Inhaled Corticosteroid Therapy in Adult Asthma. Time for a New Therapeutic Dose Terminology.


Journal

American journal of respiratory and critical care medicine
ISSN: 1535-4970
Titre abrégé: Am J Respir Crit Care Med
Pays: United States
ID NLM: 9421642

Informations de publication

Date de publication:
15 06 2019
Historique:
pubmed: 16 1 2019
medline: 25 2 2020
entrez: 16 1 2019
Statut: ppublish

Résumé

The Global Initiative for Asthma guidelines use the traditional terminology of "low," "medium," and "high" doses of inhaled corticosteroids (ICS) to define daily maintenance doses of 100 to 250 μg, >250 to 500 μg, and >500 μg, respectively, of fluticasone propionate or equivalent for adults with asthma. This concise clinical review proposes that this terminology is not evidence based and that prescribing practice based on this terminology may lead to the use of inappropriately excessive doses of ICS. Specifically, the ICS dose that achieves 80-90% of the maximum obtainable benefit is currently classified as a low dose, with the description of two higher dose levels of medium and high, which are associated with significant risk of systemic adverse effects. Asthma guidelines and clinician prescribing practice need to be modified in accordance with the currently available evidence of the dose-response relationship of ICS in adult asthma. We propose a reclassification of ICS doses based on a "standard daily dose," which is defined as 200-250 μg of fluticasone propionate or equivalent, representing the dose at which approximately 80-90% of the maximum achievable therapeutic benefit of ICS is obtained in adult asthma across the spectrum of severity. It is recommended that ICS treatment be started at these standard doses, which then represent the doses at which maintenance ICS are prescribed at step 2 and within ICS/long-acting β-agonist combination therapy at step 3. The opportunity is available to prescribe higher doses within ICS/long-acting β-agonist maintenance therapy in accordance with the stepwise approach to asthma treatment at step 4.

Identifiants

pubmed: 30645143
doi: 10.1164/rccm.201810-1868CI
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Anti-Asthmatic Agents 0
Fluticasone CUT2W21N7U

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1471-1477

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Richard Beasley (R)

1 Medical Research Institute of New Zealand, Wellington, New Zealand.
2 Victoria University of Wellington, Wellington, New Zealand.
3 Capital & Coast District Health Board, Wellington, New Zealand.

James Harper (J)

1 Medical Research Institute of New Zealand, Wellington, New Zealand.

Grace Bird (G)

1 Medical Research Institute of New Zealand, Wellington, New Zealand.

Ingrid Maijers (I)

1 Medical Research Institute of New Zealand, Wellington, New Zealand.

Mark Weatherall (M)

3 Capital & Coast District Health Board, Wellington, New Zealand.
4 University of Otago Wellington, Wellington, New Zealand; and.

Ian D Pavord (ID)

5 Oxford Respiratory, National Institute for Health Research Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH