WO2015133442A1 - 内視鏡用処置具 - Google Patents
内視鏡用処置具 Download PDFInfo
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- WO2015133442A1 WO2015133442A1 PCT/JP2015/056115 JP2015056115W WO2015133442A1 WO 2015133442 A1 WO2015133442 A1 WO 2015133442A1 JP 2015056115 W JP2015056115 W JP 2015056115W WO 2015133442 A1 WO2015133442 A1 WO 2015133442A1
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- sheath
- distal
- central axis
- curve
- lumen
- Prior art date
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1492—Probes or electrodes therefor having a flexible, catheter-like structure, e.g. for heart ablation
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/00131—Accessories for endoscopes
- A61B1/0014—Fastening element for attaching accessories to the outside of an endoscope, e.g. clips, clamps or bands
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
- A61B2017/00292—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery mounted on or guided by flexible, e.g. catheter-like, means
- A61B2017/003—Steerable
- A61B2017/00318—Steering mechanisms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00315—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for treatment of particular body parts
- A61B2018/00482—Digestive system
- A61B2018/00494—Stomach, intestines or bowel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00571—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for achieving a particular surgical effect
- A61B2018/00601—Cutting
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00571—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for achieving a particular surgical effect
- A61B2018/00607—Coagulation and cutting with the same instrument
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00982—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body combined with or comprising means for visual or photographic inspections inside the body, e.g. endoscopes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B2018/1405—Electrodes having a specific shape
- A61B2018/144—Wire
Definitions
- the present invention relates to an endoscope treatment tool.
- This application claims priority based on Japanese Patent Application No. 2014-042051 filed in Japan on March 4, 2014, the contents of which are incorporated herein by reference.
- Endoscopic sphincterotomy is known as a technique for incising the sphincter of the duodenal papilla while observing the duodenal papilla using an endoscopic device.
- Patent Literature 1 to Patent Literature 4 disclose treatment instruments used in EST.
- Patent Document 1 discloses a guide wire insertion tool provided with a funnel-shaped extension that communicates with the lumen of the catheter in order to easily insert the guide wire into the lumen of the catheter.
- Patent Document 2 discloses a high-frequency knife capable of directing an incision portion of a knife wire in a desired direction by forming a guide arm portion on a knife wire and arranging the guide arm portion in a slit formed in a sheath. Has been.
- Patent Document 3 EST can be safely performed by providing a non-insulated incision at the distal end portion of the high-frequency knife wire and an insulating portion that is insulated at a portion other than the incision.
- a treatment tool is disclosed.
- Patent Document 4 discloses a bile duct treatment catheter having a groove that communicates with the guide wire lumen from a position outside the catheter shaft and extends in the longitudinal direction of the shaft in order to easily exchange the guide wire. .
- Endoscopic sphincterotomy is known as a technique for incising the sphincter of the duodenal papilla while observing the duodenal papilla using an endoscopic device.
- Patent Document 3 discloses a treatment tool optimized for EST.
- an endoscope is disclosed. It is preferable to make an incision at a position shifted from the 12 o'clock direction toward the 11 o'clock direction in the image, and the treatment tool described in Patent Document 3 requires a complicated operation to hold the knife wire at such a position.
- the present invention has been made in view of the above-described circumstances, and an object thereof is to provide an endoscopic treatment tool and an incision system that can stably realize incision of a nipple with a small amount of bleeding.
- An endoscope treatment tool is a sheath having a central axis along a longitudinal axis, and a virtual plane provided at a distal portion of the sheath and including the central axis of the sheath.
- a first communication hole that communicates with the central axis of the sheath and opens in a direction radially away from the position of the knife wire lumen with respect to the central axis of the sheath, and the precar is more than the first communication hole.
- a second communicating hole that communicates the inner peripheral surface of the curve in the pre-curved section and the knife wire lumen on the proximal end side of the section, and the first communicating hole and the second communicating hole that protrude from the first communicating hole.
- a wire-like incision portion that extends between the first communication hole and the second communication hole and can incise the tissue, and is provided at the distal end portion of the incision portion and inserted into the knife wire lumen
- An insertable guide wire housing portion a proximal slit portion communicating from the guide wire housing portion to the outer peripheral surface of the sheath in a region proximal to the proximal end of the pre-curve portion;
- the proximal end side of the sheath communicates from the inside of the guide wire housing portion to the outer peripheral surface of the sheath.
- An inlet portion is formed so that the guide wire can be introduced.
- the proximal slit portion may be formed continuously from the proximal end of the pre-curve portion to the inlet portion.
- An endoscopic treatment tool is a sheath having a central axis along a longitudinal axis and a virtual plane provided at a distal portion of the sheath and including the central axis of the sheath.
- a pre-curve portion having a restoring force to a curved shape in which the sheath is bent, and a central axis at a position separated from the virtual plane at a tip portion of the pre-curve portion, and formed along the central axis of the sheath A knife wire lumen, an inner peripheral surface of the curved shape in the pre-curve portion that opens in a direction radially away from the position of the knife wire lumen with respect to the central axis of the sheath, and the knife wire lumen A first communication hole that communicates with the central axis of the sheath and opens in a direction radially away from the position of the knife wire lumen with respect to the central axis of the sheath.
- a second communication hole that communicates the inner peripheral surface of the curve in the pre-curve portion and the knife wire lumen, and the first communication hole is projected from the first communication hole and the second communication hole.
- a wire-like incision extending between the hole and the second communication hole and capable of incising the tissue; provided at the tip of the incision; and inserted in the knife wire lumen
- the proximal region of the pre-curve part including the distal slit part is an active curve of the endoscope apparatus.
- the contour shape of the proximal region of the pre-curve portion including the distal slit portion in a cross section perpendicular to the central axis of the sheath is circular. You may have the rigidity which deform
- incision with a small amount of bleeding can be stably performed in EST.
- FIG. 1 is an overall view of an incision system including an endoscope treatment tool according to a first embodiment of the present invention. It is a top view of the treatment tool for endoscopes concerning a first embodiment of the present invention.
- FIG. 3 is a cross-sectional view taken along line III-III in FIG. 2. It is a top view which shows the distal end part of the sheath of the treatment tool for endoscopes which concerns on 1st embodiment of this invention.
- FIG. 4 is a sectional view taken along line IV-IV in FIG. 2. It is a perspective view which shows a part of sheath in the treatment tool for endoscopes which concerns on 1st embodiment of this invention.
- FIG. 7 is a partial cross-sectional view showing a first port portion of the endoscope treatment tool according to the first embodiment of the present invention, as viewed in the direction of the line VIII-VIII shown in FIG.
- FIG. 7 is a cross-sectional view taken along line IX-IX in FIG. 6.
- FIG. 12 is a cross-sectional view taken along line XII-XII in FIG. 11.
- FIG. 7 is a cross-sectional view at the same position as the XII-XII line in FIG.
- FIG. 12 is a cross-sectional view taken along line XIII-XIII in FIG. 11. It is a figure which shows the distal part of the sheath of the treatment tool for endoscopes which concerns on 1st embodiment of this invention, and is a figure containing the fragmentary sectional view of the sheath seen from the XIV-XIV line
- FIG. 1 It is a figure which shows the positional relationship of the hook and 1st port in the state which attached the treatment tool for endoscopes which concerns on 1st embodiment of this invention to the endoscope apparatus.
- FIG. 1 It is a perspective view of the treatment tool attachment auxiliary tool which can be attached to the endoscope apparatus concerning a first embodiment of the present invention.
- FIG. 1 It is a fragmentary sectional view which shows the internal structure of the treatment tool attachment auxiliary tool shown in FIG.
- FIG. It is a figure which shows one process at the time of use of the treatment tool for endoscopes which concerns on 1st embodiment of this invention.
- FIG. 1 shows the usage condition of the treatment tool for endoscopes which concerns on 1st embodiment of this invention. It is sectional drawing which shows the state in which the flexible area
- FIG. 7 is a view showing a mode in which a guide wire is attached to the endoscope treatment tool according to the first embodiment of the present invention, and is a partial cross-sectional view taken along line VIII-VIII shown in FIG.
- FIG. 8 is a view showing another example in which a guide wire is attached to the endoscope treatment tool according to the first embodiment of the present invention, and is a partial cross-sectional view seen from the line VIII-VIII shown in FIG. It is a figure which shows one process at the time of use of the treatment tool for endoscopes which concerns on 1st embodiment of this invention.
- FIG. 1 is an overall view of an incision system 110 including an endoscope treatment tool 1 according to the present embodiment.
- an endoscope treatment tool 1 according to the present embodiment is a medical instrument that is used together with an endoscope apparatus 100 in order to incise a living tissue in a body.
- the endoscope treatment tool 1 constitutes an incision system 110 (endoscope treatment system) in a state where it is combined with the endoscope apparatus 100.
- the endoscope apparatus 100 according to the present embodiment has an active bending portion 107 (see FIG. 1).
- the active bending portion 107 is bent by the bending operation portion 107a.
- FIG. 2 is a plan view of the endoscope treatment tool 1.
- 3A is a cross-sectional view taken along line III-III in FIG.
- FIG. 3B is a plan view showing a distal end portion of the sheath 3 of the endoscope treatment tool 1.
- 4 is a cross-sectional view taken along line IV-IV in FIG.
- FIG. 5A is a perspective view showing a part of the sheath 3 in the endoscope treatment tool 1.
- FIG. 5B is a plan view showing the sheath 3.
- FIG. 6 is a plan view showing a part of the operation unit 40 of the endoscope treatment tool 1.
- FIG. 7 is a partial cross-sectional view showing the sheath 3 of the endoscope treatment tool 1 and the distal component 41 of the operation unit 40.
- FIG. 8 is a partial cross-sectional view showing the first port 49 portion of the endoscope treatment tool 1, and is a view seen in the direction of the line VIII-VIII shown in FIG. 9A is a cross-sectional view taken along line IX-IX in FIG.
- FIG. 9B is a perspective view showing the first port 49 portion of the endoscope treatment tool 1.
