WO2016017772A1 - Intraocular lens insertion instrument - Google Patents

Intraocular lens insertion instrument Download PDF

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Publication number
WO2016017772A1
WO2016017772A1 PCT/JP2015/071686 JP2015071686W WO2016017772A1 WO 2016017772 A1 WO2016017772 A1 WO 2016017772A1 JP 2015071686 W JP2015071686 W JP 2015071686W WO 2016017772 A1 WO2016017772 A1 WO 2016017772A1
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WO
WIPO (PCT)
Prior art keywords
intraocular lens
lens
nozzle body
instrument
nozzle
Prior art date
Application number
PCT/JP2015/071686
Other languages
French (fr)
Japanese (ja)
Inventor
佐藤 隆史
Original Assignee
興和株式会社
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 興和株式会社 filed Critical 興和株式会社
Priority to JP2016538445A priority Critical patent/JP7066320B2/en
Publication of WO2016017772A1 publication Critical patent/WO2016017772A1/en

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

Definitions

  • the present invention relates to an intraocular lens insertion device.
  • Intraocular lenses that are inserted as a substitute for the lens for the replacement of the human turbid lens and the correction of refraction in the treatment of cataract are being put to practical use.
  • intraocular lens insertion surgery for cataract treatment for example, a few millimeter incision wound (incision) is provided at the edge of the cornea, and the lens is crushed and removed from the incision by ultrasonic phacoemulsification The intraocular lens is inserted and fixed.
  • an insertion device in which the intraocular lens is previously loaded in a cartridge is often used.
  • the user inserts the distal end opening of the insertion tube portion provided at the distal end portion of the instrument body into the eyeball through the above-mentioned incision, and in the state where the intraocular lens is slightly deformed in the instrument body, The intraocular lens is ejected and inserted into the eyeball by pushing it out from the tip opening with a rod-like plunger.
  • the size of the incision can be reduced, and the intraocular lens can be easily inserted into the eyeball, so that the burden on the operation can be reduced.
  • an intraocular lens has a lens body and a support portion connected to the lens body.
  • the intraocular lens is folded in accordance with the inner wall shape of the insertion tube portion as the plunger moves the intraocular lens toward the distal opening side. It becomes a state.
  • the distal end portion of the insertion instrument is inclined with respect to the central axis.
  • the structure which provides what is called a bevel is proposed (for example, patent document 1).
  • the posture of the intraocular lens emitted from the distal end of the insertion device may still not be determined.
  • the user performs an operation such as changing the posture of the insertion instrument itself so that the intraocular lens is ejected in a suitable posture, or adjusting the position of the intraocular lens ejected into the eye. Take measures.
  • the technology of the present disclosure has been made in view of the above circumstances, and an object thereof is to provide an intraocular lens insertion device that can further stabilize the posture of the intraocular lens emitted from the insertion device. Is to provide.
  • the intraocular lens insertion device of the present disclosure includes a lens body and an instrument body having an insertion tube portion at the tip end of which an intraocular lens having a support portion having one end connected to the lens body via a connection portion,
  • An insertion device for an intraocular lens including a storage unit for storing an intraocular lens, provided with a slit extending in the longitudinal direction of the insertion tube portion from the opening at the front end of the insertion tube portion toward the rear end,
  • the connection part of at least one support part is relative to the central axis of the instrument main body
  • the center position in the width direction of the slit is the rear side of the optical axis of the intraocular lens in the instrument body when viewed from the center axis of the instrument body in the front view of the instrument body.
  • the intraocular lens stored in the storage unit It is arranged to be inclined at a predetermined angle in the same direction as the connection portion of the at least one support.
  • the predetermined angle coincides with the position of the connection part when the intraocular lens passes through the insertion tube part when the center position in the width direction of the slit is viewed from the central axis of the instrument body in a front view of the instrument body. It is an angle to do.
  • the intraocular lens insertion device is configured such that the predetermined angle is about 30 °. Accordingly, when a general intraocular lens is ejected into the eye using the intraocular lens insertion device disclosed herein, the intraocular lens support can be more reliably ejected from the slit, and thus the eye The posture at the time of injection of the inner lens is preferably maintained.
  • an intraocular lens insertion device that can further stabilize the posture of the intraocular lens emitted from the insertion device.
  • FIG. 1 It is a figure which shows schematic structure of the insertion instrument of the intraocular lens in one Embodiment. It is a figure which shows schematic structure of the intraocular lens in one Embodiment. It is a figure which shows schematic structure of the nozzle main body in one Embodiment. It is a figure which shows schematic structure of the positioning member in one Embodiment. It is a figure which shows schematic structure of the plunger in one Embodiment. It is a figure which shows schematic structure of the front-end
  • FIG. 1A is a plan view of the insertion instrument 1 when the stage lid 13 is opened
  • FIG. 1B is a side view of the insertion instrument 1 when the stage lid 13 is closed.
  • the insertion instrument 1 has a nozzle body 10 as an instrument body, a plunger 30 as an intraocular lens pushing member, a stage part 12 and a stage lid part 13 as a storage part for an intraocular lens.
  • the stage unit 12 is provided integrally with the nozzle body 10 or separately.
  • a plunger 30 is inserted into the nozzle body 10.
  • the intraocular lens 2 is set on the stage unit 12.
  • the stage unit 12 is formed integrally with the stage lid unit 13.
  • FIG. 1 shows a state in which the stage lid 13 is opened.
  • the nozzle body 10 of the insertion instrument 1 is formed in a cylindrical shape having a substantially rectangular cross section, and one end of the insertion tool 1 is greatly open (hereinafter, the side having the large opening is referred to as a rear end 10b), and the end on the other side. Includes a nozzle portion 15 and a tip portion 10a which are narrowed down. As shown in FIG.1 (b), the front-end
  • the plunger 30 is inserted into the nozzle body 10 and can reciprocate.
  • a slit 15 b is formed in the nozzle portion 15. Details of the slit 15b will be described later.
  • the direction from the rear end 10b of the nozzle body 10 to the front end 10a is the front direction
  • the opposite direction is the rear direction
  • the front side of the page in FIG. 1A is the upper direction
  • the reverse direction is the lower direction
  • the front side of the page is the left direction
  • the opposite direction is the right direction.
  • the upper side is the front side of the optical axis of the lens body 2a, which will be described later
  • the lower side is the rear side of the optical axis of the lens body 2a
  • the front side is the front side in the pressing direction by the plunger 30, and the rear side is pressed by the plunger 30 Corresponds to the rear side.
  • a stage portion 12 for setting the intraocular lens 2 is provided on the rear side of the nozzle portion 15 in the nozzle body 10.
  • the stage portion 12 is configured such that the upper side of the nozzle body 10 is opened by opening the stage lid portion 13.
  • a positioning member 50 is attached to the stage portion 12 from the lower side of the nozzle body 10. By this positioning member 50, the intraocular lens 2 is stably held in the stage portion 12 even before use (during transportation).
  • the intraocular lens 2 is on the stage unit 12 and the front side of the optical axis is on the upper side in a state where the stage lid unit 13 is opened and the positioning member 50 is attached to the stage unit 12. Is set as Then, after the stage lid 13 is closed, it is shipped and sold. Then, the user removes the positioning member 50 with the stage lid portion 13 closed, and then pushes the plunger 30 into the distal end side of the nozzle body 10. As a result, the intraocular lens 2 is pressed by the plunger 30 and moved to the nozzle unit 15, and then the intraocular lens 2 is injected into the eyeball from the distal end portion 10 a.
  • the nozzle body 10, the plunger 30, and the positioning member 50 in the insertion instrument 1 are formed of a resin material such as polypropylene. Polypropylene is a material with a proven track record in medical equipment and high reliability such as chemical resistance.
  • FIG. 2 is a diagram showing a schematic configuration of the intraocular lens 2.
  • 2A is a plan view and FIG. 2B is a side view.
  • the intraocular lens 2 is a so-called one-piece type.
  • the intraocular lens 2 is formed of a lens body 2a having a predetermined refractive power and two flat plate-like support portions 2b connected to the lens body 2a for holding the lens body 2a in the eyeball. Yes.
  • Some intraocular lenses have not only refractive correction but also optical functions such as astigmatism correction, bifocal (multifocal) and identity with the visual axis. In the case of an intraocular lens for correcting astigmatism, as shown in FIG.
  • a marking 2d indicating the position of the main meridian is applied to the lens.
  • a diffraction grating shape 2e appears on the lens surface. Furthermore, by shifting the center of the lens body 2a and the center of the shape 2e of the diffraction grating, it is possible to cope with the deviation of the visual axis of the individual into which the intraocular lens is inserted.
  • the support part 2b has a junction part 2c that contacts the outer edge of the lens body 2, and the junction part 2c and the lens body 2a are connected by an adhesive or the like.
  • the junction part corresponds to an example of a connection part.
  • the lens body 2a and the support portion 2b are made of a flexible resin material.
  • the intraocular lens 2 is set so that one of the two support portions 2b is disposed on the rear side of the lens body 2a and the other is disposed on the front side of the lens body. .
  • FIG. 3 shows a plan view of only the nozzle body 10.
  • the intraocular lens 2 is set on the stage unit 12. In this state, the intraocular lens 2 is pressed by the plunger 30 and ejected from the distal end portion 10a.
  • the nozzle body 10 is provided with a through-hole 10c having a cross-sectional shape that becomes smaller toward the tip according to the shape that the outer shape of the nozzle body 10 becomes thinner toward the tip.
  • the cross-sectional shape of the through hole is an oval shape (egg shape) in the embodiment diagram, it may be a circular shape or an oval shape for the convenience of the lens used or specifications.
  • the intraocular lens 2 when the intraocular lens 2 is inject
  • the tip portion 10a has a shape cut obliquely so that the upper region of the nozzle portion 15 is in front of the lower region.
  • the shape of the tip portion 10a that is obliquely cut may be linearly obliquely cut when viewed from the left-right direction, or may have a bulge outward, that is, a curved shape. It may be cut into
  • a stage groove 12 a having a width slightly larger than the diameter of the lens body 2 a of the intraocular lens 2 is formed in the stage portion 12.
  • the dimension in the front-rear direction of the stage groove 12 a is set to be larger than the maximum width dimension including the support portions 2 b extending on both sides of the intraocular lens 2.
  • a set surface 12b is formed by the bottom surface of the stage groove 12a. The vertical position of the set surface 12b is set higher than the height position of the bottom surface of the through hole 10c of the nozzle body 10, and the set surface 12b and the bottom surface of the through hole 10c are connected by a bottom slope 10d. .
  • the stage portion 12 and the stage lid portion 13 are integrally formed.
  • the stage lid portion 13 has the same size in the front-rear direction as the stage portion 12.
  • the stage lid portion 13 is connected by a thin plate-like connecting portion 14 formed by extending the side surface of the stage portion 12 to the stage lid portion 13 side.
  • the connecting portion 14 is formed to be bendable at the center portion, and the stage lid portion 13 can be closed by overlapping the stage portion 12 from above by bending the connecting portion 14.
  • ribs 13 a and 13 b are provided on the surface facing the set surface 12 b when the lid is closed in order to reinforce the stage lid 13 and stabilize the position of the intraocular lens 2. Further, a guide protrusion 13 c is provided as a guide on the upper side of the plunger 30.
  • FIG. 4 shows a schematic configuration of the positioning member 50.
  • FIG. 4A shows a plan view of the positioning member 50
  • FIG. 4B shows a left side view of the positioning member 50.
  • the positioning member 50 is configured as a separate body from the nozzle body 10, and has a structure in which a pair of side wall portions 51 are connected by a connecting portion 52.
  • a holding portion 53 is formed at the lower end of each side wall portion 51 so as to extend outward.
  • a pair of first mounting portions 54 are formed on the upper end portions of the respective side wall portions 51.
  • the pair of first mounting portions 54 are formed in an arc shape when viewed from above and project upward.
  • a first positioning portion 55 is formed on the outer peripheral side of the upper end surface of the first placement portion 54 so as to protrude. The distance between the inner diameters of the first positioning portion 55 is set to be slightly larger than the diameter dimension of the lens body 2 a of the intraocular lens 2.
  • a pair of second placement portions 56 are formed at both ends in the front-rear direction of the connecting portion 52, and the shape viewed from above is a rectangular shape and protrudes upward.
  • the height of the upper surface of the second placement unit 56 is equal to the height of the upper surface of the first placement unit 54.
  • a second positioning portion 57 that further protrudes upward over the entire left and right direction of the second placement portion 56 is formed on the outer portion of the upper surface of the second placement portion 56.
  • the distance between the inner sides of the second positioning portion 57 is set slightly larger than the diameter of the lens body 2a of the intraocular lens 2.
  • a locking claw 58 that slightly protrudes in the front-rear direction is formed on the upper end portion of the second placement portion 56 over the entire left-right direction.
  • the positioning member 50 is assembled from below the set surface 12b of the nozzle body 10.
  • the set surface 12b of the nozzle body 10 is formed with a set surface through hole 12c that penetrates the set surface 12b in the thickness direction.
  • the outer shape of the set surface through hole 12c is substantially similar to the shape of the first mounting portion 54 and the second mounting portion 56 of the positioning member 50 as viewed from above.
  • the first placement portion 54 and the second placement portion 56 are inserted into the set surface through hole 12c from the lower side of the set surface 12b, and the set surface 12b. Protrudes above.
