McFadden E R, Casale T B, Edwards T B, Kemp J P, Metzger W J, Nelson H S, Storms W W, Neidl M J
University Hospitals of Cleveland, Cleveland, OH 44106, USA.
J Allergy Clin Immunol. 1999 Jul;104(1):46-52. doi: 10.1016/s0091-6749(99)70112-0.
Optimal management of chronic, mild-to-moderate asthma with inhaled steroids may include use of the lowest possible doses, as recommended in guidelines, and a reduction in the frequency of daily administration for greater convenience. Lower doses and once daily treatment with inhaled steroids must be rigorously evaluated in controlled clinical trials.
The objective of this study was to assess the efficacy and safety of once daily treatment with budesonide in subjects with stable asthma.
Once daily budesonide was assessed in 309 adult subjects, including those who were and were not using an inhaled steroid at baseline. The subjects were stratified by inhaled steroid use and randomly assigned to one of 3 treatments: 200 microgram budesonide, 400 microgram budesonide, or placebo administered by means of Turbuhaler once daily in the morning for 6 weeks. Beyond this point, treatment was continued unchanged for another 12 weeks (maintenance) in those receiving 200 microgram budesonide once daily and placebo. In those who received 400 microgram budesonide once daily, the dose was reduced to 200 microgram once daily at week 6 and held constant for the remaining 12 weeks (400/200 microgram group). Primary efficacy endpoints were mean change from baseline in FEV1 and morning peak expiratory flow.
Once daily budesonide was well tolerated and resulted in significant improvements in all efficacy endpoints, even though baselines were well stabilized. Baseline lung function was elevated with little room for improvement; however, mean increases in FEV1 during the maintenance period were 0.10 L and 0.11 L in the 200 microgram and 400/200 microgram groups, respectively, versus a decrease of -0.09 L in the placebo arm (P <.001). Results for peak expiratory flow were similar. Significant improvements in secondary endpoints, including symptoms, beta-agonist use, and quality of life, also developed with budesonide 200 and 400 microgram once daily.
Inhaled budesonide, in doses as low as 200 microgram, may be an appropriate introductory or maintenance dose in subjects with stable, mild-to-moderate asthma.
按照指南推荐,使用吸入性糖皮质激素对慢性轻至中度哮喘进行优化管理可能包括使用尽可能低的剂量,并减少每日给药频率以提高便利性。必须在对照临床试验中对较低剂量和吸入性糖皮质激素每日一次的治疗进行严格评估。
本研究的目的是评估布地奈德每日一次治疗稳定期哮喘患者的疗效和安全性。
对309名成年受试者评估了布地奈德每日一次的治疗效果,包括基线时正在使用和未使用吸入性糖皮质激素的受试者。根据吸入性糖皮质激素的使用情况对受试者进行分层,并随机分配至3种治疗之一:200微克布地奈德、400微克布地奈德或安慰剂,通过都保装置每天早晨给药一次,持续6周。此后,接受200微克布地奈德每日一次和安慰剂治疗的受试者,治疗方案维持不变,再持续12周(维持期)。接受400微克布地奈德每日一次治疗的受试者,在第6周时剂量减至200微克每日一次,并在剩余12周内保持不变(400/200微克组)。主要疗效终点为第1秒用力呼气容积(FEV1)和晨起呼气峰值流速较基线的平均变化。
布地奈德每日一次耐受性良好,即使基线情况已充分稳定,所有疗效终点仍有显著改善。基线肺功能较高,改善空间较小;然而,在维持期,200微克组和400/200微克组的FEV1平均增加量分别为0.10升和0.11升,而安慰剂组下降了-0.09升(P<0.001)。呼气峰值流速的结果相似。布地奈德200微克和400微克每日一次治疗,包括症状、β受体激动剂使用情况和生活质量在内的次要终点也有显著改善。
对于稳定的轻至中度哮喘患者,低至200微克的吸入性布地奈德剂量可能是合适的起始或维持剂量。