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WO2013038689A1 - Intraocular lens insertion tool - Google Patents

Intraocular lens insertion tool Download PDF

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Publication number
WO2013038689A1
WO2013038689A1 PCT/JP2012/005861 JP2012005861W WO2013038689A1 WO 2013038689 A1 WO2013038689 A1 WO 2013038689A1 JP 2012005861 W JP2012005861 W JP 2012005861W WO 2013038689 A1 WO2013038689 A1 WO 2013038689A1
Authority
WO
WIPO (PCT)
Prior art keywords
intraocular lens
holding member
holding
movable
optical
Prior art date
Application number
PCT/JP2012/005861
Other languages
French (fr)
Japanese (ja)
Inventor
一晴 丹羽
鈴木 保彦
Original Assignee
株式会社メニコン
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 株式会社メニコン filed Critical 株式会社メニコン
Priority to JP2013533517A priority Critical patent/JP5980218B2/en
Publication of WO2013038689A1 publication Critical patent/WO2013038689A1/en

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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 or corneal implants; Artificial eyes
    • A61F2/16Intraocular lenses
    • A61F2/1662Instruments for inserting intraocular lenses into the eye
    • A61F2/1675Instruments for inserting intraocular lenses into the eye with a lubricated inner surface, e.g. the lubricant being coated on the inner surface or being injected through a port
    • 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 or corneal implants; Artificial eyes
    • A61F2/16Intraocular lenses
    • A61F2/1662Instruments for inserting intraocular lenses into the eye
    • A61F2/1678Instruments for inserting intraocular lenses into the eye with a separate cartridge or other lens setting part for storage of a lens, e.g. preloadable for shipping