- FIG. 10 is a cross-sectional view of the distal end portion of the sheath 3 in the first virtual plane ⁇ .
- FIG. 11 is a view of the distal portion of the sheath 3 as viewed from the direction perpendicular to the second virtual plane ⁇ .
- 12A is a cross-sectional view taken along line XII-XII in FIG.
- FIG. 13 is a cross-sectional view taken along line XIII-XIII in FIG.
- FIG. 14 is a view showing a distal portion of the sheath 3, and includes a partial cross-sectional view of the sheath 3 as seen from the line XIV-XIV shown in FIG. 12A.
- the endoscope treatment tool 1 has an insertion part 2 and an operation part 40.
- the insertion unit 2 is an elongated member that is inserted into the treatment instrument channel 104 of the endoscope apparatus 100.
- the insertion part 2 has a sheath 3 and a knife wire 30.
- the sheath 3 is an elongated member having a central axis L1 along the longitudinal axis and having flexibility.
- the sheath 3 is made of resin.
- the operation part 40 side of the endoscope treatment tool 1 is referred to as a proximal side
- the insertion part 2 is provided
- the side inserted into the body is referred to as a distal side.
- the sheath 3 has a pre-curve portion 4 in a predetermined region including the distal end 3a of the sheath 3 as shown in FIG. 3B.
- the pre-curve portion 4 is provided with a bending force in a shape curved in a predetermined direction, and has a restoring force to restore the curved shape given in advance.
- the central axis L1 of the sheath 3 in the pre-curve portion 4 is within a predetermined plane (hereinafter referred to as “first virtual plane ⁇ ”). That is, the pre-curve portion 4 has a restoring force to a curved shape in which the sheath 3 is curved along the first virtual plane ⁇ .
- the distal portion side of the pre-curve portion 4 has a drawing portion 5, and the proximal portion side of the pre-curve portion 4 has a copying deformation portion 6.
- the outer diameter of the drawing portion 5 preferably has an outer diameter slightly smaller than the outer diameter of the proximal end side of the sheath 3 and the copying deformable portion 6.
- At least a part of the drawing unit 5 is inserted into the duodenal papilla PV (see FIG. 23) of the patient to be treated. As shown in FIG. 3B, the drawing unit 5 is provided with a distal first series hole 23 and a distal second hole 24 described later.
- the copying deformation portion 6 belongs to a distal portion of the flexible region 26 described later in the present embodiment.
- a distal slit portion 10 d described later is not formed in the drawing portion 5 but is formed in the copying deformation portion 6.
- the central axis L1 is the vertical axis
- the plane perpendicular to the first virtual plane ⁇ on the central axis L1 of the sheath 3 (hereinafter referred to as “second virtual plane ⁇ ”) is the horizontal axis.
- the configuration of the sheath 3 will be described using an orthogonal coordinate system (hereinafter referred to as “virtual coordinate system”).
- virtual coordinate system On the vertical axis of the virtual coordinate system, the bending direction of the pre-curve portion 4 is the upper side.
- a first lumen 7, a second lumen 15, and a third lumen (knife wire lumen) 20 are formed inside the sheath 3.
- the first lumen 7, the second lumen 15, and the third lumen 20 are formed to extend in parallel to each other in the longitudinal direction of the sheath 3.
- Each lumen has a central axis extending substantially parallel to the central axis L1 of the sheath 3.
- the first lumen 7 is a passage portion having an inner diameter that allows the guide wire 80 to advance and retract. That is, the first lumen 7 is a lumen in which the guide wire 80 is held.
- the first lumen 7 has a central axis L7 located on the first virtual plane ⁇ and is located below the central axis L1 of the sheath 3, that is, in the third quadrant Q3 and the fourth quadrant Q4 of the virtual coordinate system. .
- the first virtual plane ⁇ crosses the internal space of the first lumen 7.
- the predetermined first virtual plane ⁇ includes the central axis L7 of the first lumen 7. Further, it can be said that the first lumen 7 is located at a position separated from the third lumen 20 in the circumferential direction.
- the first lumen 7 is exemplified as a passage for moving the guide wire 80.
- the passage is not limited to the guide wire 80 and may be used as a passage for moving another treatment instrument.
- the first lumen 7 includes an outlet portion 12 that opens to the distal end 3 a, a guide wire housing portion 9, a slit portion 10, and an inlet portion 8 that opens to the proximal end side. And having.
- the guide wire housing portion 9 is a region of the first lumen 7 where the slit portion 10 is formed and communicates with the outer peripheral surface 3 c of the sheath 3.
- the slit portion 10 has a shape in which a resin member constituting the sheath 3 is cut off in the direction of the central axis L ⁇ b> 1 of the sheath 3.
- the slit portion 10 is opened in the outer peripheral surface 3c of the sheath 3 so as to communicate the first lumen 7 and the outside of the sheath 3, and is formed by extending along the direction of the central axis L1 of the sheath 3. It is a lack. As shown in FIG.
- the slit portion 10 has a proximal slit portion 10p formed in a region proximal to the base end of the pre-curve portion 4, and the proximal slit portion 10p is formed, The torsional moment of the cross section is reduced, and the region proximal to the proximal end of the pre-curved portion 4 is configured to be easily twisted.
- the proximal slit portion 10 p extends from the proximal end of the pre-curved portion 4 to the inlet portion 8 and communicates with the opening of the inlet portion 8.
- the inlet portion 8 is opened on the proximal end side of the sheath 3 so as to communicate from the inside of the guide wire housing portion 9 to the outer peripheral surface 3c of the sheath 3, and the guide wire 80 can be introduced.
- the guide wire housing portion 9 is formed along the longitudinal axis of the sheath 3 at a position spaced from the third lumen 20 in the circumferential direction around the central axis of the sheath 3.
- the slit portion 10 may further include a distal slit portion 10d. As shown in FIG.
- the distal slit portion 10 d extends from the proximal end of the precurve portion 4 to the middle portion of the precurve portion 4 toward the distal side, and has a curved outer shape in the guide wire housing portion 9 and the precurve portion 4. It suffices if it is formed along the central axis of the sheath 3 so as to communicate with the outer peripheral surface 402 of the sheath 3. Specifically, the distal slit portion 10d is formed along the central axis L1 of the sheath 3 at a position where the outer peripheral surface of the copying deformable portion 6 and the first virtual plane ⁇ intersect.
- the position of the distal end 10a of the distal slit portion 10d is a position closer to the proximal side than the base end of the drawing portion 5 and an arbitrary position on the copying deformation portion 6 (an intermediate portion of the copying deformation portion 6). Alternatively, it is the tip of the copying deformable portion 6.
- the position of the proximal end of the distal slit portion 10 d is the base end of the pre-curve portion 4.
- the distal slit portion 10d communicates with the proximal slit portion 10p.
- the contour deformation portion 6 in which the distal slit portion 10d is formed has a rigidity in which the contour shape of the contour deformation portion 6 is easily deformed into an elliptical shape in a cross section perpendicular to the central axis L1 of the sheath 3.
- the region between the distal end 3a of the sheath 3 and the distal end 10a of the distal slit portion 10d is a high rigidity region 25 having relatively high torsional rigidity in the sheath 3.
- the region from the distal end of the proximal slit portion 10p to the tip of the notch 55 is set as a flexible region 26 having at least a relatively low torsional rigidity with respect to the high-rigidity region 25.
- the high rigidity region 25 has a higher restoring force to the predetermined curved shape in the pre-curved portion 4 than the flexible region 26.
- the high-rigidity region 25 is easy to follow the curved shape of the active bending portion 107 in the treatment instrument channel 104 curved by the active bending portion 107 of the endoscope apparatus 100, and the treatment instrument channel 104 of the endoscope apparatus 100. When it is protruded from the distal end 104a, it is restored to a curved shape suitable for incision of the treatment target site.
- the slit portion 10 includes a pair of flap portions 11 (first flap 11 a, second flap 11) that are spaced apart from each other such that the opening width of the slit portion 10 is smaller than the diameter of the guide wire 80. It has a flap 11b).
- the flap portion 11 is a pair of elastic portions that cover the guide wire housing portion 9 with a resin member constituting the sheath 3. The flap portion 11 is deformed until a gap of a size through which the guide wire 80 can pass is generated by the force of the operator when removing the guide wire 80 from the guide wire housing portion 9 through the slit portion 10.
- the inlet 8 is opened to the outer peripheral surface 3 c of the sheath 3 in the vicinity of the proximal end 7 b of the first lumen 7, which is the same as the diameter of the guide wire 80 or larger than the diameter of the guide wire 80. It is a part.
- the inlet portion 8 is an opening portion that is wider than the slit portion 10 where the inner surface 7c of the first lumen 7 is exposed to the outside due to the absence of the flap portion 11.
- the length of the inlet portion 8 in the direction of the central axis L1 of the sheath 3 is larger than the inner diameter of the guide wire housing portion 9 (first lumen 7) in the first lumen 7.
- the inlet portion 8 has a long hole shape that is long in the direction of the central axis L1 of the sheath 3.
- the shape of the inlet portion 8 may be a rectangular shape.
- the left and right ends 8 c (both ends in the circumferential direction) of the inlet portion 8 in the circumferential direction of the sheath 3 are tapered so that the opening area of the inlet portion 8 gradually increases from the guide wire housing portion 9 toward the outer peripheral surface 3 c of the sheath 3. It may have a shape (see FIG. 9A).
- the guide wire accommodating portion 9 has a circular outline except for the boundary with the slit portion 10 in a cross section orthogonal to the central axis L ⁇ b> 1 of the sheath 3. That is, the guide wire accommodating portion 9 has a substantially C-shaped contour shape in a cross section orthogonal to the central axis L ⁇ b> 1 of the sheath 3.
- the guide wire accommodating portion 9 has a clearance in a state where the guide wire 80 is inserted so that the guide wire 80 can be advanced and retracted.
