WO2011001996A1 - Forceps for endoscope - Google Patents

Forceps for endoscope Download PDF

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Publication number
WO2011001996A1
WO2011001996A1 PCT/JP2010/061101 JP2010061101W WO2011001996A1 WO 2011001996 A1 WO2011001996 A1 WO 2011001996A1 JP 2010061101 W JP2010061101 W JP 2010061101W WO 2011001996 A1 WO2011001996 A1 WO 2011001996A1
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WO
WIPO (PCT)
Prior art keywords
forceps
pair
insertion member
state
annular member
Prior art date
Application number
PCT/JP2010/061101
Other languages
French (fr)
Japanese (ja)
Inventor
鈴木一郎
Original Assignee
株式会社スズケン
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 株式会社スズケン filed Critical 株式会社スズケン
Publication of WO2011001996A1 publication Critical patent/WO2011001996A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B10/00Other methods or instruments for diagnosis, e.g. instruments for taking a cell sample, for biopsy, for vaccination diagnosis; Sex determination; Ovulation-period determination; Throat striking implements
    • A61B10/02Instruments for taking cell samples or for biopsy
    • A61B10/06Biopsy forceps, e.g. with cup-shaped jaws
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B10/00Other methods or instruments for diagnosis, e.g. instruments for taking a cell sample, for biopsy, for vaccination diagnosis; Sex determination; Ovulation-period determination; Throat striking implements
    • A61B10/02Instruments for taking cell samples or for biopsy
    • A61B10/04Endoscopic instruments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/28Surgical forceps
    • A61B17/29Forceps for use in minimally invasive surgery
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12009Implements for ligaturing other than by clamps or clips, e.g. using a loop with a slip knot
    • A61B17/12013Implements for ligaturing other than by clamps or clips, e.g. using a loop with a slip knot for use in minimally invasive surgery, e.g. endoscopic surgery
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/28Surgical forceps
    • A61B17/29Forceps for use in minimally invasive surgery
    • A61B2017/2901Details of shaft
    • A61B2017/2905Details of shaft flexible

Definitions

  • the present invention relates to an endoscopic forceps used for endoscopic tissue collection, treatment, hemostasis, treatment site marking, and the like.
  • an endoscopic forceps for performing various treatments on a living tissue in a body cavity has been provided (see, for example, Patent Document 1).
  • An endoscopic forceps is a medical device that is inserted into a body cavity through a forceps channel of an endoscope.
  • a general endoscope forceps includes a coil 92 having a cup holding portion 91 at the tip, a pair of forceps pieces 93 rotatably supported by the cup holding portion 91, and a coil 92.
  • an endoscopic forceps 9 including two operation wires 94 inserted through and an operation unit (not shown) operated by an operator.
  • a pair of forceps pieces 93 are rotatably supported by the pins 910 of the cup holding portion 91 like scissors.
  • the distal end of the operation wire 94 is locked to each of the arm portions 931 corresponding to the rear end portion of the forceps piece 93.
  • a cup shape 930 that is depressed leaving the outer peripheral edge portion 932 is formed. After the biological tissue is positioned in the gap between the pair of forceps pieces 93, the biological tissue can be cut according to the engagement of the outer peripheral edge portion 932 by closing the forceps piece 93. The cut biological tissue is accommodated in the cup shape 930 and can be collected as it is.
  • an endoscopic hemostatic clip (not shown) is known as an instrument for performing hemostasis, marking, and the like after collection or treatment of living tissue using endoscopic forceps.
  • a clip that exhibits an expanded shape in a freely deformed state like tweezers a clip closing member that opens and closes in response to axial advancement and retraction, and an insertion of the clip closing member
  • an endoscopic hemostatic clip provided with a possible cylindrical sheath (see, for example, Patent Document 2).
  • the clip and the clip closing member are supported in a detachable state.
  • the clip closed by elastic deformation is inserted and arranged in the sheath together with the clip closing member.
  • the clip closing member is retracted so that the clip protrudes, so that the clip is opened by free deformation.
  • the clip closing member is advanced to close the clip and perform hemostasis or the like.
  • the sheath can be extracted from the forceps channel by separating the clip and the clip closing member.
  • the internal tissue is quickly extracted from the forceps channel after the biological tissue is collected. It is necessary to remove the forceps for endoscope and insert a hemostatic clip for endoscope instead. Furthermore, it is necessary to promptly execute a series of operations in which the hemostatic clip for endoscope is inserted into the body cavity, the clip is opened, and then the clip is closed to stop bleeding.
  • the present invention has been made in view of the above-described conventional problems, and an object of the present invention is to provide an endoscopic forceps that can perform hemostasis, marking, and the like without being extracted from the forceps channel.
  • the present invention is a flexible cross-sectional structure composed of a first insertion member located on the inner peripheral side and a cylindrical second insertion member that can advance and retract in the axial direction relative to the first insertion member.
  • An elongated insertion part exhibiting sex;
  • An operation unit coupled to the rear end side of the first and second insertion members;
  • the first insertion member and the pair of forceps pieces can be extrapolated and moved forward in the axial direction in accordance with the advancement of the second insertion member facing the first insertion member.
  • An annular member configured to be separable by being pushed to the distal end side through a state of being extrapolated to the forceps piece
  • the second insertion member is capable of advancing and retreating in the axial direction relative to the first insertion member between a position where the pair of forceps pieces is accommodated and a position where the second insertion member protrudes toward the distal end side. While the pair of forceps pieces are in an open state in a free deformation state, the pair of forceps pieces are deformed according to a force acting from the second insertion member side when housed on the inner peripheral side of the second insertion member.
  • An endoscope forceps is configured such that when the insertion member advances in the axial direction, a state in which the living tissue is completely closed is set to such an extent that the living tissue can be cut.
  • the endoscope forceps of the present invention has the annular member that can be separated by being pushed out as the second insertion member advances. Before the annular member is separated, the pair of forceps pieces can be set only in an incompletely closed state in which the biological tissue is grasped without being cut. On the other hand, when the annular member is pushed out and separated from the distal end side of the pair of forceps pieces, the pair of forceps pieces are in the completely closed state capable of cutting the living tissue.
  • the annular member pushed through the pair of forceps pieces in the state of grasping the living tissue and pushed to the distal end side is extrapolated to the root of the cut living tissue. According to the said annular member, it fixes to a biological tissue, maintaining the state extrapolated by the cut
  • the forceps for endoscope of the present invention treatments such as collection and treatment of living tissue and treatments such as hemostasis and marking after treatment can be performed almost simultaneously. Therefore, it is not necessary to remove the forceps from the endoscope after a procedure such as collection of a living tissue and reinsert another instrument for hemostasis into the endoscope. According to the forceps for endoscope, the necessary number of insertions of the treatment tool into the endoscope can be reduced, and the treatment can be executed relatively efficiently and relatively easily.
  • the forceps piece and the annular member in the present invention can be formed of various materials such as an elastic metal such as elastic stainless steel, a shape memory alloy, a shape memory resin, and a biodegradable resin.
  • an elastic metal such as elastic stainless steel
  • a shape memory alloy such as stainless steel
  • a shape memory resin such as polymethyl methacrylate
  • a biodegradable resin such as polymethyl methacrylate
  • a configuration for heating the forceps piece is preferably provided. In this case, it becomes possible to enhance the hemostatic effect by heating the annular member with the forceps piece to exhibit the shape memory effect.
  • the second insertion member is preferably formed so as to ensure a load resistance in the compression direction. If the load resistance in the compression direction is ensured, the reliability of the operation of moving the second insertion member forward relative to the first insertion member can be increased.
  • the second insertion member can be formed of carbon fiber or a resin material alone, but may be formed of a combination of carbon fiber and a resin material. Furthermore, a metal may be disposed at the tip portion of the second insertion member, that is, the portion in contact with the annular member.
  • the pair of forceps pieces are connected to each other via an elastically deformable connecting portion, and the incompletely closed state and the completely closed state according to the elastic deformation of the connecting portion. It is preferable that a closed state can be set.
  • the opening / closing structure of the pair of forceps pieces can be simplified compared to an opening / closing structure including a shaft that supports the forceps pieces in a rotatable state. If the mechanical structure can be configured simply, the possibility of trouble occurring during use can be suppressed and the reliability can be improved.
  • the pair of forceps pieces and the connecting portion may be integrally formed of a metal material, a resin material, or the like.
  • the pair of forceps pieces, the connecting portion, and the first insertion member may be integrally formed. For example, if molding is integrally performed with a resin material, a resin composite material, or the like, assembly work is not necessary, and production efficiency can be improved.
  • the pair of forceps pieces is formed with a convex portion protruding toward the outer peripheral side in the radial direction, and the pair of forceps pieces is formed by the second insertion member. It is preferable that the completely closed state is set in accordance with the contact load that acts on the convex portion from the inner peripheral surface.
  • the pair of forceps pieces can be completely closed according to the contact between the convex portion and the inner peripheral surface of the second insertion member. According to the convex portion formed at the distal end portion of the forceps piece, the contact load from the inner peripheral surface of the second insertion member is directly applied to the meshing position located at the distal end portion of the pair of forceps pieces. And can work efficiently.
  • the said annular member is provided with elasticity, and the inner peripheral cross-sectional area in a free deformation state is smaller than the inner peripheral cross-sectional area in the extrapolation state with respect to a pair of forceps piece.
  • the diameter of the living tissue corresponding to the root is often the same as the diameter of a circumscribed circle formed by the pair of forceps pieces at that time. Therefore, when configured as described above, the annular member is firmly fixed to the living tissue by the elastic restoring force of the annular member and the living tissue that is to return to the original shape.
  • a drop-off preventing structure for preventing drop-out from the living tissue is formed on the inner peripheral surface of the annular member.
  • dropping from the living tissue can be prevented in advance, and treatments such as hemostasis and marking can be realized with higher certainty.
  • the drop-off preventing structure for example, a structure including a protrusion having a sharp shape in a certain direction like a saw tooth can be considered.
  • the annular member provided with the protrusion may be formed of a shape memory alloy or the like, and the protrusion may be configured to stand depending on the shape memory effect. In this case, a high dropout prevention effect can be exhibited according to the shape memory effect.
  • the forceps for endoscope of the present invention in a series of actions such as hemostasis and marking after collecting or treating a living tissue, the forceps for endoscope from the forceps channel of the endoscope, etc.
  • the number of times of inserting and removing can be reduced and efficient work is possible. Therefore, with this endoscopic forceps, the required skill level of the procedure can be suppressed, and the safety of the procedure can be improved.
  • FIG. 3 is a top view illustrating a forceps piece housing structure according to the first embodiment. Explanatory drawing which shows the endoscope and forceps for endoscopes in Example 1.
  • FIG. The front view which shows the cyclic
  • FIG. Sectional drawing which shows the cross-sectional structure of the annular member in Example 1 (AA arrow cross section.).
  • the perspective view which shows the accommodation structure of the forceps piece in Example 1.
  • FIG. 3 is a perspective view illustrating an operation unit in the first embodiment. Sectional drawing which shows the cross-section of the operation part in the unused state in Example 1.
  • FIG. 3 is a top view showing a forceps piece in an open state according to the first embodiment.
  • Explanatory drawing which shows a mode that the forceps piece of the state closed incompletely in Example 1 hold
  • Explanatory drawing which shows the cross-section of an operation part when the forceps piece is in the incompletely closed state in Example 1.
  • FIG. Explanatory drawing which shows the moment in which the forceps piece of the completely closed state cut
  • FIG. 3 is an explanatory diagram for explaining the mechanical superiority over the conventional forceps in the first embodiment.
  • the front view which shows the other annular member in Example 1.
  • FIG. The side view which shows the other annular member in Example 1.
  • FIG. The figure which shows the other outer sheath in Example 1.
  • FIG. The side view which shows the forceps for endoscopes in a prior art example.
  • Example 1 This example is an example relating to an endoscopic forceps 1 having a hemostatic function. The contents will be described with reference to FIGS. As shown in FIGS. 1 to 3, the endoscope forceps 1 of this example is advanced and retracted in the axial direction relative to the first insertion member 11 located on the inner peripheral side and the first insertion member 11.
  • the first and second insertion members 11 and 12 can be extrapolated with respect to the operation portion 4 to which the rear ends of the first and second insertion members 11 and 12 are connected, and the first insertion member 11 and the pair of forceps pieces 21.
  • an annular member 30 that can be separated by being pushed forward through the pair of forceps pieces 21 after being advanced in the axial direction in accordance with the advancement of the second insertion member 12 opposite to the first insertion member 12. .
  • the second insertion member 12 can advance and retreat in the axial direction relative to the first insertion member 11 between a position where the pair of forceps pieces 21 are accommodated and a position where the second insertion member 12 protrudes toward the distal end side.
  • the pair of forceps pieces 21 are in an open state in a freely deformed state, while the force acting from the inner peripheral surface of the second insertion member 12 is accommodated in the second insertion member 12 on the inner peripheral side. Accordingly, it is deformed and closed. Further, the pair of forceps pieces 21 can be set only in an incompletely closed state in which the living tissue is grasped without being cut until the annular member 30 is separated, while the annular member 30 is separated.
  • the second insertion member 12 moves forward in the axial direction to a position where the living tissue is located, the living tissue is completely closed to the extent that it can be cut. This will be described in detail below.
  • the endoscopic forceps 1 of this example is a medical device used in combination with the endoscope 100 as shown in FIG.
  • the endoscope 100 includes a tubular insertion tube 102 having flexibility, and an operation unit 103 connected to the rear end of the insertion tube 102.
  • An imaging element (not shown) for capturing an endoscopic image is disposed at the distal end of the insertion tube 102.
  • the insertion tube 102 is inserted with a control line of the imaging device, a tube for sending and sucking air and water, and a tube called a forceps channel 101 for inserting the forceps for endoscope 1. It is inserted.
  • the endoscopic forceps 1 of this example is a medical device that is inserted into a body cavity through the forceps channel 101.
  • the endoscopic forceps 1 of this example has a hemostatic function. Therefore, if this endoscopic forceps 1 is used, hemostasis can be performed without removing the forceps from the forceps channel 101 after the biological tissue is cut. That is, it is possible to treat biological tissue cutting and hemostasis after cutting almost simultaneously.
  • the endoscopic forceps 1 includes an insertion portion 10 to be inserted into the forceps channel 101 and an operation portion 4 connected to the rear end of the insertion portion 10.
