[mepolizumab对严重嗜酸性粒细胞性哮喘患者的疗效:真实研究]。

IF 0.7 Q4 RESPIRATORY SYSTEM Tuberkuloz ve Toraks-Tuberculosis and Thorax Pub Date : 2023-06-01 DOI:10.5578/tt.20239918
İsmet Bulut, Zeynep Yegin Katran, Dilek Yavuz, Ali Burkan Yıldız, Tuğçe Yakut, Cihan Örçen, Selver Seda Mersin
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引用次数: 0

摘要

简介我们分析了接受美泊利珠单抗治疗的重度嗜酸性粒细胞性哮喘患者的症状、哮喘发作、肺功能检查指标外周血嗜酸性粒细胞水平和百分比对基线、第6个月和第12个月数据的影响:回顾性审查了2018年1月至2021年12月期间我院确诊为重度嗜酸性粒细胞性哮喘并接受麦泊利单抗治疗的患者病历。调查了患者的人口统计学数据、哮喘病程、合并症(如鼻息肉、嗜酸性粒细胞性多血管炎)以及非甾体抗炎药加重的呼吸系统疾病。对开始使用麦泊利单抗治疗前以及开始治疗后第六个月和第十二个月的各种因素进行了比较。这些因素包括哮喘控制测试评分、哮喘发作频率(包括急诊入院、住院和重症监护入院)、外周血嗜酸性粒细胞水平和百分比以及肺功能测试参数。此外,还评估了预测应答者和超级应答者的临床和实验室参数:研究共纳入 21 名患者。他们的平均年龄为(50.7±11.9)岁,其中四名(19%)为男性。哮喘诊断的平均持续时间为(17.5 ± 13.7)年。14名患者(66.7%)患有特应性哮喘。4名患者(19%)患有鼻息肉,4名患者(19%)患有非哮喘。在使用mepolizumab之前,13名患者(61.9%)曾接受过奥马珠单抗治疗。接受麦泊珠单抗治疗的时间为(29.2 ± 9.9)个月。在第 6 个月和第 12 个月时,嗜酸性粒细胞的数量和百分比均出现了统计学意义上的明显下降(p 结论:尽管我们研究的患者人数有限,但麦泊珠单抗改善了严重嗜酸性粒细胞性哮喘的症状评分,减少了发作次数,并改善了肺功能检测值。
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[Effectiveness of mepolizumab in patients with severe eosinophilic asthma: In a real life study].

Introduction: We analyzed the effects of mepolizumab treatment on symptoms, asthma attacks, pulmonary function test parameters peripheral blood eosinophil level, and percentage in patients with severe eosinophilic asthma receiving mepolizumab treatment as the baseline, sixth and twelfthmonth data.

Materials and methods: The medical records of patients diagnosed with severe eosinophilic asthma and treated with mepolizumab at our clinic were retrospectively reviewed for the period between January 2018 and December 2021. Demographic data of the patients, duration of asthma disease, comorbidities such as a nasal polyp, eosinophilic granulomatous polyangiitis, and nonsteroidal anti-inflammatory drug exacerbated respiratory disease were investigated. A comparison was made of various factors before initiating mepolizumab treatment, as well as at the sixth and twelfth month after treatment initiation. These factors include asthma control test scores, frequency of asthma attacks (including emergency admissions, hospitalizations, and intensive care admissions), peripheral blood eosinophil levels and percentages, and pulmonary function test parameters. Clinic and laboratory parameters that provide a prediction of being a responder and super responder were evaluated.

Result: A total of 21 patients were included in the study. Their mean age was 50.7 ± 11.9 years, and four (19%) were males. The mean duration of asthma diagnosis was 17.5 ±13.7 years. 14 patients (66.7%) were atopic. 4 patients (19%) had nasal polyps and four patients (19%) had NERD. Before mepolizumab, 13 (61.9%) patients had received omalizumab. The duration of receiving mepolizumab treatment was 29.2 ± 9.9 months. A statistically significant decrease was observed in both the number and percentage of eosinophils at months six and 12 (p<0.01). There was a statistically significant increase in FEV1 values both as a percentage and in milliliters at month 12. There was an increase in both percentage and milliliters in FEF25-75 values, but this increase did not reach statistical significance. There was a decrease in service admissions, intensive care admissions, and emergency admissions due to asthma exacerbations. Out of 21 patients, 11 (52.4%) were classified as responders, while 10 (47.6%) were classified as super responders.

Conclusions: Although the number of patients in our study was limited, mepolizumab improved symptom scores in severe eosinophilic asthma, reduced the number of attacks, and improved pulmonary function test values.

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