An intraocular lens (IOL) is a lens implanted in the eye to treat large refractive errors. The IOLs usually consist of small optics with side structures to hold the lens in place. There are two types of IOLs. One type is inserted into the capsular bag replacing the natural crystalline lens. The other type, known as a phakic IOL is placed within the eye under the iris without removing the existing natural lens.
In the following description variations of exemplary embodiments will be described and illustrated; it is not intended to be an exhaustive description.
For purposes of clarity some descriptive and geometric designations are used. For the intraocular lens and its subparts as described herein, there is a front facing surface also referred to as an anterior (meaning facing outwardly of the eye) surface and an inner facing surface referred to as a posterior (meaning facing inwardly of the eye) surface. In general the term anterior means a direction toward the front or in front of some other part and the term posterior means a direction toward the back or behind some other part. The term “top” refers to the view looking down from above a lens as installed in the eye. The term “bottom” refers to the view looking up from below a lens as installed in the eye. The term “side” refers to the view looking horizontally from a side of the lens as installed in the eye. The term “horizontal” refers to the horizontal direction across the eye from side-to-side. The term “vertical” refers to the vertical direction of an eye from top to bottom. The term “edge” means looking in from the side, top or bottom, as the case may be.
The present invention is in the technology of the intraocular lens (IOL) in the particular aspect of that technology known as the posterior chamber phakic intraocular lens (IOL). In this technology, there are a plentitude of variables both for the function of the implant and for the means and method for its implantation. The present description of exemplary embodiments for the IOL configuration and for its method of implantation include but are not limited to the following:
1) A configuration for allowing flow of fluids between the posterior and anterior chambers of the eye, while avoiding increased risk of impeding visual acuity and the risk of increasing intraocular pressure:
2) A haptic assembly configuration and positioning of a plurality of the haptic assemblies to accomplish improved maintenance of the optic portion position aligned with the optical axis of the subject eye:
3) An embodiment of providing the haptic assemblies to extend radially angularly downwardly from the optic portion (exemplary range of about 5 degrees to 10 degrees) such that increased pressure by the sulcus contact will cause the haptic assemblies to lift the optic portion way from the crystalline lens to allow an accommodation of vision.
4) An embodiment that has an ovulated shape of the optic portion by reducing its vertical dimension which results in a smaller vertical height, less material to a lower total volume and bulk of material and a lesser vertical height such that it occupies less space when folded for insertion thereby allowing a smaller incision for the implantation process, but without any optical consequences.
5) The optic portion having a dark zone or light blocking surface as a ring around the outer diameter of the optic element of the IOL to reduce the optic element such as to block light rays on the periphery of the optic portion reducing glare and halos around lights as seen.
The optical axis OX defines the optical center of the optic element16, and as will be appreciated defines an axial center for the entire IOL 1. In the present embodiment, the surround ring 18 has a flattened portion 28 along its horizontal curvatures (at its top and bottom as seen in the figures) to flatten the circularity of the structure thereby reducing its height dimension and overall volume. The haptic bases 12 are attached to the optic portion 10 and extend symmetrically oppositely on each of the outer sides (left and right sides as seen in the figures) also referred to as the vertical sides or vertically extending sides. The haptic bases 12 in their upper and lower extension around the surround ring 18, thin to merge into the flattened portions 28 of the surround ring 18. The haptic assemblies 14 extend from the optic portion 10 (more specifically in this embodiment, from the haptic bases 12). There are four haptic assemblies 14. They each extend nominally along a radial line or radial axis RA (being a pair, RA1 and RA2 more detailed below). Each haptic assembly 14 comprises a spring element also referred to as a reversed undulation 30 which is constructed to functionally operate along its RA in resilient flexibility to compress or expand from an unflexed original posture. The reversed undulation 30 in the present exemplary structure comprises a pair of laterally oppositely extending portions each being an undulation and together defined as a reversed undulation. A first or lower undulation 32 extending to one side of the axis RA and a second or higher undulation 34 extending to the opposite side of the axis RA, the undulations 32 and 34 reconsidered to be nominally symmetrically opposite relative to the axis RA, although that symmetry need not