necessitating intensive medical care and administration of mul...
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creator | Holzer, Franz Josef Rossetti, Andrea O. Heritier-Barras, Anne-Chantal Zumsteg, Dominik Roebling, Robert Huber, Roman Lerche, Holger Kiphuth, Ines C. Bardutzky, Jürgen Bien, Christian G. Tröger, Mathias Schoch, Gaby Prüss, Harald Seeck, Margitta |
description | Background: In recent years, an increasing number of auto-antibodies (AB) have been detected in the CSF and serum of patients with new onset epilepsy. Some of these patients develop convulsive or nonconvulsive status epilepticus (AB-SE), necessitating intensive medical care and administration of multiple antiepileptic and immunomodulatory treatments of uncertain effectiveness. Objectives: In this retrospective multicenter survey we aimed to determine the spectrum of gravity, the duration and the prognosis of the disorder. In addition, we sought to identify the antibodies associated with this condition, as well as determine whether there is a most effective treatment regime. Methods: 12 European Neurology University Clinics, with extensive experience in the treatment of SE patients, were sent a detailed questionnaire regarding symptoms and treatment of AB-SE patients. Seven centers responded positively, providing a total of 13 patients above the age of 16. Results: AB-SE affects mainly women (12/13, 92%) with a variable age at onset (17–69 years, median: 25 years). The duration of the disease is also variable (10 days to 12 years, median: 2 months). Only the 3 oldest patients died (55–69 years). Most patients were diagnosed with anti NMDAR encephalitis (8/13) and had oligoclonal bands in the CSF (9/13). No specific treatment regimen (antiepileptic, immunomodulatory) was found to be clearly superior. Most of the surviving 10 patients (77%) recovered completely or nearly so within 2 years of index poststatus. Conclusion: AB-SE is a severe but potentially reversible condition. Long duration does not seem to imply fatal outcome; however, age older than 50 years at time of onset appears to be a risk factor for death. There was no evidence for an optimal antiepileptic or immunomodulatory treatment. A prospective multicenter study is warranted in order to stratify the optimal treatment algorithm, determine clear risk factors of unfavorable outcome and long-term prognosis. |
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Some of these patients develop convulsive or nonconvulsive status epilepticus (AB-SE), necessitating intensive medical care and administration of multiple antiepileptic and immunomodulatory treatments of uncertain effectiveness. Objectives: In this retrospective multicenter survey we aimed to determine the spectrum of gravity, the duration and the prognosis of the disorder. In addition, we sought to identify the antibodies associated with this condition, as well as determine whether there is a most effective treatment regime. Methods: 12 European Neurology University Clinics, with extensive experience in the treatment of SE patients, were sent a detailed questionnaire regarding symptoms and treatment of AB-SE patients. Seven centers responded positively, providing a total of 13 patients above the age of 16. Results: AB-SE affects mainly women (12/13, 92%) with a variable age at onset (17–69 years, median: 25 years). The duration of the disease is also variable (10 days to 12 years, median: 2 months). Only the 3 oldest patients died (55–69 years). Most patients were diagnosed with anti NMDAR encephalitis (8/13) and had oligoclonal bands in the CSF (9/13). No specific treatment regimen (antiepileptic, immunomodulatory) was found to be clearly superior. Most of the surviving 10 patients (77%) recovered completely or nearly so within 2 years of index poststatus. Conclusion: AB-SE is a severe but potentially reversible condition. Long duration does not seem to imply fatal outcome; however, age older than 50 years at time of onset appears to be a risk factor for death. There was no evidence for an optimal antiepileptic or immunomodulatory treatment. A prospective multicenter study is warranted in order to stratify the optimal treatment algorithm, determine clear risk factors of unfavorable outcome and long-term prognosis.