» Articles » PMID: 37386469

Physician- and Patient-reported Perspectives on Myasthenia Gravis in Europe: a Real-world Survey

Overview
Publisher Biomed Central
Specialty General Medicine
Date 2023 Jun 29
PMID 37386469
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Myasthenia gravis (MG) is a rare, chronic, debilitating, unpredictable, and potentially life-threatening neuromuscular disease. There is a lack of real-world data on disease management that could be used to further understand and address unmet patient needs and burden. We aimed to provide comprehensive real-world insights in the management of MG in five European countries.

Methods: Data were collected using the Adelphi Real World Disease Specific Programme™ in MG, a point-in-time survey of physicians and their patients with MG in France, Germany, Italy, Spain, and the United Kingdom (UK). Physician- and patient-reported clinical data were collected, including demographics, comorbidities, symptoms, disease history, treatments, healthcare resource utilization (HCRU), and quality of life outcomes.

Results: In total, 144 physicians completed 778 patient record forms from March to July 2020 in the UK, and from June to September 2020 in France, Germany, Italy and Spain. Mean patient age at symptom onset was 47.7 years, with a mean time from symptom onset to diagnosis of 332.4 days (10.97 months). At diagnosis, 65.3% of patients were classified as Myasthenia Gravis Foundation of America Class II or above. Mean number of symptoms reported at diagnosis per patient was five, with ocular myasthenia reported in at least 50% of patients. At time of survey completion, the mean number of symptoms reported per patient was five and ocular myasthenia and ptosis were each still present in more than 50% of patients. Acetylcholinesterase inhibitors were the most commonly prescribed chronic treatments in all countries. Of 657 patients treated with chronic treatment at the time of the survey, 62% continued to experience moderate-to-severe symptoms. On average, 3.1 healthcare professionals (HCPs) were involved in patient management, 6.2 consultations were made per patient with any HCP over the last 12 months, and 178 (22.9%) patients were hospitalized in the last 12 months. Overall, HCRU and disease management were similar across all countries.

Conclusions: Our findings demonstrated the high burden of MG despite current treatment options for patients with MG.

Citing Articles

Individualized Dosing of Efgartigimod in Patients With Generalized Myasthenia Gravis: Clinical Experience at a Single Center.

Silvestri N Muscle Nerve. 2025; 71(3):422-428.

PMID: 39744896 PMC: 11799394. DOI: 10.1002/mus.28334.


Assessing the effectiveness of measurement scales in evaluating the health-related quality of life in rare disease patients after treatment: a systematic review.

Dumbuya J, Ahmad B, Zeng C, Chen X, Lu J Health Qual Life Outcomes. 2024; 22(1):108.

PMID: 39696506 PMC: 11657302. DOI: 10.1186/s12955-024-02324-0.


Treatment of myasthenia gravis in france: A retrospective claims database study (STAMINA).

Tard C, Laforet P, de Pouvourville G, Crochard A, Chollet G, Nevoret C J Neurol. 2024; 271(11):7239-7249.

PMID: 39387949 PMC: 11561051. DOI: 10.1007/s00415-024-12714-5.


Advancements and prospects of novel biologicals for myasthenia gravis: toward personalized treatment based on autoantibody specificities.

Ma C, Liu D, Wang B, Yang Y, Zhu R Front Pharmacol. 2024; 15:1370411.

PMID: 38881870 PMC: 11177092. DOI: 10.3389/fphar.2024.1370411.


Astragaloside IV protects against autoimmune myasthenia gravis in rats via regulation of mitophagy and apoptosis.

Zhang J, Huang J, Lan J, Li Q, Ke L, Jiang Q Mol Med Rep. 2024; 30(1).

PMID: 38785143 PMC: 11140232. DOI: 10.3892/mmr.2024.13253.


References
1.
Mahic M, Bozorg A, Rudnik J, Zaremba P, Scowcroft A . Healthcare resource use in myasthenia gravis: a US health claims analysis. Ther Adv Neurol Disord. 2023; 16:17562864221150327. PMC: 9880582. DOI: 10.1177/17562864221150327. View

2.
Elsais A, Wyller V, Loge J, Kerty E . Fatigue in myasthenia gravis: is it more than muscular weakness?. BMC Neurol. 2013; 13:132. PMC: 3852076. DOI: 10.1186/1471-2377-13-132. View

3.
Harris L, Graham S, MacLachlan S, Exuzides A, Jacob S . Healthcare resource utilization by patients with treatment-refractory myasthenia gravis in England. J Med Econ. 2019; 22(7):691-697. DOI: 10.1080/13696998.2019.1592180. View

4.
Freimer M, Vu T, Benatar M, MacDougall J, Barohn R, Dimachkie M . Clinical Effects of the Self-administered Subcutaneous Complement Inhibitor Zilucoplan in Patients With Moderate to Severe Generalized Myasthenia Gravis: Results of a Phase 2 Randomized, Double-Blind, Placebo-Controlled, Multicenter Clinical Trial. JAMA Neurol. 2020; 77(5):582-592. PMC: 7042797. DOI: 10.1001/jamaneurol.2019.5125. View

5.
Babineaux S, Curtis B, Holbrook T, Milligan G, Piercy J . Evidence for validity of a national physician and patient-reported, cross-sectional survey in China and UK: the Disease Specific Programme. BMJ Open. 2016; 6(8):e010352. PMC: 5013497. DOI: 10.1136/bmjopen-2015-010352. View