Definitions

  • the present invention relates to an intraocular lens insertion device that is provided with a built-in intraocular lens and used to insert the built-in intraocular lens into the eye.
  • an intraocular lens insertion device an intraocular lens that is provided separately from the intraocular lens and is used by setting an intraocular lens that is separately packed at the time of treatment to the insertion device is used.
  • Some are provided with built-in.
  • the intraocular lens is sterilized and packed and stored until use.
  • Patent Document 1 Japanese Patent Application Laid-Open No. 2009-160140
  • Patent Document 2 Japanese Patent Application Laid-Open No. 2009-160140
  • a structure was proposed in which the holding members were assembled in a removable manner. According to such an insertion instrument, it is avoided that the optical part of the intraocular lens is in close contact with the inner surface of the instrument main body such as the placement part over a wide range, thereby advantageously preventing the occurrence of deformation over time. be able to.
  • the intraocular lens can be positioned and placed on the placement portion by removing the holding member from the placement portion, so that the intraocular lens can be deformed into a desired shape and inserted into the patient's sac. It is.
  • the intraocular lens is held by the holding member to prevent the occurrence of deformation at the time, it is difficult to completely stabilize the behavior of the intraocular lens when the intraocular lens is inserted into the patient's sac. was there. That is, in the so-called one-piece type intraocular lens in which the optical part and a pair of support parts extending on both sides of the optical part are integrally formed of a soft synthetic resin material, the support part is hard due to the influence of room temperature or the like. Is easy to change.
  • Patent Document 2 In order to cope with such a problem, the applicant of the present application previously described in International Patent Publication No. WO2010 / 064275 (Patent Document 2), provided with a protruding portion at an appropriate position of the insertion tube portion, the optical portion of the intraocular lens is located upward.
  • a structure has been proposed in which a so-called tacking state is developed in which a front support portion located in front of the extrusion direction is inserted into the optical portion so as to be deformed into a mountain-fold shape that is convex on the lens front surface.
  • the posture of the support portion on the front end side of the intraocular lens can be stabilized, and the behavior of the intraocular lens in the sac can be stabilized with high accuracy.
  • JP 2009-160140 A International Patent Publication No. WO2010 / 064275
  • the present invention has been made in the background as described above, and the problem to be solved is to maintain the stability of the intraocular lens for a long period of time and to control the posture of the rear support part of the intraocular lens.
  • An object of the present invention is to provide an intraocular lens insertion device having a novel structure that can be realized with a simple structure and simple operation.
  • the present inventors have superimposed the rear support portion of the intraocular lens on the front surface side (the upper surface side on the mounting surface) of the optical portion. It is possible to smoothly push out the intraocular lens from the insertion tube part and to quickly release the close contact between the optical part and the support part and to stabilize the behavior of the intraocular lens in the sac. I found something to do.
  • the rear support part of the intraocular lens is deformed so as to overlap the rear surface side (the lower surface side on the mounting surface) of the optical part, so that the rear support part is inserted between the optical parts deformed in a mountain shape.
  • the first aspect of the present invention is a cylindrical instrument body provided with a placement portion on which an intraocular lens having an optical portion and a pair of support portions extending from both sides of the optical portion is placed;
  • a holding member that is inserted from the rear end of the instrument body and pushes out the intraocular lens to an insertion tube part provided at the distal end of the instrument body, while protruding and assembled to the mounting part.
  • Intraocular provided by the member in a state where the intraocular lens is positioned and held on the mounting portion so that the pair of support portions of the intraocular lens extend to the front end side and the rear end side of the instrument body.
  • the holding member is provided with a movable portion that is slidable from the rear end side to the front end side of the holding member in a state of being engaged with the push-out member, and the movable portion slides.
  • the holding member While it is impossible to detach from the instrument main body, the support portion positioned behind the intraocular lens by the distal end portion of the pushing member is moved to the optical portion side by moving the movable portion toward the distal end side in the sliding direction.
  • the holding member including the movable part is detachable from the instrument body, and the rear support part is moved to the optical part side when the rear support part is deformed to the optical part side.
  • the movable member is provided on the mounting member for positioning and holding the intraocular lens, and the movable unit is positioned on the rear end side.
  • a locking action that makes the holding member unremovable from the instrument main body is exhibited.
  • the movable part When performing the treatment, the movable part is moved to the distal end side to release the locking action and the holding member is detached from the instrument body. By performing this separation operation, the movable part is engaged.
  • the rear support portion of the intraocular lens By the extruded member, the rear support portion of the intraocular lens is bent or curved to the optical portion side, and the rear support portion is guided to a desired position on the upper surface side or the lower surface side of the optical portion by the guide portion. it can.
  • the deformation posture of the posterior support part can be controlled to a desired shape, and the intraocular lens in the patient's sac
  • the behavior of the intraocular lens when releasing the lens can be controlled with high accuracy.
  • the holding member is detached from the instrument body by providing the movable member that slides in a state in which the intraocular lens is stably held for a long time while being engaged with the pushing member. Only by performing a series of operations, desired deformation of the rear support part toward the optical part side can be made manifest at the same time. Therefore, stable holding of the intraocular lens and control of the rear support portion can be realized with a simple structure and simple operation.
  • the guide part may be any structure as long as it can guide the rear support part approaching the optical part to the front side or the rear side of the lens.
  • the curved surface provided on the front end surface of the push-out member may constitute a guide unit that guides the front support side or the rear side as the rear support unit approaches the optical unit, or the upper or lower side provided on the instrument body
  • the guide portion may be configured by a protruding portion that protrudes toward the optical portion, and a rear support portion approaching the optical portion may be brought into contact with the protruding portion and guided to the front side or the rear side of the optical portion.
  • a gripping protrusion protrudes from the movable part, and the sliding operation of the movable part is performed by the gripping protrusion.
  • the holding member can be detached from the instrument body.
  • the sliding operation of the movable part and the detaching operation of the holding member can be performed in a series of operations while holding the gripping protrusion, and the operability can be improved.
  • the holding member is provided by providing the movable member that slides in a state in which the intraocular lens is engaged with the pushing member with respect to the holding member that stably holds the intraocular lens for a long time. Only by performing a series of operations for detachment from the main body, a desired deformation of the rear support portion toward the optical portion side can be simultaneously exhibited. That is, stable holding of the intraocular lens and control of the rear support portion can be realized with a simple structure and simple operation.
  • the side view of the insertion instrument shown in FIG. The principal part enlarged top view of the mounting part which comprises the insertion instrument shown in FIG.
  • the top view of the holding member which comprises the insertion instrument shown in FIG. The side view of the holding member shown in FIG.
  • the upper surface explanatory drawing which expands and shows the principal part of the insertion instrument shown in FIG. VII-VII longitudinal cross-sectional enlarged view of FIG.
  • the principal part enlarged top view of the mounting part of the insertion instrument of the intraocular lens as 2nd embodiment of this invention.
  • FIGS. 1 and 2 show an intraocular lens insertion device 10 as an embodiment of the present invention.
  • the intraocular lens insertion instrument 10 is made of a synthetic resin, and is inserted from a cylindrical instrument body 16 having a placement portion 14 on which the intraocular lens 12 is placed, and a rear end portion 18 of the instrument body 16.
  • the push-out member 22 that pushes the intraocular lens 12 to the insertion tube portion 20 provided at the distal end portion of the instrument main body 16 is provided, and the intraocular lens 12 is provided in advance.
  • “front” refers to the pushing direction of the pushing member 22 (left direction in FIG. 1)
  • “upward” refers to the up direction in FIG.
  • the left-right direction refers to the left-right direction in the top view of the intraocular lens insertion device 10 (upper is right and lower is left in FIG. 1).
  • the instrument main body 16 has a main body cylinder portion 24 having a substantially cylindrical shape.
  • a through-hole 26 that penetrates in the axial direction with a substantially rectangular cross-sectional shape is formed inside the main body cylinder portion 24.
  • a plate-like portion 28 that extends in a direction orthogonal to the extending direction of the main body cylinder portion 24 is integrally formed at a position slightly forward from the rear end portion of the main body cylinder portion 24.
  • FIG. 3 shows the placement unit 14.
  • the mounting portion 14 is formed with a concave groove 32 extending in the axial direction with a width that is slightly larger than the diameter of the optical portion 30 of the intraocular lens 12 shown in FIG.
  • the concave groove 32 is formed with an axial length dimension that is slightly larger than the maximum width dimension (the horizontal dimension in FIG. 1) including the pair of support portions 34, 35 of the intraocular lens 12.
  • the concave groove 32 has an opening 36 opened upward, and a mounting surface 38 is formed on the bottom surface thereof.
  • the placement surface 38 has a width dimension slightly larger than the minimum width dimension (the vertical dimension in FIG. 1) of the intraocular lens 12, and is larger than the maximum width dimension (the horizontal dimension in FIG. 1) of the intraocular lens 12. Is also a flat surface having a large axial length dimension.
  • the height position of the mounting surface 38 is located higher than the height position of the bottom surface of the through hole 26 in the main body cylinder portion 24, and the front edge of the through hole 26 in the main body cylinder portion 24 is A wall portion 40 (see FIG. 2) that extends upward from the bottom surface of the through hole 26 and is connected to the rear end edge portion of the placement surface 38 is formed.
  • the concave groove 32 communicates with the through hole 26, and the width dimension of the concave groove 32 is substantially equal to the width dimension of the through hole 26.
  • a cover member 42 as a lid is integrally formed with the instrument body 16 on the side of the concave groove 32 (on the right side in the present embodiment).
  • the cover member 42 has an axial dimension substantially equal to the axial dimension of the concave groove 32 and is formed with a width dimension slightly larger than the width dimension of the concave groove 32.
  • the cover member 42 is connected to the instrument main body 16 by a substantially thin plate-like connecting portion 44 formed by extending the upper end edge of the mounting portion 14 to the side (in the present embodiment, the right side).
  • the connecting portion 44 is thinnest at a bent portion 46 extending in the axial direction of the instrument body 16 at a substantially central portion in the width direction, and can be bent at the bent portion 46.
  • the cover member 42 is configured to be able to cover the opening 36 by bending the connecting portion 44 and overlapping the concave groove 32.
  • An engagement piece 48 is formed to project from the edge of the cover member 42 opposite to the connecting portion 44, while the end of the mounting portion 14 opposite to the cover member 42 projects outward.
  • a protruding edge 50 is formed, and an engagement notch 52 is formed at a position corresponding to the engagement piece 48 in the protruding edge 50.
  • the holding member 54 is detachably provided on the lower side of the mounting surface 38 of the mounting portion 14 having such a structure in a state where the intraocular lens 12 is positioned and held.
  • the holding member 54 is configured as a separate body from the instrument body 16, and a pair of side wall portions 56, 56 are connected by a connecting plate portion 58 formed integrally between the opposing surfaces. It is structured.
  • the separation distance of the outer surface of the side wall portion 56 is substantially equal to the radial dimension of the optical portion 30 of the intraocular lens 12.
  • a thin flat plate-like leg plate portion 60 is integrally formed at the lower end portion of the connecting plate portion 58 in a direction perpendicular to the pushing direction of the pushing member 22.
  • first holding projections 62 and 62 projecting upward with a substantially arc shape in a top view are integrally formed at the upper end portions of the respective side wall portions 56 and 56.
  • a peripheral wall 64 is integrally formed on the outer side of the upper end surface of the first holding projection 62 on the inner side of the holding member 54.
  • the separation distance of the peripheral wall 64 is slightly larger than the diameter of the optical part 30 of the intraocular lens 12.
  • a pair of second holding projections 66 and 66 projecting upward in a rectangular shape in a top view are mutually opposite in the longitudinal direction of the holding member 54 (left and right direction in FIG. 4).
  • the height position of the upper end surface of the second holding projection 66 is equal to the height position of the upper end surface of the first holding projection 62.
  • Each of the second holding projections 66 includes a projection main body 68 projecting from the connecting plate portion 58, a peripheral wall 70 projecting from the upper end surface of the projection main body 68, and the second main body projection 68 in the opposing direction of the second holding projection 66.
  • each peripheral wall 70 and each engagement portion 71 have a width dimension substantially equal to the width dimension of the projection main body 68.
  • the opening part 72 of the rectangular shape is formed in planar view at both axial ends of the connecting plate part 58, and the distance between the opposing side wall parts 74, 74 in the axial vertical direction of the opening part 72 is the side wall. The distance between the portions 56 and 56 is shorter.
  • a movable portion 78 is formed in the opening 72 separately from the holding member 54 and has a rectangular flat plate-like portion 76 that is slightly narrower than the distance between the side wall portions 74 and 74 in plan view. It is slidably assembled to the holding member 54 from the rear end side toward the front end side.
  • the movable portion 78 is formed with engaging protrusions 80 protruding from the side edge portions on both sides in the width direction over a predetermined length at the center portion in the length direction.
  • both side wall portions 74, 74 that define the opening 72 extend on both side walls 74, 74 forward in the axial direction of the holding member 54, and on the rear end side of the opening 72 and the holding member 54.
  • Long grooves 82 and 82 that are open rails are formed, respectively.
  • the movable portion 78 is inserted into the long groove 82 from the rear end side of the holding member 54, so that the movable portion 78 can move by sliding forward in the axial direction.
  • the long groove 82 is formed with an internal dimension slightly larger than the external dimension of the engaging projection 80 in the direction perpendicular to the axis (vertical direction in FIG. 4) so that the movable portion 78 can slide smoothly and does not wobble. In the axial direction, it is formed with a length dimension that can ensure a predetermined slide length.
  • the movable portion 78 is inserted into the long groove 82 from the rear end side of the holding member 54.
  • the holding member 54 having such a structure is assembled from below the placement surface 38 of the instrument body 16.
  • through holes 84 and 86 penetrating in the thickness direction are formed on the mounting surface 38 of the instrument body 16 (see FIG. 3).
  • the through holes 84 and 86 are formed to have a substantially similar shape that is slightly larger than the top view of the first holding projection 62 and the second holding projection 66 of the holding member 54.
  • the first holding projection 62 and the second holding projection 66 of the holding member 54 are inserted into the through holes 84 and 86 from the lower side of the mounting surface 38 and protruded on the mounting surface 38.
  • the engaging portion 71 provided on the second holding projection 66 is protruded on the mounting surface 38 and is locked to the upper surface of the mounting surface 38, so that the holding member 54 is attached to the instrument body 16.
  • the state where the first holding protrusion 62 and the second holding protrusion 66 are protruded from the mounting surface 38 is held from the outside.
  • a through hole 85 penetrating in the thickness direction is formed in the mounting surface 38 of the instrument body 16 (see FIG. 3).
  • the through-hole 85 is opened to a predetermined size so that the columnar protrusion 88 protruding upward (perpendicular to the paper surface) from the rectangular flat plate portion 76 constituting the movable portion 78 can perform a sliding operation described later. Yes.
  • the movable portion 78 assembled to the holding member 54 is slid rearward in the axial direction of the instrument main body 16, thereby being guided to the groove 92 formed in the front portion 90 of the main body cylinder portion 24 in the instrument main body 16.
  • the locking claw 94 provided in the rectangular flat plate portion 76 constituting the movable portion 78 is fitted into the locking hole 96 provided in the groove portion 92. That is, at the slide start end where the movable portion 78 is located on the rear end side in the sliding direction, the holding member 54 is moved to the instrument main body 16 by the engagement of the rectangular flat plate portion 76 constituting the movable portion 78 with the main body cylinder portion 24. It is engaged so that it cannot be detached.
  • the movable portion 78 assembled to the holding member 54 is slid toward the distal end side in the axial forward sliding direction of the instrument body 16, thereby moving the movable portion 78.
  • the rectangular flat plate portion 76 constituting the movable portion 78 is housed in the lower portion of the placement surface 38. At this time, it is desirable that the engagement protrusion 80 is in contact with the end portion on the front end side of the long groove 82.
  • An insertion tube portion 20 that extends toward the front in the axial direction of the instrument body 16 is integrally formed in front of the mounting portion 14.
  • the insertion tube portion 20 has a tapered shape that gradually tapers from the placement portion 14 side toward the distal end portion in the extending direction as a whole, and has a tapered shape penetrating the entire length in the extending direction.
  • a through hole 106 is formed.
  • the through-hole 106 communicates with the placement unit 14 by connecting a base end opening 108 opened to the placement unit 14 side to the placement surface 38.
  • the base end opening 108 as a whole has a flat, substantially elliptical cross section in which the bottom surface 110 is a flat surface and the top surface is a substantially arc shape.
  • the tip opening 112 provided at the tip of the through-hole 106 has an oblique opening shape in a side view with the upper surface extending forward from the bottom.
  • the bottom surface 110 is formed with an introduction protrusion 114 that extends in the axial direction of the instrument body 16 with the widthwise center portion of the bottom surface 110 interposed therebetween.
  • the introduction protrusions 114 have a linear shape that protrudes slightly upward from the bottom surface 110 and extends parallel to each other.
  • the protrusion height of the introduction protrusion 114 is gradually increased as it goes forward in the axial direction of the instrument body 16, and is flush with the bottom surface 110 at the rear end portion of the proximal end opening 108. .
  • the introduction protrusions 114 are disposed substantially in parallel with each other at a predetermined distance in the direction perpendicular to the axis of the instrument body 16 with the center in the width direction of the bottom surface 110 interposed therebetween. Is preferably slightly larger than the width of the distal end portion of the extrusion member 22, and in this embodiment, it is slightly larger than the width of the rod-shaped portion 98 of the extrusion member 22.
  • the instrument main body 16 in the present embodiment is configured as a single member in which the main body cylinder part 24, the placement part 14, the cover member 42, and the insertion cylinder part 20 are integrally molded.
  • a holding member 54 including a movable portion 78 configured separately from the main body 16 is assembled from below the placement surface 38.
  • the extrusion member 22 is inserted in the through-hole 26 from the rear of the instrument body 16 having such a structure.
  • the pushing member 22 has a substantially rod shape having an axial length dimension slightly larger than the axial length dimension of the instrument main body 16, and has a substantially cylindrical action portion 116 and a substantially rectangular rod shape.
  • the insertion part 118 is integrally formed.
  • the distal end portion of the pushing member 22 is inserted into the main body cylinder portion 24 of the device main body 16 from the rear side, and the pushing member 22 as shown in FIG.
  • the claw portion 120 is set at an initial position locked in a locking hole 124 penetrating the instrument body 16.
  • the holding member 54 is attached to the instrument body 16 from below the placement surface 38 as described above, and the movable portion 78 is set at the slide start end.
  • the holding member 54 including the movable portion 78 is assembled to the instrument body 16 so as not to be detached, and the first holding projection 62 and the second holding projection 66 of the holding member 54 are held in a state of protruding on the placement surface 38. Is done.
  • the optical unit 30 of the intraocular lens 12 is placed and held on the upper end surfaces of the first holding projection 62 and the second holding projection 66 of the holding member 54.
  • FIG. 6 only a necessary portion of the instrument main body 16 and a distal end portion of the pushing member 22 facing the intraocular lens 12, the holding member 54, and the placement portion 14 are shown for easy understanding.
  • the intraocular lens 12 has the outer peripheral portion of the optical unit 30 in contact with the first and second holding projections 62 and 66, and the central portion has the first and second holding projections 62 and 66. 66 in a non-contact state.
  • peripheral walls 64 and 70 formed on the first holding protrusion 62 and the second holding protrusion 66 are outside the optical unit 30 in the intraocular lens 12, and in particular in the present embodiment, formed on the first holding protrusion 62.
  • the peripheral wall 64 sandwiches the intraocular lens 12 on both sides in an oblique direction with respect to the axial direction of the instrument main body 16, and the peripheral wall 70 formed on the second holding projection 66 connects the intraocular lens 12 to the axis of the instrument main body 16. It is provided so as to sandwich both sides of the direction. Thereby, the amount of displacement of the intraocular lens 12 with respect to the instrument body 16 in the axial direction and the axial direction is limited, and the intraocular lens 12 can be stably held.
  • the pair of support portions 34 and 35 of the intraocular lens 12 extend from the first and second holding projections 62 and 66 of the holding member 54 to the front side and the rear side of the instrument body 16. Is placed on top.
  • the bent portion 46 is bent and the opening portion 36 of the placement portion 14 is covered with the cover member 42, so that the intraocular lens 12 is set in the instrument body 16 in the accommodated state.
  • the cover member 42 is maintained in the closed state by the engagement piece 48 being engaged with the engagement notch 52.
  • the intraocular lens 12 is accommodated in the insertion device 10. And the insertion instrument 10 in this embodiment is packaged and delivered after sterilization etc. are made in the state which accommodated the intraocular lens 12.
  • FIG. 1 is a diagrammatic representation of the intraocular lens 12.
  • the insertion instrument 10 according to the present embodiment provided with the intraocular lens 12 is used in the following manner during an operation such as a cataract.
  • a lubricant mainly composed of a viscoelastic substance such as sodium hyaluronate into the mounting portion 14 or the insertion tube portion 20.
  • a lubricant mainly composed of a viscoelastic substance such as sodium hyaluronate
  • an injection hole 126 penetrating in the thickness direction is formed in the cover member 42, and the lubricant can be injected through the injection hole 126 with the cover member 42 being closed.
  • the lubricant may be injected from, for example, the distal end opening 112 of the insertion tube portion 20, or the cover member 42 is opened once and then injected from the opening 36 of the mounting portion 14, or once the extrusion member. 22 may be pulled out from the instrument body 16 and injected from the rear end 18 of the rear end of the through hole 26.
  • the movable part 78 of the holding member 54 is moved to the instrument. From the slide start end fitted in the groove portion 92 provided in the front portion 90 of the main body cylinder portion 24 of the main body 16, toward the slide end end positioned at the lower portion of the placement surface 38 of the holding member 54. And slide forward in the axial direction.
  • the first and second holding projections 62 and 66 constituting the holding member 54 are not displaced, and only the distal end portion of the rod-like portion 98 of the pushing member 22 engaged with the movable portion 78 is slid forward in the axial direction. Therefore, the rear support part 35 of the intraocular lens 12 can be deformed to the optical part 30 side.
  • this deformation for example, as shown in FIG. 7, by providing a guide portion 128 that increases in height toward the front in the axial direction on the mounting surface 38, the rear support portion 35 is guided to the front side of the optical portion 30. can do.
  • the rear support portion 35 is guided to the rear surface side of the optical portion 30 by providing the guide portion 128 in a symmetrical shape with respect to the paper surface (not shown) on the surface of the cover member 42 facing the placement surface 38.
  • the rear support portion 35 is guided to the front surface side or the rear surface side of the optical unit 30 by providing a taper of a right shoulder downward or a right shoulder upward at the front end portion 129 of the rod-shaped portion 98 of the pushing member 22. Can do. In this way, the rear support portion 35 can be deformed into a desired shape, and the stability of the intraocular lens 12 within the sac can be improved.
  • the installation location of the guide part 128 is not limited to the illustrated example, and can be installed on the holding member 54 or the movable part 78.
  • the intraocular lens 12 can be placed on the placement surface 38 in a state of being wrapped in the above-described lubricant by pulling the holding member 54 below the instrument body 16 and removing it from the instrument body 16. It becomes.
  • the mounting surface 38 in this embodiment is a flat surface, the intraocular lens 12 can be stably mounted, and the width dimension of the concave groove 32 is the optical part of the intraocular lens 12. Since the diameter is slightly larger than 30, the rotation of the intraocular lens 12 in the circumferential direction on the placement surface 38 is also prevented.
  • a gripping protrusion 130 bent outward is integrally formed at the lower central part of the rectangular flat plate portion 76 constituting the movable part 78, and the sliding operation of the movable part 78 and the movable part are formed by the gripping protrusion 130.
  • the holding member 54 engaged with 78 can be detached from the instrument main body 16. Accordingly, the sliding operation of the movable portion 78 and the detaching operation of the holding member 54 can be performed by a series of operations while the gripping protrusion 130 is gripped, and operability can be improved.
  • the pressing plate portion 132 of the pushing member 22 is pushed into the instrument main body 16 side in a state where the distal end portion of the insertion tube portion 20 is inserted into the incision provided in the eye tissue.
  • the rod-like portion 98 at the tip of the pushing member 22 is brought into contact with the outer peripheral edge portion of the optical portion 30 of the intraocular lens 12 placed on the placing surface 38, and the intraocular lens 12 is inserted into the insertion tube portion by the pushing member 22.
  • the intraocular lens 12 is fed out from the distal end portion of the insertion tube portion 20 into the sac.
  • the maximum pushing amount of the pushing member 22 into the instrument main body 16 is limited by the distal end surface of the insertion portion 118 being locked by the wall portion 40 of the through hole 26, and the maximum pushing position is as follows.
  • the distal end portion of the pushing member 22 is projected from the distal end opening portion 112 to an appropriate length, for example, 5 to 10 mm.
  • the movable member 78 is provided in the holding member 54, when inserting the intraocular lens 12 into the patient's sac, With the intraocular lens 12 positioned and held by the holding member 54, the pushing member 22 can be brought close to the intraocular lens 12.
  • the rear support part 35 of the intraocular lens 12 is guided to either the front surface or the rear surface of the optical part 30 of the intraocular lens 12 with good reproducibility. can do. Therefore, the rear support portion 35 is deformed into a desired shape, and the behavior of the intraocular lens 12 after being inserted or inserted into the sac can be controlled and the stability in the sac can be improved. Therefore, as in the conventional structure, after the intraocular lens 12 is removed from the holding member 54, it is possible to prevent problems such as lens movement and rotation caused by pushing out the rear support portion 35 with the pushing member 22, and stable. It is possible to insert an intraocular lens.
  • the intraocular lens 12 since the intraocular lens 12 is built in the instrument body 16 in a state of being positioned and placed on the holding projections 62 and 66 of the holding member 54, stable holding during transportation and storage is possible. It becomes possible. Further, after the movable portion 78 is slid, the intraocular lens 12 can be stably placed on the placement surface 38 by withdrawing the holding member 54 from the placement portion 14. As described above, the holding member 54 can exhibit a stable support function during transportation and storage of the intraocular lens 12.
  • the rear portion of the rectangular flat plate-like portion 76 of the movable portion 78 is fitted into the groove portion 92 provided in the front portion 90 of the main body cylinder portion 24 of the instrument main body 16, and cannot be detached. Therefore, it is possible to prevent the holding member 54 including the movable portion 78 from being unexpectedly detached from the placement portion 14.
  • the holding member 54 can be quickly removed from the through holes 84 and 86, and the insertion operation by the pushing member 22 of the intraocular lens 12 can be performed with the holding member 54. Interference can be avoided and stable operation can be performed.
  • the movable portion 78 is provided with the gripping protrusion 130, the sliding operation of the movable portion 78 by the gripping protrusion 130 and the holding member 54 engaged with the movable portion 78 from the instrument main body 16.
  • the withdrawal operation is possible. Accordingly, the sliding operation of the movable portion 78 and the detaching operation of the holding member 54 can be performed by a series of operations while the gripping protrusion 130 is gripped, and the operability can be improved.
  • the intraocular lens 12 can be placed while maintaining the state in which the opening 36 of the placement portion 14 is covered by the cover member 42, the ocular lens can be prevented from falling off from the insertion device 10. At the same time, the chance of contact of the intraocular lens 12 with the outside world is reduced, and an excellent effect on hygiene can be obtained.
  • the support holding protrusion 136 that abuts the front support 34. Is provided so that the deformed shape of the front support portion 34 can be controlled.
  • members and parts that are substantially the same as those of the above-described embodiment are denoted by the same reference numerals as those of the above-described embodiment, and detailed description thereof is omitted.
  • the connecting portion 138 extends straight in the longitudinal direction of the holding member 54, and the support holding portion is held.
  • the protrusion 136 is disposed at substantially the same position as the front edge of the holding member 54. Further, as shown in FIG.
  • an accommodation hole 140 for the support portion holding projection 136 is provided through the bottom surface of the concave groove 32 of the device body 16, and the support portion holding projection 136 is passed through the accommodation hole 140. It protrudes on the mounting surface 38 in front of the intraocular lens 12 on the distal end side of the main body 16.
  • an accommodation groove that opens on the back side of the bottom surface of the recessed groove 32 may be provided so that the connecting portion 138 can be accommodated in a state where it can be bent and deformed.
  • the intraocular lens insertion device 134 of this embodiment first, the initial state shown in FIG. 8A, that is, the intraocular lens 12 is positioned and placed on the holding protrusions 62 and 66 of the holding member 54. From this state, the rear support portion 35 of the intraocular lens 12 can be deformed to the optical portion 30 side by sliding the movable portion 78 provided on the holding member 54 forward in the axial direction with respect to the instrument body 16. Thus, the desired deformed shape of the rear support portion 35 can be advantageously produced. Further, in the present embodiment, the through holes 142 and 144 for projecting the holding projections 62 and 66 that hold the intraocular lens 12 have a long hole shape extending in a predetermined length in the axial direction of the instrument body 16.
  • the movable portion 78 engaged with the holding member 54 can be further slid from FIG. 8B to FIG. 8C together with the holding member 54, and the rear support portion 35 is deformed.
  • the intraocular lens 12 can be slid while maintaining the above.
  • the support portion holding projection 136 that protrudes on the placement surface 38 through the accommodation hole 140 is immovable with respect to the instrument main body 16, so that the connecting portion 138 is curved to cause the eye to bend.
  • the inner lens 12 can be brought close to the support holding projection 136.
  • the movement of the front support portion 34 of the intraocular lens 12 can be restricted by the support portion holding protrusion 136 by sliding the holding member 54 axially forward with respect to the instrument body 16.
  • connection portion 138 has been described with a thin-walled and strip-like structure. However, a chain-like structure or a telescopic structure may be used, or the connection portion 138 may be omitted and formed separately.
  • the front support part 34 is deformed so that the front end part of the front support part 34 is deformed to the optical part 30 side, and the front end part of the rear support part 35 is placed on the front surface of the optical part 30.
  • the pushing member 22 pushes out the intraocular lens 12 from the instrument body 16. Then, a so-called tacking state in which the front support portion 34 is sandwiched between the optical portions 30 deformed so as to be convex upward can be advantageously produced, and the intraocular lens 12 is released into the sac.
  • the behavior of the front support part 34 and the optical part 30 is stabilized, and the stability of the intraocular lens 12 within the capsule can be improved.
  • the rear support portion 35 is deformed so as to be placed on the front surface of the optical portion 30, the cross-sectional area of the intraocular lens 12 pushed out from the insertion tube portion 20 is reduced, and the intraocular lens 12 is pushed out. Can be performed smoothly and with less resistance.
  • the front and rear support portions 34 and 35 can be deformed to the optical portion 30 side simply by sliding the movable portion 78 forward in the axial direction. The postures of the front and rear support portions 34 and 35 can be controlled to a desired state.
  • the rear support part 35 can be deformed so as to enter the lower surface side of the optical part 30 as in the first embodiment. This can advantageously prevent the rear support portion 35 from being damaged when the intraocular lens 12 is pushed out.
  • the engagement structure between the movable portion 78 and the pushing member 22 may be a known engagement structure as long as the engagement is released when the holding member 54 is detached from the instrument body 16. .
  • the introduction protrusion 114 provided on the bottom surface 110 of the proximal end opening 108 may be provided to extend to the portion on the placement surface 38 where the optical part 30 of the intraocular lens 12 is placed. Then, the optical unit 30 may be placed and supported also on the projecting tip of the introduction projection 114 in the state of being placed on the first and second holding projections 62 and 66.
  • 10 insertion instrument
  • 12 intraocular lens
  • 14 placement part
  • 16 instrument body
  • 18 rear end part
  • 20 insertion cylinder part
  • 22 pushing member
  • 24 body cylinder part
  • 30 optical part
  • 32 concave groove
  • 34 front support part
  • 35 rear support part
  • 38 mounting surface
  • 42 cover member
  • 54 holding member
  • 62 first holding protrusion
  • 66 second holding protrusion
  • 76 rectangular Flat plate portion
  • 78 movable portion
  • 88 columnar protrusion
  • 90 front portion
  • 92 groove portion
  • 94 locking claw
  • 96 locking hole
  • 98 rod-shaped portion
  • 100 engagement notch
  • 128 guide portion
  • 130 gripping protrusion