  • the locking claw 58 provided in the second positioning portion 57 protrudes to the set surface 12b through the set surface through hole 12c and is locked to the upper surface of the set surface 12b.
  • the positioning member 50 is assembled from the lower side of the nozzle body 10, and the first placement portion 54 and the second placement portion 56 are fixed in a state of protruding from the set surface 12b.
  • the bottom surface of the outer periphery of the lens body 2a is placed on the upper surfaces of the first placement unit 54 and the second placement unit 56. Further, the position of the lens body 2a is restricted with respect to the horizontal direction (direction horizontal to the set surface 12b) by the first positioning portion 55 and the second positioning portion 57.
  • the positioning member 50 When inserting the intraocular lens 2 into the eyeball, the positioning member 50 is removed from the nozzle body 10. Thereby, the 1st mounting part 54 and the 2nd mounting part 56 which were supporting the lens main body 2a of the intraocular lens 2 retreat from the set surface 12b, and the intraocular lens 2 can move on the set surface 12b. Placed. Then, the intraocular lens 2 is pushed forward to a predetermined position by the plunger 30.
  • the distal end portion 10a of the nozzle portion 15 of the nozzle body 10 is inserted into the incision provided in the eye tissue. Since the distal end portion 10a has an oblique opening shape, it can be easily inserted into the incision. Then, after inserting the nozzle portion 15 into the incision, the pressing plate portion 33 of the plunger 30 is again pushed into the distal end side of the nozzle body 10. As a result, the distal end of the action portion 31 of the plunger 30 comes into contact with the outer periphery of the lens body 2a of the intraocular lens 2 set on the set surface 12a, and the intraocular lens 2 is guided toward the distal end portion 10a by the plunger 30.
  • FIG. 5 shows a schematic configuration of the plunger 30.
  • the plunger 30 has a slightly larger longitudinal length than the nozzle body 10. And it forms from the action part 31 of the front end side based on a column shape, and the insertion part 32 of the rear end side based on a rectangular rod shape.
  • the action part 31 is comprised including the cylindrical part 31a made into the column shape, and the thin plate-shaped flat part 31b extended in the left-right direction of the cylindrical part 31a.
  • a notch 31 c is formed at the tip of the action part 31.
  • the notch 31c is formed in a groove shape that opens upward in the action portion 31 and penetrates in the left-right direction.
  • the groove wall on the distal end side of the notch 31 c is formed with an inclined surface that goes upward as it goes to the distal end side of the action portion 31.
  • the insertion part 32 has a substantially H-shaped cross section as a whole, and the horizontal and vertical dimensions thereof are set slightly smaller than the through hole 10 c of the nozzle body 10.
  • a disc-shaped pressing plate portion 33 is formed at the rear end of the insertion portion 32 so as to spread in the vertical and horizontal directions.
  • a claw portion 32 a that protrudes upward from the insertion portion 32 and that can move up and down by the elasticity of the material of the plunger 30 is formed at a portion of the insertion portion 32 that is ahead of the center in the front-rear direction.
  • the locking hole 10e shown in FIG. 3 provided in the thickness direction on the upper surface of the nozzle body 10 and the claw portion 32a are engaged.
  • the relative position between the nozzle body 10 and the plunger 30 in the initial state is determined.
  • the claw portion 32a and the locking hole 10e are formed at the positions where the distal end of the action portion 31 is located on the rear side of the lens body 2a of the intraocular lens 2 set on the stage portion 12 in the engaged state.
  • the support portion 2b on the rear side of the main body 2a is set so that the cutout portion 31c can be supported from below.
  • the plunger 30 is inserted into the nozzle body 10 and disposed at the initial position. Further, as described above, the positioning member 50 is attached to the nozzle body 10 from below the set surface 12b. Thereby, the 1st mounting part 54 and the 2nd mounting part 56 of the positioning member 50 are hold
  • the lens body 2 a of the intraocular lens 2 is placed and positioned on the upper surfaces of the first placement part 54 and the second placement part 56 in a state where the support part 2 b is directed in the front-rear direction of the nozzle body 10.
  • a part of the support portion 2b on the rear side of the intraocular lens 2 is sandwiched between the notches 31c of the plunger 30 and is supported by the bottom surface thereof.
  • FIG. 6 is a side view schematically showing the tip of the nozzle body 10 of the insertion instrument 1 in the present embodiment.
  • the central axis of the cylindrical nozzle portion 15 extending in the front-rear direction of the nozzle body 10 is AX (two-dot chain line in FIG. 6).
  • so-called bevel processing is performed in which the tip of the nozzle portion 15 of the nozzle body 10 is cut by a surface inclined so as to face the lower side of the nozzle portion 15 with respect to the central axis AX.
  • the opening 15a at the tip of the nozzle portion 15 is formed so as to be a so-called bevel down.
  • a slit 15b connected to the opening 15a of the nozzle portion 15 is provided.
  • the slit 15 b is a substantially V-shaped cut extending from the rear end side of the opening 15 a of the nozzle portion 15 to the rear end side of the nozzle portion 15.
  • the edge of the slit 15b has a tapered shape, and the tapered shape continues to the rear end 15c of the slit 15b. Since the edge of the slit 15b is formed in this way, the insertion property when the opening 15a and the slit 15b of the nozzle portion 15 are inserted from an incision of an eye tissue is improved.
  • the positional relationship between the intraocular lens 2 and the slit 15b when the intraocular lens 2 is set on the stage unit 12 is below the nozzle unit 15 when viewed from the central axis AX of the nozzle unit 15.
  • the slit 15b and the junction part 2c of the support part 2b on the rear end side of the nozzle body 10 are in the positional relationship on the same side. Details of the movement of the intraocular lens 2 emitted from the slit 15b will be described later.
  • FIG. 7 shows a cross section taken along line AA of FIG. 6 as viewed from the front of the nozzle body 10.
  • FIG. 7 also shows a part of the nozzle body 10 when the nozzle body 10 is viewed from the front.
  • FIG. 7 also shows an example of the lens body 2 a of the intraocular lens 2 moved to the nozzle unit 15.
  • a gap is provided between the lens body 2a of the intraocular lens 2 and the nozzle portion 15 for ease of viewing, but the lens body 2a and the inner wall of the nozzle portion 15 are actually in contact with each other.
  • the slit 15b of the nozzle portion 15 is provided so as to open by a predetermined width around a direction D2 inclined by a predetermined angle ⁇ ( ⁇ 0 °) from the lower direction D1 when viewed from the central axis AX.
  • the downward direction D1 corresponds to the rear direction of the optical axis of the lens body 2a of the intraocular lens 2 set on the stage unit 12.
  • the edge 15c of the nozzle portion 15 forming the slit 15b is formed in a tapered shape.
  • the intraocular lens 2 When the intraocular lens 2 is ejected into the eye from the tip of the nozzle body 10, when the intraocular lens 2 is pushed forward by the plunger 30 toward the tip side of the nozzle body 10, of the support portion 2 b of the intraocular lens 2.
  • the positional relationship that the junction 2c and the slit 15b of the support 2b on the rear end side of the nozzle body 10 are on the same side with respect to the downward direction of the nozzle 15 as viewed from the central axis AX of the nozzle 15 is maintained. Is done.
  • the support portion 2b of the intraocular lens 2 can be suitably emitted from the slit 15b.
  • the angle ⁇ is about 30 °, the orientation of the intraocular lens is adjusted by rotating the insertion instrument 1 or the like. It is not necessary, and an effect that the intraocular lens can be emitted in the eye while maintaining a suitable posture is expected.
  • the opening width of the slit 15b can be set as appropriate.
  • the angle ⁇ corresponds to a predetermined angle in the present embodiment.
  • FIG. 8 is a top view schematically showing the posture of the intraocular lens 2 when the intraocular lens 2 moves in the nozzle body 10 by the operation of the plunger 30 in the present embodiment.
  • the user pushes the plunger 30 toward the distal end side of the nozzle body 10, and the intraocular lens 2 is sequentially moved from FIG. 8A to FIG. 8B, FIG. 8C, FIG. Move.
  • the nozzle body 10 is indicated by a dotted line
  • the intraocular lens 2 and the plunger 30 are indicated by a solid line for ease of viewing.
  • the user operates the plunger 30 to move the intraocular lens 2 placed on the stage unit 12 to the tip side of the nozzle body 10.
  • the intraocular lens 2 is pushed by the plunger 30, and the outer edge of the lens body 2 a is in contact with the inner wall of the nozzle body 10.
  • the outer edge portion of the lens body 2 a is the through hole of the nozzle body 10 as shown in FIG.
  • the lens body 2a is folded toward the center (optical axis) according to the cross-sectional shape of 10c.
  • the support portion 2b on the distal end side of the nozzle body 10 abuts against the inner wall of the nozzle body 10, and then the lens body 2a moves and folds over the lens body 2a. In a so-called tucked state.
  • the user operates the plunger 30 to move the intraocular lens 2 in the forward direction of the nozzle body 10.
  • the lens body 2a of the intraocular lens 2 was gradually pushed out through the opening 15a or slit 15b of the nozzle portion 15 to the outside of the nozzle body 10. The part is restored from the folded state to the original state.
  • the junction portion 2c of the support portion 2b on the rear end side of the nozzle body 10 is leftward from the central axis AX in a top view inside the nozzle body 10.
  • the predetermined direction means the left direction.
  • the slit 15b of the nozzle portion 15 is the same as the junction portion 2c of the support portion 2b on the rear end side of the nozzle body 10 when viewed from the central axis AX.
  • the left side is deviated from the central axis AX.
  • the junction part of the support part 2b 2c moves to a position overlapping the slit 15b when viewed from above.
  • the plunger 30 is pushed in the front direction of the nozzle main body 10
  • the said junction part 2c is extruded to the outer side of the nozzle main body 10 from the slit 15b.
  • the plunger 30 is further pushed forward of the nozzle body 10 and protrudes from the tip of the nozzle body 10
  • the intraocular lens 2 is positioned on the rear end side of the nozzle body 10 as shown in FIG. In a state where a part of the support portion 2b is engaged with the plunger 30, the original state is restored.
  • the slit 15b is provided on the side (in this case, the right side) different from the junction part 2c of the support part 2b on the rear end side of the nozzle body 10 when viewed from the central axis AX.
  • the angle ⁇ is approximately 0 °
  • the support portion 2b and the junction portion 2c on the rear end side of the nozzle body 10 may not be pushed out of the nozzle body 10 through the slit 15b.
  • the support portion 2 b on the rear end side of the nozzle body 10 of the intraocular lens 2 is supported by a notch portion 31 c at the distal end of the plunger 30 while being curved by a predetermined amount in the nozzle body 10.
  • the support portion 2b tries to return to a natural state by the elastic restoring force until it is pushed out of the nozzle body 10. For this reason, when the support part 2b moves to the tip side of the nozzle body 10 without passing through the slit 15b, the restorative force causes the intraocular portion when the part other than the support part 2 is pushed outside the nozzle body 10. There is a possibility that the lens 2 takes an unexpected posture. As a result, the user must adjust the posture of the intraocular lens 2 by rotating the insertion instrument 1 around the central axis AX.
  • the support part 2b on the rear end side of the nozzle body 10 of the intraocular lens 2 is pushed out of the nozzle body 10 through the slit 15b, so that the intraocular lens 2 is emitted from the nozzle body 10. It is possible to suppress the above-described restoring force that is unnecessary when acting on the intraocular lens 2. As a result, a suitable posture of the intraocular lens 2 can be maintained, and the trouble of adjusting the posture of the intraocular lens 2 as described above can be saved.
  • the slit 15b of the nozzle portion 15 is formed as a substantially V-shaped cut, but the shape of the slit 15b is not limited to this, and an arbitrary shape can be adopted.
  • the slit 15b of the nozzle portion 15 is the same side as the junction portion 2c of the support portion 2b on the “rear end side” of the nozzle body 10 when viewed from the central axis AX.
  • the configuration is formed so as to deviate from the central axis AX.
  • the slit 15b of the nozzle portion 15 is the same side as the junction portion 2c of the support portion 2b of the “tip side” of the nozzle body 10 when viewed from the central axis AX.
  • it may be configured to be formed away from the central axis AX.
  • the support portion 2b on the front end side of the nozzle body 10 is in a state of being tucked in the nozzle body 10, in the nozzle body 10, similarly to the support portion 2b on the rear end side of the nozzle body 10, It is trying to return to a natural state by elastic restoring force. For this reason, when parts other than the support part 2 are inject
  • the support portions 2 b on the front end side and the rear end side of the nozzle body 10 are centered on the same side as viewed from the center axis AX.
  • the slit 15b is formed on the same side as the support portion 2b, so that a suitable posture is maintained when the intraocular lens 2 is ejected from the nozzle body 10 as described above. Can do.
  • FIG. 9 shows a modification of the intraocular lens insertion device 1 in the above embodiment.
  • FIG. 10 shows the plunger 300 of the insertion instrument 100 of this modification.
  • 10C and 10D are views showing the relationship between the plunger 300 and the insertion portion 32 when the plunger 300 is viewed from the front side or the rear side of the insertion instrument 100.
  • FIG. As shown in FIGS. 10 (c) and 10 (d), in the insertion instrument 100 of this modification, the pressing plate portion 330 of the plunger 300 is viewed when the plunger 300 is viewed from the front side or the rear side of the insertion instrument 100. It is formed to be a substantially regular hexagon.
  • the shape of the press plate part 330 can be made into a free shape as long as the operation feeling of the plunger 300 for the user is not impaired. Therefore, in consideration of the design of the insertion instrument 100, the shape of the pressing plate portion 330 can be selected as appropriate, such as a circle, a square, and other polygons.
  • FIG. 11 schematically shows a front view of the insertion instrument 100 of this modification as viewed from the front side of the insertion instrument 100.
  • the hold unit 11 has a shape in which so-called “brims” extend in the vertical direction so that the user can easily put his / her finger on the corner, and the four corners of the brim have an angle of about 5 ° to 15 °. Chamfered.
  • the hold part 11 has a vertically long octagonal shape in a front view.
  • the pressing plate portion 330 has a substantially regular hexagonal shape.

