JP5125051B2 - Medical connector - Google Patents

Medical connector Download PDF

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Publication number
JP5125051B2
JP5125051B2 JP2006279203A JP2006279203A JP5125051B2 JP 5125051 B2 JP5125051 B2 JP 5125051B2 JP 2006279203 A JP2006279203 A JP 2006279203A JP 2006279203 A JP2006279203 A JP 2006279203A JP 5125051 B2 JP5125051 B2 JP 5125051B2
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container
medical connector
peripheral surface
tube
outlet
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JP2008093211A (en
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大輔 ▲堤▼
尚継 井藤
隆彦 国重
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JMS Co Ltd
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JMS Co Ltd
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本発明は、生体に投与するための液状物を収容した容器とその液状物を生体に投与するための投与管とを接続する際に用いられる医療用接続具に関する。   The present invention relates to a medical connector used when connecting a container containing a liquid material for administration to a living body and an administration tube for administering the liquid material to the living body.

従来より、例えば、特許文献1に開示されているように、食物の嚥下に障害を有する患者に対して、液状物としての栄養剤を胃に直接注入して投与する経管栄養補給法が行われることがある。この経管栄養補給法は、消化器官を働かせることができるため、静脈に栄養剤を注入する経静脈栄養補給法に比べて患者の回復期間の短縮化が図られるという長所を有しており、広く用いられるようになってきている。   Conventionally, as disclosed in Patent Document 1, for example, a tube feeding method has been performed in which a liquid nutrient is directly injected into a stomach and administered to a patient who has a disorder in swallowing food. May be. This tube feeding method has the advantage that the recovery period of the patient can be shortened compared to the intravenous feeding method in which a nutrient is injected into the vein because the digestive organs can work. Widely used.

上記経管栄養補給法では、患者の口や鼻から胃へ挿入した投与管や、腹壁から胃壁に跨って造設された孔部から胃に挿入した投与管の上流端部を容器の出口部に接続し、該容器に収容された栄養剤を投与管により胃に導くようにしている。
実開平7−31059号公報
In the above-mentioned tube feeding method, the upstream end of the administration tube inserted into the stomach from the mouth or nose of the patient or the hole constructed from the abdominal wall to the stomach wall is used as the outlet portion of the container. And the nutrient contained in the container is guided to the stomach by the administration tube.
Japanese Utility Model Publication No. 7-31059

ところで、上記栄養剤を収容する容器としては、特許文献1にも開示されているように、樹脂製フィルムを溶着した袋状の容器や、ポリプロピレン等を円筒状に成形した容器等がある。さらに、栄養剤が予め充填されたプレフィルドタイプの容器や、患者に合わせて医療現場で調合した栄養剤を移し替え可能な容器等もある。このように容器には様々な種類があるとともに、製造メーカーも複数あることから、容器の出口部の形状は、容器の本体部分から突出する形状であるという点を除いて、互いに異なっている。このため、医療現場においては容器毎に専用の接続構造を持った接続具を用意しなければならず、これらの管理を考えると不便である。   By the way, as disclosed in Patent Document 1, there are a bag-like container in which a resin film is welded, a container in which polypropylene or the like is formed into a cylindrical shape, and the like. Furthermore, there are prefilled type containers pre-filled with nutrients, containers that can transfer nutrients formulated at the medical site according to the patient, and the like. As described above, since there are various types of containers and there are a plurality of manufacturers, the shape of the outlet portion of the container is different from each other except that the shape protrudes from the main body portion of the container. For this reason, in the medical field, it is necessary to prepare a connecting tool having a dedicated connection structure for each container, which is inconvenient when considering these controls.

これに対し、容器と投与管との接続構造を複数種の容器の出口部に対応できるように汎用性を持たせいという要求がある。しかしながら、汎用性を持たせた場合には、様々な形状の出口部に投与管を確実に接続して栄養剤の洩れを抑制するのは難しく、しかも、専用の接続構造を持ったものに比べて接続作業性が悪化することも考えられる。   On the other hand, there exists a request | requirement of having versatility so that the connection structure of a container and an administration tube can respond | correspond to the exit part of multiple types of containers. However, in the case of general versatility, it is difficult to suppress the leakage of nutrients by securely connecting the administration tube to the outlets of various shapes, and compared to those with a dedicated connection structure. Therefore, the connection workability may be deteriorated.

本発明は斯かる点に鑑みてなされたものであり、その目的とするところは、生体に投与する液状物が収容された複数種の容器の各出口部と投与管との接続作業性を良好にしながら、接続部分からの液状物の洩れを抑制することにある。   The present invention has been made in view of such a point, and the object of the present invention is to improve the connection workability between each outlet portion of a plurality of kinds of containers containing liquids to be administered to a living body and the administration tube. However, the object is to suppress leakage of the liquid from the connecting portion.

上記目的を達成するために、本発明では、容器の出口部が接続される容器接続部を柔軟なものとするとともに、この容器接続部の投与管接続部側に、該容器接続部よりも硬い把持部を設けた。   In order to achieve the above object, in the present invention, the container connecting portion to which the outlet portion of the container is connected is made flexible, and the container connecting portion is harder than the container connecting portion on the administration tube connecting portion side. A gripping part was provided.

具体的には、請求項1の発明では、液状物を収容する容器から突出するように設けられた出口部と、上記液状物を生体に導く投与管との間に配置され、上記出口部及び上記投与管を接続する医療用接続具において、上記投与管の上流端部が接続される投与管接続部と、上記容器の出口部が挿入された状態で接続される筒状をなし、挿入された状態にある上記出口部の外周面形状に対応して拡径するように変形する柔軟性を有する容器接続部と、上記容器接続部の投与管接続部側に設けられ、該容器接続部よりも硬く構成された把持部とを備え、上記容器接続部の周壁には、該容器接続部よりも硬く構成されて中心線方向に延びる骨部が埋め込まれ、上記把持部は、上記出口部が挿入される側へ向けて上記容器接続部を外側から覆うように延びる延長部を有し、上記延長部と上記容器接続部との間には、隙間が設けられ、上記延長部の先端部は、上記容器接続部における上記出口部が挿入される側の端部よりも上記投与管接続部側に位置付けられている構成とする。 Specifically, in the invention of claim 1, the outlet portion provided so as to protrude from a container that stores the liquid material and an administration tube that guides the liquid material to a living body, the outlet portion and In the medical connector for connecting the administration tube, the administration tube connecting portion to which the upstream end portion of the administration tube is connected and the tube connected to the outlet portion of the container are inserted and inserted. A container connecting portion having flexibility to deform so as to expand the diameter corresponding to the shape of the outer peripheral surface of the outlet portion in a closed state, and provided on the administration tube connecting portion side of the container connecting portion, from the container connecting portion A bone portion that is harder than the container connection portion and extends in the center line direction is embedded in the peripheral wall of the container connection portion , and the grip portion includes the outlet portion. It extends so as to cover the container connecting portion from the outside toward the insertion side. There is an extension part, and a gap is provided between the extension part and the container connection part, and the tip part of the extension part is more than the end part of the container connection part on the side where the outlet part is inserted. Is configured to be positioned on the administration tube connecting portion side .

この構成によれば、容器の出口部を容器接続部に挿入する際、作業者が把持部を持つことで、容器接続部の径方向の潰れが抑制され、さらに、硬い把持部が容器接続部の投与管接続部側にあるので、容器接続部に挿入方向の力が作用した時には、把持部によって容器接続部の投与管接続部側の変形も抑制される。これにより、柔軟な容器接続部に出口部を容易に挿入して接続することが可能になる。そして、出口部を容器接続部に挿入した状態では、容器接続部は、出口部の外周面形状に対応するように変形する。これにより、様々な形状の出口部に対し容器接続部を密着させて液状物の洩れを抑制することが可能になる。   According to this configuration, when inserting the outlet portion of the container into the container connecting portion, the operator can hold the gripping portion, so that the container connecting portion is prevented from being crushed in the radial direction, and the hard gripping portion is further connected to the container connecting portion. Therefore, when a force in the insertion direction is applied to the container connecting portion, deformation of the container connecting portion on the administration tube connecting portion side is also suppressed by the grip portion. Thereby, it becomes possible to easily insert and connect the outlet portion to the flexible container connecting portion. And in the state which inserted the exit part in the container connection part, a container connection part deform | transforms so that it may respond | correspond to the outer peripheral surface shape of an exit part. As a result, the container connecting portion can be brought into close contact with the outlet portions of various shapes, thereby suppressing the leakage of the liquid material.

尚、投与管については、統一された規格品が用いられることが多いため、投与管と投与管接続部との間からは液状物が洩れ難い。   In addition, since a standardized product is often used for the administration tube, it is difficult for the liquid material to leak from between the administration tube and the administration tube connecting portion.

