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Effectiveness of the Polish program for the treatment of severe allergic asthma with omalizumab: a single-center experience

机译:波兰使用奥马珠单抗治疗严重过敏性哮喘的计划的有效性:单中心经验

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Background A national program for the treatment of severe allergic (IgE-dependent) asthma with omalizumab (OMA) was implemented in Poland in 2013. This observational study evaluated the effectiveness of the Polish OMA program and monitored asthma control after treatment discontinuation. Methods In the first year of the program, 53 patients (23 new/30 continuing treatment) received OMA in the Barlicki Hospital, Poland. Patients were evaluated at baseline and after 16?weeks of OMA treatment by spirometry, mean dose of inhaled corticosteroids (ICS) and oral corticosteroids (OCS), number of asthma exacerbations, the Asthma Control Questionnaire (ACQ), and the Asthma Quality of Life Questionnaire (AQLQ). OMA treatment responses were determined using the global effectiveness of treatment evaluation scale. Fourteen patients ceased OMA treatment following ≥36?months of therapy and entered follow up. Results All patients treated with OMA de novo for at least 16?weeks had a decrease in asthma exacerbations and showed a good (15/16, 94?%) or an excellent (1/16, 6?%) response to treatment. We observed a reduction in OCS dose (≥5?mg/day) in 14/16 (88?%) patients. ACQ and AQLQ scores improved by ≥0.5 points in 15/16 (94?%) and 14/16 (88?%) patients, respectively. After OMA cessation, 11/14 (79?%) patients showed worsening of asthma control and severe exacerbations. Conclusions Patients in the OMA program show significant benefits, including reduced use of OCS, improved asthma control and quality of life. After OMA discontinuation, frequent severe exacerbations were observed primarily in patients whose asthma was previously uncontrolled by high OCS doses.
机译:背景技术波兰于2013年实施了一项国家治疗严重过敏性(IgE依赖性)哮喘的奥马珠单抗(OMA)的国家计划。这项观察性研究评估了波兰OMA计划的有效性,并监测了治疗中断后哮喘的控制。方法在该计划的第一年,在波兰的Barlicki医院接受了OMA治疗的53名患者(23名新患者/ 30名继续治疗)。在基线和OMA治疗16周后通过肺活量测定,吸入皮质类固醇(ICS)和口服皮质类固醇(OCS)的平均剂量,哮喘发作次数,哮喘控制问卷(ACQ)和哮喘生活质量对患者进行评估问卷(AQLQ)。使用整体疗效评估量表确定OMA治疗反应。 ≥36个月的治疗后,有14例患者停止了OMA治疗,并进行了随访。结果所有接受OMA从头治疗至少16周的患者,哮喘发作加重程度均降低,对治疗的反应良好(15/16,94%),或表现良好(1/16,6%)。我们观察到14/16(88%)的患者的OCS剂量减少了(≥5?mg /天)。 15/16(94%)和14/16(88%)的患者的ACQ和AQLQ得分分别提高了≥0.5分。停止OMA后,有11/14(79%)的患者表现出哮喘控制恶化和严重加重。结论OMA计划的患者显示出显着的益处,包括减少使用OCS,改善哮喘控制和生活质量。停用OMA后,主要在以前无法通过高OCS剂量控制哮喘的患者中观察到频繁的严重加重病情。

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