be exact. In this embodiment it can be seen that the undulations 32 and 34 have sharp direction change in the nature of a bellows shape. The term bellows in this embodiment can be seen as having a distinct change of direction almost a fold point such as in a bellows flex, wherein at a point of direction change 35 like an elbow rotation is readily available to accept the compression and expansion. The reversed undulation 30 commences from the haptic base 12 extending away from the optical axis OX along the axis RA and then connects to a haptic pad 36. The haptic pad 36 has an end surface 38 also called a haptic pad sulcus surface, that is that surface 38 is where the pressure contact from the sulcus is imposed onto and released from the haptics The positioning of the haptic assemblies 14 is set to provide symmetrical interaction upon the IOL in use by the contact with the sulcus, and therefore they are positioned symmetrical around the IOL. That symmetry is defined by the radial axis RA as being a pair of the radial axes RA1 and RA2 which cross at the optical axis OX. The axes RA1 and RA2 each extend at a selected equal angular relationship AV to a horizontal axis HX and an angle of the right angle difference to vertical axis VX which run through the optical axis OX. That angular relationship may be selected according to any desired haptic posturing and interfunction of the haptic with contact to the sulcus as described in more detail below. Each of the haptic assemblies 14 therefore extend along the axes RA1 And RA2 in axial pairs outwardly such that they are arranged symmetrically as defining paired vertical haptic symmetry VHS and paired horizontal haptic symmetry HHS as indicated schematically in
The haptic assemblies have a thickness that will not allow bending or flexing about the thickness and therefore only the flexing about the undulations 32 and 34 that define the reversed undulation 30 is allowed by which the haptic pad 38 can be moved by the sulcus, that movement being allowed by the spring flexing of the undulations 26 and 28 and nominally along the axes RA1 and RA2.
This structure of the haptics 14 provides, through operation of the reversed undulation 30 the effect of offsetting rotational force vectors that can be imposed by the sulcus pressure. Thus, the possible rotation of the lens from rotational force vectors is to be offset by the oppositely extending undulations that make up the reverse undulation.
It can be further appreciated that the reverse undulations in
Now referring to an alternative embodiment described with relation to
With further reference to this embodiment, as best seen in
With reference to
Some commonly allowed, expected or ranges of operation and construction are: Diameter across the axis E-E′ from the haptic pad sulcus surfaces 38, about 14-15 mm.
Diameter of the optic portion 10 and 110 about 7 mm.
Diameter of the optic element 16 and 116 about 5 mm.
It is considered that the foregoing described exemplary embodiments can provide a diopter range of about −1 to about −30 and +1 to +10.
The structures described above especially with relationship to the haptic configuration provide significant improvements in available use. A major aspect of that improvement is the relatively long range of the reach of the haptic pad made available by the long range of compression given by the reversed undulations. The undulations extend a small distance from the radial axis RA while allowing a relatively long radial compression range. The radial movement of the haptic is strictly controlled along the radial axis RA, allowed by the oppositely facing undulations thus provides a major advantage by allowing application to a wide range of eye anatomy, in which one haptic configuration fits a greater range of sulcus sizes than has been previously possible with a single dimensioned design that required different size lenses to be selected from. In some cases the lens was too large and bulged too much forward or other when the lens was too small was not stable in its position and moved off axis, rubbing the crystalline lens, which caused cataract.
The foregoing Detailed Description of exemplary embodiments are presented for purposes of illustration and disclosure in accordance with the requirements of the law. It is not intended to be exhaustive nor to limit the invention to the precise form(s) described, but only to enable others skilled in the art to understand how the invention may be suited for a particular use or implementation. The possibility of modifications and variations will be apparent to practitioners skilled in the art. No limitation is intended by the description of exemplary embodiments which may have included tolerances, feature dimensions, specific operating conditions, engineering specifications, or the like, and which may vary between implementations or with changes to the state of the art, and no limitation should be implied therefrom. It is intended that the scope of the invention be defined by the Claims as written and equivalents as applicable.
Number | Date | Country | |
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62904640 | Sep 2019 | US |
Number | Date | Country | |
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Parent | PCT/US2020/037306 | Jun 2020 | US |
Child | 17584014 | US |