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Adrenal function and high dose inhaled corticosteroids for asthma
  1. Panayiotis K Yiallourosa,
  2. Anthony D Milnera,
  3. Elvira Conwayb,
  4. John W Honourb
  1. aChildren’s Respiratory Unit, Division of Paediatrics, United Medical and Dental Schools of Guy’s and St Thomas’ Hospitals, University of London, London, bDepartment of Chemical Pathology, University College London Hospitals, London
  1. Professor AD Milner, Department of Paediatrics, St Thomas’ Hospital, Lambeth Palace Road, London SE1 7EH.

Abstract

OBJECTIVE To investigate effects on adrenal function of fluticasone, a recently released inhaled steroid preparation with lower systemic bioavailability than beclomethasone dipropionate.

METHODS 34 children on high doses (400-909 μg/m2/d) of inhaled beclomethasone dipropionate or budesonide were recruited into a double blind, crossover study investigating the effects on adrenal function of beclomethasone and fluticasone propionate, given using a standard spacer (Volumatic). The 24 hour excretion rates of total cortisol and cortisol metabolites were determined at baseline (after a two week run in), after six weeks treatment with an equal dose of beclomethasone, and after six weeks of treatment with half the dose of fluticasone, both given through a spacer device.

RESULTS The comparison of effects between fluticasone and beclomethasone during treatment periods, although favouring fluticasone in all measured variables, reached significance only after correction for urinary creatinine excretion (tetrahydrocortisol and 5α-tetrahydrocortisol geometric means: 424 v 341 μg/m2/d). The baseline data showed adrenal suppression in the children taking beclomethasone (total cortisol geometric means: 975 v 1542 μg/d) and a dose related suppression in the children taking budesonide. Suppressed adrenal function in the children who were taking beclomethasone at baseline subsequently improved with fluticasone and beclomethasone during treatment periods.

CONCLUSIONS Fluticasone is less likely to suppress adrenal function than beclomethasone at therapeutically equivalent doses. The baseline data also support the claim that spacer devices should be used for the administration of high doses of inhaled topical steroids.

  • inhaled corticosteroids
  • adrenal function
  • spacer devices

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