JP2005288143A - Surgical treatment tool - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To easily and surely suture tissue under the condition of using an endoscope. <P>SOLUTION: This surgical treatment tool includes: an operating part provided on one end of an insert part; and a treatment part extended from the other end of the insert part and provided with a gripping part. The operating part includes: a turning operation part for turning the treatment part; an opening and closing part for opening and closing the treatment part; and an angle changing operating part for changing the angle of extending the treatment part. The treatment part is turned around the axis of the treatment part according to the turning operation in the turning operation part, and the opening and closing operation of the gripping part is performed according to the opening and closing operation in the opening and closing part. This surgical treatment tool is provided with an angle changing means for changing the angle of the treatment part to the axis of the insert part according to the changing operation to the angle changing operation part. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a surgical treatment instrument for grasping a needle and suturing a tissue when performing, for example, coronary revascularization (CABG) of a heart under an endoscope.

  The following operations are known as operations for performing coronary revascularization of the heart under an endoscope, for example. That is, an endoscope, a surgical treatment instrument as a needle holder and forceps are inserted into the chest cavity through a trocar punctured in the chest wall, a part of the coronary artery is incised with acupuncture forceps to provide an anastomosis, A bypass operation is known in which an artery is guided to an anastomosis with grasping forceps and an internal thoracic artery is anastomosed to the anastomosis with a surgical treatment tool. For example, it is disclosed in detail in Min Invas Ther & Technol, 10: 227-230,2001.

  Further, as a surgical treatment tool used in this type of surgery, that is, as a needle driving device for grasping the needle and anastomosing the tissue, an insertion portion having a curved portion is provided at the distal end portion, and the distal end portion of the insertion portion is provided. A surgical treatment instrument having a structure provided with a jaw as a pair of treatment portions that can be opened and closed and rotated around an axis of an insertion portion is known in US Pat. No. 5,951,575 (see Patent Document 1) and the like. ing.

As described above, this surgical treatment tool has a jaw serving as a treatment part that can be opened and closed and rotated at the distal end of the insertion part, but by rotating the rotary operation dial provided in the operation part. The jaw is rotated, and on the other hand, the jaw is opened and closed by operating an opening / closing lever provided in the operation section.
U.S. Pat. No. 5,951,575 (Claim 1 and FIG. 1). Min Invas Ther & Technol, 10: 227-230,2001

  The above-described surgical treatment instrument (needle driving device) disclosed in US Pat. No. 5,951,575 (Patent Document 1) has a pair of jaws that can be opened and closed at the distal end of the insertion portion. When the jaws are closed, the pair of jaws are pulled into the cylinder part via the cable by the operation of the operation part, and the needle is gripped. Therefore, when the jaw is open and closed, the position of the jaw moves in the front-rear direction.Therefore, even if the jaw is opened and approached to the needle, the jaw position is changed when the jaw is closed to try to grip the needle. It is said that the operability is poor because it may change and may be missed.

Further, in the surgical treatment instrument described in the US Pat. No. 5,951,575, when the anastomosis is performed under the endoscope, the friction of the bearing portion that receives the rotation of the jaw when the jaw is closed. Is a configuration that increases,
(1) Holding the holding force increases the load of the turning force. (2) The surgeon must perform the rotating operation while applying the holding force. In other words, the suture needle is stably operated while performing the rotating operation. It is said that it is difficult to hold.

  Further, regarding the treatment portion having a pair of openable and closable jaws provided at the distal end of the surgical treatment instrument described in the US Pat. No. 5,951,575, the treatment portion is in relation to the insertion shaft. Although it is possible to change the angle in the extending direction, when changing the angle in the extending direction, it is necessary to slide the external sheath at the insertion portion of the surgical treatment instrument along the insertion axis. . When performing the procedure using the surgical treatment tool, when changing the angle of the treatment unit in the extending direction, the operator uses the external sheath from the state holding the operation unit to the insertion shaft. You have to move to the state of sliding along. That is, it is said that the surgeon must change the operation unit during the procedure, and it is practically difficult to change the angle in the extending direction of the treatment unit without any trouble in the procedure.

  The present invention has been made in view of the above-described points, and an object of the present invention is to provide a surgical treatment instrument capable of easily and reliably performing tissue suturing under an endoscope.

  A first surgical treatment instrument of the present invention is a treatment having an insertion part, an operation part provided at one end of the insertion part, and a clamping part provided to extend from the other end of the insertion part. A surgical instrument having a surgical operation tool, wherein the operation unit includes a rotation operation unit for performing a rotation operation of the treatment unit, an opening / closing operation unit for performing an opening / closing operation of the treatment unit, An angle change operation unit for changing an angle in the extending direction of the treatment unit, and the treatment unit rotates around an axis of the treatment unit according to the rotation operation in the rotation operation unit. And the opening / closing operation of the clamping unit is possible according to the opening / closing operation in the opening / closing operation unit, and the shaft with respect to the shaft of the insertion unit is changed according to the changing operation with respect to the angle changing operation unit. Having an angle changing means for changing the angle of the treatment section; And butterflies.

  According to a second surgical treatment tool of the present invention, in the first surgical treatment tool, the sandwiching portion includes two sandwiching members each having a flat portion, and the opening / closing operation portion performs the opening / closing operation. Accordingly, at least one of the two clamping members is moved in a direction substantially orthogonal to the plane of the plane portion, whereby the opening / closing operation of the clamping portion is possible.

  According to a third surgical treatment instrument of the present invention, in the second surgical treatment instrument, the treatment section constantly urges at least one of the two holding members in a direction in close contact with the other. And the one clamping member moves in a direction away from the other clamping member against an urging force in the close contact direction by an opening operation in the opening / closing operation.

  According to the present invention, tissue suturing under an endoscope can be easily and reliably performed, that is, a surgical operation can be easily performed by a doctor, thereby shortening the operation time and performing surgery. Improve quality, reduce the burden on patients, promote early discharge of surgical patients and eventually return to society, and improve the rotation efficiency of hospitalized patient beds to realize efficient hospital management The surgical treatment tool which enables is provided.

Embodiments of the present invention will be described below with reference to the drawings.
FIG. 1 is an external perspective view of a needle driver according to an embodiment of the present invention as seen from one side of a front face.

  As shown in FIG. 1, the needle driver 1 as a needle holder as a surgical treatment instrument according to this embodiment is provided at the distal end of the insertion portion 2, the operation portion 3, and the insertion portion 2, as will be described in detail later. A main part is constituted by the treatment part 4. In addition, although the said insertion part 2, the operation part 3, and the treatment part 4 which comprise the said needle driver 1 are explained in full detail behind, a schematic structure is demonstrated below.

  The operation unit 3 is provided with an opening / closing lever 5, a variable angle dial 6, and a rotation dial 7. The open / close lever 5 is a lever for opening and closing the treatment section 4, the variable angle dial 6 is a dial for performing an operation of changing the angle in the extending direction of the treatment section 4, and the rotary dial 7 is It is a dial for performing a turning operation of the treatment section 4.

  As shown in FIG. 2, the treatment portion 4 provided so as to extend from one end of the insertion portion 2 has a clamping portion 8 on the distal end side. When the opening / closing lever 5 is pressed, the clamping portion 8 is opened as shown in FIG. 3, and when the opening / closing lever 5 is stopped, the clamping portion 8 is closed as shown in FIG.

  By performing the opening / closing operation of the clamping part 8 with the opening / closing lever 5, it is possible to clamp / release a suture needle (not shown) having a suture for suturing the affected part with the clamping part 8.

  Further, by rotating the variable angle dial 6, as shown in FIG. 4, the angle in the extending direction of the clamping portion 8 of the treatment portion 4 is rotated within a predetermined plane including the insertion shaft 2 a of the insertion portion 2. The extension direction of the treatment section 4 can be changed to an arbitrary angle with respect to the insertion shaft 2a.

  Further, by rotating the rotary dial 7, as shown in FIG. 2, the holding portion 8 of the treatment portion 4 can be turned around the long axis of the treatment portion 4 and is sewn to the holding portion 8. By operating the rotary dial 7 with the needle held, the biological tissue can be sutured with the suture needle.

  Next, an operation process of coronary artery bypass surgery as an endoscopic anastomosis technique method using a needle driver which is a surgical treatment tool of this embodiment will be described.

In the coronary artery bypass surgery, the skin at a predetermined position on the chest (for example, the left third, fourth, and sixth intercostal positions) is incised with a scalpel.
Next, after the incision, a finger or a conical inner cannula is inserted into the outer tube of the trocar and protrudes from the end, and the incised part of the skin is expanded to form a hole on the inside of the body. At the stage of forming, the inner cannula is extracted from the outer tube of the trocar, thereby creating a port hole to the internal organ by a plurality of, for example, three trocars. Accordingly, various treatment tools can be approached into the left thoracic cavity through a plurality of trocars.

  Subsequently, one-lung ventilation is performed to secure the visual field, as applied in a normal (known) thoracoscopic procedure. That is, a tracheal tube for single-lung ventilation is inserted into the trachea, ventilation with only one (right) lung is performed, and the other (left) lung is collapsed.

  Then, an internal thoracic artery ablation procedure is performed. In the internal thoracic artery ablation procedure, although not shown, an ultrasonic treatment tool, grasping forceps, and endoscope are inserted through a plurality of trocars provided in the port hole. The ultrasonic treatment tool is connected to an ultrasonic control device that supplies and controls ultrasonic drive energy to the ultrasonic treatment tool. Further, the endoscope is connected to a light source device that supplies illumination light and a CCU (camera control unit) that performs signal processing to display the endoscopic image.

  Then, under the observation of the endoscope, the ultrasonic treatment tool is approached to the internal thoracic artery, and the pleura covering the internal thoracic artery is incised. The internal thoracic artery and its side branch are exposed from surrounding tissue using grasping forceps and an ultrasonic treatment tool, and the side branch (blood vessel) extending from the side wall of the internal thoracic artery is cut with an ultrasonic treatment tool. The internal thoracic artery is partially removed by hemostasis of the cut side branch (blood vessel) with an ultrasonic treatment tool.

Then, until the predetermined amount (for example, about 15 cm to 20 cm) of the internal thoracic artery is peeled, the region is enlarged and the pleura incision is continued, and the partial peeling is repeated.
When a predetermined amount of detachment of the internal thoracic artery is performed, hemostasis is performed at two peripheral positions at the cutting position of the internal thoracic artery with hemostatic clips. Then, instead of the ultrasonic treatment tool, the internal thoracic artery is cut at the cutting position of the internal thoracic artery between the hemostatic clips using scissors forceps, and the internal thoracic artery ablation procedure is completed.

When the internal thoracic artery ablation procedure is thus completed, an anastomosis procedure between the internal thoracic artery and the coronary artery is performed. Here, an anastomosis procedure will be described with reference to the flowchart of FIG.
As shown in FIG. 5, the anastomosis procedure between the internal thoracic artery and the coronary artery is performed by adding, for example, three port holes at a position where the approach of the various treatment tools from above to the heart can be performed in step S51. Change the insertion position of multiple trocars. Then, an endoscope is inserted through a trocar directly above the coronary artery. That is, the surgery is performed while observing from approximately right above the surgical site.

  In step S52, a plurality of trocars are inserted with a stabilizer, the needle driver 1 which is the surgical instrument of the present embodiment or other forceps, an endoscope, and grasping forceps. For example, the insertion portion 2 of the needle driver 1 is inserted into the chest cavity, and the operation portion 3 of the needle driver 1 is located outside the body cavity.