Abstract

Provided is an intraocular lens insertion instrument that can make the posture of an intraocular lens, which is ejected from the insertion instrument, more stable. An intraocular lens insertion instrument comprises: an instrument body having an insertion tube through which an intraocular lens moves, the intraocular lens having a lens body and a support section connected to the lens body via a connection section; and an intraocular lens storage section. A slit is provided that extends from an opening in a leading end of the insertion tube to a rear end thereof. The connection section of the support section is arranged so as to deviate from a central axis of the instrument body in a prescribed direction in a projection view of the body of the insertion instrument from an optical axis direction of the intraocular lens in a state where the intraocular lens is stored in the storage section. In a front view of the instrument body, when seen along the central axis of the instrument body, a width-direction position of the center of the slit is arranged tilted at a prescribed angle in the same direction as the connection section of the support section of the intraocular lens stored in the storage section with respect to a rearward direction along the optical axis of the intraocular lens in the instrument body.

Description

眼内レンズの挿入器具Intraocular lens insertion device
 本発明は、眼内レンズの挿入器具に関する。 The present invention relates to an intraocular lens insertion device.
 白内障治療においてヒト混濁水晶体の置換や屈折の補正のために水晶体の代用として挿入される眼内レンズが実用に供されている。白内障治療における眼内レンズ挿入手術においては、例えば角膜の縁に数ミリの切開の創口(切開創)が設けられ、超音波水晶体乳化吸引術などにより水晶体が粉砕されて切開創から取り除かれた後、眼内レンズが挿入及び固定される。 Intraocular lenses that are inserted as a substitute for the lens for the replacement of the human turbid lens and the correction of refraction in the treatment of cataract are being put to practical use. In intraocular lens insertion surgery for cataract treatment, for example, a few millimeter incision wound (incision) is provided at the edge of the cornea, and the lens is crushed and removed from the incision by ultrasonic phacoemulsification The intraocular lens is inserted and fixed.
 近年においては、眼内レンズを切開創より眼球内に挿入する際に、あらかじめ眼内レンズがカートリッジに装填された挿入器具が用いられる場合が多い。使用者は、器具本体の先端部に設けられた挿入筒部の先端開口を上述の切開創を通じて眼球内に挿し入れると共に、眼内レンズを器具本体内で小さく変形せしめた状態で挿入筒部の先端開口から棒状のプランジャーによって押し出すことにより、眼内レンズを眼球内に射出して挿入する。このような挿入器具を用いることにより、切開創の大きさを小さくすることができ、かつ眼内レンズを簡単に眼球内に挿入できるので、手術における負担を少なくすることができる。 In recent years, when an intraocular lens is inserted into an eyeball through an incision, an insertion device in which the intraocular lens is previously loaded in a cartridge is often used. The user inserts the distal end opening of the insertion tube portion provided at the distal end portion of the instrument body into the eyeball through the above-mentioned incision, and in the state where the intraocular lens is slightly deformed in the instrument body, The intraocular lens is ejected and inserted into the eyeball by pushing it out from the tip opening with a rod-like plunger. By using such an insertion device, the size of the incision can be reduced, and the intraocular lens can be easily inserted into the eyeball, so that the burden on the operation can be reduced.
 一般に眼内レンズは、レンズ本体とレンズ本体に接続される支持部とを有する。そして、眼内レンズを上記の挿入器具を用いて眼球内に挿入する場合、プランジャーが眼内レンズを先端開口側に移動するにつれて、眼内レンズは挿入筒部の内壁形状に合わせて折り畳まれた状態になる。このとき、一度折り畳まれた眼内レンズが挿入器具の先端から射出される際の眼内レンズの姿勢をより安定させるため、挿入器具の先端部が中心軸に対して傾いた面になっている構成、いわゆるベベルを設ける構成が提案されている(例えば特許文献1)。 Generally, an intraocular lens has a lens body and a support portion connected to the lens body. When the intraocular lens is inserted into the eyeball using the above-described insertion device, the intraocular lens is folded in accordance with the inner wall shape of the insertion tube portion as the plunger moves the intraocular lens toward the distal opening side. It becomes a state. At this time, in order to stabilize the posture of the intraocular lens when the intraocular lens once folded is emitted from the distal end of the insertion instrument, the distal end portion of the insertion instrument is inclined with respect to the central axis. The structure which provides what is called a bevel is proposed (for example, patent document 1).
特開2012-249678号公報JP 2012-249678 A
 しかしながら、従来の眼内レンズの挿入器具では、挿入器具の先端部にベベルが設けられているにすぎないため、依然として挿入器具の先端から射出される眼内レンズの姿勢が定まらない可能性がある。このため、使用者は、眼内レンズが好適な姿勢で射出されるように挿入器具自体の姿勢を変える等の操作をしたり、眼内に射出された眼内レンズの位置を調整する追加の処置等を行ったりする。 However, in the conventional intraocular lens insertion device, since the tip of the insertion device is only provided with a bevel, the posture of the intraocular lens emitted from the distal end of the insertion device may still not be determined. . For this reason, the user performs an operation such as changing the posture of the insertion instrument itself so that the intraocular lens is ejected in a suitable posture, or adjusting the position of the intraocular lens ejected into the eye. Take measures.
 本件開示の技術は、上記の事情に鑑みてなされたものであり、その目的とするところは、挿入器具から射出される眼内レンズの姿勢をより安定させることができる眼内レンズの挿入器具を提供することである。 The technology of the present disclosure has been made in view of the above circumstances, and an object thereof is to provide an intraocular lens insertion device that can further stabilize the posture of the intraocular lens emitted from the insertion device. Is to provide.
 本件開示の眼内レンズの挿入器具は、レンズ本体とレンズ本体に一端が接続部を介して接続されている支持部とを有する眼内レンズが移動する挿入筒部を先端に有する器具本体と、眼内レンズを収納する収納部とを備える眼内レンズの挿入器具であって、挿入筒部の先端の開口から後端に向かって挿入筒部の長手方向に延伸するスリットが設けられており、眼内レンズが収納部に収納された状態での挿入器具の本体の該眼内レンズの光軸方向からの投影視において、少なくとも1つの支持部の接続部は、器具本体の中心軸に対して所定方向に外れて配されており、器具本体の正面視において、スリットの幅方向の中心位置が、器具本体の中心軸から見て、器具本体にある眼内レンズの光軸の後側方向に対して、収納部に収納された眼内レンズの上記少なくとも1つの支持部の接続部と同じ方向に所定角度傾斜して配置されている。これにより、眼内レンズの支持部がスリットから押し出されるため、支持部によってレンズ本体ひいては眼内レンズの姿勢が変更される可能性を抑えることができる。ここで、所定角度は、器具本体の正面視において、スリットの幅方向の中心位置が、器具本体の中心軸から見て、眼内レンズが挿入筒部を通過する際の接続部の位置と合致するような角度である。 The intraocular lens insertion device of the present disclosure includes a lens body and an instrument body having an insertion tube portion at the tip end of which an intraocular lens having a support portion having one end connected to the lens body via a connection portion, An insertion device for an intraocular lens including a storage unit for storing an intraocular lens, provided with a slit extending in the longitudinal direction of the insertion tube portion from the opening at the front end of the insertion tube portion toward the rear end, In the projection view from the optical axis direction of the intraocular lens of the main body of the insertion instrument in a state where the intraocular lens is accommodated in the accommodating part, the connection part of at least one support part is relative to the central axis of the instrument main body The center position in the width direction of the slit is the rear side of the optical axis of the intraocular lens in the instrument body when viewed from the center axis of the instrument body in the front view of the instrument body. In contrast, the intraocular lens stored in the storage unit It is arranged to be inclined at a predetermined angle in the same direction as the connection portion of the at least one support. Thereby, since the support part of an intraocular lens is extruded from a slit, possibility that the attitude | position of a lens main body and by extension, an intraocular lens will be changed by a support part can be suppressed. Here, the predetermined angle coincides with the position of the connection part when the intraocular lens passes through the insertion tube part when the center position in the width direction of the slit is viewed from the central axis of the instrument body in a front view of the instrument body. It is an angle to do.
 好ましくは、上記の眼内レンズの挿入器具において、上記所定角度が約30°であるように構成する。これにより、本件開示の眼内レンズの挿入器具を用いて一般的な眼内レンズを眼内に射出する場合に、より確実に眼内レンズの支持部をスリットから射出することができ、ひいては眼内レンズの射出時の姿勢が好適に維持される。 Preferably, the intraocular lens insertion device is configured such that the predetermined angle is about 30 °. Accordingly, when a general intraocular lens is ejected into the eye using the intraocular lens insertion device disclosed herein, the intraocular lens support can be more reliably ejected from the slit, and thus the eye The posture at the time of injection of the inner lens is preferably maintained.
 本件開示の技術によれば、挿入器具から射出される眼内レンズの姿勢をより安定させることができる眼内レンズの挿入器具を提供することができる。 According to the technology disclosed herein, it is possible to provide an intraocular lens insertion device that can further stabilize the posture of the intraocular lens emitted from the insertion device.
一実施形態における眼内レンズの挿入器具の概略構成を示す図である。It is a figure which shows schematic structure of the insertion instrument of the intraocular lens in one Embodiment. 一実施形態における眼内レンズの概略構成を示す図である。It is a figure which shows schematic structure of the intraocular lens in one Embodiment. 一実施形態におけるノズル本体の概略構成を示す図である。It is a figure which shows schematic structure of the nozzle main body in one Embodiment. 一実施形態における位置決め部材の概略構成を示す図である。It is a figure which shows schematic structure of the positioning member in one Embodiment. 一実施形態におけるプランジャーの概略構成を示す図である。It is a figure which shows schematic structure of the plunger in one Embodiment. 一実施形態におけるノズル本体の先端の概略構成を示す図である。It is a figure which shows schematic structure of the front-end | tip of the nozzle main body in one Embodiment. 一実施形態におけるノズル本体の先端と眼内レンズを示す図である。It is a figure which shows the front-end | tip of the nozzle main body and intraocular lens in one Embodiment. 一実施形態における眼内レンズをノズル本体から射出する場合の眼内レンズの姿勢を示す模式図である。It is a schematic diagram which shows the attitude | position of the intraocular lens in the case of inject | emitting the intraocular lens in one Embodiment from a nozzle main body. 一変形例における眼内レンズの挿入器具の概略構成を示す図である。It is a figure which shows schematic structure of the insertion instrument of the intraocular lens in one modification. 一変形例におけるプランジャーの概略構成を示す図である。It is a figure which shows schematic structure of the plunger in one modification. 一変形例における眼内レンズの挿入器具と眼内レンズを示す図である。It is a figure which shows the insertion instrument and intraocular lens of the intraocular lens in one modification.
 以下に、図面を参照して本発明の実施の形態について説明する。 Hereinafter, embodiments of the present invention will be described with reference to the drawings.
 〔実施例〕
 図1に、本実施形態の挿入器具1の概略構成を示す。図1(a)はステージ蓋部13を開蓋した場合の挿入器具1の平面図、図1(b)はステージ蓋部13を閉蓋した場合の挿入器具1の側面図を示している。挿入器具1は、器具本体としてのノズル本体10と、眼内レンズの押出部材としてのプランジャー30と、眼内レンズの収納部としてのステージ部12及びステージ蓋部13を有する。ステージ部12は、ノズル本体10に一体又は別体に設けられる。ノズル本体10にはプランジャー30が挿入されている。ステージ部12には、眼内レンズ2がセットされる。ステージ部12は、ステージ蓋部13と一体に形成されている。図1には、ステージ蓋部13を開けた状態を示す。
〔Example〕
In FIG. 1, schematic structure of the insertion instrument 1 of this embodiment is shown. 1A is a plan view of the insertion instrument 1 when the stage lid 13 is opened, and FIG. 1B is a side view of the insertion instrument 1 when the stage lid 13 is closed. The insertion instrument 1 has a nozzle body 10 as an instrument body, a plunger 30 as an intraocular lens pushing member, a stage part 12 and a stage lid part 13 as a storage part for an intraocular lens. The stage unit 12 is provided integrally with the nozzle body 10 or separately. A plunger 30 is inserted into the nozzle body 10. The intraocular lens 2 is set on the stage unit 12. The stage unit 12 is formed integrally with the stage lid unit 13. FIG. 1 shows a state in which the stage lid 13 is opened.
 挿入器具1のノズル本体10は、断面略矩形の筒状に形成されており片側の端部は大きく開口し(以下、大きく開口した側を後端部10bという。)、別の側の端部には細く絞られたノズル部15と先端部10aを備える。図1(b)に示すように、先端部10aは斜めに開口している。プランジャー30は、ノズル本体10に挿入され往復運動可能である。また、ノズル部15にはスリット15bが形成されている。スリット15bの詳細については後述する。 The nozzle body 10 of the insertion instrument 1 is formed in a cylindrical shape having a substantially rectangular cross section, and one end of the insertion tool 1 is greatly open (hereinafter, the side having the large opening is referred to as a rear end 10b), and the end on the other side. Includes a nozzle portion 15 and a tip portion 10a which are narrowed down. As shown in FIG.1 (b), the front-end | tip part 10a is opening diagonally. The plunger 30 is inserted into the nozzle body 10 and can reciprocate. In addition, a slit 15 b is formed in the nozzle portion 15. Details of the slit 15b will be described later.
 以下の説明において、ノズル本体10の後端部10bから先端部10aへ向かう方向を前方向、その逆方向を後方向、図1(a)において紙面手前側を上方向、その逆方向を下方向、図1(b)において紙面手前方向を左方向、その逆方向を右方向とする。また、この場合、上側は後述するレンズ本体2aの光軸前側に、下側はレンズ本体2aの光軸後側に、前側はプランジャー30による押圧方向前側に、後側はプランジャー30による押圧方向後側に相当する。 In the following description, the direction from the rear end 10b of the nozzle body 10 to the front end 10a is the front direction, the opposite direction is the rear direction, the front side of the page in FIG. 1A is the upper direction, and the reverse direction is the lower direction. In FIG. 1B, the front side of the page is the left direction, and the opposite direction is the right direction. In this case, the upper side is the front side of the optical axis of the lens body 2a, which will be described later, the lower side is the rear side of the optical axis of the lens body 2a, the front side is the front side in the pressing direction by the plunger 30, and the rear side is pressed by the plunger 30 Corresponds to the rear side.
