Healthcare utilization of patients with hereditary angioedema treated with lanadelumab and subcutaneous C1-inhibitor concentrate.

IF 2.6 3区 医学 Q2 ALLERGY Allergy and asthma proceedings Pub Date : 2023-07-16 DOI:10.2500/aap.2023.44.230026
Marc A Riedl, David R Hinds, Patricia M Prince, Trevor M Alvord, Sara Dosenovic, Jenna F Abdelhadi, Jack R Brownrigg, Charlotte L Camp, Thomas Machnig, Aleena Banerji
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引用次数: 1

Abstract

Background: New hereditary angioedema (HAE) treatments have become available in recent years for the treatment of HAE due to C1-inhibitor (C1-INH) deficiency, including two subcutaneous (SC) options: a monoclonal antibody (lanadelumab) and a plasma-derived C1-INH concentrate (SC-C1-INH). Limited real-world data on these therapies have been reported. Objective: The objective was to describe new users of lanadelumab and SC-C1-INH, including demographics, healthcare resource utilization (HCRU), costs, and treatment patterns before and after beginning treatment. Methods: This was a retrospective cohort study that used an administrative claims data base. Two mutually exclusive cohorts of adult (ages ≥18 years) new users of lanadelumab or SC-C1-INH with ≥180 days of continuous use were identified. HCRU, costs, and treatment patterns were assessed in the 180-day period before the index date (new treatment use) and up to 365 days after the index date. HCRU and costs were calculated as annualized rates. Results: Forty-seven patients who used lanadelumab and 38 patients who used SC-C1-INH were identified. The most frequently used on-demand HAE treatments at baseline were the same for both cohorts: bradykinin B₂ antagonists (48.9% of the patients on lanadelumab, 52.6% of the patients on SC-C1-INH) and C1-INHs (40.4% of the patients on lanadelumab, 57.9% of the patients on SC-C1-INH). More than 33% of the patients continued to fill on-demand medications after treatment initiation. Annualized angioedema-associated emergency department visits and hospitalizations decreased after initiation of treatment, from 1.8 to 0.6 for the patients on lanadelumab and from 1.3 to 0.5 for the patients on SC-C1-INH. Annualized total healthcare costs after treatment initiation in the database were $866,639 and $734,460 for the lanadelumab and SC-C1-INH cohorts, respectively. Pharmacy costs accounted for >95% of these total costs. Conclusion: Although HCRU decreased after the initiation of treatment, angioedema-associated emergency department visits and hospitalizations and on-demand treatment fills were not completely eliminated. This indicates ongoing disease and treatment burden despite use of modern HAE medicines.

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lanadelumab和皮下c1抑制剂浓缩物治疗遗传性血管性水肿患者的医疗保健利用
背景:近年来,新的遗传性血管性水肿(HAE)治疗方法可用于治疗由于c1抑制剂(C1-INH)缺乏引起的HAE,包括两种皮下(SC)治疗方案:单克隆抗体(lanadelumab)和血浆来源的C1-INH浓缩物(SC-C1-INH)。关于这些疗法的真实数据有限。目的:目的是描述lanadelumab和SC-C1-INH的新使用者,包括人口统计学、医疗资源利用率(HCRU)、成本和开始治疗前后的治疗模式。方法:这是一项回顾性队列研究,使用行政索赔数据库。确定了两个相互排斥的成人(年龄≥18岁)新使用lanadelumab或SC-C1-INH且连续使用≥180天的队列。在指标日期前180天(新治疗使用)和指标日期后365天内评估HCRU、成本和治疗模式。HCRU和成本按年化率计算。结果:确定了47例使用lanadelumab的患者和38例使用SC-C1-INH的患者。基线时最常用的按需HAE治疗在两个队列中是相同的:缓激肽B₂拮抗剂(lanadelumab患者的48.9%,SC-C1-INH患者的52.6%)和c1 - inh (lanadelumab患者的40.4%,SC-C1-INH患者的57.9%)。超过33%的患者在治疗开始后继续按需服药。开始治疗后,与血管性水肿相关的急诊就诊和住院的年化次数减少,lanadelumab组从1.8次减少到0.6次,SC-C1-INH组从1.3次减少到0.5次。在数据库中,lanadelumab组和SC-C1-INH组治疗开始后的年化总医疗费用分别为866,639美元和734,460美元。药品费用占总费用的95%以上。结论:虽然HCRU在治疗开始后有所下降,但血管水肿相关的急诊就诊和住院以及按需治疗填充并未完全消除。这表明尽管使用了现代HAE药物,但仍存在疾病和治疗负担。
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来源期刊
CiteScore
5.70
自引率
35.70%
发文量
106
审稿时长
6-12 weeks
期刊介绍: Allergy & Asthma Proceedings is a peer reviewed publication dedicated to distributing timely scientific research regarding advancements in the knowledge and practice of allergy, asthma and immunology. Its primary readership consists of allergists and pulmonologists. The goal of the Proceedings is to publish articles with a predominantly clinical focus which directly impact quality of care for patients with allergic disease and asthma. Featured topics include asthma, rhinitis, sinusitis, food allergies, allergic skin diseases, diagnostic techniques, allergens, and treatment modalities. Published material includes peer-reviewed original research, clinical trials and review articles.
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