Publication:
Acute flaccid myelitis and Guillain-Barré syndrome in children: A comparative study with evaluation of diagnostic criteria

dc.contributor.authorHelfferich, Jelte
dc.contributor.authorRoodbol, Joyce
dc.contributor.authorde Wit, Marie-Claire
dc.contributor.authorBrouwer, Oebele F
dc.contributor.authorJacobs, Bart C
dc.contributor.author2016 Enterovirus D68 Acute Flaccid Myelitis Working Group
dc.contributor.authorDutch Pediatric GBS Study Group
dc.contributor.authorCabrerizo, Maria
dc.contributor.funderPrinses Beatrix Spierfondses_ES
dc.date.accessioned2023-05-09T07:53:31Z
dc.date.available2023-05-09T07:53:31Z
dc.date.issued2022-02
dc.description.abstractBackground and purpose: Differentiation between acute flaccid myelitis (AFM) and Guillain-Barré syndrome (GBS) can be difficult, particularly in children. Our objective was to improve the diagnostic accuracy by giving recommendations based on a comparison of clinical features and diagnostic criteria in children with AFM or GBS. Methods: A cohort of 26 children with AFM associated with enterovirus D68 was compared to a cohort of 156 children with GBS. The specificity of the Brighton criteria, used for GBS diagnosis, was evaluated in the AFM cohort and the specificity of the Centers for Disease Control and Prevention (CDC) AFM diagnostic criteria in the GBS cohort. Results: Children with AFM compared to those with GBS had a shorter interval between onset of weakness and nadir (3 vs. 8 days, p < 0.001), more often had asymmetric limb weakness (58% vs. 0%, p < 0.001), and less frequently had sensory deficits (0% vs. 40%, p < 0.001). In AFM, cerebrospinal fluid leukocyte counts were higher, whereas protein concentrations were lower. Spinal cord lesions on magnetic resonance imaging were only found in AFM patients. No GBS case fulfilled CDC criteria for definite AFM. Of the AFM cases, 8% fulfilled the Brighton criteria for GBS, when omitting the criterion of excluding an alternate diagnosis. Conclusions: Despite the overlap in clinical presentation, we found distinctive early clinical and diagnostic characteristics for differentiating AFM from GBS in children. Diagnostic criteria for AFM and GBS usually perform well, but some AFM cases may fulfill clinical diagnostic criteria for GBS. This underlines the need to perform diagnostic tests early to exclude AFM in children suspected of atypical GBS.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThe Prinses Beatrix Spierfonds funded the PhD project of J.R. on GBS in children (project number: W.OR12-04)es_ES
dc.format.number2es_ES
dc.format.page593-604es_ES
dc.format.volume29es_ES
dc.identifier.citationEur J Neurol. 2022 Feb;29(2):593-604.es_ES
dc.identifier.doi10.1111/ene.15170es_ES
dc.identifier.e-issn1468-1331es_ES
dc.identifier.journalEuropean journal of neurologyes_ES
dc.identifier.pubmedID34747551es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16024
dc.language.isoenges_ES
dc.publisherWiley
dc.relation.publisherversionhttps://doi.org/10.1111/ene.15170es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBrighton criteriaes_ES
dc.subjectGuillain-Barré syndromees_ES
dc.subjectAcute flaccid myelitises_ES
dc.subject.meshCentral Nervous System Viral Diseaseses_ES
dc.subject.meshGuillain-Barre Syndromees_ES
dc.subject.meshMyelitises_ES
dc.subject.meshNeuromuscular Diseaseses_ES
dc.subject.meshChildes_ES
dc.subject.meshHumanses_ES
dc.titleAcute flaccid myelitis and Guillain-Barré syndrome in children: A comparative study with evaluation of diagnostic criteriaes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication9d46c24b-57af-4d1f-9df2-67ce5c248b37
relation.isAuthorOfPublication.latestForDiscovery9d46c24b-57af-4d1f-9df2-67ce5c248b37
relation.isPublisherOfPublicationd81e762a-95f7-4917-88a1-8004b3b8caa7
relation.isPublisherOfPublication.latestForDiscoveryd81e762a-95f7-4917-88a1-8004b3b8caa7

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