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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-8-30-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-8-4-10</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Antiepileptic Drugs</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>Phenytoin and Cognitive-Motor Performance</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>04</month>
<year>1994</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>8</volume>
<issue>4</issue>
<fpage>30</fpage>
<lpage>31</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1994 The Author(s)</copyright-statement>
<copyright-year>1994</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="10.1111/j.1528-1157.1994.tb02929.x" vol="35" page="172">
<article-title>Effects of phenytoin on cognitive-motor performance in children as a function of drug concentration, seizure type, and time of medication</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Cognitive-motor function in 51 children with seizures well controlled with phenytoin (PHT) monotherapy was assessed in relation to drug concentration, seizure type, and time of medication at the Departments of Psychiatry and Pharmacology, Auckland University School of Medicine, Australia.</p>
</abstract>
<kwd-group>
<kwd>Cognitive-Motor Function</kwd>
<kwd>Phenytoin</kwd>
<kwd>Glucose Homeostasis</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Cognitive-motor function in 51 children with seizures well controlled with phenytoin (PHT) monotherapy was assessed in relation to drug concentration, seizure type, and time of medication at the Departments of Psychiatry and Pharmacology, Auckland University School of Medicine, Australia. Age ranged from 4 to 14 years, and performance was significantly better in older patients. Diagnosis (partial vs generalized epilepsy), PHT concentration levels, and change from trough to peak concentration days had little effect. Fluctuations in PHT as great as 50% had no or minimal effects on performance of tests in low therapeutic doses. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p>COMMENT. Maintenance phenytoin monotherapy, at relatively low therapeutic levels, had negligible or no effects on cognitive motor function in a group of children with well controlled seizures. Performance swings resulting from drug absorption and elimination were absent or minimal in this carefully monitored study. The importance of frequent determinations of phenytoin levels during evaluations of neuropsychological function in children is evident from the following report.</p>
<p>In a special article on the &#x201C;role of therapeutic drug monitoring in pediatric anticonvulsant drug dosing,&#x201D; Walson PD at Children&#x2019;s Hospital, Columbus, OH refers to a rapid phenytoin clearance and a first order (linear) rather than saturated kinetics observed in some children found to have unusually low serum drug levels despite doses as high as 18 mg/kg/day [<xref ref-type="bibr" rid="CIT0002">2</xref>]. The effects of rate and extent of absorption on the interpretation of phenytoin concentrations and cognitive function are often unappreciated. Various factors can modify phenytoin absorption in children, including the dose and stool frequency. Doses well tolerated in healthy children may become toxic if the patient is constipated. High dose phenytoin loading can affect glucose homeostasis, with possible changes in cognition. The hyperglycemic effect of phenytoin was first demonstrated in the Division of Neurology and Neurochemistry Laboratories at Children&#x2019;s Memorial Hospital, Chicago. [<xref ref-type="bibr" rid="CIT0003">3</xref>]</p>
</disp-quote>
</body>
<back>
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