WO2014162428A1 - Indwelling anchor device - Google Patents

Indwelling anchor device Download PDF

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Publication number
WO2014162428A1
WO2014162428A1 PCT/JP2013/059893 JP2013059893W WO2014162428A1 WO 2014162428 A1 WO2014162428 A1 WO 2014162428A1 JP 2013059893 W JP2013059893 W JP 2013059893W WO 2014162428 A1 WO2014162428 A1 WO 2014162428A1
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WO
WIPO (PCT)
Prior art keywords
anchor
hole
indwelling
elongated body
implant
Prior art date
Application number
PCT/JP2013/059893
Other languages
French (fr)
Japanese (ja)
Inventor
政克 川浦
有浦 茂樹
奈央 横井
Original Assignee
テルモ株式会社
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 テルモ株式会社 filed Critical テルモ株式会社
Priority to PCT/JP2013/059893 priority Critical patent/WO2014162428A1/en
Publication of WO2014162428A1 publication Critical patent/WO2014162428A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/0401Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/0467Instruments for cutting sutures
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/0487Suture clamps, clips or locks, e.g. for replacing suture knots; Instruments for applying or removing suture clamps, clips or locks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/06Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
    • A61B17/06066Needles, e.g. needle tip configurations
    • A61B17/06109Big needles, either gripped by hand or connectable to a handle
    • 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
    • A61F2/0004Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse
    • A61F2/0031Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra
    • A61F2/0036Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra implantable
    • A61F2/0045Support slings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B2017/00743Type of operation; Specification of treatment sites
    • A61B2017/00818Treatment of the gastro-intestinal system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/0401Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
    • A61B2017/0409Instruments for applying suture anchors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/0401Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
    • A61B2017/0464Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors for soft tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/0487Suture clamps, clips or locks, e.g. for replacing suture knots; Instruments for applying or removing suture clamps, clips or locks
    • A61B2017/0488Instruments for applying suture clamps, clips or locks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
    • A61B17/06Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
    • A61B17/06066Needles, e.g. needle tip configurations
    • A61B2017/0608J-shaped

Definitions

  • the present invention relates to an anchor indwelling device.
  • Urinary incontinence particularly stress urinary incontinence, urine leakage occurs due to abdominal pressure applied during normal exercise, laughing, coughing, sneezing, etc.
  • the cause of this is, for example, that the pelvic floor muscle, which is a muscle that supports the urethra, is loosened due to childbirth and the like.
  • Surgical therapy is effective for the treatment of urinary incontinence.
  • a band-like tissue-supporting indwelling material called a “sling”
  • the sling is placed in the body, and the sling supports the urethra (for example, Patent Document 1).
  • the operator incises the vagina 920 with a scalpel, peels off the space between the urethra 910 and the vagina 920, and uses the puncture needle or the like to remove the peeled portion and the outside. Are communicated with each other through a closing hole. Then, the sling is placed in the puncture hole formed by the puncture needle.
  • a sling what is called a “mini sling” in which a pair of anchors 810 and 820 are provided at both ends of a belt-like main body is known (see, for example, Patent Document 2).
  • one anchor 810 is inserted from the incised site to close one closing hole 931 of the pelvis 930, and the large opening of the closing hole 931 occurs from the edge of the closing hole 931.
  • the film is hooked and fixed to the closing membrane 933 by penetrating through a closing membrane (ligament tissue) 933 which is a ligamentous thin film that closes the portion.
  • the other anchor 820 is inserted from the incised portion and penetrated through the closing membrane 934 that closes the other closing hole 932, thereby being hooked and fixed to the closing membrane 934 to obtain the state shown in FIG.
  • an appropriate tension is applied to the urethra by adjusting the length of the sling between the pair of anchors 810 and 820.
  • the incision is sutured.
  • the placement of the sling 800 is completed. According to such a technique, since the portion to be punctured is shortened, there is an advantage that the burden on the patient is reduced.
  • An object of the present invention is to provide an anchor indwelling device that can indwell an anchor in a living body so that its effect is maintained over time.
  • An anchor indwelling device for fixing a living tissue supporting indwelling object used for pelvic treatment in a living body A long body, An anchor portion removably provided at the distal end of the elongated body, The anchor portion has a guide portion into which the living tissue supporting indwelling material is inserted, and is fixed to a part of the living tissue supporting indwelling material inserted into the guide portion. Ingredients.
  • the biological tissue supporting indwelling object is disposed inside the body so that at least one end is exposed outside the body, The one end of the biological tissue support indwelling object is inserted into the guide part, and the guide part is inserted into the body along the biological support indwelling object, and is fixed to the biological tissue support indwelling object in the body.
  • the anchor indwelling device according to claim 1.
  • the cylindrical elongated body having a first through hole on the inner side, and the anchor portion including the second through hole in which the guide portion communicates with the first through hole,
  • a second instrument comprising a fixing part for fixing the anchor part to the biological tissue supporting indwelling object,
  • the anchor portion is configured to be detached from the elongated body when the elongated body is moved to the proximal end side in a state where the anchor portion is fixed to the biological tissue supporting indwelling object ( The anchor indwelling device according to any one of 1) to (3).
  • the first instrument further includes an operation unit capable of switching between a restricted state for restricting detachment of the anchor portion from the long body and an allowable state for allowing detachment from the long body.
  • the anchor portion has a proximal end portion that is inserted into the first through hole and engages with a distal end portion of the elongated body, When the elongated body is moved to the proximal end side in a state where the anchor portion is fixed to the living tissue supporting indwelling object, the distal end portion of the elongated body is elastically deformed and the engagement is released.
  • the anchor portion is configured to be detached from the elongated body
  • the operation portion has a cylindrical shape and is provided on the outer periphery of the elongated body so as to be slidable. In the restricted state, the operation portion suppresses the deformation by covering a distal end portion of the elongated body, and allows the tolerance.
  • the anchor indwelling device according to (5) wherein the distal end portion of the elongated body is exposed and the deformation is allowed.
  • the first instrument further includes a guiding portion that guides the biological tissue supporting indwelling material to the first through hole through the second through hole.
  • the anchor indwelling device according to any one of the above.
  • the guiding portion is inserted into the first through hole and the second through hole so that the distal end portion and the proximal end portion are exposed from the first instrument, and the living tissue supporting indwelling is placed in the distal end portion.
  • the second instrument may further include a long insertion portion that is inserted into the first through-hole and the fixing portion is detachably provided at a distal end portion thereof.
  • the anchor indwelling device according to any one of 11).
  • Anchor detainer
  • the insertion portion has a third through hole through which the biological tissue supporting indwelling object is inserted.
  • an anchor portion can be fixed to the sling after the sling (living tissue supporting indwelling object) is placed in the living body. Therefore, for example, in the case of the treatment of urinary incontinence described above, the anchor portion can be disposed on the closing membrane without penetrating the closing membrane. As a result, it is possible to maintain the tension applied to the urethra over time without the anchors coming off or loosening from the closure membrane.
  • FIG. 1 is a side view showing a preferred embodiment of the anchor indwelling device of the present invention.
  • FIG. 2 is a cross-sectional view of a shaft included in the anchor placement device shown in FIG. 3 (a) and 3 (b) are cross-sectional views for explaining the movement of the operation portion of the shaft shown in FIG. 4 is a cross-sectional view of an insertion tool provided in the anchor placement device shown in FIG.
  • FIG. 5 is a cross-sectional view showing a distal end portion of the insertion tool shown in FIG.
  • FIGS. 6A and 6B are side views for explaining the movement of the cutting portion of the insertion tool shown in FIG.
  • FIG. 7 is a diagram illustrating an example of an implant.
  • FIG. 8 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 9 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 10 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 11 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 12 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 13 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 14 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 15 is a view for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 16 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 17 is a view for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 18 is a view for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • FIG. 19 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1.
  • 20 is a view showing a modification of the anchor indwelling device shown in FIG. 1, in which (a) is a side view and (b) is a cross-sectional view taken along the line AA in (a).
  • FIG. 21 is a side view showing an example of an implant cutting tool.
  • 22 (a) and 22 (b) are side views for explaining the movement of the cutting portion of the implant cutting tool shown in FIG.
  • FIG. 23 is a view for explaining an operation procedure of the implant cutting tool shown in FIG.
  • FIG. 24 is a view for explaining an operation procedure of the implant cutting tool shown in FIG.
  • FIG. 25 is a view for explaining an operation procedure of the implant cutting tool shown in FIG.
  • FIG. 26 is a side view showing a modified example of the implant cutting tool shown in FIG.
  • FIG. 27 is a view for explaining an operation procedure of the implant cutting tool shown in FIG.
  • FIG. 28 is a side view showing another modification of the implant cutting tool shown in FIG.
  • FIG. 29 is a diagram for explaining the prior art.
  • FIG. 1 is a side view showing a preferred embodiment of the anchor indwelling device of the present invention.
  • FIG. 2 is a cross-sectional view of a shaft included in the anchor placement device shown in FIG. 3 (a) and 3 (b) are cross-sectional views for explaining the movement of the operation portion of the shaft shown in FIG. 4 is a cross-sectional view of an insertion tool provided in the anchor placement device shown in FIG.
  • FIG. 5 is a cross-sectional view showing a distal end portion of the insertion tool shown in FIG.
  • FIGS. 6A and 6B are side views for explaining the movement of the cutting portion of the insertion tool shown in FIG.
  • FIG. 7 is a diagram illustrating an example of an implant.
  • FIG. 8 to 19 are diagrams for explaining the operation procedure of the anchor indwelling device shown in FIG. 20 is a view showing a modification of the anchor indwelling device shown in FIG. 1, in which (a) is a side view and (b) is a cross-sectional view taken along the line AA in (a).
  • the right side in FIG. 1 is referred to as “tip” and the left side is referred to as “base end”.
  • Anchor Indwelling Device 1 shown in FIG. 1 is an apparatus used when, for example, an urinary incontinence treatment for women, that is, an implant (living tissue supporting indwelling material) 9 for urinary incontinence treatment is embedded in a living body. It is.
  • the anchor detainer 1 includes a tubular shaft (first instrument) 2 and an insertion instrument (second instrument) 3 inserted into the shaft 2.
  • first instrument tubular shaft
  • second instrument insertion instrument
  • the shaft 2 includes an elongated body 21, an anchor portion 22 held at the distal end of the elongated body 21, and the anchor portion 22 being detached from the elongated body 21. It has the operation part 23 made into a possible state, the maintenance part 24 which maintains the state of the operation part 23, and the string body (guidance
  • the long body 21 has a cylindrical shape, and has a through hole (first through hole) 211 penetrating both ends. Further, a concave portion 212 that engages with the anchor portion 22 is formed on the inner peripheral surface of the distal end portion of the long body 21. The distal end portion of the long body 21 is configured to be elastically deformed and expanded in diameter by a predetermined stress, and the engagement between the long body 21 and the anchor portion 22 is released by expanding the diameter of the distal end portion. It has come to be. Further, a flange 213 protruding from the outer peripheral surface is formed at the proximal end portion of the long body 21. The flange 213 has a function of preventing the maintenance unit 24 from being detached from the long body 21.
  • the length of the long body 21 is not particularly limited, and varies depending on the treatment to be used, but is preferably about 1 to 10 cm, for example. Thereby, it becomes a size suitable for using especially when the implant for treatment of urinary incontinence is embedded in the living body.
  • the anchor portion 22 is attached to the distal end portion of the long body 21.
  • the anchor portion 22 includes a main body 221 that protrudes toward the distal end side of the long body 21, and a base end portion 222 that is provided on the base end side of the main body 221 and inserted into the through hole 211 of the long body 21.
  • the front end of the main body 221 is rounded, for example, hemispherical or semi-long. Thereby, the resistance at the time of inserting the shaft 2 in a living body can be reduced.
  • the base end portion of the main body 221 has a diameter larger than the outer periphery of the long body 21, and protrudes outward from the outer peripheral surface of the long body 21.
  • a convex portion 223 is formed on the outer periphery of the base end portion 222, and the convex portion 223 engages with the concave portion 212 of the long body 21.
  • the anchor part 22 is hold
  • the anchor portion 22 is formed with a guide portion constituted by a through hole (second through hole) 224 along the axis of the shaft 2, and the through hole 224 is a through hole at the proximal end side opening. 211 communicates.
  • the base end part of the through-hole 224 is comprised by the taper part 224a which a diameter increases gradually toward base end opening.
  • An operation unit 23 is arranged on the outer periphery of the long body 21.
  • the operation unit 23 has a cylindrical shape, and is provided so as to be slidable in the axial direction with respect to the long body 21.
  • the operation portion 23 is located on the distal end side and abuts on the anchor portion 22, and as shown in FIG. 3A, the operation portion 23 covers the distal end portion of the long body 21, and the proximal portion is located on the flange 213. As shown in FIG. 3 (b), it is possible to move to an allowable state in which the tip of the long body 21 is exposed.
  • the distal end portion of the long body 21 is covered with the operation unit 23, and therefore elastic deformation (expansion) of the distal end portion of the long body 21 is prevented. Therefore, detachment of the anchor portion 22 from the long body 21 is prevented in the restricted state.