また、容器の出口部を容器接続部に挿入して接続する際、容器接続部が中心線方向に潰れ難くなる。また、出口部を容器接続部から抜く際には、該容器接続部をこじるようにすることで、該容器接続部の周壁における骨部が埋め込まれた部分が他の部分よりも硬いので、その骨部が埋めこまれた部分を容器の出口部の外周面から離すことが可能になる。これにより、容器の出口部の外周面と容器接続部の内周面との間に空気を入れて両者の密着状態を解くことが可能になる。   Further, when the outlet portion of the container is inserted and connected to the container connecting portion, the container connecting portion is not easily crushed in the center line direction. Also, when pulling out the outlet part from the container connection part, the part where the bone part is embedded in the peripheral wall of the container connection part is harder than the other parts by twisting the container connection part. It is possible to separate the portion in which the bone portion is embedded from the outer peripheral surface of the outlet portion of the container. Thereby, it becomes possible to put air between the outer peripheral surface of the outlet portion of the container and the inner peripheral surface of the container connecting portion to unseal the contact state between them.

また、容器接続部を容器の出口部に接続する際、把持部の延長部は容器に近い所に位置することになる。従って、延長部を手で持つことで、医療用接続具における容器に近い所を持って接続作業することが可能になる。また、容器の出口部を容器接続部に挿入する際には、延長部と容器接続部との間に隙間があるため、容器接続部が拡径方向に変形するのを延長部が阻害することはない。Moreover, when connecting a container connection part to the exit part of a container, the extension part of a holding part will be located in the place near a container. Therefore, by holding the extension part by hand, it is possible to perform the connection work while holding a place close to the container in the medical connector. Further, when inserting the outlet portion of the container into the container connection portion, there is a gap between the extension portion and the container connection portion, so that the extension portion inhibits the container connection portion from being deformed in the diameter increasing direction. There is no.

請求項2の発明では、請求項1の発明において、投与管の上流端部と投与管接続部との間に配置される点滴筒を備えており、上記投与管接続部は、上記点滴筒を介して上記投与管の上流端部と接続され、上記点滴筒は把持部に固定されている構成とする。   According to a second aspect of the present invention, in the first aspect of the invention, the apparatus further comprises an infusion tube disposed between the upstream end of the administration tube and the administration tube connection portion, and the administration tube connection portion includes the infusion tube. The infusion tube is connected to the upstream end of the administration tube, and the drip tube is fixed to the gripping portion.

この構成によれば、把持部を点滴筒と一体化したことにより、作業者は容器の出口部を容器接続部に挿入する際に、把持部と一緒に点滴筒を持つことで、把持部を手の中で安定させることが可能になる。   According to this configuration, by integrating the grip portion with the infusion tube, the operator can hold the infusion tube together with the grip portion when inserting the outlet portion of the container into the container connection portion. It becomes possible to stabilize in the hand.

請求項3の発明では、請求項1または2の発明において、把持部の外周面には、平坦面部が設けられている構成とする。   According to a third aspect of the present invention, in the first or second aspect of the present invention, a flat surface portion is provided on the outer peripheral surface of the gripping portion.

この構成によれば、作業者が平坦面部に指を置いて掴むようにすることで、容器の出口部を容器接続部に挿入する際に把持部が手の中で滑り難くなる。   According to this configuration, when the operator puts his / her finger on the flat surface portion and grips it, the grip portion becomes difficult to slip in the hand when the outlet portion of the container is inserted into the container connection portion.

請求項4の発明では、請求項1から3のいずれか1つの発明において、把持部の外周面には、突出部が設けられている構成とする。   According to a fourth aspect of the present invention, in any one of the first to third aspects of the present invention, the outer peripheral surface of the gripping portion is provided with a protruding portion.

この構成によれば、容器の出口部を容器接続部に挿入する際や容器接続部から抜く際に突出部が滑り止めとなり、把持部が手の中で滑り難くなる。   According to this configuration, when the outlet portion of the container is inserted into the container connection portion or pulled out from the container connection portion, the protruding portion is prevented from slipping, and the gripping portion is difficult to slip in the hand.

請求項5の発明では、請求項1から4のいずれか1つの発明において、把持部と投与管接続部とが一体である構成とする。   According to a fifth aspect of the present invention, in any one of the first to fourth aspects of the present invention, the grip portion and the administration tube connecting portion are integrated.

この構成によれば、医療用接続具のコストダウンを図ることが可能になる。   According to this configuration, it is possible to reduce the cost of the medical connector.

請求項6の発明では、請求項1から4のいずれか1つの発明において、容器接続部と投与管接続部とが一体である構成とする。   According to a sixth aspect of the present invention, in any one of the first to fourth aspects, the container connecting portion and the administration tube connecting portion are integrated.

この構成によれば、医療用接続具のコストダウンが図られるとともに、容器接続部と投与管接続部との間で液状物の洩れを防止することが可能になる。   According to this configuration, it is possible to reduce the cost of the medical connector and to prevent leakage of the liquid material between the container connecting portion and the administration tube connecting portion.

請求項7の発明では、請求項1から6のいずれか1つの発明において、把持部は筒状に形成され、容器接続部には、上記把持部の内周面を覆う筒状の被覆部が一体成形されている構成とする。   In the invention of claim 7, in any one of claims 1 to 6, the gripping portion is formed in a cylindrical shape, and the container connecting portion has a cylindrical covering portion covering the inner peripheral surface of the gripping portion. The structure is integrally formed.

この構成によれば、容器から流入した液状物が把持部の内部を流れる際、この把持部の内周面は被覆部で覆われているので、液状物の圧力により被覆部が把持部の内周面に押し付けられることになる。このとき、被覆部は容器接続部と一体成形されていて柔軟性を有しており、一方、把持部は被覆部よりも硬いので、被覆部は把持部の内周面に密着してシール効果が得られる。これにより、液状物の洩れが抑制される。   According to this configuration, when the liquid material flowing from the container flows through the inside of the gripping portion, the inner peripheral surface of the gripping portion is covered with the covering portion. It will be pressed against the peripheral surface. At this time, the covering portion is integrally formed with the container connecting portion and has flexibility, while the gripping portion is harder than the covering portion, so that the covering portion is in close contact with the inner peripheral surface of the gripping portion and has a sealing effect. Is obtained. Thereby, leakage of the liquid material is suppressed.

請求項8の発明では、請求項7の発明において、容器接続部の被覆部の内周面は平滑面で構成されているものとする。   In the invention of claim 8, in the invention of claim 7, the inner peripheral surface of the covering portion of the container connecting portion is constituted by a smooth surface.

この構成によれば、液状物が被覆部の内部を通って流れる際、該被覆部の内周面が平滑なので、液状物が滞留し難くなる。   According to this configuration, when the liquid material flows through the inside of the covering portion, the inner peripheral surface of the covering portion is smooth, so that the liquid material does not easily stay.

請求項9の発明では、請求項7の発明において、把持部の内周面には、被覆部の厚みに対応した段部が形成され、該段部内に被覆部が位置している構成とする。   In the invention of claim 9, in the invention of claim 7, a step portion corresponding to the thickness of the covering portion is formed on the inner peripheral surface of the gripping portion, and the covering portion is located in the step portion. .

この構成によれば、液状物の流路を滑らかにすることが可能になる。   According to this configuration, the flow path of the liquid material can be made smooth.

請求項10の発明では、請求項1から9のいずれか1つの発明において、容器接続部には、把持部の外周面に固着した固着部が設けられている構成とする。   In the invention of claim 10, in any one of claims 1 to 9, the container connection portion is provided with a fixing portion fixed to the outer peripheral surface of the gripping portion.

この構成によれば、容器接続部と把持部とが分離し難くなる According to this structure, it becomes difficult to isolate | separate a container connection part and a holding part .

請求項1の発明では、請求項1の発明において、骨部の長手方向に直交する方向の断面積は、容器の出口部が挿入される側に近づくほど小さくなるように設定されている構成とする。 Configuration In the present invention of claim 1 1, in the invention according to the first cross-sectional area in a direction orthogonal to the longitudinal direction of the bone portion, which is set to be smaller as closer to the side where the outlet of the container is inserted And

この構成によれば、骨部は、容器の出口部が挿入される側に近づくほど剛性が低くなる。従って、容器の出口部が容器接続部に挿入された状態では、骨部にける剛性の低い部分の形状が出口部の外周面の形状に沿うようになり、出口部に対し容器接続部が確実に密着するようになる。   According to this configuration, the rigidity of the bone portion decreases as it approaches the side where the outlet portion of the container is inserted. Therefore, in a state where the outlet portion of the container is inserted into the container connecting portion, the shape of the portion having low rigidity in the bone portion follows the shape of the outer peripheral surface of the outlet portion, and the container connecting portion is surely connected to the outlet portion. It comes in close contact with.

請求項1の発明では、請求項1から1のいずれか1つの発明において、把持部と容器接続部とは別部材で構成され、該容器接続部には、該把持部に係合するアンカー部が設けられている構成とする。 In the invention of claim 1 2, in any one invention of claim 1 1 1, the grip portion and the container connection part consists of a separate member, the container connection portion, to engage the grip portion It is set as the structure by which the anchor part is provided.

