Wahedna I, Wong C S, Wisniewski A F, Pavord I D, Tattersfield A E
Respiratory Medicine Unit, City Hospital, Nottingham, United Kingdom.
Am Rev Respir Dis. 1993 Sep;148(3):707-12. doi: 10.1164/ajrccm/148.3.707.
It has been suggested that regular treatment with high doses of beta 2-agonists might result in poorer control of asthma and increased bronchial responsiveness. We have examined change in FEV1 (delta FEV1), bronchial reactivity, peak expiratory flow (PEF), and symptoms during and after 3 wk of regular treatment with a relatively low dose of albuterol and broxaterol, a new beta 2-agonist. Eleven subjects 18 to 50 yr of age with mild asthma inhaled albuterol (200 micrograms), broxaterol (400 micrograms), or placebo three times a day for 3 wk with a 2- to 4-wk run-in/washout period between treatments. Ipratropium bromide was allowed for symptomatic relief. The PD20 (dose of histamine causing a 20% fall in FEV1) was measured before and 11, 35, and 59 h after cessation of treatment and a bronchodilator dose-response study before and 83 h after cessation of treatment. Change from baseline after albuterol and broxaterol are compared with change after placebo. Diurnal change in PEF (amplitude % mean) increased during treatment with albuterol by 6.5% (95% CI, 1.7-12.3; p < 0.02) mainly because of a fall in morning PEF. Cessation of treatment with both beta 2-agonists was associated with a fall in FEV1 and PD20 compared with placebo.(ABSTRACT TRUNCATED AT 250 WORDS)
有人提出,长期大剂量使用β2受体激动剂可能导致哮喘控制不佳,并增加支气管反应性。我们研究了在使用相对低剂量的沙丁胺醇和新型β2受体激动剂溴沙特罗进行3周常规治疗期间及之后,第一秒用力呼气容积(ΔFEV1)、支气管反应性、呼气峰值流速(PEF)和症状的变化。11名年龄在18至50岁之间的轻度哮喘患者,每天吸入沙丁胺醇(200微克)、溴沙特罗(400微克)或安慰剂3次,共3周,治疗之间有2至4周的导入/洗脱期。可使用异丙托溴铵缓解症状。在治疗停止前以及停止后11、35和59小时测量使FEV1下降20%的组胺剂量(PD20),并在治疗停止前和停止后83小时进行支气管扩张剂剂量反应研究。将沙丁胺醇和溴沙特罗治疗后相对于基线的变化与安慰剂治疗后的变化进行比较。沙丁胺醇治疗期间,PEF的日变化(平均幅度百分比)增加了6.5%(95%可信区间,1.7 - 12.3;p < 0.02),主要是因为早晨PEF下降。与安慰剂相比,两种β2受体激动剂治疗停止均与FEV1和PD20下降有关。(摘要截断于250字)