JP6019064B2 - Ophthalmic surgical device for reaching tissue and performing capsulotomy - Google Patents

Description

  The present invention relates generally to tissue microsurgery, and more particularly to treatments and devices for reaching one tissue through another tissue layer and cutting or manipulating that tissue. For example, the procedure and device can be used to deliver an ophthalmic surgical device through the cornea to the membrane of the anterior lens capsule in the anterior chamber of the eye.

  Lens cataract is the leading cause of blindness worldwide, and surgical treatment with cataract removal is the optimal treatment. Cataracts are cloudiness that occurs in the lens of the eye or its envelope. If an opaque area occurs in the lens, the passage of light is hindered. It is assumed that the eye lens is transparent. If an opaque area occurs in the lens, such as a cataract, the lens must be removed surgically. If there is no lens in the eye, heavy corrective glasses are required to form an image on the net. However, the lens can be replaced with an artificial intraocular lens (IOL) to give better vision after removal of the cataract. There may be other reasons for replacing a lens that does not perform its function properly.

  Removal of the lens to replace the IOL is a surgical procedure that requires considerable accuracy. The lens is completely surrounded by a membrane called the capsular bag, so the surgeon must first open the sac in order to reach the lens. It is important to cut the sac in the right way. The capsular bag can be used to hold the IOL if the capsular bag is accurately cut and not damaged during removal of the cataract. IOL implantation requires the creation of a precisely centered, sized and shaped opening in the capsular bag for implant stability and optimal IOL function. It is very important to match the size of the opening of the lens capsule to the peripheral edge of the IOL. The surgeon's goal is to create a perfectly circular hole (eg 5.5 +/- 0.1 mm in diameter) in the sac that is exactly centered on the optical axis of the eye, with a tear or defect at the edge of the hole. It is to create in the state without. A tear or defect in the edge of the hole can make the capsule very weak and lose its ability to hold the IOL properly. Different IOL designs may require different diameters for the holes (eg, in the range of 4.5 +/− 0.1 mm to 5.75 +/− 0.1 mm), but what is the defined diameter? Whatever the case, for the proper outcome of cataract surgery, the accuracy of the surgeon in actually obtaining the hole is crucial. This is especially true for IOLs that are intended to provide complex optical and focusing functions.

  Creating an opening with this required level of accuracy in the capsular bag is a surgeon who controls and guides a traditional hand-held cutting instrument and attempts to follow a precise circular path on the capsular bag. This is a difficult task. Currently, to perform capsulotomy (creating an opening in the capsular bag), the surgeon typically manually creates a small tear in the anterior region of the capsular bag. In that case, the surgeon should be very careful to use a small needle-like capsulotomy and / or forceps to follow the circular path of a specific diameter centered on the optical axis of the eye. Try to expand the part. In practice, it often happens that the holes do not eventually become circular or accurate in diameter, or do not center on the optical axis. There may be radial tears at the edge of the hole that significantly weaken the capsule. As a result of these errors, the sac may not be able to properly hold the IOL and may not obtain optimal visual outcome.

  In addition to the difficulties faced by the surgeon by performing an accurate capsulotomy of the capsular bag when reaching the lens, the surgeon must also be able to reach the capsular bag itself. The lens is positioned in the anterior chamber of the eye. In order to reach the capsular bag, the surgeon must make an incision in the cornea and carefully insert a capsulotomy instrument through the incision. Of several microsurgical procedures that must pass through an incision in the first layer of tissue before it can reach the second layer of tissue behind or beneath the first layer of tissue. There is the same requirement for treatment. In order for a surgeon to manipulate a microsurgical instrument through a corneal incision, the incision must be large enough to accept such an instrument. However, the larger the incision, the greater the risk of infection, corneal distortion and other complications. Microsurgical instruments are generally not compact enough or simplified enough to make it difficult for the surgeon to minimize the size of the incision or, in some cases, an incision Risk of rupture or other damage at the site. During insertion, cutting elements or other sharp components may be exposed, requiring the surgeon to be very rigorous and causing collateral damage to the tissue when inserting the instrument through the incision Other risks arise. Furthermore, this insertion often requires multiple steps and may require complex manipulation of the instrument by the surgeon, leaving little room for error. Often, the instrument cannot be easily manipulated after insertion, and the surgeon may be forced to handle or move multiple discrete parts within a small space. Any of these problems can make it very difficult for the surgeon to reach the second layer of tissue behind the first layer, especially when the second layer is tissue in a very small area, such as in the eye. There is a possibility.

  In view of the shortcomings of existing therapeutic devices / procedures for reaching tissue such as the capsular bag and performing surgery, improved techniques and devices for performing microsurgery are required.

  Embodiments of the present invention include devices and methods for reaching the capsular bag through the cornea of the eye and performing a capsulotomy in the eye. The lens capsulotomy device includes a handpiece having a tip designed to be inserted into an incision in the cornea of the eye. The handpiece has a sliding element disposed therein and a suction cup is attached to the sliding element for movement into and out of the handpiece. A cutting element is attached to the suction cup. A compression mechanism associated with the suction cup and handpiece compresses the suction cup for placement through the tip. After inserting the tip of the device through the corneal incision, the compressed suction cup and cutting element can be ejected through the tip of the device with a single smooth motion and moved closer to the capsular bag. The suction cup and cutting element extend inside the anterior chamber to create an opening in the capsular bag.

  In operation, the surgeon compresses the suction cup and cutting element (eg, by manipulating a knob or other mechanism on the handpiece), and the surgeon places the tip of the capsulotomy device in the incision in the cornea of the eye (The tip of the capsulotomy device can also be inserted into the incision before the suction cup is compressed). The compressed suction cup is forced out through the tip of the handpiece and placed in the anterior chamber, where the suction cup extends inside the anterior chamber to a cutting position on the capsular bag. Suction can be applied to the suction cup to secure the cup to the capsular bag, pull the tissue of the capsular bag that contacts the cutting element of the suction cup, and cut a portion of the capsular bag (eg, a circular portion). Aspiration can then be reduced and the suction cup released from the capsular bag while the excised tissue fragment is still held by the suction cup while the device is removed. The device is withdrawn through the incision and removed from the eye. A cataract or other lens surgery can then be performed on the eye (ie, the lens can then be removed by the usual methods of cataract surgery).

  Other embodiments include a device and procedure for reaching a second layer of tissue behind the first layer of tissue and performing a microsurgery or therapeutic operation on the second layer, wherein the tissue is a lens It is not limited to sac or eye tissue. The surgical device includes a handpiece having a tip for insertion through an incision in the first layer of tissue and a sliding element disposed in the handpiece. A foldable structure (eg, a suction cup or other foldable device) is attached to the sliding element for movement into and out of the handpiece. A compression arm for compressing the foldable structure is positioned on the side of the foldable structure and associated with the handpiece. The manipulating mechanism operates the compression arm to compress the foldable structure through the tip of the handpiece and placed past the first layer of tissue. Once deployed, the foldable structure extends to an operable position on the second layer of tissue. Engage in microsurgery or treatment operations on the second layer of tissue using manipulable elements associated with the foldable structure. In some embodiments, the manipulable element is a cutting element used to cut a portion of the second layer of tissue.

