WO2021100441A1 - Medical device - Google Patents

Medical device Download PDF

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Publication number
WO2021100441A1
WO2021100441A1 PCT/JP2020/040898 JP2020040898W WO2021100441A1 WO 2021100441 A1 WO2021100441 A1 WO 2021100441A1 JP 2020040898 W JP2020040898 W JP 2020040898W WO 2021100441 A1 WO2021100441 A1 WO 2021100441A1
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WO
WIPO (PCT)
Prior art keywords
basket
wire
tip
medical device
curved portion
Prior art date
Application number
PCT/JP2020/040898
Other languages
French (fr)
Japanese (ja)
Inventor
寛彬 甲斐
Original Assignee
朝日インテック株式会社
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Filing date
Publication date
Application filed by 朝日インテック株式会社 filed Critical 朝日インテック株式会社
Publication of WO2021100441A1 publication Critical patent/WO2021100441A1/en

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    • 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

Definitions

  • This disclosure relates to medical devices.
  • Some medical devices for removing stones that form inside the common bile duct push, pull, or rotate a basket provided at the tip with an operating wire that extends from the hand to the tip.
  • the surgeon can expand the basket in the radial direction and collect the stones inside the basket (see, for example, Patent Document 1).
  • the common bile duct recess there are cases that are difficult to collect.
  • the operation wire extends straight from the hand side to the tip.
  • the shape of the basket is the shape of the common bile duct recess when a calculus is formed in the common bile duct recess. It may not be possible to adapt to the condition and recover the stones.
  • the present disclosure has been made to solve the above-mentioned problems, and an object of the present disclosure is to provide a medical device capable of easily recovering stones formed in the concave part of the common bile duct.
  • the medical device is formed of a plurality of wires with an operation wire and a rear end bonded to the tip of the operation wire, and is formed in the radial direction. It has an expandable and contractible basket, and the operation wire is provided with a curved portion at the tip end portion of the operation wire.
  • the tip of the operation wire follows the shape of the common bile duct recess, so that the basket can be placed near the side wall surface of the common bile duct recess and expanded, and the common bile duct recess can be formed. The resulting stones can be easily recovered.
  • the basket of the medical device is the first of a plurality of wires, which is adjacent to the circumferential direction of the basket and is provided in the bending direction of the curved portion with respect to the central axis of the basket in the expanded state of the basket. It has an inner wire and a second inner wire of the basket, and a first outer wire and a second outer wire provided in a direction opposite to the bending direction of the curved portion from the central axis of the basket, and has a cross section of the basket.
  • the distance between the first inner wire and the second inner wire may be larger than the distance between the first outer wire and the second outer wire. According to the medical device of this configuration, since the distance between the first inner wire and the second inner wire is wide, even a large-sized stone can be easily stored in the basket.
  • the curved portion of the operation wire of the medical device has a first curved portion provided at the tip end portion of the operation wire and a second curved portion provided on the rear end side of the operation wire with respect to the first curved portion. It has a curved portion, and the degree of curvature of the first curved portion may be larger than the degree of curvature of the second curved portion. According to the medical device having this configuration, the tip of the operation wire can be formed into more various shapes by providing a plurality of curved portions. As a result, even when the shape of the common bile duct recess is complicatedly curved, the tip of the operation wire can follow the shape of the common bile duct recess.
  • the basket is placed in the common bile duct recess. It can be expanded closer to the side wall surface. As a result, the stones formed in the concave part of the common bile duct can be recovered more easily.
  • the medical device has a sheath for accommodating the operation wire and the basket, and the operation wire has a curved portion at the tip of the operation wire which is curved when exposed to the outside from the cavity of the sheath.
  • the tip direction of the basket may change according to the curvature of the curved portion of the operation wire.
  • the curved portion is curved by being pushed out from the sheath, and the tip direction of the basket is changed according to the curvature, so that the inner wall of the common bile duct in the foreground and the inner wall of the concave part of the common bile duct are formed. Since the angle of the basket can be adapted to the angle formed by the bile duct, foreign matter generated in the concave part of the common bile duct can be easily collected.
  • FIG. 1 is a schematic partial vertical sectional view of the medical device 1A according to the first embodiment of the present disclosure.
  • FIG. 1 includes a portion in which the relative ratio of the sizes of the constituent members is described by a relative ratio different from the actual one. In addition, a part of each component is exaggerated and described. These points are the same for FIGS. 2 to 6.
  • the left side is the front end side of each component of the medical device 1A and the medical device 1A
  • the right side is the rear end side of each component of the medical device 1A and the medical device 1A.
  • the end portion located on the tip side is described as "tip”
  • the portion including the "tip” extending halfway from the tip toward the rear end side is described. Described as "tip”.
  • the end located on the rear end side is described as the "rear end”
  • the end portion including the "rear end” is included and is halfway from the rear end to the front end side.
  • the part extending to is described as "rear end”.
  • the medical device 1A includes a basket portion 10A, an operation wire 20A connected to a rear end portion of the basket portion 10A, a sheath 30 covering a part of the basket portion 10A and a part of the operation wire 20A, and a sheath 30. It is composed of an operation unit 40 connected to the rear end portion of the sheath 30.
  • the basket portion 10A has a tip tip 11, a rear end tip 13, and a basket 14A whose tip is connected to the tip tip 11 and whose rear end is connected to the rear end tip 13.
  • the basket 14A has a plurality of wires 12A.
  • a curved portion 21A is formed on the tip side of the operation wire 20A, and a straight portion 22A continuous from the curved portion 21A is formed on the rear end side of the curved portion 21A.
  • the sheath 30 is a tubular body having a first lumen 31 extending in the longitudinal direction of the medical device 1A formed therein.
  • a basket 14A and a rear end tip 13 which are a part of the basket portion 10A, and a part of the curved portion 21A and the straight portion 22A of the operation wire 20A are inserted into the first lumen 31.
  • the tip tip 11 which is a part of the basket portion 10A projects outward from the tip of the sheath 30.
  • the operation unit 40 has a grip portion 41 connected to the rear end portion of the sheath 30 and a handle 45 connected to the rear end portion of the operation wire 20A for operating the operation wire 20A.
  • a second lumen 42 that communicates with the first lumen 31 of the sheath 30 and extends in the longitudinal direction of the medical device 1A is formed inside the grip portion 41.
  • a part of the straight portion 22A of the operation wire 20A is inserted into the second lumen 42.
  • the operation wire 20A is inserted into the first lumen 31 of the sheath 30 and the second lumen 42 of the grip portion 41, and the rear end portion of the operation wire 20A protrudes from the rear end of the grip portion 41 and is connected to the handle 45. ing.
  • the sheath 30 preferably has a circular or oval cross-sectional shape, such as a triangle or a quadrangle, in order not to damage the inner wall of the body cavity when inserted into the body cavity. It may be rectangular.
  • the sheath 30 may be a coil body formed by spirally winding one or more elongated strands.
  • the strands constituting the coil body may be a single wire or a stranded wire formed by twisting a plurality of strands.
  • the sheath 30 may be a braid formed by crossing a plurality of elongated strands with each other to form a tubular shape, that is, by knitting a plurality of strands to form a tubular shape.
  • the material constituting the sheath 30 is preferably flexible and biocompatible because the sheath 30 is inserted into the bent body cavity, and if it is a resin material, for example, a polyamide resin, a polyolefin resin, or a polyester.
  • Resins polyurethane resins, silicone resins, fluororesins and the like can be adopted.
  • metal material for example, stainless steel such as SUS304, nickel titanium alloy, cobalt chrome alloy and the like can be adopted. Further, it may be a combination of the above resin material and metal material.
  • the operation wire 20A has a curved portion 21A provided at the tip thereof and curved in a predetermined direction, and a straight portion 22A continuous with the rear end of the curved portion 21A and extending toward the rear end side of the medical device 1A. ..
  • the curved portion 21A of the operation wire 20A is previously processed into a curved shape and the curved shape is stored, that is, the curved portion 21A is a portion that stores the curved shape.
  • FIG. 1 shows a state in which the curved portion 21A is pressed against the inner peripheral surface of the sheath 30, deformed into a substantially linear shape, and accommodated in the first lumen 31.
  • the straight portion 22A is formed in a substantially straight line shape along the longitudinal direction of the medical device 1A, and the rear end portion is connected to the tip end portion of the handle 45.
  • the material constituting the operation wire 20A is preferably flexible and biocompatible because the operation wire 20A is inserted into the bent body cavity together with the sheath 30.
  • the resin material for example, polyamide resin, polyolefin resin, polyester resin, polyurethane resin, silicone resin, fluororesin and the like can be adopted. Further, a material having rigidity for transmitting the operation of the handle 45 by the operator to the basket portion 10A is preferable.
  • the metal material for example, stainless steel such as SUS304, nickel titanium alloy, cobalt chrome alloy and the like can be adopted. As described above, the nickel titanium alloy is more preferable in view of the fact that the curved portion 21A stores the curved shape. Further, it may be a combination of the above resin material and metal material.
  • the basket portion 10A has a tip tip 11, a basket 14A, and a rear end tip 13 as described above.
  • the basket 14A is composed of a plurality of wires 12A. Each tip of the wire 12A is fixed by the tip tip 11 so as not to come apart, and the rear end is also fixed by the tip 13 so as not to come apart.
  • the wires 12A intersect each other between the tip tip 11 and the rear end tip 13. They are arranged without being twisted together.
  • the basket 14A is previously processed into an extended shape that expands in the radial direction, that is, in the direction perpendicular to the central axis C of the basket 14A (see FIG. 2A), and this extended shape is stored, that is, the basket 14A is stored.
  • each of the plurality of wires 12A constituting the basket 14A is preliminarily processed into a curved shape, and the curved shape is stored.
  • FIG. 1 shows a state in which the basket 14A is pressed by the inner peripheral surface of the sheath 30, deformed into a shape contracted in the radial direction, and housed in the first lumen 31.
  • the basket portion 10A may be configured such that only the basket 14A and the rear end tip 13 are housed in the first lumen 31 and the tip tip 11 cannot be housed in the first lumen 31.
  • a part of the tip tip 11 may be formed so as to have an outer diameter larger than the inner diameter of the tip of the sheath 30. With such a configuration, the tip end 11 is not accommodated in the first lumen 31 of the sheath 30. Therefore, even when the basket portion 10A is moved back and forth by the first lumen 31 by operating the handle 45, the tip tip 11 does not enter the first lumen 31 and get caught on the inner peripheral surface of the sheath 30. As a result, the curved portion 21A of the basket 14A and the operation wire 20A can be relatively easily moved from the state of FIG. 1 to a state of protruding from the tip of the sheath 30.
  • the tip tip 11 may be a member that can prevent the tips of the plurality of wires 12A constituting the basket 14A from being separated.
  • the tip tip 11 may be formed by welding the tips of a plurality of wires 12A to each other.
  • the trailing end tip 13 may be, for example, a brazing material or an adhesive for joining the trailing ends of the plurality of wires 12A to each other.
  • the rear end tip 13 may be formed by welding the rear ends of a plurality of wires 12A to each other.
  • the tip of the tip tip 11 may be processed into a substantially hemispherical shape by polishing, cutting, or the like so as not to damage the inside of the body.
  • the tip tip 11 may have a lumen (not shown) extending in the longitudinal direction of the medical device 1A to insert a guide wire (not shown) used in combination with the medical device 1A, that is, a through hole. ..
  • a guide wire used in combination with the medical device 1A
  • the medical device 1A can be easily inserted into the body cavity along the guide wire by passing the guide wire previously inserted into the body cavity through the lumen provided on the tip tip 11.
  • the material constituting the wire 12A is biocompatible, flexible, and elastic because the basket 14A is inserted into the body cavity and may be expanded or contracted in the bent body cavity.
