Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey

dc.authorid0000-0002-3613-0814
dc.authorid0000-0001-7462-4578
dc.authorid0000-0003-0896-8799
dc.authorid0000-0001-8869-0277
dc.contributor.authorUnver, Olcay
dc.contributor.authorTurkdogan, Dilsad
dc.contributor.authorGuler, Serhat
dc.contributor.authorKipoglu, Osman
dc.contributor.authorGungor, Mesut
dc.contributor.authorPaketci, Cem
dc.contributor.authorCarman, Kursat Bora
dc.date.accessioned2025-05-10T19:49:14Z
dc.date.issued2021
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractAim: We aim to describe the demographic characteristics, etiology, neurophysiology, imaging findings, treatment, prognosis, and prognostic factors of acute flaccid myelitis. Methods: The clinical data, laboratory test and, magnetic resonance imaging (MRI) results of pediatric patients diagnosed with acute flaccid myelitis according to the Centers for Disease Control criteria between August 1, 2016, and December 31, 2018, from 13 centers in Turkey were reviewed. Results: Of the 34 cases identified, 31 were confirmed (91.2%). Eighteen patients (55.9%) were boys. The median patient age was 4 years (interquartile range 2.5-6.9 years). Most of the patients were admitted in 2018 (n = 27). A preceding history of a febrile illness was reported in all patients, with a median of 4 days (interquartile range 3-7 days) before symptom onset. Thirty-one patients had T2 hyperintensity on spinal MRI, and 18 patients had cerebrospinal fluid pleocytosis. The most common infectious agents were entero/rhinoviruses (n = 5) in respiratory specimens. All patients except one received immunotherapy either alone or in combination. Among 27 patients with follow-up data 24 had persistent weakness. Involvement of four limbs together with an abnormal brain MRI at onset were associated with a poor prognosis. Conclusion: The number of patients with acute flaccid myelitis increased since 2012, spiking with every 2-year interval, largely in the pediatric population. The median age decreases with every outbreak. Clinicians should be aware of the clinical picture for early collection of specimens and early start of rehabilitation programs. Further studies are needed to better characterize the etiology, pathogenesis, risk factors, and treatment of this rare condition. (c) 2020 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
dc.identifier.doi10.1016/j.ejpn.2020.10.011
dc.identifier.endpage120
dc.identifier.issn1090-3798
dc.identifier.issn1532-2130
dc.identifier.pmid33218883
dc.identifier.scopusqualityQ1
dc.identifier.startpage113
dc.identifier.urihttps://doi.org/10.1016/j.ejpn.2020.10.011
dc.identifier.urihttps://hdl.handle.net/20.500.14730/11972
dc.identifier.volume30
dc.identifier.wosWOS:000637968400019
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.ispartofEuropean Journal of Paediatric Neurology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectAcute flaccid paralysis
dc.subjectEnterovirus D-68
dc.subjectPolio-like disease
dc.subjectEnterovirus
dc.titleAcute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey
dc.typeArticle

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