Infections in Biological and Targeted Synthetic Drug Use in Rheumatoid Arthritis: Where do We Stand? A Scoping Review and Meta-analysis

被引:4
作者
Bergmans, Barbara J. M. [1 ,2 ,3 ]
Gebeyehu, Biniyam Y. [1 ,4 ]
van Puijenbroek, Eugene P. [5 ,6 ]
Van Deun, Katrijn [4 ]
Kleinberg, Bennett [4 ]
Murk, Jean-Luc [2 ,3 ]
de Vries, Esther [1 ,2 ]
机构
[1] Tilburg Univ, Tranzo Tilburg Sch Social & Behav Sci, Tilburg, Netherlands
[2] Elisabeth TweeSteden Hosp, Dept Med Microbiol & Immunol, Tilburg, Netherlands
[3] Elisabeth TweeSteden Hosp, Microvida, Tilburg, Netherlands
[4] Tilburg Univ, Tilburg Sch Social & Behav Sci, Dept Methodol & Stat, Tilburg, Netherlands
[5] Netherlands Pharmacovigilance Ctr Lareb, Shertogenbosch, Netherlands
[6] Univ Groningen, Groningen Res Inst Pharm, Groningen, Netherlands
关键词
Biological; Infection; Heterogeneity; Meta-analysis; Meta-regression; Rheumatoid arthritis; Targeted synthetic drugs; QUALITY-OF-LIFE; SERIOUS INFECTIONS; MEDICAL DICTIONARY; ECONOMIC BURDEN; RISK-FACTORS;
D O I
10.1007/s40744-023-00571-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1147 / 1165
页数:19
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