  • a resin material for example, polyamide resin, polyolefin resin, polyester resin, polyurethane resin, silicone resin, fluororesin and the like can be adopted.
  • the metal material for example, stainless steel such as SUS304, nickel titanium alloy, cobalt chrome alloy and the like can be adopted.
  • the nickel titanium alloy is more preferable in view of the fact that the wire 12A stores the curved shape. Alternatively, it may be a combination of the above resin material and metal material.
  • the grip portion 41 constituting the operating portion 40 includes a liquid feeding unit 43 having a liquid feeding lumen 44.
  • the liquid feeding portion 43 is arranged at an arbitrary position of the grip portion 41, and the liquid feeding lumen 44 is defined by the inner peripheral surface thereof.
  • the liquid feeding lumen 44 communicates with the second lumen 42 of the grip portion 41. That is, the first lumen 31 of the sheath 30, the second lumen 42 of the grip portion 41, and the liquid feeding lumen 44 communicate with each other.
  • the liquid feeding portion 43 is provided so as to project from the side surface of the grip portion 41 extending in the longitudinal direction of the medical device 1A, and a spiral groove (not shown) is formed on the outer peripheral surface thereof. May have.
  • a syringe (not shown) provided with a spiral convex portion on the inner peripheral surface can be connected to the liquid feeding unit 43, and the chemical solution or the like injected from the syringe into the liquid feeding lumen 44 is seconded. It can flow into the body cavity from the tip of the sheath 30 via the lumen 42 and the first lumen 31.
  • the liquid feeding portion 43 is formed as a part of the grip portion 41, but it may be formed as a separate member and attached to the grip portion 41. Further, it may be attached to the sheath 30, in which case the liquid feeding lumen 44 communicates directly with the first lumen 31.
  • the rear end of the straight portion 22A of the operation wire 20A protrudes from the rear end of the grip portion 41 and is connected to the handle 45.
  • the handle 45 is operated by an operator and is a member for transmitting the operation by the operator to the operation wire 20A.
  • the handle 45 has two bent portions, but the shape of the handle 45 may be any shape that can be easily operated by the operator, and has a bent portion as shown in FIG. Not limited.
  • the operator grips the grip 41 and moves the handle 45 back and forth in the longitudinal direction of the medical device 1A so that the operation wire 20A and the operation wire 20A and the second lumen 42 of the grip 41 are formed by the operator.
  • the basket portion 10A can be moved back and forth. Further, by rotating the handle 45 around the operation wire 20A around the operation wire 20A, the operation wire 20A and the basket portion 10A can be rotated.
  • the material constituting the grip portion 41 and the handle 45 is preferably durable and suitable for sterilization, and may be a metal, an injection-molded resin, or a combination thereof.
  • FIG. 2A is a schematic partial vertical sectional view of a tip portion of the medical device 1A according to the first embodiment of the present disclosure.
  • FIG. 2A shows a central axis C (a virtual straight line passing through the tip 11 at the tip and the tip 13 at the rear) of the basket portion 10A.
  • FIG. 2A shows a basket portion as a result of moving the handle 45 relative to the grip portion 41 while the operator grips the grip portion 41 while the medical device 1A is in the state of FIG. 10A and the curved portion 21A of the operation wire 20A are shown in a state in which the curved portion 21A protrudes from the tip of the sheath 30.
  • the basket 14A is released from the pressing by the inner peripheral surface of the sheath 30, and is substantially perpendicular to the central axis C of the basket portion 10A. It shows a state in which the shape has changed from a shape contracted in the direction to an expanded shape. Further, the curved portion 21A of the operation wire 20A is released from the pressing by the inner peripheral surface of the sheath 30, and shows a state in which the shape is changed from a substantially linear shape to a curved shape. In FIG. 2A, the tip of the curved portion 21A is connected to the rear end tip 13.
  • the plurality of wires 12A are pushed out from the first lumen 31 and the sheath 30 is formed. It is released from the pressure by the inner peripheral surface of.
  • the wires (12Aa, 12Ab, 12Ac, 12Ad) constituting the plurality of wires 12A are curved in different directions from each other and in a direction away from the central axis C of the basket portion 10A. That is, each wire constituting the plurality of wires 12A extends radially around the central axis C of the basket portion 10A. As a result, a space is formed inside the plurality of wires 12A extending radially, and it becomes possible to take in the calculus 102 (see FIG. 3) generated in the common bile duct recess 101 described later in this space.
  • the operation wire 20A and the basket portion 10A move to the rear end side, and the basket 14A and the operation wire 20A are moved.
  • the curved portion 21A is re-accommodated in the first lumen 31 of the sheath 30.
  • the curved portion 21A of the operation wire 20A is pressed by the inner peripheral surface of the sheath 30, deforms from the curved shape to a shape close to straight (a substantially linear shape), and is accommodated in the first lumen 31.
  • each of the wires 12A of the basket 14A is pressed by the inner peripheral surface of the sheath 30, and the basket 14A contracts by deforming from a curved shape to a substantially linear shape, and follows the operation wire 20A to the first lumen 31. Be housed. As a result, the medical device 1A returns to the state shown in FIG.
  • FIG. 2B is a view obtained by observing a cross section of the tip end portion of the medical device 1A in FIG. 2A cut out by the line AA from the direction of the arrow.
  • the basket 14A consists of four wires, 12Aa, 12Ab, 12Ac and 12Ad.
  • the wire 12Aa and the wire 12Ab are arranged symmetrically with respect to the central axis C
  • the wire 12Ac and the wire 12Ad are arranged symmetrically with respect to the central axis C.
  • the wires constituting the wire 12A do not have to be arranged symmetrically with respect to the central axis C.
  • any two of the four wires 12A may be arranged symmetrically with respect to the central axis C, and the remaining two wires may be arranged asymmetrically with respect to the central axis C. ..
  • the combination of either two wires may be arranged so as to be asymmetric with respect to the central axis C.
  • the number of wires 12A is not limited to four.
  • FIG. 3 is a diagram showing a state in which an operator inserts a medical device 1A into the common bile duct 100 and collects a calculus 102 formed in a common bile duct recess 101.
  • the common bile duct recess 101 is a portion formed by rapidly expanding the diameter of a part of the common bile duct 100.
  • the common bile duct recess in FIG. 3 includes a portion different from the actual form for the purpose of explaining the medical device 1A.
  • the medical device 1A passes through the inside of an endoscope (not shown) in which the tip is inserted close to the duodenal papilla (not shown), and is inserted into the common bile duct 100 from the papilla through the inside of the endoscope in advance. It is inserted into the common bile duct 100 along a guide wire (not shown).
  • the medical device 1A is placed in the common bile duct 100 in the state shown in FIG. 1, that is, in a state where the basket 14A, the rear end tip 13, and the curved portion 21A of the operation wire 20A are housed in the first lumen 31 of the sheath 30. Will be inserted.
  • the operator grips the grip 41 with one hand and moves the handle 45 to the tip side with the other hand to move the basket 14A and the handle 45 to the tip side.
  • the curved portion 21A of the operation wire 20A is pushed out from the tip of the sheath 30.
  • the basket 14A changes from a contracted shape to an expanded shape
  • the curved portion 21A of the operation wire 20A changes from a substantially linear shape to a curved shape along the shape of the concave portion 101.
  • the operator can expand the basket 14A near the side wall surface 103 of the common bile duct recess 101.
  • the operator can accommodate the calculus 102 formed on the wall surface of the common bile duct recess 101 by the expanded basket 14A in the space inside the basket 14A extended from the gap between the adjacent wires of the plurality of wires 12A. After that, the operator pulls the handle 45 toward the rear end side and accommodates a part or all of the basket 14A in the first lumen 31 of the sheath 30 to contract the basket 14A and put the calculus 102 inside the basket 14A. Can be retained. The operator can pull the basket 14A containing the calculus 102 from the common bile duct recess 101 and the common bile duct 100 through the papilla by further pulling the handle 45 and the grip portion 41 toward the rear end side.
  • the basket 14A is made of the common bile duct recess 101.
  • the side wall surface 103 can be brought closer and expanded. As a result, the calculus 102 formed in the common bile duct recess 101 can be more easily recovered.
  • FIG. 4A is a schematic partial vertical sectional view of the basket portion 10B in the medical device 1B according to the second embodiment of the present disclosure.
  • FIG. 4B is a view of a cross section of the medical device 1B in FIG. 4A cut out by the line BB, observed from the direction of the arrow.
  • the medical device 1B according to the second embodiment and the medical device 1A according to the first embodiment differ only in the structure of the basket 14B.
  • the constituent members common to the medical device 1A according to the first embodiment are assigned the same numbers as those assigned in the first embodiment, and detailed description thereof will be given. Omit.
  • 4A and 4B are views showing a state in which the curved portion 21A of the basket 14B and the operation wire 20A protrudes from the tip of the sheath 30, and the basket 14B is released from the pressure by the inner peripheral surface of the sheath 30 and the basket portion 10B is released. It shows a state in which the shape is changed from a shape contracted in a direction substantially perpendicular to the central axis C of the above to an expanded shape. Further, the curved portion 21A of the operation wire 20A is released from the pressing by the inner peripheral surface of the sheath 30, and shows a state in which the shape is changed from a substantially linear shape to a curved shape.
  • the basket 14B has a plurality of wires 12B.
  • the plurality of wires 12B consist of a first inner wire 12Ba, a second inner wire 12Bb, a first outer wire 12Bc, and a second outer wire 12Bd.
  • the first inner wire 12Ba and the second inner wire 12Bb are adjacent to each other along the circumferential direction of the basket 14B, and in a state where the basket 14B is expanded, in the bending direction of the bending portion 21A with respect to the central axis C of the basket portion 10B. It is arranged so as to be located (in other words, it is arranged so as to be located inside the curved shape of the curved portion 21A rather than the central axis C).
  • the first outer wire 12Bc and the second outer wire 12Bd are adjacent to each other along the circumferential direction of the basket 14B, and in a state where the basket 14B is expanded, the bending direction of the bending portion 21A is larger than the central axis C of the basket portion 10B. It is arranged so as to be located in the opposite direction (in other words, it is arranged so as to be located outside the curved shape of the curved portion 21A with respect to the central axis C).
  • the distance a between the center of the cross section of the first inner wire 12Ba and the center of the cross section of the second inner wire 12Bb is the distance a of the first outer wire 12Bc. It is larger than the distance b between the center of the cross section of the second outer wire 12Bd and the center of the cross section of the second outer wire 12Bd.
  • the distance a between the center of the cross section of the first inner wire 12Ba and the center of the cross section of the second inner wire 12Bb is the cross section of the first outer wire 12Bc.
  • a larger size stone 102 can be easily accommodated inside the basket 14B as compared to a configuration in which the distance b between the center and the center of the cross section of the second outer wire 12Bd is equal.
  • FIG. 5 is a diagram showing a schematic partial vertical cross section of a tip portion of the medical device 1C according to the third embodiment of the present disclosure.
  • the medical device 1C and the medical device 1A according to the first embodiment differ only in the structure of the operation wire 20C.
  • the constituent members of the medical device 1C are assigned the same numbers as those assigned in the first embodiment, and detailed description thereof will be given. Omit.
  • the medical device 1C has an operation wire 20C instead of the operation wire 20A of the medical device 1A according to the first embodiment.
  • the operation wire 20C has a first straight portion 22Ca continuous with the rear end portion of the rear end tip 13, a curved portion 21C continuous with the rear end portion of the first straight portion 22Ca, and a curved portion 21C at the tip portion. It has a second straight portion 22Cb that is continuous with the rear end portion and extends substantially parallel to the sheath 30.
  • the curved portion 21C is formed on the tip end side of the operation wire 20C.
