ABSTRACT
Purpose
This review aims to provide an update on the clinical presentation, etiologies, complications, and treatment options in intermediate uveitis (IU).
Methods
Narrative literature review.
Results
IU affects all age groups with no clear gender predominance and has varied etiologies including systemic illnesses and infectious diseases, or pars planitis. In some instances, IU may be the sole presentation of an underlying associated condition or disease. Management of IU and its complications include administration of corticosteroids, antimetabolites, T-cell inhibitors, and/or biologics, along with surgical interventions, with varying degrees of effectiveness across literature. In particular, increasing evidence of the safety and efficacy of immunomodulatory agents and biologics has seen greater adoption of these therapies in clinical practice.
Conclusions
IU is an anatomical description of uveitis, involving intraocular inflammation of the vitreous, peripheral retinal vasculature, and pars plana. Various treatment options for intermediate uveitis are currently used in practice.
Acknowledgments
A.Y.T.T., B.K.B., K.L.Q.H, E.J.C., and V.G. report no conflicts of interest, financial, or propriety, in the subject matter or materials discussed in this manuscript. R.A. is supported by a grant from the National Medical Research Council (NMRC), Singapore, for the Clinician Scientist Award (CSA) from 2020 to 2023. He has not received funding for his work in this publication. The authors alone are responsible for the content and writing of this article. The final version of the article has been seen and approved by all authors.
Disclosure statement
No potential conflict of interest was reported by the author(s).