WO2006080113A1 - Medical appliance for treating inside of biological duct - Google Patents

Medical appliance for treating inside of biological duct Download PDF

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Publication number
WO2006080113A1
WO2006080113A1 PCT/JP2005/018665 JP2005018665W WO2006080113A1 WO 2006080113 A1 WO2006080113 A1 WO 2006080113A1 JP 2005018665 W JP2005018665 W JP 2005018665W WO 2006080113 A1 WO2006080113 A1 WO 2006080113A1
Authority
WO
WIPO (PCT)
Prior art keywords
insertion tube
tube
filter
treatment device
shape
Prior art date
Application number
PCT/JP2005/018665
Other languages
French (fr)
Japanese (ja)
Inventor
Satoshi Saito
Daisuke Kawabe
Original Assignee
Nihon University
Ir Medical Laboratory Co., Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nihon University, Ir Medical Laboratory Co., Ltd. filed Critical Nihon University
Priority to JP2007500420A priority Critical patent/JPWO2006080113A1/en
Publication of WO2006080113A1 publication Critical patent/WO2006080113A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/22Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
    • A61B17/221Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B2017/00831Material properties
    • A61B2017/00867Material properties shape memory effect
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/22Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
    • A61B17/221Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions
    • A61B2017/2212Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions having a closed distal end, e.g. a loop

Definitions

  • Intravascular treatment device Intravascular treatment device
  • the present invention relates to an in-vivo treatment device that treats the inside of a living body by capturing and removing foreign matter in the living body.
  • the in-vivo treatment device described in Patent Document 1 connects three or more alloy wires formed in a straight line to each other at both front and rear ends, and removes intermediate portions of the plurality of alloy wires. It is provided with a filter portion that is configured to be sunk in the radial direction and arranged along a substantially football-like boundary surface. Then, for example, the thrombus in the blood vessel is captured and removed by the trapping portion formed of an umbrella-like cover formed by covering the outer surface of the filter portion, for example, from the front end portion to almost the middle with an elastic film.
  • the in-vivo treatment device is inserted into an induction conduit having catheter force with the filter portion folded, and then inserted into the blood vessel together with the guide tube. Then, after reaching the target location, such as the lesion site, the front end portion of the in-vivo treatment device is sent forward in the guide tube force, and the guide tube force is also exerted, and the filter portion is projected outward. The thrombus is captured and removed from the blood vessel by the filter unit.
  • the filter part provided in the in-vivo treatment device described in Patent Document 1 may become clogged during the operation or immediately block the blood flow in the blood vessel. Therefore, in order to deal with this problem, there is an in-vivo treatment device in which the filter portion is composed of a plurality of support lines and a basket-like mesh body. In a living tube provided with such a filter unit If it is a treatment tool, it is possible to remove the thrombus without blocking the blood flow in the blood vessel.
  • Patent Document 1 JP-A-2001-212152
  • the filter portion provided in the in-vivo treatment device as described above is formed in a basket shape by weaving a mesh body having a shape memory alloy force into a plurality of support wires. For this reason, it takes time to manufacture the filter part, and the manufacturing efficiency of the in-vivo treatment device is reduced, and the cost of the in-vivo treatment device is increased.
  • the filter part is often formed of a shape memory alloy such as a nickel'titanium alloy, and is often subjected to shape memory processing in the state of projecting in the outer diameter direction. It is difficult to bond by. For this reason, when connecting the filter part and other parts of the treatment device such as a wire such as a wire, it is necessary to caulk the front and rear ends of the filter part with a metal or the like, and the step formed in the caulking part However, this contributes to the removal of the filter unit from the in-vivo treatment device. If the filter part is detached from the in-vivo treatment device in the blood vessel, the detached filter part is carried by the blood flow, and there is a possibility that the narrower downstream blood vessel is blocked.
  • a shape memory alloy such as a nickel'titanium alloy
  • the present invention has been made paying attention to the above-described problems, and can improve the manufacturing efficiency and reduce the cost, and can prevent the separation of the filter part. It is an object to provide a treatment tool.
  • the invention described in claim 1 of the present invention is an in-vivo treatment device that captures and removes a foreign substance in the in-vivo tube by a filter portion protruding in the outer diameter direction,
  • the filter part In the insertion tube, at least one place along the axial direction of the insertion tube forms the filter part
  • the filter section has a plurality of openings or slits formed in the peripheral surface of the insertion tube, and is formed between the plurality of openings or slits by contracting the filter section forming position of the insertion tube in the axial direction.
  • the shape is memorized and formed.
  • a plurality of openings or slits are formed on the peripheral surface of the insertion tube, and each filter component formed between the plurality of openings or slits is formed in the outer diameter direction of the insertion tube.
  • the filter portion is prevented from being detached from the insertion tube in the living body tube. Further, since the insertion tube and the filter portion are a single body, no step is formed at the coupling portion between the filter portion and the other components, so that the diameter of the insertion tube can be reduced.
  • the shape of the insertion tube is made of a shape memory alloy, and the shape of each filter component is stored in a state where each filter component is wound in the outer diameter direction of the insertion tube. Even when the filter is folded for a long time, the shape of the filter section is reliably restored.
  • a superelastic alloy such as a nickel titanium alloy is suitable.
  • a method of forming the opening or slit on the peripheral surface of the insertion tube a method using a laser cut is suitable.
  • the invention described in claim 2 is the invention described in claim 1, in which at least one of the opening and the slit extends along a longitudinal direction of the insertion tube. It is characterized by extending!
  • the shape of the filter constituent portion is a shape suitable for the filter portion to capture foreign matter in the biological tube. It is formed to become.
  • the invention described in claim 3 is the invention described in claim 1, wherein the filter portion is formed on a distal side which is a distal end side of the insertion tube. And a transmission part formed on the proximal side, which is the proximal end side of the insertion tube,
  • the opening of the capturing part has a smaller opening area than the opening of the transmission part.
  • the present invention in a living body tube, it passes through a transmission part formed on the proximal side of the insertion tube.
  • the trapped foreign matter is captured by the capture part that is formed on the distal side of the insertion tube and has an opening area that is narrower than the opening part of the transmission part.
  • the invention described in claim 4 is the invention described in claim 3, wherein the opening of the transmission portion extends along the longitudinal direction of the insertion tube. It is characterized by being.
  • the opening of the permeation part has a shape extending along the longitudinal direction of the insertion tube, the force of the filter component formed in each opening of the permeation part. It is formed in a shape suitable for passing through.
  • the invention according to claim 5 is the invention according to any one of claims 1 to 4, wherein the wire is movably inserted into the insertion tube. And the wire passes through the filter part and is joined to a distal side part which is the distal end side of the insertion tube.
  • the shape of the filter portion becomes an appropriate shape for capturing the foreign matter in the biological tube. Retained.
  • the invention described in claim 6 is an in-vivo treatment device that captures and removes foreign matter in a living body tube by a filter portion protruding in an outer diameter direction, and the living body
  • the filter part In the insertion tube, at least one place along the axial direction of the insertion tube forms the filter part
  • the filter part is cut into a spiral shape along the axial direction of the insertion tube on the peripheral surface of the insertion tube to form a cutting part, and the filter component formed between the cutting parts is disposed outside the insertion pipe.
  • the shape is memorized and formed in the expanded state in the radial direction,
  • the wire passes through the filter part and is joined to a distal side part which is the distal end side of the insertion tube.
  • the peripheral surface of the insertion tube is spirally cut along the axial direction of the insertion tube.
  • the insertion tube is made of a shape memory alloy, and the shape of each filter component is stored in a state in which each filter component is expanded in the outer diameter direction of the insertion tube, so that the filter unit is folded for a long time. Even in the state, the shape of the filter portion is reliably restored.
  • the shape of the filter portion is maintained in an appropriate shape for capturing foreign matter in the living tube. Is done.
  • a laser cut method is suitable.
  • the invention described in claim 7 is the invention described in claim 5 or 6, wherein the one end of the wire is connected to the proximal end side of the insertion tube.
  • the near end force is protruding.
  • the shape of the filter portion can be changed to an arbitrary shape by moving a portion protruding from the proximal end of the insertion tube of the wire inserted into the insertion tube. Is possible.
  • FIG. 1 is a diagram showing an in-vivo treatment device according to a first embodiment of the present invention.
  • FIG. 2 is a view showing the in-vivo treatment device according to the first embodiment of the present invention.
  • FIG. 3 is a view showing a state of foreign body removal work in a living body tube using the in-vivo treatment device of the first embodiment of the present invention.
  • FIG. 4 is a diagram showing a modification of the first embodiment of the present invention.
  • FIG. 5 is a diagram showing a modification of the first embodiment of the present invention.
  • FIG. 6 is a view showing a modification of the first embodiment of the present invention.
  • FIG. 7 is a view showing an in-vivo treatment device according to a second embodiment of the present invention.
  • FIG. 8 is a view showing an in-vivo treatment device according to a second embodiment of the present invention.
  • FIG. 9 is a view showing an in-vivo treatment device according to a third embodiment of the present invention.
  • FIG. 10 is a view showing an in-vivo treatment device according to a third embodiment of the present invention.
  • FIG. 11 is a cross-sectional view taken along line AA in FIG.
  • the in-vivo treatment device of this embodiment includes an insertion tube 1 as shown in FIG.
  • the insertion tube 1 has a cylindrical shape and is made of a shape memory alloy having flexibility.
  • a case where a ⁇ kel ′ titanium alloy is used as the shape memory alloy will be described as an example.
  • the insertion tube 1 has a filter portion that captures a foreign substance in the living body tube at one place along the axial direction of the insertion tube 1.
  • each opening 4 is a shape extending along the central axis CL of the insertion tube 1.
  • each opening 4 is set so that the intervals between adjacent openings 4 are equal.
  • FIG. 1B which is a development view of FIG. 1A, a case where four openings 4 are formed in the insertion tube 1 will be described as an example.
  • the shape is stored in the filter constituent portion la, and the formation of the filter portion 2 is completed.
  • the circumferential force of the insertion tube 1 is externally applied to one place along the axial direction of the insertion tube 1 by each filter component la shaped in the outer diameter direction from the circumferential surface of the insertion tube 1.
  • a filter portion 2 projecting in the radial direction is formed.
  • a biological tube is a blood vessel and a foreign substance in the biological tube is a thrombus will be described as an example.
  • the intravascular blood clot removal operation using the in-vivo treatment device of this embodiment is performed according to the following procedure.
  • the insertion tube 1 is inserted into a guide tube 6 such as a catheter catheter, the filter portion forming position 2a extends in the axial direction of the insertion tube 1, and each filter component la extends in the outer diameter direction of the insertion tube 1. It is assumed that the insertion tube 1 is displaced in the inner diameter direction while having a spring. Then, the guide tube 6 is inserted into the blood vessel 8 from the distal end side, and after the distal end of the guide tube 6 has passed through the thrombus 10, the distal force insertion tube 1 of the guide tube 6 is pushed out as shown in FIG.
  • a guide tube 6 such as a catheter catheter
  • the filter portion forming position 2a extends in the axial direction of the insertion tube 1
  • each filter component la extends in the outer diameter direction of the insertion tube 1. It is assumed that the insertion tube 1 is displaced in the inner diameter direction while having a spring.
  • the guide tube 6 is inserted into the blood vessel 8 from the distal end side, and after the distal end of the
  • the filter portion 2 since the shape is stored in the filter portion 2 in a state where the filter constituting portion la is held in the outer diameter direction of the insertion tube 1, if the distal end force insertion tube 1 of the guide tube 6 is pushed out, the filter portion 2 The shape of the portion 2 is restored, and the filter portion 2 is formed in the blood vessel 8 between the thrombus 10 and the downstream side in the blood vessel 8.
  • the insertion tube 1 is moved to the upstream side of the blood vessel 8 while rotating the insertion tube 1, and the filter portion 2 is moved from the downstream side of the blood vessel 8 to the thrombus 10. Pass through the position.
  • the insertion tube 1 may be moved upstream of the blood vessel 8 without rotating.
  • the thrombus 10 is entangled by the filter portion 2 that has passed through the position of the thrombus 10 from the downstream side of the blood vessel 8, and the entangled thrombus 10 is captured by each filter component la.
  • each filter component la has an outer diameter of the insertion tube 1.
  • the filter portion forming position 2a of the insertion tube 1 is set to the axis of the insertion tube 1.
  • the filter portion 2 can be formed by causing the filter component portion la to store the shape in a state where the filter component portion la is contracted in the direction and the filter component portion la is constricted in the outer diameter direction of the insertion tube 1.
  • the insertion tube 1 and the filter unit 2 are a single body in the in-vivo treatment device of the present embodiment, the removal of the filter unit 2 from the insertion tube 1 in the blood vessel 8 is prevented, and The safety of removing foreign substances in the body tube is improved.
  • a connecting portion between the filter portion 2 and other components such as a forceps portion is not formed, and the filter portion 2 and other components are not formed. Since no step is formed, it is possible to reduce the diameter of the insertion tube 1, and it is possible to use an in-vivo treatment tool in a thinner living tube.
