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Comparison of preferences of healthcare professionals and MS patients for attributes of disease‐modifying drugs

A best‐worst scaling

Bibliographic Data

ID19505993
AuthorsIngrid E H Kremer (0000-0003-2784-8207, Department of Health Services Research Care and Public Health Research Institute (CAPHRI) Maastricht University Maastricht The Netherlands, corresponding author), Sandra Ever (0000-0003-1026-570X, Maastricht University), Silvia M A A Evers (Department of Health Services Research Care and Public Health Research Institute (CAPHRI) Maastricht University Maastricht The Netherlands), Peter Joseph Jongen (0000-0002-9202-6309, University Medical Center Groningen), Mickaël Hiligsmann (0000-0003-4274-9258, Department of Health Services Research Care and Public Health Research Institute (CAPHRI) Maastricht University Maastricht The Netherlands)
Year2018
Volume21
Issue1
Pages171-180
Publication date2018-02-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueHealth Expectations (JOURNAL)
Journal identifiersISSN: 1369-6513 • E-ISSN: 1369-7625
PublisherWiley (PUBLISHER • GB)
DOI10.1111/hex.12599
PMID28734004
OpenAlexW2736882042
LanguageEN
Citations received1
References cited26

BACKGROUND: The choice between disease-modifying drugs (DMDs) for the treatment of multiple sclerosis (MS) becomes more often a shared decision between the patient and the neurologist and MS nurse. This study aimed to assess which DMD attributes are most important for the healthcare professionals in selecting a DMD for a patient. Subsequently, within this perspective, the neurologists' and nurses' perspectives were compared. Lastly, the healthcare professionals' perspective was compared with the patients' perspective to detect any differences that may need attention in the communication about DMDs. DESIGN: A best-worst scaling (BWS) was conducted among 27 neurologists and 33 MS nurses treating patients with MS to determine the importance of 27 DMD attributes. These attributes were identified through three focus groups with MS patients in a previous study (N=19). Relative importance scores (RISs) were estimated for each attribute. Multivariable linear regression analyses were used to compare the different perspectives. RESULTS: According to the neurologists and nurses, safety of the DMD was the most important DMD attribute in the treatment decision, closely followed by effect on disability progression, quality of life and relapse rate. Patients with MS agreed with the importance of the last three attributes, but valued safety significantly lower (b=-2.59, P<.001). CONCLUSIONS: This study suggests that, overall, neurologists and nurses regard the same DMD attributes as important as MS patients with the notable exception of safety. This study provides valuable information for the development of interventions to support shared decision making and highlights which attributes of DMDs may need additional attention

Disease · Family medicine · Health care · Health professionals · Multiple sclerosis · Patient participation · Psychiatry · Psychological intervention · Computer Science · Health Systems, Economic Evaluations, Quality of Life · Medicine · Multiple Sclerosis Research Studies · Nursing · Patient-Provider Communication in Healthcare · Psychology · Internal Medicine

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    Open Access•Terry N Flynn, Jordan J Louviere et al.•Journal of Health Economics•2007

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    Dawn Stacey, France Légaré et al.•Cochrane Database of Systematic…•2017

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Unique citing works1
Citations per year0.14
Citation span2019 - 2019 (1)
Citation velocityhistorical
Highly citedNo
Citation typesNeutral: 1

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