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Vigabatrin and high-dose prednisolone therapy for patients with West syndrome

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dc.contributor.author강훈철-
dc.contributor.author김세희-
dc.contributor.author김흥동-
dc.contributor.author윤송이-
dc.contributor.author이준수-
dc.date.accessioned2018-10-11T08:52:56Z-
dc.date.available2018-10-11T08:52:56Z-
dc.date.issued2018-
dc.identifier.issn0920-1211-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/163425-
dc.description.abstractOBJECTIVE: Hormonal therapy and vigabatrin are now accepted as the first-line or standard therapies for West syndrome (WS). However, the superiority of these drugs in terms of monotherapy or combination therapy is still in question. In this study, we designed a treatment protocol for WS and prospectively assessed the efficacy of these therapies in controlling spasms, stabilizing electroencephalography (EEG), and allowing for developmental catch-up. METHODS: In patients diagnosed with WS, vigabatrin was first administered alone for 2 weeks, and then prednisolone was administered in combination with vigabatrin if patients did not respond to vigabatrin. The detailed drug administration protocol was as follows: vigabatrin 50 mg/kg/day for 1 day, followed by vigabatrin 100 mg/kg/day for 3 days, vigabatrin 150 mg/kg/day if spasms were still present or the burden of amplitudes and epileptiform discharges (BASED) score on EEG was ≥3 on day 5; 40 mg/day of prednisolone was added if spasms were still present or the BASED score was ≥3 on day 14. The prednisolone dose was increased to 60 mg/day if spasms were still present or the BASED score was ≥3 on day 21. RESULTS: Sixty-six patients newly diagnosed with WS (median seizure onset age: 5.7 [IQR, 4.1-7.1] months, median age at diagnosis: 6.6 [IQR, 5.4-8.1] months, n = 40 [60.6%] boys) were subjected to the vigabatrin and prednisolone therapy protocol. Of the 66 patients, 22 (33.3%) patients showed resolution of spasms and a BASED score of ≤2 after vigabatrin alone, and 26 (39.4%) patients showed resolution of spasms and a BASED score of ≤2 after a combination of vigabatrin and prednisolone, for a total of 48 (72.7%) patients who were responsive to the protocol without relapse for at least 7 months after WS diagnosis. The mental and psychomotor age quotients were higher at the time of diagnosis and remained significantly higher 6 months after the diagnosis in responsive patients (p <  0.001). No serious adverse reactions leading to discontinuation or reduction of drug doses were observed. CONCLUSION: Using a treatment protocol involving vigabatrin and prednisolone for WS, 72.7% of patients showed resolution of spasms and a BASED score of ≤2. This study also found that this drug administration protocol was safe. However, further studies are warranted as this study describes results from observational study with limited sample size.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier Science Publishers-
dc.relation.isPartOfEPILEPSY RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleVigabatrin and high-dose prednisolone therapy for patients with West syndrome-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Pediatrics-
dc.contributor.googleauthorAra Ko-
dc.contributor.googleauthorSong Ee Youn-
dc.contributor.googleauthorHee Jung Chung-
dc.contributor.googleauthorSe Hee Kim-
dc.contributor.googleauthorJoon Soo Lee-
dc.contributor.googleauthorHeung Dong Kim-
dc.contributor.googleauthorHoon-Chul Kang-
dc.identifier.doi10.1016/j.eplepsyres.2018.06.013-
dc.contributor.localIdA00102-
dc.contributor.localIdA00611-
dc.contributor.localIdA01208-
dc.contributor.localIdA05368-
dc.contributor.localIdA03177-
dc.relation.journalcodeJ00796-
dc.identifier.eissn1872-6844-
dc.identifier.pmid29966811-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0920121118302481-
dc.subject.keywordInfantile spasms-
dc.subject.keywordPrednisolone-
dc.subject.keywordTreatment-
dc.subject.keywordVigabatrin-
dc.subject.keywordWest syndrome-
dc.contributor.alternativeNameKang, Hoon Chul-
dc.contributor.alternativeNameKim, Se Hee-
dc.contributor.alternativeNameKim, Heung Dong-
dc.contributor.alternativeNameYoun, Song Ee-
dc.contributor.alternativeNameLee, Joon Soo-
dc.contributor.affiliatedAuthorKang, Hoon Chul-
dc.contributor.affiliatedAuthorKim, Se Hee-
dc.contributor.affiliatedAuthorKim, Heung Dong-
dc.contributor.affiliatedAuthorYoun, Song Ee-
dc.contributor.affiliatedAuthorLee, Joon Soo-
dc.citation.volume145-
dc.citation.startPage127-
dc.citation.endPage133-
dc.identifier.bibliographicCitationEPILEPSY RESEARCH, Vol.145 : 127-133, 2018-
dc.identifier.rimsid60375-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers

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