  • the distal end portion of the long body 21 is not covered with the operation unit 23, so that the distal end portion of the long body 21 can be elastically deformed (expanded), and the anchor portion 22 can be Can be disengaged from.
  • the operation part 23 is comprised so hard that the elastic deformation of the front-end
  • the structure of the operation part 23 will not be specifically limited if the state which prevents the elastic deformation
  • a maintenance unit 24 is provided on the outer periphery of the long body 21 and between the flange 213 and the operation unit 23.
  • the maintenance part 24 is comprised by the C-shaped clip, for example, and is detachable with respect to the elongate body 21.
  • the maintenance unit 24 has a function of maintaining the operation unit 23 in a restricted state. That is, when the maintenance unit 24 is attached to the long body 21, the operation unit 23 is maintained in a restricted state, and when the maintenance unit 24 is detached from the long body 21, the operation unit 23 moves to an allowable state. It becomes possible.
  • the configuration of the maintenance unit 24 is not particularly limited as long as the operation unit 23 can be selected between a state in which the operation unit 23 is maintained in a restricted state and a state in which the operation unit 23 can move to an allowable state.
  • the string body 25 is inserted through the through holes 211 and 224.
  • the string body 25 has a distal end projecting from the distal end side opening of the through hole 224 and a proximal end projecting from the proximal end side opening of the through hole 211.
  • a holding portion 251 that holds the implant 9 is provided at the distal end portion of the string body 25.
  • the holding part 251 is configured by a ring (loop) 251 formed by the string body 25.
  • Such a string body 25 is used to guide the implant 9 into the through hole 211 as described later.
  • the configuration of the shaft 2 has been described above. It does not specifically limit as a constituent material of the elongate body 21, the anchor part 22, the operation part 23, and the maintenance part 24, For example, various resin materials and various metal materials can be used. Moreover, it does not specifically limit as a constituent material of the string 25, For example, various resin materials, fibers, etc. which have biocompatibility like a polypropylene etc. can be used.
  • the insertion tool 3 includes an insertion portion 31 having a straight rod shape, a fixing portion 32 attached to the distal end portion of the insertion portion 31, and a cylinder provided on the outer periphery of the insertion portion 31. And a cut portion 33 having a shape.
  • the insertion portion 31 has a through-hole (third through-hole) 311 that penetrates the opposite part of the outer peripheral surface.
  • the through-hole 311 extends while being inclined with respect to the axis of the insertion portion 31, and one opening 311 a and the other opening 311 b are arranged so as to be shifted in the axial direction of the insertion portion 31.
  • the implant 9 is inserted into the through hole 311 from the opening 311a located on the distal end side to the opening 311b located on the proximal end side.
  • the length of the insertion portion 31 is not particularly limited, but is preferably longer than the long body 21.
  • the fixing part 32 is provided detachably from the insertion part 31.
  • the fixing portion 32 is fixed to the anchor portion 22 during use of the anchor placement device 1, and thereby the anchor portion 22 can be fixed to the implant 9 as described later.
  • a method for fixing the fixing portion 32 to the anchor portion 22 is not particularly limited. For example, screwing, fitting, adhesion, or the like can be used. In this embodiment, as shown in FIG. 32 is pressed into the through hole 224 from the base end side to be fixed to the anchor portion 22.
  • the fixed portion 32 has a substantially conical shape as a whole, the outer diameter R1 of the distal end thereof is smaller than the inner diameter r1 of the through hole 224, and the outer diameter R2 on the proximal end side is the inner diameter of the proximal end opening of the through hole 224. It is configured to be larger than r2. By setting it as such a shape, the fixing
  • a convex portion is formed on one of the tapered portions 224a and 321 and a concave portion that engages with the convex portion is formed on the other side.
  • the fixing portion 32 may be press-fitted into the through hole 224 and the concave portion and the convex portion may be engaged.
  • a cylindrical cutting portion 33 is disposed on the outer periphery of the insertion portion 31.
  • the insertion part 31 is inserted inside the cutting part 33.
  • the cutting part 33 is provided so as to be slidable in the axial direction with respect to the insertion part 31.
  • an opening 331 is provided at the tip of the cutting part 33, and a blade part 332 is provided in the opening 331.
  • a flange 333 that protrudes to the outer periphery is provided at the base end portion of the cutting portion 33.
  • the cutting part 33 can move from the first state shown in FIG. 6A to the second state shown in FIG. 6B moved to the proximal end side.
  • the opening 311a is located on the tip side with respect to the cutting part 33, and the opening 311b is located in the opening 331. Therefore, both the openings 311a and 311b are exposed from the cutting part 33, and the blade part 332 Is located on the tip side of the opening 311b.
  • the blade portion 332 moves so as to straddle the opening 311 b, 9 is cut.
  • the configuration of the insertion tool 3 has been described above. It does not specifically limit as a constituent material of the insertion part 31, the fixing
  • the implant 9 shown in FIG. 7 is an implantable device for the treatment of female urinary incontinence, that is, a device that supports the urethra, for example, when the urethra is about to move toward the vaginal wall, It is the instrument supported in the direction (ventral side) which leaves
  • this implant 9 for example, a long object having flexibility can be used.
  • the implant 9 has a net shape, and the entire shape thereof has a band shape.
  • the implant 9 is called a “sling”.
  • the implant 9 can be constituted by, for example, a braided body in which a linear body is crossed and knitted in a net shape (lattice shape), that is, a net-like braided body.
  • the linear body include a circular cross-sectional shape, a flat cross-sectional shape, that is, a belt-like (ribbon-like) shape, and the like.
  • One end of the thread 91 is fixed to one end of the implant 9, and one end of the thread 92 is fixed to the other end.
  • the constituent material of the implant 9 is not particularly limited, and various resin materials, fibers, and the like having biocompatibility such as polypropylene can be used. Further, the constituent materials of the yarns 91 and 92 are not particularly limited, and various biomaterials such as polypropylene, fibers, and the like can be used, for example.
  • the implant 9 is not limited to the net-like one as long as the same effect can be exhibited.
  • the vagina 920 is incised with a scalpel, the puncture needle 7 is punctured from the incision portion 921, and is extracted from one buttocks to the body surface S through one closing hole 931 of the pelvis 930. To do.
  • the puncture needle 7 holds the thread 91 of the implant 9, whereby the thread 91 is exposed to the body surface S from the buttocks.
  • the puncture needle 7 is punctured from the incision 921, and is extracted from the other buttocks to the body surface S via the other closing hole 932.
  • the puncture needle 7 holds the thread 92 of the implant 9, whereby the thread 92 is exposed to the body surface S from the buttocks.
  • the threads 91 and 92 are pulled, and the implant 9 is placed between the urethra 910 and the vagina 920 as shown in FIG.
  • the shaft 2 is prepared, and the thread 91 is inserted through the ring 251 of the string body 25.
  • yarn 91 (A part of the implant 9 may be contained in the string body 25. It is the same below.) Is hold
  • the string body 25 is pulled to the proximal end side, the thread 91 is guided into the through hole 211 through the through hole 224, and further guided to the outside from the proximal end opening of the through hole 211. To do.
  • the shaft 2 is inserted into the living body along the thread 91 and the implant 9, and the anchor portion 22 is brought into contact with the closing membrane 933 as shown in FIGS. .
  • the thread 91 is inserted into the through hole 311 from the opening 311a and pulled out from the opening 311b.
  • the insertion tool 3 is inserted into the shaft 2 from the proximal end side in a state where the thread 91 is tensioned, and the fixing portion 32 is pressed against the anchor portion 22 as shown in FIG.
  • the fixing portion 32 is press-fitted into the through hole 224, and the fixing portion 32 is fixed to the anchor portion 22 in a state where the fixing portion 32 and the anchor portion 22 sandwich the implant 9. As a result, the anchor portion 22 is fixed to the implant 9.
  • the cutting unit 33 is changed from the first state to the second state by hooking a finger on the flange 333 of the cutting unit 33 and sliding the cutting unit 33 toward the proximal end side with respect to the insertion unit 31. As shown in FIG. 4, the tip portion is cut from the opening 311b of the implant 9. Thereby, the excess implant 9 is removed.
  • the insertion tool 3 is pulled out from the shaft 2.
  • the maintenance unit 24 is removed from the long body 21, and the operation unit 23 is slid toward the proximal side with respect to the long body 21 to be in an allowable state.
  • the shaft 2 is pulled out from the living body (that is, the long body 21 is moved to the proximal end side).
  • the distal end portion of the long body 21 is elastically deformed (expanded diameter), and the anchor portion 22 is detached from the long body 21, so that the anchor portion 22 abuts against the closing film 933 as shown in FIG. Indwelling in the living body.
  • the anchor part 22 is placed using the anchor placing tool 1 so as to contact the closing film 934 covering the closing hole 932.
  • the anchor portion 22 is placed in a state where the thread 92 is pulled with a predetermined force and a predetermined tension is applied to the urethra 910.
  • a predetermined procedure such as suturing is performed on the incision 921 to complete the procedure.
  • the anchor portion 22 can be inserted from the left and right buttocks and fixed to the implant 9. Therefore, the anchor part 22 does not penetrate the closing films 933 and 934 with which the anchor part 22 abuts (engages). Therefore, a large gap is not formed in the closing membranes 933 and 934 as in the prior art, and the anchor portion 22 can be reliably engaged with the closing membranes 933 and 934. As a result, the state in which a predetermined tension is applied to the urethra by the implant 9 can be reliably maintained for a long time.
  • the two anchors are placed after the yarns 91 and 92 are both exposed from the buttocks to the body surface S.
  • the present invention is not limited to this.
  • the anchor portion 22 is placed so as to contact the closing membrane 933, and then the thread 92 is exposed to the body surface S from the starboard portion so as to contact the closing membrane 934.
  • the anchor part 22 may be placed.
  • the vagina 920 is incised and the implant 9 is disposed between the urethra 910 and the vagina 920 from the incision portion 921, but the arrangement method of the implant 9 is not limited thereto.
  • a puncture member having a puncture needle 71 curved on an arc may be used.
  • a through-hole 940 is formed in the living body by protruding from the other buttocks.
  • the implant 9 is held at the tip of the puncture needle 71, and the puncture needle 71 is rotated in reverse.
  • the needle tip of the puncture needle 71 enters the body from the left groin portion of the patient, passes through the obstruction hole 931, the urethra 910 and the vagina 920, and the obstruction hole 932 in order, and then exits from the right inguinal portion to the outside of the body.
  • the puncture needle 71 is removed from the body.
  • the thread 92 is pulled to insert the implant 9 into the through hole 940. Thereby, as shown in FIG. 19, installation of the implant 9 is completed.
  • the implant 9 when the implant 9 is indwelled, it can be handled only by a minimally invasive technique such as puncture of the puncture needle 71, and it is not necessary to perform a large invasive incision or the like.
  • the patient safety is also high.
  • the anchor placement device 1 has been described above.
  • the through hole 211 is formed in the long body 21 and the through hole 224 is formed in the anchor portion 22.
  • the configuration of the long body 21 and the anchor portion 22 is not limited thereto.
  • the elongated body 21 may be provided with a groove 211 a and the anchor portion 22 may be provided with a groove 225.
  • the openings of the grooves 211a and 225 communicate with each other.
  • the operation unit 23 is provided with a slit 239 at a position corresponding to the opening of the groove 211a so that the opening of the groove 211a is exposed to the outside.
  • the implant 9 (thread 91) can be introduced into the grooves 211a and 225 through the openings of the grooves 211a and 225, the introduction of the implant 9 is facilitated. Moreover, since it is not necessary to use the string body 25 to introduce the implant 9, the operation is facilitated.
  • the opening of the groove 211a is made narrower than the internal space, and the hooking portion 214 for hooking the thread 91 is provided, thereby preventing the thread 91 introduced into the groove 211a from being detached. Thus, the movement of the shaft 2 along the yarn 91 can be performed smoothly.
  • FIG. 21 is a side view showing an example of an implant cutting tool.
  • 22 (a) and 22 (b) are side views for explaining the movement of the cutting portion of the implant cutting tool shown in FIG.
  • FIG. 22 is a side view for explaining the movement of the cutting part of the implant cutting part shown in FIG. 23 to 25 are diagrams for explaining the operation procedure of the implant cutting tool shown in FIG.
  • FIG. 26 is a side view showing a modified example of the implant cutting tool shown in FIG.
  • FIG. 27 is a view for explaining an operation procedure of the implant cutting tool shown in FIG.
  • FIG. 28 is a side view showing another modification of the implant cutting tool shown in FIG.
  • the right side in FIG. 21 is referred to as “tip”, and the left side is referred to as “base end”.
  • the implant cutting tool 4 is an instrument used for cutting the implant 9 in vivo. As shown in FIG. 21, the implant cutting tool 4 has a long main body 41 having a through-hole 411 and a cutting portion 42 that is formed in a cylindrical shape and is slidably provided on the outer periphery of the main body 41. Yes.
  • the tip of the main body 41 is rounded. Further, the opening 411 a on the distal end side of the through hole 411 is located at the distal end of the main body 41, and the opening 411 b on the proximal end side is located on the side surface of the main body 41.