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Abstract

Provided is an intraocular lens insertion tool having a novel structure whereby an intraocular lens can be stably retained over a long time and the positioning of a rear support part of the intraocular lens can be controlled, with a simple structure and easy operation. An intraocular lens insertion tool (10) comprising a cylindrical tool body (16) provided with a placement part (14) at which an intraocular lens (12) is placed, an out-pushing member (22), and a retention member (54) assembled to project out to the placement part (14), wherein a movable part (78) able to slide engaged with the out-pushing member (22) is furnished to the retention member (54), movement of the movable part (78) toward the sliding direction distal end side causes the rear support part (35) of the intraocular lens (12) to be deformed toward the optical part (30) by the distal end part of the out-pushing member (22), and a guiding part (128) for guiding is furnished to the front surface side or rear surface side of the optical part (30).

Description

眼内レンズの挿入器具Intraocular lens insertion device
 本発明は、眼内レンズを内蔵して提供されて、内蔵された眼内レンズを眼内に挿入するために用いられる、眼内レンズの挿入器具に関するものである。 The present invention relates to an intraocular lens insertion device that is provided with a built-in intraocular lens and used to insert the built-in intraocular lens into the eye.
 従来から、白内障等の手術においては、角膜(鞏膜)や水晶体前嚢部分などの眼組織に設けた切開創を通じて、嚢内の水晶体を摘出、除去した後、その水晶体に代替する眼内レンズを、前記切開創より眼内に挿入して嚢内に配する手法が採用されている。 Conventionally, in surgery such as cataract, after removing the lens in the capsule through the incision provided in the eye tissue such as cornea (capsular) and anterior lens capsule part, removing the intraocular lens to replace the lens, A technique is adopted in which the incision is inserted into the eye and placed in the sac.
 特に近年においては、特許文献1に記載の如き眼内レンズの挿入器具を用いた手法が広く採用されている。一般的には、筒状の器具本体の先端部に設けられた挿入筒部の先端開口を切開創を通じて眼内に挿し入れると共に、器具本体の後端部から挿入する押出部材で、器具本体内に載置部に収容された眼内レンズを小さく変形させて挿入筒部の先端開口部から押し出すことによって、眼内レンズが眼内に挿入される。このような挿入器具を用いれば、水晶体の摘出除去のために形成した切開創を広げることなく眼内レンズを挿入出来ることから、施術に要する手間を軽減出来ると共に、術後乱視の発生や感染の危険を低減することも出来る。 Particularly in recent years, a technique using an intraocular lens insertion device as described in Patent Document 1 has been widely adopted. In general, a push-out member that is inserted into the eye through the incision through the incision at the distal end of the insertion tube provided at the distal end of the tubular instrument body, The intraocular lens is inserted into the eye by deforming the intraocular lens housed in the mounting portion into a small shape and pushing it out from the distal end opening of the insertion tube portion. With such an insertion device, it is possible to insert an intraocular lens without expanding the incision formed for the removal of the crystalline lens, so that the labor required for the operation can be reduced, as well as the occurrence of postoperative astigmatism and infection. Risk can also be reduced.
 ところで、このような眼内レンズの挿入器具としては、眼内レンズとは別に提供されて、施術時に別途にパッキングされた眼内レンズを挿入器具にセットして用いられるものと、予め眼内レンズを内蔵した状態で提供されるものがある。そして、眼内レンズを内蔵して提供される所謂プリセットタイプの眼内レンズの挿入器具においては、眼内レンズを収容した状態で滅菌梱包され、使用時まで保管されることとなる。 By the way, as such an intraocular lens insertion device, an intraocular lens that is provided separately from the intraocular lens and is used by setting an intraocular lens that is separately packed at the time of treatment to the insertion device is used. Some are provided with built-in. In a so-called preset type intraocular lens insertion device provided with a built-in intraocular lens, the intraocular lens is sterilized and packed and stored until use.
 そこで、挿入器具内に長期間保存される眼内レンズに変形や傷を与えることがないよう、眼内レンズを安定して保持する様々な機構が提案されている。例えば、本願出願人は、先に特開2009-160140号公報(特許文献1)において、眼内レンズの載置部に突出して眼内レンズの周縁部を載置部上に位置決め保持する別体の保持部材を取り外し可能に組み付けた構造を提案した。このような挿入器具によれば、眼内レンズの光学部が載置部等の器具本体内面に広範囲に亘って密着することが回避され、それによる継時的な変形の発生を有利に防止することができる。また、施術時には、保持部材を載置部から取り外すことにより、載置部に眼内レンズを位置決めして載置できることから、眼内レンズを所望の形状に小さく変形させて患者の嚢内に挿入できるのである。 Therefore, various mechanisms for stably holding the intraocular lens have been proposed so that the intraocular lens stored in the insertion device for a long period of time is not deformed or damaged. For example, the applicant of the present application previously disclosed in Japanese Patent Application Laid-Open No. 2009-160140 (Patent Document 1), which protrudes from the intraocular lens mounting portion and positions and holds the peripheral portion of the intraocular lens on the mounting portion. A structure was proposed in which the holding members were assembled in a removable manner. According to such an insertion instrument, it is avoided that the optical part of the intraocular lens is in close contact with the inner surface of the instrument main body such as the placement part over a wide range, thereby advantageously preventing the occurrence of deformation over time. be able to. In addition, at the time of surgery, the intraocular lens can be positioned and placed on the placement portion by removing the holding member from the placement portion, so that the intraocular lens can be deformed into a desired shape and inserted into the patient's sac. It is.
 ところが、眼内レンズを保持部材により保持して継時変形の発生を防止した場合でも、眼内レンズを患者の嚢内に挿入する際の眼内レンズの挙動までも完全に安定させることが難しい場合があった。すなわち、光学部と光学部の両側に延出する一対の支持部が軟質の合成樹脂材料により一体的に形成された、所謂ワンピースタイプの眼内レンズにおいては、室温などの影響により支持部の硬さが変化し易い。そうすると、眼内レンズが押出部材により挿入筒部に向かって小さく変形される際に、支持部の姿勢が安定せず、挿入筒部から眼内レンズが嚢内に解放される際に、眼内レンズの挙動が変化するおそれがあった。 However, even when the intraocular lens is held by the holding member to prevent the occurrence of deformation at the time, it is difficult to completely stabilize the behavior of the intraocular lens when the intraocular lens is inserted into the patient's sac. was there. That is, in the so-called one-piece type intraocular lens in which the optical part and a pair of support parts extending on both sides of the optical part are integrally formed of a soft synthetic resin material, the support part is hard due to the influence of room temperature or the like. Is easy to change. Then, when the intraocular lens is deformed small toward the insertion tube part by the pushing member, the posture of the support part is not stable, and when the intraocular lens is released from the insertion tube part into the capsule, the intraocular lens There was a possibility that the behavior of the garment would change.
 かかる問題に対処するために、本願出願人は先に国際特許公開第WO2010/064275号公報(特許文献2)において、挿入筒部の適所に突状部を設けて眼内レンズの光学部が上方(レンズ前面)に凸となる山折状に変形されるようにして、押出方向の前方に位置する前方支持部を光学部に入り込ませる所謂タッキングと呼ばれる状態を発現させる構造を提案した。これにより、眼内レンズの前端側の支持部の姿勢を安定させ、眼内レンズの嚢内の挙動を高精度に安定させることが可能となる。 In order to cope with such a problem, the applicant of the present application previously described in International Patent Publication No. WO2010 / 064275 (Patent Document 2), provided with a protruding portion at an appropriate position of the insertion tube portion, the optical portion of the intraocular lens is located upward. A structure has been proposed in which a so-called tacking state is developed in which a front support portion located in front of the extrusion direction is inserted into the optical portion so as to be deformed into a mountain-fold shape that is convex on the lens front surface. As a result, the posture of the support portion on the front end side of the intraocular lens can be stabilized, and the behavior of the intraocular lens in the sac can be stabilized with high accuracy.
 なお、眼内レンズの押出方向の後方に位置する後方支持部についても、押出部材で押し出される際の姿勢を安定させることで、眼内レンズの嚢内の挙動をさらに安定させることは可能であると考えられる。しかしながら、後方支持部が光学部よりも後方側の押出部材の経路上に延び出していることから、そのような部位に、後方支持部の姿勢を規制する突起等を設けることが難しいという問題があった。また、眼内レンズを保持する保持部材に加えて、眼内レンズの後方支持部の姿勢を規制する突起を取り外し可能に設けることも考えられるが、取り外しが必要な部品点数の増加により、施術時の挿入器具の操作が複雑且つ煩雑となることから、実用性に乏しかった。更に、保持部材を取り外して眼内レンズの固定が解除されてから押出部材で後方支持部を押し進める場合、レンズが移動や回転することで押出部材と後方支持部の当接位置が変化してしまい、後方支持部の姿勢が一定に制御できないという問題があった。 In addition, it is possible to further stabilize the behavior of the intraocular lens in the sac by stabilizing the posture at the time of being pushed out by the pushing member with respect to the posterior support part located behind the pushing direction of the intraocular lens. Conceivable. However, since the rear support part extends on the path of the pushing member on the rear side of the optical part, there is a problem that it is difficult to provide a projection or the like for regulating the posture of the rear support part at such a part. there were. In addition to the holding member that holds the intraocular lens, it may be possible to provide a detachable protrusion that regulates the posture of the rear support part of the intraocular lens. However, due to the increase in the number of parts that need to be removed, Since the operation of the insertion tool becomes complicated and complicated, it was not practical. Further, when the holding member is removed and the fixation of the intraocular lens is released, and the pushing member pushes the rear support part forward, the contact position between the pushing member and the rear support part changes as the lens moves or rotates. There is a problem that the posture of the rear support portion cannot be controlled to be constant.
特開2009-160140号公報JP 2009-160140 A 国際特許公開第WO2010/064275号公報International Patent Publication No. WO2010 / 064275
 本発明は上述の如き事情を背景として為されたものであって、その解決課題とするところは、眼内レンズの長期間に亘る安定保持と眼内レンズの後方支持部の姿勢の制御を、簡単な構造且つ簡素な操作で実現することができる、新規な構造の眼内レンズの挿入器具を提供することにある。 The present invention has been made in the background as described above, and the problem to be solved is to maintain the stability of the intraocular lens for a long period of time and to control the posture of the rear support part of the intraocular lens. An object of the present invention is to provide an intraocular lens insertion device having a novel structure that can be realized with a simple structure and simple operation.
 上述の如き課題を解決するために鋭意検討を重ねた結果、本発明者等は、眼内レンズの後方支持部を光学部の前面側(載置面上の上面側)に重ね合されるように変形させることで、挿入筒部からの眼内レンズの押し出しをスムーズに行うことができると共に光学部と支持部の密着を速やかに解放することができ、嚢内での眼内レンズの挙動が安定することを見い出した。また、眼内レンズの後方支持部を光学部の後面側(載置面上の下面側)に重ね合せるように変形させることで、山折状に変形する光学部の間に後方支持部を入り込ませてタッキングさせることが可能となり、これにより、後方支持部の器具本体内の移動中の姿勢が安定し、後方支持部におけるクラック等の損傷発生を防止することができると共に、嚢内に押し出された際の眼内レンズの挙動も安定することも見い出した。これら2つのパターンにはそれぞれの特徴があるため、どちらか一方に再現性良く制御する方法が必要となる。そこで、本発明者等は、かかる新たな知見に基づいて、本発明を完成するに至ったのである。 As a result of intensive studies in order to solve the above-described problems, the present inventors have superimposed the rear support portion of the intraocular lens on the front surface side (the upper surface side on the mounting surface) of the optical portion. It is possible to smoothly push out the intraocular lens from the insertion tube part and to quickly release the close contact between the optical part and the support part and to stabilize the behavior of the intraocular lens in the sac. I found something to do. In addition, the rear support part of the intraocular lens is deformed so as to overlap the rear surface side (the lower surface side on the mounting surface) of the optical part, so that the rear support part is inserted between the optical parts deformed in a mountain shape. This makes it possible to stabilize the posture of the rear support part during movement in the instrument body, prevent the occurrence of damage such as cracks in the rear support part, and when pushed into the sac It has also been found that the behavior of the intraocular lens is stable. Since these two patterns have their respective characteristics, a method for controlling one of them with good reproducibility is required. Thus, the present inventors have completed the present invention based on such new knowledge.
 すなわち、本発明の第一の態様は、光学部と該光学部の両側から延び出す一対の支持部を有する眼内レンズが載置される載置部を備えた筒形状の器具本体と、該器具本体の後端部から挿入されて該眼内レンズを該器具本体の先端部に設けられた挿入筒部へ押し出す押出部材とを備えている一方、該載置部に突出して組み付けられた保持部材によって、該眼内レンズの該一対の支持部が該器具本体の先端側と後端側に延び出すように該眼内レンズを該載置部上に位置決め保持した状態で提供される眼内レンズの挿入器具において、前記保持部材には、前記押出部材と係合した状態で前記保持部材の後端側から先端側に向かってスライド可能な可動部が設けられており、前記可動部がスライド方向の後端側に位置する際には、前記保持部材が前記器具本体から離脱不能とされている一方、前記可動部がスライド方向先端側に移動されることにより、前記押出部材の先端部により前記眼内レンズの後方に位置する前記支持部が前記光学部側へ変形されると共に、前記可動部を含む前記保持部材が前記器具本体から離脱可能とされており、前記後方の支持部の前記光学部側への変形に際して該後方の支持部を該光学部の前面側又は後面側に案内する案内部が設けられている、ことを特徴とする眼内レンズの挿入器具を提供するものである。 That is, the first aspect of the present invention is a cylindrical instrument body provided with a placement portion on which an intraocular lens having an optical portion and a pair of support portions extending from both sides of the optical portion is placed; A holding member that is inserted from the rear end of the instrument body and pushes out the intraocular lens to an insertion tube part provided at the distal end of the instrument body, while protruding and assembled to the mounting part. Intraocular provided by the member in a state where the intraocular lens is positioned and held on the mounting portion so that the pair of support portions of the intraocular lens extend to the front end side and the rear end side of the instrument body. In the lens insertion device, the holding member is provided with a movable portion that is slidable from the rear end side to the front end side of the holding member in a state of being engaged with the push-out member, and the movable portion slides. When positioned on the rear end side in the direction, the holding member While it is impossible to detach from the instrument main body, the support portion positioned behind the intraocular lens by the distal end portion of the pushing member is moved to the optical portion side by moving the movable portion toward the distal end side in the sliding direction. And the holding member including the movable part is detachable from the instrument body, and the rear support part is moved to the optical part side when the rear support part is deformed to the optical part side. It is an object of the present invention to provide an insertion device for an intraocular lens, characterized in that a guide portion for guiding the front side or the rear side is provided.