  In operation, the surgeon applies pressure to the side of the foldable structure inside the device handpiece to compress the foldable structure (eg, by pushing a thumb or other handpiece mechanism). . The surgeon reaches the second layer of tissue behind the first layer of tissue (foldable structure) by moving the tip of the microsurgical device through the incision in the first layer of tissue. It is also possible to insert the tip of the device into the incision before the body is compressed). The procedure involves moving the sliding element in the handpiece into the tip and moving the compressed foldable structure through the tip of the handpiece and placing it past the first layer of tissue. To further include. Once deployed, the foldable structure spreads into a maneuverable configuration on the second layer of tissue. The surgeon then engages in microsurgery or therapeutic work on the second layer of tissue. In some embodiments, the microsurgical or therapeutic operation performed includes cutting a portion of the second layer of tissue (eg, using a cutting element associated with the foldable structure). Is included.

  These techniques allow surgeons to reach tissues such as the lens capsule and perform minimally invasive microsurgery on the tissues. A foldable structure / suction cup with a cutting element having a diameter greater than the length of the incision (eg, about 2 mm to 3 mm) (eg, about 5 mm to 7.5 mm) in the handpiece Because it can be compressed to a small size and smoothly placed through the tip of the handpiece, the surgeon can reach the capsular bag through a very small incision in a reversible manner. This minimizes the risk of infection and corneal distortion compared to previous techniques. During insertion of the device into the incision, the cutting element is protected within the device, avoiding collateral tissue damage and damage to the cutting element, or any element is placed with the device. Reaching the capsular bag requires only a smooth movement of placing a single suction cup with a compact and simplified device, reducing the amount of manipulation required for the surgeon to reach the tissue. The

1 is a top perspective view of a microsurgical / capsulotomy device with a suction cup in place according to an embodiment of the present invention. FIG. 1 is a top perspective view of a microsurgical / capsulotomy device when used in the anterior chamber of the eye, according to one embodiment of the present invention. FIG. 1 is a top perspective view of a microsurgical / capsulotomy device with a suction cup housed therein according to an embodiment of the present invention. FIG. 1 is an uncovered top perspective view of a microsurgical / capsulotomy device with a suction cup housed therein according to an embodiment of the present invention. FIG. 1 is an uncovered top view of a microsurgical / capsulotomy device with a suction cup housed therein according to one embodiment of the present invention. FIG. 1 is an uncovered top view of a microsurgical / capsulotomy device with a suction cup compressed, according to one embodiment of the present invention. FIG. 1 is an uncovered top view of a microsurgical / capsulotomy device with a suction cup compressed and moved into the tip, according to one embodiment of the present invention. FIG. 1 is an uncovered top view of a microsurgical / capsulotomy device with a suction cup in place according to one embodiment of the present invention. FIG. 1 is a partially exploded perspective view of a microsurgical / capsulotomy device with a suction cup in place according to an embodiment of the present invention. FIG. 1 is an exploded top perspective view of a microsurgical / capsulotomy device, with internal components also shown as an exploded perspective view, according to one embodiment of the present invention. FIG. 1 is an exploded perspective view of a portion of a compression arm and handpiece according to an embodiment of the present invention. 1 is an exploded perspective view of a sliding element and a compression arm according to an embodiment of the present invention. 1 is a top perspective view of a cutting element according to an embodiment of the present invention. FIG. 1 is a top perspective view of a cutting element in a molten (or made without tether) tether, in accordance with one embodiment of the present invention. FIG. It is a bottom perspective view of a suction cup according to an embodiment of the present invention. It is a section bottom perspective view of a suction cup by one embodiment of the present invention. FIG. 6 is a cross-sectional side view of another design of suction cup according to an embodiment of the present invention. FIG. 6 is a top perspective view of another design cutting element according to an embodiment of the present invention. FIG. 6 is an exploded top perspective view of another design of suction cup and cutting element including dual tubing, according to one embodiment of the present invention. FIG. 10 is a top perspective view of another design of a microsurgical / capsulotomy device with a suction cup housed, according to one embodiment of the present invention. FIG. 6 is a bottom perspective view of another design of a microsurgical / capsulotomy device with a suction cup in place, according to one embodiment of the present invention. FIG. 6 is a top perspective view of another design of a microsurgical / capsulotomy device with a suction cup in place, according to one embodiment of the present invention. 6 is a flow diagram illustrating preparation steps for a microsurgery / capsulotomy procedure according to one embodiment of the present invention. 6 is a flow diagram illustrating steps for a microsurgical / capsulotomy procedure according to one embodiment of the present invention. 6 is a flow diagram illustrating the continuation of steps for a microsurgery / capsulotomy procedure according to one embodiment of the present invention.

  The drawings depict only one embodiment of the invention for purposes of illustration. From the following description, it will be appreciated that alternative embodiments of the structures and methods shown herein may be used without departing from the principles of the invention described herein. Would be easily recognized by engineers.

Microsurgery / capsulotomy device This description describes an embodiment of the present invention in the context of a capsular surgery where a portion of the anterior surface of the capsular bag is cut. This technique can be used to treat cataracts by removing all or part of the lens in the lens capsule from the eye. The procedure can also be used to create a hole to reach into the lens capsule through which an artificial lens (eg, an intraocular lens or IOL) is implanted into the lens capsule. Although often described herein in terms relating to performing capsular surgery, the devices and procedures are not limited to capsular surgery, and include, among others, corneal surgery, glaucoma treatment, optic nerve microperforation. ), And may be useful for other eye treatments such as surgery involving the Descemet's membrane. In addition, the devices and procedures may be useful for delivery of pharmacological, biological and chemical entities and therapies. Devices and procedures can be used to deliver fluid in addition to aspiration, where delivery can be clearly localized (eg, with a suction cup) to limit exposure to only the desired tissue. In addition, the devices and procedures may be useful for industrial applications or other medical procedures other than the eye, such as procedures involving excision of sensitive membranes or tissue structures, perforations of the dura, etc. For industrial applications and the like, the device and procedure can also be used in vitro on tissue that has been excised and separated from the body. In these other types of applications, the procedures and devices generally function in the same manner as described for capsular surgery, but each component is arranged and sized differently to accommodate different tissues. And can be molded.

  FIG. 1 is a top perspective view of a microsurgical / capsulotomy device 1 with a suction cup / foldable structure 2 in place according to one embodiment of the present invention. Device 1 is designed to reach a second layer of tissue (eg, capsular bag) behind a first layer of tissue (eg, cornea) when performing microsurgery. The device 1 includes a handpiece 5 or structure with a housing that can be manipulated by a surgeon to perform a surgical procedure (eg, to perform a capsulotomy capsulotomy step). The handpiece includes a tip 3 for insertion through an incision in the first layer of tissue (eg, an incision in the cornea of the eye). The tip 3 is thin and simplified, and therefore the tip 3 can be easily slid into the tissue incision without tearing the incision or damaging the tissue. The tip 3 includes an opening 14 through which a foldable structure or suction cup 2 connected to the end of the shaft 19 can be placed. In FIG. 1, the handpiece 5 is shown as a long, generally cylindrical structure, but the handpiece 5 can take a variety of shapes and forms.

