MSBEST aims to develop comprehensive systematic reviews in multiple sclerosis rehabilitation to inform evidence-based care and improve the lives of people living with MS.
The MSBEST (Multiple Sclerosis Best Evidence-Based Strategies and Treatment/Therapies for Rehabilitation) project consists of a series of systematic reviews of the literature on topics in MS care and rehabilitation.
A group of researchers and clinicians in North America with expertise in MS rehabilitation initiated MSBEST. The website provides a comprehensive summary of the research, in addition to clinicians' guidance about appropriate care and rehabilitation for people living with MS. Topic reviews are freely accessible as online modules.
The MSBEST modules help translate research findings into practice, however further strategies are needed. The MSBEST leadership team in partnership with MS Canada hosted a knowledge mobilization summit in 2023, engaging experts and key stakeholders to develop knowledge mobilization priorities for MS rehabilitation. A key priority identified from the summit was the need to create an MS Rehabilitation Best Practice Guideline. The work of the MBSEST team and the next MSBEST modules will be conducted in view of this priority.
The MSBEST team would like to thank The Ralph M. Barford Foundation for their ongoing support. We would also like to acknowledge the Collaboration of Rehabilitation Research Evidence group (CORRE), the University of Saskatchewan College of Medicine, the Saskatchewan Health Authority and the Saskatchewan Health Research Foundation.
Project Leads |
|
Name |
Affiliation |
Katherine B Knox, MD, FRCPC |
Department of Physical Medicine and Rehabilitation, College of Medicine, University of Saskatchewan, Saskatoon, SK, Can |
Sarah J Donkers, BSc, MPT, MSc, PhD |
School of Rehabilitation Science, University of Saskatchewan, SK, Can |
Mark Bayley, MD, FRCPC |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Tania Bruno, MD, FRCPC |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Project coordinators |
|
Name |
Affiliation |
Ailene Kua, MSc, PMP |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Devon Ireland, BScIn Memory |
Past project coordinator Department of Physical Medicine and Rehabilitation, College of Medicine, University of Saskatchewan, Saskatoon, SK, Can |
Magdalena Mirkowski, MSc |
Past project coordinator Collaboration of Rehabilitation Research Evidence (CORRE), Parkwood Institute Research, London, ON, Can |
Project Team Members | |
Name |
Affiliation |
Eman Abdulhadi, MPT, BKin (hons), BA |
Department of Physical Medicine and Rehabilitation, College of Medicine, University of Saskatchewan, Saskatoon, SK, Can |
Afsoun Amiraslany, BSc |
College of Medicine, University of Saskatchewan, Saskatoon, SK, Can |
Mohammad Alshahrani, MD |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Melissa Andersen, BSc, MPT, MD |
Department of Physical Medicine and Rehabilitation, University of Saskatchewan, Saskatoon, SK, Can |
Deborah Backus, PT, PhD, FACRM |
Virginia C. Crawford Institute at Shepherd Center, Atlanta, Georgia, USA |
Ali Bateman MD, FRCPC, CSCN Diplomate (EMG), MSc(c) QIPS |
Parkwood Institute, St. Joseph's Health Care London, Department of Physical Medicine & Rehabilitation, Schulich School of Medicine & Dentistry, Western University, London, ON, Can |
B. Catharine Craven, MD, MSc, FRCPC |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Whitney Duff, BSc, MSc, PhD |
Department of Physical Medicine and Rehabilitation, University of Saskatchewan, Saskatoon, SK, Can |
Karen Ethans, MD, FRCPC |
Winnipeg's Health Sciences Centre, Winnipeg, MB, Can |
Marcia Finlayson, PhD |
Queen's University, Kingston, ON, Can |
Emma Le, PhD |
Department of Physical Medicine and Rehabilitation, University of Saskatchewan, Saskatoon, SK, Can |
Nancy Mayo, BSc (PT), MSc, PhD |
McGill University, Montreal, QC, Can |
Amanda McIntyre, RN MSc |
Collaboration of Rehabilitation Research Evidence (CORRE), Parkwood Institute Research, Lawson Health Research Institute, London, ON, Can |
Sarah A Morrow, MD, FRCPC, MS |
Western University, London, ON, Can |
Rob Motl, PhD |
University of Illinois, Chicago, USA |
Darren Nickel, PhD |
Department of Physical Medicine and Rehabilitation College of Medicine University of Saskatchewan, Saskatoon, SK, Can |
Colleen O'Connell, MD, FRCPC |
Stan Cassidy Centre for Rehabilitation, Fredericton NB, Can |
Eleni M. Patsakos, HBSc, MSc |
Rehabilitation Sciences Institute, Temerty Faculty of Medicine, University of Toronto, KITE Research Institute, University Health Network, Toronto, Ontario, Canada |
Michelle Ploughman, BSc, PT, MSc, PhD |
Memorial University of Newfoundland, St. John's, NL, Can |
Dale Robinson, MD, FRCPC |
Markham Stouffville Hospital, Markham, ON, Can |
Christine Short, MD, FRCPC, FACP |
Nova Scotia Rehabilitation Centre, Halifax, NS, Can |
Robert Simpson, PhD MBChB |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Abe Snaiderman, MD, FRCPC |
University Health Network-Toronto Rehabilitation Institute, Toronto, ON, Can |
Robert Teasell, MD, FRCPC |
Collaboration of Rehabilitation Research Evidence (CORRE), Parkwood Institute Research, Lawson Health Research Institute, London, ON, Can |
Daria Trojan, MD, MSc |
McGill University, Montreal, QC, Can |
Geoffrey K. Turnbull, MD |
Department of Medicine, Dalhousie University, Halifax, NS, Can |
Joy Williams, PT, DPT |
Crawford Research Institute Kaiser Permanente, Northern California, USA |
A systematic literature search is conducted following PRISMA guidelines for each module topic with the online databases PubMed, MEDLINE, CINAHL, Scopus and EMBASE. Each search is limited to articles published after January 1, 1970, investigating rehabilitation interventions for multiple sclerosis and published in English in a peer-reviewed journal. Population key words (i.e., “multiple sclerosis” or “MS”) and complication key words pertaining to a particular symptom are used in combination with intervention key words. Customized complication and intervention search terms are applied for each module with input from content expert MSBEST team members. Literature searches for individual modules are completed independently at various time points.