- the inner diameter of the guide wire accommodating portion 9 is equal to the clearance dimension. Greater than the diameter of
- the first lumen 7 has a cross section orthogonal to the central axis L1 of the sheath 3 in a region between the distal end 10a of the distal slit portion 10d and the distal end 3a of the sheath 3. It has a continuous circumferential contour, and has a distal region that restricts the movement of the guide wire 80 with respect to the radial direction of the first lumen 7.
- the distal end 3 a of the sheath 3 is provided with an outlet portion 12 that is open to communicate with the guide wire housing portion 9, and the guide wire 80 can protrude from the outlet portion 12. It is.
- the second lumen 15 is used to send a liquid such as a contrast medium from the proximal end 3b of the sheath 3 (see FIG. 2) to the distal end 3a of the sheath 3 (see FIGS. 2 and 3A). Lumen.
- the second lumen 15 can also be used as a drainage lumen for removing body fluid.
- the second lumen 15 in the pre-curve portion 4 is located in the first quadrant Q1 in the virtual coordinate system.
- a second port 62 described later is provided at the proximal end of the second lumen 15.
- the second port 62 has an opening through which liquid is introduced.
- the distal end of the second lumen 15 has an opening (distal discharge port) 17 through which liquid introduced from the second port 62 is discharged.
- the third lumen 20 is a lumen into which a knife wire 30 described later is inserted.
- the third lumen 20 is set so that the knife wire 30 can advance and retract within the third lumen 20. That is, it has a clearance with the knife wire 30 inserted, and the inner diameter of the third lumen 20 is larger than the diameter of the knife wire 30 by the clearance dimension.
- the third lumen 20 in the pre-curve portion 4 is located in the second quadrant Q2 in the virtual coordinate system.
- the second lumen 15 and the third lumen 20 are located in the curved inner surface 401 side region, and the first lumen 7 Is located in an area on the curved outer surface 402 side. That is, as shown in FIG. 3A, in the vicinity of the distal end 3 a of the sheath 3, above the vertical axis (above the first virtual plane ⁇ ) in the virtual coordinate system of the cross section orthogonal to the central axis L ⁇ b> 1 of the sheath 3.
- the third lumen 20 in the pre-curve portion 4 is located in a range between 9 o'clock and 12 o'clock.
- the third lumen 20 has a knife wire accommodating portion 22 (see FIG. 14), a distal first communication hole 23, and a distal second communication hole 24.
- the first virtual plane ⁇ traverses the wall 3 d located between the second lumen 15 and the third lumen 20 in the sheath 3.
- the wall 3d is positioned on the first virtual plane ⁇
- the second lumen 15 and the third lumen 20 are positioned on both sides of the first virtual plane ⁇ .
- the knife wire accommodating portion 22 covers the entire outer periphery of the knife wire 30 so as to hold the knife wire 30 in an electrically insulated state.
- the distal first through hole 23 is opened in the outer peripheral surface 3 c of the sheath 3 and communicated with the third lumen 20.
- the distal first series through hole 23 is located in the second quadrant Q2 in the virtual coordinate system. That is, when the upper part of the vertical axis (above the first virtual plane ⁇ ) in the virtual coordinate system of the cross section orthogonal to the central axis L1 of the sheath 3 is regarded as a clock face at 12 o'clock, the distal first series The through hole 23 is located in a range between 9 o'clock and 12 o'clock.
- the distal first series through-hole 23 communicates the curved inner surface 401 (curved inner outer peripheral surface) and the third lumen 20 in the pre-curved portion 4. Further, the distal first series through-hole 23 is formed to open at a position on the curved inner surface 401 side at the tip of the pre-curved portion 4 and spaced from the first virtual plane ⁇ . Further, the first distal through hole 23 is formed so as to open in a direction away from the position of the third lumen 20 radially outward with respect to the central axis of the sheath 3.
- the distal second communication hole 24 is disposed on a position closer to the distal side than the first distal through hole 23 and at a position separated from the first distal through hole 23.
- the distal second communication hole 24 is located in the second quadrant Q2 in the virtual coordinate system. That is, when the upper part of the vertical axis (above the first virtual plane ⁇ ) in the virtual coordinate system of the cross section orthogonal to the central axis L1 of the sheath 3 is regarded as a clock face at 12 o'clock, the distal first series
- the through hole 24 is located in the range between 9 o'clock and 12 o'clock similarly to the first series of through holes 23.
- the distal second communication hole 24 is similar to the distal first communication hole 23 in that the curved inner surface 401 (curved inner peripheral surface) and the third lumen 20 in the pre-curved portion 4 Is communicated. Further, the distal second communication hole 24 is formed so as to open at a position on the curved inner surface 401 side at the tip portion of the pre-curved portion 4 and at a position separated from the first virtual plane ⁇ . Furthermore, the first distal through hole 24 is formed to open in a direction away from the position of the third lumen 20 radially outward with respect to the central axis of the sheath 3. In addition, it is more preferable that the distal first series through hole 23 and the distal second communication hole 24 are arranged in a region where the drawing portion 5 exists.
- the distal second communication hole 24 and the distal first continuous hole 23 are located at the same position in the circumferential direction around the central axis L1 of the sheath 3. It is desirable to do it. However, the positions of the distal first communication hole 23 and the distal second communication hole 24 in the circumferential direction of the sheath 3 do not necessarily coincide with each other.
- the distal first communication hole 23 and the distal second communication hole 24 are provided so as to communicate the curved inner surface 401 and the third lumen 20 in the pre-curve part 4, and at the tip part of the pre-curve part 4. If it is open on the curved inner surface 401 side and spaced from the first virtual plane ⁇ in a direction away from the central axis L1 of the sheath 3 in the radially outward direction of the third lumen 20. Function.
- the knife wire 30 has an incision 34 for incising a treatment target site.
- the incision 34 protrudes from the distal first communication hole 23 and the distal second communication hole 24 and extends between the distal first communication hole 23 and the distal second communication hole 24.
- the knife wire 30 preferably includes a conductive core wire 31 and an insulating coating 32 that covers the core wire 31.
- the knife wire 30 includes a distal fixing member (fixing portion) 37.
- the insulating coating 32 is made of, for example, polytetrafluoroethylene (PTFE), tetrafluoroethylene hexafluoropropylene resin (FEP), polyethylene, polyolefin, polyamide, vinyl chloride, latex, natural rubber, polysulfone, polyphenylsulfone,
- PTFE polytetrafluoroethylene
- FEP tetrafluoroethylene hexafluoropropylene resin
- polyethylene polyolefin
- polyamide polyamide
- vinyl chloride vinyl chloride
- latex latex
- natural rubber polysulfone
- polyphenylsulfone polyphenylsulfone
- the outer surface of the core wire 31 is coated or covered with a resin such as polyetherimide, POM, PEEK, polycarbonate, ABS, or a synthetic resin material thereof.
- the incision 34 is a portion of the entire length of the knife wire 30 that is not covered with the insulating coating 32 (see FIG. 13) and is arranged outside the sheath 3.
- the incision part 34 can incise a living tissue when a high-frequency current supplied to the core wire 31 is passed through the connector 73.
- the incision part 34 desirably has a bending part 36 to be described later in addition to the knife bending part 35.
- the proximal end of the knife wire 30 is fixed to the slider portion 71 of the handle portion 67 in the operation portion 40 (see FIG. 2).
- a knife wire 30 is inserted into the third lumen 20 and fixed to the third lumen 20 by a distal fixing member 37.
- the core wire 31 of the knife wire 30 may be covered with an insulating coating 32 from the proximal end of the knife wire 30 to the proximal end of the incision 34.
- the knife bending portion 35 is located in the region between the distal first communication hole 23 and the distal second communication hole 24 in the virtual coordinate system. Two quadrants Q2 and the inside of the curve in the pre-curve portion 4 are arranged. As shown in FIG. 11, FIG. 12A, FIG. 13, and FIG. 14, a bent portion 36 is formed at the distal end 35 a of the knife bending portion 35. In the knife bending portion 35, a maximum portion 35 c is formed between the distal first series hole 23 and the distal second communication hole 24.
- the maximum portion 35 c of the knife bending portion 35 has a curved shape that connects the distal first continuous hole 23 and the distal second communication hole 24 at a position separated from the first virtual plane ⁇ .
- the maximum portion 35 c of the knife curved portion 35 is closer to the distal first series hole 23 than the center between the distal first series hole 23 and the distal second communication hole 24 in the direction of the central axis L1 of the sheath 3. In position.
- the distal first series through-hole 23 extends from the outer peripheral surface 3c of the pre-curved portion 4 at the position of the curved inner surface 401 in the pre-curved portion 4 (sheath 3) as shown in FIG. 12B. It may be formed by cutting. Specifically, the distal first series passage hole 23 is a notch cut out so as to communicate with the third lumen 20 from the outer peripheral surface 3c of the pre-curve portion 4 at the position of the second quadrant (between 9 o'clock and 12 o'clock). The notch part 29 may be sufficient.
- the distal second communication hole 24 is also formed by cutting away from the outer peripheral surface 3 c of the pre-curved portion 4 at the position of the curved inner surface 401 in the pre-curved portion 4 (sheath 3). May be. Specifically, it may be a cutout portion 29 cut out so as to communicate with the third lumen 20 from the outer peripheral surface 3c of the pre-curve portion 4 at a position in the second quadrant (between 9 o'clock and 12 o'clock).
- the bent portion 36 is bent in a direction away from the first virtual plane ⁇ .
- the knife bending portion 35 contacts the outer peripheral surface 3c of the sheath 3 while intersecting the first virtual plane ⁇ within the range of the second quadrant Q2 in the virtual coordinate system defined by the first virtual plane ⁇ and the second virtual plane ⁇ .
- the maximum portion 35c is located on the knife curved portion 35 so as to reach the distal second communication hole 24 from the distal first series of through holes 23 on a virtual plane substantially parallel to the tangential plane. Curved away from the plane ⁇ .
- the maximum portion 35c may be curved so as to be inclined with respect to the first virtual plane ⁇ and the second virtual plane ⁇ so as to approach the second virtual plane ⁇ as the distance from the bent portion 36 increases.