</description><identifier>ISSN: 0014-3022</identifier><identifier>EISSN: 1421-9913</identifier><identifier>DOI: 10.1159/000341143</identifier><identifier>PMID: 23051892</identifier><identifier>CODEN: EUNEAP</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Adolescent ; Adult ; Age ; Aged ; Algorithms ; Antibodies ; Autoantibodies ; Autoantibodies - blood ; Autoantibodies - cerebrospinal fluid ; Autoantibodies - immunology ; Cerebrospinal fluid ; Electroencephalography ; Encephalitis ; Epilepsy ; Female ; Geriatrics ; Glutamic acid receptors ; Humans ; Immunomodulation ; Inventories ; Male ; Middle Aged ; N-Methyl-D-aspartic acid receptors ; Original Paper ; Prognosis ; Retrospective Studies ; Risk Factors ; Seizures - complications ; Seizures - drug therapy ; Seizures - immunology ; Seizures - physiopathology ; Status Epilepticus - diagnosis ; Status Epilepticus - drug therapy ; Status Epilepticus - immunology ; Status Epilepticus - physiopathology ; Surveys and Questionnaires ; Treatment Outcome ; Young Adult</subject><ispartof>European neurology, 2012-11, Vol.68 (5), p.310-317</ispartof><rights>2012 S. Karger AG, Basel</rights><rights>Copyright © 2012 S. Karger AG, Basel.</rights><rights>Copyright (c) 2012 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-747b04c7e640fd09e305ce2a969d44b7c9748344b47dd393cf0ef93bdfa73ec23</citedby><cites>FETCH-LOGICAL-c402t-747b04c7e640fd09e305ce2a969d44b7c9748344b47dd393cf0ef93bdfa73ec23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2429,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23051892$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holzer, Franz Josef</creatorcontrib><creatorcontrib>Rossetti, Andrea O.</creatorcontrib><creatorcontrib>Heritier-Barras, Anne-Chantal</creatorcontrib><creatorcontrib>Zumsteg, Dominik</creatorcontrib><creatorcontrib>Roebling, Robert</creatorcontrib><creatorcontrib>Huber, Roman</creatorcontrib><creatorcontrib>Lerche, Holger</creatorcontrib><creatorcontrib>Kiphuth, Ines C.</creatorcontrib><creatorcontrib>Bardutzky, Jürgen</creatorcontrib><creatorcontrib>Bien, Christian G.</creatorcontrib><creatorcontrib>Tröger, Mathias</creatorcontrib><creatorcontrib>Schoch, Gaby</creatorcontrib><creatorcontrib>Prüss, Harald</creatorcontrib><creatorcontrib>Seeck, Margitta</creatorcontrib><title>Antibody-Mediated Status Epilepticus: A Retrospective Multicenter Survey</title><title>European neurology</title><addtitle>Eur Neurol</addtitle><description>Background: In recent years, an increasing number of auto-antibodies (AB) have been detected in the CSF and serum of patients with new onset epilepsy. Some of these patients develop convulsive or nonconvulsive status epilepticus (AB-SE), necessitating intensive medical care and administration of multiple antiepileptic and immunomodulatory treatments of uncertain effectiveness. Objectives: In this retrospective multicenter survey we aimed to determine the spectrum of gravity, the duration and the prognosis of the disorder. In addition, we sought to identify the antibodies associated with this condition, as well as determine whether there is a most effective treatment regime. Methods: 12 European Neurology University Clinics, with extensive experience in the treatment of SE patients, were sent a detailed questionnaire regarding symptoms and treatment of AB-SE patients. Seven centers responded positively, providing a total of 13 patients above the age of 16. Results: AB-SE affects mainly women (12/13, 92%) with a variable age at onset (17–69 years, median: 25 years). The duration of the disease is also variable (10 days to 12 years, median: 2 months). Only the 3 oldest patients died (55–69 years). Most patients were diagnosed with anti NMDAR encephalitis (8/13) and had oligoclonal bands in the CSF (9/13). No specific treatment regimen (antiepileptic, immunomodulatory) was found to be clearly superior. Most of the surviving 10 patients (77%) recovered completely or nearly so within 2 years of index poststatus. Conclusion: AB-SE is a severe but potentially reversible condition. Long duration does not seem to imply fatal outcome; however, age older than 50 years at time of onset appears to be a risk factor for death. There was no evidence for an optimal antiepileptic or immunomodulatory treatment. A prospective multicenter study is warranted in order to stratify the optimal treatment algorithm, determine clear risk factors of unfavorable outcome and long-term prognosis.