TY - JOUR
T1 - Prevention of glucocorticoid morbidity in giant cell arteritis
AU - Buttgereit, Frank
AU - Matteson, Eric L.
AU - Dejaco, Christian
AU - Dasgupta, Bhaskar
N1 - Funding Information:
Disclosure statement: F.B. has received grants, personal fees and non-financial support from Horizon Pharmaceuticals and Mundipharma and personal fees from Roche outside of the submitted work. C.D. has received personal fees from Merck Sharp and Dohme, Pfizer, Union Chimique Belge, Abbvie, Roche, Novartis, Sandoz, Eli Lilly, Celgene, Bristol-Myers Squibb (BMS) and Astro Pharma outside of the submitted work. E.L.M. has received grants from Genentech, BMS, and Eli Lilly. B.D. has received honoraria for consultancies on Advisory Boards for Roche, GSK, BMS and Mundipharma.
Funding Information:
Medical writing assistance in the preparation of this manuscript was provided by Melanie Sweetlove and Sara Dugan, PhD, of ApotheCom (Yardley, PA, USA). Support for this assistance was funded by F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Publisher Copyright:
© The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Glucocorticoids are the mainstay of treatment for GCA. Patients often require long-term treatment that may be associated with numerous adverse effects, depending on the dose and the duration of treatment. Trends in recent decades for glucocorticoid use in GCA suggest increasing cumulative doses and longer exposures. Common adverse events (AEs) reported in glucocorticoid-treated GCA patients include osteoporosis, hypercholesterolaemia, hypertension, posterior subcapsular cataract, infections, diabetes mellitus, Cushingoid appearance, adrenal insufficiency and aseptic necrosis of bone. AEs considered most worrisome by patients and rheumatologists include weight gain, psychological effects, osteoporosis, cardiometabolic complications and infections. The challenge is to maximize the benefit-risk ratio by giving the maximum glucocorticoid treatment necessary to control GCA initially and then to prevent relapse but to give the minimum treatment possible to avoid glucocorticoid-related AEs. We discuss the safety issues associated with long-term glucocorticoid use in patients with GCA and strategies for preventing glucocorticoid-related morbidity.
AB - Glucocorticoids are the mainstay of treatment for GCA. Patients often require long-term treatment that may be associated with numerous adverse effects, depending on the dose and the duration of treatment. Trends in recent decades for glucocorticoid use in GCA suggest increasing cumulative doses and longer exposures. Common adverse events (AEs) reported in glucocorticoid-treated GCA patients include osteoporosis, hypercholesterolaemia, hypertension, posterior subcapsular cataract, infections, diabetes mellitus, Cushingoid appearance, adrenal insufficiency and aseptic necrosis of bone. AEs considered most worrisome by patients and rheumatologists include weight gain, psychological effects, osteoporosis, cardiometabolic complications and infections. The challenge is to maximize the benefit-risk ratio by giving the maximum glucocorticoid treatment necessary to control GCA initially and then to prevent relapse but to give the minimum treatment possible to avoid glucocorticoid-related AEs. We discuss the safety issues associated with long-term glucocorticoid use in patients with GCA and strategies for preventing glucocorticoid-related morbidity.
KW - Adverse events
KW - Giant cell arteritis
KW - Glucocorticoids
KW - Morbidity
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U2 - 10.1093/rheumatology/kex459
DO - 10.1093/rheumatology/kex459
M3 - Article
C2 - 29982779
AN - SCOPUS:85042609290
SN - 1462-0324
VL - 57
SP - ii11-ii21
JO - Rheumatology (United Kingdom)
JF - Rheumatology (United Kingdom)
ER -