DOSE OF INHALED BUDESONIDE REQUIRED TO PRODUCE CLINICAL SUPPRESSION OF PLASMA-CORTISOL
- 1 July 1987
- journal article
- research article
- Vol. 71 (1) , 10-14
Abstract
Increasing doses of budesonide, each dose given for a minimum of 1 month, were administered via a Nebuhaler to 14 patients. Two consecutive abnormally low fasting morning plasma cortisol values, taken 2 weeks apart, were accepted as evidence of hypothalamo-pituitary-adrenal (HPA) hypofunction. Data from nine of the 14 patients entering the study were available for analysis. One patient developed HPA hypofunction while inhaling 2.4 mg budesonide per day and another retained normal HPA function on a dose of 12 mg. In the remaining patients, intermediate doses resulted in suppression, or the patients were withdrawn unsuppressed for other reasons (n = 3). The results in this small patient sample suggest that budesonide administered via the Nebuhaler in doses up to 1.6 mg daily does not significantly affect plasma cortisol.This publication has 4 references indexed in Scilit:
- Improvement of pressurised aerosol deposition with Nebuhaler spacer device.Thorax, 1984
- Use of Spacers to Facilitate Inhaled Corticosteroid Treatment of Asthma1–4American Review of Respiratory Disease, 1984
- Topical and systemic glucocorticoid potencies of budesonide and beclomethasone dipropionate in manEuropean Journal of Clinical Pharmacology, 1982
- DEPOSITION OF PRESSURIZED SUSPENSION AEROSOLS INHALED THROUGH EXTENSION DEVICESPublished by Elsevier ,1981