UCB Pharma, 208 Bath Road, Slough, SL1 3WE, UK.
UCB Pharma, Morrisville, NC, USA.
Orphanet J Rare Dis. 2023 Jun 29;18(1):169. doi: 10.1186/s13023-023-02727-0.
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.
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.
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.
Our findings demonstrated the high burden of MG despite current treatment options for patients with MG.
重症肌无力(MG)是一种罕见的、慢性的、使人虚弱的、不可预测的、潜在危及生命的神经肌肉疾病。目前缺乏有关疾病管理的真实世界数据,这些数据可用于进一步了解和解决未满足的患者需求和负担。我们的目的是在五个欧洲国家提供 MG 管理的全面真实世界的见解。
使用 Adelphi 真实世界疾病专项计划™在 MG 中收集数据,这是一项针对法国、德国、意大利、西班牙和英国(UK)的医生及其 MG 患者的时点调查。收集了医生和患者报告的临床数据,包括人口统计学、合并症、症状、疾病史、治疗、医疗保健资源利用(HCRU)和生活质量结果。
在英国,共有 144 名医生在 2020 年 3 月至 7 月期间完成了 778 份患者病历,在法国、德国、意大利和西班牙则在 2020 年 6 月至 9 月期间完成了。患者症状发作时的平均年龄为 47.7 岁,从症状发作到诊断的平均时间为 332.4 天(10.97 个月)。在诊断时,65.3%的患者被归类为美国重症肌无力基金会(Myasthenia Gravis Foundation of America)Ⅱ级或以上。每位患者在诊断时报告的症状平均为五个,至少有 50%的患者存在眼肌型肌无力。在调查完成时,每位患者报告的症状平均为五个,50%以上的患者仍存在眼肌型肌无力和上睑下垂。乙酰胆碱酯酶抑制剂是所有国家最常用的慢性治疗药物。在接受调查时接受慢性治疗的 657 名患者中,62%继续经历中重度症状。平均有 3.1 名医疗保健专业人员(HCP)参与患者管理,在过去 12 个月中,每位患者与任何 HCP 的就诊次数为 6.2 次,在过去 12 个月中有 178 名(22.9%)患者住院。总体而言,所有国家的 HCRU 和疾病管理相似。
尽管目前有治疗 MG 的选择,但我们的研究结果表明 MG 的负担仍然很高。