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Tolerance of glucocorticoids in giant cell arteritis: a study of patient-reported adverse events.

Authors :
de Boysson H
Barakat C
Dumont A
Boutemy J
Martin Silva N
Maigné G
Nguyen A
Lavergne A
Castan P
Gallou S
Sultan A
Deshayes S
Aouba A
Source :
Rheumatology (Oxford, England) [Rheumatology (Oxford)] 2022 Aug 30; Vol. 61 (9), pp. 3567-3575.
Publication Year :
2022

Abstract

Objective: To assess patients' self-reported glucocorticoid (GC)-related adverse events (AEs) in a GCA population.<br />Methods: A questionnaire was sent to the 100 patients most recently diagnosed with GCA in a tertiary centre. This questionnaire included open- and close-ended questions on the disease and GC effects. Eight primary AE areas were analysed: cardiovascular, metabolic, muscle, cognitive and psychologic, bone, cutaneous and hairiness, infective and visual complications. Including derivative subitems from preceding areas, a total of 18 GC-related AEs were analysed separately and according to GC duration.<br />Results: Ninety patients were analysed and 89 (99%) reported at least one GC-related AE [median 6 (range 1-11)]. Cognitive and psychological changes, primarily insomnia (72%), affected 90% of patients. Cutaneous changes and muscle loss affected 70% of patients, with frequent impairment of physical autonomy (P = 0.007) associated with this event. Metabolic issues, especially weight gain (40%) and diabetes mellitus (20%), affected 49% of patients. Conversely, vision troubles and bone fractures were mentioned by 42% and 9% of patients, respectively, and more frequently in patients who received GCs for >18 months (P = 0.01 and P = 0.007, respectively). Cardiovascular changes and infections affected 30% and 26% of patients, respectively.<br />Conclusion: This real-life study of GC tolerance assessed using a self-evaluation provides pragmatic and updated data reminding us that GC tolerance remains more noteworthy than ever. This study suggests carefully monitoring GC-related AEs during follow-up and encourages GC-sparing strategies in some patients.<br /> (© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1462-0332
Volume :
61
Issue :
9
Database :
MEDLINE
Journal :
Rheumatology (Oxford, England)
Publication Type :
Academic Journal
Accession number :
34919673
Full Text :
https://doi.org/10.1093/rheumatology/keab921