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Sjogren’s syndrome and severe ocular surface disease can make the eyes feel painfully dry, sensitive, gritty, and unstable. Vision may fluctuate because the tear film and corneal surface are not healthy enough to provide a clear optical surface. For selected patients, scleral lenses may help protect the ocular surface during wear and improve functional vision.
Dr. Edward Boshnick evaluates complex dry eye and ocular surface disease with attention to the tear film, cornea, eyelids, inflammation, previous treatments, and the patient’s ability to safely handle specialty lenses. Scleral lenses are not a replacement for medical dry eye care, but they may be an important part of a broader care plan.
Sjogren’s syndrome can reduce tear production and contribute to ocular surface inflammation. Patients may experience burning, foreign body sensation, redness, light sensitivity, blurred vision, mucus, eye fatigue, and difficulty tolerating contact lenses or windy environments.
Severe ocular surface disease can also occur with graft-versus-host disease, Stevens-Johnson syndrome, neurotrophic keratitis, exposure keratopathy, autoimmune disease, prior surgery, or chronic inflammation. These conditions require careful diagnosis and ongoing medical supervision.
Scleral lenses are custom gas-permeable lenses that rest on the sclera and vault over the cornea. Before insertion, the bowl of the lens is filled with preservative-free saline, creating a fluid reservoir over the front surface of the eye during lens wear.
Scleral lenses do not eliminate Sjogren’s syndrome or ocular surface disease. They may help manage symptoms and visual function for selected patients while the underlying condition is also treated.
The evaluation includes dry eye symptoms, systemic diagnoses, medications, previous treatments, contact lens history, pain or light sensitivity, and daily visual demands.
The cornea, conjunctiva, eyelids, tear film, and ocular surface staining pattern are evaluated because these findings influence lens safety, comfort, and wearing time.
Diagnostic fitting helps evaluate comfort, vault, landing, fluid reservoir, vision, and how the ocular surface responds. Severe ocular surface disease may require conservative wearing schedules and close follow-up.
Some patients also need prescription dry eye therapy, lid treatment, serum tears, punctal occlusion, systemic care, or co-management with a corneal specialist, rheumatologist, oncologist, or other physician.
The fitting process may take multiple visits. Patients need training in insertion, removal, cleaning, disinfection, filling solution, wearing time, and warning signs that require prompt attention. Follow-up visits are important because dry eye and ocular surface disease can change over time.
Some patients experience improved comfort and more stable vision during wear. Others may need additional ocular surface treatment before lens wear is successful. Dense scarring, active inflammation, infection risk, poor handling ability, or severe epithelial fragility may limit candidacy.
They may help selected Sjogren’s patients by protecting the ocular surface during wear and maintaining a fluid reservoir over the cornea. A specialty evaluation is needed to determine candidacy.
No. Scleral lenses do not eliminate Sjogren’s syndrome or the underlying autoimmune process. They may help manage eye comfort and visual function as part of a broader care plan.
Some patients with severe ocular surface disease from these conditions are evaluated for scleral lenses or prosthetic scleral devices. These cases require careful medical supervision and individualized fitting.
Fogging can be related to inflammation, tear debris, lens fit, solution issues, or ocular surface disease. Follow-up care helps determine whether the lens design, filling solution, or medical treatment plan should be adjusted.
This page is educational and is not a diagnosis or treatment plan. A specialty examination is needed to determine whether scleral lenses are appropriate for Sjogren’s syndrome or severe ocular surface disease.

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