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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-6-70-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-6-9-9</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>Carbamazepine Acute Toxicity</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>09</month>
<year>1992</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>07</month>
<year>2016</year>
</pub-date>
<volume>6</volume>
<issue>9</issue>
<fpage>70</fpage>
<lpage>71</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1992 The Author(s)</copyright-statement>
<copyright-year>1992</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="10.1016/S0022-3476(05)81208-9" vol="121" page="295">
<article-title>Acute toxic reaction to carbamazepine: clinical effects and serum concentrations</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The clinical toxic effects and serum concentrations after ingestion of carbamazepine are reported in 82 pediatric patients from the Intensive Care Unit, Royal Children&#x2019;s Hospital, Melbourne, Australia.</p>
</abstract>
<kwd-group>
<kwd>Carbamazepine</kwd>
<kwd>Myocardial</kwd>
<kwd>Drowsiness</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The clinical toxic effects and serum concentrations after ingestion of carbamazepine are reported in 82 pediatric patients from the Intensive Care Unit, Royal Children&#x2019;s Hospital, Melbourne, Australia. Two died, 1 of cardiac failure and 1 of aspiration pneumonitis with septicemia. In 10 patients in deep coma with a Glasgow Coma Scale (GCS) of 3-4, the mean serum level was 213 <italic>&#x0075;</italic>mol/L. The serum carbamazepine level was related to the depth of coma, convulsions, hypotension caused by myocardial failure and conduction defects, and to the requirement for mechanical ventilation. In 27 patients with moderate coma (GCS 5-8) the mean serum level of carbamazepine was 112 <italic>&#x0075;</italic>mol/L; convulsions occurred in 2 patients in this group. In 45 patients with mildly depressed consciousness (GCS 9-15) the serum level was 73 <italic>&#x0075;</italic>mol/L and symptoms included drowsiness (80%), ataxia (53%), nystagmus (38%), vomiting (17%), and dystonia (7%). Patients with carbamazepine serum levels greater than 150 <italic>&#x0075;</italic>mol/L may require intensive life support. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><bold>COMMENT.</bold> In a study from the University of Cincinnati, Ohio, the administration of activated charcoal resulted in a statistically significant reduction in carbamazepine half-life but the time to complete recovery from overdose was not affected [<xref ref-type="bibr" rid="CIT0002">2</xref>]. The authors recommend no more than 2 to 3 doses (1 gram per kilogram) of activated charcoal in order to prevent formation of concretions and continued absorption of the drug. Prolonged repeated use of activated charcoal after carbamazepine overdose in comatose patients is not beneficial and carries a hazard of aspiration.</p>
</disp-quote>
</body>
<back>
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</article>