  • the insertion part 10 has a double cross-sectional structure of an inner sheath that is the first insertion member 11 and an outer sheath that is the second insertion member 12.
  • the inner sheath 11 is a cylindrical elongated tube made of a resin material.
  • the outer sheath 12 is a thin, cylindrical, elongated tube made of a carbon composite material.
  • the insertion portion 10 in which the inner sheath 11 is inserted and disposed with respect to the outer sheath 12 has flexibility.
  • a treatment portion 20 including a pair of forceps pieces 21 is integrally formed at the distal end of the inner sheath 11.
  • the outer sheath 12 is formed so that the inner sheath 11 and the treatment portion 20 can be inserted.
  • the inner diameter of the outer sheath 12 is set larger than the outer diameter of the inner sheath 11 so that the outer sheath 12 can smoothly advance and retreat in an extrapolated state with respect to the inner sheath 11.
  • the outer sheath 12 of this example made of a carbon composite material, it is easy to set a high load resistance in the compression direction, and an operation force for advancing in the axial direction relative to the inner sheath 11 can be efficiently transmitted.
  • the outer sheath 12 of this example has a convex portion 121 that protrudes to the inner peripheral side on the inner peripheral surface that is a predetermined distance from the tip.
  • the annular member 30 is a component that is placed in the body cavity for hemostasis at the cut site.
  • the annular member 30 is an annular component having elasticity made of a resin material. As shown in FIG. 4, the annular member 30 in a freely deformed state has a shape such that a circular ring is crushed sideways, and its inner peripheral shape has a slit shape.
  • the annular member 30 extrapolated to the living tissue is elastically deformed so as to approach a circular shape, and is fixed to the living tissue with high certainty by an elastic restoring force for returning to the original shape.
  • a drop-off preventing structure is formed on the inner peripheral surface of the annular member 30.
  • the drop-off prevention structure of this example is a structure in which a plurality of protrusions 31 having a sharp shape in a certain direction like saw teeth are formed.
  • the protrusion 31 bites into the living tissue, and the effect of preventing the dropout is effectively exhibited.
  • a T bar 251 for retracting the annular member 30 is engaged with the distal end surface of the annular member 30.
  • the T bar 251 is connected to the operation unit 4 via an operation wire 252 inserted and disposed in the inner sheath 11.
  • the T bar 251 is formed of a resin material having appropriate flexibility so that it can be bent. Note that an insertion hole (not shown) is drilled in the outer peripheral wall corresponding to the middle in the axial direction of the inner sheath 11. The operation wire 252 is taken out into the gap between the outer sheath 12 and the inner sheath 11 through the insertion hole.
  • the treatment unit 20 is a part that cuts a living tissue. Similar to the inner sheath 11, the treatment portion 20 of this example is made of a resin material and is integrally formed at the tip of the inner sheath 11. The treatment portion 20 is shaped such that a pair of forceps pieces 21 are connected via a connecting portion 23.
  • the forceps piece 21 has a cup shape 215 that is obtained by vertically dividing a hollow cylindrical shape along the axial direction into two parts. The outer peripheral edge of the cup shape 215 in the forceps piece 21 forms a cutting tooth 210.
  • the connecting portion 23 has a shape that is obtained by bending a substantially rectangular flat plate.
  • the forceps pieces 21 are connected so as to extend from the portions corresponding to both ends of the connecting portion 23.
  • the distal end of the inner sheath 11 is coupled to the coupling portion 23.
  • the pair of forceps pieces 21 are opened at an angle of about 90 degrees.
  • the connecting portion 23 made of a resin material can be elastically deformed so that the opening angle of the bent portion varies. If the opening angle of the bent portion is elastically deformed until it becomes substantially zero, the pair of forceps pieces 21 face each other with a substantially constant gap therebetween, and the gap is closed incompletely so that the living tissue can be grasped. Can be set (to be described later with reference to FIG. 11).
  • the connecting portion 23 in the incompletely closed state can be further elastically deformed so as to bring the forceps pieces 21 closer to each other.
  • a completely closed state in which the living tissue can be cut by the engagement of the cutting teeth 210 can be set (described later with reference to FIG. 13).
  • a convex portion 211 protruding toward the outer peripheral side in the radial direction is formed on a portion located in the opening / closing direction (vertical direction in FIG. 1).
  • the connecting portion 23 is formed with a slope 232 that smoothly extends to the outer peripheral surface of the forceps piece 21 as the width corresponding to the opening and closing direction gradually approaches the forceps piece 21 side.
  • the convex portion 211 is formed so as to come into contact with the inner peripheral surface when the outer sheath 12 advances to a predetermined position.
  • the inclined surface 232 is formed so as to contact the convex portion 121 disposed on the inner peripheral surface of the outer sheath 12 when the convex portion 211 contacts the inner peripheral surface of the outer sheath 12.
  • the operation unit 4 includes a substantially cylindrical shaft portion 41, and a bottomed substantially cylindrical slider that is extrapolated in a state in which the shaft portion 41 can advance and retreat in the axial direction. 42 and a biasing spring 43 that biases the slider 42 toward the forward side so as to push the slider 42 against the shaft portion 41.
  • an operation ring 410 on which an operator places a finger is extended.
  • the rear end of the inner sheath 11 is fixed to the shaft portion 41, while the rear end of the outer sheath 12 is fixed to the slider 42.
  • the outer sheath 12 can be advanced and retracted in the axial direction relative to the inner sheath 11. If the outer sheath 12 is retracted relative to the inner sheath 11, the treatment portion 20 can be projected to open the pair of forceps pieces 21. If the outer sheath 12 is advanced relative to the inner sheath 11, the treatment portion 20 can be accommodated in the outer sheath 12 and the pair of forceps pieces 21 can be closed.
  • the urging spring 43 is disposed in a compressed state in the gap between the bottom 427 of the slider 42 and the tip end surface 411 of the shaft portion 41.
  • the biasing spring 43 is arranged in a state of being extrapolated to the inner sheath 11.
  • the urging spring 43 urges the slider 42 forward with respect to the shaft portion 41.
  • This urging force is a reaction force against the backward operation of the slider 42 that attempts to open the forceps piece 21.
  • an appropriate operating force can be set when the forceps piece 21 is opened by the backward operation of the slider 42.
  • the rear end of the inner sheath 11 is fixed to a front end surface 411 that is opposite to the operation ring 410 in the end surface of the shaft portion 41.
  • a groove 415 having a rectangular cross section extends along the axial direction. The groove 415 opens on the rear end surface 412 on the operation ring 410 side, but does not reach the opposite end surface 411, and the groove end 416 is positioned in front of the groove 415.
  • a pair of two operation rings 420 are installed on the outer peripheral surface of the slider 42 so as to protrude on both sides in the radial direction.
  • a through hole 426 for inserting the inner sheath 11 is formed in the bottom 427 of the slider 42.
  • the rear end of the outer sheath 12 and the rear end of the operation wire 252 extending from the T bar 251 are fixed.
  • the operation wire 252 is taken out to the outer peripheral side of the inner sheath 11 from an insertion hole (not shown) drilled in the outer peripheral surface of the inner sheath 11.
  • convex portions 421 and 422 that engage with the groove 415 of the shaft portion 41 are formed at two locations along the axial direction.
  • the convex portion 421 is a convex portion that always engages with the groove portion 415 regardless of the advance / retreat position of the slider 42.
  • the slider 42 is restricted from rotating relative to the shaft portion 41 in accordance with the engagement between the convex portion 421 and the groove 415.
  • the convex portion 422 is a convex portion for separating from the groove 415 when the slider 42 is advanced with respect to the shaft portion 41 and positioned at the tip side of the shaft portion 41, and then restricting the slider 42 from retreating. is there.
  • the convex portion 422 is formed at the tip of a rectangular piece 423 that forms part of the outer peripheral wall of the slider 42.
  • the rectangular piece 423 is a portion connected to the main body side of the slider 42 through only one side of the root like a diving plate.
  • the rectangular piece 423 is separated from the surroundings by a substantially U-shaped slit 424 formed in the outer peripheral wall of the slider 42.
  • the rectangular piece 423 can be rotated by elastic deformation around one side of the base located on the bottom 427 side.
  • the convex portion 422 has a protruding shape formed by an inclined surface 422T located on the front end surface 411 side and a right-angle surface 422V located on the rear end surface 412 side.
  • the rectangular piece 423 is formed with a protruding portion 425 that protrudes in a dome shape toward the inner peripheral side, similar to the protruding portion 422.
  • the protruding portion 425 is arranged closer to the base side of the rectangular piece 423 than the convex portion 422.
  • the position where the protruding portion 425 engages with the groove end 416 is the urging position of the slider 42 by the urging spring 43.
  • the urging spring 43 is set so as to urge the slider 42 until the protruding portion 425 reaches the groove end 416 in an unused state, and to generate an urging force such that the protruding portion 425 does not exceed the groove end 416.
  • the state in which the protrusion 425 is positioned at the groove end 416 as shown in FIG. 8 corresponds to the unused state shown in FIGS. 1, 2, and 6.
  • the distal end surface of the outer sheath 12 is located deeper on the retreat side by the width of the annular member 30 than the convex portion 211.
  • the T bar 251 connected to the distal end of the operation wire 252 is locked to the distal end surface of the annular member 30.
  • the state where the convex portion 422 is positioned at the groove end 416 corresponds to a state where the living tissue is incompletely closed to the extent that the living tissue can be grasped, as will be described later with reference to FIG.
  • the state in which the convex portion 422 is positioned on the distal end side of the shaft portion 41 beyond the groove end 416 corresponds to a state in which the living tissue is completely closed to the extent that it can be cut as described later with reference to FIG. is doing.
  • the unused endoscope forceps 1 can be inserted into a body cavity through the forceps channel 101 of the endoscope 100.
  • the operation portion 4 is operated so as to retract the slider 42 with respect to the shaft portion 41.
  • the relative position between the slider 42 and the shaft portion 41 in the unoperated state is such that the convex portion 422 is accommodated in the groove 415 as shown in FIG. Since the projecting portion 422 can be retracted along the groove 415, the retracting of the slider 42 with respect to the shaft portion 41 is allowed.
  • the slider 42 is connected to the rear end of the outer sheath 12 and the operation wire 252. Therefore, if the slider 42 is retracted as described above, the outer sheath 12 and the operation wire 252 can be retracted with respect to the inner sheath 11. If the operation wire 252 is retracted, the annular member 30 can be retracted by the T bar 251 connected to the tip.
  • the pair of forceps pieces 21 can be protruded.
  • the pair of forceps pieces 21 protruding from the annular member 30 and the outer sheath 12 are opened according to the free deformation of the connecting portion 23 as shown in FIGS.
  • the T bar 251 is accommodated so as to be bent and deformed and dragged into the inner sheath 11. Thereby, the locking relationship between the annular member 30 and the T bar is released.
  • the slider 42 is advanced with respect to the shaft portion 41 in a state where the living tissue is positioned in the gap between the pair of forceps pieces 21. Accordingly, the outer sheath 12 can be advanced relative to the inner sheath 11 and the forceps piece 21 can be closed. If the outer sheath 12 is advanced to the front of the convex portion 211, as shown in FIG. 11, the pair of forceps pieces 21 returns to the incompletely closed state. In the incompletely closed state, the living tissue can be grasped with high reliability by the pair of forceps pieces 21. At this time, in the operation part 4, as shown in FIG. 12, the convex part 422 contacts the groove end 416, and an axial reaction force is generated. The operator of the operation unit 4 can grasp with high certainty that the incompletely closed state is set according to the reaction force in the axial direction.
  • the operation wire 252 does not have axial rigidity. Therefore, the operation wire 252 sags as the slider 42 advances with respect to the shaft portion 41. The T bar 251 connected to the distal end of the operation wire 252 is left as it is inside the inner sheath 11.
  • the annular member 30 When the incompletely closed state is reached, the annular member 30 is positioned on the outer periphery of the living tissue grasped by the forceps piece 21. If the slider 42 is further advanced, the outer sheath 12 can be advanced beyond the convex portion 211.
  • the convex portion 121 comes into contact with the inclined surface 232 of the treatment portion 20 at the same time as the distal end of the outer sheath 12 gets over the convex portion 211. Yes.
  • a contact load that acts on the convex portion 211 from the inner peripheral surface of the outer sheath 12 and a contact load that acts on the slope 232 from the convex portion 121 are generated. These contact loads act as a force for bringing the pair of forceps pieces 21 closer to each other. With these forces, the pair of forceps pieces 21 are completely closed, and the living tissue is cut.
  • the operation unit 4 is in a state in which the convex portion 422 has moved forward over the groove end 416.
  • the right-angle surface 422V of the convex portion 422 is engaged with the tip surface 411 of the shaft portion 41, the retreat of the slider 42 is restricted.
  • the state in which the pair of forceps pieces 21 are completely closed is firmly maintained, and the cut biological tissue can be held with high reliability.
  • the separated annular member 30 is extrapolated to the living tissue corresponding to the root portion of the cut living tissue.
  • the living tissue that hits the root portion is bound by the annular member 30.
  • a drop-off preventing structure including the protrusion 31 (FIG. 5) is formed as described above.
  • the protrusion 31 bites into the living tissue, and the annular member 30 can be fixed with high reliability.
  • the inner peripheral shape of the annular member 30 in a state where the root portion is tightly bound is close to a circular shape with respect to the slit-shaped inner peripheral shape (FIG. 4) in a freely deformed state.
  • an elastic force is generated in the annular member 30 to return to the original shape.
  • an elastic force is generated to return the bound biological tissue to its original state.
  • the elastic force of the annular member 30 and the elastic force of the biological tissue work effectively because the annular member 30 is firmly fixed to the biological tissue.
  • the endoscopic forceps 1 accommodates a living tissue in a cup shape 215 inside a pair of forceps pieces 21. If the insertion part 10 of the forceps 1 for endoscope is extracted from the forceps channel 101, the cut biological tissue can be collected. On the other hand, the annular member 30 is firmly fixed to the cut portion in the body cavity as described above. Therefore, bleeding from the cut surface of the living tissue can be suppressed with high certainty.
