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dc.contributor.authorTurgut, Nilda
dc.contributor.authorAltunan, Bengü
dc.contributor.authorGündoğdu, Aksoy
dc.date.accessioned2022-05-11T14:40:18Z
dc.date.available2022-05-11T14:40:18Z
dc.date.issued2020
dc.identifier.issn1300-8773
dc.identifier.urihttps://doi.org/10.5455/NYS.20200307085847
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8932
dc.description.abstractIntroduction: Multiple sclerosis (MS) and neuromyelitis optica spectrum disorders (NMOSD) are idiopathic, autoimmune, and central nervous system inflammatory diseases. The similarity in the clinical course of both diseases creates difficulties in the differential diagnosis. Pattern reversal visual evoked potentials (VEP) are used at this stage. This study aimed to investigate VEP’s role in the differential diagnosis of MS and NMOSD when the patients apply with acute optic neuritis. Method: The data of 15 relapsing-remitting MS patients (RRMS) and 10 NMOSD patients (1 seropositive patient) presenting with blurred vision and who were diagnosed with acute optic neuritis were retrospectively analyzed. Demographic, disease, and VEP characteristics of the patients were recorded. Results: According to retrospective data obtained from NMOSD patients, the mean P100 latency was 117.3 ± 12.3, and the mean amplitude was 6.1 ± 3.5. When the VEP characteristics obtained from 15 RRMS patients were evaluated, the P100 latency was 131.7 ± 17.3, and the mean P100 amplitude was 8.0 ± 3.0. P100 latency was significantly prolonged in the RRMS group than the NMOSD group, and amplitude was significantly lower in the NMOSD group than the RRMS group. Discussion: Differentiating NMOSD patients with optic neuritis from MS in the early period is very important for preventing permanent visual damage, initiating appropriate treatment, planning treatment, and predicting prognosis. VEP findings in early-stage acute optic neuritis can be used to differentiate clinically challenging both seropositive and seronegative NMOSD patients from patients with MS. © 2020, Istanbul Universitesi. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherIstanbul Universitesien_US
dc.identifier.doi10.5455/NYS.20200307085847
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeuromyelitis optica spectrum disordersen_US
dc.subjectP100 amplitudeen_US
dc.subjectP100 latencyen_US
dc.subjectPattern reversal visual evoked potentialsen_US
dc.subjectRelapsing-remitting multiple sclerosisen_US
dc.subjectaquaporin 4 antibodyen_US
dc.subjectimmunoglobulin Gen_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectArticleen_US
dc.subjectblurred visionen_US
dc.subjectclinical articleen_US
dc.subjectcomparative studyen_US
dc.subjectdisease durationen_US
dc.subjectelectrical potential parametersen_US
dc.subjectExpanded Disability Status Scaleen_US
dc.subjectfemaleen_US
dc.subjecthumanen_US
dc.subjectlatent perioden_US
dc.subjectmaleen_US
dc.subjectmultiple sclerosisen_US
dc.subjectmyelooptic neuropathyen_US
dc.subjectneurophysiologyen_US
dc.subjectoccipital cortexen_US
dc.subjectoptic neuritisen_US
dc.subjectprognosisen_US
dc.subjectretrospective studyen_US
dc.subjecttreatment planningen_US
dc.subjectvisual evoked potentialen_US
dc.titleThe comparison of vep parameters in neuromyelitis optica spectrum disorders and multiple sclerosis patients with acute optic neuritisen_US
dc.title.alternativeAkut optik nöritli multipl skleroz ve nöromiyelitis optika spektrum bozuklukları hasta-larında vep parametrelerinin karşılaştırılması]en_US
dc.typearticleen_US
dc.relation.ispartofYeni Symposiumen_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Nöroloji Ana Bilim Dalıen_US
dc.identifier.volume58en_US
dc.identifier.issue1en_US
dc.identifier.startpage1en_US
dc.identifier.endpage4en_US
dc.institutionauthorTurgut, Nilda
dc.institutionauthorAltunan, Bengü
dc.institutionauthorGündoğdu, Aksoy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid6603040523
dc.authorscopusid57211906388
dc.authorscopusid57220069864
dc.identifier.scopus2-s2.0-85096779124en_US


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