Transfer equipment

JP2025001222APending Publication Date: 2025-01-08TERUMO KK
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Patent Information

Application Number
JP2023100698
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Filing Date
2023-06-20
Publication Date
2025-01-08

AI Technical Summary

Benefits of technology

【0011】 本発明によれば、移送器具の支持部に一対の突出部を設けることで、外筒内に収容したときに効果的に支持部を湾曲変形させることができる。そのため、支持部に載置された医療用シートを外筒内に効率的に収容することができる。移送器具を使用する直前まで支持部の基端支持部が外筒内に挿入されているため、第2位置において支持部を展開した際、塑性変形した一対の突出部の形状が効果的に維持される。

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Abstract

To provide transfer equipment capable of storing a medical sheet in an external cylinder efficiently.SOLUTION: In transfer equipment 10 in a state before use, a base end support part 34 of a first support part 26 is inserted into a tip opening 80 of an external cylinder 22, and a tip support par 42 of the first support part 26 protrudes from the tip opening 80 of the external cylinder 22 in the tip direction. Both side parts 341 in a width direction of the base end support part 34 are opposed to each other on the reverse face of the first support part 26, and are plastically deformed in the state of protruding downward so as to be away from a lumen of the external cylinder 22. When the first support part 26 is developed at a second position of the transfer equipment 10, the first support part 26 has a pair of protrusions 37, in which both side parts 341 in the width direction are plastically deformed and protruded upward from a first support surface 261.SELECTED DRAWING: Figure 3
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Description

[Technical field]

[0001] The present invention relates to a transfer device for transferring a medical sheet to a treatment target part of a living body. [Background technology]

[0002] Patent Document 1 discloses, for example, a transfer device for transferring a medical sheet (cell sheet) used in organ transplantation to a treatment target part of a living body. This transfer device comprises an outer tube, a shaft movable inside the outer tube, and a support part provided at the tip of the shaft and capable of protruding from the tip of the outer tube. The support part has a sheet support for placing the medical sheet. With the transfer device, with the medical sheet placed on the support surface of the sheet support, the shaft is slid relative to the outer tube, thereby drawing the medical sheet together with the sheet support into the outer tube and storing it within the outer tube. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] International Publication No. 2022 / 080459 Summary of the Invention [Problem to be solved by the invention]

[0004] It is desirable to efficiently contain the medical sheet within the barrel. [Means for solving the problem]

[0005] (1) An aspect of the present invention is a transfer device for transferring a medical sheet to a treatment target part of a living body, comprising an outer tube having a distal opening, a shaft extending in the axial direction of the outer tube and disposed inside the outer tube so as to be movable along the axial direction, and a carrier member having a sheet-shaped support part disposed at the distal end of the shaft, wherein the support part has a support surface capable of holding the medical sheet and a back surface opposite to the support surface, and the width of the support part in a direction perpendicular to the extension direction of the shaft is greater than the inner peripheral length of the outer tube, and at a first position where the shaft is moved in a base end direction relative to the outer tube so that the support part is contained within the outer tube, the support part is contained within the outer tube in a curved and deformed state, and at a second position where the shaft is moved in a distal direction relative to the outer tube so that the support part protrudes from the distal opening of the outer tube, the support part is exposed in the distal direction from the outer tube. and when the support part is moved relatively in the base end direction with respect to the outer cylinder with the medical sheet placed on the support part, the support part is guided toward the tip opening of the outer cylinder and the support part is deformed into a curved shape so that both sides in the width direction of the support part protrude toward the support surface, in an initial state before use, a base end support part constituting the base end side of the support part is inserted into the tip opening of the outer cylinder and a tip support part constituting the tip side of the support part protrudes in the tip direction from the tip opening of the outer cylinder and is plastically deformed in a state where both sides in the width direction of the base end support part face each other on the back surface and protrude downward so as to be away from the inner cavity of the outer cylinder, and when the support part is deployed at the second position, the support part has a pair of protrusions whose both sides in the width direction are plastically deformed and protrude upward from the support surface.

[0006] According to this transfer device, by providing the pair of protrusions on the support part, the support part can be effectively curved and deformed when the support part is housed in the outer tube. Therefore, the medical sheet placed on the support part can be efficiently housed in the outer tube. Since the base end support part of the support part is inserted in the outer tube until just before the transfer device is used, the shape of the pair of plastically deformed protrusions is effectively maintained when the support part is deployed in the second position.

[0007] (2) In the transfer device described in (1) above, the support portion may be provided at a boundary between the support surface and the protruding portion and may have a bent portion where the protruding portion is bent relative to the support surface.

[0008] With this configuration, the bent portion can effectively shape the protruding portion relative to the support surface. The protruding portion can be formed at a predetermined position on the first support portion.

[0009] (3) In the transfer device described in (1) or (2) above, the pair of protrusions may contact each other on the back surface when the support portion is housed within the outer cylinder.

