The present invention relates to devices for delivering an intraocular lens (IOL) into an eye and, more particularly, to IOL injector cartridges that reduce compressive stresses in IOLs while being delivered.
A cataract is a clouding of the eye's lens that impairs a person's vision and, if left untreated, causes blindness. Cataracts cause half of all cases of blindness and 33% of visual impairment worldwide. By age 80, more than half of all Americans have cataracts. As a result, each year approximately 1.4 million people in the United States alone undergo cataract surgery, whereby the clouded lens is removed and replaced with an intraocular lens (IOL) implant.
Intraocular lenses (IOLs) are commonly implanted in the eye as a replacement for the natural crystalline lens after cataract surgery. The IOL provides the light focusing function originally undertaken by the crystalline lens. Insertion of an IOL for the treatment of cataracts is the most commonly performed ophthalmic surgical procedure.
A typical IOL includes a disc-shaped optic or lens body for focusing light toward the retina of the eye. In addition, the IOL also includes one or more fixation members or haptics extending outward from the optic for securing and centering the IOL in the desired position within the chamber of the eye. The IOL is implanted directly into the eye through a small incision in a way that reduces trauma and expedites post-surgery healing. To fit through this small incision, modern IOLs are designed to be deformed, e.g., rolled, folded or the like, to a relatively small profile prior to insertion into the eye and then allowed to return to their original shape within the eye.
A useful technique for inserting an IOL into the eye includes use of an IOL injector. Injectors for delivering IOLs into the eye typically employ a syringe-like handpiece and a cartridge having a hollow injection tube or cannula through which the folded IOL is passed using a push rod. The cartridges are often made of disposable materials, such as plastics, and remain in a sterile package until ready for coupling with the handpiece, and may be pre-loaded with an IOL or not.
The cartridge injection tube includes a small diameter distal tip that is insertable into the incision within the eye. A push rod urges the IOL through the injection tube into the eye. The distal end of the cartridge is beveled into a sharp point that enables insertion through the corneal incision and facilitates expulsion and manipulation of the IOL into the capsular bag.
It is advantageous to only make a small incision in the eye when inserting an IOL. Accordingly, an injection tube that tapers to a small diameter tip is typically used. As the IOL progresses down the injection tube, increased force is needed. Many inserters use a screw-type device to advance the push rod for better mechanical advantage, though this involves a stop and start advancement as a proximal dial is rotated and re-gripped by the user in several discreet steps. Also, the IOL or the cartridge tip may be damaged during insertion due to push rod/IOL interaction or high compressive forces. Then, as the IOL is being expelled, the resistant force dramatically decreases. Consequently, the expelled IOL tends to pop open into place within the eye, and there is an increased risk of damaging the eye.
In view of the above, there is a need for a cartridge that requires less force to pass an IOL through and/or will create less compressive stress on the IOL.
The present application provides an intraocular lens (IOL) injector cartridge for receiving and delivering an intraocular lens having an optic to the inner eye, comprising a main body extending along a longitudinal axis from a proximal opening for receiving the intraocular lens to a distal end which defines a distal opening smaller than the intraocular lens through which the intraocular lenses expelled. The main body may have a narrowing lumen extending from the proximal opening to the distal opening, wherein the lumen further has a discontinuity or step formed in a midsection thereof and extending longitudinally for at least 0.2 cm, such as 0.2-0.5 cm, whereby the discontinuity or step facilitates a stress-optimized spiral rolling-up or folding of the optic of the intraocular lens.
Another IOL injector cartridge disclosed herein has a main body extending along a longitudinal axis from a proximal opening for receiving the intraocular lens to a distal end which defines a distal opening smaller than the intraocular lens through which the intraocular lenses expelled. The main body has a funnel portion with a plurality of axial grooves formed in an outer surface thereof, the axial grooves being spaced apart around the outer surface.
A still further IOL injector cartridge has a main body extending along a longitudinal axis from a proximal opening for receiving the intraocular lens to a distal end which defines a distal opening smaller than the intraocular lens through which the intraocular lenses expelled. The main body has a narrowing lumen extending from the proximal opening to the distal opening, wherein the lumen defines a luminal shape at the distal end which deviates from an oval of equivalent aspect ratio with a tension ΣH of 1.2 on top/bottom and a tension ΣW of 1.4 on each side. This results in a luminal shape at the distal end of the cartridge which deviates from a standard oval of equivalent aspect ratio such that the luminal shape is larger than the standard oval between equatorial points.
IOLs as disclosed herein may have one or more of the attributes described above.
