AU720114B2 - Deformable intraocular lens injecting device - Google Patents

Deformable intraocular lens injecting device Download PDF

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Publication number
AU720114B2
AU720114B2 AU53098/96A AU5309896A AU720114B2 AU 720114 B2 AU720114 B2 AU 720114B2 AU 53098/96 A AU53098/96 A AU 53098/96A AU 5309896 A AU5309896 A AU 5309896A AU 720114 B2 AU720114 B2 AU 720114B2
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AU
Australia
Prior art keywords
lens
plunger tip
tip portion
apparatus according
portion
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Ceased
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AU53098/96A
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AU5309896A (en
Inventor
Vladimir Feingold
John R. Wolf
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Staar Surgical Co Inc
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Staar Surgical Co Inc
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Priority to US40353095A priority Critical
Priority to US08/403530 priority
Application filed by Staar Surgical Co Inc filed Critical Staar Surgical Co Inc
Priority to PCT/US1996/003409 priority patent/WO1996028122A1/en
Publication of AU5309896A publication Critical patent/AU5309896A/en
Assigned to STAAR SURGICAL COMPANY, INC. reassignment STAAR SURGICAL COMPANY, INC. Alteration of Name(s) of Applicant(s) under S113 Assignors: FEINGOLD, VLADIMIR, WOLF, JOHN R.
Publication of AU720114B2 publication Critical patent/AU720114B2/en
Application granted granted Critical
Anticipated expiration legal-status Critical
Application status is Ceased legal-status Critical

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/14Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
    • A61F2/16Intraocular lenses
    • A61F2/1662Instruments for inserting intraocular lenses into the eye
    • A61F2/1664Instruments for inserting intraocular lenses into the eye for manual insertion during surgery, e.g. forceps-like instruments

Description

This invention relates to a deformable intraocular lens injecting device for use with a lens cartridge. Specifically, the present invention is directed to the tip structure of a plunger of the deformable intraocular lens injecting device configured to prevent damage to a trailing haptic of a deformable intraocular lens loaded in the lens cartridge, which lens cartridge is loaded into the lens injecting device.

Staar Surgical Company of Monrovia, California has been actively producing and selling deformable intraocular lens since the early 1980s.

Dr. Mozzocco who affiliated with Staar Surgical Company invented and patented the first commercially successful deformable intraocular lens.

Dr. Mozzocco also developed a number of methods techniques) and devices for implantation of deformable intraocular lens.

Staar Surgical Company began distributing a deformable intraocular lens surgical implantation system in 1986, which included a device that 15 became known as the "Staar Shooter" for use with disposable plastic lens o cartridges. An example of the prior art "Staar Shooter" device is shown in Figures 34-40. It is important to note the plunger tip of this device was a cylindrical shaped, and had a flat circular end face, as shown in Figure 42.

*go• o o°° •o go• o* o ITO 28/4/98 WO 96/28122 PCT/US96/03409 The Staar Shooter device was used by surgeons in the United States and around the world in tens of thousands of deformable intraocular lens implantation surgical procedures.

Even though the "Staar Shooter" device performed very well and was highly accepted and used by practicing surgeons, the device could potentially be improperly operated. For example, in a small number of incidences, the trailing haptic of the deformable intraocular lens was damaged by being caught between the plunger tip and inner wall of the passageway through the lens cartridge during insertion. Specifically, there existed a small clearance between the outer diameter of the plunger tip and the inner wall of the passageway through the lens cartridge allowing the trailing haptic to potentially enter into a void space created by the small clearance, and then become wedged and further wedged as the plunger tip was forced through the passageway in the lens cartridge. The forces due to this wedging action were significant in some cases to cause permanent deformation of the trailing haptic due to tensile and shear stress applied to the trailing haptic.

Another potential for damage to the trailing haptic could occur with the "Staar Shooter", if the deformable intraocular lens was improperly loaded into the lens cartridge.

Specifically, the entire deformable intraocular lens including the trailing haptic needed to be loaded into the lens cartridge prior to loading the lens cartridge into the lens injecting device.

A surgeon or surgical support staff personnel could potentially improperly load the deformable intraocular lens with the trailing haptic at least partially extending out of the passageway of the lens cartridge. If the deformable intraocular lens was improperly loaded in this manner, the trailing haptic could easily be damaged by the tip of the plunger of the "Staar Shooter" by being caught between the circular edge of the end face of the plunger tip and the circular edge of the opening into the passageway. If the trailing haptic became caught in this manner and further force was applied to the plunger, the circular edge of the end face of the plunger tip and the circular end of the opening in the passageway could cut into the trailing haptic potentially permanently damaging the same.