  • FIG. 5 is a diagram showing a state in which a part of the basket portion 10A, the first straight portion 22Ca, the curved portion 21C, and the second straight portion 22Cb of the operation wire 20C protrudes from the tip of the sheath 30. It shows a state in which the basket 14A is released from the pressure by the inner peripheral surface of the sheath 30 and changes from a shape contracted in a direction substantially perpendicular to the central axis C (see FIG. 2A) of the basket portion 10A to an expanded shape. Further, the curved portion 21C of the operation wire 20C is released from the pressing by the inner peripheral surface of the sheath 30, and shows a state in which the shape is changed from a substantially linear shape to a curved shape. Even with such a configuration, the same effect as that of the medical device 1A according to the first embodiment can be obtained.
  • FIG. 6 is a schematic partial vertical sectional view of a tip portion of the medical device 1D according to the fourth embodiment of the present disclosure.
  • the medical device 1D according to the fourth embodiment and the medical device 1A according to the first embodiment differ only in the structure of the operation wire 20D.
  • the constituent members of the medical device 1D are assigned the same numbers as those assigned in the first embodiment, and detailed explanations thereof will be given. Omit.
  • the medical device 1D has an operating wire 20D, and the operating wire 20D has two curved portions.
  • the operation wire 20D includes a first straight portion 22Da continuous with the rear end portion of the rear end tip 13, and a first curved portion 21Da continuous with the rear end portion of the first straight portion 22Da.
  • the second straight portion 22Db continuous with the rear end portion of the first curved portion 21Da
  • the second curved portion 21Db continuous with the rear end portion of the second straight portion 22Db
  • the second curved portion 21Db has a third straight portion 22Dc continuous to the end.
  • the degree of curvature of the first curved portion 21Da is larger than the degree of curvature of the second curved portion 21Db.
  • the degree of curvature can be defined by, for example, the minimum radius of curvature.
  • the minimum radius of curvature of the second curved portion 21Da is smaller than the minimum radius of curvature of the second curved portion 21Db.
  • the radius of curvature of the curved portion is the radius of the circle when the local degree of bending of the curved portion is approximated to a circle.
  • the minimum radius of curvature is the radius of the circle at the point where the radius of the circle is the smallest. Note that FIG. 6 shows the basket portion 10A, the first straight portion 21Da of the operation wire 20D, the first curved portion 21Da, the second straight portion 22Db, the second curved portion 21Db, and the third straight portion 22Dc.
  • FIG. 2A It is a figure which shows the state which a part protruded from the tip of a sheath 30, and the basket 14A is released from the pressure by the inner peripheral surface of a sheath 30, and is in the direction substantially perpendicular to the central axis C (see FIG. 2A) of a basket part 10A. It shows a state in which the shape has changed from a contracted shape to an expanded shape. Further, the first curved portion 21Da and the second curved portion 21Db of the operation wire 20D are released from the pressing by the inner peripheral surface of the sheath 30, and the state of changing from a substantially linear shape to a curved shape is shown.
  • the side wall surface 103 of the common bile duct recess 101 is curved so as to slip under the duct of the common bile duct 100, and the space formed thereby.
  • the basket 14A can be expanded closer to the side wall surface 103 of the common bile duct recess 101.
  • the calculus 102 formed in the common bile duct recess 101 can be recovered more easily. Note that FIG.
  • first curved portion 21Da and second curved portion 21Db having different degrees of curvature
  • the number of curved portions is not limited to two and three. It may be the above. In that case, the degree of curvature of the curved portion located on the front end side may be larger than the degree of curvature of the curved portion located on the rear end side.
  • the present disclosure is not limited to the configuration of the above-described embodiment, but is indicated by the scope of claims, and is intended to include all modifications within the meaning and scope equivalent to the scope of claims. Will be done.
  • a part of the configuration of the above-described embodiment may be deleted or replaced with another configuration, or another configuration may be added to the configuration of the above-described embodiment.
  • the operation wire 20A of the medical device 1B according to the second embodiment instead of the operation wire 20C of the medical device 1C according to the third embodiment, or the operation wire 20D of the medical device 1D according to the fourth embodiment. May be applied.
  • the degree of curvature of the first curved portion 21Da may be smaller than the degree of curvature of the second curved portion 21Db.

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  • Surgery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Medical Informatics (AREA)
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  • Surgical Instruments (AREA)

Abstract

Provided is a medical device that makes it easy to recover a foreign object formed in a recess of the common bile duct. A medical device 1A comprises: a manipulation wire 20A; and a basket 14A that has a rear end joined to a leading end of the manipulation wire 20A and that is formed from a plurality of wires 12A so as to be expandable/contractable in the radial direction of the leading end of the manipulation wire 20A. The manipulation wire 20A has a curved portion 21A being curved at the leading end of the manipulation wire 20A.

Description

医療用デバイスMedical device
 本開示は、医療用デバイスに関する。 This disclosure relates to medical devices.
 総胆管の内部に生じる結石を除去するための医療用デバイスには、手元から先端部まで延びる操作ワイヤによって、先端部に設けられたバスケットを押し引き、または回転させるものがある。術者は、バスケットを径方向に拡張し、バスケット内部に結石を内包して回収することができる(例えば、特許文献1参照)。
 また、難渋症例の一例として、総胆管の一部に内腔の直径が急激に拡大する凹部(以下、総胆管凹部と記載する)が存在し、その総胆管凹部に結石が生じたため、結石の回収が困難な症例がある。
Some medical devices for removing stones that form inside the common bile duct push, pull, or rotate a basket provided at the tip with an operating wire that extends from the hand to the tip. The surgeon can expand the basket in the radial direction and collect the stones inside the basket (see, for example, Patent Document 1).
In addition, as an example of a difficult case, there is a recess in a part of the common bile duct where the diameter of the lumen rapidly expands (hereinafter referred to as the common bile duct recess), and a calculus is formed in the common bile duct recess. There are cases that are difficult to collect.
 特許文献1に記載の内視鏡用処置具は、操作ワイヤが手元側から先端まで真直ぐに伸びている。 In the endoscopic treatment tool described in Patent Document 1, the operation wire extends straight from the hand side to the tip.
特許第6188997号Patent No. 6188997
 特許文献1に記載の、操作ワイヤが手元側から先端まで真直ぐに伸びている内視鏡用処置具においては、総胆管凹部に結石が生じている場合に、バスケットの形状が総胆管凹部の形状に適応することができず、結石を回収することができない場合がある。 In the endoscopic treatment tool described in Patent Document 1 in which the operation wire extends straight from the hand side to the tip, the shape of the basket is the shape of the common bile duct recess when a calculus is formed in the common bile duct recess. It may not be possible to adapt to the condition and recover the stones.
 本開示は上述した課題を解決するためになされたものであり、総胆管凹部に生じた結石を容易に回収可能な医療用デバイスを提供することを目的とする。 The present disclosure has been made to solve the above-mentioned problems, and an object of the present disclosure is to provide a medical device capable of easily recovering stones formed in the concave part of the common bile duct.
 上記の目的を達成するために、本開示の一形態に係る医療用デバイスは、操作ワイヤと、操作ワイヤの先端部に後端部が接合されるとともに、複数のワイヤから形成され、径方向に拡縮可能なバスケットと、を有し、操作ワイヤは、操作ワイヤの先端部に湾曲部を備える。本形態の医療用デバイスによると、操作ワイヤの先端部が総胆管凹部の形状に沿うことで、バスケットを総胆管凹部の側壁面近くに配置し、拡張することが可能であり、総胆管凹部に生じた結石を容易に回収可能となる。 In order to achieve the above object, the medical device according to one embodiment of the present disclosure is formed of a plurality of wires with an operation wire and a rear end bonded to the tip of the operation wire, and is formed in the radial direction. It has an expandable and contractible basket, and the operation wire is provided with a curved portion at the tip end portion of the operation wire. According to the medical device of this embodiment, the tip of the operation wire follows the shape of the common bile duct recess, so that the basket can be placed near the side wall surface of the common bile duct recess and expanded, and the common bile duct recess can be formed. The resulting stones can be easily recovered.
上記の形態に係る医療用デバイスのバスケットは、複数のワイヤのうち、バスケットの周方向に隣接し、バスケットが拡張した状態において、バスケットの中心軸よりも湾曲部の湾曲方向に設けられる、第1の内側ワイヤ及び第2の内側ワイヤと、バスケットの中心軸よりも湾曲部の湾曲方向と反対方向に設けられる、第1の外側ワイヤ及び第2の外側ワイヤと、を有し、バスケットの横断面における、第1の内側ワイヤ及び第2の内側ワイヤの距離が、第1の外側ワイヤ及び第2の外側ワイヤの距離よりも大きくてもよい。本構成の医療用デバイスによると、第1の内側ワイヤ及び第2の内側ワイヤの距離が大きく開いていることで、サイズの大きな結石でもバスケット内部に容易に収容することができる。 The basket of the medical device according to the above embodiment is the first of a plurality of wires, which is adjacent to the circumferential direction of the basket and is provided in the bending direction of the curved portion with respect to the central axis of the basket in the expanded state of the basket. It has an inner wire and a second inner wire of the basket, and a first outer wire and a second outer wire provided in a direction opposite to the bending direction of the curved portion from the central axis of the basket, and has a cross section of the basket. The distance between the first inner wire and the second inner wire may be larger than the distance between the first outer wire and the second outer wire. According to the medical device of this configuration, since the distance between the first inner wire and the second inner wire is wide, even a large-sized stone can be easily stored in the basket.
上記の形態に係る医療用デバイスの操作ワイヤの湾曲部は、操作ワイヤの先端部に設けられる第1の湾曲部と、第1の湾曲部よりも操作ワイヤの後端側に設けられる第2の湾曲部と、を有し、第1の湾曲部の湾曲度合いが、第2の湾曲部の湾曲度合いよりも大きくてもよい。本構成の医療用デバイスによると、湾曲部を複数設けることで、操作ワイヤの先端部をより多様な形状に形成することができる。これにより、総胆管凹部の形状が複雑に湾曲している場合においても、操作ワイヤの先端部が総胆管凹部の形状に沿うことができる。また、総胆管凹部において、総胆管凹部の側壁面が総胆管の管路の下に潜り込むように湾曲し、それにより形成された空間に結石が生じている場合においても、バスケットを総胆管凹部の側壁面により一層接近させて拡張させることが可能となる。この結果、総胆管凹部に生じた結石をより一層容易に回収可能となる。 The curved portion of the operation wire of the medical device according to the above embodiment has a first curved portion provided at the tip end portion of the operation wire and a second curved portion provided on the rear end side of the operation wire with respect to the first curved portion. It has a curved portion, and the degree of curvature of the first curved portion may be larger than the degree of curvature of the second curved portion. According to the medical device having this configuration, the tip of the operation wire can be formed into more various shapes by providing a plurality of curved portions. As a result, even when the shape of the common bile duct recess is complicatedly curved, the tip of the operation wire can follow the shape of the common bile duct recess. In addition, in the common bile duct recess, even when the side wall surface of the common bile duct recess is curved so as to slip under the duct of the common bile duct and stones are formed in the space formed by the curved side wall surface, the basket is placed in the common bile duct recess. It can be expanded closer to the side wall surface. As a result, the stones formed in the concave part of the common bile duct can be recovered more easily.
上記の形態に係る医療用デバイスは、操作ワイヤ及びバスケットを収容するシースを有し、操作ワイヤは、操作ワイヤの先端部に、シースの内腔から外部に露出するときに湾曲する湾曲部を有し、バスケットの先端方向が、操作ワイヤの湾曲部の湾曲に従って変化していてもよい。本構成の医療用デバイスによると、湾曲部がシースから外部に押し出されることにより湾曲し、その湾曲に従って、バスケットの先端方向が変化することで、手前の総胆管の内壁と、総胆管凹部の内壁とが成す角度にバスケットの角度を適応させることができるため、総胆管凹部に生じた異物を容易に回収可能となる。 The medical device according to the above embodiment has a sheath for accommodating the operation wire and the basket, and the operation wire has a curved portion at the tip of the operation wire which is curved when exposed to the outside from the cavity of the sheath. However, the tip direction of the basket may change according to the curvature of the curved portion of the operation wire. According to the medical device of this configuration, the curved portion is curved by being pushed out from the sheath, and the tip direction of the basket is changed according to the curvature, so that the inner wall of the common bile duct in the foreground and the inner wall of the concave part of the common bile duct are formed. Since the angle of the basket can be adapted to the angle formed by the bile duct, foreign matter generated in the concave part of the common bile duct can be easily collected.