  • the endoscopic forceps 1 of this example is an endoscopic forceps having a hemostatic function. If this endoscopic forceps 1 is used, cutting of a living tissue and hemostasis and hemostasis can be performed almost simultaneously, so that bleeding and the like can be suppressed to a minimum and the burden on the human body side can be suppressed. Furthermore, since it is not necessary to quickly remove the endoscopic forceps 1 from the forceps channel 101 after cutting the living tissue and immediately insert the hemostatic clip for endoscope to stop the hemostasis, it is possible to suppress the burden on the treatment side.
  • the mechanical superiority of the endoscopic forceps 1 of this example will be described in comparison with the conventional endoscopic forceps 9 with reference to FIG.
  • a fulcrum is set on the pin 910
  • an action point is set on the tip of the forceps piece 93
  • a force point is set on the arm portion 931. Due to the demand for a smaller diameter, it is difficult to ensure a long length between the pin 910 and the arm portion 931, and in general, there is a tendency to be shorter than the length between the forceps piece 93 and the pin 910. Therefore, it is necessary to apply a force larger than that required for the forceps piece 93 to the arm portion 931.
  • the load acting on the engagement structure between the operation wire 252 and the arm portion 931, the pin 910 that is a fulcrum, and the like is increased, causing a mechanical trouble.
  • the positional relationship among the force point set at the convex portion 211, the action point set at the tip of the forceps piece 21, and the fulcrum set at the connecting portion 23 is the same as in the conventional endoscope. It is completely different from the forceps for mirrors. That is, in the endoscopic forceps 1 of this example, the force point and the action point are arranged on the same side with respect to the fulcrum and at substantially the same position. Therefore, the force acting on the force point can be directly transmitted to the action point. Unlike the conventional case, since there is no possibility that an excessive load acts on the fulcrum or the like, the possibility of causing a mechanical trouble is extremely reduced.
  • the annular member 30 in which the inner peripheral shape in the free deformation state exhibits a linear slit shape is employed.
  • the annular member 30 in which the inner peripheral shape in the free deformation state exhibits a cross shape is used. It can also be adopted.
  • the annular member 30 provided with the side wall which exhibits the mesh structure like knitting is also employable.
  • the mesh structure is an effective structure for ensuring strength. If the annular member 30 has a mesh structure, it is possible to secure the strength that can withstand the pushing force when extrapolated into the living tissue while suppressing dimensions such as thickness.
  • the material of the annular member 30 various materials such as elastic stainless steel, shape memory alloy, shape memory resin, and biodegradable resin can be adopted.
  • a configuration for heating the forceps piece 21 is preferably provided.
  • the shape memory effect can be exhibited by heating the annular member with the forceps piece 21.
  • the protrusion 31 is configured to stand on the inner peripheral side due to the shape memory effect, the effect of the drop-off prevention mechanism is further enhanced.
  • the annular member 30 may be formed of a biodegradable resin. Since it is decomposed in nature after being discharged from the body, the impact on the environment can be suppressed.
  • a metal ring may be disposed at the tip of the outer sheath 12.
  • the strength of the distal end portion of the outer sheath 12 can be secured high. If the strength of the outer sheath 12 is ensured, a force can be applied to the forceps piece 21 more efficiently.
  • This example is an example in which the treatment portion 20 is integrally formed at the tip of the inner sheath 11.
  • the treatment portion may be formed separately from the inner sheath 11.
  • a method for fixing a separate treatment portion to the distal end of the inner sheath for example, there are a method for fixing via a support pin or the like, a method for bonding, and the like.
  • a method of joining there are various methods such as adhesive joining, welding joining, caulking joining, and fitting.
  • this example is an example in which the outer sheath 12 advances in accordance with the pushing operation of the slider 42 with respect to the shaft portion 41, that is, the advancement of the slider 42 with respect to the shaft portion 41.
  • the outer sheath 12 may be configured to advance in accordance with the pushing operation of the shaft portion 41 with respect to the slider 42, that is, with the advancement of the shaft portion 41 with respect to the slider 42. If the outer sheath 12 and the rear end of the operation wire 252 are connected to the shaft portion 41 and the rear end of the inner sheath 11 is connected to the slider 42, the outer sheath 12 is moved according to the pushing operation of the shaft portion 41 as described above. The annular member 30 can be pushed out and separated by being advanced.
  • the groove 120 may be disposed opposite to the inner peripheral surface of the outer sheath 12.
  • the groove 120 extends along the axial direction and opens at the distal end surface of the outer sheath 12.
  • the circumferential position of the groove 120 can be matched with the convex portion 211 of the forceps piece 21, and the convex portion 121 of the outer sheath 12 can be It can be located on both sides of the connecting portion 23.
  • the annular member 30 can be pushed out and separated while picking up without cutting the living tissue. It can be applied to treatments such as hemostasis and marking of a living body site where bleeding has occurred like a hemostatic forceps.
  • An endoscopic forceps in which the convex portion 211 of the forceps piece 21 and the convex portion 121 of the outer sheath 12 are omitted and the right-angle surface 422V of the convex portion 422 of the slider 42 is changed to an inclined surface is also useful.
  • This endoscopic forceps is an instrument in which the cutting function is omitted from the endoscopic forceps of the present invention.
  • the living tissue is picked up by the pair of forceps pieces 41 by advancing the outer sheath 12 in the axial direction relative to the inner sheath 11 by the advancement of the slider 42 relative to the shaft portion 41.
  • the annular member 30 can be moved without being cut.
  • the slider 42 is allowed to move backward with respect to the shaft portion 41, and the pinched biological tissue can be released.
  • Such endoscopic forceps are useful for procedures such as hemostasis and marking.

Abstract

A forceps for an endoscope, having a blood stanching function, the forceps being capable of treatment such as blood stanching without being extracted from a forceps channel. A forceps (1) for an endoscope, comprising: a flexible elongated insertion section (10) having a double structure in a cross-section thereof and comprising a first insertion member (11) and a second insertion member (12); a pair of forceps elements (21) held at the tip of the first insertion member (11); and a ring-shaped annular member (30) which is separable by being advanced in the axial direction in response to the advance of the second insertion member (12), which faces the first insertion member (11), and then extruded to the tip side after being brought to a state in which the annular member (30) is fitted over the pair of forceps elements (21). In a state before the annular member (30) is separated, the pair of forceps elements (21) can be set only to a state in which the pair is in an incompletely closed state in which the pair can hold an organism tissue without cutting the organism tissue, while in a state in which the second insertion section (12) is advanced in the axial direction to a position at which the annular member (30) becomes separated, the pair of forceps elements (21) is in a completely closed state in which the pair can cut the organism tissue.

Description

内視鏡用鉗子Endoscopy forceps
 本発明は、内視鏡的な組織採取・治療・止血・治療部位マーキング等に利用される内視鏡用鉗子に関する。 The present invention relates to an endoscopic forceps used for endoscopic tissue collection, treatment, hemostasis, treatment site marking, and the like.
 従来より、例えば、体腔内の生体組織に対して各種の処置を行うための内視鏡用鉗子が提供されている(例えば、特許文献1参照。)。内視鏡用鉗子は、内視鏡の鉗子チャンネルを通して体腔内に挿入される医療機器である。一般的な内視鏡用鉗子としては、図20に示すごとく、先端にカップ保持部91を設けたコイル92と、カップ保持部91により回動支持された一対の鉗子片93と、コイル92内に挿通配置された2本の操作ワイヤ94と、オペレータが操作する操作部(図示略)と、を備えた内視鏡用鉗子9が知られている。 Conventionally, for example, an endoscopic forceps for performing various treatments on a living tissue in a body cavity has been provided (see, for example, Patent Document 1). An endoscopic forceps is a medical device that is inserted into a body cavity through a forceps channel of an endoscope. As shown in FIG. 20, a general endoscope forceps includes a coil 92 having a cup holding portion 91 at the tip, a pair of forceps pieces 93 rotatably supported by the cup holding portion 91, and a coil 92. There is known an endoscopic forceps 9 including two operation wires 94 inserted through and an operation unit (not shown) operated by an operator.
 この内視鏡用鉗子9では、カップ保持部91のピン910により一対の鉗子片93がハサミのごとく回動支持されている。鉗子片93の後端部分に当たるアーム部931には、それぞれ、操作ワイヤ94の先端が係止されている。操作部の操作により操作ワイヤ94を進退させると、一対の鉗子片93がハサミのごとく開閉する。 In this endoscopic forceps 9, a pair of forceps pieces 93 are rotatably supported by the pins 910 of the cup holding portion 91 like scissors. The distal end of the operation wire 94 is locked to each of the arm portions 931 corresponding to the rear end portion of the forceps piece 93. When the operation wire 94 is advanced and retracted by operating the operation unit, the pair of forceps pieces 93 open and close like scissors.
 閉じた状態の一対の鉗子片93が相互に当接する表面には、外周縁部932を残して陥没するカップ形状930が形成されている。一対の鉗子片93の間隙に生体組織を位置させた後、鉗子片93を閉じれば外周縁部932の噛み合わせに応じて生体組織を切断可能である。切断された生体組織は、カップ形状930の内部に収容され、そのまま採取可能である。 On the surface where the pair of forceps pieces 93 in a closed state contact each other, a cup shape 930 that is depressed leaving the outer peripheral edge portion 932 is formed. After the biological tissue is positioned in the gap between the pair of forceps pieces 93, the biological tissue can be cut according to the engagement of the outer peripheral edge portion 932 by closing the forceps piece 93. The cut biological tissue is accommodated in the cup shape 930 and can be collected as it is.
 また、内視鏡用鉗子による生体組織の採取や治療等の実施後に止血やマーキング等を実施するための器具として図示しない内視鏡用止血クリップが知られている。一般的な内視鏡用止血クリップとしては、ピンセットのごとく自由変形状態において拡開形状を呈するクリップと、軸方向の進退に応じてクリップを開閉させるクリップ閉塞部材と、このクリップ閉塞部材を内挿可能な円筒状のシースと、を備えた内視鏡用止血クリップがある(例えば、特許文献2参照。)。内視鏡用止血クリップでは、クリップ及びクリップ閉塞部材が切り離し可能な状態で支持されている。 In addition, an endoscopic hemostatic clip (not shown) is known as an instrument for performing hemostasis, marking, and the like after collection or treatment of living tissue using endoscopic forceps. As a general endoscopic hemostatic clip, a clip that exhibits an expanded shape in a freely deformed state like tweezers, a clip closing member that opens and closes in response to axial advancement and retraction, and an insertion of the clip closing member There is an endoscopic hemostatic clip provided with a possible cylindrical sheath (see, for example, Patent Document 2). In the hemostatic clip for endoscope, the clip and the clip closing member are supported in a detachable state.
 鉗子チャンネルへの挿入状態では、弾性変形により閉じた状態のクリップがクリップ閉塞部材と共にシースに内挿配置されている。生体組織の切断箇所を処置するに当たっては、まず、クリップが突出するようにクリップ閉塞部材を後退させることで、自由変形によりクリップを開いた状態にする。開いた状態のクリップの内側に切断箇所を位置させた後、クリップ閉塞部材を前進させることでクリップを閉じて止血等を行うことができる。止血等の処置後では、クリップ及びクリップ閉塞部材を切り離すことで鉗子チャンネルからシースを抜き取り可能である。 In the inserted state into the forceps channel, the clip closed by elastic deformation is inserted and arranged in the sheath together with the clip closing member. In treating the cut portion of the living tissue, first, the clip closing member is retracted so that the clip protrudes, so that the clip is opened by free deformation. After the cut portion is positioned inside the open clip, the clip closing member is advanced to close the clip and perform hemostasis or the like. After treatment such as hemostasis, the sheath can be extracted from the forceps channel by separating the clip and the clip closing member.
 上記のような内視鏡用鉗子及び内視鏡用止血クリップを用いて経内視鏡的に生体組織の採取等を実施するに当たっては、生体組織の採取等を行った後に鉗子チャンネルから素早く内視鏡用鉗子を抜き取り、代わりに内視鏡用止血クリップを挿入する必要がある。さらに、内視鏡用止血クリップを体腔内へ挿入した後にクリップを開き、その後、クリップを閉じて止血するという一連の操作を速やかに実行する必要がある。 When performing the endoscopic forceps and endoscopic hemostasis clip as described above to collect biological tissue, etc., endoscopically, the internal tissue is quickly extracted from the forceps channel after the biological tissue is collected. It is necessary to remove the forceps for endoscope and insert a hemostatic clip for endoscope instead. Furthermore, it is necessary to promptly execute a series of operations in which the hemostatic clip for endoscope is inserted into the body cavity, the clip is opened, and then the clip is closed to stop bleeding.
 しかしながら、上記従来の経内視鏡的な生体組織の採取等を行うための器具では、次のような問題がある。すなわち、組織採取に伴い、ときに出血し止血処理を施術しなければならないケースがあり、その際には、上記内視鏡用鉗子を抜き取り、内視鏡用止血クリップを素早く挿入するために補助者が必要となったり、全長1mを超えるものもある内視鏡用止血クリップの挿入を時間をかけずに素早い操作で行わなければならないという問題がある。 However, there are the following problems with the above-described conventional instrument for collecting a bioendoscopic tissue. In other words, there are cases where bleeding and bleeding must be performed as the tissue is collected. In such cases, the above-mentioned endoscopic forceps are removed, and the endoscopic hemostatic clip is quickly inserted. There is a problem that the insertion of the hemostatic clip for an endoscope, which requires a person or has a total length exceeding 1 m, must be performed quickly without taking time.
特開2005-58344号公報JP 2005-58344 A 特開2000-254143号公報JP 2000-254143 A
 本発明は、上記従来の問題点に鑑みてなされたものであり、鉗子チャンネルから抜き取ることなく止血やマーキング等の処置を行うことができる内視鏡用鉗子を提供しようとするものである。 The present invention has been made in view of the above-described conventional problems, and an object of the present invention is to provide an endoscopic forceps that can perform hemostasis, marking, and the like without being extracted from the forceps channel.
