TY - JOUR
T1 - Infections in biological and targeted synthetic drug use in rheumatoid arthritis
T2 - Where do we stand? A scoping review and meta-analysis
AU - Bergmans, B.J.M.
AU - Gebeyehu, B.Y.
AU - van Puijenbroek, E.P.
AU - Van Deun, K.
AU - Kleinberg, B.
AU - Murk, J.
AU - de Vries, E.
PY - 2023
Y1 - 2023
N2 - IntroductionThe advent of biological and targeted synthetic therapies has revolutionized rheumatoid arthritis (RA) treatment. However, this has come at the price of an increased risk of infections. The aim of this study was to present an integrated overview of both serious and non-serious infections, and to identify potential predictors of infection risk in RA patients using biological or targeted synthetic drugs.MethodsWe systematically reviewed available literature from PubMed and Cochrane and performed multivariate meta-analysis with meta-regression on the reported infections. Randomized controlled trials and prospective and retrospective observational studies including patient registry studies were analyzed, combined as well as separately.We excluded studies focusing on viral infections only.ResultsInfections were not reported in a standardized manner. Meta-analysis showed significant heterogeneity that persisted after forming subgroups by study design and follow-up duration. Overall, the pooled proportions of patients experiencing an infection during a study were 0.30 (95% CI, 0.28-0.33) and 0.03 (95% CI, 0.028-0.035) for any kind of infections or serious infections only, respectively. We found no potential predictors that were consistent across all study subgroups.ConclusionsThe high heterogeneity and the inconsistency of potential predictors between studies show that we do not yet have a complete picture of infection risk in RA patients using biological or targeted synthetic drugs. Besides, we found non-serious infections outnumbered serious infections by a factor 10:1, but only a few studies have focused on their occurrence. Future studies should apply a uniform method of infectious adverse event reporting and also focus on non-serious infections and their impact on treatment decisions and quality of life.
AB - IntroductionThe advent of biological and targeted synthetic therapies has revolutionized rheumatoid arthritis (RA) treatment. However, this has come at the price of an increased risk of infections. The aim of this study was to present an integrated overview of both serious and non-serious infections, and to identify potential predictors of infection risk in RA patients using biological or targeted synthetic drugs.MethodsWe systematically reviewed available literature from PubMed and Cochrane and performed multivariate meta-analysis with meta-regression on the reported infections. Randomized controlled trials and prospective and retrospective observational studies including patient registry studies were analyzed, combined as well as separately.We excluded studies focusing on viral infections only.ResultsInfections were not reported in a standardized manner. Meta-analysis showed significant heterogeneity that persisted after forming subgroups by study design and follow-up duration. Overall, the pooled proportions of patients experiencing an infection during a study were 0.30 (95% CI, 0.28-0.33) and 0.03 (95% CI, 0.028-0.035) for any kind of infections or serious infections only, respectively. We found no potential predictors that were consistent across all study subgroups.ConclusionsThe high heterogeneity and the inconsistency of potential predictors between studies show that we do not yet have a complete picture of infection risk in RA patients using biological or targeted synthetic drugs. Besides, we found non-serious infections outnumbered serious infections by a factor 10:1, but only a few studies have focused on their occurrence. Future studies should apply a uniform method of infectious adverse event reporting and also focus on non-serious infections and their impact on treatment decisions and quality of life.
KW - Biological
KW - Heterogeneity
KW - Infection
KW - Meta-analysis
KW - Meta-regression
KW - Rheumatoid arthritis
KW - Targeted synthetic drugs
UR - http://www.scopus.com/inward/record.url?scp=85162992150&partnerID=8YFLogxK
U2 - 10.1007/s40744-023-00571-z
DO - 10.1007/s40744-023-00571-z
M3 - Article
C2 - 37365454
SN - 2198-6576
VL - 10
SP - 1147
EP - 1165
JO - Rheumatology and Therapy
JF - Rheumatology and Therapy
IS - 5
ER -