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首页> 外文期刊>Medical principles and practice: international journal of the Kuwait University, Health Science Centre >'Real-life' Efficacy and Safety Aspects of 4-Year Omalizumab Treatment for Asthma
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'Real-life' Efficacy and Safety Aspects of 4-Year Omalizumab Treatment for Asthma

机译:奥马珠单抗治疗哮喘4年的“实际”疗效和安全性方面

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Objective: To evaluate the long-term efficacy and safety of omalizumab in asthma in a real-life setting. Subjects and Methods: This 4-year observational study included 65 patients treated with omalizumab during clinic visits; treatment response was rated as excellent, good, and partial based on a modified physician’s Global Evaluation of Treatment Effectiveness (mGETE) scale of emergency room visits (ERV), hospitalization, use of oral corticosteroids, inhaled corticosteroid (ICS)/long-acting β-agonist (LABA) dose, and short-acting β-agonist rescue. The following tests were done: forced expiratory volume in 1 s (FEV1) and the asthma control test (ACT). Measurements were performed 1 month before therapy and at 16 weeks, 1 year, and 4 years of treatment. Statistical analyses were done using the Wilcoxon signed-rank test, Spearman rank correlation, and McNemar χ2 test. Results: The dropout rate was 15 (18.5%): 8 nonresponders (10.0%); 2 patients died (2.5%), and 5 were lost to follow-up (6.25%). Treatment response was excellent in 35 (53.8%); good in 23 (35.4%), and partial in 7 patients (10.8%). The number of excellent responders increased from 35 (53.8%) at 16 weeks to 48 (73.8%) at the 4-year follow-up. The number of patients who did not require ERV improved from 0 to 59 (90.8%), and the lowest rate of hospitalization was 1 in year 4 ( p 1 level from 55.6 ± 10.6 to 76.63 ± 10.34 at year 4. Conclusion: In this study, omalizumab therapy resulted in better asthma control, and was effective and well tolerated as an add-on therapy for patients with moderate-to-severe asthma.
机译:目的:在实际生活中评估奥马珠单抗在哮喘中的长期疗效和安全性。受试者与方法:这项为期4年的观察性研究包括65位在临床就诊期间接受奥马珠单抗治疗的患者。根据经修改的医师对急诊室就诊(ERV),住院,口服皮质类固醇,吸入皮质类固醇(ICS)/长效β的整体治疗效果评估(mGETE)量表,治疗反应被评为优秀,良好和部分评估激动剂(LABA)剂量和短效β激动剂抢救。进行了以下测试:1 s内呼气量(FEV 1 )和哮喘控制测试(ACT)。在治疗前1个月以及治疗的16周,1年和4年进行测量。使用Wilcoxon符号秩检验,Spearman秩相关和McNemarχ 2 检验进行统计分析。结果:辍学率为15(18.5%):8位无反应者(10.0%); 2例患者死亡(2.5%),5例失访(6.25%)。 35例的治疗反应极佳(53.8%); 23例(35.4%)为好,7例为部分(10.8%)。出色的响应者数量从16周的35(53.8%)增加到4年随访的48(73.8%)。不需要ERV的患者数量从0增至59(90.8%),住院率最低的是第4年1(p 1 水平从55.6±10.6增至第4年的76.63±10.34)。结论:在这项研究中,奥马珠单抗疗法可更好地控制哮喘,并且作为中重度哮喘患者的附加疗法有效且耐受性良好。

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