de Benedictis F M, Tuteri G, Pazzelli P, Niccoli A, Mezzetti D, Vaccaro R
Pediatric Dept, University of Perugia, Italy.
Eur Respir J. 1996 Oct;9(10):2099-103. doi: 10.1183/09031936.96.09102099.
Since the optimal dose of salmeterol in asthmatic children has not yet been clearly defined, we compared the efficacy and duration of the protective effect of two doses of salmeterol (25 and 50 micrograms) against exercise-induced bronchoconstriction. Twelve children (aged 7-14 yrs) with asthma were studied in a double-blind, cross-over, placebo-controlled design. On three separate days, exercise tests were performed 1 h and 12 h after administration of the drug. Pulmonary function measurements were performed before drug inhalation, before every exercise test and 1, 5, 10, 15 and 30 min after the end of exercise. The response was expressed as maximal decrease in forced expiratory volume in one second (FEV1). Both doses of salmeterol provided significant bronchodilation for up to 12 h, with no difference between them. Maximal exercise-induced decrease in FEV1 (% fall) 1 h after pretreatment was (mean +/- SD) 35 +/- 16, 10 +/- 10 and 4 +/- 3% for placebo, 25 and 50 micrograms salmeterol, respectively. At 12 h after pretreatment these values were 31 +/- 14, 19 +/- 12 and 15 +/- 13%, respectively. Individual protection against exercise-induced bronchoconstriction at 1 and 12 h did not vary between the dosages (p < 0.05), even though the protection obtained by 25 micrograms at 12 h was no longer significant versus placebo. We conclude that 25 micrograms of inhaled salmeterol provides equally effective long-lasting bronchodilation and acute protection against exercise-induced bronchoconstriction as 50 micrograms, and may be a suitable dose for most asthmatic children.
由于哮喘儿童中沙美特罗的最佳剂量尚未明确界定,我们比较了两剂量沙美特罗(25微克和50微克)对运动诱发性支气管收缩的保护作用的疗效和持续时间。采用双盲、交叉、安慰剂对照设计对12名患有哮喘的儿童(7 - 14岁)进行了研究。在三个不同的日子里,于给药后1小时和12小时进行运动试验。在药物吸入前、每次运动试验前以及运动结束后1、5、10、15和30分钟进行肺功能测量。反应以一秒用力呼气容积(FEV1)的最大下降值表示。两剂量的沙美特罗均提供长达12小时的显著支气管扩张作用,两者之间无差异。预处理后1小时,安慰剂、25微克和50微克沙美特罗组运动诱发的FEV1最大下降值(%下降)分别为(均值±标准差)35±16、10±10和4±3%。预处理后12小时,这些值分别为31±14、19±12和15±13%。尽管25微克剂量在12小时时获得的保护作用与安慰剂相比不再显著,但各剂量在1小时和12小时对运动诱发性支气管收缩的个体保护作用并无差异(p<0.05)。我们得出结论,25微克吸入用沙美特罗与50微克一样,能提供同样有效的长效支气管扩张作用以及对运动诱发性支气管收缩的急性保护作用,可能是大多数哮喘儿童的合适剂量。