[0010] This arrangement allows for compact storage of the support within the barrel when the delivery device is in the first position. Effect of the Invention

[0011] According to the present invention, by providing a pair of protrusions on the support part of the transfer device, the support part can be effectively curved and deformed when housed in the outer tube. Therefore, the medical sheet placed on the support part can be efficiently housed in the outer tube. Since the base end support part of the support part is inserted into the outer tube until just before the transfer device is used, the shape of the pair of plastically deformed protrusions is effectively maintained when the support part is deployed in the second position. [Brief description of the drawings]

[0012] [Figure 1] FIG. 1 is a perspective view of a delivery device according to an embodiment of the present invention. [Diagram 2] FIG. 2 is an exploded perspective view of the delivery device of FIG. [Diagram 3] FIG. 3 is a plan view of the tip of the delivery device of FIG. [Figure 4] FIG. 4 is a vertical cross-sectional view taken along line IV-IV in FIG. [Diagram 5] FIG. 5 is a cross-sectional view taken along line VV in FIG. [Figure 6] FIG. 6 is a schematic diagram showing a medical instrument package containing a delivery instrument prior to use. [Figure 7] FIG. 7 is a plan view of the distal end of the delivery device of FIG. [Figure 8] FIG. 8 is a cross-sectional view taken along line VIII-VIII in FIG. [Figure 9] FIG. 9 is a flow chart showing the steps of a method for transferring a medical sheet using the transfer device of FIG. [Figure 10] FIG. 10 is a first explanatory view of the sheet placing step. [Figure 11] FIG. 11 is a second explanatory view of the sheet placing step. [Figure 12] FIG. 12 is a first explanatory view of the accommodation step. [Figure 13] FIG. 13 is a cross-sectional view taken along line XIII-XIII in FIG. [Figure 14] FIG. 14 is an explanatory diagram of the arrangement process. [Figure 15] FIG. 15 is a first explanatory diagram of the development process. [Figure 16] FIG. 16 is an explanatory diagram of the movement process. [Figure 17] FIG. 17 is an explanatory diagram of the removal step. [Figure 18] FIG. 18 is a plan view showing a first support portion according to a modified example. [Figure 19] FIG. 19 is a cross-sectional view taken along line XIX-XIX in FIG. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] As shown in Fig. 1, the transfer device 10 according to this embodiment is a medical device for transferring a medical sheet 300 to a treatment target part of a living body. The transfer device 10 is used, for example, in the treatment of severe heart failure caused by ischemic heart disease. In this case, the medical sheet 300 is transplanted to a transplant target part 402 of a heart 400 (a treatment target part of a living body) (see Figs. 14 to 17). The transfer device 10 can attach multiple medical sheets 300 to the transplant target part 402.

[0014] Such medical sheet 300 includes pharmaceuticals for medical use, regenerative medicine products, medical devices, etc. The medical sheet 300 is formed in a sheet shape such as a film or membrane (gel-like substance). The medical sheet 300 may be reinforced by applying fibrin or the like. Regenerative medicine products containing cells include, for example, cell sheets (sheet-shaped cell cultures), spheroids, etc. The cell sheet can be formed by culturing autologous cells or allogeneic cells. The cells constituting the cell sheet include, for example, somatic stem cells (adult stem cells), mesenchymal stem cells, or cardiomyocytes derived from iPS cells (induced pluripotent stem cells). The somatic stem cells preferably include skeletal myoblasts (myoblast cells).

[0015] The medical sheet 300 may contain a tissue adhesive, a local anesthetic, etc. The thickness of the medical sheet 300 is, for example, about 100 μm, and the diameter of the medical sheet 300 is, for example, about 60 mm. However, the thickness and diameter (size) of the medical sheet 300 can be set appropriately.

[0016] The medical sheet 300 may be a sheet to be transplanted into an organ (such as the lung, liver, pancreas, kidney, small intestine, or esophagus) other than the heart 400. Furthermore, the medical sheet 300 may be a sheet for preventing adhesions, for example, so long as it is for medical use.

[0017] 1 and 2, the transportation instrument 10 includes an instrument body 12, an endoscope 14, and a fixing member 16. The instrument body 12 includes a first carrier member 18, a second carrier member 20, and an outer cylinder 22. Note that the transportation instrument 10 is not limited to including the endoscope 14.

[0018] In FIG. 2, the first carrier member 18 includes a first shaft 24 and a first support 26 .

[0019] The first shaft 24 is a tubular body (a circular tube member in this embodiment) having a first lumen 28. The first lumen 28 opens at the tip (the end in the direction of the arrow X1) of the first shaft 24 and at the base end (the end in the direction of the arrow X2) of the first shaft 24. An airtight valve body 55 that is in close contact with the outer circumferential surface of the second shaft 48 is provided at the base end of the first shaft 24. A marker 551 is provided on the outer circumferential surface of the valve body 55. When using the transfer device 10, the user can see the marker 551. Note that the first shaft 24 is not limited to a tubular body, and may not be a tubular body.