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Algorithms</subject><subject>Antibodies</subject><subject>Autoantibodies</subject><subject>Autoantibodies - blood</subject><subject>Autoantibodies - cerebrospinal fluid</subject><subject>Autoantibodies - immunology</subject><subject>Cerebrospinal fluid</subject><subject>Electroencephalography</subject><subject>Encephalitis</subject><subject>Epilepsy</subject><subject>Female</subject><subject>Geriatrics</subject><subject>Glutamic acid receptors</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>Inventories</subject><subject>Male</subject><subject>Middle Aged</subject><subject>N-Methyl-D-aspartic acid receptors</subject><subject>Original Paper</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Seizures - complications</subject><subject>Seizures - drug therapy</subject><subject>Seizures - immunology</subject><subject>Seizures - physiopathology</subject><subject>Status Epilepticus - diagnosis</subject><subject>Status Epilepticus - drug therapy</subject><subject>Status Epilepticus - immunology</subject><subject>Status Epilepticus - physiopathology</subject><subject>Surveys and Questionnaires</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0014-3022</issn><issn>1421-9913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqN0c1LwzAUAPAgipvTg3eRghc9VPPVpfE2xnTChuD0XNrkVTq7tuZjsP_ejM0dPEkOScgv7yXvIXRJ8D0hiXzAGDNOCGdHqE84JbGUhB2jPsaExwxT2kNn1i7DNpEiPUU9ynBCUkn7aDpqXFW0ehPPQVe5Ax0tXO68jSZdVUPnKuXtYzSK3sCZ1nagXLWGaO7rcAKNAxMtvFnD5hydlHlt4WI_D9DH0-R9PI1nr88v49EsVhxTFwsuCsyVgCHHpcYSwksU0FwOpea8EEoKnrKw4kJrJpkqMZSSFbrMBQNF2QDd7uJ2pv32YF22qqyCus4baL3NCE2ESGgq5T8oxYlgPBkGevOHLltvmvCRjDBCWRh0m_tup1QohTVQZp2pVrnZZARn205kh04Ee72P6IsV6IP8LX0AVzvwlZtPMAewv_8D7q-KKQ</recordid><startdate>201211</startdate><enddate>201211</enddate><creator>Holzer, Franz Josef</creator><creator>Rossetti, Andrea O.</creator><creator>Heritier-Barras, Anne-Chantal</creator><creator>Zumsteg, Dominik</creator><creator>Roebling, Robert</creator><creator>Huber, Roman</creator><creator>Lerche, Holger</creator><creator>Kiphuth, Ines C.</creator><creator>Bardutzky, Jürgen</creator><creator>Bien, Christian G.</creator><creator>Tröger, Mathias</creator><creator>Schoch, Gaby</creator><creator>Prüss, Harald</creator><creator>Seeck, Margitta</creator><general>S. Karger AG</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>201211</creationdate><title>Antibody-Mediated Status Epilepticus: A Retrospective Multicenter Survey</title><author>Holzer, Franz Josef ; Rossetti, Andrea O. ; Heritier-Barras, Anne-Chantal ; Zumsteg, Dominik ; Roebling, Robert ; Huber, Roman ; Lerche, Holger ; Kiphuth, Ines C. ; Bardutzky, Jürgen ; Bien, Christian G. ; Tröger, Mathias ; Schoch, Gaby ; Prüss, Harald ; Seeck, Margitta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-747b04c7e640fd09e305ce2a969d44b7c9748344b47dd393cf0ef93bdfa73ec23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Algorithms</topic><topic>Antibodies</topic><topic>Autoantibodies</topic><topic>Autoantibodies - blood</topic><topic>Autoantibodies - cerebrospinal fluid</topic><topic>Autoantibodies - immunology</topic><topic>Cerebrospinal fluid</topic><topic>Electroencephalography</topic><topic>Encephalitis</topic><topic>Epilepsy</topic><topic>Female</topic><topic>Geriatrics</topic><topic>Glutamic acid receptors</topic><topic>Humans</topic><topic>Immunomodulation</topic><topic>Inventories</topic><topic>Male</topic><topic>Middle Aged</topic><topic>N-Methyl-D-aspartic acid receptors</topic><topic>Original Paper</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Seizures - complications</topic><topic>Seizures - drug therapy</topic><topic>Seizures - immunology</topic><topic>Seizures - physiopathology</topic><topic>Status Epilepticus - diagnosis</topic><topic>Status Epilepticus - drug therapy</topic><topic>Status Epilepticus - immunology</topic><topic>Status Epilepticus - physiopathology</topic><topic>Surveys and Questionnaires</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holzer, Franz Josef</creatorcontrib><creatorcontrib>Rossetti, Andrea O.</creatorcontrib><creatorcontrib>Heritier-Barras, Anne-Chantal</creatorcontrib><creatorcontrib>Zumsteg, Dominik</creatorcontrib><creatorcontrib>Roebling, Robert</creatorcontrib><creatorcontrib>Huber, Roman</creatorcontrib><creatorcontrib>Lerche, Holger</creatorcontrib><creatorcontrib>Kiphuth, Ines C.