WO2012140768A1 - Orifice médical, contenant de nutriment employant celui-ci et ensemble de fourniture de nutriment - Google Patents

Orifice médical, contenant de nutriment employant celui-ci et ensemble de fourniture de nutriment Download PDF

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Publication number
WO2012140768A1
WO2012140768A1 PCT/JP2011/059291 JP2011059291W WO2012140768A1 WO 2012140768 A1 WO2012140768 A1 WO 2012140768A1 JP 2011059291 W JP2011059291 W JP 2011059291W WO 2012140768 A1 WO2012140768 A1 WO 2012140768A1
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WO
WIPO (PCT)
Prior art keywords
flow path
opening member
medical port
tubular portion
path opening
Prior art date
Application number
PCT/JP2011/059291
Other languages
English (en)
Japanese (ja)
Inventor
沖山忠
▲堤▼大輔
上原康賢
Original Assignee
株式会社ジェイ・エム・エス
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 株式会社ジェイ・エム・エス filed Critical 株式会社ジェイ・エム・エス
Priority to CN201180070095.9A priority Critical patent/CN103491926B/zh
Priority to SG2013076153A priority patent/SG194470A1/en
Priority to KR1020137028596A priority patent/KR101799138B1/ko
Priority to PCT/JP2011/059291 priority patent/WO2012140768A1/fr
Priority to JP2013509713A priority patent/JP5920340B2/ja
Publication of WO2012140768A1 publication Critical patent/WO2012140768A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14—Details; Accessories therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14—Details; Accessories therefor
    • A61J1/1406—Septums, pierceable membranes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14—Details; Accessories therefor
    • A61J1/1475—Inlet or outlet ports
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14—Details; Accessories therefor
    • A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D33/00—Details of, or accessories for, sacks or bags
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/05—Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
    • A61J1/10—Bag-type containers

Definitions

  • the present invention relates to a medical port that is fixed to a container body portion of a container for a nutrient solution and that allows the inside and outside of the container body portion to communicate with each other, a nutrient solution container in which the medical port is fixed to the container body portion, and a nutrient solution Regarding supply set.
  • Enteral nutrition therapy and parenteral nutrition therapy are known as methods for administering nutrition and drugs to patients without oral administration.
  • enteral nutrition therapy a tube passed from the patient's nasal cavity to the stomach or duodenum (commonly called a “nasal tube”) or a gastric fistula formed on the patient's abdomen (percutaneousaneEndoscopic treatment).
  • a liquid (generally referred to as “enteral nutrition”) such as a nutrient, liquid food, or drug is administered via a tube (commonly referred to as “PEG tube”) inserted in a “Gastrostomy”.
  • infusion liquid containing nutritional components such as glucose and drug components is administered via an infusion line (liquid feeding circuit) inserted into a patient's vein.
  • FIG. 15 shows a schematic configuration diagram of an example of an enteral nutrition set used in conventional enteral nutrition therapy.
  • the container body 101 of the nutrient solution container 100 is filled with a nutrient solution.
  • a thin film (not shown) is attached to the mouth portion 102 through which the nutrient of the container main body 101 flows out, and the inside of the container main body 101 is sealed.
  • the plastic connecting needle 104 is pierced into the cap 105 attached to the mouth, and the thin film is pierced. Thereby, the nutrient can be sent into the body through the tube connected to the connecting needle 104.
  • FIG. 16 shows a schematic configuration diagram of an example of an infusion set used in conventional parenteral nutrition therapy.
  • the bag body 111 of the bag 110 is filled with a liquid material containing nutritional components and pharmaceutical components.
  • the connection needle 114 is punctured into the connection needle port 113. Thereby, a liquid substance can be sent into the body through a tube connected to the connection needle 114 (see Patent Document 1).
  • the present invention solves the above-mentioned problem of erroneous connection, and makes it possible to provide a nutrient container that can be sanitized with a simple operation for supplying a liquid such as a nutrient, and a medical port using the same.
  • a container for nutrients and a nutrient supply set were provided.
  • the medical port of the present invention is A medical port fixed to the container body of the nutrient container and capable of communicating inside and outside of the container body,
  • the medical port is A top surface portion facing inside the container main body portion in a state where the medical port is fixed to the container main body portion; a side wall portion arranged on one main surface side of the top surface portion and fixed to the container main body portion;
  • a port body portion including a mounting portion including a tubular portion having a through-hole that protrudes on the opposite side of the top surface portion from the side wall portion and communicates with a space surrounded by the side wall portion; It is attached to the port main body, and is disposed on an extension line of the through hole in the container main body in a state where the medical port is fixed to the container main body, and the liquid substance in the container main body is used for the nutrient
  • a thin film that blocks outflow from the container A flow path opening member mounted on the mounting portion;
  • a connection holding part that is provided in the port main body part or the flow path opening member and that
  • the flow path opening member can take a first mounting state and a second mounting state with respect to the mounting portion; In the first attachment state, the flow path opening member with respect to the attachment portion is held such that the tip of the puncture portion does not contact the thin film or is in contact with the thin film but does not press the thin film The wearing state of is maintained, In the second mounting state, the flow path with respect to the mounting portion is maintained such that the thin film is broken by the puncture portion and the inner peripheral surface of the tubular portion is kept in contact with the outer peripheral surface of the tubular portion. The mounting state of the opening member is maintained.
  • the nutrient solution container of the present invention includes a container body portion including a flexible bag-like member and the medical port of the present invention fixed to the container body portion.
  • the nutrient solution supply set of the present invention includes the nutrient solution container of the present invention, a connector having an engagement portion that can be engaged with the connection holding portion of the medical port, and a liquid feeding tube connected to the connector. Including a liquid delivery circuit.
  • a liquid feeding circuit used for parenteral nutrition therapy is erroneously connected to a nutrient container, and supply of a liquid substance such as a nutrient is a simple operation. It is possible to provide a medical port that makes it possible to provide a sanitary nutrient container, and a nutrient container and nutrient supply set using the medical port.
  • FIG. 1 is a front view showing an example of a nutrient container according to Embodiment 1.
  • FIG. 2A is an enlarged perspective view showing an example of the medical port of the present invention constituting the nutrient solution container shown in FIG.
  • FIG. 2B is a plan view of the medical port shown in FIG. 2A.
  • FIG. 2C is a bottom view of the medical port shown in FIG. 2A.
  • 2D is a side view of the medical port shown in FIG. 2A.
  • FIG. 2E is another side view of the medical port shown in FIG. 2A.
  • 2F is a cross-sectional view of the medical port shown in FIG. 2A.
  • FIG. 2G is a partially enlarged view of the medical port shown in FIG. 2F.