 本態様に従う構造とされた眼内レンズの挿入器具においては、載置部上に眼内レンズを位置決め保持する保持部材に可動部が設けられており、該可動部が後端側に位置する際には、保持部材を器具本体から離脱不能とするロック作用が発揮される。これにより、施術前の挿入器具の輸送中等に、保持部材が器具本体から離脱して眼内レンズの安定保持が阻害される不具合を未然に防止することができる。 In the intraocular lens insertion device structured according to this aspect, the movable member is provided on the mounting member for positioning and holding the intraocular lens, and the movable unit is positioned on the rear end side. In this case, a locking action that makes the holding member unremovable from the instrument main body is exhibited. Thereby, it is possible to prevent a problem that the holding member is detached from the main body of the instrument and the stable holding of the intraocular lens is hindered during the transportation of the insertion instrument before the operation.
 また、施術を行う際には、可動部を先端側に移動させてロック作用を解除して保持部材を器具本体から離脱させることとなるが、この離脱作動を行うことにより、可動部と係合した押出部材により、眼内レンズの後方支持部を光学部側へ屈曲乃至は湾曲変形させ、しかも、案内部により後方支持部を光学部の上面側又下面側の所望の位置に案内させることができる。これにより、実際に押出部材を押し出して眼内レンズを器具本体から患者の嚢内に挿入する場合に、後方支持部の変形姿勢を所望の形状に制御することができ、患者の嚢内に眼内レンズを解放する際の眼内レンズの挙動を高精度に制御することができる。 When performing the treatment, the movable part is moved to the distal end side to release the locking action and the holding member is detached from the instrument body. By performing this separation operation, the movable part is engaged. By the extruded member, the rear support portion of the intraocular lens is bent or curved to the optical portion side, and the rear support portion is guided to a desired position on the upper surface side or the lower surface side of the optical portion by the guide portion. it can. Accordingly, when the intraocular lens is actually inserted from the instrument body into the patient's sac by extruding the pushing member, the deformation posture of the posterior support part can be controlled to a desired shape, and the intraocular lens in the patient's sac The behavior of the intraocular lens when releasing the lens can be controlled with high accuracy.
 このように、本態様によれば、眼内レンズを長期間に亘り安定保持する保持部材に対して押出部材に係合した状態でスライドする可動部を設けることにより、保持部材を器具本体から離脱させる一連の作業を行うことのみにより、後方支持部の光学部側への所望の変形をも同時に発現させることができるのである。従って、簡単な構造且つ簡素な操作で、眼内レンズの安定保持と後方支持部の制御を実現できる。 Thus, according to this aspect, the holding member is detached from the instrument body by providing the movable member that slides in a state in which the intraocular lens is stably held for a long time while being engaged with the pushing member. Only by performing a series of operations, desired deformation of the rear support part toward the optical part side can be made manifest at the same time. Therefore, stable holding of the intraocular lens and control of the rear support portion can be realized with a simple structure and simple operation.
 なお、案内部は、光学部に接近する後方支持部をレンズ前面側又は後面側に案内できる構造であれば何れでもよい。例えば、押出部材の先端面に設けた湾曲面により、後方支持部を光学部に接近させるにつれて前面側又は後面側に案内する案内部を構成してもよいし、器具本体に設けた上方又は下方に突出する突起部により案内部を構成し、光学部に接近する後方支持部を該突起部に当接させて光学部の前面側又は後面側に案内するようにしてもよい。 Note that the guide part may be any structure as long as it can guide the rear support part approaching the optical part to the front side or the rear side of the lens. For example, the curved surface provided on the front end surface of the push-out member may constitute a guide unit that guides the front support side or the rear side as the rear support unit approaches the optical unit, or the upper or lower side provided on the instrument body The guide portion may be configured by a protruding portion that protrudes toward the optical portion, and a rear support portion approaching the optical portion may be brought into contact with the protruding portion and guided to the front side or the rear side of the optical portion.
 本発明の第二の態様は、前記第一の態様に記載の眼内レンズの挿入器具において、前記可動部には把持突起が突出して設けられており、該把持突起により該可動部のスライド操作と前記保持部材の前記器具本体からの離脱操作が可能とされているものである。 According to a second aspect of the present invention, in the intraocular lens insertion device according to the first aspect, a gripping protrusion protrudes from the movable part, and the sliding operation of the movable part is performed by the gripping protrusion. The holding member can be detached from the instrument body.
 本態用によれば、把持突起を把持したまま、可動部のスライド操作と保持部材の離脱操作を一連の動作で行うことができ、操作性の向上を図ることができる。 According to this embodiment, the sliding operation of the movable part and the detaching operation of the holding member can be performed in a series of operations while holding the gripping protrusion, and the operability can be improved.
 本発明の眼内レンズの挿入器具によれば、眼内レンズを長期間に亘り安定保持する保持部材に対して押出部材に係合した状態でスライドする可動部を設けることにより、保持部材を器具本体から離脱させる一連の作業を行うことのみにより、後方支持部の光学部側への所望の変形をも同時に発現させることができる。すなわち、簡単な構造且つ簡素な操作で、眼内レンズの安定保持と後方支持部の制御を実現できるのである。 According to the intraocular lens insertion device of the present invention, the holding member is provided by providing the movable member that slides in a state in which the intraocular lens is engaged with the pushing member with respect to the holding member that stably holds the intraocular lens for a long time. Only by performing a series of operations for detachment from the main body, a desired deformation of the rear support portion toward the optical portion side can be simultaneously exhibited. That is, stable holding of the intraocular lens and control of the rear support portion can be realized with a simple structure and simple operation.
本発明の第一の実施形態としての眼内レンズの挿入器具の上面図。The top view of the insertion instrument of the intraocular lens as 1st embodiment of this invention. 図1に示す挿入器具の側面図。The side view of the insertion instrument shown in FIG. 図1に示す挿入器具を構成する載置部の要部拡大上面図。The principal part enlarged top view of the mounting part which comprises the insertion instrument shown in FIG. 図1に示す挿入器具を構成する保持部材の上面図。The top view of the holding member which comprises the insertion instrument shown in FIG. 図4に示す保持部材の側面図。The side view of the holding member shown in FIG. 図1に示す挿入器具の要部を拡大して示す上面説明図。The upper surface explanatory drawing which expands and shows the principal part of the insertion instrument shown in FIG. 図6のVII-VII縦断面拡大図。VII-VII longitudinal cross-sectional enlarged view of FIG. 本発明の第二の実施形態としての眼内レンズの挿入器具の載置部の要部拡大上面図。The principal part enlarged top view of the mounting part of the insertion instrument of the intraocular lens as 2nd embodiment of this invention. 図8に示す挿入器具を構成する保持部材の上面図。The top view of the holding member which comprises the insertion instrument shown in FIG.
 以下、本発明を更に具体的に明らかにするために、本発明の実施形態について、図面を参照しつつ、詳細に説明する。 Hereinafter, in order to clarify the present invention more specifically, embodiments of the present invention will be described in detail with reference to the drawings.
 先ず、図1および図2に、本発明の一実施形態としての眼内レンズの挿入器具10を示す。眼内レンズの挿入器具10は合成樹脂製とされており、眼内レンズ12が載置される載置部14を備えた筒形状の器具本体16と、器具本体16の後端部18から挿入されて眼内レンズ12を器具本体16の先端部に設けられた挿入筒部20へ押し出す押出部材22とを備えており、予め眼内レンズ12を内蔵して提供される。なお、以下の説明において、前方とは、押出部材22の押出方向(図1中、左方向)を言うものとし、上方とは、図2中、上方向を言うものとする。また、左右方向とは、眼内レンズの挿入器具10の上面視における左右方向(図1中、上方が右、下方が左)を言うものとする。 First, FIGS. 1 and 2 show an intraocular lens insertion device 10 as an embodiment of the present invention. The intraocular lens insertion instrument 10 is made of a synthetic resin, and is inserted from a cylindrical instrument body 16 having a placement portion 14 on which the intraocular lens 12 is placed, and a rear end portion 18 of the instrument body 16. The push-out member 22 that pushes the intraocular lens 12 to the insertion tube portion 20 provided at the distal end portion of the instrument main body 16 is provided, and the intraocular lens 12 is provided in advance. In the following description, “front” refers to the pushing direction of the pushing member 22 (left direction in FIG. 1), and “upward” refers to the up direction in FIG. The left-right direction refers to the left-right direction in the top view of the intraocular lens insertion device 10 (upper is right and lower is left in FIG. 1).
 より詳細には、器具本体16は、略筒形状とされた本体筒部24を有している。本体筒部24の内部には、略矩形断面形状をもって軸方向に貫通する貫通孔26が形成されている。また、本体筒部24の後端部からやや前方の部位には、本体筒部24の延出方向と直交する向きに広がる板状部28が一体的に形成されている。 More specifically, the instrument main body 16 has a main body cylinder portion 24 having a substantially cylindrical shape. A through-hole 26 that penetrates in the axial direction with a substantially rectangular cross-sectional shape is formed inside the main body cylinder portion 24. Further, a plate-like portion 28 that extends in a direction orthogonal to the extending direction of the main body cylinder portion 24 is integrally formed at a position slightly forward from the rear end portion of the main body cylinder portion 24.
 さらに、器具本体16における本体筒部24の前方には、載置部14が形成されている。図3に、載置部14を示す。載置部14には、図1に示す眼内レンズ12の光学部30の径寸法より僅かに大きな幅寸法をもって軸方向に延びる凹状溝32が形成されている。凹状溝32は、眼内レンズ12の一対の支持部34,35を含む最大幅寸法(図1における左右方向寸法)よりもやや大きな軸方向長さ寸法をもって形成されている。 Furthermore, a mounting portion 14 is formed in front of the main body cylinder portion 24 in the instrument main body 16. FIG. 3 shows the placement unit 14. The mounting portion 14 is formed with a concave groove 32 extending in the axial direction with a width that is slightly larger than the diameter of the optical portion 30 of the intraocular lens 12 shown in FIG. The concave groove 32 is formed with an axial length dimension that is slightly larger than the maximum width dimension (the horizontal dimension in FIG. 1) including the pair of support portions 34, 35 of the intraocular lens 12.
 ここにおいて、凹状溝32は上方に開口せしめられた開口部36を有する一方、その底面には載置面38が形成されている。載置面38は、眼内レンズ12の最小幅寸法(図1における上下方向寸法)よりも僅かに大きな幅寸法を有すると共に、眼内レンズ12の最大幅寸法(図1における左右方向寸法)よりも大きな軸方向長さ寸法を有する平坦面とされている。なお、載置面38の高さ位置は、本体筒部24における貫通孔26の底面の高さ位置よりも上方に位置しており、本体筒部24における貫通孔26の前端縁部には、貫通孔26の底面から上方に延び出して載置面38の後端縁部に接続する壁部40(図2参照)が形成されている。このようにして、凹状溝32は貫通孔26と連通されており、凹状溝32の幅寸法が貫通孔26の幅寸法と略等しくされている。 Here, the concave groove 32 has an opening 36 opened upward, and a mounting surface 38 is formed on the bottom surface thereof. The placement surface 38 has a width dimension slightly larger than the minimum width dimension (the vertical dimension in FIG. 1) of the intraocular lens 12, and is larger than the maximum width dimension (the horizontal dimension in FIG. 1) of the intraocular lens 12. Is also a flat surface having a large axial length dimension. In addition, the height position of the mounting surface 38 is located higher than the height position of the bottom surface of the through hole 26 in the main body cylinder portion 24, and the front edge of the through hole 26 in the main body cylinder portion 24 is A wall portion 40 (see FIG. 2) that extends upward from the bottom surface of the through hole 26 and is connected to the rear end edge portion of the placement surface 38 is formed. Thus, the concave groove 32 communicates with the through hole 26, and the width dimension of the concave groove 32 is substantially equal to the width dimension of the through hole 26.
 そして、凹状溝32の側方(本実施形態においては、右側)には、蓋体としてのカバー部材42が器具本体16と一体形成されている。カバー部材42は、凹状溝32の軸方向寸法と略等しい軸方向寸法を有すると共に、凹状溝32の幅寸法よりもやや大きな幅寸法をもって形成されている。更に、カバー部材42は、載置部14の上端縁部が側方(本実施形態においては、右側)に延び出して形成された略薄板形状の連結部44によって器具本体16と連結されている。連結部44は、幅方向略中央部分を器具本体16の軸方向に延びる屈曲部46において最も薄肉とされており、屈曲部46で折り曲げ可能とされている。これにより、カバー部材42は、連結部44を折り曲げて凹状溝32に重ね合わせ、開口部36を覆蓋することが出来るようにされている。 A cover member 42 as a lid is integrally formed with the instrument body 16 on the side of the concave groove 32 (on the right side in the present embodiment). The cover member 42 has an axial dimension substantially equal to the axial dimension of the concave groove 32 and is formed with a width dimension slightly larger than the width dimension of the concave groove 32. Further, the cover member 42 is connected to the instrument main body 16 by a substantially thin plate-like connecting portion 44 formed by extending the upper end edge of the mounting portion 14 to the side (in the present embodiment, the right side). . The connecting portion 44 is thinnest at a bent portion 46 extending in the axial direction of the instrument body 16 at a substantially central portion in the width direction, and can be bent at the bent portion 46. Thus, the cover member 42 is configured to be able to cover the opening 36 by bending the connecting portion 44 and overlapping the concave groove 32.
 そして、カバー部材42における連結部44と反対側の縁部には、係合片48が突出形成されている一方、載置部14におけるカバー部材42と反対側の端部には、外側に突出する突出縁部50が形成されており、かかる突出縁部50における係合片48と対応する位置には、係合切欠52が形成されている。 An engagement piece 48 is formed to project from the edge of the cover member 42 opposite to the connecting portion 44, while the end of the mounting portion 14 opposite to the cover member 42 projects outward. A protruding edge 50 is formed, and an engagement notch 52 is formed at a position corresponding to the engagement piece 48 in the protruding edge 50.
 このような構造とされた載置部14の載置面38の下側には、眼内レンズ12を位置決め保持した状態で保持部材54が取外し可能に設けられている。図4および図5に示すように、保持部材54は器具本体16と別体として構成されており、一対の側壁部56,56が対向面間に一体形成された連結板部58で連結された構造とされている。ここにおいて、側壁部56における外側面の離隔距離は、眼内レンズ12の光学部30の径寸法と略等しくされている。また、連結板部58の下端部には、押出部材22の押出方向に対して垂直方向に、薄肉平板形状の脚板部60が一体形成されている。 The holding member 54 is detachably provided on the lower side of the mounting surface 38 of the mounting portion 14 having such a structure in a state where the intraocular lens 12 is positioned and held. As shown in FIGS. 4 and 5, the holding member 54 is configured as a separate body from the instrument body 16, and a pair of side wall portions 56, 56 are connected by a connecting plate portion 58 formed integrally between the opposing surfaces. It is structured. Here, the separation distance of the outer surface of the side wall portion 56 is substantially equal to the radial dimension of the optical portion 30 of the intraocular lens 12. Further, a thin flat plate-like leg plate portion 60 is integrally formed at the lower end portion of the connecting plate portion 58 in a direction perpendicular to the pushing direction of the pushing member 22.
