<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="article-commentary" dtd-version="1.0" xml:lang="en">
<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-2014-28-8-3</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-28-8-3</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>Oral Prednisolone vs. IM Corticotropin and Hypsarrhythmia<xref ref-type="fn" rid="fn1">&#x002A;</xref> in West Syndrome</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 contrib-type="author">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0798-0131</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>John J.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Ann &#x0026; Robert H. Lurie Children&#x0027;s Hospital of Chicago, 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>
<fn id="fn1">
<label>&#x002A;</label>
<p><italic>Hypsarrhythmia</italic> was originally spelled with one &#x2018;r&#x2019; by the Drs Gibbs who coined the term in 1952 [<xref ref-type="bibr" rid="CIT0007">7</xref>]. They wished to emphasize that &#x201C;the term applied to a <italic>specific</italic> type of electroencephalographic abnormality&#x201D; [<xref ref-type="bibr" rid="CIT0008">8</xref>], and feared that their definition would be confused by a literal translation of the two &#x2018;r&#x2019; Greek root, &#x201C;mountainous arrhythmia&#x201D; [<xref ref-type="bibr" rid="CIT0009">9</xref>]. The one &#x2018;r&#x2019; spelling was the rule in the 1950s-60s [<xref ref-type="bibr" rid="CIT0010">10</xref>]. The two &#x2018;r&#x2019; spelling became convention in the literature by the mid 1970s [<xref ref-type="bibr" rid="CIT0011">11</xref>], with the Gibbs&#x2019; intended meaning faithfully maintained and accepted for both spellings today.</p>
</fn>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>08</month>
<year>2014</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>31</day>
<month>10</month>
<year>2015</year>
</pub-date>
<volume>28</volume>
<issue>8</issue>
<fpage>59</fpage>
<lpage>60</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2014 The Author(s)</copyright-statement>
<copyright-year>2014</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/j.pediatrneurol.2014.03.014" vol="51" page="24">
<article-title>The efficacy of moderate-to-high dose oral prednisolone versus low-to-moderate dose intramuscular corticotropin for improvement of hypsarrhythmia in West syndrome: a randomized, single-blind, parallel clinical trial</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators at University of Columbo, Sri Lanka, studied the efficacy of oral prednisolone (40-60 mg/day) and intramuscular adrenocorticotrophin hormone (40-60 IU synthetic ACTH every other day) for 14 days in improving hypsarrhythmia in children (age 2 mos-2 yrs) with previously untreated West syndrome.</p>
</abstract>
<kwd-group>
<kwd>Hypsarrhythmia</kwd>
<kwd>Weight Gain</kwd>
<kwd>Abdominal Distension</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators at University of Columbo, Sri Lanka, studied the efficacy of oral prednisolone (40-60 mg/day) and intramuscular adrenocorticotrophin hormone (40-60 IU synthetic ACTH every other day) for 14 days in improving hypsarrhythmia in children (age 2 mos-2 yrs) with previously untreated West syndrome. Children with tuberous sclerosis were excluded. Eighty of 92 patients (48 randomized to prednisolone and 44 to ACTH) completed the evaluation. Hypsarrhythmia severity score significantly improved with hormonal therapy (p &#x003C; 0.01); improvement in the prednisolone arm was significantly greater than that in the ACTH arm (p&#x003C; 0.01). The score system adapted from Kramer et al [<xref ref-type="bibr" rid="CIT0001">1</xref>], with a maximum of 16, employed a 10-sec segment of the most representative record. Frequent crying, irritability, weight gain, increased appetite, and abdominal distension were more common with prednisolone (but not significantly). Clinical outcome assessment (spasm control) is ongoing. [<xref ref-type="bibr" rid="CIT0002">2</xref>]</p>
<p>COMMENTARY. Comparative studies of the efficacy of prednisolone and ACTH are difficult to evaluate because of the variations and imbalance of dosages employed. The relative optimum dosages are not known. An editorial suggests that the reported EEG improvement following prednisolone may be at least as good as synthetic ACTH but the superiority of prednisolone is still unclear. Study limitations include brevity of the EEG, especially during sleep, and lack of clinical and developmental outcomes [<xref ref-type="bibr" rid="CIT0003">3</xref>]. After ACTH, oral corticosteroids remain the second most commonly used treatment for infantile spasms (with the exception of vigabatrin for patients with tuberous sclerosis).</p>