  • FIG. 2H is a partially enlarged view for explaining another example of the medical port of the present invention.
  • 3A is a perspective cross-sectional view illustrating a flow path opening member of the medical port illustrated in FIG. 2A.
  • 3B is a bottom view of the flow path opening member shown in FIG. 3A.
  • FIG. 3C is a perspective cross-sectional view illustrating another example of the flow path opening member.
  • FIG. 3D is a perspective cross-sectional view illustrating another example of the flow path opening member.
  • FIG. 3E is a perspective cross-sectional view illustrating another example of the flow path opening member.
  • FIG. 3F is a perspective cross-sectional view illustrating another example of the flow path opening member.
  • FIG. 3G is a perspective cross-sectional view illustrating another example of the flow path opening member.
  • FIG. 4A is a cross-sectional view illustrating a state immediately before a liquid feeding circuit is connected to the medical port illustrated in FIG. 2A.
  • 4B is a cross-sectional view illustrating a state in which the liquid feeding circuit is being attached to the medical port illustrated in FIG. 2A and the thin film has been broken by the flow path opening member.
  • FIG. 4C shows a state in which the liquid feeding circuit is being attached to the medical port shown in FIG. 2A, and the protruding portion of the medical port is in the insertion part of the connector of the liquid feeding circuit. It is sectional drawing explaining a mode that it inserted completely.
  • FIG. 4D is a partially enlarged view of FIG. 4C.
  • FIG. 5A is a perspective view of an example of a connector connected to the medical port shown in FIG. 2A.
  • FIG. 5B is a plan view of the connector shown in FIG. 5A.
  • FIG. 5C is a bottom view of the connector shown in FIG. 5A.
  • FIG. 5D is a side view of the connector shown in FIG. 5A.
  • FIG. 5E is another side view of the connector shown in FIG. 5A.
  • FIG. 6 is a partial perspective view illustrating an example of a nutrient container according to the second embodiment.
  • FIG. 7A is an enlarged perspective view showing an example of the medical port of the present invention that constitutes the nutrient container shown in FIG. 6.
  • FIG. 7B is a plan view of the medical port shown in FIG. 7A.
  • FIG. 7C is a bottom view of the medical port shown in FIG. 7A.
  • FIG. 7D is a side view of the medical port shown in FIG. 7A.
  • FIG. 7E is another side view of the medical port shown in FIG. 7A.
  • FIG. 7F is a cross-sectional view of the medical port shown in FIG. 7A.
  • FIG. 8A is a partially enlarged schematic cross-sectional view of the medical port shown in FIG. 7A.
  • FIG. 8B is a partially enlarged cross-sectional view of the medical port shown in FIG. 7A.
  • FIG. 9A is a perspective cross-sectional view illustrating a flow path opening member of the medical port illustrated in FIG. 7A.
  • FIG. 9B is a bottom view of the flow path opening member shown in FIG. 9A.
  • FIG. 10A is a cross-sectional view showing a state where the thin film is broken by the flow path opening member of the medical port shown in FIG. 7A.
  • FIG. 10B is a cross-sectional view showing a state where the liquid feeding circuit is being attached to the medical port shown in FIG. 10A.
  • FIG. 11A is a cross-sectional view illustrating an example of a medical port according to the third embodiment.
  • FIG. 11B is a partially enlarged schematic cross-sectional view of the medical port shown in FIG. 11A.
  • FIG. 12 is a front view showing an example of a nutrient container according to the fourth embodiment.
  • FIG. 13A is a perspective view of a protective cover constituting the nutrient solution container shown in FIG. 12.
  • FIG. 13B is a top view of the protective cover shown in FIG. 13A.
  • FIG. 13C is a bottom view of the protective cover shown in FIG. 13A.
  • FIG. 13D is a side view of the protective cover shown in FIG. 13A.
  • FIG. 13E is another perspective view of the protective cover shown in FIG. 13A.
  • FIG. 14 is a front view showing another example of the nutrient solution container of the present invention.
  • FIG. 15 is a schematic configuration diagram of an example of an enteral nutrition set used in conventional enteral nutrition therapy.
  • FIG. 16 is a schematic configuration diagram of an example of an infusion set used for conventional parenteral nutrition therapy.
  • the communication portion further includes a rib
  • the tubular portion further includes an annular groove formed on the inner peripheral surface of which the rib can be fitted. The first mounting state is maintained by fitting the rib and the annular groove.
  • the communication portion when the rib is the first rib, the communication portion further includes a second rib disposed at a position farther from the puncture portion than the first rib.
  • the second rib is fitted not only in the second mounting state but also in the annular groove by fitting the second rib and the annular groove. It is preferable because it is possible to confirm that the second mounting state has been reached by the vibration at the time. Further, it is preferable that the first mounting state can be changed to the second mounting state by a simple operation of simply pressing the communicating portion in the axial direction.
  • the port main body portion when the tubular portion is a first tubular portion, is disposed so as to surround the first tubular portion, and on the side opposite to the side wall portion side of the top surface portion. It further includes a second tubular portion that protrudes and has a linear rib formed on the outer peripheral surface thereof.
  • the channel opening member is disposed so as to surround the first cylindrical portion, is disposed outside the second tubular portion, and is an upper surface portion of the channel opening member. It further includes a second tubular portion that protrudes from the port main body portion and has a linear groove formed on the inner peripheral surface thereof.
  • the longitudinal direction of the filament rib is the same as the axial direction of the second tubular portion, and the filament rib is slidably inserted into the filament groove.
  • the linear rib is inserted into the linear groove, the flow path opening member is prevented from rotating around its central axis. Therefore, it is easy to perform an operation of pushing the flow path opening member toward the thin film side and a connection operation between the connector and the medical port.
  • the port main body portion when the tubular portion is a first tubular portion, is disposed so as to surround the first tubular portion, and on the side opposite to the side wall portion side of the top surface portion. It further includes a second tubular portion that protrudes and has a linear groove formed on its outer peripheral surface. Further, when the tubular portion is the first tubular portion, the flow path opening member is disposed so as to surround the first tubular portion, and is disposed outside the second tubular portion, from the upper surface portion of the flow path opening member. It further includes a second cylindrical portion that protrudes toward the port main body and has a linear rib formed on the inner peripheral surface thereof.
  • the longitudinal direction of the linear groove is the same as the axial direction of the second tubular portion, and the linear rib is slidably inserted into the linear groove.
  • the linear rib is inserted into the linear groove, the flow path opening member is prevented from rotating around its central axis. Therefore, it is easy to perform an operation of pushing the flow path opening member toward the thin film side and a connection operation between the connector and the medical port.