この構成によれば、把持部と容器接続部とを各々に適した材料で構成した場合に、両者が強固に一体化される。   According to this configuration, when the gripping portion and the container connection portion are made of materials suitable for each, the two are firmly integrated.

請求項1の発明によれば、容器接続部を柔軟に構成し、この容器接続部の投与管接続部側に容器接続部よりも硬い把持部を設けたので、把持部を持つことで容器の出口部の接続作業性を良好にしながら、複数種の容器の各出口部と投与管とを確実に接続して液状物の洩れを抑制することができる。   According to the invention of claim 1, the container connecting portion is configured flexibly, and the gripping portion harder than the container connecting portion is provided on the administration tube connecting portion side of the container connecting portion. While improving the connection workability of the outlet portion, each outlet portion of the plurality of types of containers and the administration tube can be reliably connected to suppress leakage of the liquid material.

また、容器接続部の周壁に中心線方向に延びる骨部を埋め込むことで、容器の出口部を容器接続部に挿入して接続する際、容器接続部が中心線方向に潰れ難くなり、接続作業性をより一層良好にすることができる。また、容器の出口部を容器接続部から抜く際には、該容器接続部をこじるようにすることで、容器の出口部の外周面と容器接続部の内周面との間に空気を入れて両者の密着状態を解くことができ、容器の出口部を小さい力で容易に抜くことができる。   Also, by embedding a bone portion extending in the center line direction in the peripheral wall of the container connection portion, when the outlet portion of the container is inserted and connected to the container connection portion, the container connection portion is not easily crushed in the center line direction, and the connection work The property can be further improved. In addition, when pulling out the outlet of the container from the container connecting part, air is introduced between the outer peripheral surface of the outlet part of the container and the inner peripheral surface of the container connecting part by twisting the container connecting part. Thus, the close contact state of the two can be released, and the outlet portion of the container can be easily pulled out with a small force.

請求項2の発明によれば、投与管の上流端部と投与管接続部との間に配置した点滴筒を把持部と一体化したので、接続作業の際、把持部を手の中で安定させることができ、接続作業性をより一層良好にすることができる。   According to the invention of claim 2, since the drip tube arranged between the upstream end portion of the administration tube and the administration tube connecting portion is integrated with the gripping portion, the gripping portion is stabilized in the hand during the connection work. Therefore, the connection workability can be further improved.

請求項3、4の発明によれば、容器の出口部を容器接続部に挿入する際や容器接続部から抜く際に把持部が手の中で滑り難くなるので、接続作業性をより一層良好にすることができる。   According to the third and fourth aspects of the invention, the gripping portion is less likely to slip in the hand when the outlet portion of the container is inserted into the container connecting portion or when being pulled out of the container connecting portion, so that the connection workability is further improved. Can be.

請求項5の発明によれば、把持部と投与管接続部とを一体にしたので、医療用接続具のコストダウンを図ることができる。   According to invention of Claim 5, since the holding | grip part and the administration pipe | tube connection part were united, the cost reduction of a medical connection tool can be aimed at.

請求項6の発明によれば、容器接続部と投与管接続部とを一体にしたので、医療用接続具のコストダウンを図ることができるとともに、液状物の洩れを防止することができる。   According to the sixth aspect of the present invention, since the container connecting portion and the administration tube connecting portion are integrated, the cost of the medical connecting device can be reduced, and the leakage of the liquid substance can be prevented.

請求項7の発明によれば、把持部を筒状に形成し、容器接続部に、該把持部の内周面を覆う被覆部を一体成形したので、把持部及び投与管接続部と、容器接続部とを別部材で構成した場合に、液状物の洩れを防止することができる。   According to the invention of claim 7, since the gripping portion is formed in a cylindrical shape, and the covering portion covering the inner peripheral surface of the gripping portion is integrally formed on the container connecting portion, the gripping portion, the administration tube connecting portion, the container When the connecting portion is formed of a separate member, the liquid material can be prevented from leaking.

請求項8の発明によれば、被覆部の内周面を平滑面で構成したので、液状物をスムーズに流すことができる。これにより、液状物の滞留を抑制することができる。   According to the eighth aspect of the invention, since the inner peripheral surface of the covering portion is configured as a smooth surface, the liquid material can flow smoothly. Thereby, retention of a liquid substance can be suppressed.

請求項9の発明によれば、被覆部を把持部の内周面に形成した段部内に位置付けたので、液状物の流路を滑らかに構成でき、液状物の滞留を抑制することができる。   According to invention of Claim 9, since the coating | coated part was located in the step part formed in the internal peripheral surface of a holding part, the flow path of a liquid substance can be comprised smoothly and the retention of a liquid substance can be suppressed.

請求項10の発明によれば、別部材で構成した投与管接続部と容器接続部とを分離し難くすることができ、医療用接続具の破損を抑止できる。   According to the invention of claim 10, it is possible to make it difficult to separate the administration tube connecting portion and the container connecting portion, which are constituted by separate members, and it is possible to suppress damage to the medical connection tool.

請求項11の発明によれば、骨部の剛性を、容器の出口部が挿入される側に近づくほど低くできる、これにより、容器の出口部が容器接続部に挿入された状態で、骨部における剛性の低い部分が出口部の外周面の形状に沿う形状となり、出口部に対し容器接続部を確実に密着させて液密性を確保できる。 According to the invention of claim 11, the rigidity of the bone portion can be lowered as it approaches the side where the outlet portion of the container is inserted, whereby the bone portion is inserted in the state where the outlet portion of the container is inserted into the container connecting portion. The portion with low rigidity in the shape is in conformity with the shape of the outer peripheral surface of the outlet portion, and the container connection portion can be securely adhered to the outlet portion to ensure liquid tightness.

請求項1の発明によれば、容器接続部に、把持部に係合するアンカー部を設けたので、容器接続部と把持部とを強固に一体化して両者が分離するのを防止でき、医療用接続具の破損を防止できる。 According to the present invention 2, the container connecting portion, is provided with the anchor portion engaged with the grip portion, can be prevented and a gripping portion container connecting portion and firmly integrated to each other are separated, Damage to medical connectors can be prevented.

以下、本発明の実施形態を図面に基づいて詳細に説明する。尚、以下の好ましい実施形態の説明は、本質的に例示に過ぎず、本発明、その適用物或いはその用途を制限することを意図するものではない。   Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. It should be noted that the following description of the preferred embodiment is merely illustrative in nature, and is not intended to limit the present invention, its application, or its use.

図1は、本発明の参考例1に係る医療用接続具1を示すものである。医療用接続具1は、図2に示すように、経管栄養補給法に用いられる栄養剤を収容した容器Aと、栄養剤を患者の胃に導くための投与管Bとを接続するためのものである。上記容器Aは、樹脂製フィルムを溶着してなる袋状のものであり、患者のベッド周りに配置されたイルリガートル台等(図示せず)に吊り下げるための吊り下げ用孔A1を有している。この容器Aの出口部A2は、ポリプロピレン等の硬質樹脂材を筒状に成形してなるものであり、容器Aの本体部分から突出している。尚、容器Aとしては、袋状のもの以外にも樹脂を円筒状に成形してなるものもあり、また、患者に合わせて医療現場で調合した栄養剤を移し替えることができる蓋付きの容器もある。これら複数種の容器Aの出口部A2の形状は、統一した規格がないため、互いに異なっている。   FIG. 1 shows a medical connector 1 according to Reference Example 1 of the present invention. As shown in FIG. 2, the medical connector 1 is for connecting a container A containing a nutrient used for tube feeding and an administration tube B for guiding the nutrient to the patient's stomach. Is. The container A has a bag-like shape formed by welding a resin film, and has a suspension hole A1 for suspending it on an irrigator platform (not shown) arranged around the patient's bed. Yes. The outlet portion A2 of the container A is formed by molding a hard resin material such as polypropylene into a cylindrical shape, and protrudes from the main body portion of the container A. In addition to the bag-shaped container, the container A includes a resin molded into a cylindrical shape, and a container with a lid that can transfer nutrients prepared at the medical site according to the patient. There is also. The shapes of the outlet portions A2 of the plurality of types of containers A are different from each other because there is no unified standard.

上記投与管Bは、例えば、ポリ塩化ビニル等で構成されている。投与管Bの下流端部は、患者の口や鼻から食道を経由させて胃に挿入されるようになっており、上流端部が上記医療用接続具1を介して容器Aの出口部A2に接続されるようになっている。尚、患者に腹膜から胃壁に跨って栄養剤投与用の孔部が造設されている場合には、投与管Bの先端部をその孔部に挿入するようにすればよい。また、栄養剤を投与管Bにより腸へ直接導くようにしてもよい。また、投与管Bの途中には、流量調整用のロールクランプCが設けられている。   The administration tube B is made of, for example, polyvinyl chloride. The downstream end portion of the administration tube B is inserted into the stomach from the patient's mouth and nose via the esophagus, and the upstream end portion is the outlet portion A2 of the container A via the medical connector 1. To be connected to. If the patient has a hole for administration of nutrients extending from the peritoneum to the stomach wall, the distal end of the administration tube B may be inserted into the hole. Further, the nutrient may be guided directly to the intestine through the administration tube B. In the middle of the administration tube B, a roll clamp C for adjusting the flow rate is provided.

