Characteristics and healthcare utilization of patients with myasthenia gravis exacerbation

IF 3.6 3区 医学 Q1 CLINICAL NEUROLOGY Journal of the Neurological Sciences Pub Date : 2024-11-22 DOI:10.1016/j.jns.2024.123322
Cynthia Z. Qi , Yilu Lin , Yuebing Li , Tuan Vu , Femke De Ruyck , Deborah Gelinas , Lizheng Shi
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Abstract

Purpose

This retrospective cohort study describes the characteristics of patients with myasthenia gravis (MG) who developed exacerbations (MG-E) and compares their healthcare utilization (HRU) to patients who did not experience exacerbations (MG-O).

Method

De-identified data from patients who had ≥2 MG-related diagnostic code submissions were extracted from the National Veterans Affairs Health Care Network electronic health records between 1999 and 2022. Descriptive statistics, Kaplan-Meier analysis, and per-patient per-year (PPPY) HRU were used to compare the two patient groups.

Results

About 34 % (3603/10,718) of patients with MG developed exacerbations over a median follow-up of 6.8 years. Approximately 52 % of the MG-E cohort had 3 or more exacerbations over the study period, averaging 1.34 (SD 2.50) exacerbations per year. The MG-E cohort had a higher incidence of early-onset MG (7.72 % vs. 4.05 %; p < 0.0001) and higher mean Charlson Comorbidity Index scores before a diagnosis of MG (0.86 vs. 0.59; p < 0.0001). Relative to patients of other racial groups with MG-E, Hispanic and African Americans had higher cumulative incidence of exacerbations over time (p < 0.0001). Additionally, MG-E patients were five times more likely to be intubated compared to MG-O patients (p < 0.0001). Increased PPPY HRU was observed in patients with MG-E compared to patients with MG-O (outpatient visit: 25.05 vs. 14.08; inpatient admission: 0.47 vs. 0.14; ED visit: 0.69 vs. 0.26; ICU stay: 0.08 vs. 0.02, respectively; p < 0.001).

Conclusion

Approximately one-third of patients diagnosed with MG experienced exacerbations, with higher incidences seen among Hispanic and African Americans. MG-E was associated with higher HRU and a higher intubation risk.
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重症肌无力加重患者的特点及保健利用
目的:本回顾性队列研究描述了重症肌无力(MG)患者发生加重(MG- e)的特征,并比较了他们的医疗保健利用率(HRU)与未发生加重(MG- o)的患者。方法从1999年至2022年的国家退伍军人事务卫生保健网络电子健康记录中提取≥2例mg相关诊断代码提交的患者的识别数据。采用描述性统计、Kaplan-Meier分析和人均年HRU (PPPY)对两组患者进行比较。结果在中位随访6.8年期间,约34% (3603/10,718)MG患者出现加重。大约52%的MG-E队列在研究期间有3次或3次以上的加重,平均每年加重1.34次(标准差2.50)。MG- e组早发性MG发生率较高(7.72% vs 4.05%;p & lt;0.0001)和MG诊断前较高的Charlson共病指数(0.86 vs 0.59;p & lt;0.0001)。相对于其他种族的MG-E患者,西班牙裔和非裔美国人随着时间的推移有更高的累积恶化发生率(p <;0.0001)。此外,MG-E患者插管的可能性是MG-O患者的5倍(p <;0.0001)。MG-E患者与MG-O患者相比,PPPY HRU升高(门诊访问量:25.05 vs 14.08;住院率:0.47 vs. 0.14;ED访视:0.69 vs 0.26;ICU住院时间:分别为0.08 vs 0.02;p & lt;0.001)。结论:大约三分之一被诊断为MG的患者经历了急性发作,其中西班牙裔和非裔美国人的发病率更高。MG-E与较高的HRU和插管风险相关。
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
Journal of the Neurological Sciences
Journal of the Neurological Sciences 医学-临床神经学
CiteScore
7.60
自引率
2.30%
发文量
313
审稿时长
22 days
期刊介绍: The Journal of the Neurological Sciences provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. JNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials). JNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism.
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