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Serial Nerve Conduction Studies in Guillain-Barré Syndrome: Its Usefulness and Precise Timing

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dc.contributor.authorLee, Hyung-Soo-
dc.contributor.authorSuh, Bum Chun-
dc.contributor.authorKim, Jong Kuk-
dc.contributor.authorKim, Byung-Jo-
dc.contributor.authorNam, Tai-Seung-
dc.contributor.authorOh, Jeeyoung-
dc.contributor.authorBae, Jong Seok-
dc.contributor.authorShin, Kyong Jin-
dc.contributor.authorKim, Seung Woo-
dc.contributor.authorKim, Seung Min-
dc.contributor.authorShin, Ha Young-
dc.date.accessioned2024-12-06T03:36:18Z-
dc.date.available2024-12-06T03:36:18Z-
dc.date.created2025-01-24-
dc.date.issued2024-03-
dc.identifier.issn0736-0258-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201174-
dc.description.abstractSupplemental Digital Content is Available in the Text. Purpose:Nerve conduction study (NCS) is essential for subclassifying Guillain-Barre syndrome (GBS). It is well known that the GBS subclassification can change through serial NCSs. However, the usefulness of serial NCSs is debatable, especially in patients with early stage GBS.Methods:Follow-up NCS data within 3 weeks (early followed NCS, EFN) and within 3 to 10 weeks (late-followed NCS, LFN) were collected from 60 patients with GBS who underwent their first NCS (FN) within 10 days after symptom onset. Each NCS was classified into five subtypes (normal, demyelinating, axonal, inexcitable, and equivocal), according to Hadden's and Rajabally's criteria. We analyzed the frequency of significant changes in classification (SCCs) comprising electrodiagnostic aggravation and subtype shifts between demyelinating and axonal types according to follow-up timing.Results:Between FN and EFN, 33.3% of patients with Hadden's criteria and 18.3% with Rajabally's criteria showed SCCs. Between FN and LFN, 23.3% of patients with Hadden's criteria and 21.7% with Rajabally's criteria showed SCCs, of which 71.4% (Hadden's criteria) and 46.2% (Rajabally's criteria) already showed SCCs from the EFN. The conditions of delayed SCCs between EFN and LFN were very early FN, mild symptoms at the FN, or persistent electrophysiological deterioration 3 weeks after symptom onset.Conclusions:A substantial proportion of patients with GBS showed significant changes in neurophysiological classification at the early stage. Serial NCS may be helpful for precise neurophysiological classification. This study suggests that follow-up NCSs should be performed within 3 weeks of symptom onset in patients with GBS in whom FN was performed within 10 days of symptom onset.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherLippincott Williams & Wilkins-
dc.relation.isPartOfJOURNAL OF CLINICAL NEUROPHYSIOLOGY-
dc.relation.isPartOfJOURNAL OF CLINICAL NEUROPHYSIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleSerial Nerve Conduction Studies in Guillain-Barré Syndrome: Its Usefulness and Precise Timing-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorLee, Hyung-Soo-
dc.contributor.googleauthorSuh, Bum Chun-
dc.contributor.googleauthorKim, Jong Kuk-
dc.contributor.googleauthorKim, Byung-Jo-
dc.contributor.googleauthorNam, Tai-Seung-
dc.contributor.googleauthorOh, Jeeyoung-
dc.contributor.googleauthorBae, Jong Seok-
dc.contributor.googleauthorShin, Kyong Jin-
dc.contributor.googleauthorKim, Seung Woo-
dc.contributor.googleauthorKim, Seung Min-
dc.contributor.googleauthorShin, Ha Young-
dc.identifier.doi10.1097/WNP.0000000000000985-
dc.relation.journalcodeJ04646-
dc.identifier.eissn1537-1603-
dc.identifier.pmid38436391-
dc.subject.keywordGuillain-Barre syndrome-
dc.subject.keywordNerve conduction studies-
dc.subject.keywordAcute inflammatory demyelinating polyneuropathy-
dc.subject.keywordAcute motor axonal neuropathy-
dc.subject.keywordSerial nerve conduction study-
dc.contributor.alternativeNameKim, Seung Min-
dc.contributor.affiliatedAuthorKim, Seung Woo-
dc.contributor.affiliatedAuthorKim, Seung Min-
dc.contributor.affiliatedAuthorShin, Ha Young-
dc.identifier.scopusid2-s2.0-85186869800-
dc.identifier.wosid001179512900013-
dc.citation.volume41-
dc.citation.number3-
dc.citation.startPage278-
dc.citation.endPage284-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL NEUROPHYSIOLOGY, Vol.41(3) : 278-284, 2024-03-
dc.identifier.rimsid84575-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorGuillain-Barre syndrome-
dc.subject.keywordAuthorNerve conduction studies-
dc.subject.keywordAuthorAcute inflammatory demyelinating polyneuropathy-
dc.subject.keywordAuthorAcute motor axonal neuropathy-
dc.subject.keywordAuthorSerial nerve conduction study-
dc.subject.keywordPlusEARLY ELECTRODIAGNOSTIC FINDINGS-
dc.subject.keywordPlusSYNDROME SUBTYPES-
dc.subject.keywordPlusPATTERNS-
dc.subject.keywordPlusCRITERIA-
dc.subject.keywordPlusFAILURE-
dc.subject.keywordPlusBLOCK-
dc.subject.keywordPlusSETS-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalResearchAreaNeurosciences & Neurology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers

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