WO2015146484A1 - Body cavity access tool - Google Patents

Body cavity access tool Download PDF

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Publication number
WO2015146484A1
WO2015146484A1 PCT/JP2015/055864 JP2015055864W WO2015146484A1 WO 2015146484 A1 WO2015146484 A1 WO 2015146484A1 JP 2015055864 W JP2015055864 W JP 2015055864W WO 2015146484 A1 WO2015146484 A1 WO 2015146484A1
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WO
WIPO (PCT)
Prior art keywords
retractor
body cavity
retracting
annular member
treatment instrument
Prior art date
Application number
PCT/JP2015/055864
Other languages
French (fr)
Japanese (ja)
Inventor
秀司 北城
卓也 宮崎
慶弘 宮澤
Original Assignee
秀司 北城
株式会社トップ
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 秀司 北城, 株式会社トップ filed Critical 秀司 北城
Priority to JP2016510172A priority Critical patent/JP6378318B2/en
Publication of WO2015146484A1 publication Critical patent/WO2015146484A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/34Trocars; Puncturing needles
    • A61B17/3417Details of tips or shafts, e.g. grooves, expandable, bendable; Multiple coaxial sliding cannulas, e.g. for dilating
    • A61B17/3421Cannulas
    • A61B17/3423Access ports, e.g. toroid shape introducers for instruments or hands
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/34Trocars; Puncturing needles
    • A61B17/3462Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/02Surgical instruments, devices or methods, e.g. tourniquets for holding wounds open; Tractors
    • A61B17/0293Surgical instruments, devices or methods, e.g. tourniquets for holding wounds open; Tractors with ring member to support retractor elements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/34Trocars; Puncturing needles
    • A61B17/3462Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals
    • A61B2017/3464Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals with means acting on inner surface of valve or seal for expanding or protecting, e.g. inner pivoting fingers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/34Trocars; Puncturing needles
    • A61B17/3462Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals
    • A61B2017/3466Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals for simultaneous sealing of multiple instruments

Definitions

  • the present invention relates to a body cavity access device for introducing a treatment instrument that is attached to a retracted part when performing treatment while accessing the body cavity.
  • Patent Document 1 Japanese Patent Document 1
  • the retractor includes an inner annular member disposed in the body cavity, an outer annular member disposed outside the body, and the inner annular member fixed to one opening.
  • a flexible, tubular retractor member having an outer annular member fixed to the other opening.
  • the funnel-shaped treatment instrument introduction section functions as a protective lining and introduction path when the treatment instrument is introduced into the body cavity through the retractor.
  • a closure is attached to the outer annular member of the retractor attached to the retractor. Thereby, the opening part outside the body of the retracting member is closed.
  • the occlusion portion has an insertion portion for allowing the treatment tool to pass while maintaining the airtightness of the occlusion.
  • a retractor used in a body cavity access device one having a retractable member that can be wound with an outer annular member is known (for example, see Patent Document 2).
  • the retractor is wound around the outer annular member, thereby fixing the retractor to the retracted portion.
  • an inner annular member provided with a retractor having the inner annular member, the outer annular member, and the retracting member as described above, and a closing portion attached to the outer annular member, and disposed in the body cavity.
  • a string-like member for pulling out See, for example, Patent Document 3).
  • one end of the retracting member is fixed to the outer annular member, the intermediate portion is folded back with the inner annular member inside, and the other end is led out of the outer annular member. Therefore, the retracting member is doubled when mounted on the retracting portion. In this state, one end of the string-like member is fixed to the inner annular member, and extends from the outer peripheral side of the outer annular member to the outside of the retractor body through a doubled retracting member.
  • One end of the string-like member is fixed to the frame of the closing portion, and starting from this, the outside of the double retractable member passes while being folded back at the end on the inner annular member side, and the other end is the body of the retractor It may extend outward.
  • the end of the string-like member extending to the outside of the retractor is fixed to the ring member or is in a free state. By pulling up the extended end of the string-like member, the inner annular member can be taken out of the body cavity from the body cavity through the retracting portion.
  • the string-like member is led out through the inside of the treatment instrument introduction portion arranged inside the retracting member, but in that case, the string-like member passes between the treatment instrument introduction portion and the blocking portion or the outer annular member. Since the member is derived, there is a concern that the airtightness deteriorates similarly.
  • An object of the present invention is to provide a body cavity access device that can take out an inner annular member via a string-like member without causing deterioration of airtightness and damage of a retracted portion in view of the problems of the conventional technology. is there.
  • the body cavity access device of the present invention has an inner annular member disposed on the body cavity side of the retracting portion, an outer annular member disposed on the outer side of the retracting portion, and the inner annular member fixed to one opening,
  • a retractor having a flexible and tubular retractor member in which the outer annular member is fixed to the other opening, and inserted into the retractor mounted on the retractor, and into the body cavity of the treatment instrument
  • a funnel-shaped treatment instrument introduction section constituting an introduction path and an insertion section through which the treatment instrument is passed in an airtight state, and is attached to the outer annular member to block the retractor in an airtight manner
  • a gripping member that is gripped to pull out the inner annular member disposed on the body cavity side of the retracting portion, and one end is fixed to the inner annular member, and the other end is fixed to the gripping member
  • the retractor comprising a string-like member and attached to the retracting portion In a state where the treatment instrument introducing portion is inserted and the retractor is
  • the string-like member between the inner annular member of the retractor and the gripping member passes through the inside of the retracting member of the retractor, and the gripping member is the body.
  • a retractor is attached to the retracting portion in a state of being arranged on the outside.
  • the gripping member is disposed outside the body in the retractor.
  • the treatment instrument introducing portion is inserted into the retractor from the outside of the retractor body.
  • the string-like member is placed on the path from the grasping member to the inner annular member through the retractor and the treatment instrument introducing portion.
  • the closure part in which the treatment tool is disposed through the insertion part is attached to the outer annular member of the retractor while the distal end side of the treatment tool is inserted into the treatment tool introduction part. This completes the mounting of the body cavity access device to the retracted portion.
  • the gripping member is located in a portion where the airtightness is maintained by the closing, and the string-like member is connected to the retracting member and the treatment instrument introducing portion from the inner annular member. It arrange
  • the occlusion part is removed from the outer annular member together with the treatment instrument. Thereafter, the treatment instrument introducing portion is extracted from the retractor, and the gripping member is moved away from the retracting portion, whereby the inner annular member in the body cavity is pulled out of the body together with the retracting member via the string member.
  • the string-like member is located inside the retracting member and does not directly contact the retracting portion, so that the retracting portion is not damaged. Therefore, according to the present invention, it is possible to take out the inner annular member via the string-like member without causing deterioration of airtightness and damage to the wound portion.
  • the grasping member is disposed concentrically with the retracting portion on the outside of the retractor mounted on the retracting portion, and then inserted into the retractor and the retractor It may be comprised by the annular pulling member fixed by being pinched
  • the inner annular member when removing the body cavity access device, after removing the treatment instrument introducing portion from the retractor, the inner annular member is pulled out of the body by moving the handle member in a direction away from the retracting portion. Therefore, the inner annular member can be reliably taken out by the pulling member.
  • the gripping member may be constituted by the treatment instrument introducing portion, and the other end of the string-like member may be fixed to a portion outside the body of the treatment instrument introducing portion. According to this, since the treatment instrument introducing portion can be used as a grasping member, the configuration of the body cavity access device can be simplified.
  • the gripping member may be constituted by the outer annular member, and the other end of the string-like member may be fixed to the outer annular member. According to this, since the outer annular member can also be used as a gripping member, the configuration of the body cavity access device can be simplified.
  • the retractor is configured such that the inner annular member is disposed on the body cavity side of the retracting portion, and the outer annular member is disposed on the body outer side of the retracting portion, and the outer annular member is wound around the winding shaft.
  • the wound member is fixed to the wound part by winding a part of the wound member outside the body in one or the other winding direction, and the treatment instrument introducing part is arranged according to the winding direction. You may have the shape suitable for the shape which a member exhibits.
  • the treatment instrument introducing portion has a shape that matches the shape of the retractor corresponding to the winding direction of the retracting member, it is possible to arbitrarily select the winding direction of the retracting member or the shape of the retractor. it can.
  • FIG. 2 is a perspective cross-sectional view showing a state where the body cavity access device according to the first embodiment of the present invention is attached to a patient's wound part. It is sectional drawing which shows a mode when the retractor of the body cavity access device of FIG. 1 is mounted
  • FIG. 6 is a cross-sectional view showing a state where the retractor of the body cavity access device of FIG. 5 is attached to the retractor or when the retractor is removed from the retractor. It is sectional drawing which shows the state with which the body cavity access device concerning 4th Embodiment of this invention was mounted
  • a body cavity access device 1 includes a retractor 5 that is provided on a body wall 2 of a patient and that maintains a retractor 4 that leads into the body cavity 3 in an open state.
  • the retractor 5 includes an inner annular member 9 disposed on the body cavity 3 side of the retracting portion 4, an outer annular member 10 disposed on the outer side of the retracting portion 4, and the inner annular member 9 fixed to one opening. And a flexible retracting member 11 having the outer annular member 10 fixed to the other opening.
  • the pulling member 8 functions as a gripping member that is gripped in order to pull out the inner annular member 9 disposed on the body cavity side of the retracting portion 4 to the outside of the body.
  • the outer annular member 10 and the inner annular member 9 are both elastically deformable by a predetermined external force, are circular in a free state, and typically have substantially the same diameter.
  • the retracting member 11 is formed of an elastic thin film made of polyurethane, for example.
  • the retracting member 11 has a cylindrical shape and has a diameter smaller than the outer diameter of the outer annular member 10 and the inner annular member 9.
  • the outer annular member 10 is made of, for example, silicone rubber and has a substantially rectangular cross-sectional shape.
  • the inner annular member 9 is made of, for example, silicone rubber and has a substantially circular cross-sectional shape.
  • the retractor 5 has the inner annular member 9 disposed on the body cavity side of the retracting portion 4 and the outer annular member 10 disposed on the body outer side of the retracting portion 4, and the retracting member 11 using the outer annular member 10 as a winding shaft. By winding a part of the outside of the body, the retractable member 11 can be attached to the retracting portion 4 while the substantial length of the retracting member 11 corresponds to the thickness of the body wall 2.
  • the blocking portion 7 includes a disc-shaped canopy member 12, a first film member 17 and a second film member 18 stacked on the front and back surfaces of the canopy member 12, and a first film member 17 and a second film member 18, respectively.
  • a mounting ring 13 for mounting the stacked canopy member 12 on the outer annular member 10 in an airtight manner is provided.
  • the canopy member 12 is made of a soft resin having flexibility, and is formed by laminating two sheet members (gel sheets) 14 a and 14 b having the same diameter as the inner diameter of the outer annular member 10.
  • the canopy member 12 may be composed of three or more sheet members.
  • the soft resin for example, silicone rubber, polyurethane, or polyethylene can be used.
  • the sheet members 14a and 14b are provided with a plurality of slit portions 16 penetrating in the thickness direction in order to introduce the columnar treatment instrument into the body cavity 3.
  • Each slit portion 16 of the sheet member 14a is orthogonal to the corresponding slit portion 16 of the sheet member 14b in a cross shape.
  • the first film member 17 and the second film member 18 are made of another soft resin that has elasticity and is slidable with respect to the soft resin constituting the sheet members 14a and 14b, and is larger than the diameter of the canopy member 12. Has a diameter.