  • the inside of the insertion tube 1 can be a passage through which a liquid such as a thrombolytic agent can pass. For this reason, even if the clot 10 is clogged by the thrombus 10 during the removal of the thrombus 10, the thrombolytic agent is pumped from the outside of the insertion tube 1 to the filter unit 2 to remove the filter unit 2. It is possible to eliminate clogging of 2. Therefore, the thrombus 10 in the blood vessel 8 can be removed more effectively.
  • the insertion tube 1 is made of a shape memory alloy. Since the shape is stored in a state where the filter portion 2 is formed, the insertion tube 1 is inserted into the guide tube 6 even when the insertion tube 1 is inserted into the guide tube 6 for a long time with the filter portion 2 folded. The shape of the filter part 2 is reliably restored when it comes out of the box.
  • each opening 4 may be formed at an arbitrary angle with respect to the central axis CL of the insertion tube 1. Further, each opening 4 may have a shape extending while meandering along the longitudinal direction of the insertion tube 1.
  • each opening 4 formed in the insertion tube 1 shown in FIG. 4 (b), which is a development view of FIGS. 4 (a) and 4 (a) is inserted into the insertion tube 1 as shown in the figure. It is formed with an angle of 10 degrees with respect to the central axis CL.
  • each opening 4 formed in the insertion tube 1 shown in FIG. 5 (b), which is an exploded view of FIG. 5 (a) and FIG. 5 (a), is inserted as shown in the figure. It is formed with an angle of 19 degrees with respect to the central axis CL of the tube 1. In this way, each opening 4 is formed at an arbitrary angle with respect to the central axis CL of the insertion tube 1, thereby complicating the shape of the filter unit 2. Increases efficiency.
  • the shape of the opening 4 may be a wide variety of shapes as shown in Figs. 6 (a) to 6 (h). That is, the shape of the opening 4 may be any shape as long as the filter portion 2 is formed in a shape capable of capturing foreign matter in the living body tube. Although not particularly shown, the opening 4 may be a slit. In this case, all the openings 4 may be slits, or the openings 4 and the slits may be mixed.
  • the intervals between the adjacent openings 4 are set to be equal intervals, but the present invention is not limited to this, and the filter unit 2 is formed so as to capture foreign substances in the in-vivo tube. If it is an interval,
  • the in-vivo treatment device of the present embodiment is configured to include only the insertion tube 1, it is not limited to this. That is, a flexible wire may be movably inserted into the insertion tube 1 and the wire may be connected to the distal side portion of the insertion tube 1 through the filter unit 2. In this case, the shape force of the filter unit 2 is held in an appropriate shape for capturing the thrombus 10. Further, the end of the wire may be configured such that the proximal end force of the insertion tube 1 also protrudes. In this case, it is possible to change the shape of the filter portion 2 to an arbitrary shape by moving the portion of the wire that also projects the proximal end force of the insertion tube 1. Further, an introduction member having a shape that facilitates insertion of the insertion tube 1 into the blood vessel 8 such as a shape that decreases in diameter toward the distal end may be connected to the distal end portion of the insertion tube 1. ,.
  • the filter unit 2 is formed only at one location along the axial direction of the insertion tube 1.
  • the present invention is not limited to this, and the axial direction of the insertion tube 1 is not limited thereto. Filter 2 at multiple locations along the line.
  • the insertion tube 1 has a cylindrical shape.
  • the present invention is not limited to this, and a passage through which liquid can pass is formed inside the insertion tube 1.
  • it may be formed in a substantially cylindrical shape whose cross section is elliptical.
  • each filter component la is placed in a state in which each filter component la is bent in the outer diameter direction of the insertion tube 1.
  • the force that memorizes the shape is not limited to this. That is, when forming the filter portion 2, the shape of the entire insertion tube 1 may be stored in a state where each filter component la is held in the outer diameter direction of the insertion tube 1.
  • the case where the blood vessel 8 is the blood vessel 8 has been described as an example.
  • the present invention is not limited to this and can be applied to other biological tubes such as a bile duct.
  • the case where the foreign substance in the living body tube is the thrombus 10 has been described as an example.
  • the present invention is not limited to this and can be applied to other foreign substances such as gallstones.
  • the insertion tube 1 provided in the in-vivo treatment device of the present embodiment has the same configuration as that of the first embodiment described above except for the configuration of the filter unit 2.
  • the filter portion 2 includes a capture portion 12 formed on the distal side that is the distal end side of the insertion tube 1 and a proximal end side of the insertion tube 1. And a transmission part 14 formed on the distal side.
  • the peripheral surface of the insertion tube 1 is opened by laser cutting to form a plurality of openings 4 a in the capturing part 12 and a plurality of openings 4 b in the transmission part 14.
  • each opening 4a of the trapping part 12 is contracted in the axial direction of the insertion pipe 1 at the filter part forming position 2a of the insertion pipe 1, and the trapping part constituting part 12a formed between the openings 4a is inserted.
  • a rectangular shape is formed by one laser cut so that the capturing portion constituting portion 12a has a mesh shape.
  • each opening 4a is formed such that its opening area is narrower than the opening area of each opening 4b of the transmission part 14.
  • the opening 4b of the transmission portion 14 is contracted in the axial direction of the insertion tube 1 at the filter portion forming position 2a of the insertion tube 1, and the transmission portion constituting portion 14a formed between the openings 4b is provided. Formed by laser cutting so that the transmission portion constituting portion 14a formed between the openings 4b is formed in a columnar shape along the axial direction of the insertion tube 1 in a state where the insertion tube 1 is constricted in the outer diameter direction. .
  • the shape of each opening 4b extends along the axial direction of the insertion tube 1, and the width along the circumferential direction of the insertion tube 1 gradually increases the proximal force of the insertion tube 1 toward the distal side. The shape becomes narrower.
  • the filter portion forming position 2a of the insertion tube 1 is contracted in the axial direction of the insertion tube 1, and the capturing portion constituting portion 12a and the transmission portion constituting portion 14a are connected to the insertion tube 1.
  • the shape is stored in the capturing part constituting part 12a and the transmissive part constituting part 14a in a state where it is bent in the outer diameter direction, and the formation of the filter part 2 is completed.
  • the insertion tube 1 is disposed at one place along the axial direction of the insertion tube 1 by the capturing portion constituting portion 12a and the transmission portion constituting portion 14a having a shape sandwiched from the peripheral surface of the insertion tube 1 in the outer diameter direction.
  • a filter portion 2 is formed which projects in the outer diameter direction from the peripheral surface 1.
  • the intravascular blood clot removal operation using the in-vivo treatment device of this embodiment is performed according to the following procedure. Do along.
  • the insertion tube 1 is inserted into the guide tube, and the trapping portion constituting portion 12a and the transmitting portion constituting portion 14a are extended in the axial direction of the insertion tube 1 while the filter portion forming position 2a extends in the outer diameter direction of the insertion tube 1. It is assumed that the insertion tube 1 is displaced in the inner diameter direction while having a spring. Then, this guide tube is inserted into the living body tube at the distal end side force, and after the distal end of the guide tube passes through the foreign matter, the insertion tube 1 is pushed out from the distal end of the guide tube.
  • the tip force of the guide tube is also reduced.
  • the shape of the filter portion 2 is restored, and the filter portion 2 is formed between the foreign substance and the downstream side in the biological tube in the biological tube.
  • the insertion tube 1 is moved to the upstream side of the biological tube, and the filter unit 2 passes through the position of the foreign substance from the downstream side of the biological tube. Let At this time, the foreign matter on the upstream side of the filter unit 2 passes through the transmission unit 14 and is captured by the capture unit 12.
  • the insertion tube 1 is moved to the upstream side of the living body tube, the insertion tube 1 is stored in the guide tube, and the trapping portion constituting portion 12a and the transmitting portion constituting portion 14a are formed as filter portions.
  • the position 2a extends in the axial direction of the insertion tube 1 and is displaced in the inner diameter direction of the insertion tube 1 while having a spring in the outer diameter direction of the insertion tube 1, the guide tube and the insertion tube 1 are Withdrawing from the living body tube, the foreign substance removing operation in the living body tube is completed.
  • each opening 4a of the capturing unit 12 is narrower than the opening area of each opening 4b of the transmitting unit 14, the transmitting unit 14 is used.
  • the foreign matter that has passed through is captured by the capturing unit 12 located on the downstream side in the biological tube, and the efficiency of the foreign matter removal work in the biological tube is improved.
  • each opening 4b of the transmission part 14 has an opening area larger than that of the opening 4a of the capturing part 12, it is possible to ensure a sufficient fluid flow in the living body tube.
  • each opening 4a of the capturing part 12 has a different opening area, and the opening area of the opening 4a located on the distal end side of the insertion tube 1 is set to be proximal to the insertion tube 1.
  • a configuration may be adopted in which the opening area of the opening 4a located on the end side is narrower.
  • the in-vivo treatment device of the present embodiment is above the filter unit 2 in the in-vivo tube.
  • the foreign substance on the flow side passes through the permeation section 14 and is captured and removed by the capture section 12, it is not limited thereto. That is, after the guide tube is moved to the upstream side of the biological tube, the insertion tube 1 is rotated and moved to the upstream side of the biological tube, and the filter unit 2 is passed through the position of the force foreign substance on the downstream side of the biological tube, A method of using the filter unit 2 that has passed through the position of the foreign substance from the downstream side of the biological tube may be used.
  • the in-vivo treatment device of the present embodiment includes an insertion tube 1 and a wire 16 that is movably inserted into the insertion tube 1.
  • the insertion tube 1 has a cylindrical shape and is formed of a flexible shape memory alloy.
  • the insertion tube 1 has a filter portion 2 that captures a foreign substance in the living body tube at one place along the axial direction of the insertion tube 1.
  • a cutting portion 18 that is cut in a spiral shape along the axial direction of the insertion tube 1 is formed on the peripheral surface of the insertion tube 1 by laser cutting.
  • the filter component la formed between the cut portions 18 is expanded in the outer diameter direction of the insertion tube 1. The shape is stored, and the formation of the filter unit 2 is completed.
  • the shape of the filter portion 2 is a shape in which the distal side force of the insertion tube 1 also expands toward the proximal side of the insertion tube 1.
  • the outer diameter of the insertion tube 1 from the circumferential surface of the insertion tube 1 is increased by the filter component la having a shape expanded from the circumferential surface of the insertion tube 1 to the outer diameter direction.
  • a filter part 2 projecting in the direction is formed.
  • the wire 16 is formed of a flexible wire, one end of which is connected to the distal side lb which is the distal end side of the insertion tube 1, and the other end 16a is the insertion tube.
  • the proximal end lc force which is the base end of 1, also protrudes.
  • one end of the wire 16 and the distal side lb are joined together by applying force together.
  • a gap 20 is formed between the inner diameter surface Id of the insertion tube 1 and the wire 16.
  • the in-vivo foreign body removal operation using the in-vivo treatment device of the present embodiment is performed according to the following procedure.
  • the portion of the wire 16 that also projects the proximal end lc force of the insertion tube 1 is moved to reduce the diameter of the filter component la in the inner diameter direction of the insertion tube 1.
  • the insertion tube 1 is inserted into the biological tube from the distal end side, and after the distal end of the insertion tube 1 has passed through the foreign matter, the shape of the filter unit 2 is restored, and the foreign matter and the downstream side of the biological tube in the biological tube.
  • the filter part 2 is formed between the two.
  • the shape of the filter portion 2 is memorized in a state where the diameter of the filter component la is expanded in the outer diameter direction of the insertion tube 1, so that the shape of the filter portion 2 is surely ensured in the living body tube. Restored.
  • the insertion tube 1 is rotated and moved to the upstream side of the biological tube, and the filter unit 2 is passed through the position of the foreign substance on the downstream side of the biological tube.
  • the foreign matter is entangled by the filter unit 2 that has passed through the position of the foreign matter from the downstream side of the biological tube, and the entangled foreign matter is captured by the filter component la.
  • the insertion tube 1 is moved to the upstream side of the living body tube and pulled out from the living body tube, and the foreign substance removing operation in the living body tube is completed.
  • the filter part 2 can be formed by storing the shape in a state where the filter component la is expanded in the outer diameter direction of the insertion tube 1, the manufacturing efficiency of the in-vivo treatment device is improved. In addition, manufacturing costs can be reduced.
  • the insertion tube 1 and the wire 16 are coupled by caulking the distal side portion lb of the insertion tube 1 and the wire 16, the conventional living body
  • the forceps for connecting the filter portion 2 and other components, which have been formed in the intravascular treatment tool, are formed only on the distal side portion lb of the insertion tube 1. For this reason, the risk that the distal side portion lb of the insertion tube 1 and the filter portion 2 are detached from other components in the biological tube is reduced, and the safety of the foreign substance removal work in the biological tube is improved.
  • one end of the wire 16 is coupled to the distal side lb of the insertion tube 1, and the other end 16a of the wire 16 is It protrudes from the proximal end lc of the insertion tube 1.
  • the shape force of the filter unit 2 is held in a shape suitable for trapping foreign matter in the biological tube, and the work efficiency of the foreign matter removal work in the biological tube is improved.
  • the shape of the filter unit 2 can be changed to an arbitrary shape, so that the foreign matter in the biological tube The work efficiency of the removal work is improved.
