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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-18-75</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-18-10-3</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Seizure Disorders</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Risk of Status Epilepticus in Epilepsy</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Children&#x0027;s Memorial Hospital, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>10</month>
<year>2004</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>03</month>
<year>2016</year>
</pub-date>
<volume>18</volume>
<issue>10</issue>
<fpage>75</fpage>
<lpage>76</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2004 The Author(s)</copyright-statement>
<copyright-year>2004</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="doi" xlink:href="10.1212/01.WNL.0000138425.54223.DC" vol="63" page="1027">
<article-title>Status epilepticus after the initial diagnosis of epilepsy in children</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The occurrence of status epilepticus (SE) after the initial diagnosis of epilepsy was determined in a prospective community-based cohort study of 613 children at Montefiore Medical Center, Bronx, NY; Yale Medical School, New Haven, CT; and BIOS/NIU, DeKalb, IL.</p>
</abstract>
<kwd-group>
<kwd>Encephalopathic Disorder</kwd>
<kwd>Status Epilepticus</kwd>
<kwd>Initial Diagnosis</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The occurrence of status epilepticus (SE) after the initial diagnosis of epilepsy was determined in a prospective community-based cohort study of 613 children at Montefiore Medical Center, Bronx, NY; Yale Medical School, New Haven, CT; and BIOS/NIU, DeKalb, IL. During a median follow-up of 8 years, 58 (9.5%) had 1 or &#x003E;1 episode of SE, the first occurring a median of 2.5 years after initial diagnosis (range, &#x003C;1 month to 8.8 years). Thirty three had only one episode, 8 had 2 episodes, and 16 had 3 or more episodes. Of 56 patients with previous SE, 18 (32.1%) had at least one further episode during follow-up compared to 40 of 557 (7.2%) without history of SE (P&#x003C;0.0001). Factors associated with a risk of SE included SE before initial diagnosis of epilepsy, younger age at onset (3 fold increased risk at age &#x003C;1 year vs 10+ years) and symptomatic etiology. In those with no SE before initial diagnosis, the risk of SE during follow-up was 14% in the symptomatic etiology group vs 2.6% in the idiopathic group. In those with previous SE, the relative risks for symptomatic/idiopathic groups were 52% vs 37%. Overall, 13 (2.1%) died, and the risk of dying was greater in children who had previous SE (5/56 [8.9%]) vs 8/557 [1.4%] who did not (P=0.0002). Death in those with previous SE was usually associated with an underlying cause, eg neurodegenerative or encephalopathic disorder. Children who experienced SE during follow-up were less likely to be in 3-year remission (19.6% vs 65.3%; P&#x003C;0.0001) and much more likely to have intractable seizures (47.4% vs 8.9%; P&#x003C;0.0001). [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. The risk of status epilepticus (SE) in children with an initial diagnosis of epilepsy is approximately 10%. The risk is increased in children with a previous history of status, in younger age groups, and in those with symptomatic etiology. Data regarding antiepileptic drug levels in patients with SE would be of interest. The authors recommend abortive therapy in the home for patients at high risk of SE. A poor outcome of SE in a Netherlands study was related to inadequate AED therapy, as well as medical complications (eg respiratory insufficiency, cardiac arrhythmias), and a duration of SE greater than 4 hours [<xref ref-type="bibr" rid="CIT0002">2</xref>]. Noncompliance with antiepileptic drug therapy or inadequate instruction regarding the use of rectal diazepam in the home were the explanations for the admission of 8 children with SE at the University Hospital of Wales, Cardiff, UK. [<xref ref-type="bibr" rid="CIT0003">3</xref>]</p>
<p>In a previous study by the current group of authors, SE was the first seizure in 38 (11%) of 342 children followed for a mean of 72 months after a first idiopathic unprovoked seizure (Shinnar S, et al. <bold>Dev Med Child Neurol</bold> 1995;37 (suppl 72): 116 (abstract)). At follow-up, 127 (37%) had experienced a seizure recurrence, including 42% of those who presented with status and 37% of those with a brief first seizure. SE did not adversely affect outcome in this cohort of idiopathic cases. The importance of seizure prevention or abortive therapy is stressed in both US and UK literature, especially in symptomatic epilepsies.</p>
</body>
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