Bird John A, Near Aimee M, Wang Julie, Seetasith Arpamas, Garmo Vincent, Ko Stella, Zhao Xiaohui, Doshi Riddhi, Wang Elizabeth J, Gupta Sachin, Fleischer David M
UT Southwestern Medical Center, Dallas, Tex.
IQVIA, Durham, NC.
J Allergy Clin Immunol Glob. 2025 May 7;4(3):100491. doi: 10.1016/j.jacig.2025.100491. eCollection 2025 Aug.
Patients with comorbid asthma and food allergy (FA) are at increased risk of adverse outcomes for both conditions. Omalizumab, a biologic for moderate to severe persistent asthma, received recent approval for FA.
We sought to compare FA-, asthma/FA-related, and all-cause health care resource utilization and costs before and after omalizumab initiation among patients with asthma and FA.
This study retrospectively analyzed data from IQVIA PharMetrics Plus claims among patients who were 6 years or older, had asthma and FA (medical claim for FA or anaphylactic reaction due to food), had initiated omalizumab between 2018 and 2021, and had 12 months of data before (baseline) and after (follow-up) omalizumab initiation (index date).
Of 523 patients who initiated omalizumab (mean age, 33.1 years; 71.5% female), the prevalence of FA-related (12.4% vs 4.8%), asthma/FA-related (25.0% vs 15.5%), and all-cause (44.6% vs 30.2%; all < .0001) emergency department visits reduced at follow-up versus baseline. Significant reductions were also observed for the prevalence of hospitalizations (FA: 1.5% vs 0.2%; asthma/FA: 12.3% vs 7.4%; all-cause: 13.2% vs 7.5%) and total FA-related health care costs per patient ($1600 vs $1502; all < .0001). The total asthma/FA-related ($5,966 vs $5,683, = .8375) and all-cause ($24,874 vs $27,298, = .6724) health care costs were similar from baseline to follow-up after excluding the omalizumab costs.
FA-related, asthma/FA-related, and all-cause emergency department visits and hospitalizations significantly reduced in the 12 months after omalizumab initiation. These results provide valuable and timely real-world evidence that omalizumab has the potential to reduce the acute care utilization in patients with comorbid asthma and FA.
合并哮喘和食物过敏(FA)的患者出现两种病症不良后果的风险增加。奥马珠单抗是一种用于治疗中度至重度持续性哮喘的生物制剂,最近被批准用于治疗食物过敏。
我们试图比较哮喘和食物过敏患者在开始使用奥马珠单抗之前和之后,与食物过敏、哮喘/食物过敏相关以及全因的医疗资源利用情况和费用。
本研究回顾性分析了IQVIA PharMetrics Plus数据库中6岁及以上、患有哮喘和食物过敏(食物过敏或食物引起的过敏反应的医疗记录)、在2018年至2021年期间开始使用奥马珠单抗、且在开始使用奥马珠单抗前(基线)和后(随访)有12个月数据(索引日期)的患者的数据。
在523例开始使用奥马珠单抗的患者中(平均年龄33.1岁;71.5%为女性),与食物过敏相关的(12.4%对4.8%)、哮喘/食物过敏相关的(25.0%对15.5%)以及全因的(44.6%对30.2%;均P<0.0001)急诊就诊率在随访时较基线时降低。住院率(食物过敏:1.5%对0.2%;哮喘/食物过敏:12.3%对7.4%;全因:13.2%对7.5%)以及每位患者与食物过敏相关的总医疗费用(1600美元对1502美元;均P<0.0001)也有显著降低。排除奥马珠单抗费用后,从基线到随访,与哮喘/食物过敏相关的总医疗费用(5966美元对5683美元,P = 0.8375)和全因总医疗费用(24874美元对27298美元,P = 0.6724)相似。
在开始使用奥马珠单抗后的12个月内,与食物过敏相关的、哮喘/食物过敏相关的以及全因的急诊就诊和住院情况显著减少。这些结果提供了有价值且及时的真实世界证据,表明奥马珠单抗有可能减少合并哮喘和食物过敏患者的急性护理利用。