  • a passage through which a liquid such as a thrombolytic agent can pass through the void portion 20 formed between the inner diameter surface Id of the insertion tube 1 and the wire 16 is provided. It is possible to For this reason, since it is possible to send a liquid such as a thrombolytic agent from the proximal end lc of the insertion tube 1 into the living body tube via the filter unit 2, it is possible to more effectively remove foreign substances in the living tube. Is possible.
  • the insertion tube 1 is inserted into the insertion tube 1 while the filter component 1a has a spring in the outer diameter direction of the insertion tube 1 as in the first embodiment. Insert the guide tube into the living body tube from the distal end side after the foreign substance has passed through the foreign body, and then push the insertion tube 1 from the distal end of the guide tube. It is good also as a structure to take out.
  • the shape of the filter unit 2 is a shape that expands from the distal side of the insertion tube 1 toward the proximal side of the insertion tube 1.
  • the shape of the insertion tube 1 is not limited to a shape that expands toward the distal side of the insertion tube 1 from the proximal side of the insertion tube 1.
  • the force is such that the other end portion 16a of the wire 16 protrudes from the proximal end lc of the insertion tube 1.
  • the wire is not limited to this.
  • the other end 16a of 16 may be stored in the insertion tube 1!
  • a chamfered portion may be provided on the peripheral edge 22 of the insertion tube 1 of the filter component la.
  • the risk of damaging the inside of the living body can be reduced in the foreign body removing work in the living body, and the safety of the removing work in the living body can be improved.
  • an opening and a cutting portion are formed by laser cutting on a part of the peripheral surface of the insertion tube. The work accuracy was verified.
  • an insertion tube having the same configuration as that described in the first embodiment was created.
  • the insertion tube uses a nickel-titanium alloy pipe with a diameter of 0.458mm and a circumference of 1.438mm.
  • a slit-shaped opening with a width of 0.03mm is parallel to the central axis of the insertion tube by laser cutting. 24 locations were formed.
  • 24 filter components having a width of 0.02992 mm were formed in the insertion tube.
  • an insertion tube having the same configuration as that described in the third embodiment was created.
  • a nickel-titanium alloy pipe having an outer diameter of 0.4 mm and an inner diameter of 0.2 mm was used as the insertion tube, and a steel wire having an outer diameter of 0.18 mm was used as the wire.
  • the insertion tube was provided with a laser cut to form a cut portion having a width of 50 m in a spiral shape and a width between adjacent cut portions of 200 ⁇ m.
  • the insertion tube provided in the in-vivo treatment device of each embodiment described above can be created by forming an opening and a cut portion by laser cutting on a cylindrical nickel-titanium alloy pipe. It was confirmed that.
  • the present invention it is possible to improve the production efficiency and cost of an in-vivo treatment device, and to prevent the filter unit from being disengaged from the in-vivo treatment device force within the in-vivo tube, so that the inside of the in-vivo tube can be prevented. Occlusion can be prevented.

Abstract

A medical appliance for treating the inside of a biological duct enabling an increase in manufacturing efficiency and a reduction in cost. A filter part (2) is formed at a position along the axial direction of a cylindrical insertion tube (1) formed of a shape memory alloy. The filter part (2) is formed by forming a plurality of openings (4) in the peripheral surface of the insertion tube (1) by laser cutting, contracting the filter part formed portion (2a) of the insertion tube (1) in the axial direction of the insertion tube (1), and in the state of each filter formed part (1a) of the insertion tube (1)formed between the opening parts (4) deflected in the radial outer direction of the insertion tube (1), storing the shape of the filter part in each filter formed part (1a).

Description

明 細 書  Specification
生体管内治療具  Intravascular treatment device
技術分野  Technical field
[0001] 本発明は、生体管内にある異物を捕捉して除去することにより生体管内を治療する 生体管内治療具に関する。  The present invention relates to an in-vivo treatment device that treats the inside of a living body by capturing and removing foreign matter in the living body.
背景技術  Background art
[0002] 従来から、血管等の生体管内を治療する場合には、生体管の壁面から血栓等の異 物を捕捉して除去する方法が多く用いられている。ここで、生体管として血管を想定 し、異物として血栓を想定した場合、血管の壁面から除去された血栓は血流によって 運ばれ、より細!、下流の血管を閉塞するおそれがある。  Conventionally, when treating the inside of a biological tube such as a blood vessel, many methods for capturing and removing foreign matters such as a thrombus from the wall surface of the biological tube have been used. Here, when a blood vessel is assumed as the living body tube and a thrombus is assumed as the foreign body, the thrombus removed from the wall surface of the blood vessel is carried by the blood flow, and there is a possibility that the downstream blood vessel may be blocked.
このような問題に対応するために、特許文献 1に記載されているような生体管内治 療具を血管内へ挿入して、血管内の血栓を捕捉して除去する治療方法がある。  In order to cope with such a problem, there is a treatment method in which a medical treatment device in a living tube as described in Patent Document 1 is inserted into a blood vessel, and a thrombus in the blood vessel is captured and removed.
[0003] 特許文献 1に記載されている生体管内治療具は、直線状に形成された 3本以上の 合金線を前後両端で互 ヽに結合するとともに、これら複数の合金線の途中部分を外 径方向に橈ませて、略フットボール状の境界面に沿って配置させて構成されたフィル タ部を備えている。そして、フィルタ部の外面の、例えば、前端部からほぼ中間までを 弾性皮膜によって覆うことにより形成した傘状カバーからなる捕捉部によって、血管 内の血栓を捕捉して除去して 、る。  [0003] The in-vivo treatment device described in Patent Document 1 connects three or more alloy wires formed in a straight line to each other at both front and rear ends, and removes intermediate portions of the plurality of alloy wires. It is provided with a filter portion that is configured to be sunk in the radial direction and arranged along a substantially football-like boundary surface. Then, for example, the thrombus in the blood vessel is captured and removed by the trapping portion formed of an umbrella-like cover formed by covering the outer surface of the filter portion, for example, from the front end portion to almost the middle with an elastic film.
[0004] ここで、上記生体管内治療具は、フィルタ部を畳んだ状態でカテーテル力 なる誘 導管内に差し込まれた後、誘導管と共に血管内に差し込まれる。そして、病変部位 等、目的の場所に到達した後、生体管内治療具の前端部分を誘導管力 前方に送 り出してフィルタ部を誘導管力も出し、フィルタ部を外径方向に張り出した状態として 、このフィルタ部によって血栓を捕捉して血管内から除去する。  [0004] Here, the in-vivo treatment device is inserted into an induction conduit having catheter force with the filter portion folded, and then inserted into the blood vessel together with the guide tube. Then, after reaching the target location, such as the lesion site, the front end portion of the in-vivo treatment device is sent forward in the guide tube force, and the guide tube force is also exerted, and the filter portion is projected outward. The thrombus is captured and removed from the blood vessel by the filter unit.
し力しながら、特許文献 1に記載の生体管内治療具に備えられて 、るフィルタ部で は、作業中に目詰まりが生じやすぐ血管内の血流を遮断してしまうことがある。そこ で、この問題に対応するため、フィルタ部を、複数本の支柱線とバスケット状のメッシ ュ体とから構成した生体管内治療具がある。このようなフィルタ部を備えた生体管内 治療具であれば、血管内の血流を遮断することなぐ血栓の除去を行うことが可能で ある。 However, the filter part provided in the in-vivo treatment device described in Patent Document 1 may become clogged during the operation or immediately block the blood flow in the blood vessel. Therefore, in order to deal with this problem, there is an in-vivo treatment device in which the filter portion is composed of a plurality of support lines and a basket-like mesh body. In a living tube provided with such a filter unit If it is a treatment tool, it is possible to remove the thrombus without blocking the blood flow in the blood vessel.
特許文献 1 :特開平 2001— 212152号公報  Patent Document 1: JP-A-2001-212152
発明の開示  Disclosure of the invention
[0005] し力しながら、上述したような生体管内治療具に備えられるフィルタ部は、複数本の 支柱線に形状記憶合金力 なるメッシュ体を編みこむことにより、バスケット状に形成 されている。このため、フィルタ部の製造に手間がかかり、生体管内治療具の製造効 率が低下してしまうとともに、生体管内治療具のコストが増加してしまう。  [0005] However, the filter portion provided in the in-vivo treatment device as described above is formed in a basket shape by weaving a mesh body having a shape memory alloy force into a plurality of support wires. For this reason, it takes time to manufacture the filter part, and the manufacturing efficiency of the in-vivo treatment device is reduced, and the cost of the in-vivo treatment device is increased.
また、フィルタ部は、ニッケル 'チタン合金等の形状記憶合金によって形成される場 合が多ぐ外径方向に張り出した状態で形状記憶加工を施すことが多いが、この種の 形状記憶合金は接着による結合が困難である。このため、フィルタ部と、ワイヤ等の 生体管内治療具を構成する他の部分とを結合する際は、フィルタ部の前後両端を金 属等でかしめる必要があり、かしめ部分に形成された段差が、フィルタ部が生体管内 治療具から離脱する一因となる。血管内においてフィルタ部が生体管内治療具から 離脱すると、離脱したフィルタ部が血流によって運ばれ、より細い下流の血管を閉塞 するおそれがある。  In addition, the filter part is often formed of a shape memory alloy such as a nickel'titanium alloy, and is often subjected to shape memory processing in the state of projecting in the outer diameter direction. It is difficult to bond by. For this reason, when connecting the filter part and other parts of the treatment device such as a wire such as a wire, it is necessary to caulk the front and rear ends of the filter part with a metal or the like, and the step formed in the caulking part However, this contributes to the removal of the filter unit from the in-vivo treatment device. If the filter part is detached from the in-vivo treatment device in the blood vessel, the detached filter part is carried by the blood flow, and there is a possibility that the narrower downstream blood vessel is blocked.
[0006] 本発明は、上述のような問題点に着目してなされたもので、製造効率の向上及びコ ストの低減が可能であるとともに、フィルタ部の離脱を防止することが可能な生体管内 治療具を提供することを課題とする。  [0006] The present invention has been made paying attention to the above-described problems, and can improve the manufacturing efficiency and reduce the cost, and can prevent the separation of the filter part. It is an object to provide a treatment tool.
前記課題を解決するために、本発明のうち、請求項 1に記載した発明は、生体管内 にある異物を外径方向に張り出したフィルタ部により捕捉して除去する生体管内治療 具であって、  In order to solve the above-mentioned problem, the invention described in claim 1 of the present invention is an in-vivo treatment device that captures and removes a foreign substance in the in-vivo tube by a filter portion protruding in the outer diameter direction,
前記生体管内に挿入される形状記憶合金製の挿入管を備え、  An insertion tube made of a shape memory alloy to be inserted into the biological tube;
前記挿入管は、当該挿入管の軸方向に沿った少なくとも一箇所が前記フィルタ部 を形成し、  In the insertion tube, at least one place along the axial direction of the insertion tube forms the filter part,
前記フィルタ部は、前記挿入管の周面に複数の開口部またはスリットが形成され、 且つ前記挿入管のフィルタ部形成位置を軸方向に収縮させて前記複数の開口部ま たはスリット間に形成されたフィルタ構成部を挿入管の外径方向へ橈ませた状態に 形状が記憶されて形成されることを特徴とするものである。 The filter section has a plurality of openings or slits formed in the peripheral surface of the insertion tube, and is formed between the plurality of openings or slits by contracting the filter section forming position of the insertion tube in the axial direction. In the state where the filtered filter part is folded in the outer diameter direction of the insertion tube The shape is memorized and formed.
[0007] 本発明によれば、挿入管の周面に複数の開口部またはスリットを形成し、複数の開 口部またはスリット間に形成された各フィルタ構成部を挿入管の外径方向へ橈ませた 状態で、各フィルタ構成部に形状を記憶させることにより、生体管内にある異物を捕 捉するフィルタ部を形成することで、生体管内治療具の製造効率向上及びコスト低減 が可能となる。  [0007] According to the present invention, a plurality of openings or slits are formed on the peripheral surface of the insertion tube, and each filter component formed between the plurality of openings or slits is formed in the outer diameter direction of the insertion tube. In this state, by storing the shape in each filter component, and forming a filter unit that captures foreign substances in the living tube, the manufacturing efficiency of the in-vivo treatment device can be improved and the cost can be reduced.
また、挿入管とフィルタ部とがー体であるため、生体管内においてフィルタ部が挿入 管から離脱することが防止される。また、挿入管とフィルタ部とがー体であることにより 、フィルタ部と他の構成部分との結合部に段差が形成されないため、挿入管を小径 化することが可能となる。  Further, since the insertion tube and the filter portion are a single body, the filter portion is prevented from being detached from the insertion tube in the living body tube. Further, since the insertion tube and the filter portion are a single body, no step is formed at the coupling portion between the filter portion and the other components, so that the diameter of the insertion tube can be reduced.
[0008] また、挿入管を形状記憶合金製とし、各フィルタ構成部を挿入管の外径方向へ橈ま せた状態で各フィルタ構成部に形状を記憶させて 、るため、フィルタ部を長時間折り 畳んだ状態とした場合でも、フィルタ部の形状が確実に復元される。 [0008] Further, the shape of the insertion tube is made of a shape memory alloy, and the shape of each filter component is stored in a state where each filter component is wound in the outer diameter direction of the insertion tube. Even when the filter is folded for a long time, the shape of the filter section is reliably restored.
