Healthcare Resource Utilization in Patients Receiving Omalizumab for Allergic Asthma in a Real-World Setting.

Biologics in therapy Pub Date : 2014-12-01 Epub Date: 2014-11-05 DOI:10.1007/s13554-014-0019-z
Gert-Jan Braunstahl, Janice Canvin, Guy Peachey, Chien-Wei Chen, Panayiotis Georgiou
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引用次数: 20

Abstract

Introduction: Inadequately controlled asthma is associated with increased healthcare resource utilization. The eXpeRience registry was initiated to evaluate real-world outcomes in patients receiving omalizumab for uncontrolled persistent allergic asthma. The current analysis of data from the eXpeRience registry focuses on healthcare resource utilization and on absences from work or school.

Methods: The eXpeRience was a 2-year, multinational, non-interventional, observational registry conducted to investigate real-world outcomes among patients receiving omalizumab in accordance with country-specific prescribing criteria for the treatment of uncontrolled persistent allergic asthma. Asthma-related healthcare resource utilization (hospitalizations, emergency room visits or unscheduled-asthma-related doctor visits or interventions) and absences from work or school were assessed pre-treatment (12-month data were collected retrospectively at baseline) and at months 12 and 24 after the initiation of omalizumab treatment. Serious adverse event (SAE) data were also assessed.

Results: A total of 943 patients (mean age 45 years; female 65%) were enrolled in the registry. Overall, the mean (standard deviation [SD]) number of asthma-related medical healthcare uses per patient decreased from 6.2 (6.97) during the pre-treatment period to 1.0 (1.96) and 0.5 (1.28) at months 12 and 24, respectively. The mean (SD) number of work or school days missed due to asthma was also lower at months 12 (3.5 [17.28] and 1.6 [4.28], respectively) and 24 (1.0 [4.66] and 1.9 [5.46], respectively) compared with the pre-treatment period (26.4 [49.61] and 20.7 [27.49], respectively). The nature and frequency of SAEs in the eXpeRience registry were comparable to that seen in interventional clinical trials with omalizumab.

Conclusion: The results of the eXpeRience registry indicate that omalizumab is associated with reductions in healthcare utilization, and in the number of days of absence from work or school, in patients with uncontrolled persistent allergic asthma in the real-world setting.

Funding: Novartis Pharma AG, Basel, Switzerland.

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在现实世界中接受奥玛珠单抗治疗过敏性哮喘患者的医疗资源利用
简介:哮喘控制不充分与医疗资源利用率增加有关。eXpeRience注册是为了评估接受omalizumab治疗不受控制的持续性过敏性哮喘患者的真实结果。目前对eXpeRience注册表数据的分析侧重于医疗保健资源利用和缺勤情况。方法:该研究是一项为期2年、跨国、非介入性、观察性注册研究,旨在调查根据国家特定处方标准接受奥玛珠单抗治疗不受控制的持续性过敏性哮喘患者的现实结果。在治疗前(在基线时回顾性收集12个月的数据)和开始奥玛单抗治疗后的12个月和24个月,评估哮喘相关医疗资源的利用(住院、急诊室就诊或未安排的哮喘相关医生就诊或干预)和缺勤情况。严重不良事件(SAE)数据也进行了评估。结果:共943例患者(平均年龄45岁;女性(65%)登记在册。总体而言,每位患者与哮喘相关的医疗保健使用的平均(标准差[SD])数量分别从治疗前的6.2(6.97)下降到12个月和24个月时的1.0(1.96)和0.5(1.28)。与治疗前(26.4[49.61]和20.7[27.49])相比,12个月时因哮喘而缺勤的平均(SD)天数(分别为3.5[17.28]和1.6[4.28])和24天(分别为1.0[4.66]和1.9[5.46])也较低。在eXpeRience注册表中,SAEs的性质和频率与使用omalizumab的介入性临床试验中所见的相当。结论:eXpeRience注册的结果表明,omalizumab与现实环境中不受控制的持续性过敏性哮喘患者的医疗保健利用率和缺勤或缺课天数的减少有关。资助:诺华制药公司,巴塞尔,瑞士。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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