These and other situations could potentially occur resulting in permanent damage to the trailing haptic. The resulting permanent damage to the trailing haptic is costly, since the damaged deformable intraocular lens must be discarded. Further, if the physician did not realize that the trailing haptic was actually damaged during insertion, the damage deformable 4- 4-00;10!1AM:PETER MAXWELL ASSOCIATES :612 92479945 4/ 16 3 intraocular lens must then be retrieved from the patient's eye potentially causing eye damage and complications.

According to the invention there is provided a deformable intraocular lens injecting apparatus for inserting a deformable intraocular lens into the eye through a relatively small incision made in the ocular tissue, said apparatus comprising: a body portion and a nozzle portion, said nozzle portion configured for insertion through the relatively small incision made in the ocular tissue, said nozzle portion having a lens delivery passageway extending therethrough, S 10 a plunger having a plunger tip movably disposed in said lens delivery passageway, said plunger tip being defined by a distal plunger tip portion extending to a proximal plunger tip portion, said distal plunger tip portion having a substantially constant transverse cross-sectional size and shape, said S. constant transverse cross-sectional size of said distal plunger tip being less 15 than a transverse cross-sectional size of said proximal plunger tip portion, said distal plunger tip portion having a sufficient length and configured to provide a sufficient side clearance space for accommodating the trailing haptic of the deformable intraocular lens, said side clearance space extending from a front edge of said distal plunger tip portion to said proximal plunger tip portion defining the clearance space between said distal plunger tip portion and an inner wall of said lens delivery passageway to accommodate the trailing haptic of the deformable intraocular lens to prevent damage to the trailing haptic during insertion, and said proximal plunger tip portion having a transverse cross-sectional size sightly less relative to a transverse cross-sectional size of said lens delivery passageway.

31/03/00 04/04 '00 TUE 11:20 [TX/RX NO 8186] 4- 4-00;10:19AM;PETER MAXWELL ASSOCIATES :612 92479945 5/ 16 4 The present invention is, therefore, directed to improved deformable intraocular lens injecting devices having specially designed plunger tip configurations each providing a side clearance between the plunger tip and inner wall of the lens cartridge to accommodate the trailing haptic of the deformable intraocular lens to prevent damage thereto during insertion.

The side clearance allows the end of the plunger tip to be placed in direct contact with the deformable intraocular lens when loaded in the lens cartridge without contacting or contacting the trailing haptic of the deformable intraocular lens in a manner that could potentially damage the same during 10 insertion.

The side clearance between the plunger tip and inner wall of the passageway through the lens cartridge allows the trailing haptic to be received or accommodated in the void space created by the side clearance in a manner that the trailing haptic is not subject to tensile or shear stresses during the 15 insertion mode. Specifically, the trailing haptic is accommodated so that it cannot be caught between the plunger tip and inner wall of the passageway through the lens cartridge that could potentially compress the trailing haptic by wedge action, twist the trailing haptic causing shear stresses inside the trailing haptic resulting in substantial strain and potential permanently deformation by exceeding the elastic limits of the material used to make the trailing haptic.

Further, the side clearance is preferable made to enclosed or captivate the trailing haptic to maintaining the trailing haptic in a certain configuration and again protect it during insertion.

The lens is inserted by lubricating the surface of a deformable intraocular lens with surgically compatible lubricant, and loading the deformable intraocular lens into a lens cartridge in 31103/00 04/04 '00 TUE 11:20 [TX/RX NO 8186] 4a the opened position. The lens cartridge is closed while condensing the deformable intraocular lens by a folding action into a shape so that it can be forced through the passageway in the cartridge. The lens cartridge is inserted into the lens injecting device with the plunger retracted.

The plunger is moved forward in a sliding manner by pushing the plunger forward while holding the lens cartridge still. This action forces the deformable intraocular lens from the lens holding portion of the lens cartridge into the nozzle portion. At this point the threads of the threaded end cap of the plunger engage with the threads of the threaded 0 90 a

S/

28/4/98 WO 96/28122 PCT/US96/03409 sleeve. The threaded end cap is rotate slightly to engage the threads. The device is now ready for the implantation process.

The nozzle portion of the lens cartridge is placed through a small incision in the eye.

The threaded end cap of the plunger is rotated or dialed to further advance the deformable intraocular lens forward through the nozzle portion and into the eye. The threaded end cap is further dialed to exposed the tip of the plunger within the eye and push the deformable intraocular lens into position. The tip can be used to also rotate the lens within the eye for positioning of the haptics.

BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a perspective view of one embodiment of the surgical implantation device according to the present invention with a lens cartridge positioned in the lens injecting device for implantation of deformable lens structures for placement in the eye.

Fig. 2 is a perspective view of the surgical implantation device shown in Figure 1 with the plunger retracted, and with the lens cartridge removed.

Fig. 3 is a side view of the surgical implantation device shown in Figure 2 with the plunger in the extended position.

Fig. 4 is a side elevational view of the surgical implantation device shown in Figure 1.

Fig. 5 is a detailed longitudinal cross-sectional view of the surgical implantation device shown in Figure 4.