- the maximum portion 35c may be curved so as to be inclined with respect to the first virtual plane ⁇ and the second virtual plane ⁇ so as to be separated from the second virtual plane ⁇ as the distance from the bent portion 36 increases.
- the maximum portion 35c may extend substantially parallel to the second virtual plane ⁇ . As shown in FIGS.
- the orientation of the distal end 35a of the knife bending portion 35 is as follows. Although the orientation is preferably along the plane perpendicular to the central axis L1 of the sheath 3, it is slightly closer to the proximal side of the sheath 3 than the plane perpendicular to the central axis L1 of the sheath 3 (longitudinal axis of the sheath 3). It may be the orientation that was given.
- the bent portion 36 is distal in the direction substantially parallel to the tangent to the outer peripheral surface 3c of the sheath 3 in the second quadrant Q2 in the virtual coordinate system defined by the first virtual plane ⁇ and the second virtual plane ⁇ .
- the knife wire 30 protruding from the first through hole 23 may have a shape bent with respect to the protruding direction.
- the incision portion 34 may have a bent portion that is bent in a direction away from the first virtual plane ⁇ from the direction in which the distal first through hole 23 opens.
- the bent portion 36 has a bent shape in which the core wire 31 extending from the knife curved portion 35 toward the distal end 30 a of the knife wire 30 is bent toward the distal first through hole 23 in the knife wire 30. This is a portion where the core wire 31 is bent.
- the bent portion 36 may be covered with the insulating coating 32.
- the distal fixing member 37 is provided at the distal end 30 a of the knife wire 30 and is fixed to the inside of the third lumen 20. That is, the distal fixing member 37 fixes the knife wire 30 and the pre-curve part 4 while being inserted into the pre-curve part 4.
- the distal fixing member 37 is connected to the inner peripheral surface 20c of the third lumen 20 in the pre-curved portion 4 by friction, adhesion, or other connection methods. Since the distal fixing member 37 is fixed inside the third lumen 20 (pre-curved portion 4), the distal portion of the knife wire 30 does not come out of the distal first through hole 23.
- the knife wire 30 Since the knife wire 30 is fixed to the pre-curved portion 4, when the knife wire 30 is pulled toward the proximal end side, the drawing portion 5 in the vicinity where the distal first through hole 23 is provided is moved toward the proximal end side. It is attracted and curved more greatly than the curved shape previously imparted to the drawing portion 5. In other words, the knife wire 30 has a function of bending and deforming the drawing unit 5 beyond a predetermined bending angle, in addition to a function of cutting the treatment target site.
- the operation unit 40 illustrated in FIG. 2 is a part that is gripped by the operator, and is disposed at the proximal end 2b of the insertion unit 2 (the proximal end 3b of the sheath 3). Various operations for operating the endoscope treatment tool 1 are input to the operation unit 40.
- the operation unit 40 includes a distal component 41, a flexible coupling 58, a proximal component 61, and a handle 67.
- the distal component portion 41 is a member arranged on the most distal side in the operation portion 40.
- the distal component 41 has a connecting part 45 to the endoscope device 100 and a connecting part 48 to the sheath 3.
- the connecting portion 45 has a hook 46.
- the hook 46 is a locking portion that can be locked to the grip portion 102 provided in the endoscope apparatus 100.
- the hook 46 is an elastic member formed in a C shape so as to surround a part of the outer peripheral surface of the grip portion 102 provided in the endoscope apparatus 100.
- the hook 46 can press the outer surface of the grip portion 102 of the endoscope apparatus 100 by the restoring force that the hook 46 itself restores to a C shape. As a result, the hook 46 can be engaged with the grip portion 102 of the endoscope apparatus 100.
- the connecting portion 48 is a cylindrical portion formed in a substantially cylindrical shape having an inner diameter into which the proximal end 3 b and the vicinity thereof of the sheath 3 can be inserted, and has a first port 49. Further, the connecting portion 48 fixes the operating portion 40 to the sheath 3 at the proximal end 3b of the sheath 3 and its vicinity so that the opening directions of the first port 49 and the inlet portion 8 coincide. As a result, the sheath 3 is prevented from rotating around its longitudinal axis and from coming off from the tubular portion. As a method for fixing the operation unit 40 and the sheath 3, a known fixing method can be appropriately employed.
- the first port 49 is a port that serves as an entrance when the guide wire 80 (see FIG. 25) is introduced into the first lumen 7.
- the first port 49 has an inner opening edge portion 50, an outer opening edge portion 51, a tapered portion 52, and a notch portion 55.
- FIG. 15 is a diagram illustrating a positional relationship between the first port 49 and the operation unit 40 in a state where the endoscope treatment tool 1 is attached to the endoscope apparatus 100.
- FIG. FIG. 16 is a diagram illustrating a positional relationship between the hook 46 and the first port 49 in a state where the endoscope treatment tool 1 is attached to the endoscope apparatus 100.
- the opening of the first port 49 is the bending operation portion of the endoscope device 100 in a state where the operation portion 40 is locked to the grip portion 102 of the endoscope device 100 by a hook (locking portion) 46.
- the positional relationship between the opening of the first port 49 and the hook 46 is determined so as to face the 107a side.
- the bending operation unit 107 a is an operation unit that can actively operate the active bending unit 107 provided at the distal end portion of the endoscope apparatus 100.
- the active bending portion 107 actively bends and deforms the treatment instrument channel disposed in the endoscope insertion portion that is inserted into the body.
- the first port 49 only needs to be formed with a through-hole whose axial direction intersects with a virtual plane that penetrates along the axis substantially parallel to the longitudinal axis of the grip portion 102.
- the endoscope treatment tool 1 may be fixed to the endoscope apparatus 100 so as to extend in a direction substantially parallel to the direction in which the forceps plug 103 of the endoscope apparatus 100 extends.
- the first port 49 is used.
- the axial direction through which the through hole penetrates (the direction of the central axis L3 described later) is a positional relationship of twist with respect to the longitudinal axis of the grip portion 102 of the endoscope apparatus 100. In the present embodiment, as shown in FIG.
- first a straight direction from the surface defined by the inner opening edge 50 toward the surface defined by the outer opening edge 51 (hereinafter referred to as “first”
- the direction of the central axis L3 of the opening of the port 49 is referred to as “the direction of the central axis L3”), as shown in FIG. That is, in the cross section of the operation portion 40 of the endoscope treatment tool 100 shown in FIG. 9A, it passes through the central axis L7 of the first lumen 7 and between the inner opening edge portions 50 and between the outer opening edge portions 51.
- the direction of the central axis L3 of the opening of the first port 49 that passes between them is substantially parallel to the direction of the central axis L4 of the circle surrounding the grip portion 102 in the hook 46.
- the opening of the first port 49 is formed so as to open around the central axis L3 of the opening of the first port 49 orthogonal to the central axis L1 of the sheath 3, as shown in FIG. 9A.
- the central axis L3 of the 49 openings and the central axis L4 of the circle surrounding the grip portion 102 of the endoscope apparatus 100 are substantially parallel.
- the operator grips the grip portion 102 of the endoscope apparatus 100 and operates the endoscope apparatus 100 in a state where the operation section 40 is attached and locked to the endoscope apparatus 100 by the hook 46.
- the opening of the first port 49 is directed in a direction (see FIG. 20) visible to the operator.
- the notch portion 55 is a portion where the notch is formed so as to be substantially C-shaped when the connecting portion 48 is viewed in a cross section orthogonal to the central axis L1 of the sheath 3. It is. Further, the notch 55 communicates with the opening of the first port 49.
- the notch 55 is such that the diameter of the connecting portion 48 is larger than the diameter of the guide wire 80 by a clearance that allows the guide wire 80 to move so that the guide wire 80 can move from the inlet portion 8 to the slit portion 10.
- the gap in the notch portion 55 is provided along the slit portion 10 of the sheath 3.
- the notch 55 has an inner surface 55 c that can contact the outer peripheral surface 3 c of the sheath 3, and holds the outer peripheral surface 3 c of the sheath 3.
- the flexible connecting portion 58 is a member that connects the distal component portion 41 and the proximal component portion 61, and has flexibility.
- the flexible coupling part 58 buffers the twist generated between the distal component part 41 and the proximal component part 61. That is, when the operation unit 40 and the endoscope apparatus 100 are connected by the hook 46, the flexible connection unit 58 is operated by the operation of the operation unit 40 and the operation of the endoscope apparatus 100. And torsion occurring between the proximal component 61 and the proximal component 61 is buffered.
- the flexible connecting portion 58 has a communication passage 59 for feeding liquid and a communication passage 60 for knife wire inside.
- the communication passage 59 for liquid feeding communicates with the second lumen 15.
- the knife wire communication passage 60 communicates with the third lumen 20.
- the proximal component 61 has a second port 62.
- the second port 62 is a port to which a syringe containing liquid is connected.
- a syringe filled with the contrast agent is connected to the second port 62.
- the proximal end 62b of the second port 62 has a connector structure that can be connected to a syringe having a luer lock structure.
- the distal end 62 a of the second port 62 communicates with a liquid-feeding communication passage 59 (see FIG. 7) formed in the flexible connection portion 58.
- the handle fixing portion 64 is provided to fix the handle portion 67 to the flexible connecting portion 58 in a predetermined connection state.
- the knife wire passage 66 is a passage through which the knife wire 30 is inserted so as to be movable forward and backward, communicating with the knife wire connecting passage 60 in the flexible connecting portion 58.
- the handle portion 67 is a portion where an input for the operator to operate the knife wire 30 is performed.
- the handle portion 67 has a shaft portion 68 and a slider portion 71.
- the shaft portion 68 is fixed to the handle fixing portion 64 of the proximal component portion 61.
- the slider part 71 is slidably connected along the longitudinal axis of the shaft part 68.
- the shaft portion 68 has a rod-shaped portion 69 and a ring portion 70.
- the rod-like portion 69 is coaxial with the center axis L5 of the handle fixing portion 64 or extends linearly along the center axis L5 of the handle fixing portion 64.
- the ring part 70 is formed at the proximal end of the rod-like part 69.
