den Otter Joost J, van Schayck Constant P, Folgering Hans T M, van den Boom Guido, Akkermans Reinier P M, van Weel Chris
Department of General Practice, Dekkerswald UMC St Radboud Nijmegen, Nijmegen, The Netherlands.
Eur J Gen Pract. 2007;13(2):89-91. doi: 10.1080/13814780701377455.
Asthma is generally accepted as an inflammatory disease that needs steroid treatment. However, when to start with inhaled steroids remains unclear. A study was undertaken to determine when inhaled corticosteroids should be introduced as the first treatment step.
To investigate the effectiveness of early introduction of inhaled steroids on decline in lung function in steroid-naïve subjects with a rapid decline in lung function in general practice.
Patients with signs/symptoms suspect of asthma (i.e., persistent and/or recurrent respiratory symptoms) and a decline in forced expiratory volume in 1 s (FEV(1)) during 1-year monitoring of 0.080 l or more and reversible obstruction (> or =10% predicted) or bronchial hyperresponsiveness (PC(20)< or =8 mg/ml) were studied. They had been identified in a population screening aiming to detect subjects at risk for chronic obstructive pulmonary disease (COPD) or asthma.
A placebo-controlled, randomized, double-blind study.
75 subjects out of a random population of 1155 were found eligible, and 45 were willingly to participate. Subjects were randomly treated with placebo or fluticasone propionate 250 microg b.i.d., and FEV(1) and PC(20) were monitored over a 2-year period.
The primary outcome measure was decline in FEV(1); the secondary outcome measure was bronchial hyperresponsiveness (PC(20)).
22 subjects were randomly allocated to the active group with inhaled corticosteroids and 23 to placebo. Change of FEV(1) in the active treated group was +43 ml in post-bronchodilator FEV(1) (p =0.341) and +62 ml/year (p =0.237) in pre-bronchodilator FEV(1) after 1 year, and -22 ml (p =0.304) for post-bronchodilator FEV(1) and -9.4 ml (p =0.691) for pre-bronchodilator FEV(1) after 2 years, compared to placebo. The effect on PC(20) was almost one dose-step (p =0.627) after 1 year and one dose-step (p =0.989) after 2 years.
In this study, the early introduction of inhaled corticosteroids in newly diagnosed asthmatic subjects with rapid decline in lung function did not prove to be either clinically relevant or statistically significant in reversing the decline in FEV(1). For PC(20), no significant changes were detected.
哮喘通常被认为是一种需要类固醇治疗的炎症性疾病。然而,何时开始使用吸入性类固醇仍不明确。开展了一项研究以确定何时应将吸入性皮质类固醇作为首个治疗步骤引入。
研究在基层医疗中肺功能快速下降的未使用过类固醇的受试者中,早期引入吸入性类固醇对肺功能下降的有效性。
对有哮喘疑似体征/症状(即持续性和/或复发性呼吸道症状)且在1年监测期间1秒用力呼气量(FEV₁)下降0.080升或更多、存在可逆性阻塞(≥预测值的10%)或支气管高反应性(PC₂₀≤8毫克/毫升)的患者进行了研究。他们是在一项旨在检测慢性阻塞性肺疾病(COPD)或哮喘风险受试者的人群筛查中被识别出来的。
一项安慰剂对照、随机、双盲研究。
在1155名随机人群中,75名受试者符合条件,45名愿意参与。受试者被随机给予安慰剂或丙酸氟替卡松250微克,每日两次,并在2年期间监测FEV₁和PC₂₀。
主要结果指标是FEV₁的下降;次要结果指标是支气管高反应性(PC₂₀)。
22名受试者被随机分配到吸入性皮质类固醇治疗的活性组,23名被分配到安慰剂组。活性治疗组在支气管扩张剂后FEV₁中,1年后的变化为+43毫升(p = 0.341),支气管扩张剂前FEV₁中每年变化为+62毫升(p = 0.237),2年后支气管扩张剂后FEV₁为 -22毫升(p = 0.304),支气管扩张剂前FEV₁为 -9.4毫升(p = 0.691),与安慰剂组相比。对PC₂₀的影响在1年后几乎是一个剂量级(p = 0.627),2年后是一个剂量级(p = 0.989)。
在本研究中,对于新诊断的肺功能快速下降的哮喘受试者,早期引入吸入性皮质类固醇在逆转FEV₁下降方面未被证明具有临床相关性或统计学显著性。对于PC₂₀,未检测到显著变化。