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Utility of portable spirometry in a pediatric emergency department in children with acute exacerbation of asthma.

机译:便携式肺活量测定仪在小儿急症哮喘儿童急诊中的应用。

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OBJECTIVES: The primary purpose of this study was to determine if portable spirometers can be successfully used in an emergency department (ED) in children with an acute exacerbation of asthma. The secondary purpose of this study was to determine if a validated clinical asthma score (CAS) correlates with the spirometry results in children with an acute exacerbation of asthma. METHODS: Children between the ages of 6 and 17 years who presented to an urban free-standing children's hospital ED with an acute exacerbation of asthma were enrolled in our study. On arrival, the CAS was recorded and then portable spirometry was performed. Attempts were continued until acceptable and reproducible flow loop measurements were obtained or until the patient was unable to perform further attempts. Outcomes included success at spirometry and correlation of spirometry with the CAS. RESULTS: A total of 101 patients were enrolled in this study. Of those patients, only 35 (35%) were able to successfully perform portable spirometry. Successful spirometry attempts were associated with older age (10.4 vs. 8.9, p = .01), lower respiratory rates (24.8 vs. 30.2, p = .001), lower heart rates (110 vs. 124, p = .004), and lower CASs (8.4 vs. 9.7, p = .001). Increasing asthma severity correlated with a decreased likelihood of successfully obtaining a useful forced expiratory volume in 1 second (FEV(1)) measurement (p = .013). Compared with cases of mild asthma, a patient with moderate asthma is 33% less likely to be able to perform spirometry, and a patient with severe asthma 93% less likely to perform spirometry. The CAS correlated poorly with the more objective measure of FEV(1)% predicted in those with mild asthma. CONCLUSION: Many children are incapable of using portable spirometry for the evaluation of acute exacerbations of asthma in the ED. The clinical asthma scoring system demonstrated poor correlation with portable spirometry measurements in terms of severity classification.
机译:目的:本研究的主要目的是确定便携式肺活量计是否可以成功用于哮喘急性加重患儿的急诊科(ED)。这项研究的第二个目的是确定在患有哮喘急性发作的儿童中,经过验证的临床哮喘评分(CAS)是否与肺活量测定结果相关。方法:本研究纳入了6至17岁的儿童,这些儿童曾就诊于城市独立儿童医院ED,患有哮喘急性发作。到达后,记录CAS,然后进行便携式肺活量测定。继续尝试直到获得可接受的和可重复的流量环测量结果,或者直到患者无法进行进一步尝试为止。结果包括肺活量测定的成功以及肺活量测定与CAS的相关性。结果:总共101例患者参加了这项研究。在这些患者中,只有35(35%)人能够成功进行便携式肺活量测定。成功的肺活量测定尝试与年龄较大(10.4 vs. 8.9,p = .01),较低的呼吸频率(24.8 vs. 30.2,p = .001),较低的心率(110 vs 124,p = .004)相关,以及较低的CAS(8.4与9.7,P = 0.001)。哮喘严重程度的增加与1秒内成功获得有用的强制呼气量(FEV(1))的可能性降低有关(p = .013)。与轻度哮喘患者相比,中度哮喘患者进行肺活量测定的可能性要低33%,重度哮喘患者进行肺活量测定的可能性要低93%。 CAS与较轻度哮喘患者中预测的FEV(1)%的更客观测量值相关性较差。结论:许多儿童无法使用便携式肺活量测定法来评估急诊室的哮喘急性发作。临床哮喘评分系统在严重性分类方面与便携式肺活量测定法的相关性较差。

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