なお、形状記憶合金としては、ニッケル 'チタン合金等の超弾性合金が好適である 。また、挿入管の周面に開口部またはスリットを形成する方法としては、レーザーカツ トによる方法が好適である。  As the shape memory alloy, a superelastic alloy such as a nickel titanium alloy is suitable. Further, as a method of forming the opening or slit on the peripheral surface of the insertion tube, a method using a laser cut is suitable.
[0009] 次に、本発明のうち、請求項 2に記載した発明は、請求項 1に記載した発明であつ て、前記開口部またはスリットのうち少なくとも一方は、前記挿入管の長手方向に沿つ て延びて!/ヽることを特徴とするものである。 [0009] Next, of the present invention, the invention described in claim 2 is the invention described in claim 1, in which at least one of the opening and the slit extends along a longitudinal direction of the insertion tube. It is characterized by extending!
本発明によれば、複数の開口部またはスリットを挿入管の長手方向に沿って延びる 形状とすることにより、フィルタ構成部の形状が、フィルタ部が生体管内の異物を捕捉 するために好適な形状となるように形成される。  According to the present invention, by forming the plurality of openings or slits in a shape extending along the longitudinal direction of the insertion tube, the shape of the filter constituent portion is a shape suitable for the filter portion to capture foreign matter in the biological tube. It is formed to become.
[0010] 次に、本発明のうち、請求項 3に記載した発明は、請求項 1に記載した発明であつ て、前記フィルタ部は、前記挿入管の先端側となる遠位側に形成される捕捉部と挿 入管の基端側となる近位側に形成される透過部とからなり、 [0010] Next, of the present invention, the invention described in claim 3 is the invention described in claim 1, wherein the filter portion is formed on a distal side which is a distal end side of the insertion tube. And a transmission part formed on the proximal side, which is the proximal end side of the insertion tube,
前記捕捉部の開口部は、前記透過部の開口部よりも開口面積が狭いことを特徴と するものである。  The opening of the capturing part has a smaller opening area than the opening of the transmission part.
本発明によれば、生体管内において、挿入管の近位側に形成される透過部を通過 した異物が、挿入管の遠位側に形成され透過部の開口部よりも開口面積が狭い開 口部が設けられている捕捉部によって捕捉されるため、生体管内における異物除去 作業の効率が向上する。 According to the present invention, in a living body tube, it passes through a transmission part formed on the proximal side of the insertion tube. The trapped foreign matter is captured by the capture part that is formed on the distal side of the insertion tube and has an opening area that is narrower than the opening part of the transmission part. To do.
[0011] 次に、本発明のうち、請求項 4に記載した発明は、請求項 3に記載した発明であつ て、前記透過部の開口部は、前記挿入管の長手方向に沿って延びていることを特徴 とするちのである。  [0011] Next, of the present invention, the invention described in claim 4 is the invention described in claim 3, wherein the opening of the transmission portion extends along the longitudinal direction of the insertion tube. It is characterized by being.
本発明によれば、透過部の開口部が、挿入管の長手方向に沿って延びる形状とな つているため、透過部の各開口部に形成されるフィルタ構成部力 生体管内の異物 が透過部を通過するために好適な形状となるように形成される。  According to the present invention, since the opening of the permeation part has a shape extending along the longitudinal direction of the insertion tube, the force of the filter component formed in each opening of the permeation part. It is formed in a shape suitable for passing through.
[0012] 次に、本発明のうち、請求項 5に記載した発明は、請求項 1から 4のうちいずれか 1 項に記載した発明であって、前記挿入管内へ移動自在に挿通されるワイヤを備え、 前記ワイヤは、前記フィルタ部を通過して前記挿入管の先端側となる遠位側部と結 合されて!/ヽることを特徴とするちのである。 [0012] Next, of the present invention, the invention according to claim 5 is the invention according to any one of claims 1 to 4, wherein the wire is movably inserted into the insertion tube. And the wire passes through the filter part and is joined to a distal side part which is the distal end side of the insertion tube.
本発明によれば、挿入管内に、フィルタ部を通過して挿入管の遠位側部とワイヤが 結合されているため、フィルタ部の形状が生体管内の異物を捕捉するために適切な 形状に保持される。  According to the present invention, since the distal side portion of the insertion tube and the wire are connected to each other through the filter portion in the insertion tube, the shape of the filter portion becomes an appropriate shape for capturing the foreign matter in the biological tube. Retained.
[0013] 次に、本発明のうち、請求項 6に記載した発明は、生体管内にある異物を外径方向 に張り出したフィルタ部によって捕捉して除去する生体管内治療具であって、 前記生体管内に挿入される形状記憶合金製の挿入管と、当該挿入管内へ移動自 在に挿通されるワイヤと、を備え、  [0013] Next, among the present inventions, the invention described in claim 6 is an in-vivo treatment device that captures and removes foreign matter in a living body tube by a filter portion protruding in an outer diameter direction, and the living body An insertion tube made of a shape memory alloy to be inserted into the tube, and a wire that is inserted into the insertion tube so as to move.
前記挿入管は、当該挿入管の軸方向に沿った少なくとも一箇所が前記フィルタ部 を形成し、  In the insertion tube, at least one place along the axial direction of the insertion tube forms the filter part,
前記フィルタ部は、前記挿入管の周面に当該挿入管の軸方向に沿って螺旋状に 切断されて切断部が形成され、且つ前記切断部間に形成されたフィルタ構成部を揷 入管の外径方向へ拡径させた状態に形状が記憶されて形成され、  The filter part is cut into a spiral shape along the axial direction of the insertion tube on the peripheral surface of the insertion tube to form a cutting part, and the filter component formed between the cutting parts is disposed outside the insertion pipe. The shape is memorized and formed in the expanded state in the radial direction,
前記ワイヤは、前記フィルタ部を通過して前記挿入管の先端側となる遠位側部と結 合されて!/ヽることを特徴とするちのである。  The wire passes through the filter part and is joined to a distal side part which is the distal end side of the insertion tube.
[0014] 本発明によれば、挿入管の周面に、挿入管の軸方向に沿って螺旋状に切断された 切断部を形成し、切断部間に形成された各フィルタ構成部を挿入管の外径方向へ 拡径させた状態で、各フィルタ構成部に形状を記憶させることにより、生体管内にあ る異物を捕捉するフィルタ部を形成することが可能となるため、生体管内治療具の製 造効率向上及びコスト低減が可能となる。 [0014] According to the present invention, the peripheral surface of the insertion tube is spirally cut along the axial direction of the insertion tube. By forming a cut portion and storing the shape in each filter component in a state where each filter component formed between the cut portions is expanded in the outer diameter direction of the insertion tube, foreign matter in the living body tube Therefore, it is possible to improve the manufacturing efficiency and reduce the cost of the in-vivo treatment device.
また、挿入管を形状記憶合金製とし、各フィルタ構成部を挿入管の外径方向へ拡 径させた状態で各フィルタ構成部に形状を記憶させて 、るため、フィルタ部を長時間 折り畳んだ状態とした場合でも、フィルタ部の形状が確実に復元される。  In addition, the insertion tube is made of a shape memory alloy, and the shape of each filter component is stored in a state in which each filter component is expanded in the outer diameter direction of the insertion tube, so that the filter unit is folded for a long time. Even in the state, the shape of the filter portion is reliably restored.
[0015] また、挿入管内に、フィルタ部を通過して挿入管の遠位側部とワイヤが結合されて いるため、フィルタ部の形状が生体管内の異物を捕捉するために適切な形状に保持 される。  [0015] In addition, since the insertion tube is connected to the distal side portion of the insertion tube and the wire through the filter portion, the shape of the filter portion is maintained in an appropriate shape for capturing foreign matter in the living tube. Is done.
なお、挿入管の周面に切断部を形成する方法としては、レーザーカットによる方法 が好適である。  As a method for forming the cut portion on the peripheral surface of the insertion tube, a laser cut method is suitable.
次に、本発明のうち、請求項 7に記載した発明は、請求項 5または 6に記載した発明 であって、前記ワイヤは、当該ワイヤの一方の端部が前記挿入管の基端側となる近 位端力 突出していることを特徴とするものである。  Next, of the present invention, the invention described in claim 7 is the invention described in claim 5 or 6, wherein the one end of the wire is connected to the proximal end side of the insertion tube. The near end force is protruding.
[0016] 本発明によれば、挿入管内に挿通されているワイヤのうち、挿入管の近位端から突 出している部分を移動させることにより、フィルタ部の形状を任意の形状に変化させる ことが可能となる。 [0016] According to the present invention, the shape of the filter portion can be changed to an arbitrary shape by moving a portion protruding from the proximal end of the insertion tube of the wire inserted into the insertion tube. Is possible.
図面の簡単な説明  Brief Description of Drawings
[0017] [図 1]本発明の第一実施形態の生体管内治療具を示す図である。 [0017] FIG. 1 is a diagram showing an in-vivo treatment device according to a first embodiment of the present invention.
[図 2]本発明の第一実施形態の生体管内治療具を示す図である。  FIG. 2 is a view showing the in-vivo treatment device according to the first embodiment of the present invention.
[図 3]本発明の第一実施形態の生体管内治療具を用いた生体管内の異物除去作業 の状態を示す図である。  FIG. 3 is a view showing a state of foreign body removal work in a living body tube using the in-vivo treatment device of the first embodiment of the present invention.
[図 4]本発明の第一実施形態の変形例を示す図である。  FIG. 4 is a diagram showing a modification of the first embodiment of the present invention.
[図 5]本発明の第一実施形態の変形例を示す図である。  FIG. 5 is a diagram showing a modification of the first embodiment of the present invention.
[図 6]本発明の第一実施形態の変形例を示す図である。  FIG. 6 is a view showing a modification of the first embodiment of the present invention.
[図 7]本発明の第二実施形態の生体管内治療具を示す図である。  FIG. 7 is a view showing an in-vivo treatment device according to a second embodiment of the present invention.
[図 8]本発明の第二実施形態の生体管内治療具を示す図である。 圆 9]本発明の第三実施形態の生体管内治療具を示す図である。 FIG. 8 is a view showing an in-vivo treatment device according to a second embodiment of the present invention. [9] FIG. 9 is a view showing an in-vivo treatment device according to a third embodiment of the present invention.
圆 10]本発明の第三実施形態の生体管内治療具を示す図である。  [10] FIG. 10 is a view showing an in-vivo treatment device according to a third embodiment of the present invention.
[図 11]図 9の A— A線断面図である。  FIG. 11 is a cross-sectional view taken along line AA in FIG.
符号の説明  Explanation of symbols
1 挿入管  1 Insertion tube
2 フィルタ部  2 Filter section
4 開口部  4 opening
6 案内管  6 Guide tube
8 血管  8 blood vessels
10 血栓  10 Thrombus
12 捕捉部  12 Trapping part
14 透過部  14 Transmission part
16 ワイヤ  16 wires
18 切断部  18 Cutting part
20 空隙部  20 Cavity
22 縁部  22 Edge
CL 挿入管の中心軸線  Center axis of CL insertion tube
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0019] 次に、本発明の第一の実施形態について図面を参照しつつ説明する。  Next, a first embodiment of the present invention will be described with reference to the drawings.
まず、図 1及び図 2を参照して本実施形態の構成を説明する。  First, the configuration of the present embodiment will be described with reference to FIG. 1 and FIG.
本実施形態の生体管内治療具は、図 1に示すような挿入管 1を備えている。  The in-vivo treatment device of this embodiment includes an insertion tube 1 as shown in FIG.
図 1 (a)に示すように、挿入管 1は円筒形状をなしており、可撓性を有する形状記憶 合金によって形成されている。なお、本実施形態では、形状記憶合金として、 -ッケ ル 'チタン合金を用いた場合を例にして説明する。  As shown in FIG. 1 (a), the insertion tube 1 has a cylindrical shape and is made of a shape memory alloy having flexibility. In the present embodiment, a case where a −kel ′ titanium alloy is used as the shape memory alloy will be described as an example.
[0020] また、挿入管 1は、挿入管 1の軸方向に沿った一箇所が、生体管内にある異物を捕 捉するフィルタ部を形成して 、る。 [0020] In addition, the insertion tube 1 has a filter portion that captures a foreign substance in the living body tube at one place along the axial direction of the insertion tube 1.
以下に、フィルタ部の形成方法について説明する。  Below, the formation method of a filter part is demonstrated.
まず、挿入管 1の周面をレーザーカットによって開口し、挿入管 1の周面に複数の 開口部 4を形成する。各開口部 4の形状は、挿入管 1の中心軸線 CLに沿って延びた 形状とする。また、各開口部 4は、隣り合う開口部 4同士の間隔が等間隔となるように 設定する。なお、本実施形態では、図 1 (a)の展開図である図 1 (b)に示すように、挿 入管 1に、四つの開口部 4が形成されている場合を例として説明する。 First, the peripheral surface of the insertion tube 1 is opened by laser cutting, and a plurality of surfaces are inserted into the peripheral surface of the insertion tube 1. Opening 4 is formed. The shape of each opening 4 is a shape extending along the central axis CL of the insertion tube 1. In addition, each opening 4 is set so that the intervals between adjacent openings 4 are equal. In this embodiment, as shown in FIG. 1B, which is a development view of FIG. 1A, a case where four openings 4 are formed in the insertion tube 1 will be described as an example.
