Keratoconus

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Keratoconus Treatment

The condition known as keratoconus occurs when the cornea, the transparent, dome-shaped front surface of the eye, thins and eventually swells outward into a cone shape. Blurred vision and possible light and glare sensitivity are caused by a conical cornea.

Environmental and genetic factors are risk factors, but the causes are unknown. About 10% of keratoconus sufferers also have a parent who has the disorder.

Following are main risk factors:

  1. History of family member with keratoconus
  2. Habit of vigorous rubbing eyes
  3. associated certain conditions, such as retinitis pigmentosa, Down syndrome, Ehlers-Danlos syndrome, hay fever and asthma.

Diagnosis

To diagnose keratoconus, ophthalmologist will review your medical and family history and conduct an eye exam. Tests to diagnose keratoconus include:

  • Eye refraction to measure patient eyes to check for vision problems
  • Slit-lamp examination
  • Keratometry determines the basic shape of your cornea. High K readings are suggestive of Keratoconus.
  • Computerized corneal mapping.Special photographic tests, such as optical coherence tomography and corneal topography to record images of patient cornea to create a detailed shape map of cornea’s surface. The tests can also measure the thickness of your cornea.

Treatment for keratoconus depends on the severity of condition and how quickly the condition is progressing.

Mild to moderate keratoconus can be treated with eyeglasses or special contact lenses. Patients using rigid or scleral contact lenses need to make sure to have them fitted by an ophthalmologist with experience in treating keratoconus. Patients also need to have regular checkups to determine whether the fitting remains satisfactory.

Treatment

A process called corneal collagen cross-linking fortifies chemical bonds in the cornea by using UV light and a photosensitiser. The goal of the treatment is to stop ectasia, which is characterised by gradual and asymmetrical changes in corneal shape.

Advanced cases need surgery

Corneal inserts.  (intracorneal ring segments)

improve vision and support the cornea’s shape by flattening the cone.

Corneal inserts can lessen the need for a corneal transplant, restore a more normal corneal shape, and slow the progression of keratoconus. Contact lens fitting and tolerance may also be improved by this procedure. The procedure can be regarded as a temporary measure because the corneal inserts can be taken out if necessary.

Cornea transplant.

Patients will probably require a corneal transplant (keratoplasty) if they have severe thinning or corneal scarring.

A full-thickness corneal transplant is called penetrating keratoplasty. A full-thickness section of your central cornea is removed during this procedure, and donor tissue is used in its place.

The endothelium, the cornea’s inner lining, is preserved during a deep anterior lamellar keratoplasty (DALK). It helps prevent this vital inner lining from being rejected, which can happen with a full-thickness transplant.

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