Note that the stabilizer is a treatment tool that suppresses the pulsation effect of the heart, and is disclosed in, for example, US Pat. No. 5,807,243, and the detailed description thereof is omitted.
Next, in step S53, the pericardium is incised to expose the epicardial surface, and in step S54, the pulsation effect of the heart near the target coronary artery is suppressed by the stabilizer.

Steps S51 through S54 are anastomosis procedure preparation steps in the anastomosis procedure.
Then, while suppressing the pulsation effect of the heart with the stabilizer, the tourniquet is inserted in the step S56 to close the internal thoracic artery, the internal thoracic artery is closed with the tourniquet, and then the portion with the hemostatic clip in step S57 is attached. In step S58, the cut surface of the internal thoracic artery is trimmed to a predetermined shape using scissors forceps.

Steps S55 to S58 are the internal thoracic artery preparation step in the anastomosis procedure.
In step S59, the central part of the coronary artery is closed with a tourniquet. Next, in step S60, the epicardium covering the coronary artery is incised with a beaver knife (or micro knife) having a round tip to expose the coronary artery, and in step S61, the side wall of the coronary artery is pointed out with a pointed micro knife. An incision is made and a predetermined amount is opened with scissors forceps to form an anastomosis.

  In step S62, the shunt is inserted into the coronary artery from the coronary artery anastomosis. In step S63, the tourniquet is loosened, and the coronary artery is unblocked. This ensures blood flow in the coronary artery.

Steps S59 to S63 are the coronary artery preparation step in the anastomosis procedure.
In step S64, the needle driver 1 which is the surgical treatment instrument of this embodiment is inserted, and the angle in the extending direction of the clamping portion 8 of the treatment portion 4 of the needle driver 1 is adjusted.

  Thereafter, in step S65, a blood vessel anastomosis (suture) procedure between the internal thoracic artery and the coronary artery is performed by the needle driver 1 which is the surgical treatment instrument of the present embodiment. In the vascular anastomosis (suture) procedure between the internal thoracic artery and the coronary artery, the angle in the extending direction of the clamping part 8 of the treatment part 4 is readjusted according to the situation while continuing the continuous suture between the internal thoracic artery and the coronary artery. To do.

  Specifically, as shown in FIG. 6, the treatment section 4 at the tip of the needle driver 1 is accessed near the heart 1002 via a trocar 1001 inserted through the chest wall 1000, and the internal thoracic artery ( When continuous stitching between the cut surface (not shown) and the anastomosis opening 1004 of the coronary artery 1003 is performed, the pulsation effect of the heart 1002 is suppressed by the stabilizer 1005 as described above. Therefore, the stabilizer 1005 may interfere with the approach of the clamping portion 8 of the treatment portion 4 to the suture portion between the cut surface of the internal thoracic artery and the anastomosis opening 1004 of the coronary artery 1003.

  Therefore, as shown in FIG. 7, by rotating the variable angle dial 6 provided in the operation unit 3, the extending direction of the clamping unit 8 of the treatment unit 4 when the needle driver 1 is inserted or continuously stitched. Is adjusted to a desired angle.

  In the needle driver 1 of the present embodiment, since the variable angle dial 6 is provided in the operation unit 3, the operator can change the angle variable dial 6 while maintaining the grip state without changing the grip state in the operation unit 3. Can be rotated, the angle in the extending direction of the clamping part 8 of the treatment part 4 of the needle driver 1 can be readjusted without any trouble in the procedure, and interference by the stabilizer 1005 can be avoided.

Then, before the end of the vascular anastomosis (suture) procedure between the internal thoracic artery and the coronary artery, in step S66, after removing the shunt placed in the coronary artery and adding 12-needle suture, In step S67, a yarn ligation technique is performed.
Steps S64 to S67 are the internal thoracic artery-coronary artery anastomosis step in the anastomosis procedure.

Next, the structure of the needle driver 1 which is the above-described surgical treatment tool as a needle holder will be described with reference to the drawings.
As described above, FIG. 1 is an external perspective view of a needle driver according to an embodiment of the present invention as seen from one side of the front, and FIG. 8 is an external perspective view of the needle driver from the other side of the back. It is.

  9 to 12 are respectively a front view of the needle driver of the present embodiment, FIG. 10 is a left side view of the needle driver of the present embodiment as viewed from one side (left side), and FIG. These are the right view which looked at the needle driver of this embodiment from the other side (right side), and FIG. 12 is the rear view of the needle driver of this embodiment.

  The needle driver 1 includes an insertion portion 2, an operation portion 3 provided at one end (base end side) of the insertion portion 2, and a treatment portion provided to extend from the other end of the insertion portion 2. 4 constitutes a main part.

  The insertion portion 2 has a substantially cylindrical shape having a predetermined length. The operation portion 3 is a member having a substantially rectangular parallelepiped shape that is integrally disposed coaxially with the long axis of the insertion portion 2 on the proximal end side of the insertion portion 2, and is held by an operator with one hand. Thus, the shape can be operated as described later.

  The operation unit 3 includes an opening / closing lever 5 as an opening / closing operation unit for opening / closing the treatment unit 4 and an angle changing operation unit for changing the angle of the treatment unit 4 in the extending direction. The variable angle dial 6 and a rotation dial 7 as a rotation operation unit for rotating the treatment unit 4 are provided.

  As will be described in detail later, the proximal end portion of the opening / closing lever 5 is pivotally supported on one side of the proximal end portion of the operation portion 3, while the free end portion of the opening / closing lever 5 faces toward the distal end side of the operation portion 3. And is biased in a direction away from the exterior portion of the operation portion 3 by a biasing force of a spring 33 described later.

  As will be described in detail later, one end of the base end side of the pulling wire (not shown in FIGS. 8 to 12) is connected to an opening / closing base member (not shown in FIGS. 8 to 12) engaged with the opening / closing lever 5. The urging force of the spring 33 is applied to the open / close lever 5 via the pulling wire.

  The treatment section 4 provided so as to extend from one end of the insertion section 2 has a sandwiching section 8 on the distal end side, and the axial direction of the sandwiching section 8, that is, the extending direction of the treatment section 4 is inserted. It is variable within a predetermined angle range with respect to the axial direction of the portion 2. In other words, the needle driver 1 is provided with angle changing means for changing the angle in the extending direction of the treatment portion 4 with respect to the axis of the insertion portion 2.

Next, the internal structure of the needle driver 1 will be described with reference to the drawings.
First, the structure of the tip part of the needle driver 1 will be described.
13 to 17 are views for explaining the structure of the distal end portion including the treatment portion 4 of the needle driver 1.

  FIG. 13 is a side view of the distal end portion including the treatment portion 4 of the needle driver 1. FIG. 14 is a rear view of the distal end portion including the treatment portion 4 of the needle driver 1. FIG. 15 is a cross-sectional view of the distal end portion including the treatment portion 4 of the needle driver 1. Specifically, FIG. 15 is a cross-sectional view taken along line IX-IX in FIG. 16 and 17 are cross-sectional views of the distal end portion of the needle driver 1. Specifically, FIG. 16 is a cross-sectional view taken along line XVI-XVI in FIG. 14, and FIG. 17 is a cross-sectional view taken along line XVII-XVII in FIG.

  The insertion portion 2 has a sheath 11 that is a stainless steel pipe, that is, a cylindrical member. A stainless steel distal end fixing member 12 is fixed to the distal end side of the sheath 11, that is, the treatment portion 4 side. The distal end fixing member 12 includes, on the proximal end side of the distal end fixing member 12, that is, the sheath 11 side, a cylindrical fitting portion that fits the inner peripheral surface of the sheath 11, and the distal end side of the distal end fixing member 12, that is, the clamping portion. On the 8th side, there is a channel shape portion having a space inside and a cross-sectional shape orthogonal to the axis of the insertion portion 2 having a channel shape.

  In the sheath 11, a rotating power transmission pipe 13 made of stainless steel is inserted as a shaft member. The rotational power transmission pipe 13 is a pipe for transmitting rotational power to the tip portion. A stainless-steel puller wire 14 is inserted into the rotating power transmission pipe 13 for opening and closing the clamping unit 8 described later.

  The pulling wire 14 is a line member that is pulled to the operation unit 3 side in order to perform the opening operation of the clamping unit 8, and is configured flexibly by knitting a thin stainless steel wire. Further, in order to reduce the sliding resistance inside and make it easy to advance and retreat, the wire surface may be coated with a fluorine-based resin.

  The fitting portion of the distal end fixing member 12 is a rod-shaped member having a substantially circular cross-section perpendicular to the axis of the insertion portion 2, but is fixed by a stainless set screw 16 (described later) as shown in FIG. The portion to be formed has a semi-cylindrical shape with a substantially semicircular cross-sectional shape. A rotational power transmission pipe 13 and a stainless bending force transmission rod 15 are inserted at positions substantially symmetrical with respect to the axis of the fitting portion of the tip fixing member 12. The turning power transmission pipe 13 is inserted so as to be rotatable and slidable about the shaft of the turning power transmission pipe 13 as a rotation center, and the bending force transmission rod 15 made of stainless steel as a rod member is in the axial direction of the bending force transmission rod 15. It is inserted to be able to advance and retreat.

  The sheath 11 and the distal end fixing member 12 are fixed by a set screw 16 made of stainless steel, and the distal end portion of the sheath 11 and the distal end fixing member 12 are fixed with an adhesive such as an epoxy resin adhesive. Yes.

  A stainless-steel rotational power transmission coil 17 is fixed to the tip of the rotational power transmission pipe 13. The rotational power transmission coil 17 is a flexible coil for transmitting rotational power to the distal end portion of the insertion portion 2. A pulling wire 14 is inserted into the rotational power transmission coil 17. Since the rotational power transmission pipe 13 is made of metal, the rotational power by the rotational operation of the rotational dial 7 in the operation unit 3 can be reliably transmitted to the rotational power transmission coil 17.

  The rotational power transmission coil 17 connected to the rotational power transmission pipe 13 has a triple winding close contact structure configured by overlapping three coils. A second coil is wound in a direction opposite to the winding direction of the lowermost coil so as to be superimposed on the lowermost coil, and the winding direction of the second coil is superimposed on the lowermost coil. A third coil is provided in the opposite winding direction (the same winding direction as the bottommost coil).

  Both ends of the rotational power transmission coil 17 are brazed and cut after being brazed. As a result, the thickness at both ends is thinner than the thickness at the center. Both end portions are fixed to the rotating power transmission pipe 13 and the rotating portion base member 25 by brazing, respectively.

Each of the bending force transmission rods 15 is connected to the bending portion base member 20 via a stainless steel link joint 18 and an H-shaped link member 19.
FIG. 18 is a perspective view for explaining the internal structure of the distal end portion in which the distal end fixing member 12 is omitted by a dotted line. As shown in FIG. 18, the H-type link member 19 has an H-shape having two arm portions 19a and 19b on both sides of the base portion. One of the two arm portions 19a has a longer arm portion than the other two arm portions 19b.