 そして、それぞれの側壁部56,56の上端部には、上面視において略円弧形状をもって上方に突出する第一保持突起62,62が一体形成されている。更に、第一保持突起62の上端面における外側部分で、保持部材54の内方側には、周壁64が一体的に突出形成されている。ここにおいて、周壁64の離隔距離は、眼内レンズ12の光学部30の径寸法よりも僅かに大きくされている。 Further, first holding projections 62 and 62 projecting upward with a substantially arc shape in a top view are integrally formed at the upper end portions of the respective side wall portions 56 and 56. Further, a peripheral wall 64 is integrally formed on the outer side of the upper end surface of the first holding projection 62 on the inner side of the holding member 54. Here, the separation distance of the peripheral wall 64 is slightly larger than the diameter of the optical part 30 of the intraocular lens 12.
 また、連結板部58の軸方向両端部には、上面視において矩形状をもって上方に突出する一対の第二保持突起66,66が保持部材54の長手方向(図4中、左右方向)で相互に離隔して対向位置するように一体形成されている。ここにおいて、第二保持突起66の上端面の高さ位置は、第一保持突起62の上端面の高さ位置と等しくされている。各第二保持突起66は、連結板部58から突出する突起本体部68と、突起本体部68上端面から突出する周壁70と、突起本体部68上部側面において第二保持突起66の対向方向の外方端側で突出して設けられた係合部71から構成されている。かかる周壁70,70の対向方向での離隔距離は、眼内レンズ12の光学部30の径寸法よりも僅かに大きくされている。さらに、各周壁70と各係合部71は、突起本体部68の幅寸法と略等しい幅寸法を有している。 In addition, a pair of second holding projections 66 and 66 projecting upward in a rectangular shape in a top view are mutually opposite in the longitudinal direction of the holding member 54 (left and right direction in FIG. 4). Are integrally formed so as to be opposed to each other. Here, the height position of the upper end surface of the second holding projection 66 is equal to the height position of the upper end surface of the first holding projection 62. Each of the second holding projections 66 includes a projection main body 68 projecting from the connecting plate portion 58, a peripheral wall 70 projecting from the upper end surface of the projection main body 68, and the second main body projection 68 in the opposing direction of the second holding projection 66. It is comprised from the engaging part 71 which protruded and provided in the outward end side. The separation distance in the facing direction of the peripheral walls 70 and 70 is slightly larger than the diameter of the optical part 30 of the intraocular lens 12. Further, each peripheral wall 70 and each engagement portion 71 have a width dimension substantially equal to the width dimension of the projection main body 68.
 さらに、連結板部58の軸方向両端部には、平面視で矩形状の開口部72が形成されており、開口部72の軸垂直方向の対向する側壁部74,74間の距離は、側壁部56,56間の距離よりも短くされている。そして、開口部72に、保持部材54とは別体形成され、平面視において側壁部74,74間の距離よりも僅かに狭幅の矩形平板状部76を有する可動部78が、保持部材54の後端側から先端側に向かって、保持部材54に対してスライド可能に組み付けられている。 Furthermore, the opening part 72 of the rectangular shape is formed in planar view at both axial ends of the connecting plate part 58, and the distance between the opposing side wall parts 74, 74 in the axial vertical direction of the opening part 72 is the side wall. The distance between the portions 56 and 56 is shorter. A movable portion 78 is formed in the opening 72 separately from the holding member 54 and has a rectangular flat plate-like portion 76 that is slightly narrower than the distance between the side wall portions 74 and 74 in plan view. It is slidably assembled to the holding member 54 from the rear end side toward the front end side.
 より詳細には、可動部78には、幅方向両側の側縁部から突出する係合突起80が、その長さ方向中央部分で所定長さに亘って形成されている。一方、開口部72を画成する両側壁部74,74には、両側壁部74,74を保持部材54の軸方向で前方に向かって延びると共に開口部72および保持部材54の後端側に開口するレールたる長溝82,82がそれぞれ形成されている。そして、可動部78が保持部材54の後端側から長溝82内に差し込まれることにより、可動部78が軸方向前方にスライドして移動できるようになっている。長溝82は、可動部78が滑らかにスライドでき且つぐらつかないように、軸垂直方向(図4における上下方向)の係合突起80の外形寸法よりも僅かに大きな内法寸法で形成されている一方、軸方向には所定のスライド長を確保できる長さ寸法で形成されている。 More specifically, the movable portion 78 is formed with engaging protrusions 80 protruding from the side edge portions on both sides in the width direction over a predetermined length at the center portion in the length direction. On the other hand, both side wall portions 74, 74 that define the opening 72 extend on both side walls 74, 74 forward in the axial direction of the holding member 54, and on the rear end side of the opening 72 and the holding member 54. Long grooves 82 and 82 that are open rails are formed, respectively. The movable portion 78 is inserted into the long groove 82 from the rear end side of the holding member 54, so that the movable portion 78 can move by sliding forward in the axial direction. The long groove 82 is formed with an internal dimension slightly larger than the external dimension of the engaging projection 80 in the direction perpendicular to the axis (vertical direction in FIG. 4) so that the movable portion 78 can slide smoothly and does not wobble. In the axial direction, it is formed with a length dimension that can ensure a predetermined slide length.
 図3および図4(a)に示すように、始めに、可動部78が保持部材54の後端側から長溝82内に差し込まれる。次に、このような構造とされた保持部材54が、器具本体16の載置面38の下側から組み付けられる。具体的には、器具本体16の載置面38には、厚さ方向に貫通する貫通孔84,86が形成されている (図3参照)。かかる貫通孔84,86は、保持部材54の第一保持突起62および第二保持突起66の上面視よりも僅かに大きな略相似形状をもって形成されている。そして、保持部材54の第一保持突起62および第二保持突起66が、載置面38の下側から貫通孔84,86に挿通せしめられて、載置面38上に突出せしめられる。これにより、第二保持突起66に設けられた係合部71が載置面38上に突出せしめられて、載置面38の上面に係止せしめられることによって、保持部材54が器具本体16の外側から組み付けられ、第一保持突起62および第二保持突起66が載置面38から突出せしめられた状態が保持されることとなる。 3 and 4A, first, the movable portion 78 is inserted into the long groove 82 from the rear end side of the holding member 54. Next, the holding member 54 having such a structure is assembled from below the placement surface 38 of the instrument body 16. Specifically, through holes 84 and 86 penetrating in the thickness direction are formed on the mounting surface 38 of the instrument body 16 (see FIG. 3). The through holes 84 and 86 are formed to have a substantially similar shape that is slightly larger than the top view of the first holding projection 62 and the second holding projection 66 of the holding member 54. Then, the first holding projection 62 and the second holding projection 66 of the holding member 54 are inserted into the through holes 84 and 86 from the lower side of the mounting surface 38 and protruded on the mounting surface 38. As a result, the engaging portion 71 provided on the second holding projection 66 is protruded on the mounting surface 38 and is locked to the upper surface of the mounting surface 38, so that the holding member 54 is attached to the instrument body 16. The state where the first holding protrusion 62 and the second holding protrusion 66 are protruded from the mounting surface 38 is held from the outside.
 また、器具本体16の載置面38には、厚さ方向に貫通する貫通孔85が形成されている (図3参照)。かかる貫通孔85は、可動部78を構成する矩形平板状部76から上方(紙面垂直方向)に突出する柱状突起88が後述するスライド動作を支障なく出来るように、所定の大きさに開口されている。 Further, a through hole 85 penetrating in the thickness direction is formed in the mounting surface 38 of the instrument body 16 (see FIG. 3). The through-hole 85 is opened to a predetermined size so that the columnar protrusion 88 protruding upward (perpendicular to the paper surface) from the rectangular flat plate portion 76 constituting the movable portion 78 can perform a sliding operation described later. Yes.
 そして、このような保持部材54に組み付けられた可動部78を器具本体16の軸方向後方にスライドすることにより、器具本体16における本体筒部24の前方部90に形成された溝部92に案内され、可動部78を構成する矩形平板状部76に設けられた係止爪94が、溝部92に設けられた係止孔96に嵌め込まれる。すなわち、可動部78がスライド方向の後端側に位置するスライド開始端においては、可動部78を構成する矩形平板状部76の本体筒部24への係合により、保持部材54が器具本体16から離脱不能に係合されている。さらに、可動部78がスライド開始端に位置された状態では、図6(a)に示すように、可動部78を構成する矩形平板状部76から上方(紙面垂直方向)に突出する柱状突起88に、押出部材22の棒状部98の先端に形成された係合切欠100が嵌め込まれている。なお、可動部78がスライド方向の先端側に移動され、可動部78を構成する矩形平板状部76が、本体筒部24の前方部90に形成された溝部92から抜け出すスライド終了端においては、可動部78を含む保持部材54が載置部14から離脱できるようになっている。 Then, the movable portion 78 assembled to the holding member 54 is slid rearward in the axial direction of the instrument main body 16, thereby being guided to the groove 92 formed in the front portion 90 of the main body cylinder portion 24 in the instrument main body 16. The locking claw 94 provided in the rectangular flat plate portion 76 constituting the movable portion 78 is fitted into the locking hole 96 provided in the groove portion 92. That is, at the slide start end where the movable portion 78 is located on the rear end side in the sliding direction, the holding member 54 is moved to the instrument main body 16 by the engagement of the rectangular flat plate portion 76 constituting the movable portion 78 with the main body cylinder portion 24. It is engaged so that it cannot be detached. Further, in a state where the movable portion 78 is positioned at the slide start end, as shown in FIG. 6A, a columnar protrusion 88 that protrudes upward (in the direction perpendicular to the paper surface) from the rectangular flat plate portion 76 constituting the movable portion 78. Further, an engagement notch 100 formed at the tip of the rod-like portion 98 of the push member 22 is fitted. In addition, at the slide end end where the movable portion 78 is moved to the front end side in the sliding direction and the rectangular flat plate portion 76 constituting the movable portion 78 comes out from the groove portion 92 formed in the front portion 90 of the main body cylinder portion 24, The holding member 54 including the movable portion 78 can be detached from the placement portion 14.
 次に、図3(b)および図4(b)に示すように、保持部材54に組み付けられた可動部78を器具本体16の軸方向前方スライド方向先端側にスライドすることにより、可動部78が器具本体16に形成された溝部92から抜け出すことが出来ると共に、可動部78を構成する矩形平板状部76の軸方向前方に設けられた係止爪102が、保持部材54の脚板部60に設けられた係止孔104に嵌め込まれ、保持部材54に係合される。すなわち、スライド終了端においては、可動部78を含む保持部材54が載置部14から離脱できるようになっている。なお、図5に示すように、可動部78を構成する矩形平板状部76は、載置面38の下部に収納されているようになっている。また、この時、係合突起80が長溝82の先端側端部に当接していることが望ましい。 Next, as shown in FIGS. 3 (b) and 4 (b), the movable portion 78 assembled to the holding member 54 is slid toward the distal end side in the axial forward sliding direction of the instrument body 16, thereby moving the movable portion 78. Can be removed from the groove 92 formed in the instrument main body 16, and the locking claw 102 provided in the axially forward direction of the rectangular flat plate portion 76 constituting the movable portion 78 is provided on the leg plate portion 60 of the holding member 54. It is fitted into the provided locking hole 104 and engaged with the holding member 54. That is, the holding member 54 including the movable portion 78 can be detached from the placement portion 14 at the slide end end. As shown in FIG. 5, the rectangular flat plate portion 76 constituting the movable portion 78 is housed in the lower portion of the placement surface 38. At this time, it is desirable that the engagement protrusion 80 is in contact with the end portion on the front end side of the long groove 82.
 載置部14の前方には、器具本体16の軸方向前方に向かって延び出す挿入筒部20が一体形成されている。挿入筒部20は、全体として載置部14側から延出方向の先端部に行くに連れて次第に先細となるテーパ形状を有しており、延出方向の全長に亘って貫通するテーパ形状の通孔106が形成されている。 An insertion tube portion 20 that extends toward the front in the axial direction of the instrument body 16 is integrally formed in front of the mounting portion 14. The insertion tube portion 20 has a tapered shape that gradually tapers from the placement portion 14 side toward the distal end portion in the extending direction as a whole, and has a tapered shape penetrating the entire length in the extending direction. A through hole 106 is formed.
 通孔106は、載置部14側に開口した基端開口部108が載置面38と接続されることによって載置部14と連通されている。基端開口部108は、全体として、底面110が平坦面とされて、上面が略円弧形状とされた扁平な略楕円形状断面とされている。通孔106の先端部に設けられた先端開口部112は、上面が底面よりも前方に延び出された側方視において斜めの開口形状とされている。 The through-hole 106 communicates with the placement unit 14 by connecting a base end opening 108 opened to the placement unit 14 side to the placement surface 38. The base end opening 108 as a whole has a flat, substantially elliptical cross section in which the bottom surface 110 is a flat surface and the top surface is a substantially arc shape. The tip opening 112 provided at the tip of the through-hole 106 has an oblique opening shape in a side view with the upper surface extending forward from the bottom.
 また、底面110には、底面110の幅方向中央部分を挟んで器具本体16の軸方向に延びる導入突部114が形成されている。導入突部114は、底面110から僅かに上方に突出して互いに平行に延びる線形状とされている。導入突部114の突出高さは、器具本体16の軸方向前方に行くに連れて次第に高くされており、基端開口部108の後端部では底面110と面一となるようにされている。 In addition, the bottom surface 110 is formed with an introduction protrusion 114 that extends in the axial direction of the instrument body 16 with the widthwise center portion of the bottom surface 110 interposed therebetween. The introduction protrusions 114 have a linear shape that protrudes slightly upward from the bottom surface 110 and extends parallel to each other. The protrusion height of the introduction protrusion 114 is gradually increased as it goes forward in the axial direction of the instrument body 16, and is flush with the bottom surface 110 at the rear end portion of the proximal end opening 108. .
 更にまた、導入突部114は、底面110の幅方向の中央を挟んで器具本体16の軸直角方向で互いに所定距離を隔てて略平行に配設されており、かかる導入突部114の離隔距離は、押出部材22の先端部の幅寸法よりも僅かに大きい寸法とされることが好ましく、特に本態様においては、押出部材22の棒状部98の幅寸法よりも僅かに大きくされている。 Furthermore, the introduction protrusions 114 are disposed substantially in parallel with each other at a predetermined distance in the direction perpendicular to the axis of the instrument body 16 with the center in the width direction of the bottom surface 110 interposed therebetween. Is preferably slightly larger than the width of the distal end portion of the extrusion member 22, and in this embodiment, it is slightly larger than the width of the rod-shaped portion 98 of the extrusion member 22.
 以上のように、本実施形態における器具本体16は、本体筒部24、載置部14、カバー部材42、および挿入筒部20が一体成形された単一の部材として構成されており、かかる器具本体16とは別体として構成された可動部78を含む保持部材54が載置面38の下方から組み付けられるようになっている。 As described above, the instrument main body 16 in the present embodiment is configured as a single member in which the main body cylinder part 24, the placement part 14, the cover member 42, and the insertion cylinder part 20 are integrally molded. A holding member 54 including a movable portion 78 configured separately from the main body 16 is assembled from below the placement surface 38.