 本開示によると、総胆管凹部に生じた結石を容易に回収可能な医療用デバイスを提供することができる。 According to the present disclosure, it is possible to provide a medical device capable of easily recovering a stone formed in a concave part of the common bile duct.
本開示の第1実施形態に係る医療用デバイスの概略部分縦断面図であり、バスケットがシースの内部に収容され、収縮した状態を示す図である。It is a schematic partial vertical cross-sectional view of the medical device which concerns on 1st Embodiment of this disclosure, and is the figure which shows the state which the basket was housed in the sheath, and was contracted. 本開示の第1実施形態に係る医療用デバイスの先端部の概略部分縦断面図であり、バスケットがシースの外部に露出し、拡張した状態を示す図である。It is a schematic partial vertical sectional view of the tip part of the medical device which concerns on 1st Embodiment of this disclosure, and is the figure which shows the state which the basket is exposed to the outside of the sheath, and is expanded. 本開示の第1実施形態に係る医療用デバイスの先端部の概略横断面図であり、図2AにおけるA-A線によって切り取られた断面を矢印の方向から観察した図である。It is a schematic cross-sectional view of the tip portion of the medical device which concerns on 1st Embodiment of this disclosure, and is the figure which observed the cross section cut by the line AA in FIG. 2A from the direction of an arrow. 本開示の第1実施形態に係る医療用デバイスが総胆管に挿入され、総胆管凹部に生じた結石を回収する状態を示す図である。It is a figure which shows the state which the medical device which concerns on 1st Embodiment of this disclosure is inserted into a common bile duct, and collects the calculus generated in the common bile duct recess. 本開示の第2実施形態に係る医療用デバイスの先端部の概略部分縦断面図である。It is a schematic partial vertical sectional view of the tip part of the medical device which concerns on 2nd Embodiment of this disclosure. 本開示の第2実施形態に係る医療用デバイスの先端部の概略横断面図であり、図4AにおけるB-B線によって切り取られた断面を矢印の方向から観察した図である。It is a schematic cross-sectional view of the tip portion of the medical device which concerns on 2nd Embodiment of this disclosure, and is the figure which observed the cross section cut by the line BB in FIG. 4A from the direction of an arrow. 本開示の第3実施形態に係る医療用デバイスの先端部の概略部分縦断面図である。It is a schematic partial vertical sectional view of the tip part of the medical device which concerns on 3rd Embodiment of this disclosure. 本開示の第4実施形態に係る医療用デバイスの先端部の概略部分縦断面図である。It is a schematic partial vertical sectional view of the tip part of the medical device which concerns on 4th Embodiment of this disclosure.
本開示の実施形態に係る医療用デバイスについて図面を参照して説明する。本開示は、当該図面に記載の実施形態にのみ限定されるものではない。 The medical device according to the embodiment of the present disclosure will be described with reference to the drawings. The present disclosure is not limited to the embodiments described in the drawings.
<第1実施形態>
図1は、本開示の第1実施形態に係る医療用デバイス1Aの概略部分縦断面図である。 
<First Embodiment>
FIG. 1 is a schematic partial vertical sectional view of the medical device 1A according to the first embodiment of the present disclosure.
図1は、説明の便宜上、各構成部材の大きさの相対比を実際とは異なる相対比で記載している部分を含んでいる。また、各構成部材の一部を誇張して記載している部分を含んでいる。これらの点は、図2から図6についても同様である。 For convenience of explanation, FIG. 1 includes a portion in which the relative ratio of the sizes of the constituent members is described by a relative ratio different from the actual one. In addition, a part of each component is exaggerated and described. These points are the same for FIGS. 2 to 6.
図1において、左側は医療用デバイス1A及び医療用デバイス1Aの各構成部材の先端側であり、右側は医療用デバイス1A及び医療用デバイス1Aの各構成部材の後端側である。また、医療用デバイス1A及び医療用デバイス1Aの各構成部材について、先端側に位置する端部を「先端」と記載し、「先端」を含み先端から後端側に向かって中途まで延びる部位を「先端部」と記載する。同様に、医療用デバイス1A及び医療用デバイス1Aの各構成部材について、後端側に位置する端部を「後端」と記載し、「後端」を含み後端から先端側に向かって中途まで延びる部位を「後端部」と記載する。これらの点は、図2B及び図4Bは除いて、図2から図6についても同様である。 In FIG. 1, the left side is the front end side of each component of the medical device 1A and the medical device 1A, and the right side is the rear end side of each component of the medical device 1A and the medical device 1A. Further, for each component of the medical device 1A and the medical device 1A, the end portion located on the tip side is described as "tip", and the portion including the "tip" extending halfway from the tip toward the rear end side is described. Described as "tip". Similarly, for each component of the medical device 1A and the medical device 1A, the end located on the rear end side is described as the "rear end", and the end portion including the "rear end" is included and is halfway from the rear end to the front end side. The part extending to is described as "rear end". These points are the same for FIGS. 2 to 6 except for FIGS. 2B and 4B.
図1において、医療用デバイス1Aは、バスケット部10A、バスケット部10Aの後端部に接続された操作ワイヤ20A、バスケット部10Aの一部及び操作ワイヤ20Aの一部の外周を覆うシース30、及びシース30の後端部に接続された操作部40、から構成されている。 In FIG. 1, the medical device 1A includes a basket portion 10A, an operation wire 20A connected to a rear end portion of the basket portion 10A, a sheath 30 covering a part of the basket portion 10A and a part of the operation wire 20A, and a sheath 30. It is composed of an operation unit 40 connected to the rear end portion of the sheath 30.
バスケット部10Aは、先端チップ11と、後端チップ13と、先端が先端チップ11に接続されるとともに後端が後端チップ13に接続されたバスケット14Aと、を有している。バスケット14Aは、複数のワイヤ12Aを有している。
操作ワイヤ20Aには、先端側に湾曲部21Aが形成され、湾曲部21Aより後端側に湾曲部21Aから連続するストレート部22Aが形成されている。
The basket portion 10A has a tip tip 11, a rear end tip 13, and a basket 14A whose tip is connected to the tip tip 11 and whose rear end is connected to the rear end tip 13. The basket 14A has a plurality of wires 12A.
A curved portion 21A is formed on the tip side of the operation wire 20A, and a straight portion 22A continuous from the curved portion 21A is formed on the rear end side of the curved portion 21A.
シース30は、内部に、医療用デバイス1Aの長手方向に延びる第1のルーメン31が形成された管状体である。第1のルーメン31には、バスケット部10Aの一部であるバスケット14A及び後端チップ13、並びに、操作ワイヤ20Aの湾曲部21A及びストレート部22Aの一部が挿入されている。バスケット部10Aの一部である先端チップ11は、シース30の先端から外部に突出している。 The sheath 30 is a tubular body having a first lumen 31 extending in the longitudinal direction of the medical device 1A formed therein. A basket 14A and a rear end tip 13 which are a part of the basket portion 10A, and a part of the curved portion 21A and the straight portion 22A of the operation wire 20A are inserted into the first lumen 31. The tip tip 11 which is a part of the basket portion 10A projects outward from the tip of the sheath 30.
操作部40は、シース30の後端部に接続された把持部41と、操作ワイヤ20Aの後端部に接続された、操作ワイヤ20Aを操作するためのハンドル45と、を有している。
把持部41の内部には、シース30の第1のルーメン31に連通するとともに、医療用デバイス1Aの長手方向に延びる第2のルーメン42が形成されている。第2のルーメン42には操作ワイヤ20Aのストレート部22Aの一部が挿入されている。
操作ワイヤ20Aは、シース30の第1のルーメン31及び把持部41の第2のルーメン42に挿入され、操作ワイヤ20Aの後端部は、把持部41の後端から突出し、ハンドル45に接続されている。
The operation unit 40 has a grip portion 41 connected to the rear end portion of the sheath 30 and a handle 45 connected to the rear end portion of the operation wire 20A for operating the operation wire 20A.
Inside the grip portion 41, a second lumen 42 that communicates with the first lumen 31 of the sheath 30 and extends in the longitudinal direction of the medical device 1A is formed. A part of the straight portion 22A of the operation wire 20A is inserted into the second lumen 42.
The operation wire 20A is inserted into the first lumen 31 of the sheath 30 and the second lumen 42 of the grip portion 41, and the rear end portion of the operation wire 20A protrudes from the rear end of the grip portion 41 and is connected to the handle 45. ing.
シース30は、体腔内に挿入されたときに、体腔内の内壁を傷つけないようにするために、横断面の形状が円形や楕円形であることが好ましいが、三角形または四角形のような、多角形であってもよい。 The sheath 30 preferably has a circular or oval cross-sectional shape, such as a triangle or a quadrangle, in order not to damage the inner wall of the body cavity when inserted into the body cavity. It may be rectangular.
シース30は、細長い一つ又は複数の素線を螺旋状に巻くことにより形成されるコイル体であってもよい。この場合、コイル体を構成する素線は、単一の線でも複数の素線を撚り合わせて形成される撚り線であってもよい。また、シース30は、細長い複数の素線を互いに交差させて筒状に形成される、即ち、複数の素線を編むことによって筒状に形成される編組であってもよい。
シース30を構成する材料としては、シース30が屈曲した体腔に挿入されることから、可撓性および生体適合性を有することが好ましく、樹脂材料であれば、例えば、ポリアミド樹脂、ポリオレフィン樹脂、ポリエステル樹脂、ポリウレタン樹脂、シリコーン樹脂、フッ素樹脂等を採用することができる。金属材料であれば、例えば、SUS304などのステンレス鋼、ニッケルチタン合金、コバルトクロム合金等を採用することができる。また、上記の樹脂材料、金属材料の組み合わせであってもよい。
The sheath 30 may be a coil body formed by spirally winding one or more elongated strands. In this case, the strands constituting the coil body may be a single wire or a stranded wire formed by twisting a plurality of strands. Further, the sheath 30 may be a braid formed by crossing a plurality of elongated strands with each other to form a tubular shape, that is, by knitting a plurality of strands to form a tubular shape.
The material constituting the sheath 30 is preferably flexible and biocompatible because the sheath 30 is inserted into the bent body cavity, and if it is a resin material, for example, a polyamide resin, a polyolefin resin, or a polyester. Resins, polyurethane resins, silicone resins, fluororesins and the like can be adopted. As for the metal material, for example, stainless steel such as SUS304, nickel titanium alloy, cobalt chrome alloy and the like can be adopted. Further, it may be a combination of the above resin material and metal material.
操作ワイヤ20Aは、その先端部に設けられた所定の方向に湾曲する湾曲部21Aと、湾曲部21Aの後端に連続し、医療用デバイス1Aの後端側に向かって延びるストレート部22Aを有する。操作ワイヤ20Aの湾曲部21Aは、予め、湾曲形状に加工され、その湾曲形状が記憶させられている、即ち、湾曲部21Aは湾曲形状を記憶している部位である。図1は、湾曲部21Aがシース30の内周面に押圧され、略直線形状に変形させられて第1のルーメン31に収容された状態を示している。ストレート部22Aは、医療用デバイス1Aの長手方向に沿うように、略直線形状に形成されており、後端部は、ハンドル45の先端部に接続されている。 The operation wire 20A has a curved portion 21A provided at the tip thereof and curved in a predetermined direction, and a straight portion 22A continuous with the rear end of the curved portion 21A and extending toward the rear end side of the medical device 1A. .. The curved portion 21A of the operation wire 20A is previously processed into a curved shape and the curved shape is stored, that is, the curved portion 21A is a portion that stores the curved shape. FIG. 1 shows a state in which the curved portion 21A is pressed against the inner peripheral surface of the sheath 30, deformed into a substantially linear shape, and accommodated in the first lumen 31. The straight portion 22A is formed in a substantially straight line shape along the longitudinal direction of the medical device 1A, and the rear end portion is connected to the tip end portion of the handle 45.