  The structure disposed through the tip of the handpiece 5 can be a suction cup 2 as shown in FIG. However, any other type of foldable, foldable or compressible structure that can be folded can be used. For example, the structure 2 can have other shapes necessary to function with a particular tissue type. Device 1 provides a mechanism for delivering any type or shape of foldable structure through a smaller opening to allow the device to be folded in an orderly manner. Thus, when referring to a “suction cup” throughout this description, it is possible to replace it with other types of foldable devices. Furthermore, the suction cup 2 shown in FIG. 1 is designed to be folded mainly along one axis, in particular, still flat inside the device 1 (as described in more detail below). It is mainly compressed horizontally while staying in a stable state. However, different suction cups or foldable structure types can also be compressed to fold along different axes or to be placed against various tissue types. In some embodiments, the suction cup is folded along only one axis, and in other embodiments, the suction cup is folded along more than one axis.

  The device 1 further comprises an operating mechanism comprising a knob 8 connected to the sliding part / sliding element 7 via a groove 9 in the housing of the handpiece 5, which is operated by the surgeon. By pushing the knob 8, it can be moved back and forth. A part of the sliding portion 7 is shown at the end of the handpiece 5 opposite to the tip 3. The surgeon can operate the knob 8 by reciprocating along the groove 9. As shown in FIG. 1, the groove 9 in the housing can restrict the movement of the sliding portion 7 to the foremost position and the last position. In some embodiments, a storage latch 12 holds the slide 7 in its shipping position prior to use. It is also possible to move components within the device using operating mechanisms other than knob 8, such as levers, buttons to be depressed, switches, rotatable knobs, flaps and the like.

  In use, the handpiece 5 can be connected to a hose that leads to a control system that provides air flow and suction (eg, via a hose barb 10). The handpiece 5 can also be connected to a wire leading to a control system that supplies current (eg, with an electrical connector 11) and performs electrical measurements. The device 1 further includes a lumen in the slide 7 so that fluid can be transferred from the hose barb 10 to the suction cup 2. The electrical connector 11 can also be connected to an electrical circuit in the lumen of the sliding portion 7. The lubrication holes 4 provide a viscoelastic (usually used inside the eye during cataract surgery) for the suction cup 2 and the passage through which the suction cup 2 slides. Appropriate lubricants can be applied. In some embodiments, all or part of device 1 is disposable.

  FIG. 2 is a top perspective view of the microsurgical / capsulotomy device 1 when used in the anterior chamber of the eye 100 according to one embodiment of the present invention. The portion of the eye 100 shown in FIG. 2 includes the sclera 102, cornea 101, iris 103, and capsular bag 104. The device 1 shown in FIG. 2 has been used by an ophthalmic surgeon to perform a capsulotomy, one of the steps typically performed in cataract surgery. The sac 104 is a transparent film that contains the lens of the eye 100. In FIG. 2, an incision 105 has been made through the cornea 101 by the surgeon. The insertion tip 3 of the device 1 has a narrow leading edge (13, see FIG. 3) for mechanically finding and entering the corneal incision 105. In FIG. 2, the tip 3 of the device 1 has already been inserted through the incision 105 of the cornea 101, and the suction cup 2 and the shaft 19 are pushed through the lumen of the insertion tip 3 (see FIG. 3, FIG. 3). ing. When the system applies suction through the hose barb 10, the capsular bag is forced against the suction cup 2 and the cutting element contained therein (shown in FIGS. 13, 14 and 18).

  A circular hole is drilled in the anterior capsule 104 so that the lens can be removed and the IOL can be inserted. In some embodiments, the diameter of the circular opening in the sac 104 or other tissue is about 5 mm to 7.5 mm. However, in other embodiments desired for various surgical procedures, other diameter openings can be created (eg, 1 mm, 2 mm, 3 mm, 4 mm, 8 mm, 9 mm, 10 mm, 15 mm, 20 mm, etc.). . A circular piece of excised membrane can be held in the suction cup 2 by suction and removed from the eye 100 together with the device 1. After the device 1 is removed from the eye 100, the excised tissue can be disposed of. The remaining capsular bag can be left intact, and therefore it has the structural health necessary to hold the IOL.

  In some embodiments, the device 1 does not include a cutting element. In such embodiments, the device 1 can include one or more other operable elements for therapeutic tasks. For example, the device 1 can include a tissue manipulation mechanism for grasping or manipulating tissue. As another example, the device 1 is a mechanism for ablating tissue, stretching tissue, conditioning tissue, stabilizing tissue, supplying fluid to tissue, or performing other operations on tissue. Can be included.

  FIG. 3 is a top perspective view of the microsurgical / capsulotomy device 1 in a housed configuration with the suction cup 2 housed inside, according to one embodiment of the present invention. In some embodiments, the device 1 is shipped to the customer in this retracted configuration to protect the suction cup 2 during shipment. The knob 8 is opposite to the proximal end of the device 1 in the groove 9 (as compared to FIG. 1 where the knob 8 is shown at the distal end of the groove 9 when the suction cup 2 is unrolled from the tip 3). At the end. The storage latch 12 is engaged with the detent (22, FIG. 5) at the sliding portion 7. The storage latch 12 is designed to prevent unintentional movement (e.g., during shipping), but to release under an intended force that exceeds a predetermined threshold. FIG. 3 also shows the leading edge 13 of the insertion tip 3 inserted through the tissue incision and the lumen 14 of the insertion tip 3 through which the suction cup 2 can enter and exit the device 1. .

  4 is an uncovered top perspective view of the microsurgical / capsulotomy of the lower half 5A of the housing of the hand piece 5 of the device 1 with the suction cup 2 housed therein, according to one embodiment of the present invention. FIG. The suction cup 2 is attached to the sliding portion 7 through the shaft 19 in the handpiece 5 so as to move in and out of the handpiece 5. The sliding part 7 was seen at the proximal end of the handpiece 5 opposite the suction cup 2 in FIGS. 1 and 3, but in FIG. FIG. 4 also shows a knob 8 attached to the sliding part 7 (attached through a groove 9 in the housing of the handpiece 5 as shown in FIGS. 1 and 3). The surgeon can apply force to the knob 8 and slide the knob 8 distally along the groove 9 to move the slide 7 distally within the handpiece 5. This causes the suction cup 2 to slide out through the tip 3 to position relative to the second layer of tissue in the first layer (eg, relative to the capsular bag in the anterior chamber). .