  • this another soft resin for example, polyurethane, polyvinyl chloride, or polyethylene can be used.
  • the end portions of the first film member 17 and the second film member 18 are bonded to each other so as to sandwich the canopy member 12 therebetween.
  • the first film member 17 is provided with a circular hole 19 for allowing a treatment instrument passed through each slit portion 16 to pass through at a position overlapping the center position of each slit portion 16 of the sheet member 14a.
  • the circular hole 19 has a diameter in the range of 40 to 90% of the diameter of the treatment instrument.
  • the second film member 18 includes a slit portion 20 for passing a treatment instrument passed through each slit portion 16 at a position corresponding to each slit portion 16 of the sheet member 14b.
  • the slit portion 20 is orthogonal to the corresponding slit portion 16 of the sheet member 14 b and has the same length as the slit portion 16.
  • the circular hole 19 of the first membrane member 17, the slit portion 16 of the sheet members 14a and 14b, and the slit portion 20 of the second membrane member 18 constitute an insertion portion 21 through which the treatment instrument is passed while maintaining airtightness.
  • the mounting ring 13 is made of, for example, natural rubber or polyurethane, has a substantially U-shaped cross section, and can be mounted on the outer annular member 10 of the retractor 5.
  • the mounting ring 13 is bonded to the end portions of the first film member 17 and the second film member 18 so that the canopy member 12 is positioned outside the body of the outer annular member 10 when the mounting ring 13 is mounted on the outer annular member 10. .
  • the treatment instrument introducing unit 6 is inserted into the retractor 5 attached to the retracting unit 4 and constitutes an introduction path into the body cavity of the treatment instrument while protecting the retracting member 11.
  • the treatment instrument introducing portion 6 has a funnel shape, and is adjacent to the cylindrical portion 22 that contacts the outlet side of the funnel, the conical portion 23 adjacent to the inlet side of the cylindrical portion 22, and the outer side of the conical portion 23. And an annular wall portion 24.
  • the treatment instrument introducing portion 6 has a shape and a size that are substantially contained in a space formed by the retractor 5 attached to the retracting portion 4 and the closing portion 7 that closes the retractor 5. Therefore, the annular wall 24 has a slightly smaller diameter and a slightly shorter axial length than the outer annular member 10 of the retractor 5.
  • the cylindrical portion 22 has an inner diameter that is slightly smaller than the diameter of the retractable portion 4 opened by the retractor 5, but larger than the outer diameter of the treatment instrument to be introduced. For example, it has an inner diameter that allows three treatment tools having a diameter of about 5 mm to pass through.
  • the length of the cylindrical portion 22 is approximately the same as the thickness of the body wall 2.
  • An elastic material such as polyurethane, polyvinyl chloride, or polyethylene is used as the material constituting the treatment instrument introduction unit 6.
  • one end of the string-like member T is fixed to the inner annular member 9 of the retractor 5, and the other end is fixed to the fixing portion 25 of the pulling member 8.
  • the retractor 5 is attached to the retractable portion 4 in a state in which the string-like member T passes through the inside of the retractor 5 and the handle member 8 is separated above the outer annular member 10.
  • the length of the string-like member T is shorter than the shortest possible length in the state where the handle member 8 is arranged as shown by the two-dot chain line in FIG. 2 with respect to the retractor 5 attached to the retracting portion 4. Is set to a length having a sufficient margin.
  • the retractor 5 when performing a surgical operation on a patient using the body cavity access device 1, first, the retractor 5 is attached to the retractable portion 4 provided in advance. That is, in a state where the string-like member T passes through the inside of the retractor 5 and the handle member 8 is separated above the outer annular member 10, the inner annular member 9 of the retractor 5 is bent and the body cavity 3 extends from the retracted portion 4. And inserted into the body cavity 3. Thereby, the inner side annular member 9 is arrange
  • the retracting member 11 is expanded in the radial direction to form an opening having a desired diameter.
  • the length of the retracting member 11 is made to correspond to the thickness of the body wall 2.
  • the handle member 8 is arranged inside the portion located outside the body of the retracting member 11 so as to be substantially concentric with the outer annular member 10 and the retracting portion 4. That is, the pulling member 8 is arranged at a position as shown by a two-dot chain line in FIG.
  • the treatment instrument introducing portion 6 is inserted into the retractor 5.
  • the cylindrical portion 22 of the treatment instrument introducing portion 6 is inserted into the opening formed by the retracting member 11.
  • the treatment instrument introduction unit 6 is in a state of being fitted (fit) to a region extending from the outside of the retractor 5 to the portion of the retracting unit 4.
  • the pulling member 8 is sandwiched and fixed between the retractor 5 and the treatment instrument introducing portion 6, and the string-like member T is introduced from the retractor 5 and the treatment instrument starting from the fixing portion 25 of the pulling member 8. It will be in the state arrange
  • the closed portion 7 in which a few treatment tools for surgery are arranged through the insertion portion 21 is attached to the outer annular member 10. That is, the closure 7 is attached to the retractor 5 by covering the outer annular member 10 with the attachment ring 13. This attachment is performed such that the distal end sides of the respective treatment instruments are bundled and the distal end side is introduced into the body cavity 3 from the cylindrical portion 22 of the treatment instrument introduction section 6.
  • the inside of the body cavity 3 is in an airtight state, and it becomes possible to perform an operation using each treatment instrument.
  • the string-like member T is located on the side of the body cavity 3 of the obstruction 7 as shown in FIG. 1, so that the airtight state of the body cavity 3 deteriorates due to the presence of the string-like member T as in the prior art. It is not.
  • the treatment tool introduction unit 6 prevents the wound member 11 and the wound part 4 from being damaged by the treatment tool.
  • the blocking portion 7 is removed from the outer annular member 10 together with the treatment instrument.
  • the treatment instrument introducing portion 6 is extracted from the retractor 5. Further, by moving the pulling member 8 in the direction away from the retracting portion 4, the inner annular member 9 is pulled out from the body cavity 3 together with the retracting member 11 via the string-like member T.
  • the treatment instrument introduction unit 6 since the treatment instrument introduction unit 6 is made of an elastic material, the treatment instrument introduction unit 6 can cope with external force with high followability.
  • the cylindrical portion 22 of the treatment instrument introduction section 6 has a diameter that allows three treatment instruments to be passed together, for example, two bending forceps are introduced into the body cavity 3 as treatment instruments by the body cavity access instrument 1. Even so, it is possible to maintain a high degree of freedom in the insertion / extraction operation and the turning operation of each bending forceps.
  • the blocking part 7 can maintain airtightness even if a plurality of treatment tools are passed through the insertion part 21, it is not necessary to ensure airtightness by using a trocar check valve. For this reason, a treatment tool can be directly passed through the closing part 7 without using a trocar. Therefore, the operability is not deteriorated due to the mutual interference (fighting) of the trocar. Thereby, a some treatment tool can be arrange
  • the treatment instrument introduction section 6 is inserted into the retractor 5 before the closure section 7 is attached to the retractor 5, the treatment instrument is attached to the body cavity using a trocar even when a bending forceps is used as the treatment instrument.
  • the wound part 4 can be prevented from being damaged by the treatment tool.
  • damage of the retractable member 11 by a treatment tool can also be prevented.
  • such an effect can be obtained by a simple operation by simply inserting the treatment instrument introducing portion 6 into the retractor 5.
  • the treatment instrument introducing portion 6 that can be configured as an integrally molded product of an elastic material enables a very low cost.
  • the retracting portion 4 and the retracting member 11 can be protected.
  • the pulling member 8 used as a tab for pulling out the retracting member 11 together with the inner annular member 9 is fixed on the treatment instrument introducing portion 6 after being arranged on the retracting member 11, so that it is stable during the operation period. In this state, it can be left at the arrangement position.
  • the pulling member 8 is located outside the body in the retractor 5, and the string member T is treated from the inner annular member 9 to the retracting member 11. It arrange
  • the string-like member T is present inside the closure part 7 and the retractor 5, and is not led out from between the treatment instrument introduction part 6 and the closure part 7 or the outer annular member 10, The airtightness due to the blocking portion 7 is not impaired by the string member T.
  • FIG. 3 shows a body cavity access device according to the second embodiment of the present invention.
  • the same reference numerals are given to the same elements as those in FIG.
  • the winding direction of the retracting member 11 by the outer annular member 10 in the retractor 5 is opposite to the case of the body cavity access device 1 of FIG. 1.
  • the retracting member 11 of the retractor 5 has an isosceles triangular shape having a smaller apex angle than the case of FIG. 1 inside the outer annular member 10. A cross-sectional shape is formed.
  • the outer shape of the conical portion 28 in the treatment instrument introducing portion 27 of the body cavity access device 26 is a conical shape that matches the shape of the retracting member 11 having the cross-sectional shape.
  • the cylindrical portion 30 and the annular wall portion 29 adjacent to the conical portion 28 also have a shape and a size that match the shape of the retractor 5.
  • a pulling member 8 that is operated when the retractor 5 is removed from the retracting portion 4 is provided, and a string-like member T is provided between the pulling member 8 and the inner annular member 9.
  • the pulling member 8 is disposed in the retractor 5 in the same manner as described above, and is fixed by the treatment instrument introducing portion 6.
  • the cylindrical portion 30 of the treatment instrument introduction section 27 is slightly smaller than the diameter of the retractable section 4 opened by the retractor 5, but a treatment instrument having a diameter of about 5 [mm] is provided. It has a diameter that can be passed through all together. Therefore, as shown in FIG. 4, a plurality of bending forceps 31 is inserted into the body cavity as a treatment tool through the obstruction portion 7 and the treatment tool introduction portion 27 by the body cavity access device 26 attached to the retractable portion 4 and used. can do.
  • the degree of freedom of the insertion / extraction operation and the turning operation of each bending forceps 31 can be kept high.
  • the treatment instrument introducing portion 27 can prevent the bent portion of the bending forceps 31 from coming into contact with the retracting portion 4 and the retracting member 11 of the retractor 5 to cause damage.
  • the retracting member 11 of the retractor 5 can be wound up in the opposite direction to the case of the first embodiment.
  • FIG. 5 shows a body cavity access device according to a third embodiment of the present invention. 5, the same elements as those in FIG. 1 are denoted by the same reference numerals.
  • the treatment instrument introducing portion 6 is used as a grasping member that is grasped to pull out the inner annular member 9 disposed on the body cavity 3 side of the retracting portion 4 to the outside of the body.
  • one end of the string-like member T is fixed to the inner annular member 9, and the other end is fixed to a portion outside the body of the treatment instrument introducing portion 6 through the inside of the retracting member 11.
  • the other end of the string-like member T is fixed to the fixing portion 25 of the annular wall portion 24.
  • the length of the string-like member T is such that the other end is fixed from the portion of the inner annular member 9 to which one end is fixed in a state where the treatment instrument introducing portion 6 is inserted into the retractor 5 attached to the retracting portion 4.
  • the length is set to have a sufficient margin than the shortest length of the annular wall portion 24 reaching the fixed portion 25.
  • the string-like member T passes through the inside of the retracting member 11 to the fixing portion 25 of the treatment instrument introducing portion 6. It will be in the extended state. Therefore, most of the string-like member T is in a state of being sandwiched between the retracting member 11 and the treatment instrument introducing portion 6.
  • the treatment instrument introducing portion 6 is extracted from the retractor 5, and further moved away from the retracting portion 4, thereby the string-like member T is removed.
  • the inner annular member 9 is pulled out from the body cavity 3 together with the retracting member 11.