Features and advantages of the present invention will become appreciated as the same become better understood with reference to the specification, claims, and appended drawings wherein:
The present application discloses a number of improvements to the prior art IOL cartridge 20, as will be explained. It should be understood that though the improvements are discussed separately in sequence, one or more can easily be combined in one IOL cartridge. Furthermore, the advances inherent in these improvements may be applied to a variety of IOL cartridges other than the illustrated embodiment.
As best seen in the sectional view of
It is also important to note that these are merely examples, and there are many ways to increase the flexural capacity of the funnel portion 72. For instance, a material modification coupled with grooves 74 of lesser depth (e.g., 20% or more of the thickness) of the grooves 74 may also work. Also, non-linear grooves 74 or grooves that are non-uniform around the funnel portion 72 are contemplated. For instance, grooves 74 having a teardrop shape along the axial direction may enable the flexure and thus compressive stresses to be better controlled. Also, any grooves 74 should be contoured to avoid sharp corners which act as stress risers and potential sites for cracking under the highest stresses. Ultimately, one goal is to ensure more uniform flexure along the funnel portion 72 as the IOL passes through, which in turn exerts uniform compressive stress on the lens. Smoothing spikes in such stresses may require a more nuanced shape for the funnel portion 72, and various solutions are possible. 3D modeling and the use of FEA techniques will likely be used to fine tune these flexures/stresses.
The ribbed/grooved funnel portion 72 provides support to the portion of the cartridge experiencing high outward stresses to ensure that there is not excessive flexure resulting in rupture of the material during lens delivery. Though some such flexing could be produced simply by thinning the funnel wall, the risk of rupture is also increased. Moreover, by simply thinning the cartridge wall in the funnel portion 72 a thin-walled mold is required, which would be difficult because of the need for an increase in the packing pressure of the mold. The grooves/ribs in the funnel portion 72 of the cartridge allow the molded material to maintain its ductility in the section of the cartridge in which there is sometimes brittle cracking. It is the increased packing pressure needed to mold a very thin part that induces residual stress in the cartridge, making the tip material more brittle. The ribbed/grooved funnel portion 72 provides flexibility without introducing such negative effects.
Initially, as seen in
Providing the discontinuity or step 92 thus facilitates folding of the IOL 94 by camming one facing edge underneath the other. Prior art cartridges mostly have inner lumens that are symmetric across the central vertical plane which causes the optic to fold symmetrically about the vertical plane at the mid-section of the optic during the compression stage of delivery. When the free side edges of the IOL come into direct contact, just after section 10B, they briefly cause high compressive forces within the optic. A geometric stiffening of the optic occurs as the opposite side edges of the optic body meet, and this geometric state will increase resistance to further deformation as the plunger rod pushes the optic forward. Modeling indicates that the optic must in fact buckle before it can advance further, leading to a spike in the applied force required to push the optic forward. Typically, one free edges or the other is ultimately forced to fold under, whereupon the IOL continues down the cartridge lumen and is fully folded. However, the high compressive forces at the point at which the free edges contact each other sometimes leads to damage of the optic, such as surface defects, or even damage of the wall of the cartridge. Sometimes, the optic even becomes stuck within the cartridge lumen because of the symmetric folding. Removing this behavior could result in a smoother transition from the optic being held in the flat state to it being full compressed in the inserter tip, and removal of the spike in applied force could enable development of a push style insertion device that would involve a single continuous forward motion for delivery rather than the intermittent stops required in a screw-type device as a dial is rotated and re-gripped by the user in several discreet steps.
Providing a simple surface feature on the internal lumen of the cartridge such as the step 92 provides a positional offset for each edge of the IOL optic, camming one edge inside the other, with one side being biased upwards by approximately 0.1 mm and the other biased downwards by an equal amount. This feature may develop along a longitudinal midsection of the cartridge and then recedes, as will be seen below, such that the proximal and distal segments of the cartridge lumen have a left/right mirror symmetry, but at the point where the optic edges would otherwise meet the feature is present and is at its maximum size with the greatest bias between the left and the right sides. As the IOL progresses beyond this point a spiral folding pattern will be affected in the optic cross-section, and this configuration will remain through the optic compression process while the inserter geometry gradually returns to a left/right symmetric shape.
The discontinuity or step 92 is expected to reduce the peak force that occurs during delivery, possibly enabling a constant linear push style delivery system and potentially reducing strain in the optic to enable a smaller final tip size and thereby a slightly smaller incision in the eye. Additional potential benefits include a reduction in surface damage or tears due to the reduction in localized strain in the regions where the optic folds as well as a reduction of the likelihood of delivery failures.