操作ワイヤ20Aを構成する材料としては、操作ワイヤ20Aがシース30とともに屈曲した体腔に挿入されることから、可撓性および生体適合性を有することが好ましい。樹脂材料であれば、例えば、ポリアミド樹脂、ポリオレフィン樹脂、ポリエステル樹脂、ポリウレタン樹脂、シリコーン樹脂、フッ素樹脂等を採用することができる。また、術者によるハンドル45の操作を、バスケット部10Aに伝達するための剛性を有する材料が好ましい。金属材料であれば、例えば、SUS304などのステンレス鋼、ニッケルチタン合金、コバルトクロム合金等を採用することができる。前述したように、湾曲部21Aが湾曲形状を記憶していることを踏まえると、ニッケルチタン合金がより好ましい。また、上記の樹脂材料、金属材料の組み合わせであってもよい。 The material constituting the operation wire 20A is preferably flexible and biocompatible because the operation wire 20A is inserted into the bent body cavity together with the sheath 30. As the resin material, for example, polyamide resin, polyolefin resin, polyester resin, polyurethane resin, silicone resin, fluororesin and the like can be adopted. Further, a material having rigidity for transmitting the operation of the handle 45 by the operator to the basket portion 10A is preferable. As for the metal material, for example, stainless steel such as SUS304, nickel titanium alloy, cobalt chrome alloy and the like can be adopted. As described above, the nickel titanium alloy is more preferable in view of the fact that the curved portion 21A stores the curved shape. Further, it may be a combination of the above resin material and metal material.
バスケット部10Aは、上述したように先端チップ11と、バスケット14Aと、後端チップ13と、を有する。バスケット14Aは複数のワイヤ12Aから成る。ワイヤ12Aのそれぞれの先端は、ばらけないように先端チップ11により固定され、後端も、ばらけないように後端チップ13により固定されている。図1の状態において、即ち、バスケット14A及び後端チップ13がシース30の第1のルーメン31に収容された状態において、ワイヤ12Aは、先端チップ11と後端チップ13との間では、互いに交差することなく、又、互いに撚り合されることなく配置されている。
バスケット14Aは、予め、径方向、即ち、バスケット14Aの中心軸Cに垂直な方向に拡張した拡張形状に加工され(図2A参照)、この拡張形状が記憶させられている、即ち、バスケット14Aは、径方向へ拡張した形状を記憶している部位である。具体的には、バスケット14Aを構成する複数のワイヤ12Aのそれぞれが、予め、湾曲形状に加工され、この湾曲形状を記憶している。図1は、バスケット14Aがシース30の内周面によって押圧され、径方向に収縮した形状に変形させられて第1のルーメン31に収容された状態を示している。
The basket portion 10A has a tip tip 11, a basket 14A, and a rear end tip 13 as described above. The basket 14A is composed of a plurality of wires 12A. Each tip of the wire 12A is fixed by the tip tip 11 so as not to come apart, and the rear end is also fixed by the tip 13 so as not to come apart. In the state of FIG. 1, that is, in the state where the basket 14A and the rear end tip 13 are housed in the first lumen 31 of the sheath 30, the wires 12A intersect each other between the tip tip 11 and the rear end tip 13. They are arranged without being twisted together.
The basket 14A is previously processed into an extended shape that expands in the radial direction, that is, in the direction perpendicular to the central axis C of the basket 14A (see FIG. 2A), and this extended shape is stored, that is, the basket 14A is stored. , A part that memorizes the shape that expands in the radial direction. Specifically, each of the plurality of wires 12A constituting the basket 14A is preliminarily processed into a curved shape, and the curved shape is stored. FIG. 1 shows a state in which the basket 14A is pressed by the inner peripheral surface of the sheath 30, deformed into a shape contracted in the radial direction, and housed in the first lumen 31.
バスケット部10Aは、バスケット14Aと後端チップ13のみが第1のルーメン31に収容され、先端チップ11が第1のルーメン31に収容できないように構成されてもよい。具体的には、先端チップ11の一部が、シース30の先端の内径よりも大きい外径を有するように形成されてもよい。このような構成とすると、先端チップ11がシース30の第1のルーメン31に収容されない。そのため、ハンドル45の操作によって第1のルーメン31でバスケット部10Aを進退させた場合でも、先端チップ11が第1のルーメン31に入り込んでシース30の内周面に引っ掛かってしまうことがない。この結果、図1の状態から、比較的容易に、バスケット14A及び操作ワイヤ20Aの湾曲部21Aをシース30の先端から突出した状態へと移行させることができる。 The basket portion 10A may be configured such that only the basket 14A and the rear end tip 13 are housed in the first lumen 31 and the tip tip 11 cannot be housed in the first lumen 31. Specifically, a part of the tip tip 11 may be formed so as to have an outer diameter larger than the inner diameter of the tip of the sheath 30. With such a configuration, the tip end 11 is not accommodated in the first lumen 31 of the sheath 30. Therefore, even when the basket portion 10A is moved back and forth by the first lumen 31 by operating the handle 45, the tip tip 11 does not enter the first lumen 31 and get caught on the inner peripheral surface of the sheath 30. As a result, the curved portion 21A of the basket 14A and the operation wire 20A can be relatively easily moved from the state of FIG. 1 to a state of protruding from the tip of the sheath 30.
先端チップ11は、バスケット14Aを構成する複数のワイヤ12Aのそれぞれの先端をばらけないようにできる部材であればよく、たとえば、複数のワイヤ12Aのそれぞれの先端を互いに接合するためのろう材や接着材であってもよい。また、先端チップ11を複数のワイヤ12Aの先端を互いに溶接することによって形成してもよい。同様に、後端チップ13は、たとえば、複数のワイヤ12Aのそれぞれの後端を互いに接合するためのろう材や接着材であってもよい。また、後端チップ13を、複数のワイヤ12Aの後端を互いに溶接することによって形成してもよい。また、先端チップ11の先端を、体内を傷つけないように、研磨加工、切削加工などにより、略半球形状に加工してもよい。 The tip tip 11 may be a member that can prevent the tips of the plurality of wires 12A constituting the basket 14A from being separated. For example, a brazing material for joining the tips of the plurality of wires 12A to each other. It may be an adhesive. Further, the tip tip 11 may be formed by welding the tips of a plurality of wires 12A to each other. Similarly, the trailing end tip 13 may be, for example, a brazing material or an adhesive for joining the trailing ends of the plurality of wires 12A to each other. Further, the rear end tip 13 may be formed by welding the rear ends of a plurality of wires 12A to each other. Further, the tip of the tip tip 11 may be processed into a substantially hemispherical shape by polishing, cutting, or the like so as not to damage the inside of the body.
先端チップ11は、医療用デバイス1Aと併用されるガイドワイヤ(不図示)を挿通するために、医療由デバイス1Aの長手方向に延びるルーメン(不図示)、即ち貫通孔を有していてもよい。この場合、先行して体腔内に挿入されたガイドワイヤを先端チップ11に設けられたルーメンに通すことで、ガイドワイヤに沿って医療用デバイス1Aを体腔内に容易に挿入することができる。 The tip tip 11 may have a lumen (not shown) extending in the longitudinal direction of the medical device 1A to insert a guide wire (not shown) used in combination with the medical device 1A, that is, a through hole. .. In this case, the medical device 1A can be easily inserted into the body cavity along the guide wire by passing the guide wire previously inserted into the body cavity through the lumen provided on the tip tip 11.
ワイヤ12Aを構成する材料としては、バスケット14Aが体腔内に挿入されること、また、屈曲した体腔内で拡縮させられる場合があることから、生体適合性、可撓性、及び弾性を有することが好ましく、樹脂材料であれば、例えば、ポリアミド樹脂、ポリオレフィン樹脂、ポリエステル樹脂、ポリウレタン樹脂、シリコーン樹脂、フッ素樹脂等を採用することができる。金属材料であれば、例えば、SUS304などのステンレス鋼、ニッケルチタン合金、コバルトクロム合金等を採用することができる。前述したように、ワイヤ12Aが湾曲形状を記憶していることを踏まえると、ニッケルチタン合金がより好ましい。または、上記の樹脂材料、金属材料の組み合わせであってもよい。 The material constituting the wire 12A is biocompatible, flexible, and elastic because the basket 14A is inserted into the body cavity and may be expanded or contracted in the bent body cavity. Preferably, as a resin material, for example, polyamide resin, polyolefin resin, polyester resin, polyurethane resin, silicone resin, fluororesin and the like can be adopted. As for the metal material, for example, stainless steel such as SUS304, nickel titanium alloy, cobalt chrome alloy and the like can be adopted. As described above, the nickel titanium alloy is more preferable in view of the fact that the wire 12A stores the curved shape. Alternatively, it may be a combination of the above resin material and metal material.
操作部40を構成する把持部41は、送液ルーメン44を有する送液部43を備える。送液部43は、把持部41の任意の場所に配置され、その内周面により送液ルーメン44が規定される。送液ルーメン44は、把持部41の第2のルーメン42と連通する。即ち、シース30の第1のルーメン31、把持部41の第2のルーメン42、及び送液ルーメン44は連通している。 The grip portion 41 constituting the operating portion 40 includes a liquid feeding unit 43 having a liquid feeding lumen 44. The liquid feeding portion 43 is arranged at an arbitrary position of the grip portion 41, and the liquid feeding lumen 44 is defined by the inner peripheral surface thereof. The liquid feeding lumen 44 communicates with the second lumen 42 of the grip portion 41. That is, the first lumen 31 of the sheath 30, the second lumen 42 of the grip portion 41, and the liquid feeding lumen 44 communicate with each other.
送液部43は、例えば、図1に示すように、医療用デバイス1Aの長手方向に延びる把持部41の側面から突出するように設けられ、その外周面に、螺旋状の溝(不図示)を有していても良い。この場合、内周面に螺旋状の凸部が設けられているシリンジ(不図示)を送液部43に接続することができ、シリンジから送液ルーメン44に注入した薬液等を、第2のルーメン42、及び第1のルーメン31を介して、シース30の先端から体腔内へと流入させることができる。 As shown in FIG. 1, the liquid feeding portion 43 is provided so as to project from the side surface of the grip portion 41 extending in the longitudinal direction of the medical device 1A, and a spiral groove (not shown) is formed on the outer peripheral surface thereof. May have. In this case, a syringe (not shown) provided with a spiral convex portion on the inner peripheral surface can be connected to the liquid feeding unit 43, and the chemical solution or the like injected from the syringe into the liquid feeding lumen 44 is seconded. It can flow into the body cavity from the tip of the sheath 30 via the lumen 42 and the first lumen 31.
図1においては、送液部43は、把持部41の一部として形成されているが、別部材として形成し、把持部41に取り付けてもよい。また、シース30に取り付けてもよく、その場合、送液ルーメン44は、第1のルーメン31に直接連通することになる。 In FIG. 1, the liquid feeding portion 43 is formed as a part of the grip portion 41, but it may be formed as a separate member and attached to the grip portion 41. Further, it may be attached to the sheath 30, in which case the liquid feeding lumen 44 communicates directly with the first lumen 31.