  • the retracting portion 4 is not damaged by the string-like member T.
  • the treatment instrument introduction unit 6 can be used as a grasping member, the configuration of the body cavity access device 32 can be simplified. Other points are the same as those in the first embodiment of FIG.
  • FIG. 7 shows a body cavity access device according to the fourth embodiment of the present invention.
  • the same elements as those in FIG. 3 or FIG. the winding direction of the retracting member 11 by the outer annular member 10 in the retractor 5 is opposite to the case of the body cavity access device 32 of FIG. 5.
  • the retracting member 11 of the retractor 5 has an isosceles triangular shape having a smaller apex angle than that of FIG. A cross-sectional shape is formed.
  • the outer shape of the conical portion 28 in the treatment instrument introducing portion 27 of the body cavity access device 33 is a conical shape that matches the shape of the retracting member 11 having the cross-sectional shape.
  • the cylindrical portion 30 adjacent to the conical portion 28 and the fixing portion 25 of the annular wall portion 29 also have a shape and dimensions that match the shape of the retractor 5.
  • Other points of the body cavity access device 33 are the same as those of the body cavity access device 32 of FIG.
  • a treatment instrument introducing portion having a shape suitable for the shape of the retractor corresponding to the winding direction of the retractable member can be employed. . Therefore, it is possible to select the desired winding direction of the retracting member or the shape of the retractor with emphasis on either the winding direction of the retracting member or the shape of the retractor.
  • FIG. 8 shows a body cavity access device according to the fifth embodiment of the present invention.
  • the same elements as those in FIG. 1 are denoted by the same reference numerals.
  • the outer annular member 10 is used as a gripping member that is gripped in order to pull out the inner annular member 9 disposed on the body cavity 3 side of the retractable portion 4 to the outside of the body.
  • one end of the string-like member T is fixed to the inner annular member 9, and the other end is fixed to the fixing portion 25 of the outer annular member 10 through the inside of the retracting member 11.
  • the length of the string-like member T is such that the other end is fixed from the portion of the inner annular member 9 to which one end is fixed in a state where the treatment instrument introducing portion 6 is inserted into the retractor 5 attached to the retracting portion 4.
  • the outer annular member 10 is set to a length that has a sufficient margin than the shortest length to the fixed portion 25 of the outer annular member 10.
  • the inner annular member 9 is disposed on the body cavity 3 side of the retractor 4, and the retractor 11 is wound around the outer annular member 10 as an axis.
  • the string-like member T is also wound up by the outer annular member 10 from the fixed portion 25 side. Thereby, the remaining portion of the string-like member T that has not been wound is in a state of extending to the inner annular member 9 through the inside of the retracting member 11.
  • the string-like member T is not led out of the body cavity access device 34 through the space between the retractor 5 and the occlusion portion 7 in a state where the body cavity access device 34 is attached to the retractable portion 4.
  • the airtightness of the body cavity access device 34 due to the occlusion portion 7 does not deteriorate.
  • the outer annular member 10 can be used as a gripping member, the configuration of the body cavity access device 34 can be simplified. Other points are the same as those in the first embodiment of FIG.
  • the retractor may not be of a type in which a part of the retracting member is wound up by the outer annular member as long as the closing part and the treatment instrument introducing part can be attached.
  • the pulling member does not need to be completely closed in a ring shape, and a part thereof may be open. Further, the pulling member does not need to be a perfect circle, and may be a polygonal shape or an elliptical shape.

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  • Health & Medical Sciences (AREA)
  • Surgery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medical Informatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pathology (AREA)
  • Molecular Biology (AREA)
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Abstract

Provided is a body cavity access tool (1), comprising a retractor (5), a funnel-shaped instrument introduction part (6), and a closing part (7). The retractor (5) further comprises an inner-side ring-shaped member (9) which is to be positioned within a body cavity (3), and an outer-side ring-shaped member (10) which is to be positioned outside the body. Both members (9, 10) are coupled with a flexible cylindrical retraction member (11). The retraction member (11) passes through a body wall (2). The instrument introduction part (6) is inserted in the retractor (5). The closing part (7) is mounted on the outer-side ring-shaped member (10). The closing part further comprises an insertion part (21). The instrument is to be inserted in the body cavity (3), passing through the insertion part (21) and the instrument introduction part (6). A handle member (8) is positioned outside the body and within the retractor (5). The handle member (8) and the inner-side ring-shaped member (9) are coupled with a thread-shaped member (T). After an operation, it is possible, by pulling upward on the handle member (8), to remove the inner-side ring-shaped member (9) from the body cavity (3).

Description

体腔アクセス器具Body cavity access device
 本発明は、体腔内にアクセスして処置を行うときに開創部に装着される処置具導入用の体腔アクセス器具に関する。 The present invention relates to a body cavity access device for introducing a treatment instrument that is attached to a retracted part when performing treatment while accessing the body cavity.
 従来、このような体腔アクセス器具として、開創部を開いた状態にするための開創器と、開創器に挿入される漏斗状の処置具導入部とを備えたものが知られている(例えば、特許文献1参照)。 Conventionally, as such a body cavity access device, one having a retractor for opening the retractor and a funnel-shaped treatment instrument introducing unit inserted into the retractor is known (for example, Patent Document 1).
 特許文献1に記載の体腔アクセス器具においては、開創器は、体腔内に配置される内側環状部材と、体外側に配置される外側環状部材と、一方の開口部に内側環状部材が固定され、他方の開口部に外側環状部材が固定された可撓性で筒状の開創部材とを備える。 In the body cavity access device described in Patent Document 1, the retractor includes an inner annular member disposed in the body cavity, an outer annular member disposed outside the body, and the inner annular member fixed to one opening. A flexible, tubular retractor member having an outer annular member fixed to the other opening.
 漏斗状の処置具導入部は、開創器を通して処置具を体腔内に導入する際の保護ライニング及び導入路として機能する。開創部に取り付けられた開創器の外側環状部材には閉塞部が取り付けられる。これにより、開創部材の体外側の開口部が閉塞される。閉塞部は、この閉塞の気密性を維持しつつ処置具を通すための挿通部を有する。 The funnel-shaped treatment instrument introduction section functions as a protective lining and introduction path when the treatment instrument is introduced into the body cavity through the retractor. A closure is attached to the outer annular member of the retractor attached to the retractor. Thereby, the opening part outside the body of the retracting member is closed. The occlusion portion has an insertion portion for allowing the treatment tool to pass while maintaining the airtightness of the occlusion.
 なお、体腔アクセス器具において使用される開創器としては、外側環状部材で巻取り可能な開創部材を有するものも知られている(例えば、特許文献2参照)。かかる開創器においては、内側環状部材が体腔内に配置された後、外側環状部材で開創部材を巻き取ることにより、開創器が開創部に固定される。 In addition, as a retractor used in a body cavity access device, one having a retractable member that can be wound with an outer annular member is known (for example, see Patent Document 2). In such a retractor, after the inner annular member is disposed in the body cavity, the retractor is wound around the outer annular member, thereby fixing the retractor to the retracted portion.
 一方、体腔アクセス器具として、上述のような内側環状部材、外側環状部材、及び開創部材を有する開創器と、外側環状部材に取り付けられる閉塞部とを備えるとともに、体腔内に配置された内側環状部材を引き出すための紐状部材を備えたものも知られている(例えば、特許文献3参照)。 On the other hand, as a body cavity access device, an inner annular member provided with a retractor having the inner annular member, the outer annular member, and the retracting member as described above, and a closing portion attached to the outer annular member, and disposed in the body cavity. There is also known one provided with a string-like member for pulling out (see, for example, Patent Document 3).
 特許文献3の体腔アクセス器具では、開創部材は、一端が外側環状部材に固定され、中間部が内側環状部材を内側にして折り返されて、他端が外側環状部材の外側に導出される。したがって、開創部材は、開創部に装着された状態では、二重になっている。この状態において、紐状部材は、一端が内側環状部材に固定され、そこから二重になった開創部材の間を経て、外側環状部材の外周側から、開創器の体外側に延出される。 In the body cavity access device of Patent Document 3, one end of the retracting member is fixed to the outer annular member, the intermediate portion is folded back with the inner annular member inside, and the other end is led out of the outer annular member. Therefore, the retracting member is doubled when mounted on the retracting portion. In this state, one end of the string-like member is fixed to the inner annular member, and extends from the outer peripheral side of the outer annular member to the outside of the retractor body through a doubled retracting member.
 紐状部材は、その一端が閉塞部の枠に固定され、これを起点として、二重の開創部材の外側を、内側環状部材側の端部で折り返しつつ通過し、他端側が開創器の体外側に延出している場合もある。開創器の体外側に延出した紐状部材の端部は、リング部材に固定され、又はフリー状態とされる。紐状部材の延出した端部を引き上げることにより、開創部を通して内側環状部材を、体腔内から体外へ取り出すことができる。 One end of the string-like member is fixed to the frame of the closing portion, and starting from this, the outside of the double retractable member passes while being folded back at the end on the inner annular member side, and the other end is the body of the retractor It may extend outward. The end of the string-like member extending to the outside of the retractor is fixed to the ring member or is in a free state. By pulling up the extended end of the string-like member, the inner annular member can be taken out of the body cavity from the body cavity through the retracting portion.
特開2010-207579号公報JP 2010-207579 A 特開2013-55993号公報JP 2013-55993 A 特表2009-501045号公報Special table 2009-501045 gazette
 上記の特許文献1の体腔アクセス器具や、これに特許文献2の開創器を適用したものにおいても、特許文献3におけるような紐状部材を採用し、内側環状部材を、体腔内から容易に取り出すことができるようにするのが好ましいと考えられる。 Even in the above-described body cavity access device of Patent Document 1 and the retractor of Patent Document 2 applied thereto, a string-like member as in Patent Document 3 is adopted, and the inner annular member is easily taken out from the body cavity. It would be preferable to be able to do so.
 この場合、特許文献1や2の開創器の開創部材は、特許文献3の開創部材のように二重に折り畳まれるものではないので、体腔アクセス器具を開創部に装着するとき、紐状部材は、開創部材の外側又は内側を経て開創部の上方に導出されることになる。紐状部材が開創部材の外側を経て導出される場合には、紐状部材が開創部と直接接触する。このため、内側環状部材を紐状部材で引っ張り出すとき、紐状部材により開創部に損傷を与えるおそれがある。 In this case, since the retracting member of the retractor of Patent Documents 1 and 2 is not double-folded like the retracting member of Patent Document 3, when the body cavity access device is attached to the retracting part, the string member is Then, it is led out above the retracting portion through the outside or inside of the retracting member. When the string member is led out through the outside of the retracting member, the string member is in direct contact with the retracting portion. For this reason, when pulling out an inner side annular member with a string-like member, there exists a possibility that a wound part may be damaged by a string-like member.
 一方、紐状部材が開創部材の内側を経て導出される場合には、開創部材の体外側端部に固定された外側環状部材と閉塞部との間を通して紐状部材が導出されることになるので、閉塞部による気密性が劣化するおそれがある。 On the other hand, when the string-like member is led out through the inside of the retracting member, the string-like member is led out between the outer annular member fixed to the body outer end of the retracting member and the closing portion. Therefore, there is a possibility that the airtightness due to the blocking portion is deteriorated.