 そして、このような構造とされた器具本体16の後方から、押出部材22が貫通孔26に挿し入れられている。押出部材22は、器具本体16の軸方向長さ寸法よりもやや大きな軸方向長さ寸法を有する略ロッド形状とされており、略円柱形状とされた作用部116と、略矩形ロッド形状とされた挿通部118が一体形成されている。 And the extrusion member 22 is inserted in the through-hole 26 from the rear of the instrument body 16 having such a structure. The pushing member 22 has a substantially rod shape having an axial length dimension slightly larger than the axial length dimension of the instrument main body 16, and has a substantially cylindrical action portion 116 and a substantially rectangular rod shape. The insertion part 118 is integrally formed.
 このような構造とされた眼内レンズの挿入器具10においては、先ず、押出部材22の先端部分が器具本体16の本体筒部24に後方から挿入されて、図1に示すように押出部材22の爪部120が器具本体16に貫設された係止孔124に係止された初期位置にセットされる。それと共に、保持部材54が、前述のように、載置面38の下方から器具本体16に取り付けられて、可動部78がスライド開始端にセットされる。これにより、可動部78を含む保持部材54が器具本体16に離脱不能に組み付けられて、保持部材54の第一保持突起62および第二保持突起66が載置面38上に突出した状態に保持される。 In the intraocular lens insertion device 10 having such a structure, first, the distal end portion of the pushing member 22 is inserted into the main body cylinder portion 24 of the device main body 16 from the rear side, and the pushing member 22 as shown in FIG. The claw portion 120 is set at an initial position locked in a locking hole 124 penetrating the instrument body 16. At the same time, the holding member 54 is attached to the instrument body 16 from below the placement surface 38 as described above, and the movable portion 78 is set at the slide start end. Accordingly, the holding member 54 including the movable portion 78 is assembled to the instrument body 16 so as not to be detached, and the first holding projection 62 and the second holding projection 66 of the holding member 54 are held in a state of protruding on the placement surface 38. Is done.
 そして、図6および図7に示すように、眼内レンズ12の光学部30が保持部材54の第一保持突起62および第二保持突起66の上端面に載置され、保持されている。なお、図6においては、理解を容易とするために、器具本体16の必要部分と眼内レンズ12、保持部材54および載置部14内に臨む押出部材22の先端部分のみを示す。かかる載置状態において、眼内レンズ12は、光学部30の外周部分が第一及び第二保持突起62,66に接触状態とされており、中央部分はこれら第一及び第二保持突起62,66に対して非接触状態で保持されている。 6 and 7, the optical unit 30 of the intraocular lens 12 is placed and held on the upper end surfaces of the first holding projection 62 and the second holding projection 66 of the holding member 54. In FIG. 6, only a necessary portion of the instrument main body 16 and a distal end portion of the pushing member 22 facing the intraocular lens 12, the holding member 54, and the placement portion 14 are shown for easy understanding. In such a mounted state, the intraocular lens 12 has the outer peripheral portion of the optical unit 30 in contact with the first and second holding projections 62 and 66, and the central portion has the first and second holding projections 62 and 66. 66 in a non-contact state.
 さらに、第一保持突起62および第二保持突起66に形成された周壁64、70が、眼内レンズ12における光学部30の外側にあり、特に本実施形態においては、第一保持突起62に形成された周壁64が眼内レンズ12を器具本体16の軸方向に対する斜め方向の両側を挟んでいると共に、第二保持突起66に形成された周壁70が、眼内レンズ12を器具本体16の軸方向の両側を挟むように設けられている。これにより、眼内レンズ12の器具本体16に対する軸方向および軸直方向の変位量を制限して、眼内レンズ12を安定して保持出来るようになっている。 Furthermore, the peripheral walls 64 and 70 formed on the first holding protrusion 62 and the second holding protrusion 66 are outside the optical unit 30 in the intraocular lens 12, and in particular in the present embodiment, formed on the first holding protrusion 62. The peripheral wall 64 sandwiches the intraocular lens 12 on both sides in an oblique direction with respect to the axial direction of the instrument main body 16, and the peripheral wall 70 formed on the second holding projection 66 connects the intraocular lens 12 to the axis of the instrument main body 16. It is provided so as to sandwich both sides of the direction. Thereby, the amount of displacement of the intraocular lens 12 with respect to the instrument body 16 in the axial direction and the axial direction is limited, and the intraocular lens 12 can be stably held.
 なお、眼内レンズ12の一対の支持部34,35は、保持部材54の第一及び第二保持突起62,66から器具本体16の前方側及び後方側に延び出すように、載置面38上に置かれている。 The pair of support portions 34 and 35 of the intraocular lens 12 extend from the first and second holding projections 62 and 66 of the holding member 54 to the front side and the rear side of the instrument body 16. Is placed on top.
 そして、屈曲部46が屈曲されて、カバー部材42によって載置部14の開口部36が覆蓋されることによって、眼内レンズ12が器具本体16内に収容状態でセットされる。なお、カバー部材42は、係合片48が係合切欠52に係合されることによって、閉状態に維持される。 Then, the bent portion 46 is bent and the opening portion 36 of the placement portion 14 is covered with the cover member 42, so that the intraocular lens 12 is set in the instrument body 16 in the accommodated state. The cover member 42 is maintained in the closed state by the engagement piece 48 being engaged with the engagement notch 52.
 以上のようにして、眼内レンズ12が挿入器具10内に収容される。そして、本実施形態における挿入器具10は、眼内レンズ12を収容した状態で殺菌処理等がなされた後に、梱包されて配送される。 As described above, the intraocular lens 12 is accommodated in the insertion device 10. And the insertion instrument 10 in this embodiment is packaged and delivered after sterilization etc. are made in the state which accommodated the intraocular lens 12. FIG.
 このように、眼内レンズ12を内蔵して提供された、本実施形態における挿入器具10は、白内障等の手術に際して、以下のように用いられる。 As described above, the insertion instrument 10 according to the present embodiment provided with the intraocular lens 12 is used in the following manner during an operation such as a cataract.
 梱包から取り出した後、始めに、ヒアルロン酸ナトリウム等の粘弾性物質を主成分とする潤滑剤を載置部14や挿入筒部20の内部に注入することが望ましい。特に本実施形態においては、カバー部材42に厚さ方向に貫通する注入孔126が形成されており、かかる注入孔126を通じて、カバー部材42を閉じた状態で潤滑剤が注入出来るようになっているが、潤滑剤の注入は、例えば、挿入筒部20の先端開口部112から注入したり、一旦カバー部材42を開いて、載置部14の開口部36から注入したり、或いは、一旦押出部材22を器具本体16から引き抜いて、貫通孔26の後端の後端部18から注入するなどしても良い。 After removing from the package, it is desirable to first inject a lubricant mainly composed of a viscoelastic substance such as sodium hyaluronate into the mounting portion 14 or the insertion tube portion 20. Particularly in this embodiment, an injection hole 126 penetrating in the thickness direction is formed in the cover member 42, and the lubricant can be injected through the injection hole 126 with the cover member 42 being closed. However, the lubricant may be injected from, for example, the distal end opening 112 of the insertion tube portion 20, or the cover member 42 is opened once and then injected from the opening 36 of the mounting portion 14, or once the extrusion member. 22 may be pulled out from the instrument body 16 and injected from the rear end 18 of the rear end of the through hole 26.
 次に、眼内レンズ12の光学部30が保持部材54の第一保持突起62および第二保持突起66の上端面に載置および保持された状態で、保持部材54の可動部78を、器具本体16の本体筒部24の前方部90に設けられた溝部92に嵌め込まれたスライド開始端から、保持部材54の載置面38の下部に位置するスライド終了端に向かって、載置面38に沿って軸方向前方にスライドさせる。スライド時には、保持部材54を構成する第一および第二保持突起62,66は変位せず、可動部78に係合された押出部材22の棒状部98の先端部だけが軸方向前方にスライドされるので、眼内レンズ12の後方支持部35を光学部30側に変形させることができる。この変形に際して、例えば、図7に示すように、載置面38上に軸方向前方に向かって高さを増す案内部128を設けることにより、後方支持部35を光学部30の前面側に案内することができる。同様にして、カバー部材42の載置面38と対向する面に、案内部128を紙面に対して対称形状に設ける(図示しない)ことにより、後方支持部35を光学部30の後面側に案内することもできる。あるいは、押出部材22の棒状部98の先端部129に軸方向前方に右肩下がり又は右肩上がりのテーパを設けることにより、後方支持部35を光学部30の前面側又は後面側に案内することができる。このように、後方支持部35を所望の形状に変形させることができ、眼内レンズ12の嚢内での安定性の向上を図ることができるのである。なお、案内部128の設置箇所は例示のものに限定されず、保持部材54や可動部78に設置することも可能である。 Next, in a state where the optical part 30 of the intraocular lens 12 is placed and held on the upper end surfaces of the first holding protrusion 62 and the second holding protrusion 66 of the holding member 54, the movable part 78 of the holding member 54 is moved to the instrument. From the slide start end fitted in the groove portion 92 provided in the front portion 90 of the main body cylinder portion 24 of the main body 16, toward the slide end end positioned at the lower portion of the placement surface 38 of the holding member 54. And slide forward in the axial direction. At the time of sliding, the first and second holding projections 62 and 66 constituting the holding member 54 are not displaced, and only the distal end portion of the rod-like portion 98 of the pushing member 22 engaged with the movable portion 78 is slid forward in the axial direction. Therefore, the rear support part 35 of the intraocular lens 12 can be deformed to the optical part 30 side. At the time of this deformation, for example, as shown in FIG. 7, by providing a guide portion 128 that increases in height toward the front in the axial direction on the mounting surface 38, the rear support portion 35 is guided to the front side of the optical portion 30. can do. Similarly, the rear support portion 35 is guided to the rear surface side of the optical portion 30 by providing the guide portion 128 in a symmetrical shape with respect to the paper surface (not shown) on the surface of the cover member 42 facing the placement surface 38. You can also Alternatively, the rear support portion 35 is guided to the front surface side or the rear surface side of the optical unit 30 by providing a taper of a right shoulder downward or a right shoulder upward at the front end portion 129 of the rod-shaped portion 98 of the pushing member 22. Can do. In this way, the rear support portion 35 can be deformed into a desired shape, and the stability of the intraocular lens 12 within the sac can be improved. In addition, the installation location of the guide part 128 is not limited to the illustrated example, and can be installed on the holding member 54 or the movable part 78.
 そして、保持部材54を器具本体16の下方に引き抜いて、器具本体16から取り外すことにより、眼内レンズ12を上述の潤滑剤に包まれた状態で載置面38上に載置することが可能となる。なお、本実施形態における載置面38は平坦面とされていることから、眼内レンズ12を安定して載置することが出来ると共に、凹状溝32の幅寸法が眼内レンズ12の光学部30の径寸法より僅かに大きい程度とされていることから、載置面38上での眼内レンズ12の周方向の回転も阻止されるようになっている。なお、可動部78を構成する矩形平板状部76の下部中央部には、外側に向けて屈曲された把持突起130が一体形成されており、把持突起130により可動部78のスライド操作並びに可動部78と係合した保持部材54の器具本体16からの離脱操作が可能となっている。これにより、把持突起130を把持したまま、可動部78のスライド操作と保持部材54の離脱操作を一連の動作で行うことができ、操作性の向上を図ることができる。 The intraocular lens 12 can be placed on the placement surface 38 in a state of being wrapped in the above-described lubricant by pulling the holding member 54 below the instrument body 16 and removing it from the instrument body 16. It becomes. In addition, since the mounting surface 38 in this embodiment is a flat surface, the intraocular lens 12 can be stably mounted, and the width dimension of the concave groove 32 is the optical part of the intraocular lens 12. Since the diameter is slightly larger than 30, the rotation of the intraocular lens 12 in the circumferential direction on the placement surface 38 is also prevented. A gripping protrusion 130 bent outward is integrally formed at the lower central part of the rectangular flat plate portion 76 constituting the movable part 78, and the sliding operation of the movable part 78 and the movable part are formed by the gripping protrusion 130. The holding member 54 engaged with 78 can be detached from the instrument main body 16. Accordingly, the sliding operation of the movable portion 78 and the detaching operation of the holding member 54 can be performed by a series of operations while the gripping protrusion 130 is gripped, and operability can be improved.
 続いて、眼組織に設けた切開創に挿入筒部20の先端部分を挿入せしめた状態で、押出部材22の押圧板部132を器具本体16側に押し込む。これにより、載置面38に載置された眼内レンズ12の光学部30の外周縁部に押出部材22先端の棒状部98が当接され、押出部材22によって眼内レンズ12が挿入筒部20に向けて案内され、挿入筒部20の先端部分から嚢内に眼内レンズ12が送り出される。なお、押出部材22の器具本体16への最大押し込み量は、挿通部118の先端面が貫通孔26の壁部40で係止されることで制限されるようになっており、かかる最大押し込み位置で、押出部材22の先端部が先端開口部112から適当な長さ、例えば5~10mm外方に突出せしめられるようになっている。 Subsequently, the pressing plate portion 132 of the pushing member 22 is pushed into the instrument main body 16 side in a state where the distal end portion of the insertion tube portion 20 is inserted into the incision provided in the eye tissue. Thereby, the rod-like portion 98 at the tip of the pushing member 22 is brought into contact with the outer peripheral edge portion of the optical portion 30 of the intraocular lens 12 placed on the placing surface 38, and the intraocular lens 12 is inserted into the insertion tube portion by the pushing member 22. The intraocular lens 12 is fed out from the distal end portion of the insertion tube portion 20 into the sac. Note that the maximum pushing amount of the pushing member 22 into the instrument main body 16 is limited by the distal end surface of the insertion portion 118 being locked by the wall portion 40 of the through hole 26, and the maximum pushing position is as follows. Thus, the distal end portion of the pushing member 22 is projected from the distal end opening portion 112 to an appropriate length, for example, 5 to 10 mm.
 このような本実施形態に従う構造とされた眼内レンズの挿入器具10においては、保持部材54に可動部78が設けられていることから、眼内レンズ12を患者の嚢内に挿入する際に、眼内レンズ12が保持部材54により位置決め保持された状態で、押出部材22を眼内レンズ12に接近させることができる。これにより、眼内レンズ12が保持部材54により位置決め保持された状態で、眼内レンズ12の後方支持部35を、眼内レンズ12の光学部30の前面又は後面のどちらかに再現性良く案内することができる。それ故、所望の形状に後方支持部35を変形させて、押出時や嚢内に挿入された後の眼内レンズ12の挙動の制御や嚢内での安定性の向上を図ることができるのである。従って、従来構造の如き、眼内レンズ12を保持部材54の保持から取り外した後に、押出部材22で後方支持部35を押し出すことによるレンズの移動や回転といった問題を防止することができ、安定した眼内レンズの挿入が可能となるのである。 In the intraocular lens insertion device 10 configured according to this embodiment, since the movable member 78 is provided in the holding member 54, when inserting the intraocular lens 12 into the patient's sac, With the intraocular lens 12 positioned and held by the holding member 54, the pushing member 22 can be brought close to the intraocular lens 12. Thus, with the intraocular lens 12 positioned and held by the holding member 54, the rear support part 35 of the intraocular lens 12 is guided to either the front surface or the rear surface of the optical part 30 of the intraocular lens 12 with good reproducibility. can do. Therefore, the rear support portion 35 is deformed into a desired shape, and the behavior of the intraocular lens 12 after being inserted or inserted into the sac can be controlled and the stability in the sac can be improved. Therefore, as in the conventional structure, after the intraocular lens 12 is removed from the holding member 54, it is possible to prevent problems such as lens movement and rotation caused by pushing out the rear support portion 35 with the pushing member 22, and stable. It is possible to insert an intraocular lens.
