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dc.contributor.authorHartley, H
dc.contributor.authorLane, S
dc.contributor.authorPizer, B
dc.contributor.authorBunn, Lisa
dc.contributor.authorCarter, B
dc.contributor.authorCassidy, E
dc.contributor.authorKumar, R
dc.date.accessioned2021-06-08T09:15:49Z
dc.date.issued2021-07-07
dc.identifier.issn0256-7040
dc.identifier.issn1433-0350
dc.identifier.urihttp://hdl.handle.net/10026.1/17232
dc.descriptionNo embargo required.
dc.description.abstract

<jats:title>Abstract</jats:title><jats:sec> <jats:title>Purpose</jats:title> <jats:p>To report the course of ataxia in children up to 2 years post-operatively, following surgical resection of a posterior fossa tumour (PFT).</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>Thirty-five children, (median age 9 years, range 4–15) having resection of PFT, were assessed using the Scale for the Assessment and Rating of Ataxia (SARA), Brief Ataxia Rating Scale (BARS) and the mobility domain of the Paediatric Evaluation of Disability Index (PEDI-m) at initial post-operative period (baseline), 3 months, 1 year and 2 years post-operatively.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>Baseline median scores of the SARA and BARS were 8.5 (range 0–35.5), and 7 (0–25) respectively. Ataxia improved at 3 months (median SARA and BARS reduction 3.5 and 4, respectively). Additional gradual improvements in SARA were recorded at 1 (median reduction 2) and 2 years post-operatively (median reduction 0.5). Median baseline PEDI-m was 54.75 (range 15.2–100) with improvement at 3 months (median increase 36.95) and small improvement at 1 year (median increase 2.5) and 2 years (median increase 5.8). Children with medulloblastoma and midline tumours (median baseline SARA 10 and 11, respectively) demonstrated more severe ataxia than children with low-grade gliomas and unilateral tumours (median baseline SARA 7.5 and 6.5, respectively).</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>The largest improvement in ataxia scores and functional mobility scores is demonstrated within the first 3 months post-operatively, but ongoing gradual improvement is observed at 2 years. Children with medulloblastoma and midline tumour demonstrated higher ataxia scores long term.</jats:p> </jats:sec>

dc.format.extent2831-2838
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherSpringer (part of Springer Nature)
dc.subjectPaediatrics
dc.subjectCerebellum
dc.subjectRehabilitation
dc.titleAtaxia and mobility in children following surgical resection of posterior fossa tumour: A longitudinal cohort study
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000671924000004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue9
plymouth.volume37
plymouth.publication-statusPublished
plymouth.journalChild's Nervous System
dc.identifier.doi10.1007/s00381-021-05246-0
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Health Professions
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Health and Community
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeGermany
dcterms.dateAccepted2021-04-23
dc.rights.embargodate2021-7-23
dc.identifier.eissn1433-0350
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1007/s00381-021-05246-0
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2021-07-07
rioxxterms.typeJournal Article/Review


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