 本発明は、内周側に位置する第1の挿入部材、及び当該第1の挿入部材に相対して軸方向に進退可能な筒状の第2の挿入部材よりなる断面二重構造の可撓性を呈する細長い挿入部と、
 上記第1の挿入部材の先端側に保持された一対の鉗子片と、
 上記第1及び上記第2の挿入部材の後端側に連結された操作部と、
 上記第1の挿入部材及び上記一対の鉗子片に対して外挿可能であると共に、上記第1の挿入部材に相対する上記第2の挿入部材の前進に応じて軸方向に前進し上記一対の鉗子片に外挿された状態を経て先端側に押し出されて分離可能なように構成された環状部材と、を備え、
 上記第2の挿入部材は、上記一対の鉗子片を収容する位置と先端側に突出させる位置との間で上記第1の挿入部材に相対して軸方向に進退可能であり、
 上記一対の鉗子片は、自由変形状態において開いた状態となる一方、上記第2の挿入部材の内周側に収容されたときに当該第2の挿入部材側から作用する力に応じて変形して閉じた状態となり、
 かつ、上記環状部材が分離されるまでの間は生体組織を切断せずに把持する程度の不完全に閉じた状態のみ設定可能である一方、上記環状部材が分離される位置まで上記第2の挿入部材が軸方向に前進したとき、生体組織を切断可能な程度に完全に閉じた状態が設定されるように構成されていることを特徴とする内視鏡用鉗子にある。
The present invention is a flexible cross-sectional structure composed of a first insertion member located on the inner peripheral side and a cylindrical second insertion member that can advance and retract in the axial direction relative to the first insertion member. An elongated insertion part exhibiting sex;
A pair of forceps pieces held on the distal end side of the first insertion member;
An operation unit coupled to the rear end side of the first and second insertion members;
The first insertion member and the pair of forceps pieces can be extrapolated and moved forward in the axial direction in accordance with the advancement of the second insertion member facing the first insertion member. An annular member configured to be separable by being pushed to the distal end side through a state of being extrapolated to the forceps piece,
The second insertion member is capable of advancing and retreating in the axial direction relative to the first insertion member between a position where the pair of forceps pieces is accommodated and a position where the second insertion member protrudes toward the distal end side.
While the pair of forceps pieces are in an open state in a free deformation state, the pair of forceps pieces are deformed according to a force acting from the second insertion member side when housed on the inner peripheral side of the second insertion member. Closed,
In addition, until the annular member is separated, it is possible to set only an incompletely closed state in which the living tissue is grasped without being cut, while the second member is separated to the position where the annular member is separated. An endoscope forceps is configured such that when the insertion member advances in the axial direction, a state in which the living tissue is completely closed is set to such an extent that the living tissue can be cut.
 本発明の内視鏡用鉗子は、上記第2の挿入部材の前進に応じて押し出されて分離可能な上記環状部材を有している。この環状部材が分離される前では、上記一対の鉗子片について、生体組織を切断せずに把持する程度の上記不完全に閉じた状態のみ設定可能である。一方、上記環状部材が上記一対の鉗子片の先端側に押し出されて分離されたとき、上記一対の鉗子片は、生体組織を切断可能な上記完全に閉じた状態となる。 The endoscope forceps of the present invention has the annular member that can be separated by being pushed out as the second insertion member advances. Before the annular member is separated, the pair of forceps pieces can be set only in an incompletely closed state in which the biological tissue is grasped without being cut. On the other hand, when the annular member is pushed out and separated from the distal end side of the pair of forceps pieces, the pair of forceps pieces are in the completely closed state capable of cutting the living tissue.
 生体組織を把持した状態の上記一対の鉗子片を通り越して先端側に押し出された上記環状部材は、切断された生体組織の根元に外挿される。上記環状部材によれば、切断された生体組織に外挿された状態を維持しつつ生体組織に固定される。このように生体組織に上記環状部材を移設すれば、切断箇所からの出血を止めたり、切断箇所をマーキングできる。さらに、この環状部材は、生体組織の切断とほぼ同時に生体組織に移設される。そのため、止血効果を備えた環状部材であれば、生体組織の切断に伴う出血を最小限に抑制できる。また、マーキングのための環状部材であれば、切断箇所を位置精度高く正確にマーキングできる。 The annular member pushed through the pair of forceps pieces in the state of grasping the living tissue and pushed to the distal end side is extrapolated to the root of the cut living tissue. According to the said annular member, it fixes to a biological tissue, maintaining the state extrapolated by the cut | disconnected biological tissue. If the annular member is transferred to the living tissue in this way, bleeding from the cut portion can be stopped or the cut portion can be marked. Further, the annular member is transferred to the living tissue almost simultaneously with the cutting of the living tissue. Therefore, if it is a cyclic | annular member provided with the hemostatic effect, the bleeding accompanying the cutting | disconnection of a biological tissue can be suppressed to the minimum. Moreover, if it is an annular member for marking, a cutting location can be accurately marked with high positional accuracy.
 このように本発明の内視鏡用鉗子によれば、生体組織の採取や治療等の処置と、処置後の止血やマーキング等の処置と、をほぼ同時に遂行し得る。そのため、生体組織の採取等の処置後に鉗子を内視鏡から抜き取り、止血のための別の器具を内視鏡に挿入し直す必要がない。この内視鏡用鉗子によれば、内視鏡への処置具の挿入する必要回数を減らすことができ、極めて効率良く、比較的簡便に処置を実行できる。 Thus, according to the forceps for endoscope of the present invention, treatments such as collection and treatment of living tissue and treatments such as hemostasis and marking after treatment can be performed almost simultaneously. Therefore, it is not necessary to remove the forceps from the endoscope after a procedure such as collection of a living tissue and reinsert another instrument for hemostasis into the endoscope. According to the forceps for endoscope, the necessary number of insertions of the treatment tool into the endoscope can be reduced, and the treatment can be executed relatively efficiently and relatively easily.
 本発明における鉗子片及び環状部材は、弾性ステンレス等の弾性金属、形状記憶合金、形状記憶樹脂、生分解性樹脂等、様々な材料により形成できる。特に、形状記憶合金や形状記憶樹脂よりなる環状部材を採用した場合には、鉗子片を加温する構成を設けることが良い。この場合には、鉗子片により環状部材を加温して形状記憶効果を発揮させ、止血効果を高めること等が可能になる。 The forceps piece and the annular member in the present invention can be formed of various materials such as an elastic metal such as elastic stainless steel, a shape memory alloy, a shape memory resin, and a biodegradable resin. In particular, when an annular member made of a shape memory alloy or a shape memory resin is employed, a configuration for heating the forceps piece is preferably provided. In this case, it becomes possible to enhance the hemostatic effect by heating the annular member with the forceps piece to exhibit the shape memory effect.
 また、上記第2の挿入部材は、圧縮方向の耐荷重を確保できるように形成することが好ましい。圧縮方向の耐荷重を確保すれば、上記第1の挿入部材に相対して上記第2の挿入部材を前進させる操作の確実性を高めることができる。上記第2の挿入部材は、カーボンファイバー、あるいは樹脂材料のみにより形成することもできるが、カーボンファイバーと樹脂材料との組合せにより形成しても良い。さらに、上記第2の挿入部材の先端部分、すなわち上記環状部材に接する部分に金属を配置することも良い。 The second insertion member is preferably formed so as to ensure a load resistance in the compression direction. If the load resistance in the compression direction is ensured, the reliability of the operation of moving the second insertion member forward relative to the first insertion member can be increased. The second insertion member can be formed of carbon fiber or a resin material alone, but may be formed of a combination of carbon fiber and a resin material. Furthermore, a metal may be disposed at the tip portion of the second insertion member, that is, the portion in contact with the annular member.
 また、上記一対の鉗子片は、弾性的に変形可能な連結部を介して相互に連結されていると共に、該連結部の弾性的な変形に応じて上記不完全に閉じた状態及び上記完全に閉じた状態を設定可能であることが好ましい。
 この場合には、例えば、各鉗子片を回動可能な状態で支持する軸を含む開閉構造等に比べ、上記一対の鉗子片の開閉構造を簡略化できる。機械的な構造をシンプルに構成できれば、使用に際してトラブルが発生するおそれを抑制でき信頼性を向上できる。上記一対の鉗子片及び上記連結部を、金属材料や樹脂材料等により一体的に成形することも良い。
In addition, the pair of forceps pieces are connected to each other via an elastically deformable connecting portion, and the incompletely closed state and the completely closed state according to the elastic deformation of the connecting portion. It is preferable that a closed state can be set.
In this case, for example, the opening / closing structure of the pair of forceps pieces can be simplified compared to an opening / closing structure including a shaft that supports the forceps pieces in a rotatable state. If the mechanical structure can be configured simply, the possibility of trouble occurring during use can be suppressed and the reliability can be improved. The pair of forceps pieces and the connecting portion may be integrally formed of a metal material, a resin material, or the like.
 また、上記一対の鉗子片、上記連結部及び上記第1の挿入部材は、一体的に成形されていることも良い。
 例えば、樹脂材料や樹脂複合材料等により一体的に成形すれば、組付作業が不要となり、生産効率を向上できる。
The pair of forceps pieces, the connecting portion, and the first insertion member may be integrally formed.
For example, if molding is integrally performed with a resin material, a resin composite material, or the like, assembly work is not necessary, and production efficiency can be improved.
 また、上記一対の鉗子片のうちの少なくともいずれか一方の先端部分には、径方向外周側に向けて突出する凸部が形成されており、上記一対の鉗子片は、上記第2の挿入部材の内周面から上記凸部に作用する当接荷重に応じて上記完全に閉じた状態が設定されることが好ましい。
 この場合には、上記凸部と上記第2の挿入部材の内周面との当接に応じて上記一対の鉗子片を完全に閉じた状態にできる。上記鉗子片の先端部分に形成された上記凸部によれば、上記一対の鉗子片の先端部分に位置する噛み合わせ箇所に上記第2の挿入部材の内周面からの当接荷重を直接的かつ効率的に作用できる。
Further, at least one of the pair of forceps pieces is formed with a convex portion protruding toward the outer peripheral side in the radial direction, and the pair of forceps pieces is formed by the second insertion member. It is preferable that the completely closed state is set in accordance with the contact load that acts on the convex portion from the inner peripheral surface.
In this case, the pair of forceps pieces can be completely closed according to the contact between the convex portion and the inner peripheral surface of the second insertion member. According to the convex portion formed at the distal end portion of the forceps piece, the contact load from the inner peripheral surface of the second insertion member is directly applied to the meshing position located at the distal end portion of the pair of forceps pieces. And can work efficiently.
 また、上記環状部材は、弾性を備えており、自由変形状態における内周断面積が、上記一対の鉗子片に対する外挿状態における内周断面積よりも小さいことが好ましい。
 一般的に、上記一対の鉗子片により生体組織を把持した場合、その根元に当たる生体組織の直径は、そのときの一対の鉗子片がなす外接円の直径と同程度になることが多い。それ故、上記のごとく構成した場合、元の形状に戻ろうとする上記環状部材及び生体組織の弾性復帰力により、上記環状部材が生体組織に強固に固定される。
Moreover, it is preferable that the said annular member is provided with elasticity, and the inner peripheral cross-sectional area in a free deformation state is smaller than the inner peripheral cross-sectional area in the extrapolation state with respect to a pair of forceps piece.
Generally, when a living tissue is grasped by the pair of forceps pieces, the diameter of the living tissue corresponding to the root is often the same as the diameter of a circumscribed circle formed by the pair of forceps pieces at that time. Therefore, when configured as described above, the annular member is firmly fixed to the living tissue by the elastic restoring force of the annular member and the living tissue that is to return to the original shape.
 また、上記環状部材の内周面には、生体組織からの脱落を防止するための脱落防止構造が形成されていることが好ましい。
 この場合には、生体組織からの脱落を未然に防止でき、一層、確実性高く止血やマーキング等の処置を実現できる。上記脱落防止構造としては、例えば、鋸の歯のごとく一定方向に尖った形状を呈する突起を備えた構造等が考えられる。さらに、この突起を備えた環状部材を形状記憶合金等により形成し、形状記憶効果に応じて上記突起が起立するように構成することも良い。この場合には、形状記憶効果に応じて、高い脱落防止効果が発揮され得る。
Moreover, it is preferable that a drop-off preventing structure for preventing drop-out from the living tissue is formed on the inner peripheral surface of the annular member.
In this case, dropping from the living tissue can be prevented in advance, and treatments such as hemostasis and marking can be realized with higher certainty. As the drop-off preventing structure, for example, a structure including a protrusion having a sharp shape in a certain direction like a saw tooth can be considered. Further, the annular member provided with the protrusion may be formed of a shape memory alloy or the like, and the protrusion may be configured to stand depending on the shape memory effect. In this case, a high dropout prevention effect can be exhibited according to the shape memory effect.
 本発明の内視鏡用鉗子によれば、生体組織の採取や治療等を行った後に止血やマーキング等の処置を行うという一連の行為において、内視鏡の鉗子チャンネルから内視鏡用鉗子等を抜き差しする回数を減らすことができ効率的な作業が可能である。それ故、この内視鏡用鉗子では、要求される手技の熟練度合いを抑制でき、処置の安全性を向上させることができる。 According to the forceps for endoscope of the present invention, in a series of actions such as hemostasis and marking after collecting or treating a living tissue, the forceps for endoscope from the forceps channel of the endoscope, etc. The number of times of inserting and removing can be reduced and efficient work is possible. Therefore, with this endoscopic forceps, the required skill level of the procedure can be suppressed, and the safety of the procedure can be improved.