 また、本実施形態では、眼内レンズ12が保持部材54の保持突起62,66上に位置決め載置された状態で器具本体16に内蔵されていることから、輸送時や保管時の安定保持が可能となる。また、可動部78をスライドさせた後、保持部材54を載置部14から引き抜くことにより、載置面38に眼内レンズ12を安定して載置することができる。このように保持部材54によって、眼内レンズ12の輸送時や保管時の安定した担持機能を発現することができる。 Further, in this embodiment, since the intraocular lens 12 is built in the instrument body 16 in a state of being positioned and placed on the holding projections 62 and 66 of the holding member 54, stable holding during transportation and storage is possible. It becomes possible. Further, after the movable portion 78 is slid, the intraocular lens 12 can be stably placed on the placement surface 38 by withdrawing the holding member 54 from the placement portion 14. As described above, the holding member 54 can exhibit a stable support function during transportation and storage of the intraocular lens 12.
 さらに、可動部78のスライド開始端では、可動部78の矩形平板状部76の後方部が、器具本体16の本体筒部24の前方部90に設けられた溝部92に嵌め込まれ離脱不能とされていることから、可動部78を含む保持部材54の予期せぬ載置部14からの離脱を未然に防止することができる。また、可動部78をスライド終了端に移動した後には、貫通孔84,86から保持部材54を速やかに離脱させることができ、眼内レンズ12の押出部材22による挿入操作を保持部材54との干渉を回避して安定して行うことができる。 Further, at the slide start end of the movable portion 78, the rear portion of the rectangular flat plate-like portion 76 of the movable portion 78 is fitted into the groove portion 92 provided in the front portion 90 of the main body cylinder portion 24 of the instrument main body 16, and cannot be detached. Therefore, it is possible to prevent the holding member 54 including the movable portion 78 from being unexpectedly detached from the placement portion 14. In addition, after the movable portion 78 is moved to the slide end, the holding member 54 can be quickly removed from the through holes 84 and 86, and the insertion operation by the pushing member 22 of the intraocular lens 12 can be performed with the holding member 54. Interference can be avoided and stable operation can be performed.
 また、本実施形態では、可動部78には把持突起130が設けられていることから、把持突起130により可動部78のスライド操作並びに可動部78と係合した保持部材54の器具本体16からの離脱操作が可能となっている。これにより、把持突起130を把持したまま、可動部78のスライド操作と保持部材54の離脱操作を一連の動作で行うことができ、操作性の向上を図ることができるのである。 Further, in this embodiment, since the movable portion 78 is provided with the gripping protrusion 130, the sliding operation of the movable portion 78 by the gripping protrusion 130 and the holding member 54 engaged with the movable portion 78 from the instrument main body 16. The withdrawal operation is possible. Accordingly, the sliding operation of the movable portion 78 and the detaching operation of the holding member 54 can be performed by a series of operations while the gripping protrusion 130 is gripped, and the operability can be improved.
 なお、カバー部材42によって載置部14の開口部36を覆蓋せしめた状態を維持して眼内レンズ12の載置を行えることから、眼内レンズの挿入器具10からの脱落を抑えることが出来ると共に、眼内レンズ12の外界との接触の機会も軽減されて、衛生面上も優れた効果を得ることが出来るのである。 Since the intraocular lens 12 can be placed while maintaining the state in which the opening 36 of the placement portion 14 is covered by the cover member 42, the ocular lens can be prevented from falling off from the insertion device 10. At the same time, the chance of contact of the intraocular lens 12 with the outside world is reduced, and an excellent effect on hygiene can be obtained.
 次に、図8および図9を用いて、本発明の第二の実施形態としての眼内レンズの挿入器具134の要部を説明する。第二の実施形態は、第一の実施形態の眼内レンズの挿入器具10に対して、眼内レンズ12が押出部材22により押し出される際に、前方支持部34に当接する支持部保持突起136を設けて、前方支持部34の変形形状を制御可能とするものである。なお、以下の説明において、前述の実施形態と実質的に同様の部材および部位については、前述の実施形態と同様の符号を付することによって、詳細な説明を省略する。 Next, the main part of the intraocular lens insertion device 134 according to the second embodiment of the present invention will be described with reference to FIGS. In the second embodiment, when the intraocular lens 12 is pushed out by the pushing member 22 with respect to the intraocular lens insertion device 10 of the first embodiment, the support holding protrusion 136 that abuts the front support 34. Is provided so that the deformed shape of the front support portion 34 can be controlled. In the following description, members and parts that are substantially the same as those of the above-described embodiment are denoted by the same reference numerals as those of the above-described embodiment, and detailed description thereof is omitted.
 より詳細には、図9に示すように、本実施形態の眼内レンズの挿入器具134においては、保持部材54に対して支持部保持突起136が容易に湾曲変形可能な薄肉短冊状の連結部138を介して側壁部56に一体的に連結されている。図9(a)に示すように、保持部材54と支持部保持突起136の離隔距離が最大となる初期状態では、連結部138が保持部材54の長手方向にストレートに延びており、支持部保持突起136が保持部材54の前方側端縁部と略同じ位置に配設されている。また、図9(b)に示すように、連結部138が湾曲変形された後には、保持部材54と支持部保持突起136の離隔距離が最小となり、支持部保持突起136が保持部材54の前方側端縁部よりも後方側に入り込んで位置される。 More specifically, as shown in FIG. 9, in the intraocular lens insertion device 134 of the present embodiment, a thin strip-like connecting portion in which the support holding projection 136 can be easily curved and deformed with respect to the holding member 54. It is integrally connected to the side wall part 56 via 138. As shown in FIG. 9A, in the initial state in which the separation distance between the holding member 54 and the support holding protrusion 136 is maximum, the connecting portion 138 extends straight in the longitudinal direction of the holding member 54, and the support holding portion is held. The protrusion 136 is disposed at substantially the same position as the front edge of the holding member 54. Further, as shown in FIG. 9B, after the connecting portion 138 is curved and deformed, the separation distance between the holding member 54 and the supporting portion holding projection 136 is minimized, and the supporting portion holding projection 136 is positioned in front of the holding member 54. It is located in the rear side of the side edge portion.
 一方、図8に示すように、器具本体16の凹状溝32の底面を貫通して、支持部保持突起136の収容孔140が設けられており、かかる収容孔140を通じて支持部保持突起136が器具本体16の先端部側となる眼内レンズ12の前方の載置面38上に突出されるようになっている。また、図示は省略するが、凹状溝32の底面の裏面側に開口する収容凹溝を設けて、連結部138を屈曲変形可能な状態で収容するようにしてもよい。 On the other hand, as shown in FIG. 8, an accommodation hole 140 for the support portion holding projection 136 is provided through the bottom surface of the concave groove 32 of the device body 16, and the support portion holding projection 136 is passed through the accommodation hole 140. It protrudes on the mounting surface 38 in front of the intraocular lens 12 on the distal end side of the main body 16. In addition, although not shown, an accommodation groove that opens on the back side of the bottom surface of the recessed groove 32 may be provided so that the connecting portion 138 can be accommodated in a state where it can be bent and deformed.
 このような本実施形態の眼内レンズの挿入器具134においては、先ず、図8(a)に示す初期状態、即ち、眼内レンズ12が保持部材54の保持突起62,66上に位置決め載置された状態から、保持部材54に設けられた可動部78を器具本体16に対して軸方向前方にスライドさせることにより、眼内レンズ12の後方支持部35を光学部30側に変形させることができ、後方支持部35の所望の変形形状を有利に生ぜしめることができる。さらに、本実施形態では、眼内レンズ12を保持する保持突起62,66を突出させるための貫通孔142,144が、器具本体16の軸方向に所定長さで延びる長孔形状とされている。これにより、保持部材54と係合された可動部78は保持部材54と一緒に、図8(b)から図8(c)までさらにスライドさせることができるようになり、後方支持部35の変形を維持したまま、眼内レンズ12をスライドできるのである。今回のスライドの際には、収容孔140を通じて載置面38上突出された支持部保持突起136が器具本体16に対して移動不能とされていることから、連結部138が湾曲させることで眼内レンズ12を支持部保持突起136に接近させることができる。すなわち、保持部材54を器具本体16に対して軸方向前方にスライドさせることにより、眼内レンズ12の前方支持部34の移動を支持部保持突起136により制限することができるのである。このように、前方および後方支持部34,35を光学部30側に変形するようにした後、器具本体16から支持部保持突起136を含む保持部材54を一括して下方に引き抜いて、器具本体16から取り外すことができるのである。なお、ここでは、連結部138として薄肉厚かつ短冊状の構造で説明を行ったが、鎖状の構造やテレスコピック構造でもよいし、仮に連結部138がなく別体として形成しても構わない。 In the intraocular lens insertion device 134 of this embodiment, first, the initial state shown in FIG. 8A, that is, the intraocular lens 12 is positioned and placed on the holding protrusions 62 and 66 of the holding member 54. From this state, the rear support portion 35 of the intraocular lens 12 can be deformed to the optical portion 30 side by sliding the movable portion 78 provided on the holding member 54 forward in the axial direction with respect to the instrument body 16. Thus, the desired deformed shape of the rear support portion 35 can be advantageously produced. Further, in the present embodiment, the through holes 142 and 144 for projecting the holding projections 62 and 66 that hold the intraocular lens 12 have a long hole shape extending in a predetermined length in the axial direction of the instrument body 16. . Accordingly, the movable portion 78 engaged with the holding member 54 can be further slid from FIG. 8B to FIG. 8C together with the holding member 54, and the rear support portion 35 is deformed. The intraocular lens 12 can be slid while maintaining the above. At the time of this slide, the support portion holding projection 136 that protrudes on the placement surface 38 through the accommodation hole 140 is immovable with respect to the instrument main body 16, so that the connecting portion 138 is curved to cause the eye to bend. The inner lens 12 can be brought close to the support holding projection 136. In other words, the movement of the front support portion 34 of the intraocular lens 12 can be restricted by the support portion holding protrusion 136 by sliding the holding member 54 axially forward with respect to the instrument body 16. As described above, after the front and rear support portions 34 and 35 are deformed to the optical portion 30 side, the holding member 54 including the support portion holding projection 136 is collectively pulled out from the device main body 16, and the device main body is pulled out downward. 16 can be removed. Here, the connection portion 138 has been described with a thin-walled and strip-like structure. However, a chain-like structure or a telescopic structure may be used, or the connection portion 138 may be omitted and formed separately.
 このように、前方支持部34の先端部を光学部30側に変形するようにすると共に、後方支持部35の先端部が光学部30の前面上に載置されるように変形させた後、押出部材22により眼内レンズ12の器具本体16からの押し出しを行う。そうすると、上方に凸となるように変形される光学部30の間に前方支持部34が挟み込まれる所謂タッキングの状態を有利に生ぜしめることができ、眼内レンズ12が嚢内にリリースされる際の前方支持部34や光学部30の挙動が安定化されて、眼内レンズ12の嚢内での安定性の向上を図ることができる。一方、後方支持部35が光学部30の前面上に載置されるように変形されることから、挿入筒部20から押し出される眼内レンズ12の断面積が小さくされて眼内レンズ12の押出をスムーズに且つ少ない抵抗で行うことができる。上述の如く、可動部78を軸方向前方にスライドするだけで、前方および後方支持部34,35を光学部30側に変形できる構造とすることにより、極めて容易に、押し出し前に眼内レンズ12の前方および後方支持部34,35の姿勢を望ましい状態に制御できるのである。 In this way, the front support part 34 is deformed so that the front end part of the front support part 34 is deformed to the optical part 30 side, and the front end part of the rear support part 35 is placed on the front surface of the optical part 30. The pushing member 22 pushes out the intraocular lens 12 from the instrument body 16. Then, a so-called tacking state in which the front support portion 34 is sandwiched between the optical portions 30 deformed so as to be convex upward can be advantageously produced, and the intraocular lens 12 is released into the sac. The behavior of the front support part 34 and the optical part 30 is stabilized, and the stability of the intraocular lens 12 within the capsule can be improved. On the other hand, since the rear support portion 35 is deformed so as to be placed on the front surface of the optical portion 30, the cross-sectional area of the intraocular lens 12 pushed out from the insertion tube portion 20 is reduced, and the intraocular lens 12 is pushed out. Can be performed smoothly and with less resistance. As described above, the front and rear support portions 34 and 35 can be deformed to the optical portion 30 side simply by sliding the movable portion 78 forward in the axial direction. The postures of the front and rear support portions 34 and 35 can be controlled to a desired state.
 以上、本発明の複数の実施形態について詳述してきたが、これはあくまでも例示であって、本発明は、かかる実施形態における具体的な記載によって、何等、限定的に解釈されるものではない。例えば、第二の実施形態にかかる眼内レンズの挿入器具134おいても、第一の実施形態と同様、後方支持部35を光学部30の下面側に入り込ませるように変形させることもでき、これにより眼内レンズ12押出の際の後方支持部35の傷付き等を有利に防止できる。また、可動部78と押出部材22の係合構造は、保持部材54の器具本体16からの離脱の際に係合が解除されるものであれば、公知の係合構造の採用も可能である。 Although a plurality of embodiments of the present invention have been described in detail above, this is merely an example, and the present invention is not construed as being limited by the specific description in the embodiments. For example, also in the intraocular lens insertion device 134 according to the second embodiment, the rear support part 35 can be deformed so as to enter the lower surface side of the optical part 30 as in the first embodiment. This can advantageously prevent the rear support portion 35 from being damaged when the intraocular lens 12 is pushed out. In addition, the engagement structure between the movable portion 78 and the pushing member 22 may be a known engagement structure as long as the engagement is released when the holding member 54 is detached from the instrument body 16. .
 また、基端開口部108の底面110に設けられた導入突部114は、載置面38における眼内レンズ12の光学部30が載置される部分まで延長して設けるようにしてもよい。そして、光学部30が、第一及び第二保持突起62,66への載置状態において導入突部114の突出先端部へも載置されて支持されるようにしてもよい。 In addition, the introduction protrusion 114 provided on the bottom surface 110 of the proximal end opening 108 may be provided to extend to the portion on the placement surface 38 where the optical part 30 of the intraocular lens 12 is placed. Then, the optical unit 30 may be placed and supported also on the projecting tip of the introduction projection 114 in the state of being placed on the first and second holding projections 62 and 66.
10:挿入器具、12:眼内レンズ、14:載置部、16:器具本体、18:後端部、20:挿入筒部、22:押出部材、24:本体筒部、30:光学部、32:凹状溝、34:前方支持部、35:後方支持部、38:載置面、42:カバー部材、54:保持部材、62:第一保持突起、66:第二保持突起、76:矩形平板状部、78:可動部、88:柱状突起、90:前方部、92:溝部、94:係止爪、96:係止孔、98:棒状部、100:係合切欠、128:案内部、130:把持突起 10: insertion instrument, 12: intraocular lens, 14: placement part, 16: instrument body, 18: rear end part, 20: insertion cylinder part, 22: pushing member, 24: body cylinder part, 30: optical part, 32: concave groove, 34: front support part, 35: rear support part, 38: mounting surface, 42: cover member, 54: holding member, 62: first holding protrusion, 66: second holding protrusion, 76: rectangular Flat plate portion, 78: movable portion, 88: columnar protrusion, 90: front portion, 92: groove portion, 94: locking claw, 96: locking hole, 98: rod-shaped portion, 100: engagement notch, 128: guide portion , 130: gripping protrusion

