Backer V, Bach-Mortensen N, Becker U, Brink L, Howitz P, Hansen K K, Jensen D W, Laursen E M
Dept. of Medicine B, Laboratory of Respiratory Physiology, State University Hospital, Copenhagen, Denmark.
Allergy. 1989 Apr;44(3):209-13. doi: 10.1111/j.1398-9995.1989.tb02264.x.
The ability of the new generation H1-receptor antagonist, astemizole, to prevent histamine-induced airway obstruction and exercise-induced asthma (EIA) was studied in 20 children with asthma. The study was a randomised clinically controlled trial of oral astemizole versus placebo in a cross-over study. In each of the two treatment periods the children were tested at days 0, 6, 15 and 22 of therapy. The two treatment periods were separated by a washout period of 50 days, and at each visit a bronchial challenge with increasing concentrations of histamine followed by an exercise test was performed, and peak flow and asthmatic symptom score were recorded daily. The children tolerated significantly higher mean concentrations of histamine when treated with astemizole compared with placebo (P less than 0.001). Astemizole postponed the response to exercise, but no change in the maximal response was found. No differences between the treatment periods were found regarding frequency of asthmatic symptoms or the daily recording of peak flow.
在20名哮喘患儿中研究了新一代H1受体拮抗剂阿司咪唑预防组胺诱发的气道阻塞和运动诱发性哮喘(EIA)的能力。该研究是一项口服阿司咪唑与安慰剂的随机临床对照交叉试验。在两个治疗期的每一期中,在治疗的第0、6、15和22天对患儿进行测试。两个治疗期之间有50天的洗脱期,每次就诊时先进行递增浓度组胺的支气管激发试验,随后进行运动试验,并每日记录峰值流速和哮喘症状评分。与安慰剂相比,患儿接受阿司咪唑治疗时能耐受显著更高的组胺平均浓度(P小于0.001)。阿司咪唑延迟了对运动的反应,但未发现最大反应有变化。在哮喘症状频率或峰值流速的每日记录方面,各治疗期之间未发现差异。