Arnold Donald H, Gebretsadik Tebeb, Abramo Thomas J, Hartert Tina V
Department of Pediatrics, Division of Emergency Medicine, Vanderbilt University School of Medicine, Nashville, TN, USA.
J Asthma. 2012 Feb;49(1):29-35. doi: 10.3109/02770903.2011.637599. Epub 2011 Dec 1.
There is limited information on performance rates for tests of lung function and inflammation in pediatric patients with acute asthma exacerbations. We sought to examine how frequently pediatric patients with acute asthma exacerbations could perform noninvasive lung function and exhaled nitric oxide (FE(NO)) testing and participant characteristics associated with successful performance.
We studied a prospective convenience sample aged 5-17 years with acute asthma exacerbations in a pediatric emergency department. Participants attempted spirometry for percent predicted forced expiratory volume in 1 second (%FEV(1)), airway resistance (Rint), and FE(NO) testing before treatment. We examined overall performance rates and the associations of age, gender, race, and baseline acute asthma severity score with successful test performance.
Among 573 participants, age was (median [interquartile range]) 8.8 [6.8, 11.5] years, 60% were male, 57% were African-American, and 58% had Medicaid insurance. Tests were performed successfully by the following [n (%)]: full American Thoracic Society-European Respiratory Society criteria spirometry, 331 (58%); Rint, 561 (98%); and FE(NO), 354 (70% of 505 attempted test). Sixty percent with mild-moderate exacerbations performed spirometry compared to 17% with severe exacerbations (p = .0001). Participants aged 8-12 years (67%) were more likely to perform spirometry than those aged 5-7 years (48%) (OR = 2.23, 95% CI: 1.45-3.11) or 13-17 years (58%) (OR = 1.61, 95% CI: 1.00-2.59).
There is clinically important variability in performance of these tests during acute asthma exacerbations. The proportion of patients with severe exacerbations able to perform spirometry (17%) limits its utility. Almost all children with acute asthma can perform Rint testing, and further development and validation of this technology is warranted.
关于急性哮喘加重期儿科患者肺功能和炎症检测的执行率信息有限。我们试图研究急性哮喘加重期儿科患者进行无创肺功能和呼出一氧化氮(FE(NO))检测的频率以及与检测成功相关的参与者特征。
我们在儿科急诊科对5至17岁急性哮喘加重期的前瞻性便利样本进行了研究。参与者在治疗前尝试进行肺活量测定,以测定1秒用力呼气容积占预计值的百分比(%FEV(1))、气道阻力(Rint)和FE(NO)检测。我们检查了总体执行率以及年龄、性别、种族和基线急性哮喘严重程度评分与检测成功之间的关联。
在573名参与者中,年龄(中位数[四分位间距])为8.8[6.8,11.5]岁,60%为男性,57%为非裔美国人,58%有医疗补助保险。以下检测成功进行的情况[n(%)]为:符合美国胸科学会-欧洲呼吸学会完整标准的肺活量测定,331例(58%);Rint,561例(98%);FE(NO),354例(占50五项尝试检测的70%)。轻度至中度加重期的患者中有60%进行了肺活量测定,而重度加重期的患者中这一比例为17%(p = 0.0001)。8至12岁的参与者(67%)比5至7岁的参与者(48%)(OR = 2.23,95%CI:1.45 - 3.11)或13至17岁的参与者(58%)(OR = 1.61,95%CI:1.00 - 2.59)更有可能进行肺活量测定。
在急性哮喘加重期,这些检测的执行情况存在临床上重要的变异性。重度加重期能够进行肺活量测定的患者比例(17%)限制了其效用。几乎所有急性哮喘儿童都能进行Rint检测,因此有必要对该技术进行进一步开发和验证。