Nelson Harold S
National Jewish Medical and Research Center, Denver, CO 80206, USA.
J Allergy Clin Immunol. 2006 Jan;117(1):3-16; quiz 17. doi: 10.1016/j.jaci.2005.10.013.
Short-acting beta(2)-agonists are effective in relieving acute symptoms of asthma and in the short-term prevention of symptoms from stimuli, such as exercise. They are ineffective when used on a regular schedule to improve asthma control. Long-acting beta(2)-agonists, on the other hand, provide sustained bronchodilation and improve asthma control. Regular use of long-acting beta(2)-agonists is not associated with significant tolerance to their bronchodilator action, impairment in the response to albuterol, decreased baseline pulmonary function, increased response to methacholine, or increased risk of adverse cardiac events. Case-control studies do not suggest an increased risk for death or intensive care unit admissions with use of long-acting beta(2)-agonists. In prospective studies in which there has been an increase in asthma deaths or serious asthma exacerbations, this increased risk has not been observed in subjects using inhaled corticosteroids. Where increased deaths have occurred in relation to either short- or long-acting beta(2)-agonists, the events have not occurred equally throughout the exposed population. This suggests that these outcomes were not a direct toxic effect of the drugs and increases the possibility that they resulted from an interaction between relief of symptoms by beta(2)-agonists and delay in seeking medical care.
短效β₂受体激动剂可有效缓解哮喘急性症状,并在短期内预防运动等刺激引发的症状。但定期使用时,它们对改善哮喘控制无效。另一方面,长效β₂受体激动剂可提供持续的支气管舒张作用,改善哮喘控制。定期使用长效β₂受体激动剂不会对其支气管舒张作用产生明显耐受,不会影响对沙丁胺醇的反应,不会降低基线肺功能,不会增加对乙酰甲胆碱的反应,也不会增加不良心脏事件的风险。病例对照研究未提示使用长效β₂受体激动剂会增加死亡风险或入住重症监护病房的风险。在前瞻性研究中,尽管哮喘死亡或严重哮喘加重有所增加,但在使用吸入性糖皮质激素的受试者中未观察到这种风险增加。在与短效或长效β₂受体激动剂相关的死亡增加的情况中,并非在所有暴露人群中均同等发生此类事件。这表明这些结果并非药物的直接毒性作用,增加了它们是由β₂受体激动剂缓解症状与延迟就医之间的相互作用导致的可能性。