図1、図3〜図5に示すように、上記医療用接続具1は、全体として筒状をなしており、軟質部材10からなる容器接続部11と、硬質部材12からなる把持部13及び投与管接続部14と、点滴筒15とを備えている。この医療用接続具1は、図2に示す使用状態で、容器接続部11が上部に位置しており、この容器接続部11の下方に点滴筒15が位置している。尚、この参考例1の説明では、使用状態で上となる方を単に「上」といい、下となる方を単に「下」というものとする。   As shown in FIGS. 1 and 3 to 5, the medical connector 1 has a tubular shape as a whole, and includes a container connecting portion 11 made of a soft member 10, a gripping portion 13 made of a hard member 12, and An administration tube connection portion 14 and an infusion tube 15 are provided. In the state of use shown in FIG. 2, the medical connector 1 has the container connecting portion 11 located at the upper portion, and the drip tube 15 located below the container connecting portion 11. In the description of Reference Example 1, the upper side in the usage state is simply referred to as “upper”, and the lower side is simply referred to as “lower”.

上記硬質部材12は、ポリプロピレン等の樹脂材を大略円筒状に形成してなるものである。この硬質部材12の材料としては、他にも、例えば、アクリロニトリルブタジエンスチレン樹脂(ABS樹脂)、ポリカーボネートや硬質ポリ塩化ビニル等が挙げられが、これらに限定されるものではない。図5に示すように、この硬質部材12の上半部で上記把持部13が構成され、下半部で上記投与管接続部14が構成されている。把持部13の外周面における周方向に180゜離れた2箇所には、平坦面部13aがそれぞれ形成されている。これら平坦面部13a、13aは、互いに同じ形状とされ、把持部13の上下方向中間部から上縁部に亘って形成されている。把持部13における平坦面部13aが形成された部位は、他の部位に比べて薄肉となっている。平坦面部13aの下縁部には、下方へ行くほど把持部13の径方向外側に位置するように傾斜した傾斜面部13bが連続している。尚、上記平坦面部13aの数は、2つに限られるものではなく、任意に設定することができる。   The hard member 12 is formed by forming a resin material such as polypropylene in a substantially cylindrical shape. Other examples of the material of the hard member 12 include, but are not limited to, acrylonitrile butadiene styrene resin (ABS resin), polycarbonate, hard polyvinyl chloride, and the like. As shown in FIG. 5, the grip 13 is formed in the upper half of the hard member 12, and the administration tube connection 14 is formed in the lower half. Flat surface portions 13 a are respectively formed at two positions 180 ° apart in the circumferential direction on the outer peripheral surface of the grip portion 13. The flat surface portions 13 a and 13 a have the same shape as each other, and are formed from the intermediate portion in the vertical direction of the grip portion 13 to the upper edge portion. The site | part in which the flat surface part 13a in the holding part 13 was formed is thin compared with another site | part. An inclined surface portion 13b that is inclined so as to be located on the radially outer side of the gripping portion 13 is continued to the lower edge portion of the flat surface portion 13a as it goes downward. The number of the flat surface portions 13a is not limited to two and can be arbitrarily set.

図1及び図3に示すように、上記把持部13の外周面における平坦面部13a、13aの間には、それぞれ、把持部13の中心線方向に延びる2本の凹条部13cが周方向に離れて形成されている。これら凹条部13cは、把持部13の下縁部から上縁部に亘って形成されている。   As shown in FIGS. 1 and 3, between the flat surface portions 13 a and 13 a on the outer peripheral surface of the grip portion 13, there are two concave strip portions 13 c extending in the center line direction of the grip portion 13 in the circumferential direction. Are formed apart. These concave strip portions 13 c are formed from the lower edge portion of the grip portion 13 to the upper edge portion.

図5に示すように、上記把持部13の内周面における下部近傍には、段部13dが形成されている。この段部13dの深さは、後述する容器接続部11の被覆部11bの厚さと同じに設定されている。また、把持部13の断面形状は、上縁部から段部13dまで略同じに設定されており、従って、把持部13の内周面は、上縁部から段部13dまで平滑面で構成されている。把持部13の内周面における段部13dよりも下側は、下方へ行くほど小径となるテーパー面部13eで構成されている。   As shown in FIG. 5, a step portion 13 d is formed near the lower portion of the inner peripheral surface of the grip portion 13. The depth of the stepped portion 13d is set to be the same as the thickness of a covering portion 11b of the container connecting portion 11 described later. Further, the cross-sectional shape of the gripping portion 13 is set to be substantially the same from the upper edge portion to the stepped portion 13d. Therefore, the inner peripheral surface of the gripping portion 13 is constituted by a smooth surface from the upper edge portion to the stepped portion 13d. ing. A lower side of the inner peripheral surface of the gripping portion 13 than the step portion 13d is configured by a tapered surface portion 13e having a smaller diameter as it goes downward.

上記投与管接続部14は、内筒部14aと外筒部14bとを備えた2重筒構造とされている。内筒部14aの内周面は、上記把持部13のテーパー面部13eに連なっている。この内筒部14aの内部は、把持部13の内部に連通している。外筒部14bの肉厚は、内筒部14aの肉厚よりも薄く設定され、また、外筒部14bの下端部は、内筒部14aの下端部よりも上方に位置している。外筒部14bの外周面には、外方へ突出して周方向に延びる第1環状壁14cが設けられている。この第1環状壁14cの外縁部には、下方へ延びる第2環状壁14dが設けられている。   The administration tube connection part 14 has a double cylinder structure including an inner cylinder part 14a and an outer cylinder part 14b. The inner peripheral surface of the inner cylinder portion 14 a is continuous with the tapered surface portion 13 e of the grip portion 13. The inside of the inner cylinder portion 14 a communicates with the inside of the grip portion 13. The thickness of the outer cylinder part 14b is set thinner than the thickness of the inner cylinder part 14a, and the lower end part of the outer cylinder part 14b is located above the lower end part of the inner cylinder part 14a. A first annular wall 14c that protrudes outward and extends in the circumferential direction is provided on the outer peripheral surface of the outer cylindrical portion 14b. A second annular wall 14d extending downward is provided at the outer edge of the first annular wall 14c.

上記投与管接続部14の下部に上記点滴筒15が固定され、投与管接続部14と点滴筒15が一体化されている。点滴筒15は、無色透明なポリプロピレン等からなる一体成形品であり、下方へ行くほど小径となるように形成されている。点滴筒15の上端部には、径方向外方へ突出して周方向に延びるフランジ15aが設けられている。フランジ15aの上面の内周側には、上記外筒部14bと第2環状壁14dとの間に位置する環状の溶着部15bが設けられている。この溶着部15bの全周が外筒部14b、第1及び第2環状壁14c、14dに溶着されている。フランジ15aの上面の外周側は、第2環状壁14dの下端部に当接するようになっている。尚、投与管接続部14と点滴筒15とは、接着剤等を用いて接着してもよいし、一体成形するようにしてもよい。   The infusion tube 15 is fixed to the lower part of the administration tube connecting portion 14, and the administration tube connecting portion 14 and the infusion tube 15 are integrated. The drip tube 15 is an integrally molded product made of colorless and transparent polypropylene or the like, and is formed to have a smaller diameter as it goes downward. A flange 15 a that protrudes radially outward and extends in the circumferential direction is provided at the upper end of the drip tube 15. An annular welded portion 15b located between the outer cylindrical portion 14b and the second annular wall 14d is provided on the inner peripheral side of the upper surface of the flange 15a. The entire circumference of the welded portion 15b is welded to the outer tube portion 14b and the first and second annular walls 14c and 14d. The outer peripheral side of the upper surface of the flange 15a comes into contact with the lower end of the second annular wall 14d. The administration tube connecting portion 14 and the drip tube 15 may be adhered using an adhesive or the like, or may be integrally formed.

図1にも示すように、上記点滴筒15の下端面には、投与管Bの上流端部が嵌入する嵌入溝15cが形成されている。投与管Bは、嵌入溝15cに嵌入された状態で、点滴筒15を介して投与管接続部14に接続された状態となって把持部13の内部と連通する。投与管Bは、統一された規格品であるため、嵌入溝15cの形状は、洩れが起こり難い所定形状とされている。   As shown in FIG. 1, a fitting groove 15 c into which the upstream end of the administration tube B is fitted is formed on the lower end surface of the infusion tube 15. The administration tube B is connected to the administration tube connection portion 14 via the infusion tube 15 in a state where the administration tube B is inserted into the insertion groove 15 c and communicates with the inside of the gripping portion 13. Since the administration tube B is a standardized product, the shape of the insertion groove 15c is a predetermined shape that hardly leaks.

