Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/16380
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Tai, Geneieve | - |
dc.contributor.author | Corben, Louise A | - |
dc.contributor.author | Yiu, Eppie M | - |
dc.contributor.author | Delatycki, Martin B | - |
dc.date | 2016-09-28 | - |
dc.date.accessioned | 2016-10-23T23:21:14Z | - |
dc.date.available | 2016-10-23T23:21:14Z | - |
dc.date.issued | 2017-07 | - |
dc.identifier.citation | Acta Neurologica Scandinavica 2017; 136(1): 41-46 | en_US |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/16380 | - |
dc.description.abstract | OBJECTIVES: The Medical Outcomes Study 36 item Short-Form Health Survey (SF-36) is one of the most commonly used patient reported outcome measure. This study aimed to examine the relationship between SF-36 version 2 (SF-36V2) summary scores and Friedreich ataxia (FRDA) clinical characteristics, and to investigate the responsiveness of the scale, in comparison with the Friedreich Ataxia Rating Scale (FARS), over 1, 2 and 3 years. MATERIALS AND METHODS: Descriptive statistics were used to examine the characteristics of the cohort at baseline and years 1, 2 and 3. Correlations between FRDA clinical characteristics and SF-36V2 summary scores were reported. Responsiveness was measured using paired t tests. RESULTS: We found significant correlations between the physical component summary (PCS) of the SF-36V2 and various FRDA clinical parameters but none for the mental component summary. No significant changes in the SF-36V2 were seen over 1 or 2 years; however, PCS scores at Year 3 were significantly lower than at baseline (-3.3, SD [7.6], P=.01). FARS scores were found to be significantly greater at Years 1, 2 and 3 when compared to baseline. CONCLUSIONS: Our findings suggest that despite physical decline, individuals with FRDA have relatively stable mental well-being. This study demonstrates that the SF-36V2 is unlikely to be a useful tool for identifying clinical change in FRDA therapeutic trials. | en_US |
dc.subject | Friedreich ataxia | en_US |
dc.subject | Health status | en_US |
dc.subject | Rating Scales | en_US |
dc.subject | SF-36 | en_US |
dc.title | A longitudinal study of the SF-36 version 2 in Friedreich ataxia | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Acta Neurologica Scandinavica | en_US |
dc.identifier.affiliation | Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville, Victoria, Australia | en_US |
dc.identifier.affiliation | School of Psychological Science, Faculty of Medicine, Nursing and Health Sciences, Monash University, Clayton, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Occupational Therapy, Monash Health, Clayton, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Neurology, Royal Children's Hospital, Parkville, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Clinical Genetics, Austin Health, Heidelberg, Victoria, Australia | en_US |
dc.identifier.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/27679455 | en_US |
dc.identifier.doi | 10.1111/ane.12693 | en_US |
dc.type.content | Text | en_US |
dc.type.austin | Journal Article | en_US |
local.name.researcher | Delatycki, Martin B | |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | Clinical Genetics | - |
Appears in Collections: | Journal articles |
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