 ノズル本体10の後端部10b付近には、板状に迫り出し、使用者がプランジャー30をノズル本体10の先端側に押し込む際に指を掛けるホールド部11が一体的に設けられている。また、ノズル本体10におけるノズル部15の後側には、眼内レンズ2をセットするステージ部12が設けられている。このステージ部12は、ステージ蓋部13を開蓋することでノズル本体10の上側が開放されるようになっている。また、ステージ部12には、ノズル本体10の下側から位置決め部材50が取り付けられている。この位置決め部材50によって、使用前(輸送中)においてもステージ部12内で眼内レンズ2が安定して保持されている。 In the vicinity of the rear end portion 10b of the nozzle body 10, there is integrally provided a holding portion 11 that protrudes in a plate shape and hooks a finger when the user pushes the plunger 30 into the front end side of the nozzle body 10. A stage portion 12 for setting the intraocular lens 2 is provided on the rear side of the nozzle portion 15 in the nozzle body 10. The stage portion 12 is configured such that the upper side of the nozzle body 10 is opened by opening the stage lid portion 13. Further, a positioning member 50 is attached to the stage portion 12 from the lower side of the nozzle body 10. By this positioning member 50, the intraocular lens 2 is stably held in the stage portion 12 even before use (during transportation).
 すなわち、挿入器具1においては、製造時に、ステージ蓋部13が開蓋し位置決め部材50がステージ部12に取り付けられた状態で、眼内レンズ2がステージ部12に、光軸前側が上になるようにセットされる。そして、ステージ蓋部13を閉蓋させた後出荷され、販売される。そして、使用者はステージ蓋部13を閉蓋したままで位置決め部材50を取り外し、その後プランジャー30をノズル本体10の先端側に押し込む。これにより、プランジャー30によって眼内レンズ2を押圧し、ノズル部15まで移動させた上で、先端部10aより眼内レンズ2を眼球内に射出する。なお、挿入器具1におけるノズル本体10、プランジャー30、位置決め部材50はポリプロピレンなどの樹脂の素材で形成される。ポリプロピレンは医療用機器において実績があり、耐薬品性などの信頼性も高い素材である。 That is, in the insertion instrument 1, the intraocular lens 2 is on the stage unit 12 and the front side of the optical axis is on the upper side in a state where the stage lid unit 13 is opened and the positioning member 50 is attached to the stage unit 12. Is set as Then, after the stage lid 13 is closed, it is shipped and sold. Then, the user removes the positioning member 50 with the stage lid portion 13 closed, and then pushes the plunger 30 into the distal end side of the nozzle body 10. As a result, the intraocular lens 2 is pressed by the plunger 30 and moved to the nozzle unit 15, and then the intraocular lens 2 is injected into the eyeball from the distal end portion 10 a. In addition, the nozzle body 10, the plunger 30, and the positioning member 50 in the insertion instrument 1 are formed of a resin material such as polypropylene. Polypropylene is a material with a proven track record in medical equipment and high reliability such as chemical resistance.
 図2は、眼内レンズ2の概略構成を示した図である。図2(a)は平面図、図2(b)は側面図を示す。眼内レンズ2は、いわゆるワンピース型である。眼内レンズ2は、所定の屈折力を有するレンズ本体2aと、レンズ本体2aに連結された、レンズ本体2aを眼球内で保持するための平板状の2本の支持部2bとから形成されている。なお、眼内レンズは、屈折矯正はもとより、乱視矯正や遠近両用(多焦点)および視軸との同一性などの光学的機能を有するものもある。乱視矯正の眼内レンズ場合は、図2(c)に示すように、主経線の位置を示すマーキング2dがレンズに施される。また、多焦点レンズの場合は、レンズ面に回折格子の形状2eが現れる。さらにまた、レンズ本体2aの中心と回折格子の形状2eの中心をズラすことで、眼内レンズを挿入される個々人がもつ視軸のズレにも対応し得る。一方、支持部2bはレンズ本体2の外縁に当接するジャンクション部2cを有し、ジャンクション部2cとレンズ本体2aとが接着剤等によって接続されている。なお、ジャンクション部が接続部の一例に相当する。レンズ本体2a及び支持部2bは可撓性の樹脂材料から形成されている。本実施例における挿入器具1内では、2つの支持部2bのうちの1つが、レンズ本体2aの後側、もう1つがレンズ本体の前側に配置されるように、眼内レンズ2がセットされる。 FIG. 2 is a diagram showing a schematic configuration of the intraocular lens 2. 2A is a plan view and FIG. 2B is a side view. The intraocular lens 2 is a so-called one-piece type. The intraocular lens 2 is formed of a lens body 2a having a predetermined refractive power and two flat plate-like support portions 2b connected to the lens body 2a for holding the lens body 2a in the eyeball. Yes. Some intraocular lenses have not only refractive correction but also optical functions such as astigmatism correction, bifocal (multifocal) and identity with the visual axis. In the case of an intraocular lens for correcting astigmatism, as shown in FIG. 2C, a marking 2d indicating the position of the main meridian is applied to the lens. In the case of a multifocal lens, a diffraction grating shape 2e appears on the lens surface. Furthermore, by shifting the center of the lens body 2a and the center of the shape 2e of the diffraction grating, it is possible to cope with the deviation of the visual axis of the individual into which the intraocular lens is inserted. On the other hand, the support part 2b has a junction part 2c that contacts the outer edge of the lens body 2, and the junction part 2c and the lens body 2a are connected by an adhesive or the like. The junction part corresponds to an example of a connection part. The lens body 2a and the support portion 2b are made of a flexible resin material. In the insertion instrument 1 in the present embodiment, the intraocular lens 2 is set so that one of the two support portions 2b is disposed on the rear side of the lens body 2a and the other is disposed on the front side of the lens body. .
 図3にはノズル本体10のみの平面図を示す。前述した図1に示したようにノズル本体10においては、眼内レンズ2はステージ部12にセットされる。そして、その状態でプランジャー30によって眼内レンズ2が押圧されて先端部10aから射出される。なお、ノズル本体10の内部には、ノズル本体10の外形が先端にいくほど細くなっているという形状に応じて断面形状も先端にいくほど小さくなっている貫通孔10cが設けられている。なお、貫通孔の断面形状は実施例図ではオーバル形状(卵形)になっているが使用レンズや仕様の都合で円形や長円形としても何ら差し支えない。そして、眼内レンズ2が射出される際は、眼内レンズ2は、ノズル本体10内の貫通孔10cの断面形状の変化に応じて変形して折り畳まれた状態となり、患者の眼球に形成された切開創に入り易い形に変形した上で射出される。 FIG. 3 shows a plan view of only the nozzle body 10. As shown in FIG. 1 described above, in the nozzle body 10, the intraocular lens 2 is set on the stage unit 12. In this state, the intraocular lens 2 is pressed by the plunger 30 and ejected from the distal end portion 10a. The nozzle body 10 is provided with a through-hole 10c having a cross-sectional shape that becomes smaller toward the tip according to the shape that the outer shape of the nozzle body 10 becomes thinner toward the tip. In addition, although the cross-sectional shape of the through hole is an oval shape (egg shape) in the embodiment diagram, it may be a circular shape or an oval shape for the convenience of the lens used or specifications. And when the intraocular lens 2 is inject | emitted, the intraocular lens 2 will be in the state which deform | transformed and folded according to the change of the cross-sectional shape of the through-hole 10c in the nozzle main body 10, and is formed in a patient's eyeball. After being transformed into a shape that makes it easy to enter an incision, it is injected.
 また、先端部10aは、ノズル部15の上側の領域が下側の領域より前側になるように斜めにカットされた形状となっている。なお、この先端部10aの斜めにカットされた形状については、左右方向から見て直線的に斜めにカットされていてもよいし、外側に膨らみを持つように、すなわち曲面形状となるように斜めにカットされていてもよい。 Further, the tip portion 10a has a shape cut obliquely so that the upper region of the nozzle portion 15 is in front of the lower region. Note that the shape of the tip portion 10a that is obliquely cut may be linearly obliquely cut when viewed from the left-right direction, or may have a bulge outward, that is, a curved shape. It may be cut into
 ステージ部12には、眼内レンズ2のレンズ本体2aの径より僅かに大きな幅を有するステージ溝12aが形成されている。ステージ溝12aの前後方向の寸法は、眼内レンズ2の両側に延びる支持部2bを含む最大幅寸法よりも大きく設定されている。また、ステージ溝12aの底面によってセット面12bが形成されている。セット面12bの上下方向位置は、ノズル本体10の貫通孔10cの底面の高さ位置よりも上方に設定されており、セット面12bと貫通孔10cの底面とは底部斜面10dによって連結されている。 A stage groove 12 a having a width slightly larger than the diameter of the lens body 2 a of the intraocular lens 2 is formed in the stage portion 12. The dimension in the front-rear direction of the stage groove 12 a is set to be larger than the maximum width dimension including the support portions 2 b extending on both sides of the intraocular lens 2. A set surface 12b is formed by the bottom surface of the stage groove 12a. The vertical position of the set surface 12b is set higher than the height position of the bottom surface of the through hole 10c of the nozzle body 10, and the set surface 12b and the bottom surface of the through hole 10c are connected by a bottom slope 10d. .
 ステージ部12とステージ蓋部13とは一体に形成されている。ステージ蓋部13はステージ部12と同等の前後方向の寸法を有している。ステージ蓋部13は、ステージ部12の側面がステージ蓋部13側に延出して形成された薄板状の連結部14によって連結されている。連結部14は中央部で屈曲可能に形成されており、ステージ蓋部13は、連結部14を屈曲させることでステージ部12に上側から重なり閉蓋することができる。 The stage portion 12 and the stage lid portion 13 are integrally formed. The stage lid portion 13 has the same size in the front-rear direction as the stage portion 12. The stage lid portion 13 is connected by a thin plate-like connecting portion 14 formed by extending the side surface of the stage portion 12 to the stage lid portion 13 side. The connecting portion 14 is formed to be bendable at the center portion, and the stage lid portion 13 can be closed by overlapping the stage portion 12 from above by bending the connecting portion 14.
 ステージ蓋部13において、閉蓋時にセット面12bと対向する面には、ステージ蓋部13を補強し、眼内レンズ2の位置を安定させるためにリブ13a及び13bが設けられている。また、プランジャー30の上側のガイドとして案内突起13cが設けられている。 In the stage lid 13, ribs 13 a and 13 b are provided on the surface facing the set surface 12 b when the lid is closed in order to reinforce the stage lid 13 and stabilize the position of the intraocular lens 2. Further, a guide protrusion 13 c is provided as a guide on the upper side of the plunger 30.
 ステージ部12のセット面12bの下側には、位置決め部材50が取外し可能に設けられている。図4に、位置決め部材50の概略構成を示す。図4(a)は位置決め部材50の平面図を示し、図4(b)は位置決め部材50の左側面図を示している。位置決め部材50はノズル本体10と別体として構成されており、一対の側壁部51が連結部52で連結された構造とされている。それぞれの側壁部51の下端には、外側に向けて延出して広がる保持部53が形成されている。 A positioning member 50 is detachably provided below the set surface 12b of the stage portion 12. FIG. 4 shows a schematic configuration of the positioning member 50. FIG. 4A shows a plan view of the positioning member 50, and FIG. 4B shows a left side view of the positioning member 50. The positioning member 50 is configured as a separate body from the nozzle body 10, and has a structure in which a pair of side wall portions 51 are connected by a connecting portion 52. A holding portion 53 is formed at the lower end of each side wall portion 51 so as to extend outward.
 そして、それぞれの側壁部51の上端部には、上方から見た形状が円弧形状であり上側に突出した一対の第一載置部54が形成されている。さらに、第一載置部54の上端面における外周側には、第一位置決め部55が突出して形成されている。第一位置決め部55の内径どうしの距離は、眼内レンズ2のレンズ本体2aの径寸法よりも僅かに大きく設定されている。 Further, a pair of first mounting portions 54 are formed on the upper end portions of the respective side wall portions 51. The pair of first mounting portions 54 are formed in an arc shape when viewed from above and project upward. Further, a first positioning portion 55 is formed on the outer peripheral side of the upper end surface of the first placement portion 54 so as to protrude. The distance between the inner diameters of the first positioning portion 55 is set to be slightly larger than the diameter dimension of the lens body 2 a of the intraocular lens 2.
 また、連結部52の前後方向の両端には、上方から見た形状が矩形状であり上側に突出した一対の第二載置部56が形成されている。第二載置部56の上面の高さは、第一載置部54の上面の高さと同等になっている。さらに、第二載置部56の上面において外側の部分には、第二載置部56の左右方向の全体にわたって上側にさらに突出する第二位置決め部57が形成されている。第二位置決め部57の内側どうしの離隔は、眼内レンズ2のレンズ本体2aの径寸法よりも僅かに大きく設定されている。加えて、第二載置部56の上端部には左右方向の全体にわたり、前後方向に僅かに突出した係止爪58が形成されている。 Further, a pair of second placement portions 56 are formed at both ends in the front-rear direction of the connecting portion 52, and the shape viewed from above is a rectangular shape and protrudes upward. The height of the upper surface of the second placement unit 56 is equal to the height of the upper surface of the first placement unit 54. Further, a second positioning portion 57 that further protrudes upward over the entire left and right direction of the second placement portion 56 is formed on the outer portion of the upper surface of the second placement portion 56. The distance between the inner sides of the second positioning portion 57 is set slightly larger than the diameter of the lens body 2a of the intraocular lens 2. In addition, a locking claw 58 that slightly protrudes in the front-rear direction is formed on the upper end portion of the second placement portion 56 over the entire left-right direction.
 上記の位置決め部材50は、ノズル本体10のセット面12bの下側から組み付けられる。ノズル本体10のセット面12bには、厚さ方向にセット面12bを貫通するセット面貫通孔12cが形成されている。セット面貫通孔12cの外形は、位置決め部材50の第一載置部54及び第二載置部56を上側から見た形状に対し僅かに大きな略相似形状とされている。そして、位置決め部材50がノズル本体10に取り付けられる際には、第一載置部54及び第二載置部56が、セット面12bの下側からセット面貫通孔12cに挿入され、セット面12bの上側に突出する。 The positioning member 50 is assembled from below the set surface 12b of the nozzle body 10. The set surface 12b of the nozzle body 10 is formed with a set surface through hole 12c that penetrates the set surface 12b in the thickness direction. The outer shape of the set surface through hole 12c is substantially similar to the shape of the first mounting portion 54 and the second mounting portion 56 of the positioning member 50 as viewed from above. When the positioning member 50 is attached to the nozzle body 10, the first placement portion 54 and the second placement portion 56 are inserted into the set surface through hole 12c from the lower side of the set surface 12b, and the set surface 12b. Protrudes above.
 その際、第二位置決め部57に設けられた係止爪58がセット面貫通孔12cを介してセット面12bに突出し、セット面12bの上面に係止される。このことによって、位置決め部材50がノズル本体10の下側から組み付けられ、第一載置部54及び第二載置部56がセット面12bから突出した状態で固定される。そして、眼内レンズ2がセット面12bにセットされる際には、レンズ本体2aの外周部底面が、第一載置部54及び第二載置部56の上面に載置される。また、レンズ本体2aは第一位置決め部55及び第二位置決め部57によって水平方向(セット面12bに水平な方向)に対して位置規制される。 At that time, the locking claw 58 provided in the second positioning portion 57 protrudes to the set surface 12b through the set surface through hole 12c and is locked to the upper surface of the set surface 12b. As a result, the positioning member 50 is assembled from the lower side of the nozzle body 10, and the first placement portion 54 and the second placement portion 56 are fixed in a state of protruding from the set surface 12b. When the intraocular lens 2 is set on the setting surface 12b, the bottom surface of the outer periphery of the lens body 2a is placed on the upper surfaces of the first placement unit 54 and the second placement unit 56. Further, the position of the lens body 2a is restricted with respect to the horizontal direction (direction horizontal to the set surface 12b) by the first positioning portion 55 and the second positioning portion 57.