  • the implant 9 is inserted into the through hole 411.
  • the length of the through hole 411 is not particularly limited, but is preferably about 1 to 3 cm.
  • An opening 421 is provided at the tip of the cutting part 42, and a blade part 422 is provided in the opening 421. Further, a flange 423 that protrudes to the outer periphery is provided at the proximal end portion of the cutting portion 42.
  • the cutting part 42 can move from the first state shown in FIG. 22A to the second state shown in FIG. 22B moved to the base end side. In the first state, the opening 411b of the through hole 411 is exposed from the cutting part 42, and the blade part 422 is located on the tip side of the opening 411b. Therefore, when the cutting portion 42 is changed from the first state to the second state in a state where the implant 9 is inserted through the through-hole 411, the portion of the implant 9 drawn out from the opening 411b can be cut.
  • Such an implant cutting tool 4 is used as follows. First, as shown in FIG. 23, the implant 9 is placed in the living body. The method for arranging the implant is the same as that described above. Next, after the cut portion is set to the first state, the thread 91 is inserted into the through hole 411 from the opening 411a of the through hole 411 and pulled out from the opening 411b. Next, the thread 91 is stretched, and the implant cutting tool 4 is inserted into the living body along the thread 91 and the implant 9, and the distal end portion is brought into contact with the closing membrane 933 as shown in FIG. Next, the portion of the implant 9 protruding from the opening 411b is cut by sliding the cutting portion 42 to the proximal end side. Then, as shown in FIG. 25, the implant cutting tool 4 is pulled out from the living body. According to such an implant cutting tool 4, an extra portion of the implant 9 can be easily cut in vivo.
  • the implant cutting tool 4 does not place an anchor portion, unlike the anchor placement tool 1 described above.
  • the implant 9 including the threads 91 and 92
  • surrounding biological tissues such as the closing membranes 933 and 934 and muscle tissue
  • an anchor effect can be exerted and necessary tension is applied to the urethra 910. Can do.
  • a positioning marker 424 that determines the insertion depth of the implant cutting tool 4 into the living body may be provided in the cutting part 42.
  • the positioning marker 424 is configured by a flange. By having such a positioning marker 424, as shown in FIG. 27, when the implant cutting tool 4 is inserted into a living body, the positioning marker 424 comes into contact with the body surface S, and thus further insertion is restricted. Therefore, the insertion depth of the implant cutting tool 4 can be accurately controlled.
  • the cutting part 42 may be omitted. That is, as shown in FIG. 28, the implant cutting tool 4 may be composed of only the main body 41. In this case, for example, a portion exposed from the body surface of the implant 9 may be cut with a cutting tool such as a scissors.
  • the anchor indwelling device of the present invention is an anchor indwelling device for fixing a living tissue supporting indwelling material used for pelvic treatment in a living body, and is detachable from a long body and a distal end portion of the long body.
  • An anchor portion provided on the living body tissue, the anchor portion having a guide portion into which the living tissue supporting indwelling material is inserted, and a part of the living tissue supporting indwelling material inserted into the guide portion It is characterized by being fixed. Therefore, for example, after the implant is placed in the living body, the anchor portion can be fixed to the implant.
  • the anchor portion can be used as the closing membrane without penetrating the closing membrane. Can be arranged. As a result, it is possible to maintain the tension applied to the urethra over time without the anchors coming off or loosening from the closure membrane. Therefore, the anchor indwelling device of the present invention has industrial applicability.

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Abstract

This indwelling anchor device (1) is for fixing, in the body, a biological tissue-supporting indwelling object used in intrapelvic treatment, and is provided with an elongate body (21) and an anchor unit (22) which is detachably provided on the tip of the elongate body (21). The anchor unit (22) has a guide unit (through-hole (224)) in which the biological tissue-supporting indwelling object is inserted, and is fixed to a part of the biological tissue-supporting indwelling object inserted into the through-hole (224). This biological tissue-supporting indwelling object is arranged in the body such that at least one end thereof is exposed outside of the body, and the through-hole (224) is inserted into the body along the biological tissue-supporting indwelling object and is fixed, inside of the body, to the biological tissue-supporting indwelling object.

Description

アンカー留置具Anchor detainer
 本発明は、アンカー留置具に関するものである。 The present invention relates to an anchor indwelling device.
 尿失禁、特に、腹圧性尿失禁になると、通常の運動中や、笑い、咳、くしゃみ等により腹圧がかかることで、尿漏れが生じる。この原因は、例えば、出産等により、尿道を支える筋肉である骨盤底筋が緩むこと等が挙げられる。 Urinary incontinence, particularly stress urinary incontinence, urine leakage occurs due to abdominal pressure applied during normal exercise, laughing, coughing, sneezing, etc. The cause of this is, for example, that the pelvic floor muscle, which is a muscle that supports the urethra, is loosened due to childbirth and the like.
 尿失禁の治療には、外科的療法が有効であり、例えば、「スリング」と呼ばれる帯状の生体組織支持用留置物を用い、スリングを体内に留置し、そのスリングで尿道を支持する(例えば、特許文献1参照)。スリングを体内に留置するには、図29に示すように術者がメスで膣920を切開し、尿道910と膣920の間を剥離し、穿刺針等を用いて、その剥離した部位と外部とを閉鎖孔を介し連通させる。そして、穿刺針によって形成された穿刺孔にスリングを留置する。 Surgical therapy is effective for the treatment of urinary incontinence. For example, using a band-like tissue-supporting indwelling material called a “sling”, the sling is placed in the body, and the sling supports the urethra (for example, Patent Document 1). In order to place the sling in the body, as shown in FIG. 29, the operator incises the vagina 920 with a scalpel, peels off the space between the urethra 910 and the vagina 920, and uses the puncture needle or the like to remove the peeled portion and the outside. Are communicated with each other through a closing hole. Then, the sling is placed in the puncture hole formed by the puncture needle.
 ここで、スリングとして、帯状の本体の両端に一対のアンカー810、820が設けられた「ミニスリング」と呼ばれるものが知られている(例えば、特許文献2参照)。当該構成のスリングを用いた場合、まず、一方のアンカー810を、前記切開した部位から挿入して骨盤930の一方の閉鎖孔931を閉鎖し、閉鎖孔931の縁から起こって閉鎖孔931の大部分を閉鎖する靱帯性の薄膜である閉鎖膜(靭帯組織)933に貫通させることによって閉鎖膜933に引っ掛けて固定する。これと共に、他方のアンカー820を、前記切開した部位から挿入して他方の閉鎖孔932を閉鎖する閉鎖膜934に貫通させることによって閉鎖膜934に引っ掛けて固定し、図29に示す状態とする。次に、一対のアンカー810、820間にあるスリングの長さを調整して尿道に適切なテンションを付与する。その後、前記切開部を縫合する。これにより、スリング800の留置が終了する。このような手技によれば、穿刺される部分が短くなるため、患者への負担が小さくなるという利点がある。しかしながら、このような手技では、大きいアンカー810、820が閉鎖膜933、934を貫通するため、閉鎖膜933、934に大きな隙間が形成されてしまい、アンカー810、820が閉鎖膜933、934から外れたり、緩んだりし、尿道へ付与されるテンションが低下すると言った問題がある。 Here, as a sling, what is called a “mini sling” in which a pair of anchors 810 and 820 are provided at both ends of a belt-like main body is known (see, for example, Patent Document 2). In the case of using the sling having the above configuration, first, one anchor 810 is inserted from the incised site to close one closing hole 931 of the pelvis 930, and the large opening of the closing hole 931 occurs from the edge of the closing hole 931. The film is hooked and fixed to the closing membrane 933 by penetrating through a closing membrane (ligament tissue) 933 which is a ligamentous thin film that closes the portion. At the same time, the other anchor 820 is inserted from the incised portion and penetrated through the closing membrane 934 that closes the other closing hole 932, thereby being hooked and fixed to the closing membrane 934 to obtain the state shown in FIG. Next, an appropriate tension is applied to the urethra by adjusting the length of the sling between the pair of anchors 810 and 820. Thereafter, the incision is sutured. Thereby, the placement of the sling 800 is completed. According to such a technique, since the portion to be punctured is shortened, there is an advantage that the burden on the patient is reduced. However, in such a procedure, since the large anchors 810 and 820 penetrate the closing membranes 933 and 934, a large gap is formed in the closing membranes 933 and 934, and the anchors 810 and 820 are detached from the closing membranes 933 and 934. There is a problem that the tension applied to the urethra is reduced.
特開2010-99499号公報JP 2010-99499 A 特表2005-536316号公報JP 2005-536316 A
 本発明の目的は、生体内へアンカーを、その効果が経時的に維持されるように留置することのできるアンカー留置具を提供することにある。 An object of the present invention is to provide an anchor indwelling device that can indwell an anchor in a living body so that its effect is maintained over time.
 このような目的は、下記(1)~(15)の本発明により達成される。
 (1) 骨盤内治療に使用する生体組織支持用留置物を生体内に固定するためのアンカー留置具であって、
 長尺体と、
 前記長尺体の先端部に離脱自在に設けられたアンカー部と、を備え、
 前記アンカー部は、前記生体組織支持用留置物が挿入されるガイド部を有し、前記ガイド部に挿入された前記生体組織支持用留置物の一部と固定されることを特徴とするアンカー留置具。
Such an object is achieved by the present inventions (1) to (15) below.
(1) An anchor indwelling device for fixing a living tissue supporting indwelling object used for pelvic treatment in a living body,
A long body,
An anchor portion removably provided at the distal end of the elongated body,
The anchor portion has a guide portion into which the living tissue supporting indwelling material is inserted, and is fixed to a part of the living tissue supporting indwelling material inserted into the guide portion. Ingredients.
 (2) 前記生体組織支持用留置物は、少なくとも一端が体外へ露出するように体内へ配置され、
 前記生体組織支持用留置物の前記一端が前記ガイド部へ挿入され、前記ガイド部は、前記生体支持用留置物に沿って体内に挿入され、体内にて前記生体組織支持用留置物に固定される請求項1に記載のアンカー留置具。
(2) The biological tissue supporting indwelling object is disposed inside the body so that at least one end is exposed outside the body,
The one end of the biological tissue support indwelling object is inserted into the guide part, and the guide part is inserted into the body along the biological support indwelling object, and is fixed to the biological tissue support indwelling object in the body. The anchor indwelling device according to claim 1.
 (3)前記ガイド部は、貫通孔である上記(1)または(2)に記載のアンカー留置具。 (3) The anchor placement device according to (1) or (2), wherein the guide portion is a through hole.
 (4) 内側に第1貫通孔を有する筒状の前記長尺体と、前記ガイド部が前記第1貫通孔と連通する第2貫通孔で構成された前記アンカー部とを備え、前記第2貫通孔を介して前記第1貫通孔に生体組織支持用留置物が挿入される第1器具と、
 前記第2貫通孔を介して前記第1貫通孔に前記生体組織支持用留置物が挿入された状態にて、前記第1貫通孔を介して、基端側から前記アンカー部に固定され、前記アンカー部を前記生体組織支持用留置物に固定する固定部を備える第2器具と、を有し、
 前記アンカー部が前記生体組織支持用留置物に固定された状態にて、前記長尺体を基端側へ移動させると、前記長尺体から前記アンカー部が離脱するよう構成されている上記(1)ないし(3)のいずれか1項に記載のアンカー留置具。
(4) The cylindrical elongated body having a first through hole on the inner side, and the anchor portion including the second through hole in which the guide portion communicates with the first through hole, A first instrument in which a living tissue supporting indwelling object is inserted into the first through hole via a through hole;
With the biological tissue supporting indwelling object inserted into the first through-hole through the second through-hole, the anchor is fixed to the anchor portion from the base end side through the first through-hole, A second instrument comprising a fixing part for fixing the anchor part to the biological tissue supporting indwelling object,
The anchor portion is configured to be detached from the elongated body when the elongated body is moved to the proximal end side in a state where the anchor portion is fixed to the biological tissue supporting indwelling object ( The anchor indwelling device according to any one of 1) to (3).
 (5) 前記第1器具は、さらに、前記長尺体からの前記アンカー部の離脱を規制する規制状態と、前記長尺体からの離脱を許容する許容状態とを切り替えることのできる操作部を有している上記(4)に記載のアンカー留置具。 (5) The first instrument further includes an operation unit capable of switching between a restricted state for restricting detachment of the anchor portion from the long body and an allowable state for allowing detachment from the long body. The anchor indwelling device according to (4) above.
