Tracking myasthenia gravis severity over time: Insights from the French health insurance claims database.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY European Journal of Neurology Pub Date : 2024-11-04 DOI:10.1111/ene.16518
Shahram Attarian, Jean-Philippe Camdessanché, Andoni Echaniz-Laguna, Mariana Ciumas, Cécile Blein, Benjamin Grenier, Guilhem Solé
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Abstract

Background and purpose: Few data are available on the course of myasthenia gravis (MG) regarding disease severity and stability over time in real-world settings. This study used the French National Health Insurance Database (SNDS) to assess markers of disease severity in patients with MG longitudinally.

Methods: All patients with MG-related claims in the SNDS between 2013 and 2020 were identified. Patients were followed for up to 8 years after the first claim. Intensive care unit (ICU) stays, treatment with intravenous immunoglobulin (IVIg) or plasma exchange (PE), and death were documented throughout the follow-up period. Standardized mortality rates were estimated, and mortality-related variables were identified using a Cox model.

Results: In all, 14,459 individuals constituted the full study population, including 6354 incident patients. In the incident population, 2199 (34.6%) were admitted to ICUs at least once, principally during the first year after the index date (N = 1477; 23.3%). This proportion decreased progressively to reach 3.0% in the seventh year. A total of 2817 patients received IVIg and 432 PE, again principally in the first year. In the full study population, the standardized mortality rate was 1.08 (95% confidence interval [CI] 1.03-1.13), being lower in men (0.95, 95% CI 0.89-1.02) than in women (1.15, 95% CI 1.07-1.23) and in patients aged >65 years (1.06, 95% CI 1.01-1.11) than in younger patients (1.50, 95% CI 1.24-1.76). Male gender, older age and higher comorbidity were independently associated with mortality.

Conclusions: A subgroup of patients with MG require ICU admission and rescue therapy with IVIg or PE, indicative of poor disease control. New therapies are needed to improve disease control and reduce disease burden.

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随时间追踪肌无力严重程度:法国医疗保险索赔数据库的启示。
背景和目的:关于重症肌无力(MG)的病程、疾病严重程度以及在现实世界中的长期稳定性,目前鲜有相关数据。本研究利用法国国家医疗保险数据库(SNDS)对重症肌无力患者的疾病严重程度指标进行纵向评估:方法:确定2013年至2020年期间SNDS中所有与MG相关的索赔患者。在首次报销后,对患者进行长达8年的随访。在整个随访期间记录重症监护室(ICU)的住院情况、静脉注射免疫球蛋白(IVIg)或血浆置换(PE)的治疗情况以及死亡情况。我们估算了标准化死亡率,并使用 Cox 模型确定了与死亡率相关的变量:总共有 14459 人构成了完整的研究人群,其中包括 6354 名事件患者。在发病人群中,有 2199 人(34.6%)至少入住过一次重症监护病房,主要是在发病日期后的第一年(N = 1477;23.3%)。这一比例在第七年逐渐下降至 3.0%。共有 2817 名患者接受了 IVIg 治疗,432 名患者接受了 PE 治疗,同样主要集中在第一年。在全部研究人群中,标准化死亡率为 1.08(95% 置信区间 [CI] 1.03-1.13),男性(0.95,95% CI 0.89-1.02)低于女性(1.15,95% CI 1.07-1.23),年龄大于 65 岁的患者(1.06,95% CI 1.01-1.11)低于年轻患者(1.50,95% CI 1.24-1.76)。男性、高龄和较高的合并症与死亡率密切相关:有一部分 MG 患者需要入住 ICU 并接受 IVIg 或 PE 的抢救治疗,这表明患者的病情控制不佳。需要新的疗法来改善疾病控制并减轻疾病负担。
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
European Journal of Neurology
European Journal of Neurology 医学-临床神经学
CiteScore
9.70
自引率
2.00%
发文量
418
审稿时长
1 months
期刊介绍: The European Journal of Neurology is the official journal of the European Academy of Neurology and covers all areas of clinical and basic research in neurology, including pre-clinical research of immediate translational value for new potential treatments. Emphasis is placed on major diseases of large clinical and socio-economic importance (dementia, stroke, epilepsy, headache, multiple sclerosis, movement disorders, and infectious diseases).
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