上記軟質部材10は、上記硬質部材12及び点滴筒15を構成する材料よりも柔らかく、かつ、ゴム弾性を有する熱可塑性エラストマーを円筒状に形成してなるものである。この軟質部材10の材料としては、他にも、例えば、軟質ポリ塩化ビニル等が挙げられるが、これらに限定されるものではない。この軟質部材10は容器接続部11を構成するものであり、図5に示すように、容器Aの出口部A2が挿入される挿入孔11fを有する厚肉な本体部11aと、本体部11aの下端部から上記把持部13の内周面を被覆するように下方へ延びる筒状の被覆部11bとで構成されている。つまり、容器接続部11の投与管接続部14側に把持部13が位置している。また、上記容器接続部11が有する柔軟性は、複数種の容器Aで出口部A2の外径や形状が異なる場合に、これら出口部A2を挿入する際に容易に変形し、かつ、完全に挿入した状態で出口部A2の外周面形状に対応して該外周面に沿うように変形する程度の柔軟性である。   The soft member 10 is formed by forming a thermoplastic elastomer in a cylindrical shape that is softer than the material constituting the hard member 12 and the drip tube 15 and has rubber elasticity. Other examples of the material of the soft member 10 include, but are not limited to, soft polyvinyl chloride. This soft member 10 constitutes the container connecting portion 11, and as shown in FIG. 5, a thick main body portion 11a having an insertion hole 11f into which the outlet portion A2 of the container A is inserted, and the main body portion 11a. It is comprised by the cylindrical coating | coated part 11b extended below so that the inner peripheral surface of the said holding | grip part 13 may be coat | covered from a lower end part. That is, the gripping portion 13 is located on the administration tube connecting portion 14 side of the container connecting portion 11. Further, the flexibility of the container connecting portion 11 is easily deformed when the outlet portion A2 is inserted when the outer diameter and the shape of the outlet portion A2 are different among a plurality of types of containers A, and completely. It is flexible enough to be deformed along the outer peripheral surface corresponding to the outer peripheral surface shape of the outlet portion A2 in the inserted state.

上記本体部11aの内周面は、下方へ向かって僅かに縮径しながら延びるテーパー面で構成されている。この本体部11aの内径は、上記した複数種の容器Aのうち、出口部A2の外径が最も小さい容器Aに対応するように、該容器Aの出口部A2の外径よりも小さめに設定されている。従って、容器接続部11に出口部A2を挿入すると、該容器接続部11の周壁が伸びるとともに、拡径する。   The inner peripheral surface of the main body portion 11a is configured by a tapered surface that extends while slightly reducing the diameter downward. The inner diameter of the main body portion 11a is set to be smaller than the outer diameter of the outlet portion A2 of the container A so as to correspond to the container A having the smallest outer diameter of the outlet portion A2 among the plurality of types of containers A described above. Has been. Therefore, when the outlet portion A2 is inserted into the container connecting portion 11, the peripheral wall of the container connecting portion 11 extends and the diameter increases.

被覆部11bの内周面は、上記把持部13の内周面に沿って延びる平滑面で構成されている。図1、図3及び図4に示すように、本体部11aの外周面には、複数の凹み部11cが周方向に離れて形成されている。また、本体部11aの下端部には、把持部13の各平坦面部13aの上部に固着した固着部11dが設けられている。図5に示すように、固着部11dと被覆部11bとで把持部13の上部が挟まれている。一方、本体部11aの上縁部には、径方向外方へ突出して周方向に延びる突条部11eが形成されている。   The inner peripheral surface of the covering portion 11 b is a smooth surface extending along the inner peripheral surface of the grip portion 13. As shown in FIGS. 1, 3, and 4, a plurality of recessed portions 11 c are formed on the outer peripheral surface of the main body portion 11 a so as to be separated in the circumferential direction. In addition, a fixing portion 11d fixed to the upper portion of each flat surface portion 13a of the grip portion 13 is provided at the lower end portion of the main body portion 11a. As shown in FIG. 5, the upper portion of the gripping portion 13 is sandwiched between the fixing portion 11d and the covering portion 11b. On the other hand, on the upper edge portion of the main body portion 11a, a ridge portion 11e protruding outward in the radial direction and extending in the circumferential direction is formed.

次に、上記医療用接続具1を製造する要領について説明する。まず、硬質部材12及び点滴筒15を別々に成形しておく。そして、点滴筒15の溶着部15bを投与管接続部14に溶着する。次いで、容器接続部11を成形する成形型(図示せず)内に把持部13を配置し、この成形型内のキャビティに材料を射出する。これにより、把持部13と一体化した容器接続部11が得られ、この容器接続部11の被覆部11bは把持部13の内周面に溶着しているとともに、固着部11dは平坦面部13aに溶着している。   Next, a procedure for manufacturing the medical connector 1 will be described. First, the hard member 12 and the drip tube 15 are formed separately. Then, the welding portion 15 b of the drip tube 15 is welded to the administration tube connecting portion 14. Next, the gripping portion 13 is placed in a mold (not shown) for molding the container connection portion 11 and the material is injected into the cavity in the mold. As a result, the container connecting portion 11 integrated with the gripping portion 13 is obtained. The covering portion 11b of the container connecting portion 11 is welded to the inner peripheral surface of the gripping portion 13, and the fixing portion 11d is attached to the flat surface portion 13a. Welding.

次に、上記のように構成された医療用接続具1を用いて容器Aと投与管Bとを接続する要領について説明する。まず、作業者は、把持部13を手で持ち、図3に矢印で示すように、容器Aの出口部A2を容器接続部11の挿入孔11fに挿入する。このとき、作業者が平坦面部13a、13aに指を置いて把持部13を掴むようにすることで、把持部13が手の中で滑り難くなる。さらに、硬質部材12に点滴筒15を直接固定して把持部13と点滴筒15とを一体化しているため、作業者は、把持部13と一緒に点滴筒15を持つことで、把持部13を手の中で安定させることが可能になる。   Next, the point which connects the container A and the administration pipe | tube B using the medical connector 1 comprised as mentioned above is demonstrated. First, the operator holds the grip portion 13 by hand, and inserts the outlet portion A2 of the container A into the insertion hole 11f of the container connection portion 11 as indicated by an arrow in FIG. At this time, when the operator puts his / her finger on the flat surface portions 13a and 13a so as to grip the grip portion 13, the grip portion 13 becomes difficult to slip in the hand. Further, since the drip tube 15 is directly fixed to the hard member 12 and the gripping unit 13 and the drip tube 15 are integrated, the operator can hold the drip tube 15 together with the gripping unit 13, thereby holding the gripping unit 13. Can be stabilized in the hand.

上記作業者が容器接続部11よりも硬い把持部13を持つことで、容器接続部11の潰れが抑制され、図5に仮想線で示すように、出口部A2を容器接続部11の深い所まで挿入可能となる。出口部A2を挿入する際には、出口部A2の外径が容器接続部11の内径よりも大きく設定されているため、挿入方向に押さえ付けられた容器接続部11には、中心線方向の圧縮力が強く作用することになる。このとき、把持部13が硬いので、該把持部13によって容器接続部11の投与管接続部14側の変形が抑制される。これにより、容器接続部11に出口部A2を容易に挿入して接続することが可能になる。そして、出口部A2を容器接続部11に完全に挿入した状態では、容器接続部11は、ゴム弾性を有していることから、出口部A2の外周面形状に対応するように変形して拡径し、容器接続部11の内周面と出口部A2の外周面とが全周に亘って密着する。このようにして、様々な形状の出口部A2に対し容器接続部11を密着させて栄養剤の洩れを抑制することが可能になる。また、投与管Bの上流端部は、点滴筒15の嵌入溝15cに嵌入させる。これにより、投与管接続部14は、点滴筒15を介して投与管Bの上流端部と接続される。この投与管Bを接続するタイミングは、容器Aの出口部A2を接続した後であってもよいし、出口部A2を接続する前であってもよい。   Since the worker has the grip portion 13 that is harder than the container connection portion 11, the container connection portion 11 is prevented from being crushed, and the outlet portion A <b> 2 is located deep in the container connection portion 11 as indicated by a virtual line in FIG. 5. Can be inserted. When the outlet part A2 is inserted, the outer diameter of the outlet part A2 is set larger than the inner diameter of the container connection part 11, so that the container connection part 11 pressed in the insertion direction has a centerline direction. A compressive force acts strongly. At this time, since the grip portion 13 is hard, the grip portion 13 suppresses deformation of the container connection portion 11 on the administration tube connection portion 14 side. Thereby, it becomes possible to easily insert and connect the outlet portion A2 to the container connecting portion 11. In a state where the outlet portion A2 is completely inserted into the container connecting portion 11, the container connecting portion 11 has rubber elasticity, so that it is deformed and expanded so as to correspond to the outer peripheral surface shape of the outlet portion A2. The inner peripheral surface of the container connecting portion 11 and the outer peripheral surface of the outlet portion A2 are in close contact with each other over the entire periphery. In this manner, it is possible to prevent leakage of nutrients by bringing the container connection portion 11 into close contact with the outlet portion A2 having various shapes. Further, the upstream end portion of the administration tube B is fitted into the fitting groove 15 c of the infusion tube 15. As a result, the administration tube connecting portion 14 is connected to the upstream end portion of the administration tube B via the drip tube 15. The timing of connecting the administration tube B may be after connecting the outlet part A2 of the container A or before connecting the outlet part A2.