実施例1における、鉗子片の収容構造を示す側面図。The side view which shows the accommodation structure of the forceps piece in Example 1. FIG. 実施例1における、鉗子片の収容構造を示す上面図。FIG. 3 is a top view illustrating a forceps piece housing structure according to the first embodiment. 実施例1における、内視鏡及び内視鏡用鉗子を示す説明図。Explanatory drawing which shows the endoscope and forceps for endoscopes in Example 1. FIG. 実施例1における、自由変形状態の環状部材を示す正面図。The front view which shows the cyclic | annular member of the free deformation state in Example 1. FIG. 実施例1における、環状部材の断面構造を示す断面図(A-A線矢視断面。)。Sectional drawing which shows the cross-sectional structure of the annular member in Example 1 (AA arrow cross section.). 実施例1における、鉗子片の収容構造を示す斜視図。The perspective view which shows the accommodation structure of the forceps piece in Example 1. FIG. 実施例1における、操作部を示す斜視図。FIG. 3 is a perspective view illustrating an operation unit in the first embodiment. 実施例1における、未使用状態における操作部の断面構造を示す断面図。Sectional drawing which shows the cross-section of the operation part in the unused state in Example 1. FIG. 実施例1における、開口状態の鉗子片を示す側面図。The side view which shows the forceps piece of the open state in Example 1. FIG. 実施例1における、開口状態の鉗子片を示す上面図。FIG. 3 is a top view showing a forceps piece in an open state according to the first embodiment. 実施例1における、不完全に閉じた状態の鉗子片が生体組織を把持する様子を示す説明図。Explanatory drawing which shows a mode that the forceps piece of the state closed incompletely in Example 1 hold | maintains a biological tissue. 実施例1における、鉗子片が不完全に閉じた状態にあるときの操作部の断面構造を示す説明図。Explanatory drawing which shows the cross-section of an operation part when the forceps piece is in the incompletely closed state in Example 1. FIG. 実施例1における、完全に閉じた状態の鉗子片が生体組織を切断する瞬間を示す説明図。Explanatory drawing which shows the moment in which the forceps piece of the completely closed state cut | disconnects a biological tissue in Example 1. FIG. 実施例1における、鉗子片が完全に閉じた状態にあるときの操作部の断面構造を示す説明図。Explanatory drawing which shows the cross-section of an operation part when the forceps piece is in the completely closed state in Example 1. FIG. 実施例1における、環状部材が生体組織を緊縛する様子を示す説明図。Explanatory drawing which shows a mode that the cyclic | annular member in Example 1 binds a biological tissue. 実施例1における、従来の鉗子に対する力学的な優位性を説明するための説明図。FIG. 3 is an explanatory diagram for explaining the mechanical superiority over the conventional forceps in the first embodiment. 実施例1における、その他の環状部材を示す正面図。The front view which shows the other annular member in Example 1. FIG. 実施例1における、その他の環状部材を示す側面図。The side view which shows the other annular member in Example 1. FIG. 実施例1における、その他のアウターシースを示す図。The figure which shows the other outer sheath in Example 1. FIG. 従来例における、内視鏡用鉗子を示す側面図。The side view which shows the forceps for endoscopes in a prior art example.
 本発明の実施の形態につき、以下の実施例を用いて具体的に説明する。
(実施例1)
 本例は、止血機能を備えた内視鏡用鉗子1に関する例である。この内容について、図1~図18を用いて説明する。
 本例の内視鏡用鉗子1は、図1~図3に示すように、内周側に位置する第1の挿入部材11、及びこの第1の挿入部材11に相対して軸方向に進退可能な筒状の第2の挿入部材12よりなる断面二重構造の可撓性を呈する細長い挿入部10と、第1の挿入部材11の先端側に保持された一対の鉗子片21と、第1及び第2の挿入部材11、12の後端が連結された操作部4と、第1の挿入部材11及び一対の鉗子片21に対して外挿可能であると共に、第1の挿入部材11に相対する第2の挿入部材12の前進に応じて軸方向に前進し一対の鉗子片21に外挿された状態を経て先端側に押し出されて分離可能な環状部材30と、を備えている。
 第2の挿入部材12は、一対の鉗子片21を収容する位置と、先端側に突出させる位置との間で第1の挿入部材11に相対して軸方向に進退可能である。
 一対の鉗子片21は、自由変形状態において開いた状態となる一方、第2の挿入部材12に内周側に収容されたときに当該第2の挿入部材12の内周面から作用する力に応じて変形して閉じた状態となる。
 さらに、一対の鉗子片21は、環状部材30が分離されるまでの間は生体組織を切断せずに把持する程度の不完全に閉じた状態のみ設定可能である一方、環状部材30が分離される位置まで第2の挿入部材12が軸方向に前進したとき、生体組織を切断可能な程度に完全に閉じた状態となる。
 以下、この内容について、詳しく説明する。
The embodiment of the present invention will be specifically described with reference to the following examples.
Example 1
This example is an example relating to an endoscopic forceps 1 having a hemostatic function. The contents will be described with reference to FIGS.
As shown in FIGS. 1 to 3, the endoscope forceps 1 of this example is advanced and retracted in the axial direction relative to the first insertion member 11 located on the inner peripheral side and the first insertion member 11. A long and narrow insertion portion 10 having a double-section flexible structure composed of a cylindrical second insertion member 12, a pair of forceps pieces 21 held on the distal end side of the first insertion member 11, The first and second insertion members 11 and 12 can be extrapolated with respect to the operation portion 4 to which the rear ends of the first and second insertion members 11 and 12 are connected, and the first insertion member 11 and the pair of forceps pieces 21. And an annular member 30 that can be separated by being pushed forward through the pair of forceps pieces 21 after being advanced in the axial direction in accordance with the advancement of the second insertion member 12 opposite to the first insertion member 12. .
The second insertion member 12 can advance and retreat in the axial direction relative to the first insertion member 11 between a position where the pair of forceps pieces 21 are accommodated and a position where the second insertion member 12 protrudes toward the distal end side.
The pair of forceps pieces 21 are in an open state in a freely deformed state, while the force acting from the inner peripheral surface of the second insertion member 12 is accommodated in the second insertion member 12 on the inner peripheral side. Accordingly, it is deformed and closed.
Further, the pair of forceps pieces 21 can be set only in an incompletely closed state in which the living tissue is grasped without being cut until the annular member 30 is separated, while the annular member 30 is separated. When the second insertion member 12 moves forward in the axial direction to a position where the living tissue is located, the living tissue is completely closed to the extent that it can be cut.
This will be described in detail below.
 本例の内視鏡用鉗子1は、図3に示すごとく、内視鏡100と組み合わせて使用される医療機器である。内視鏡100は、可撓性を備えた管状の挿入管102と、挿入管102の後端に連結された操作部103と、を備えている。挿入管102の先端には、内視鏡像を撮像するための撮像素子(図示略)が配設されている。挿入管102には、撮像素子の制御線や、空気や水を送ったり吸い込んだりするための管が挿通されているほか、内視鏡用鉗子1を挿入するための鉗子チャンネル101と呼ばれる管が挿通されている。 The endoscopic forceps 1 of this example is a medical device used in combination with the endoscope 100 as shown in FIG. The endoscope 100 includes a tubular insertion tube 102 having flexibility, and an operation unit 103 connected to the rear end of the insertion tube 102. An imaging element (not shown) for capturing an endoscopic image is disposed at the distal end of the insertion tube 102. The insertion tube 102 is inserted with a control line of the imaging device, a tube for sending and sucking air and water, and a tube called a forceps channel 101 for inserting the forceps for endoscope 1. It is inserted.
 本例の内視鏡用鉗子1は、鉗子チャンネル101を通して体腔内へ挿入される医療機器である。特に、本例の内視鏡用鉗子1は、止血機能を備えている。それ故、この内視鏡用鉗子1を用いれば、生体組織の切断後、鉗子チャンネル101から鉗子を抜き取ることなく、そのまま止血を行うことができる。つまり、生体組織の切断及び切断後の止血を、ほぼ同時に処置することが可能である。 The endoscopic forceps 1 of this example is a medical device that is inserted into a body cavity through the forceps channel 101. In particular, the endoscopic forceps 1 of this example has a hemostatic function. Therefore, if this endoscopic forceps 1 is used, hemostasis can be performed without removing the forceps from the forceps channel 101 after the biological tissue is cut. That is, it is possible to treat biological tissue cutting and hemostasis after cutting almost simultaneously.
 内視鏡用鉗子1は、図1~図3に示すごとく、鉗子チャンネル101に挿入される挿入部10と、挿入部10の後端に連結された操作部4と、を備えている。
 挿入部10は、第1の挿入部材11であるインナーシースと、第2の挿入部材12であるアウターシースと、の断面二重構造を呈している。インナーシース11は、樹脂材料よりなる筒状の細長い管である。アウターシース12は、カーボン複合材料よりなる薄肉筒状の細長い管である。アウターシース12に対してインナーシース11を内挿配置した挿入部10は、可撓性を備えている。
As shown in FIGS. 1 to 3, the endoscopic forceps 1 includes an insertion portion 10 to be inserted into the forceps channel 101 and an operation portion 4 connected to the rear end of the insertion portion 10.
The insertion part 10 has a double cross-sectional structure of an inner sheath that is the first insertion member 11 and an outer sheath that is the second insertion member 12. The inner sheath 11 is a cylindrical elongated tube made of a resin material. The outer sheath 12 is a thin, cylindrical, elongated tube made of a carbon composite material. The insertion portion 10 in which the inner sheath 11 is inserted and disposed with respect to the outer sheath 12 has flexibility.
 インナーシース11の先端には、図1及び図2に示すごとく、一対の鉗子片21を含む処置部20が一体的に形成されている。 As shown in FIGS. 1 and 2, a treatment portion 20 including a pair of forceps pieces 21 is integrally formed at the distal end of the inner sheath 11.
 アウターシース12は、インナーシース11及び処置部20を内挿可能なように形成されている。アウターシース12の内径は、インナーシース11に対する外挿状態において滑らかに進退できるよう、インナーシース11の外径よりも大径に設定されている。カーボン複合材料よりなる本例のアウターシース12によれば、圧縮方向の耐荷重を高く設定し易く、インナーシース11に相対して軸方向に前進させるための操作力を効率良く伝達可能である。さらに、本例のアウターシース12は、先端から所定距離の位置に当たる内周面に内周側に突出する凸部121を有している。 The outer sheath 12 is formed so that the inner sheath 11 and the treatment portion 20 can be inserted. The inner diameter of the outer sheath 12 is set larger than the outer diameter of the inner sheath 11 so that the outer sheath 12 can smoothly advance and retreat in an extrapolated state with respect to the inner sheath 11. According to the outer sheath 12 of this example made of a carbon composite material, it is easy to set a high load resistance in the compression direction, and an operation force for advancing in the axial direction relative to the inner sheath 11 can be efficiently transmitted. Furthermore, the outer sheath 12 of this example has a convex portion 121 that protrudes to the inner peripheral side on the inner peripheral surface that is a predetermined distance from the tip.
 環状部材30は、切断箇所の止血のために体腔内に留置される部品である。環状部材30は、樹脂材料よりなる弾性を備えた環状の部品である。自由変形状態の環状部材30は、図4に示すごとく、円形状のリングを横に潰したような形状を呈し、その内周形状はスリット状を呈している。生体組織に外挿された環状部材30は、円形状に近づくように弾性変形し、元の形状に復帰しようとする弾性復帰力により確実性高く生体組織に固定される。 The annular member 30 is a component that is placed in the body cavity for hemostasis at the cut site. The annular member 30 is an annular component having elasticity made of a resin material. As shown in FIG. 4, the annular member 30 in a freely deformed state has a shape such that a circular ring is crushed sideways, and its inner peripheral shape has a slit shape. The annular member 30 extrapolated to the living tissue is elastically deformed so as to approach a circular shape, and is fixed to the living tissue with high certainty by an elastic restoring force for returning to the original shape.
 環状部材30の内周面には、図5に示すごとく、脱落防止構造が形成されている。本例の脱落防止構造は、鋸の歯のごとく一定方向に尖った形状の突起31が複数形成された構造である。この一定方向とは逆向き(図中、挿入方向。)に挿入された環状部材30では、突起31が生体組織に食い込み、脱落防止効果が効果的に発揮される。 As shown in FIG. 5, a drop-off preventing structure is formed on the inner peripheral surface of the annular member 30. The drop-off prevention structure of this example is a structure in which a plurality of protrusions 31 having a sharp shape in a certain direction like saw teeth are formed. In the annular member 30 inserted in the direction opposite to the certain direction (in the drawing direction, in the drawing), the protrusion 31 bites into the living tissue, and the effect of preventing the dropout is effectively exhibited.
 未使用状態における内視鏡用鉗子1では、図1、図2及び図6に示すごとく、環状部材30を後退させるためのTバー251が環状部材30の先端面に係合している。Tバー251は、インナーシース11に挿通配置された操作ワイヤ252を介して操作部4に連結されている。このTバー251は、屈曲可能なように適度な柔軟性を備えた樹脂材料により形成されている。なお、インナーシース11の軸方向の中間に当たる外周壁には、図示しない挿通孔が穿孔されている。操作ワイヤ252は、この挿通孔を介して、アウターシース12とインナーシース11との間隙に取り出されている。 In the endoscope forceps 1 in the unused state, as shown in FIGS. 1, 2, and 6, a T bar 251 for retracting the annular member 30 is engaged with the distal end surface of the annular member 30. The T bar 251 is connected to the operation unit 4 via an operation wire 252 inserted and disposed in the inner sheath 11. The T bar 251 is formed of a resin material having appropriate flexibility so that it can be bent. Note that an insertion hole (not shown) is drilled in the outer peripheral wall corresponding to the middle in the axial direction of the inner sheath 11. The operation wire 252 is taken out into the gap between the outer sheath 12 and the inner sheath 11 through the insertion hole.
 処置部20は、図1及び図2に示すごとく、生体組織の切断等を行う部分である。本例の処置部20は、インナーシース11と同様、樹脂材料よりなり、インナーシース11の先端に一体成形されている。処置部20は、連結部23を介して一対の鉗子片21が連結されるよう成形されている。鉗子片21は、中空円柱形状を軸方向に沿って縦割して2分割したようなカップ形状215を呈している。鉗子片21におけるカップ形状215の外周縁部が切断歯210を形成している。 As shown in FIGS. 1 and 2, the treatment unit 20 is a part that cuts a living tissue. Similar to the inner sheath 11, the treatment portion 20 of this example is made of a resin material and is integrally formed at the tip of the inner sheath 11. The treatment portion 20 is shaped such that a pair of forceps pieces 21 are connected via a connecting portion 23. The forceps piece 21 has a cup shape 215 that is obtained by vertically dividing a hollow cylindrical shape along the axial direction into two parts. The outer peripheral edge of the cup shape 215 in the forceps piece 21 forms a cutting tooth 210.
 連結部23は、略矩形状の平板を折り曲げたような形状を呈する。鉗子片21は、連結部23の両端に当たる部分から延設されるように連結されている。連結部23には、インナーシース11の先端が連結されている。なお、自由変形状態の処置部20は、一対の鉗子片21が約90度程度の角度で開口している。 The connecting portion 23 has a shape that is obtained by bending a substantially rectangular flat plate. The forceps pieces 21 are connected so as to extend from the portions corresponding to both ends of the connecting portion 23. The distal end of the inner sheath 11 is coupled to the coupling portion 23. In the treatment portion 20 in the free deformation state, the pair of forceps pieces 21 are opened at an angle of about 90 degrees.
