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Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey

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 provid...

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Autores principales: Mahic, Milada, Bozorg, Ali, DeCourcy, Jonathan, Golden, Keisha, Gibson, Gregor, Taylor, Christian, Scowcroft, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308674/
https://www.ncbi.nlm.nih.gov/pubmed/37386469
http://dx.doi.org/10.1186/s13023-023-02727-0
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author Mahic, Milada
Bozorg, Ali
DeCourcy, Jonathan
Golden, Keisha
Gibson, Gregor
Taylor, Christian
Scowcroft, Anna
author_facet Mahic, Milada
Bozorg, Ali
DeCourcy, Jonathan
Golden, Keisha
Gibson, Gregor
Taylor, Christian
Scowcroft, Anna
author_sort Mahic, Milada
collection PubMed
description 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.
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spelling pubmed-103086742023-06-30 Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey Mahic, Milada Bozorg, Ali DeCourcy, Jonathan Golden, Keisha Gibson, Gregor Taylor, Christian Scowcroft, Anna Orphanet J Rare Dis Research 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. BioMed Central 2023-06-29 /pmc/articles/PMC10308674/ /pubmed/37386469 http://dx.doi.org/10.1186/s13023-023-02727-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mahic, Milada
Bozorg, Ali
DeCourcy, Jonathan
Golden, Keisha
Gibson, Gregor
Taylor, Christian
Scowcroft, Anna
Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey
title Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey
title_full Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey
title_fullStr Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey
title_full_unstemmed Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey
title_short Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world survey
title_sort physician- and patient-reported perspectives on myasthenia gravis in europe: a real-world survey
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308674/
https://www.ncbi.nlm.nih.gov/pubmed/37386469
http://dx.doi.org/10.1186/s13023-023-02727-0
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