Abstract

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.

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