[0021] 次に、図 2に示すように、挿入管 1のフィルタ部形成位置 2aを挿入管 1の軸方向に 収縮させるとともに、挿入管 1のうち各開口部 4間に形成されるフィルタ構成部 laを、 挿入管 1の外径方向に橈ませた状態で、フィルタ構成部 laに形状を記憶させて、フィ ルタ部 2の形成を終了する。 Next, as shown in FIG. 2, the filter configuration in which the filter portion forming position 2a of the insertion tube 1 is contracted in the axial direction of the insertion tube 1 and is formed between the openings 4 in the insertion tube 1 In a state where the portion la is constricted in the outer diameter direction of the insertion tube 1, the shape is stored in the filter constituent portion la, and the formation of the filter portion 2 is completed.
上述の方法によって、挿入管 1の軸方向に沿った一箇所には、挿入管 1の周面から 外径方向へ橈んだ形状の各フィルタ構成部 laにより、挿入管 1の周面力 外径方向 に張り出したフィルタ部 2が形成される。各フィルタ構成部 laは、挿入管 1の内径方向 への負荷を受けると、フィルタ部形成位置 2aが挿入管 1の軸方向に伸長するとともに 、挿入管 1の外径方向へのばねを有しながら挿入管 1の内径方向へ変位し、挿入管 1の内径方向への負荷から開放されると、挿入管 1の外径方向へ橈んだ形状へ復元 する。  By the above-described method, the circumferential force of the insertion tube 1 is externally applied to one place along the axial direction of the insertion tube 1 by each filter component la shaped in the outer diameter direction from the circumferential surface of the insertion tube 1. A filter portion 2 projecting in the radial direction is formed. When each filter component la receives a load in the inner diameter direction of the insertion tube 1, the filter portion forming position 2 a extends in the axial direction of the insertion tube 1 and has a spring in the outer diameter direction of the insertion tube 1. However, when it is displaced in the inner diameter direction of the insertion tube 1 and released from the load in the inner diameter direction of the insertion tube 1, the shape is restored to the shape of the insertion tube 1 in the outer diameter direction.
[0022] 次に、図 3を参照して、本実施形態の作用 ·効果について説明する。なお、本実施 形態では、生体管を血管とし、生体管内の異物を血栓とした場合を例にあげて説明 する。  Next, operations and effects of the present embodiment will be described with reference to FIG. In the present embodiment, a case where a biological tube is a blood vessel and a foreign substance in the biological tube is a thrombus will be described as an example.
本実施形態の生体管内治療具を用いた血管内の血栓除去作業は、以下の手順に 沿って行う。  The intravascular blood clot removal operation using the in-vivo treatment device of this embodiment is performed according to the following procedure.
まず、挿入管 1をカテーテルカゝらなる案内管 6内に挿入し、フィルタ部形成位置 2a が挿入管 1の軸方向に伸長するとともに、各フィルタ構成部 laが挿入管 1の外径方 向へのばねを有しながら挿入管 1の内径方向へ変位した状態とする。そして、案内管 6を先端側から血管 8内に挿入して、案内管 6の先端が血栓 10を通過した後、図 3に 示すように、案内管 6の先端力 挿入管 1を押し出す。このとき、フィルタ部 2には、フ ィルタ構成部 laを挿入管 1の外径方向に橈ませた状態で形状が記憶されているため 、案内管 6の先端力 挿入管 1を押し出すと、フィルタ部 2の形状が復元して、血管 8 内において、血栓 10と血管 8内の下流側との間にフィルタ部 2が形成される。 [0023] 次に、案内管 6を血管 8の上流側に移動させた後、挿入管 1を回転させつつ血管 8 の上流側に移動させて、フィルタ部 2を血管 8の下流側から血栓 10の位置を通過さ せる。なお、挿入管 1を回転させずに血管 8の上流側に移動させてもよい。このとき、 血管 8の下流側から血栓 10の位置を通過したフィルタ部 2によって、血栓 10が絡め 取られ、絡め取られた血栓 10は各フィルタ構成部 laによって捕捉される。 First, the insertion tube 1 is inserted into a guide tube 6 such as a catheter catheter, the filter portion forming position 2a extends in the axial direction of the insertion tube 1, and each filter component la extends in the outer diameter direction of the insertion tube 1. It is assumed that the insertion tube 1 is displaced in the inner diameter direction while having a spring. Then, the guide tube 6 is inserted into the blood vessel 8 from the distal end side, and after the distal end of the guide tube 6 has passed through the thrombus 10, the distal force insertion tube 1 of the guide tube 6 is pushed out as shown in FIG. At this time, since the shape is stored in the filter portion 2 in a state where the filter constituting portion la is held in the outer diameter direction of the insertion tube 1, if the distal end force insertion tube 1 of the guide tube 6 is pushed out, the filter portion 2 The shape of the portion 2 is restored, and the filter portion 2 is formed in the blood vessel 8 between the thrombus 10 and the downstream side in the blood vessel 8. Next, after moving the guide tube 6 to the upstream side of the blood vessel 8, the insertion tube 1 is moved to the upstream side of the blood vessel 8 while rotating the insertion tube 1, and the filter portion 2 is moved from the downstream side of the blood vessel 8 to the thrombus 10. Pass through the position. The insertion tube 1 may be moved upstream of the blood vessel 8 without rotating. At this time, the thrombus 10 is entangled by the filter portion 2 that has passed through the position of the thrombus 10 from the downstream side of the blood vessel 8, and the entangled thrombus 10 is captured by each filter component la.
そして、案内管 6を移動させずに挿入管 1のみを血管 8の上流側へ移動させて、挿 入管 1を案内管 6内へ格納して、各フィルタ構成部 laが挿入管 1の外径方向へのば ねを有しながら挿入管 1の内径方向へ変位した状態とした後、案内管 6及び挿入管 1 を血管 8内から引き抜いて、血管 8内における血栓 10の除去作業を終了する。  Then, without moving the guide tube 6, only the insertion tube 1 is moved to the upstream side of the blood vessel 8, the insertion tube 1 is stored in the guide tube 6, and each filter component la has an outer diameter of the insertion tube 1. After the guide tube 6 and the insertion tube 1 are pulled out from the blood vessel 8, the removal of the thrombus 10 in the blood vessel 8 is completed. .
[0024] したがって、本実施形態の生体管内治療具であれば、挿入管 1の周面に複数の開 口部 4を形成した後、挿入管 1のフィルタ部形成位置 2aを挿入管 1の軸方向に収縮さ せるとともに、フィルタ構成部 laを挿入管 1の外径方向に橈ませた状態で、フィルタ 構成部 laに形状を記憶させることによって、フィルタ部 2を形成することが可能である ため、生体管内治療具の製造効率向上及び製造コスト低減が可能となる。  [0024] Therefore, in the in-vivo treatment device of the present embodiment, after forming a plurality of openings 4 on the peripheral surface of the insertion tube 1, the filter portion forming position 2a of the insertion tube 1 is set to the axis of the insertion tube 1. The filter portion 2 can be formed by causing the filter component portion la to store the shape in a state where the filter component portion la is contracted in the direction and the filter component portion la is constricted in the outer diameter direction of the insertion tube 1. In addition, it is possible to improve the manufacturing efficiency and reduce the manufacturing cost of the in-vivo treatment device.
また、本実施形態の生体管内治療具であれば、挿入管 1とフィルタ部 2がー体であ るので、血管 8内において、挿入管 1からフィルタ部 2が離脱することが防止され、生 体管内の異物除去作業の安全性が向上する。また、従来の生体管内治療具に形成 されて 、た力しめ部のような、フィルタ部 2と他の構成部分との結合部が形成されず、 フィルタ部 2と他の構成部分との間に段差が形成されることがないため、挿入管 1を小 径ィ匕することが可能となり、より細い生体管における生体管内治療具の使用が可能と なる。  In addition, since the insertion tube 1 and the filter unit 2 are a single body in the in-vivo treatment device of the present embodiment, the removal of the filter unit 2 from the insertion tube 1 in the blood vessel 8 is prevented, and The safety of removing foreign substances in the body tube is improved. In addition, since it is formed in a conventional in-vivo treatment device, a connecting portion between the filter portion 2 and other components such as a forceps portion is not formed, and the filter portion 2 and other components are not formed. Since no step is formed, it is possible to reduce the diameter of the insertion tube 1, and it is possible to use an in-vivo treatment tool in a thinner living tube.
[0025] さらに、本実施形態の生体管内治療具であれば、挿入管 1の内部を、血栓溶解剤 等の液体が通過可能な通路とすることが可能となる。このため、血栓 10の除去作業 中に、血栓 10によってフィルタ部 2に目詰まりが生じた場合であっても、挿入管 1の外 部からフィルタ部 2へ血栓溶解剤を圧送して、フィルタ部 2の目詰まりを解消すること が可能となる。したがって、より効果的に血管 8内の血栓 10を除去することが可能とな る。  [0025] Further, in the in-vivo treatment device of the present embodiment, the inside of the insertion tube 1 can be a passage through which a liquid such as a thrombolytic agent can pass. For this reason, even if the clot 10 is clogged by the thrombus 10 during the removal of the thrombus 10, the thrombolytic agent is pumped from the outside of the insertion tube 1 to the filter unit 2 to remove the filter unit 2. It is possible to eliminate clogging of 2. Therefore, the thrombus 10 in the blood vessel 8 can be removed more effectively.
また、本実施形態の生体管内治療具であれば、挿入管 1が形状記憶合金製であり 、フィルタ部 2が形成された状態で形状が記憶されているため、フィルタ部 2を畳んだ 状態で、案内管 6内に挿入管 1を長期間挿入した場合でも、挿入管 1を案内管 6から 出したときに、フィルタ部 2の形状が確実に復元される。 Further, in the case of the in-vivo treatment device of the present embodiment, the insertion tube 1 is made of a shape memory alloy. Since the shape is stored in a state where the filter portion 2 is formed, the insertion tube 1 is inserted into the guide tube 6 even when the insertion tube 1 is inserted into the guide tube 6 for a long time with the filter portion 2 folded. The shape of the filter part 2 is reliably restored when it comes out of the box.
[0026] なお、本実施形態の生体管内治療具では、各開口部 4の形状を、挿入管 1の中心 軸線 CLに沿って延びる形状に形成した力 これに限定されるものではない。すなわ ち、図 4及び図 5に示すように、各開口部 4を、挿入管 1の中心軸線 CLに対して任意 の角度を付けて形成してもよい。また、各開口部 4を、挿入管 1の長手方向に沿って 蛇行しながら延びる形状としてもよい。ここで、図 4 (a)及び図 4 (a)の展開図である図 4 (b)に示す挿入管 1に形成されている各開口部 4は、図中に示すように、挿入管 1の 中心軸線 CLに対して 10度の角度を付けて形成されている。また、図 5 (a)及び図 5 ( a)の展開図である図 5 (b)に示す挿入管 1に形成されて!、る各開口部 4は、図中に示 すように、挿入管 1の中心軸線 CLに対して 19度の角度を付けて形成されている。こ のように、各開口部 4を、挿入管 1の中心軸線 CLに対して任意の角度を付けて形成 することにより、フィルタ部 2の形状が複雑ィ匕するため、生体管内における異物の除 去効率が向上する。 [0026] In the in-vivo treatment device of the present embodiment, the force formed in the shape of each opening 4 along the central axis CL of the insertion tube 1 is not limited to this. That is, as shown in FIGS. 4 and 5, each opening 4 may be formed at an arbitrary angle with respect to the central axis CL of the insertion tube 1. Further, each opening 4 may have a shape extending while meandering along the longitudinal direction of the insertion tube 1. Here, each opening 4 formed in the insertion tube 1 shown in FIG. 4 (b), which is a development view of FIGS. 4 (a) and 4 (a), is inserted into the insertion tube 1 as shown in the figure. It is formed with an angle of 10 degrees with respect to the central axis CL. In addition, each opening 4 formed in the insertion tube 1 shown in FIG. 5 (b), which is an exploded view of FIG. 5 (a) and FIG. 5 (a), is inserted as shown in the figure. It is formed with an angle of 19 degrees with respect to the central axis CL of the tube 1. In this way, each opening 4 is formed at an arbitrary angle with respect to the central axis CL of the insertion tube 1, thereby complicating the shape of the filter unit 2. Increases efficiency.
[0027] また、開口部 4の形状は、図 6 (a)〜 (h)に示すような多種多様な形状であってもよ い。すなわち、開口部 4の形状は、フィルタ部 2が生体管内にある異物を捕捉可能な 形状に形成されるものであれば、どのような形状であってもよい。また、特に図示しな いが、開口部 4をスリットとしてもよい。この場合、全ての開口部 4をスリットとしてもよく 、開口部 4とスリットとが混在する構成としてもよい。  [0027] The shape of the opening 4 may be a wide variety of shapes as shown in Figs. 6 (a) to 6 (h). That is, the shape of the opening 4 may be any shape as long as the filter portion 2 is formed in a shape capable of capturing foreign matter in the living body tube. Although not particularly shown, the opening 4 may be a slit. In this case, all the openings 4 may be slits, or the openings 4 and the slits may be mixed.