- the ring part 70 is an annular part through which an operator can pass a finger.
- the slider portion 71 may include a connector 73 that can be connected to a high-frequency power supply device and a finger hook portion 74. Two rings 75 through which an operator's finger can be passed are formed in the finger hook portion 74.
- the connector 73 is electrically connected to the proximal end of the knife wire 30.
- the finger hook portion 74 can be used to advance and retract the knife wire 30 by passing an operator's finger through the two rings 75 and 70.
- FIG. 17 is a perspective view of a treatment instrument attachment assisting tool 90 that can be attached to the endoscope apparatus 100.
- FIG. 18 is a partial cross-sectional view showing the internal structure of the treatment instrument attachment assisting tool 90.
- the treatment instrument attachment assisting tool 90 includes an assisting instrument main body 91, a discharge pipe 92, and a plug 93.
- the auxiliary tool main body 91 has a cylindrical shape that can be fixed to the forceps plug 103 of the endoscope apparatus 100.
- the discharge pipe 92 is in communication with the internal space of the auxiliary tool main body 91.
- the plug 93 is disposed on the extension line of the central axis of the treatment instrument channel 104 from the proximal opening of the treatment instrument channel 104 in the forceps plug 103.
- the auxiliary tool body 91 has a mounting structure that can be connected to the forceps plug 103 in a watertight manner.
- the discharge pipe 92 can be connected to a pipe line connected to a drainage container (not shown).
- the plug 93 is a flexible member having an opening or a cut that is close to the outer peripheral surface 3 c of the sheath 3.
- the treatment tool attachment assisting tool 90 is fixed to the forceps plug 103 of the endoscope apparatus 100 before the treatment tool for endoscope 1 is inserted into the treatment tool channel 104 (see FIG. 20). ).
- the liquid that has flowed back through the treatment instrument channel 104 of the endoscope apparatus 100 from the distal side toward the proximal side is mainly a discharge pipe 92. Flow into.
- FIG. 2 shows an example in which the endoscope treatment tool 1 according to the present embodiment is used together with the endoscope apparatus 100.
- FIG. 19 is a diagram illustrating a process during use of the endoscope treatment tool 1.
- a side-view type endoscope apparatus 100 suitable for observing the duodenal papilla PV is used.
- the side-view type endoscope apparatus 100 includes, for example, a cylindrical member 101, a grip portion 102, a forceps plug 103, a treatment instrument channel 104, a raising base 105, and an imaging unit 106.
- the cylindrical member 101 is a part inserted into the body.
- the grip portion 102 is disposed at the proximal end of the cylindrical member 101.
- the forceps plug 103 is disposed on a part of the grip portion 102.
- the treatment instrument channel 104 communicates with the forceps plug 103 and is disposed inside the cylindrical member 101.
- the elevator 105 is used to change the direction of the treatment instrument or the like protruding from the treatment instrument channel 104 at the distal end 104a of the treatment instrument channel 104 in a direction orthogonal to the central axis L8 of the cylindrical member 101. It is provided so as to be movable in the opening from which the tool is projected.
- the imaging field is directed to the imaging unit 106 in a direction orthogonal to the central axis L8 of the cylindrical member 101.
- the imaging unit 106 is provided adjacent to an opening from which the treatment tool projects.
- the endoscope treatment tool 1 includes a mode in which an operator of the endoscope apparatus 100 and an operator of the endoscope treatment tool 1 are different from each other, and a grip portion of the endoscope apparatus 100
- the hook 46 is connected to 102 so that one operator can use the endoscope apparatus 100 by operating the endoscope treatment tool 1 in an appropriate manner.
- the endoscope treatment tool 1 A case of using the endoscope treatment tool 1 will be described.
- the operator performs a known procedure on the endoscope apparatus 100 as a treatment target site as shown in FIG. Guide to the PV and observe the treatment target site using the endoscope apparatus 100.
- the treatment tool attachment assisting tool 90 may be attached to the forceps plug 103 or may not be attached.
- FIG. 20 is a diagram of a state in which the endoscope treatment tool 1 is attached to the endoscope apparatus 100 as seen from the viewpoint of the operator of the endoscope apparatus 100.
- the hook 46 is attached to the grip portion 102 of the endoscope apparatus 100 with the treatment tool attachment assisting tool 90 fixed to the forceps plug 103.
- the sheath 3 of the endoscope treatment tool 1 according to the present embodiment is inserted into the treatment tool channel 104 (see FIG. 1) of the endoscope apparatus 100 via the treatment tool attachment assisting tool 90.
- the operation unit 40 of the endoscope treatment tool 1 is connected to the endoscope apparatus 100 by a hook 46.
- the operator of the endoscope treatment tool 1 holds the endoscope apparatus 100 in, for example, the left hand and the sheath 3 in, for example, the right hand, and moves the sheath 3 in and out of the forceps plug 103 of the endoscope apparatus 100. Can do.
- FIG. 21 is a diagram illustrating a process during use of the endoscope treatment tool 1.
- FIG. 22 is a cross-sectional view showing a state where the flexible region of the sheath 3 is located on the inner surface of the treatment instrument channel at the curved portion.
- FIG. 23 is a schematic diagram showing the endoscope treatment tool 1 according to the present embodiment reflected in an endoscope image captured using the endoscope apparatus 100. As shown in FIG. 21, when the operator operates the sheath 3, the distal end 3a of the sheath 3 protrudes from the distal end 104a (opening) of the treatment instrument channel 104, and as shown in FIG. Images are taken by the imaging unit 106 of the endoscope apparatus 100.
- the operator passes the high-rigidity region 25 through the treatment instrument channel 104 bent by the active bending portion 107 of the endoscope apparatus 100.
- the curved shape of the pre-curved portion 4 is imitated in the treatment instrument channel 104 curved by the active bending portion 107 or the raising base 105.
- the pre-curve part 4 including the high-rigidity region 25 is passively rotated about the central axis L1.
- the proximal slit portion 10p the region closer to the proximal side than the proximal end of the pre-curved portion 4 is easily twisted.
- the high-rigidity region 25 in the pre-curve portion 4 passively rotates within the treatment instrument channel 104 so as to follow the curved shape of the treatment instrument channel 104 that is curved by the active bending portion 107 of the endoscope apparatus 100. Furthermore, the rotational resistance due to the region closer to the proximal side than the high-rigidity region 25 can be reduced. Thereafter, the operator causes the high-rigidity region 25 to protrude from the distal end 104a of the treatment instrument channel 104 of the endoscope apparatus 100.
- the high rigidity region 25 including the drawing unit 5 is caused to enter the imaging field of the imaging unit 106 of the endoscope apparatus 100. Since the rotational resistance due to the region proximal to the high-rigidity region 25 is reduced, the high-rigidity region 25 is projected from the distal end 104a of the treatment instrument channel 104 of the endoscope apparatus 100, and then the drawing unit 5 is used as it is.
- the incision 34 projecting from the distal first through hole 23 and the distal second communication hole 24 is directed in the direction closer to the 11 o'clock direction than the 12 o'clock direction. Easily protruding.
- the endoscope treatment tool 1 according to the present embodiment is applied to the side-view type endoscope apparatus 100 to incise the duodenal papilla PV, it is possible to incise a position with less bleeding.
- the proximal end 3b of the sheath 3 is not actively rotated about the central axis L1 of the sheath 3 as a rotation center, the high-rigidity region 25 is curved in the active bending portion 107 and the raising base 105 of the endoscope apparatus 100.
- the distal end 3a of the sheath 3 becomes a position curved in the 12 o'clock direction in the endoscopic image.
- the outer peripheral surface of the copying deformation unit 6 of the pre-curve unit 4 is pressed by the elevator 105 as shown in FIG. 21.
- the position of the pressed surface 4x pressed by the raising base 105 in the outer peripheral surface of the copying deformation portion 6 of the pre-curve portion 4 is the position of the outer peripheral surface of the copying deformation portion 6 of the pre-curve portion 4.
- the flexible region 26 is located at a site where the treatment instrument channel 104 is curved by the active bending unit 107 of the endoscope apparatus 100. positioned.
- the copying deformable portion 6 is pressed by the inner surface of the treatment instrument channel 104 having a shape bent by the active bending portion 107. Since the distal deformation portion 6d is formed in the copying deformation portion 6, when an external force is applied to the outer peripheral surface of the copying deformation portion, the contour shape of the copying deformation portion 6 in the cross section orthogonal to the central axis L1 of the sheath 3 is Easy to deform.
- the formation of the distal slit portion 10d reduces the resistance caused by deformation when the contour shape of the copying deformable portion 6 is to be deformed into an elliptical shape. Therefore, when the outer peripheral surface of the copying deformable portion 6 is pressed by the inner surface of the treatment instrument channel 104, the contour shape of the copying deforming portion 6 becomes slightly elliptical.
- the copying deforming portion 6 is slightly elliptical, the copying deforming portion 6 is difficult to rotate in the treatment instrument channel 104 bent by the active bending portion 107 of the endoscope apparatus 100. Therefore, the incision 34 projecting from the distal first through hole 23 and the distal second communication hole 24 can easily maintain a state of projecting in a direction closer to 11 o'clock than 12 o'clock. This effect is remarkable when an external force such as a reaction force from the tissue is received.
- the incision portion 34 Protrudes from the distal first through hole 23 and the distal second communication hole 24 in a direction closer to the 11 o'clock direction than the 12 o'clock direction.
- the operator advances the sheath 3 in the treatment instrument channel 104 while confirming that the incision 34 is directed in the direction between 11 o'clock and 12 o'clock on the endoscopic image.
- the distal end 3a of the sheath 3 reaches the opening of the duodenal papilla PV and is inserted into the duodenal papilla PV.
- the operator When positioning for inserting the distal end 3 a of the sheath 3 into the duodenal papilla PV is difficult, the operator inserts the guide wire 80 into the first lumen 7 from the first port 49 of the operation unit 40.
- the distal end 80 a of the guide wire 80 may protrude from the distal end 7 a of the first lumen 7.
