首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Administration of budesonide once daily by means of turbuhaler to subjects with stable asthma.
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Administration of budesonide once daily by means of turbuhaler to subjects with stable asthma.

机译:每天用turbuhaler给予布地奈德稳定哮喘患者一次。

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BACKGROUND: 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. OBJECTIVES: The objective of this study was to assess the efficacy and safety of once daily treatment with budesonide in subjects with stable asthma. METHODS: 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. RESULTS: 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. CONCLUSION: 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.
机译:背景:吸入类固醇对慢性,轻度至中度哮喘的最佳管理可能包括按照指南中的建议使用最低剂量,并减少每日给药的频率,以提供更大的便利。在受控的临床试验中必须严格评估小剂量和每日一次吸入类固醇的治疗。目的:本研究的目的是评估每日一次布地奈德治疗稳定哮喘患者的疗效和安全性。方法:在309名成人受试者中评估了布地奈德的每日使用量,其中包括基线时使用和未使用吸入类固醇的受试者。通过吸入类固醇的使用将受试者分层,并随机分配至以下3种治疗方法之一:200微克布地奈德,400微克布地奈德或安慰剂,每天早上一次,通过Turbuhaler给药,持续6周。超过这一点,每天接受一次200毫克布地奈德和安慰剂治疗的患者继续治疗12周(维持)。在那些每天接受一次400微克布地奈德治疗的患者中,剂量在第6周减少到每天一次200毫克,并在剩余的12周内保持不变(400/200毫克)。主要功效终点为FEV1和早晨峰值呼气流量相对于基线的平均变化。结果:即使基线稳定,每天一次布地奈德的耐受性良好,所有功效终点均得到显着改善。基线肺功能升高,改善空间很小;然而,在维持期间,FEV1的平均增加在200微克和400/200微克组中分别为0.10 L和0.11 L,而在安慰剂组中为-0.09 L(P <.001)。峰值呼气流量的结果相似。布地奈德200和400微克每天一次也可改善次要终点的显着改善,包括症状,使用β激动剂和改善生活质量。结论:对于稳定,轻度至中度哮喘的患者,吸入布地奈德的剂量低至200微克,可能是适当的入门剂量或维持剂量。

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