Literature DB >> 10465863

Comparative efficacy and safety of inhaled corticosteroids in asthma.

L D Jackson1, D Polygenis, R A McIvor, I Worthington.   

Abstract

Current guidelines emphasize the efficacy of inhaled corticosteroids for anti-inflammatory activity in asthma, and recommend higher doses and earlier initiation of therapy than previous guidelines. Concern over possible side effects with long term use has prompted an evaluation of the available literature to determine the optimal dose that may be administered without fear that significant side effects might occur (e.g., growth retardation in children, adrenal suppression, reduction in bone mineral density, cataract formation). Regular treatment with the following drugs in adults and children, respectively, is unlikely to result in any clinically significant effects on the above parameters: beclomethasone dipropionate less than 1500 micrograms and 400 micrograms, budesonide less than 1600 micrograms and 400 micrograms, flunisolide less than 2000 micrograms and 1000 micrograms, fluticasone propionate approximately 500 micrograms and 200 micrograms, and triamcinolone acetonide less than 1600 micrograms and 1200 micrograms. Systemic effects are influenced by potency and bioavailability. Inhaled corticosteroids owe their favourable safety profile to a high topical to systemic potency ratio compared with that of oral corticosteroids. In terms of relative topical potency, fluticasone propionate is more potent than budesonide, which is more potent than beclomethasone dipropionate, which is more potent than flunisolide and triamcinolone acetonide. The delivery device has an important influence on the amount of drug reaching the patient. A spacer device attached to a metered dose inhaler or a Turbuhaler reduces oropharyngeal deposition and increases lung deposition. As a result, a dosage reduction may be possible, and local side effects of dysphonia and oral candidiasis may be reduced. Patients requiring continued high doses by the inhaled route should be monitored for systemic effects and be considered for osteoporosis prevention therapy if appropriate.

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Year:  1999        PMID: 10465863

Source DB:  PubMed          Journal:  Can J Clin Pharmacol        ISSN: 1198-581X


  4 in total

1.  Equivalent pharmacokinetics of the active metabolite of ciclesonide with and without use of the AeroChamber Plus spacer for inhalation.

Authors:  Anton Drollmann; Ruediger Nave; Volker W Steinijans; Eugen Baumgärtner; Thomas D Bethke
Journal:  Clin Pharmacokinet       Date:  2006       Impact factor: 6.447

2.  Lower oropharyngeal deposition of inhaled ciclesonide via hydrofluoroalkane metered-dose inhaler compared with budesonide via chlorofluorocarbon metered-dose inhaler in healthy subjects.

Authors:  Ruediger Nave; Karl Zech; Thomas D Bethke
Journal:  Eur J Clin Pharmacol       Date:  2005-04-12       Impact factor: 2.953

Review 3.  Inhaled ciclesonide versus inhaled budesonide or inhaled beclomethasone or inhaled fluticasone for chronic asthma in adults: a systematic review.

Authors:  Matthew J Dyer; David M G Halpin; Ken Stein
Journal:  BMC Fam Pract       Date:  2006-06-05       Impact factor: 2.497

4.  Molecular dissection of an inhibitor targeting the HIV integrase dependent preintegration complex nuclear import.

Authors:  Kylie M Wagstaff; Stephen Headey; Sushama Telwatte; David Tyssen; Anna C Hearps; David R Thomas; Gilda Tachedjian; David A Jans
Journal:  Cell Microbiol       Date:  2018-09-27       Impact factor: 3.715

  4 in total

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