 開創部材の内側に配置される処置具導入部の内側を経て紐状部材を導出することも考えられるが、その場合にも、処置具導入部と閉塞部や外側環状部材との間を通して紐状部材が導出されることになるので、同様に気密性の劣化が懸念される。 It is also conceivable that the string-like member is led out through the inside of the treatment instrument introduction portion arranged inside the retracting member, but in that case, the string-like member passes between the treatment instrument introduction portion and the blocking portion or the outer annular member. Since the member is derived, there is a concern that the airtightness deteriorates similarly.
 本発明の目的は、かかる従来技術の課題に鑑み、気密性の劣化や開創部の損傷を生じさせることなく紐状部材を介して内側環状部材を取り出すことができる体腔アクセス器具を提供することにある。 An object of the present invention is to provide a body cavity access device that can take out an inner annular member via a string-like member without causing deterioration of airtightness and damage of a retracted portion in view of the problems of the conventional technology. is there.
 本発明の体腔アクセス器具は、開創部の体腔側に配置される内側環状部材と、該開創部の体外側に配置される外側環状部材と、該内側環状部材が一方の開口部に固定され、該外側環状部材が他方の開口部に固定された可撓性で筒状の開創部材とを有する開創器と、前記開創部に装着された前記開創器に挿入され、処置具の体腔内への導入路を構成する漏斗状の処置具導入部と、前記処置具が気密を保持した状態で通される挿通部を有し、前記外側環状部材に取り付けられて前記開創器を気密に閉塞する閉塞部と、前記開創部の体腔側に配置された前記内側環状部材を体外に引き出すために把持される把持部材と、一端が前記内側環状部材に固定され、他端が前記把持部材に固定された紐状部材とを備え、前記開創部に装着された前記開創器に前記処置具導入部が挿入され、前記開創器が前記閉塞部により閉塞された状態で、前記把持部材は、前記開創器内の体外側に位置し、かつ前記紐状部材は、前記内側環状部材から前記開創部材と前記処置具導入部との間を経て前記把持部材に到るように配置されることを特徴とする。 The body cavity access device of the present invention has an inner annular member disposed on the body cavity side of the retracting portion, an outer annular member disposed on the outer side of the retracting portion, and the inner annular member fixed to one opening, A retractor having a flexible and tubular retractor member in which the outer annular member is fixed to the other opening, and inserted into the retractor mounted on the retractor, and into the body cavity of the treatment instrument A funnel-shaped treatment instrument introduction section constituting an introduction path and an insertion section through which the treatment instrument is passed in an airtight state, and is attached to the outer annular member to block the retractor in an airtight manner A gripping member that is gripped to pull out the inner annular member disposed on the body cavity side of the retracting portion, and one end is fixed to the inner annular member, and the other end is fixed to the gripping member The retractor comprising a string-like member and attached to the retracting portion In a state where the treatment instrument introducing portion is inserted and the retractor is closed by the closing portion, the gripping member is located outside the body in the retractor, and the string-like member is the inner annular member It arrange | positions so that it may reach to the said holding member through between the said retractable member and the said treatment tool introduction part.
 本発明において、体腔アクセス器具を開創部に装着する際には、まず、開創器の内側環状部材と把持部材との間の紐状部材が開創器の開創部材の内側を通り、把持部材が体外側に配置された状態で、開創部に開創器を装着する。このとき、把持部材は、開創器内の体外側に配置される。そして、処置具導入部を、開創器の体外側から開創器に挿入する。 In the present invention, when the body cavity access device is attached to the retracting portion, first, the string-like member between the inner annular member of the retractor and the gripping member passes through the inside of the retracting member of the retractor, and the gripping member is the body. A retractor is attached to the retracting portion in a state of being arranged on the outside. At this time, the gripping member is disposed outside the body in the retractor. Then, the treatment instrument introducing portion is inserted into the retractor from the outside of the retractor body.
 これにより、紐状部材が、把持部材から開創器と処置具導入部との間を経て内側環状部材に到る経路上に配置された状態となる。次に、処置具が挿通部を通して配置された閉塞部を、処置具の先端側を処置具導入部に挿入しながら、開創器の外側環状部材に取り付ける。これにより、体腔アクセス器具の開創部への装着が完了する。 Thus, the string-like member is placed on the path from the grasping member to the inner annular member through the retractor and the treatment instrument introducing portion. Next, the closure part in which the treatment tool is disposed through the insertion part is attached to the outer annular member of the retractor while the distal end side of the treatment tool is inserted into the treatment tool introduction part. This completes the mounting of the body cavity access device to the retracted portion.
 この間、開創器が閉塞部により閉塞された状態では、把持部材は、該閉塞により気密が保持された部分に位置し、かつ紐状部材は、内側環状部材から開創部材と処置具導入部との間を経て把持部材に到るように配置される。このため、紐状部材は、外側環状部材と閉塞部との間を介して開創器の外側に導出されることはない。したがって、閉塞部が開創器を閉塞した状態では、体腔側の外部に対する気密性が劣化することはない。 During this time, in a state where the retractor is closed by the closing portion, the gripping member is located in a portion where the airtightness is maintained by the closing, and the string-like member is connected to the retracting member and the treatment instrument introducing portion from the inner annular member. It arrange | positions so that it may reach a holding member after a gap. For this reason, a string-like member is not derived | led-out outside the retractor through between an outer side annular member and an obstruction | occlusion part. Therefore, in a state where the occlusion portion closes the retractor, the airtightness with respect to the outside on the body cavity side does not deteriorate.
 開創部から体腔アクセス器具を取り外す際には、まず、処置具とともに閉塞部を外側環状部材から取り外す。その後、処置具導入部を開創器から抜き取り、さらに把持部材を開創部から離れる方向に移動させることにより、紐状部材を介して、体腔内の内側環状部材を開創部材とともに体外に引き出す。 When removing the body cavity access device from the retracted part, first, the occlusion part is removed from the outer annular member together with the treatment instrument. Thereafter, the treatment instrument introducing portion is extracted from the retractor, and the gripping member is moved away from the retracting portion, whereby the inner annular member in the body cavity is pulled out of the body together with the retracting member via the string member.
 このとき、紐状部材は、開創部材の内側に位置し、開創部に直接接触することはないので、開創部に損傷を与えることはない。したがって、本発明によれば、気密性の劣化や開創部の損傷を生じさせることなく、紐状部材を介して内側環状部材を取り出すことができる。 At this time, the string-like member is located inside the retracting member and does not directly contact the retracting portion, so that the retracting portion is not damaged. Therefore, according to the present invention, it is possible to take out the inner annular member via the string-like member without causing deterioration of airtightness and damage to the wound portion.
 本発明において、前記把持部材は、前記開創部に装着された前記開創器の体外側に開創部と同心状に配置され、その後に該開創器に挿入される前記処置具導入部と該開創器の前記開創部材との間に挟まれて固定される環状の引手部材で構成されてもよい。 In the present invention, the grasping member is disposed concentrically with the retracting portion on the outside of the retractor mounted on the retracting portion, and then inserted into the retractor and the retractor It may be comprised by the annular pulling member fixed by being pinched | interposed between the said retracting members.
 この場合、体腔アクセス器具を取り外す際には、処置具導入部を開創器から抜き取った後、引手部材を開創部から離れる方向に移動させることにより、内側環状部材が体外に引き出される。したがって、引手部材により確実に内側環状部材を取り出すことができる。 In this case, when removing the body cavity access device, after removing the treatment instrument introducing portion from the retractor, the inner annular member is pulled out of the body by moving the handle member in a direction away from the retracting portion. Therefore, the inner annular member can be reliably taken out by the pulling member.
 本発明において、前記把持部材は、前記処置具導入部で構成され、前記紐状部材の他端は、該処置具導入部の体外側の部分に固定されてもよい。これによれば、処置具導入部を把持部材としても利用できるので、体腔アクセス器具の構成を簡便なものとすることができる。 In the present invention, the gripping member may be constituted by the treatment instrument introducing portion, and the other end of the string-like member may be fixed to a portion outside the body of the treatment instrument introducing portion. According to this, since the treatment instrument introducing portion can be used as a grasping member, the configuration of the body cavity access device can be simplified.
 本発明において、前記把持部材は、前記外側環状部材で構成され、前記紐状部材の他端は、該外側環状部材に固定されてもよい。これによれば、外側環状部材を把持部材としても利用できるので、体腔アクセス器具の構成を簡便なものとすることができる。 In the present invention, the gripping member may be constituted by the outer annular member, and the other end of the string-like member may be fixed to the outer annular member. According to this, since the outer annular member can also be used as a gripping member, the configuration of the body cavity access device can be simplified.
 本発明において、前記開創器は、前記内側環状部材が前記開創部の体腔側に配置され、前記外側環状部材が前記開創部の体外側に配置された状態で、前記外側環状部材を巻取り軸として一方又は他方の巻取り方向に前記開創部材の体外側の一部を巻き取ることによって前記開創部に固定されるものであり、前記処置具導入部は、前記巻取り方向に応じて前記開創部材が呈する形状に適合した形状を有してもよい。 In the present invention, the retractor is configured such that the inner annular member is disposed on the body cavity side of the retracting portion, and the outer annular member is disposed on the body outer side of the retracting portion, and the outer annular member is wound around the winding shaft. As described above, the wound member is fixed to the wound part by winding a part of the wound member outside the body in one or the other winding direction, and the treatment instrument introducing part is arranged according to the winding direction. You may have the shape suitable for the shape which a member exhibits.
 これによれば、処置具導入部が、開創部材の巻取り方向に対応する開創器の形状に適合した形状を有するので、開創部材の巻取り方向又は開創器の形状を任意に選択することができる。 According to this, since the treatment instrument introducing portion has a shape that matches the shape of the retractor corresponding to the winding direction of the retracting member, it is possible to arbitrarily select the winding direction of the retracting member or the shape of the retractor. it can.
本発明の第1実施形態に係る体腔アクセス器具が患者の開創部に装着された状態を示す斜視断面図である。FIG. 2 is a perspective cross-sectional view showing a state where the body cavity access device according to the first embodiment of the present invention is attached to a patient's wound part. 図1の体腔アクセス器具の開創器が開創部に装着されたとき又は開創器を開創部から取り外すときの様子を示す断面図である。It is sectional drawing which shows a mode when the retractor of the body cavity access device of FIG. 1 is mounted | worn with a retractor, or when removing a retractor from a retractor. 本発明の第2実施形態に係る体腔アクセス器具が患者の開創部に装着された状態を示す断面図である。It is sectional drawing which shows the state with which the body cavity access device concerning 2nd Embodiment of this invention was mounted | worn with the patient's wound part. 図3の体腔アクセス器具を介して屈曲鉗子を用いる様子を示す断面図である。It is sectional drawing which shows a mode that a bending forceps is used via the body cavity access device of FIG. 本発明の第3実施形態に係る体腔アクセス器具が患者の開創部に装着された状態を示す斜視断面図である。It is a perspective sectional view showing the state where the body cavity access device concerning a 3rd embodiment of the present invention was equipped in the retracted part of a patient. 図5の体腔アクセス器具の開創器が開創部に装着されたとき又は開創器を開創部から取り外すときの様子を示す断面図である。FIG. 6 is a cross-sectional view showing a state where the retractor of the body cavity access device of FIG. 5 is attached to the retractor or when the retractor is removed from the retractor. 本発明の第4実施形態に係る体腔アクセス器具が患者の開創部に装着された状態を示す断面図である。It is sectional drawing which shows the state with which the body cavity access device concerning 4th Embodiment of this invention was mounted | worn with the patient's wound part. 本発明の第5実施形態に係る体腔アクセス器具が患者の開創部に装着された状態を示す斜視断面図である。It is a perspective sectional view showing the state where the body cavity access device concerning a 5th embodiment of the present invention was equipped in the retracted part of a patient.