  FIG. 4 also shows a part of the compression mechanism associated with the suction cup 2 and the handpiece 5. In the design of device 1, the mechanism includes two compression arms 15 attached to an arm base 21 (shown in FIG. 5) designed to move relative to the handpiece 5 and the slide 7. The compression mechanism also includes a latch arm 18 (shown more clearly in FIG. 6) that surrounds the position where the knob 8 is attached to the sliding portion 7. Using a compression mechanism, the suction cup 2 is compressed to a smaller cross section between the distal end portions 16 of the compression arm 15, and as a result, after the distal end portion 3 is inserted into the tissue incision, the suction cup 2 is moved to the handpiece 5. It becomes possible to arrange | position through the front-end | tip part 3 of this. Since the suction cup 2 is compressed, it can easily pass through the tip without tearing the incision or causing damage to the incision. When the distal end 16 of the compression arm 15 is moved distally against the inclined surface 17 narrowing inside the side wall of the housing in the device 1, it is moved toward each other and compresses the suction cup 2.

  FIG. 5 is an uncovered top view of the entire microsurgical / capsulotomy device 1 with the suction cup 2 housed therein, according to one embodiment of the present invention. In FIG. 5, the compression mechanism comprising the arm base 21, the compression arm 15 and the latch arm 18 can be seen more clearly. In the design of FIG. 5, the arm base 21 is positioned around the sliding portion 7 so as to move along the sliding portion 7, but the arm base can be slid with respect to the sliding portion 7. It can also be designed by other methods (for example, the arm base can be connected to the sliding portion 7 so that it can slide in the groove of the sliding portion 7). The compression arm 15 is positioned on the side surface of the suction cup 2 and attached to the arm base 21. In the housed position of FIG. 5, the arm 15 is separated and does not contact the suction cup 2, and the knob 8 is positioned at the most proximal position in the latch arm 18 of the compression mechanism. FIG. 5 further shows a bent part 20 of the arm, where the arm 15 bends and moves the arm tip 16 toward each other to compress the suction cup 2. FIG. 5 also shows a detent 22 in the slide 7 where the storage latch 12 is engaged with the detent 22 in the stowed position in order to ship the device 1 safely. In FIG. 5 both electrical connectors 11A and 11B can be seen for supplying current to the cutting element of the suction cup 2 (where the cutting element is an electrical element).

  FIG. 6 is an uncovered top view of the microsurgical / capsulotomy device 1 with the suction cup compressed (2B), according to one embodiment of the present invention. When the knob 8 is moved by applying an external force, the knob 8 slides along the groove 9 on the outside of the handpiece 5 and inside the latch arm 18 on the inside. FIG. 6 shows a latch boss 27, which is an attachment receptacle through which the knob 8 is attached to the sliding portion 7. A latch boss projecting on both the top and bottom surfaces of the sliding portion 7 (only the top surface is shown) is located in the latch arm 18 at a position at the proximal end of the latch arm 18 (close to the arm base 21). To the distal end of the latch arm 18 (towards the insertion tip 3). This movement of the knob 8 (moving the latch boss 27 within the latch arm 18) moves both the sliding part 7 (including the suction cup 2) and the compression mechanism distally. The arm 15 slides distally within the handpiece 5 until it contacts the first portion 24 of the ramp 17 where the tip 16 of the arm 15 narrows. The inclined surface 17 presses the distal end portion 16 of the arm 15 inward toward each other, and compresses the suction cup 2. As the arm 15 continues to move distally, the tip 16 slides along the ramp 17 and is pushed further inward until the suction cup 2 reaches the end 23 of the narrow ramp 17 where it is fully compressed. It is. The arm base 21 contacts one or more arm stops 26 (eg, molded into the top and bottom housings of the handpiece 5) so that the compression mechanism is further within the device 1. Prevent moving.

  Since the suction cup 2 and the tip of the arm advance together, the surfaces of the inclined surfaces 17 that approach each other cause the arm 15 to move the arm 15 by a predetermined amount (for example, like tweezers) that compresses the suction cup 2 to a desired width. ) Push towards each other. Accordingly, there is no or limited frictional resistance against the elastomeric suction cup 2. If the suction cups 2 slide directly against the side walls approaching each other, friction can cause the suction cups 2 to deform rearward and prevent proper lateral compression. By using a rigid tweezer tip 16 between the approaching side walls and the suction cup 2, pure lateral compression is possible.

  FIG. 7 is an uncovered top view of the microsurgical / capsulotomy device 1 with the suction cup compressed (2B) and moved to the tip 3 according to one embodiment of the present invention. FIG. 7 shows the device 1 after changing the orientation of the arm latch 18 to release the grip on the latch boss 27. At this point, the knob 8 can still slide further along the groove 9 to move the slide 7 further distally, but the compression mechanism is such that the arm base 21 contacts the arm stop 26. To move further distally. The latch arm 18 includes an opening at the distal end, and after the arm 15 reaches the end of its travel range, the latch boss 27 (not shown here, connected to the knob 8) passes through the opening. It becomes possible to move. When the suction cup 2 is disposed in the distal end portion 3, the latch boss 27 can move through the opening and continue the movement of the sliding portion 7. It is at this point that the surgeon typically inserts the tip 3 through the corneal incision after the suction cup 2 is compressed and moved to the tip 3.

  FIG. 8 is an uncovered top view of the microsurgical / capsulotomy device 1 with the suction cup 2 in place according to one embodiment of the present invention. In this view, the elastomeric suction cup 2 has been fully deployed, unfolded and returned to its previous shape when it was housed. The sliding part 7 is moved distally. The most proximal end of the sliding part 7 wider than the remaining part of the sliding part 7 is in contact with the arm base 21. Therefore, the suction cup 2 cannot be moved further. The knob 8 is also shown fully moved to the distal end of the groove 9.

  FIG. 9 is a partially exploded perspective view of the microsurgical / capsulotomy device 1 with the suction cup 2 in place according to one embodiment of the present invention. This figure shows the various components of the device 1 in the deployed state and also shows both the upper half 5B and the lower half 5A of the housing of the handpiece 5. The latch boss 27 is moved distally away from the latch arm 18 and the knob 8 is moved to the distal end of the groove 9. The sliding part 7 is moved distally until it comes into contact with the arm base 21. Also seen is the bottom housing 5A with the sliding portion 7 and compression mechanism removed. A groove 28 in the bottom housing 5A allows movement of the latch boss 27 on that side of the device 1. Also seen in FIG. 9 is an arm stop 26 in the bottom housing 5A that prevents further movement of the arm base 21 after the suction cup 2 is fully compressed. Further, in FIG. 9, the bending position 20 of the arm can be seen more clearly.

