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美国医疗保险优势人群:使用糠酸氟替卡松/乌美溴铵/维兰特罗(FF/UMEC/VI)起始治疗前后接受吸入性糖皮质激素/长效β2受体激动剂(ICS/LABA)治疗的哮喘患者的结局

Medicare Advantage Population in the United States: Outcomes of Patients with Asthma Treated with ICS/LABA Before and After Initiation with Fluticasone Furoate/Umeclidinium/Vilanterol (FF/UMEC/VI).

作者信息

Baptist Alan P, Germain Guillaume, Klimek Jacob, Laliberté François, Schell Robert C, Forero-Schwanhaeuser Sergio, Moore Alison, Noorduyn Stephen G, Paczkowski Rosirene

机构信息

Division of Allergy and Clinical Immunology, Henry Ford Health and MI State University Health Sciences, One Ford Place, 3A32, Detroit, MI, 48202, USA.

Group d'Analyse, Ltée, Montreal, QC, Canada.

出版信息

Adv Ther. 2025 Feb;42(2):1061-1074. doi: 10.1007/s12325-024-03083-6. Epub 2024 Dec 23.

Abstract

INTRODUCTION

The clinical benefits of fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) have been demonstrated in clinical trials. There is limited evidence regarding the effectiveness and economic outcomes associated with FF/UMEC/VI use in US clinical practice. This real-world study assessed asthma-related exacerbations, healthcare resource utilization (HRU), and healthcare costs among a Medicare Advantage-insured population before and after initiation of FF/UMEC/VI in patients with asthma previously treated with an inhaled corticosteroid/long-acting β-agonist (ICS/LABA).

METHODS

De-identified data were obtained from the Komodo Health database (01/01/2016-12/31/2023) for adults with asthma who received prior ICS/LABA treatment and had ≥ 12 months of continuous Medicare Advantage coverage both pre- and post-FF/UMEC/VI initiation (index date). Rates of asthma-related exacerbations and HRU were compared using rate ratios (RR) from Poisson regressions. Healthcare costs were calculated per patient per year (PPPY) and compared using mean cost differences from generalized linear models.

RESULTS

In total, 2598 Medicare Advantage-insured patients who initiated FF/UMEC/VI for asthma were included. The mean ± SD age was 67.9 ± 12.3 years; 75.5% were female. The rate of overall asthma-related exacerbations was 31% lower in the post- versus pre-initiation period (RR 0.69; 95% CI 0.65, 0.73; p < 0.001) and included a 24% lower rate of inpatient/emergency department (IP/ED)-defined exacerbations (RR 0.76; 95% CI 0.68, 0.85; p < 0.001) and a 34% lower rate of systemic corticosteroid (SCS)-defined exacerbations (RR 0.66; 95% CI 0.61, 0.71; p < 0.001). Asthma-related ED visits (RR 0.69; 95% CI 0.60, 0.80; p < 0.001) and asthma-related outpatient (OP) visits (RR 0.77; 95% CI 0.71, 0.84; p < 0.001) were both lower, and the mean reduction in cost was $411 PPPY (95% CI $575, $248; p < 0.001), after FF/UMEC/VI initiation.

CONCLUSIONS

Initiation of FF/UMEC/VI after ICS/LABA treatment among Medicare Advantage-insured patients with asthma was associated with reduced rates of asthma-related exacerbations, ED and OP visits, and healthcare costs, highlighting the benefits of therapy escalation among this patient population.

摘要

简介

糠酸氟替卡松/乌美溴铵/维兰特罗(FF/UMEC/VI)的临床益处已在临床试验中得到证实。关于FF/UMEC/VI在美国临床实践中的有效性和经济结果的证据有限。这项真实世界研究评估了在先前接受吸入性糖皮质激素/长效β受体激动剂(ICS/LABA)治疗的哮喘患者中,开始使用FF/UMEC/VI前后,医疗保险优势计划参保人群中与哮喘相关的急性加重、医疗资源利用(HRU)和医疗费用。

方法

从科莫多健康数据库(2016年1月1日至2023年12月31日)获取去识别化数据,对象为患有哮喘且之前接受过ICS/LABA治疗、在开始使用FF/UMEC/VI前后(索引日期)均有≥12个月连续医疗保险优势计划覆盖的成年人。使用泊松回归的率比(RR)比较与哮喘相关的急性加重率和HRU。计算每位患者每年的医疗费用(PPPY),并使用广义线性模型的平均费用差异进行比较。

结果

总共纳入了2598名开始使用FF/UMEC/VI治疗哮喘的医疗保险优势计划参保患者。平均年龄±标准差为67.9±12.3岁;75.5%为女性。与哮喘相关的总体急性加重率在开始使用FF/UMEC/VI后较使用前降低了31%(RR 0.69;95%置信区间0.65,0.73;p<0.001),其中住院/急诊科(IP/ED)定义的急性加重率降低了24%(RR 0.76;95%置信区间0.68,0.85;p<0.001),全身性糖皮质激素(SCS)定义的急性加重率降低了34%(RR 0.66;95%置信区间0.61,0.71;p<0.001)。与哮喘相关的急诊科就诊(RR 0.69;95%置信区间0.60,0.80;p<0.001)和与哮喘相关的门诊就诊(RR 0.77;95%置信区间0.71,0.84;p<0.001)均减少,开始使用FF/UMEC/VI后,平均费用降低为411美元/PPPY(95%置信区间575美元,248美元;p<0.001)。

结论

在医疗保险优势计划参保的哮喘患者中,在ICS/LABA治疗后开始使用FF/UMEC/VI与哮喘相关急性加重率、急诊科和门诊就诊次数以及医疗费用的降低相关,突出了该患者群体治疗升级的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e79/11787182/13a84e5934ff/12325_2024_3083_Fig1_HTML.jpg

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