 (6) 前記アンカー部は、前記第1貫通孔に挿入され、前記長尺体の先端部と係合する基端部を有し、
 前記アンカー部が前記生体組織支持用留置物に固定された状態にて、前記長尺体を基端側へ移動させると、前記長尺体の先端部が弾性変形して前記係合が解除され、前記アンカー部が前記長尺体から離脱するように構成され、
 前記操作部は、筒状をなし、前記長尺体の外周に摺動可能に設けられており、前記規制状態では、前記長尺体の先端部を覆うことにより前記変形を抑制し、前記許容状態では、前記長尺体の先端部を露出させ、前記変形を許容する上記(5)に記載のアンカー留置具。
(6) The anchor portion has a proximal end portion that is inserted into the first through hole and engages with a distal end portion of the elongated body,
When the elongated body is moved to the proximal end side in a state where the anchor portion is fixed to the living tissue supporting indwelling object, the distal end portion of the elongated body is elastically deformed and the engagement is released. The anchor portion is configured to be detached from the elongated body,
The operation portion has a cylindrical shape and is provided on the outer periphery of the elongated body so as to be slidable. In the restricted state, the operation portion suppresses the deformation by covering a distal end portion of the elongated body, and allows the tolerance. In the state, the anchor indwelling device according to (5), wherein the distal end portion of the elongated body is exposed and the deformation is allowed.
 (7) 前記第1器具は、さらに、前記操作部を前記規制状態に維持する維持部を有している上記(6)に記載のアンカー留置具。 (7) The anchor indwelling device according to (6), wherein the first instrument further includes a maintenance unit that maintains the operation unit in the restricted state.
 (8) 前記維持部は、前記長尺体から離脱自在に設けられている上記(7)に記載のアンカー留置具。 (8) The anchor indwelling device according to (7), wherein the maintenance unit is provided so as to be detachable from the elongated body.
 (9) 前記第1器具は、さらに、前記第2貫通孔を介して前記第1貫通孔へ前記生体組織支持用留置物を誘導する誘導部を有している上記(4)ないし(8)のいずれか1項に記載のアンカー留置具。 (9) The above (4) to (8), wherein the first instrument further includes a guiding portion that guides the biological tissue supporting indwelling material to the first through hole through the second through hole. The anchor indwelling device according to any one of the above.
 (10) 前記誘導部は、先端部および基端部がそれぞれ前記第1器具から露出するように、前記第1貫通孔および前記第2貫通孔に挿通され、先端部に前記生体組織支持用留置物を保持する保持部が設けられた紐体で構成されている上記(9)に記載のアンカー留置具。 (10) The guiding portion is inserted into the first through hole and the second through hole so that the distal end portion and the proximal end portion are exposed from the first instrument, and the living tissue supporting indwelling is placed in the distal end portion. The anchor indwelling device according to (9), which is configured by a string body provided with a holding portion for holding an object.
 (11) 前記保持部は、前記紐体で形成された輪である上記(10)に記載のアンカー留置具。 (11) The anchor indwelling device according to (10), wherein the holding portion is a ring formed of the string body.
 (12) 前記第2器具は、さらに、前記第1貫通孔に挿入され、先端部に前記固定部が脱離自在に設けられた長尺な挿入部を有している上記(4)ないし(11)のいずれか1項に記載のアンカー留置具。 (12) The second instrument may further include a long insertion portion that is inserted into the first through-hole and the fixing portion is detachably provided at a distal end portion thereof. The anchor indwelling device according to any one of 11).
 (13) 前記挿入具の長さは、前記長尺体の長さよりも長い上記(12)に記載のアンカー留置具。 (13) The anchor placement device according to (12), wherein a length of the insertion tool is longer than a length of the elongated body.
 (14) 前記第2器具は、さらに、前記アンカー部よりも基端側にて、前記生体組織支持用留置物を切断する切断部を有している上記(12)または(13)に記載のアンカー留置具。 (14) The second instrument according to (12) or (13), further including a cutting portion that cuts the living tissue supporting indwelling object on a proximal end side with respect to the anchor portion. Anchor detainer.
 (15) 前記挿入部は、前記生体組織支持用留置物が挿通される第3貫通孔を有し、
 前記切断部は、前記第3貫通孔の一方の開口を跨ぐように移動させることのできる刃部を有している上記(14)に記載のアンカー留置具。
(15) The insertion portion has a third through hole through which the biological tissue supporting indwelling object is inserted.
The anchor indwelling device according to (14), wherein the cutting portion has a blade portion that can be moved so as to straddle one opening of the third through hole.
 本発明によれば、例えば、スリング(生体組織支持用留置物)を生体内に留置した後に、スリングにアンカー部を固定することができる。そのため、例えば、前述した尿失禁の治療の場合には、閉鎖膜を貫通させることなくアンカー部を閉鎖膜に配置することができる。その結果、アンカーが閉鎖膜から外れたり、緩んだりすることがなく、尿道へ付与されるテンションを経時的に維持することができる。 According to the present invention, for example, an anchor portion can be fixed to the sling after the sling (living tissue supporting indwelling object) is placed in the living body. Therefore, for example, in the case of the treatment of urinary incontinence described above, the anchor portion can be disposed on the closing membrane without penetrating the closing membrane. As a result, it is possible to maintain the tension applied to the urethra over time without the anchors coming off or loosening from the closure membrane.
図1は、本発明のアンカー留置具の好適な実施形態を示す側面図である。FIG. 1 is a side view showing a preferred embodiment of the anchor indwelling device of the present invention. 図2は、図1に示すアンカー留置具が備えるシャフトの断面図である。FIG. 2 is a cross-sectional view of a shaft included in the anchor placement device shown in FIG. 図3(a)および(b)は、それぞれ、図2に示すシャフトが有する操作部の動きを説明する断面図である。3 (a) and 3 (b) are cross-sectional views for explaining the movement of the operation portion of the shaft shown in FIG. 図4は、図1に示すアンカー留置具が備える挿入具の断面図である。4 is a cross-sectional view of an insertion tool provided in the anchor placement device shown in FIG. 図5は、図4に示す挿入具の先端部を示す断面図である。FIG. 5 is a cross-sectional view showing a distal end portion of the insertion tool shown in FIG. 図6(a)および(b)は、それぞれ、図4に示す挿入具が有する切断部の動きを説明する側面図である。FIGS. 6A and 6B are side views for explaining the movement of the cutting portion of the insertion tool shown in FIG. 図7は、インプラントの一例を示す図である。FIG. 7 is a diagram illustrating an example of an implant. 図8は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 8 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図9は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 9 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図10は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 10 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図11は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 11 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図12は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 12 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図13は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 13 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図14は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 14 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図15は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 15 is a view for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図16は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 16 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図17は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 17 is a view for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図18は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 18 is a view for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図19は、図1に示すアンカー留置具の操作手順を説明するための図である。FIG. 19 is a diagram for explaining an operation procedure of the anchor indwelling device shown in FIG. 1. 図20は、図1に示すアンカー留置具の変形例を示す図であり、(a)が側面図、(b)が(a)中のA-A線断面図である。20 is a view showing a modification of the anchor indwelling device shown in FIG. 1, in which (a) is a side view and (b) is a cross-sectional view taken along the line AA in (a). 図21は、インプラント切断具の一例を示す側面図である。FIG. 21 is a side view showing an example of an implant cutting tool. 図22(a)および(b)は、それぞれ、図21に示すインプラント切断具が有する切断部の動きを説明する側面図である。22 (a) and 22 (b) are side views for explaining the movement of the cutting portion of the implant cutting tool shown in FIG. 図23は、図21に示すインプラント切断具の操作手順を説明するための図である。FIG. 23 is a view for explaining an operation procedure of the implant cutting tool shown in FIG. 図24は、図21に示すインプラント切断具の操作手順を説明するための図である。FIG. 24 is a view for explaining an operation procedure of the implant cutting tool shown in FIG. 図25は、図21に示すインプラント切断具の操作手順を説明するための図である。FIG. 25 is a view for explaining an operation procedure of the implant cutting tool shown in FIG. 図26は、図21に示すインプラント切断具の変形例を示す側面図である。FIG. 26 is a side view showing a modified example of the implant cutting tool shown in FIG. 図27は、図26に示すインプラント切断具の操作手順を説明するための図である。FIG. 27 is a view for explaining an operation procedure of the implant cutting tool shown in FIG. 図28は、図21に示すインプラント切断具の他の変形例を示す側面図である。FIG. 28 is a side view showing another modification of the implant cutting tool shown in FIG. 図29は、従来技術の説明するための図である。FIG. 29 is a diagram for explaining the prior art.
 以下、本発明のアンカー留置具を添付図面に示す好適な実施形態に基づいて詳細に説明する。 Hereinafter, the anchor indwelling device of the present invention will be described in detail based on preferred embodiments shown in the accompanying drawings.
 図1は、本発明のアンカー留置具の好適な実施形態を示す側面図である。図2は、図1に示すアンカー留置具が備えるシャフトの断面図である。図3(a)および(b)は、それぞれ、図2に示すシャフトが有する操作部の動きを説明する断面図である。図4は、図1に示すアンカー留置具が備える挿入具の断面図である。図5は、図4に示す挿入具の先端部を示す断面図である。図6(a)および(b)は、それぞれ、図4に示す挿入具が有する切断部の動きを説明する側面図である。図7は、インプラントの一例を示す図である。図8ないし図19は、それぞれ、図1に示すアンカー留置具の操作手順を説明するための図である。図20は、図1に示すアンカー留置具の変形例を示す図であり、(a)が側面図、(b)が(a)中のA-A線断面図である。なお、以下では、説明の便宜上、図1中の右側を「先端」、左側を「基端」と言う。 FIG. 1 is a side view showing a preferred embodiment of the anchor indwelling device of the present invention. FIG. 2 is a cross-sectional view of a shaft included in the anchor placement device shown in FIG. 3 (a) and 3 (b) are cross-sectional views for explaining the movement of the operation portion of the shaft shown in FIG. 4 is a cross-sectional view of an insertion tool provided in the anchor placement device shown in FIG. FIG. 5 is a cross-sectional view showing a distal end portion of the insertion tool shown in FIG. FIGS. 6A and 6B are side views for explaining the movement of the cutting portion of the insertion tool shown in FIG. FIG. 7 is a diagram illustrating an example of an implant. 8 to 19 are diagrams for explaining the operation procedure of the anchor indwelling device shown in FIG. 20 is a view showing a modification of the anchor indwelling device shown in FIG. 1, in which (a) is a side view and (b) is a cross-sectional view taken along the line AA in (a). In the following, for convenience of explanation, the right side in FIG. 1 is referred to as “tip” and the left side is referred to as “base end”.
 1.アンカー留置具
 図1に示すアンカー留置具1は、例えば、女性の尿失禁の治療、すなわち、尿失禁の治療用のインプラント(生体組織支持用留置物)9を生体内に埋設する際に用いる装置である。
1. Anchor Indwelling Device The anchor indwelling device 1 shown in FIG. 1 is an apparatus used when, for example, an urinary incontinence treatment for women, that is, an implant (living tissue supporting indwelling material) 9 for urinary incontinence treatment is embedded in a living body. It is.
 図1に示すように、アンカー留置具1は、管状のシャフト(第1器具)2と、シャフト2内に挿入される挿入具(第2器具)3とで構成されている。以下、シャフト2および挿入具3について順に説明する。 As shown in FIG. 1, the anchor detainer 1 includes a tubular shaft (first instrument) 2 and an insertion instrument (second instrument) 3 inserted into the shaft 2. Hereinafter, the shaft 2 and the insertion tool 3 will be described in order.
 (シャフト)
 図1および図2に示すように、シャフト2は、長尺状の長尺体21と、長尺体21の先端部に保持されたアンカー部22と、アンカー部22を長尺体21から離脱可能な状態とする操作部23と、操作部23の状態を維持する維持部24と、長尺体21内に挿通された紐体(誘導部)25とを有している。
(shaft)
As shown in FIGS. 1 and 2, the shaft 2 includes an elongated body 21, an anchor portion 22 held at the distal end of the elongated body 21, and the anchor portion 22 being detached from the elongated body 21. It has the operation part 23 made into a possible state, the maintenance part 24 which maintains the state of the operation part 23, and the string body (guidance | derivation part) 25 penetrated in the elongate body 21.
 長尺体21は、円筒状をなし、その内部に両端を貫通する貫通孔(第1貫通孔)211を有している。また、長尺体21の先端部の内周面には、アンカー部22と凹凸係合する凹部212が形成されている。長尺体21の先端部は、所定の応力によって弾性変形して拡径するように構成されており、先端部が拡径することによって、長尺体21とアンカー部22との係合が解除されるようになっている。また、長尺体21の基端部には、外周面から突出するフランジ213が形成されている。このフランジ213は、長尺体21からの維持部24の離脱を防止する役目を有している。長尺体21の長さとしては、特に限定されず、用いる治療によっても異なるが、例えば、1~10cm程度であるのが好ましい。これにより、特に、尿失禁の治療用のインプラントを生体内に埋設する際に用いるのに適したサイズとなる。 The long body 21 has a cylindrical shape, and has a through hole (first through hole) 211 penetrating both ends. Further, a concave portion 212 that engages with the anchor portion 22 is formed on the inner peripheral surface of the distal end portion of the long body 21. The distal end portion of the long body 21 is configured to be elastically deformed and expanded in diameter by a predetermined stress, and the engagement between the long body 21 and the anchor portion 22 is released by expanding the diameter of the distal end portion. It has come to be. Further, a flange 213 protruding from the outer peripheral surface is formed at the proximal end portion of the long body 21. The flange 213 has a function of preventing the maintenance unit 24 from being detached from the long body 21. The length of the long body 21 is not particularly limited, and varies depending on the treatment to be used, but is preferably about 1 to 10 cm, for example. Thereby, it becomes a size suitable for using especially when the implant for treatment of urinary incontinence is embedded in the living body.