 以下、図面を用いて本発明の実施形態を説明する。図1に示すように、第1実施形態に係る体腔アクセス器具1は、患者の体壁2に設けられて体腔3内に通じる開創部4を開いた状態に維持するための開創器5と、開創器5に挿入される処置具導入部6と、開創器5を体外側において閉塞するための閉塞部7と、開創器5を開創部4から取り外すときに操作される引手部材8とを備える。 Hereinafter, embodiments of the present invention will be described with reference to the drawings. As shown in FIG. 1, a body cavity access device 1 according to the first embodiment includes a retractor 5 that is provided on a body wall 2 of a patient and that maintains a retractor 4 that leads into the body cavity 3 in an open state. A treatment instrument introducing portion 6 to be inserted into the retractor 5, a closing portion 7 for closing the retractor 5 outside the body, and a pulling member 8 that is operated when the retractor 5 is removed from the retractable portion 4. .
 開創器5は、開創部4の体腔3側に配置される内側環状部材9と、開創部4の体外側に配置される外側環状部材10と、一方の開口部に内側環状部材9が固定され、他方の開口部に外側環状部材10が固定された可撓性の開創部材11とを有する。引手部材8は、開創部4の体腔側に配置された内側環状部材9を体外に引き出すために把持される把持部材として機能する。 The retractor 5 includes an inner annular member 9 disposed on the body cavity 3 side of the retracting portion 4, an outer annular member 10 disposed on the outer side of the retracting portion 4, and the inner annular member 9 fixed to one opening. And a flexible retracting member 11 having the outer annular member 10 fixed to the other opening. The pulling member 8 functions as a gripping member that is gripped in order to pull out the inner annular member 9 disposed on the body cavity side of the retracting portion 4 to the outside of the body.
 外側環状部材10及び内側環状部材9は、いずれも所定の外力により弾性変形自在となっており、自由状態では円形となり、典型的には、ほぼ同一の直径を有する。開創部材11は、例えば、ポリウレタンからなる弾性を有する薄膜で形成される。 The outer annular member 10 and the inner annular member 9 are both elastically deformable by a predetermined external force, are circular in a free state, and typically have substantially the same diameter. The retracting member 11 is formed of an elastic thin film made of polyurethane, for example.
 開創器5が開創部4に装着されていない状態では、開創部材11は、筒状の形態を有し、外側環状部材10及び内側環状部材9の外径よりも小さい直径を有する。 In a state where the retractor 5 is not mounted on the retracting portion 4, the retracting member 11 has a cylindrical shape and has a diameter smaller than the outer diameter of the outer annular member 10 and the inner annular member 9.
 外側環状部材10は、例えば、シリコーンゴムで構成され、ほぼ長方形の断面形状を有する。内側環状部材9は、例えば、シリコーンゴムで構成され、ほぼ円形の断面形状を有する。開創器5は、内側環状部材9が開創部4の体腔側に配置され、外側環状部材10が開創部4の体外側に配置された状態で、外側環状部材10を巻取り軸として開創部材11の体外側の一部を巻き取ることにより、開創部材11の実質的な長さを体壁2の厚さに対応させながら、開創部4に装着することができる。 The outer annular member 10 is made of, for example, silicone rubber and has a substantially rectangular cross-sectional shape. The inner annular member 9 is made of, for example, silicone rubber and has a substantially circular cross-sectional shape. The retractor 5 has the inner annular member 9 disposed on the body cavity side of the retracting portion 4 and the outer annular member 10 disposed on the body outer side of the retracting portion 4, and the retracting member 11 using the outer annular member 10 as a winding shaft. By winding a part of the outside of the body, the retractable member 11 can be attached to the retracting portion 4 while the substantial length of the retracting member 11 corresponds to the thickness of the body wall 2.
 閉塞部7は、円盤状の天蓋部材12と、天蓋部材12の表面及び裏面にそれぞれ積層された第1膜部材17及び第2膜部材18と、第1膜部材17及び第2膜部材18が積層された天蓋部材12を外側環状部材10に気密に装着するための装着リング13とを備える。 The blocking portion 7 includes a disc-shaped canopy member 12, a first film member 17 and a second film member 18 stacked on the front and back surfaces of the canopy member 12, and a first film member 17 and a second film member 18, respectively. A mounting ring 13 for mounting the stacked canopy member 12 on the outer annular member 10 in an airtight manner is provided.
 天蓋部材12は、可撓性を有する軟質樹脂で構成され、外側環状部材10の内径と同程度の直径を有する2枚のシート部材(ゲルシート)14a及び14bを積層して形成される。天蓋部材12は、3枚以上のシート部材で構成されてもよい。軟質樹脂としては、例えば、シリコーンゴム、ポリウレタン、又はポリエチレンを用いることができる。 The canopy member 12 is made of a soft resin having flexibility, and is formed by laminating two sheet members (gel sheets) 14 a and 14 b having the same diameter as the inner diameter of the outer annular member 10. The canopy member 12 may be composed of three or more sheet members. As the soft resin, for example, silicone rubber, polyurethane, or polyethylene can be used.
 シート部材14a及び14bは、円柱状の処置具を体腔3内に導入するために厚さ方向に貫通したスリット部16を複数箇所に備える。シート部材14aの各スリット部16は、シート部材14bの対応するスリット部16と十字をなして直交する。 The sheet members 14a and 14b are provided with a plurality of slit portions 16 penetrating in the thickness direction in order to introduce the columnar treatment instrument into the body cavity 3. Each slit portion 16 of the sheet member 14a is orthogonal to the corresponding slit portion 16 of the sheet member 14b in a cross shape.
 第1膜部材17及び第2膜部材18は、伸縮性を有するとともにシート部材14a及び14bを構成する軟質樹脂に対して滑り性を有する別の軟質樹脂からなり、天蓋部材12の直径よりも大きい直径を有する。該別の軟質樹脂としては、例えば、ポリウレタン、ポリ塩化ビニル、又はポリエチレンを用いることができる。第1膜部材17及び第2膜部材18は、その間で天蓋部材12を挟持するように、その端部が互いに接着される。 The first film member 17 and the second film member 18 are made of another soft resin that has elasticity and is slidable with respect to the soft resin constituting the sheet members 14a and 14b, and is larger than the diameter of the canopy member 12. Has a diameter. As this another soft resin, for example, polyurethane, polyvinyl chloride, or polyethylene can be used. The end portions of the first film member 17 and the second film member 18 are bonded to each other so as to sandwich the canopy member 12 therebetween.
 第1膜部材17は、シート部材14aの各スリット部16の中心位置と重なる位置に、各スリット部16に通される処置具を通過させるための円孔19を備える。円孔19は、処置具の直径の40~90%の範囲の直径を有する。 The first film member 17 is provided with a circular hole 19 for allowing a treatment instrument passed through each slit portion 16 to pass through at a position overlapping the center position of each slit portion 16 of the sheet member 14a. The circular hole 19 has a diameter in the range of 40 to 90% of the diameter of the treatment instrument.
 第2膜部材18は、シート部材14bの各スリット部16に対応する位置に、各スリット部16に通される処置具を通過させるためのスリット部20を備える。スリット部20は、シート部材14bの対応するスリット部16と直交し、スリット部16と同程度の長さを有する。 The second film member 18 includes a slit portion 20 for passing a treatment instrument passed through each slit portion 16 at a position corresponding to each slit portion 16 of the sheet member 14b. The slit portion 20 is orthogonal to the corresponding slit portion 16 of the sheet member 14 b and has the same length as the slit portion 16.
 第1膜部材17の円孔19、シート部材14a及び14bのスリット部16、及び第2膜部材18のスリット部20により、気密性を維持しつつ処置具が通される挿通部21が構成される。 The circular hole 19 of the first membrane member 17, the slit portion 16 of the sheet members 14a and 14b, and the slit portion 20 of the second membrane member 18 constitute an insertion portion 21 through which the treatment instrument is passed while maintaining airtightness. The
 装着リング13は、例えば、天然ゴムやポリウレタンで構成され、断面がほぼU字形状であって、開創器5の外側環状部材10に装着可能である。装着リング13は、外側環状部材10に装着されたときに外側環状部材10の体外側に天蓋部材12が位置するように、第1膜部材17及び第2膜部材18の端部が接着される。 The mounting ring 13 is made of, for example, natural rubber or polyurethane, has a substantially U-shaped cross section, and can be mounted on the outer annular member 10 of the retractor 5. The mounting ring 13 is bonded to the end portions of the first film member 17 and the second film member 18 so that the canopy member 12 is positioned outside the body of the outer annular member 10 when the mounting ring 13 is mounted on the outer annular member 10. .
 処置具導入部6は、開創部4に装着された開創器5に挿入され、開創部材11を保護しつつ、処置具の体腔内への導入路を構成する。処置具導入部6は、漏斗状の形状を有し、漏斗の出口側に当たる筒状部22と、筒状部22の入り口側に隣接した円錐部23と、円錐部23の体外側に隣接する環状壁部24とを備える。 The treatment instrument introducing unit 6 is inserted into the retractor 5 attached to the retracting unit 4 and constitutes an introduction path into the body cavity of the treatment instrument while protecting the retracting member 11. The treatment instrument introducing portion 6 has a funnel shape, and is adjacent to the cylindrical portion 22 that contacts the outlet side of the funnel, the conical portion 23 adjacent to the inlet side of the cylindrical portion 22, and the outer side of the conical portion 23. And an annular wall portion 24.
 処置具導入部6は、開創部4に装着された開創器5及びこれを閉塞する閉塞部7が形成する空間内にほぼ収まる形状及び寸法を有する。したがって、環状壁部24は、開創器5の外側環状部材10よりやや小さい径及びやや短い軸方向長さを有する。 The treatment instrument introducing portion 6 has a shape and a size that are substantially contained in a space formed by the retractor 5 attached to the retracting portion 4 and the closing portion 7 that closes the retractor 5. Therefore, the annular wall 24 has a slightly smaller diameter and a slightly shorter axial length than the outer annular member 10 of the retractor 5.
 筒状部22は、開創器5で開かれた開創部4の径よりやや小さいが、導入される処置具の外径よりも大きい内径を有する。例えば、直径が5[mm]程度の処置具を3本まとめて通すことができる内径を有する。筒状部22の長さは、体壁2の厚さと同程度である。処置具導入部6を構成する素材としては、ポリウレタン、ポリ塩化ビニル、ポリエチレン等の弾性素材が用いられる。 The cylindrical portion 22 has an inner diameter that is slightly smaller than the diameter of the retractable portion 4 opened by the retractor 5, but larger than the outer diameter of the treatment instrument to be introduced. For example, it has an inner diameter that allows three treatment tools having a diameter of about 5 mm to pass through. The length of the cylindrical portion 22 is approximately the same as the thickness of the body wall 2. An elastic material such as polyurethane, polyvinyl chloride, or polyethylene is used as the material constituting the treatment instrument introduction unit 6.
 図2に示すように、紐状部材Tは、開創器5の内側環状部材9に一端が固定され、他端は、引手部材8の固定部25に固定される。そして、開創部4に対する開創器5の装着は、紐状部材Tが開創器5の内側を通り、引手部材8が外側環状部材10の上方に離された状態で行われる。 2, one end of the string-like member T is fixed to the inner annular member 9 of the retractor 5, and the other end is fixed to the fixing portion 25 of the pulling member 8. The retractor 5 is attached to the retractable portion 4 in a state in which the string-like member T passes through the inside of the retractor 5 and the handle member 8 is separated above the outer annular member 10.