<p>
<bold>ACTH vs Predisolone for Spasms Post Vigabatrin Failure</bold>. According to the experience at the Hospital for Sick Children, Toronto, Canada, when vigabatrin is ineffective and ACTH unavailable, short-term prednisolone is recommended. While ACTH is more likely to provide short-term relief from spasms, prednisolone is equally effective in the long-term resolution of spasms [<xref ref-type="bibr" rid="CIT0004">4</xref>].</p>
<p>
<bold>Infantile spasms and vitamin B12 deficiency</bold>. Investigators in Ankara, Turkey, report two unrelated infants with infantile spasms associated with vitamin B12 deficiency related to maternal nutritional deficiency. After a month of treatment with ACTH, phenobarbital and vitamin B12, both infants&#x2019; abnormalities resolved. After 3 months, the EEG was normal and ACTH and phenobarbital were discontinued. At 9 months following treatment with vitamin B12, psychomotor developments are improved and the EEG remains normal. For diagnostic clarity, initial treatment with vitamin B12 alone would have been preferred. However, vitamin B12 deficiency should be considered as a cause of infantile spasms in an infant whose mother has severe nutritional deficiency [<xref ref-type="bibr" rid="CIT0005">5</xref>, <xref ref-type="bibr" rid="CIT0006">6</xref>].</p>
<p>* Hypsarrhythmia was originally spelled with one ‘r’ by the Drs Gibbs who coined the term in 1952
[<xref ref-type="bibr" rid="CIT0007">7</xref>]. They wished to emphasize that “the term applied to a
specific type of electroencephalographic abnormality” [<xref ref-type="bibr" rid="CIT0008"
>8</xref>], and feared that their definition would be confused by a literal translation of the two
‘r’ Greek root, “mountainous arrhythmia” [<xref ref-type="bibr" rid="CIT0009">9</xref>]. The one ‘r’
spelling was the rule in the 1950s-60s [<xref ref-type="bibr" rid="CIT0010">10</xref>]. The two ‘r’
spelling became convention in the literature by the mid 1970s [<xref ref-type="bibr" rid="CIT0011"
>11</xref>], with the Gibbs’ intended meaning faithfully maintained and accepted for both spellings
today.</p>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kramer</surname>
<given-names>U</given-names>
</name>
<name>
<surname>Sue</surname>
<given-names>WC</given-names>
</name>
<name>
<surname>Mikati</surname>
<given-names>MA</given-names>
</name>
</person-group>
<article-title>Hypsarrhythmia: frequency of variant patterns and correlation with etiology and outcome</article-title>
<source>Neurology</source>
<year>1997</year>
<month>Jan</month>
<volume>48</volume>
<issue>1</issue>
<fpage>197</fpage>
<lpage>203</lpage>
<pub-id pub-id-type="doi">10.1212/WNL.48.1.197</pub-id>
</element-citation>
</ref>
<ref id="CIT0002">
<label>2</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Wanigasinghe</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Arambepola</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Sri Ranganathan</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Sumanasena</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Muhandiram</surname>
<given-names>EC</given-names>
</name>
</person-group>
<article-title>The efficacy of moderate-to-high dose oral prednisolone versus low-to-moderate dose intramuscular corticotropin for improvement of hypsarrhythmia in West syndrome: a randomized, single-blind, parallel clinical trial</article-title>
<source>Pediatr Neurol</source>
<year>2014</year>
<month>Jul</month>
<volume>51</volume>
<issue>1</issue>
<fpage>24</fpage>
<lpage>30</lpage>
<pub-id pub-id-type="doi">10.1016/j.pediatrneurol.2014.03.014</pub-id>
<pub-id pub-id-type="pmid">24938136</pub-id>
</element-citation>
</ref>
<ref id="CIT0003">
<label>3</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Mytinger</surname>
<given-names>JR</given-names>
</name>
<name>
<surname>Heyer</surname>
<given-names>GL</given-names>
</name>
</person-group>
<article-title>Oral corticosteroids versus adrenocorticotropic hormone for infantile spasms--an unfinished story</article-title>
<source>Pediatr Neurol</source>
<year>2014</year>
<month>Jul</month>
<volume>51</volume>
<issue>1</issue>
<fpage>13</fpage>
<lpage>4</lpage>
<pub-id pub-id-type="doi">10.1016/j.pediatrneurol.2014.05.025</pub-id>
<pub-id pub-id-type="pmid">24938134</pub-id>
</element-citation>
</ref>
<ref id="CIT0004">
<label>4</label>
<element-citation publication-type="confproc">
<person-group person-group-type="author">
<name>