また、本実施形態の生体管内治療具では、隣り合う開口部 4同士の間隔を等間隔 としたが、これに限定されるものではなぐフィルタ部 2が生体管内にある異物を捕捉 可能に形成される間隔であればょ 、。  Further, in the in-vivo treatment device of the present embodiment, the intervals between the adjacent openings 4 are set to be equal intervals, but the present invention is not limited to this, and the filter unit 2 is formed so as to capture foreign substances in the in-vivo tube. If it is an interval,
[0028] また、本実施形態の生体管内治療具では、挿入管 1のみを備える構成としたが、こ れに限定されるものではない。すなわち、挿入管 1内へ、可撓性を有するワイヤを移 動自在に挿通し、このワイヤを、フィルタ部 2を通過して挿入管 1の遠位側部と連結す る構成としてもよい。この場合、フィルタ部 2の形状力 血栓 10を捕捉するために適切 な形状に保持される。 また、上記ワイヤの端部が、挿入管 1の近位端力も突出する構成としてもよい。この 場合、ワイヤのうち、挿入管 1の近位端力も突出する部分を移動させることにより、フィ ルタ部 2の形状を任意の形状に変形させることが可能となる。また、挿入管 1の先端 部に、例えば、先端へ向けて縮径する形状等の、挿入管 1の血管 8内への挿入が容 易となるような形状の導入部材を連結してもよ 、。 [0028] Further, although the in-vivo treatment device of the present embodiment is configured to include only the insertion tube 1, it is not limited to this. That is, a flexible wire may be movably inserted into the insertion tube 1 and the wire may be connected to the distal side portion of the insertion tube 1 through the filter unit 2. In this case, the shape force of the filter unit 2 is held in an appropriate shape for capturing the thrombus 10. Further, the end of the wire may be configured such that the proximal end force of the insertion tube 1 also protrudes. In this case, it is possible to change the shape of the filter portion 2 to an arbitrary shape by moving the portion of the wire that also projects the proximal end force of the insertion tube 1. Further, an introduction member having a shape that facilitates insertion of the insertion tube 1 into the blood vessel 8 such as a shape that decreases in diameter toward the distal end may be connected to the distal end portion of the insertion tube 1. ,.
[0029] また、本実施形態の生体管内治療具では、挿入管 1の軸方向に沿った一箇所のみ にフィルタ部 2を形成したが、これに限定されるものではなぐ挿入管 1の軸方向に沿 つた複数箇所にフィルタ部 2をしてもょ 、。 [0029] In the in-vivo treatment device of the present embodiment, the filter unit 2 is formed only at one location along the axial direction of the insertion tube 1. However, the present invention is not limited to this, and the axial direction of the insertion tube 1 is not limited thereto. Filter 2 at multiple locations along the line.
また、本実施形態の生体管内治療具では、挿入管 1を円筒形状としたが、これに限 定されるものではなく、挿入管 1の内部に液体が通過可能な通路が形成されて ヽれ ば、例えば断面が楕円形状となるような、略円筒形状に形成してもよい。  In the in-vivo treatment device of the present embodiment, the insertion tube 1 has a cylindrical shape. However, the present invention is not limited to this, and a passage through which liquid can pass is formed inside the insertion tube 1. For example, it may be formed in a substantially cylindrical shape whose cross section is elliptical.
[0030] また、本実施形態の生体管内治療具では、フィルタ部 2を形成する際に、各フィル タ構成部 laを挿入管 1の外径方向に橈ませた状態で、各フィルタ構成部 laに形状を 記憶させた力 これに限定されるものではない。すなわち、フィルタ部 2を形成する際 に、各フィルタ構成部 laを挿入管 1の外径方向に橈ませた状態で、挿入管 1全体に 形状を記憶させてもよい。 [0030] Further, in the in-vivo treatment device of the present embodiment, when the filter unit 2 is formed, each filter component la is placed in a state in which each filter component la is bent in the outer diameter direction of the insertion tube 1. The force that memorizes the shape is not limited to this. That is, when forming the filter portion 2, the shape of the entire insertion tube 1 may be stored in a state where each filter component la is held in the outer diameter direction of the insertion tube 1.
また、本実施形態では、生体管を血管 8とした場合を例にあげて説明したが、これ に限定されるものではなぐ胆管等の他の生体管に対しても適用可能である。また、 本実施形態では、生体管内にある異物を血栓 10とした場合を例にあげて説明したが 、これに限定されるものではなぐ胆石等の他の異物に対しても適用可能である。  In this embodiment, the case where the blood vessel 8 is the blood vessel 8 has been described as an example. However, the present invention is not limited to this and can be applied to other biological tubes such as a bile duct. In this embodiment, the case where the foreign substance in the living body tube is the thrombus 10 has been described as an example. However, the present invention is not limited to this and can be applied to other foreign substances such as gallstones.
[0031] 次に、本発明の第二実施形態を、図 7及び図 8を参照して説明する。なお、上述し た第一実施形態と同様の構成については同一符号を付し、その説明は省略する。 本実施形態の生体管内治療具に備えられている挿入管 1は、フィルタ部 2の構成を 除き、上述した第一実施形態と同様の構成と同様である。 Next, a second embodiment of the present invention will be described with reference to FIG. 7 and FIG. In addition, the same code | symbol is attached | subjected about the structure similar to 1st embodiment mentioned above, and the description is abbreviate | omitted. The insertion tube 1 provided in the in-vivo treatment device of the present embodiment has the same configuration as that of the first embodiment described above except for the configuration of the filter unit 2.
挿入管 1の展開図である図 7に示すように、フィルタ部 2は、挿入管 1の先端側となる 遠位側に形成される捕捉部 12と、挿入管 1の基端側となる近位側に形成される透過 部 14とから形成されている。  As shown in FIG. 7, which is a development view of the insertion tube 1, the filter portion 2 includes a capture portion 12 formed on the distal side that is the distal end side of the insertion tube 1 and a proximal end side of the insertion tube 1. And a transmission part 14 formed on the distal side.
[0032] 以下、フィルタ部 2の形成方法について説明する。 まず、挿入管 1の周面をレーザーカットによって開口して、捕捉部 12に複数の開口 部 4aを形成し、透過部 14に複数の開口部 4bを形成する。 Hereinafter, a method for forming the filter portion 2 will be described. First, the peripheral surface of the insertion tube 1 is opened by laser cutting to form a plurality of openings 4 a in the capturing part 12 and a plurality of openings 4 b in the transmission part 14.
次に、捕捉部 12の各開口部 4aを、挿入管 1のフィルタ部形成位置 2aを挿入管 1の 軸方向に収縮させるとともに、各開口部 4a間に形成される捕捉部構成部 12aを挿入 管 1の外径方向に橈ませた状態で、捕捉部構成部 12aが網目状となるように、レーザ 一カットによって矩形状に形成する。ここで、各開口部 4aは、その開口面積が透過部 14の各開口部 4bの開口面積よりも狭くなるように形成する。  Next, each opening 4a of the trapping part 12 is contracted in the axial direction of the insertion pipe 1 at the filter part forming position 2a of the insertion pipe 1, and the trapping part constituting part 12a formed between the openings 4a is inserted. In a state where the tube 1 is squeezed in the outer diameter direction, a rectangular shape is formed by one laser cut so that the capturing portion constituting portion 12a has a mesh shape. Here, each opening 4a is formed such that its opening area is narrower than the opening area of each opening 4b of the transmission part 14.
[0033] また、透過部 14の開口部 4bを、挿入管 1のフィルタ部形成位置 2aを挿入管 1の軸 方向に収縮させるとともに、各開口部 4b間に形成される透過部構成部 14aを挿入管 1の外径方向に橈ませた状態で、各開口部 4b間に形成される透過部構成部 14aが 挿入管 1の軸方向に沿った支柱状となるように、レーザーカットによって形成する。各 開口部 4bの形状は、挿入管 1の軸方向に沿って延びる形状とし、挿入管 1の周方向 に沿った幅が、挿入管 1の近位側力も遠位側へ向けて段階的に狭くなる形状とする。 [0033] Further, the opening 4b of the transmission portion 14 is contracted in the axial direction of the insertion tube 1 at the filter portion forming position 2a of the insertion tube 1, and the transmission portion constituting portion 14a formed between the openings 4b is provided. Formed by laser cutting so that the transmission portion constituting portion 14a formed between the openings 4b is formed in a columnar shape along the axial direction of the insertion tube 1 in a state where the insertion tube 1 is constricted in the outer diameter direction. . The shape of each opening 4b extends along the axial direction of the insertion tube 1, and the width along the circumferential direction of the insertion tube 1 gradually increases the proximal force of the insertion tube 1 toward the distal side. The shape becomes narrower.
[0034] そして、図 8に示すように、挿入管 1のフィルタ部形成位置 2aを挿入管 1の軸方向に 収縮させるとともに、捕捉部構成部 12a及び透過部構成部 14aを、挿入管 1の外径方 向に橈ませた状態で、捕捉部構成部 12a及び透過部構成部 14aに形状を記憶させ て、フィルタ部 2の形成を終了する。 Then, as shown in FIG. 8, the filter portion forming position 2a of the insertion tube 1 is contracted in the axial direction of the insertion tube 1, and the capturing portion constituting portion 12a and the transmission portion constituting portion 14a are connected to the insertion tube 1. The shape is stored in the capturing part constituting part 12a and the transmissive part constituting part 14a in a state where it is bent in the outer diameter direction, and the formation of the filter part 2 is completed.
上述の方法によって、挿入管 1の軸方向に沿った一箇所には、挿入管 1の周面から 外径方向へ橈んだ形状の捕捉部構成部 12a及び透過部構成部 14aにより、挿入管 1の周面カゝら外径方向に張り出したフィルタ部 2が形成される。捕捉部構成部 12a及 び透過部構成部 14aは、挿入管 1の内径方向への負荷を受けると、フィルタ部形成 位置 2aが挿入管 1の軸方向に伸長するとともに、挿入管 1の外径方向へのばねを有 しながら挿入管 1の内径方向へ変位し、挿入管 1の内径方向への負荷力 開放され ると、挿入管 1の外径方向へ橈んだ形状へ復元する。  By the above-described method, the insertion tube 1 is disposed at one place along the axial direction of the insertion tube 1 by the capturing portion constituting portion 12a and the transmission portion constituting portion 14a having a shape sandwiched from the peripheral surface of the insertion tube 1 in the outer diameter direction. A filter portion 2 is formed which projects in the outer diameter direction from the peripheral surface 1. When receiving part 12a and permeation part constituting part 14a are loaded in the inner diameter direction of insertion tube 1, filter part forming position 2a extends in the axial direction of insertion pipe 1, and outer diameter of insertion pipe 1 is increased. When it is displaced in the inner diameter direction of the insertion tube 1 while having a spring in the direction and the load force in the inner diameter direction of the insertion tube 1 is released, the shape of the insertion tube 1 is restored to the shape of the outer diameter.
[0035] その他の構成は、上述した第一の実施形態と同様である。 Other configurations are the same as those of the first embodiment described above.
次に、本実施形態の作用'効果について説明する。なお、上述した第一の実施形 態と同様の作用 ·効果については詳細な説明は省略する。  Next, the effect | action effect of this embodiment is demonstrated. Detailed description of the same operations and effects as those of the first embodiment described above will be omitted.
本実施形態の生体管内治療具を用いた血管内の血栓除去作業は、以下の手順に 沿って行う。 The intravascular blood clot removal operation using the in-vivo treatment device of this embodiment is performed according to the following procedure. Do along.
まず、挿入管 1を案内管内に挿入して、捕捉部構成部 12a及び透過部構成部 14a を、フィルタ部形成位置 2aが挿入管 1の軸方向に伸長するとともに、挿入管 1の外径 方向へのばねを有しながら挿入管 1の内径方向へ変位した状態とする。そして、この 案内管を先端側力 生体管内に挿入して、案内管の先端が異物を通過した後、案内 管の先端カゝら挿入管 1を押し出す。このとき、フィルタ部 2には、捕捉部構成部 12a及 び透過部構成部 14aを挿入管 1の外径方向に橈ませた状態で形状が記憶されてい るため、案内管の先端力も挿入管 1を押し出すと、フィルタ部 2の形状が復元して、生 体管内において、異物と生体管内の下流側との間にフィルタ部 2が形成される。  First, the insertion tube 1 is inserted into the guide tube, and the trapping portion constituting portion 12a and the transmitting portion constituting portion 14a are extended in the axial direction of the insertion tube 1 while the filter portion forming position 2a extends in the outer diameter direction of the insertion tube 1. It is assumed that the insertion tube 1 is displaced in the inner diameter direction while having a spring. Then, this guide tube is inserted into the living body tube at the distal end side force, and after the distal end of the guide tube passes through the foreign matter, the insertion tube 1 is pushed out from the distal end of the guide tube. At this time, since the shape is stored in the filter portion 2 with the capturing portion constituting portion 12a and the transmissive portion constituting portion 14a being squeezed in the outer diameter direction of the insertion tube 1, the tip force of the guide tube is also reduced. When 1 is pushed out, the shape of the filter portion 2 is restored, and the filter portion 2 is formed between the foreign substance and the downstream side in the biological tube in the biological tube.
