多灶性运动神经病变患者的特征、治疗模式、医疗资源利用和费用:一项美国索赔数据库队列研究

IF 2.3 Q2 ECONOMICS
Journal of Health Economics and Outcomes Research Pub Date : 2025-06-26 eCollection Date: 2025-01-01 DOI:10.36469/001c.140817
Nikhil Khandelwal, Marie Sanchirico, Ade Ajibade, Kiraat Munshi, Michelle Vu, Nicole Engel-Nitz, Christina Steiger, Amy J Anderson, Chafic Karam
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引用次数: 0

摘要

背景:多灶性运动神经病(MMN)是一种罕见的缓慢进展的神经疾病,其特征是不对称肢体无力,无感觉异常。由于临床症状与肌萎缩侧索硬化症(ALS)等疾病相似,MMN经常被误诊,这使得诊断和治疗具有挑战性。目的:本研究评估了美国MMN的患者特征、治疗模式和经济负担。方法:使用Optum研究数据库,回顾性分析2016年至2020年期间(首次诊断相关索赔日期=索引日期)有≥1个MMN诊断代码的诊断或非诊断医疗索赔的患者,并连续纳入12个月的索引前和索引后。该组中MMN患者使用更具体的标准进行鉴定;≥2 MMN非诊断性索赔,间隔≥30天,随访期间无后续ALS诊断。所有不符合这些标准的患者都被纳入MMN-mimic队列。结果包括治疗模式、鉴别诊断、医疗保健利用和费用。结果:904例患者中,37%有MMN, 63%有MMN模拟症状。MMN患者明显比MMN模拟组患者年轻(平均64.9岁vs 66.8岁;p = .047)。在指数前,MMN患者接受MMN相关药物治疗的比例明显高于MMN模拟组(20.5% vs 9.0%;70%的患者有≥1个鉴别诊断。MMN组的全因总成本高于MMN模拟组(平均预指数分别为58 974 vs 48 132) [P = .100];平均后指数为74 187 vs 50 652 [P = .002]);与mmn相关的医疗费用也显著增加(平均预指数,23 625 vs 12 890 [P = .011];讨论:本研究表明,大多数最初诊断为MMN的患者在随后的评估/随访后出现了另一种疾病,MMN患者的费用较高。许多MMN患者没有接受IVIG,这表明治疗不足或诊断代码的错误归属是常见的。结论:需要对MMN的准确诊断进行进一步的教育,以确保患者获得指南推荐的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics, Treatment Patterns, Healthcare Resource Utilization, and Costs Among Patients with Multifocal Motor Neuropathy: A US Claims Database Cohort Study.

Background: Multifocal motor neuropathy (MMN) is a rare, slowly progressive nerve disorder characterized by asymmetric limb weakness without sensory abnormalities. MMN is often misdiagnosed due to similarities in clinical symptoms with conditions including amyotrophic lateral sclerosis (ALS), making diagnosis and treatment challenging. Objectives: This study assessed patient characteristics, treatment patterns, and the economic burden of MMN in the United States. Methods: Using the Optum Research Database, this retrospective analysis included patients with ≥1 diagnostic or nondiagnostic medical claim with an MMN diagnosis code between 2016 and 2020 (date of first diagnosis-related claim =index date), and continuous enrollment for 12 months preindex and postindex. Patients with MMN within this group were identified using more specific criteria; ≥2 MMN nondiagnostic claims separated by ≥30 days, with no subsequent ALS diagnosis during follow-up. All patients who did not meet these criteria were included in the MMN-mimic cohort. Outcomes included treatment patterns, differential diagnoses, healthcare utilization, and costs. Results: Of 904 patients identified, 37% had MMN and 63% had an MMN-mimic condition. Patients with MMN were significantly younger than patients in the MMN-mimic cohort (mean, 64.9 vs 66.8 years; P = .047). At preindex, significantly more patients with MMN received MMN-related medications than patients in the MMN-mimic cohort (20.5% vs 9.0%, respectively; P < .001). Intravenous immunoglobulin (IVIG) was the most common MMN-related medication. At postindex, more patients with MMN used IVIG (28.0%) compared with preindex (16.4%). In the 12 months preindex and postindex, >70% of patients had ≥1 differential diagnosis. The MMN cohort had higher all-cause total costs than the MMN-mimic cohort (mean preindex, 58 974 v s 48 132, respectively [P = .100]; mean postindex, 74 187 v s 50 652 [P = .002]); they also had significantly higher MMN-related healthcare costs (mean preindex, 23 625 v s 12 890 [P = .011]; mean postindex, 39 521 v s 11 938 [P < .001]). Discussion: This study showed that most patients with initial MMN diagnoses had an alternative disorder after subsequent evaluation/follow-up, and patients with MMN incurred higher costs. Many patients with MMN did not receive IVIG, suggesting that undertreatment or misattribution of diagnosis codes are common. Conclusions: Further education is needed regarding accurate diagnosis of MMN to ensure patient access to guideline-recommended treatment.

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