  • the port main body portion when the tubular portion is the first tubular portion, the port main body portion is disposed so as to surround the first tubular portion, and protrudes to the side opposite to the side wall portion side of the top surface portion. And the 2nd tubular part by which the 1st collar part was formed in the front-end
  • the flow path opening member when the tubular portion is the first tubular portion, the flow path opening member is disposed so as to surround the first tubular portion, and is disposed outside the second tubular portion, from the upper surface portion of the flow path opening member. It further includes a second tubular portion that protrudes toward the port body portion and that has a second collar portion that is engageable with the first collar portion at the distal end portion thereof.
  • the communication portion further includes a male screw formed on the outer peripheral surface thereof.
  • the first tubular portion further includes a female screw formed on the inner peripheral surface thereof and capable of being screwed with the male screw of the communication portion.
  • the surface facing the female screw at the end of the male screw start side is in contact with the surface facing the female screw, and the second collar is closer to the top surface than the first collar. Be placed.
  • the flow passage opening member is rotated around its central axis, and the male screw and the female screw are screwed together to perform the second operation from the first mounting state. It can be put into a mounted state, which is preferable.
  • the flow path opening member is rotated several times around the central axis, and the screw thread is fitted in the screw groove, so that the holding of the second mounting state is stable. Furthermore, if the operation of rotating the flow path opening member around its central axis is not performed, it is not possible to change from the first mounting state to the second mounting state, so an external force is applied to the communicating portion when not desired, The possibility that the thin film is pierced by the puncture portion is low, which is preferable.
  • the communication part further includes a male screw formed on the outer peripheral surface thereof.
  • the tubular portion further includes a female screw formed on the inner peripheral surface thereof and capable of screwing with the male screw.
  • the flow channel opening member In the first mounting state, the flow channel opening member cannot be removed from the tubular portion unless the flow channel opening member is rotated around its central axis in the direction opposite to the direction in which the male screw and the female screw are screwed together.
  • the screwing start side of the male screw and the screwing start side of the female screw are screwed together.
  • the flow passage opening member is rotated around its central axis, and the male screw and the female screw are screwed together to perform the second operation from the first mounting state. It can be put into a mounted state, which is preferable. Further, in the second mounting state, the flow path opening member is rotated several times around the central axis, and the screw thread is fitted in the screw groove, so that the holding of the second mounting state is stable.
  • the communication portion includes a plurality of flow paths, and a plurality of holes are formed on the end surface opposite to the thin film side of the communication portion.
  • the communicating portion includes a protruding portion at an end opposite to the thin film side, and a hole constituting a part of each flow path is formed in the protruding portion.
  • the fact that a plurality of holes are formed on the end face means that one hole is partitioned into a plurality of small holes, and it is difficult to insert a connecting needle having a sharp tip into the hole.
  • the communicating part has a structure in which a connecting needle with a sharp tip is difficult to be inserted into the communicating part, the parenteral nutrition therapy that sends a liquid material into the body exclusively by piercing the connecting object with a sharp tip
  • the problem of erroneous connection, in which the liquid supply circuit for use is erroneously connected to the nutrient container used for enteral nutrition therapy, is more reliably solved.
  • the communication portion includes a partition wall disposed on the thin film side of the protruding portion and disposed so as to separate the spaces in the extending direction of the holes.
  • the communication portion is lighter than the case where the outer shape of the communication portion is substantially cylindrical, and the flow path opening member is easily molded, which is preferable.
  • the medical port further includes a protective cover that covers the flow passage opening member in the first mounting state and includes an engaging portion that can be engaged with the connection holding portion.
  • a protective cover that covers the flow passage opening member in the first mounting state and includes an engaging portion that can be engaged with the connection holding portion.
  • Embodiment 1 In Embodiment 1, an example of the medical port of the present invention and an example of the nutrient solution container of the present invention using the medical port will be described with reference to FIGS. 1 to 5E.
  • FIG. 1 is a front view showing an example of a nutrient container according to the present embodiment.
  • 2A is an enlarged perspective view showing an example of the medical port 13 of the present embodiment constituting the nutrient solution container shown in FIG. 1, and
  • FIG. 2B is a plan view of the medical port 13,
  • FIG. Fig. 2D is a side view of the medical port 13
  • Fig. 2E is another side view of the medical port 13
  • Fig. 2F is a cross-sectional view of the medical port 13.
  • FIG. 2G is a partially enlarged view of the medical port 13 shown in FIG. 2F.
  • the direction parallel to the central axis 19n of the flow path opening member 19 is set as shown in FIG.
  • the long axis direction of the top surface 17 orthogonal to the Z axis and the Z axis is taken as the X axis
  • the direction perpendicular to the Z axis and the X axis is taken as the Y axis.
  • the Z-axis direction is called “vertical direction”
  • the Z-axis arrow side that is, the upper side in FIG. 2A
  • the opposite side ie, the lower side in FIG. It is called “lower side” or “proximal side”.
  • the nutrient solution container 10 includes a container main body portion 11 including a flat bag-like flexible bag-shaped member 29, and a liquid material (including a nutrient solution filled in the container main body portion 11 ( (Not shown) and a medical port 13 fixed to the lower end of the container body 11.
  • a suspending portion 28 for suspending the nutrient solution container 10 on a stand or the like is provided above the flexible bag-shaped member 29.
  • the container body 11 is formed, for example, by stacking two soft resin sheets 16a and 16b and heat-sealing (thermally bonding) their outer peripheral edges to each other.
  • Reference numeral 2 in FIG. 1 indicates a heat seal region (portion to which dots are added in FIG. 1) of the two soft resin sheets 16a and 16b.
  • the medical port 13 is fixed to the container body 11 by being sandwiched between the soft resin sheets 16a and 16b.
  • the medical port 13 is integrated with the soft resin sheets 16a and 16b by heat-sealing the heat seal region 2 of the soft resin sheets 16a and 16b while being disposed between the soft resin sheets 16a and 16b. Can do.
  • the soft resin sheets 16a and 16b are not particularly limited, and conventionally known soft resin sheets used for, for example, medical soft containers can be used. Specifically, for example, a single-layer sheet made of vinyl chloride resin, polyethylene, ethylene-vinyl acetate copolymer, polyester, polybutadiene, polypropylene, polyamide, ethylene-methacrylate copolymer, or the like, or two layers of the above-mentioned single-layer sheet The laminated sheet laminated
  • the layer structure of the laminated sheet include nylon / polyethylene, nylon / polypropylene, polyethylene terephthalate / polyethylene, polyethylene terephthalate / polypropylene, polypropylene / polyethylene, nylon / polypropylene / polyethylene, and the like.