上記出口部A2と投与管Bとが接続具1を介して接続されると、容器Aの栄養剤は、出口部A2から把持部13内及び内筒部14aを流れて点滴筒15内に滴下し、この点滴筒15から投与管Bを介して胃へ導入される。   When the outlet part A2 and the administration tube B are connected via the connector 1, the nutrient in the container A flows from the outlet part A2 into the gripping part 13 and the inner cylinder part 14a and drops into the infusion tube 15 Then, it is introduced from the infusion tube 15 into the stomach via the administration tube B.

また、被覆部11bの内周面を平滑面とし、さらに、把持部13の内周面に被覆部11bの肉厚に対応した段差13dを形成し、この段差13d内に被覆部11bを位置付けたので、出口部A2から流入した栄養剤が点滴筒15にスムーズに流れる。   Further, the inner peripheral surface of the covering portion 11b is a smooth surface, and further, a step 13d corresponding to the thickness of the covering portion 11b is formed on the inner peripheral surface of the gripping portion 13, and the covering portion 11b is positioned in the step 13d. Therefore, the nutrient that has flowed in from the outlet portion A <b> 2 flows smoothly into the drip tube 15.

以上説明したように、この参考例1に係る医療用接続具1によれば、容器接続部11を柔軟に構成し、この容器接続部11の投与管接続部14側に容器接続部11よりも硬い把持部13を設けたので、把持部13を持つことで容器Aの出口部A2の接続作業性を良好にしながら、複数種の容器Aの出口部A2を投与管Bに確実に接続して栄養剤の洩れを抑制することができる。   As described above, according to the medical connector 1 according to the first reference example, the container connecting portion 11 is configured flexibly, and the container connecting portion 11 is closer to the administration tube connecting portion 14 than the container connecting portion 11. Since the rigid gripping portion 13 is provided, the outlet portion A2 of the plurality of types of containers A is securely connected to the administration tube B while the gripping portion 13 is provided to improve the connection workability of the outlet portion A2 of the container A. The leakage of nutrients can be suppressed.

また、把持部13を構成する硬質部材12に点滴筒15を固定して、該把持部13と点滴筒15とを一体化したので、接続作業の際、把持部13を手の中で安定させることができる。さらに、把持部13に平坦面部13aを設けたことで、把持部13が手の中で滑り難くなる。これらのことにより、接続作業性をより一層良好にすることができる。   In addition, since the drip tube 15 is fixed to the hard member 12 constituting the gripping portion 13 and the gripping portion 13 and the drip tube 15 are integrated, the gripping portion 13 is stabilized in the hand during the connection work. be able to. Furthermore, by providing the grip portion 13 with the flat surface portion 13a, the grip portion 13 becomes difficult to slip in the hand. By these things, connection workability | operativity can be made still better.

また、把持部13と投与管接続部14と一体成形しているので、部品点数を削減できる。この場合に、把持部13及び投与管接続部14と、容器接続部11とを各々に適した材料で構成でき、容器接続部11の柔軟性と把持部13の十分な硬さとを両立することができる。   Moreover, since the holding part 13 and the administration pipe connection part 14 are integrally formed, the number of parts can be reduced. In this case, the holding part 13 and the administration tube connecting part 14 and the container connecting part 11 can be made of materials suitable for each, and both the flexibility of the container connecting part 11 and the sufficient hardness of the holding part 13 can be achieved. Can do.

また、把持部13を筒状に形成し、容器管接続部11に、該把持部13の内周面を覆う柔軟な被覆部11bを設けたので、栄養剤の洩れを防止することができる。   Further, since the gripping portion 13 is formed in a cylindrical shape and the flexible covering portion 11b that covers the inner peripheral surface of the gripping portion 13 is provided in the container pipe connection portion 11, leakage of nutrients can be prevented.

また、被覆部11bの内周面を平滑にするとともに、被覆部11bを把持部13の段部13d内に位置付けるようにしたので、栄養剤をスムーズに流すことができる。これにより、栄養剤が医療用接続具1の中で滞留するのを抑制できる。   Further, since the inner peripheral surface of the covering portion 11b is smoothed and the covering portion 11b is positioned in the stepped portion 13d of the gripping portion 13, the nutrient can be flowed smoothly. Thereby, it can suppress that a nutrient is retained in the medical connector 1.

また、把持部13の外周面に固着部11dを固着させたことにより、容器接続部11と投与管接続部14とを分離し難くすることができる。   Further, by fixing the fixing portion 11d to the outer peripheral surface of the gripping portion 13, it is possible to make it difficult to separate the container connecting portion 11 and the administration tube connecting portion 14.

また、図6に示す参考例2のように、把持部13の外周面に突出部20を設けてもよい。この突出部20は、把持部13の中心線方向に延びる板状をなしており、周方向に離れて2つ設けられている。このように把持部13に突出部20を設けることで、容器Aの出口部A2を容器接続部11に挿入する際に把持部13を持つことで突出部20が滑り止めとなり、把持部13が手の中で滑り難くなる。これにより、容器Aの出口部A2の接続作業性をより一層良好にすることができる。尚、この変形例1において、把持部13に突出部20と共に平坦面部を設けてもよい。また、突出部20の形状や数は、任意に設定することができる。   Moreover, you may provide the protrusion part 20 in the outer peripheral surface of the holding part 13 like the reference example 2 shown in FIG. The projecting portion 20 has a plate shape extending in the center line direction of the grip portion 13, and two protruding portions 20 are provided apart in the circumferential direction. By providing the protruding portion 20 in the gripping portion 13 in this way, the protruding portion 20 becomes non-slip by having the gripping portion 13 when the outlet portion A2 of the container A is inserted into the container connecting portion 11, and the gripping portion 13 It becomes difficult to slip in the hands. Thereby, the connection workability | operativity of exit part A2 of the container A can be made still better. In the first modification, the grip portion 13 may be provided with a flat surface portion together with the protruding portion 20. Moreover, the shape and number of the protrusions 20 can be arbitrarily set.

また、点滴筒15の形状は、図7に示す参考例3のように形成してもよい。この点滴筒15は、例えばポリ塩化ビニル等で構成されている。   Further, the shape of the drip tube 15 may be formed as in Reference Example 3 shown in FIG. The drip tube 15 is made of, for example, polyvinyl chloride.

図8は、本発明の参考例4に係る医療用接続具1を示すものである。この参考例4の医療用接続具1は、点滴筒15が硬質部材12から分離している点と把持部13に突出部22が設けられている点で参考例1のものと異なっており、以下、参考例1のものと同じ部分には同じ符号を付し、異なる部分を詳細に説明する。   FIG. 8 shows a medical connector 1 according to Reference Example 4 of the present invention. The medical connector 1 of this reference example 4 is different from that of the reference example 1 in that the drip tube 15 is separated from the hard member 12 and that the protruding portion 22 is provided on the grip portion 13. Hereinafter, the same parts as those in Reference Example 1 are denoted by the same reference numerals, and different parts will be described in detail.

上記突出部22は、把持部13の外周面から突出して上下方向に延びる板状をなしており、周方向に離れて2つ設けられている。また、点滴筒15の上端開口部は、樹脂製のキャップ部材21で閉塞されている。このキャップ部材21の略中心部には、貫通孔(図示せず)が形成され、この貫通孔の周縁部から上方へ筒部21aが突出している。   The protruding portion 22 has a plate shape protruding from the outer peripheral surface of the gripping portion 13 and extending in the vertical direction, and two protruding portions 22 are provided in the circumferential direction. The upper end opening of the drip tube 15 is closed with a resin cap member 21. A through hole (not shown) is formed at a substantially central portion of the cap member 21, and the cylindrical portion 21 a protrudes upward from the peripheral portion of the through hole.

上記硬質部材12における把持部13よりも下側が投与管接続部14である。硬質部材12と点滴筒15との間には、接続具1の構成部材である上部管16が配置されている。この上部管16は、投与管Bと同様に構成された柔軟性を有するものであり、上部管16の上流端部が投与管接続部14に設けられた筒部に外嵌合して接続され、上部管16の下流端部が上記キャップ部材21の筒部21aに外嵌合して接続されている。また、投与管Bの上流端部は、点滴筒15の下流端部に接続されている。つまり、投与管Bは、点滴筒15及び上部管16を介して投与管接続部14に接続された状態となっている。   The administration tube connecting portion 14 is below the grip portion 13 in the hard member 12. Between the hard member 12 and the drip tube 15, an upper tube 16 that is a constituent member of the connector 1 is disposed. The upper tube 16 has the same flexibility as that of the administration tube B, and the upstream end portion of the upper tube 16 is externally fitted and connected to a cylindrical portion provided in the administration tube connection portion 14. The downstream end portion of the upper pipe 16 is externally fitted and connected to the cylindrical portion 21 a of the cap member 21. The upstream end of the administration tube B is connected to the downstream end of the infusion tube 15. That is, the administration tube B is connected to the administration tube connection portion 14 via the infusion tube 15 and the upper tube 16.