To better illustrate the particular placement of the discontinuity or step 92,
In practice, the step 92 should be approximately the same radial dimension as the thickness of the optic edge, which is larger in lower power lenses. IOL optics are typically biconvex, and thus the thicknesses at the axial center are greater than that at the outer edge. IOL optics have thicknesses at the axial center which typically range between 0.35-0.50 mm (sometimes up to 0.7 mm), and thus the thickness at the outer edge of the IOL optic is less than 0.35-0.70 mm. Accordingly, the radial dimension of the step 92 may be between 0.25 to 0.5 mm. While the present description anticipates that the haptics will be folded within the lens during insertion, the benefits of the inserter geometry described herein could also be recognized if either the leading or trailing haptic, or both, were not contained within the fold of the lens.
Alternatively, the step 92 may be formed by a single cam member that has a relatively short axial profile and acts as a sudden ramp at a location where the side edges of the IOL would otherwise collide head-on. The cam or step 92 must be located where the edges meet, not too soon or too late, or the camming effect will be negligible. The elongated nature of the illustrated step 92 is mainly a constraint of the manufacturing process. The cartridge is injection molded, and thus the internal surface has to have smooth transitions so that a) the material can flow in the mold cavity b) the part can be easily removed from the mold core and c) to avoid complex mold core designs. If other manufacturing techniques are considered such as 3D printing, then the step 92 could be more abrupt and without transitions. For instance, the “step” could be created by halting narrowing on one side of the central vertical plane while the other side continues to narrow. In such a case, the spiral would cause the lens on the side which is not narrowed to move to the outside of the other side.
The start location of the step 92 corresponds to the point at which the IOL optic free edges 96a, 96b meet, or slightly before they meet, and as such may vary depending on IOL optic diameter and configuration of the cartridge lumen 88. In general, the point at which the free edges 96a, 96b meet is when the circumference of the cartridge lumen 88 is about equal to a given IOL optic diameter, since the optic rolls upon itself to form a tube. IOL optic diameters range between 6-7 mm, and thus the central point along the longitudinal step 92 is where the circumference of the cartridge lumen 88 is between 6-7 mm. The end point of the step 92 is desirably after the free edges overlap by a minimum amount, such as 1-2 mm or by an angular amount such as 20-45°. Though the preferred start/stop is as described above, the start could be before the free edges abut and the stop could be beyond the overlaps cited.
In addition to reducing stresses and strains during IOL folding in the middle of the cartridge, it is important to also do so at the extreme distal end of the cartridge tip where the IOL is compressed to its maximum amount. During the process of inserting an IOL the optic is compressed through a small injector tip before delivery into the eye. The lens shape is biconvex in cross-section and typically inserter cross-sections are circular, which may result in significant variation in localized strain across the cross-section. The inventors have determined that there may be an optimal cross-sectional shape for the inserter such that strain across the lens when the lens is fully compressed in the tip is normalized across the cross-section.
Strain is a unitless expression, and in terms of strain on an IOL lens within a cartridge, a positive value means parts of the lens bulk are being stretched apart whereas a negative value means they are being compressed. Ideally, as a lens is pressed into a narrowing inserter tip, all regions of the lens will be undergoing compression and have negative strain. Instead, it has been found that some regions are in fact undergoing a stretching force, or tension. That is, strain is not all compressive and certainly not uniform across the lens midsection in a round lumen. Consequently, an inserter geometry that provides a more even strain distribution, where no parts of the cross-section are in a state of tension, is desirable.
The discontinuity or step 122 is again formed in the interior wall 128, projecting inward in generally oval-shaped lumen 130. The step 122 is formed as a V-shaped rib that extends longitudinally along the wall 129, gradually decreasing in profile until it disappears once again so that the lumen 130 is smooth. The step 122 extends axially along one side wall of the inner lumen 130 for a certain distance, with a minimum of at least about 0.2 cm
More particularly, the step 122 includes two curved faces 132, 134 on each side of an apex ridge 136. The step 122 may commence suddenly, and have a front or leading end transverse to the longitudinal axis through the cartridge 120, or the step may begin gradually such that the apex ridge 136 increases in size from nothing to a maximum, and then decreases as shown moving distally through the lumen 130. The two curved faces 132, 134 facilitate folding or curling of the IOL edges as the IOL is pushed through the cartridge 120, as described below with respect to
Initially, as seen in
The V-shaped step 122 may be symmetric such that the two curved faces 132, 134 on each side of an apex ridge 136 are identical in size and shape. However, to facilitate a first edge 142a folding under the second edge 142b, the left-hand face 132 is preferably steeper in angle than the right-hand face 134 so that the first edge 142a is cammed inward sooner, and dives under the second edge 142b. A similar result may be achieved by positioning the step slightly off-center. That is, the step 122 is symmetric or asymmetric in shape, and centered at the vertical midline or positioned off-center. Likewise, the slopes of each face 132, 134 may be planar, for a V-shaped step 122, or convexly curved for a more wave-shaped step. The term midsection as used herein may be read as referring to the general area at or near the vertical midline.
