Uveitis Registries – A Digital Tool for Patient Care, Education, Research, and Collaboration

ABSTRACT

Purpose

Clinical registries are increasingly important in research and clinical advancement. This review explores and compares current uveitis registries and recommends future directions on how uveitis registries can complement one another for synergistic effect and benefit.

Methods

From a systematic search, 861 citations were screened for longitudinal, non-interventional, and multicenter uveitis-specific registries. Additional registries were identified via consultations with uveitis experts. Characteristics of all registries were analyzed and compared.

Results

Four registries were identified: Treatment Exit Options for Non-infectious Uveitis, AutoInflammatory Disease Alliance International Registry, Ocular Autoimmune Systemic Inflammatory Infectious Study, and Fight Uveitis Blindness!. Despite certain differences, these registries have the overarching goal of collecting large quantities of real-world, high-quality patient data to improve the understanding of uveitis.

Conclusion

The four uveitis registries share similar goals and collect clinical data from overlapping geographical regions. There is vast potential for collaboration, including data sharing to further augment datasets for analysis.

KEYWORDS:

• AIDA
• FUB
• OASIS
• registry
• TOFU
• uveitis

Acknowledgments

There are no acknowledgments nor funding details to declare.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

Dr Rupesh Agrawal is funded by National Medical Research Council (NMRC, Singapore) for his clinician-scientist [grant:CSAINV19nov-0007].