 長尺体21の先端部には、アンカー部22が装着されている。アンカー部22は、長尺体21の先端側に突出して設けられた本体221と、本体221の基端側に設けられ、長尺体21の貫通孔211に挿入された基端部222とを有している。本体221の先端部は、例えば、半球状、半長状等に丸みを帯びている。これにより、シャフト2を生体に挿入する際の抵抗を低減することができる。また、本体221の基端部は、長尺体21の外周より大きい径を有し、長尺体21の外周面よりも外側へ突出している。 An anchor portion 22 is attached to the distal end portion of the long body 21. The anchor portion 22 includes a main body 221 that protrudes toward the distal end side of the long body 21, and a base end portion 222 that is provided on the base end side of the main body 221 and inserted into the through hole 211 of the long body 21. Have. The front end of the main body 221 is rounded, for example, hemispherical or semi-long. Thereby, the resistance at the time of inserting the shaft 2 in a living body can be reduced. Further, the base end portion of the main body 221 has a diameter larger than the outer periphery of the long body 21, and protrudes outward from the outer peripheral surface of the long body 21.
 一方、基端部222の外周には凸部223が形成されており、この凸部223が長尺体21の凹部212と凹凸係合している。これにより、アンカー部22が長尺体21に保持され、アンカー部22の意図しない離脱が防止される。また、アンカー部22には、シャフト2の軸に沿った貫通孔(第2貫通孔)224で構成されたガイド部が形成されており、この貫通孔224は、基端側開口にて貫通孔211と連通している。また、貫通孔224の基端部は、基端開口へ向けて径が漸増するテーパ部224aで構成されている。 On the other hand, a convex portion 223 is formed on the outer periphery of the base end portion 222, and the convex portion 223 engages with the concave portion 212 of the long body 21. Thereby, the anchor part 22 is hold | maintained at the elongate body 21, and the unintentional detachment | leave of the anchor part 22 is prevented. Further, the anchor portion 22 is formed with a guide portion constituted by a through hole (second through hole) 224 along the axis of the shaft 2, and the through hole 224 is a through hole at the proximal end side opening. 211 communicates. Moreover, the base end part of the through-hole 224 is comprised by the taper part 224a which a diameter increases gradually toward base end opening.
 長尺体21の外周には、操作部23が配置されている。操作部23は、円筒状をなしており、長尺体21に対して、その軸方向に摺動可能に設けられている。操作部23は、先端側に位置してアンカー部22に当接し、図3(a)に示すように、長尺体21の先端部を覆う規制状態と、基端側に位置してフランジ213に当接し、図3(b)に示すように、長尺体21の先端部を露出させる許容状態とに移動可能である。 An operation unit 23 is arranged on the outer periphery of the long body 21. The operation unit 23 has a cylindrical shape, and is provided so as to be slidable in the axial direction with respect to the long body 21. The operation portion 23 is located on the distal end side and abuts on the anchor portion 22, and as shown in FIG. 3A, the operation portion 23 covers the distal end portion of the long body 21, and the proximal portion is located on the flange 213. As shown in FIG. 3 (b), it is possible to move to an allowable state in which the tip of the long body 21 is exposed.
 規制状態では、長尺体21の先端部が操作部23で覆われているため、長尺体21の先端部の弾性変形(拡径)が阻止される。そのため、規制状態では、長尺体21からのアンカー部22の脱離が防止される。一方、許容状態では、長尺体21の先端部が操作部23で覆われていないため、長尺体21の先端部の弾性変形(拡径)が可能となり、アンカー部22を長尺体21から離脱させることができる。なお、操作部23は、規制状態にて、長尺体21の先端部の弾性変形を阻止できる程度に硬質に構成されている。操作部23の構成は、長尺体21の先端部の弾性変形を阻止する状態と、許容する状態とをとることができれば、特に限定されない。 In the regulated state, the distal end portion of the long body 21 is covered with the operation unit 23, and therefore elastic deformation (expansion) of the distal end portion of the long body 21 is prevented. Therefore, detachment of the anchor portion 22 from the long body 21 is prevented in the restricted state. On the other hand, in the permissible state, the distal end portion of the long body 21 is not covered with the operation unit 23, so that the distal end portion of the long body 21 can be elastically deformed (expanded), and the anchor portion 22 can be Can be disengaged from. In addition, the operation part 23 is comprised so hard that the elastic deformation of the front-end | tip part of the elongate body 21 can be prevented in a regulation state. The structure of the operation part 23 will not be specifically limited if the state which prevents the elastic deformation | transformation of the front-end | tip part of the elongate body 21 and the state to accept | permit are taken.
 長尺体21の外周であって、フランジ213と操作部23との間には、維持部24が設けられている。維持部24は、例えば、C字状のクリップで構成されており、長尺体21に対して着脱自在となっている。維持部24は、操作部23を規制状態に維持する機能を有している。すなわち、維持部24を長尺体21に装着した状態では、操作部23が規制状態に維持され、維持部24を長尺体21から離脱させた状態では、操作部23が、許容状態に移動可能となる。このような維持部24を設けることによって、アンカー部22の意図しない離脱等、アンカー留置具1の誤操作を防止することができる。なお、維持部24の構成としては、操作部23が規制状態に保たれる状態と、許容状態に移動可能な状態とを選択することができれば、特に限定されない。 A maintenance unit 24 is provided on the outer periphery of the long body 21 and between the flange 213 and the operation unit 23. The maintenance part 24 is comprised by the C-shaped clip, for example, and is detachable with respect to the elongate body 21. As shown in FIG. The maintenance unit 24 has a function of maintaining the operation unit 23 in a restricted state. That is, when the maintenance unit 24 is attached to the long body 21, the operation unit 23 is maintained in a restricted state, and when the maintenance unit 24 is detached from the long body 21, the operation unit 23 moves to an allowable state. It becomes possible. By providing such a maintenance part 24, it is possible to prevent erroneous operation of the anchor indwelling tool 1, such as unintentional detachment of the anchor part 22. The configuration of the maintenance unit 24 is not particularly limited as long as the operation unit 23 can be selected between a state in which the operation unit 23 is maintained in a restricted state and a state in which the operation unit 23 can move to an allowable state.
 貫通孔211、224には、紐体25が挿通されている。紐体25は、その先端が貫通孔224の先端側開口から突出し、その基端が貫通孔211の基端側開口から突出している。また、紐体25の先端部には、インプラント9を保持する保持部251が設けられている。保持部251は、紐体25で形成された輪(ループ)251で構成されている。このような紐体25は、後述するように、インプラント9を貫通孔211内へ誘導するのに用いられる。 The string body 25 is inserted through the through holes 211 and 224. The string body 25 has a distal end projecting from the distal end side opening of the through hole 224 and a proximal end projecting from the proximal end side opening of the through hole 211. In addition, a holding portion 251 that holds the implant 9 is provided at the distal end portion of the string body 25. The holding part 251 is configured by a ring (loop) 251 formed by the string body 25. Such a string body 25 is used to guide the implant 9 into the through hole 211 as described later.
 以上、シャフト2の構成について説明した。長尺体21、アンカー部22、操作部23および維持部24の構成材料としては、特に限定されず、例えば、各種樹脂材料、各種金属材料を用いることができる。また、紐体25の構成材料としては、特に限定されず、例えば、ポリプロピレン等のような生体適合性を有する各種樹脂材料、繊維等を用いることができる。 The configuration of the shaft 2 has been described above. It does not specifically limit as a constituent material of the elongate body 21, the anchor part 22, the operation part 23, and the maintenance part 24, For example, various resin materials and various metal materials can be used. Moreover, it does not specifically limit as a constituent material of the string 25, For example, various resin materials, fibers, etc. which have biocompatibility like a polypropylene etc. can be used.
 (挿入具)
 図1および図4に示すように、挿入具3は、真っ直ぐな棒状をなす挿入部31と、挿入部31の先端部に装着された固定部32と、挿入部31の外周に設けられた筒状の切断部33とを有している。
(Insert tool)
As shown in FIG. 1 and FIG. 4, the insertion tool 3 includes an insertion portion 31 having a straight rod shape, a fixing portion 32 attached to the distal end portion of the insertion portion 31, and a cylinder provided on the outer periphery of the insertion portion 31. And a cut portion 33 having a shape.
 挿入部31は、外周面の対向する部位を貫通する貫通孔(第3貫通孔)311を有している。貫通孔311は、挿入部31の軸に対して傾斜して延在しており、一方の開口311aと他方の開口311bとが挿入部31の軸方向にずれて配置されている。貫通孔311には、先端側に位置する開口311aから基端側に位置する開口311bへインプラント9が挿通される。 The insertion portion 31 has a through-hole (third through-hole) 311 that penetrates the opposite part of the outer peripheral surface. The through-hole 311 extends while being inclined with respect to the axis of the insertion portion 31, and one opening 311 a and the other opening 311 b are arranged so as to be shifted in the axial direction of the insertion portion 31. The implant 9 is inserted into the through hole 311 from the opening 311a located on the distal end side to the opening 311b located on the proximal end side.
 挿入部31の長さとしては、特に限定されないが、長尺体21よりも長いことが好ましい。これにより、挿入具3をシャフト2に挿入した状態で、挿入部31の基端部が貫通孔211から露出するため、挿入具3の操作性が向上する。 The length of the insertion portion 31 is not particularly limited, but is preferably longer than the long body 21. Thereby, in the state which inserted the insertion tool 3 in the shaft 2, since the base end part of the insertion part 31 is exposed from the through-hole 211, the operativity of the insertion tool 3 improves.
 固定部32は、挿入部31から離脱自在に設けられている。この固定部32は、アンカー留置具1の使用中にて、アンカー部22に固定され、これにより、後述するように、アンカー部22をインプラント9に固定することができる。固定部32をアンカー部22に固定する方法としては、特に限定されず、例えば、螺合、嵌合、接着などを用いることができるが、本実施形態では、図5に示すように、固定部32を基端側から貫通孔224に圧入することによって、アンカー部22に固定する。 The fixing part 32 is provided detachably from the insertion part 31. The fixing portion 32 is fixed to the anchor portion 22 during use of the anchor placement device 1, and thereby the anchor portion 22 can be fixed to the implant 9 as described later. A method for fixing the fixing portion 32 to the anchor portion 22 is not particularly limited. For example, screwing, fitting, adhesion, or the like can be used. In this embodiment, as shown in FIG. 32 is pressed into the through hole 224 from the base end side to be fixed to the anchor portion 22.
 固定部32は、全体的に略円錐形状とされ、その先端部の外径R1が貫通孔224の内径r1よりも小さく、その基端側の外径R2が貫通孔224の基端開口の内径r2よりも大きく構成されている。このような形状とすることにより、円滑に、固定部32を貫通孔224に圧入することができる。また、固定部32の軸方向の途中には、先端へ向けて外径が漸減するテーパ部321が設けられており、このテーパ部321のテーパ角は、貫通孔224のテーパ部224aとほぼ等しくなっている。これにより、固定部32がアンカー部22に固定されている状態にて、後述するように、固定部32とアンカー部22でインプラント9をより強固に挟持することができる。 The fixed portion 32 has a substantially conical shape as a whole, the outer diameter R1 of the distal end thereof is smaller than the inner diameter r1 of the through hole 224, and the outer diameter R2 on the proximal end side is the inner diameter of the proximal end opening of the through hole 224. It is configured to be larger than r2. By setting it as such a shape, the fixing | fixed part 32 can be press-fit in the through-hole 224 smoothly. Further, a taper portion 321 whose outer diameter gradually decreases toward the tip is provided in the middle of the fixed portion 32 in the axial direction, and the taper angle of the taper portion 321 is substantially equal to the taper portion 224a of the through hole 224. It has become. Thereby, in the state where the fixing portion 32 is fixed to the anchor portion 22, as will be described later, the implant 9 can be more firmly held between the fixing portion 32 and the anchor portion 22.
 なお、固定部32をアンカー部22により確実に固定するために、例えば、テーパ部224aおよび321のうちの一方に凸部を形成するとともに、他方に前記凸部と係合する凹部を形成し、固定部32を貫通孔224に圧入するとともに、凹部と凸部とを係合させてもよい。 In order to securely fix the fixing portion 32 by the anchor portion 22, for example, a convex portion is formed on one of the tapered portions 224a and 321 and a concave portion that engages with the convex portion is formed on the other side. The fixing portion 32 may be press-fitted into the through hole 224 and the concave portion and the convex portion may be engaged.