<surname>Jones</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Snead</surname>
<given-names>OC</given-names>
<suffix>3rd</suffix>
</name>
<name>
<surname>Boyd</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Go</surname>
<given-names>C</given-names>
</name>
</person-group>
<article-title>Adrenocorticotropic hormone versus prednisolone in the treatment of infantile spasms post vigabatrin failure</article-title>
<source>J Child Neurol</source>
<year>2014</year>
<month>Jun</month>
<day>25</day>
<pub-id pub-id-type="doi">10.1177/0883073814533148</pub-id>
<pub-id pub-id-type="pmid">24965788</pub-id>
</element-citation>
</ref>
<ref id="CIT0005">
<label>5</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Malbora</surname>
<given-names>B</given-names>
</name>
<name>
<surname>Yuksel</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Aksoy</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Ozkan</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>Two infants with infantile spasms associated with vitamin B12 deficiency</article-title>
<source>Pediatr Neurol</source>
<year>2014</year>
<month>Jul</month>
<volume>51</volume>
<issue>1</issue>
<fpage>144</fpage>
<lpage>6</lpage>
<pub-id pub-id-type="doi">10.1016/j.pediatrneurol.2014.03.001</pub-id>
<pub-id pub-id-type="pmid">24810877</pub-id>
</element-citation>
</ref>
<ref id="CIT0006">
<label>6</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Erol</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Alehan</surname>
<given-names>F</given-names>
</name>
<name>
<surname>G&#x00FC;m&#x00FC;s</surname>
<given-names>A</given-names>
</name>
</person-group>
<article-title>West syndrome in an infant with vitamin B12 deficiency in the absence of macrocytic anaemia</article-title>
<source>Dev Med Child Neurol</source>
<year>2007</year>
<month>Oct</month>
<volume>49</volume>
<issue>10</issue>
<fpage>774</fpage>
<lpage>6</lpage>
<pub-id pub-id-type="doi">10.1111/j.1469-8749.2007.00774.x</pub-id>
<pub-id pub-id-type="pmid">17880648</pub-id>
</element-citation>
</ref>
<ref id="CIT0007">
<label>7</label>
<element-citation publication-type="confproc">
<person-group person-group-type="author">
<name>
<surname>Gibbs</surname>
<given-names>FA</given-names>
</name>
<name>
<surname>Gibbs</surname>
<given-names>EL</given-names>
</name>
</person-group>
<article-title>Atlas of Electroencephalography</article-title>
<year>1952</year>
<volume>2</volume>
<publisher-loc>Reading, MA</publisher-loc>
<publisher-name>Addison-Wesley</publisher-name>
</element-citation>
</ref>
<ref id="CIT0008">
<label>8</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Gibbs</surname>
<given-names>FA</given-names>
</name>
</person-group>
<article-title>Infantile Spasms and Hypsarrhythmia or Hypsarhythmia</article-title>
<source>DMCN</source>
<year>1965</year>
<month>Jun</month>
<volume>7</volume>
<issue>3</issue>
<fpage>329</fpage>
<pub-id pub-id-type="doi">10.1111/j.1469-8749.1965.tb10947.x</pub-id>
<pub-id pub-id-type="pmid">14343238</pub-id>
</element-citation>
</ref>
<ref id="CIT0009">
<label>9</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Mac Keith</surname>
<given-names>R</given-names>
</name>
</person-group>
<article-title>Infantile spasms and hypsarrhythmia or hypsarhythmia</article-title>
<source>Dev Med Child Neurol</source>
<year>1965</year>
<month>Apr</month>
<volume>7</volume>
<issue>2</issue>
<fpage>204</fpage>
<pub-id pub-id-type="doi">10.1111/j.1469-8749.1965.tb10916.x</pub-id>
</element-citation>
</ref>
<ref id="CIT0010">
<label>10</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Millichap</surname>
<given-names>JG</given-names>
</name>
<name>
<surname>Bickford</surname>
<given-names>RG</given-names>
</name>
</person-group>
<article-title>Infantile Spasms, Hypsarhythmia, and Mental Retardation: Response to Corticotropin and Its Relation to Age and Etiology in 21 Patients</article-title>
<source>JAMA</source>
<year>1962</year>
<volume>182</volume>
<issue>5</issue>
<fpage>523</fpage>
<lpage>527</lpage>
<pub-id pub-id-type="doi">10.1001/jama.1962.03050440015004</pub-id>
</element-citation>
</ref>
<ref id="CIT0011">
<label>11</label>
<mixed-citation publication-type="webpage" publication-format="web">
<source>Google Books: Ngram. Incidence of &#x2018;hypsarrhythmia&#x2019; and &#x2018;hypsarhythmia&#x2019;</source> [Internet].
<publisher-loc>Mountain View, CA</publisher-loc>:
<publisher-name>Google</publisher-name>;
cited
[<date-in-citation content-type="access-date"
iso-8601-date="2007-02-22">2014 Oct 1</date-in-citation>].
Available from: <uri>https://goo.gl/Di9QqE</uri>.
</mixed-citation>
</ref>
</ref-list>
</back>
</article>