Description of Baseline Characteristics of Pediatric Allergic Asthma Patients Including those Initiated on Omalizumab.

IF 2.3 Q1 OTORHINOLARYNGOLOGY
Allergy & Rhinology Pub Date : 2018-04-09 eCollection Date: 2018-01-01 DOI:10.1177/2152656718763387
Abhishek Kavati, Dominic Pilon, Benjamin Ortiz, Brandee Paknis, Ashok Vegesna, Bradd Schiffman, Maryia Zhdanava, Patrick Lefebvre, Brian Stone
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引用次数: 0

Abstract

Background: Indication of omalizumab in the United States was recently extended to include pediatric (6-11 years) uncontrolled moderate-to-severe allergic asthma patients.

Objective: The purpose of this study was to describe baseline characteristics of this population from a real-world dataset.

Methods: Allergic asthma patients and uncontrolled moderate-to-severe allergic asthma patients, aged 6-11 years, were identified in the Allergy Partners Network Electronic Medical Records (2007-2016). The index date for allergic asthma patients was the latest between the second asthma-related visit and the allergic status confirmation. Uncontrolled moderate-to-severe allergic asthma patients were stratified into omalizumab-exposed (index date) or omalizumab-unexposed (index date randomly generated) groups. Characteristics were evaluated during the 12-month preindex period.

Results: A total of 5806 allergic asthma, 37 omalizumab-exposed, and 2620 omalizumab-unexposed patients were selected (mean age approximately 9 years). Allergic asthma and omalizumab-unexposed patients were predominantly white (70.2% and 61.2%) whereas the majority of omalizumab-exposed were African Americans (62.2%). Mean immunoglobulin E was 782.0 IU/ml in allergic asthma patients (available in 2.2%), 1134.4 IU/ml in omalizumab-exposed (available in 100.0%), and 746.1 IU/ml in omalizumab-unexposed (available in 3.1%). Allergic asthma patients were less severe than omalizumab-exposed and omalizumab-unexposed based on the forced expiratory volume in 1 s as a percentage of predicted value (FEV1% predicted) and the Childhood Asthma Control Test (C-ACT). FEV1% predicted was below normal (<80%) in 42.4% of omalizumab-exposed and 39.1% of omalizumab-unexposed patients, also 63.6% of omalizumab-exposed and 46.7% of omalizumab-unexposed had uncontrolled asthma (C-ACT score <20). In African American omalizumab-exposed patients, FEV1% predicted was below normal in 47.6% and 55.0% had uncontrolled asthma.

Conclusions: In a real-world setting, pediatric patients with uncontrolled moderate-to-severe allergic asthma have a significant disease burden as shown by high rates of poor lung function, disease control, and symptoms. Currently available treatments could help improve disease management in this population.

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儿童过敏性哮喘患者(包括开始使用奥马珠单抗的患者)的基线特征描述。
背景:美国最近将奥马珠单抗的适应症扩展至儿童(6-11 岁)未获控制的中重度过敏性哮喘患者:最近,奥马珠单抗在美国的适应症扩大到了未得到控制的中重度过敏性哮喘儿童患者(6-11 岁):方法:过敏性哮喘患者和未受控制的中度至重度过敏性哮喘患者均可使用奥马珠单抗:过敏伙伴网络电子病历(2007-2016 年)中确定了 6-11 岁的过敏性哮喘患者和未受控制的中重度过敏性哮喘患者。过敏性哮喘患者的指数日期是第二次哮喘相关就诊和过敏状态确认之间的最近日期。未受控制的中重度过敏性哮喘患者被分为接触奥马珠单抗组(指数日期)和未接触奥马珠单抗组(指数日期随机生成)。对指数前 12 个月期间的特征进行了评估:共选取了 5806 名过敏性哮喘患者、37 名暴露于奥马珠单抗的患者和 2620 名未暴露于奥马珠单抗的患者(平均年龄约为 9 岁)。过敏性哮喘和暴露于奥马珠单抗的患者主要是白人(70.2% 和 61.2%),而暴露于奥马珠单抗的患者大多数是非裔美国人(62.2%)。过敏性哮喘患者的免疫球蛋白 E 平均值为 782.0 IU/ml(2.2% 的患者有此数据),奥马珠单抗暴露患者的免疫球蛋白 E 平均值为 1134.4 IU/ml(100.0% 的患者有此数据),奥马珠单抗未暴露患者的免疫球蛋白 E 平均值为 746.1 IU/ml(3.1% 的患者有此数据)。根据1秒内用力呼气容积占预测值的百分比(FEV1%预测值)和儿童哮喘控制测试(C-ACT),过敏性哮喘患者的病情没有接触过奥马珠单抗和未接触过奥马珠单抗的患者严重。47.6%的患者FEV1%预测值低于正常(1%预测值低于正常),55.0%的患者哮喘未得到控制:在现实世界中,未受控制的中度至重度过敏性哮喘儿童患者的肺功能、疾病控制和症状均较差,这表明他们承受着巨大的疾病负担。目前可用的治疗方法有助于改善这一人群的疾病管理。
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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来源期刊
Allergy & Rhinology
Allergy & Rhinology OTORHINOLARYNGOLOGY-
CiteScore
3.30
自引率
4.50%
发文量
11
审稿时长
15 weeks
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