この参考例4に係る医療用接続具1によっても、参考例1と同様に、容器Aの出口部A2の接続作業性を良好にしながら、複数種の容器Aの出口部A2を投与管Bに確実に接続して栄養物の洩れを抑制することができる。また、硬質部材12と点滴筒15との間に上部管16を設けたので、この上部管16を曲げて、硬質部材12と点滴筒15との相対位置を変えることができ、使用時の利便性が向上する。   Similarly to the reference example 1, the medical connector 1 according to the reference example 4 improves the connection workability of the outlet part A2 of the container A, and the outlet parts A2 of the plural kinds of containers A to the administration tube B. It can be connected securely to prevent leakage of nutrients. In addition, since the upper tube 16 is provided between the hard member 12 and the drip tube 15, the upper tube 16 can be bent to change the relative position between the hard member 12 and the drip tube 15, which is convenient for use. Improves.

また、この参考例4の把持部13に参考例1と同様な平坦面部を設けることも可能である。また、突出部22は省略することもできる。   Further, it is possible to provide a flat surface portion similar to that of the reference example 1 to the grip portion 13 of the reference example 4. Moreover, the protrusion part 22 can also be abbreviate | omitted.

《発明の実施形態1》
図9及び図10は、本発明の実施形態1に係る医療用接続具1を示すものである。この実施形態1の医療用接続具1は、軟質部材10及び硬質部材12の形状が参考例1のものと異なっており、以下、参考例1のものと同じ部分には同じ符号を付し、異なる部分を詳細に説明する。
Embodiment 1 of the Invention
9 and 10 show the medical connector 1 according to Embodiment 1 of the present invention. The medical connector 1 of Embodiment 1 is different in the shape of the soft member 10 and the hard member 12 from that of Reference Example 1, and hereinafter, the same reference numerals are given to the same parts as those of Reference Example 1, Different parts will be described in detail.

上記硬質部材12には、図10及び図11にも示すように、該硬質部材12の内周面における中心線方向略中央部近傍から上方へ突出する2つの骨部30、30が、周方向に約180゜離れて2つ形成されている。骨部30、30は、硬質部材12の内周面から内方へ所定寸法離れており、その全体が軟質部材10の容器接続部11の周壁に埋め込まれて一体化している。骨部30、30は、該容器接続部11の中心線方向の潰れを防止するためのものである。各骨部30は、容器接続部11の上端部まで延びる細長い形をしており、図9に示すように、その上端面が容器接続部11の上端面から露出している。骨部30の長手方向に直交する方向の断面形状は、該容器接続部11の周方向に沿う円弧を描く形状とされている。また、骨部30の肉厚は、上方へ行くほど薄くされている。つまり、骨部30の長手方向に直交する方向の断面積は、上方へ行くほど、すなわち出口部A2の挿入側に近づくほど、小さくなるように設定されている。このため、骨部30は、上方へ行くほど剛性が低くなり、よって、骨部30の上側部分は、出口部A2が挿入された状態で、該出口部A2の外周面形状に沿うように変形する。これにより、容器接続部11を出口部A2の外周面に密着させることができ、栄養剤の洩れを防止できる。   As shown in FIGS. 10 and 11, the hard member 12 has two bone portions 30, 30 projecting upward from the vicinity of the substantially central portion in the center line direction on the inner peripheral surface of the hard member 12. Are formed at a distance of about 180 °. The bone parts 30, 30 are separated from the inner peripheral surface of the hard member 12 by a predetermined dimension inward, and the whole is embedded in the peripheral wall of the container connecting part 11 of the soft member 10 and integrated. The bone portions 30 are for preventing the container connecting portion 11 from being crushed in the center line direction. Each bone portion 30 has an elongated shape extending to the upper end portion of the container connection portion 11, and its upper end surface is exposed from the upper end surface of the container connection portion 11 as shown in FIG. 9. The cross-sectional shape in the direction orthogonal to the longitudinal direction of the bone portion 30 is a shape that draws an arc along the circumferential direction of the container connecting portion 11. Moreover, the thickness of the bone part 30 is made thin, so that it goes upwards. That is, the cross-sectional area in the direction orthogonal to the longitudinal direction of the bone part 30 is set to be smaller as it goes upward, that is, as it approaches the insertion side of the outlet part A2. For this reason, the rigidity of the bone part 30 decreases as it goes upward. Therefore, the upper part of the bone part 30 is deformed so as to follow the outer peripheral surface shape of the outlet part A2 with the outlet part A2 inserted. To do. Thereby, the container connection part 11 can be closely_contact | adhered to the outer peripheral surface of exit part A2, and the leakage of a nutrient can be prevented.

上記硬質部材12の把持部13には、図12にも示すように、容器接続部11の外方で該容器接続部11側へ向けて延びる延長部31が形成されている。この延長部31の上端部は、容器接続部11の上端部よりも下方に位置していて、延長部31は、全体として容器接続部11の略下半部を取り囲む円筒形状をなしている。図9及び図10に示すように、延長部31の内周面と容器接続部11の外周面との間には、全周に亘って隙間32が形成されている。この隙間32は、容器Aの出口部A2を容器接続部11に挿入する際に容器接続部11の拡径方向の変形を許容するためのものである。   As shown in FIG. 12, the holding portion 13 of the hard member 12 is formed with an extension portion 31 extending toward the container connection portion 11 outside the container connection portion 11. The upper end portion of the extension portion 31 is located below the upper end portion of the container connection portion 11, and the extension portion 31 has a cylindrical shape surrounding the substantially lower half portion of the container connection portion 11 as a whole. As shown in FIGS. 9 and 10, a gap 32 is formed over the entire circumference between the inner peripheral surface of the extension portion 31 and the outer peripheral surface of the container connection portion 11. The gap 32 is for allowing deformation of the container connecting portion 11 in the diameter increasing direction when the outlet portion A2 of the container A is inserted into the container connecting portion 11.

図10に示すように、硬質部材12の内周面には、内方へ向けて突出する突出部12aが形成されている。この突出部12aには、硬質部材12の中心線方向に貫通する貫通孔33が形成されている。この貫通孔33内には、容器接続部11を構成する軟質樹脂材が流れ込んでいる。この貫通孔33に流れこんだ樹脂材は該貫通孔33の下側で広がった形状で固化しており、この樹脂材が、本発明における把持部13に係合するアンカー部34を構成している。   As shown in FIG. 10, a protruding portion 12 a that protrudes inward is formed on the inner peripheral surface of the hard member 12. A through hole 33 penetrating in the center line direction of the hard member 12 is formed in the protruding portion 12a. A soft resin material constituting the container connecting portion 11 flows into the through hole 33. The resin material that has flowed into the through-hole 33 is solidified in a shape that spreads below the through-hole 33, and this resin material constitutes an anchor portion 34 that engages with the grip portion 13 in the present invention. Yes.

図9や図11に示すように、上記把持部13の外周面には、僅かに窪んだ窪み部35が周方向に互いに離れて複数形成されている。窪み部35は、上下方向に細長い形状とされている。尚、この窪み部35の形状や数は、任意に設定することができる。   As shown in FIGS. 9 and 11, a plurality of recessed portions 35 that are slightly recessed are formed on the outer peripheral surface of the grip portion 13 so as to be separated from each other in the circumferential direction. The hollow portion 35 has an elongated shape in the vertical direction. In addition, the shape and number of this hollow part 35 can be set arbitrarily.

次に、この実施形態1に係る医療用接続具1の容器接続部11に容器Aの出口部A2を挿入する場合について説明する。作業者が把持部13を手で持った際には、把持部13の外周面に複数の窪み部13が形成されていることから、これら窪み部13が滑り止めとなって、医療用接続具1が手の中で滑り難い。また、把持部13の延長部31は容器Aの出口部A2に近い所に位置することになる。従って、延長部31を手で持つことで、接続具1における出口部A2に近い所を持つことが可能になる。このとき、延長部31は硬質な樹脂材で構成されていることから変形し難い。   Next, a case where the outlet portion A2 of the container A is inserted into the container connecting portion 11 of the medical connector 1 according to the first embodiment will be described. When the operator holds the grip portion 13 by hand, since the plurality of recess portions 13 are formed on the outer peripheral surface of the grip portion 13, these recess portions 13 serve as slip stoppers, and the medical connector 1 is hard to slip in the hand. Further, the extension part 31 of the gripping part 13 is located in a place near the outlet part A2 of the container A. Therefore, by holding the extension part 31 by hand, it is possible to have a place close to the outlet part A2 in the connector 1. At this time, since the extension part 31 is comprised with the hard resin material, it is hard to deform | transform.

