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雾化器与储雾罐装置给药的支气管扩张剂对急性喘息婴儿的疗效比较

Efficacy of bronchodilators administered by nebulizers versus spacer devices in infants with acute wheezing.

作者信息

Closa R M, Ceballos J M, Gómez-Papí A, Galiana A S, Gutiérrez C, Martí-Henneber C

机构信息

Hospital Universitario de Tarragona Joan XXIII, Universidad Rovira i Virgili, Spain.

出版信息

Pediatr Pulmonol. 1998 Nov;26(5):344-8. doi: 10.1002/(sici)1099-0496(199811)26:5<344::aid-ppul7>3.0.co;2-f.

Abstract

The aim of this study was to compare the response of infants with acute wheezing to treatments with inhaled terbutaline when administered by nebulizer or by metered-dose inhaler and spacer device (MDI-spacer). Thirty-four infants between the ages of 1 and 24 months who were seen in our emergency department for acute wheezing were studied in a double-blind, randomized trial. The participants received two treatments of terbutaline at 20-min intervals, either by a nebulizer (2 mg/dose in 2.8 mL of 0.9% saline solution) or by an MDI-spacer device (0.5 mg/dose). The outcome measure was a clinical score, based on respiratory rate, degree of wheezing, retractions, degree of cyanosis, color, and pulse oximetry data measured before treatment, 20 min after the first treatment, and again 20 min after the second treatment. There was no difference in the rate of improvement in the clinical score between infants who received terbutaline by nebulizer and those who received it by MDI-spacer. We conclude that MDI-spacers and nebulizers are equally effective means of delivering beta-2 agonists to infants and small children with acute wheezing.

摘要

本研究的目的是比较雾化吸入特布他林与使用定量气雾剂和储物罐装置(MDI-储物罐)给急性喘息婴儿治疗时的反应。在一项双盲随机试验中,对在我们急诊科就诊的34名1至24个月大的急性喘息婴儿进行了研究。参与者每隔20分钟接受两次特布他林治疗,一次通过雾化器(2毫克/剂量,溶于2.8毫升0.9%盐溶液中),另一次通过MDI-储物罐装置(0.5毫克/剂量)。观察指标是一个临床评分,基于治疗前、首次治疗后20分钟以及第二次治疗后20分钟测量的呼吸频率、喘息程度、凹陷、发绀程度、肤色和脉搏血氧饱和度数据。通过雾化器接受特布他林治疗的婴儿与通过MDI-储物罐接受治疗的婴儿在临床评分改善率上没有差异。我们得出结论,MDI-储物罐和雾化器是向患有急性喘息的婴幼儿输送β-2激动剂的同样有效的方式。

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