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A randomised controlled trial of the clinical effectiveness, safety and cost-effectiveness of adalimumab in combination with methotrexate for the treatment of juvenile idiopathic arthritis associated…

Overview of attention for article published in Trials, January 2014
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Title
A randomised controlled trial of the clinical effectiveness, safety and cost-effectiveness of adalimumab in combination with methotrexate for the treatment of juvenile idiopathic arthritis associated uveitis (SYCAMORE Trial)
Published in
Trials, January 2014
DOI 10.1186/1745-6215-15-14
Pubmed ID
Authors

Athimalaipet V Ramanan, Andrew D Dick, Diana Benton, Sandrine Compeyrot-Lacassagne, Dalia Dawoud, Ben Hardwick, Helen Hickey, Dyfrig Hughes, Ashley Jones, Patricia Woo, Clive Edelsten, Michael W Beresford, The SYCAMORE Trial Management Group

Abstract

Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children. Children with JIA are at risk of inflammation of the uvea in the eye (uveitis). Overall, 20% to 25% of paediatric uveitis is associated with JIA. Major risk factors for development of uveitis in JIA are oligoarticular pattern of arthritis, an age at onset of arthritis of less than seven years of age, and antinuclear antibody positivity. In the initial stages of mild to moderate inflammation the uveitis is asymptomatic. This has led to current practice of screening all children with JIA for uveitis. Approximately 12% to 38% of patients with JIA develop uveitis in seven years following onset of arthritis. In 30% to 50% of children with JIA-associated uveitis structural complications are present at diagnosis. Furthermore about 50% to 75% of those with severe uveitis will eventually develop visual impairment secondary to ocular complications such as cataract and glaucoma. Defining the severity of inflammation and structural complications in uveitis patients is now possible following Standardised Uveitis Nomenclature (SUN) guidelines, and modified to incorporate the consensus of end point and outcome criteria into the design of randomised trials. Despite current screening and therapeutic options (pre-biologics) 10% to 15% of children with JIA-associated uveitis may develop bilateral visual impairment and certified legally blind. To date, there remains no controlled trial evidence of benefits of biologic therapy.

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The data shown below were compiled from readership statistics for 203 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Canada 2 <1%
Brazil 2 <1%
Spain 2 <1%
Denmark 1 <1%
Germany 1 <1%
Unknown 195 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 32 16%
Student > Ph. D. Student 24 12%
Student > Master 23 11%
Student > Bachelor 21 10%
Other 13 6%
Other 40 20%
Unknown 50 25%
Readers by discipline Count As %
Medicine and Dentistry 91 45%
Pharmacology, Toxicology and Pharmaceutical Science 11 5%
Nursing and Health Professions 9 4%
Agricultural and Biological Sciences 7 3%
Biochemistry, Genetics and Molecular Biology 4 2%
Other 28 14%
Unknown 53 26%