The illustrations show the second edge 142b essentially remaining in place at the point at which the edges abut, with all folding movement due to further movement of the first edge 142a. This is due to compressive forces within the lumen 130, and may change depending on the particular geometry of the step 122 or other factors.
It should be noted that the desired shape as in section
The process was to create an ellipse with an aspect ratio and then add an additional degree of freedom by allowing the curve to deviate (i.e., expand) from this construction curve in each quadrant. The aspect ratio is the proportion of the horizontal to the vertical dimension of the cross-section along the equatorial axes. The aspect ratio of the ellipse was first optimized, and then the final curve was created with a spline fixed to be tangent to the ellipse where it intersected with the horizontal and vertical axes but could deviate between those two points based on a start and an end tension. The cross-sectional shape was created in a SolidWorks CAD application as a parametrically defined set of four curves (ellipse quadrants) created with a spline with defined tensions on the top and side having start and end points coincident with the quadrants of the ellipse with a specified width and aspect ratio. This curve was then mirrored horizontally and vertically to create the final cross-sectional shape that was swept to create the internal geometry of the inserter. For any given aspect ratio and set of tensions the width of the tip was modified such that the internal cross-sectional area would match that of the nominal current inserter design. These parameters can represent a broad range of shapes, a subset of which includes circles and ellipses.
Evaluation of the nominal case and each design contender was performed with a simple 2-D plane stress finite element model in an MSC Marc Mentat application, where the lens cross-section was shrunk with a thermal load and then expanded back to the nominal size inside the constraint of a tip having the internal shape of the current design. The sidewall thickness was constant and equal to that of the nominal design. Both the major principal strain and the maximum principal shear value of strain were used as the optimization goals, the range and absolute maximum value of each was to be minimized.
The nominal circular case, with a 1.46 mm diameter and 1.67 mm2 cross-sectional area, showed a substantial variation in strain across the cross-section when a biconvex lens of approximately the same cross-sectional area as a current 20 diopter Tecnis IOL was compressed to fill it. It is believed that in an ideal situation the strain would have been consistent, with all sections of the lens under equal compressive strain. However, the major principal value of elastic strain was found to range from −0.486 to +0.813. That is, portions of the cross-section were placed into a state of tensile rather than compressive strain, and this effectively lessened the efficiency of the compression. The shear strain varied from 0.097 to 0.619.
After an optimization process using SolidWorks, as explained above, a cross-sectional shape was determined that resulted in a strain variation of −0.485 to −0.216, meaning that all portions of the lens were under compressive strain and the total range of strain had been reduced by approximately 80%. The peak shear strain was reduced substantially to 0.39, with a range of 0.012 to 0.39 representing a 35% reduction. This optimal shape had a width of 1.57 mm and a height of 1.31 mm (aspect ratio 1.2), a side tension of 1.4 and a top tension of 1.2. Again, these tensions are used to define in SolidWorks a spline curve relative to a regular elliptical shape. Of course, the ranges of aspect ratio, tensions or the size and position of the discontinuity may differ while still realizing relatively even compression and no tension. Therefore, an aspect ratio in the range of about 1.1 to 1.3 is believed suitable. Higher diopter lenses might perform better at an aspect ratio just above 1.4, however the surgeon needs to retain the ability to rotate the cartridge tip inside the wound without creating any additional stretching from a tip that is wider than it is tall. A higher aspect ratio might lead to more stretching in this case and therefore may not be preferable. Further, extending the range below 1.1 would not result in significant benefits as the geometry becomes functionally identical to a circular cross-section.
A graphical representation of one proposed geometry is seen in
After testing using the finite element model as explained above, more uniform stress in the simulated lens was seen with certain modified ovals. The modification is perhaps best expressed by looking at one quadrant of
The potential impact of this geometry in the cross-section of the inserter tip could be a reduction of the needed cross-sectional area of the tip, thereby reducing the incision size required for delivery, and it may also reduce possible damage to the lens because of the reductions in strain and shear that are exhibited on the lens during the delivery process.
While the invention has been described in its preferred embodiments, it is to be understood that the words which have been used are words of description and not of limitation. Therefore, changes may be made within the appended claims without departing from the true scope of the invention.
The present application claims priority to Provisional Application No. 63/266,932, filed on Jan. 19, 2022, the contents of which are expressly incorporated herein by reference.
Number | Date | Country | |
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63266932 | Jan 2022 | US |