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Extreme intraocular pressure and steroid-dependent iritis
Thomas W Samuelson1, Marshall J Huang, Christine L Larsen
1Minneapolis, Minnesota.
Journal of Cataract and Refractive Surgery
|December 27, 2022
Summary
This case study discusses managing elevated intraocular pressure (IOP) in a patient with chronic uveitis and juvenile rheumatoid arthritis. Aggressive medical therapy was required to control the high IOP, highlighting challenges in steroid-induced glaucoma management.
Area of Science:
- Ophthalmology
- Glaucoma Research
- Uveitis Management
Background:
- A 50-year-old female with a history of chronic polyarticular juvenile rheumatoid arthritis and uveitis presented with markedly elevated intraocular pressure (IOP) in the left eye.
- The patient required ongoing topical steroid therapy, which complicated IOP management, and had previously received a sub-Tenon injection of triamcinolone.
- Despite aggressive medical therapy, including acetazolamide and topical anti-inflammatories, the IOP remained elevated.
Purpose of the Study:
- To describe the management of a complex case of elevated intraocular pressure (IOP) in a patient with co-existing chronic uveitis and juvenile rheumatoid arthritis.
- To evaluate the effectiveness of intensified medical therapy in controlling steroid-induced glaucoma in a challenging clinical scenario.
- To discuss the interplay between chronic inflammation, topical steroid use, and intraocular pressure management.
Main Methods:
- A 50-year-old female patient with a history of chronic inflammatory conditions and topical steroid use was evaluated for refractory elevated intraocular pressure (IOP).
- The patient's medical regimen was optimized, including substitutions in topical steroids and the addition of multiple IOP-lowering agents.
- Ophthalmic examinations, including gonioscopy, intraocular pressure measurements, and optical coherence tomography (OCT) of the retinal nerve fiber layer, were performed.
Main Results:
- The patient presented with an intraocular pressure (IOP) of 44 mm Hg in the left eye, which showed only slight improvement with initial medical adjustments.
- Following substitution of loteprednol for prednisolone acetate and addition of brimonidine, nepafenac, and a latanoprost/netarsudil combination, the IOP in the left eye decreased to 31 mm Hg.
- Despite the reduction, the IOP remained elevated, necessitating continued aggressive medical management. Visual fields and optic nerve appearance were stable.
Conclusions:
- Managing elevated intraocular pressure (IOP) in patients with chronic uveitis and concurrent steroid use presents significant challenges.
- Intensified medical therapy, including a combination of anti-inflammatory and IOP-lowering agents, is crucial for controlling refractory glaucoma in such cases.
- Close monitoring of IOP and optic nerve health is essential in patients with complex inflammatory eye conditions requiring long-term steroid treatment.
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