通过脉冲振荡测量系统和肺活量测定法评估患有囊性纤维化的儿童和青少年的支气管扩张反应。

IF 2
Tayná Castilho, José Dirceu Ribeiro, Renata Maba Gonçalves Wamosy, Juliana Cardoso, Gabriela Castilhos Ducati, Camila Isabel Santos Schivinski
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引用次数: 0

摘要

目的:研究支气管扩张剂对囊性纤维化儿童和青少年呼吸力学和肺功能的影响:研究支气管扩张剂对囊性纤维化儿童和青少年呼吸力学和肺功能的影响:横断面研究,对象为临床病情稳定的 6 至 15 岁囊性纤维化儿童和青少年。参与者在吸入支气管扩张剂之前和之后 15 分钟接受脉冲振荡测量和肺活量评估。采用Kolmogorov-Smirnov检验验证样本分布,采用学生t检验和Wilcoxon检验比较吸入支气管扩张剂前后的数据:研究共纳入54人,平均年龄为(9.7±2.8)岁。分析表明,吸入支气管扩张剂后,脉冲振荡计和肺活量参数有明显改善。然而,根据美国胸科学会(ATS)和欧洲呼吸学会(ERS)的建议(2020 年和 2021 年),这种改善不足以将其归类为支气管扩张剂反应:使用支气管扩张剂药物可改善囊性纤维化儿童和青少年的呼吸力学和肺功能参数;然而,根据美国胸科学会(ATS)/欧洲呼吸学会(ERS)的建议,大多数患者并未表现出支气管扩张剂反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bronchodilator response assessment through impulse oscillometry system and spirometry in children and adolescents with cystic fibrosis.

Bronchodilator response assessment through impulse oscillometry system and spirometry in children and adolescents with cystic fibrosis.

Bronchodilator response assessment through impulse oscillometry system and spirometry in children and adolescents with cystic fibrosis.

Objective: To investigate the effect of bronchodilator on the respiratory mechanics and pulmonary function of children and adolescents with cystic fibrosis.

Methods: Cross-sectional study on clinically stable children and adolescents with cystic fibrosis aged from six to 15 years. Participants underwent impulse oscillometry and spirometry evaluations before and 15 minutes after bronchodilator inhalation. The Kolmogorov-Smirnov test was applied to verify the sample distribution, and the Student's t-test and Wilcoxon test were used to compare the data before and after bronchodilator inhalation.

Results: The study included 54 individuals with a mean age of 9.7±2.8 years. The analysis showed a statistically significant improvement in impulse oscillometry and spirometry parameters after bronchodilator inhalation. However, according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) recommendations (2020 and 2021), this improvement was not sufficient to classify it as a bronchodilator response.

Conclusions: The use of bronchodilator medication improved respiratory mechanics and pulmonary function parameters of children and adolescents with cystic fibrosis; however, most patients did not show bronchodilator response according to ATS/ERS recommendations.

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