scholarly journals Demographic Characteristics of Participants in Rheumatoid Arthritis Randomized Clinical Trials

2019 ◽  
Vol 2 (11) ◽  
pp. e1914745 ◽  
Author(s):  
Adrienne Strait ◽  
Francine Castillo ◽  
Sonam Choden ◽  
Jing Li ◽  
Evans Whitaker ◽  
...  
2006 ◽  
Vol 12 (Supplement) ◽  
pp. S43-S44
Author(s):  
Carlos Abud-Mendoza ◽  
L W Moreland ◽  
K Bahrt ◽  
J-C Becker ◽  
R Aranda ◽  
...  

2012 ◽  
Vol 4 (4) ◽  
pp. 213-223 ◽  
Author(s):  
Ennio Giulio Favalli ◽  
Francesca Pregnolato ◽  
Martina Biggioggero ◽  
Pier Luigi Meroni

Objectives: All biologic agents approved for the treatment of rheumatoid arthritis (RA) have been tested versus methotrexate (MTX) for efficacy on damage progression in several randomized clinical trials (RCTs), but direct head-to-head comparisons have never been conducted. The purpose of this investigation is to analyse data coming from main RA RCTs and to perform an indirect comparison. Methods: A systematic review of literature from 1988 to 2011 was conducted. Only randomized, double-blind, controlled, comparative trials, with evaluation of radiographic progression were included. The radiographic score was standardized and mean difference in the percentage of the annual radiographic progression rate was used as the effect measure. Heterogeneity between studies was estimated by I2 test. For each trial, the effect was plotted according to its standard error in a funnel plot. Results: Of 44 potentially relevant trials, 12 RCTs were included in the study. In order to optimize RCTs comparison, studies were stratified in early and late RA group. Main population characteristics were similar in both early and late RA groups, whereas the standardized baseline radiographic score value significantly differs among trials in both early (range 2.7–21.9) and late (range 23.46–75) RA groups. The standardized annual estimated progression is similar across the late RA group. Strong evidence of heterogeneity ( I2 = 97%, p = 0.00001) but no asymmetry of the funnel plot was observed in the early RA group. Total mean difference was −16.28 (95% confidence interval [CI] −24.42 to −8.14). For the late RA group a random model was used ( I2 = 99%, p = 0.00001) and a total mean difference of −39.25 (95% CI −53.77 to −24.73) was found. Conclusions: All biologic agents provide a favourable effect on disease progression both in early and late RA. The significant heterogeneity among various RCTs did not allow an effective comparison of the performance of biologic agents in each study.


2013 ◽  
Vol 53 (5) ◽  
pp. 419-430
Author(s):  
Marina Amaral de Ávila Machado ◽  
Alessandra Almeida Maciel ◽  
Lívia Lovato Pires de Lemos ◽  
Juliana Oliveira Costa ◽  
Adriana Maria Kakehasi ◽  
...  

2021 ◽  
Vol 97 (4) ◽  
pp. 113-119
Author(s):  
Maria N. Chamurlieva ◽  
Yulia L. Korsakova ◽  
Stefka G. Radenska-Lopovok ◽  
Tatiana V. Korotaeva

Biological disease-modifying anti-rheumatic drugs (bDMARDs) are widely used for the treatment of chronic inflammatory rheumatic diseases. Since the introduction of tumor necrosis factor alpha (TNF-) inhibitors, the treatment of rheumatoid arthritis has been revolutionized. The approach of targeting TNF- has considerably improved the success of the treatment of rheumatoid arthritis. Their effectiveness has been extensively proven in randomized clinical trials and in clinical practice. Randomized clinical trials and post-marketing studies proved that patients undergoing TNF- inhibitors therapy are at increased risk of infectious disease, bacterial, viral, fungal, opportunistic, oncology and skin adverse effects such as psoriasis and angiitis of the skin. In this case report drug-induced cutaneous vasculitis developing during TNF- inhibitor (Etanercept) treatment for rheumatoid arthritis is described.


2015 ◽  
Vol 35 (8) ◽  
pp. 1423-1430 ◽  
Author(s):  
Mercedes de Jorge ◽  
Sonia Parra ◽  
Jenny de la Torre-Aboki ◽  
Gabriel Herrero-Beaumont

2020 ◽  
Vol 3 (4) ◽  
pp. e203842 ◽  
Author(s):  
Joseph M. Unger ◽  
Charles D. Blanke ◽  
Michael LeBlanc ◽  
William E. Barlow ◽  
Riha Vaidya ◽  
...  

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