 樹脂材料よりなる連結部23は、折曲げ部分の開き角が変動するように弾性変形可能である。折り曲げ部分の開き角が略ゼロになるまで弾性変形させれば、一対の鉗子片21が略一定の隙間を空けた状態で相互に対面し、その隙間に生体組織を把持可能な不完全に閉じた状態を設定できる(図11を参照して後述する)。不完全に閉じた状態における連結部23は、さらに、鉗子片21を相互に接近させるように弾性変形可能である。このように鉗子片21を相互に接近させる弾性変形によれば、切断歯210の噛み合わせにより生体組織を切断できる完全に閉じた状態を設定できる(図13を参照して後述する)。 The connecting portion 23 made of a resin material can be elastically deformed so that the opening angle of the bent portion varies. If the opening angle of the bent portion is elastically deformed until it becomes substantially zero, the pair of forceps pieces 21 face each other with a substantially constant gap therebetween, and the gap is closed incompletely so that the living tissue can be grasped. Can be set (to be described later with reference to FIG. 11). The connecting portion 23 in the incompletely closed state can be further elastically deformed so as to bring the forceps pieces 21 closer to each other. Thus, according to the elastic deformation that causes the forceps pieces 21 to approach each other, a completely closed state in which the living tissue can be cut by the engagement of the cutting teeth 210 can be set (described later with reference to FIG. 13).
 鉗子片21の先端部分の外周面のうち、その開閉方向(図1における上下方向)に位置する部分には、径方向外周側に突出する凸部211が形成されている。また、連結部23には、上記開閉方向に当たる幅が鉗子片21側に近づくに伴って次第に拡大していき鉗子片21の外周面に滑らかに連なる斜面232が形成されている。凸部211は、アウターシース12が所定の位置まで前進した際にその内周面と当接するように形成されている。斜面232は、凸部211がアウターシース12の内周面に当接するとき、アウターシース12の内周面に配設された上記凸部121に当接するように形成されている。凸部211及び斜面232を開閉方向に押圧すれば、一対の鉗子片21を相互に接近させ、上記完全に閉じた状態を設定できる。 Of the outer peripheral surface of the distal end portion of the forceps piece 21, a convex portion 211 protruding toward the outer peripheral side in the radial direction is formed on a portion located in the opening / closing direction (vertical direction in FIG. 1). In addition, the connecting portion 23 is formed with a slope 232 that smoothly extends to the outer peripheral surface of the forceps piece 21 as the width corresponding to the opening and closing direction gradually approaches the forceps piece 21 side. The convex portion 211 is formed so as to come into contact with the inner peripheral surface when the outer sheath 12 advances to a predetermined position. The inclined surface 232 is formed so as to contact the convex portion 121 disposed on the inner peripheral surface of the outer sheath 12 when the convex portion 211 contacts the inner peripheral surface of the outer sheath 12. By pressing the convex portion 211 and the inclined surface 232 in the opening / closing direction, the pair of forceps pieces 21 can be brought close to each other and the completely closed state can be set.
 操作部4は、図3、図7及び図8に示すごとく、略円柱状の軸部41と、軸部41に対して軸方向に進退可能な状態で外挿される有底略円筒状のスライダ42と、軸部41に対してスライダ42を押し出すように前進側に付勢する付勢スプリング43と、を備えている。軸部41の後端には、オペレータが指をかける操作リング410が延設されている。 As shown in FIGS. 3, 7, and 8, the operation unit 4 includes a substantially cylindrical shaft portion 41, and a bottomed substantially cylindrical slider that is extrapolated in a state in which the shaft portion 41 can advance and retreat in the axial direction. 42 and a biasing spring 43 that biases the slider 42 toward the forward side so as to push the slider 42 against the shaft portion 41. At the rear end of the shaft portion 41, an operation ring 410 on which an operator places a finger is extended.
 軸部41にインナーシース11の後端が固定されている一方、スライダ42にはアウターシース12の後端が固定されている。軸部41に対してスライダ42を進退させれば、インナーシース11に相対してアウターシース12を軸方向に進退させることができる。インナーシース11に相対してアウターシース12を後退させれば、処置部20を突出させて一対の鉗子片21を開口させることができる。インナーシース11に相対してアウターシース12を前進させれば、アウターシース12に処置部20を収容して一対の鉗子片21を閉じさせることができる。 The rear end of the inner sheath 11 is fixed to the shaft portion 41, while the rear end of the outer sheath 12 is fixed to the slider 42. By moving the slider 42 forward and backward with respect to the shaft portion 41, the outer sheath 12 can be advanced and retracted in the axial direction relative to the inner sheath 11. If the outer sheath 12 is retracted relative to the inner sheath 11, the treatment portion 20 can be projected to open the pair of forceps pieces 21. If the outer sheath 12 is advanced relative to the inner sheath 11, the treatment portion 20 can be accommodated in the outer sheath 12 and the pair of forceps pieces 21 can be closed.
 付勢スプリング43は、スライダ42の底427と軸部41の先端面411との間隙に圧縮状態で配置されている。付勢スプリング43は、インナーシース11に外挿された状態で配置されている。この付勢スプリング43は、軸部41に相対してスライダ42を前進側に付勢する。この付勢力は、鉗子片21を開口させようとするスライダ42の後退操作に対する反力となる。この付勢スプリング43によれば、スライダ42の後退操作により鉗子片21を開口させる際の適度な操作力を設定できる。 The urging spring 43 is disposed in a compressed state in the gap between the bottom 427 of the slider 42 and the tip end surface 411 of the shaft portion 41. The biasing spring 43 is arranged in a state of being extrapolated to the inner sheath 11. The urging spring 43 urges the slider 42 forward with respect to the shaft portion 41. This urging force is a reaction force against the backward operation of the slider 42 that attempts to open the forceps piece 21. According to the urging spring 43, an appropriate operating force can be set when the forceps piece 21 is opened by the backward operation of the slider 42.
 軸部41の端面のうち、上記操作リング410とは反対側に当たる先端面411には、インナーシース11の後端が固定されている。軸部41の外周面には、断面矩形状の溝415が軸方向に沿って延設されている。この溝415は、操作リング410側の後端面412に開口する一方、反対側の先端面411には到達しておらずその手前に溝端416が位置している。 The rear end of the inner sheath 11 is fixed to a front end surface 411 that is opposite to the operation ring 410 in the end surface of the shaft portion 41. On the outer peripheral surface of the shaft portion 41, a groove 415 having a rectangular cross section extends along the axial direction. The groove 415 opens on the rear end surface 412 on the operation ring 410 side, but does not reach the opposite end surface 411, and the groove end 416 is positioned in front of the groove 415.
 スライダ42の外周面には、図3、図7及び図8に示すごとく、径方向両側に突出するように立設された2本1組の操作リング420が取り付けられている。また、スライダ42の底427には、インナーシース11を挿通させるための貫通孔426が穿設されている。底427には、アウターシース12の後端及び上記Tバー251から延設された操作ワイヤ252の後端が固定されている。なお、上記のごとく操作ワイヤ252は、インナーシース11の外周面に穿孔された挿通孔(図示略)よりインナーシース11の外周側に取り出されている。 As shown in FIGS. 3, 7 and 8, a pair of two operation rings 420 are installed on the outer peripheral surface of the slider 42 so as to protrude on both sides in the radial direction. A through hole 426 for inserting the inner sheath 11 is formed in the bottom 427 of the slider 42. To the bottom 427, the rear end of the outer sheath 12 and the rear end of the operation wire 252 extending from the T bar 251 are fixed. As described above, the operation wire 252 is taken out to the outer peripheral side of the inner sheath 11 from an insertion hole (not shown) drilled in the outer peripheral surface of the inner sheath 11.
 スライダ42の内周面には、軸部41の溝415に係合する凸部421、422が軸方向に沿って2箇所、形成されている。凸部421は、スライダ42の進退位置によらず常に溝部415に係合する凸部である。スライダ42は、凸部421と溝415との係合に応じて軸部41に対する相対回転が規制されている。凸部422は、軸部41に対してスライダ42を前進させたときに溝415から離脱して軸部41の先端側に位置し、その後、スライダ42の再後退を規制するための凸部である。 On the inner peripheral surface of the slider 42, convex portions 421 and 422 that engage with the groove 415 of the shaft portion 41 are formed at two locations along the axial direction. The convex portion 421 is a convex portion that always engages with the groove portion 415 regardless of the advance / retreat position of the slider 42. The slider 42 is restricted from rotating relative to the shaft portion 41 in accordance with the engagement between the convex portion 421 and the groove 415. The convex portion 422 is a convex portion for separating from the groove 415 when the slider 42 is advanced with respect to the shaft portion 41 and positioned at the tip side of the shaft portion 41, and then restricting the slider 42 from retreating. is there.
 凸部422は、スライダ42の外周壁の一部をなす矩形片423の先端に形成されている。矩形片423は、飛び込み板のごとく根元の1辺のみを介してスライダ42の本体側に連結された部分である。矩形片423は、スライダ42の外周壁に穿設された略U字状のスリット424により周囲から切り離されている。矩形片423は、底427側に位置する根元の1辺を中心とした弾性変形により回動可能である。凸部422は、先端面411側に位置する傾斜面422Tと、後端面412側に位置する直角面422Vと、により形成された突出形状である。 The convex portion 422 is formed at the tip of a rectangular piece 423 that forms part of the outer peripheral wall of the slider 42. The rectangular piece 423 is a portion connected to the main body side of the slider 42 through only one side of the root like a diving plate. The rectangular piece 423 is separated from the surroundings by a substantially U-shaped slit 424 formed in the outer peripheral wall of the slider 42. The rectangular piece 423 can be rotated by elastic deformation around one side of the base located on the bottom 427 side. The convex portion 422 has a protruding shape formed by an inclined surface 422T located on the front end surface 411 side and a right-angle surface 422V located on the rear end surface 412 side.
 矩形片423には、凸部422と同様、内周側に向けてドーム状に突出する突出部425が形成されている。突出部425は、凸部422よりも矩形片423の根元側に近く配置されている。この突出部425が溝端416に係合する位置が、上記付勢スプリング43によるスライダ42の付勢位置となる。付勢スプリング43は、未使用状態において突出部425が溝端416に達するまでスライダ42を付勢し、かつ、突出部425が溝端416を超えない程度の付勢力が生じるように設定されている。 The rectangular piece 423 is formed with a protruding portion 425 that protrudes in a dome shape toward the inner peripheral side, similar to the protruding portion 422. The protruding portion 425 is arranged closer to the base side of the rectangular piece 423 than the convex portion 422. The position where the protruding portion 425 engages with the groove end 416 is the urging position of the slider 42 by the urging spring 43. The urging spring 43 is set so as to urge the slider 42 until the protruding portion 425 reaches the groove end 416 in an unused state, and to generate an urging force such that the protruding portion 425 does not exceed the groove end 416.
 ここで、突出部425あるいは凸部422の位置と、処置部20の状態との関係について説明する。
 図8のごとく突出部425が溝端416に位置する状態は、図1、図2及び図6に示す未使用状態に対応している。未使用状態の処置部20では、アウターシース12の先端面が、凸部211よりも環状部材30の幅分、後退側に奥まって位置している。さらに、この未使用状態では、上記のごとく、操作ワイヤ252の先端に連結されたTバー251が環状部材30の先端面に係止されている。
Here, the relationship between the position of the protrusion part 425 or the convex part 422 and the state of the treatment part 20 will be described.
The state in which the protrusion 425 is positioned at the groove end 416 as shown in FIG. 8 corresponds to the unused state shown in FIGS. 1, 2, and 6. In the treatment portion 20 in the unused state, the distal end surface of the outer sheath 12 is located deeper on the retreat side by the width of the annular member 30 than the convex portion 211. Further, in this unused state, as described above, the T bar 251 connected to the distal end of the operation wire 252 is locked to the distal end surface of the annular member 30.
 凸部422が溝端416に位置する状態(図12)は、図11を参照して後述する通り、生体組織を把持可能な程度に不完全に閉じた状態に対応している。
 凸部422が溝端416を超えて軸部41の先端側に位置する状態(図14)は、図13を参照して後述する通り、生体組織を切断可能な程度に完全に閉じた状態に対応している。
The state where the convex portion 422 is positioned at the groove end 416 (FIG. 12) corresponds to a state where the living tissue is incompletely closed to the extent that the living tissue can be grasped, as will be described later with reference to FIG.
The state in which the convex portion 422 is positioned on the distal end side of the shaft portion 41 beyond the groove end 416 (FIG. 14) corresponds to a state in which the living tissue is completely closed to the extent that it can be cut as described later with reference to FIG. is doing.
 次に、上記のように構成された内視鏡用鉗子1の使用方法について説明する。図1、図2及び図6に示すごとく未使用状態の内視鏡用鉗子1は、内視鏡100の鉗子チャンネル101を通して体腔内に挿入可能である。
 切断対象の生体組織に対して内視鏡用鉗子1の処置部20を接近させた後、軸部41に対してスライダ42を後退させるように操作部4を操作する。未操作状態におけるスライダ42と軸部41との相対位置は、図8に示すごとく溝415に凸部422が収容された状態となっている。凸部422は溝415に沿って後退可能であるため、軸部41に対するスライダ42の後退が許容される。
Next, a method of using the endoscope forceps 1 configured as described above will be described. As shown in FIGS. 1, 2, and 6, the unused endoscope forceps 1 can be inserted into a body cavity through the forceps channel 101 of the endoscope 100.
After the treatment portion 20 of the endoscopic forceps 1 is brought close to the biological tissue to be cut, the operation portion 4 is operated so as to retract the slider 42 with respect to the shaft portion 41. The relative position between the slider 42 and the shaft portion 41 in the unoperated state is such that the convex portion 422 is accommodated in the groove 415 as shown in FIG. Since the projecting portion 422 can be retracted along the groove 415, the retracting of the slider 42 with respect to the shaft portion 41 is allowed.
 スライダ42には、アウターシース12及び操作ワイヤ252の後端が連結されている。それ故、上記のようにスライダ42を後退操作すれば、インナーシース11に対してアウターシース12及び操作ワイヤ252を後退させることができる。操作ワイヤ252を後退させれば、先端に連結されたTバー251により環状部材30を後退させることができる。 The slider 42 is connected to the rear end of the outer sheath 12 and the operation wire 252. Therefore, if the slider 42 is retracted as described above, the outer sheath 12 and the operation wire 252 can be retracted with respect to the inner sheath 11. If the operation wire 252 is retracted, the annular member 30 can be retracted by the T bar 251 connected to the tip.