Fig. 6 is a detailed transverse cross-sectional view of the surgical implantation device, as indicated in Figure Fig. 7 is a detailed end view of the surgical implantation device, as indicated in Figure Fig. 8 is an enlarged detailed left side elevational view of the tip of the plunger in the spacial orientation as shown in Figure 1.

Fig. 9 is an enlarged detailed end view of the tip shown in Figure 8.

Fig. 10 is an enlarged detailed top-planar view of the tip of the plunger.

WO 96/28122 PCITUS96/03409 Fig. 11 is an enlarged detailed right side elevational view of the tip of the plunger in the spacial orientation, as shown in Figure 4.

Fig. 12 is an enlarged detailed bottom view of the tip of the plunger in the spacial orientation, as shown in Figure 1.

Fig. 13 is a perspective view of a deformable intraocular lens for use in the present invention.

Fig. 14 is a perspective view of another type of deformable intraocular lens for use in the present invention.

Fig. 15 is a side view of the lens shown in Figure 13.

Fig. 16 is a perspective view of the lens cartridge shown in the open position to allow a deformable intraocular lens to be loaded therein.

Fig. 16A is another perspective view of the lens cartridge shown in the open position.

Fig. 17 is a rear end elevational view of the lens cartridge shown in the open position.

Fig. 18 is a front end elevational view of the lens cartridge shown in the open position.

Fig. 19 is a rear end elevational view of the lens cartridge shown in the closed position.

Fig. 20 is a front end elevational view of the lens cartridge shown in the closed position.

Fig. 20A is a detailed end view of the nozzle portion showing three slots of different length equally spaced about the circumference of the tip.

Fig. 20B is a detailed perspective view of the tip showing the three slots of different length.

Fig. 21 is a top planar view of the lens cartridge shown in the open position.

Fig. 22 is a side elevational view of the lens cartridge shown in the closed position.

Fig. 23 is a rear end elevational view of the lens cartridge shown in the closed position.

Fig. 24 is a broken away side view of the device showing the lens cartridge in relationship to the plunger in the retracted position.

WO 96/28122 PCT/US96/03409 Fig. 25 is a broken away side view of the surgical implantation device showing the lens cartridge in relationship to the plunger in a partially extended position.

Fig. 26 is a broken away side view of the device showing the lens cartridge in relationship to the plunger in a fully extended position.

Fig. 27 is a perspective view showing the device positioning a deformable intraocular lens within the eye.

Fig. 28 is a cross-sectional view of an eye showing the positioning of the deformable intraocular lens into position in the eye by the surgical implantation device.

Fig. 29 is a cross-sectional view of an eye showing the positioning of the deformable intraocular lens into a different position in the eye by the surgical implantation device.

Fig. 30 is a side elevational view of an alternative embodiment of the lens cartridge provided with a beveled tip.

Fig. 31 is a rear end elevational view of another alternative embodiment of the lens cartridge provided with grooves in the passageway to facilitate folding the deformable intraocular lens in an open position.

Fig. 32 is a rear end elevational view of another alternative embodiment of the lens cartridge provided with grooves in the passageway to facilitate folding the deformable intraocular lens in a closed position.

Fig. 33A is a front end elevational view of the nozzle portion of an alternative embodiment of the lens cartridge.

Fig. 33B is a front end elevational view of the nozzle portion of a further alternative embodiment of the lens cartridge.

Fig. 34 is a detailed side elevational view of another embodiment of the plunger tip contacting with the deformable intraocular lens inside the lens injecting passageway.

Fig. 35 is a detailed end elevational view of the plunger tip shown in Fig. 34.

Fig. 36 is a detailed side elevational view of a further embodiment of the plunger tip contacting with the deformable intraocular lens inside the lens injecting passageway.

Fig. 37 is a detailed end elevational view of the plunger tip shown in Fig. 36.

WO 96128122 PCT/US96/03409 Fig. 38 is a detailed side elevational view of an even further embodiment of the plunger tip contacting with the deformable intraocular lens inside the lens injecting passageway.

Fig. 39 is a detailed end elevational view of the plunger tip shown in Fig. 38.

Fig. 40 is a detailed side elevational view of another further embodiment of the plunger tip contacting with the deformable intraocular lens inside the lens injecting passageway.

Fig. 41 is a detailed end elevational view of the plunger tip shown in Fig. Fig. 42 is a detailed side elevational view of a prior art plunger tip.

Fig. 43 is a perspective view of a prior art lens injecting device.

Fig. 44 is a longitudinal side cross-sectional view of the prior art lens injecting device shown in Fig. 43.

Fig. 45 is a side elevational view of a prior art disposable plastic lens cartridge.

Fig. 46 is a longitudinal cross-sectional view of the lens cartridge shown in Fig. DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS A device according to the present invention comprises a deformable intraocular lens injecting device having a plunger tip configured to provide a side clearance between the plunger tip and inner wall of a lens injecting passageway.