  FIG. 10 is another exploded top perspective view of the microsurgical / capsulotomy device 1 with the internal components shown separated, according to one embodiment of the present invention. In this figure, the sliding part 7 and the compression mechanism are also separated from each other. In this embodiment, the sliding part 7 comprises a bottom half 7A and a top part with deep grooves 29, 30 for receiving a fluid suction lumen 31 and electrical conductors (eg wires, not shown). Has half 7B. The suction cup 2 and the shaft 19 are shown separately from the sliding portion 7 (although the suction cup 2, the shaft 19 and the sliding portion 7 can be a single part). 11 and suction component 10 are shown removed from device 1. Electrical pins 11 connect to deep grooves 29, 30 that can accommodate electrical wires therein. The hose connection unit 10 is connected to a fluid suction lumen 31 for performing suction on the suction cup 2.

  FIG. 11 is an exploded perspective view of a portion of the compression arm and handpiece according to one embodiment of the present invention. FIG. 11 shows a diagram of the components of the housing and compression mechanism to make their functions look better. The nail 34 in the upper housing 5B engages with the hole 35 in the lower housing 5A to facilitate assembly. The protruding storage latch feature 12 engages the detent (22, FIG. 12) at the slide 7 when the handpiece 5 is in its shipping configuration. Both the front edge 25 and the rear edge 32 of the arm attachment 21 are shown. A narrowed portion 33 of the housing to which the tip 3 connects is also shown.

  FIG. 12 is an exploded perspective view of the sliding element 7 and the compression arm 15 according to one embodiment of the present invention. FIG. 12 shows an illustration of the sliding portion 7 and the compression components until the sliding portion 7 is in a fully positioned configuration until the trailing edge 32 of the arm base contacts the leading edge 35 of the sliding portion base. It is shown to show how it can move through the lumen 34 inside the arm base 21.

Cutting Element and Suction Cup Design FIG. 13 is a top perspective view of the cutting element 50 according to one embodiment of the present invention. In the embodiment of FIG. 13, the cutting element 50 is an electrode that cuts the capsular membrane, but other designs are possible (eg, a sharp knife, or multiple sharp knives or teeth). In use, current can flow through rigid lead 53A, 90 degree arc lead 51A, electrode arc lead connection 52A and then into electrode ring 54. Half of the current flows clockwise around the ring 54 and half flows counterclockwise, leading to the connection 52B and entering the 90 degree arc lead 51B. Eventually, current flows out through the rigid lead 53B. This design advantageously allows the continuous ring 54 to be heated so that a portion of the tissue is evenly heated and disconnected. Since the current travels through the connection 52A to the ring 54 and travels in both directions along the ring 54 (current flows from one point of the ring through the ring in only one direction, so the tissue is not heated very uniformly The current is distributed evenly on both sides of the electrode (as opposed to a ring), heating the tissue more evenly. This is just one example of electrode configuration and current path. Several other designs can also be used.

  The rigid leads 53A, 53B, anchor tabs 56, 59, and 90 degree arc leads 51A, 51B can be overmolded with an elastomer (eg, silicone or polyurethane). The gap 55 separating the rigid leads 53A and 53B can be filled with an elastomer for overmolding, and a short circuit of current between the rigid leads 53A and 53B can be prevented. For fluid flow and suction, a lumen can be included in the rigid lead, and thus the lumen is usually not filled with an elastomer. The dissolvable tethers 57, 58 can be designed as very thin ligaments that harden the electrodes in order to treat the electrodes to maintain their shape prior to overmolding. After overmolding, a defined series of currents can be applied and the tether can be melted into an open circuit. Components with larger cross-sections are typically unaffected by the current required to melt the smaller cross-sectional tethers 57,58. This melting process can be performed at the factory prior to shipping. In order to ensure that each unit is properly manufactured, the voltage applied for quality control purposes, the resulting current, and the resistance (before and after) may be monitored and recorded. Optionally, the electrodes can be made without using a tether.

  FIG. 14 is a top perspective view of a cutting element with or without tethers 57, 58 removed according to one embodiment of the present invention. FIG. 14 shows the electrodes where the tethers 57, 58 have been blown away, leaving the non-conductive gaps 57x, 58x.

  FIG. 15 is a bottom perspective view of the suction cup 2 according to one embodiment of the present invention. The suction cup 2 has a roof 66 and an opening 60 in the center. The suction cup 2 also has an internal channel 61 delimited on both sides by an inner diameter (ID) wall 67 and an outer diameter (OD) wall 68. The electrode ring 54 is positioned on the other side of the OD wall 68.

  When the suction cup 2 faces the capsular bag 104 and suction is applied through the lumen 62, the pressure in the flow path 61 of the suction cup 2 can be reduced. Lumen 62 connects through a shaft 63, device 1 and hose barb 10 to a suction mechanism for applying suction. The outer diameter (OD) lip 64 and inner diameter (ID) lip 65 of the suction cup 2 can be pulled against the capsular membrane 104 to form a low leakage seal, and therefore the pressure in the flow path 61 is predetermined. It can be further reduced to the value of. A vacuum seal to the tissue can also be provided by aspiration. To allow the suction cup 2 to be fixed relative to the tissue, or to allow the tissue to be separated using a cutting element, portions of the tissue can be pulled further into the suction cup 2 by suction. The applied suction force can stretch the capsular membrane over the edge of the cutting element, creating a high tensile stress condition just on the circle where cutting is desired. During removal, suction can also be used to hold the cut portion of the tissue inside the device 1. Since the cutting element is directly incorporated into the device 1 that also provides suction capability, the device 1 can be used in a one-step procedure to perform a capsulotomy.

  The OD lip 64 of the suction cup 2 has a flare skirt-like design extending from the edge around the outer peripheral edge of the suction cup 2. The flare skirt shape allows the suction cup 2 to be supported on the curved surface of the sac 104 with a small force, and the suction cup 2 can be vacuum sealed against the sac 104 for a cutting procedure. It becomes possible.

  FIG. 16 is a cross-sectional bottom perspective view of a suction cup according to an embodiment of the present invention. Anchor tab 56 of cutting element 50 is embedded in the overmolded elastomer. A rigid lead 53B is shown inside the shaft 63 of the suction cup 2. The lead 53B is electrically connected to the electrode ring 54. In order to perform suction, the lumen 62 of the shaft 63 is connected to the flow path 61 of the suction cup 2.

  FIG. 17 is a cross-sectional side view of another design of suction cup 70 (eg, a central ridge or dual channel suction cup design) according to one embodiment of the present invention. FIG. 17 shows the exposed electrode ring 54 held by a supporting elastomeric ridge 71 located in the center of the channel 61. This creates two suction channels 73, 72, so that the capsular membrane 104 can be forced to extend over the edge of the electrode 54.

