首页> 外文期刊>The journal of asthma >Effect of omalizumab as add-on therapy on asthma-related quality of life in severe allergic asthma: A Brazilian study (QUALITX)
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Effect of omalizumab as add-on therapy on asthma-related quality of life in severe allergic asthma: A Brazilian study (QUALITX)

机译:奥马珠单抗作为附加疗法对严重变应性哮喘中与哮喘相关的生活质量的影响:一项巴西研究(QUALITX)

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Objective. To assess the impact of omalizumab as an add-on therapy to standard treatment with inhaled corticosteroids (ICS) and long-acting beta-2 agonists (LABA) on asthma-related quality of life (QoL) in patients with severe allergic asthma. Methods. This was a 20-week, randomized, open-label, study involving Brazilian patients (>12 years) with severe persistent allergic asthma inadequately controlled despite regular treatment with, at least, ICS (≥500 μg/day fluticasone or equivalent) + LABA. The primary objective was to assess the mean change from baseline in overall Asthma-related Quality of Life Questionnaire (AQLQ) score in omalizumab-treated patients compared with the control group. Secondary outcome measures included rescue medication use, incidence of asthma exacerbations, perception of treatment efficacy among patients, mean change from baseline in AQLQ score, and >1.5-point increase in overall AQLQ score. Results. In the omalizumab group, overall AQLQ score was 3.2 (0.9) (mean [SD]) at baseline and 4.4 (1.3) at week 20 versus 3.0 (1.0) at baseline and 3.0 (1.1) at week 20 in the control group. Mean change from baseline on overall AQLQ score at week 20 in the omalizumab group was 1.2 (0.2) versus 0 (0.1) in the control group, showing a significant increase in scores from baseline in the omalizumab group (p <.001). There was also a statistically significant difference (p <.001) in the number of patients who showed a >1.5-point increase from baseline in overall AQLQ score after 20 weeks, thus indicating a better QoL in the omalizumab group. There was no significant difference with respect to the use of rescue medication, incidence of asthma exacerbation, and adverse events between treatment groups. The global evaluation of treatment effectiveness was significantly better for omalizumab (p <.001). Conclusion. Omalizumab was well tolerated and significantly improved the overall AQLQ score. Hence, it is a potential add-on therapy for severe persistent allergic asthma not controlled by standard prescribed treatment in Brazilian patients.
机译:目的。评估奥马珠单抗作为吸入性糖皮质激素(ICS)和长效β-2激动剂(LABA)的标准治疗的补充疗法对严重过敏性哮喘患者与哮喘相关的生活质量(QoL)的影响。方法。这是一项为期20周,随机,开放标签的研究,研究对象是尽管定期接受至少ICS(≥500μg/天氟替卡松或同等剂量)+ LABA的常规治疗,但仍未充分控制严重持续性过敏性哮喘的巴西患者(> 12岁) 。主要目标是评估与对照组相比,在接受奥马珠单抗治疗的患者中,与哮喘相关的生活质量调查问卷(AQLQ)总体得分与基线相比的平均变化。次要结局指标包括急救药物的使用,哮喘急性发作的发生率,患者对治疗效果的认识,AQLQ得分与基线相比的平均变化以及AQLQ总体得分增加> 1.5分。结果。在奥马珠单抗组中,AQLQ总体评分在基线时为3.2(0.9)(平均值[SD]),在第20周时为4.4(1.3),而在基线时为3.0(1.0),在第20周时为3.0(1.1)。奥马珠单抗组在第20周时,与基线相比,AQLQ总体得分的平均变化为1.2(0.2),而对照组为0(0.1),表明奥马珠单抗组的基线得分显着增加(p <.001)。在20周后,总AQLQ得分比基线增加> 1.5点的患者数量也有统计学上的显着差异(p <.001),因此表明奥马珠单抗组的QoL更好。治疗组之间在使用急救药物,哮喘急性发作和不良事件方面无显着差异。对于奥马珠单抗,治疗效果的整体评估明显更好(p <.001)。结论。奥马珠单抗耐受性良好,可显着改善总体AQLQ评分。因此,在巴西患者中,这是不受标准处方治疗控制的严重持续性过敏性哮喘的潜在附加疗法。

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