 紐状部材Tの長さは、開創部4に装着された開創器5に対して引手部材8が図2中の2点鎖線で示されるように配置された状態において、とり得る最短の長さよりも十分に余裕を有する長さに設定される。 The length of the string-like member T is shorter than the shortest possible length in the state where the handle member 8 is arranged as shown by the two-dot chain line in FIG. 2 with respect to the retractor 5 attached to the retracting portion 4. Is set to a length having a sufficient margin.
 この構成において、体腔アクセス器具1を用いて患者の手術を行う場合には、まず、予め設けられた開創部4に開創器5を装着する。すなわち、紐状部材Tが開創器5の内側を通り、引手部材8が外側環状部材10の上方に離された状態で、開創器5の内側環状部材9を撓めて開創部4から体腔3内に挿入し、体腔3内で展開させる。これにより、内側環状部材9が、開創部4の体腔3側に配置され、開創器5の外側環状部材10は、体外側に位置した状態となる。 In this configuration, when performing a surgical operation on a patient using the body cavity access device 1, first, the retractor 5 is attached to the retractable portion 4 provided in advance. That is, in a state where the string-like member T passes through the inside of the retractor 5 and the handle member 8 is separated above the outer annular member 10, the inner annular member 9 of the retractor 5 is bent and the body cavity 3 extends from the retracted portion 4. And inserted into the body cavity 3. Thereby, the inner side annular member 9 is arrange | positioned at the body cavity 3 side of the retracting part 4, and the outer side annular member 10 of the retractor 5 will be in the state located in the body outer side.
 そして、外側環状部材10を把持し、外側環状部材10を軸として開創部材11を巻き取ることにより、開創部材11を径方向に拡張して所望の大きさの直径を有する開口部を形成するとともに、開創部材11の長さを体壁2の厚さに対応させる。これにより、開創器5の装着が完了し、図2に示すような状態となる。 Then, by holding the outer annular member 10 and winding the retracting member 11 around the outer annular member 10 as an axis, the retracting member 11 is expanded in the radial direction to form an opening having a desired diameter. The length of the retracting member 11 is made to correspond to the thickness of the body wall 2. Thereby, mounting | wearing of the retractor 5 is completed and it will be in a state as shown in FIG.
 次に、開創部材11の体外側に位置する部分の内側に、引手部材8を、外側環状部材10や開創部4とほぼ同心となるように配置する。すなわち、引手部材8は、図2において、2点鎖線で示すような位置に配置される。 Next, the handle member 8 is arranged inside the portion located outside the body of the retracting member 11 so as to be substantially concentric with the outer annular member 10 and the retracting portion 4. That is, the pulling member 8 is arranged at a position as shown by a two-dot chain line in FIG.
 次に、処置具導入部6を、開創器5に挿入する。このとき、開創部材11で形成されている開口部に、処置具導入部6の筒状部22が挿入される。これにより、処置具導入部6は、開創器5の体外側から開創部4の部分に到る領域に適合(フィット)した状態となる。また、引手部材8は、開創器5と処置具導入部6との間に挟まれて固定され、紐状部材Tは、引手部材8の固定部25を起点として、開創器5と処置具導入部6との間を通り、さらに開創器5の内側を通って内側環状部材9に到る経路上に配置された状態となる。 Next, the treatment instrument introducing portion 6 is inserted into the retractor 5. At this time, the cylindrical portion 22 of the treatment instrument introducing portion 6 is inserted into the opening formed by the retracting member 11. As a result, the treatment instrument introduction unit 6 is in a state of being fitted (fit) to a region extending from the outside of the retractor 5 to the portion of the retracting unit 4. Further, the pulling member 8 is sandwiched and fixed between the retractor 5 and the treatment instrument introducing portion 6, and the string-like member T is introduced from the retractor 5 and the treatment instrument starting from the fixing portion 25 of the pulling member 8. It will be in the state arrange | positioned on the path | route which passes between between the parts 6 and further passes through the inside of the retractor 5, and reaches the inner annular member 9.
 次に、手術用の2、3本の処置具が挿通部21を通して配置された閉塞部7を、外側環状部材10に取り付ける。すなわち、装着リング13で外側環状部材10を被覆することにより、閉塞部7を開創器5に装着する。この装着は、各処置具の先端側を束ねて処置具導入部6の筒状部22から該先端側が体腔3内に導入されるようにして行われる。 Next, the closed portion 7 in which a few treatment tools for surgery are arranged through the insertion portion 21 is attached to the outer annular member 10. That is, the closure 7 is attached to the retractor 5 by covering the outer annular member 10 with the attachment ring 13. This attachment is performed such that the distal end sides of the respective treatment instruments are bundled and the distal end side is introduced into the body cavity 3 from the cylindrical portion 22 of the treatment instrument introduction section 6.
 これにより、体腔3内が気密状態となり、各処置具を用いた手術を行うことができる状態となる。手術が行われる間、紐状部材Tは、図1のように、閉塞部7の体腔3側に位置するので、従来のように紐状部材Tの存在によって体腔3の気密状態が劣化するおそれはない。また、この間、処置具導入部6により、処置具による開創部材11や開創部4の損傷が防止される。 Thereby, the inside of the body cavity 3 is in an airtight state, and it becomes possible to perform an operation using each treatment instrument. During the operation, the string-like member T is located on the side of the body cavity 3 of the obstruction 7 as shown in FIG. 1, so that the airtight state of the body cavity 3 deteriorates due to the presence of the string-like member T as in the prior art. It is not. In addition, during this time, the treatment tool introduction unit 6 prevents the wound member 11 and the wound part 4 from being damaged by the treatment tool.
 手術が完了し、体腔アクセス器具1を開創部4から取り外す際には、まず、閉塞部7を、処置具とともに、外側環状部材10から取り外す。次に、処置具導入部6を開創器5から抜き取る。さらに、引手部材8を開創部4から離れる方向に移動させることにより、紐状部材Tを介して、内側環状部材9を、開創部材11とともに体腔3内から引き出す。 When the operation is completed and the body cavity access device 1 is removed from the retracting portion 4, first, the blocking portion 7 is removed from the outer annular member 10 together with the treatment instrument. Next, the treatment instrument introducing portion 6 is extracted from the retractor 5. Further, by moving the pulling member 8 in the direction away from the retracting portion 4, the inner annular member 9 is pulled out from the body cavity 3 together with the retracting member 11 via the string-like member T.
 このとき、紐状部材Tが常に開創部材11の内側に位置するので、紐状部材Tにより開創部4が損傷を受けることはない。内側環状部材9の取り出しが終了すると、体腔アクセス器具1の取り外しが完了する。 At this time, since the string-like member T is always located inside the retracting member 11, the retracting portion 4 is not damaged by the string-like member T. When the removal of the inner annular member 9 is completed, the removal of the body cavity access device 1 is completed.
 本実施形態によれば、処置具導入部6が弾性素材で構成されるので、処置具導入部6は、外力に対して高い追従性で対応することができる。また、処置具導入部6の筒状部22が、処置具を3本まとめて通すことができる径を有するので、体腔アクセス器具1により処置具として例えば2本の屈曲鉗子を体腔3内に導入しても、各屈曲鉗子の挿抜動作や旋回動作の自由度を高く維持することができる。 According to this embodiment, since the treatment instrument introduction unit 6 is made of an elastic material, the treatment instrument introduction unit 6 can cope with external force with high followability. In addition, since the cylindrical portion 22 of the treatment instrument introduction section 6 has a diameter that allows three treatment instruments to be passed together, for example, two bending forceps are introduced into the body cavity 3 as treatment instruments by the body cavity access instrument 1. Even so, it is possible to maintain a high degree of freedom in the insertion / extraction operation and the turning operation of each bending forceps.
 また、閉塞部7は、挿通部21を経て複数の処置具が通されても気密性を維持できるので、トロカーの逆止弁を利用して気密性を確保する必要がない。このため、トロカーを介することなく直接、処置具を閉塞部7に通すことができる。したがって、トロカーの相互干渉(ファイティング)による操作性の悪化を招来することはない。これにより、閉塞部7を介して複数の処置具を近接させて配置し、処置具の操作性を向上させることができる。 Moreover, since the blocking part 7 can maintain airtightness even if a plurality of treatment tools are passed through the insertion part 21, it is not necessary to ensure airtightness by using a trocar check valve. For this reason, a treatment tool can be directly passed through the closing part 7 without using a trocar. Therefore, the operability is not deteriorated due to the mutual interference (fighting) of the trocar. Thereby, a some treatment tool can be arrange | positioned through the obstruction | occlusion part 7, and the operativity of a treatment tool can be improved.
 また、閉塞部7を開創器5に装着する前に処置具導入部6を開創器5に挿入するようにしたので、処置具として屈曲鉗子を用いる場合でも、トロカーを利用して処置具を体腔3内に挿入する場合と同様に、処置具による開創部4の損傷を防止することができる。また、処置具による開創部材11の損傷も防止することができる。また、このような効果を、処置具導入部6を開創器5に挿入するだけの簡単な操作により得ることができる。 In addition, since the treatment instrument introduction section 6 is inserted into the retractor 5 before the closure section 7 is attached to the retractor 5, the treatment instrument is attached to the body cavity using a trocar even when a bending forceps is used as the treatment instrument. Similarly to the case of insertion into 3, the wound part 4 can be prevented from being damaged by the treatment tool. Moreover, damage of the retractable member 11 by a treatment tool can also be prevented. In addition, such an effect can be obtained by a simple operation by simply inserting the treatment instrument introducing portion 6 into the retractor 5.
 また、その際に、何種類かの素材や部品で構成される可撓性トロカーを複数利用する場合に比べて、弾性素材の一体成形品として構成できる処置具導入部6により、非常に低いコストで開創部4や開創部材11を保護することができる。 Further, at that time, compared with the case where a plurality of flexible trocars composed of several kinds of materials and parts are used, the treatment instrument introducing portion 6 that can be configured as an integrally molded product of an elastic material enables a very low cost. Thus, the retracting portion 4 and the retracting member 11 can be protected.
 また、内側環状部材9とともに開創部材11を引き出すためのタブとして利用される引手部材8は、開創部材11上に配置された後、処置具導入部6により固定されるので、手術期間中、安定した状態で、その配置位置に留置させておくことができる。 In addition, the pulling member 8 used as a tab for pulling out the retracting member 11 together with the inner annular member 9 is fixed on the treatment instrument introducing portion 6 after being arranged on the retracting member 11, so that it is stable during the operation period. In this state, it can be left at the arrangement position.
 また、体腔アクセス器具1が開創部4に装着された状態では、引手部材8は、開創器5内の体外側に位置し、かつ紐状部材Tは、内側環状部材9から開創部材11と処置具導入部6との間を経て引手部材8に到るように配置される。このため、紐状部材Tが、閉塞部7及び開創器5の内側に存在し、処置具導入部6と閉塞部7や外側環状部材10との間から外部に導出されることがないので、閉塞部7による気密性が紐状部材Tによって損なわれることもない。 Further, in the state where the body cavity access device 1 is mounted on the retracting portion 4, the pulling member 8 is located outside the body in the retractor 5, and the string member T is treated from the inner annular member 9 to the retracting member 11. It arrange | positions so that it may reach the handle member 8 through between the tool introduction parts 6. FIG. For this reason, the string-like member T is present inside the closure part 7 and the retractor 5, and is not led out from between the treatment instrument introduction part 6 and the closure part 7 or the outer annular member 10, The airtightness due to the blocking portion 7 is not impaired by the string member T.