  • a laminated sheet for example, biaxially stretched polypropylene (OPP) / unstretched polypropylene (CPP) in which the same kind of resin having different grades (for example, film forming method, mechanical properties, or composition) is laminated. Good.
  • OPP biaxially stretched polypropylene
  • CPP unstretched polypropylene
  • the surface on the side to be heat-sealed is made of a material having easy heat-sealability (for example, polypropylene).
  • the thickness of the soft resin sheets 16a and 16b is not particularly limited, but is about 0.1 to 0.6 mm, for example. It is preferable that the soft resin sheets 16a and 16b have translucency (or translucency) because the liquid material in the flexible bag-like member 29 can be visually recognized from the outside. More preferably, the soft resin sheets 16a and 16b are transparent.
  • the pressure in the container main body 11 decreases as the liquid filled in the container main body 11 flows out of the medical port 13.
  • the bag-like member of the container body 11 is the flexible bag-like member 29 formed of a soft material such as a soft resin sheet, the flexible bag-like member 29 is deformed with the outflow of the liquid substance, Liquid outflow continues.
  • the medical port 13 includes a port main body portion 22 and a flow path opening member 19 attached to the port main body portion 22.
  • the flow path opening member 19 is molded separately from the port main body 22 and attached to the port main body 22.
  • the port main body portion 22 of the medical port 13 includes a base portion 20 and a mounting portion 21 to which the flow path opening member 19 is mounted.
  • the base 20 is erected in parallel with the Z axis from one main surface of the top surface portion 17 to the lower side, including a surface parallel to the XY plane, and the base body portion 11 (see FIG. 1).
  • a side wall 18 that can be fixed to the inner surface. Therefore, for example, a cylindrical space 20a (see FIG. 2F) surrounded by the side wall portion 18 is present below the top surface portion 17 of the port body portion 22 (on the side opposite to the mounting portion 21).
  • the space 20 a communicates with the inside of the container main body 11 in a state where the medical port 13 is fixed to the container main body 11. As shown in FIG. 1, in the state where the medical port 13 is fixed to the container main body 11 (see FIG. 1), the entire mounting portion 21 and the flow path opening member 19 are disposed outside the container main body 11. In addition, at least a part of the port main body 22 is disposed in the container main body 11.
  • the mounting portion 21 includes a tubular portion 21a and a second tubular portion 21b that protrude above the top surface portion 17 (on the side opposite to the side wall portion 18 side of the top surface portion 17).
  • the second tubular portion 21b is disposed around the first tubular portion 21a and is disposed away from the first tubular portion 21a.
  • the first tubular portion 21a has a through hole 21e that penetrates the top surface portion 17 in the vertical direction (thickness direction), and the through hole 21e communicates with a space 20a below the through hole 21e.
  • the alternate long and short dash line 151 is the central axis of the first tubular portion 21a and the second tubular portion 21b, and coincides with the central axis 19n (see FIG. 2A) of the flow path opening member 19. In the example shown in FIGS. 2A to 2F, the alternate long and short dash line 151 is orthogonal to the top surface portion 17.
  • An annular groove 211 that can be fitted to the first rib 198 and the second rib 199 (see FIG. 4A) of the communication portion 19a of the flow passage opening member 19 described later is formed on the inner surface in the vicinity of the upper end of the first tubular portion 21a. Has been.
  • a pair of filament ribs 21c are formed on the outer peripheral surface of the second tubular portion 21b.
  • the pair of linear ribs 21c are symmetric with respect to the central axis 151 of the second tubular portion 21b.
  • the longitudinal direction of each filament rib 21c is the same direction as the central axis direction of the second tubular portion 21b.
  • the pair of linear ribs 21c are slidably received on the inner peripheral surface of the second cylindrical portion 19c of the flow passage opening member 19 described later.
  • a pair of linear grooves 190a is formed, and each linear groove 190a receives a part of each linear rib 21c.
  • the flow path opening member 19 is prevented from rotating around the central axis 19n (see FIG. 2A). Therefore, the lock protrusion 197 (see FIGS. 2D and 2E) is fitted into the lock recess 321g (see FIG. 5A) of the connector 25 of the liquid feeding circuit 27 (see FIG. 5A and the like) to be described later, and the claw portion 19e and the connector 25 are connected. It is easy to perform a rotation operation performed when the engagement wall 321d is engaged.
  • the pair of linear ribs 21c and the pair of linear grooves 190a also function as a guide when the flow path opening member 19 moves to the top surface portion 17 side.
  • the second tubular portion 21b has the linear rib 21c and the second cylindrical portion 19c has the linear groove 190a.
  • the second tubular portion 21b has a pair of linear grooves 21d on its outer peripheral surface, and the second cylindrical portion 19c is on its inner peripheral surface.
  • a pair of linear ribs 190b may be provided, and the linear ribs 190b may be slidably inserted into the linear grooves 21d.
  • the shape of the outer peripheral surface 18a of the side wall portion 18 surrounding the space 20a as viewed along the Z-axis direction is a substantially rhombus, and the widths at both ends of the substantially rhombus in the X direction are the tips. It gradually becomes narrower toward. Therefore, the side wall 18 is sandwiched between the two soft resin sheet materials 16a and 16b (see FIG. 1) constituting the container body 11, and the medical port 13 is fixed to the soft resin sheets 16a and 16b by heat sealing.
  • the sealing failure is suppressed at the boundary between the portion where the soft resin sheets 16a and 16b are in close contact with each other and the portion where the soft resin sheets 16a and 16b and the side wall portion 18 are in close contact with each other.
  • the liquid material flows between the through hole 21e and the space 20a.
  • a shielding film 16 is attached. Therefore, as shown in FIG. 1, even if the nutrient solution container 10 is directed so that the medical port 13 faces downward, the liquid in the nutrient solution container 10 leaks out of the nutrient solution container 10. Absent. Since the thin film 16 is attached to the lower surface 17a of the top surface portion 17 so as to close the through hole 21e, it can be said that the thin film 16 is disposed on an extension line of the through hole 21e.
  • Examples of the material of the thin film 16 include aluminum foil, a laminated film made of paper and aluminum foil, and a resin film containing the same resin as that contained in the base 20.
  • the resin film may be either a single layer film or a laminated film composed of a plurality of layers. Among these, from the viewpoint of ensuring high adhesion to the base portion 20 of the port body portion 22 of the thin film 16 by heat welding, a resin film containing the same resin as that contained in the port body portion 22 on the surface in contact with the port body portion 22 is preferable.
  • the thin film 16 may be transparent, translucent, or opaque, but in FIG. 2C, dots are attached to the thin film 16 for easy understanding (the same applies to FIG. 7C and the like). .