 眼内レンズ2を眼球内に挿入する際は、位置決め部材50をノズル本体10から取り外す。これにより、眼内レンズ2のレンズ本体2aを支持していた第一載置部54および第二載置部56がセット面12bから後退し、眼内レンズ2がセット面12b上に移動可能に載置される。そして、プランジャー30によって、眼内レンズ2が所定の位置まで推し進められる。 When inserting the intraocular lens 2 into the eyeball, the positioning member 50 is removed from the nozzle body 10. Thereby, the 1st mounting part 54 and the 2nd mounting part 56 which were supporting the lens main body 2a of the intraocular lens 2 retreat from the set surface 12b, and the intraocular lens 2 can move on the set surface 12b. Placed. Then, the intraocular lens 2 is pushed forward to a predetermined position by the plunger 30.
 続いて、眼組織に設けた切開創に、ノズル本体10のノズル部15における先端部10aを挿入する。先端部10aは、斜めの開口形状を有しているので、切開創への挿入を容易に行なうことができる。そして、切開創にノズル部15を挿入した後に、再度プランジャー30の押圧板部33をノズル本体10の先端側に押し込む。これにより、セット面12aにセットされた眼内レンズ2のレンズ本体2a外周にプランジャー30の作用部31の先端が当接し、プランジャー30によって眼内レンズ2が先端部10aに向けて案内される。 Subsequently, the distal end portion 10a of the nozzle portion 15 of the nozzle body 10 is inserted into the incision provided in the eye tissue. Since the distal end portion 10a has an oblique opening shape, it can be easily inserted into the incision. Then, after inserting the nozzle portion 15 into the incision, the pressing plate portion 33 of the plunger 30 is again pushed into the distal end side of the nozzle body 10. As a result, the distal end of the action portion 31 of the plunger 30 comes into contact with the outer periphery of the lens body 2a of the intraocular lens 2 set on the set surface 12a, and the intraocular lens 2 is guided toward the distal end portion 10a by the plunger 30. The
 次に、図5に、プランジャー30の概略構成を示す。プランジャー30は、ノズル本体10よりもやや大きな前後方向長さを有している。そして、円柱形状を基本とした先端側の作用部31と、矩形ロッド形状を基本とした後端側の挿通部32とから形成されている。そして、作用部31は、円柱形状とされた円柱部31aと、円柱部31aの左右方向に広がる薄板状の扁平部31bとを含んで構成されている。 Next, FIG. 5 shows a schematic configuration of the plunger 30. The plunger 30 has a slightly larger longitudinal length than the nozzle body 10. And it forms from the action part 31 of the front end side based on a column shape, and the insertion part 32 of the rear end side based on a rectangular rod shape. And the action part 31 is comprised including the cylindrical part 31a made into the column shape, and the thin plate-shaped flat part 31b extended in the left-right direction of the cylindrical part 31a.
 作用部31の先端部分には、切欠部31cが形成されている。この切欠部31cは、図5(a)に示すように、作用部31の上方向に開口し左右方向に貫通する溝状に形成されている。また、図5(b)に示すように、切欠部31cの先端側の溝壁は作用部31の先端側に行くに連れて上方に向かう傾斜面で形成されている。一方、挿通部32は、全体的に概略H字状の断面を有しており、その左右方向及び上下方向の寸法は、ノズル本体10の貫通孔10cよりも僅かに小さく設定されている。また、挿通部32の後端には、上下左右方向に広がる円板状の押圧板部33が形成されている。 A notch 31 c is formed at the tip of the action part 31. As shown in FIG. 5A, the notch 31c is formed in a groove shape that opens upward in the action portion 31 and penetrates in the left-right direction. Further, as shown in FIG. 5B, the groove wall on the distal end side of the notch 31 c is formed with an inclined surface that goes upward as it goes to the distal end side of the action portion 31. On the other hand, the insertion part 32 has a substantially H-shaped cross section as a whole, and the horizontal and vertical dimensions thereof are set slightly smaller than the through hole 10 c of the nozzle body 10. In addition, a disc-shaped pressing plate portion 33 is formed at the rear end of the insertion portion 32 so as to spread in the vertical and horizontal directions.
 挿通部32の前後方向の中央より先側の部分には、挿通部32の上側に向けて突出し、プランジャー30の素材の弾性により上下に移動可能な爪部32aが形成されている。そして、プランジャー30がノズル本体10に挿入された際には、ノズル本体10の上面において厚さ方向に設けられた図3に示す係止孔10eと爪部32aが係合し、このことにより初期状態におけるノズル本体10とプランジャー30との相対位置が決定される。なお、爪部32aと係止孔10eの形成位置は、係合状態において、作用部31の先端が、ステージ部12にセットされた眼内レンズ2のレンズ本体2aの後側に位置し、レンズ本体2aの後側の支持部2bを切欠部31cが下方から支持可能な場所に位置するよう設定されている。 A claw portion 32 a that protrudes upward from the insertion portion 32 and that can move up and down by the elasticity of the material of the plunger 30 is formed at a portion of the insertion portion 32 that is ahead of the center in the front-rear direction. When the plunger 30 is inserted into the nozzle body 10, the locking hole 10e shown in FIG. 3 provided in the thickness direction on the upper surface of the nozzle body 10 and the claw portion 32a are engaged. The relative position between the nozzle body 10 and the plunger 30 in the initial state is determined. It should be noted that the claw portion 32a and the locking hole 10e are formed at the positions where the distal end of the action portion 31 is located on the rear side of the lens body 2a of the intraocular lens 2 set on the stage portion 12 in the engaged state. The support portion 2b on the rear side of the main body 2a is set so that the cutout portion 31c can be supported from below.
 上記のように構成された挿入器具1の眼内レンズ2の収納前においては、プランジャー30がノズル本体10に挿入されて初期位置に配置される。また、上記の通り、位置決め部材50が、セット面12bの下方からノズル本体10に取り付けられる。これにより、位置決め部材50の第一載置部54及び第二載置部56がセット面12bに突出した状態に保持される。 Before the intraocular lens 2 of the insertion instrument 1 configured as described above is stored, the plunger 30 is inserted into the nozzle body 10 and disposed at the initial position. Further, as described above, the positioning member 50 is attached to the nozzle body 10 from below the set surface 12b. Thereby, the 1st mounting part 54 and the 2nd mounting part 56 of the positioning member 50 are hold | maintained in the state protruded to the set surface 12b.
 次に、眼内レンズ2のレンズ本体2aが支持部2bをノズル本体10の前後方向に向けた状態で第一載置部54および第二載置部56の上面に載置され位置決めされる。この状態において、眼内レンズ2の後側の支持部2bの一部がプランジャー30の切欠部31cに挟まれ、その底面によって支持された状態となる。 Next, the lens body 2 a of the intraocular lens 2 is placed and positioned on the upper surfaces of the first placement part 54 and the second placement part 56 in a state where the support part 2 b is directed in the front-rear direction of the nozzle body 10. In this state, a part of the support portion 2b on the rear side of the intraocular lens 2 is sandwiched between the notches 31c of the plunger 30 and is supported by the bottom surface thereof.
 図6は、本実施形態における挿入器具1のノズル本体10の先端部を模式的に示す側面図である。図7のノズル本体10の正面図にも示すように、ノズル本体10の前後方向に延びる円筒形状のノズル部15の中心軸をAX(図6中の二点鎖線)とする。図6に示すように、ノズル本体10のノズル部15の先端が中心軸AXに対してノズル部15の下方を向くよう傾いた面でカットされる、いわゆるベベル加工が施されている。これにより、ノズル部15の先端の開口15aは、いわゆるベベルダウンとなるよう形成される。 FIG. 6 is a side view schematically showing the tip of the nozzle body 10 of the insertion instrument 1 in the present embodiment. As shown in the front view of the nozzle body 10 in FIG. 7, the central axis of the cylindrical nozzle portion 15 extending in the front-rear direction of the nozzle body 10 is AX (two-dot chain line in FIG. 6). As shown in FIG. 6, so-called bevel processing is performed in which the tip of the nozzle portion 15 of the nozzle body 10 is cut by a surface inclined so as to face the lower side of the nozzle portion 15 with respect to the central axis AX. Thereby, the opening 15a at the tip of the nozzle portion 15 is formed so as to be a so-called bevel down.
 本実施形態では、図6に示すように、ノズル部15の開口15aと接続するスリット15bが設けられている。スリット15bは、ノズル部15の開口15aの後端側からノズル部15の後端側に延びる略V字形状の切り込みである。図7を参照しながら後述するように、スリット15bは縁がテーパ状に形成されており、当該テーパ形状はスリット15bの後端部15cに至るまで続いている。スリット15bの縁がこのように形成されているため、ノズル部15の開口15aおよびスリット15bを、眼組織の切開創から挿入する際の刺入性が向上する。 In the present embodiment, as shown in FIG. 6, a slit 15b connected to the opening 15a of the nozzle portion 15 is provided. The slit 15 b is a substantially V-shaped cut extending from the rear end side of the opening 15 a of the nozzle portion 15 to the rear end side of the nozzle portion 15. As will be described later with reference to FIG. 7, the edge of the slit 15b has a tapered shape, and the tapered shape continues to the rear end 15c of the slit 15b. Since the edge of the slit 15b is formed in this way, the insertion property when the opening 15a and the slit 15b of the nozzle portion 15 are inserted from an incision of an eye tissue is improved.
 このため、本実施形態では、眼内レンズ2をステージ部12にセットしたときの眼内レンズ2とスリット15bとの位置関係が、ノズル部15の中心軸AXから見て、ノズル部15の下方向に対して、スリット15bとノズル本体10の後端側の支持部2bのジャンクション部2cとが同じ側にある位置関係となる。なお、スリット15bから射出される眼内レンズ2の動きの詳細については後述する。 Therefore, in the present embodiment, the positional relationship between the intraocular lens 2 and the slit 15b when the intraocular lens 2 is set on the stage unit 12 is below the nozzle unit 15 when viewed from the central axis AX of the nozzle unit 15. With respect to the direction, the slit 15b and the junction part 2c of the support part 2b on the rear end side of the nozzle body 10 are in the positional relationship on the same side. Details of the movement of the intraocular lens 2 emitted from the slit 15b will be described later.
 図7に、図6のA-A線による断面をノズル本体10の正面から見た図を示す。図7には、ノズル本体10を正面から見たときのノズル本体10の一部も示している。また、図7には、ノズル部15に移動された眼内レンズ2のレンズ本体2aの一例も示している。なお、図7では、見やすさのために眼内レンズ2のレンズ本体2aとノズル部15との間に隙間を設けているが、実際はレンズ本体2aとノズル部15の内壁とが接している。 FIG. 7 shows a cross section taken along line AA of FIG. 6 as viewed from the front of the nozzle body 10. FIG. 7 also shows a part of the nozzle body 10 when the nozzle body 10 is viewed from the front. FIG. 7 also shows an example of the lens body 2 a of the intraocular lens 2 moved to the nozzle unit 15. In FIG. 7, a gap is provided between the lens body 2a of the intraocular lens 2 and the nozzle portion 15 for ease of viewing, but the lens body 2a and the inner wall of the nozzle portion 15 are actually in contact with each other.
 図7に示すように、ノズル部15のスリット15bは、中心軸AXから見て下方向D1から所定の角度θ(≠0°)だけ傾斜した方向D2を中心として所定幅だけ開口するように設けられている。ここで下方向D1は、ステージ部12にセットされた眼内レンズ2のレンズ本体2aの光軸後側方向に相当する。また、図7に示すように、ノズル部15の中心軸AXに垂直な断面において、スリット15bを形成するノズル部15の縁15cがテーパ状に形成されている。 As shown in FIG. 7, the slit 15b of the nozzle portion 15 is provided so as to open by a predetermined width around a direction D2 inclined by a predetermined angle θ (≠ 0 °) from the lower direction D1 when viewed from the central axis AX. It has been. Here, the downward direction D1 corresponds to the rear direction of the optical axis of the lens body 2a of the intraocular lens 2 set on the stage unit 12. Further, as shown in FIG. 7, in the cross section perpendicular to the central axis AX of the nozzle portion 15, the edge 15c of the nozzle portion 15 forming the slit 15b is formed in a tapered shape.
 眼内レンズ2をノズル本体10の先端から眼内に射出する際は、眼内レンズ2がプランジャー30によってノズル本体10の先端側に押し進められるときに、眼内レンズ2の支持部2bのうちノズル本体10の後端側の支持部2bのジャンクション部2cとスリット15bとが、ノズル部15の中心軸AXから見て、ノズル部15の下方向に対して同じ側にあるという位置関係が維持される。眼内レンズ2のレンズ本体2aと支持部2bとの相対的な位置関係、眼内レンズ2がステージ部12にセットされたときのジャンクション部2cの位置、ノズル部15内における眼内レンズ2の折り畳み状態等を考慮して角度θを設定することで、眼内レンズ2の支持部2bを好適にスリット15bから射出することができる。 When the intraocular lens 2 is ejected into the eye from the tip of the nozzle body 10, when the intraocular lens 2 is pushed forward by the plunger 30 toward the tip side of the nozzle body 10, of the support portion 2 b of the intraocular lens 2. The positional relationship that the junction 2c and the slit 15b of the support 2b on the rear end side of the nozzle body 10 are on the same side with respect to the downward direction of the nozzle 15 as viewed from the central axis AX of the nozzle 15 is maintained. Is done. The relative positional relationship between the lens body 2 a and the support portion 2 b of the intraocular lens 2, the position of the junction portion 2 c when the intraocular lens 2 is set on the stage portion 12, and the intraocular lens 2 in the nozzle portion 15. By setting the angle θ in consideration of the folded state or the like, the support portion 2b of the intraocular lens 2 can be suitably emitted from the slit 15b.
 一般的な眼内レンズを本実施形態の挿入器具1を用いて眼内に射出する場合、角度θは約30°とすると、挿入器具1を回転させるなどして眼内レンズの姿勢を調整する必要なく、眼内レンズを好適な姿勢で維持して眼内に射出できる効果が期待される。なお、スリット15bの開口幅は適宜設定することができる。ここで、角度θは、本実施例において所定角度に相当する。 When a general intraocular lens is injected into the eye using the insertion instrument 1 of the present embodiment, if the angle θ is about 30 °, the orientation of the intraocular lens is adjusted by rotating the insertion instrument 1 or the like. It is not necessary, and an effect that the intraocular lens can be emitted in the eye while maintaining a suitable posture is expected. The opening width of the slit 15b can be set as appropriate. Here, the angle θ corresponds to a predetermined angle in the present embodiment.
 図8は、本実施形態において、プランジャー30の操作によって眼内レンズ2がノズル本体10内を移動する際の眼内レンズ2の姿勢を模式的に示す上面図である。図8では、使用者がプランジャー30をノズル本体10の先端側に押し込み、眼内レンズ2が図8(a)から図8(b)、(c)、(d)、(e)と順次移動していく。なお、図8では、見やすさのためノズル本体10を点線にて示し、眼内レンズ2およびプランジャー30を実線にて示す。 FIG. 8 is a top view schematically showing the posture of the intraocular lens 2 when the intraocular lens 2 moves in the nozzle body 10 by the operation of the plunger 30 in the present embodiment. In FIG. 8, the user pushes the plunger 30 toward the distal end side of the nozzle body 10, and the intraocular lens 2 is sequentially moved from FIG. 8A to FIG. 8B, FIG. 8C, FIG. Move. In FIG. 8, the nozzle body 10 is indicated by a dotted line, and the intraocular lens 2 and the plunger 30 are indicated by a solid line for ease of viewing.