  FIG. 18 is a top perspective view of another design cutting element 200 according to an embodiment of the present invention. In use, current can flow from the rigid lead 53A through the connection lead 203A into the electrode ring 201. A portion of the current can travel around the ring 201 and the remaining portion can go through the gap material 204 to the connection lead 203B. The portion flowing through the gap 204 can be zero if the material of the gap 204 is not conductive. However, if the gap is sufficiently small, the cutting action of heat from the discharge can be designed to fill the gap so that a complete circular capsular piece is cut. If the gap material is conductive, the gap 204 will have the same power loss per millimeter of circumference that occurs around the ring 201 (by having the appropriate length, width and thickness). It can be designed to obtain a uniform heating and cutting action for a complete circle. Exemplary structures can include electroformed nickel or steel in rigid leads 53A and 53B and gap 204. The electrode ring 201 can be electroformed gold or nickel, or etched stainless steel. FIG. 18 also shows an anchor tab 202 similar to the tab 56 shown in FIG. In the embodiment of FIGS. 13, 15 and 18, the cutting element is a circular cutting element attached to the underside of the suction cup. However, in different types of surgical procedures where differently shaped incisions are desired in the tissue, the cutting element may take other shapes (eg, oval, square, rectangular, irregular and other shapes). Can take. Similarly, the suction cup can take other forms.

  Embodiments of device 1 can be used with electrical, mechanical, and combined electromechanical cutting elements, but other designs can be used. The electrical cutting element functions as a resistor. Very short electrical pulses heat the element quickly (eg, up to over 500 ° C., eg, 600 ° C., 700 ° C., 800 ° C., 900 ° C., 1000 ° C., 1200 ° C., 1500 ° C., etc.). In some embodiments, the heating process continues for several microseconds (eg, less than 10 microseconds), but in other embodiments the heating time may be different (eg, 1 microsecond, 5 microseconds, 10 microseconds). Seconds, 20 microseconds, 1 millisecond, 5 milliseconds, etc.). The duration of the discharge is too short for heat to travel more than a few microns by conduction from the cutting element, so for a few microseconds a thin layer of water trapped between the sac and the cutting element Absorbs energy and forms vapor. The vapor expands rapidly at high pressure, increasing the tensile stress in the sac until it is sufficient to tear the sac. Since the current is applied for only a few microseconds, it does not burn the tissue as in the case of ablation instruments, and therefore the device 1 causes the tissue to burn in the patient's eye, possibly incidental to adjacent tissue. The risks associated with damaging, applying heat very long, and other problems are avoided. Further, the electrical cutting element of device 1 differs from ablation devices that often require tweezers to remove the detached portion, completing the tissue separation and releasing the detached portion from the sac 104. Further, in some embodiments, the cutting element has a mass of less than 0.35 milligrams, thus eliminating the bulky heating elements typically found with cautery devices.

  If the cutting element is mechanical, the element has one or more extremely sharp micro teeth (or a knife or mechanism for cutting other tissues), and the micro teeth have a suction force past the teeth Pulling on the membrane just cuts off a small piece of pie, and a hole is made in the sac. Mechanical knife devices used to perform capsulotomy in the past use a knife to stretch tissue and provide sufficient force against the cutting edge. In contrast, in this device, the reaction force required to cut with the mechanical cutting element of device 1 arises from the suction supplied by the device. Aspiration pulls the tissue perpendicular to the cutting edge, so there is no lateral distortion away from where the cutting is supposed to proceed, making it possible to reproduce accurate micro cuts It can be carried out. In addition, the cutting knives used in the past can make a complete cut with the cutting element, as opposed to often requiring multiple paths. The cutting element may be a continuous ring similar to that shown in FIGS. 13, 14 and 18 or a non-continuous ring.

  If the cutting element is a combined electromechanical cutting element, the cutting element may be one microtooth (or optionally multiple) or other mechanism for severing tissue that creates an initial tear in the sac Have As described previously, the design of an electrical cutting element to apply a short electrical pulse is used to propagate the tear. Also, the lower vapor pressure required for an intact sac can propagate the tear and complete the sac incision.

  FIG. 19 is an exploded top perspective view of another design 80 suction cup and cutting element including dual tubing in accordance with an embodiment of the present invention. The design is shown in both assembled and unassembled conditions. The design 80 of FIG. 19 includes two sections of tubing 86A, 86B (eg, stainless steel tubing) assembled into a rigid polymer shaft 84. FIG. Molded ends 87 of tubing 86A, 86B are coupled to electrode 85 and overmolded with elastomer 81 to form a suction cup 82 having a shaft 83 that holds the tubing. Other shapes may include two concentric conductive tubes separated by an insulating layer, one tube and adjacent wires isolated from each other, a non-conductive tube having two adjacent wires, etc. .

Other Microsurgery / Sactomy Device Design FIG. 20 is a top perspective view of another design of the microsurgery / sactomy device 90 with a suction cup housed, according to one embodiment of the present invention. In FIG. 20, the device 90 is in a housed (or shipped) configuration with a suction cup 99 protected within the device. This design is an external compression mechanism handpiece design 90. The operating mechanism includes a piston 97 for moving the suction cup 99 from the device 90, and the compression mechanism includes an external slidable ring / member 94 and a compression arm 93 attached to the housing of the handpiece 95. . The slidable ring 94 slides distally toward the suction cup 99 over the compression arms 93 positioned on both sides of the suction cup 99 and pushes the tips 92 of the arms 93 together to suck the suction cup 99. Is slidably attached to the handpiece 95 so as to compress.

  The suction cup 99 is further attached to a shaft 199 that connects to a sliding element in the device 90 connected to the piston 97. The piston 97 is manipulated or pushed distally towards the suction cup 99 to push the sliding element distally inside the device 90. This causes shaft 199 and suction cup 99 to move distally. The tip of the device 90 has two inserts disposed at the tip of the handpiece to maintain the compressed suction cup in a flattened position as the suction cup is moved from the tip to the tissue. Finger portion 91 (eg, two lips that can be designed to be compliant). In the embodiment of FIG. 20, the finger portions 91 are tilted inward toward each other at the tip and are pushed together to form a wedge portion for sliding reliably through the incision. The finger portion 91 is configured to be separated by pressure due to the suction cup 99 moving forward and out of the handpiece 95. In the embodiment of FIG. 20, the distal portion of handpiece 94 is designed to have an upper flat portion and a lower flat portion that also help keep suction cup 99 flat during placement. The compression arm 93 is designed to slide between the upper and lower portions to compress the suction cup 99 laterally. The hose connector 96 for performing suction on the suction cup 99 is only slightly visible in FIG.

  21 is a bottom perspective view of the microsurgical / capsulotomy device 90 of the design of FIG. 20 with the suction cup 99 positioned according to one embodiment of the present invention. This figure shows a hose connector 96 that provides fluid and / or suction to the suction cup (in a manner similar to that performed on device 1), and the electricity that supplies current to the device and to the cutting element in suction cup 99. Connector 98 is shown more appropriately. The cutting element in device 90 can be any of the cutting element designs described above. If the cutting element in device 1 or 90 is not electrical, the electrical connections and components may not be included in the design.

  22 is a top perspective view of the microsurgical / capsulotomy device 90 of the design of FIGS. 20 and 21 with the suction cup 99 in place, according to one embodiment of the present invention. After placement, the suction cup 99 has spread and returned to its previous shape.