  The bending portion base member 20 has a cylindrical portion 20a on the distal end side, protrudes from the side surface portion and the bottom portion of the proximal end portion of the cylindrical portion 20a on the proximal end side, and extends toward the bending transmission rod 15. It has the extended part 20b extended. An opening is provided on the distal end side of the cylindrical portion 20a. As shown in FIG. 18, a part of the extended portion 20b is sandwiched between two longer arm portions 19a of the H-shaped link member 19 and is connected by a pin 21 penetrating the extended portion 20b. ing. The pin 21 is fixed by laser welding at the end of the H-shaped link member 19, but the extended portion 20 b is rotatable about the axis of the pin 21.

  Further, as shown in FIG. 18, a pin that penetrates one hole of the link joint 18 so that a part of the link joint 18 is sandwiched between the other two arm portions 19 b, which is the shorter one of the H-type link member 19. 22 are connected. The link joint 18 has a substantially rectangular parallelepiped shape and is formed with three holes. The pin 22 is fixed by laser welding at the end of the H-shaped link member 19, but the link joint 18 is rotatable about the axis of the pin 22 as a rotation center.

  The link joint 18 further has a hole portion into which the bending force transmission rod 15 can be inserted. The bending force transmission rod 15 inserted into the hole is connected by a pin 23 that penetrates the bending force transmission rod 15. The pin 23 has an axis in a direction perpendicular to the axis of the pin 22. The pin 23 is fixed at the end of the link joint 18 by laser welding.

  The extending portion 20 b of the bending portion base member 20 is disposed in the space inside the channel-shaped portion of the distal end portion fixing member 12, and the extending portion 20 b and the distal end portion fixing member 12 are on both sides of the distal end portion fixing member 12. The curved portion base member 20 is connected by pins 24 that are inserted from opposite positions on the surface, and the bending portion base member 20 is rotatable about a common axis of these two pins 24.

  Accordingly, as shown in FIG. 19, when the bending force transmission rod 15 advances and retreats in the axial direction of the operation unit 3 by rotating the angle variable dial 6 of the operation unit 3, the bending unit base is set with the pin 24 as the rotation center. The member 20 rotates. FIG. 19 is a perspective view for explaining the internal structure of the distal end portion in which the distal end fixing member 12 is omitted by a dotted line. The pins 21, 22, 23, and 24 are each made of stainless steel. A mechanism by which the bending force transmission rod 15 advances and retreats in the axial direction of the operation unit 3 by rotating the variable angle dial 6 of the operation unit 3 will be described later.

  Returning to FIG. 15, in the cylindrical portion 20 a of the bending portion base member 20, the cylindrical rotating portion base member 25 can rotate around the axis of the rotating portion base member 25 as a rotation center. It is inserted. The rotating part base member 25 has an opening on the distal end side and a bottom on the proximal end side. A hole is formed in the bottom portion on the proximal end side of the rotating portion base member 25, and the distal end portion of the rotational power transmission coil 17 is inserted into the hole, and is fixed by brazing as described above.

  As described above, the rotational power transmission coil 17 is fixed to the rotational force transmission pipe 13 by brazing on the proximal end side, and is fixed to the rotating portion base member 25 on the distal end side. The distal end portion of the rotational force transmission coil 17 is inserted into the bottom portion on the proximal end side of the rotating portion base member 25 and brazed. The proximal end portion of the rotational force transmission coil 17 is inserted and brazed into a step portion formed inside the distal end portion of the rotational force transmission pipe 13. Therefore, when the rotational force transmission pipe 13 is rotated about the rotational force transmission pipe 13 as the rotational center, the rotational force transmission coil 17 and the rotational force are rotated so as to transmit the rotational amount of the rotational force transmission pipe 13 to the treatment unit 4. The part base member 25 also rotates in the same manner.

  The rotating part base member 25 is made of stainless steel, and a wire retaining member 26 is inserted into the rotating part base member 25. The wire retaining member 26 is made of stainless steel and is a cylindrical member having a flange portion on the proximal end side.

  A hole through which the pulling wire 14 can be inserted is provided at the bottom of the proximal end side of the wire retaining member 26. A cylindrical wire retaining member 27 made of stainless steel is inserted into the cylindrical portion on the distal end side of the wire retaining member 26. The wire retaining member 27 is a cylindrical member that is provided at the tip of the pulling wire 14 and prevents the pulling wire 14 from being pulled out.

  The pulling wire 14 is inserted into the cylinder of the wire retaining member 27, and the wire retaining member 27 and the pulling wire 14 are fixed by brazing. The wire retaining member 27 is brought into contact with and caught by the bottom portion on the distal end side of the wire retaining member 26 so that when the pulling wire 14 is pulled toward the operation unit 3 side, the wire retaining member is pulled. 26 can be moved to the operation unit 3 side.

  The distal end portion of the treatment portion 4 is provided with a clamping portion 8 including two clamping members that clamp the needle. Next, the configuration of the clamping portion 8 will be described. FIG. 20 is a rear view of the distal end portion of the needle driver 1. FIG. 21 is a sectional view taken along line XXI-XXI in FIG. 22 is a cross-sectional view taken along line XXII-XXII in FIG.

  A part of a movable clamping piece 28 made of stainless steel, which is one clamping member, is fitted into the rotating part base member 25. The movable clamping piece 28 has a substantially cylindrical shape having two cutout portions 28a and 28b, and the wire in the rotating portion base member 25 is bonded to the end portion of the base end portion with an adhesive such as an epoxy resin adhesive. It is fixed to the retaining member 26. The distal end portion of the movable holding piece 28 has a flat portion for holding the needle. Here, the plane of the flat portion is orthogonal to the axis of the substantially cylindrical movable holding piece 28.

Further, as shown in FIGS. 21 and 22, a convex portion 26 a is formed on a part of the cylindrical portion of the wire retaining member 26, and on the other hand, on the inner peripheral surface on the proximal end side of the movable clamping piece 28. A convex portion 28c is also formed in part. After fitting each convex part so that it does not collide with a part where there is no convex part of the other party, rotate it around the axis so that the convex parts overlap each other in the axial direction of the tip part, and adhesive as described above Thus, the wire retaining member 26 and the movable clamping piece 28 are fixed. By doing so, when the pulling wire 14 is pulled and moved to the operation unit 3 side, the movable holding piece 28 is also moved to the operation unit 3 side together with the wire retaining member 26.
A stainless steel tip clamping piece attachment member 29 is fixed to the tip of the rotating portion base member 25 by a pin 30.

23 to 26 are diagrams for explaining the configuration of the clamping unit 8.
FIG. 23 is a perspective view showing the appearance of the treatment portion at the distal end portion. FIG. 24 is a diagram showing the internal configuration of the clamping unit, and is a perspective view showing the rotating unit base member omitted. FIG. 25 is a diagram showing an internal configuration of the clamping unit, and is a perspective view in which a rotating unit base member and a bending unit base member are partially omitted. FIG. 26 is a view showing the internal configuration of the clamping unit, and is a perspective view showing the rotating unit base member, the bending unit base member, and the movable clamping piece partially omitted.

  As shown in FIG. 15 and FIG. 24 to FIG. 26, the distal end clamping piece mounting member 29 has a T-shaped portion on the proximal end side and a rod-shaped portion on the distal end side. The T-shaped portion on the proximal end side has an extending portion 29 a that extends in a direction orthogonal to the axis of the rotating portion base member 25. The extending portion 29a is slidably inserted into the two cutout portions 28a and 28b of the movable holding piece 28, and the extending portion 29a and the rotating portion base member 25 are formed of the extending portion. It is fixed by a pin 30 that penetrates 29a. The pin 30 is fixed to the rotating portion base member 25 at the end portion by laser welding.

  A stainless steel tip clamping piece 31, which is one clamping member, is fixed to the distal end portion of the tip clamping piece mounting member 29 by a stainless steel pin 32. The pin 32 is fixed to the tip clamping piece 31 by laser welding at the end. The front end clamping piece 31 has an annular shape and has a flat portion parallel to the flat portion of the front end portion of the movable holding piece 28. Therefore, as will be described later, in accordance with the opening / closing operation with respect to the opening / closing lever 5, the needle is sandwiched between the planar portion of the tip sandwiching piece 31 and the planar portion of the movable sandwiching piece 28.

  Anti-slip processing is applied to the surfaces of the flat portion of the tip holding piece 31 and the flat portion of the movable holding piece 28, which are holding surfaces for holding the needle. Non-slip processing includes electrical discharge machining, knurling, and processing of spraying diamond fine powder onto metal plating.

  An inward flange is provided at the distal end portion of the cylindrical movable sandwiching piece 28, and the distal end of the extending portion 29a of the distal end sandwiching piece mounting member 29 facing the inner side surface of the inward flange portion and the inner side surface thereof. Between the side surfaces, the stainless steel spring 33 is compressed and provided so as to be interposed in the rod-shaped portion of the tip clamping piece mounting member 29. Therefore, the spring 33 constitutes a part of a biasing means that always biases at least one of the two clamping members in a direction in close contact with the other.

Next, operation | movement of the treatment part 4 of the needle driver 1 comprised as mentioned above is demonstrated.
First, the opening / closing operation | movement of the clamping part 8 is demonstrated. FIG. 27 to FIG. 29 are views showing a state in which the clamping unit 8 of the treatment unit 4 of the needle driver 1 is opened. FIG. 27 is a perspective view showing a state in which the holding portion 8 of the treatment portion 4 of the needle driver 1 is opened. FIG. 28 is a rear view showing a state in which the holding portion 8 of the treatment portion 4 of the needle driver 1 is opened. FIG. 29 is a cross-sectional view showing a state in which the holding portion 8 of the treatment portion 4 of the needle driver 1 is opened.

  Since the tip clamping piece attachment member 29 is fixed to the rotating portion base member 25, the tip clamping piece 31 fixed to the tip clamping piece attachment member 29 is fixed to the turning portion base member 25. Has a positional relationship. In other words, the tip clamping piece 31 has a positional relationship fixed in the major axis direction with respect to the bending portion base member 20.

  On the other hand, when the opening / closing lever 5 is opened, that is, when the opening / closing lever 5 is pushed and the pulling wire 14 is pulled, it is fixed and hooked to the wire retaining member 26 that can move to the operation unit 3 side. The movable clamping piece 28 can move toward the operation unit 3, which is a direction away from the tip clamping piece 31, while resisting the force applied in the direction in which the spring 33 extends. Accordingly, when the pulling wire 14 is pulled, the movable clamping piece 28 moves in the direction indicated by the arrow in FIG. 27 by an amount corresponding to the forward / backward movement of the pulling wire 14. That is, against the biasing force in the direction of tightly contacting the distal end clamping piece 31 that is the other clamping member by the spring 33, the movable clamping piece 28 that is one clamping member is opened by the opening operation in the opening / closing operation. It moves to the direction away from the front-end | tip clamping piece 31 located in the front-end | tip part. At this time, as shown in FIG. 29, the spring 33 is further compressed as compared with the state where the opening / closing lever 5 is not opened as shown in FIG. 15, and the opening / closing lever 5 is not pushed and opened. The pulling wire 14 is pulled toward the treatment section 4 by the urging force of the spring 33 in the direction in which the movable holding piece 28 is brought into close contact with the distal end holding piece 31 by the extension force of the spring 33. As a result, in the clamping part 8, the needle located between the flat part of the tip clamping piece 31 and the flat part of the movable clamping piece 28 is clamped.

