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美国为多发性硬化症急性加重期患者开具促肾上腺皮质激素注射液时保险拒付的后果

Consequences of Insurance Denials Among U.S. Patients Prescribed Repository Corticotropin Injection for Acute Exacerbations of Multiple Sclerosis.

作者信息

Rice J Bradford, Panaccio Mary P, White Alan, Simes Mark, Billmyer Emma, Downes Nathaniel, Niewoehner John, Wan George J

机构信息

Analysis Group Inc., Boston, MA, USA.

Mallinckrodt Pharmaceuticals, Bedminster, NJ, USA.

出版信息

Neurol Ther. 2021 Jun;10(1):149-167. doi: 10.1007/s40120-020-00219-y. Epub 2020 Nov 10.

Abstract

INTRODUCTION

Repository corticotropin injection (RCI; Acthar Gel) is indicated for the treatment of acute exacerbations of multiple sclerosis (MS) in adults. Despite the well-documented clinical and economic benefits of RCI, many patients are denied use of the therapy by third-party payers. This study aims to understand the demographic and clinical characteristics of MS relapse patients who received a prescription for RCI from their physicians and then were either approved or denied treatment by their insurers. The study compares measurable clinical outcomes and healthcare resource utilization (HCRU) between approved and denied cohorts.

METHODS

A retrospective analysis of adults experiencing MS relapse from January 2015 to December 2018 was conducted using a de-identified open-source claims database [Symphony Health Integrated Dataverse (IDV)]. Patients were identified using ICD codes for MS and considered to have relapsing/remitting type according to established claims-based methodology. Clinical characteristics and HCRU were analyzed during the year preceding ("baseline") and the year following ("follow-up") each patient's index date, defined as the date of a patient's first approved RCI claim (for patients with ≥ 1 approved claim) or first denied RCI claim (for patients with only denied claims). Baseline characteristics were reported with unadjusted differences and p values indicating the significance of characteristics between the two cohorts. For outcomes, match-adjusted results were reported using propensity matching to account for underlying differences between cohorts.

RESULTS

The study sample included 1902 MS relapse patients with at least one claim for RCI. At baseline, approved patients were slightly older compared to denied patients (mean age 48.0 vs. 47.2), had higher rates of hemiplegia/paraplegia (6.7% vs. 3.3%), greater mobility impairment (17% vs. 11.5%), more exacerbation episodes (66.2% vs. 59.9%), and a higher number of physical therapy/rehab claims (23.5 vs. 14.0), respectively. Outcomes among the matched sample show an increased use of corticosteroids for patients denied access to RCI compared to approved patients (51.1% vs. 42.4%), more exacerbation episodes (36.6% vs. 28.2%), and an increased number of physical therapy/rehab claims (11.5% vs. 9.9%), respectively.

CONCLUSION

The results of this study may aid providers and payers in evaluating scenarios where RCI may be beneficial and improve quality of care for patients experiencing MS relapse.

摘要

引言

储存型促肾上腺皮质激素注射液(RCI;Acthar Gel)适用于治疗成人多发性硬化症(MS)的急性加重期。尽管RCI在临床和经济方面的益处已有充分记录,但许多患者被第三方支付方拒绝使用该疗法。本研究旨在了解那些从医生处获得RCI处方但随后被保险公司批准或拒绝治疗的MS复发患者的人口统计学和临床特征。该研究比较了获批和被拒队列之间可测量的临床结局和医疗资源利用(HCRU)情况。

方法

使用一个去识别化的开源索赔数据库[交响乐健康综合数据集(IDV)],对2015年1月至2018年12月经历MS复发的成年人进行回顾性分析。根据国际疾病分类(ICD)编码识别患者,并根据既定的基于索赔的方法将其视为复发/缓解型。在每位患者的索引日期之前(“基线”)和之后(“随访”)的一年中分析临床特征和HCRU,索引日期定义为患者首次获批RCI索赔的日期(对于有≥1次获批索赔的患者)或首次被拒RCI索赔的日期(对于只有被拒索赔的患者)。报告基线特征时采用未调整的差异和p值,以表明两个队列之间特征的显著性。对于结局,使用倾向匹配报告匹配调整后的结果,以考虑队列之间的潜在差异。

结果

研究样本包括1902例至少有一次RCI索赔的MS复发患者。在基线时,获批患者比被拒患者年龄稍大(平均年龄48.0岁对47.2岁),偏瘫/截瘫发生率更高(6.7%对3.3%),行动能力受损更严重(17%对11.5%),加重发作次数更多(66.2%对59.9%),物理治疗/康复索赔次数更多(23.5次对14.0次)。匹配样本中的结局显示,与获批患者相比,被拒用RCI的患者使用皮质类固醇的比例增加(51.1%对42.4%),加重发作次数更多(36.6%对28.2%),物理治疗/康复索赔次数增加(11.5%对9.9%)。

结论

本研究结果可能有助于医疗服务提供者和支付方评估RCI可能有益的情况,并改善MS复发患者的护理质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed62/8140003/96eaef110fb7/40120_2020_219_Fig1_HTML.jpg

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