A graded dose assessment of the efficacy of beclomethasone dipropionate aerosol for severe chronic asthma

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Abstract

In a 26-wk double-blind controlled study of 34 patients whose asthma had been poorly controlled despite oral steroids, valuable clinical and pulmonary function improvement was derived by adding beclomethasone aerosol to the prednisone regimen. The amount of improvement correlated linearly with beclomethasone dosage over the range 200 to 1,600 μg/day. These patients required relatively high dosage. Success in achieving asymptomatic status was only 26% with the conventional 400 μg/day and 60% at 1,600 μg/day. Oropharyngeal candidiasis was also dose-related but did not prohibit the use of high-dosage beclomethasone. Respiratiory infections, physical signs, blood glucose, and electrolytes were unaffected by the drug. A dose-related suppression of cortisol secretion was demonstrated, but about 14 of the group had normal plasma cortisol even at 1,600 μg/day plus the oral prednisone. An individualized risk-benefit assessment seems a better basis for choosing an optimal beclomethasone regimen for each patient than adherence to a conventionalized fixed dosage of 400 μg/day. This requires definition of: (1) a specific goal of treatment in the individual patient and the beclomethasone dosage required to achieve it; (2) the adrenocortical functional response of that particular patient to the desired dose of beclomethasone; and (3) the presence and degree of any dose-limiting constraints such as preexisting complications of steroid use.

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    Supported by grants from Schering (Canada) Ltd., the Medical Associates of Victoria Hospital, the Ontario Respiratory Disease Foundation, and the London-Middlesex Christmas Seals Undergraduate Research Fellowship Fund.

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