The present invention can be applied to the plunger tip of a separate deformable intraocular lens injecting device to be used with a separate lens cartridge two-piece system such as disclosed herein), or can be applied to the plunger tip of an intraocular lens injecting device having a lens injecting passageway itself one-piece system such as disclosed in U.S. patent 5,275,604 to Rheinish, fully incorporated by reference herein).

A preferred embodiment of a deformable intraocular lens surgical implantation device 10 according to the present invention is shown in Figures 1-3. The surgical implantation device 10 comprises a lens cartridge 12 disposed within a lens injecting device 13. The lens injecting device comprising a lens injecting body 14 with a side receiver 15, and a movable plunger 16. In Figure 1, the side receiver 15 is defined by an opening 17 through the wall 9 of the lens injecting body 14 of the size and shape shown in Figures 1 and 2. The opening 17 is defined by parallel edges 17a, 17a, which are sufficiently spaced apart to allow the lens cartridge 12 to be loaded into the side receiver 15 of the lens injecting device 13, tapered edges 1 7b, clamping edges 17c, and stop edge 17d. In Figure 1, the lens cartridge 12 is positioned in the side receiver 15 between the clamping edges 17c with the plunger extending through the lens cartridge 12 in a position, for example, after a lens implantation procedure.

In Figure 2, the lens cartridge 12 is shown removed from the lens injecting device 13 with the plunger 16 in a retracted position for allowing the lens cartridge 12 containing a loaded lens and its haptic to be inserted within the lens injecting device 13. In Figure 3, the lens injecting device 13 is shown with the plunger 16 in the extended position without the lens cartridge 12 for purposes of illustration of the components.

The plunger 16 is fitted with a threaded end cap 18 at one end, and fitted with a tip 20 at an opposite end. The threaded end cap 18 is a °a :00 provided with a plurality of grooves 22 to a allow a person to tightly grip the cap 18 with his or her finger tips. The threaded end cap 18 is received i: within a threaded sleeve 24 of the lens injecting body 14. The threaded end cap 18 can be a separate component attached to the lens injecting device 13, or integral therewith, as shown in the construction is Figure The plunger 16 is installed within the lens injecting device 13 in a manner to allow the plunger 16 to be reciprocated therein. In the illustrated embodiment, the plunger 16 is supported for sliding movement within the lens injecting device 13 by guide 26, as shown in Figures 5 and 6. The outer dimension of the guide 26 is approximately the same size as the inner dimensions of the lens injecting body 14 to allow the guide to be 28/4/98 inserted within the lens injecting body 14. During construction, the guide 26 is inserted within the lens injecting device 13, and locked into position by pin 28 inserted into a predrilled hole in both the wall of the lens injecting device 13 and guide 26. In an alternative embodiment, the guide 26 is deleted and the pin 28 is utilized to prevent rotation of the plunger 16 by the pin 28 riding along the flat side of the plunger 16, as shown in Fig. The cross-sectional shape of the plunger 16 as well as the shape of the inner surface of the guide 26 are approximately a half-circle, as shown in Figure 6. This arrangement prevents the plunger 16 from rotating within the lens injecting device 13 to maintain the orientation of the tip 20 relative to the lens injecting device 13 during operation.

The threaded end cap 18 is connected to the plunger 16 in a manner to allow the threaded end cap 18 to be rotated relative to the plunger 16.

For example, the left end of the plunger 16 (Figure 5) is provided with a 15 threaded extension 30, which is secured to the threaded end cap 18 by a •nut 32. Specifically, the threaded end cap 18 can be made with external *o threads 34 and a longitudinal centre bore 36 that ends on the right side of the threaded end cap 18 leaving an end wall 38.

The end wall 38 is provided with a hole slightly larger than the outer 20 diameter of the threaded extension 30 to allow the threaded end cap 18 to go freely rotate on the plunger 16 while being secured to the end of the 9 lO plunger 16. During construction, the nut 32 is inserted through the centre bore 36 and threaded onto the extension 30 to secure the threaded end cap 18 to the plunger 16. A curved end cap 40 is press fitted into the end 25 of the centre bore 36, and seal the centre bore 36 to prevent debris from entering therein during use. Alternatively, the threaded extension 30 can Ibe replaced with an interference type connection snap fit type) 28/4/98 11 between the modified extension and threaded end cap 18 to facilitate quick assembly.

The details of the tip arrangement are shown in Figures 8 to 12. The plunger 16 is manufactured with an extension 42 supporting tip 20. The tip 20 structure provides means for inserting the deformable intraocular lens into the eye and manipulating the lens within the eye after the insertion step. For example, the tip 20 is faceted in the manner shown in the figures. Specifically, the left side of the tip 20 shown in Figure 8 is provided with a flat surface facet 44, conical surface 46, and cylindrical surface 48. The right side of the tip 20 is provided with a concave surface facet 47, conical surface 46, and cylindrical surface 48. (See Figs 8 to The end face of the tip 20 is designed to push the lens into position once inserted into the eye. For example, the end face is defined by a concave cylindrical surface 52 shown in Figure 8.