- the operator first inserts the distal end 80a of the guide wire 80 into the duodenal papilla PV, and then the operator inserts the distal end 3a of the sheath 3 along the guide wire 80 into the duodenum. Can be inserted into the nipple PV.
- the operator discharges the contrast agent from the second port 62 and passes the contrast agent into the bile duct through the duodenal papilla PV from the distal outlet 17 of the second lumen 15 of the sheath 3. It may be introduced.
- the contrast agent By introducing the contrast agent, the operator can easily grasp the travel of the bile duct, the presence or absence of stones, the position and size thereof, and the like.
- FIG. 24 is a schematic diagram showing an endoscopic image in a process of treatment using the endoscope treatment tool 1.
- the operation portion 40 is in a state where the distal portion (drawing portion 5) of the sheath 3 is disposed in the duodenal papilla PV by a predetermined length. Is moved in the direction of the central axis of the rod-shaped portion 69 of the shaft portion 68, that is, in the direction of the central axis L5 of the handle fixing portion 46 (see FIG. 2).
- the knife wire 30 moves toward the proximal end of the knife wire 30, and the distal end 30 a of the knife wire 30 moves through the portion of the distal first through hole 23 of the sheath 3 in the proximal direction.
- the force to make arises.
- the portion of the sheath 3 near the distal end 3 a is bent and deformed between the distal first series hole 23 and the distal second communication hole 24.
- the incision 34 of the knife wire 30 is stretched in an arc shape with respect to the sheath 3.
- the knife bending portion 35 (see FIG. 12A) is arranged in the second quadrant Q2 in the virtual coordinate system. Therefore, when the bending direction of the pre-curve unit 4 captured by the imaging unit 106 as an endoscopic image is set to 12 o'clock, the knife bending unit 35 is located at a position deviated closer to 11 o'clock than 12 o'clock. It contacts the opening of the nipple PV.
- the operator supplies a high frequency current from the high frequency power supply device to the knife wire 30 through the connector 73 of the operation portion 40.
- the tissue in contact with the knife bending portion 35 is incised by the high-frequency current.
- the knife bending portion 35 is bent in a natural state where no external force is applied to the knife bending portion 35.
- the knife bending portion 35 is gradually deformed from a curved shape in a natural state to a linear shape by moving the knife wire 30 toward the proximal end 68 b of the shaft portion 68 by the slider portion 71.
- the knife bending portion 35 is gradually deformed from a curved shape in a natural state to a linear shape along a linear direction connecting the distal first series through hole 23 and the distal second communication hole 24.
- the curvature radius of the pre-curve portion 4 is set large, the knife wire 30 is gradually deformed from a linear shape to a curved shape.
- the bending state of the knife bending portion 35 is changed by the movement of the knife wire 30 using the slider portion 71.
- the duodenal papilla PV Since the position avoiding the main blood vessel in the duodenal papilla PV is set to be reflected from the 11 o'clock direction on the endoscopic image, the duodenal papilla PV is incised by the knife bending portion 35 at this 11 o'clock direction position. An incision can be made with a small amount of bleeding due to incision of the duodenal papilla PV.
- the operator connects a syringe containing a contrast medium to the second port 62 as necessary, and the contrast medium is transferred from the second port 62 through the second lumen 15 to the duodenal papilla PV. Discharge inside.
- the route to the calculus to be removed can be grasped on the X-ray image by the contrast medium discharged into the duodenal papilla PV.
- the opening of the first port 49 is directed to the proximal side of the endoscope apparatus 100. Therefore, the operator can insert the distal end of the guide wire 80 toward the first lumen 7 in a state where the first lumen 7 of the sheath 3 is visible through the first port 49.
- the first port 49 has a long hole shape that is long in the direction of the long axis L2 extending in the linear direction connecting the distal end 48a of the connecting portion 48 to the sheath 3 and the proximal end 48b of the connecting portion 48 to the sheath 3. It has a shaped opening.
- the guide wire 80 inserted into the first port 49 can be advanced and retracted in a direction substantially along the central axis L7 of the first lumen 7 (a direction slightly inclined with respect to the central axis L7 of the first lumen 7). It is.
- the guide wire 80 can be easily advanced and retracted with the right hand of the operator, and the occurrence of buckling of the guide wire 80 can be prevented.
- the right hand changes the sheath 3 from the guide wire 80 and inserts the guide wire 80 into the first port 49 with the right hand. It is easy to advance and retreat according to the endoscope treatment tool 1 according to the present embodiment.
- the already inserted guide wire 80 is used.
- the angle-type guide wire 80 may be replaced.
- the operator projects the guide wire 80 from the distal end 3a of the sheath 3 and guides the guide wire 80 to a desired position in the bile duct. At this time, if necessary, the operator rotates the guide wire 80 around its central axis, so that the distal end 80a of the guide wire 80 is inserted into a desired branch at the bifurcation of the bile duct. 80 may be moved.
- FIG. 27 is a diagram illustrating a process during use of the endoscope treatment tool 1. As shown in FIG. 27, the guide wire 80 is inserted, for example, until the distal end 80a of the guide wire 80 is located at a position that has advanced to some depth beyond the calculus to be removed from the bile duct.
- FIG. 28 is a diagram illustrating a process of removing the endoscope treatment tool 1 from the endoscope apparatus 100 while leaving the guide wire 80 attached to the endoscope treatment tool 1.
- FIG. 29 is a diagram illustrating a process of separating the sheath 3 and the guide wire 80 of the endoscope treatment tool 1.
- FIG. 30 is a diagram illustrating an example of a treatment performed after the endoscope treatment tool 1 is removed. After the guide wire 80 reaches a predetermined position, the endoscope treatment tool 1 is removed with the guide wire 80 left in the body. This is performed in order to introduce a known endoscopic stone removing tool (basket forceps, balloon or the like) for removing a stone into the bile duct instead of the endoscope treatment tool 1 according to the present embodiment. .
- a known endoscopic stone removing tool basic forceps, balloon or the like
- the notch part 55 is passed through.
- the guide wire 80 is removed.
- the operator does not change the position of the distal end 80 a of the guide wire 80, and moves away from the notch 55 from the proximal end 55 b of the notch 55 of the first port 49 through the inside of the notch 55.
- the guide wire 80 is moved relative to the first port 49 to the distal end 55a. In the process in which the guide wire 80 passes through the notch 55 of the first port 49, the guide wire 80 is gradually taken out of the sheath 3 from the guide wire housing portion 9 through the slit portion 10.
- the operator moves the sheath 3 toward the proximal end of the treatment instrument channel 104 while supporting the guide wire 80 so that the position of the guide wire 80 does not move.
- the sheath 3 is gradually removed from the guide wire 80.
- the operator When the outlet 12 (see FIG. 10) of the first lumen 7 in the sheath 3 reaches the position of the forceps plug 103, the operator resists the force that the guide wire 80 tries to move toward the proximal end 80b. While supporting the guide wire 80, the sheath 3 is moved toward the proximal end 80 b of the guide wire 80. The operator pulls out the outlet 12 of the sheath 3 from the forceps plug 103 without changing the position of the guide wire 80 in the body. Thereafter, the operator moves the distal portion of the sheath 3 where the outlet portion 12 of the sheath 3 is disposed toward the proximal end 80 b of the guide wire 80 and removes the sheath 3 from the guide wire 80.
- the operator attaches the above-described known endoscope stone removing tool (for example, the basket forceps 120 shown in FIG. 30) to the guide wire 80, and this endoscope stone.
- the removal tool is guided through the treatment tool channel 104 of the endoscope apparatus 100 to the stone to be removed.
- the operator who operates the endoscope treatment tool 1 holds the operation unit 40 of the endoscope treatment tool 1 in one hand, and the guide wire 80 to the opening of the first port 49 with the opposite hand. And the position of the guide wire 80 can be adjusted.
- the operator of the endoscope apparatus 100 and the operator of the endoscope treatment tool 1 coordinate each other's operations so that the endoscope apparatus 100 and the endoscope treatment tool 1 can be operated by one operator. It is possible to proceed with the same treatment as in the above example operated by.
- the endoscope treatment tool 1 has the first lumen 7 through the opening of the first port 49 when the hook 46 is attached to the grip portion 102 of the endoscope apparatus 100. Since the first port 49 is arranged in such a direction that the inner surface 7c can be seen, the hook 46 is attached to the grip portion 102 of the endoscope apparatus 100, and the endoscope apparatus 100 and the endoscope treatment tool 1 are used alone. In this case, the guide wire 80 can be easily inserted into the opening of the first port 49.
- the first port 49 is arranged in the above-described direction, so that the guide wire 80 is inserted into the first lumen 7 from the opening of the first port 49.
- the guide wire 80 can be easily advanced and retracted and rotated by a single operator while holding the grip portion 102 of the endoscope apparatus 100.
- the opening of the first port 49 is an oval opening, even if it is an angle type guide wire 80 having a curved distal end, the distal end can be easily introduced into the first lumen 7.
- the sheath 3 is configured to have the first lumen 7 as the guide wire lumen and the second lumen 15 as the liquid feeding lumen in addition to the third lumen 20.
- Lumen is not an essential component.
- At least the above-described distal first through hole 23 and the distal second communication hole 24 are formed in the third lumen, and the incision 34 has the above-described configuration with the third lumen 20 and the distal first through hole 23. And what is necessary is just the structure inserted in the distal 2nd communicating hole 24.
- FIG. below the modification 1 of the treatment tool 1 for endoscopes which concerns on this embodiment is shown.
- FIG. 31 is a schematic diagram showing the configuration of this modification.
- the position of the distal end of the proximal slit portion 10 p may be at a position spaced from the base end 4 b of the pre-curved portion 4.
- the distal slit portion 10d does not exist or does not communicate with the distal slit portion 10d.