 図4に示すように、挿入部31の外周には、円筒状の切断部33が配置されている。言い換えれば、切断部33の内側に挿入部31が挿入されている。また、切断部33は、挿入部31に対して、その軸方向に摺動可能に設けられている。また、切断部33の先端部には、開口331が設けられており、さらに、開口331内には、刃部332が設けられている。また、切断部33の基端部には、外周へ突出するフランジ333が設けられている。切断部33は、図6(a)に示す第1状態から、基端側に移動した図6(b)に示す第2状態へと移動することができる。第1状態では、開口311aが切断部33よりも先端側に位置し、開口311bが開口331内に位置しているため、開口311a、311bが共に切断部33から露出し、また、刃部332が開口311bよりも先端側に位置している。貫通孔311へインプラント9を挿通した状態にて、第1状態から第2状態とすべく、切断部33を基端側へ移動させると、刃部332が開口311bを跨ぐように移動し、インプラント9を切断する。このようにインプラント9を切断することによって、インプラント9の不要部が生体内に残留することを防止することができる。 As shown in FIG. 4, a cylindrical cutting portion 33 is disposed on the outer periphery of the insertion portion 31. In other words, the insertion part 31 is inserted inside the cutting part 33. The cutting part 33 is provided so as to be slidable in the axial direction with respect to the insertion part 31. In addition, an opening 331 is provided at the tip of the cutting part 33, and a blade part 332 is provided in the opening 331. Further, a flange 333 that protrudes to the outer periphery is provided at the base end portion of the cutting portion 33. The cutting part 33 can move from the first state shown in FIG. 6A to the second state shown in FIG. 6B moved to the proximal end side. In the first state, the opening 311a is located on the tip side with respect to the cutting part 33, and the opening 311b is located in the opening 331. Therefore, both the openings 311a and 311b are exposed from the cutting part 33, and the blade part 332 Is located on the tip side of the opening 311b. In a state where the implant 9 is inserted into the through-hole 311, when the cutting portion 33 is moved to the proximal end side so as to change from the first state to the second state, the blade portion 332 moves so as to straddle the opening 311 b, 9 is cut. By cutting the implant 9 in this way, unnecessary portions of the implant 9 can be prevented from remaining in the living body.
 以上、挿入具3の構成について説明した。挿入部31、固定部32および切断部33の構成材料としては、特に限定されず、例えば、各種樹脂材料、各種金属材料を用いることができる。 The configuration of the insertion tool 3 has been described above. It does not specifically limit as a constituent material of the insertion part 31, the fixing | fixed part 32, and the cutting part 33, For example, various resin materials and various metal materials can be used.
 2.アンカー留置具の使用方法
 まず、アンカー留置具1の使用方法について説明するのに先立って、インプラント9について説明する。
2. Method for Using Anchor Indwelling Device First, the implant 9 will be described prior to describing the method for using the anchor indwelling device 1.
 図7に示すインプラント9は、女性の尿失禁の治療のための埋設可能な器具、すなわち、尿道を支持する器具、例えば、尿道が膣壁側に移動しようとしたときに、その尿道を膣壁から離間する方向(腹側)へ支持する器具である。このインプラント9としては、例えば、可撓性を有する長尺物を用いることができる。 The implant 9 shown in FIG. 7 is an implantable device for the treatment of female urinary incontinence, that is, a device that supports the urethra, for example, when the urethra is about to move toward the vaginal wall, It is the instrument supported in the direction (ventral side) which leaves | separates from. As this implant 9, for example, a long object having flexibility can be used.
 インプラント9は、網状をなしており、その全体形状は、帯状をなしている。インプラント9は、「スリング」と呼ばれている。インプラント9は、例えば、線状体を交差させて網状(格子状)に編んだもの、すなわち、網状の編組体で構成することができる。線状体としては、例えば、その横断面形状が円形のものや、横断面形状が扁平形状のもの、すなわち帯状(リボン状)のもの等が挙げられる。また、インプラント9の一方の端部には、糸91の一方の端部が固定され、他方の端部には、糸92の一方の端部が固定されている。 The implant 9 has a net shape, and the entire shape thereof has a band shape. The implant 9 is called a “sling”. The implant 9 can be constituted by, for example, a braided body in which a linear body is crossed and knitted in a net shape (lattice shape), that is, a net-like braided body. Examples of the linear body include a circular cross-sectional shape, a flat cross-sectional shape, that is, a belt-like (ribbon-like) shape, and the like. One end of the thread 91 is fixed to one end of the implant 9, and one end of the thread 92 is fixed to the other end.
 インプラント9の構成材料としては、特に限定されず、例えば、ポリプロピレン等のような生体適合性を有する各種樹脂材料、繊維等を用いることができる。また、糸91、92の構成材料としては、それぞれ、特に限定されず、例えば、ポリプロピレン等のような生体適合性を有する各種樹脂材料、繊維等を用いることができる。 The constituent material of the implant 9 is not particularly limited, and various resin materials, fibers, and the like having biocompatibility such as polypropylene can be used. Further, the constituent materials of the yarns 91 and 92 are not particularly limited, and various biomaterials such as polypropylene, fibers, and the like can be used, for example.
 なお、インプラント9としては、同様の効果を発揮することができれば、前記網状のものに限定されない。 The implant 9 is not limited to the net-like one as long as the same effect can be exhibited.
 次に、アンカー留置具1の使用方法について説明する。
 まず、図8に示すように、メスで膣920を切開し、穿刺針7を切開部921から穿刺して、骨盤930の一方の閉鎖孔931を介して一方の鼠蹊部から体表面Sに抜去する。穿刺針7には、インプラント9の糸91が保持されており、これにより、糸91が鼠蹊部から体表面Sに露出する。次に、穿刺針7を切開部921から穿刺して、他方の閉鎖孔932を介して他方の鼠蹊部から体表面Sに抜去する。穿刺針7には、インプラント9の糸92が保持されており、これにより、糸92が鼠蹊部から体表面Sに露出する。次に、糸91、92を引っ張り、図9に示すように、インプラント9を尿道910と膣920との間に配置する。
Next, the usage method of the anchor indwelling tool 1 is demonstrated.
First, as shown in FIG. 8, the vagina 920 is incised with a scalpel, the puncture needle 7 is punctured from the incision portion 921, and is extracted from one buttocks to the body surface S through one closing hole 931 of the pelvis 930. To do. The puncture needle 7 holds the thread 91 of the implant 9, whereby the thread 91 is exposed to the body surface S from the buttocks. Next, the puncture needle 7 is punctured from the incision 921, and is extracted from the other buttocks to the body surface S via the other closing hole 932. The puncture needle 7 holds the thread 92 of the implant 9, whereby the thread 92 is exposed to the body surface S from the buttocks. Next, the threads 91 and 92 are pulled, and the implant 9 is placed between the urethra 910 and the vagina 920 as shown in FIG.
 次に、シャフト2を用意し、紐体25の輪251に糸91を挿通する。これにより、紐体25に糸91(インプラント9の一部が含まれていてもよい。以下同様である。)が保持される。次に、図10に示すように、紐体25を基端側へ引っ張り、貫通孔224を介して糸91を貫通孔211内に誘導し、さらに、貫通孔211の基端開口から外部へ誘導する。 Next, the shaft 2 is prepared, and the thread 91 is inserted through the ring 251 of the string body 25. Thereby, the thread | yarn 91 (A part of the implant 9 may be contained in the string body 25. It is the same below.) Is hold | maintained. Next, as shown in FIG. 10, the string body 25 is pulled to the proximal end side, the thread 91 is guided into the through hole 211 through the through hole 224, and further guided to the outside from the proximal end opening of the through hole 211. To do.
 次に、糸91を張った状態で、シャフト2を糸91およびインプラント9に沿わせて生体内へ挿入し、図11および図12に示すように、閉鎖膜933にアンカー部22を当接させる。次に、挿入具3を用意し、切断部33を第1状態とした後、糸91を開口311aから貫通孔311内に挿入し、開口311bから外部へ引き出す。次に、糸91を張った状態で、挿入具3をシャフト2に基端側から挿入し、図13に示すように、固定部32をアンカー部22に押し付ける。これにより、固定部32が貫通孔224に圧入され、固定部32とアンカー部22とでインプラント9を挟持した状態で、固定部32がアンカー部22に固定される。その結果、アンカー部22がインプラント9に固定される。 Next, in a state where the thread 91 is stretched, the shaft 2 is inserted into the living body along the thread 91 and the implant 9, and the anchor portion 22 is brought into contact with the closing membrane 933 as shown in FIGS. . Next, after preparing the insertion tool 3 and setting the cutting part 33 in the first state, the thread 91 is inserted into the through hole 311 from the opening 311a and pulled out from the opening 311b. Next, the insertion tool 3 is inserted into the shaft 2 from the proximal end side in a state where the thread 91 is tensioned, and the fixing portion 32 is pressed against the anchor portion 22 as shown in FIG. Accordingly, the fixing portion 32 is press-fitted into the through hole 224, and the fixing portion 32 is fixed to the anchor portion 22 in a state where the fixing portion 32 and the anchor portion 22 sandwich the implant 9. As a result, the anchor portion 22 is fixed to the implant 9.
 次に、例えば、切断部33のフランジ333に指を引っ掛けて切断部33を挿入部31に対して基端側へスライドさせることによって、切断部33を第1状態から第2状態とし、図14に示すように、インプラント9の開口311bから先の部分を切断する。これにより、余分なインプラント9が除去される。 Next, for example, the cutting unit 33 is changed from the first state to the second state by hooking a finger on the flange 333 of the cutting unit 33 and sliding the cutting unit 33 toward the proximal end side with respect to the insertion unit 31. As shown in FIG. 4, the tip portion is cut from the opening 311b of the implant 9. Thereby, the excess implant 9 is removed.
 次に、挿入具3をシャフト2から引き抜く。次に、図15に示すように、長尺体21から維持部24を外し、操作部23を長尺体21に対して基端側へスライドさせて許容状態とする。そして、シャフト2を生体から引き抜く(すなわち、長尺体21を基端側へ移動させる)。この時、長尺体21の先端部が弾性変形(拡径)し、長尺体21からアンカー部22が離脱するため、図16に示すように、アンカー部22が閉鎖膜933に当接した状態で生体内に留置さる。 Next, the insertion tool 3 is pulled out from the shaft 2. Next, as shown in FIG. 15, the maintenance unit 24 is removed from the long body 21, and the operation unit 23 is slid toward the proximal side with respect to the long body 21 to be in an allowable state. Then, the shaft 2 is pulled out from the living body (that is, the long body 21 is moved to the proximal end side). At this time, the distal end portion of the long body 21 is elastically deformed (expanded diameter), and the anchor portion 22 is detached from the long body 21, so that the anchor portion 22 abuts against the closing film 933 as shown in FIG. Indwelling in the living body.
 次に、図17に示すように、閉鎖孔931と同様に、アンカー留置具1を用いて、閉鎖孔932を覆う閉鎖膜934に当接するようにアンカー部22を留置する。この際、糸92を所定の力で引っ張り、尿道910に対して所定のテンションが加わった状態でアンカー部22を留置する。これにより、両アンカー部22が閉鎖膜933、934に引っ掛かることによって、インプラント9によって、尿道910へテンションが加わった状態が維持される。最後に、切開部921を縫合等の所定の処置を行って手技が終了する。 Next, as shown in FIG. 17, similarly to the closing hole 931, the anchor part 22 is placed using the anchor placing tool 1 so as to contact the closing film 934 covering the closing hole 932. At this time, the anchor portion 22 is placed in a state where the thread 92 is pulled with a predetermined force and a predetermined tension is applied to the urethra 910. Thereby, the state in which the tension is applied to the urethra 910 by the implant 9 is maintained by the two anchor portions 22 being hooked on the closing membranes 933 and 934. Finally, a predetermined procedure such as suturing is performed on the incision 921 to complete the procedure.
 以上、説明したように、アンカー留置具1によれば、左右鼠蹊部からアンカー部22を挿入し、インプラント9に固定することができる。そのため、アンカー部22が当接(係合)する閉鎖膜933、934をアンカー部22が貫通することが無い。したがって、従来のように閉鎖膜933、934に大きな隙間が形成されず、アンカー部22を閉鎖膜933、934に確実に係合させることができる。その結果、インプラント9によって尿道に所定のテンションがかかった状態を確実にかつ長期間維持することができる。 As described above, according to the anchor placement device 1, the anchor portion 22 can be inserted from the left and right buttocks and fixed to the implant 9. Therefore, the anchor part 22 does not penetrate the closing films 933 and 934 with which the anchor part 22 abuts (engages). Therefore, a large gap is not formed in the closing membranes 933 and 934 as in the prior art, and the anchor portion 22 can be reliably engaged with the closing membranes 933 and 934. As a result, the state in which a predetermined tension is applied to the urethra by the implant 9 can be reliably maintained for a long time.
 なお、上述の手技では、糸91、92を共に鼠蹊部から体表面Sに露出させてから、2つのアンカーを留置しているが、これに限定されず、例えば、糸91を左鼠蹊部から体表面Sに露出させた後、閉鎖膜933に当接するようにアンカー部22を留置し、次いで、糸92を右鼠蹊部から体表面Sに露出させた後、閉鎖膜934に当接するようにアンカー部22を留置してもよい。 In the above-described procedure, the two anchors are placed after the yarns 91 and 92 are both exposed from the buttocks to the body surface S. However, the present invention is not limited to this. After being exposed to the body surface S, the anchor portion 22 is placed so as to contact the closing membrane 933, and then the thread 92 is exposed to the body surface S from the starboard portion so as to contact the closing membrane 934. The anchor part 22 may be placed.