 まず、使用者がプランジャー30を操作して、ステージ部12に載置されている眼内レンズ2をノズル本体10の先端側に移動させる。図8(a)に示すように、眼内レンズ2はプランジャー30に押され、レンズ本体2aの外縁がノズル本体10の内壁と接する。そして、眼内レンズ2がプランジャー30に押されてさらにノズル本体10の先端側に移動する際に、図8(b)に示すように、レンズ本体2aの外縁部がノズル本体10の貫通孔10cの断面形状に合わせてレンズ本体2aの中心(光軸)に向かって折り畳まれる。また、眼内レンズ2の2本の支持部2bのうちノズル本体10の先端側の支持部2bは、ノズル本体10の内壁に当接した後、レンズ本体2aが移動するとともにレンズ本体2aに折り重なる、いわゆるタッキングされた状態となる。 First, the user operates the plunger 30 to move the intraocular lens 2 placed on the stage unit 12 to the tip side of the nozzle body 10. As shown in FIG. 8A, the intraocular lens 2 is pushed by the plunger 30, and the outer edge of the lens body 2 a is in contact with the inner wall of the nozzle body 10. When the intraocular lens 2 is pushed by the plunger 30 and further moves to the tip side of the nozzle body 10, the outer edge portion of the lens body 2 a is the through hole of the nozzle body 10 as shown in FIG. The lens body 2a is folded toward the center (optical axis) according to the cross-sectional shape of 10c. Of the two support portions 2b of the intraocular lens 2, the support portion 2b on the distal end side of the nozzle body 10 abuts against the inner wall of the nozzle body 10, and then the lens body 2a moves and folds over the lens body 2a. In a so-called tucked state.
 そして、眼内レンズ2がプランジャー30に押されてノズル本体10の先端側に移動すると、タッキングされていた支持部2bが、スリット15bからノズル本体10の外側に押し出され、図8(c)に示すように折り曲げられない自然な状態に戻る。 Then, when the intraocular lens 2 is pushed by the plunger 30 and moves to the tip side of the nozzle body 10, the tacked support portion 2b is pushed out of the nozzle body 10 from the slit 15b, and FIG. It returns to the natural state where it cannot be bent as shown in FIG.
 図8(c)に示す状態から、使用者はプランジャー30を操作して眼内レンズ2をノズル本体10の前方向に移動する。このとき、図8(d)に示すように、眼内レンズ2のレンズ本体2aは、ノズル部15の開口15aまたはスリット15bを経由してノズル本体10の外側に徐々に押し出され、押し出された部分は、折り畳み状態から元の状態へと復元していく。 From the state shown in FIG. 8C, the user operates the plunger 30 to move the intraocular lens 2 in the forward direction of the nozzle body 10. At this time, as shown in FIG. 8 (d), the lens body 2a of the intraocular lens 2 was gradually pushed out through the opening 15a or slit 15b of the nozzle portion 15 to the outside of the nozzle body 10. The part is restored from the folded state to the original state.
 本実施形態では、眼内レンズ2の2本の支持部2bのうちノズル本体10の後端側の支持部2bのジャンクション部2cが、ノズル本体10内の上面視において中心軸AXから左方向に外れた位置を移動する。この場合、所定方向とは左方向を意味することになる。また、図7に示すように、ノズル本体10の正面視において、ノズル部15のスリット15bの幅方向の中心位置O、すなわち点線D2とD3とが交わる位置は、ノズル本体10の下方向に対して角度θだけ左方向に傾斜した方向に位置する。さらに、図8に示すように、ノズル本体10の上面視においては、ノズル部15のスリット15bは、中心軸AXから見て、ノズル本体10の後端側の支持部2bのジャンクション部2cと同様、左側に中心軸AXから外れて形成されている。 In the present embodiment, of the two support portions 2b of the intraocular lens 2, the junction portion 2c of the support portion 2b on the rear end side of the nozzle body 10 is leftward from the central axis AX in a top view inside the nozzle body 10. Move out of position. In this case, the predetermined direction means the left direction. Further, as shown in FIG. 7, the center position O in the width direction of the slit 15 b of the nozzle portion 15, that is, the position where the dotted lines D <b> 2 and D <b> 3 intersect, Is located in a direction inclined leftward by an angle θ. Further, as shown in FIG. 8, when the nozzle body 10 is viewed from the top, the slit 15b of the nozzle portion 15 is the same as the junction portion 2c of the support portion 2b on the rear end side of the nozzle body 10 when viewed from the central axis AX. The left side is deviated from the central axis AX.
 このため、本実施形態では、眼内レンズ2が、プランジャー30に押されて、ノズル本体10の後端側の支持部2bがノズル本体10の先端に移動すると、当該支持部2bのジャンクション部2cが、上面視においてスリット15bと重なり合う位置に移動する。そして、プランジャー30がノズル本体10の前方向に押し込まれるとともに、当該ジャンクション部2cは、スリット15bからノズル本体10の外側に押し出される。プランジャー30がさらにノズル本体10の前方向に押し込まれてノズル本体10の先端から突出した状態になると、図8(e)に示すように、眼内レンズ2は、ノズル本体10の後端側の支持部2bの一部がプランジャー30と係合した状態で、元の状態に復元する。 For this reason, in this embodiment, when the intraocular lens 2 is pushed by the plunger 30 and the support part 2b on the rear end side of the nozzle body 10 moves to the tip of the nozzle body 10, the junction part of the support part 2b 2c moves to a position overlapping the slit 15b when viewed from above. And while the plunger 30 is pushed in the front direction of the nozzle main body 10, the said junction part 2c is extruded to the outer side of the nozzle main body 10 from the slit 15b. When the plunger 30 is further pushed forward of the nozzle body 10 and protrudes from the tip of the nozzle body 10, the intraocular lens 2 is positioned on the rear end side of the nozzle body 10 as shown in FIG. In a state where a part of the support portion 2b is engaged with the plunger 30, the original state is restored.
 ここで、仮にスリット15bが、中心軸AXから見て、ノズル本体10の後端側の支持部2bのジャンクション部2cと異なる側(この場合は右側)に設けられている場合や、上記の説明で角度θが略0°となるように設けられている場合、ノズル本体10の後端側の支持部2bおよびジャンクション部2cが、スリット15bを通ってノズル本体10の外側に押し出されない可能性がある。図8に示すように、眼内レンズ2のノズル本体10の後端側の支持部2bは、ノズル本体10内では所定量湾曲した状態でプランジャー30先端の切欠部31cに支持されている。 Here, if the slit 15b is provided on the side (in this case, the right side) different from the junction part 2c of the support part 2b on the rear end side of the nozzle body 10 when viewed from the central axis AX, the above description is given. In the case where the angle θ is approximately 0 °, the support portion 2b and the junction portion 2c on the rear end side of the nozzle body 10 may not be pushed out of the nozzle body 10 through the slit 15b. There is. As shown in FIG. 8, the support portion 2 b on the rear end side of the nozzle body 10 of the intraocular lens 2 is supported by a notch portion 31 c at the distal end of the plunger 30 while being curved by a predetermined amount in the nozzle body 10.
 したがって、当該支持部2bは、ノズル本体10の外側に押し出されるまでは、弾性復元力により自然な状態に戻ろうとする。このため、当該支持部2bがスリット15bを通らずにノズル本体10の先端側に移動する場合、支持部2以外の部分がノズル本体10の外側に押し出される際に当該復元力が原因で眼内レンズ2が予期せぬ姿勢になる可能性がある。この結果、使用者は、挿入器具1を中心軸AX回りに回転させるなどして眼内レンズ2の姿勢を調整しなければならない。一方、本実施形態では、眼内レンズ2のノズル本体10の後端側の支持部2bが、スリット15bからノズル本体10の外側に押し出されることで、眼内レンズ2がノズル本体10から射出される際に不要な上記復元力が眼内レンズ2に作用することを抑制できる。その結果、眼内レンズ2の好適な姿勢を維持することができ、上記のような眼内レンズ2の姿勢の調整を行う手間を省くことができる。 Therefore, the support portion 2b tries to return to a natural state by the elastic restoring force until it is pushed out of the nozzle body 10. For this reason, when the support part 2b moves to the tip side of the nozzle body 10 without passing through the slit 15b, the restorative force causes the intraocular portion when the part other than the support part 2 is pushed outside the nozzle body 10. There is a possibility that the lens 2 takes an unexpected posture. As a result, the user must adjust the posture of the intraocular lens 2 by rotating the insertion instrument 1 around the central axis AX. On the other hand, in this embodiment, the support part 2b on the rear end side of the nozzle body 10 of the intraocular lens 2 is pushed out of the nozzle body 10 through the slit 15b, so that the intraocular lens 2 is emitted from the nozzle body 10. It is possible to suppress the above-described restoring force that is unnecessary when acting on the intraocular lens 2. As a result, a suitable posture of the intraocular lens 2 can be maintained, and the trouble of adjusting the posture of the intraocular lens 2 as described above can be saved.
 以上が本実施形態に関する説明であるが、上記の挿入部などの構成は、上記の実施形態に限定されるものではなく、本発明の技術的思想と同一性を失わない範囲内において種々の変更が可能である。例えば、上記の説明では、ノズル部15のスリット15bは略V字形状の切り込みとして形成されているが、スリット15bの形状はこれに限られず任意の形状を採用することができる。 The above is the description of the present embodiment, but the configuration of the insertion portion and the like is not limited to the above-described embodiment, and various modifications can be made within the scope that does not lose the technical idea of the present invention. Is possible. For example, in the above description, the slit 15b of the nozzle portion 15 is formed as a substantially V-shaped cut, but the shape of the slit 15b is not limited to this, and an arbitrary shape can be adopted.
 また、上記の説明では、ノズル本体10の上面視において、ノズル部15のスリット15bが、中心軸AXから見て、ノズル本体10の「後端側」の支持部2bのジャンクション部2cと同じ側に、中心軸AXから外れて形成されている構成とした。ただし、当該構成の代わりに、ノズル本体10の上面視において、ノズル部15のスリット15bが、中心軸AXから見て、ノズル本体10の「先端側」の支持部2bのジャンクション部2cと同じ側に、中心軸AXから外れて形成されている構成としてもよい。上記の通り、ノズル本体10の先端側の支持部2bは、ノズル本体10内でタッキングされた状態であるため、ノズル本体10内では、ノズル本体10の後端側の支持部2bと同様に、弾性復元力により自然な状態に戻ろうとしている。このため、支持部2以外の部分が射出される際に支持部2の復元力が原因で眼内レンズ2が予期せぬ姿勢になる可能性がある。したがって、ノズル本体10の先端側の支持部2bのジャンクション部2cから先にノズル本体10から射出されるようにスリット15bが形成されることで、眼内レンズ2がノズル本体10から射出される際に好適な姿勢を維持することができ、上記のような眼内レンズ2の姿勢の調整を行う手間を省くことができる。 In the above description, when the nozzle body 10 is viewed from the top, the slit 15b of the nozzle portion 15 is the same side as the junction portion 2c of the support portion 2b on the “rear end side” of the nozzle body 10 when viewed from the central axis AX. In addition, the configuration is formed so as to deviate from the central axis AX. However, instead of this configuration, when the nozzle body 10 is viewed from the top, the slit 15b of the nozzle portion 15 is the same side as the junction portion 2c of the support portion 2b of the “tip side” of the nozzle body 10 when viewed from the central axis AX. In addition, it may be configured to be formed away from the central axis AX. As described above, since the support portion 2b on the front end side of the nozzle body 10 is in a state of being tucked in the nozzle body 10, in the nozzle body 10, similarly to the support portion 2b on the rear end side of the nozzle body 10, It is trying to return to a natural state by elastic restoring force. For this reason, when parts other than the support part 2 are inject | emitted, the restoring force of the support part 2 may cause the intraocular lens 2 to be in an unexpected posture. Therefore, when the intraocular lens 2 is emitted from the nozzle body 10 by forming the slit 15b so as to be emitted from the nozzle body 10 first from the junction portion 2c of the support portion 2b on the distal end side of the nozzle body 10. Therefore, it is possible to save the trouble of adjusting the posture of the intraocular lens 2 as described above.
 さらに、ステージ部12にセットされた眼内レンズ2について、ノズル本体10の上面視において、ノズル本体10の先端側および後端側の支持部2bが、中心軸AXから見て同じ側に中心軸AXから外れている場合は、これら支持部2bと同じ側にスリット15bを形成することで、上記と同様に、眼内レンズ2がノズル本体10から射出される際に好適な姿勢を維持することができる。 Further, with respect to the intraocular lens 2 set on the stage unit 12, when the nozzle body 10 is viewed from above, the support portions 2 b on the front end side and the rear end side of the nozzle body 10 are centered on the same side as viewed from the center axis AX. When it is off the AX, the slit 15b is formed on the same side as the support portion 2b, so that a suitable posture is maintained when the intraocular lens 2 is ejected from the nozzle body 10 as described above. Can do.
 以下に上記の実施形態の変形例を示す。なお、以下の説明において各構成要素は、上記の実施形態における構成要素に対応するものについては、同一の符号を付し、特に言及しない限りその説明を省略する。 The following is a modification of the above embodiment. In the following description, components corresponding to the components in the above-described embodiment are denoted by the same reference numerals, and the description thereof is omitted unless otherwise specified.
 図9に、上記の実施形態における眼内レンズの挿入器具1の変形例を示す。また、図10に、本変形例の挿入器具100のプランジャー300を示す。なお、図10(c)、10(d)は、プランジャー300を挿入器具100の前側あるいは後側から見たときのプランジャー300と挿通部32との関係を示す図である。図10(c)、(d)に示すように、本変形例の挿入器具100において、プランジャー300の押圧板部330は、プランジャー300を挿入器具100の前側あるいは後側から見たときに略正六角形となるように形成されている。なお、押圧板部330の形状は、使用者にとってのプランジャー300の操作感を損なわない範囲で自由な形状とすることができる。したがって、挿入器具100のデザイン性などを考慮して、押圧板部330の形状は円形、正方形、その他の多角形など、適宜選択することができる。 FIG. 9 shows a modification of the intraocular lens insertion device 1 in the above embodiment. FIG. 10 shows the plunger 300 of the insertion instrument 100 of this modification. 10C and 10D are views showing the relationship between the plunger 300 and the insertion portion 32 when the plunger 300 is viewed from the front side or the rear side of the insertion instrument 100. FIG. As shown in FIGS. 10 (c) and 10 (d), in the insertion instrument 100 of this modification, the pressing plate portion 330 of the plunger 300 is viewed when the plunger 300 is viewed from the front side or the rear side of the insertion instrument 100. It is formed to be a substantially regular hexagon. In addition, the shape of the press plate part 330 can be made into a free shape as long as the operation feeling of the plunger 300 for the user is not impaired. Therefore, in consideration of the design of the insertion instrument 100, the shape of the pressing plate portion 330 can be selected as appropriate, such as a circle, a square, and other polygons.
 図11に、本変形例の挿入器具100を挿入器具100の前側から見たときの正面図を模式的に示す。なお、図11では、見やすさのため、挿入器具100の各部間の大きさの比率は実際の挿入器具とは異なっている。図11に示すように、ホールド部11は使用者が指を掛けやすいように、上下方向にいわゆる「つば」が延びた形状になっており、つばの四隅には5°~15°程度の角度で面取りが施されている。これにより、ホールド部11は正面視において縦長の八角形形状になっている。さらに、図11にも示すように、押圧板部330は略正六角形の形状になっている。 FIG. 11 schematically shows a front view of the insertion instrument 100 of this modification as viewed from the front side of the insertion instrument 100. In FIG. 11, for ease of viewing, the size ratio between the parts of the insertion instrument 100 is different from that of the actual insertion instrument. As shown in FIG. 11, the hold unit 11 has a shape in which so-called “brims” extend in the vertical direction so that the user can easily put his / her finger on the corner, and the four corners of the brim have an angle of about 5 ° to 15 °. Chamfered. Thereby, the hold part 11 has a vertically long octagonal shape in a front view. Furthermore, as shown in FIG. 11, the pressing plate portion 330 has a substantially regular hexagonal shape.
1  挿入器具
2  眼内レンズ
2a  レンズ本体
2b  支持部
2c  ジャンクション部
10  ノズル本体
15  ノズル部
15a  ノズル部の開口
15b  ノズル部のスリット
30  プランジャー
DESCRIPTION OF SYMBOLS 1 Insertion tool 2 Intraocular lens 2a Lens main body 2b Support part 2c Junction part 10 Nozzle main body 15 Nozzle part 15a Nozzle part opening 15b Nozzle part slit 30 Plunger