[0020] The first shaft 24 extends in the axial direction of the outer cylinder 22 and is disposed inside the outer cylinder 22 so as to be movable along the axial direction. The first shaft 24 is made of, for example, a resin material. The constituent material of the first shaft 24 is not particularly limited, but examples thereof include polyethylene, polypropylene, fluororesin, polyethylene terephthalate, polymethyl methacrylate, polyamide resin, polystyrene, polycarbonate, polyimide, polyetherimide, polyether ether ketone, polyvinyl chloride, ABS resin, polyamide elastomer, and polyester elastomer. The first shaft 24 may be made of a metal material.

[0021] The first shaft 24 may be flexible. The first shaft 24 may have a flexible tube portion capable of retaining a bent shape. In this case, the first shaft 24 can be bent into an appropriate shape within the body cavity and can retain the bent shape.

[0022] As shown in Figs. 2 to 4, the first support part 26 is attached to the tip part of the first shaft 24. The first support part 26 is made of, for example, a resin material. The first support part 26 is capable of holding a medical sheet 300. The first support part 26 is formed by folding a flexible resin sheet material (film material) into a predetermined shape. The first support part 26 is formed, for example, by forming the sheet material into a predetermined shape using a sheet forming die. The thickness of the sheet material is not particularly limited, but is preferably set to, for example, 100 µm or more and 200 µm or less. The first support part 26 has a first joint part 30 and a first support body 32.

[0023] The constituent material of the first support section 26 is not particularly limited, but is preferably transparent, and examples of the constituent material include polyethylene, polycarbonate, polyamide, polystyrene, polypropylene, polyacetal resin, polyimide, polyetherimide, polyether ether ketone, polyethylene terephthalate, fluororesin, etc. The first support section 26 may be in a mesh shape.

[0024] In Fig. 4, the first joint part 30 is bonded to the inner circumferential surface of the tip part of the first shaft 24 by an adhesive. The adhesive is not particularly limited, but examples thereof include a UV adhesive, a hot melt adhesive, and an instant adhesive (e.g., a cyanoacrylate instant adhesive). The first joint part 30 may be heat fused to the inner circumferential surface of the first shaft 24. The first support part 26 may be detachable from the tip part of the first shaft 24.

[0025] As shown in FIG. 2, the first support body 32 extends from the first joint portion 30 in the distal direction. The first support body 32 has a base end support portion 34, an intermediate support portion 36, a pair of first protrusions 38, a pair of second protrusions 40, and a distal support portion 42. The first support body 32 has a first support surface 261. The marker 551 is arranged so that the marker 551 of the first shaft 24 faces upward when the first support surface 261 faces upward. That is, the marker 551 allows the user to confirm the direction of the first support surface 261 in the first support portion 26.

[0026] 3, the base end support part 34 is formed to be wider in the extension direction. In other words, both sides in the width direction of the base end support part 34 are tapered toward the first joint part 30. The intermediate support part 36 is formed to be tapered so that the width gradually decreases from the tip toward the base end (arrow X2 direction).

[0027] The tip support portion 42 is connected to the tip of the intermediate support portion 36 and the tips of the pair of second protrusions 40. The tip support portion 42 protrudes in an arc shape toward the tip direction (arrow X1 direction). That is, when viewed from a direction perpendicular to the first support surface 261 shown in FIG. 3, the tip support portion 42 of the first support portion 26 is in the shape of an arc connecting the pair of second protrusions 40.

[0028] 4, the base end support portion 34 extends from the tip of the first joint portion 30 toward the tip direction (arrow X1 direction) so as to generally follow the axis Ax of the first shaft 24. The intermediate support portion 36 extends from the tip of the base end support portion 34 toward the tip direction (arrow X1 direction) to intersect with the axis Ax of the first shaft 24 and toward the tip direction of the first support portion 26 (arrow X1 direction).

[0029] 2 and 3, the pair of first protrusions 38 protrude upward (in the direction of arrow Y) and inward in the width direction of the intermediate support part 36 from both sides in the width direction of the intermediate support part 36 perpendicular to the moving direction of the first shaft 24. The pair of first protrusions 38 are connected to the base end support part 34. The first protrusions 38 are arc-shaped and bulge outward in a convex manner in a direction away from the first support surface 261.

[0030] 3, the pair of second protrusions 40 are respectively connected to the tips of the pair of first protrusions 38. The pair of second protrusions 40 protrude upward and outward in the width direction from both sides of the intermediate support part 36. The second protrusions 40 are formed with a smaller curvature than the first protrusions 38. The second protrusions 40 protrude lower from the first support surface 261 than the first protrusions 38.

[0031] As shown in FIG. 3, hereinafter, the combined portion of the first protrusion 38 and the second protrusion 40 of the first support portion 26 is referred to as the "protrusion 37". Therefore, a pair of protrusions 37 is provided on both sides of the width direction of the first support portion 26. In FIG. 3, the direction perpendicular to the axial direction of the first shaft 24 (W direction) is the width direction of the first support portion 26. The W direction is also the width direction of other components (such as the outer tube 22). In this embodiment, the first support portion 26 has a pair of protrusions 37, and W1 in FIG. 3 is the width of the portion where the width of the first support portion 26 is maximum when the first support portion 26 is developed in a planar state. That is, the width W1 of the first support portion 26 is the maximum width of the first support portion 26P in a planar state before the pair of protrusions 37 are formed (before bending). The width W1 of the first support portion 26 is greater than the inner circumferential length L of the outer tube 22 (see FIG. 13). 13, the inner peripheral length L of the outer cylinder 22 is the length of the inner peripheral surface along the circumferential direction of the outer cylinder 22 (L=2πR). R is the radius of the inner cavity 78 of the outer cylinder 22.