[0036] 次に、案内管を生体管の上流側に移動させた後、挿入管 1を生体管の上流側に移 動させて、フィルタ部 2を生体管の下流側から異物の位置を通過させる。このとき、フ ィルタ部 2よりも上流側にある異物が、透過部 14を通過して捕捉部 12によって捕捉さ れる。 Next, after moving the guide tube to the upstream side of the biological tube, the insertion tube 1 is moved to the upstream side of the biological tube, and the filter unit 2 passes through the position of the foreign substance from the downstream side of the biological tube. Let At this time, the foreign matter on the upstream side of the filter unit 2 passes through the transmission unit 14 and is captured by the capture unit 12.
そして、案内管を移動させずに挿入管 1のみを生体管の上流側へ移動させて、挿 入管 1を案内管内へ格納し、捕捉部構成部 12a及び透過部構成部 14aを、フィルタ 部形成位置 2aが挿入管 1の軸方向に伸長するとともに、挿入管 1の外径方向へのば ねを有しながら挿入管 1の内径方向へ変位した状態とした後、案内管及び挿入管 1 を生体管内から引き抜いて、生体管内における異物の除去作業を終了する。  Then, without moving the guide tube, only the insertion tube 1 is moved to the upstream side of the living body tube, the insertion tube 1 is stored in the guide tube, and the trapping portion constituting portion 12a and the transmitting portion constituting portion 14a are formed as filter portions. After the position 2a extends in the axial direction of the insertion tube 1 and is displaced in the inner diameter direction of the insertion tube 1 while having a spring in the outer diameter direction of the insertion tube 1, the guide tube and the insertion tube 1 are Withdrawing from the living body tube, the foreign substance removing operation in the living body tube is completed.
[0037] したがって、本実施形態の生体管内治療具であれば、捕捉部 12の各開口部 4aの 開口面積が、透過部 14の各開口部 4bの開口面積よりも狭いため、透過部 14を通過 した異物が、生体管内において下流側に位置する捕捉部 12によって捕捉され、生 体管内における異物除去作業の効率が向上する。 [0037] Therefore, in the in-vivo treatment device of the present embodiment, since the opening area of each opening 4a of the capturing unit 12 is narrower than the opening area of each opening 4b of the transmitting unit 14, the transmitting unit 14 is used. The foreign matter that has passed through is captured by the capturing unit 12 located on the downstream side in the biological tube, and the efficiency of the foreign matter removal work in the biological tube is improved.
また、透過部 14の各開口部 4bは捕捉部 12の開口部 4aよりも開口面積が広いため 、生体管内における流体の流れを十分に確保することが可能となる。  Further, since each opening 4b of the transmission part 14 has an opening area larger than that of the opening 4a of the capturing part 12, it is possible to ensure a sufficient fluid flow in the living body tube.
[0038] なお、特に図示しないが、捕捉部 12の各開口部 4aをそれぞれ異なる開口面積とし 、挿入管 1の遠位端側に位置する開口部 4aの開口面積を、挿入管 1の近位端側に 位置する開口部 4aの開口面積よりも狭くした構成としてもよい。 [0038] Although not particularly illustrated, each opening 4a of the capturing part 12 has a different opening area, and the opening area of the opening 4a located on the distal end side of the insertion tube 1 is set to be proximal to the insertion tube 1. A configuration may be adopted in which the opening area of the opening 4a located on the end side is narrower.
また、本実施形態の生体管内治療具は、生体管内において、フィルタ部 2よりも上 流側にある異物を、透過部 14を通過して捕捉部 12によって捕捉して除去する使用 方法としたが、これに限定されるものではない。すなわち、案内管を生体管の上流側 に移動させた後、挿入管 1を回転させつつ生体管の上流側に移動させて、フィルタ 部 2を生体管の下流側力 異物の位置を通過させ、生体管の下流側から異物の位 置を通過したフィルタ部 2によって異物を絡め取る使用方法としてもよい。 Further, the in-vivo treatment device of the present embodiment is above the filter unit 2 in the in-vivo tube. Although the foreign substance on the flow side passes through the permeation section 14 and is captured and removed by the capture section 12, it is not limited thereto. That is, after the guide tube is moved to the upstream side of the biological tube, the insertion tube 1 is rotated and moved to the upstream side of the biological tube, and the filter unit 2 is passed through the position of the force foreign substance on the downstream side of the biological tube, A method of using the filter unit 2 that has passed through the position of the foreign substance from the downstream side of the biological tube may be used.
[0039] その他の作用'効果は、上述した第一の実施形態と同様である。 [0039] Other effects are the same as in the first embodiment described above.
次に、本発明の第三の実施形態について図面を参照しつつ説明する。なお、上述 した第一及び第二実施形態と同様の構成については同一符号を付して説明する。 まず、図 9から図 11を参照して本実施形態の構成を説明する。  Next, a third embodiment of the present invention will be described with reference to the drawings. In addition, the same code | symbol is attached | subjected and demonstrated about the structure similar to 1st and 2nd embodiment mentioned above. First, the configuration of this embodiment will be described with reference to FIGS.
図 9に示すように、本実施形態の生体管内治療具は、挿入管 1と、挿入管 1内へ移 動自在に挿通されるワイヤ 16とを備えて 、る。  As shown in FIG. 9, the in-vivo treatment device of the present embodiment includes an insertion tube 1 and a wire 16 that is movably inserted into the insertion tube 1.
[0040] 挿入管 1は、円筒形状をなしており、可撓性を有する形状記憶合金によって形成さ れている。 [0040] The insertion tube 1 has a cylindrical shape and is formed of a flexible shape memory alloy.
また、挿入管 1は、挿入管 1の軸方向に沿った一箇所が、生体管内にある異物を捕 捉するフィルタ部 2を形成して 、る。  In addition, the insertion tube 1 has a filter portion 2 that captures a foreign substance in the living body tube at one place along the axial direction of the insertion tube 1.
以下、フィルタ部 2の形成方法について説明する。  Hereinafter, a method for forming the filter portion 2 will be described.
まず、挿入管 1の周面に、挿入管 1の軸方向に沿って螺旋状に切断される切断部 1 8を、レーザーカットによって形成する。次に、図 10に示すように、挿入管 1のうち各 切断部 18間に形成されるフィルタ構成部 laを挿入管 1の外径方向へ拡径させた状 態で、フィルタ構成部 laに形状を記憶させて、フィルタ部 2の形成を終了する。  First, a cutting portion 18 that is cut in a spiral shape along the axial direction of the insertion tube 1 is formed on the peripheral surface of the insertion tube 1 by laser cutting. Next, as shown in FIG. 10, in the insertion tube 1, the filter component la formed between the cut portions 18 is expanded in the outer diameter direction of the insertion tube 1. The shape is stored, and the formation of the filter unit 2 is completed.
[0041] ここで、フィルタ部 2の形状は、挿入管 1の遠位側力も挿入管 1の近位側へ向けて拡 径する形状とする。 [0041] Here, the shape of the filter portion 2 is a shape in which the distal side force of the insertion tube 1 also expands toward the proximal side of the insertion tube 1.
上述の方法によって、挿入管 1の軸方向に沿った一箇所には、挿入管 1の周面から 外径方向へ拡径した形状のフィルタ構成部 laにより、挿入管 1の周面から外径方向 に張り出したフィルタ部 2が形成される。フィルタ構成部 laは、挿入管 1の内径方向へ の負荷を受けると、挿入管 1の外径方向へのばねを有しながら挿入管 1の内径方向 へ変位し、挿入管 1の内径方向への負荷から開放されると、挿入管 1の外径方向へ 橈んだ形状へ復元する。 [0042] ワイヤ 16は、可撓性の線材によって形成されており、一方の端部が挿入管 1の先端 側となる遠位側部 lbと結合されており、他方の端部 16aが挿入管 1の基端部となる近 位端 lc力も突出している。ここで、ワイヤ 16の一方の端部と遠位側部 lbとは、両者を 力しめることによって結合されて 、る。 By the above-described method, at one location along the axial direction of the insertion tube 1, the outer diameter of the insertion tube 1 from the circumferential surface of the insertion tube 1 is increased by the filter component la having a shape expanded from the circumferential surface of the insertion tube 1 to the outer diameter direction. A filter part 2 projecting in the direction is formed. When receiving a load in the inner diameter direction of the insertion tube 1, the filter component la displaces in the inner diameter direction of the insertion tube 1 while having a spring in the outer diameter direction of the insertion tube 1, and moves toward the inner diameter direction of the insertion tube 1. When the load is released, the shape of the insertion tube 1 is restored to the shape of the outer diameter. [0042] The wire 16 is formed of a flexible wire, one end of which is connected to the distal side lb which is the distal end side of the insertion tube 1, and the other end 16a is the insertion tube. The proximal end lc force, which is the base end of 1, also protrudes. Here, one end of the wire 16 and the distal side lb are joined together by applying force together.
図 11に示すように、挿入管 1の内径面 Idとワイヤ 16との間には、空隙部 20が形成 されている。  As shown in FIG. 11, a gap 20 is formed between the inner diameter surface Id of the insertion tube 1 and the wire 16.
[0043] その他の構成は、上述した第一の実施形態と同様である。  Other configurations are the same as those in the first embodiment described above.
次に、本実施形態の作用'効果について説明する。  Next, the effect | action effect of this embodiment is demonstrated.
本実施形態の生体管内治療具を用いた生体内の異物除去作業は、以下の手順に 沿って行う。  The in-vivo foreign body removal operation using the in-vivo treatment device of the present embodiment is performed according to the following procedure.
まず、ワイヤ 16のうち挿入管 1の近位端 lc力も突出している部分を移動させて、フィ ルタ構成部 laを挿入管 1の内径方向へ縮径させる。次に、挿入管 1を先端側から生 体管内に挿入し、挿入管 1の先端が異物を通過した後、フィルタ部 2の形状を復元さ せ、生体管内において、異物と生体管内の下流側との間にフィルタ部 2を形成する。 このとき、フィルタ部 2〖こは、フィルタ構成部 laを挿入管 1の外径方向に拡径させた状 態で形状が記憶されているため、生体管内において、フィルタ部 2の形状が確実に 復元される。  First, the portion of the wire 16 that also projects the proximal end lc force of the insertion tube 1 is moved to reduce the diameter of the filter component la in the inner diameter direction of the insertion tube 1. Next, the insertion tube 1 is inserted into the biological tube from the distal end side, and after the distal end of the insertion tube 1 has passed through the foreign matter, the shape of the filter unit 2 is restored, and the foreign matter and the downstream side of the biological tube in the biological tube. The filter part 2 is formed between the two. At this time, the shape of the filter portion 2 is memorized in a state where the diameter of the filter component la is expanded in the outer diameter direction of the insertion tube 1, so that the shape of the filter portion 2 is surely ensured in the living body tube. Restored.
[0044] 次に、挿入管 1を回転させつつ生体管の上流側に移動させて、フィルタ部 2を生体 管の下流側力 異物の位置を通過させる。このとき、生体管の下流側から異物の位 置を通過したフィルタ部 2によって異物が絡め取られ、絡め取られた異物はフィルタ 構成部 laによって捕捉される。  [0044] Next, the insertion tube 1 is rotated and moved to the upstream side of the biological tube, and the filter unit 2 is passed through the position of the foreign substance on the downstream side of the biological tube. At this time, the foreign matter is entangled by the filter unit 2 that has passed through the position of the foreign matter from the downstream side of the biological tube, and the entangled foreign matter is captured by the filter component la.
そして、挿入管 1を生体管の上流側へ移動させて生体管内から引き抜き、生体管 内における異物の除去作業を終了する。  Then, the insertion tube 1 is moved to the upstream side of the living body tube and pulled out from the living body tube, and the foreign substance removing operation in the living body tube is completed.
[0045] したがって、本実施形態の生体管内治療具であれば、挿入管 1の周面に、レーザ 一カットによって、挿入管 1の軸方向に沿った螺旋状の切断部 18を形成した後、フィ ルタ構成部 laを挿入管 1の外径方向に拡径させた状態で形状を記憶させることによ り、フィルタ部 2を形成することが可能であるため、生体管内治療具の製造効率向上 及び製造コスト低減が可能となる。 また、本実施形態の生体管内治療具であれば、挿入管 1の遠位側部 lbとワイヤ 16 とをかしめることにより、挿入管 1とワイヤ 16とを結合しているため、従来の生体管内 治療具に形成されていた、フィルタ部 2と他の構成部分とを結合する力しめ部が、挿 入管 1の遠位側部 lbにのみ形成される。このため、生体管内において、挿入管 1の 遠位側部 lb及びフィルタ部 2が他の構成部分から離脱する危険性が低減され、生体 管内の異物除去作業の安全性が向上する。 Therefore, in the in-vivo treatment device of the present embodiment, after forming the helical cut portion 18 along the axial direction of the insertion tube 1 on the peripheral surface of the insertion tube 1 by one laser cut, Since the filter part 2 can be formed by storing the shape in a state where the filter component la is expanded in the outer diameter direction of the insertion tube 1, the manufacturing efficiency of the in-vivo treatment device is improved. In addition, manufacturing costs can be reduced. Further, in the case of the in-vivo treatment device of the present embodiment, since the insertion tube 1 and the wire 16 are coupled by caulking the distal side portion lb of the insertion tube 1 and the wire 16, the conventional living body The forceps for connecting the filter portion 2 and other components, which have been formed in the intravascular treatment tool, are formed only on the distal side portion lb of the insertion tube 1. For this reason, the risk that the distal side portion lb of the insertion tube 1 and the filter portion 2 are detached from other components in the biological tube is reduced, and the safety of the foreign substance removal work in the biological tube is improved.
