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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorAlemañ Díez, Jose
dc.contributor.authorLópez Diego, Verónica
dc.contributor.authorSalvadó Figueras, Maria
dc.contributor.authorLlaurado, Arnau
dc.contributor.authorQuintana, Manuel
dc.contributor.authorGratacòs-Viñola, Margarida
dc.contributor.authorVidal-Taboada, jose M
dc.contributor.authorRestrepo Vera, Juan Luis
dc.contributor.authorSánchez-Tejerina, Daniel
dc.contributor.authorSotoca, Javier
dc.contributor.authorRaguer, Núria
dc.contributor.authorJuntas Morales, Raúl
dc.date.accessioned2024-05-13T08:09:14Z
dc.date.available2024-05-13T08:09:14Z
dc.date.issued2024-04-08
dc.identifier.citationLlauradó A, Quintana M, Gratacós-Viñola M, Vidal-Taboada JM, Restrepo-Vera JL, Alemañ J, et al. Gait Assessment in Chronic Inflammatory Demyelinating Polyradiculoneuropathy. Acta Neurol Scand. 2024 Apr 8;2024:7037704.
dc.identifier.issn1600-0404
dc.identifier.urihttps://hdl.handle.net/11351/11451
dc.descriptionAssessment; Chronic inflammatory demyelinating polyradiculoneuropathy
dc.description.abstractBackground and Aims. Gait impairment is a common manifestation of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). However, clinicians lack an effective monitoring tool, as no gait test has been validated for CIDP. The aim of this study was to determine the usefulness of three tests in monitoring the clinical course of patients with CIDP: Timed Up and Go (TUG), 10-Meter Walk Test (10MWT), and 30-Second Chair Stand (30SCS). Methods. This is a prospective, single-center observational study. We included newly diagnosed CIDP patients starting treatment or relapsed CIDP patients requiring new treatment. We monitored the clinical course using CIDP-validated clinical scales and correlated changes in clinical status with the results of the gait tests. A ROC curve was developed, and we chose the cut-off point on each scale with the best specificity and sensitivity to detect change in clinical status. Results. A total of 20 patients have been recruited. The 3 tests show a statistical correlation with objective clinical improvement. In patients who have showed clinical improvement during the follow-up examination, a mean reduction of 4.8 seconds in TUG and 2.6 in 10MWT and a gain of 3 repetitions in 30SCS have been observed. The optimal cut-off points for each test were seconds, seconds, and repetition. The TUG test has the highest sensitivity (82.6%), and the 30SCS test has the highest specificity (100%) for detecting clinical improvement. Conclusions. The study found that the TUG and 30SCS tests could become effective tools for monitoring treatment response in CIDP patients.
dc.language.isoeng
dc.publisherWiley
dc.publisherHindawi
dc.relation.ispartofseriesActa Neurologica Scandinavica;2024
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectMarcadors bioquímics
dc.subjectMedicaments immunosupressors - Tractament
dc.subjectTrastorns de la marxa
dc.subjectSistema nerviós - Malalties - Tractament
dc.subjectMalalties autoimmunitàries - Tractament
dc.subject.meshPolyradiculoneuropathy, Chronic Inflammatory Demyelinating
dc.subject.meshBiomarkers
dc.subject.meshImmunosuppressive Agents
dc.subject.meshGait Disorders, Neurologic
dc.titleGait Assessment in Chronic Inflammatory Demyelinating Polyradiculoneuropathy
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1155/2024/7037704
dc.subject.decspolirradiculoneuropatía desmielinizante inflamatoria crónica
dc.subject.decsbiomarcadores
dc.subject.decsinmunosupresores
dc.subject.decstrastornos neurológicos de la marcha
dc.relation.publishversionhttps://doi.org/10.1155/2024/7037704
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Llauradó A, Quintana M, Vidal-Taboada JM, Restrepo-Vera JL, Alemañ J, López-Diego V, Salvadó M, Sanchez-Tejerina D, Sotoca J, Juntas-Morales R] Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Gratacós-Viñola M, Raguer N] Servei de Neurofisiologia Clínica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.wos001205923300001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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