PMID- 26564998 OWN - NLM STAT- MEDLINE DCOM- 20180117 LR - 20220410 IS - 1477-0970 (Electronic) IS - 1352-4585 (Print) IS - 1352-4585 (Linking) VI - 22 IP - 10 DP - 2016 Sep TI - A comparative analysis of Patient-Reported Expanded Disability Status Scale tools. PG - 1349-58 LID - 10.1177/1352458515616205 [doi] AB - BACKGROUND: Patient-Reported Expanded Disability Status Scale (PREDSS) tools are an attractive alternative to the Expanded Disability Status Scale (EDSS) during long term or geographically challenging studies, or in pressured clinical service environments. OBJECTIVES: Because the studies reporting these tools have used different metrics to compare the PREDSS and EDSS, we undertook an individual patient data level analysis of all available tools. METHODS: Spearman's rho and the Bland-Altman method were used to assess correlation and agreement respectively. RESULTS: A systematic search for validated PREDSS tools covering the full EDSS range identified eight such tools. Individual patient data were available for five PREDSS tools. Excellent correlation was observed between EDSS and PREDSS with all tools. A higher level of agreement was observed with increasing levels of disability. In all tools, the 95% limits of agreement were greater than the minimum EDSS difference considered to be clinically significant. However, the intra-class coefficient was greater than that reported for EDSS raters of mixed seniority. The visual functional system was identified as the most significant predictor of the PREDSS-EDSS difference. CONCLUSION: This analysis will (1) enable researchers and service providers to make an informed choice of PREDSS tool, depending on their individual requirements, and (2) facilitate improvement of current PREDSS tools. CI - (c) The Author(s), 2015. FAU - Collins, Christian DE AU - Collins CD AD - Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK. FAU - Ivry, Ben AU - Ivry B AD - Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK. FAU - Bowen, James D AU - Bowen JD AD - Multiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, WA, USA. FAU - Cheng, Eric M AU - Cheng EM AD - Department of Neurology, David Geffen School of Medicine, VA Greater Los Angeles Healthcare System, University of California, Los Angeles (UCLA), Los Angeles, CA, USA. FAU - Dobson, Ruth AU - Dobson R AD - Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK. FAU - Goodin, Douglas S AU - Goodin DS AD - Department of Neurology, University of California, San Francisco (UCSF), San Francisco, CA, USA. FAU - Lechner-Scott, Jeannette AU - Lechner-Scott J AD - Hunter Medical Research Institute, The University of Newcastle, Australia and Department of Neurology, John Hunter Hospital, Newcastle, NSW, Australia. FAU - Kappos, Ludwig AU - Kappos L AD - Departments of Medicine, Clinical Research, Biomedicine and Biomedical Engineering, University Hospital Basel, Basel, Switzerland. FAU - Galea, Ian AU - Galea I AD - Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK/Wessex Neurosciences Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK I.Galea@soton.ac.uk. LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20151112 PL - England TA - Mult Scler JT - Multiple sclerosis (Houndmills, Basingstoke, England) JID - 9509185 SB - IM MH - *Disability Evaluation MH - Humans MH - Multiple Sclerosis/*physiopathology MH - *Patient Reported Outcome Measures PMC - PMC5015760 OTO - NOTNLM OT - Expanded disability status scale OT - Kurtzke scale OT - Neurostatus OT - Patient-reported Expanded Disability Status Scale OT - multiple sclerosis OT - patient reported OT - self administered COIS- The author(s) declared no potential conflicts of interest with respect to the research, authorship and/or publication of this article. EDAT- 2015/11/14 06:00 MHDA- 2018/01/18 06:00 PMCR- 2016/09/08 CRDT- 2015/11/14 06:00 PHST- 2015/07/09 00:00 [received] PHST- 2015/09/30 00:00 [accepted] PHST- 2015/11/14 06:00 [entrez] PHST- 2015/11/14 06:00 [pubmed] PHST- 2018/01/18 06:00 [medline] PHST- 2016/09/08 00:00 [pmc-release] AID - 1352458515616205 [pii] AID - 10.1177_1352458515616205 [pii] AID - 10.1177/1352458515616205 [doi] PST - ppublish SO - Mult Scler. 2016 Sep;22(10):1349-58. doi: 10.1177/1352458515616205. Epub 2015 Nov 12.