Next, the rotation operation will be described.
When the rotary dial 7 is rotated in a state where the needle is clamped or in a state where the needle is not clamped, the rotational power transmission pipe 13 which is a shaft member rotates around the shaft as a rotation center. The rotating power transmission pipe 17 fixed to the rotating power transmission pipe 13 rotates, and the rotating portion base member 25 fixed to the rotating power transmission pipe 17 also rotates. Since the rotational power transmission pipe 13 is rotated according to the amount of rotation of the rotation dial 7, the amount of rotation corresponding to the amount of rotation of the rotation dial 7 is transmitted to the treatment unit 4. As a result, the tip clamping piece 31 and the movable clamping piece 28 constituting the clamping unit 8 rotate together in conjunction with the rotating unit base member 25.

Further, since the movable holding piece 28 and the wire retaining member 26 are fixed, and the extending portion 29a of the tip holding piece attaching member 29 is inserted into the notches 28a and 28b, The moving part base member 25 and the wire retaining member 26 cooperate to rotate together.

  At this time, the pulling wire 14 and the wire retaining member 27 fixed to the pulling wire 14 are slidable with respect to the wire retaining member 26. Even if it rotates, the pulling wire 14 and the wire retaining member 27 do not rotate together with the rotating part base member 25.

Next, the angle variable operation will be described.
FIG. 30 is a cross-sectional view when the treatment portion 4 of the needle driver 1 is bent as shown in FIG. When the bending force transmission rod 15 is pulled toward the operation unit 3 from the state shown in FIG. 15 by rotating the variable angle dial 6, the bending portion base member is formed by the link joint 18 and the H-shaped link 19. 20 is rotated about the pin 24 as a rotation center.

  The bending amount of the treatment section 4, that is, the bending angle, changes as the bending force transmission rod 15 advances and retreats according to the rotation amount of the variable angle dial 6. Therefore, as described above, the surgeon can perform the treatment by setting the treatment portion 4 to a desired angle with respect to the axis of the insertion portion 2 according to the state of the operation.

  The angle of the axis of the treatment section 4, that is, the axis perpendicular to the sandwiching surfaces of the distal end sandwiching piece 31 and the movable sandwiching piece 28 of the sandwiching section 8 with respect to the axis of the insertion section 2 is in the range of about 0 to 92 degrees Although it can be changed, the angle change range can be variously changed by adjusting the positional relationship of each member.

Here, the curved rotation center position of the treatment portion 4 of the needle driver 1 will be described with reference to FIGS. 31 to 35.
31 to 33,
l: Distance in the longitudinal direction of the insertion portion between the surface where the rotational power transmission coil 17 and the rotational power transmission pipe 13 are joined and the central axis of the pin 24 (curved rotation center)
r: Radius of the coil guide provided on the bending portion base member 20
k: Distance between the rotation center O of the coil guide and the pin 24 in the horizontal and vertical directions
Point A (r, 0): Point at which the rotational power transmission coil 17 contacts the distal end side of the coil guide provided on the bending portion base member 20
Point B (X1, Y1): Point closest to the bending force transmission rod 15 on the surface where the rotational power transmission coil 17 and the rotational power transmission pipe 13 are joined.
Point C (X2, Y2): The point where the rotating power transmission coil 17 and the coil guide provided on the bending portion base member 20 contact each other.
θ: Angle between the insertion section and the tip (0 to -90 degrees), bending angle
L: Length of point A to point C to point B of the rotational power transmission coil 17
t: A gap between the bending portion base member 20 and the rotating portion base member 25
It is.

  L changes as the treatment section 4 is bent. This length change appears as a gap t between the bending portion base member 20 and the rotation portion base member 25. When the change in the gap t is large, the following situation occurs.

(1) The needle holding part at the tip is difficult to work as it moves forward and backward in the long axis direction of the holding part
(2) When L is further increased from the state where the gap t becomes 0, the rotating portion base member 25 is pressed against the bending portion base member 20, so that the force required for rotation increases.
(3) The gripping force decreases when the gap t increases, and the gripping part opens when the gap t further increases. Under such circumstances (1) to (3), it is necessary to minimize the change in the length of L due to bending. There is.

Therefore, in this embodiment, the bending rotation center position of the treatment section 4 is set as follows, and the change in the length of L accompanying the bending is suppressed.
That is, by setting r, l, k, L at the bending angle θ is obtained. R, l, and k are adjusted so that the change in L is small (in the process of obtaining L, the coordinate values X1, Y1, X2, and Y2 of points B and C are used).

Coordinate value of point B
X1 = (r−k) cos θ + lsin θ + k
Y1 = (r−k) sin θ−l cos θ−k
Coordinate value of point C
^{X2 = (r 2 -Y1Y2) /} X1
^{Y2 = [r 2 Y1 + {} r 4 Y1 2 - (X1 2 + Y1 2) (r 4 -r 2 X1 2)} 1/2] / (X1 2 + Y1 2) (X1 ≧ 0)
or
^{Y2 = [r 2 Y1- {r} 4 Y1 2 - (X1 2 + Y1 2) (r 4 -r 2 X1 2)} 1/2] / (X1 2 + Y1 2) (X1 <0)
Coil inner length L
L = racos (X2 / r) + {(X1-X2) 2 + (Y1-Y2) 2} 1/2 ( function actually theta)
By appropriately setting the rotation center position of the curve by the above equations, the change in L is suppressed to a small value.

For example,
k = πr / 4 (the distance between the radius center O of the coil guide and the center of curvature rotation is √2πr / 4)
As a result, the change in L is 0 when θ is 0 ° and −90 °.

In the condition of r = 3 [mm] and l = 6.4 [mm]
When k = 2.3561, the change in L when θ is 0 ° and −90 ° is 0, and the change in L when θ is changed from 0 ° to −90 ° is shown in FIG. Thus, it is possible to keep the change in L to about 0.2 [mm] when bending in this range.

  For reference, FIG. 35 shows the change in L when k = 3. At this time, the length change of L in the curved range from 0 ° to 90 ° becomes as large as about 1.3 [mm], and it can be seen that the position of the rotation center is important.

Next, the operation unit in the embodiment of the present invention will be described.
FIG. 36 is a front view of the needle driver of the present embodiment, and FIG. 37 is a rear view of the needle driver of the present embodiment. FIG. 38 is a side view of the main part of the operation unit 3 of the needle driver according to the present embodiment as viewed from one side (left side). FIG. 39 shows the operation unit 3 in XXXVII-XXXVII in FIG. It is the principal part sectional drawing cut out and shown in figure, and is the figure which looked at the said operation part 3 from the back side.

  Further, FIG. 40 is a perspective view of a main part of the needle driver according to the above embodiment in which the rotary dial 7, the angle variable dial 6 and the open / close lever 5 are omitted from the exterior portion of the operation unit 3. FIG. 41 is an enlarged perspective view of a main part of the needle driver of the above-described embodiment, in which the rotary dial 7 and the variable angle dial 6 are shown without the exterior part of the operation part 3, and the treatment part 4 is curved. FIG. 42 is an enlarged perspective view of the main part of the needle driver according to the above-described embodiment, in which the rotary dial 7 and the variable angle dial 6 are shown with the exterior portion of the operation unit 3 omitted. The initial state (not curved) is shown. Further, FIG. 43 is an enlarged perspective view of a main part of the needle driver according to the above embodiment in which the opening / closing lever 5 is shown without the exterior part of the operation part 3, and shows a state when the treatment part 4 is closed. 44 is an enlarged perspective view of a main part of the opening / closing lever 5 in the needle driver of the above embodiment, with the exterior portion of the operation unit 3 omitted, and shows a state when the treatment unit 4 is opened.

  As described above, the needle driver 1 as a needle holder, which is a surgical treatment instrument of the present embodiment, is composed mainly of the insertion portion 2, the operation portion 3, and the treatment portion 4 provided at the distal end of the insertion portion 2. However, the operation unit 3 includes operation mechanisms for various operations in the treatment unit 4 and is integrally disposed on the proximal end side of the insertion unit 2 (see FIG. 36 and FIG. 37).

Hereinafter, the operation part 3 in the needle driver 1 of this embodiment is demonstrated.
As shown in FIGS. 36 to 40, the operating portion 3 is integrally disposed coaxially with the long axis of the insertion portion 2 on the proximal end side of the insertion portion 2, and has an approximately rectangular parallelepiped shape. 131.

On one side of the operation unit 3, an opening / closing lever 5 having a base end portion of the operation unit 3 as a rotation center is disposed so as to be swingable toward one side of the operation unit 3.
The opening / closing lever 5 is a lever as an opening / closing operation unit for opening / closing the treatment unit 4, and can swing around a shaft 151 provided on one side of the proximal end of the operation unit 3. The free end portion extends from the proximal end portion of the operation portion 3 toward the distal end side.

  Further, a link 152 (described later) is installed in the middle of the free end portion between the opening / closing operation mechanism 171 provided in the exterior member 131, and further toward the direction away from the exterior member 131 via the link 152. Thus, the biasing force of the spring 33 described above is applied.

  Further, in the middle of the exterior member 131 in the long axis direction, in the vicinity of the free end portion of the opening / closing lever 5, toward the one side (left side in FIG. 36), the surgeon's finger placement convex portion. 133 is projected. The height in the projecting direction of the finger placement convex portion 133 is determined to an appropriate value according to the swing range of the free end portion of the open / close lever 5, that is, according to the maximum separation position of the tip portion. . Specifically, in this embodiment, before and after the operator operates the opening / closing lever 5 with a predetermined finger (assuming a thumb in the needle driver 1 of this embodiment), the finger is temporarily It is assumed that the operating portion 3 is gripped by abutting the finger placement convex portion 133, so that the needle driver 1 can be gripped more stably when the opening / closing lever 5 is not operated, and reliable. The procedure can be realized.

  Returning to FIG. 36, in the middle of the exterior member 131 in the major axis direction, a convex portion 132 in which a dial operation unit 101 to be described later is provided is provided toward the other side (right side in FIG. 36). Projected.

  An opening groove 136a for exposing the variable angle dial 6 and an opening groove 137a for the rotating dial 7 are formed along the long axis direction of the exterior member 131 on the front side of the convex portion 132 (see FIG. 36). ing. The opening groove 136a and the opening groove 137a are arranged along the major axis direction of the exterior member 131 at positions closer to the other side surface (right side surface in FIG. 36) and closer to the center, respectively. Although arranged, the opening groove 136a is arranged closer to the proximal end side of the operation unit 3 than the opening groove 137a.

  On the other hand, at the positions facing the opening groove 136a and the opening groove 137a on the back side of the convex portion 132 (see FIG. 37), the opening groove 136b for exposing the variable angle dial 6 and the rotation dial 7 are respectively provided. An opening groove 137b is formed.

  From the opening grooves 136a and 136b and the opening grooves 137a and 137b, the variable angle dial 6 and the rotary dial 7 are arranged so as to expose a part of their circumferential surfaces.

  That is, the variable angle dial 6 and the rotary dial 7 that are exposed and disposed in the open grooves 136a and 136b and the open grooves 137a and 137b, respectively, have the variable angle dial 6 closer to the proximal end side of the operation unit 3. Therefore, it is arranged at a position outside the operation unit 3.

  Next, the angle variable dial 6 as an angle changing operation part for changing the angle in the extending direction of the treatment part 4 and the turning as a turning operation part for turning the treatment part 4 The dial 7 and its peripheral part will be described with reference to FIGS.

  From the middle in the long axis direction of the operation unit 3 toward the insertion unit 2 side, that is, on the convex portion 132, the rotation dial 7 constituting the rotation operation mechanism of the treatment unit 4 and the angle of the treatment unit 4 An angle variable dial 6 constituting a variable operation mechanism is provided.