  • the method for adhering the thin film 16 to the port main body 22 is appropriately selected according to the material of the thin film 16 and the material of the port main body 22.
  • the flow path opening member 19 of the medical port 13 has a communication portion 19a partially inserted into the through hole 21e, and a first tubular shape.
  • a portion 19b, a second cylindrical portion 19c, an upper surface portion 19d, and a pair of claw portions 19e are included.
  • the pair of claw portions 19e protrudes outward (in a direction parallel to the XY plane) from the outer peripheral surface of the upper surface portion 19d, for example, and the second cylindrical portion 19c It is provided around.
  • the opposite surface of the pair of claws 19e on the top surface 17 side and the outer surface (upper surface) of the upper surface portion 19d are in the same plane.
  • the pair of claw portions 19e have locking projections 197 (on the surfaces facing the top surface portion 17) that can be fitted into lock recesses 321g (see FIG. 5A) of the connector 25 of the liquid feeding circuit 27 (see FIG. 4A and the like) described later. 2D and 2E). That is, the pair of claw portions 19e function as a connection holding portion that can hold a connection state with a connector 25 of a liquid feeding circuit 27 (see FIG. 5B or the like) described later.
  • the first cylindrical part 19b and the second cylindrical part 19c are arranged in this order around the communication part 19a, the first cylindrical part 19b is from the communication part 19a, and the second cylindrical part 19c is the first cylinder. Each of them is arranged away from the shape portion 19b.
  • the alternate long and short dash line 151 is the central axis of the first tubular portion 21a (see FIG. 2F), but also coincides with the central axes of the communication portion 19a, the first cylindrical portion 19b, and the second cylindrical portion 19c.
  • the communication portion 19a, the first tubular portion 19b, and the second tubular portion 19c are connected to each other by an upper surface portion 19d. Therefore, in the second mounting state, the flow path opening member 19 is combined with the tight contact of the inner peripheral surface of the first tubular portion 19b with the outer peripheral surface of the first tubular portion 21a, and the puncture portion 194 of the communication portion 19a. Even when the thin film 16 is broken and the liquid material filled in the container main body 11 (see FIG. 1) flows into the channel opening member 19 side, the channel 211e (see FIG. 3e) of the communication portion 19a of the channel opening member 19 It has a structure that prevents liquids from leaking from other locations.
  • the communication portion 19a includes a protruding portion 191 at the end opposite to the puncture portion 194 side.
  • the protruding portion 191 has a circular planar shape and protrudes above the upper surface portion 19d (on the side opposite to the first cylindrical portion 19b of the upper surface portion 19d), and is inside a connector 25 (see FIG. 4A and the like) described later. Inserted into.
  • a plurality of holes 192 penetrating in the thickness direction are formed in the protruding portion 191.
  • the communication portion 19a has a plurality of spaces (through holes 21e) on the thin film 16 side below the protrusions 191 (on the side close to the thin film 16) (see FIG. 2F and the like).
  • a plurality of partition walls 193 are provided. The partition walls 193 are arranged so as to separate the spaces (through holes 21e) in the extending direction of the holes 192 from each other. Therefore, in order to connect the connector 25 of the liquid delivery circuit 27 (see FIG. 4A, etc.) to the medical port 13, the channel opening member 19 is pushed into the thin film 16 side by the connector 25, and the thin film 16 is broken by the puncture portion 194.
  • a plurality of spaces 196 and a plurality of holes 192 which are formed by having a plurality of partition walls 193 and open to the space 20a of the port body portion 22 (base portion 20) It functions as a plurality of flow paths 211e (see FIG. 3B) that can cause the liquid material filled in the portion 11 to flow out of the nutrient container (in the direction of arrow X (see FIG. 3A)).
  • the channel opening member 19 shown in FIGS. 3A and 3B has four partition walls 193 and thus has four channels. Since the four partition walls 193 are arranged at an equal angle along the circumferential direction and are integrated with each other, as shown in FIG. 3B, it can be seen when the flow path opening member 19 is viewed from the bottom surface side.
  • the outer shape of the partition body composed of the plurality of partition walls 193 is substantially a cross.
  • the communication part 19a of the flow path opening member 19 has a puncture part 194 on the side close to the thin film 16 in both axial direction (Z-axis direction) ends.
  • the tip of the puncture portion 194 is sharp enough to break through the thin film 16.
  • each of the plurality of partition walls 193 has an inclined surface 195 inclined toward the tip on the thin film side of the communication portion 19a, and each inclined surface 195 corresponds to the communication portion 19a.
  • a puncture portion 194 that converges at the tip on the thin film side and can break through the thin film 16 is formed.
  • each partition wall 193 includes a first rib 198 and a second rib 199 formed on the side thereof. That is, the 1st rib 198 and the 2nd rib 199 are formed in the surface facing the internal peripheral surface of the 1st tubular part of the communication part 19a.
  • the plurality of first ribs 198 are arranged along a single circumference centered on a predetermined point on the central axis 151 and separated from the tip of the communication portion 19a by the thin film 16 side.
  • the plurality of second ribs 199 are further away from the tip on the thin film 16 side of the communication portion 19a than the plurality of first ribs 198, and have another single circumference centered on another predetermined point on the central axis 151. Are arranged along.
  • FIG. 4A shows a state where the first rib 198 is fitted into the annular groove 211
  • FIG. 4B shows a state where the second rib 199 is fitted into the annular groove 211.
  • the material other than the thin film 16 of the medical port 13 is not particularly limited, but is harder than the material of the soft resin sheets 16a and 16b.
  • polyethylene (PE), polypropylene (PP), polyacetal (POM), polyethylene terephthalate. (PET), polycarbonate (PC), etc. are mentioned.
  • FIG. 5A is a perspective view showing a schematic configuration of an example of a connector 25 connected to the medical port of the present invention
  • FIG. 5B is a plan view of the connector 25 shown in FIG. 5A
  • FIG. 5A is a bottom view of the connector 25 shown in FIG. 5A
  • FIG. 5D is a side view of the connector 25 shown in FIG. 5A
  • FIG. 5E is another side view of the connector 25 shown in FIG. 6A.
  • the female connector 25 includes an insertion portion 33, a liquid feeding tube connection portion 30, a collar portion 32, and a grip portion 31.
  • the connector 25 is connected to the medical port 13 attached to the mouth portion 12 of the container body 11, so that a flexible liquid feeding tube 26 (FIG. 4A) connected to the inside of the container body 11 and the connector 25. (See FIG. 4C and the like).
