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dc.contributor.authorÇetiner, Mustafa
dc.contributor.authorSeyit, Murat
dc.contributor.authorAkdağ, Gönül
dc.contributor.authorDemirbaş, Hayri
dc.contributor.authorTemel, Özge
dc.contributor.authorCanbaz Kabay, Sibel
dc.date.accessioned2021-05-05T22:11:54Z
dc.date.available2021-05-05T22:11:54Z
dc.date.issued2019
dc.identifier.issn1301-062X
dc.identifier.urihttps://doi.org/10.4274/tnd.galenos.2019.34445
dc.identifier.urihttps://hdl.handle.net/20.500.12933/225
dc.description2-s2.0-85073417514en_US
dc.description.abstractObjective: We aimed to evaluate the demographic, clinical, laboratory and electrophysiological findings of patients with inpatient Guillain-Barré syndrome in our clinics and to investigate the effect of these parameters on the prognosis of the disease. Materials and Methods: Between January 2014 and April 2018, file records of patients admitted to our clinics with the diagnosis of Guillain-Barré syndrome were retrospectively reviewed. Demographic characteristics, clinical, laboratory and electrophysiological findings of the patients at the time of admission were recorded. Patients were clinically graded according to the Hughes classification at the time of admission and on the 3rd month after discharge. Results: In the study, 25 of the 51 patients were male (49%) and 26 were female (51%) and the mean age was 54.21±17.32 years. According to clinical and electrophysiologic diagnosis, 34 patients (66.7%) had acute inflammatory demyelinating polyradiculoneuropathy, 9 patients (17.6%) had acute motor axonal neuropathy, 6 patients (11.8%) had acute motor sensory axonal neuropathy and 2 patients (3.9%) had Miller Fisher syndrome. According to Hughes scoring on the 3rd month after discharge, 31 patients (60.8%) had in good prognosis (Hughes score ?2) and 20 patients (39.2%) had in poor prognosis group (Hughes score >2). In the comparison between the two groups according to clinical, demographic, and laboratory parameters, older age (?50), high Hughes score at admission, weakness in extremities as first complaint, the presence of complications, need for mechanical ventilation and presence of gastroenteritis as a leading infection were evaluated as prognostic factors. Conclusion: The most common variant of Guillain-Barré syndrome in our study was acute inflammatory demyelinating polyradiculoneuropathy. Older age (?50), high Hughes score at admission, weakness in extremities as the first symptom, presence of complications, need for mechanical ventilation, and presence of gastroenteritis as a precursor infection were poor prognostic factors. © 2019 by Turkish Neurological Society.en_US
dc.language.isoengen_US
dc.publisherTurkish Neurosurgical Societyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectClinical findingsen_US
dc.subjectGuillain-Barré syndromeen_US
dc.subjectPrognosisen_US
dc.titleFactors associated with prognosis in patients with guillain-barré syndrome [Guillain-Barré Sendromlu Hastalarda Prognozla İlişkili Faktörler]en_US
dc.typearticleen_US
dc.departmentAFSÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Nöroloji Ana Bilim Dalı
dc.contributor.institutionauthorDemirbaş, Hayri
dc.identifier.doi10.4274/tnd.galenos.2019.34445
dc.identifier.volume25en_US
dc.identifier.issue3en_US
dc.identifier.startpage140en_US
dc.identifier.endpage145en_US
dc.relation.journalTurk Noroloji Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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