15 Suitable deformable intraocular lens for use in the present invention o are shown in Figures 13 15. The deformable intraocular lens 54 shown in Figures 13 and 15 includes a lens body 56 with attachment means defined by a pair of haptics 58 each having one end anchored in the lens portion 56 and a free end for attachment to the eye tissue. The deformable 20 intraocular lens 60 shown in Figure 14 includes a lens body 62 and te *attachment means defined by a pair of lateral lobes 64 of the lens portion 62.

The details of the preferred lens cartridge 12 as shown in Figures 16 20. The lens cartridge 12 comprises a lens holding portion 66 extending to a transition portion 67 and an implantation nozzle portion 68. When the lens cartridge 12 is in a closed position, a continuous circular or oval 28/4/98 11a passageway of the same diameter extends through the lens holding portion 66 through the transition portion 67 and through the implantation nozzle portion 68. The lens cartridge 12 is preferably made of injection moulded plastic such as polypropylene. The lens holding portion 66 is defined by a fixed portion 70 and a movable portion 72. The fixed portion 70 is fixed relative to the implantation nozzle portion 68, and is defined by a tubular portion 74 and extension 76. The movable portion 72 is movable relative to the fixed portion 70 for opening and closing the lens holding portion.

The movable portion 72 is defined by a tubular portion 78 and extension 80. A hinge 82 is provided between the fixed portion 70 and movable portion 72. The hinge 82 is defined by reducing the thickness of the walls of the tubular portions 74 and 78 at the hinge 82, as shown in Figures 17, 18 and 19. The hinge 82 runs the length of the lens holding portion 66 to allow the extension 76 and 80 to be split apart, or brought together open and close, respectively, the lens holding portion 66.

The tubular portion 78 of the movable portion 72 is provided with a boo. sealing edge 84, which is exposed when the lens cartridge 12 is opened, as shown in Figure 16A, and seals with a similar sealing edge 86 (See Figure i 17) of the transition portion 67 when the lens cartridge 12 is closed.

The end of the nozzle tip 69 is provided with three equally spaced slots 87a, 87b and 87c of different length provided about the circumference thereof, as shown in Figures 20A and 20B. The slot 87a boeo positioned at the top of the nozzle tip 69 is the shortest, slot 87c on the right side of the nozzle tip 69 is the longest, and slot 87b on the left side is o o 25 of medium length. The slots 87a, 87b, 87c cause the lens 54 to rotate as it exits the nozzle tip 69.

28/4/98 WO 96/28122 PCTIUS96/03409 Other embodiments of the lens cartridge 12 according to the present invention are shown in Figures 30-33.

The lens cartridge 12 shown in Figure 30 is provided with a beveled tip 94 to facilitate entry of the tip through the incision in the eye during implantation. The beveled tip 94 can be set at approximately forty-five (45) degrees relative to the passageway through the lens cartridge 12.

The embodiment of the lens cartridge 12 shown in Figures 31 and 32 is provided with a set of grooves 96 provided inside the passageway therethrough. The grooves accommodate the edges of the lens being loaded into the lens cartridge 12 to facilitate bending of the lens.

Specifically, the edges of the lens are placed in the grooves 96 to prevent relative slippage of the edges with the inner surface of the passageway through the lens cartridge 12 when the lens cartridge 12 is being folded into the closed position.

The embodiments of the lens cartridge 12 shown in Figures 33A and 33B each have a nozzle portion 68' having an oval cross-section with slots 87' differently position as shown, respectively, again to facilitate entry through an incision in the eye. Alternatively, the crosssection can be two half circles set apart and connected together rather than oval.

The various features of the lens cartridges 12 shown in Figures 16-21 and 30-33 can be used in various combinations to achieved an optimum design for a particular application.

However, all of these features are typically considered improvements of the basic combination.

The components of the device 10, except for the lens cartridge 12, are preferably fabricated from autoclavable material such as stainless steel or from a disposable rigid plastic such as medical grade ABS or the like.

ALTERNATIVE PLUNGER TIP CONFIGURATIONS Additional embodiments of plunger tips are shown in Figures 34 to 41. These plunger tips all provide a side clearance between the plunger tip and lens insertion passageway to accommodate the trailing haptic.

WO 96/28122 PCT/US96/03409 In Fig. 34, a plunger tip 100 is shown contacting with the deformable intraocular lens 54 in the lens injecting passageway p while accommodating the trailing haptic 58b between plunger tip 100 and inner surface wall of the lens injecting passageway P.

