Albertson Timothy E, Sutter Mark E, Chan Andrew L
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, School of Medicine, University of California, Davis, PSSB 3400, 4150 V Street, Sacramento, CA, 95817, USA,
Clin Rev Allergy Immunol. 2015 Feb;48(1):114-25. doi: 10.1007/s12016-014-8448-5.
Patients presenting to the emergency department (ED) or clinic with acute exacerbation of asthma (AEA) can be very challenging varying in both severity and response to therapy. High-dose, frequent or continuous nebulized short-acting beta2 agonist (SABA) therapy that can be combined with a short-acting muscarinic antagonist (SAMA) is the backbone of treatment. When patients do not rapidly clinically respond to SABA/SAMA inhalation, the early use of oral or parenteral corticosteroids should be considered and has been shown to impact the immediate need for ICU admission or even the need for hospital admission. Adjunctive therapies such as the use of intravenous magnesium and helium/oxygen combination gas for inhalation and for driving a nebulizer to deliver a SABA and or SAMA should be considered and are best used early in the treatment plan if they are likely to impact the patients' clinical course. The use of other agents such as theophylline, leukotriene modifiers, inhaled corticosteroids, long-acting beta2 agonist, and long-acting muscarinic antagonist currently does not play a major role in the immediate treatment of AEA in the clinic or the ED but is an important therapeutic option for physicians to be aware of and to consider initiating at the time of discharge from clinic, hospital, or ED to reduce later clinical worsening and readmission to the ED and hospital. A comprehensive summary is provided of the currently available respiratory pharmaceuticals approved for asthma and other airway syndromes. Clinicians must be prepared to use the entire spectrum of medications available for the treatment of acute asthma exacerbations and the agents that should be initiated to prevent worsening or additional exacerbations. They need to be familiar with the major potential drug toxicities associated with their use.
因哮喘急性加重(AEA)而前往急诊科(ED)或诊所就诊的患者,其严重程度和对治疗的反应各不相同,治疗起来颇具挑战性。高剂量、频繁或持续雾化吸入短效β2激动剂(SABA)疗法,可联合短效毒蕈碱拮抗剂(SAMA),是治疗的基础。当患者对SABA/SAMA吸入治疗没有迅速产生临床反应时,应考虑早期使用口服或胃肠外糖皮质激素,且已证明这会影响到立即入住重症监护病房的必要性,甚至影响到住院的必要性。应考虑使用辅助疗法,如静脉注射镁剂以及氦/氧混合气体吸入,用于驱动雾化器以输送SABA和/或SAMA,如果这些疗法可能会影响患者的临床病程,则最好在治疗方案早期使用。目前,使用氨茶碱、白三烯调节剂、吸入性糖皮质激素、长效β2激动剂和长效毒蕈碱拮抗剂等其他药物,在诊所或急诊科对AEA的即时治疗中并不起主要作用,但对于医生来说,这是一个重要的治疗选择,应在患者从诊所、医院或急诊科出院时考虑启动,以减少后续临床症状恶化以及再次前往急诊科和医院就诊的情况。本文提供了目前已批准用于哮喘和其他气道综合征的呼吸道药物的全面总结。临床医生必须准备好使用可用于治疗急性哮喘加重的全谱药物以及应启动使用以预防病情恶化或再次加重的药物。他们需要熟悉与这些药物使用相关的主要潜在药物毒性。