Sa544 THE BURDEN OF WORK PRODUCTIVITY AND ACTIVITY IMPAIRMENT IN CROHN'S DISEASE, ULCERATIVE COLITIS, PSORIASIS AND PSORIATIC ARTHRITIS

2021 ◽  
Vol 160 (6) ◽  
pp. S-543
Author(s):  
David Hudesman ◽  
Philip Mease ◽  
Mark Lebwohl ◽  
Anita M. Loughlin ◽  
Page C. Moore ◽  
...  
2020 ◽  
Vol 158 (6) ◽  
pp. S-442
Author(s):  
Sheri Volger ◽  
Ilia Tikhonov ◽  
Connie Lin ◽  
Christopher D. O'Brien ◽  
Colleen W. Marano ◽  
...  

2011 ◽  
Vol 14 (6) ◽  
pp. 859-861 ◽  
Author(s):  
Mercedes Vergara ◽  
Antònia Montserrat ◽  
Francesc Casellas ◽  
Albert Villoria ◽  
David Suarez ◽  
...  

2019 ◽  
Vol 47 (6) ◽  
pp. 568-578 ◽  
Author(s):  
L. S. Kruglova ◽  
A. N. Lvov ◽  
A. V. Kagramanova ◽  
O. V. Knyazev

Psoriasis and inflammatory bowel disease (IBD) are multifactorial chronic immuno-inflammatory potentially disabling disorders with similar genetic factors and immunological pathways, in particular, genetic polymorphisms of IL-23R, which determines the signal IL-12/23-mediated pathway of immunopathogenesis. The emergence of genetically engineered biological agents has changed the prognosis for both psoriasis and IBD. The intersection of the therapeutic spectrum in psoriasis and IBD is a very important point when choosing the management strategy for these patients. Infliximab and adalimumab are effective in the treatment of psoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitis (evidence level 1A). Ustekinumab demonstrates effectiveness in the treatment of psoriasis, psoriatic arthritis (evidence level 1A) and Crohn's disease (evidence level 1B). Etanercept and secukinumab have been shown to be effective against psoriasis, psoriatic arthritis (evidence level 1A) and ineffective and even associated with exacerbation risk in Crohn's disease and ulcerative colitis. Inhibition of regulatory cytokines IL-12/23 also has a number of advantages compared to the blockade of effector cytokines (TNF-α, IL-17) due to potentially long-term and stable treatment results and less frequent administration.


2012 ◽  
Vol 6 ◽  
pp. S115 ◽  
Author(s):  
F. Gomollón Garcia ◽  
Y. Gonzalez Lama ◽  
J. Hinojosa ◽  
M. Iglesias ◽  
M. Maroto ◽  
...  

2011 ◽  
Vol 25 (9) ◽  
pp. 492-496 ◽  
Author(s):  
David G Binion ◽  
Edouard Louis ◽  
Bas Oldenburg ◽  
Parvez Mulani ◽  
Arielle G Bensimon ◽  
...  

OBJECTIVE: To assess the effect of adalimumab on work productivity and indirect costs in patients with Crohn’s disease (CD) using a meta-analysis of clinical trials.METHODS: Study-level results were pooled from all clinical trials of adalimumab for moderate to severe CD in which work productivity outcomes were evaluated. Work Productivity and Activity Impairment Questionnaire outcomes (absenteeism, presenteeism and total work productivity impairment [TWPI]) were extracted from adalimumab trials. Meta-analyses were used to estimate pooled averages and 95% CIs of one-year accumulated reductions in work productivity impairment with adalimumab. Pooled averages were multiplied by the 2008 United States national average annual salary ($44,101) to estimate per-patient indirect cost savings during the year following adalimumab initiation.RESULTS: The four included trials (ACCESS, CARE, CHOICE and EXTEND) represented a total of 1202 employed adalimumab-treated patients at baseline. Each study followed patients for a minimum of 20 weeks. Pooled estimates (95% CIs) of one-year accumulated work productivity improvements were as follows: −9% (−10% to −7%) for absenteeism; −22% (−26% to −18%) for presenteeism; and −25% (−30% to −20%) for TWPI. Reductions in absenteeism and TWPI translated into per-patient indirect cost savings (95% CI) of $3,856 ($3,183 to $4,529) and $10,964 ($8,833 to $13,096), respectively.CONCLUSION: Adalimumab provided clinically meaningful improvements in work productivity among patients with moderate to severe CD, which may translate into substantial indirect cost savings from an employer’s perspective.


2020 ◽  
Vol 14 (Supplement_1) ◽  
pp. S460-S460 ◽  
Author(s):  
A Geldhof ◽  
S Volger ◽  
C B Lin ◽  
C O’Brien ◽  
I Tikhonov

Abstract Background Ustekinumab (UST) is indicated for psoriasis (PSO), psoriatic arthritis (PsA), Crohn’s disease (CD), and ulcerative colitis (UC). The recommended dose in CD/UC is generally higher than in PSO/PsA. No adverse pregnancy outcomes were observed in preclinical studies.1 Here we present pregnancy outcomes from spontaneous reporting, clinical studies and registries. Methods This dataset includes pregnancies with maternal exposure to UST during pregnancy or within 3 months prior to conception reported to the manufacturer through April 2019. Results Overall, 478 maternal pregnancies (334 PSO, 124 CD, 11 UC, 9 PsA) were identified. Mean maternal age was 30.5 years. Most pregnancies (71.3%) resulted in live births (LB, [including 20 preterm births; PTB]). Spontaneous abortion (SA) was reported in 18.4% of cases. Congenital anomalies (CA) were reported in 3.8% (3.3% major CA [MCA]). Pregnancies with UST exposure throughout gestation (12.1%) resulted in 55 (94.8%) LB including 4 (7.3%) PTB, and 5 (8.6%) MCA. Among pregnancies with exposure in Trimester 1 (66.5%), 207 (65.1%) LB including 11 (5.3%) PTB, and 2 (0.6%) MCA were reported. Among PSO/PsA maternal pregnancies, rates were 72.3% LB, 2.0% CA (1.4% MCA), and 16.9% SA; among CD/UC maternal pregnancies, rates were 68.9% LB, 4.4% MCA and 22.2% SA. Conclusion Pregnancy outcome data following maternal exposure to UST showed that the prevalence of live births, spontaneous abortions and congenital anomalies were consistent with the general population and TNFi therapies. Pregnancy outcomes in women with CD/UC and PSO/PsA were generally comparable. No apparent safety signals were noted with exposure throughout pregnancy. Reference


2008 ◽  
Vol 30 (2) ◽  
pp. 393-404 ◽  
Author(s):  
Margaret C. Reilly ◽  
Laetitia Gerlier ◽  
Yves Brabant ◽  
Martin Brown

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