Claims (3)

  1.  レンズ本体と前記レンズ本体に一端が接続部を介して接続されている支持部とを有する眼内レンズが移動する挿入筒部を先端に有する器具本体と、
     前記眼内レンズを収納する収納部と
    を備える眼内レンズの挿入器具であって、
     前記挿入筒部の先端の開口から後端に向かって前記挿入筒部の長手方向に延伸するスリットが設けられており、
     前記眼内レンズが前記収納部に収納された状態での前記挿入器具の本体の該眼内レンズの光軸方向からの投影視において、少なくとも1つの前記支持部の接続部は、前記器具本体の中心軸に対して所定方向に外れて配されており、
     前記器具本体の正面視において、前記スリットの幅方向の中心位置が、前記器具本体の中心軸から見て、前記器具本体にある前記眼内レンズの光軸の後側方向に対して、前記収納部に収納された前記眼内レンズの前記少なくとも1つの支持部の接続部と同じ方向に所定角度傾斜して配置されている
    眼内レンズの挿入器具。
    An instrument main body having an insertion tube part at the tip of which an intraocular lens moves, the lens main body and a support part having one end connected to the lens main body via a connection part;
    An intraocular lens insertion device comprising a storage unit for storing the intraocular lens,
    A slit extending in the longitudinal direction of the insertion cylinder part from the opening at the front end of the insertion cylinder part toward the rear end is provided,
    In a projection view from the optical axis direction of the intraocular lens of the body of the insertion instrument in a state where the intraocular lens is housed in the housing part, at least one connecting part of the support part is provided on the body of the instrument. Disposed in a predetermined direction with respect to the central axis,
    In the front view of the instrument main body, the center position in the width direction of the slit is stored in the rear direction of the optical axis of the intraocular lens in the instrument main body when viewed from the central axis of the instrument main body. An intraocular lens insertion device disposed at a predetermined angle in the same direction as the connection portion of the at least one support portion of the intraocular lens housed in a portion.
  2.  前記所定角度は約30°である請求項1に記載の眼内レンズの挿入器具。 The intraocular lens insertion device according to claim 1, wherein the predetermined angle is about 30 °.
  3.  前記挿入器具の流通前に、前記収納部に前記眼内レンズが収納されている
    ことを特徴とする請求項1または請求項2に記載の眼内レンズの挿入器具。
    The intraocular lens insertion device according to claim 1 or 2, wherein the intraocular lens is housed in the housing portion before the insertion device is distributed.
PCT/JP2015/071686 2014-07-30 2015-07-30 Intraocular lens insertion instrument WO2016017772A1 (en)

