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美国成人全身性重症肌无力患者静脉注射免疫球蛋白的真实世界应用模式。

Real-world utilization patterns of intravenous immunoglobulin in adults with generalized myasthenia gravis in the United States.

机构信息

argenx US Inc., 33 Arch Street, 32nd Floor, Boston, MA 02110, USA.

argenx US Inc., 33 Arch Street, 32nd Floor, Boston, MA 02110, USA.

出版信息

J Neurol Sci. 2022 Dec 15;443:120480. doi: 10.1016/j.jns.2022.120480. Epub 2022 Oct 28.

Abstract

OBJECTIVE

To evaluate real-world utilization patterns of intravenous immunoglobulin (IVIg) among patients with generalized myasthenia gravis (gMG) over 3 years post-IVIg initiation.

METHODS

Patients with gMG who initiated IVIg treatment were identified from a United States claims database (Symphony Health's Integrated Dataverse [IDV]®, January 1, 2014 - December 31, 2019). The frequency of subsequent IVIg treatment and associated cost during the year post-IVIg initiation were analyzed. Usage patterns of IVIg and concomitant gMG treatments during the year preceding and 3 years post-IVIg initiation were compared.

RESULTS

Among 1225 patients with gMG who initiated IVIg treatment, 706 patients (57.6%) received 1 to 5 IVIg treatment courses (intermittent IVIg users), and 519 patients (42.4%) received ≥6 IVIg treatment courses (chronic IVIg users) within the subsequent year. Mean annual medical cost per patient was nearly 2.5-fold higher for chronic vs. intermittent IVIg users ($161,478 vs. $64,888, p < 0.001). The proportion of patients using corticosteroids and nonsteroidal immunosuppressive treatments (NSISTs) was not reduced over the 3-year follow-up period following IVIg initiation, even for patients who continued annual chronic IVIg for 3 consecutive years post-initiation.

CONCLUSIONS

Nearly half of patients with gMG received chronic and multiple IVIg treatment courses within the first year once initiating IVIg treatment, indicating higher usage than expected. For all IVIg initiators, the proportion of patients using corticosteroids and NSISTs did not decrease over 3 years despite IVIg initiation.

摘要

目的

评估静脉注射免疫球蛋白(IVIg)在全身性重症肌无力(gMG)患者起始 IVIg 治疗后 3 年的真实世界应用模式。

方法

从美国索赔数据库(Symphony Health 的 Integrated Dataverse [IDV]®,2014 年 1 月 1 日至 2019 年 12 月 31 日)中确定起始 IVIg 治疗的 gMG 患者。分析起始 IVIg 治疗后 1 年内 IVIg 治疗的频率和相关费用。比较起始 IVIg 治疗前 1 年和 3 年内 IVIg 治疗期间的 IVIg 和同时进行的 gMG 治疗的使用模式。

结果

在 1225 例起始 IVIg 治疗的 gMG 患者中,706 例(57.6%)患者接受了 1 至 5 个 IVIg 治疗疗程(间歇性 IVIg 使用者),519 例(42.4%)患者在随后的 1 年内接受了≥6 个 IVIg 治疗疗程(慢性 IVIg 使用者)。与间歇性 IVIg 使用者相比,慢性 IVIg 使用者的每位患者年均医疗费用高近 2.5 倍($161,478 与$64,888,p<0.001)。起始 IVIg 治疗后 3 年的随访期间,使用皮质类固醇和非甾体免疫抑制治疗(NSISTs)的患者比例并未降低,即使是起始 IVIg 治疗后连续 3 年每年接受慢性 IVIg 治疗的患者也是如此。

结论

一旦开始 IVIg 治疗,近一半的 gMG 患者在起始 IVIg 治疗后的 1 年内接受了慢性和多次 IVIg 治疗,这表明使用量高于预期。对于所有 IVIg 起始者,尽管开始 IVIg 治疗,但在 3 年内使用皮质类固醇和 NSISTs 的患者比例并未降低。

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