Literature DB >> 33424485

"I Will Respect the Autonomy of My Patient": A Scoping Review of Shared Decision Making in Multiple Sclerosis.

Anne Christin Rahn, Alessandra Solari, Heleen Beckerman, Richard Nicholas, David Wilkie, Christoph Heesen, Andrea Giordano.   

Abstract

BACKGROUND: Patient autonomy is a bioethical principle that was strengthened in the revised Declaration of Geneva. Shared decision making (SDM) is particularly relevant in the management of multiple sclerosis (MS) because many preference-sensitive decisions have to be made during the disease course. We aimed to summarize the available evidence on SDM in the MS field and to inform future research and practice.
METHODS: We performed a scoping review by searching MEDLINE (past 5 years). Studies were included if they reported primary/secondary research and focused on SDM related to people with MS. Data were grouped into topics, with results presented in narrative form.
RESULTS: From 865 references, we included 55 studies conducted mostly in Europe. Half of the studies were observational, followed by qualitative (20%), mixed-methods (17%), randomized controlled trials (RCTs, 5%), quasi-experimental (5%), and reviews (4%). Most studies addressed people with relapsing-remitting MS (85%); the remaining addressed health care professionals, patients' significant others, or a combination. We identified five main topics: decisions on disease-modifying drugs, decisions on chronic cerebrospinal venous insufficiency treatment, information provision and patient education, health literacy, and risk knowledge.
CONCLUSIONS: The high proportion of included studies on SDM in MS in Europe suggests an earlier adoption of these concepts in this area. Decisions on disease-modifying drugs was the prevalent topic. Only 5% of studies were RCTs, indicating that more research is needed to study the effectiveness of SDM interventions. Studies addressing people with primary and secondary progressive MS are also needed.
© 2020 Consortium of Multiple Sclerosis Centers.

Entities:  

Keywords:  Decision aids; Multiple sclerosis (MS); Patient Autonomy; Rehabilitation; Shared decision making (SDM)

Year:  2020        PMID: 33424485      PMCID: PMC7780705          DOI: 10.7224/1537-2073.2020-027

Source DB:  PubMed          Journal:  Int J MS Care        ISSN: 1537-2073


  71 in total

1.  An information aid for newly diagnosed multiple sclerosis patients improves disease knowledge and satisfaction with care.

Authors:  A Solari; V Martinelli; M Trojano; A Lugaresi; F Granella; A Giordano; M Messmer Uccelli; R D'Alessandro; E Pucci; P Confalonieri; C Borreani
Journal:  Mult Scler       Date:  2010-09-21       Impact factor: 6.312

2.  A discrete choice experiment to determine UK patient preference for attributes of disease modifying treatments in Multiple Sclerosis.

Authors:  Catherine Bottomley; Andrew Lloyd; Gary Bennett; Nicholas Adlard
Journal:  J Med Econ       Date:  2017-06-14       Impact factor: 2.448

3.  Scoping studies: advancing the methodology.

Authors:  Danielle Levac; Heather Colquhoun; Kelly K O'Brien
Journal:  Implement Sci       Date:  2010-09-20       Impact factor: 7.327

4.  Evaluation of a Novel Preference Assessment Tool for Patients with Multiple Sclerosis.

Authors:  Nananda F Col; Andrew J Solomon; Vicky Springmann; Carolina Ionete; Enrique Alvarez; Brenda Tierman; Christen Kutz; Idanis Berrios Morales; Carolyn Griffin; Long H Ngo; David E Jones; Glenn Phillips; Ashli Hopson; Lori Pbert
Journal:  Int J MS Care       Date:  2018 Nov-Dec

5.  Information provision for people with multiple sclerosis.

Authors:  Sascha Köpke; Alessandra Solari; Anne Rahn; Fary Khan; Christoph Heesen; Andrea Giordano
Journal:  Cochrane Database Syst Rev       Date:  2018-10-14

6.  Dietary Interventions in Multiple Sclerosis: Development and Pilot-Testing of an Evidence Based Patient Education Program.

Authors:  Karin Riemann-Lorenz; Marlene Eilers; Gloria von Geldern; Karl-Heinz Schulz; Sascha Köpke; Christoph Heesen
Journal:  PLoS One       Date:  2016-10-20       Impact factor: 3.240

7.  Comparison of preferences of healthcare professionals and MS patients for attributes of disease-modifying drugs: A best-worst scaling.

Authors:  Ingrid E H Kremer; Silvia M A A Evers; Peter J Jongen; Mickaël Hiligsmann
Journal:  Health Expect       Date:  2017-07-21       Impact factor: 3.377

8.  Initiating disease-modifying treatments in multiple sclerosis: Measuring the decision process using decisional conflict and decisional regret scales.

Authors:  D D Wilkie; A Solari; R Nicholas
Journal:  Mult Scler J Exp Transl Clin       Date:  2019-02-27

9.  Chronic cerebrospinal venous insufficiency in patients with multiple sclerosis.

Authors:  P Zamboni; R Galeotti; E Menegatti; A M Malagoni; G Tacconi; S Dall'Ara; I Bartolomei; F Salvi
Journal:  J Neurol Neurosurg Psychiatry       Date:  2008-12-05       Impact factor: 10.154

10.  Resilience, trust, and civic engagement in the post-CCSVI era.

Authors:  Shelly Benjaminy; Andrew Schepmyer; Judy Illes; Anthony Traboulsee
Journal:  BMC Health Serv Res       Date:  2018-05-16       Impact factor: 2.655

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  1 in total

Review 1.  Treatment Challenges in Multiple Sclerosis - A Continued Role for Glatiramer Acetate?

Authors:  Massimiliano Mirabella; Pietro Annovazzi; Wallace Brownlee; Jeffrey A Cohen; Christoph Kleinschnitz; Christian Wolf
Journal:  Front Neurol       Date:  2022-04-15       Impact factor: 4.086

  1 in total

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