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Abstract
Description
前記近位スリット部は、前記プリカーブ部の基端から前記入口部まで連続的に形成されていてもよい。
図1に示すように、本実施形態に係る内視鏡用処置具1は、体内において生体組織の切開をするために内視鏡装置100とともに使用される医療器具である。内視鏡用処置具1は、内視鏡装置100と組み合わされた状態で切開システム110(内視鏡処置システム)を構成する。本実施形態に係る内視鏡装置100は、能動湾曲部107(図1参照)を有している。能動湾曲部107は、湾曲操作部107aによって湾曲動作される。
さらに、第一ルーメン7は、第三ルーメン20に対して周方向に離間した位置にあるとも言える。なお、本実施形態では、ガイドワイヤ80を移動させる通路として第一ルーメン7を使用することを例示したが、ガイドワイヤ80に限らず別の処置具を移動させる通路として使用しても良い。
好ましくは、近位スリット部10pは、プリカーブ部4の基端から入口部8まで延びており、入口部8の開口と連通している。入口部8は、シース3の近位端側においてガイドワイヤ収容部9の内部からシース3の外周面3cまで連通するように開口されており、ガイドワイヤ80を導入可能である。
ガイドワイヤ収容部9は、第三ルーメン20からシース3の中心軸周りの周方向に離間した位置にシース3の長手軸に沿って形成されている。
スリット部10は、更に、遠位スリット部10dを有しても良い。遠位スリット部10dは、図5Bに示すように、プリカーブ部4の基端から遠位側に向かってプリカーブ部4の途中部分まで延び、ガイドワイヤ収容部9とプリカーブ部4における湾曲形状の外側の外周面402とが連通するようにシース3の中心軸に沿って形成されていればよい。具体的には、遠位スリット部10dは、倣い変形部6の外周面と第一仮想平面αとが交差する位置に、シース3の中心軸L1に沿って形成されている。遠位スリット部10dの遠位端10aの位置は、ドローイング部5の基端よりも近位側の位置であって、且つ倣い変形部6上の任意の位置(倣い変形部6の途中部分)または倣い変形部6の先端である。遠位スリット部10dの近位端の位置は、プリカーブ部4の基端である。好ましくは、遠位スリット部10dは、近位スリット部10pと連通している。遠位スリット部10dが形成された倣い変形部6は、外力が加わると、シース3の中心軸L1に直交する断面において倣い変形部6の輪郭形状は楕円形状に変形しやすい剛性を有する。
シース3の中心軸L1方向における入口部8の長さは、第一ルーメン7におけるガイドワイヤ収容部9(第一ルーメン7)の内径よりも大きい。すなわち、入口部8は、シース3の中心軸L1方向に長い長穴形状を有する。なお、入口部8の形状は、矩形形状であってもよい。入口部8の形状が矩形形状であると、入口部8を形成する加工が容易である。シース3の周方向における入口部8の左右端8c(周方向の両端)は、ガイドワイヤ収容部9からシース3の外周面3cへ向かって入口部8の開口面積が漸次大きくなるように広がるテーパー形状を有していてもよい(図9A参照)。
プリカーブ部4における第二ルーメン15は、上記の仮想座標系における第一象限Q1に位置している。
第三ルーメン20は、ナイフワイヤ収容部22(図14参照)と、遠位第一連通孔23と、遠位第二連通孔24とを有する。
ナイフ湾曲部35は、第一仮想平面α及び第二仮想平面βによって規定される仮想座標系における第二象限Q2の範囲内で第一仮想平面αと交差してシース3の外周面3cに接する接平面に対して略平行な仮想平面上を、遠位第一連通孔23から遠位第二連通孔24へ達するように、且つ、極大部35cがナイフ湾曲部35上において最も第一仮想平面αから離れるように、湾曲している。
たとえば、極大部35cは、屈曲部36から離れるにしたがって第二仮想平面βに近づくように第一仮想平面α及び第二仮想平面βに対して傾斜するように湾曲していてもよい。この他、極大部35cは、屈曲部36から離れるにしたがって第二仮想平面βから離れるように第一仮想平面α及び第二仮想平面βに対して傾斜するように湾曲していてもよい。極大部35cは、第二仮想平面βに略平行に延びていてもよい。
図11及び図12Aに示すように、シース3の中心軸L1に対して直交する方向からナイフ湾曲部35の遠位端35aを見たときに、ナイフ湾曲部35の遠位端35aの向きは、シース3の中心軸L1に直交する面に沿った向きであることが好ましいが、シース3の中心軸L1(シース3の長手軸)に直交する面よりもややシース3の近位側に向けられた向きでもよい。
屈曲部36は、ナイフワイヤ30において、ナイフ湾曲部35からナイフワイヤ30の遠位端30aへ向かって延びる芯線31が遠位第一連通孔23へ向けて屈曲された屈曲形状となるように芯線31が折り曲げられた部位である。屈曲部36は、絶縁被膜32に覆われていてもよい。
操作部40は、遠位構成部41と、可撓連結部58と、近位構成部61と、ハンドル部67とを有する。
本実施形態では、図8に示すように、第一ポート49の開口において内側開口縁部50により規定される面から外側開口縁部51により規定される面へ向かう直線方向(以下、「第一ポート49の開口の中心軸L3方向」と称する。)は、図16に示すように、フック46において把持部102を囲む円の中心軸L4方向とは、略平行である。すなわち、図9Aに示された内視鏡用処置具100の操作部40の断面において、第一ルーメン7の中心軸L7を通り、内側開口縁部50同士の間と外側開口縁部51同士の間とを通る第一ポート49の開口の中心軸L3方向は、フック46において把持部102を囲む円の中心軸L4方向とは、略平行である。その結果、第一ポート49の開口は、図9Aに示すように、シース3の中心軸L1と直交する第一ポート49の開口の中心軸L3を中心として開口するように形成され、第一ポート49の開口の中心軸L3と、内視鏡装置100の把持部102を囲む円の中心軸L4とが略平行である。この結果、フック46によって操作部40が内視鏡装置100に取り付けられ、係止された状態で、操作者が内視鏡装置100の把持部102を把持して内視鏡装置100を操作する通常の位置関係において第一ポート49の開口は、操作者に視認可能な方向(図20参照)に向けられる。
図1及び図19に示すように、本実施形態では、十二指腸乳頭PVを観察するのに適した側視型の内視鏡装置100が使用される。
側視型の内視鏡装置100は、たとえば、筒状部材101と、把持部102と、鉗子栓103と、処置具チャンネル104と、起上台105と、撮像部106とを備える。筒状部材101は体内に挿入される部分である。把持部102は、筒状部材101の近位端に配されている。鉗子栓103は、把持部102の一部に配されている。処置具チャンネル104は、鉗子栓103と連通され筒状部材101の内部に配されている。起上台105は、処置具チャンネル104の遠位端104aにおいて処置具チャンネル104から突出される処置具等の向きを筒状部材101の中心軸L8に対して直交する方向へと変えるために、処置具が突出される開口部内を移動可能に設けられている。撮像部106は、筒状部材101の中心軸L8に対して直交する方向へ撮像視野が向けられている。撮像部106は、処置具が突出される開口部に隣接して設けられている。
まず、内視鏡用処置具1が内視鏡装置100に取り付けられていない状態で、操作者は、図19に示すように公知の手技により内視鏡装置100を処置対象部位である十二指腸乳頭PVまで案内し、内視鏡装置100を用いて処置対象部位を観察する。このとき、処置具取付補助具90は鉗子栓103に取り付けられていてもよいし、取り付けられていなくてもよい。
処置対象部位の観察後、図20に示すように、処置具取付補助具90が鉗子栓103に固定された状態で、フック46が内視鏡装置100の把持部102に取り付けられる。さらに、内視鏡装置100の処置具チャンネル104(図1参照)に処置具取付補助具90を介して本実施形態に係る内視鏡用処置具1のシース3が挿入される。内視鏡用処置具1の操作部40は内視鏡装置100に対してフック46により連結されている。そのため、内視鏡用処置具1の操作者は、内視鏡装置100をたとえば左手、シース3をたとえば右手に持って、内視鏡装置100の鉗子栓103に対してシース3を出し入れする操作ができる。
図21に示すように、操作者によるシース3の操作により、シース3の遠位端3aは、処置具チャンネル104の遠位端104a(開口部)から突出され、図23に示すように、内視鏡装置100の撮像部106により撮像される。
側視型の内視鏡装置100を利用した十二指腸乳頭PVに対するESTの手技においては、内視鏡装置100が撮像した画像を、画像の上部中央を12時とする時計の文字盤と見立てた場合、内視鏡装置100が撮像した画像における11時と12時との間に十二指腸乳頭PVの切開対象部位が写るように撮像部の向きを合わせる。この状態で、十二指腸乳頭PVの開口部から十二指腸乳頭PVを拡張するように切開することで、十二指腸乳頭PVにおいて結石等を通過させるための通路を形成する。
その後、操作者は、高剛性領域25を内視鏡装置100の処置具チャンネル104の遠位端104aから突出させる。
図24は、内視鏡用処置具1を用いた処置の一過程における内視鏡画像を示す模式図である。
図24に示すように、シース3が十二指腸乳頭PV内に導入されたあと、シース3の遠位部分(ドローイング部5)が所定長さだけ十二指腸乳頭PV内に配された状態で、操作部40におけるスライダ部71を軸部68の近位端68b方向へ軸部68の棒状部69の中心軸方向、すなわち、ハンドル固定部46の中心軸L5方向(図2参照)へ移動させる。これにより、ナイフワイヤ30は、ナイフワイヤ30の近位端方向へと移動し、ナイフワイヤ30の遠位端30aはシース3の遠位第一連通孔23の部分を近位方向へと移動させる力が生じる。これにより、シース3の遠位端3a近傍の部分は、遠位第一連通孔23と遠位第二連通孔24との間で湾曲変形される。また、ナイフワイヤ30の切開部34は、シース3に対して弓状に張られる。
十二指腸乳頭PVにおける主要な血管を避けた位置が内視鏡画像上の11時方向よりに映るように設定し、この11時方向の位置でナイフ湾曲部35により十二指腸乳頭PVが切開されるので、十二指腸乳頭PVの切開による出血量が少ない状態で切開ができる。
すなわち、操作者が内視鏡装置100を左手に持ちシース3を右手で進退させた状態から、右手はシース3からガイドワイヤ80に持ち替えてガイドワイヤ80を右手で第一ポート49に挿入したり進退させたりすることが、本実施形態に係る内視鏡用処置具1によれば容易である。
ガイドワイヤ80が所定の位置に達した後、体内にガイドワイヤ80が残された状態で内視鏡用処置具1が抜去される。これは、結石を除去するための公知の内視鏡用結石除去具(バスケット鉗子やバルーン等)を本実施形態に係る内視鏡用処置具1に代えて胆管内に導入するために行われる。
この例では、内視鏡用処置具1を操作する操作者は、内視鏡用処置具1の操作部40を片手に持ち、反対の手で、第一ポート49の開口へのガイドワイヤ80の挿入及びガイドワイヤ80の位置調整をすることができる。内視鏡装置100の操作者と内視鏡用処置具1の操作者とは、互いの操作を協調させることで、内視鏡装置100と内視鏡用処置具1とを一人の操作者が操作する上記の例と同様の処置を進めることができる。