</creatorcontrib><creatorcontrib>Bardutzky, Jürgen</creatorcontrib><creatorcontrib>Bien, Christian G.</creatorcontrib><creatorcontrib>Tröger, Mathias</creatorcontrib><creatorcontrib>Schoch, Gaby</creatorcontrib><creatorcontrib>Prüss, Harald</creatorcontrib><creatorcontrib>Seeck, Margitta</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 Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma 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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Science Database</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 China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>European neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holzer, Franz Josef</au><au>Rossetti, Andrea O.</au><au>Heritier-Barras, Anne-Chantal</au><au>Zumsteg, Dominik</au><au>Roebling, Robert</au><au>Huber, Roman</au><au>Lerche, Holger</au><au>Kiphuth, Ines C.</au><au>Bardutzky, Jürgen</au><au>Bien, Christian G.</au><au>Tröger, Mathias</au><au>Schoch, Gaby</au><au>Prüss, Harald</au><au>Seeck, Margitta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibody-Mediated Status Epilepticus: A Retrospective Multicenter Survey</atitle><jtitle>European neurology</jtitle><addtitle>Eur Neurol</addtitle><date>2012-11</date><risdate>2012</risdate><volume>68</volume><issue>5</issue><spage>310</spage><epage>317</epage><pages>310-317</pages><issn>0014-3022</issn><eissn>1421-9913</eissn><coden>EUNEAP</coden><abstract>Background: In recent years, an increasing number of auto-antibodies (AB) have been detected in the CSF and serum of patients with new onset epilepsy. Some of these patients develop convulsive or nonconvulsive status epilepticus (AB-SE), necessitating intensive medical care and administration of multiple antiepileptic and immunomodulatory treatments of uncertain effectiveness. Objectives: In this retrospective multicenter survey we aimed to determine the spectrum of gravity, the duration and the prognosis of the disorder. In addition, we sought to identify the antibodies associated with this condition, as well as determine whether there is a most effective treatment regime. Methods: 12 European Neurology University Clinics, with extensive experience in the treatment of SE patients, were sent a detailed questionnaire regarding symptoms and treatment of AB-SE patients. Seven centers responded positively, providing a total of 13 patients above the age of 16. Results: AB-SE affects mainly women (12/13, 92%) with a variable age at onset (17–69 years, median: 25 years). The duration of the disease is also variable (10 days to 12 years, median: 2 months). Only the 3 oldest patients died (55–69 years). Most patients were diagnosed with anti NMDAR encephalitis (8/13) and had oligoclonal bands in the CSF (9/13). No specific treatment regimen (antiepileptic, immunomodulatory) was found to be clearly superior. Most of the surviving 10 patients (77%) recovered completely or nearly so within 2 years of index poststatus. Conclusion: AB-SE is a severe but potentially reversible condition. Long duration does not seem to imply fatal outcome; however, age older than 50 years at time of onset appears to be a risk factor for death. There was no evidence for an optimal antiepileptic or immunomodulatory treatment. A prospective multicenter study is warranted in order to stratify the optimal treatment algorithm, determine clear risk factors of unfavorable outcome and long-term prognosis.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>23051892</pmid><doi>10.1159/000341143</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age Aged Algorithms Antibodies Autoantibodies Autoantibodies - blood Autoantibodies - cerebrospinal fluid Autoantibodies - immunology Cerebrospinal fluid Electroencephalography Encephalitis Epilepsy Female Geriatrics Glutamic acid receptors Humans Immunomodulation Inventories Male Middle Aged N-Methyl-D-aspartic acid receptors Original Paper Prognosis Retrospective Studies Risk Factors Seizures - complications Seizures - drug therapy Seizures - immunology Seizures - physiopathology Status Epilepticus - diagnosis Status Epilepticus - drug therapy Status Epilepticus - immunology Status Epilepticus - physiopathology Surveys and Questionnaires Treatment Outcome Young Adult |
title | Antibody-Mediated Status Epilepticus: A Retrospective Multicenter Survey |
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