[0032] The first support body 32 has a front surface 461 that faces upward (in the direction of arrow Y) and includes the first support surface 261, and a back surface 462 that is the opposite surface to the front surface 461. The first support surface 261 is a flat surface that is continuous with the upper surface of the base end support part 34, the intermediate support part 36, and the upper surfaces of the tip support part 42. A lubricant may be applied to the first support surface 261 so that a second support part 50 of the second carrier member 20, which will be described later, can slide smoothly on the first support surface 261.

[0033] As shown in FIG. 2, the second carrier member 20 includes a second shaft 48 , a second support portion 50 , and a hub 52 .

[0034] The second shaft 48 is a tubular body (a circular tube member in this embodiment) having a second lumen 57. The length of the second shaft 48 along the axial direction is longer than the length of the first shaft 24 along the axial direction. The second shaft 48 is inserted into the first lumen 28 of the first shaft 24 (see Figs. 1 and 4). In other words, the distal end of the second shaft 48 protrudes in the distal direction (arrow X1 direction) from the distal end opening of the first shaft 24. The proximal end of the second shaft 48 protrudes in the proximal direction (arrow X2 direction) from the proximal end opening of the first shaft 24 (see Fig. 1). The second shaft 48 extends along the first shaft 24 and is provided movably along the first shaft 24. The second shaft 48 is not limited to a tubular body and may not be a tubular body.

[0035] The second shaft 48 is configured so as to be able to follow the shape of the first support portion 26. As the constituent material of the second shaft 48, for example, a material that is more flexible than the constituent material of the first shaft 24 is selected. Specifically, as the constituent material of the second shaft 48, for example, polyamide elastomer, polyester elastomer, polyurethane elastomer, polyvinyl chloride, polybutadiene, silicone rubber, metal coil (including composite with resin), etc. can be mentioned. The second shaft 48 is flexible.

[0036] 4, the second shaft 48 has a carrier holding portion 54 and a pressing portion 56 formed by the tip portion of the second shaft 48. The pressing portion 56 is formed from an elastic body such as an elastomer material. The pressing portion 56 presses the first support portion 26 against the inner surface of the outer tube 22 in a state in which the first support portion 26 is housed inside the outer tube 22.

[0037] The tip of the carrier holding part 54 has a pressing surface 58. The carrier holding part 54 is capable of pressing the outer peripheral end surface of the medical sheet 300 supported by the first support part 26 in the tip direction (arrow X1 direction) with the pressing surface 58. In this embodiment, the pressing part 56 is provided with the carrier holding part 54 that supports the second support part 50. The carrier holding part 54 has a pressing surface 58 and an attachment hole 60.

[0038] In Fig. 4, the pressing surface 58 is provided on the tip surface of the carrier holding part 54. An attachment hole 60 opens in the pressing surface 58. The second support part 50 is attached to the pressing surface 58. The pressing surface 58 presses the outer peripheral end surface of the medical sheet 300 in the tip direction (the direction of the arrow X1) (see Fig. 16).

[0039] 2 to 4, the second support part 50 is configured in a flexible sheet shape. The second support part 50 has a second joint part 70 and a second support body 72. The second joint part 70 is provided at the base end of the second support part 50. The second joint part 70 is provided at the base end of the second support body 72. The second joint part 70 is inserted into the mounting hole 60 of the carrier holding part 54 and is, for example, bonded. The second joint part 70 may be bonded to the mounting hole 60 of the carrier holding part 54 by an appropriate bonding method other than bonding. Furthermore, the second support part 50 may be molded integrally with the carrier holding part 54.

[0040] The second support body 72 extends from the second joint 70 in the tip direction (the direction of arrow X1). The length of the second support body 72 in the extending direction from the second joint 70 is shorter than the length of the first support body 32 in the extending direction from the first joint 30. A second support surface 74 for placing the medical sheet 300 on is provided on the upper surface of the second support body 72. The second support surface 74 is a flat surface. The second support body 72 is smaller than the first support body 32. In other words, the area of ​​the second support surface 74 is smaller than the area of ​​the first support surface 261.

[0041] In FIG. 2, the hub 52 is attached to the proximal end of the second shaft 48 .