The plunger tip 100 comprises a distal plunger tip portion 102 having a cylindrical shape and a proximal plunger tip portion 104 having a cylindrical shape, as shown in Figs.

34 and 35. The distal plunger tip portion 102 is offset a distance D from the proximal plunger tip portion 104 to provide a larger side clearance on one side of the distal plunger tip portion 102 than on an opposite side thereof. The orientation of the offset of the distal plunger tip portion 102 relative to the proximal plunger tip portion 104 can be varied to accommodate the trailing haptic due to its location and orientation inside the lens injecting passageway P depending on the folding technique and placement technique of the deformable intraocular lens inside the lens injecting passageway P. Further, the trailing haptic can be configured so as to at least partially wrap around the distal plunger tip portion 102. The cross-sectional shapes of the distal and proximal plunger tip portions can be varied.

In Fig. 36, a plunger tip 200 is shown contacting with the deformable intraocular lens 54 in the lens injecting passageway P while accommodating the trailing haptic 58b between plunger tip 200 and inner surface wall of the lens injecting passageway P.- The plunger tip 200 comprises a side groove 202 having an end portion 204 for accommodating the trailing haptic 58b, as shown in Figs. 36 and 37. The location of the side groove 202 around the periphery of the plunger tip 200 can be varied to accommodate the trailing haptic 58b due to its location and orientation inside the lens injecting passageway P depending on the folding technique and placement technique of the deformable intraocular lens 54 into the lens injecting passageway P.

The shape of the side groove 204 when viewing the side of the plunger tip 200 can be varied from rectangular to triangular, parallelogram shaped, curved edges, partial circular shaped and other suitable shapes. Further, the depth of the side groove 204 can be increased or decreased. In addition, the cross-sectional shape of the side groove 204 can be changed from half circle to rectangular, triangular, C-shaped, parallelogram and other suitable crosssectional shapes.

14 In Fig. 38, a plunger tip 300 is shown contacting with the deformable intraocular lens 54 in the lens injecting passageway P while accommodating the trailing haptic 58b between plunger tip 300 and inner surface wall of the lens injecting passageway P.

The plunger tip 300 comprises a side facet 302 having an end portion 304 for accommodating the trailing haptic 58b, as shown in Figs.

38 and 39. The location of the side facet 302 around the periphery of the plunger tip 300 can be varied to accommodate the trailing haptic 58b due to its location and orientation inside the lens injecting passageway P depending on the folding technique and placement technique of the deformable intraocular lens 54 into the lens injecting passageway P.

The shape of the side facet 304 when viewing the side of the plunger tip 300 can be varied from rectangular to triangular, parallelogram shaped, curved edges, partial circular and other suitable shapes. Further, the depth of the side facet 304 can be increased or decreased. In addition, the cross-sectional shape of the side facet 304 can be changed from half q circle to rectangular, triangular, C-shaped, parallelogram and other suitable cross-sectional shapes. The number of facets and type of facets can also be varied depending on the requirement for the particular lens injection 20 application.

In Fig. 40B, a plunger tip 400 is shown contacting with the deformable intraocular lens 54 in the lens injecting passageway P while accommodating the trailing haptic 58b between plunger tip 400 and inner ol surface wall of the lens injecting passageway P.

S 25 The plunger tip 400 comprises a cylindrical distal plunger tip portion 402 concentric with a cylindrical proximal plunger tip portion 404, as Xshown in Figs. 40 and 41. The location of the length of the cylindrical 28/4/98 14a distal plunger tip portion 402 can be varied. Further, the cross-sectional shapes of the distaland proximal plunger tip portions can be varied.

The end faces of the plunger tips in the embodiments shown in Figs.

34 to 41 are flat planar circular end faces. The configuration of these end faces can be varied to include one or more concave, convex, faceted, curved surface configuration and peripheral shapes depending on the particular lens injection application.

Se i o S

S

28/4/98 WO 96/28122 PCT/US96/03409 METHODS OF IMPLANTATION The surgical procedure begins by coating the lens with a surgically compatible lubricant, and loading the lens into the lens cartridge 12. For example, as shown in Figure 21, a lens 54 having a lens body 56, a leading haptic 58a is loaded into the lens cartridge 12 while a trailing haptic 58b remains trailing outside the lens cartridge 12 in the manner shown.

Specifically, the lens 54 is loaded downwardly into the opened lens cartridge 12 until it sits on the inner surfaces of the tubular portions 74 and 78, for example, with a pair of tweezers.

The outer circumferential surface edges of the lens 54 are held by edges 88 and 90 of the tubular portions 74 and 78, respectively. The rear edge of the lens 54 is placed approximately at the rear edge of the lens cartridge 12. The lens 54 is further manipulated to situate the haptics 58a and 58b in the manner shown. Specifically, haptic 54a is positioned in a leading position and the other haptic 54b is positioned in a trailing position outside the lens cartridge with respect to the direction of implantation, as indicated by the arrow.

