Keratoconus, often referred to as “KC,” is a sight-threatening eye disease in which the typically round dome-shaped cornea progressively thins and weakens, causing the development of a cone-like bulge and blurry or distorted vision. This can result in significant visual loss and may lead to a corneal
transplant if left untreated.
Symptoms
Keratoconus typically first appears in individuals who are in their late teens or early twenties, but can affect older adults too. Each eye may be affected differently. In the early stages of keratoconus, people might experience:
Mildly blurred vision
Frequent prescription changes
Excessive eye rubbing
Difficulty seeing at night
Frequent headaches
Vision that cannot be fully corrected with glasses or contact lenses
The cornea is responsible for focusing most of the light that comes into the eye. Therefore, abnormalities of the cornea, such as keratoconus, can have a major impact on how an individual sees the world, making simple tasks such as driving a car or reading a book very difficult.
Keratoconus:
Can result in significant vision loss
May lead to corneal transplant in severe cases
Affects both males and females
Affects all ethnicities with some studies showing higher incidence rates among Asian, black, and
Hispanic populations
10% of people with KC have affected relatives
An estimated 5-30% of people with Down syndrome are also affected by keratoconus
You can find more information at www.livingwithkeratoconus.com.
What Is iLink Corneal Cross-Linking?
iLink corneal cross-linking is the only FDA-approved cross-linking treatment for progressive keratoconus. It is a minimally invasive outpatient procedure that combines the use of ultraviolet light and specially formulated eye drops to stiffen and strengthen the cornea that has been weakened by disease or
refractive surgery. Cross-linking is considered the standard of care around the world for progressive keratoconus and corneal ectasia following refractive surgery.
Corneal Cross-Linking
Creates new corneal collagen cross-links
Results in a shortening and thickening of the collagen fibrils
Leads to the stiffening and strengthening of the cornea
Does Insurance Cover iLink Corneal Cross-Linking?
The medical necessity of FDA-approved iLink™ corneal cross-linking has become widely recognized. As a result, the procedure is covered by over 95% of commercial insurance providers.
For additional information on insurance coverage and to view the latest list of insurers that are known to have policies that cover cross-linking, visit the Insurance Information page on LivingwithKeratoconus.com.
What Technology Is Used At Whitsett Vision Group?
At Whitsett Vision Group, we use iLink cross-linking technology , the only FDA-approved technology to slow or halt the progression of keratoconus.
The iLink Procedure is performed with the KXL UVA irradiation machine and Photrexa drops. Photrexa eye drops are applied to the cornea, and then the KXL machine is used to administer ultraviolet (UV) light, which helps to stiffen and strengthen corneas weakened by keratoconus.
You will be awake during the procedure. The procedure itself typically lasts about an hour.
You will be given a mild oral sedative to help you feel relaxed, and numbing drops will be applied to your eyes.
Riboflavin eye drops will be applied to your eye, and then shine a specific type of UV light onto your cornea. This will be repeated several times in order to strength the collagen fibers in your eye.
After the procedure, you may experience increased sensitivity to light, and/or some mild discomfort that could be described as a gritty or burning sensation. This generally improves within a few hours.