Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/172764
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dc.contributor.authorCarmona-Iragui, Maria-
dc.contributor.authorSantos, Telma-
dc.contributor.authorVidela, Sebas-
dc.contributor.authorFernández, Susana-
dc.contributor.authorBenejam, Bessy-
dc.contributor.authorVidela, Laura-
dc.contributor.authorAlcolea, Daniel-
dc.contributor.authorBlennow, Kaj-
dc.contributor.authorBlesa González, Rafael-
dc.contributor.authorLleo, Alberto-
dc.contributor.authorFortea Ormaechea, Juan-
dc.date.accessioned2020-12-18T16:51:47Z-
dc.date.available2020-12-18T16:51:47Z-
dc.date.issued2017-10-01-
dc.identifier.issn1387-2877-
dc.identifier.urihttp://hdl.handle.net/2445/172764-
dc.description.abstractBackground: Alzheimer's disease (AD) is the main medical problem in older adults with Down syndrome (DS). Studies of cerebrospinal fluid (CSF) AD biomarkers are limited and the feasibility of lumbar puncture (LP) is controversial in this population. Objective: to analyze the frequency of complications after a LP in DS. Methods: we collected data from 80 adults with DS that underwent a LP within the Down Alzheimer Barcelona Neuroimaging Initiative. Demographics, cognitive status, headache history, and presence of complications after the LP were recorded in every subject. In 53 of them (active group), this information was collected following a semi-structured and validated protocol that actively looks for complications. Other variables related to the LP procedure were also recorded. A telephone interview to the caregiver was performed 5-7 days after the procedure to ask about complications. Data from 27 subjects (clinical practice group), from whom the presence of complications was obtained in a medical follow-up visit within the three months after the LP, were also included. Results: there were no adverse events in 90% of our participants. The most frequent complication was headache (6.25%); only one subject reported a typical post-lumbar puncture headache with moderate severity that required analgesic treatment. Dizziness (3.75%) and back pain (1.25%) were also reported. All the participants that reported complications belonged to the active group. Conclusion: LP can be safely performed to study CSF biomarkers in DS. The reported complications are qualitatively similar to the general population, but are less frequently reported, even when actively searched for.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherIOS Press-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3233/JAD-160827-
dc.relation.ispartofJournal of Alzheimer's Disease, 2017, vol. 55, num. 4, p. 1489-1496-
dc.relation.urihttps://doi.org/10.3233/JAD-160827-
dc.rights(c) Carmona-Iragui, Maria et al., 2017-
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)-
dc.subject.classificationLíquid cefalorraquidi-
dc.subject.classificationMalaltia d'Alzheimer-
dc.subject.classificationSíndrome de Down-
dc.subject.classificationPunció lumbar-
dc.subject.otherCerebrospinal fluid-
dc.subject.otherAlzheimer's disease-
dc.subject.otherDown syndrome-
dc.subject.otherSpinal puncture-
dc.titleFeasibility of lumbar puncture in the study of cerebrospinal fluid biomarkers for Alzheimer disease in subjects with Down syndrome-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec697988-
dc.date.updated2020-12-18T16:51:47Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid27858714-
Appears in Collections:Articles publicats en revistes (Patologia i Terapèutica Experimental)

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