Myasthenia gravis in Spain: A survey of specialized neurologists to uncover unmet needs


Por: Cortés-Vicente, E, Casasnovas, C, Juntas, R, Sevilla, T, Pardo, J, de Rivera, FR, Sola, AG

Publicada: 1 abr 2026
Resumen:
Introduction: Myasthenia gravis (MG) is a neuromuscular autoimmune disease that requires prompt diagnosis and management by neurologists. The challenges of MG management are associated with the diagnostic process and the selection of an effective form of therapy enabling long-term remission of the disease. The objective of this study was to assess the state of MG in Spain to identify unaddressed needs in the clinical progression, diagnosis, and treatment approaches. Methods: A survey was distributed via email between 19 July and 25 October 2022 to neurologists belonging to the Spanish Society of Neurology. A comprehensive descriptive analysis was conducted on all collected data. Results: In total, 69 completed surveys, representing 64 Spanish hospitals, were analyzed and included in the results. The study identified that economic difficulties, such as departmental budgets, have led to a lack of access to antibody testing during diagnosis. Furthermore, corti-costeroids were found to achieve the best clinical response, despite also being associated with a higher frequency of adverse effects. The results show that 34% of patients with MG present active symptoms. Eighteen percent have symptoms that limit their daily activities. Additionally, 29% of patients have requested an unscheduled follow-up visit within the last year. Conclusions: Several areas present unmet needs in terms of improving access to diagnostic assays, residual disease burden in treated patients, and the management and diagnosis of MG. (c) 2025 Sociedad Espanola de Neurolog & imath;a. Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).

Filiaciones:
Cortés-Vicente, E:
 Hosp Santa Creu i St Pau, Dept Neurol, Neuromuscular Dis Unit, Barcelona, Spain

 Biomed Res Inst St Pau, Neuromuscular Dis Lab, Barcelona, Spain

 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Madrid, Spain

Casasnovas, C:
 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Madrid, Spain

 Hosp Univ Bellvitge, Neurol Dept, Neuromuscular Unit, Hosp Llobregat, Barcelona, Spain

 Bellvitge Biomed Res Inst IDIBELL, Neurometab Dis Grp, Barcelona, Spain

Juntas, R:
 Hosp Univ Vall Dhebron, Neurol Dept, Neuromuscular Dis Unit, Barcelona, Spain

Sevilla, T:
 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Madrid, Spain

 Hosp Univ & Politecn Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, Spain

 Inst Fe, Ataxia & Neuromuscular Disorders Res Grp, Valencia, Spain

 Valencia Univ, Med Dept, Valencia, Spain

Pardo, J:
 Hosp Clin, Neurol Dept, Santiago De Compostela, Spain

de Rivera, FR:
 Hosp Univ Paz, Neurol Unit, Madrid, Spain

 Univ Autonoma Madrid, Ciudad Univ Cantoblanco, Madrid, Spain

 Inst Invest Hosp Univ Paz, Madrid, Spain

Sola, AG:
 Hosp Univ Clin San Carlos, Inst Neurosci, Dept Neurol, Neuromuscular Dis Unit, Madrid, Spain
ISSN: 02134853





NEUROLOGIA
Editorial
ELSEVIER ESPANA SLU, AV JOSEP TARRADELLAS, 20-30, 1ERA PLANTA, BARCELONA, CP-08029, SPAIN, España
Tipo de documento: Article
Volumen: 41 Número: 3
Páginas:
WOS Id: 001740918500001
imagen Green Submitted, gold

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