The global patient-reported outcomes for multiple sclerosis initiative: bridging the gap between clinical research and care – updates at the 2023 plenary event

Altres autors/es

Institut Català de la Salut

[Zaratin P] Research Department, Italian Multiple Sclerosis Foundation, Genoa, Italy. [Samadzadeh S] Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Experimental and Clinical Research Center, Berlin, Germany. Institute of Regional Health Research and Molecular Medicine, University of Southern Denmark, Odense, Denmark. Department of Neurology, The Center for Neurological Research, Næstved-Slagelse-Ringsted Hospitals, Slagelse, Denmark. [Seferoğlu M] Department of Neurology, Bursa Faculty of Medicine, Bursa Yüksek İhtisas Training and Research Hospital, University of Health Sciences, Bursa, Türkiye. [Ricigliano V] Sorbonne Université, Paris Brain Institute, ICM, CNRS, Inserm, Paris, France. Neurology Department, Pitié-Salpêtrière Hospital, APHP, Paris, France. [dos Santos Silva J] Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States. Programa de Pós Graduação Stricto Senso em Neurologia, Department of Neurology, Fluminense Federal University, Niterói, Brazil. [Tunc A] Department of Neurology, Sakarya University Faculty of Medicine, Sakarya, Türkiye. [Montalban X] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain

Vall d'Hebron Barcelona Hospital Campus

Data de publicació

2024-07-11T10:07:17Z

2024-07-11T10:07:17Z

2024-06-20

Resum

Digital health; Multiple sclerosis progression; Patient engagement


Salut digital; Progressió de l'esclerosi múltiple; Compromís del pacient


Salud digital; Progresión de la esclerosis múltiple; Compromiso del paciente


Significant advancements have been achieved in delineating the progress of the Global PROMS (PROMS) Initiative. The PROMS Initiative, a collaborative endeavor by the European Charcot Foundation and the Multiple Sclerosis International Federation, strives to amplify the influence of patient input on MS care and establish a cohesive perspective on Patient-Reported Outcomes (PROs) for diverse stakeholders. This initiative has established an expansive, participatory governance framework launching four dedicated working groups that have made substantive contributions to research, clinical management, eHealth, and healthcare system reform. The initiative prioritizes the global integration of patient (For the purposes of the Global PROMS Initiative, the term “patient” refers to the people with the disease (aka People with Multiple Sclerosis – pwMS): any individual with lived experience of the disease. People affected by the disease/Multiple Sclerosis: any individual or group that is affected by the disease: E.g., family members, caregivers will be also engaged as the other stakeholders in the initiative). insights into the management of MS care. It merges subjective PROs with objective clinical metrics, thereby addressing the complex variability of disease presentation and progression. Following the completion of its second phase, the initiative aims to help increasing the uptake of eHealth tools and passive PROs within research and clinical settings, affirming its unwavering dedication to the progressive refinement of MS care. Looking forward, the initiative is poised to continue enhancing global surveys, rethinking to the relevant statistical approaches in clinical trials, and cultivating a unified stance among ‘industry’, regulatory bodies and health policy making regarding the application of PROs in MS healthcare strategies.

Tipus de document

Article


Versió publicada

Llengua

Anglès

Matèries i paraules clau

Esclerosi múltiple - Prognosi; Telemedicina; Pacients - Satisfacció; Avaluació de resultats (Assistència sanitària); ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Investigative Techniques::Epidemiologic Methods::Data Collection::Surveys and Questionnaires::Health Care Surveys::Patient Reported Outcome Measures; PUBLIC HEALTH::Health Care (Public Health)::Delivery of Health Care::Health Care (Public Health)::Health Care (Public Health)::Telemedicine; DISEASES::Nervous System Diseases::Autoimmune Diseases of the Nervous System::Demyelinating Autoimmune Diseases, CNS::Multiple Sclerosis; DISEASES::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Progression; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::métodos epidemiológicos::recopilación de datos::encuestas y cuestionarios::encuestas sobre atención a la salud::medidas de resultados percibidos por los pacientes; SALUD PÚBLICA::atención a la salud (salud pública)::prestación sanitaria::atención a la salud (salud pública)::atención a la salud (salud pública)::telemedicina; ENFERMEDADES::enfermedades del sistema nervioso::enfermedades autoinmunitarias del sistema nervioso::enfermedades autoinmunes desmielinizantes del SNC::esclerosis múltiple; ENFERMEDADES::afecciones patológicas, signos y síntomas::procesos patológicos::atributos de la enfermedad::progresión de la enfermedad

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Frontiers Media

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