Therapeutic efficacy of omalizumab in children with moderate-to-severe allergic asthma combined with chronic sinusitis.

IF 3.3 Q2 ALLERGY Frontiers in allergy Pub Date : 2023-10-16 eCollection Date: 2023-01-01 DOI:10.3389/falgy.2023.1236798
Weikun Chong, Hailang Li, Juan Wang
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Abstract

Background: Omalizumab has been approved for treating moderate-to-severe asthma in children aged over 6 years. Its application to asthmatic children with other allergic diseases has been rarely explored. The present study aims to explore the therapeutic efficacy of omalizumab in children with moderate-to-severe allergic asthma combined with chronic sinusitis.

Methods: The clinical data of children diagnosed with moderate-to-severe allergic asthma combined with chronic sinusitis and treated with omalizumab between September 2020 and April 2022 were retrospectively analyzed. Lung function indexes such as Childhood Asthma Control Test (C-ACT) scores, fractional exhaled nitric oxide (FeNO), and forced expiratory volume in the first second (FEV1) percent predicted (FEV1%pred), small airway function indexes, and the clinical symptoms of chronic sinusitis were analyzed.

Results: A total of 26 children were observed for 16 weeks. After 16 weeks of omalizumab treatment, the significantly increased C-ACT scores (15.57 ± 3.25 points vs. 24.98 ± 5.21 points, F = 15.7112, P < 0.001) and decreased FeNO (31.55 ± 15.57 ppb vs. 19.86 ± 9.80 ppb, F = 4.4265, P = 0.0022), compared with those at baseline, were suggestive of well-controlled symptoms of asthma and improved lung function. FEV1%pred and FEV1/forced vital capacity (FVC) ratio (the ratio of the forced expiratory volume in the first 1 s to the forced vital capacity) increased after omalizumab treatment, although no significant differences were detected (P = 0.9954 and 0.9382, respectively). Peak expiratory flow (PEF) percent predicted (PEF%pred) and forced expiratory flow at 75% of FVC (FEF75%), 50% of FVC (FEF50%), and 25%-75% of FVC (FEF25%-75%) significantly increased after omalizumab treatment (P = 0.0477, <0.001, <0.001, and <0.001, respectively). Visual analog scale scores significantly decreased after omalizumab treatment (6.40 ± 2.98 points vs. 0.85 ± 0.40 points, t = 27.2419, P < 0.001), suggesting alleviation in the clinical symptoms of chronic sinusitis.

Conclusion: In this study, it was found that omalizumab can effectively alleviate clinical symptoms and improve lung function and quality of life in children with moderate-to-severe allergic asthma combined with chronic sinusitis.

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奥马珠单抗治疗儿童中重度过敏性哮喘合并慢性鼻窦炎的疗效。
背景:奥马珠单抗已被批准用于治疗6岁以上儿童的中重度哮喘。它在患有其他过敏性疾病的哮喘儿童中的应用很少被探索。本研究旨在探讨奥马珠单抗治疗儿童中重度过敏性哮喘合并慢性鼻窦炎的疗效。方法:回顾性分析2020年9月至2022年4月期间诊断为中重度过敏性哮喘合并慢性鼻窦炎并接受奥马珠单抗治疗的儿童的临床数据。分析了肺功能指标,如儿童哮喘控制测试(C-ACT)评分、呼出一氧化氮(FeNO)分数、预测的前一秒用力呼气量(FEV1)百分比(FEV1%pred)、小气道功能指标和慢性鼻窦炎的临床症状。结果:共观察了26名儿童16周。奥马珠单抗治疗16周后,C-ACT评分显著增加(15.57 ± 3.25分对24.98分 ± 5.21分,F = 15.7112,P F = 4.4265,P = 0.0022),与基线时相比,表明哮喘症状得到了很好的控制,肺功能得到了改善。FEV1%pred和FEV1/用力肺活量(FVC)比(前1 s与强迫肺活量的比值)增加,但没有发现显著差异(P = 分别为0.9954和0.9382)。奥马珠单抗治疗后,预测呼气峰流量百分比(PEF%pred)和75%FVC(FEF75%)、50%FVC(FEF50%)和25%-75%FVC的用力呼气流量显著增加(P = 0.0477吨 = 27.2419,P 结论:本研究发现奥马珠单抗能有效缓解中重度过敏性哮喘合并慢性鼻窦炎患儿的临床症状,改善肺功能和生活质量。
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