[0042] 1 and 2, the outer tube 22 is a cylindrical member having a cavity 78. The cavity 78 has a tip opening 80 that opens at the tip (end in the direction of arrow X1) of the outer tube 22. The cavity 78 opens at the base end (end in the direction of arrow X2) of the outer tube 22. The outer tube 22 is flexible. The outer tube 22 may be made of the same material as the first shaft 24 described above. The first shaft 24 is inserted into the cavity 78 of the outer tube 22. The length of the outer tube 22 in the axial direction is shorter than the length of the first shaft 24 in the axial direction. The base end of the outer tube 22 is provided with an airtight valve body 84 that is in close contact with the outer circumferential surface of the first shaft 24.

[0043] 2 and 4, the tip surface of the outer cylinder 22 extends along a direction perpendicular to the axial direction of the outer cylinder 22. In FIG.

[0044] As shown in Fig. 2, the endoscope 14 has a long endoscope body 86. The tip of the endoscope body 86 is fixed to the outer peripheral surface of the outer tube 22 by a fixing member 16 (see Fig. 1). An objective lens 88 provided on the tip surface of the endoscope body 86 faces the tip direction of the outer tube 22 (the direction of the arrow X1). The tip of the endoscope body 86 is fixed to a middle part of the outer tube 22 in the axial direction. However, the tip of the endoscope body 86 may be fixed to the tip of the outer tube 22.

[0045] The fixing member 16 includes, for example, a fixed cylinder 90 and a fixed tube 92. The fixed cylinder 90 is made of, for example, a hard resin material. The endoscope main body 86 can be inserted into the inner cavity of the fixed cylinder 90. The fixed cylinder 90 is arranged along the longitudinal direction of the outer cylinder 22. The fixed tube 92 is a tube for fixing the fixed cylinder 90 to a predetermined position of the outer cylinder 22. The fixed tube 92 is, for example, a heat shrink tube. The method of fixing the tip portion of the endoscope main body 86 to the outer cylinder 22 can be set appropriately.

[0046] As shown in FIG. 6, before use, the transport instrument 10 is contained in a packaging body 94 to form a medical instrument package P. Before use, the packaging body 94 of the medical instrument package P is sealed. In the unopened medical instrument package P before opening the packaging body 94, as shown in FIG. 7, the base end support part 34 of the first support part 26 of the transport instrument 10 is inserted into the inside of the outer tube 22 through the tip opening 80. The state of FIG. 7 in which the base end support part 34 of the first support part 26 is inserted into the inside of the outer tube 22 is the initial position of the transport instrument 10. As shown in FIG. 8, in the unopened state (initial position) of the medical instrument package P, the front surface 461 of the first support part 26 is curved so that the back surface 462 of the first support part 26 is curved so that the outside, and both widthwise side parts 341 of the base end support part 34 of the first support part 26P are curved along the inner cavity 78 of the outer tube 22. At the back surface 462 of the first support portion 26P, the width direction side portions 341 of the base end support portion 34 face each other in contact with each other and are curved in a state of protruding downward so as to be away from the inner cavity 78 of the outer cylinder 22. Note that the width direction side portions 341 of the base end support portion 34 are not limited to a case in which the back surfaces 462 are in contact with each other. The base end support portion 34 may be curved and deformed in a state in which the back surface 462 of one width direction side portion 341 and the back surface 462 of the other width direction side portion 341 are not in contact with each other.

[0047] 7, when the medical instrument package P is in an unopened state, the distal support part 42 of the first support part 26 is disposed in the distal direction (the direction of the arrow X1) of the outer cylinder 22 and is exposed to the outside of the outer cylinder 22. As shown in Fig. 7, the first support part 26 is tapered from the distal support part 42 toward the proximal support part 34. Like the first support part 26, the proximal end part of the second support part 50 is also curved along the first support part 26 on the inside of the first support part 26 (the surface 461 side).

[0048] 6, when manufacturing a medical instrument package P, a transfer instrument 10 having a first support part 26P before the protrusion 37 is formed is prepared. From a state (second position) in which the first and second support parts 26, 50 are deployed toward the distal end of the outer tube 22, the first and second carrier members 18, 20 are moved toward the proximal end relative to the outer tube 22 to an initial position in which the proximal end support part 34 of the first support part 26 is inserted into the interior through the distal opening 80 of the outer tube 22. Both widthwise side parts 341 of the proximal end support part 34 of the first support part 26 are curved along the inner cavity 78 of the outer tube 22.

[0049] Next, the transfer instrument 10 is housed in the packaging body 94 in the initial position, and the packaging body 94 is closed. The transfer instrument 10 housed in the packaging body 94 is sterilized. Examples of the sterilization include steam sterilization, radiation sterilization, ethylene oxide gas (EOG) sterilization, and hydrogen peroxide sterilization. At this time, the first support part 26 is heated by the sterilization, and both widthwise sides 341 of the base end support part 34 are plastically deformed in a curved shape. A pair of first protrusions 38 are shaped from the base end support part 34 to the intermediate support part 36 by the plastic deformation. A pair of first protrusions 38 bent with respect to the first support surface 261 is formed in the first support part 26. Furthermore, when radiation sterilization is performed, the molecular structure of the first support part 26 is changed by crosslinking and the like in addition to heating, and the shaping of the first protrusions 38 is further promoted.

