首页> 外文期刊>Respiration: International Review of Thoracic Diseases >Tidal volume forced expiration in asthmatic infants: reproducibility and reversibility tests.
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Tidal volume forced expiration in asthmatic infants: reproducibility and reversibility tests.

机译:哮喘婴儿的潮气量强迫到期:可重复性和可逆性测试。

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Background: The tidal volume forced expiration technique used in infants is considered as the first practical noninvasive method of assessing airway physiology in infants. However, its role has been discussed mainly due to the high variability of the derived parameters. Objectives: The aim of the study was to assess the reproducibility of a complete measurement with the tidal volume forced expiration technique in infants as measured by the maximal flow at FRC (Vdot;(max)FRC). A second aim was to evaluate the bronchial reversibility test in infant asthma. Methods: Thirty infants with asthma were investigated with the tidal volume forced expiration technique twice with 10 min in between and a third time 10 min after inhalation of terbutalin 0.5 mg. Results: The mean Vdot;(max)FRC in the first investigation was 285 ml.s(-1) (coefficient of variation 57%), unchanged in the second investigation and significantly lower than the mean predicted value of 404 ml.s(-1). The relative difference between the 2 investigations of Vdot;(max)FRC was mean 10.5% (SD 8.4) of the absolute Vdot;(max)FRC value and independent of the size of this Vdot;(max)FRC value. The 95% confidence interval for individual changes would then be up to 27% (mean + 2 SD). The infants with the lowest Vdot;(max)FRC percent predicted decreased further in Vdot;(max)FRC after inhalation of the bronchodilator (p < 0.05). Conclusions: The tidal volume forced expiration technique was able to measure flow at late expiration with the same reproducibility as seen with spirometry in adults, even if the flow was low. We found the technique acceptable for clinical practice and research, but the results from reversibility tests are difficult to interpret. A significant change of Vdot;(max)FRC would, however, be 27% or more. Copyright 2002 S. Karger AG, Basel
机译:背景:用于婴儿的潮气量强制呼气技术被认为是评估婴儿气道生理的第一种实用的非侵入性方法。然而,由于导出参数的高度可变性,已经对其作用进行了讨论。目的:该研究的目的是评估采用潮气量强制呼气技术对婴儿进行完整测量的可重复性,该测量通过FRC处的最大流量(Vdot(max)FRC)进行测量。第二个目的是评估婴儿哮喘中的支气管可逆性测试。方法:采用潮气量强制呼气技术,对30例哮喘患儿进行了两次调查,两次间吸气时间分别为10分钟和吸入0.5 mg特布他林后10分钟的第三次。结果:第一次研究的平均Vdot(max)FRC为285 ml.s(-1)(变异系数为57%),在第二次研究中未发生变化,并且显着低于平均预测值404 ml.s(-1)。 -1)。 V点(最大)FRC的两次研究之间的相对差是绝对V点(最大)FRC值的平均值的10.5%(SD 8.4),并且与该V点(最大)FRC值的大小无关。单个更改的95%置信区间将达到27%(平均值+ 2 SD)。预计最低V点(最大)FRC百分比的婴儿在吸入支气管扩张剂后,V点(最大)FRC进一步降低(p <0.05)。结论:潮气量强制呼气技术即使在低通气量时,也能以与肺活量测定法相同的可重复性测量晚期通气量。我们发现该技术可用于临床实践和研究,但是可逆性测试的结果难以解释。但是,V max(最大)FRC的显着变化将是27%或更大。版权所有2002 S. Karger AG,巴塞尔

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