  • An alternate long and short dash line 150 is the central axis of the insertion portion 33 and the liquid feeding tube connection portion 30.
  • the central axis 151 of the first tubular portion 21 a and the flow path opening member 19 It coincides with the central axis 19n.
  • the direction of the central axis 150 is the vertical direction, and the upper side (side connected to the medical port) of FIG. 5A is called “upper side”, and the lower side of the page is called “lower side”.
  • the connector 25 has a generally cylindrical shape as a whole, and the insertion portion 33 near the upper end thereof has a large inner diameter that is equal to or slightly smaller than the maximum outer diameter of the protruding portion 191 of the medical port 13 (see FIG. 3A and the like).
  • a small-diameter portion 33b having a diameter portion 33a and having an inner diameter smaller than the outer diameter of the projecting portion 191 (see FIG. 4A and the like) of the flow path opening member 19 and the inner diameter of the large-diameter portion 33a is provided below the large-diameter portion 33a.
  • the protruding portion 191 of the medical port 13 is pushed into the insertion portion 33 of the connector 25 so that the connector 25 and the medical port 13 are connected.
  • the outer peripheral surface of the protruding portion 191 is in close contact with the inner peripheral surface of the large-diameter portion 33a. Therefore, the medical port 13 and the connector 25 can be reliably connected without causing leakage of the liquid material (see FIG. 4D).
  • the insertion part 33 of the connector 25 has the level
  • the step surface 33c contacts the end surface 191a of the protruding portion 191 (see FIG. 4D).
  • a substantially cylindrical liquid feeding tube connecting portion 30 is provided below the small diameter portion 33b.
  • a pair of flanges 32 are formed around and above the large diameter portion 33a.
  • the pair of collar portions 32 are symmetric with respect to the central axis 150.
  • the collar portion 32 includes an arc-shaped wall 321 substantially extending along a cylindrical surface having the central axis 150 as a central axis, and a lower end of the arc-shaped wall 321 extending in a direction perpendicular to the central axis 151 and an upper end of the large-diameter portion 33a. It has a connecting part 322 that connects.
  • the arc-shaped wall 321 includes a passing region 321a, an engaging region 321b, and a non-passing region 321c due to the difference in the shape of the inner peripheral surface facing the central axis 151.
  • the inner peripheral surface of the passing region 321a is a part of a cylindrical surface having a diameter DF21
  • the inner peripheral surface of the non-passing region 321c is a part of a cylindrical surface having a diameter DF23 (DF23 ⁇ DF21). is there.
  • the engaging region 321b between the passing region 321a and the non-passing region 321c has an engaging wall 321d extending in the circumferential direction so as to connect the upper end of the passing region 321a and the upper end of the non-passing region 321c. It is provided as an engaging part that can engage with the claw part 19e of the medical port 13.
  • An inner peripheral surface of the engagement wall 321d facing the central axis 150 is a part of a cylindrical surface having a diameter DF22 (DF22 ⁇ DF21). Since the engaging region 321b includes the engaging wall 321d, the region between the engaging wall 321d and the crossing portion 322 is depressed in a concave shape.
  • the region between the engaging wall 321d and the crossing portion 322 is recessed from the central shaft 150 in the radial direction relative to the engaging wall 321d to form the concave portion 321e.
  • the non-passing region 321c adjacent to the engaging region 321b in the circumferential direction protrudes in the direction of the central axis 151 relative to the concave portion 321e, and constitutes a convex portion 321f.
  • a lock recess 321g that is recessed in a concave shape is formed on the lower surface (the surface on the recess 321e side, the surface facing the crossover portion 322) of the end of the engagement wall 321d on the non-passing region 321c side.
  • a through hole 220 (see FIG. 5C) that penetrates in the thickness direction of the crossover portion 322 is formed in a portion of the crossover portion 322 that faces the engagement wall 321d, but the through hole 220 may not be formed. Good.
  • a pair of grip portions 31 are formed around the insertion portion 33 so as to protrude outward from the outer peripheral surface of the insertion portion 33 (a direction orthogonal to the central axis 150).
  • the rotation operation is performed with the pair of grip portions 31.
  • FIG. 4A shows a state immediately before a liquid feeding circuit 27 including a connector 25 and a flexible liquid feeding tube 26 connected to the connector 25 is connected to the medical port 13, and
  • FIG. 4C shows a state in which the thin film 16 is broken while the liquid supply circuit 27 is being connected to the medical port 13, and the protrusion 191 of the medical port 13 is inserted into the insertion portion of the connector 25. 33 (see FIG. 5A) is shown completely inserted.
  • the first rib 198 is fitted in the annular groove 211, and the tip of the puncture portion 194 is attached to the thin film 16. They are not in contact with each other or are in contact with the thin film 16 but are not pressed against the thin film 16 (first mounting state).
  • the first rib 198 and the annular groove 211 can be fitted together by pressing the flow path opening member 19 toward the thin film 16 while pressing the projecting portion 191 into the connector 25.
  • the flow path opening member 19 is pushed into the thin film 16 side and is fitted into the second rib 199 and the annular groove 211. That is, the channel opening member 19 is moved to the container body 11 side by an operation for connecting the connector 25 to the medical port 13.
  • the thin film 16 is broken by the puncture portion 194, and the inner peripheral surface of the first tubular member 19b is in close contact with the outer peripheral surface of the first tubular portion 21a.
  • the flow path opening member 19 is mounted on the port main body portion 22 so as not to cause liquid leakage (second mounting state).
  • the outer peripheral surface 191 b of the protruding portion 191 is in close contact with the large diameter portion 33 a of the connector 25.
  • the second rib 199 can be reliably fitted to the annular groove 211, which is preferable.
  • the lock protrusion 197 (see FIG. 2E, etc.) It slides on the surface 321h while being pressed against the surface 321h on the crossing portion 322 side of the engaging wall 321d, and then fits into the lock recess 321g (see FIG. 5A).
  • the state in which the connector 25 is connected to the medical port 13 can be stably held by fitting the lock protrusion 197 and the lock recess 321g.
  • the connector 25 is provided with a convex portion 321f (see FIG. 5A) adjacent to the lock concave portion 321g in which the lock projection 197 is accommodated, the lock projection 197 of the medical port 13 is allowed to enter the lock concave portion 321g. If the claw portion 19e (see FIG. 2E and the like) is moved until it comes into contact with the convex portion 321f, the claw portion 19e and the engagement wall 321d can be reliably engaged.
  • the rotation of the connector 25 with respect to the medical port 13 is restricted by the claw portion 19e of the medical port 13 coming into contact with the convex portion 321f of the connector 25.