  Both the rotary dial 7 and the variable angle dial 6 are incorporated in the dial operation unit 101 and are disposed so as to be rotatable at predetermined positions.

  Note that the outer peripheral surfaces of the variable angle dial 6 and the rotary dial 7 are knurled in this embodiment in consideration of operability.

  The dial operation unit 101 includes a pedestal 102 made of aluminum or the like, holding protrusions 111, 113, and 114 suspended from the pedestal 102, and a member 112 that connects the holding protrusions 111 and 113. The rotation unit 7, the variable angle dial 6, and the bevel gear units 123 and 121 that engage with the rotation dial 7 and the variable angle dial 6, respectively, are incorporated in the configured holding unit.

  The pedestal 102 is a hard plate-like member having a substantially strip shape. A holding projection 111 is integrally suspended by a screw or the like at one end thereof, and a holding projection 113 at the other end. Is integrally suspended by screws or the like as described above. Further, the holding projection piece 111 and the holding projection piece 113 are connected by a connecting member 112 in which a step corresponding to the arrangement position of the variable angle dial 6 and the rotary dial 7 is formed. The connecting member 112 is fixed to the holding protrusions 111 and 113 by screws 118 and 119, respectively.

  In addition, an inner bevel gear 61 and an inner bevel gear 71 are disposed coaxially with respect to the angle variable dial 6 and the rotation dial 7, respectively. It is designed to rotate integrally with the moving dial 7.

  Further, the inner bevel gear 61 and the inner bevel gear 71 are integrally formed with a rotation shaft 6a and a rotation shaft 7a, which are rotation shafts common to the variable angle dial 6 and the rotation dial 7, and these rotation shafts. 6a and the rotation shaft 7a are pivotally supported by shaft holes 112a and 112b formed in the connecting member 112, respectively.

  Further, the bevel gear 122 in the bevel gear unit 121 meshes with the inner bevel gear 61, and the bevel gear 124 in the bevel gear unit 123 meshes with the inner bevel gear 71, respectively.

  The bevel gear 122 is integrally fixed to the distal end portion of the large-diameter rotating shaft 126, and the base end portion of the rotating shaft 126 is pivotally supported by a bearing portion 113a formed on the holding projection 113. Has been. On the other hand, the bevel gear 124 is integrally fixed to the distal end portion of the large-diameter rotating shaft 127, and the base end portion of the rotating shaft 127 is rotatable to the bearing portion 111 a formed on the holding projection piece 111. Is pivotally supported.

  Hereinafter, a power conversion mechanism for transmitting the turning power of the variable angle dial 6 to the treatment section 4 and a power conversion mechanism for transmitting the turning power of the rotary dial 7 to the treatment section 4 will be described.

First, the power conversion mechanism related to the variable angle dial 6 will be described.
In the bevel gear unit 121, a worm screw 125 is integrally extended coaxially with the rotation shaft 126 at the center of the base end surface of the rotation shaft 126 that is rotatably supported by the bearing portion 113 a. . The other end of the worm screw 125 is pivotally supported by a holding protrusion 114 that is suspended from the pedestal 102.

  The worm screw 125 is engaged with a moving member 161 that is screwed into the worm screw 125 and is disposed so as to be movable in the long axis direction of the operation unit 3. The moving member 161 is a nut member having an outer peripheral surface having a rectangular shape, and its bottom side is slidably in contact with the pedestal 102. Further, the moving member 161 is screwed into the worm screw 125 with appropriate friction. As the worm screw 125 rotates, the moving member 161 moves on the base 102 in the major axis direction of the appropriate operation unit 3 of the operation unit 3. It comes to slide on. That is, the worm screw 125 and the moving member 161 have a cam-cam follower relationship.

  The variable angle dial 6, the inner bevel gear 61, and the worm screw 125 are configured with a predetermined reduction ratio, and the rotation of the variable angle dial 6 is used for the movement of the moving member 161 with an appropriate reduction ratio. The Rukoto.

  Further, a projecting piece 162 projects from one side of the moving member 161 and moves in the long axis direction of the operation unit 3 as the moving member 161 moves. An engaging hole 162a is formed at the tip of the projecting piece 162, and one end of a connecting rod 163 extending toward the inserting portion 2 is fitted and fixed to the engaging hole 162a. Further, an insertion hole 162b of the pulling wire 14 is formed on the base end side of the projecting piece 162 and on the extension of the rotating shaft of the bevel gear 124. And the pulling wire 14 extended from the insertion part 2 can move freely within the said insertion hole 162b, without being influenced by the position of the said protrusion 162, and the presence or absence of a movement.

  On the other hand, the other end of the connecting rod 163 is fitted and fixed in an engaging hole 164a formed in the connecting portion 164 with the bending force transmitting rod 15 described above. The connecting rod 163 is fitted to one end of the connecting portion 164 from the proximal end side of the operation portion 3, and the bending force transmitting rod 15 is fitted and fixed to the engaging hole 164b at the other end. Thereby, in conjunction with the movement of the moving member 161, the connecting portion 164 moves in the long axis direction of the operation portion 3 via the projecting piece 162 and the connecting rod 163, that is, the rotation of the angle variable dial 6 is rotated. Accordingly, the bending force transmission rod 15 moves in the long axis direction of the operation unit 3.

  The connecting portion 164 is formed with the guide groove 164c that engages with the above-described rotating power transmission pipe 13, and the connecting portion 164 is guided by the rotating power transmission pipe 13 and moves in the long axis direction of the operation portion 3. It is like that.

  FIG. 41 is a view showing a state when the moving member 161 is positioned on the most proximal side of the operation unit 3, and at this time, the treatment unit 4 is in a curved state. FIG. 42 is a view showing a state where the moving member 161 is positioned on the most distal end side of the operation unit 3. At this time, the treatment unit 4 maintains an initial state in which it does not bend.

  Here, the operation of the power conversion mechanism related to the variable angle dial 6 and the treatment unit 4 accompanying the operation of the variable angle dial 6 will be described from the standpoint of an operator.

  When the surgeon rotates the variable angle dial 6, as described above, the inner bevel gear 61, the bevel gear unit 121, the worm screw 125, the moving member 161, and the projecting piece 162 are moved according to the rotation amount of the variable angle dial 6. The bending force transmission rod 15 moves (advances and retreats) in the long axis direction of the operation unit 3. As the bending force transmission rod 15 advances and retreats, the bending amount of the treatment section 4, that is, the bending angle changes (see FIG. 4). Thereby, as described above, the surgeon can perform the treatment by setting the treatment portion 4 to a desired angle with respect to the axis of the insertion portion 2 according to the state of the operation.

Next, a power conversion mechanism related to the rotary dial 7 will be described.
Returning to FIG. 40, as described above, the bevel gear 124 meshes with the inner bevel gear 71 that rotates integrally with the rotation dial 7, and the bevel gear 124 is integrated with the distal end portion of the large-diameter rotation shaft 127. The base end portion of the rotating shaft 127 is pivotally supported by a bearing portion 111 a formed on the holding projection piece 111. One end of the rotating power transmission pipe 13 is coaxially fixed integrally to the base end surface of the rotating shaft 127, and the rotating power transmission pipe 13 rotates integrally with the rotation of the bevel gear 124. It is like that.

  An insertion hole 127 a for inserting the pulling wire 14 is formed at the center of the rotating shaft 127. The distal end portion of the rotational power transmission pipe 13 extending from the insertion portion 2 is fitted into the insertion hole 127 a, and the distal end portion of the rotational power transmission pipe 13 is screwed and inserted from the outer peripheral surface of the rotating shaft 127. The inside of the insertion hole 127a is fixed by the screw that is made. That is, the pulling wire 14 extended from the insertion portion 2 in the rotating power transmission pipe 13 is exposed from the distal end surface of the rotating power transmission pipe 13 and further extends toward an opening / closing operation mechanism 171 described later. Note that the pulling wire 14 extending from the insertion portion 2 can freely move along the rotating power transmission pipe 13 without being affected by the rotation of the rotation shaft 127.

  Here, the operation of the power conversion mechanism according to the rotary dial 7 and the treatment section 4 accompanying the operation of the rotary dial 7 will be described from the standpoint of the surgeon.

  When the operator rotates the rotary dial 7 in a state where the needle is clamped in the treatment unit 4 or in a state where the needle is not clamped, the inner bevel gear 71 and the bevel gear 124 move, and the rotational power transmission pipe 13 rotates. Move. Thereby, the rotating power transmission pipe 17 fixed to the rotating power transmission pipe 13 rotates, and the rotating part base member 25 fixed to the rotating power transmission pipe 17 also rotates. That is, the rotational power transmission pipe 13 rotates according to the rotational amount of the rotational dial 7, and the rotational power of the rotational dial 7 is transmitted to the treatment unit 4. As a result, the tip clamping piece 31 and the movable clamping piece 28 that constitute the clamping unit 8 rotate together with the rotating unit base member 25.

  Next, the opening / closing lever 5 as an opening / closing operation part for opening / closing the treatment part 4 and its peripheral part will be described with reference to FIGS. 39 to 44.

  As described above, on one side of the operation unit 3, the open / close lever 5 that opens and closes the treatment unit 4 is swingably disposed on the shaft 151. The opening / closing lever 5 is a lever as an opening / closing operation unit for opening / closing the treatment unit 4, and can swing around a shaft 151 provided on one side of the proximal end of the operation unit 3. The free end portion extends from the proximal end portion of the operation portion 3 toward the distal end side.

  Further, a link 152 (described later) is installed in the middle of the free end portion between the opening / closing operation mechanism 171 provided in the exterior member 131, and further toward the direction away from the exterior member 131 via the link 152. Thus, the biasing force of the spring 33 described above is applied.

  The opening / closing operation mechanism 171 includes an opening / closing operation base member 172 slidably disposed in the long axis direction of the operation unit 3 inside the proximal end side of the operation unit 3, and the end of the pulling wire 14. A holding member for the engaging piece 14a fixed to the pulling wire 14, which is a pulling wire holding member 173 that moves according to the movement of the opening / closing operation base member 172, the opening / closing operation base member 172, and the opening / closing lever 5 and the like.

  The opening / closing operation base member 172 has a substantially rectangular shape, and is slidably disposed in a guide groove 139 formed in the major axis direction inside the proximal end side of the operation portion 3. The pulling wire holding member 173 is a holding member for the engagement piece 14a in the pulling wire 14 having a prismatic shape, and a long hole 173b is formed in the long axis direction. The long hole 173b is assembled to one side of the opening / closing operation base member 172 with a screw 176. When the pulling wire holding member 173 is assembled to the opening / closing operation base member 172, the pulling wire holding member 173 can be adjusted so as to obtain an optimum tension of the pulling wire 14. That is, when attaching the pulling wire holding member 173, the position of the pulling wire holding member 173 is adjusted so as to absorb the variation in the length of the pulling wire 14 and to give the pulling wire 14 an appropriate deflection. Install.

  A holding portion 173 a for sandwiching the engaging piece 14 a in the pulling wire 14 is formed on the distal end side of the opening / closing operation base member 172. An opening 173c is formed on one surface of the operation portion 3 in the short axis direction of the holding portion 173a. After the engagement piece 14a of the pulling wire 14 is inserted from the opening 173c, the engagement piece 14a Movement in the long axis direction is restricted.

