Myopic corneal ring with central accommodating portion

Abstract

A bio-compatible corneal ring for myopic correction and accommodation for presbyopia. The corneal ring is made from a bio-compatible material with a lens body having an inner and outer circular edge. The inner circular edge forms an opening in the lens body. The posterior surface of the lens body has a uniform radii of curvature between the inner and outer circular edges. The anterior surface has two radii of curvatures providing for correction of myopia. The first radii of curvature extends from near the outer circular edge to a junction point before the inner circular edge. The second radii of curvature extends from the junction point and continues to the inner circular edge. The inner and outer circular edges have a thickness of less than about 0.020 mm, but preferably are about 0.010 mm or less.

Description

[0001] This application is a continuation of U.S. Ser. No. 10 / 610,000, filed Jun. 30, 2003, which is a continuation of U.S. Ser. No. 10 / 053,178, filed Oct. 7, 2001, now U.S. Pat. No. 6,623,522, and claims priority thereto.FIELD OF THE INVENTION [0002] The field of this invention relates to prosthetic implants designed to be implanted in the cornea for modifying the cornea curvature and altering the corneal refractive power for correcting myopia and accommodating for presbyopia. BACKGROUND OF THE INVENTION [0003] It is well known that anomalies in the shape of the eye can be the cause of visual disorders. Normal vision occurs when light passes through and is refracted by the cornea, the lens, and other portions of the eye, and converges at or near the retina. [0004] In a myopic or near-sighted eye, the cornea is too steeply curved for the length of the eye. This curvature causes light rays to converge at a point before it reaches the retina. Distant objects, therefore, appear out-of-...

AI Technical Summary

Benefits of technology

[0010] The corneal implant, when placed under a lamellar dissection made in the cornea (such as a corneal flap), to relieve tension of Bowman's membrane, alters the outer surface of the cornea to correct the refractive error of the eye. By relieving the pressure and subsequent implantation of the device, the pressure points which typically are generated in present corneal surgeries are eliminated, and hence reduces risk to patients of extrusion of implants. Unlike an implant placed in an intact cornea where corneal tissue can be deflected anteriorly or posteriorly leading to unpredictable refractive correction, proper relief of the pressure due to dissection of the Bowman's membrane ensures that all the corneal changes take place at the anterior surface.

[0014] The refractive index of the implant material should be in the range of 1.36-1.39, which is substantially similar to that of the cornea (1.376). This substantially similar refractive index prevents optical aberrations due to edge effects at the cornea-implant interface.

Problems solved by technology

It is well known that anomalies in the shape of the eye can be the cause of visual disorders.

However, with the loss of lens elasticity, the eye muscles cannot bend or focus the lens needed for clear vision of near objects.

Few persons of older age, however, are able to adjust to the use of contact lenses.

This is especially true as many older persons have trouble inserting and removing the contacts on a daily basis from their eyes.

Although these corneal implants attempt to correct for the myopic condition, they do not adequately accommodate for presbyopia.

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