 また、上述の手技では、膣920を切開してその切開部921から、尿道910と膣920との間にインプラント9を配置しているが、インプラント9の配置方法は、これに限定されない。例えば、円弧上に湾曲した穿刺針71を有する穿刺部材を用いてもよい。具体的に説明すると、まず、図18に示すように、穿刺針71を一方の鼠蹊部に穿刺し、閉鎖孔932、尿道910と膣920との間、閉鎖孔931を順に通過させた後、他方の鼠蹊部から体外に突出させ、生体に貫通孔940を形成する。次に、穿刺針71の先端部にインプラント9を保持し、穿刺針71を逆に回転させる。これにより、穿刺針71の針先は、患者の左鼠径部から体内に入り、閉鎖孔931、尿道910と膣920との間、閉鎖孔932を順に通過した後、右鼠径部から体外に出て、穿刺針71が体外に抜去される。インプラント9を穿刺針71から外した後、糸92を引っ張って、インプラント9を貫通孔940に挿入する。これにより、図19に示すように、インプラント9の設置が完了する。 Further, in the above procedure, the vagina 920 is incised and the implant 9 is disposed between the urethra 910 and the vagina 920 from the incision portion 921, but the arrangement method of the implant 9 is not limited thereto. For example, a puncture member having a puncture needle 71 curved on an arc may be used. Specifically, as shown in FIG. 18, first, after puncturing the puncture needle 71 into one of the buttocks and passing through the closing hole 931, between the urethra 910 and the vagina 920 in order, A through-hole 940 is formed in the living body by protruding from the other buttocks. Next, the implant 9 is held at the tip of the puncture needle 71, and the puncture needle 71 is rotated in reverse. Thereby, the needle tip of the puncture needle 71 enters the body from the left groin portion of the patient, passes through the obstruction hole 931, the urethra 910 and the vagina 920, and the obstruction hole 932 in order, and then exits from the right inguinal portion to the outside of the body. Thus, the puncture needle 71 is removed from the body. After removing the implant 9 from the puncture needle 71, the thread 92 is pulled to insert the implant 9 into the through hole 940. Thereby, as shown in FIG. 19, installation of the implant 9 is completed.
 このような方法によれば、インプラント9を留置する際、その穿刺針71の穿刺等の低侵襲の手技のみで対応することができ、侵襲の大きい切開等を行わなくてよいので、患者の負担が少なく、また、患者の安全性も高い。 According to such a method, when the implant 9 is indwelled, it can be handled only by a minimally invasive technique such as puncture of the puncture needle 71, and it is not necessary to perform a large invasive incision or the like. The patient safety is also high.
 以上、アンカー留置具1について説明した。アンカー留置具1では、長尺体21に貫通孔211が形成され、アンカー部22に貫通孔224が形成されていたが、長尺体21およびアンカー部22の構成としては、これに限定されず、例えば、貫通孔211、224に替えて、図20(a)に示すように、長尺体21に溝211aが設けられ、アンカー部22に溝225が設けられていてもよい。溝211a、225の開口同士は、連通している。この場合、操作部23には、溝211aの開口が外部へ露出するように、溝211aの開口に対応する位置にスリット239が設けられる。このような構成では、溝211a、225の開口を介してインプラント9(糸91)を溝211a、225内へ導入することができるため、インプラント9の導入が容易となる。また、インプラント9を導入するのに紐体25を用いる必要がないため、その操作が容易となる。特に、図20(b)に示すように、溝211aの開口を内部空間に対して狭くし、糸91を引っ掛ける引掛け部214を設けることによって、溝211a内へ導入した糸91の離脱が抑制され、糸91に沿ったシャフト2の移動をスムーズに行うことができる。 The anchor placement device 1 has been described above. In the anchor indwelling device 1, the through hole 211 is formed in the long body 21 and the through hole 224 is formed in the anchor portion 22. However, the configuration of the long body 21 and the anchor portion 22 is not limited thereto. For example, instead of the through holes 211 and 224, as shown in FIG. 20A, the elongated body 21 may be provided with a groove 211 a and the anchor portion 22 may be provided with a groove 225. The openings of the grooves 211a and 225 communicate with each other. In this case, the operation unit 23 is provided with a slit 239 at a position corresponding to the opening of the groove 211a so that the opening of the groove 211a is exposed to the outside. In such a configuration, since the implant 9 (thread 91) can be introduced into the grooves 211a and 225 through the openings of the grooves 211a and 225, the introduction of the implant 9 is facilitated. Moreover, since it is not necessary to use the string body 25 to introduce the implant 9, the operation is facilitated. In particular, as shown in FIG. 20B, the opening of the groove 211a is made narrower than the internal space, and the hooking portion 214 for hooking the thread 91 is provided, thereby preventing the thread 91 introduced into the groove 211a from being detached. Thus, the movement of the shaft 2 along the yarn 91 can be performed smoothly.
 3.インプラント切断具
 次に、インプラント切断具について説明する。
3. Implant Cutting Tool Next, the implant cutting tool will be described.
 図21は、インプラント切断具の一例を示す側面図である。図22(a)および(b)は、それぞれ、図21に示すインプラント切断具が有する切断部の動きを説明する側面図である。図22は、図21に示すインプラント切断部が有する切断部の動きを説明する側面図である。図23ないし図25は、それぞれ、図21に示すインプラント切断具の操作手順を説明するための図である。図26は、図21に示すインプラント切断具の変形例を示す側面図である。図27は、図26に示すインプラント切断具の操作手順を説明するための図である。図28は、図21に示すインプラント切断具の他の変形例を示す側面図である。なお、以下では、説明の便宜上、図21中の右側を「先端」、左側を「基端」と言う。 FIG. 21 is a side view showing an example of an implant cutting tool. 22 (a) and 22 (b) are side views for explaining the movement of the cutting portion of the implant cutting tool shown in FIG. FIG. 22 is a side view for explaining the movement of the cutting part of the implant cutting part shown in FIG. 23 to 25 are diagrams for explaining the operation procedure of the implant cutting tool shown in FIG. FIG. 26 is a side view showing a modified example of the implant cutting tool shown in FIG. FIG. 27 is a view for explaining an operation procedure of the implant cutting tool shown in FIG. FIG. 28 is a side view showing another modification of the implant cutting tool shown in FIG. In the following, for convenience of explanation, the right side in FIG. 21 is referred to as “tip”, and the left side is referred to as “base end”.
 インプラント切断具4は、生体内にてインプラント9を切断するのに用いられる器具である。図21に示すように、インプラント切断具4は、貫通孔411を有する長尺な本体41と、筒状をなし、本体41の外周に摺動可能に設けられた切断部42とを有している。 The implant cutting tool 4 is an instrument used for cutting the implant 9 in vivo. As shown in FIG. 21, the implant cutting tool 4 has a long main body 41 having a through-hole 411 and a cutting portion 42 that is formed in a cylindrical shape and is slidably provided on the outer periphery of the main body 41. Yes.
 本体41の先端部は、丸みを帯びている。また、貫通孔411の先端側の開口411aは、本体41の先端に位置し、基端側の開口411bは、本体41の側面に位置している。貫通孔411には、インプラント9が挿入される。貫通孔411の長さとしては、特に限定されないが、1~3cm程度であるのが好ましい。 The tip of the main body 41 is rounded. Further, the opening 411 a on the distal end side of the through hole 411 is located at the distal end of the main body 41, and the opening 411 b on the proximal end side is located on the side surface of the main body 41. The implant 9 is inserted into the through hole 411. The length of the through hole 411 is not particularly limited, but is preferably about 1 to 3 cm.
 切断部42の先端部には、開口421が設けられており、さらに、開口421内には刃部422が設けられている。また、切断部42の基端部には、外周へ突出するフランジ423が設けられている。切断部42は、図22(a)に示す第1状態から、基端側に移動した図22(b)に示す第2状態へと移動することができる。第1状態では、貫通孔411の開口411bが切断部42から露出しているとともに、刃部422が開口411bよりも先端側に位置している。そのため、貫通孔411にインプラント9が挿通されている状態で、切断部42を第1状態から第2状態とすると、開口411bから引き出されている部分のインプラント9を切断することができる。 An opening 421 is provided at the tip of the cutting part 42, and a blade part 422 is provided in the opening 421. Further, a flange 423 that protrudes to the outer periphery is provided at the proximal end portion of the cutting portion 42. The cutting part 42 can move from the first state shown in FIG. 22A to the second state shown in FIG. 22B moved to the base end side. In the first state, the opening 411b of the through hole 411 is exposed from the cutting part 42, and the blade part 422 is located on the tip side of the opening 411b. Therefore, when the cutting portion 42 is changed from the first state to the second state in a state where the implant 9 is inserted through the through-hole 411, the portion of the implant 9 drawn out from the opening 411b can be cut.
 このようなインプラント切断具4は、次のようにして使用する。まず、図23に示すように、インプラント9を生体内に配置する。インプラントの配置方法は、前述した方法と同様である。次に、切断部を第1状態とした後、糸91を貫通孔411の開口411aから貫通孔411へ挿入し、開口411bから外へ引き出す。次に、糸91を張って、インプラント切断具4を糸91およびインプラント9に沿わせて生体内へ挿入し、図24に示すように、閉鎖膜933に先端部を当接させる。次に、切断部42を基端側にスライドさせることによって、開口411bから飛び出した部分のインプラント9を切断する。そして、図25に示すように、インプラント切断具4を生体から引き抜く。このようなインプラント切断具4によれば、インプラント9の余分な部分を生体内にて簡単に切断することができる。 Such an implant cutting tool 4 is used as follows. First, as shown in FIG. 23, the implant 9 is placed in the living body. The method for arranging the implant is the same as that described above. Next, after the cut portion is set to the first state, the thread 91 is inserted into the through hole 411 from the opening 411a of the through hole 411 and pulled out from the opening 411b. Next, the thread 91 is stretched, and the implant cutting tool 4 is inserted into the living body along the thread 91 and the implant 9, and the distal end portion is brought into contact with the closing membrane 933 as shown in FIG. Next, the portion of the implant 9 protruding from the opening 411b is cut by sliding the cutting portion 42 to the proximal end side. Then, as shown in FIG. 25, the implant cutting tool 4 is pulled out from the living body. According to such an implant cutting tool 4, an extra portion of the implant 9 can be easily cut in vivo.
 なお、インプラント切断具4では、前述したアンカー留置具1とは異なってアンカー部を留置しない。しかしながら、インプラント9(糸91、92を含む)が閉鎖膜933、934や筋組織等の周囲の生体組織に絡み付くことによって、アンカー効果を発揮することができ、尿道910に必要なテンションを与えることができる。 Note that the implant cutting tool 4 does not place an anchor portion, unlike the anchor placement tool 1 described above. However, when the implant 9 (including the threads 91 and 92) is entangled with surrounding biological tissues such as the closing membranes 933 and 934 and muscle tissue, an anchor effect can be exerted and necessary tension is applied to the urethra 910. Can do.
 インプラント切断具4の変形例として、図26に示すように、切断部42に、インプラント切断具4の生体への挿入深さを定める位置決めマーカー424が設けられていてもよい。位置決めマーカー424は、フランジで構成されている。このような位置決めマーカー424を有することによって、図27に示すように、インプラント切断具4を生体に挿入すると、位置決めマーカー424が体表面Sに当接することによって、それ以上の挿入が規制される。そのため、インプラント切断具4の挿入深さを正確に制御することができる。 As a modification of the implant cutting tool 4, as shown in FIG. 26, a positioning marker 424 that determines the insertion depth of the implant cutting tool 4 into the living body may be provided in the cutting part 42. The positioning marker 424 is configured by a flange. By having such a positioning marker 424, as shown in FIG. 27, when the implant cutting tool 4 is inserted into a living body, the positioning marker 424 comes into contact with the body surface S, and thus further insertion is restricted. Therefore, the insertion depth of the implant cutting tool 4 can be accurately controlled.
 また、インプラント切断具4の他の変形例として、切断部42を省略してもよい。すなわち、図28に示すように、インプラント切断具4が本体41のみで構成されていてもよい。この場合には、例えば、鋏等の切断具によって、インプラント9の体表から露出している部分を切断すればよい。 Further, as another modification of the implant cutting tool 4, the cutting part 42 may be omitted. That is, as shown in FIG. 28, the implant cutting tool 4 may be composed of only the main body 41. In this case, for example, a portion exposed from the body surface of the implant 9 may be cut with a cutting tool such as a scissors.
 以上、本発明のアンカー留置具を、図示の実施形態に基づいて説明したが、本発明はこれに限定されるものではなく、各部の構成は、同様の機能を有する任意の構成のものに置換することができる。また、本発明に、他の任意の構成物が付加されていてもよい。 As mentioned above, although the anchor indwelling device of this invention was demonstrated based on embodiment of illustration, this invention is not limited to this, The structure of each part is substituted by the thing of the arbitrary structures which have the same function. can do. In addition, any other component may be added to the present invention.