以下に、本実施形態に係る内視鏡用処置具1の変形例1を示す。
本発明の第一実施形態の変形例1について説明する。図31は、本変形例の構成を示す模式図である。図31に示すように、たとえば、近位スリット部10pの遠位端の位置は、プリカーブ部4の基端4bから離間した位置にあってもよい。この場合、遠位スリット部10dは存在しないか、もしくは、遠位スリット部10dとは連通していない。
2 挿入部
3 シース
3c 外周面
4 プリカーブ部
7 第一ルーメン(ガイドワイヤルーメン)
10 スリット部
20 第三ルーメン(ナイフワイヤルーメン)
23 第一連通孔
24 第二連通孔
34 切開部
80 ガイドワイヤ
107 能動湾曲部
α 第一仮想平面(仮想平面)
Claims (4)
- 長手軸に沿って中心軸を有するシースと、
前記シースの遠位部に設けられ、前記シースの前記中心軸を含む仮想平面に沿って前記シースが湾曲する湾曲形状への復元力を有するプリカーブ部と、
前記プリカーブ部の先端部で前記仮想平面から離間した位置に中心軸を有し、前記シースの中心軸に沿って形成されたナイフワイヤルーメンと、
前記シースの中心軸に対して前記ナイフワイヤルーメンの位置から径方向外方に離間する方向に開口して前記プリカーブ部における湾曲形状の内側の外周面と前記ナイフワイヤルーメンとを連通する第1連通孔と、
前記シースの中心軸に対して前記ナイフワイヤルーメンの位置から径方向外方に離間する方向に開口して前記第1連通孔よりも前記プリカーブ部の近位端部側で前記プリカーブ部における湾曲の内側の外周面と前記ナイフワイヤルーメンとを連通する第2連通孔と、
前記第1連通孔および前記第2連通孔から突出されて前記第1連通孔および前記第2連通孔の間を跨って延設されて組織を切開可能なワイヤ状の切開部と、
前記切開部の先端部に設けられ、前記ナイフワイヤルーメン内に挿入された状態で前記切開部と前記ナイフワイヤルーメンとを固定する固定部と、
前記ナイフワイヤルーメンから前記シースの中心軸周りの周方向に離間した位置に前記シースの長手軸に沿って形成されてガイドワイヤを挿入可能なガイドワイヤ収容部と、
前記プリカーブ部の基端よりも近位側の領域において前記ガイドワイヤ収容部から前記シースの外周面まで連通された近位スリット部と、
前記プリカーブ部の基端から遠位側に向かって前記プリカーブ部の途中部分まで前記ガイドワイヤ収容部と前記プリカーブにおける湾曲の外側の外周面が連通された遠位スリット部と、
前記シースの遠位端から前記遠位スリット部の遠位端まで延び、前記プリカーブ部の基端よりも近位側の領域に対して相対的に捻れ剛性が高い高剛性領域と、
を有する内視鏡用処置具。 - 前記シースの近位端側には前記ガイドワイヤ収容部の内部から前記シースの外周面まで連通するように開口されて前記ガイドワイヤを導入可能な入口部が形成され、
前記近位スリット部は、前記プリカーブ部の基端から前記入口部まで連続的に形成されている
請求項1に記載の内視鏡用処置具。 - 長手軸に沿って中心軸を有するシースと、
前記シースの遠位部に設けられ、前記シースの中心軸を含む仮想平面に沿って前記シースが湾曲する湾曲形状への復元力を有するプリカーブ部と、
前記プリカーブ部の先端部で前記仮想平面から離間した位置に中心軸を有し、前記シースの中心軸に沿って形成されたナイフワイヤルーメンと、
前記シースの中心軸に対して前記ナイフワイヤルーメンの位置から径方向外方に離間する方向に開口して前記プリカーブ部における湾曲形状の内側の外周面と前記ナイフワイヤルーメンとを連通する第1連通孔と、
前記シースの中心軸に対して前記ナイフワイヤルーメンの位置から径方向外方に離間する方向に開口して前記第1連通孔よりも前記プリカーブ部の近位端部側で前記プリカーブ部における湾曲の内側の外周面と前記ナイフワイヤルーメンとを連通する第2連通孔と、
前記第1連通孔および前記第2連通孔から突出されて前記第1連通孔および前記第2連通孔の間を跨って延設されて組織を切開可能なワイヤ状の切開部と、
前記切開部の先端部に設けられ、前記ナイフワイヤルーメン内に挿入された状態で前記切開部と前記ナイフワイヤルーメンとを固定する固定部と、
前記ナイフワイヤルーメンから前記シースの中心軸周りの周方向に離間した位置に前記シースの長手軸に沿って形成されてガイドワイヤを挿入可能なガイドワイヤ収容部と、
前記プリカーブ部の基端から遠位側に向かって前記プリカーブ部の途中部分まで前記ガイドワイヤ収容部と前記プリカーブにおける湾曲の外側の外周面が連通するように前記シースの中心軸に沿って形成された遠位スリット部と、
を有する内視鏡用処置具。 - 前記遠位スリット部を含む前記プリカーブ部の近位領域は、前記内視鏡装置の能動湾曲部によって湾曲変形される処置具チャンネルの内壁から力を受けることによって、前記シースの中心軸に対して直交する断面において前記遠位スリット部を含む前記プリカーブ部の近位領域の輪郭形状は円形から楕円形に変形する剛性を有する
請求項3に記載の内視鏡用処置具。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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EP15758398.0A EP3115012A4 (en) | 2014-03-04 | 2015-03-02 | Treatment instrument for endoscope |
JP2015546356A JP5911652B2 (ja) | 2014-03-04 | 2015-03-02 | 内視鏡用処置具 |
CN201580007713.3A CN106028992A (zh) | 2014-03-04 | 2015-03-02 | 内窥镜用处理器具 |
US15/223,888 US20160331454A1 (en) | 2014-03-04 | 2016-07-29 | Treatment tool for endoscope |
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JP2014042051 | 2014-03-04 | ||
JP2014-042051 | 2014-03-04 |
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US15/223,888 Continuation US20160331454A1 (en) | 2014-03-04 | 2016-07-29 | Treatment tool for endoscope |
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WO2015133442A1 true WO2015133442A1 (ja) | 2015-09-11 |
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PCT/JP2015/056115 WO2015133442A1 (ja) | 2014-03-04 | 2015-03-02 | 内視鏡用処置具 |
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US (1) | US20160331454A1 (ja) |
EP (1) | EP3115012A4 (ja) |
JP (1) | JP5911652B2 (ja) |
CN (1) | CN106028992A (ja) |
WO (1) | WO2015133442A1 (ja) |
Cited By (4)
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JP6004556B1 (ja) * | 2016-03-08 | 2016-10-12 | 敦 三並 | 手術用ナイフ付き超音波プローブ用シース |
JP2017153698A (ja) * | 2016-03-01 | 2017-09-07 | オリンパス株式会社 | 内視鏡処置具 |
WO2021186519A1 (ja) * | 2020-03-16 | 2021-09-23 | オリンパス株式会社 | 電子モジュール、電子モジュールの製造方法および内視鏡 |
CN112867457B (zh) * | 2018-10-19 | 2024-06-07 | 奥林巴斯株式会社 | 内窥镜用处置器具 |
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JP6165397B1 (ja) * | 2015-11-16 | 2017-07-19 | オリンパス株式会社 | 処置具挿通具 |
KR20190059911A (ko) * | 2016-10-22 | 2019-05-31 | 오퍼튜니티 / 디스커버리 엘엘씨 | 일회용 피복 디바이스 |
KR102090363B1 (ko) * | 2017-03-06 | 2020-03-17 | 한양대학교 에리카산학협력단 | 연성 메커니즘 |
WO2018220850A1 (ja) * | 2017-06-02 | 2018-12-06 | オリンパス株式会社 | 内視鏡用穿刺針 |
WO2019049229A1 (ja) | 2017-09-06 | 2019-03-14 | オリンパス株式会社 | 高周波処置具および内視鏡システム |
WO2019075707A1 (zh) * | 2017-10-20 | 2019-04-25 | 周震华 | 大通道直***内窥镜 |
CN112040894B (zh) * | 2018-04-19 | 2024-05-28 | 奥林巴斯株式会社 | 医疗设备 |
US20240058024A1 (en) * | 2023-10-03 | 2024-02-22 | Mohammad Fayyaz | Multi-purpose medical device for streamlined biliary and other interventions. |
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WO2021186519A1 (ja) * | 2020-03-16 | 2021-09-23 | オリンパス株式会社 | 電子モジュール、電子モジュールの製造方法および内視鏡 |
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Also Published As
Publication number | Publication date |
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EP3115012A4 (en) | 2017-11-08 |
EP3115012A1 (en) | 2017-01-11 |
JP5911652B2 (ja) | 2016-04-27 |
US20160331454A1 (en) | 2016-11-17 |
JPWO2015133442A1 (ja) | 2017-04-06 |
CN106028992A (zh) | 2016-10-12 |
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