[0050] In addition, the medical instrument package P may be manufactured by placing the transfer instrument 10 in the initial position after sterilization. In this case, the transfer instrument 10 is sterilized in a state where the first and second support parts 26, 50 are deployed toward the distal end of the outer tube 22 (second position). Then, the first support part 26 and the second support part 50 are moved toward the proximal end relative to the outer tube 22, and the proximal support part 34 of the first support part 26 is inserted into the distal opening 80 of the outer tube 22 and curved. Next, the transfer instrument 10 in this state is housed in a packaging body 94, and the packaging body 94 is closed. When the medical instrument package P is in an unopened state, the proximal support part 34 of the transfer instrument 10 is inserted into the outer tube 22 for a certain long time before use, so that the pair of first protrusions 38 are shaped in the first support part 26.

[0051] Next, a method for transferring the medical sheet 300 to a treatment target part of a living body will be described. Specifically, as shown in Fig. 14 to Fig. 17, a method for transferring the medical sheet 300 to a transplant target part 402 of a heart 400 (treatment target part of a living body) by thoracoscopic surgery will be described. As shown in Fig. 9, the transfer method according to this embodiment includes a preparation step, a sheet placement step, a storage step, a positioning step, a deployment step, a movement step, and a removal step.

[0052] First, in a preparation step (step S1), the transfer device 10 according to the present embodiment described above is prepared. In the preparation step, after a user opens the medical device package P and takes out the transfer device 10, the first shaft 24 and the second shaft 48 are moved in the distal direction (arrow X1 direction) relative to the outer tube 22, and the first support part 26 and the second support part 50 are brought into a state (second position) in which they are protruding in the distal direction from the distal opening 80 of the outer tube 22. Each of the first and second support parts 26, 50 is exposed in the distal direction (arrow X1 direction) from the outer tube 22 and deployed, and the second support part 50 is placed on the first support surface 261 of the first support part 26. That is, the second support part 50 is placed in a retracted position overlapping the first support surface 261 of the first support part 26. At this time, the base end part of the carrier holding part 54 is inserted into the first inner cavity 28 of the first shaft 24. As the first support portion 26 protrudes in the distal direction from the distal end opening 80 of the outer cylinder 22, a pair of first protrusions 38 protruding upward relative to the first support surface 261 are formed on the first support portion 26 (see FIG. 5). When the transfer device 10 is in a state prior to use, the pair of first protrusions 38 are shaped to protrude upward relative to the first support surface 261.

[0053] 10, the medical sheet 300 placed in the petri dish 401 is placed on the second support surface 74. The medical sheet 300 protrudes outward from the second support portion 50 when placed on the second support surface 74. The first support surface 261 supports the protruding portion 302 of the medical sheet 300 that protrudes outward from the second support portion 50.

[0054] Thereafter, in the accommodation step (step S3 in FIG. 9), the medical sheet 300 is accommodated in the outer cylinder 22 together with the first support part 26 and the second support part 50 to a accommodated position (first position) as shown in FIG. 12. Specifically, the first shaft 24 of the first carrier member 18 and the second shaft 48 of the second carrier member 20 are moved together in the base end direction (the direction of the arrow X2) relative to the outer cylinder 22.

[0055] Then, the base end support portion 34 (see FIG. 2) of the first support portion 26 is drawn in the base end direction from the tip opening 80 of the outer tube 22. At this time, the tapered both sides of the base end support portion 34 come into contact with the tip opening 80 of the outer tube 22, so that a force acts on the base end support portion 34 to curl the base end support portion 34 along the circumferential direction of the outer tube 22. Therefore, the base end support portion 34 is smoothly drawn into the outer tube 22 while curling. At this time, the first support portion 26 is accommodated in the outer tube 22 while curling into a cone shape such that the tip side has a large diameter and the base end support portion 34 has a small diameter.

[0056] When the base end support portion 34 of the first support portion 26 is deformed, a force acts on the intermediate support portion 36 of the first support portion 26 to curl up along the circumferential direction of the outer tube 22, so that the intermediate support portion 36 (see FIG. 2) is drawn into the outer tube 22 while curling up. At this time, the intermediate support portion 36 is deformed into a cylindrical shape along the inner surface of the outer tube 22. Each of the pair of first protrusions 38 is curved so that the surface 461 of the first support portion 26 is on the inside and the back surface 462 of the first support portion 26 is on the outside. As shown in FIG. 13, the back surfaces 462 on both sides in the width direction of the first support portion 26 come into contact with each other on a virtual line D extending perpendicular to the central axis of the outer tube 22. One first protrusion 38 and the other first protrusion 38 come into contact with each other and are accommodated downward (first support surface 261, surface 461).

[0057] As a result, the back surface 462 of the first support portion 26 is curved in intimate contact with the inner surface of the outer tube 22, and each of the first protrusions 38 is further curved so as to be folded back toward the center of the outer tube 22, and the free end of each of the first protrusions 38 is disposed below the central axis of the outer tube 22. In other words, the first support portion 26 is curved into a heart shape along the inner surface of the outer tube 22.

