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UVESCREEN1: A randomised feasibility study of imaging-based uveitis screening for children with juvenile idiopathic
Sonali Dave1, Jugnoo S Rahi1,2,3,4,5, Harry Petrushkin2,4,6
1Population, Policy and Practice Programme, UCL GOS Institute of Child Health, London, United Kingdom.
Insights
Optical coherence tomography (AS-OCT) shows promise for detecting childhood uveitis in Juvenile Idiopathic Arthritis (JIA) patients, potentially improving surveillance and reducing the need for frequent, distant eye exams.
Area of Science:
- Ophthalmology
- Pediatric Rheumatology
- Medical Imaging
Background:
- Juvenile Idiopathic Arthritis (JIA) patients face unpredictable risks of anterior uveitis, a vision-threatening condition.
- Current surveillance involves frequent, often inconvenient, expert slit lamp examinations (SLE).
- Optical coherence tomography of the ocular anterior segment (AS-OCT) is a sensitive uveitis detection tool but not standard care.
Purpose of the Study:
- To assess the feasibility of a randomized controlled trial (RCT) comparing AS-OCT to SLE for uveitis surveillance in JIA.
- To gather proof-of-concept data for a larger-scale trial on AS-OCT efficacy.
Main Methods:
- A feasibility RCT involving 80 children (2-12 years) with recent JIA diagnoses.
- Participants randomized to AS-OCT or SLE surveillance.
- Outcomes include feasibility, clinical metrics, quality of life (PedsQL), and resource use.
Main Results:
- Feasibility metrics (recruitment, attrition) will be assessed.
- Clinical outcomes (uveitis diagnosis) at 12 months will be compared.
- AS-OCT findings will be compared to SLE ('gold standard') at 6 and 12 months.
Conclusions:
- This study will inform a larger RCT on AS-OCT's role in JIA uveitis surveillance.
- AS-OCT may offer a more convenient and effective alternative to current screening methods.
- Improved surveillance could lead to earlier detection and treatment of childhood uveitis.
Abstract:
Children with Juvenile Idiopathic Arthritis (JIA) are at a currently unpredictable risk of a blinding, often asymptomatic, co-existent eye disorder, anterior uveitis which requires prompt treatment. The unpredictability of this insidious disorder commits children with JIA to three-monthly expert clinical examinations in specialist eye centres often located far from their homes. Optical coherence tomography of the ocular anterior segment (AS-OCT) has been shown to be an acceptable, repeatable and sensitive modality for uveitis detection, but is not standard care. This feasibility randomised controlled trial (RCT) aims to inform a future full-scale RCT comparing current routine practice (expert slit lamp examination, SLE) to AS-OCT for the surveillance of uveitis in children at risk. Eighty children aged between 2 and 12 years old and diagnosed with JIA within the preceding year will be included. Participants with an existing diagnosis of uveitis, other ocular co-morbidities or those unable to complete examinations or provide informed assent will be excluded. Participants will be randomised to SLE (control) or AS-OCT (intervention) examination at a frequency consistent with the current national programme for childhood uveitis surveillance. Children in the intervention arm will also have standard examination at 6 and 12 months after study entrance. Outcomes of interest will be feasibility (recruitment and attrition rates), clinical metrics (proportion diagnosed with uveitis or other ocular disorders at 12 months after study entrance), quality of life outcomes (PedsQL), and resource use. Additionally, comparative analysis of AS-OCT versus SLE ('gold standard' reference testing) findings at 6 and 12 months for those in the intervention arm will provide the proof-of-concept data necessary to develop and undertake a larger scale trial. Trial registration: This trial has been registered with clinicaltrails.gov (NCT05984758).
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