操作ワイヤ20Aのストレート部22Aの後端部は把持部41の後端から突出し、ハンドル45に接続されている。ハンドル45は術者によって操作され、この術者による操作を操作ワイヤ20Aに伝達するための部材である。図1において、ハンドル45は2つの屈曲部を有しているが、ハンドル45の形状は、術者が容易に操作できるものであればよく、図1に示すような、屈曲部を有する形状に限られない。 The rear end of the straight portion 22A of the operation wire 20A protrudes from the rear end of the grip portion 41 and is connected to the handle 45. The handle 45 is operated by an operator and is a member for transmitting the operation by the operator to the operation wire 20A. In FIG. 1, the handle 45 has two bent portions, but the shape of the handle 45 may be any shape that can be easily operated by the operator, and has a bent portion as shown in FIG. Not limited.
術者は、把持部41を把持し、医療用デバイス1Aの長手方向にハンドル45を前後させることで、シース30の第1のルーメン及び把持部41の第2のルーメン42において、操作ワイヤ20A及びバスケット部10Aを前後に移動させることができる。また、ハンドル45を操作ワイヤ20Aを中心として操作ワイヤ20Aの周りに回転させることで、操作ワイヤ20A及びバスケット部10Aを回転させることができる。 The operator grips the grip 41 and moves the handle 45 back and forth in the longitudinal direction of the medical device 1A so that the operation wire 20A and the operation wire 20A and the second lumen 42 of the grip 41 are formed by the operator. The basket portion 10A can be moved back and forth. Further, by rotating the handle 45 around the operation wire 20A around the operation wire 20A, the operation wire 20A and the basket portion 10A can be rotated.
把持部41及びハンドル45を構成する材料としては、耐久性を有し、滅菌処理に適していることが好ましく、金属、射出成形された樹脂、又はそれらの組み合わせであってもよい。 The material constituting the grip portion 41 and the handle 45 is preferably durable and suitable for sterilization, and may be a metal, an injection-molded resin, or a combination thereof.
図2Aは、本開示の第1実施形態に係る医療用デバイス1Aの先端部の概略部分縦断面図である。図2Aにはバスケット部10Aの中心軸C(先端チップ11と後端チップ13を通る仮想の直線)が記載されている。図2Aは、医療用デバイス1Aが図1の状態にあるときに、術者が把持部41を把持した状態で、ハンドル45を把持部41に対して先端側に相対移動させた結果、バスケット部10A及び操作ワイヤ20Aの湾曲部21Aがシース30の先端から突出した状態を示す図であり、バスケット14Aがシース30の内周面による押圧から解放され、バスケット部10Aの中心軸Cに略垂直な方向に収縮した形状から拡張した形状へ変化した状態を示している。また、操作ワイヤ20Aの湾曲部21Aがシース30の内周面による押圧から解放され、略直線形状から湾曲形状に変化した状態を示している。図2Aにおいて、湾曲部21Aの先端部は後端チップ13に接続されている。 FIG. 2A is a schematic partial vertical sectional view of a tip portion of the medical device 1A according to the first embodiment of the present disclosure. FIG. 2A shows a central axis C (a virtual straight line passing through the tip 11 at the tip and the tip 13 at the rear) of the basket portion 10A. FIG. 2A shows a basket portion as a result of moving the handle 45 relative to the grip portion 41 while the operator grips the grip portion 41 while the medical device 1A is in the state of FIG. 10A and the curved portion 21A of the operation wire 20A are shown in a state in which the curved portion 21A protrudes from the tip of the sheath 30. The basket 14A is released from the pressing by the inner peripheral surface of the sheath 30, and is substantially perpendicular to the central axis C of the basket portion 10A. It shows a state in which the shape has changed from a shape contracted in the direction to an expanded shape. Further, the curved portion 21A of the operation wire 20A is released from the pressing by the inner peripheral surface of the sheath 30, and shows a state in which the shape is changed from a substantially linear shape to a curved shape. In FIG. 2A, the tip of the curved portion 21A is connected to the rear end tip 13.
図2Aに示すように、医療用デバイス1Aが図1の状態にあるときに、ハンドル45を先端側に移動させると、複数のワイヤ12Aは、第1のルーメン31から外部に押し出され、シース30の内周面による押圧から解放される。このとき、複数のワイヤ12Aを構成するそれぞれのワイヤ(本実施形態においては、12Aa、12Ab、12Ac、12Ad)が互いに異なる方向であって、バスケット部10Aの中心軸Cから離れる方向に湾曲する。即ち、複数のワイヤ12Aを構成するそれぞれのワイヤがバスケット部10Aの中心軸Cを中心に放射状に拡がる。これにより、放射状に拡がった複数のワイヤ12Aの内側に空間が形成され、この空間に後述の総胆管凹部101に生じた結石102(図3参照)を取り込むことが可能となる。 As shown in FIG. 2A, when the medical device 1A is in the state of FIG. 1 and the handle 45 is moved toward the tip side, the plurality of wires 12A are pushed out from the first lumen 31 and the sheath 30 is formed. It is released from the pressure by the inner peripheral surface of. At this time, the wires (12Aa, 12Ab, 12Ac, 12Ad) constituting the plurality of wires 12A are curved in different directions from each other and in a direction away from the central axis C of the basket portion 10A. That is, each wire constituting the plurality of wires 12A extends radially around the central axis C of the basket portion 10A. As a result, a space is formed inside the plurality of wires 12A extending radially, and it becomes possible to take in the calculus 102 (see FIG. 3) generated in the common bile duct recess 101 described later in this space.
医療用デバイス1Aが図2Aの状態にあるときに、術者がハンドル45を後端側に移動させると、操作ワイヤ20Aとバスケット部10Aが後端側に移動し、バスケット14A及び操作ワイヤ20Aの湾曲部21Aがシース30の第1のルーメン31に再び収容される。このとき、操作ワイヤ20Aの湾曲部21Aは、シース30の内周面により押圧され、湾曲形状から真直ぐに近い形状(略直線形状)に変形し、第1のルーメン31に収容される。また、バスケット14Aのワイヤ12Aのそれぞれがシース30の内周面により押圧され、湾曲形状から略直線形状に変形することでバスケット14Aが収縮し、操作ワイヤ20Aに追従して第1のルーメン31に収容される。この結果、医療用デバイス1Aは、図1の状態に戻る。 When the operator moves the handle 45 to the rear end side while the medical device 1A is in the state of FIG. 2A, the operation wire 20A and the basket portion 10A move to the rear end side, and the basket 14A and the operation wire 20A are moved. The curved portion 21A is re-accommodated in the first lumen 31 of the sheath 30. At this time, the curved portion 21A of the operation wire 20A is pressed by the inner peripheral surface of the sheath 30, deforms from the curved shape to a shape close to straight (a substantially linear shape), and is accommodated in the first lumen 31. Further, each of the wires 12A of the basket 14A is pressed by the inner peripheral surface of the sheath 30, and the basket 14A contracts by deforming from a curved shape to a substantially linear shape, and follows the operation wire 20A to the first lumen 31. Be housed. As a result, the medical device 1A returns to the state shown in FIG.
図2Bは、図2Aにおける医療用デバイス1Aの先端部のA-A線によって切り取られた断面を、矢印の方向から観察した図である。 FIG. 2B is a view obtained by observing a cross section of the tip end portion of the medical device 1A in FIG. 2A cut out by the line AA from the direction of the arrow.
図2A及び図2Bにおいては、バスケット14Aは12Aa、12Ab、12Ac、12Adの4本のワイヤから成る。図2A及び図2Bにおいて、4本のワイヤ12Aのうちワイヤ12Aaとワイヤ12Abが中心軸Cに対して対称に配置されており、かつ、ワイヤ12Acとワイヤ12Adが中心軸Cに対して対称に配置されている。尚、ワイヤ12Aを構成するそれぞれのワイヤは、中心軸Cに対して対称に配置されなくてもよい。具体的には、4本のワイヤ12Aのうちいずれか2つのワイヤを中心軸Cに対して対称に配置し、かつ、残りの2つのワイヤを中心軸Cに対して非対称に配置してもよい。または、いずれの2つのワイヤの組み合わせも中心軸Cに対して非対称となるように配置してもよい。また、ワイヤ12Aの数も4本に限定されない。 In FIGS. 2A and 2B, the basket 14A consists of four wires, 12Aa, 12Ab, 12Ac and 12Ad. In FIGS. 2A and 2B, of the four wires 12A, the wire 12Aa and the wire 12Ab are arranged symmetrically with respect to the central axis C, and the wire 12Ac and the wire 12Ad are arranged symmetrically with respect to the central axis C. Has been done. The wires constituting the wire 12A do not have to be arranged symmetrically with respect to the central axis C. Specifically, any two of the four wires 12A may be arranged symmetrically with respect to the central axis C, and the remaining two wires may be arranged asymmetrically with respect to the central axis C. .. Alternatively, the combination of either two wires may be arranged so as to be asymmetric with respect to the central axis C. Further, the number of wires 12A is not limited to four.
図3は、術者が、医療用デバイス1Aを総胆管100に挿入し、総胆管凹部101に生じた結石102を回収する様子を示した図である。尚、総胆管凹部101とは、総胆管100の一部の直径が急激に拡大してできた部位である。図3における総胆管凹部は、医療用デバイス1Aの説明のために、実際の形態とは異なる部分を含む FIG. 3 is a diagram showing a state in which an operator inserts a medical device 1A into the common bile duct 100 and collects a calculus 102 formed in a common bile duct recess 101. The common bile duct recess 101 is a portion formed by rapidly expanding the diameter of a part of the common bile duct 100. The common bile duct recess in FIG. 3 includes a portion different from the actual form for the purpose of explaining the medical device 1A.
医療用デバイス1Aは、十二指腸の乳頭(不図示)近くまで先端部が挿入された内視鏡(不図示)の内部を通り、予め内視鏡の内部を経由して乳頭から総胆管100に挿入されたガイドワイヤ(不図示)に沿って総胆管100に挿入される。尚、医療用デバイス1Aは、図1に示す状態、即ち、バスケット14A、後端チップ13、操作ワイヤ20Aの湾曲部21Aがシース30の第1のルーメン31に収容された状態で総胆管100に挿入される。医療用デバイス1Aが総胆管100の凹部101に到達した後、術者は、一方の手で把持部41を把持し、もう一方の手でハンドル45を先端側に移動させることにより、バスケット14A及び操作ワイヤ20Aの湾曲部21Aをシース30の先端から押し出す。このとき、バスケット14Aが収縮形状から拡張形状に変化するとともに操作ワイヤ20Aの湾曲部21Aが、略直線形状から凹部101の形状に沿うように湾曲形状に変化する。この結果、術者は、総胆管凹部101の側壁面103近くにバスケット14Aを拡張させることができる。術者は、拡張したバスケット14Aによって総胆管凹部101の壁面に生じた結石102を、複数のワイヤ12Aの隣り合うワイヤの隙間から拡張したバスケット14Aの内部の空間に収容することができる。その後、術者はハンドル45を後端側に引っ張ってバスケット14Aの一部又は全部をシース30の第1のルーメン31に収容することで、バスケット14Aを収縮させ、結石102をバスケット14Aの内部に保持することができる。術者は、ハンドル45及び把持部41を更に後端側に引くことで、結石102を内包するバスケット14Aを、総胆管凹部101及び総胆管100から乳頭を通って引き抜くことができる。 The medical device 1A passes through the inside of an endoscope (not shown) in which the tip is inserted close to the duodenal papilla (not shown), and is inserted into the common bile duct 100 from the papilla through the inside of the endoscope in advance. It is inserted into the common bile duct 100 along a guide wire (not shown). The medical device 1A is placed in the common bile duct 100 in the state shown in FIG. 1, that is, in a state where the basket 14A, the rear end tip 13, and the curved portion 21A of the operation wire 20A are housed in the first lumen 31 of the sheath 30. Will be inserted. After the medical device 1A reaches the recess 101 of the common bile duct 100, the operator grips the grip 41 with one hand and moves the handle 45 to the tip side with the other hand to move the basket 14A and the handle 45 to the tip side. The curved portion 21A of the operation wire 20A is pushed out from the tip of the sheath 30. At this time, the basket 14A changes from a contracted shape to an expanded shape, and the curved portion 21A of the operation wire 20A changes from a substantially linear shape to a curved shape along the shape of the concave portion 101. As a result, the operator can expand the basket 14A near the side wall surface 103 of the common bile duct recess 101. The operator can accommodate the calculus 102 formed on the wall surface of the common bile duct recess 101 by the expanded basket 14A in the space inside the basket 14A extended from the gap between the adjacent wires of the plurality of wires 12A. After that, the operator pulls the handle 45 toward the rear end side and accommodates a part or all of the basket 14A in the first lumen 31 of the sheath 30 to contract the basket 14A and put the calculus 102 inside the basket 14A. Can be retained. The operator can pull the basket 14A containing the calculus 102 from the common bile duct recess 101 and the common bile duct 100 through the papilla by further pulling the handle 45 and the grip portion 41 toward the rear end side.
