支气管收缩
乙酰甲胆碱
吸入
医学
肺活量测定
哮喘
支气管扩张
麻醉
支气管扩张剂
内科学
呼吸道疾病
肺
作者
Chizu Habukawa,Kazuhito Murakami,Hiroyuki Mochizuki,Satoru Takami,Reiko Muramatsu,Hiromi Tadaki,Satomi Hagiwara,Takahisa Mizuno,Hirokazu Arakawa,Yukio Nagasaka
出处
期刊:Respirology
[Wiley]
日期:2010-03-29
卷期号:15 (3): 485-490
被引量:18
标识
DOI:10.1111/j.1440-1843.2010.01706.x
摘要
ABSTRACT A breath sound analyser was used to detect bronchoconstriction without wheezing during methacholine inhalation challenge in children. The highest frequency of inspiratory breath sounds increased significantly during bronchoconstriction and decreased after inhalation of a bronchodilator. The highest frequency of inspiratory breaths sounds was correlated with bronchial reactivity. Background and objective: It is difficult for clinicians to identify changes in breath sounds caused by bronchoconstriction when wheezing is not audible. A breath sound analyser can identify changes in the frequency of breath sounds caused by bronchoconstriction. The present study aimed to identify the changes in the frequency of breath sounds during bronchoconstriction and bronchodilatation using a breath sound analyser. Methods: Thirty‐six children (8.2 ± 3.7 years; males : females, 22 : 14) underwent spirometry, methacholine inhalation challenge and breath sound analysis. Methacholine inhalation challenge was performed and baseline respiratory resistance, minimum dose of methacholine (bronchial sensitivity) and speed of bronchoconstriction in response to methacholine (Sm: bronchial reactivity) were calculated. The highest frequency of inspiratory breath sounds (HFI), the highest frequency of expiratory breath sounds (HFE) and the percentage change in HFI and HFE were determined. The HFI and HFE were compared before methacholine inhalation (pre‐HFI and pre‐HFE), when respiratory resistance reached double the baseline value (max HFI and max HFE), and after bronchodilator inhalation (post‐HFI and post‐HFE). Results: Breath sounds increased during methacholine‐induced bronchoconstriction. Max HFI was significantly greater than pre‐HFI ( P < 0.001), and decreased to the basal level after bronchodilator inhalation. Post‐HFI was significantly lower than max HFI ( P < 0.001). HFI and HFE were also significantly changed ( P < 0.001). The percentage change in HFI showed a significant correlation with the speed of bronchoconstriction in response to methacholine ( P = 0.007). Conclusions: Methacholine‐induced bronchoconstriction significantly increased HFI, and the increase in HFI was correlated with bronchial reactivity.
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