原发性睫状肌运动障碍患者支气管阻塞的可逆性,为吸入疗法的矫正提供依据

Y. Mizernitskiy, A. Novak, T. N. Pronkina, E. S. Ryngachenko, L. V. Sokolova, S. Diakova, I. E. Zorina, P. A. Shatokha, A. R. Shudueva
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When comparing the FEV1 indicator in children with the presence of allergic burden (n=63) and in the absence of it (n=37), it was found that in patients with markers of atopy, obstructive changes identified during spirometry were 14.2% more common ( p≤0.05). Reversibility of bronchial obstruction was recorded in 24% (n=24), of which 87.5% (n=21) of patients had markers of atopy (p≤0.05). In children with concomitant allergic burden and a decrease in FEV1, reversibility of obstruction was detected in 48.4% (n=15) of cases (p≤0.05). It was revealed that in patients with the presence of atopy markers and a decrease in FEV1≤80%, reversibility of obstruction occurs 42.8% more often compared to the group of patients with a normal level of FEV1 (p≤0.05).Conclusions. The vast majority of patients with primary ciliary dyskinesia (n=63) have markers of atopy, mainly due to an isolated increase in total IgE in the blood serum (p≤0.05). 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引用次数: 0

摘要

目的:评估原发性睫状肌运动障碍患者支气管阻塞的可逆性。评估原发性睫状肌运动障碍患者支气管阻塞的可逆性,分为伴有和不伴有过敏性炎症两组,目的是区别对待吸入疗法和支气管扩张剂处方的有效性。对吸入支气管扩张剂前后的 FEV1 结果进行回顾性分析,并研究阻塞的可逆性与是否存在过敏性标志物的关系。在 100 名患者中,63%(n=63)有特异性标记物;37%(n=37)没有这些标记物(p≤0.05)。在比较有过敏性负担(63 人)和无过敏性负担(37 人)儿童的 FEV1 指标时发现,在有过敏性标志物的患者中,肺活量测定中发现的阻塞性变化比无过敏性标志物的患者多 14.2% (p≤0.05)。支气管阻塞的可逆性记录为 24%(n=24),其中 87.5%(n=21)的患者有过敏标记物(p≤0.05)。在同时伴有过敏负荷和 FEV1 下降的儿童中,48.4%(15 人)的病例检测到阻塞的可逆性(p≤0.05)。研究显示,与 FEV1 水平正常的患者组相比,存在特应性标记物且 FEV1 下降≤80%的患者中,阻塞可逆性发生率为 42.8%(p≤0.05)。绝大多数原发性睫状肌运动障碍患者(63 人)都有特应性指标,主要是由于血清中总 IgE 的单独增加(p≤0.05)。与无过敏症的儿童组相比,有过敏症的儿童中发现 FEV1 下降≤80%的比例要高出 14.2%(p≤0.05)。在绝大多数过敏表型患者中,使用支气管扩张剂进行测试后都能观察到阻塞的可逆性。因此,建议所有患有原发性睫状肌运动障碍和存在特应性标记物的患者接受支气管扩张剂测试,如果发现阻塞可逆,建议在治疗中添加支气管扩张剂药物。
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Reversibility of bronchial obstruction in patients with primary ciliary dyskinesia to justify correction of inhalation therapy
Purpose. To assess the reversibility of bronchial obstruction in patients with primary ciliary dyskinesia in groups with and without concomitant allergic inflammation, with the aim of a differentiated approach to inhalation therapy and the validity of prescribing bronchodilators.Material and methods. Retrospective analysis of the results of FEV1 before and after inhalation of a bronchodilator and study of the dependence of the reversibility of obstruction on the presence of atopy markers.Results. Of 100 patients, 63% (n=63) had atopy markers; 37% (n=37) did not have these markers (p≤0.05). When comparing the FEV1 indicator in children with the presence of allergic burden (n=63) and in the absence of it (n=37), it was found that in patients with markers of atopy, obstructive changes identified during spirometry were 14.2% more common ( p≤0.05). Reversibility of bronchial obstruction was recorded in 24% (n=24), of which 87.5% (n=21) of patients had markers of atopy (p≤0.05). In children with concomitant allergic burden and a decrease in FEV1, reversibility of obstruction was detected in 48.4% (n=15) of cases (p≤0.05). It was revealed that in patients with the presence of atopy markers and a decrease in FEV1≤80%, reversibility of obstruction occurs 42.8% more often compared to the group of patients with a normal level of FEV1 (p≤0.05).Conclusions. The vast majority of patients with primary ciliary dyskinesia (n=63) have markers of atopy, mainly due to an isolated increase in total IgE in the blood serum (p≤0.05). A decrease in FEV1≤80% in children with allergies was detected 14.2% more often compared to the group of children without it (p≤0.05). In the vast majority of patients with an allergic phenotype, reversibility of obstruction was observed after a test with a bronchodilator. Thus, all patients with primary ciliary dyskinesia and the presence of atopy markers are recommended to undergo a test with a bronchodilator, and if reversibility of obstruction is detected, it is advisable to add a bronchodilator drug to therapy.
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