  • the claw part 19e and the engagement wall 321d can be reliably engaged by the simple operation of rotating the connector 25 with respect to the medical port 13 until the rotation is restricted.
  • connection between the medical port 13 and the connector 25 may be held by various known structures.
  • the claw portion 19e including the lock projection 197 of the medical port 13 that is a connection holding portion (see FIG. 3E and the like). ) And an engagement wall 321d including the lock recess 321g of the connector 25 (see FIG. 8A) may be used.
  • the connection holding portion is provided in the flow path opening member 19, but may be provided in the port main body portion 22.
  • the hardness measured based on JIS-K7202 is preferably R40 to R140 from the viewpoint of improving the connection workability of the flexible liquid feeding tube 26 to the connector 25, and R50 to R100. Is more preferable.
  • the form of the flow path opening member 19 is not limited to that shown in FIGS. 3A and 3B.
  • the flow path opening member 19 has three holes 192 in the protruding portion 191, three partition walls 193 on the thin film side of the protruding portion 191, and three flow paths. You may have.
  • the flow path opening member 19 has two holes 192 in the protrusion 191 and one partition wall 193 on the thin film side of the protrusion 191 and has two flow paths. It may be.
  • the communication portion 19a of the flow path opening member 19 has a substantially cylindrical shape, and has 2 to 4 holes 192, so that the inner cavity is divided into 2 to 4 holes. It may have 2 to 4 flow paths.
  • the 1st rib 198 and the 2nd rib 199 are formed in the surface facing the internal peripheral surface of the 1st tubular part of the communication part 19a, ie, the outer peripheral surface of the communication part 19a.
  • the medical port 13 may not include the second tubular portion 21b and the second tubular portion 19c.
  • FIG. 6 is a front view of an example of the nutrient solution container 10 of the present embodiment.
  • FIG. 7A is an enlarged perspective view showing an example of the medical port 43 of the present embodiment constituting the nutrient solution container shown in FIG. 6, and FIG. 7B is a plan view of the medical port 43, FIG. Is a bottom view of the medical port 43, FIG. 7D is a side view of the medical port 43, FIG. 7E is another side view of the medical port 43, and FIG. 7F is a view of the medical port shown in FIG. 2A.
  • It is sectional drawing. 8A is a partial enlarged cross-sectional schematic view of the medical port 43, FIG. 8B is a partial enlarged cross-sectional view of the medical port 43, and FIG. 9A illustrates the flow path opening member 19 of the medical port 43.
  • FIG. 9B is a perspective sectional view
  • FIG. 9B is a bottom view of the flow path opening member 19 shown in FIG. 9A.
  • the medical port 43 and the nutrient solution container 10 of this embodiment are different from those of Embodiment 1 except that the holding structure for the first tubular portion 21a of the flow path opening member 19 is different. It has the same configuration as the medical port and the nutrient solution container 10, and the same members are denoted by the same member numbers and the description thereof is omitted. Further, the liquid feeding circuit 27 shown in FIG. 10B has the same configuration as the liquid feeding circuit 27 connected to the medical port of the first embodiment. 8A is a cross-sectional view, but hatching is not included for easy understanding.
  • the communication portion 19a of the flow path opening member 19 is formed on the outer peripheral surface (the surface facing the inner peripheral surface of the first tubular portion 21a of the communication portion 19a).
  • the male screw 200 is included. As shown in FIGS. 9A and 9B, each part of the male screw 200 is formed on the side surface of the partition wall 193 (the surface facing the inner peripheral surface of the first tubular portion 21a), so the male screw 200 is discontinuous.
  • the first tubular portion 21a includes a female screw 212 that is formed on the inner peripheral surface of the first tubular portion 21a and can be screwed into the male screw 200.
  • the 2nd tubular part 21b contains the 1st collar part 211b formed in the front-end
  • the male screw 200 in the first wearing state, may or may not be fitted to the female screw 212 unless the thin film 16 is pierced by the puncture portion 194.
  • the surface 200a facing the female screw 212 at the end of the male screw 200 on the screwing start side is in contact with the surface 212a facing the male screw 200 on the screwing start side of the female screw 212, for example. Therefore, if the flow path opening member 19 is not rotated about its central axis, the surface 200a and the surface 212a collide even if a force that can be pressed against the thin film 16 is applied to the flow path opening member 19. This prevents the flow path opening member 19 from being pushed into the thin film 16 side. Unless the flow path opening member 19 is rotated around the central axis with respect to the first tubular portion 21a, the thin film 16 is not pierced by the communicating portion 19a.
  • the second collar portion 191c is disposed closer to the top surface portion 17 (see FIG. 9A) than the first collar portion 211b, and the second collar portion 191c is The flow path opening member 19 cannot be removed from the mounting portion 21 unless it gets over the first flange portion 211b. In the first mounting state, the second flange part 191c may be locked to the first flange part 211b.
  • the grasping portion 31 is grasped to be connected to the medical port 43.
  • the lock protrusion 197 see FIG. 7D, FIG. 7E, etc.
  • the lock protrusion 197 is brought into contact with the surface 321h of the engaging wall 321d on the crossing portion 322 as the connector 25 rotates. It slides on the surface 321h while being pressed down, and then fits into the lock recess 321g (see FIG. 5A).
  • the state in which the connector 25 is connected to the medical port 43 can be stably held by fitting the lock protrusion 197 and the lock recess 321g.
  • FIG. 11A is a cross-sectional view showing an example of the medical port of the present embodiment
  • FIG. 11B is a partially enlarged schematic cross-sectional view of the medical port shown in FIG. 11A.
  • the medical device of Embodiment 2 except that the channel opening member 19 does not include the second tubular portion and the mounting portion does not include the second tubular portion.
  • the same member is given the same member number, and the description thereof is omitted.
  • 11A and 11B show the medical port 53 in the first mounting state, but the flow path opening member 19 is rotated around its central axis, for example, one or more times, and the screw 200 starts to be screwed.
  • the side is screwed with the screwing start side of the female screw 212, and a part of the screwing start side of the male screw is in the screw groove of the female screw 212. Therefore, if the flow passage opening member 19 is not rotated around its central axis in the direction opposite to the rotational direction in which the male screw 200 is screwed to the female screw 212, the flow passage opening member 19 is moved to the first tubular portion (tubular portion). It cannot be removed from 21a (first wearing state).
  • the thin film 16 is not pierced by the puncture portion 194 of the communication portion 19a.
  • FIG. 12 is a front view of an example of a nutrient container according to the present embodiment.
  • the medical port 43 has the same configuration as the medical port and nutrient solution container except that a protective cover 60 for protecting the flow path opening member 19 is attached to the medical port 43.