  The link 152 is rotatably disposed on a shaft 172a disposed on the distal end side of the opening / closing operation base member 172 and a shaft 153 disposed in the middle of the free end of the opening / closing lever 5. ing. As a result, the opening / closing operation base member 172 slides on the guide groove 139 via the link 152 in accordance with the swing of the opening / closing lever 5 about the shaft 151 as the rotation center.

  On the other hand, the pulling wire 14 is applied with a biasing force that pulls the pulling wire 14 toward the trap by the spring 33 described above, whereby the opening / closing operation base member 172 is inserted into the inserting portion 2. Is biased to the side. Further, the opening / closing lever 5 is biased by the biasing force via the link 152 in a direction in which the free end portion is separated from the exterior member 131.

  When the opening / closing lever 5 thus urged is pressed against the urging force, the opening / closing operation base member 172 is displaced to the proximal end side of the operation portion 3 via the link 152, and this opening / closing operation base member Along with the displacement of 172, a pulling force to the proximal end side of the operation unit 3 is applied to the pulling wire 14 via the pulling wire holding member 173. Then, the pulling wire 14 to which the tensile force is applied is appropriately moved toward the proximal end after passing through appropriate play.

  In other words, the open / close lever 5 is normally disposed at a position where the free end portion thereof is separated from the exterior member 131 by the urging force of the spring 33. When the operator presses the free end toward the operation unit 3 during use, the traction wire 14 is moved toward the base end of the operation unit 3 after a certain amount of play. The treatment section 4 is opened as the wire 14 moves.

  FIG. 43 shows a state when the opening / closing lever 5 is in a normal state, and at this time, the treatment section 4 is closed. FIG. 44 shows a state when the open / close lever 5 is pressed, and at this time, the treatment section 4 is in an opened state.

Here, the action of the treatment section 4 accompanying the operation of the opening / closing lever 5 will be described from the standpoint of the surgeon.
When the operator presses the opening / closing lever 5 in the normal state (the initial state shown in FIG. 43) in FIG. 44 (the pressing state shown in FIG. 44), the opening / closing operation base member 172 is connected to the operation unit 3 via the link 152. As a result, the pulling wire 14 is pulled and moved toward the proximal end side of the operation portion 3 and the treatment portion 4 is opened (see FIG. 3). When the surgeon appropriately holds the suture needle between the opened treatment portion 4 and then releases the pressing of the opening / closing lever 5, the pulling wire 14 is pulled by the urging force of the spring 33 so that the insertion portion 2 is pulled to the link. The opening / closing lever 5 is again swung in a direction away from the exterior member 131 via 152.

  Thereafter, the operator can perform a bending operation or a rotation operation of the desired treatment section 4 by rotating the angle variable dial 6 or the rotation dial 7.

  Further, as described above, in the needle driver 1 of the present embodiment, the finger placement convex portion 133 is formed in the vicinity of the distal end of the opening / closing lever 5, and the operator does not perform the operation of the opening / closing lever 5. In this case, the finger related to the opening / closing lever 5 can be brought into contact with the finger placement convex portion 133. By bringing the finger into contact with the finger placement convex portion 133, it is possible to prevent the opening / closing lever 5 from being operated unintentionally, and to hold the operation portion 3 more reliably. Therefore, the turning operation of the variable angle dial 6 or the turning dial 7 can be executed more stably.

  In the present embodiment, the rotational displacement direction of the variable angle dial 6 and the rotational dial 7 is a direction parallel to the major axis direction of the operation unit 3. It may be set in an appropriate direction according to the operating range.

  In the present embodiment, the rotation dial 7 and the angle variable dial 6 are arranged with the positional relationship as described above. However, the present invention is not limited to this, and for example, the rotation dial 7 and the angle variable dial 6 are offset. It may be arranged in a row without.

  Furthermore, in this embodiment, the meshing relationship between the inner bevel gear 61 or the inner bevel gear 71 and the bevel gear unit 121 or the bevel gear unit 123 is such that the shafts are arranged with an intersection angle of about 90 degrees. Not limited to this, the angle variable dial 6 and the rotary dial 7 may be appropriately changed according to the arrangement positions of the dials 6 and 7.

Next, a modification of the above-described embodiment will be described. FIG. 45 is an external perspective view of the needle driver 1A according to the modified example as seen from the oblique front view.
The feature of this modification is in the operation unit and the treatment unit. First, the operation unit will be described first. As shown in FIG. 45, the first feature of the operation unit is that a finger hanger member 501 and a palm hanger member 502 are provided on the operation unit 3A.

  The finger hooking member 501 is made of plastic, and is a member for allowing the middle finger to be hooked when the operation unit 3A is gripped. The finger hooking member 501 fixed to the operation portion 3A by screwing or the like has two projecting portions 501a and 501b that project in a direction perpendicular to or substantially perpendicular to the long axis of the operation portion 3A. A middle finger can be placed between the two protrusions 501a and 501b. The protruding amount of the protruding portion 501a on the distal end side of the operating portion 3A from the surface of the operating portion 3A is smaller than the protruding amount of the protruding portion 501b on the proximal end side. The position where the middle finger of the finger hook member 501 is placed is substantially the same position as the variable angle dial 6 and the rotary dial 7 in the major axis direction of the operation unit 3A, or is closer to the base end than the variable angle dial 6 and the rotary dial 7. In the position. In other words, the position where the middle finger of the finger hooking member 501 is placed is substantially the same position as the position where the variable angle dial 6 and the rotation dial 7 are provided or the base end side of the position. Yes.

  The palm member 502 is provided closer to the proximal end side of the operation unit 3A than the finger member 501. The palm member 502 is made of plastic, and is a member having a projecting portion for allowing a root portion between the thumb and the index finger to be hung when the operation portion 3A is gripped.

  Further, the rotary dial 7 is disposed in a bare state on the surface of the exterior member of the operation unit 3A. This is because the finger length (in this case, the length of the index finger) varies depending on the individual, so that the turning operation of the turning dial 7 is facilitated regardless of the finger length.

  FIG. 46 is a view for explaining a state where the needle driver 1A of FIG. 45 according to the modification is gripped. As shown in FIG. 46, the surgeon places the middle finger MF between the two protrusions 501a and 501b by placing the base portion between the thumb FF and the index finger IF on the palm member 502 and placing the middle finger MF between the two protrusions 501a and 501b. The needle driver 1A can be firmly and stably gripped. As shown in FIG. 46, the operator can operate the rotary dial 7 and the variable angle dial 6 with the index finger IF while holding the needle driver 1A, and operate the opening / closing operation button 508 with the thumb FF. can do.

  Further, since the palm member 502 extends obliquely from the side of the operation portion 3A toward the proximal end side, the operator can be brought into close contact with the palm when the palm member 502 is gripped. Can firmly hold the needle driver 1A.

  As shown in FIG. 47, the palm member 502A may be larger than the palm member 502 in FIG. FIG. 47 is an external perspective view of the needle driver 1 </ b> A according to another modification of the present modification as seen from the front oblique measurement. In particular, a plurality of holes 502a are formed in a plastic palm member 502A larger than the palm member 502 in FIG. 45 for weight reduction. The palm member 502A protrudes obliquely from the side of the operation portion 3A toward the distal end side. However, since the palm member 502A and the palm are in close contact with each other when gripped, the operator holds the needle driver 1A. It can be gripped firmly and stably.

Furthermore, the palm members 502 and 502A in FIGS. 45 and 46 may be omitted. Even when the palm members 502 and 502A are not provided, the surgeon can grasp the needle driver 1A without wobbling to some extent, that is, stably. This is because, even when the palm members 502 and 502A are not provided, when the rotation dial 7 is rotated by the index finger IF, the two protruding portions 501a and 501b are rotated by the index finger IF. This is because the middle finger MF functions as a support portion for supporting the finger hooking member 501 in the direction opposite to the rotation direction of the rotation dial 7 with respect to any of the rotation directions. For example, in FIG. 46, when the palm member 502 is not provided, when the index finger IF is moved in the IFF direction on the distal end side of the needle driver 1A and the rotation dial 7 is rotated, the middle finger MF contacts the protruding portion 501b, The protruding portion 501b functions as a support portion. Similarly, when the index finger IF is moved in the IFB direction on the proximal end side of the needle driver 1A to rotate the rotation dial 7, the middle finger MF contacts the protruding portion 501a, and the protruding portion 501a functions as a support portion.
In addition, the position of the palm member 502 in the major axis direction of the operation unit 3A can be adjusted. That is, the operation unit 3 </ b> A has an interval adjustment mechanism for adjusting the interval between the finger hanging member 501 and the palm hanging member 502. This is to cope with differences in the hand size, finger length, etc. of the operator of the needle driver 1A.

  Note that, as described above, in the present modification, the rotation dial 7 is provided outside the operation unit 3A, so that it corresponds to differences in the size of the operator's hand, finger length, and the like. The interval adjusting mechanism may not be provided. However, with this distance adjustment mechanism, as shown in FIG. 1, even if only a part of the rotary dial 7 protrudes from the surface of the operation unit 3, Accordingly, the position of the palm member 502 can be adjusted so that the rotation dial 7 can be easily operated.

  A long counterbore hole 503 is formed on the proximal end side of the operation portion 3A. As shown in FIG. 48, the long counterbore hole 503 has a seat portion 503 a with which the screw head of the adjustment screw 504 comes into contact. FIG. 48 is a partial cross-sectional view of the operation unit 3A of the present modification. A long hole 506 smaller than the inner diameter of the long counterbore hole 503 is formed in the seat portion 503a. A long hole 507 into which the protruding portion 502a of the palm hanging member 502 is formed is formed on the surface of the operation portion 3A opposite to the long counterbore hole 503. The adjustment screw 504 is inserted from the long counterbore hole 503, and the screw portion of the adjustment screw 504 is screwed into the hole 502b of the projecting portion 502a in which the female screw is formed. It is fixed to the part 3A. At the time of fixing, by adjusting the position of the adjustment screw 504 in the long hole 506 in the long axis direction of the operation portion 3A, the position of the palm hanging member 502 in the long axis direction of the operation portion 3A is adjusted by the operator's hand. It can be adjusted according to the size.

Next, the second feature of the operation unit is that, as shown in FIG. 45, the treatment unit 4 is opened and closed by a push button.
An opening / closing push button 508 for opening / closing the treatment section 4 is provided on the operation section 3A. The open / close push button 508 is made of plastic or aluminum. The open / close push button 508 is between the finger hanging member 501 and the palm hanging member 502 in the major axis direction of the operation unit 3A, and is on the opposite side of the finger hanging member 501 and the palm hanging member 502 (the same side as the rotary dial 7). It is arranged. Further, as shown in FIG. 46, the open / close push button 508 is disposed at a position where the operator can perform the push-down operation of the open / close push button 508 with the thumb FF while holding the needle driver 1A.

  FIG. 49 is an external view showing a state where the open / close push button 508 is pushed down. FIG. 50 is a view for explaining an opening / closing operation mechanism of the treatment section 4 by the opening / closing push button 508. The open / close push button 508 is pushed into the operation unit 3A in accordance with the push-down operation. That is, the open / close push button 508 is pushed down in a direction orthogonal to the opening of the hole provided in the exterior member of the operation unit 3A. Further, since the open / close push button 508 has the flange portion 508a that contacts the inside of the exterior member 131, it does not come off the exterior member even when it is not pressed.