 スライダ42の後退操作に応じて環状部材30及びアウターシース12を後退させれば、一対の鉗子片21を突出させることができる。環状部材30及びアウターシース12から突出する一対の鉗子片21は、図9及び図10に示すごとく、連結部23の自由変形に応じて開いた状態となる。一方、Tバー251は、屈曲変形してインナーシース11の内部に引きずり込まれるように収容される。これにより、環状部材30とTバーとの係止関係が解かれる。 If the annular member 30 and the outer sheath 12 are retracted according to the retreat operation of the slider 42, the pair of forceps pieces 21 can be protruded. The pair of forceps pieces 21 protruding from the annular member 30 and the outer sheath 12 are opened according to the free deformation of the connecting portion 23 as shown in FIGS. On the other hand, the T bar 251 is accommodated so as to be bent and deformed and dragged into the inner sheath 11. Thereby, the locking relationship between the annular member 30 and the T bar is released.
 一対の鉗子片21の間隙に生体組織を位置させた状態で、軸部41に対してスライダ42を前進させる。これによりインナーシース11に相対してアウターシース12を前進させ、鉗子片21を閉じることができる。アウターシース12を凸部211の手前まで前進させれば、図11に示すごとく、一対の鉗子片21が不完全に閉じた状態に復帰する。不完全に閉じた状態では、一対の鉗子片21により生体組織を確実性高く把持できる。このとき、操作部4においては、図12に示すごとく、凸部422が溝端416に接触し、軸方向の反力が発生する。操作部4の操作者は、この軸方向の反力に応じて上記不完全に閉じた状態が設定された旨を確実性高く把握できる。 The slider 42 is advanced with respect to the shaft portion 41 in a state where the living tissue is positioned in the gap between the pair of forceps pieces 21. Accordingly, the outer sheath 12 can be advanced relative to the inner sheath 11 and the forceps piece 21 can be closed. If the outer sheath 12 is advanced to the front of the convex portion 211, as shown in FIG. 11, the pair of forceps pieces 21 returns to the incompletely closed state. In the incompletely closed state, the living tissue can be grasped with high reliability by the pair of forceps pieces 21. At this time, in the operation part 4, as shown in FIG. 12, the convex part 422 contacts the groove end 416, and an axial reaction force is generated. The operator of the operation unit 4 can grasp with high certainty that the incompletely closed state is set according to the reaction force in the axial direction.
 なお、アウターシース12とは相違し、操作ワイヤ252については軸方向の剛性が確保されていない。それ故、操作ワイヤ252は、軸部41に対するスライダ42の前進に応じてたるみを生じる。操作ワイヤ252の先端に連結されたTバー251は、インナーシース11の内部にそのまま取り残される。 Note that, unlike the outer sheath 12, the operation wire 252 does not have axial rigidity. Therefore, the operation wire 252 sags as the slider 42 advances with respect to the shaft portion 41. The T bar 251 connected to the distal end of the operation wire 252 is left as it is inside the inner sheath 11.
 上記不完全に閉じた状態になったとき、環状部材30は、鉗子片21により把持された生体組織の外周に位置する。スライダ42をさらに前進させれば、凸部211を超えてアウターシース12を前進させることができる。本例の内視鏡用鉗子1では、図13に示すごとく、アウターシース12の先端が凸部211を乗り越えると同時に、処置部20の斜面232に対して凸部121が当接するようになっている。このとき、アウターシース12の内周面から凸部211に作用する当接荷重、及び凸部121から斜面232に作用する当接荷重が発生する。これらの当接荷重は、一対の鉗子片21を相互に接近させる力として作用する。これらの力により一対の鉗子片21が完全に閉じた状態となり生体組織が切断される。 When the incompletely closed state is reached, the annular member 30 is positioned on the outer periphery of the living tissue grasped by the forceps piece 21. If the slider 42 is further advanced, the outer sheath 12 can be advanced beyond the convex portion 211. In the endoscopic forceps 1 of this example, as shown in FIG. 13, the convex portion 121 comes into contact with the inclined surface 232 of the treatment portion 20 at the same time as the distal end of the outer sheath 12 gets over the convex portion 211. Yes. At this time, a contact load that acts on the convex portion 211 from the inner peripheral surface of the outer sheath 12 and a contact load that acts on the slope 232 from the convex portion 121 are generated. These contact loads act as a force for bringing the pair of forceps pieces 21 closer to each other. With these forces, the pair of forceps pieces 21 are completely closed, and the living tissue is cut.
 このとき、操作部4は、図14に示すごとく、凸部422が溝端416を乗り超えて前進し切った状態となる。この状態では、軸部41の先端面411に凸部422の直角面422Vが係合するため、スライダ42の再後退が規制される。一対の鉗子片21が完全に閉じた状態が強固に維持され、切断した生体組織が確実性高く保持され得る。 At this time, as shown in FIG. 14, the operation unit 4 is in a state in which the convex portion 422 has moved forward over the groove end 416. In this state, since the right-angle surface 422V of the convex portion 422 is engaged with the tip surface 411 of the shaft portion 41, the retreat of the slider 42 is restricted. The state in which the pair of forceps pieces 21 are completely closed is firmly maintained, and the cut biological tissue can be held with high reliability.
 分離された環状部材30は、図15に示すごとく、切断された生体組織の根元部分に当たる生体組織に外挿される。根元部分に当たる生体組織は、環状部材30により緊縛される。環状部材30の内周面には、上記のごとく突起31(図5)を含む脱落防止構造が形成されている。突起31が生体組織に食い込み、環状部材30は確実性高く固定され得る。 As shown in FIG. 15, the separated annular member 30 is extrapolated to the living tissue corresponding to the root portion of the cut living tissue. The living tissue that hits the root portion is bound by the annular member 30. On the inner peripheral surface of the annular member 30, a drop-off preventing structure including the protrusion 31 (FIG. 5) is formed as described above. The protrusion 31 bites into the living tissue, and the annular member 30 can be fixed with high reliability.
 さらに、自由変形状態のスリット状の内周形状(図4)に対して、上記根元部分を緊縛した状態の環状部材30では、その内周形状が円形状に近づいている。このとき環状部材30には元の形状に戻ろうとする弾性力が発生している。また、緊縛された生体組織についても元の状態に戻ろうとする弾性力が発生している。環状部材30の弾性力及び生体組織の弾性力は、環状部材30が生体組織に強固に固定されるために有効に作用する。 Furthermore, the inner peripheral shape of the annular member 30 in a state where the root portion is tightly bound is close to a circular shape with respect to the slit-shaped inner peripheral shape (FIG. 4) in a freely deformed state. At this time, an elastic force is generated in the annular member 30 to return to the original shape. In addition, an elastic force is generated to return the bound biological tissue to its original state. The elastic force of the annular member 30 and the elastic force of the biological tissue work effectively because the annular member 30 is firmly fixed to the biological tissue.
 内視鏡用鉗子1は、一対の鉗子片21の内部のカップ形状215に生体組織を収容している。鉗子チャンネル101から内視鏡用鉗子1の挿入部10を抜き取れば、切断した生体組織を回収できる。一方、体腔内の切断箇所には、上記のごとく強固に環状部材30が固定されている。そのため、生体組織の切断面からの出血を確実性高く抑制できる。 The endoscopic forceps 1 accommodates a living tissue in a cup shape 215 inside a pair of forceps pieces 21. If the insertion part 10 of the forceps 1 for endoscope is extracted from the forceps channel 101, the cut biological tissue can be collected. On the other hand, the annular member 30 is firmly fixed to the cut portion in the body cavity as described above. Therefore, bleeding from the cut surface of the living tissue can be suppressed with high certainty.
 以上の通り、本例の内視鏡用鉗子1は、止血機能を備えた内視鏡用鉗子である。この内視鏡用鉗子1を利用すれば、生体組織の切断等と止血とをほぼ同時に処置できるため、出血等を最小限に近く抑制でき、人体側の負担を抑制できる。さらに、生体組織の切断後に鉗子チャンネル101から内視鏡用鉗子1を素早く抜き取り、直ちに内視鏡用止血クリップを挿入して止血を行う必要がなくなるため、処置を行う側の負担を抑制できる。 As described above, the endoscopic forceps 1 of this example is an endoscopic forceps having a hemostatic function. If this endoscopic forceps 1 is used, cutting of a living tissue and hemostasis and hemostasis can be performed almost simultaneously, so that bleeding and the like can be suppressed to a minimum and the burden on the human body side can be suppressed. Furthermore, since it is not necessary to quickly remove the endoscopic forceps 1 from the forceps channel 101 after cutting the living tissue and immediately insert the hemostatic clip for endoscope to stop the hemostasis, it is possible to suppress the burden on the treatment side.
 なお、本例に代えて、環状部材30を利用してマーキングを行うこともできる。本例と同様、生体組織の切断後に鉗子チャンネル101から内視鏡用鉗子1を素早く抜き取り、直ちに別の器具を挿入してマーキングを行う必要がなくなるため、処置を行う側の負担を抑制できる。 In addition, it can replace with this example and can also mark using the annular member 30. FIG. Similarly to this example, it is not necessary to quickly remove the endoscopic forceps 1 from the forceps channel 101 after cutting the living tissue and immediately insert another instrument to perform marking, so that the burden on the treatment side can be suppressed.
 次に、本例の内視鏡用鉗子1の力学的な優位性について、図16を参照して従来の内視鏡用鉗子9と対比して説明する。従来の内視鏡用鉗子9においては、ピン910に支点、鉗子片93の先端に作用点、アーム部931に力点が設定される。小径化の要請により、ピン910-アーム部931間の長さを長く確保することは難しく、一般には、鉗子片93-ピン910間の長さよりも短くなる傾向にある。それ故、鉗子片93で必要とされる力よりも大きな力をアーム部931に作用する必要がある。従来の内視鏡用鉗子9では、操作ワイヤ252とアーム部931との係合構造や、支点であるピン910等に作用する負荷が大きくなり、機械的なトラブルの原因となっている。 Next, the mechanical superiority of the endoscopic forceps 1 of this example will be described in comparison with the conventional endoscopic forceps 9 with reference to FIG. In the conventional endoscopic forceps 9, a fulcrum is set on the pin 910, an action point is set on the tip of the forceps piece 93, and a force point is set on the arm portion 931. Due to the demand for a smaller diameter, it is difficult to ensure a long length between the pin 910 and the arm portion 931, and in general, there is a tendency to be shorter than the length between the forceps piece 93 and the pin 910. Therefore, it is necessary to apply a force larger than that required for the forceps piece 93 to the arm portion 931. In the conventional endoscopic forceps 9, the load acting on the engagement structure between the operation wire 252 and the arm portion 931, the pin 910 that is a fulcrum, and the like is increased, causing a mechanical trouble.
 一方、本例の内視鏡用鉗子1では、凸部211に設定される力点、鉗子片21の先端に設定される作用点、連結部23に設定される支点の位置関係が従来の内視鏡用鉗子とは全く異なっている。すなわち、本例の内視鏡用鉗子1では、支点に対して同じ側、かつ、ほぼ同じ位置に力点と作用点が配置されている。それ故、力点に作用する力が直接的に作用点に伝達され得る。従来とは相違し、支点等に過大な荷重が作用するおそれがないため、機械的なトラブルを発生するおそれが極めて少なくなっている。 On the other hand, in the endoscopic forceps 1 of this example, the positional relationship among the force point set at the convex portion 211, the action point set at the tip of the forceps piece 21, and the fulcrum set at the connecting portion 23 is the same as in the conventional endoscope. It is completely different from the forceps for mirrors. That is, in the endoscopic forceps 1 of this example, the force point and the action point are arranged on the same side with respect to the fulcrum and at substantially the same position. Therefore, the force acting on the force point can be directly transmitted to the action point. Unlike the conventional case, since there is no possibility that an excessive load acts on the fulcrum or the like, the possibility of causing a mechanical trouble is extremely reduced.
 なお、本例では、自由変形状態における内周形状が直線的なスリット形状を呈する環状部材30を採用したが、図17に示すごとく自由変形状態における内周形状が十字状を呈する環状部材30を採用することもできる。また、図18に示すごとく、編み込んだようなメッシュ構造を呈する側壁を備えた環状部材30を採用することもできる。一般的に、メッシュ構造は、強度を確保するために有効な構造である。メッシュ構造の環状部材30であれば、厚み等の寸法を抑制しつつ、生体組織に外挿する際の押込み力に耐え得る強度を確保できる。 In this example, the annular member 30 in which the inner peripheral shape in the free deformation state exhibits a linear slit shape is employed. However, as shown in FIG. 17, the annular member 30 in which the inner peripheral shape in the free deformation state exhibits a cross shape is used. It can also be adopted. Moreover, as shown in FIG. 18, the annular member 30 provided with the side wall which exhibits the mesh structure like knitting is also employable. In general, the mesh structure is an effective structure for ensuring strength. If the annular member 30 has a mesh structure, it is possible to secure the strength that can withstand the pushing force when extrapolated into the living tissue while suppressing dimensions such as thickness.
 また、環状部材30の材質としては、弾性ステンレス、形状記憶合金、形状記憶樹脂、生分解性樹脂等、様々な材質を採用することができる。特に、形状記憶合金製あるいは形状記憶樹脂製の環状部材を採用した場合には、鉗子片21を加温する構成を設けることが良い。この場合には、鉗子片21により環状部材を加温して形状記憶効果を発揮させることができる。形状記憶効果により上記突起31が内周側に起立するように構成すれば、上記脱落防止機構による効果が一層、高くなる。
 また、生分解性樹脂により環状部材30を形成することも良い。体外排出後に自然界で分解されるため、環境に与える影響を抑制できる。
As the material of the annular member 30, various materials such as elastic stainless steel, shape memory alloy, shape memory resin, and biodegradable resin can be adopted. In particular, when an annular member made of a shape memory alloy or a shape memory resin is employed, a configuration for heating the forceps piece 21 is preferably provided. In this case, the shape memory effect can be exhibited by heating the annular member with the forceps piece 21. If the protrusion 31 is configured to stand on the inner peripheral side due to the shape memory effect, the effect of the drop-off prevention mechanism is further enhanced.
Further, the annular member 30 may be formed of a biodegradable resin. Since it is decomposed in nature after being discharged from the body, the impact on the environment can be suppressed.