Subsequently, the lens holding portion 66 of the lens cartridge 12 is closed about the lens 54 by forcing the extensions 76 and 80 together with his or her finger tips. The inner surfaces of the tubular portions 74 and 78 bend and fold the lens 54 when the extensions 76 and 80 are forced together, as shown in Figures 22 and 23. Due to the resilient nature of the deformable intraocular lens 54, the lens 54 conforms to the curved inner surfaces of the tubular portions 74 and 78 without damage thereto, as shown in Figure 23.

The lens cartridge 12 containing the loaded lens 54 is inserted between the edges 17a, 17a of the opening 17 into the lens cartridge receiver 15 of the lens injecting device 13. As the lens cartridge 12 is moved forward, the extensions 76 and 80 move past the tapered edges 17b, 17b and come to a stop position between the clamping edges 17c, 17c when front portions of the extensions 76 and 80 contact with the stop edge 17d. The clamping edges 17c prevent rotation of the lens cartridge 12 inside the lens injecting device 13.

The user pushes the threaded end cap 18 forward while securing the lens injecting body 14 from movement, forcing the plunger 16 forward within the lens injecting device 13.

As the plunger 16 is moved forward, the tip 20 enters into the rear of the lens cartridge 12 and misses the trailing haptic 58B until the tip makes contact with the loaded lens 54, as 16 shown in Figure 24. As the plunger 16 is moved forward in this manner, the lens 54 previously lubricated, is forced into the implantation nozzle portion 68 of the lens cartridge 12, as shown in Figure Once the deformable intraocular lens 54 enters the implantation nozzle portion 68, the threads of the end cap 18 contact with the threads of the sleeve 24 stopping further movement of the plunger 16 forward in this manner. The end cap 18 is slightly rotated to engage the threads of the end cap 18 with the threads of the sleeve 24. At this point, the surgical implantation device is ready for the implantation step. The nozzle tip 69 of the nozzle portion 68 is inserted through the incision 92 in the eye 94, and the end cap 18 is rotated to continue the forward movement of the plunger 16 by continued rotation of the end cap 18 relative to the lens injecting body 14 to expel the lens from the nozzle tip 69 into the interior of the eye, as shown in Figure 26. This manner of screw advancement for moving the plunger 16 forward provides for precise control and accuracy concerning forcing the lens 54 through the remaining portion of the tip 68 -be into the eye during the implantation procedure. The deformed lens after o exiting the nozzle portion 16 returns to its original configuration, full size and fixed focal length.

After the lens is inserted into the eye, the end cap 18 is further rotated to fully expose the tip 20 of the plunger 16, as shown in Figures 28 and 29, to allow the lens to be pushed forward, side manipulated to rotate too: the lens, and pushed down to properly position the lens within the eye ocwithout the aid of other surgical instruments.

25 The configuration of the tip 20 is important during the implantation process. The faceted tip 20 provides a clearance between the tip 20 and 4 the inner surface of the passageway through the lens cartridge 12 to 28/4/98 16a accommodate the trailing haptic 58b during movement of the lens within the lens cartridge 19, as shown in Figures 25 and 26. Specifically, there exists a sufficient clearance between the flat surface facet 44 and the inner wall of the passageway through the lens cartridge 12. During the implantation process, the trailing haptic 58b floats around in the space between the extension 42 of the tip 20 and the inner wall of the passageway, as shown in Figure 25. This prevents any chance of damage to the trailing haptic, for example, by being caught between the tip 20 and the lens 54 during b o E. a too 28/4/98 WO 96/28122 PCT1US96/03409 the implantation process. The leading haptic 58a moves through the passageway unimpeded during the implantation process preventing any damage thereto.

Claims (13)