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Citations (10)

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JPS63197453A (en) * 1986-11-07 1988-08-16 ザ・クーパー・カンパニー・インク Instrument and method for inserting compressive intraocular lens
US5123905A (en) * 1991-06-07 1992-06-23 Kelman Charles D Intraocular lens injector
JPH05103808A (en) * 1991-06-13 1993-04-27 Canon Star Kk Transplantation device of intraocular lens
JP2001502563A (en) * 1996-09-26 2001-02-27 ボシュ アンド ロム サージカル,インコーポレイテッド Method and apparatus for inserting a flexible membrane into the eye
JP2003513750A (en) * 1999-10-29 2003-04-15 アラーガン・セイルズ・インコーポレイテッド Rotatable IOL insertion device and method of using the same
WO2005070341A1 (en) * 2004-01-27 2005-08-04 Hoya Corporation Intraocular lens inserting device and cartridge thereof
JP2007503872A (en) * 2003-08-28 2007-03-01 ボシュ・アンド・ロム・インコーポレイテッド Preloaded IOL injector
US20110144654A1 (en) * 2006-09-22 2011-06-16 Lenstec, Inc. System and Method for Storing, Shipping and Injecting Ocular Devices
JP2013013457A (en) * 2011-06-30 2013-01-24 Nidek Co Ltd Intraocular lens insertion instrument
JP2014100558A (en) * 2012-10-26 2014-06-05 Santen Pharmaceut Co Ltd Intraocular lens injector

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63197453A (en) * 1986-11-07 1988-08-16 ザ・クーパー・カンパニー・インク Instrument and method for inserting compressive intraocular lens
US5123905A (en) * 1991-06-07 1992-06-23 Kelman Charles D Intraocular lens injector
JPH05103808A (en) * 1991-06-13 1993-04-27 Canon Star Kk Transplantation device of intraocular lens
JP2001502563A (en) * 1996-09-26 2001-02-27 ボシュ アンド ロム サージカル,インコーポレイテッド Method and apparatus for inserting a flexible membrane into the eye
JP2003513750A (en) * 1999-10-29 2003-04-15 アラーガン・セイルズ・インコーポレイテッド Rotatable IOL insertion device and method of using the same
JP2007503872A (en) * 2003-08-28 2007-03-01 ボシュ・アンド・ロム・インコーポレイテッド Preloaded IOL injector
WO2005070341A1 (en) * 2004-01-27 2005-08-04 Hoya Corporation Intraocular lens inserting device and cartridge thereof
US20110144654A1 (en) * 2006-09-22 2011-06-16 Lenstec, Inc. System and Method for Storing, Shipping and Injecting Ocular Devices
JP2013013457A (en) * 2011-06-30 2013-01-24 Nidek Co Ltd Intraocular lens insertion instrument
JP2014100558A (en) * 2012-10-26 2014-06-05 Santen Pharmaceut Co Ltd Intraocular lens injector

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