Claims (2)

  1.  光学部と該光学部の両側から延び出す一対の支持部を有する眼内レンズが載置される載置部を備えた筒形状の器具本体と、該器具本体の後端部から挿入されて該眼内レンズを該器具本体の先端部に設けられた挿入筒部へ押し出す押出部材とを備えている一方、該載置部に突出して組み付けられた保持部材によって、該眼内レンズの該一対の支持部が該器具本体の先端側と後端側に延び出すように該眼内レンズを該載置部上に位置決め保持した状態で提供される眼内レンズの挿入器具において、
     前記保持部材には、前記押出部材と係合した状態で前記保持部材の後端側から先端側に向かってスライド可能な可動部が設けられており、
     前記可動部がスライド方向の後端側に位置する際には、前記保持部材が前記器具本体から離脱不能とされている一方、
     前記可動部がスライド方向先端側に移動されることにより、前記押出部材の先端部により前記眼内レンズの後方に位置する前記支持部が前記光学部側へ変形されると共に、前記可動部を含む前記保持部材が前記器具本体から離脱可能とされており、
     前記後方の支持部の前記光学部側への変形に際して該後方の支持部を該光学部の前面側又は後面側に案内する案内部が設けられている、
    ことを特徴とする眼内レンズの挿入器具。
    A cylindrical instrument body provided with a placement part on which an intraocular lens having an optical part and a pair of support parts extending from both sides of the optical part is placed, and inserted from the rear end part of the instrument body A push-out member that pushes the intraocular lens to an insertion tube provided at the distal end of the instrument body, and the pair of intraocular lenses by the holding member that protrudes and is assembled to the mounting portion. In the intraocular lens insertion device provided in a state where the intraocular lens is positioned and held on the mounting portion so that the support portion extends to the front end side and the rear end side of the device main body,
    The holding member is provided with a movable portion that is slidable from the rear end side to the front end side of the holding member in a state of being engaged with the pushing member,
    When the movable part is located on the rear end side in the sliding direction, the holding member is not removable from the instrument body,
    When the movable portion is moved to the distal end side in the sliding direction, the support portion positioned behind the intraocular lens is deformed to the optical portion side by the distal end portion of the push-out member and includes the movable portion. The holding member is removable from the instrument body;
    A guide part is provided for guiding the rear support part to the front side or the rear side of the optical part when the rear support part is deformed to the optical part side.
    An intraocular lens insertion device.
  2.  前記可動部には把持突起が突出して設けられており、該把持突起により該可動部のスライド操作と前記保持部材の前記器具本体からの離脱操作が可能とされている請求項1に記載の眼内レンズの挿入器具。 The eye according to claim 1, wherein a gripping protrusion protrudes from the movable part, and the sliding operation of the movable part and the detachment operation of the holding member from the instrument main body are enabled by the gripping protrusion. Inner lens insertion device.
PCT/JP2012/005861 2011-09-15 2012-09-13 Intraocular lens insertion tool WO2013038689A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017093164A1 (en) * 2015-12-03 2017-06-08 Carl Zeiss Meditec Ag Intraocular lens cartridge comprising a lid, and injector comprising a cartridge
WO2017093161A1 (en) * 2015-12-03 2017-06-08 Carl Zeiss Meditec Ag Intraocular lens cartridge comprising a lubricant feed duct, and injector comprising a cartridge
EP3547960A4 (en) * 2017-02-07 2020-01-01 RxSight, Inc. Intraocular lens inserter cartridge with an iol-guiding structrure
US11013593B2 (en) 2018-12-02 2021-05-25 Rxsight, Inc. Light adjustable lens tracking system and method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007152010A (en) * 2005-12-08 2007-06-21 Hoya Corp Intraocular lens insertion device
WO2007080869A1 (en) * 2006-01-13 2007-07-19 Hoya Corporation Instrument for inserting intraocular lens

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7156854B2 (en) * 2003-05-28 2007-01-02 Alcon, Inc. Lens delivery system
US8435289B2 (en) * 2005-02-11 2013-05-07 Abbott Medical Optics Inc. Rapid exchange IOL insertion apparatus and methods of using
JP4908977B2 (en) * 2006-09-05 2012-04-04 興和株式会社 Intraocular lens insertion device

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007152010A (en) * 2005-12-08 2007-06-21 Hoya Corp Intraocular lens insertion device
WO2007080869A1 (en) * 2006-01-13 2007-07-19 Hoya Corporation Instrument for inserting intraocular lens

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017093164A1 (en) * 2015-12-03 2017-06-08 Carl Zeiss Meditec Ag Intraocular lens cartridge comprising a lid, and injector comprising a cartridge
WO2017093161A1 (en) * 2015-12-03 2017-06-08 Carl Zeiss Meditec Ag Intraocular lens cartridge comprising a lubricant feed duct, and injector comprising a cartridge
US10675148B2 (en) 2015-12-03 2020-06-09 Carl Zeiss Meditec Ag Intraocular lens cartridge having a lubricant feed duct and injector incorporating said cartridge
EP3547960A4 (en) * 2017-02-07 2020-01-01 RxSight, Inc. Intraocular lens inserter cartridge with an iol-guiding structrure
US11083568B2 (en) 2017-02-07 2021-08-10 Rxsight, Inc. Intraocular lens inserter cartridge with an IOL-guiding structure
US11013593B2 (en) 2018-12-02 2021-05-25 Rxsight, Inc. Light adjustable lens tracking system and method

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