  • the same member is given the same member number, and the description thereof is omitted.
  • the flow path opening member 19 is protected by the protective cover 60, it is possible to prevent external force from being applied to the flow path opening member 19 when not desired. Therefore, when it is not desired, an external force is applied to the flow channel opening member 19, the flow channel opening member 19 is pushed into the container main body 11 side, and the thin film 16 (see FIG. 7F etc.) by the communication portion 19a pushed into the container main body portion 11 side. ) Can be prevented from being broken through.
  • the protective cover 60 can be engaged with the cover main body 61 covering the flow path opening member 19 and the claw portion 19e of the medical port 43 (see FIGS. 7D and 7E). And a pair of flange portions 62 including the wall 621d as the engaging portion.
  • the engagement wall 621d of the flange portion 62 of the protective cover 60 has the same structure as the engagement wall 321d of the flange portion 32 of the connector 25 shown in FIGS. 5A to 5E.
  • the protective cover 60 is covered from the outer surface side of the top surface portion 17 so that the flow path opening member 19 and the mounting portion 21 are accommodated in the cover main body 61, and the protective cover 60 is rotated around its central axis to obtain a medical port. If the lock protrusion 197 (see FIG. 3E, etc.) of the 43 claw portions 19e is fitted into a lock recess 621g formed on the lower surface (surface on the recess 618 side) of the end of the non-passage region 621c of the engagement wall 621d. The state in which the protective cover 60 is attached to the medical port 43 can be stably maintained.
  • the flange 62 of the protective cover 60 abuts the protective cover 60 on the top surface 17 of the medical port 13 when the flow path opening member 19 is mounted on the medical port 13 in the first mounting state.
  • An arcuate wall 621 is included. Therefore, holding
  • the protective cover 60 can also be attached to the medical port of the first to third embodiments.
  • the protective cover 60 is removed from the medical port 43, a force for moving the communication portion 19a toward the thin film 16 is applied to break the thin film 16, and the liquid feeding circuit 27 (see FIG. 10B) is connected to the medical port 43. Only (see FIG. 10B), the liquid can be supplied to the patient.
  • the liquid feeding circuit connected to the pressure sensor is connected to a flow rate regulator for adjusting the flow rate of the liquid material flowing through the liquid feeding tube 26 by pressing the liquid feeding tube 26, a drip tube, a nasal tube fixed to the patient, etc. It may further include components provided in a liquid feeding circuit used for conventionally known enteral nutrition therapy, such as a connector that can be used and a cover of the connector.
  • the container body 11 of the nutrient solution container 10 shown in FIGS. 1, 6, and 12 is filled with a liquid material (not shown) such as a nutrient solution, which is shown in FIG.
  • the nutrient container 40 may be an empty container in which the container body 11 is not filled with a liquid material.
  • the container main body 11 of the nutrient solution container 10 has an opening 23, a zip 23 a that reversibly opens and closes the opening 23 across the width of the opening 23. (It is an engaging part that can be freely opened and closed. It is also called “chuck seal”).
  • a hanging part (not shown) may be provided above the opening 23.
  • a medical port of a nutrient container suitable for enteral nutrition therapy, a nutrient container using the same, and a nutrient supply set including the nutrient container and a liquid feeding circuit are provided. it can.

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Abstract

La présente invention porte sur un orifice médical qui est fixé à une partie de corps de contenant d'un contenant de nutriment et permet une communication entre l'intérieur et l'extérieur de la partie de corps du contenant. L'orifice médical comprend : une partie de corps d'orifice (22) ; un film mince (16) fixé à la partie de corps d'orifice, pour bloquer l'écoulement de liquide à l'intérieur de la partie de corps de contenant vers l'extérieur du contenant de nutriment ; un élément d'ouverture de trajet d'écoulement (19) qui est fixé à une partie de fixation (21) de la partie de corps d'orifice ; et un élément de maintien de liaison (19e) qui peut maintenir un état de liaison avec un élément de liaison. L'élément d'ouverture de trajet d'écoulement comprend : une partie de communication (19a) qui comprend une partie de perçage (194) et un trajet d'écoulement pour permettre à un liquide qui remplit la partie de corps de contenant de s'écouler vers l'extérieur du contenant de nutriment ; et une partie cylindrique (19b), et l'élément d'ouverture de trajet d'écoulement (19) peut adopter un premier état de fixation et un second état de fixation par rapport à la partie de fixation (21).
PCT/JP2011/059291 2011-04-14 2011-04-14 Orifice médical, contenant de nutriment employant celui-ci et ensemble de fourniture de nutriment WO2012140768A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CN201180070095.9A CN103491926B (zh) 2011-04-14 2011-04-14 医疗用端口、使用该医疗用端口的营养剂用容器以及营养剂供给组件
SG2013076153A SG194470A1 (en) 2011-04-14 2011-04-14 Medical port, nutrient container employing same, and nutrient supply set
KR1020137028596A KR101799138B1 (ko) 2011-04-14 2011-04-14 의료용 포트, 및 그것을 이용한 영양제용 용기와 영양제 공급 세트
PCT/JP2011/059291 WO2012140768A1 (fr) 2011-04-14 2011-04-14 Orifice médical, contenant de nutriment employant celui-ci et ensemble de fourniture de nutriment
JP2013509713A JP5920340B2 (ja) 2011-04-14 2011-04-14 医療用ポート、およびそれを用いた栄養剤用容器並びに栄養剤供給セット

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PCT/JP2011/059291 WO2012140768A1 (fr) 2011-04-14 2011-04-14 Orifice médical, contenant de nutriment employant celui-ci et ensemble de fourniture de nutriment

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FR3047474A1 (fr) * 2016-02-09 2017-08-11 Union Plastic Dispositif d’obturation
WO2020115989A1 (fr) * 2018-12-05 2020-06-11 イーエヌ大塚製薬株式会社 Connecteur
WO2023081991A1 (fr) * 2021-11-13 2023-05-19 Santos Leite Ronaldo Couvercle fixe pour emballage à longue durée de vie avec accès pour équipement de nutrition entérale en vue d'une utilisation par système fermé
US11674614B2 (en) 2020-10-09 2023-06-13 Icu Medical, Inc. Fluid transfer device and method of use for same

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JP2016052345A (ja) * 2014-09-02 2016-04-14 株式会社ジェイ・エム・エス 半固形化栄養剤用アダプター
JP7174953B2 (ja) * 2019-03-28 2022-11-18 大成化工株式会社 シリンジ用の調製補助具

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CN103491926A (zh) 2014-01-01
JPWO2012140768A1 (ja) 2014-07-28
CN103491926B (zh) 2016-05-18

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