Selection Criteria
Articles are included if they meet the following criteria:
(1) ≥ 3 adults (≥ 18 years) with multiple sclerosis in the study sample
(2) ≥50% of included participants have a diagnosis of multiple sclerosis, unless the results are stratified by disorder
Case studies/reports, abstracts, editorials/commentaries, protocols, reviews, qualitative studies, and assessment tool evaluations/psychometric analyses are excluded. Additional module specific exclusion/inclusion criteria are detailed in the introduction of each module.
Methodological quality of randomized controlled trials (RCTs) was assessed using the Physiotherapy Evidence Database (PEDro) tool. The PEDro scale consists of 11 items; the first item relates to external validity and the remaining ten items assess internal validity. One point was given for each satisfied criterion (items 2-11) with the exception of the first item, which was given a yes or no, yielding a maximum score of ten. A higher score is representative of a study with better methodological quality. Studies included in this review using a non-RCT design (prospective controlled trials, cohort studies, case controls, pre-post tests, post-tests, and case series) were not assigned a PEDro score.
Data from journal articles included in each module were extracted to form evidence summary tables. The journal article extraction format is described below:
Research findings were summarized by creating levels of evidence to determine the strength of the evidence for each rehabilitation intervention. The levels of evidence presented throughout each module were determined according to the levels of evidence by Sackett et al. (2000). The original system proposed by Sackett et al. (2000) has been modified to reduce the original ten categories into a less complex system comprised of five levels (see Table 1 below). Level 1 evidence pertains to high quality RCTs (PEDro≥6) and has been divided into two subcategories, Level 1a (more than one RCT with a PEDro score of ≥6) and 1b (a single RCT with a PEDro score of ≥6), based on the number of RCTs supporting the evidence statement.
Using this system, RCTs received priority when formulating concluding statements. Conclusions were easily formed when the results of multiple studies were in agreement. In cases where RCTs differed in terms of results and methodological quality, the results of the study (or studies) with higher PEDro score(s) were more heavily weighted to arrive at the final conclusions. In cases where studies of equal methodological quality reported conflicting results, final conclusions were deemed to be conflicting or inconclusive. In cases where the results of a single study of higher quality conflicted with those of several studies of inferior quality, the authors needed to make a more difficult judgment. In these cases, we attempted to provide rationale for our decision in order to make the process as transparent as possible. Readers are always encouraged to be a critical consumer of all the material presented in MSBEST.
Table 1. Modified Sackett Scale
Level |
Research Design |
Description |
Level 1a |
Randomized Controlled Trial (RCT) |
More than 1 Higher RCT, PEDro ≥ 6 Includes within-subjects comparison with randomized conditions and cross-over designs |
Level 1b |
RCT |
1 Higher RCT with PEDro ≥ 6 |
Level 2 |
RCT |
Lower RCT, PEDro < 6 |
Prospective controlled trial |
Prospective controlled trial (not randomized) |
|
Cohort |
Prospective longitudinal study using at least 2 similar groups with one exposed to a particular condition |
|
Level 3 |
Case Control |
Retrospective study comparing conditions, using historical controls |
Level 4 |
Pre-Post Test |
Prospective trial with a baseline measure, intervention, and a post-test using a single group of subjects |
Post-Test |
Prospective intervention study using a post intervention measure only (no pre-test or baseline measurement) with one or more groups |
|
Case Series |
Retrospective study usually collecting variables from a chart review |
|
Level 5 |
Observational |
Study using cross-sectional analysis to interpret relations |
Clinical Consensus |
Expert opinion without explicit critical appraisal, or based on physiology, biomechanics, or “first principles” |
|
Case Report |
Pre-post or case series involving one subject |
References
Sackett, D., Straus, S., Richardson, W., Rosenberg, W., & Haynes, R. (2000). Evidence-Based Medicine: How to Practice and Teach EBM. Toronto, ON: Churchill Livingstone.
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