What Is Keratoconus?
Keratoconus, often referred to as “KC,” is a non-inflammatory eye condition in which the typically round dome-shaped cornea progressively thins and weakens, causing the development of a cone-like bulge and optical irregularity of the cornea.
This causes “static” in your vision and can result in significant visual impairment.
Keratoconus typically first appears in individuals who are in their late teens or early 20s, and may progress for 10to 20 years and then slow or stabilize. Each eye may be affected differently.
In the early stages of keratoconus, people might experience:
- Slight blurring of vision
- Distortion of vision
- Increased sensitivity to light
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.
In keratoconus care, early detection is critical because of the condition’s progressive nature. Your optometrist plays a key role in the diagnosis of keratoconus because the sooner they identify the signs and symptoms, the sooner they can refer you for treatment that can slow or halt disease progression to help preserve your vision.
- Can result in significant vision loss
- May lead to corneal transplant in severe cases
- Affects both males and females
- Affects all ethnicities
- 0% of people with KC have affected relatives
- People with Down syndrome are 20 times more likely to be affected
The American Academy of Ophthalmology Corneal Ectasia Preferred Practice Pattern recommends prompt referral of patients who have been diagnosed with progressive keratoconus by their optometrist to a trusted ophthalmologist who can perform corneal cross-linking.
What is iLink?
iLink™ corneal cross-linking is a minimally invasive outpatient procedure that combines the use of ultraviolet light and specially formulated eye drops to stiffen and strengthen corneas that have 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.
Is iLink™ Covered by Insurance?
The medical necessity of iLink™ has become widely recognized. As a result, commercial insurance coverage for iLink™ is now over 95% in the United States for covered lives.
Only iLink™ is approved by the FDA and is covered by insurance. Typically, non–FDA-approved procedures are not covered by insurance and have not been proven safe and effective.
- Creates new corneal collagen cross-links
- Results in a shortening and thickening of the collagen fibrils
- Leads to the stiffening of the cornea
Under the conditions used for iLink™ corneal cross-linking, specially formulated pharmaceutical-strength riboflavin eye drops called Photrexa ® (riboflavin 5’-phosphate ophthalmic solution) and Photrexa ® Viscous (riboflavin 5’-phosphate in 20% dextran ophthalmic solution) help enable the cross-linking reaction.
iLink™ corneal cross-linking applies an artificial source of UV light from a machine called the KXL ® System once the cornea has been soaked in the Photrexa ® and Photrexa ® Viscous eye drops.
This process works to stiffen the cornea by increasing the number of molecular bonds, or cross-links, in the collagen. Combining Riboflavin and UV Light Using Photrexa ® and Photrexa ® Viscous riboflavin eye drops, combined with ultraviolet light from the KXL ® system, the iLink™ procedure stiffens and strengthens the cornea to slow or halt progressive keratoconus
Is Cross-Linking Right for Me?
Patients who have been diagnosed with progressive keratoconus or corneal ectasia following refractive surgery should be promptly referred to an ophthalmologist who can perform corneal cross-linking.
Our practice partnerswith an ophthalmologist who performs iLink™ corneal cross-linking. This ensures that you can be confident thatyou are receiving the only FDA-approved cross-linking procedure.
Speak with your doctor about the risks and benefits of iLink™ to determine if it may be right for you.The goal of iLink™ is to slow or halt the progression of keratoconus to help preserve patients’ vision.
Typically, within 1 or 2 months after an iLink™ procedure, patients will return to their optometrist for ongoing monitoring and overall vision care.
Only iLink™ is approved by the FDA for the treatment of progressive keratoconus and backed by robust clinical studies. Other unapproved cross-linking procedures have not been rigorously studied and are not supported by the same standards of clinical efficacy and safety.
Additionally, non–FDA-approved cross-linking procedures may be associated with greater out-of-pocket costs for patients.