[0058] The heart shape refers to a generally circular shape consisting of a convexly curved shape on one side and two convexly curved shapes on the other side opposite to the one side. When a heart shape is formed in the inner cavity 78 of the tubular body (outer cylinder 22), the two convexly curved shapes protruding to the other side along the inner surface of the tubular body approach each other and part of the circumferential surface comes into contact with each other, so that the overall outline becomes a generally circular shape along the inner surface of the tubular body (see the shape of the first support part 26 in FIG. 13).

[0059] As the first support part 26 is curved and deformed, the second support part 50 is also curved and deformed along the first support part 26 on the inside (surface 461 side) of the first support part 26. As the first support part 26 and the second support part 50 are curved and deformed, the medical sheet 300 is deformed into a shape corresponding to the shapes of the first support body 32 and the second support body 72, and the medical sheet 300 is contained within the outer cylinder 22.

[0060] 12, the accommodating step is completed when the entire first support part 26 is completely inserted into the outer tube 22. When the accommodating step is completed, a part of the first support part 26 may protrude from the tip opening 80 of the outer tube 22. In this case, the state in which a part of the first support part 26 protrudes from the tip opening 80 of the outer tube 22 is the first position of the first support part 26.

[0061] Thereafter, in a placement step (step S4 in FIG. 9), as shown in FIG. 14, the transfer instrument 10 is inserted into the thoracic cavity 410 through the incision 409 in the chest 408. At this time, the tip of the transfer instrument 10 is positioned near the transplant target portion 402 in the heart 400, and the tip of the endoscope 14 is positioned inside the thoracic cavity 410. Note that before inserting the transfer instrument 10 into the thoracic cavity 410, a liquid supply instrument (not shown) may be connected to the connection port of the hub 52 to introduce liquid (e.g., physiological saline).

[0062] Next, in the unfolding step (step S5 in FIG. 9), the first support part 26, the second support part 50, and the medical sheet 300 are unfolded as shown in FIG. 15. Specifically, in the unfolding step, the first shaft 24 is grasped and moved in the distal direction (arrow X1 direction) relative to the outer tube 22. As a result, the valve body 55 of the first shaft 24 moves the second shaft 48 together with the first shaft 24 in the distal direction (arrow X1 direction). Then, the first support part 26 exposed from the distal opening 80 of the outer tube 22 returns to its original shape by a restoring force. In the second position where the first support part 26 is unfolded, the second support part 50 spreads out in a planar shape.

[0063] In the unfolding step, the second carrier member 20 has the second support surface 74, on which the medical sheet 300 is placed, positioned entirely above the first support surface 261. At this time, the medical sheet 300 is supported by the first support surface 261 and the second support surface 74. This makes it possible to prevent wrinkles from forming in the protruding portion 302 of the medical sheet 300 before the medical sheet 300 is transferred to the transplantation target portion 402 of the heart 400.

[0064] 16, in the movement step (step S6 in FIG. 9), the second carrier member 20 is moved in the distal direction (arrow X1 direction) relative to the first carrier member 18, so that the second support part 50 on which the medical sheet 300 is placed moves from the retracted position to the advanced position, and the second support part 50 protrudes in the distal direction (arrow X1 direction) beyond the tip of the first support part 26. Specifically, in the movement step, the second shaft 48 is moved in the distal direction relative to the first shaft 24.

[0065] As a result, the second support part 50 moves in the distal direction (direction of arrow X1) relative to the first support part 26. At this time, when the pressing surface 58 of the carrier holding part 54 (pressing part 56) presses the outer peripheral end face of the medical sheet 300 in the distal direction, the entire medical sheet 300 is positioned further distally than the first support part 26. In this moving step, the medical sheet 300 is moved above the transplant target part 402 of the heart 400, and the overhanging part 302 of the medical sheet 300 is brought into contact with the transplant target part 402.

[0066] Then, in the removal step (step S7 in FIG. 9), as shown in FIG. 17, the second carrier member 20 is moved from the second position to the first position to remove the second support part 50 from between the transplantation target part 402 and the medical sheet 300. This brings the entire medical sheet 300 into contact with the surface of the transplantation target part 402. This completes the transfer of the medical sheet 300 to the transplantation target part 402. Thereafter, the transferring instrument 10 is removed from the chest 408 with the first support part 26 and the second support part 50 housed within the outer cylinder 22.

[0067] This embodiment provides the following advantages.

[0068] As shown in Fig. 7, in an initial state before the use of the transfer device 10 (when the medical device package P is unopened), the base end support part 34 of the first support part 26 is inserted into the tip opening 80 of the outer tube 22, and the tip support part 42 of the first support part 26 protrudes from the tip opening 80 of the outer tube 22 in the tip direction (arrow X1 direction). As shown in Fig. 8, on the back surface 462 of the first support part 26, both widthwise side parts 341 of the base end support part 34 face each other and are plastically deformed in a state of protruding downward so as to be separated from the inner cavity 78 of the outer tube 22. As shown in Fig. 3, when the first support part 26 is deployed in the second position of the transfer device 10, both widthwise side parts 341 of the first support part 26 are plastically deformed to have a pair of protrusions 37 protruding upward from the first support surface 261.