 本発明のアンカー留置具は、骨盤内治療に使用する生体組織支持用留置物を生体内に固定するためのアンカー留置具であって、長尺体と、前記長尺体の先端部に離脱自在に設けられたアンカー部と、を備え、前記アンカー部は、前記生体組織支持用留置物が挿入されるガイド部を有し、前記ガイド部に挿入された前記生体組織支持用留置物の一部と固定されることを特徴とする。そのため、例えば、インプラントを生体内に留置した後に、インプラントにアンカー部を固定することができ、例えば、前述した尿失禁の治療の場合には、閉鎖膜を貫通させることなくアンカー部を閉鎖膜に配置することができる。その結果、アンカーが閉鎖膜から外れたり、緩んだりすることがなく、尿道へ付与されるテンションを経時的に維持することができる。
 したがって、本発明のアンカー留置具は、産業上の利用可能性を有する。
The anchor indwelling device of the present invention is an anchor indwelling device for fixing a living tissue supporting indwelling material used for pelvic treatment in a living body, and is detachable from a long body and a distal end portion of the long body. An anchor portion provided on the living body tissue, the anchor portion having a guide portion into which the living tissue supporting indwelling material is inserted, and a part of the living tissue supporting indwelling material inserted into the guide portion It is characterized by being fixed. Therefore, for example, after the implant is placed in the living body, the anchor portion can be fixed to the implant. For example, in the case of the treatment of urinary incontinence described above, the anchor portion can be used as the closing membrane without penetrating the closing membrane. Can be arranged. As a result, it is possible to maintain the tension applied to the urethra over time without the anchors coming off or loosening from the closure membrane.
Therefore, the anchor indwelling device of the present invention has industrial applicability.
 1      アンカー留置具
 2      シャフト
 21     長尺体
 211    貫通孔
 211a   溝
 212    凹部
 213    フランジ
 22     アンカー部
 221    本体
 222    基端部
 223    凸部
 224    貫通孔
 224a   テーパ部
 225    溝
 23     操作部
 239    スリット
 24     維持部
 25     紐体
 251    保持部(輪)
 3      挿入具
 31     挿入部
 311    貫通孔
 311a   開口
 311b   開口
 32     固定部
 321    テーパ部
 33     切断部
 331    開口
 332    刃部
 333    フランジ
 4      インプラント切断具
 41     本体
 411    貫通孔
 411a   開口
 411b   開口
 42     切断部
 421    開口
 422    刃部
 423    フランジ
 424    マーカー
 7、71   穿刺針
 810    アンカー
 820    アンカー
 9      インプラント
 91     糸
 92     糸
 910    尿道
 920    膣
 921    切開部
 930    骨盤
 931    閉鎖孔
 932    閉鎖孔
 933    閉鎖膜
 934    閉鎖膜
 940    貫通孔
 R1     外径
 R2     外径
 r1     内径
 r2     内径
 S      体表面
DESCRIPTION OF SYMBOLS 1 Anchor detainer 2 Shaft 21 Long body 211 Through- hole 211a Groove 212 Recess 213 Flange 22 Anchor part 221 Main body 222 Base end part 223 Convex part 224 Through-hole 224a Taper part 225 Groove 23 Operation part 239 Slit 24 Maintenance part 25 String body 251 Holding part (ring)
DESCRIPTION OF SYMBOLS 3 Insertion tool 31 Insertion part 311 Through- hole 311a Opening 311b Opening 32 Fixing part 321 Taper part 33 Cutting part 331 Opening 332 Blade part 333 Flange 4 Implant cutting tool 41 Main body 411 Through- hole 411a Opening 411b Opening part 421 Cutting part 42 423 flange 424 marker 7, 71 puncture needle 810 anchor 820 anchor 9 implant 91 thread 92 thread 910 urethra 920 vagina 921 incision 930 pelvis 931 closure hole 932 closure hole 933 closure membrane 934 closure membrane 940 outer diameter R1 outer diameter R2 outer diameter R1 Inner diameter r2 Inner diameter S Body surface

Claims (15)

  1.  骨盤内治療に使用する生体組織支持用留置物を生体内に固定するためのアンカー留置具であって、
     長尺体と、
     前記長尺体の先端部に離脱自在に設けられたアンカー部と、を備え、
     前記アンカー部は、前記生体組織支持用留置物が挿入されるガイド部を有し、前記ガイド部に挿入された前記生体組織支持用留置物の一部と固定されることを特徴とするアンカー留置具。
    An anchor indwelling device for fixing a living tissue supporting indwelling object used for pelvic treatment in a living body,
    A long body,
    An anchor portion removably provided at the distal end of the elongated body,
    The anchor portion has a guide portion into which the living tissue supporting indwelling material is inserted, and is fixed to a part of the living tissue supporting indwelling material inserted into the guide portion. Ingredients.
  2.  前記生体組織支持用留置物は、少なくとも一端が体外へ露出するように体内へ配置され、
     前記生体組織支持用留置物の前記一端が前記ガイド部へ挿入され、前記ガイド部は、前記生体支持用留置物に沿って体内に挿入され、体内にて前記生体組織支持用留置物に固定される請求項1に記載のアンカー留置具。
    The biological tissue supporting indwelling object is disposed inside the body so that at least one end is exposed outside the body,
    The one end of the biological tissue support indwelling object is inserted into the guide part, and the guide part is inserted into the body along the biological support indwelling object, and is fixed to the biological tissue support indwelling object in the body. The anchor indwelling device according to claim 1.
  3.  前記ガイド部は、貫通孔である請求項1または2に記載のアンカー留置具。 The anchor placement device according to claim 1 or 2, wherein the guide portion is a through hole.
  4.  内側に第1貫通孔を有する筒状の前記長尺体と、前記ガイド部が前記第1貫通孔と連通する第2貫通孔で構成された前記アンカー部とを備え、前記第2貫通孔を介して前記第1貫通孔に生体組織支持用留置物が挿入される第1器具と、
     前記第2貫通孔を介して前記第1貫通孔に前記生体組織支持用留置物が挿入された状態にて、前記第1貫通孔を介して、基端側から前記アンカー部に固定され、前記アンカー部を前記生体組織支持用留置物に固定する固定部を備える第2器具と、を有し、
     前記アンカー部が前記生体組織支持用留置物に固定された状態にて、前記長尺体を基端側へ移動させると、前記長尺体から前記アンカー部が離脱するよう構成されている請求項1ないし3のいずれか1項に記載のアンカー留置具。
    The cylindrical elongated body having a first through hole on the inner side, and the anchor portion including the second through hole in which the guide portion communicates with the first through hole, and the second through hole A first instrument in which a living tissue supporting indwelling object is inserted into the first through-hole,
    With the biological tissue supporting indwelling object inserted into the first through-hole through the second through-hole, the anchor is fixed to the anchor portion from the base end side through the first through-hole, A second instrument comprising a fixing part for fixing the anchor part to the biological tissue supporting indwelling object,
    The anchor portion is configured to be detached from the elongated body when the elongated body is moved to the proximal end side in a state where the anchor portion is fixed to the biological tissue supporting indwelling object. The anchor indwelling device according to any one of 1 to 3.
  5.  前記第1器具は、さらに、前記長尺体からの前記アンカー部の離脱を規制する規制状態と、前記長尺体からの離脱を許容する許容状態とを切り替えることのできる操作部を有している請求項4に記載のアンカー留置具。 The first instrument further includes an operation unit capable of switching between a restricting state for restricting detachment of the anchor portion from the long body and an allowable state for allowing detachment from the long body. The anchor detainer according to claim 4.
  6.  前記アンカー部は、前記第1貫通孔に挿入され、前記長尺体の先端部と係合する基端部を有し、
     前記アンカー部が前記生体組織支持用留置物に固定された状態にて、前記長尺体を基端側へ移動させると、前記長尺体の先端部が弾性変形して前記係合が解除され、前記アンカー部が前記長尺体から離脱するように構成され、
     前記操作部は、筒状をなし、前記長尺体の外周に摺動可能に設けられており、前記規制状態では、前記長尺体の先端部を覆うことにより前記変形を抑制し、前記許容状態では、前記長尺体の先端部を露出させ、前記変形を許容する請求項5に記載のアンカー留置具。
    The anchor portion is inserted into the first through hole, and has a proximal end portion that engages with a distal end portion of the elongated body,
    When the elongated body is moved to the proximal end side in a state where the anchor portion is fixed to the living tissue supporting indwelling object, the distal end portion of the elongated body is elastically deformed and the engagement is released. The anchor portion is configured to be detached from the elongated body,
    The operation portion has a cylindrical shape and is slidably provided on an outer periphery of the elongated body. In the restricted state, the operation portion is configured to suppress the deformation by covering a distal end portion of the elongated body, and The anchor indwelling device according to claim 5, wherein in the state, the distal end portion of the elongated body is exposed to allow the deformation.
  7.  前記第1器具は、さらに、前記操作部を前記規制状態に維持する維持部を有している請求項6に記載のアンカー留置具。 The anchor indwelling device according to claim 6, wherein the first instrument further includes a maintenance unit that maintains the operation unit in the restricted state.
  8.  前記維持部は、前記長尺体から離脱自在に設けられている請求項7に記載のアンカー留置具。 The anchor indwelling device according to claim 7, wherein the maintenance unit is provided so as to be detachable from the elongated body.
  9.  前記第1器具は、さらに、前記第2貫通孔を介して前記第1貫通孔へ前記生体組織支持用留置物を誘導する誘導部を有している請求項4ないし8のいずれか1項に記載のアンカー留置具。 9. The device according to claim 4, wherein the first instrument further includes a guide portion that guides the biological tissue supporting indwelling material to the first through hole through the second through hole. The anchor indwelling device described.
  10.  前記誘導部は、先端部および基端部がそれぞれ前記第1器具から露出するように、前記第1貫通孔および前記第2貫通孔に挿通され、先端部に前記生体組織支持用留置物を保持する保持部が設けられた紐体で構成されている請求項9に記載のアンカー留置具。 The guide portion is inserted into the first through hole and the second through hole so that the distal end portion and the proximal end portion are exposed from the first instrument, and the biological tissue supporting indwelling object is held at the distal end portion. The anchor indwelling device according to claim 9, wherein the anchor indwelling device is configured by a string body provided with a holding portion.
  11.  前記保持部は、前記紐体で形成された輪である請求項10に記載のアンカー留置具。 The anchor indwelling device according to claim 10, wherein the holding portion is a ring formed of the string body.
  12.  前記第2器具は、さらに、前記第1貫通孔に挿入され、先端部に前記固定部が脱離自在に設けられた長尺な挿入部を有している請求項4ないし11のいずれか1項に記載のアンカー留置具。 The said 2nd instrument is further inserted in the said 1st through-hole, and has the elongate insertion part by which the said fixing | fixed part was provided detachably in the front-end | tip part. The anchor indwelling device according to item.
  13.  前記挿入具の長さは、前記長尺体の長さよりも長い請求項12に記載のアンカー留置具。 The anchor placement tool according to claim 12, wherein the length of the insertion tool is longer than the length of the elongated body.
  14.  前記第2器具は、さらに、前記アンカー部よりも基端側にて、前記生体組織支持用留置物を切断する切断部を有している請求項12または13に記載のアンカー留置具。 The anchor indwelling device according to claim 12 or 13, wherein the second instrument further has a cutting part for cutting the living tissue supporting indwelling object at a proximal end side with respect to the anchor part.
  15.  前記挿入部は、前記生体組織支持用留置物が挿通される第3貫通孔を有し、
     前記切断部は、前記第3貫通孔の一方の開口を跨ぐように移動させることのできる刃部を有している請求項14に記載のアンカー留置具。
    The insertion portion has a third through-hole through which the living tissue support indwelling object is inserted,
    The anchor indwelling tool according to claim 14, wherein the cutting portion has a blade portion that can be moved so as to straddle one opening of the third through hole.
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JP2012510863A (en) * 2008-12-05 2012-05-17 ボストン サイエンティフィック サイムド,インコーポレイテッド Insertion device and method for delivery of mesh carriers

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CN107049600A (en) * 2017-05-26 2017-08-18 西安医学院第二附属医院 A kind of ear drum membrane therapeutic system
CN107049600B (en) * 2017-05-26 2023-09-22 西安医学院第二附属医院 Eardrum membrane treatment device
DE102018103977A1 (en) * 2018-02-22 2019-08-22 Rz-Medizintechnik Gmbh Fixing device for fixing a Ligaturbands and device for inserting and fixing a Ligaturbands in a fixing device
EP3711708A1 (en) * 2019-03-18 2020-09-23 Marian Devonec Adjustable, reversible and removable device combining suspension and tensioning for treating urinary incontinence
FR3093912A1 (en) * 2019-03-18 2020-09-25 Marian Devonec READJUSTABLE, REVERSIBLE AND REMOVABLE SUSPENSION AND TENSIONING DEVICE FOR THE TREATMENT OF URINARY INCONTINENCE

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