  Furthermore, as shown in FIGS. 48 and 50, the opening / closing push button 508 is formed with a groove portion 508b along the long axis direction of the operation portion 3A. One end of the link 152A is disposed in the groove 508 so as to be rotatable around the axis of the shaft 153A. An engagement piece 14a fixed to the pulling wire 14 at the end of the pulling wire 14 is fixed to the other end of the link 152A. A curved surface portion 509 is formed at the tip of the other end of the link 152A to which the engagement piece 14a is fixed.

  One end of the link 152A in the groove portion 508 is located closer to the distal end side in the major axis direction of the operation portion 3A, that is, closer to the treatment portion 4 than the other end to which the engagement piece 14a is fixed. In other words, in the link 152A, one end of the link 152A in the groove 508 is inclined with respect to the major axis of the operation unit 3A from the proximal end side toward the distal end side with respect to the other end to which the engagement piece 14a is fixed. It is provided to be located in the direction. In this state, the curved surface portion 509 of the link 152A is in contact with or located in the vicinity of the sliding portion 510 formed inside the exterior member of the operation portion 3A. When the open / close push button 508 is pressed down, the other end of the link 152A to which the engagement piece 14a is fixed moves more proximally in the long axis direction of the operation portion 3A.

  Specifically, when the open / close push button 508 is pressed down, the link 152A moves toward the inside of the operation unit 3A, but the other end of the link 152A is in contact with the sliding unit 510 inside the operation unit 3A. Slide. That is, when the open / close push button 508 is depressed, as shown in FIG. 48, the curved surface portion 509 of the link 152A has the surface of the sliding portion 510 having a surface substantially parallel to the long axis direction of the operation portion 3 on the proximal side. Move towards. As a result, the pulling wire 14 is pulled toward the proximal end side of the operation unit 3A, so that the clamping unit 8 is opened.

  Therefore, according to the configuration of the operation unit 3A described above, the surgeon can firmly hold the operation unit 3A and can open the holding unit 8 by pressing the open / close push button 508 with the thumb FF.

  Next, a treatment unit according to a modification will be described. As shown in FIG. 51, the feature of the treatment part is that each of the two clamping members has a disk-shaped part.

FIG. 51 is a side view of the treatment section 4 according to a modification.
As shown in FIG. 51, the clamping member 29A is made of metal and has a disk-like flange portion 513 on the distal end side. The disc-shaped flange portion 513 is formed integrally with the clamping member 29A. The sandwiching member 29A is a member in which the tip sandwiching piece 31 and the tip sandwiching piece mounting member 29 in the above-described embodiment are integrated, and the tip sandwiching piece 31 portion is formed in a thin disk shape. Further, a curved surface portion 513 a is formed in the peripheral portion on the distal end side of the disk-shaped flange portion 513. Note that the peripheral portion on the distal end side of the disc-shaped flange portion 513 may be a slope portion instead of a curved portion.

The other clamping member 28A is also made of metal, and is a member having a disc-shaped flange portion 512 on the distal end side. The disc-shaped flange portion 512 is formed integrally with the clamping member 28A. The sandwiching member 28A is a member in which the shaft portion of the movable sandwiching piece 28 in the above-described embodiment is slightly narrowed and the tip side portion is formed into a thin disk shape. Furthermore, a curved surface portion 512 a is formed in the peripheral portion on the proximal end side of the disc-shaped flange portion 512.
As described above, the sandwiching member 29 </ b> A and the sandwiching member 28 </ b> A are each configured to include a thin, substantially disk-shaped portion that forms a flat portion.

  The thickness of the flange portions 512 and 513 in the major axis direction of the operation portion 3A is 0.5 mm or less. The planar portions of the clamping member 29A, which is the tip clamping piece, and the clamping member 28A, which is the movable clamping piece, have a surface shape that is anti-slip processed by electric discharge machining or the like so that the clamped needle can be firmly clamped. Yes.

  In addition, the rotating part base member 25A into which a part of the proximal end side of the sandwiching member 28A is fitted is formed longer than the rotating part base member 25 according to the above-described embodiment. As shown by a dotted line in FIG. 51, the clamping member 28A is pressed toward the distal end side with respect to the rotating portion base member 25A. By depressing the open / close push button 508, the pulling wire 14 is pulled toward the operation unit 3, and the movable holding piece 28A moves to the proximal side as shown in FIG. 51. As a result, the holding unit 8 is opened.

  The diameters of the flange portions 512 and 513 are equal to each other. A diameter d1 of the flange portions 512 and 513 is larger than a diameter d2 of the cylindrical portion 20a of the bending portion base member 20. That is, the diameter d1 of the flange portions 512 and 513 is larger than the diameter of members other than the flange portions 512 and 513 in the treatment portion 4. FIGS. 52 to 55 are views for explaining an operation of clamping a needle using the needle driver 1 according to the embodiment and the needle driver 1A according to the modification. FIG. 52 to FIG. 55 are diagrams for explaining a pinching operation when a needle is placed on a living tissue and held again during surgery, for example. 52 and 54 are diagrams for explaining an operation of holding a needle using the needle driver 1 according to the embodiment. 53 and 55 are diagrams for explaining an operation of clamping a needle using a needle driver 1A according to a modification of the embodiment.

  As shown in FIG. 52, in the case of the needle driver 1, when the needle 511 is to be clamped in a state in which the clamp unit 8 is bent with respect to the insertion unit 2, due to the thickness of the tip clamp unit 31, Depending on the bending angle and the state of the body cavity wall, the needle 511 is difficult to abut on the flat portion of the tip clamping piece 31, so that it may be difficult to clamp the needle 511 placed on the body cavity wall. On the other hand, as shown in FIG. 53, in the case of the needle driver 1A, if the needle 511 is to be clamped in a state where the clamp portion 8 is bent with respect to the insertion portion 2, the flange portion 513 of the clamp member 29A Since the thickness is small, the needle 511 is easily brought into contact with the flat surface portion of the flange portion 513. Furthermore, since the curved portion 513a is formed in the peripheral portion on the distal end side of the flange portion 513, the needle 511 is easily brought into contact with the flat portion of the flange portion 513. In the case shown in FIG. 53, it is sufficient that at least only the flange portion 513 on the front end side is a thin disk.

Further, as shown in FIGS. 54 and 55, depending on the bending angle of each holding portion 8 of the needle driver 1, 1A, the axial direction of the holding portion 8 may be substantially parallel to the wall surface of the body cavity. As shown in FIG. 54, in the case of the needle driver 1, since the diameter of the curved portion base member 20 of the sandwiching portion 8 is larger than the diameter of the distal end sandwiching portion 31, the needle 511 is brought into contact with the flat portion of the distal end sandwiching piece 31. It is difficult to pinch the needle 511 in some cases. On the other hand, as shown in FIG. 55, in the case of the needle driver 1A, the diameters of the flange portion 513 of the holding member 29A and the flange portion 512 of the holding member 28A are the largest when the holding portion 8 is bent. Since the diameter of the member, here, the curved portion base member 20 is larger, the needle 511 is easily brought into contact between the flat portions of the flange portions 513 and 512.
Therefore, according to the configuration of the clamping unit 8A described above, the surgeon can easily clamp the needle regardless of the bending angle of the clamping unit 8A or the state of the body cavity wall.

  The present invention is not limited to the above-described embodiments, and various changes and modifications can be made without departing from the scope of the present invention.

[Appendix]
(Additional Item 1) The other clamping member is positioned at a distal end of the treatment section, and the one clamping member is always attached to the other clamping member by the biasing means. The surgical treatment instrument according to claim 3, wherein the surgical treatment instrument is biased.

(Additional Item 2) The rotation operation unit transmits a rotation amount to the treatment unit by a rotation operation with the axis of the shaft member as a rotation center.
The surgical treatment instrument according to claim 1, wherein the treatment unit rotates the treatment unit in accordance with a rotation operation of the shaft member.

(Additional Item 3) The shaft member is a cylindrical member,
The opening / closing operation portion transmits an opening / closing amount to the treatment portion by an advance / retreat operation of a wire member inserted into the cylindrical member,
The surgical treatment instrument according to claim 2, wherein the treatment section opens and closes the treatment section in accordance with the advance / retreat operation of the wire member.

(Additional Item 4) The angle change operation unit transmits the amount of angle change to the angle change means by the advance / retreat operation of the bar member,
The said angle change means changes the said angle of the said extension direction of the said treatment part according to the said advancing / retreating operation | movement of the said bar member. The Claims 1-3 or the appendix 1 to the appendix The surgical treatment tool according to any one of 3 above.

(Supplementary Item 5) The surgical operation according to Additional Item 4, wherein the angle changing unit includes a coil length change suppressing unit that reduces a change in the length of the coil member connected to the rod member. Treatment tool.

(Additional Item 6) The coil length change suppression means is approximately (√2πr / 4) away from the radius center of the coil member, where π is the circumference ratio and r is the radius of the coil member. The surgical treatment tool according to appendix 5, wherein the coil has a curved center at a position.

(Additional Item 7)
An operation part provided at one end of the insertion part;
A treatment portion provided to extend from the other end of the insertion portion and having a clamping portion;
A surgical treatment instrument comprising:
The operation unit includes a rotation operation unit for rotating the treatment unit, and an opening / closing operation unit for opening / closing the treatment unit,
The treatment section can be rotated around an axis of the treatment section in accordance with the rotation operation in the rotation operation section, and the clamping section in accordance with the opening / closing operation in the opening / closing operation section Can be opened and closed,
The rotation operation unit transmits a rotation amount to the treatment unit by a rotation operation with the axis of the shaft member as a rotation center,
The surgical treatment instrument, wherein the treatment section rotates the treatment section in accordance with a rotation operation of the shaft member.

(Additional Item 8) The sandwiching portion includes two sandwiching members each having a planar portion, and at least one of the two sandwiching members is connected to the planar portion according to the opening / closing operation in the opening / closing operation portion. The surgical instrument according to Additional Item 7, wherein the clamping unit can be opened and closed by moving in a direction substantially orthogonal to a plane.

(Additional Item 9) The shaft member is a cylindrical member,
The opening / closing operation portion transmits an opening / closing amount to the treatment portion by an advance / retreat operation of a wire member or a rod member inserted into the cylindrical member,
The surgical treatment tool according to appendix 8, wherein the treatment portion opens and closes the treatment portion according to the advance / retreat operation of the wire member.

(Additional Item 10) The treatment section includes an urging unit that constantly urges at least one of the two holding members in a direction in close contact with the other.
Supplementary Item 6 or Supplementary Item 9, wherein the one clamping member moves in a direction away from the other clamping member against an urging force in the close contact direction by an opening operation in the opening / closing operation. The surgical treatment instrument described in 1.

(Additional Item 11) The other holding member is positioned at a distal end portion of the treatment portion, and the one holding member is always attached to the other holding member by the urging means. The surgical treatment tool according to item 10, wherein the surgical treatment tool is biased.

(Additional Item 12) The surgical instrument according to Additional Item 8, wherein each of the two holding members has a disk-shaped portion having the planar portion.

(Additional Item 13) The surgical treatment instrument according to Additional Item 8, wherein each of the disk-shaped portions of the two holding members is thin.

(Additional Item 14) The surgical peripheral according to Additional Item 8, wherein, of the two clamping members, a peripheral portion on a distal end side of the disc-shaped portion of the distal end side clamping member is a curved surface portion or a slope portion. Treatment tool.