[0069] Thus, by providing the pair of protrusions 37 on the first support part 26, the first support part 26 can be effectively curved and deformed when the first support part 26 is housed in the outer tube 22. Therefore, the medical sheet 300 placed on the first support part 26 can be efficiently housed in the outer tube 22. Because the base end support part 34 of the first support part 26 is inserted in the outer tube 22 until immediately before the transfer device 10 is used, the shape of the pair of plastically deformed protrusions 37 is effectively maintained when the first support part 26 is deployed in the distal end direction of the outer tube 22 at the second position.

[0070] 8, with first support part 26 housed within outer tube 22, a pair of protrusions 37 (first protrusions 38) come into contact with each other on rear surface 462 of first support part 26. This allows first support part 26 to be housed compactly within outer tube 22 when transportation device 10 is in the first position, as shown in FIG.

[0071] As shown in Fig. 18, first support part 26A of transfer device 10A according to the modified example has a pair of bent parts 444. The pair of bent parts 444 is provided on each of the pair of protruding parts 37 (first protruding parts 38). Each of the pair of bent parts 444 bends the pair of protruding parts 37 toward first support surface 261 (middle support part 36) of first support part 26A (see Fig. 19).

[0072] When manufacturing the medical instrument package P, the base end support part 34 of the first support part 26A is inserted into the interior of the outer tube 22 through the distal end opening 80, so that both widthwise side parts 341 of the base end support part 34 of the first support part 26A are curved along the inner cavity 78 of the outer tube 22, using the pair of bent parts 444 as base points. With the base end support part 34 inserted and curved within the outer tube 22, a sterilization process is performed on the transfer instrument 10A. The shape of the pair of protrusions 37 from the base end support part 34 to the intermediate support part 36 is effectively maintained by the heat generated during the sterilization process.

[0073] This modified example has the following advantages.

[0074] 19, first support portion 26A is provided at the boundary between first support surface 261 and protruding portion 37, and has bent portion 444 where protruding portion 37 is bent relative to first support surface 261. This allows protruding portion 37 to be effectively shaped relative to first support surface 261 by bent portion 444. Protruding portion 37 can be formed at a predetermined position in first support portion 26A. Bent portion 444 allows protruding portion 37 to be bent at a stable position relative to first support surface 261.

[0075] The present invention is not limited to the above disclosure, and various configurations can be adopted without departing from the gist of the present invention. [Explanation of symbols]

[0076] 10, 10A...Transportation equipment 18...First carrier member 22…Outer cylinder 24…First shaft 26, 26A...1st support part 34...Proximal support part 37...Protruding part 38...first protrusion 42...Tip support part 261...1st support surface 300…Medical sheets 402…Transplant target area 462...Back side

Claims

1. A transfer device for transferring a medical sheet to a treatment target part of a living body, An outer cylinder having a tip opening; a carrier member including a shaft extending in an axial direction of the outer cylinder and disposed inside the outer cylinder so as to be movable along the axial direction, and a sheet-shaped support portion disposed at a tip end of the shaft; Equipped with The support portion has a support surface capable of holding the medical sheet, A back surface opposite to the support surface; having The support portion has a width in a direction perpendicular to an extension direction of the shaft that is greater than an inner peripheral length of the outer cylinder, At a first position where the shaft is moved in a proximal direction relative to the outer cylinder so that the support portion is accommodated in the outer cylinder, the support portion is accommodated in the outer cylinder in a curved and deformed state, At a second position where the shaft is moved in a distal direction relative to the outer tube so that the support portion protrudes from the distal opening of the outer tube, the support portion is exposed in the distal direction from the outer tube and deployed, the support portion protrudes in the distal direction from the distal end of the outer cylinder, and when the support portion is moved in the base end direction relative to the outer cylinder with the medical sheet placed on the support portion, the support portion is guided toward the distal opening of the outer cylinder, and the support portion is deformed into a curved shape so that both sides in the width direction of the support portion protrude toward the support surface, In an initial state before use, a base end support part constituting a base end side of the support part is inserted into the tip opening of the outer tube, a tip support part constituting a tip side of the support part protrudes in a tip direction from the tip opening of the outer tube, and both widthwise side portions of the base end support part face each other on the back surface and are plastically deformed in a state of protruding downward so as to be separated from the inner cavity of the outer tube, A transfer device in which, when the support portion is deployed at the second position, the support portion has a pair of protrusions that protrude upward from the support surface by plastically deforming both sides in the width direction.

2. 2. The transfer device of claim 1, A transfer device, wherein the support portion is provided at the boundary between the support surface and the protrusion, and has a bent portion where the protrusion is bent relative to the support surface.

3. 2. The transfer device of claim 1, A transfer device in which the pair of protrusions contact each other on the back surface when the support portion is housed within the outer cylinder.

Citation Information

Patent Citations

  • Device for adhering sheetlike material within living body

    WO2022080459A1