 図3は、本発明の第2実施形態に係る体腔アクセス器具を示す。図3において、図1中の要素と同一の要素については同一の符号が付されている。この体腔アクセス器具26では、図1の体腔アクセス器具1の場合とは、開創器5における外側環状部材10による開創部材11の巻き取り方向が逆である。このため、体腔アクセス器具26が開創部4に装着された状態では、開創器5の開創部材11は、外側環状部材10の内側において、図1の場合よりも頂角が小さい二等辺三角形状の断面形状を形成する。 FIG. 3 shows a body cavity access device according to the second embodiment of the present invention. In FIG. 3, the same reference numerals are given to the same elements as those in FIG. In this body cavity access device 26, the winding direction of the retracting member 11 by the outer annular member 10 in the retractor 5 is opposite to the case of the body cavity access device 1 of FIG. 1. For this reason, in a state where the body cavity access device 26 is mounted on the retracting portion 4, the retracting member 11 of the retractor 5 has an isosceles triangular shape having a smaller apex angle than the case of FIG. 1 inside the outer annular member 10. A cross-sectional shape is formed.
 したがって、体腔アクセス器具26の処置具導入部27における円錐部28の外形は、上記断面形状を有する開創部材11の形状に適合するような円錐状のものとなっている。また、円錐部28に隣接する筒状部30及び環状壁部29も、開創器5の形状に適合した形状及び寸法を有する。 Therefore, the outer shape of the conical portion 28 in the treatment instrument introducing portion 27 of the body cavity access device 26 is a conical shape that matches the shape of the retracting member 11 having the cross-sectional shape. In addition, the cylindrical portion 30 and the annular wall portion 29 adjacent to the conical portion 28 also have a shape and a size that match the shape of the retractor 5.
 本実施形態の場合も、開創器5を開創部4から取り外すときに操作される引手部材8が設けられ、引手部材8と内側環状部材9との間に紐状部材Tが設けられる。引手部材8は、上述と同様にして開創器5内に配置され、処置具導入部6により固定される。 Also in this embodiment, a pulling member 8 that is operated when the retractor 5 is removed from the retracting portion 4 is provided, and a string-like member T is provided between the pulling member 8 and the inner annular member 9. The pulling member 8 is disposed in the retractor 5 in the same manner as described above, and is fixed by the treatment instrument introducing portion 6.
 また、本実施形態の場合も、処置具導入部27の筒状部30は、開創器5で開かれた開創部4の径よりやや小さいが、直径が5[mm]程度の処置具を3本まとめて通すことができる径を有する。したがって、図4に示すように、開創部4に装着された体腔アクセス器具26により、閉塞部7及び処置具導入部27を介し、処置具として複数の屈曲鉗子31を体腔内まで挿入し、使用することができる。 Also in the present embodiment, the cylindrical portion 30 of the treatment instrument introduction section 27 is slightly smaller than the diameter of the retractable section 4 opened by the retractor 5, but a treatment instrument having a diameter of about 5 [mm] is provided. It has a diameter that can be passed through all together. Therefore, as shown in FIG. 4, a plurality of bending forceps 31 is inserted into the body cavity as a treatment tool through the obstruction portion 7 and the treatment tool introduction portion 27 by the body cavity access device 26 attached to the retractable portion 4 and used. can do.
 この場合も、各屈曲鉗子31の挿抜操作や旋回操作の自由度を高く保つことができる。また、このとき、屈曲鉗子31の屈曲部が開創部4や、開創器5の開創部材11に接触してこれらに損傷が生じるのを、処置具導入部27により防止することができる。 Also in this case, the degree of freedom of the insertion / extraction operation and the turning operation of each bending forceps 31 can be kept high. At this time, the treatment instrument introducing portion 27 can prevent the bent portion of the bending forceps 31 from coming into contact with the retracting portion 4 and the retracting member 11 of the retractor 5 to cause damage.
 体腔アクセス器具26の他の点については、図1及び図2の体腔アクセス器具1の場合と同様であり、第1実施形態の場合と同様の効果を得ることができる。また、本実施形態によれば、開創器5の開創部材11を、第1実施形態の場合と逆方向に巻き取ることができる。 Other points of the body cavity access device 26 are the same as those of the body cavity access device 1 of FIGS. 1 and 2, and the same effects as those of the first embodiment can be obtained. Moreover, according to this embodiment, the retracting member 11 of the retractor 5 can be wound up in the opposite direction to the case of the first embodiment.
 図5は、本発明の第3実施形態に係る体腔アクセス器具を示す。図5において、図1中の要素と同一の要素については同一の符号が付されている。この体腔アクセス器具32では、開創部4の体腔3側に配置された内側環状部材9を体外に引き出すために把持される把持部材として、処置具導入部6が用いられる。 FIG. 5 shows a body cavity access device according to a third embodiment of the present invention. 5, the same elements as those in FIG. 1 are denoted by the same reference numerals. In this body cavity access device 32, the treatment instrument introducing portion 6 is used as a grasping member that is grasped to pull out the inner annular member 9 disposed on the body cavity 3 side of the retracting portion 4 to the outside of the body.
 図6に示すように、紐状部材Tは、内側環状部材9に一端が固定され、他端は、開創部材11の内側を経て処置具導入部6の体外側の部分に固定される。本実施形態では、紐状部材Tの他端は、環状壁部24の固定部25に固定される。紐状部材Tの長さは、開創部4に装着された開創器5に処置具導入部6が挿入された状態において、一端が固定された内側環状部材9の部分から他端が固定された環状壁部24の固定部25に至る最短の長さよりも十分に余裕を有する長さに設定される。 6, one end of the string-like member T is fixed to the inner annular member 9, and the other end is fixed to a portion outside the body of the treatment instrument introducing portion 6 through the inside of the retracting member 11. In the present embodiment, the other end of the string-like member T is fixed to the fixing portion 25 of the annular wall portion 24. The length of the string-like member T is such that the other end is fixed from the portion of the inner annular member 9 to which one end is fixed in a state where the treatment instrument introducing portion 6 is inserted into the retractor 5 attached to the retracting portion 4. The length is set to have a sufficient margin than the shortest length of the annular wall portion 24 reaching the fixed portion 25.
 体腔アクセス器具32を開創部4に装着するに際し、処置具導入部6を開創器5に挿入するとき、紐状部材Tは、開創部材11の内側を経て処置具導入部6の固定部25まで延びた状態となる。したがって、紐状部材Tの大部分は、開創部材11と処置具導入部6との間に挟まれた状態となる。 When the treatment tool introducing portion 6 is inserted into the retractor 5 when the body cavity access device 32 is attached to the retracting portion 4, the string-like member T passes through the inside of the retracting member 11 to the fixing portion 25 of the treatment instrument introducing portion 6. It will be in the extended state. Therefore, most of the string-like member T is in a state of being sandwiched between the retracting member 11 and the treatment instrument introducing portion 6.
 体腔アクセス器具32を開創部4から取り外す際には、図6のように、処置具導入部6を開創器5から抜き取り、さらに開創部4から離れる方向に移動させることにより、紐状部材Tを介して、内側環状部材9を、開創部材11とともに体腔3内から引き出す。このとき、紐状部材Tは常に開創部材11の内側に位置するので、紐状部材Tにより開創部4が損傷を受けることはない。 When removing the body cavity access device 32 from the retracting portion 4, as shown in FIG. 6, the treatment instrument introducing portion 6 is extracted from the retractor 5, and further moved away from the retracting portion 4, thereby the string-like member T is removed. The inner annular member 9 is pulled out from the body cavity 3 together with the retracting member 11. At this time, since the string-like member T is always located inside the retracting member 11, the retracting portion 4 is not damaged by the string-like member T.
 また、紐状部材Tは、処置具導入部6が開創器5に挿入された状態では、内側環状部材9側の一部は、開創部材11の内側に位置し、他の部分は開創部材11と処置具導入部6との間に位置する。すなわち、閉塞部7が開創器5を閉塞しているとき、紐状部材Tは、開創器5と閉塞部7との間を介して体腔アクセス器具32の外側に導出されることはないので、閉塞部7による体腔アクセス器具32の気密性が劣化することはない。 Further, in the state where the treatment instrument introducing portion 6 is inserted into the retractor 5, a part of the string-like member T on the inner annular member 9 side is located inside the retracting member 11, and the other part is the retracting member 11. And the treatment instrument introduction part 6. That is, when the occlusion part 7 occludes the retractor 5, the string member T is not led out of the body cavity access device 32 through the space between the retractor 5 and the occlusion part 7. The airtightness of the body cavity access device 32 due to the occlusion 7 does not deteriorate.
 本実施形態によれば、処置具導入部6を把持部材としても利用できるので、体腔アクセス器具32の構成を簡便なものとすることができる。他の点については、図1の第1実施形態の場合と同様である。 According to the present embodiment, since the treatment instrument introduction unit 6 can be used as a grasping member, the configuration of the body cavity access device 32 can be simplified. Other points are the same as those in the first embodiment of FIG.
 図7は、本発明の第4実施形態に係る体腔アクセス器具を示す。図7において、図3又は図5中の要素と同一の要素については同一の符号が付されている。この体腔アクセス器具33では、図5の体腔アクセス器具32の場合とは、開創器5における外側環状部材10による開創部材11の巻き取り方向が逆である。このため、体腔アクセス器具33が開創部4に装着された状態では、開創器5の開創部材11は、外側環状部材10の内側において、図1の場合よりも頂角が小さい二等辺三角形状の断面形状を形成する。 FIG. 7 shows a body cavity access device according to the fourth embodiment of the present invention. In FIG. 7, the same elements as those in FIG. 3 or FIG. In this body cavity access device 33, the winding direction of the retracting member 11 by the outer annular member 10 in the retractor 5 is opposite to the case of the body cavity access device 32 of FIG. 5. For this reason, in the state where the body cavity access device 33 is mounted on the retracting portion 4, the retracting member 11 of the retractor 5 has an isosceles triangular shape having a smaller apex angle than that of FIG. A cross-sectional shape is formed.
 したがって、体腔アクセス器具33の処置具導入部27における円錐部28の外形は、上記断面形状を有する開創部材11の形状に適合するような円錐状のものとなっている。また、円錐部28に隣接する筒状部30及び環状壁部29の固定部25も、開創器5の形状に適合した形状及び寸法を有する。体腔アクセス器具33の他の点については、図5の体腔アクセス器具32の場合と同様である。 Therefore, the outer shape of the conical portion 28 in the treatment instrument introducing portion 27 of the body cavity access device 33 is a conical shape that matches the shape of the retracting member 11 having the cross-sectional shape. In addition, the cylindrical portion 30 adjacent to the conical portion 28 and the fixing portion 25 of the annular wall portion 29 also have a shape and dimensions that match the shape of the retractor 5. Other points of the body cavity access device 33 are the same as those of the body cavity access device 32 of FIG.
