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Oral steroid-sparing effect of two doses of nebulized fluticasone propionate and placebo in patients with severe chronic asthma.

机译:两次雾化丙酸氟替卡松和安慰剂对严重慢性哮喘患者的口服类固醇保护作用。

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Inhaled steroids, delivered by metered dose aerosol and dry powder inhalers, have proved effective in reducing the need for oral steroids in patients with oral steroid-dependant asthma. This randomized, double-blind study, compared the efficacy and tolerability of nebulized fluticasone propionate (FP Nebules), 2 mg b.d. (FP 4 mg) and 0.5 mg b.d. (FP 1 mg) with placebo, on the reduction of oral steroid requirement in 301 adult patients with oral steroid-dependent asthma. Primary efficacy was assessed by the reduction in daily oral steroid dose. Secondary efficacy parameters included daily diary card peak expiratory flow (PEF), day and night-time symptoms and clinic lung function measurements. Safety was assessed by adverse event monitoring and serum cortisol levels. After 12 weeks of treatment the adjusted mean +/- SEM reduction in oral prednisolone was significantly greater in the FP 4 mg group (4.44 +/- 0.98 mg day-1) compared with FP 1 mg (2.16 +/- 1.00 mg day-1, P = 0.039) and placebo (1.20 +/- 1.02 mg day-1, P = 0.004). A higher percentage of patients discontinued the use of oral steroids with FP 4 mg (37%) compared with FP 1 mg (26%, P = 0.038) and placebo (18%, P < 0.001). Following treatment, the adjusted mean morning PEF showed a trend in favour of FP 4 mg (280 +/- 41 min-1) compared with placebo (270 +/- 51 min-1, P = 0.053) and the evening PEF was significantly higher with FP 4 mg (305 +/- 41 min-1) compared with FP 1 mg (292 +/- 41 min-1, P = 0.010). FP 4 mg resulted in a significantly higher percentage of days when the patients were free from daytime (P = 0.036) and night-time (P = 0.021) wheeze, compared with placebo. Significantly fewer patients withdrew from the FP 4 mg group compared with the other two groups (vs. FP 1 mg, P = 0.003; vs. placebo, P = 0.032). All three treatments were well tolerated and the incidence of adverse events was similar between the groups. FP Nebules at a daily dose of between 1 and 4 mg are a safe and effective means of reducing the oral steroid requirement of patients with chronic oral steroid dependent asthma.
机译:经证实,通过口服剂量的气雾剂和干粉吸入器提供的吸入类固醇可有效减少口服类固醇依赖型哮喘患者对口服类固醇的需求。这项随机,双盲研究比较了雾化丙酸氟替卡松(FP Nebules)2 mg b.d.的疗效和耐受性。 (FP 4 mg)和0.5 mg b.d. (FP 1毫克)与安慰剂,可降低301位口服类固醇依赖性哮喘成年患者的口服类固醇需求。通过减少每日口服类固醇剂量评估主要疗效。次要疗效参数包括每日日记卡最大呼气流量(PEF),日夜症状和临床肺功能测量。通过不良事件监测和血清皮质醇水平评估安全性。治疗12周后,与FP 1 mg(2.16 +/- 1.00 mg-day)相比,FP 4 mg组(4.44 +/- 0.98 mg day-1)口服泼尼松龙的调整后平均+/- SEM降低幅度明显更大。 1,P = 0.039)和安慰剂(1.20 +/- 1.02 mg day-1,P = 0.004)。与FP 1 mg(26%,P = 0.038)和安慰剂(18%,P <0.001)相比,FP 4 mg(37%)停用口服类固醇的患者比例更高。治疗后,与安慰剂(270 +/- 51 min-1,P = 0.053)相比,调整后的早晨PEF平均显示出倾向于FP 4 mg(280 +/- 41 min-1)的趋势,并且夜间PEF显着FP 4 mg(305 +/- 41 min-1)高于FP 1 mg(292 +/- 41 min-1,P = 0.010)。与安慰剂相比,FP 4 mg可使患者白天(P = 0.036)和夜间(P = 0.021)喘息的天数百分比显着更高。与其他两组相比,从FP 4 mg组退出的患者显着减少(vs. FP 1 mg,P = 0.003;与安慰剂相比,P = 0.032)。三种疗法的耐受性都很好,两组之间不良事件的发生率相似。日剂量为1至4 mg的FP星云是一种安全有效的方法,可减少患有慢性口服类固醇依赖性哮喘的患者对口服类固醇的需求。

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