以上のように、医療用デバイス1Aによると、操作ワイヤ20Aの先端部に設けられた湾曲部21Aが総胆管凹部101の形状に沿うように湾曲しているため、バスケット14Aを総胆管凹部101の側壁面103により接近させて拡張させることが可能となる。この結果、総胆管凹部101に生じた結石102をより容易に回収可能となる。 As described above, according to the medical device 1A, since the curved portion 21A provided at the tip of the operation wire 20A is curved so as to follow the shape of the common bile duct recess 101, the basket 14A is made of the common bile duct recess 101. The side wall surface 103 can be brought closer and expanded. As a result, the calculus 102 formed in the common bile duct recess 101 can be more easily recovered.
<第2実施形態>
図4Aは、本開示の第2実施形態に係る医療用デバイス1Bにおけるバスケット部10Bの概略部分縦断面図である。
<Second Embodiment>
FIG. 4A is a schematic partial vertical sectional view of the basket portion 10B in the medical device 1B according to the second embodiment of the present disclosure.
図4Bは、図4Aにおける医療用デバイス1BのB-B線によって切り取られた断面を、矢印の方向から観察した図である。第2実施形態に係る医療用デバイス1Bと第1実施形態に係る医療用デバイス1Aとは、バスケット14Bの構造のみが相違する。医療用デバイス1Bの各構成部材のうち、第1実施形態に係る医療用デバイス1Aと共通する構成部材については、第1実施形態において付されている番号と同じ番号を付し、その詳細説明を省略する。 FIG. 4B is a view of a cross section of the medical device 1B in FIG. 4A cut out by the line BB, observed from the direction of the arrow. The medical device 1B according to the second embodiment and the medical device 1A according to the first embodiment differ only in the structure of the basket 14B. Among the constituent members of the medical device 1B, the constituent members common to the medical device 1A according to the first embodiment are assigned the same numbers as those assigned in the first embodiment, and detailed description thereof will be given. Omit.
図4A及び図4Bは、バスケット14B及び操作ワイヤ20Aの湾曲部21Aがシース30の先端から突出した状態を示す図であり、バスケット14Bがシース30の内周面による押圧から解放され、バスケット部10Bの中心軸Cに略垂直な方向に収縮した形状から拡張した形状へ変化した状態を示している。また、操作ワイヤ20Aの湾曲部21Aがシース30の内周面による押圧から解放され、略直線形状から湾曲形状に変化した状態を示している。 4A and 4B are views showing a state in which the curved portion 21A of the basket 14B and the operation wire 20A protrudes from the tip of the sheath 30, and the basket 14B is released from the pressure by the inner peripheral surface of the sheath 30 and the basket portion 10B is released. It shows a state in which the shape is changed from a shape contracted in a direction substantially perpendicular to the central axis C of the above to an expanded shape. Further, the curved portion 21A of the operation wire 20A is released from the pressing by the inner peripheral surface of the sheath 30, and shows a state in which the shape is changed from a substantially linear shape to a curved shape.
図4A及び図4Bにおいて、バスケット14Bは、複数のワイヤ12Bを有する。複数のワイヤ12Bは、第1の内側ワイヤ12Ba、第2の内側ワイヤ12Bb、第1の外側ワイヤ12Bc、及び、第2の外側ワイヤ12Bdから成る。第1の内側ワイヤ12Baと第2の内側ワイヤ12Bbは、バスケット14Bの周方向に沿って隣接し、バスケット14Bが拡張した状態において、バスケット部10Bの中心軸Cよりも湾曲部21Aの湾曲方向に位置するように配置されている(換言すると、中心軸Cよりも湾曲部21Aの湾曲形状の内側に位置するように配置されている)。第1の外側ワイヤ12Bcと第2の外側ワイヤ12Bdは、バスケット14Bの周方向に沿って隣接し、バスケット14Bが拡張した状態において、バスケット部10Bの中心軸Cよりも湾曲部21Aの湾曲方向の反対方向に位置するように配置されている(換言すると、中心軸Cよりも湾曲部21Aの湾曲形状の外側に位置するように配置されている)。図4Bに示されるように、バスケット14Bが拡張した状態では第1の内側ワイヤ12Baの横断面の中心と第2の内側ワイヤ12Bbの横断面の中心との距離aは、第1の外側ワイヤ12Bcの横断面の中心と第2の外側ワイヤ12Bdの横断面の中心との距離bよりも大きい。 In FIGS. 4A and 4B, the basket 14B has a plurality of wires 12B. The plurality of wires 12B consist of a first inner wire 12Ba, a second inner wire 12Bb, a first outer wire 12Bc, and a second outer wire 12Bd. The first inner wire 12Ba and the second inner wire 12Bb are adjacent to each other along the circumferential direction of the basket 14B, and in a state where the basket 14B is expanded, in the bending direction of the bending portion 21A with respect to the central axis C of the basket portion 10B. It is arranged so as to be located (in other words, it is arranged so as to be located inside the curved shape of the curved portion 21A rather than the central axis C). The first outer wire 12Bc and the second outer wire 12Bd are adjacent to each other along the circumferential direction of the basket 14B, and in a state where the basket 14B is expanded, the bending direction of the bending portion 21A is larger than the central axis C of the basket portion 10B. It is arranged so as to be located in the opposite direction (in other words, it is arranged so as to be located outside the curved shape of the curved portion 21A with respect to the central axis C). As shown in FIG. 4B, when the basket 14B is expanded, the distance a between the center of the cross section of the first inner wire 12Ba and the center of the cross section of the second inner wire 12Bb is the distance a of the first outer wire 12Bc. It is larger than the distance b between the center of the cross section of the second outer wire 12Bd and the center of the cross section of the second outer wire 12Bd.
この構成によると、バスケット14Bが拡張したときに第1の内側ワイヤ12Baの横断面の中心と第2の内側ワイヤ12Bbの横断面の中心との距離aが第1の外側ワイヤ12Bcの横断面の中心と第2の外側ワイヤ12Bdの横断面の中心との距離bと等しくなる構成に比べ、より大きなサイズの結石102をバスケット14Bの内部に容易に収容することができる。 According to this configuration, when the basket 14B is expanded, the distance a between the center of the cross section of the first inner wire 12Ba and the center of the cross section of the second inner wire 12Bb is the cross section of the first outer wire 12Bc. A larger size stone 102 can be easily accommodated inside the basket 14B as compared to a configuration in which the distance b between the center and the center of the cross section of the second outer wire 12Bd is equal.
<第3実施形態>
図5は、本開示の第3実施形態に係る医療用デバイス1Cの先端部の概略部分縦断面を示す図である。
医療用デバイス1Cと第1実施形態に係る医療用デバイス1Aとは、操作ワイヤ20Cの構造のみが相違する。医療用デバイス1Cの各構成部材のうち、第1実施形態に係る医療用デバイス1Aと共通する構成部材については、第1実施形態において付されている番号と同じ番号を付し、その詳細説明を省略する。
<Third Embodiment>
FIG. 5 is a diagram showing a schematic partial vertical cross section of a tip portion of the medical device 1C according to the third embodiment of the present disclosure.
The medical device 1C and the medical device 1A according to the first embodiment differ only in the structure of the operation wire 20C. Among the constituent members of the medical device 1C, the constituent members common to the medical device 1A according to the first embodiment are assigned the same numbers as those assigned in the first embodiment, and detailed description thereof will be given. Omit.
図5において、医療用デバイス1Cは、第1実施形態に係る医療用デバイス1Aの操作ワイヤ20Aに替えて操作ワイヤ20Cを有する。操作ワイヤ20Cは、先端部に、後端チップ13の後端部に連続する第1のストレート部22Caと、第1のストレート部22Caの後端部に連続する湾曲部21Cと、湾曲部21Cの後端部に連続し、シース30と略平行に延びる第2のストレート部22Cbと、を有する。言い換えると、湾曲部21Cは、操作ワイヤ20Cの先端側に形成されている。
尚、図5は、バスケット部10A、操作ワイヤ20Cの第1のストレート部22Ca、湾曲部21C、及び第2のストレート部22Cbの一部がシース30の先端から突出した状態を示す図であり、バスケット14Aがシース30の内周面による押圧から解放され、バスケット部10Aの中心軸C(図2A参照)に略垂直な方向に収縮した形状から拡張した形状へ変化した状態を示している。また、操作ワイヤ20Cの湾曲部21Cがシース30の内周面による押圧から解放され、略直線形状から湾曲形状に変化した状態を示している。このような構成によっても、第1実施形態に係る医療用デバイス1Aと同様の効果を奏することができる。
In FIG. 5, the medical device 1C has an operation wire 20C instead of the operation wire 20A of the medical device 1A according to the first embodiment. The operation wire 20C has a first straight portion 22Ca continuous with the rear end portion of the rear end tip 13, a curved portion 21C continuous with the rear end portion of the first straight portion 22Ca, and a curved portion 21C at the tip portion. It has a second straight portion 22Cb that is continuous with the rear end portion and extends substantially parallel to the sheath 30. In other words, the curved portion 21C is formed on the tip end side of the operation wire 20C.
FIG. 5 is a diagram showing a state in which a part of the basket portion 10A, the first straight portion 22Ca, the curved portion 21C, and the second straight portion 22Cb of the operation wire 20C protrudes from the tip of the sheath 30. It shows a state in which the basket 14A is released from the pressure by the inner peripheral surface of the sheath 30 and changes from a shape contracted in a direction substantially perpendicular to the central axis C (see FIG. 2A) of the basket portion 10A to an expanded shape. Further, the curved portion 21C of the operation wire 20C is released from the pressing by the inner peripheral surface of the sheath 30, and shows a state in which the shape is changed from a substantially linear shape to a curved shape. Even with such a configuration, the same effect as that of the medical device 1A according to the first embodiment can be obtained.
<第4実施形態>
図6は、本開示の第4実施形態に係る医療用デバイス1Dの先端部の概略部分縦断面図である。第4実施形態に係る医療用デバイス1Dと第1実施形態に係る医療用デバイス1Aとは、操作ワイヤ20Dの構造のみが相違する。医療用デバイス1Dの各構成部材のうち、第1実施形態に係る医療用デバイス1Aと共通する構成部材については、第1実施形態において付されている番号と同じ番号を付し、その詳細説明を省略する。
<Fourth Embodiment>
FIG. 6 is a schematic partial vertical sectional view of a tip portion of the medical device 1D according to the fourth embodiment of the present disclosure. The medical device 1D according to the fourth embodiment and the medical device 1A according to the first embodiment differ only in the structure of the operation wire 20D. Among the constituent members of the medical device 1D, the constituent members common to the medical device 1A according to the first embodiment are assigned the same numbers as those assigned in the first embodiment, and detailed explanations thereof will be given. Omit.
