Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/3081
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorINOCENTE, C. O.-
dc.contributor.authorARNULF, I.-
dc.contributor.authorBASTUJI, H.-
dc.contributor.authorTHIBAULT-STOLL, A.-
dc.contributor.authorRAOUX, A.-
dc.contributor.authorREIMAO, R.-
dc.contributor.authorLIN, J-S-
dc.contributor.authorFRANCO, P.-
dc.date.accessioned2013-10-11T21:30:45Z-
dc.date.available2013-10-11T21:30:45Z-
dc.date.issued2012-
dc.identifier.citationJOURNAL OF SLEEP RESEARCH, v.21, suppl.1, Special Issue, p.317-317, 2012-
dc.identifier.issn0962-1105-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/3081-
dc.description.abstractObjectives: Narcolepsy is a rare disabling sleep disorder characterized by excessive daytime sleepiness and cataplexy (sudden loss of muscle tone). Drugs such as pitolisant, which block histamine H3 autoreceptors, constitute a newly identified class of stimulants because they increase brain histamine and enhance wakefulness in animal and human adult narcolepsy. Methods: We report our experience with the off-label use of Pitolisant in four teenagers with narcolepsy/cataplexy with severe daytime sleepiness, refractory to available treatments (modafinil, methylphenidate, mazindol, sodium oxybate, and D-amphetamine). Results: All teenagers developed their disease during childhood (11.3–2.4 years; 50% boys) and were 17.3–0.8 years old at the time of pitolisant therapy. Pitolisant treatment was increased from 10 to 30 mg (n = 1) and 40 mg (n = 3). The adapted Epworth Sleepiness Score decreased from 14.3 T 1.1 to 9.5 to 2.9 (P = 0.03) with pitolisant alone to 7 T 3.4 when combined with mazindol (n = 1), methylphenidate (n = 1), or sodium oxybate plus modafinil (n = 1). Mean sleep onset latency increased from 31 T 14 to 36 to 8 min (P = 0.21) on the maintenance of wakefulness test. The severity and frequency of cataplexy were slightly improved. Adverse effects were minor (insomnia, headache, hot flushes, leg pain, and hallucinations) and transitory, except for insomnia, which persisted in two teenagers. The benefit was maintained after a mean of 13 months. Conclusions: Pitolisant could constitute an acceptable alternative for the treatment of refractory sleepiness in teenagers with narcolepsy.-
dc.language.isoeng-
dc.publisherWILEY-BLACKWELL-
dc.relation.ispartofJournal of Sleep Research-
dc.rightsrestrictedAccess-
dc.titlePitolisant, an inverse agonist of the histamine H3 receptor: an alternative stimulant for narcolepsy-cataplexy in teenagers with refractory sleepiness-
dc.typeconferenceObject-
dc.rights.holderCopyright WILEY-BLACKWELL-
dc.description.conferencedateSEP 04-08, 2012-
dc.description.conferencelocalParis, FRANCE-
dc.description.conferencename21st Congress of the European-Sleep-Research-Society-
dc.subject.wosClinical Neurology-
dc.subject.wosNeurosciences-
dc.type.categorymeeting abstract-
dc.type.versionpublishedVersion-
hcfmusp.author.externalINOCENTE, C. O.:Univ Lyon, Lyon, France-
hcfmusp.author.externalARNULF, I.:Hosp Pitie Salpetriere, Paris, France-
hcfmusp.author.externalBASTUJI, H.:Univ Lyon, Lyon, France-
hcfmusp.author.externalTHIBAULT-STOLL, A.:Clin Sainte Barbe, Strasbourg, France-
hcfmusp.author.externalRAOUX, A.:Hop Femme Mere Enfant, Lyon, France-
hcfmusp.author.externalLIN, J-S:Univ Lyon, Lyon, France-
hcfmusp.author.externalFRANCO, P.:Univ Lyon, Lyon, France-
hcfmusp.description.beginpage317-
hcfmusp.description.endpage317-
hcfmusp.description.issuesuppl 1-
hcfmusp.description.issueSpecial Issue-
hcfmusp.description.volume21-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000307963201334-
hcfmusp.publisher.cityHOBOKEN-
hcfmusp.publisher.countryUSA-
dc.description.indexMEDLINE-
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