Views of Multiple Sclerosis Patients About Key Elements for a Decision Aid: A Qualitative Study

Altres autors/es

Institut Català de la Salut

[Robles-Sanchez MA] Centre d'Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca Multidisciplinari d'Infermeria, Vall d'Hebron Institut de Recerca (VHIR), Barcelona, Spain. Faculty of Nursing, University of Girona, Girona, Spain. [Moharra M] Agency for Health Quality and Assessment of Catalonia (AQuAS), Department of Health of Catalonia, Barcelona, Spain. [Bosch-Farré C] Faculty of Nursing, University of Girona, Girona, Spain. [Hernández-Leal MJ] Department of Community, Maternity and Pediatric Nursing, School of Nursing, University of Navarra, Pamplona, Spain. Program in Medical Sciences, University of La Frontera, Temuco, Chile. Millennium Nucleus on Sociomedicine (SocioMed), Santiago, Chile. [Montalban X] Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain. [Sastre-Garriga J] Centre d'Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Data de publicació

2023-09-19T09:02:02Z

2023-09-19T09:02:02Z

2023-10

Resum

Multiple Sclerosis


Esclerosi múltiple


Esclerosis múltiple


BACKGROUND: Patients with multiple sclerosis (MS) may experience decisional conflict during treatment choice. Shared decision making (SDM), whereby patients and health professionals, primarily nurses, collaborate in making decisions, reduces this decisional conflict. It requires understanding large amounts of information and may be complex, especially when decisions affect patients' autonomy and quality and prolongation of life. Patient decision aids are tools in facilitating SDM. This study aimed to identify the key elements from the perspective of patients with relapsing-remitting MS to create a patient decision aid in the Spanish sociocultural context. METHODS: This is a qualitative study using focus groups led by a clinical nurse specialist. Semistructured interviews included healthcare needs and demands, the SDM process, and general characteristics of a peer support program. After the transcription of interview recordings, data were analyzed by thematic analysis and a constructivist naturalistic approach. RESULTS: Patients with MS (27) from Spain participated in 4 focus groups of 90 to 120 minutes each. Three overarching themes were identified: information access to sufficient high-quality data; knowledge of available treatment options, including efficacy, adverse effects, frequency, administration route, and the impact on daily life; decision-making role, engaged versus nonengaged patients. The former require support in facilitating their active involvement in decisions, whereas the latter prefer more passive health models. CONCLUSION: The needs identified by patients with relapsing-remitting MS regarding treatment choice in the Spanish setting align with those reported by other studies. The identified themes provide valuable information to design and develop a virtual patient decision aid jointly by clinical MS nurses and patients according to the International Patient Decision Aid Standards Collaboration criteria. This aid will help improve understanding between nurses and patients during SDM and facilitate the process.

Tipus de document

Article


Versió publicada

Llengua

Anglès

Publicat per

Wolters Kluwer Health

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