Medical Research Institute of New Zealand, Wellington, New Zealand; Capital and Coast District Health Board, Wellington, New Zealand; Division of Respiratory Medicine, School of Clinical Sciences, University of Nottingham, Nottingham, United Kingdom.
Medical Research Institute of New Zealand, Wellington, New Zealand; Capital and Coast District Health Board, Wellington, New Zealand.
J Allergy Clin Immunol Pract. 2014 Nov-Dec;2(6):751-8. doi: 10.1016/j.jaip.2014.06.001. Epub 2014 Jul 25.
Predictors of asthma exacerbations, poor asthma control, or extreme β-agonist overuse may be of clinical utility in the management of asthma.
To investigate characteristics that predict subsequent adverse outcomes in asthma.
An independent 24-week, randomized controlled trial of 303 adult patients with asthma who are at risk, which compared the efficacy of SMART (single budesonide-formoterol inhaler as maintenance and reliever therapy) with a fixed-dose regimen with salbutamol as reliever ("Standard"). Inhaled medication use was measured by electronic monitoring. Baseline characteristics that were predictors of subsequent severe asthma exacerbations, poor asthma control (Asthma Control Questionnaire -5 score ≥1.5), and "extreme" β-agonist overuse (>16 budesonide-formoterol actuations/d in SMART and >32 salbutamol actuations/d in Standard) were assessed by multivariate analyses.
FEV₁ % predicted (rate ratio [RR] 1.14 [95% CI, 1.03-1.27] per 10% lower), more previous exacerbations (RR 1.15 [95% CI, 1.01-1.31]), Standard therapy (RR 1.62 [95% CI, 1.07-2.47]), and female sex (RR 2.18 [95% CI, 1.29-3.67]) were associated with future severe exacerbations. Asthma Control Questionnaire--5 (regression coefficient 0.20 [95% CI, 0.13-0.27] per 0.5 points higher) and age (regression coefficient 0.09 [95% CI, 0.01-0.17] per decade older) were associated with future poorly controlled asthma. Higher reliever use (RR 1.63 [95% CI, 1.36-1.95] per categorical score in Asthma Control Questionnaire question no. 6), Māori ethnicity (RR 2.20 [95% CI, 1.43-3.38]) and FEV₁ % predicted (RR 1.16 [95% CI, 1.03-1.31] per 10% lower) were associated with future extreme β-agonist overuse.
Future severe asthma exacerbations, poor asthma control, and extreme β-agonist overuse are predicted by different baseline clinical and demographic characteristics and management approaches in at-risk asthma.
预测哮喘恶化、哮喘控制不佳或过度使用β-激动剂的因素可能对哮喘管理具有临床应用价值。
研究可预测哮喘后续不良结局的特征。
这是一项独立的、为期 24 周的、对 303 名患有哮喘且存在风险的成年患者进行的随机对照试验,比较 SMART(单一布地奈德福莫特罗吸入剂作为维持和缓解治疗)与沙丁胺醇固定剂量作为缓解药物(“标准”)的疗效。通过电子监测来测量吸入药物的使用情况。采用多变量分析评估预测随后发生严重哮喘恶化、哮喘控制不佳(哮喘控制问卷-5 评分≥1.5)和“过度”β-激动剂使用(SMART 中>16 次布地奈德福莫特罗剂量/天和标准中>32 次沙丁胺醇剂量/天)的基线特征。
FEV₁%预测值(每降低 10%的比率比[RR]为 1.14[95%CI,1.03-1.27])、既往加重次数较多(RR 1.15[95%CI,1.01-1.31])、标准治疗(RR 1.62[95%CI,1.07-2.47])和女性(RR 2.18[95%CI,1.29-3.67])与未来严重加重有关。哮喘控制问卷-5(每提高 0.5 分的回归系数为 0.20[95%CI,0.13-0.27])和年龄(每增加十年的回归系数为 0.09[95%CI,0.01-0.17])与未来控制不佳的哮喘有关。更高的缓解药物使用(哮喘控制问卷第 6 题每增加一个分类评分的 RR 为 1.63[95%CI,1.36-1.95])、毛利人种族(RR 2.20[95%CI,1.43-3.38])和 FEV₁%预测值(每降低 10%的 RR 为 1.16[95%CI,1.03-1.31])与未来过度使用β-激动剂有关。
在存在风险的哮喘患者中,未来严重哮喘恶化、哮喘控制不佳和过度使用β-激动剂是由不同的基线临床和人口统计学特征以及管理方法预测的。