 なお、アウターシース12の先端部分に金属製のリングを配置することも良い。この場合には、アウターシース12の先端部の強度を高く確保できるようになる。アウターシース12の強度を確保すれば、鉗子片21に対してさらに効率良く力を作用できるようになる。 A metal ring may be disposed at the tip of the outer sheath 12. In this case, the strength of the distal end portion of the outer sheath 12 can be secured high. If the strength of the outer sheath 12 is ensured, a force can be applied to the forceps piece 21 more efficiently.
 なお、本例は、インナーシース11の先端に処置部20を一体成形した例である。これに代えて、インナーシース11とは別体で処置部を形成することも良い。インナーシースの先端に別体の処置部を固定する方法としては、例えば、支持ピン等を介して固定する方法や、接合する方法等がある。接合する方法としては、接着接合、溶着接合、かしめ接合、嵌合等、様々な方法がある。 This example is an example in which the treatment portion 20 is integrally formed at the tip of the inner sheath 11. Instead of this, the treatment portion may be formed separately from the inner sheath 11. As a method for fixing a separate treatment portion to the distal end of the inner sheath, for example, there are a method for fixing via a support pin or the like, a method for bonding, and the like. As a method of joining, there are various methods such as adhesive joining, welding joining, caulking joining, and fitting.
 また、本例は、軸部41に対するスライダ42の押出し操作、すなわち軸部41に対するスライダ42の前進に応じてアウターシース12が前進する例である。これに代えて、スライダ42に対する軸部41の押込み操作、すなわち、スライダ42に対する軸部41の前進に応じてアウターシース12が前進するように構成しても良い。アウターシース12及び操作ワイヤ252の後端を軸部41に連結すると共に、インナーシース11の後端をスライダ42に連結すれば、上記のような軸部41の押込み操作に応じてアウターシース12を前進させ、環状部材30を押し出し分離できるようになる。 Further, this example is an example in which the outer sheath 12 advances in accordance with the pushing operation of the slider 42 with respect to the shaft portion 41, that is, the advancement of the slider 42 with respect to the shaft portion 41. Instead of this, the outer sheath 12 may be configured to advance in accordance with the pushing operation of the shaft portion 41 with respect to the slider 42, that is, with the advancement of the shaft portion 41 with respect to the slider 42. If the outer sheath 12 and the rear end of the operation wire 252 are connected to the shaft portion 41 and the rear end of the inner sheath 11 is connected to the slider 42, the outer sheath 12 is moved according to the pushing operation of the shaft portion 41 as described above. The annular member 30 can be pushed out and separated by being advanced.
 なお、図19に示すごとく、アウターシース12の内周面に溝120を対向配置することも良い。溝120は、軸方向に沿って延設され、アウターシース12の先端面に開口している。この場合には、インナーシース11に相対してアウターシース12を90度回転させることで、溝120の周方向位置を鉗子片21の凸部211に合致できると共に、アウターシース12の凸部121を連結部23の両脇に位置させることができる。この状態であれば、インナーシース11に相対してアウターシース12を軸方向に前進させたとき、前記の不完全に閉じた状態が実現されるのみである。生体組織を切断することなくつまみ上げながら環状部材30を押し出して分離できるようになる。止血鉗子のごとく出血を生じた生体部位の止血や、マーキング等の処置に適用できる。 In addition, as shown in FIG. 19, the groove 120 may be disposed opposite to the inner peripheral surface of the outer sheath 12. The groove 120 extends along the axial direction and opens at the distal end surface of the outer sheath 12. In this case, by rotating the outer sheath 12 by 90 degrees relative to the inner sheath 11, the circumferential position of the groove 120 can be matched with the convex portion 211 of the forceps piece 21, and the convex portion 121 of the outer sheath 12 can be It can be located on both sides of the connecting portion 23. In this state, when the outer sheath 12 is advanced in the axial direction relative to the inner sheath 11, the incompletely closed state is only realized. The annular member 30 can be pushed out and separated while picking up without cutting the living tissue. It can be applied to treatments such as hemostasis and marking of a living body site where bleeding has occurred like a hemostatic forceps.
 なお、鉗子片21の凸部211及びアウターシース12の凸部121を省略すると共に、スライダ42の凸部422の直角面422Vを傾斜面に変更した内視鏡用鉗子も有用である。この内視鏡用鉗子は、本発明の内視鏡用鉗子から切断機能を省いた器具となる。この内視鏡用鉗子では、軸部41に相対したスライダ42の前進によりインナーシース11に相対してアウターシース12を軸方向に前進させることにより、一対の鉗子片41により生体組織をつまみあげつつ切断せずに環状部材30を移設できる。さらに、直角面422Vに代わる末広がりの傾斜面であれば、軸部41に対するスライダ42の後退が許容され、つまんだ生体組織をリリースできる。このような内視鏡用鉗子は、止血やマーキング等の処置に有用である。 An endoscopic forceps in which the convex portion 211 of the forceps piece 21 and the convex portion 121 of the outer sheath 12 are omitted and the right-angle surface 422V of the convex portion 422 of the slider 42 is changed to an inclined surface is also useful. This endoscopic forceps is an instrument in which the cutting function is omitted from the endoscopic forceps of the present invention. In this endoscopic forceps, the living tissue is picked up by the pair of forceps pieces 41 by advancing the outer sheath 12 in the axial direction relative to the inner sheath 11 by the advancement of the slider 42 relative to the shaft portion 41. The annular member 30 can be moved without being cut. Furthermore, if the inclined surface is a divergent slope instead of the right-angled surface 422V, the slider 42 is allowed to move backward with respect to the shaft portion 41, and the pinched biological tissue can be released. Such endoscopic forceps are useful for procedures such as hemostasis and marking.
 以上、実施例1のごとく本発明の具体例を詳細に説明したが、これらの具体例は、特許請求の範囲に包含される技術の一例を開示しているにすぎない。言うまでもなく、具体例の構成や数値等によって、特許請求の範囲が限定的に解釈されるべきではない。特許請求の範囲は、公知技術や当業者の知識等を利用して上記具体例を多様に変形あるいは変更した技術を包含している。 Although specific examples of the present invention have been described in detail as in the first embodiment, these specific examples merely disclose an example of the technology included in the scope of the claims. Needless to say, the scope of the claims should not be construed as limited by the configuration, numerical values, or the like of the specific examples. The scope of the claims includes techniques obtained by variously modifying or changing the above specific examples using known techniques, knowledge of those skilled in the art, and the like.
 1 内視鏡用鉗子
 10 挿入部
 100 内視鏡
 101 鉗子チャンネル
 11 第1の挿入部材、インナーシース
 12 第2の挿入部材、アウターシース
 20 処置部
 21 鉗子片
 211 凸部
 23 連結部
 232 斜面
 251 Tバー
 252 操作ワイヤ
 30 環状部材
 31 突起
 4 操作部
 41 軸部
 415 溝
 416 溝端
 43 付勢スプリング
 42 スライダ
 421、422 凸部
 425 突出部
DESCRIPTION OF SYMBOLS 1 Endoscopic forceps 10 Insertion part 100 Endoscope 101 Forceps channel 11 1st insertion member, inner sheath 12 2nd insertion member, outer sheath 20 Treatment part 21 Forceps piece 211 Convex part 23 Connection part 232 Slope 251 T Bar 252 Operation wire 30 Annular member 31 Protrusion 4 Operation part 41 Shaft part 415 Groove 416 Groove end 43 Energizing spring 42 Slider 421, 422 Protrusion part 425 Projection part

Claims (6)

  1.  内周側に位置する第1の挿入部材、及び当該第1の挿入部材に相対して軸方向に進退可能な筒状の第2の挿入部材よりなる断面二重構造の可撓性を呈する細長い挿入部と、
     上記第1の挿入部材の先端側に保持された一対の鉗子片と、
     上記第1及び上記第2の挿入部材の後端側に連結された操作部と、
     上記第1の挿入部材及び上記一対の鉗子片に対して外挿可能であると共に、上記第1の挿入部材に相対する上記第2の挿入部材の前進に応じて軸方向に前進し上記一対の鉗子片に外挿された状態を経て先端側に押し出されて分離可能なように構成された環状部材と、を備え、
     上記第2の挿入部材は、上記一対の鉗子片を収容する位置と先端側に突出させる位置との間で上記第1の挿入部材に相対して軸方向に進退可能であり、
     上記一対の鉗子片は、自由変形状態において開いた状態となる一方、上記第2の挿入部材の内周側に収容されたときに当該第2の挿入部材側から作用する力に応じて変形して閉じた状態となり、
     かつ、上記環状部材が分離されるまでの間は生体組織を切断せずに把持する程度の不完全に閉じた状態のみ設定可能である一方、上記環状部材が分離される位置まで上記第2の挿入部材が軸方向に前進したとき、生体組織を切断可能な程度に完全に閉じた状態が設定されるように構成されていることを特徴とする内視鏡用鉗子。
    A slender body having a flexible double-section structure composed of a first insertion member located on the inner peripheral side and a cylindrical second insertion member that can advance and retreat relative to the first insertion member in the axial direction. An insertion part;
    A pair of forceps pieces held on the distal end side of the first insertion member;
    An operation unit coupled to the rear end side of the first and second insertion members;
    The first insertion member and the pair of forceps pieces can be extrapolated and moved forward in the axial direction in accordance with the advancement of the second insertion member facing the first insertion member. An annular member configured to be separable by being pushed to the distal end side through a state of being extrapolated to the forceps piece,
    The second insertion member is capable of advancing and retreating in the axial direction relative to the first insertion member between a position where the pair of forceps pieces is accommodated and a position where the second insertion member protrudes toward the distal end side.
    While the pair of forceps pieces are in an open state in a free deformation state, the pair of forceps pieces are deformed according to a force acting from the second insertion member side when housed on the inner peripheral side of the second insertion member. Closed,
    In addition, until the annular member is separated, it is possible to set only an incompletely closed state in which the living tissue is grasped without being cut, while the second member is separated to the position where the annular member is separated. An endoscopic forceps configured to set a state in which the insertion member is completely closed to an extent that allows cutting of a living tissue when the insertion member advances in the axial direction.
  2.  請求項1において、上記一対の鉗子片は、弾性的に変形可能な連結部を介して相互に連結されていると共に、該連結部の弾性的な変形に応じて上記不完全に閉じた状態及び上記完全に閉じた状態が設定され得るように構成されていることを特徴とする内視鏡用鉗子。 2. The pair of forceps pieces according to claim 1, wherein the pair of forceps pieces are connected to each other via an elastically deformable connecting portion, and the incompletely closed state according to the elastic deformation of the connecting portion and An endoscopic forceps characterized in that the completely closed state can be set.
  3.  請求項2において、上記一対の鉗子片、上記連結部及び上記第1の挿入部材は、一体的に成形されていることを特徴とする内視鏡用鉗子。 3. The endoscope forceps according to claim 2, wherein the pair of forceps pieces, the connecting portion, and the first insertion member are integrally formed.
  4.  請求項1~3のいずれか1項において、上記一対の鉗子片のうちの少なくともいずれか一方の先端部分には、径方向外周側に向けて突出する凸部が形成されており、上記一対の鉗子片は、上記第2の挿入部材の内周面から上記凸部に作用する当接荷重に応じて上記完全に閉じた状態が設定されるように構成されていることを特徴とする内視鏡用鉗子。 4. The projection of claim 1, wherein at least one of the pair of forceps pieces has a protruding portion that protrudes toward a radially outer peripheral side. The forceps piece is configured so that the completely closed state is set according to the contact load acting on the convex portion from the inner peripheral surface of the second insertion member. Mirror forceps.
  5.  請求項1~4のいずれか1項において、上記環状部材は、弾性を備えており、自由変形状態における内周断面積が、上記一対の鉗子片に対する外挿状態における内周断面積よりも小さいことを特徴とする内視鏡用鉗子。 5. The annular member according to claim 1, wherein the annular member has elasticity, and an inner peripheral cross-sectional area in a freely deformed state is smaller than an inner peripheral cross-sectional area in an extrapolated state with respect to the pair of forceps pieces. An endoscopic forceps characterized by the above.
  6.  請求項1~5のいずれか1項において、上記環状部材の内周面には、生体組織からの脱落を防止するための脱落防止構造が形成されていることを特徴とする内視鏡用鉗子。 The endoscopic forceps according to any one of claims 1 to 5, wherein a drop-off preventing structure is formed on the inner peripheral surface of the annular member for preventing the drop-off from the living tissue. .
PCT/JP2010/061101 2009-06-30 2010-06-30 Forceps for endoscope WO2011001996A1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI452974B (en) * 2011-10-07 2014-09-21 Nat Univ Chung Hsing Electricity generating device and shoe-pad having an electricity generating device
CN113825457A (en) * 2019-05-20 2021-12-21 株式会社钟化 Forceps for endoscope

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US5922002A (en) * 1989-12-05 1999-07-13 Yoon; Inbae Surgical instrument with jaws and movable internal biopsy device and method for use thereof
JP2000014634A (en) * 1998-07-02 2000-01-18 Olympus Optical Co Ltd Endoscope system
GB2375306A (en) * 2001-05-08 2002-11-13 Stephen Addison Hall Biopsy forceps
JP2005103140A (en) * 2003-10-01 2005-04-21 Olympus Corp Insertion aid for treatment of large intestine whole layer resection, and medical instrument system thereof
JP2008149142A (en) * 2006-12-14 2008-07-03 Ethicon Endo Surgery Inc Tissue clamp for endoluminal local excision of tissue

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Publication number Priority date Publication date Assignee Title
US5922002A (en) * 1989-12-05 1999-07-13 Yoon; Inbae Surgical instrument with jaws and movable internal biopsy device and method for use thereof
JP2000014634A (en) * 1998-07-02 2000-01-18 Olympus Optical Co Ltd Endoscope system
GB2375306A (en) * 2001-05-08 2002-11-13 Stephen Addison Hall Biopsy forceps
JP2005103140A (en) * 2003-10-01 2005-04-21 Olympus Corp Insertion aid for treatment of large intestine whole layer resection, and medical instrument system thereof
JP2008149142A (en) * 2006-12-14 2008-07-03 Ethicon Endo Surgery Inc Tissue clamp for endoluminal local excision of tissue

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI452974B (en) * 2011-10-07 2014-09-21 Nat Univ Chung Hsing Electricity generating device and shoe-pad having an electricity generating device
CN113825457A (en) * 2019-05-20 2021-12-21 株式会社钟化 Forceps for endoscope

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