[0046] さらに、本実施形態の生体管内治療具であれば、ワイヤ 16の一方の端部が、挿入 管 1の遠位側部 lbと結合されており、ワイヤ 16の他方の端部 16aが挿入管 1の近位 端 lcから突出している。このため、フィルタ部 2の形状力 生体管内において異物を 捕捉するために好適な形状に保持され、生体管内の異物除去作業の作業効率が向 上する。また、ワイヤ 16のうち、挿入管 1の近位端 lcから突出している部分を移動さ せることにより、フィルタ部 2の形状を任意の形状に変形させることが可能となるため、 生体管内の異物除去作業の作業効率が向上する。  [0046] Further, in the in-vivo treatment device of the present embodiment, one end of the wire 16 is coupled to the distal side lb of the insertion tube 1, and the other end 16a of the wire 16 is It protrudes from the proximal end lc of the insertion tube 1. For this reason, the shape force of the filter unit 2 is held in a shape suitable for trapping foreign matter in the biological tube, and the work efficiency of the foreign matter removal work in the biological tube is improved. In addition, by moving the portion of the wire 16 that protrudes from the proximal end lc of the insertion tube 1, the shape of the filter unit 2 can be changed to an arbitrary shape, so that the foreign matter in the biological tube The work efficiency of the removal work is improved.
[0047] また、本実施形態の生体管内治療具であれば、挿入管 1の内径面 Idとワイヤ 16と の間に形成された空隙部 20を、血栓溶解剤等の液体が通過可能な通路とすること が可能である。このため、挿入管 1の近位端 lcから、フィルタ部 2を介して、生体管内 に血栓溶解剤等の液体を送り込むことが可能であるため、より効果的に生体管内の 異物を除去することが可能となる。  [0047] Further, in the in-vivo treatment device of the present embodiment, a passage through which a liquid such as a thrombolytic agent can pass through the void portion 20 formed between the inner diameter surface Id of the insertion tube 1 and the wire 16 is provided. It is possible to For this reason, since it is possible to send a liquid such as a thrombolytic agent from the proximal end lc of the insertion tube 1 into the living body tube via the filter unit 2, it is possible to more effectively remove foreign substances in the living tube. Is possible.
なお、本実施形態の生体管内治療具では、上述した第一の実施形態と同様に、挿 入管 1を、フィルタ構成部 1 aが挿入管 1の外径方向へのばねを有しながら挿入管 1の 内径方向へ変位した状態で案内管内に挿入し、この案内管を先端側から生体管内 に挿入して、案内管の先端が異物を通過した後、案内管の先端から挿入管 1を押し 出す構成としてもよい。  In the in-vivo treatment device of this embodiment, the insertion tube 1 is inserted into the insertion tube 1 while the filter component 1a has a spring in the outer diameter direction of the insertion tube 1 as in the first embodiment. Insert the guide tube into the living body tube from the distal end side after the foreign substance has passed through the foreign body, and then push the insertion tube 1 from the distal end of the guide tube. It is good also as a structure to take out.
[0048] また、本実施形態の生体管内治療具では、フィルタ部 2の形状を、挿入管 1の遠位 側から挿入管 1の近位側へ向けて拡径する形状としたが、これに限定されるものでは なぐ挿入管 1の近位側カゝら挿入管 1の遠位側へ向けて拡径する形状としてもょ 、。 さらに、本実施形態の生体管内治療具では、ワイヤ 16の他方の端部 16aが挿入管 1の近位端 lcから突出している構成とした力 これに限定されるものではなぐワイヤ 16の他方の端部 16aが挿入管 1内に格納される構成としてもよ!ヽ。 [0048] In the in-vivo treatment device of the present embodiment, the shape of the filter unit 2 is a shape that expands from the distal side of the insertion tube 1 toward the proximal side of the insertion tube 1. The shape of the insertion tube 1 is not limited to a shape that expands toward the distal side of the insertion tube 1 from the proximal side of the insertion tube 1. Furthermore, in the in-vivo treatment device of the present embodiment, the force is such that the other end portion 16a of the wire 16 protrudes from the proximal end lc of the insertion tube 1. The wire is not limited to this. The other end 16a of 16 may be stored in the insertion tube 1!
[0049] また、フィルタ構成部 laの挿入管 1の周面側の縁部 22に面取り部を設けてもよい。 [0049] Further, a chamfered portion may be provided on the peripheral edge 22 of the insertion tube 1 of the filter component la.
この場合、生体管内の異物除去作業において、生体管内を損傷させる危険性が低 減され、生体管内の異物除去作業の安全性が向上する。  In this case, the risk of damaging the inside of the living body can be reduced in the foreign body removing work in the living body, and the safety of the removing work in the living body can be improved.
その他の作用 ·効果は、上述した第一の実施形態と同様である。  Other functions and effects are the same as those of the first embodiment described above.
[実施例]  [Example]
上述した第一及び第三実施形態において説明したものと同様の構成を有する生体 管内治療具の作成において、挿入管の周面の一部に、レーザーカットによって開口 部及び切断部を形成し、その作業精度を検証した。  In creating an in-vivo treatment device having the same configuration as that described in the first and third embodiments described above, an opening and a cutting portion are formed by laser cutting on a part of the peripheral surface of the insertion tube. The work accuracy was verified.
[0050] まず、上述した第一の実施形態で説明したものと同様の構成を有する挿入管を作 成した。挿入管は、直径 0. 458mm,円周 1. 438mmのニッケル 'チタン合金製のパ ィプを用い、幅 0. 03mmのスリット状の開口部を、レーザーカットによって、挿入管の 中心軸線と平行に 24箇所形成した。その結果、挿入管には、幅 0. 02992mmのフィ ルタ構成部が 24箇所形成された。  [0050] First, an insertion tube having the same configuration as that described in the first embodiment was created. The insertion tube uses a nickel-titanium alloy pipe with a diameter of 0.458mm and a circumference of 1.438mm. A slit-shaped opening with a width of 0.03mm is parallel to the central axis of the insertion tube by laser cutting. 24 locations were formed. As a result, 24 filter components having a width of 0.02992 mm were formed in the insertion tube.
次に、上述した第三の実施形態で説明したものと同様の構成を有する挿入管を作 成した。挿入管は、外径 0. 4mm、内径 0. 2mmのニッケル 'チタン合金製のパイプ を用い、ワイヤは、外径 0. 18mmの鋼線を用いた。挿入管には、レーザーカットによ つて、幅 50 mの切断部を螺旋状に形成するとともに、隣り合う切断部同士の幅が 2 00 μ mとなる う〖こ設けた。  Next, an insertion tube having the same configuration as that described in the third embodiment was created. A nickel-titanium alloy pipe having an outer diameter of 0.4 mm and an inner diameter of 0.2 mm was used as the insertion tube, and a steel wire having an outer diameter of 0.18 mm was used as the wire. The insertion tube was provided with a laser cut to form a cut portion having a width of 50 m in a spiral shape and a width between adjacent cut portions of 200 μm.
[0051] したがって、上述した各実施形態の生体管内治療具に備えられる挿入管は、円筒 形状をなすニッケル 'チタン合金製のパイプに、レーザーカットによって開口部及び 切断部を形成することにより作成可能であることが確認された。  [0051] Therefore, the insertion tube provided in the in-vivo treatment device of each embodiment described above can be created by forming an opening and a cut portion by laser cutting on a cylindrical nickel-titanium alloy pipe. It was confirmed that.
産業上の利用の可能性  Industrial applicability
[0052] 本発明によれば、生体管内治療具の製造効率の向上及びコストの低減が可能とな るとともに、生体管内においてフィルタ部が生体管内治療具力 離脱することが防止 され、生体管内が閉塞されることが防止可能となる。 [0052] According to the present invention, it is possible to improve the production efficiency and cost of an in-vivo treatment device, and to prevent the filter unit from being disengaged from the in-vivo treatment device force within the in-vivo tube, so that the inside of the in-vivo tube can be prevented. Occlusion can be prevented.

Claims

請求の範囲 The scope of the claims
[1] 生体管内にある異物を外径方向に張り出したフィルタ部により捕捉して除去する生 体管内治療具であって、  [1] An in-vivo treatment device that captures and removes a foreign substance in a living body tube by a filter portion protruding in an outer diameter direction.
前記生体管内に挿入される形状記憶合金製の挿入管を備え、  An insertion tube made of a shape memory alloy to be inserted into the biological tube;
前記挿入管は、当該挿入管の軸方向に沿った少なくとも一箇所が前記フィルタ部 を形成し、  In the insertion tube, at least one place along the axial direction of the insertion tube forms the filter part,
前記フィルタ部は、前記挿入管の周面に複数の開口部またはスリットが形成され、 且つ前記挿入管のフィルタ部形成位置を軸方向に収縮させて前記複数の開口部ま たはスリット間に形成されたフィルタ構成部を挿入管の外径方向へ橈ませた状態に 形状が記憶されて形成されることを特徴とする生体管内治療具。  The filter section has a plurality of openings or slits formed in the peripheral surface of the insertion tube, and is formed between the plurality of openings or slits by contracting the filter section forming position of the insertion tube in the axial direction. An in-vivo treatment device, wherein a shape is stored and formed in a state in which the formed filter component is constricted in the outer diameter direction of the insertion tube.
[2] 前記開口部またはスリットのうち少なくとも一方は、前記挿入管の長手方向に沿って 延びて 、ることを特徴とする請求項 1に記載した生体管内治療具。  [2] The in-vivo treatment device according to claim 1, wherein at least one of the opening and the slit extends along a longitudinal direction of the insertion tube.
[3] 前記フィルタ部は、前記挿入管の先端側となる遠位側に形成される捕捉部と挿入 管の基端側となる近位側に形成される透過部とからなり、 [3] The filter portion includes a capturing portion formed on a distal side that is a distal end side of the insertion tube and a transmission portion formed on a proximal side that is a proximal end side of the insertion tube.
前記捕捉部の開口部は、前記透過部の開口部よりも開口面積が狭いことを特徴と する請求項 1に記載した生体管内治療具。  The in-vivo treatment device according to claim 1, wherein an opening area of the capturing portion is smaller than an opening area of the transmitting portion.
[4] 前記透過部の開口部は、前記挿入管の長手方向に沿って延びて!/ヽることを特徴と する請求項 3に記載した生体管内治療具。 [4] The in-vivo treatment device according to [3], wherein the opening of the transmission portion extends along the longitudinal direction of the insertion tube.
[5] 前記挿入管内へ移動自在に挿通されるワイヤを備え、 [5] comprising a wire that is movably inserted into the insertion tube,
前記ワイヤは、前記フィルタ部を通過して前記挿入管の先端側となる遠位側部と結 合されていることを特徴とする請求項 1から 4のうちいずれか 1項に記載した生体管内 治療具。  5. The living tube according to claim 1, wherein the wire passes through the filter portion and is coupled to a distal side portion which is a distal end side of the insertion tube. Treatment tool.
[6] 生体管内にある異物を外径方向に張り出したフィルタ部によって捕捉して除去する 生体管内治療具であって、  [6] An in-vivo treatment device that captures and removes foreign matter in a living body tube by a filter portion protruding in the outer diameter direction,
前記生体管内に挿入される形状記憶合金製の挿入管と、当該挿入管内へ移動自 在に挿通されるワイヤと、を備え、  An insertion tube made of a shape memory alloy that is inserted into the living body tube, and a wire that is inserted into the insertion tube so as to move.
前記挿入管は、当該挿入管の軸方向に沿った少なくとも一箇所が前記フィルタ部 を形成し、 前記フィルタ部は、前記挿入管の周面に当該挿入管の軸方向に沿って螺旋状に 切断されて切断部が形成され、且つ前記切断部間に形成されたフィルタ構成部を揷 入管の外径方向へ拡径させた状態に形状が記憶されて形成され、 In the insertion tube, at least one place along the axial direction of the insertion tube forms the filter part, The filter part is cut into a spiral shape along the axial direction of the insertion tube on the peripheral surface of the insertion tube to form a cutting part, and the filter component formed between the cutting parts is disposed outside the insertion pipe. The shape is memorized and formed in the expanded state in the radial direction,
前記ワイヤは、前記フィルタ部を通過して前記挿入管の先端側となる遠位側部と結 合されていることを特徴とする生体管内治療具。  The in-vivo treatment device according to claim 1, wherein the wire passes through the filter portion and is joined to a distal side portion which is a distal end side of the insertion tube.
前記ワイヤは、当該ワイヤの一方の端部が前記挿入管の基端側となる近位端から 突出していることを特徴とする請求項 5または 6に記載した生体管内治療具。  The in-vivo treatment device according to claim 5 or 6, wherein one end of the wire protrudes from a proximal end that is a proximal end side of the insertion tube.
PCT/JP2005/018665 2005-01-26 2005-10-07 Medical appliance for treating inside of biological duct WO2006080113A1 (en)

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