 本実施形態によれば、図5の実施形態と併せて考えると、処置具導入部として、開創部材の巻取り方向に対応する開創器の形状に適合した形状を有するものを採用することができる。したがって、開創部材の巻取り方向又は開創器の形状のいずれかを重視して、所望の開創部材の巻取り方向又は開創器の形状を選択することができる。 According to the present embodiment, when considered in conjunction with the embodiment of FIG. 5, a treatment instrument introducing portion having a shape suitable for the shape of the retractor corresponding to the winding direction of the retractable member can be employed. . Therefore, it is possible to select the desired winding direction of the retracting member or the shape of the retractor with emphasis on either the winding direction of the retracting member or the shape of the retractor.
 図8は、本発明の第5実施形態に係る体腔アクセス器具を示す。図8において、図1中の要素と同一の要素については同一の符号が付されている。この体腔アクセス器具34では、開創部4の体腔3側に配置された内側環状部材9を体外に引き出すために把持される把持部材として、外側環状部材10が用いられる。 FIG. 8 shows a body cavity access device according to the fifth embodiment of the present invention. In FIG. 8, the same elements as those in FIG. 1 are denoted by the same reference numerals. In this body cavity access device 34, the outer annular member 10 is used as a gripping member that is gripped in order to pull out the inner annular member 9 disposed on the body cavity 3 side of the retractable portion 4 to the outside of the body.
 図8に示すように、紐状部材Tは、内側環状部材9に一端が固定され、他端は、開創部材11の内側を経て外側環状部材10の固定部25に固定される。紐状部材Tの長さは、開創部4に装着された開創器5に処置具導入部6が挿入された状態において、一端が固定された内側環状部材9の部分から他端が固定された外側環状部材10の固定部25に至る最短の長さよりも十分に余裕を有する長さに設定される。 8, one end of the string-like member T is fixed to the inner annular member 9, and the other end is fixed to the fixing portion 25 of the outer annular member 10 through the inside of the retracting member 11. The length of the string-like member T is such that the other end is fixed from the portion of the inner annular member 9 to which one end is fixed in a state where the treatment instrument introducing portion 6 is inserted into the retractor 5 attached to the retracting portion 4. The outer annular member 10 is set to a length that has a sufficient margin than the shortest length to the fixed portion 25 of the outer annular member 10.
 体腔アクセス器具34を取付けるために開創部4に開創器5を装着する際には、内側環状部材9が開創部4の体腔3側に配置され、外側環状部材10を軸として開創部材11が巻き取られる。これに伴って、紐状部材Tも固定部25側から、外側環状部材10により巻き取られる。これにより、紐状部材Tの巻き取られていない残りの部分は、開創部材11の内側を経て内側環状部材9まで延びた状態となる。 When the retractor 5 is attached to the retractor 4 to attach the body cavity access device 34, the inner annular member 9 is disposed on the body cavity 3 side of the retractor 4, and the retractor 11 is wound around the outer annular member 10 as an axis. Taken. Accordingly, the string-like member T is also wound up by the outer annular member 10 from the fixed portion 25 side. Thereby, the remaining portion of the string-like member T that has not been wound is in a state of extending to the inner annular member 9 through the inside of the retracting member 11.
 その後、開創部4に装着された開創器5に処置具導入部6が挿入されると、紐状部材Tの巻き取られていない残りの部分は、内側環状部材9側の一部を除き、大部分が開創器5の開創部材11と、処置具導入部6との間に挟まれた状態となる。 After that, when the treatment instrument introducing portion 6 is inserted into the retractor 5 attached to the retractable portion 4, the remaining portion of the string-like member T that is not wound is removed except for a portion on the inner annular member 9 side, Most of the state is sandwiched between the retracting member 11 of the retractor 5 and the treatment instrument introducing portion 6.
 体腔アクセス器具34を取り外すために開創部4から開創器5を抜き取る際には、上述の外側環状部材10を軸とする開創部材11の巻取りが解除され、これに伴って、紐状部材Tも開創部材11の内側に沿って延びた状態となる。その後、開創部4から離れる方向に外側環状部材10を移動させることにより、紐状部材Tを介して、内側環状部材9を、開創部材11とともに体腔3内から引き出すことができる。このとき、紐状部材Tは常に開創部材11の内側に位置するので、紐状部材Tにより開創部4が損傷を受けることはない。 When the retractor 5 is withdrawn from the retracting portion 4 in order to remove the body cavity access device 34, the winding of the retracting member 11 with the outer annular member 10 as an axis is released, and accordingly, the string member T Is also extended along the inside of the retracting member 11. Thereafter, by moving the outer annular member 10 in the direction away from the retracting portion 4, the inner annular member 9 can be pulled out from the body cavity 3 together with the retracting member 11 via the string-like member T. At this time, since the string-like member T is always located inside the retracting member 11, the retracting portion 4 is not damaged by the string-like member T.
 また、紐状部材Tは、体腔アクセス器具34が開創部4に装着された状態では、開創器5と閉塞部7との間を介して体腔アクセス器具34の外側に導出されることはないので、閉塞部7による体腔アクセス器具34の気密性が劣化することはない。 In addition, the string-like member T is not led out of the body cavity access device 34 through the space between the retractor 5 and the occlusion portion 7 in a state where the body cavity access device 34 is attached to the retractable portion 4. In addition, the airtightness of the body cavity access device 34 due to the occlusion portion 7 does not deteriorate.
 本実施形態によれば、外側環状部材10を把持部材としても利用できるので、体腔アクセス器具34の構成を簡便なものとすることができる。他の点については、図1の第1実施形態の場合と同様である。 According to the present embodiment, since the outer annular member 10 can be used as a gripping member, the configuration of the body cavity access device 34 can be simplified. Other points are the same as those in the first embodiment of FIG.
 以上、本発明の実施形態について説明したが、本発明は、実施形態に限定されない。例えば、開創器は、閉塞部及び処置具導入部を取り付けることが可能なものであれば、外側環状部材で開創部材の一部を巻き取る形式のものでなくてもよい。 As mentioned above, although embodiment of this invention was described, this invention is not limited to embodiment. For example, the retractor may not be of a type in which a part of the retracting member is wound up by the outer annular member as long as the closing part and the treatment instrument introducing part can be attached.
 また、引手部材は、完全に環状に閉じたものである必要はなく、一部が開いていてもよい。また、引手部材は、真円である必要はなく、多角形状や楕円形状のものであってもよい。 Further, the pulling member does not need to be completely closed in a ring shape, and a part thereof may be open. Further, the pulling member does not need to be a perfect circle, and may be a polygonal shape or an elliptical shape.
 1、26、32、33、34…体腔アクセス器具、3…体腔、4…開創部、5…開創器、6…処置具導入部(把持部材)、7…閉塞部、8…引手部材(把持部材)、9…内側環状部材、10…外側環状部材(把持部材)、11…開創部材、T…紐状部材。 1, 26, 32, 33, 34 ... body cavity access device, 3 ... body cavity, 4 ... retractor, 5 ... retractor, 6 ... treatment instrument introduction part (gripping member), 7 ... obstruction part, 8 ... handle member (gripping) Member), 9 ... inner annular member, 10 ... outer annular member (gripping member), 11 ... retracting member, T ... string-like member.

Claims (5)

  1.  開創部の体腔側に配置される内側環状部材と、該開創部の体外側に配置される外側環状部材と、該内側環状部材が一方の開口部に固定され、該外側環状部材が他方の開口部に固定された可撓性で筒状の開創部材とを有する開創器と、
     前記開創部に装着された前記開創器に挿入され、処置具の体腔内への導入路を構成する漏斗状の処置具導入部と、
     前記処置具が気密を保持した状態で通される挿通部を有し、前記外側環状部材に取り付けられて前記開創器を気密に閉塞する閉塞部と、
     前記開創部の体腔側に配置された前記内側環状部材を体外に引き出すために把持される把持部材と、
     一端が前記内側環状部材に固定され、他端が前記把持部材に固定された紐状部材とを備え、
     前記開創部に装着された前記開創器に前記処置具導入部が挿入され、前記開創器が前記閉塞部により閉塞された状態で、前記把持部材は、前記開創器内の体外側に位置し、かつ前記紐状部材は、前記内側環状部材から前記開創部材と前記処置具導入部との間を経て前記把持部材に到るように配置されることを特徴とする体腔アクセス器具。
    An inner annular member disposed on the body cavity side of the retracting portion, an outer annular member disposed on the outer side of the retracting portion, the inner annular member fixed to one opening, and the outer annular member serving as the other opening A retractor having a flexible and tubular retractor fixed to the portion;
    A funnel-shaped treatment instrument introduction portion that is inserted into the retractor attached to the wound portion and constitutes an introduction path into the body cavity of the treatment instrument;
    An occlusion part that has an insertion part that is passed through in a state where the treatment instrument is kept airtight, and is attached to the outer annular member to airtightly close the retractor;
    A gripping member gripped to pull out the inner annular member disposed on the body cavity side of the retracting portion;
    A string-like member having one end fixed to the inner annular member and the other end fixed to the gripping member;
    In the state where the treatment instrument introducing portion is inserted into the retractor attached to the retractor and the retractor is closed by the closing portion, the grasping member is located outside the body in the retractor, The string-like member is disposed so as to reach the grasping member from the inner annular member through the retracting member and the treatment instrument introducing portion.
  2.  請求項1に記載の体腔アクセス器具において、
     前記把持部材は、前記開創部に装着された前記開創器の体外側に配置される環状の引手部材で構成されることを特徴とする体腔アクセス器具。
    The body cavity access device of claim 1.
    The body cavity access device, wherein the grasping member is constituted by an annular pulling member disposed on the outside of the body of the retractor mounted on the retracting portion.
  3.  請求項1に記載の体腔アクセス器具において、
     前記把持部材は、前記処置具導入部で構成され、前記紐状部材の他端は、該処置具導入部の体外側の部分に固定されることを特徴とする体腔アクセス器具。
    The body cavity access device of claim 1.
    The grasping member is constituted by the treatment instrument introducing portion, and the other end of the string-like member is fixed to a portion outside the body of the treatment instrument introducing portion.
  4.  請求項1に記載の体腔アクセス器具において、
     前記把持部材は、前記外側環状部材で構成され、前記紐状部材の他端は、該外側環状部材に固定されることを特徴とする体腔アクセス器具。
    The body cavity access device of claim 1.
    The grasping member is constituted by the outer annular member, and the other end of the string-like member is fixed to the outer annular member.
  5.  請求項1に記載の体腔アクセス器具において、
     前記開創器は、前記内側環状部材が前記開創部の体腔側に配置され、前記外側環状部材が前記開創部の体外側に配置された状態で、前記外側環状部材を巻取り軸として一方又は他方の巻取り方向に前記開創部材の体外側の一部を巻き取ることによって前記開創部に固定されるものであり、
     前記処置具導入部は、前記巻取り方向に応じて前記開創部材が呈する形状に適合した形状を有することを特徴とする体腔アクセス器具。
    The body cavity access device of claim 1.
    In the retractor, the inner annular member is arranged on the body cavity side of the retracting portion, and the outer annular member is arranged on the outer side of the retracting portion, and one or the other is used with the outer annular member as a winding shaft. Is fixed to the retracting part by winding a part of the retracting member outside the body in the winding direction of
    The treatment tool introduction part has a shape adapted to the shape exhibited by the retracting member according to the winding direction.
PCT/JP2015/055864 2014-03-27 2015-02-27 Body cavity access tool WO2015146484A1 (en)

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JP2009501045A (en) * 2005-07-15 2009-01-15 アトロポス・リミテッド Wound retractor
JP2011509767A (en) * 2008-01-22 2011-03-31 アプライド メディカル リソーシーズ コーポレイション Surgical instrument access device
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