Surgical Procedure FIG. 23 is a flow diagram illustrating various preparation steps for a microsurgical / capsulotomy procedure, including procedures that can be used with devices 1, 90, according to one embodiment of the present invention. In the case of FIGS. 23-25, each step may vary between various procedures, including having additional steps or steps different from those shown, and performing each step in a different order. Also good.

  In FIG. 23, the surgeon / user connects (2300) the device to a connector to a non-disposable control system. The connector allows suction to be transmitted to the device lumen and current to the device electrode (ie, when the cutting element is an electrode). A computer associated with the control system checks the electrical and fluidic viability of the device. During this self-check, the computer can measure the electrical resistance of the electrode (2302). By alarm or other notification mechanism (e.g. light, beep, vibration, text display on screen, etc.) if it exceeds the acceptable range for a suitable or fully functional / acceptable device The user is notified to replace the device (2304) and the computer does not run the surgical program until the problem is remedied. If the resistance is within an appropriate and acceptable range, the operation can proceed. The computer continues to measure resistance at predetermined intervals (eg, once per second) (2302). Similarly, if a measurement indicates a problem, an alarm can alert the user (2304) and the treatment can be stopped. Units previously used in the surgical procedure have a higher resistance than is acceptable, and therefore prevent the computer from accidentally using a used or damaged unit. Please keep in mind.

  Also, during the self-checking procedure, the relationship between air flow and pressure can be measured by a computer (2306, ie, clean dry filtered air can be blown through a suction cup for this test). If not within an acceptable range, an alarm or other notification system informs the user to replace the device or correct the problem (2308), and the computer will continue to operate until the problem is corrected. Do not run the program. This is done at least after the plug-in and before the user has the prospect of moving to any other step. After the preparation step is complete (2310), the device is ready for use.

  FIG. 24 is a flow diagram illustrating steps for a microsurgical / capsulotomy procedure according to one embodiment of the present invention. The user can inject a lubricant (eg, a viscoelastic body) into the suction cup for lubrication (2400). Viscoelastic bodies are commonly used in cataract surgery to keep the anterior chamber of the eye inflated. The user compresses (2402) the suction cup by manipulating the device (eg, via knob 8 or slidable ring 94). In the case of device 1, the user pushes the knob 8 along the groove 9 to move the entire suction cup / compression mechanism to the entrance of the insertion tip 3, thereby moving the compression arm distally and moving the arm to the handpiece 5. Step 2402 is carried out by pressing the inner wall of the tube and moving the arms inward toward each other to compress the suction cup 2. For device 90, the user performs step 2402 by sliding slidable ring 94 distally over compression arm 93 and pressing arm 93 together to compress suction cup 99. The user can then further manipulate the device to move the lubricated and compressed suction cup into the insertion tip of the device (2404). For device 1, the user performs step 2404 by pushing the knob 8 further along the groove 9 and moving the suction cup 2 distally into the tip 3. For device 90, the user performs step 2404 by pushing piston 97 and moving suction cup 99 to the tip of the device.

  The user moves / inserts (2406) the tip of the capsulotomy device through an incision in tissue (eg, the cornea of the eye). In some embodiments of the procedure, one or both of steps 2402 and 2404 are performed prior to step 2406, thus compressing the suction cup (2402) after inserting the tip through the incision (2406), And / or moved into the insertion tip (2404). The user removes the compressed suction cup through the tip of the handpiece and places it in tissue (eg, in the capsular bag in the anterior chamber) (2408). The suction cup extends to the cutting position (eg, over the lens capsule) inside the tissue (eg, past the cornea and into the anterior chamber of the eye). In the case of devices such as devices 1 and 90, the suction cup is attached to the sliding element, so placing the compressed suction cup moves the sliding element distally and causes the suction cup in the handpiece to move. Includes moving through the tip and moving to the tissue. The user can then position the suction cup by centering it over the tissue (2410), ascertain the direction of pitch and roll, and position the suction cup against the tissue (eg, capsular bag). The user activates suction (2412) and pulls the suction cup against the tissue, thereby pressing the cutting element against the tissue (eg, the capsular bag membrane).

  The user can confirm that the desired low-leakage suction seal is established by moving the device horizontally or vertically (eg, by 0.25 mm) and confirming that the lens moves with the device. (2414). The user can also perform one or more system checks on the suction cup seal. The control computer can also verify that a low-leakage seal has been established by reading 2416 a flow sensor that should indicate little or no liquid flow in the suction line. . In the suction line, the pressure sensor is also monitored (2418) because the computer typically reaches a low threshold pressure before proceeding to the surgical program. If a problem is indicated by reading (2416) or monitoring (2418), the user can be notified (2417, 2419) to correct the problem. The user then begins using the device to subsequently cut tissue using the cutting element. If there is no electrical cutting element in the device, the user continues to non-electrically cut tissue (2420). For example, a user can cut (2420) the tissue by suction applied to the suction cup to pull the tissue in contact with a mechanical cutting element (eg, sharp blade (s)). If there is an electrical cutting element in the device, the procedure moves to FIG. 25 for the electrical cutting step.

  FIG. 25 is a flow diagram illustrating the continuation of the steps for a microsurgery / capsulotomy procedure according to one embodiment of the present invention. The user requests a discharge for disconnection (2500) (eg, by pressing a button, by word of speech recognition software, or by any type of user interface). The control computer makes one recent measurement of the electrode resistance, pressure and flow sensors (2502). If all conditions are within range, a cut is made (2503) and a discharge is applied. If not, the user is notified (2504) and can take action to remedy the problem. The discharge for surgery can include multiple stages such as: 1) degassing (eg, keeping the electrode from 60 ° C. to 99 ° C.), 2) thermal tangling ( For example, keeping the electrode from 60 ° C. to 99 ° C.), 3) discharging for cutting (eg heating the electrode from 200 ° C. to 1000 ° C.), and / or 4) spikes for electrode modification (eg 1 Short current spikes that melt the components of one or more electrodes). After discharging, the system checks the resistance of the electrode (2506). If the resistance exceeds the expected post-discharge range, an alarm informs the user that an abnormality has occurred and informs the user to take appropriate diagnostic action (2508). Otherwise, the user can proceed to the next step.

  The user then reduces the suction applied to the suction cup (2510). The suction vacuum is weakened and the user can pull the suction cup away from the tissue. If the excised piece of membrane is sucked into the shaft lumen, the suction can be stopped completely. Otherwise, some suction can be maintained at the level necessary to ensure that the piece is retained and removed from the eye with the device. The user then unplugs the device from the tissue (eg, from the eye) (2512).

Device Manufacture A variety of different mechanisms can be used to manufacture device components. For example, the handpiece components can be made by injection molding plastic. The suction cup can be made by overmolding a suitable elastomer (eg, silicone or polyurethane) over the electrodes and shafts positioned in the mold, but other materials can be used. . The suction cup is designed to be foldable into a small cross-section and can therefore be inserted through a corneal incision (eg, an incision with a length of less than 2 to 3 mm), in which case the placement Later, it can quickly return to its circular shape. The thinner the wall, the harder the material (higher durometer). The size of the suction cup can range from about 4.5 mm to about 7 mm in diameter, and the height typically ranges from about 0.5 mm to about 1.5 mm. The design and size range of the suction cup and the entire device can be varied to suit the surgical procedure being performed.

