Risdiplam utilization, adherence, and associated health care costs for patients with spinal muscular atrophy: a United States retrospective claims database analysis.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-12-30 DOI:10.1186/s13023-024-03399-0
Anish Patel, Walter Toro, Min Yang, Wei Song, Raj Desai, Mingchen Ye, Nadia Tabatabaeepour, Omar Dabbous
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Abstract

Background: Spinal muscular atrophy (SMA) is a genetic neuromuscular disease associated with progressive loss of motor function. Risdiplam, a daily oral therapy, was approved in the United States for the treatment of SMA. Risdiplam's effectiveness depends on patient adherence to the treatment regimen. This retrospective claims database analysis assessed real-world treatment adherence and persistence, and all-cause health care costs by adherence status, for patients with SMA receiving risdiplam. Outcomes were summarized by SMA types (1-4) and age groups (0-2, 3-5, 6-17, and ≥ 18 years).

Results: 86 patients with ≥ 1 SMA diagnosis, risdiplam treatment, and ≥ 6 months of continuous enrollment after the index date (SMA diagnosis) were identified in the IQVIA PharMetrics® Plus database (01/01/2020-06/30/2022). One patient had SMA type 1 (a 1-year-old boy), 18 had type 2 (mean ± SD age: 7.9 ± 5.7 years; 61% female), 47 had type 3 (17.3 ± 10.2 years; 55% female), and 20 had type 4 (38.2 ± 11.6 years; 55% female). The mean proportion of days covered (PDC) with risdiplam was 0.89 overall, ranging from 0.88 for SMA type 4 to 0.97 for type 1. The majority (83.7%) of patients were adherent to risdiplam (PDC ≥0.80), ranging from 75.0% for type 4 to 100% for type 1. Adherence ranged from 76.5% among 6-12-year-olds to 100% among 0-2-year-olds. Compared with adherent patients, nonadherent patients had higher median total health care costs by $335,049 for type 2, $41,204 for type 3, and $12,223 for type 4. Among adherent patients, patients with PDC between 0.90 and 1.00 had lower costs compared with patients with PDC between 0.80 and 0.90.

Conclusions: Nonadherence to risdiplam was observed in the first year of treatment, especially for patients with SMA type 4 and patients aged 6-12 years. Nonadherence was associated with higher all-cause health care costs, with the most pronounced cost difference for SMA type 2. For adherent patients, those who were highly adherent incurred lower health care costs. These findings underscore the importance of treatment adherence and persistence for patients with SMA receiving risdiplam, particularly for younger children and those with greater disease severity.

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脊髓性肌萎缩症患者的利斯普仑使用、依从性和相关医疗费用:美国回顾性索赔数据库分析
背景:脊髓性肌萎缩症(SMA)是一种遗传性神经肌肉疾病,与进行性运动功能丧失相关。Risdiplam是一种每日口服药物,在美国被批准用于治疗SMA。利斯迪普兰的有效性取决于患者对治疗方案的坚持。这项回顾性索赔数据库分析评估了接受瑞西泮治疗的SMA患者的现实治疗依从性和持久性,以及根据依从状态确定的全因医疗保健成本。结果按SMA类型(1-4)和年龄组(0-2岁、3-5岁、6-17岁和≥18岁)进行汇总。结果:在IQVIA PharMetrics®Plus数据库(2020年1月1日- 2022年6月30日)中确定了86例SMA诊断≥1例、瑞斯地平治疗且在索引日期(SMA诊断)后连续入组≥6个月的患者。1例1岁男童,18例2型(平均±SD年龄:7.9±5.7岁;女性61%),3型47例(17.3±10.2岁;女性占55%),4型20例(38.2±11.6岁;55%的女性)。risdiplam的平均覆盖天数(PDC)比例总体为0.89,从4型SMA的0.88到1型SMA的0.97不等。大多数(83.7%)患者坚持使用瑞地普兰(PDC≥0.80),从4型的75.0%到1型的100%不等。依从性从6-12岁的76.5%到0-2岁的100%不等。与依从性患者相比,非依从性患者的总医疗费用中位数较高,2型为335,049美元,3型为41,204美元,4型为12,223美元。在坚持治疗的患者中,PDC值在0.90 - 1.00之间的患者比PDC值在0.80 - 0.90之间的患者成本更低。结论:在治疗的第一年观察到利地普兰的不依从,特别是对于4型SMA患者和6-12岁的患者。不依从性与较高的全因医疗保健费用相关,2型SMA患者的费用差异最为明显。对于依从性患者,高度依从性患者的医疗费用较低。这些研究结果强调了接受瑞地普兰治疗的SMA患者的治疗依从性和持久性的重要性,特别是对于年幼的儿童和疾病严重程度较高的患者。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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