(Additional Item 15) The diameter of each of the disk-shaped portions of the two clamping members is larger than the diameter of a portion other than the disk-shaped portion in the treatment portion. Surgical instrument.

(Additional Item 16)
A treatment portion provided at one end of the insertion portion and provided with a clamping portion that is rotatable around one axis and that can be opened and closed and bent;
An operation portion provided at the other end of the insertion portion;
A rotational power transmission mechanism that is provided between the operation unit and the treatment unit along the insertion unit, and transmits a rotational force for rotating the treatment unit from the operation unit to the treatment unit;
An opening / closing force transmission mechanism that is provided between the operation unit and the treatment unit along the insertion unit and transmits an opening / closing force for opening / closing the clamping unit from the operation unit to the treatment unit;
A bending force transmission mechanism which is provided between the operation unit and the treatment unit along the insertion unit and transmits a bending force for bending the clamping unit from the operation unit to the treatment unit;
An opening / closing operation mechanism provided in the operation unit, for applying the opening / closing force;
A rotation operation mechanism provided in the operation unit for applying the turning force;
A bending operation mechanism provided in the operation unit for applying the bending force;
A finger hook provided at the operation portion, substantially at the same position as the position at which the turning operation mechanism and the bending operation mechanism are provided, or at a base end side from the position; Surgical treatment tool.

(Additional Item 17) The surgical instrument according to Additional Item 16, wherein the finger-hanging portion has two protrusions, and a finger can be hooked between the two protrusions. .

(Additional Item 18) The additional item 16 or the additional item 17, further comprising a palm hanging portion provided on the operation portion and provided on a proximal end side with respect to a position where the finger hanging portion is provided. The surgical treatment instrument described in 1.

(Additional Item 19) The surgical treatment tool according to Additional Item 18, wherein the palm hanging portion is provided with at least one hole.

(Additional Item 20) The surgical treatment instrument according to Additional Item 18 or 19, further comprising a position adjustment mechanism that adjusts a position of the palm hanging portion in a major axis direction of the operation portion.

(Additional Item 21) The surgical treatment instrument according to any one of Additional Item 16 to Additional Item 20, wherein the opening / closing operation mechanism includes a push button.

(Additional Item 22) The surgical treatment instrument according to any one of Additional Item 16 to Additional Item 21, wherein the rotation operation mechanism includes a dial provided on an exterior surface of the operation unit.

(Additional Item 23) A luminal organ anastomosis technique method for anastomosing a transplanted luminal organ to a transplanted luminal organ,
A first anastomosis opening forming step of forming a first anastomosis opening in the transplanted lumen organ;
A second opening forming step of forming a second anastomosis opening for anastomosing the first anastomosis opening in the transplanted luminal organ;
A curved suture needle connected to an end of a suture thread is clamped so as to be openable and closable, and the suture needle is rotated by a surgical treatment instrument having a clamping part capable of rotating the suture needle on a clamping surface. A luminal organ suturing step of suturing one anastomosis opening and the second anastomosis opening with the suture;
An extension direction angle adjusting step of adjusting an angle in the extension direction of the holding portion, the angle of the extension direction being adjustable on a surface including the insertion axis of the surgical treatment instrument. Cavity organ anastomosis technique method.

It is the external appearance perspective view which looked at the needle driver which is one embodiment of the present invention from the front diagonal one side. It is a 1st figure explaining the effect | action of the treatment part in the needle driver of the said embodiment. It is a 2nd figure explaining the effect | action of the treatment part in the needle driver of the said embodiment. It is a 3rd figure explaining the effect | action of the treatment part in the needle driver of the embodiment. It is a flowchart which shows the flow of the anastomosis technique of the internal thoracic artery and coronary artery using the needle driver of the said embodiment. It is the principal part enlarged front view which showed one state in the anastomosis technique of the internal thoracic artery and coronary artery using the needle driver of the said embodiment. It is the principal part enlarged front view which showed the other state in the anastomosis technique of the internal thoracic artery and coronary artery using the needle driver of the said embodiment. It is the external appearance perspective view which looked at the needle driver of the embodiment from the back diagonally other side. It is a front view of the needle driver of the embodiment. It is the left view which looked at the needle driver of the embodiment from one side. It is the right view which looked at the needle driver of the embodiment from the other side (right side). It is a rear view of the needle driver of the embodiment. It is a side view of the front-end | tip part containing the treatment part in the needle driver of the embodiment. It is a rear view of the front-end | tip part containing the treatment part in the needle driver of the said embodiment. It is sectional drawing along the IX-IX line of FIG. It is sectional drawing along the XVI-XVI line | wire of FIG. It is sectional drawing along the XVII-XVII line of FIG. It is the principal part expansion perspective view which showed the internal structure of the front-end | tip part in the said needle driver which abbreviate | omitted and showed the front-end | tip fixing member in the needle driver of the embodiment. It is the principal part expansion perspective view which showed the internal structure of the front-end | tip part in the said needle driver which abbreviate | omitted and showed the front-end | tip fixing member in the needle driver of the embodiment. It is a rear view of the front-end | tip part in the needle driver of the said embodiment. It is sectional drawing along the XXI-XXI line of FIG. It is sectional drawing along the XXII-XXII line of FIG. It is the principal part expansion perspective view which showed the external appearance of the treatment part in the needle driver of the said embodiment. It is the principal part expansion perspective view which partially omitted some members in the needle driver of the embodiment, and showed an internal structure. It is the principal part expansion perspective view which partially omitted some members in the needle driver of the embodiment, and showed an internal structure. It is the principal part expansion perspective view which partially omitted some members in the needle driver of the embodiment, and showed an internal structure. It is the principal part expansion perspective view which showed the state which the clamping part of the treatment part in the needle driver of the said embodiment opened. It is a rear view of the said treatment part and peripheral part when the clamping part of the treatment part in the needle driver of the embodiment opens. It is sectional drawing which showed the said treatment part and peripheral part when the clamping part of the treatment part in the needle driver of the said embodiment opens. It is sectional drawing which showed the said treatment part and peripheral part when the treatment part in the needle driver of the said embodiment is curved. It is a 1st figure explaining the curvature center of the treatment part in the needle driver of the embodiment. It is a 2nd figure explaining the curvature center of the treatment part in the needle driver of the embodiment. It is a 3rd figure explaining the curve center of the treatment part in the needle driver of the embodiment. It is a 4th figure explaining the curvature center of the treatment part in the needle driver of the embodiment. It is a 5th figure explaining the curvature center of the treatment part in the needle driver of the embodiment. It is a front view of the needle driver of the embodiment. It is a rear view of the needle driver of the embodiment. It is the principal part side view which looked at the operation part in the needle driver of the embodiment from one side. It is principal part sectional drawing which cut and showed the operation part in the needle driver of the said embodiment by XXXVII-XXXVII in FIG. It is the principal part perspective view which abbreviate | omitted the exterior part of the said operation part, and showed the rotation dial, the angle variable dial, and the opening / closing lever in the needle driver of the said embodiment. It is the principal part expansion perspective view which omitted the exterior part of the said operation part, and shows the state when a treatment part is curved, in the rotation dial and angle variable dial in the needle driver of the embodiment. It is the principal part expansion perspective view which omitted the exterior part of the said operation part, and shows the state at the time of the initial stage (it does not curve) of the rotation part and angle variable dial in the needle driver of the said embodiment. It is the principal part expansion perspective view which showed the opening-and-closing lever in the needle driver of the embodiment except the exterior part of the operation part, and shows a state when a treatment part is closed. It is the principal part expansion perspective view which showed the opening-and-closing lever in the needle driver of the embodiment except the exterior part of the operation part, and shows a state when a treatment part is opened. It is the external appearance perspective view seen from the front diagonal measurement of the needle driver which concerns on the modification of the said embodiment. It is a figure for demonstrating the state by which the needle driver which concerns on the modification of the said embodiment was hold | gripped. It is the external appearance perspective view seen from the front diagonal measurement of the needle driver which concerns on other deformation | transformation of the modification of the said embodiment. It is a fragmentary sectional view of the operation part of the modification of the embodiment. It is an external view which shows the state by which the opening / closing pushbutton of the operation part of the modification of the said embodiment was pushed down. It is a figure for demonstrating the opening / closing operation | movement mechanism of the treatment part by the opening / closing pushbutton of the operation part of the modification of the said embodiment. It is a side surface of the treatment part which concerns on the modification of the said embodiment. It is a figure for demonstrating the operation | movement which clamps a needle | hook using the needle driver which concerns on the said embodiment. It is a figure for demonstrating the operation | movement which clamps a needle | hook using the needle driver which concerns on the modification of the said embodiment. It is another figure for demonstrating the operation | movement which clamps a needle | hook using the needle driver which concerns on the said embodiment. It is another figure for demonstrating the operation | movement which clamps a needle | hook using the needle driver which concerns on the modification of the said embodiment.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 ... Needle driver 2 ... Insertion part 3 ... Operation part 4 ... Treatment part 5 ... Opening / closing lever 6 ... Variable angle dial 7 ... Turning dial 8 ... Clamping part 11 ... Sheath 12 ... Tip fixing member 13 ... Rotation power transmission pipe 14 ... Pulling wire 15 ... bending force transmission rod 16 ... set screw 17 ... rotational power transmission coil 18 ... link joint 19 ... H-type link 21, 22, 23, 24, 30, 32 ... pin 25 ... rotating part base member 26 ... wire Retainer receiving member 27 ... Wire retaining member 28 ... Movable clamping piece 29 ... Tip clamping piece mounting member 31 ... Tip clamping piece 33 ... Spring 61 ... Inner bevel gear 71 ... Inner bevel gear 101 ... Dial operation unit 121 ... Bevel gear unit 122 ... Bevel gear 123 ... Bevel gear unit 124 ... Bevel gear 125 ... Worm screw 126 ... Rotating shaft 127 ... Rotating shaft 31 ... outer member 132 ... protrusions 133 ... finger every projection 152 ... link 161 ... moving member 171 ... opening and closing mechanism 172 ... opening and closing operation for the base member 173 ... pulling wire holding member
Attorney Susumu Ito

Claims (3)

An insertion part;
An operation part provided at one end of the insertion part;
A treatment portion provided to extend from the other end of the insertion portion and having a clamping portion;
A surgical treatment instrument comprising:
The operation unit performs a change operation of a rotation operation unit for performing a rotation operation of the treatment unit, an opening / closing operation unit for performing an opening / closing operation of the treatment unit, and an extending direction angle of the treatment unit. An angle change operation unit for
The treatment section can be rotated around the axis of the treatment section in accordance with the rotation operation in the rotation operation section, and the clamping section in accordance with the opening / closing operation in the opening / closing operation section Can be opened and closed,
A surgical treatment tool comprising angle changing means for changing the angle of the treatment section with respect to the axis of the insertion section in response to a change operation on the angle change operation section. The sandwiching portion includes two sandwiching members each having a planar portion, and at least one of the two sandwiching members is approximately relative to the plane of the planar portion in accordance with the opening / closing operation in the opening / closing operation portion. The surgical treatment tool according to claim 1, wherein the clamping unit can be opened and closed by moving in a direction orthogonal to each other. The treatment section has a biasing means that constantly biases at least one of the two clamping members in a direction in close contact with the other,
The said one clamping member moves to the direction spaced apart from said other clamping member by resisting the urging | biasing force of the said close direction by the opening operation in the said opening / closing operation. Surgical instrument.

Images