Cited by 243Rheumatoid Arthritis Research and TherapiesAdrenal Hormones and DisordersPharmacovigilance and Adverse Drug Reactions

Adverse events of low- to medium-dose oral glucocorticoids in inflammatory diseases: a meta-analysis

Hoes, J N, Jacobs, J W G, Verstappen, S M M, Bijlsma, J W J, Van der Heijden, G J M G·2009·Annals of the Rheumatic Diseases

Abstract

Objectives To systematically analyse the literature on reported adverse events of low- to medium-dose glucocorticoids during >or=1 month for inflammatory diseases.Methods Data were systematically retrieved and selected from PUBMED, EMBASE and CINAHL databases (6097 hits).Results A total of 28 studies (2382 patients) met the inclusion criteria. The risk of adverse events over all studies was 150 per 100 patient-years (95% confidence interval (CI) 132 to 169). Psychological and behavioural adverse events (eg, minor mood disturbances) were most frequently reported, followed by gastrointestinal events (eg, dyspepsia, dysphagia). In 14 studies comprising 796 patients with rheumatoid arthritis the risk of adverse events was 43/100 patient-years (95% CI 30 to 55), in 4 studies of 167 patients with polymyalgia rheumatica the risk of adverse events was 80/100 patient-years (95% CI 15 to 146), and in 10 studies of 1419 patients with inflammatory bowel disease the risk of adverse events was 555/100 patient-years (95% CI 391 to 718). High rates of adverse events were reported in high-quality studies with short follow-up, notably in studies of patients with inflammatory bowel disease.Conclusions The risk of adverse events depends on study design and disease. Studies on inflammatory bowel disease were often of short duration with frequent documentation of adverse events which resulted in higher adverse event rates whereas, in studies of rheumatoid arthritis, the longer follow-up may have resulted in lower adverse event rates. In most studies aimed at efficacy of glucocorticoids or other drugs, adverse events were not systematically assessed. Clear guidelines on assessment of adverse events are lacking.

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Crossref · 10.1136/ard.2008.100008

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Authors
Hoes, J. N., Jacobs, J. W. G., Verstappen, S. M. M., Bijlsma, J. W. J., & Van der Heijden, G. J. M. G.
Affiliations
University Medical Center Utrecht (NL)
Corresponding author
Jacobs, J W G
Venue
Annals of the Rheumatic Diseases
Publisher
Elsevier BV
Published
2009-12
Volume
68
Issue
12
Pages
1833-1838
ISSN
0003-4967 (ISSN-L)
OpenAlex
W2122641956
Cited by
243
References
14
Citations by year
2026: 7 · 2025: 9 · 2024: 16 · 2023: 14 · 2022: 13 · 2021: 19 · 2020: 13 · 2019: 15 · 2018: 16 · 2017: 13 · 2016: 14 · 2015: 9 · 2014: 15 · 2013: 19 · 2012: 14
FWCI
8.52
Type
journal article
Language
en
Open access
closed
Locations
  • Annals of the Rheumatic Diseases (publishedVersion)
  • PubMed (publishedVersion)
  • HighWire Press Open Archive (submittedVersion)
  • Research Explorer (The University of Manchester) (submittedVersion)
Topics
  • Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pharmacovigilance and Adverse Drug Reactions
Keywords
oral corticosteroids, adverse events, low-dose glucocorticoids, inflammatory diseases, rheumatoid arthritis, polymyalgia rheumatica, inflammatory bowel disease, gastrointestinal adverse effects, mood disturbance, long-term corticosteroid therapy
MeSH terms
Arthritis, Rheumatoid, Mental Disorders, Dose-Response Relationship, Drug, Gastrointestinal Diseases, Glucocorticoids, Humans, Inflammation, Polymyalgia Rheumatica, Inflammatory Bowel Diseases

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