Epidemiology and patient characteristics of the US myasthenia gravis population: real-world evidence from a large insurance claims database.

IF 2.1 Q3 CLINICAL NEUROLOGY
BMJ Neurology Open Pub Date : 2025-06-23 eCollection Date: 2025-01-01 DOI:10.1136/bmjno-2025-001076
Lesley-Ann Miller-Wilson, Joel Arackal, Yuriy Edwards, Jennifer Schwinn, Kristen Elizabeth Rockstein, Brett Venker, Richard J Nowak
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Abstract

Background: The epidemiology of myasthenia gravis (MG), a rare autoimmune disease, is not completely understood. This retrospective claims analysis assessed the epidemiologic rates of MG in the USA and the characteristics of the incident and prevalent MG populations.

Methods: Patients with MG were identified using Inovalon closed claims data; those with ≥2 International Classification of Diseases, 10th Revision (ICD-10) codes for MG from 2016 to 2019, separated by ≥30 days, were eligible. Patients in the prevalent cohort had continuous insurance coverage from January to December 2019. Patients in the incident cohort had continuous insurance coverage from January 2018 to December 2019 and no MG claims before 2019. Incidence and prevalence rates were adjusted using US census data. Treatment utilisation was assessed in both cohorts and grouped by provider type. Exacerbations were identified using ICD-10 code G70.01; codes occurring ≤30 days following a previous exacerbation code were considered as part of a single event.

Results: The incident cohort included 1442 patients (adjusted incidence: 4.3 per 100000); the prevalent cohort included 14 373 patients (adjusted prevalence: 35.7 per 100 000). In 2019, approximately two-thirds of patients in both cohorts (incident, 67.7%; prevalent, 61.6%) received MG treatments, most commonly acetylcholinesterase inhibitors, followed by oral steroids. Among incident patients with ≥1 year of continuous follow-up (n=1204), 32.1% (n=387) experienced ≥1 exacerbation, with 50% (n=194) having ≥2 exacerbations and 41% (n=159) having an exacerbation as the index MG event.

Conclusions: Estimates of MG incidence and prevalence were comparable to findings from two recent US studies. Acetylcholinesterase inhibitors and corticosteroids remain widely used. Exacerbations occurred in >30% of incident patients with ≥1 year of continuous follow-up, including 13% who had a relapse as their index event. These results highlight the need for earlier detection and use of more effective therapies in the treatment paradigm to achieve sustained disease control.

美国重症肌无力人群的流行病学和患者特征:来自大型保险索赔数据库的真实世界证据。
背景:重症肌无力(MG)是一种罕见的自身免疫性疾病,其流行病学尚未完全了解。本回顾性索赔分析评估了美国MG的流行病学发生率以及发病率和流行人群的特征。方法:使用Inovalon封闭索赔数据对MG患者进行识别;2016 - 2019年《国际疾病分类第十版(ICD-10)》MG编码≥2条,间隔≥30天者入选。流行队列中的患者从2019年1月至12月连续投保。事件队列中的患者在2018年1月至2019年12月期间连续投保,并且在2019年之前没有MG索赔。发病率和患病率使用美国人口普查数据进行调整。在两个队列中评估治疗利用情况,并按提供者类型分组。使用ICD-10代码G70.01识别加重;在前一次加重后≤30天发生的症状被视为单一事件的一部分。结果:事件队列纳入1442例患者(调整后的发病率:4.3 / 100000);流行队列包括14373例患者(调整患病率:35.7 / 100000)。在2019年,两个队列中约有三分之二的患者(事件,67.7%;(61.6%)接受MG治疗,最常见的是乙酰胆碱酯酶抑制剂,其次是口服类固醇。在连续随访≥1年的事件患者(n=1204)中,32.1% (n=387)的急性发作≥1次,其中50% (n=194)的急性发作≥2次,41% (n=159)的急性发作为MG事件的指标。结论:MG发病率和流行率的估计值与美国最近两项研究的结果相当。乙酰胆碱酯酶抑制剂和皮质类固醇仍被广泛使用。在连续随访≥1年的事件患者中,有30%的患者出现加重,其中13%的患者以复发为主要事件。这些结果强调需要在治疗范式中更早发现和使用更有效的治疗方法,以实现持续的疾病控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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