  The cutting element can be made from a variety of materials. The metallic component of the electrode can be made by electroforming of a suitable metal such as nickel, gold, steel, copper, platinum, iridium. The connection between the electrode in the shaft and the lead can be made by electroplating or welding. Typically, in the case of an electrical cutting element, the material for the cutting element is conductive, and in the case of a mechanical cutting element, the material is sufficiently hard to pierce the membrane. In the case of both electrical and mechanical cutting elements, the material is generally sufficiently elastic to return to its previous shape after being compressed and passed through the tissue incision, Or it is soft enough to be pushed back into a circular shape by a polymer support ring and / or by a suction cup in which the cutting element is mounted. For example, in the case of an electrical cutting element, the material may be spring steel, stainless steel, titanium nickel alloy, graphite, nitinol (a “shape memory alloy” of NiTi alloy), nickel, nickel-chromium alloy, tungsten, molybdenum, or the element It can include those made by photochemical etching, such as any other material that allows it to return to its previous form. Other materials for electrical cutting elements include suitably shaped conductive particles (eg, silver, gold, graphite, which can establish contact with each other and remain in contact with each other for the duration of the discharge. Conductive elastomers are included, including elastomers (eg, silicone or polyurethane) mixed with copper and the like. Other examples of materials for an electrical cutting element include a very thin wire (eg, about 1 or 2 micron diameter) compliant that can be secured to an elastomeric support ring to create a conductive element. Mesh is included. As another example, materials such as highly conductive metals (eg, gold, aluminum, copper, etc.) can be used for electrical cutting elements made by sputtering metal onto a polymeric support. Can be used to make very thin (eg 1 micron) elements deposited by RF plasma sputtering and having a resistance in the usable range (eg 1 to 10 ohms) be able to.

  The material used for the mechanical cutting element can include, inter alia, a photochemically etched metal (eg stainless steel) or a relatively hard plastic (eg phenolic resin). It is possible to etch discontinuous micro teeth from single crystal silicon. Photochemical etching can be used to make cutting elements having a thickness of, for example, 25 microns, or 12.5 microns, or 5 microns.

  The above description is included to explain the operation of the embodiment and is not intended to limit the scope of the present invention. The scope of the present invention is limited only by the following claims. From the foregoing discussion, many variations that still fall within the spirit and scope of the invention will become apparent to those skilled in the relevant art. As used herein, reference to “one embodiment” or “an embodiment” means that a particular element, function, structure, or feature described in connection with that embodiment is at least It is meant to be included in one embodiment. Although the phrase “in one embodiment” appears in various places throughout this specification, it does not necessarily refer to the same embodiment.

1 Device 2 Suction cup 5 Handpiece 7 Sliding part

Claims (15)

A capsulotomy device for reaching the lens capsule through the cornea of the eye,
With handpieces,
A suction cup in contact with the handpiece;
A compression mechanism associated with the suction cup, the compression mechanism comprising an arm attached to an arm base, wherein the arm and the arm base are designed to be movable relative to the handpiece; Positioned to allow placement of the suction cup through the corneal incision and configured to provide lateral compression of the suction cup during placement of the suction cup through the incision The suction cup is configured to extend to a cutting position on the lens capsule inside the anterior chamber;
To cut a portion of the lens capsule, and a cutting element mounted to the suction cup device.   2. The suction cup of claim 1, further comprising one or more suction elements connected to the suction cup to apply suction to the suction cup and secure the suction cup relative to the capsular bag. Devices.   The cutting element is an electrical cutting element that is connected to the electrical cutting element and sends a current to an electrical lead that heats the electrical cutting element to ablate a portion of the tissue of the capsular bag The device of claim 1, further comprising one or more electrical elements for.   The electrical cutting element is mounted around the lower surface of the suction cup, and the electrical cutting element conducts two currents so as to conduct current uniformly around the portion of the capsular bag. 4. The device of claim 3, further comprising a continuous ring configured to allow even distribution on both sides to travel in the opposite direction.   The electrical cutting element comprises an upper ring and a lower ring, the upper ring is connected to the electrical lead, and the lower ring is connected to the upper ring at two positions on opposite sides of the lower ring. Connecting, current is transmitted from the upper ring to the lower ring through one of the positions, and then travels on both sides of the lower ring to the position on the opposite side of the lower ring, and the current The device of claim 4, wherein the device is evenly distributed around the lower ring in contact with the capsular bag.   The said suction cup is further equipped with the flare skirt-shaped part extended from the edge of the said suction cup so that the said suction cup may be fixed with respect to the said lens capsule, and a vacuum seal may be formed. The device described. Said arm of said compression mechanism is one of two arms attached to the arm base, the two arms, when the compression mechanism is moved distally, prior Symbol suction cups, and the The device according to claim 1, wherein the device is positioned on both sides of the suction cup for lateral compression of a cutting element mounted in the suction cup. Further comprising a sliding element slidably disposed to move relative to the handpiece;
The two arms move distally with the sliding element, press the arms against the inner wall of the handpiece, and move the arms inward toward each other to compress the suction cup. The device according to claim 7, wherein the device is slidably attached to the sliding element.   The two arms are attached to the housing of the handpiece and slidably attached to the housing so as to slide distally over the arm and push the arms together to compress the suction cup The device of claim 7, further comprising a slidable member formed.   Moving the sliding element distally in response to an external force to move the suction cup in the handpiece through the tip of the handpiece and move it to the capsular bag in the anterior chamber. 9. The device of claim 8, further comprising a piston connected to an end of a sliding element opposite the suction cup and slidably associated with the handpiece. Further comprising an operating mechanism slidable along a slot in the housing of the handpiece to move the compression mechanism distally to effect lateral compression of the suction cup and the cutting element. The device of claim 8. The operating mechanism moves the sliding element distally in response to an external force, moves the suction cup in the handpiece out through the tip of the handpiece, and enters the lens capsule in the anterior chamber. The device of claim 11 , further comprising a knob connected to a side of the sliding element through the slot of the housing of the handpiece for positioning relative to the handpiece. Said compression mechanism is responsive to an external force to said knob moves the suction cup distally to compress, according to claim 12, characterized in that it comprises two arms attached to the arm base Devices.   The tip of the handpiece is adapted to maintain the compressed suction cup in a flattened position as the compressed suction cup is moved from the tip of the handpiece into the anterior chamber. The device according to claim 1, further comprising two insertion finger portions disposed in the portion.   The insertion finger portion is inclined toward each other inward at the distal end portion of the finger portion, and the distal end portion is pushed together so as to surely slide through the incision portion of the cornea 15. The device of claim 14, wherein the finger portion is configured to be separated by pressure as the suction cup advances and exits the handpiece.