 図6において、医療用デバイス1Dは操作ワイヤ20Dを有し、操作ワイヤ20Dは2つの湾曲部を有する。具体的には、操作ワイヤ20Dは、後端チップ13の後端部に連続する第1のストレート部22Daと、第1のストレート部22Daの後端部に連続する第1の湾曲部21Daと、第1の湾曲部21Daの後端部に連続する第2のストレート部22Dbと、第2のストレート部22Dbの後端部に連続する第2の湾曲部21Dbと、第2の湾曲部21Dbの後端部に連続する第3のストレート部22Dcを有する。第2の湾曲部21Dbの湾曲度合いより、第1の湾曲部21Daの湾曲度合いの方が大きい。湾曲度合は、例えば、最小の曲率半径によって規定することができる。湾曲度合を最小の曲率半径で定義する場合、第2の湾曲部21Dbの最小の曲率半径より、第2の湾曲部21Daの最小の曲率半径が小さい。  In FIG. 6, the medical device 1D has an operating wire 20D, and the operating wire 20D has two curved portions. Specifically, the operation wire 20D includes a first straight portion 22Da continuous with the rear end portion of the rear end tip 13, and a first curved portion 21Da continuous with the rear end portion of the first straight portion 22Da. After the second straight portion 22Db continuous with the rear end portion of the first curved portion 21Da, the second curved portion 21Db continuous with the rear end portion of the second straight portion 22Db, and the second curved portion 21Db. It has a third straight portion 22Dc continuous to the end. The degree of curvature of the first curved portion 21Da is larger than the degree of curvature of the second curved portion 21Db. The degree of curvature can be defined by, for example, the minimum radius of curvature. When the degree of curvature is defined by the minimum radius of curvature, the minimum radius of curvature of the second curved portion 21Da is smaller than the minimum radius of curvature of the second curved portion 21Db.
 湾曲部の曲率半径とは、湾曲部の局所的な曲がり具合を円に近似したときの、その円の半径である。最小の曲率半径とは、上記円の半径が最も小さくなる点における円の半径である。
尚、図6は、バスケット部10A、操作ワイヤ20Dの第1のストレート部21Da、第1の湾曲部21Da、第2のストレート部22Db、第2の湾曲部21Db、及び第3のストレート部22Dcの一部がシース30の先端から突出した状態を示す図であり、バスケット14Aがシース30の内周面による押圧から解放され、バスケット部10Aの中心軸C(図2A参照)に略垂直な方向に収縮した形状から拡張した形状へ変化した状態を示している。また、操作ワイヤ20Dの第1の湾曲部21Da及び第2の湾曲部21Dbがシース30の内周面による押圧から解放され、略直線形状から湾曲形状に変化した状態を示している。
The radius of curvature of the curved portion is the radius of the circle when the local degree of bending of the curved portion is approximated to a circle. The minimum radius of curvature is the radius of the circle at the point where the radius of the circle is the smallest.
Note that FIG. 6 shows the basket portion 10A, the first straight portion 21Da of the operation wire 20D, the first curved portion 21Da, the second straight portion 22Db, the second curved portion 21Db, and the third straight portion 22Dc. It is a figure which shows the state which a part protruded from the tip of a sheath 30, and the basket 14A is released from the pressure by the inner peripheral surface of a sheath 30, and is in the direction substantially perpendicular to the central axis C (see FIG. 2A) of a basket part 10A. It shows a state in which the shape has changed from a contracted shape to an expanded shape. Further, the first curved portion 21Da and the second curved portion 21Db of the operation wire 20D are released from the pressing by the inner peripheral surface of the sheath 30, and the state of changing from a substantially linear shape to a curved shape is shown.
本構成によると、図3のような総胆管凹部101の縦断面図において、総胆管凹部101の側壁面103が総胆管100の管路の下に潜り込むように湾曲し、それにより形成された空間に結石102が生じている場合においても、バスケット14Aを総胆管凹部101の側壁面103により一層接近させて拡張させることが可能となる。この結果、総胆管凹部101に生じた結石102をより一層容易に回収可能となる。
 尚、図6では、湾曲度合が異なる2つの湾曲部(第1の湾曲部21Da及び第2の湾曲部21Db)を有する操作ワイヤ20Dを例示したが、湾曲部は2つに限られず、3つ以上であってもよい。その場合、先端側に位置する湾曲部の湾曲度合いの方が、後端側に位置する湾曲部の湾曲度合いより大きくてもよい。
According to this configuration, in the vertical cross-sectional view of the common bile duct recess 101 as shown in FIG. 3, the side wall surface 103 of the common bile duct recess 101 is curved so as to slip under the duct of the common bile duct 100, and the space formed thereby. Even when a calculus 102 is formed in the bile duct 102, the basket 14A can be expanded closer to the side wall surface 103 of the common bile duct recess 101. As a result, the calculus 102 formed in the common bile duct recess 101 can be recovered more easily.
Note that FIG. 6 illustrates an operation wire 20D having two curved portions (first curved portion 21Da and second curved portion 21Db) having different degrees of curvature, but the number of curved portions is not limited to two and three. It may be the above. In that case, the degree of curvature of the curved portion located on the front end side may be larger than the degree of curvature of the curved portion located on the rear end side.
なお、本開示は、上述した実施形態の構成に限定されるものではなく、特許請求の範囲によって示され、特許請求の範囲と均等の意味および範囲内での全ての変更が含まれることが意図される。例えば、上述した実施形態の構成のうちの一部を削除したり、他の構成に置換してもよく、上述した実施形態の構成に他の構成を追加等してもよい。
例えば、第2実施形態に係る医療用デバイス1Bの操作ワイヤ20Aに替えて第3実施形態に係る医療用デバイス1Cの操作ワイヤ20C、又は、第4実施形態に係る医療用デバイス1Dの操作ワイヤ20Dを適用してもよい。また、第4実施形態においては、第2の湾曲部21Dbの湾曲度合いより、第1の湾曲部21Daの湾曲度合いの方が小さくてもよい。
It should be noted that the present disclosure is not limited to the configuration of the above-described embodiment, but is indicated by the scope of claims, and is intended to include all modifications within the meaning and scope equivalent to the scope of claims. Will be done. For example, a part of the configuration of the above-described embodiment may be deleted or replaced with another configuration, or another configuration may be added to the configuration of the above-described embodiment.
For example, instead of the operation wire 20A of the medical device 1B according to the second embodiment, the operation wire 20C of the medical device 1C according to the third embodiment, or the operation wire 20D of the medical device 1D according to the fourth embodiment. May be applied. Further, in the fourth embodiment, the degree of curvature of the first curved portion 21Da may be smaller than the degree of curvature of the second curved portion 21Db.
1A、1B、1C、1D:医療用デバイス
10A、10B:バスケット部
11:先端チップ
12A、12B:ワイヤ
13:後端チップ
14A、14B:バスケット
20A、20C、20D:操作ワイヤ
21A:湾曲部
22A:ストレート部
30:シース
31:第1のルーメン
40:操作部
41:把持部
42:第2のルーメン
43:送液部
44:送液ルーメン
45:ハンドル
100:総胆管
101:総胆管凹部
102:結石
103:総胆管凹部の側壁面
1A, 1B, 1C, 1D: Medical device 10A, 10B: Basket part 11: Tip tip 12A, 12B: Wire 13: Rear end tip 14A, 14B: Basket 20A, 20C, 20D: Operation wire 21A: Curved part 22A: Straight part 30: Sheath 31: First lumen 40: Operation part 41: Grip part 42: Second lumen 43: Liquid feeding part 44: Liquid feeding lumen 45: Handle 100: Common bile duct 101: Common bile duct recess 102: Calculus 103: Side wall surface of the common bile duct recess

Claims (4)

  1.  操作ワイヤと、
     前記操作ワイヤの先端部に後端部が接合されるとともに、複数のワイヤから形成され、径方向に拡縮可能なバスケットと、を有し、
     前記操作ワイヤは、前記操作ワイヤの先端部に湾曲部を備える、医療用デバイス。
    With the operation wire
    It has a basket formed from a plurality of wires and expandable and contractible in the radial direction, while the rear end portion is joined to the tip end portion of the operation wire.
    The operation wire is a medical device having a curved portion at the tip of the operation wire.
  2. 前記バスケットは、
    前記複数のワイヤのうち、前記バスケットの周方向に隣接し、前記バスケットが拡張した状態において、前記バスケットの中心軸よりも前記湾曲部の湾曲方向に設けられる、第1の内側ワイヤ及び第2の内側ワイヤと、
    前記バスケットの中心軸よりも前記湾曲部の湾曲方向と反対方向に設けられる、第1の外側ワイヤ及び第2の外側ワイヤと、を有し、
    前記バスケットの横断面における、前記第1の内側ワイヤ及び第2の内側ワイヤの距離が、前記第1の外側ワイヤ及び第2の外側ワイヤの距離よりも大きい、
    請求項1に記載の医療用デバイス。
    The basket
    Of the plurality of wires, the first inner wire and the second inner wire which are adjacent to the circumferential direction of the basket and are provided in the bending direction of the curved portion with respect to the central axis of the basket in a state where the basket is expanded. With the inner wire,
    It has a first outer wire and a second outer wire provided in a direction opposite to the bending direction of the bending portion with respect to the central axis of the basket.
    The distance between the first inner wire and the second inner wire in the cross section of the basket is larger than the distance between the first outer wire and the second outer wire.
    The medical device according to claim 1.
  3.  前記操作ワイヤの前記湾曲部は、前記操作ワイヤの先端部に設けられる第1の湾曲部と、
    前記第1の湾曲部よりも前記操作ワイヤの後端側に設けられる第2の湾曲部と、を有し、
    前記第1の湾曲部の湾曲度合いが、前記第2の湾曲部の湾曲度合いよりも大きい、
    請求項1又は2に記載の医療用デバイス。
    The curved portion of the operation wire includes a first curved portion provided at the tip end portion of the operation wire and a first curved portion.
    It has a second curved portion provided on the rear end side of the operation wire with respect to the first curved portion.
    The degree of curvature of the first curved portion is larger than the degree of curvature of the second curved portion.
    The medical device according to claim 1 or 2.
  4. 前記医療用デバイスは、
    前記操作ワイヤ及び前記バスケットを収容するシースを有し、
    前記操作ワイヤは、前記操作ワイヤの先端部に、前記シースの内腔から外部に露出するときに湾曲する湾曲部を有し、
    前記バスケットの先端方向が、前記操作ワイヤの湾曲部の湾曲に従って変化する、
    請求項1乃至3のいずれか1項に記載の医療用デバイス。
     
    The medical device is
    It has a sheath for accommodating the operating wire and the basket.
    The operating wire has a curved portion at the tip of the operating wire that curves when exposed to the outside from the lumen of the sheath.
    The tip direction of the basket changes according to the curvature of the curved portion of the operating wire.
    The medical device according to any one of claims 1 to 3.
PCT/JP2020/040898 2019-11-20 2020-10-30 Medical device WO2021100441A1 (en)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130211415A1 (en) * 2012-02-09 2013-08-15 Boston Scientific Scimed, Inc. Steerable tissue manipulation medical devices and related methods of use
US20160089170A1 (en) * 2014-09-30 2016-03-31 Boston Scientific Scimed, Inc. Invertable medical retrieval devices and methods
JP2017176672A (en) * 2016-03-31 2017-10-05 日本ゼオン株式会社 Basket-type medical treatment instrument and use method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130211415A1 (en) * 2012-02-09 2013-08-15 Boston Scientific Scimed, Inc. Steerable tissue manipulation medical devices and related methods of use
US20160089170A1 (en) * 2014-09-30 2016-03-31 Boston Scientific Scimed, Inc. Invertable medical retrieval devices and methods
JP2017176672A (en) * 2016-03-31 2017-10-05 日本ゼオン株式会社 Basket-type medical treatment instrument and use method thereof

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