Severe asthma: oral corticosteroid alternatives and the need for optimal referral pathways.


Journal

The Journal of asthma : official journal of the Association for the Care of Asthma
ISSN: 1532-4303
Titre abrégé: J Asthma
Pays: England
ID NLM: 8106454

Informations de publication

Date de publication:
04 2021
Historique:
pubmed: 14 1 2020
medline: 1 10 2021
entrez: 14 1 2020
Statut: ppublish

Résumé

Patients with severe asthma require high-dose inhaled corticosteroids, with or without add-on treatments, to maintain asthma control. Because symptom control remains unsatisfactory in some patients despite these therapies, maintenance therapy with oral corticosteroids (OCS) remains considered a treatment option by physicians. Besides physician-diagnosed exacerbations, many patients intermittently self-medicate with OCS during episodes of worsening symptoms or as a prevention of such episodes. However, long-term OCS use is associated with several comorbidities that may decrease health-related quality of life, worsen prognosis, and should ideally require monitoring and management. In this review, we discuss the adverse effects of OCS use, the OCS-sparing effect of biologics in severe asthma, and the need for optimal referral pathways to ensure the best outcomes for those at-risk asthma patients. PubMed. Studies with results on the OCS-sparing effect of biologics in adult severe asthma were selected. Chronic and intermittent OCS use in asthma is associated with considerable adverse effects in asthma. Omalizumab, mepolizumab, benralizumab, and dupilumab reduce the need for OCS in severe asthma, while also reducing the exacerbation rate and improving several patient-related outcomes. Targeted biologic therapies have revolutionized the treatment of uncontrolled severe asthma by reducing or even eliminating the need for OCS and improving other major outcomes. Novel agents are now rapidly increasing the therapeutic armamentarium, but additional efforts are needed to optimize referral pathways in order to ensure sustainable access to these therapies.

Identifiants

pubmed: 31928102
doi: 10.1080/02770903.2019.1705335
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Adrenergic beta-2 Receptor Agonists 0
Anti-Asthmatic Agents 0
Antibodies, Monoclonal, Humanized 0
Delayed-Action Preparations 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

448-458

Auteurs

Didier Cataldo (D)

Department of Respiratory Diseases, CHU Liège, GIGA-Research, University of Liège, Liège, Belgium.

Renaud Louis (R)

Department of Respiratory Diseases, CHU Liège, GIGA-Research, University of Liège, Liège, Belgium.

Alain Michils (A)

Chest Department, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Rudi Peché (R)

Department of Respiratory Medicine, University Hospital Vésale, Montigny-le-Tilleul, Belgium.

Charles Pilette (C)

Department of Pulmonary Medicine, Cliniques Universitaires St Luc, and Institute of Experimental and Clinical Research, Université Catholique de Louvain, Brussels, Belgium.

Florence Schleich (F)

Department of Respiratory Diseases, CHU Liège, GIGA-Research, University of Liège, Liège, Belgium.

Vincent Ninane (V)

Department of Respiratory Medicine, University Hospital Saint-Pierre, Université Libre de Bruxelles, Belgium.

Shane Hanon (S)

Respiratory Division, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel (VUB), Brussels, Belgium.

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Classifications MeSH