[奥玛珠单抗对未控制支气管哮喘患者的附加效应]。

Yoshinori Minami, Satoshi Endo, Shunsuke Okumur, Takaaki Sasaki, Yasushi Yamamoto, Toshiyuki Ogasa, Shinobu Osanai, Yoshinobu Ohsaki
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引用次数: 0

摘要

大剂量吸入皮质类固醇对大多数支气管哮喘患者有效,但在某些患者亚群中往往难以获得充分控制。Omalizumab最近成为治疗支气管哮喘的一种有前景的药物。为了评估其附加效应,我们对不受控制的特应性哮喘患者给予omalizumab治疗超过16周,并对他们进行问卷调查。研究人群包括9例患者,尽管给予高剂量吸入皮质类固醇和其他疾病控制药物,但仍有频繁的哮喘症状。我们使用哮喘健康问卷-33- japan和哮喘控制测试对疾病控制进行评分,并以回顾性的方式评估短效β - 2激动剂用于急救和滴注茶碱和/或全身类固醇的频率。治疗16周后哮喘评分显著提高。使用缓解剂和滴注的频率也有所下降。即使在没有检测到空气过敏原特异性IgE抗体的患者中也存在这些趋势。未观察到统计学上显著的副作用。我们的研究通过简单的问卷评估证实了omalizumab的附加效应。需要进一步的研究来阐明omalizumab治疗是否适用于没有特异性IgE抗体的患者。
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[The add-on effect of omalizumab on patients with uncontrolled bronchial asthma].

A high-dose administration of inhaled corticosteroid is effective in the majority of patients with bronchial asthma, but is often difficult to attain sufficient control in certain subsets of patients. Omalizumab has recently emerged as a promising drug for bronchial asthma. To assess its add-on effect we administered omalizumab to patients with uncontrolled atopic asthma for more than 16 weeks and gave them questionnaires. The study population comprised 9 patients with frequent asthmatic symptoms despite the administration of high-dose inhaled corticosteroid and other disease controllers. We scored disease control using the Asthma Health Questionnaire-33-Japan and the Asthma Control Test, and evaluated the frequencies of short-acting beta2-agonist use for rescue and drip infusion of theophyllines and/or systemic steroids in a retrospective fashion. Asthmatic scores were significantly improved after 16 weeks of omalizumab therapy. The frequencies of reliever use and drip infusion were also decreased. These trends were present even in patients in whom no aeroallergen-specific IgE antibodies were detected. No statistically significant side effects were observed. Our study confirmed the add-on effect of omalizumab based on evaluation by simple questionnaires. Further studies are needed to clarify whether omalizumab therapy is suitable for patients without specific IgE antibodies.

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