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Vigabatrin and high-dose prednisolone therapy for patients with West syndrome
DC Field | Value | Language |
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dc.contributor.author | 강훈철 | - |
dc.contributor.author | 김세희 | - |
dc.contributor.author | 김흥동 | - |
dc.contributor.author | 윤송이 | - |
dc.contributor.author | 이준수 | - |
dc.date.accessioned | 2018-10-11T08:52:56Z | - |
dc.date.available | 2018-10-11T08:52:56Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 0920-1211 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/163425 | - |
dc.description.abstract | OBJECTIVE: 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.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier Science Publishers | - |
dc.relation.isPartOf | EPILEPSY RESEARCH | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Vigabatrin and high-dose prednisolone therapy for patients with West syndrome | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Pediatrics | - |
dc.contributor.googleauthor | Ara Ko | - |
dc.contributor.googleauthor | Song Ee Youn | - |
dc.contributor.googleauthor | Hee Jung Chung | - |
dc.contributor.googleauthor | Se Hee Kim | - |
dc.contributor.googleauthor | Joon Soo Lee | - |
dc.contributor.googleauthor | Heung Dong Kim | - |
dc.contributor.googleauthor | Hoon-Chul Kang | - |
dc.identifier.doi | 10.1016/j.eplepsyres.2018.06.013 | - |
dc.contributor.localId | A00102 | - |
dc.contributor.localId | A00611 | - |
dc.contributor.localId | A01208 | - |
dc.contributor.localId | A05368 | - |
dc.contributor.localId | A03177 | - |
dc.relation.journalcode | J00796 | - |
dc.identifier.eissn | 1872-6844 | - |
dc.identifier.pmid | 29966811 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0920121118302481 | - |
dc.subject.keyword | Infantile spasms | - |
dc.subject.keyword | Prednisolone | - |
dc.subject.keyword | Treatment | - |
dc.subject.keyword | Vigabatrin | - |
dc.subject.keyword | West syndrome | - |
dc.contributor.alternativeName | Kang, Hoon Chul | - |
dc.contributor.alternativeName | Kim, Se Hee | - |
dc.contributor.alternativeName | Kim, Heung Dong | - |
dc.contributor.alternativeName | Youn, Song Ee | - |
dc.contributor.alternativeName | Lee, Joon Soo | - |
dc.contributor.affiliatedAuthor | Kang, Hoon Chul | - |
dc.contributor.affiliatedAuthor | Kim, Se Hee | - |
dc.contributor.affiliatedAuthor | Kim, Heung Dong | - |
dc.contributor.affiliatedAuthor | Youn, Song Ee | - |
dc.contributor.affiliatedAuthor | Lee, Joon Soo | - |
dc.citation.volume | 145 | - |
dc.citation.startPage | 127 | - |
dc.citation.endPage | 133 | - |
dc.identifier.bibliographicCitation | EPILEPSY RESEARCH, Vol.145 : 127-133, 2018 | - |
dc.identifier.rimsid | 60375 | - |
dc.type.rims | ART | - |
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