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学龄前儿童哮喘与非哮喘患者的血压计和肺量计支气管扩张剂反应。

Oscillometric and spirometric bronchodilator response in preschool children with and without asthma.

机构信息

Department of Pediatrics, CHA University School of Medicine, Seongnam, Republic of Korea.

出版信息

Can Respir J. 2012 Jul-Aug;19(4):273-7. doi: 10.1155/2012/560323.

Abstract

BACKGROUND

Bronchodilator responses (BDR) are routinely used in the diagnosis and management of asthma; however, their acceptability and repeatability have not been evaluated using quality control criteria for preschool children.

OBJECTIVES

To compare conventional spirometry with an impulse oscillometry system (IOS) in healthy and asthmatic preschool children.

METHODS

Data from 30 asthmatic children and 29 controls (two to six years of age) who underwent IOS and spirometry before and after salbutamol administration were analyzed.

RESULTS

Stable asthmatic subjects significantly differed versus controls in their spirometry-assessed BDR (forced expiratory volume in 1 s [FEV1], forced vital capacity and forced expiratory flow at 25% to 75% of forced vital capacity) as well as their IOS-assessed BDR (respiratory resistance at 5 Hz [Rrs5], respiratory reactance at 5 Hz and area under the reactance curve). However, comparisons based on the area under the ROC curve for ΔFEV1 %initial versus ΔRrs5 % initial were 0.82 (95% CI 0.71 to 0.93) and 0.75 (95% CI 0.62 to 0.87), respectively. Moreover, the sensitivity and specificity for ΔFEV1 >=9% were 0.53 and 0.93, respectively. Importantly, sensitivity increased to 0.63 when either ΔFEV1 >=9% or ΔRrs5 >=29% was considered as an additional criterion for the diagnosis of asthma.

CONCLUSION

The accuracy of asthma diagnosis in preschool children may be increased by combining spirometry with IOS when measuring BDR.

摘要

背景

支气管扩张剂反应(BDR)通常用于哮喘的诊断和管理;然而,它们的可接受性和可重复性尚未使用质量控制标准来评估学龄前儿童。

目的

比较常规肺量计和脉冲振荡系统(IOS)在健康和哮喘学龄前儿童中的应用。

方法

对 30 名哮喘儿童和 29 名对照者(2 至 6 岁)进行 IOS 和肺量计检查,这些儿童在沙丁胺醇给药前后均进行了检查。

结果

稳定的哮喘儿童在 IOS 评估的 BDR(1 秒用力呼气量 [FEV1]、用力肺活量和用力呼气流量在 25%至 75%用力肺活量时)和肺量计评估的 BDR(5 Hz 时的呼吸阻力 [Rrs5]、5 Hz 时的呼吸电抗和电抗曲线下面积)方面与对照组明显不同。然而,基于初始 ΔFEV1%与初始 ΔRrs5%的 ROC 曲线下面积的比较,分别为 0.82(95%可信区间为 0.71 至 0.93)和 0.75(95%可信区间为 0.62 至 0.87)。此外,ΔFEV1>=9%的敏感性和特异性分别为 0.53 和 0.93。重要的是,当将 ΔFEV1>=9%或 ΔRrs5>=29%作为哮喘诊断的附加标准时,敏感性增加至 0.63。

结论

当通过测量 BDR 将肺量计与 IOS 结合使用时,可提高学龄前儿童哮喘诊断的准确性。

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