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哮喘治疗:吸入型β-受体激动剂。

Asthma treatment: inhaled beta-agonists.

作者信息

Sears M R

机构信息

St Joseph's Hospital and McMaster University, Hamilton, Canada.

出版信息

Can Respir J. 1998 Jul-Aug;5 Suppl A:54A-9A.

PMID:9753519
Abstract

Short acting beta-agonists provide symptom relief with a rapid onset of bronchodilation, and protect against exercise-induced asthma and the early asthmatic response to allergen. They remain the most commonly prescribed form of therapy in asthma. However, regular use as maintenance therapy for chronic asthma is no longer recommended. Frequent use increases airway hyper-responsiveness to allergen and nonspecific challenge, and in some studies has been associated with decreased control of asthma. Excessive use of short acting beta-agonists is associated with a higher risk of fatal or near-fatal asthma, with a dose-response relationship. High doses of short acting beta-agonist in combination with oxygen and corticosteroid therapy remains the most appropriate treatment for acute severe asthma in the emergency room situation. The long acting beta-agonists salmeterol and formoterol provide more prolonged bronchodilation, greater reduction of symptoms, increased lung function and reduced need for short acting beta-agonists. Although there is no significant tachyphylaxis to the bronchodilator effects, bronchoprotective effects diminish with time, even when patients are also treated with corticosteroids. The concern that long acting beta-agonists may mask inflammation and, hence, increase the risk of exacerbations was addressed in a recent four-arm parallel group study. The exacerbation rate was highest in those receiving low dose corticosteroid and was progressively lower in those with low dose corticosteroid plus formoterol, moderate dose budesonide alone and moderate dose budesonide plus formoterol. Both budesonide and formoterol independently decreased the risk of exacerbations. Short acting beta-agonists are recommended for use only as needed, which should be relatively infrequent. Long acting beta-agonists are indicated in individuals whose asthma is not well controlled on moderate doses of inhaled corticosteroid, and are complementary to, not a replacement for, inhaled corticosteroid therapy.

摘要

短效β受体激动剂能迅速缓解症状,使支气管迅速扩张,预防运动诱发的哮喘以及对过敏原的早期哮喘反应。它们仍是哮喘治疗中最常用的处方药物形式。然而,不再推荐将其常规用作慢性哮喘的维持治疗。频繁使用会增加气道对过敏原和非特异性刺激的高反应性,并且在一些研究中与哮喘控制不佳有关。过度使用短效β受体激动剂与致命或近乎致命哮喘的较高风险相关,存在剂量反应关系。在急诊情况下,高剂量短效β受体激动剂联合氧气和皮质类固醇疗法仍是急性重症哮喘最适当的治疗方法。长效β受体激动剂沙美特罗和福莫特罗能提供更持久的支气管扩张作用,更有效地减轻症状,改善肺功能,并减少对短效β受体激动剂的需求。尽管对支气管扩张作用不存在明显的快速耐受性,但支气管保护作用会随时间减弱,即使患者同时接受皮质类固醇治疗也是如此。近期一项四组平行分组研究探讨了长效β受体激动剂可能掩盖炎症从而增加病情加重风险的问题。接受低剂量皮质类固醇治疗的患者病情加重率最高,而接受低剂量皮质类固醇加福莫特罗、中等剂量布地奈德单药治疗以及中等剂量布地奈德加福莫特罗治疗的患者病情加重率逐渐降低。布地奈德和福莫特罗均能独立降低病情加重的风险。推荐仅在需要时使用短效β受体激动剂,这种情况应相对较少。长效β受体激动剂适用于吸入中等剂量皮质类固醇后哮喘仍控制不佳的患者,是吸入皮质类固醇疗法的补充,而非替代疗法。

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