  1. 4- 4-00;10:19AM;PETER MAXWELL ASSOCIATES :612 92479945 B/ is 18 THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:- 1. A deformable intraocular lens injecting apparatus for inserting a deformable intraocular lens into the eye through a relatively small incision made in the ocular tissue, said apparatus comprising: a body portion and a nozzle portion, said nozzle portion configured for insertion through the relatively small incision made in the ocular tissue, said nozzle portion having a lens delivery passageway extending therethrough, a plunger having a plunger tip movably disposed in said lens delivery passageway, said plunger tip being defined by a distal plunger tip portion extending to a proximal plunger tip portion, said distal plunger tip portion i having a substantially constant transverse cross-sectional size and shape, said constant transverse cross-sectional size of said distal plunger tip being less than a transverse cross-sectional size of said proximal plunger tip portion, said distal plunger tip portion having a sufficient length and configured to provide a sufficient side clearance space for accommodating the trailing haptic of the deformable intraocular lens, said side clearance space extending from a front edge of said distal plunger tip portion to said proximal plunger tip portion defining the clearance space between said distal plunger tip portion and an inner wall of said lens delivery passageway to accommodate the trailing haptic of the deformable intraocular lens to prevent damage to the trailing haptic during insertion, and said proximal plunger tip portion having a transverse cross-sectional size sightly less relative to a transverse cross-sectional size of said lens delivery passageway. 31/03100 04/04 '00 TUE 11:20 [TX/RX NO 8186] 4- 4-00;10:19AM;PETER MAXWELL ASSOCIATES 612 9 2 47 99 45 7 1 6 19 2. An apparatus according to Claim 1, wherein said proximal plunger tip portion is cylindrical. 3. An apparatus according to Claim 2, wherein said distal plunger tip portion is cylindrical. 4. An apparatus according to Claim 3, wherein said cylindrical distal plunger tip portion is aligned relative to said cylindrical proximal plunger tip portion.
  2. 5. An apparatus according to Claim 3, wherein said cylindrical distal plunger tip portion is located off-axis relative to a centered longitudinal axis of said cylindrical proximal plunger tip portion. 6 An apparatus according to Claim 1, wherein said distal plunger tip *5*4 portion is provided with a groove to provide side clearance to accommodate the trailing haptic of the deformable intraocular lens.
  3. 7. An apparatus according to Claim 6, wherein said distal plunger tip portion is cylindrical.
  4. 8. An apparatus according to Claim 7, wherein said proximal plunger tip portion is cylindrical.
  5. 9. An apparatus according to Claim 8, wherein said cylindrical proximal plunger tip portion and said cylindrical distal plunger tip portion have a constant outer diameter. 31/03100 04/04 '00 TUE 11:20 TX/RX NO 8186] 04/04 '00 TUE 11:20 [TX/RX NO 8186] 4- 4-00;10:19AM;PETER MAXWELL ASSOCIATES ;612 92479945 8/ 16 S C C An apparatus according to Claim 1, wherein said distal plunger tip portion is provided with a flat side facet.
  6. 11. An apparatus according to Claim 10, wherein said distal plunger tip portion is cylindrical.
  7. 12. An apparatus according to Claim 11, wherein said proximal plunger tip portion is cylindrical.
  8. 13. An apparatus according to Claim 12, wherein said cylindrical distal plunger tip portion and said proximal plunger tip portion have a constant diameter.
  9. 14. An apparatus according to Claim 1, wherein the lens injecting apparatus is defined by at least two separate components including a lens injecting device having a lens cartridge receiver and a lens cartridge. An apparatus according to Claim 14, wherein said lens cartridge includes a lens holding portion connected to said nozzle portion.
  10. 16. An apparatus according to Claim 1 or Claim 15, wherein said lens delivery passageway is provided with at least one groove.
  11. 17. An apparatus according to Claim 16, wherein said lens delivery passageway is provided with a pair of opposed grooves. 31103/00 04/04 '00 TU 11:20 TX/RX NO 8186] 04/04 '00 TUE 11:20 [TXIRX NO 8186] 4- 4-00;10!19AM;PETER MAXWELL ASSOCIATES 612 92479945 9/ 16 21
  12. 18. An apparatus according to any one of Claims 1, 16 and 17 wherein said lens delivery passageway includes an inwardly tapering portion. Dated this 31 day of March, 2000 STAAR SURGICAL COMPANY, INC Patent Attorneys for the Applicant PETER MAXWELL ASSOCIATES 4. 9' .9 99 9 9 .9 .9 9 i S. 9 9 S 9 9 9 9*99 9 9
  13. 999. *99* S *999 9 *.99 '9 9599 31103/00 04/04 '00 TUE 11:20 [TX/RX NO 8186]
AU53098/96A 1995-03-14 1996-03-13 Deformable intraocular lens injecting device Ceased AU720114B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US40353095A true 1995-03-14 1995-03-14
US08/403530 1995-03-14
PCT/US1996/003409 WO1996028122A1 (en) 1995-03-14 1996-03-13 Deformable intraocular lens injecting device

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AU5309896A AU5309896A (en) 1996-10-02
AU720114B2 true AU720114B2 (en) 2000-05-25

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EP (1) EP0957848A4 (en)
JP (2) JPH11506357A (en)
KR (1) KR100461880B1 (en)
CN (1) CN1185100A (en)
AU (1) AU720114B2 (en)
CA (1) CA2215182A1 (en)
WO (1) WO1996028122A1 (en)

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Also Published As

Publication number Publication date
JPH11506357A (en) 1999-06-08
WO1996028122A1 (en) 1996-09-19
CN1185100A (en) 1998-06-17
EP0957848A4 (en) 2001-05-02
KR19980702942A (en) 1998-09-05
JP2006297146A (en) 2006-11-02
KR100461880B1 (en) 2005-08-29
JP4317858B2 (en) 2009-08-19
EP0957848A1 (en) 1999-11-24
CA2215182A1 (en) 1996-09-19
AU5309896A (en) 1996-10-02

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