Inês Margarido , Inês V. Carvalho , Cátia Oliveira , Danna Krupka , Miguel Duarte , Nathalia Barros , Luís Ruano , Manuel Salavisa , Sónia Batista , Joana Guimarães , Maria José Sá , José Vale , Luís Isidoro
{"title":"PERSIMS: Comparing doctors and patients PERSpectives on quality of life In Multiple Sclerosis","authors":"Inês Margarido , Inês V. Carvalho , Cátia Oliveira , Danna Krupka , Miguel Duarte , Nathalia Barros , Luís Ruano , Manuel Salavisa , Sónia Batista , Joana Guimarães , Maria José Sá , José Vale , Luís Isidoro","doi":"10.1016/j.jocn.2025.111313","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Advances in Multiple Sclerosis (MS) therapy have improved prognosis, but significant disability can still occur. Understanding the perspectives of doctors and patients on how MS and its treatment impact quality of life (QoL) is crucial. We aimed to explore the perceptions of MS patients and neurologists on MS symptoms, treatment, and their impact on QoL.</div></div><div><h3>Methods</h3><div>A cross-sectional online survey was conducted, targeting adult patients with MS and physicians experienced in MS care. Patients’ quality of life (QoL) was assessed using the MS Quality of Life (MSQOL-54) scale.</div></div><div><h3>Results</h3><div>252 patients and 53 doctors completed the survey. Relapses in the previous year were associated with lower physical (p = 0.026) and mental (p = 0.022) health scores. Being satisfied with disease-modifying treatment (DMT) and being involved in its choice were also associated with higher physical (both p < 0.001) and mental (p = 0.024 and p = 0.002, respectively) health scores; these scores were not different in patients under moderate versus high-efficacy DMTs (physical p = 0.582 and mental p = 0.180). Patients’ and doctors’ perspectives differ in what they value for QoL. Patients prioritized mental health (p = 0.024), while doctors focused on the impact of physical aspects on QoL (p = 0.030 and p = 0.004). Patients valued information about social support (p < 0.001) more than doctors and considered fatigue more challenging to discuss (p = 0.039), whereas doctors highlighted sexual dysfunction as difficult to address (p < 0.001). Doctors prioritized workplace adaptations (p = 0.041), while patients preferred faster access to healthcare to improve QoL (p < 0.001).</div></div><div><h3>Conclusion</h3><div>Incorporating patient-reported outcomes in MS care is essential to align treatment plans with patients’ priorities and improve their QoL.</div></div>","PeriodicalId":15487,"journal":{"name":"Journal of Clinical Neuroscience","volume":"137 ","pages":"Article 111313"},"PeriodicalIF":1.9000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0967586825002851","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Advances in Multiple Sclerosis (MS) therapy have improved prognosis, but significant disability can still occur. Understanding the perspectives of doctors and patients on how MS and its treatment impact quality of life (QoL) is crucial. We aimed to explore the perceptions of MS patients and neurologists on MS symptoms, treatment, and their impact on QoL.
Methods
A cross-sectional online survey was conducted, targeting adult patients with MS and physicians experienced in MS care. Patients’ quality of life (QoL) was assessed using the MS Quality of Life (MSQOL-54) scale.
Results
252 patients and 53 doctors completed the survey. Relapses in the previous year were associated with lower physical (p = 0.026) and mental (p = 0.022) health scores. Being satisfied with disease-modifying treatment (DMT) and being involved in its choice were also associated with higher physical (both p < 0.001) and mental (p = 0.024 and p = 0.002, respectively) health scores; these scores were not different in patients under moderate versus high-efficacy DMTs (physical p = 0.582 and mental p = 0.180). Patients’ and doctors’ perspectives differ in what they value for QoL. Patients prioritized mental health (p = 0.024), while doctors focused on the impact of physical aspects on QoL (p = 0.030 and p = 0.004). Patients valued information about social support (p < 0.001) more than doctors and considered fatigue more challenging to discuss (p = 0.039), whereas doctors highlighted sexual dysfunction as difficult to address (p < 0.001). Doctors prioritized workplace adaptations (p = 0.041), while patients preferred faster access to healthcare to improve QoL (p < 0.001).
Conclusion
Incorporating patient-reported outcomes in MS care is essential to align treatment plans with patients’ priorities and improve their QoL.
期刊介绍:
This International journal, Journal of Clinical Neuroscience, publishes articles on clinical neurosurgery and neurology and the related neurosciences such as neuro-pathology, neuro-radiology, neuro-ophthalmology and neuro-physiology.
The journal has a broad International perspective, and emphasises the advances occurring in Asia, the Pacific Rim region, Europe and North America. The Journal acts as a focus for publication of major clinical and laboratory research, as well as publishing solicited manuscripts on specific subjects from experts, case reports and other information of interest to clinicians working in the clinical neurosciences.