そして、出口部A2を容器接続部11に挿入していくと、該容器接続部11が拡径方向に変形する。このとき、容器接続部11と延長部31との間に隙間32があるため、延長部31が容器接続部11の変形を阻害することはなく、出口部A2を容器接続部11の深いところまで確実に挿入できる。   When the outlet portion A2 is inserted into the container connection portion 11, the container connection portion 11 is deformed in the diameter increasing direction. At this time, since there is a gap 32 between the container connection part 11 and the extension part 31, the extension part 31 does not hinder the deformation of the container connection part 11, and the outlet part A2 extends to the deep part of the container connection part 11. Can be inserted securely.

一方、上記のようにして挿入された出口部A2を容器接続部11から抜く際には、出口部A2の外周面と容器接続部11の内周面とが全周に亘って密着しているので、抜き難いことがある。このような場合では、把持部13や点滴筒15を持って、図13に矢印Yで示すように、1つの骨部30が出口部A2の外周面から離れる方向に、容器接続部11をこじるようにする。これにより、容器接続部11の周壁のうち、当該骨部30に対応する部位が該骨部30によって硬くなっているため、容器接続部11の外周面から簡単に離れ、容器接続部11の内周面と出口部A2の外周面との間に空気導入用の空間Sが形成される。この空間Sから空気が入ると、容器接続部11の内周面と出口部A2の外周面との密着状態が解かれるので、出口部A2を小さな力で容易に抜くことができる。   On the other hand, when the outlet portion A2 inserted as described above is pulled out from the container connecting portion 11, the outer peripheral surface of the outlet portion A2 and the inner peripheral surface of the container connecting portion 11 are in close contact with each other. So it may be difficult to pull out. In such a case, holding the gripping part 13 and the infusion tube 15, as shown by the arrow Y in FIG. 13, the container connecting part 11 is squeezed in the direction in which one bone part 30 is separated from the outer peripheral surface of the outlet part A2. Like that. Thereby, since the site | part corresponding to the said bone part 30 is hardened by this bone part 30 among the surrounding walls of the container connection part 11, it leaves | separates easily from the outer peripheral surface of the container connection part 11, and the inside of the container connection part 11 An air introduction space S is formed between the peripheral surface and the outer peripheral surface of the outlet portion A2. When air enters from the space S, the contact state between the inner peripheral surface of the container connecting portion 11 and the outer peripheral surface of the outlet portion A2 is released, so that the outlet portion A2 can be easily pulled out with a small force.

この実施形態1に係る医療用接続具1によっても、参考例1と同様に、容器Aの出口部A2の接続作業性を良好にしながら、複数種の容器Aの出口部A2を投与管Bに確実に接続して栄養物の洩れを抑制することができる。   Similarly to the reference example 1, the medical connector 1 according to the first embodiment also improves the connection workability of the outlet part A2 of the container A, and the outlet parts A2 of the plural kinds of containers A to the administration tube B. It can be connected securely to prevent leakage of nutrients.

また、容器接続部11にアンカー部34を設けたことにより、容器接続部11と把持部13とを強固に一体化して両者が分離するのを防止でき、接続具1の破損を未然に防ぐことができる。   Moreover, by providing the anchor part 34 in the container connecting part 11, the container connecting part 11 and the grip part 13 can be firmly integrated to prevent them from being separated, and the breakage of the connector 1 can be prevented. Can do.

《発明の実施形態2》
図14は、本発明の実施形態2に係る医療用接続具1を示すものである。この実施形態2の医療用接続具1は、硬質部材11及び点滴筒15の形状が参考例1のものと異なっており、以下、参考例1のものと同じ部分には同じ符号を付し、異なる部分を詳細に説明する。
<< Embodiment 2 of the Invention >>
FIG. 14 shows a medical connector 1 according to Embodiment 2 of the present invention. The medical connector 1 of Embodiment 2 is different in the shape of the rigid member 11 and the drip tube 15 from that of Reference Example 1, and hereinafter, the same parts as those of Reference Example 1 are denoted by the same reference numerals, Different parts will be described in detail.

硬質部材12には、図15や図16にも示すように、実施形態1と同様な細長い骨部30が6つ形成されている。これら骨部30の周方向の間隔は等しく設定されている。また、把持部13の下半部は、上半部よりも小径の小径部40とされている。この把持部13の外周面には、図17にも示すように、上下方向に延びる板状の突出部41が周方向に互いに離れて複数形成されている。また、図15に示すように、硬質部材12には実施形態1と同様な貫通孔33が形成され、この貫通孔33に流れ込んだ樹脂材は、把持部13の外周面に固着してアンカー部34を構成している。   As shown in FIGS. 15 and 16, the rigid member 12 has six elongated bone portions 30 similar to those in the first embodiment. The intervals in the circumferential direction of these bone portions 30 are set equal. Further, the lower half portion of the gripping portion 13 is a small diameter portion 40 having a smaller diameter than the upper half portion. As shown in FIG. 17, a plurality of plate-like protrusions 41 extending in the vertical direction are formed on the outer peripheral surface of the grip portion 13 so as to be separated from each other in the circumferential direction. Further, as shown in FIG. 15, the hard member 12 has a through hole 33 similar to that of the first embodiment, and the resin material that has flowed into the through hole 33 is fixed to the outer peripheral surface of the gripping portion 13 to be anchor portions. 34 is constituted.

また、投与管接続部14には、点滴筒15の内部へ向けて突出する管部14eが設けられている。図14に示すように、点滴筒15の両端部は、中間部に比べて小径に形成されている。   In addition, the administration tube connection portion 14 is provided with a tube portion 14 e that protrudes toward the inside of the infusion tube 15. As shown in FIG. 14, both end portions of the drip tube 15 are formed to have a smaller diameter than the intermediate portion.

この実施形態2に係る医療用接続具1によっても、参考例1と同様に、容器Aの出口部A2の接続作業性を良好にしながら、複数種の容器Aの出口部A2を投与管Bに確実に接続して栄養物の洩れを抑制することができる。   Similarly to the reference example 1, the medical connector 1 according to the second embodiment also improves the connection workability of the outlet part A2 of the container A, and the outlet parts A2 of the plurality of types of containers A to the administration tube B. It can be connected securely to prevent leakage of nutrients.

尚、上記実施形態1、2では、容器接続部11をエラストマーで構成しているが、容器接続部11は、これに限られるものではなく、例えば、ゴムやシリコーンのように、出口部A2の外周面形状に対応するように変形する柔軟性を有する材料であればよい。   In the first and second embodiments, the container connecting portion 11 is made of an elastomer. However, the container connecting portion 11 is not limited to this, and for example, the outlet portion A2 is made of rubber or silicone. Any material may be used as long as it is flexible so as to correspond to the shape of the outer peripheral surface.

また、上記実施形態1、2では、把持部13と投与管接続部14とを一体成形しているが、これらは別部材で構成してもよい。また、把持部13は、容器接続部11よりも硬く変形し難い材料であればよく、樹脂以外の金属材料で構成してもよい。   In the first and second embodiments, the grasping portion 13 and the administration tube connecting portion 14 are integrally formed, but they may be formed of separate members. Moreover, the holding part 13 should just be a material harder than a container connection part 11, and it is hard to deform | transform, and may be comprised with metal materials other than resin.

また、上記実施形態1、2では、容器接続部11の周壁に、該容器接続部11よりも硬く構成された骨部30を埋め込むようにしているが、この骨部30の数は、2つや6つに限られるものではなく、1つであってもよいし、3つ以上であってもよい。また、骨部30の長手方向の寸法は、容器接続部11の周壁の上下方向中間部に達する程度に短くしてもよい。また、骨部30を設ける場合には、容器接続部11を、透光性を有する材料で構成することで、骨部30を容器接続部11の外側から目視できるようにしてもよい。こうすることで、出口部A2を容器接続部11から抜くときに、作業者が骨部30の位置を確認できるので、上述した容器接続部11のこじる方向が分かり易く、作業性をより一層向上できる。また、同様な効果を得るために、容器接続部11の外周面に、骨部30の位置を示す目印を設けてもよい。   Moreover, in the said Embodiment 1, 2, although the bone part 30 comprised more rigidly than this container connection part 11 is embedded in the surrounding wall of the container connection part 11, the number of these bone parts 30 is two. The number is not limited to six, and may be one or three or more. Moreover, the dimension in the longitudinal direction of the bone part 30 may be shortened so as to reach the middle part in the vertical direction of the peripheral wall of the container connecting part 11. Moreover, when providing the bone part 30, you may make it visible from the outer side of the container connection part 11 by comprising the container connection part 11 with the material which has translucency. By doing so, the operator can confirm the position of the bone portion 30 when the outlet portion A2 is pulled out from the container connecting portion 11, so that the direction in which the container connecting portion 11 is twisted is easy to understand and the workability is further improved. it can. In order to obtain the same effect, a mark indicating the position of the bone part 30 may be provided on the outer peripheral surface of the container connecting part 11.

以上説明したように、本発明に係る医療用接続具は、例えば、経管栄養補給法の栄養剤を収容した容器と投与管とを接続する際に用いることができる。   As described above, the medical connector according to the present invention can be used, for example, when connecting a container containing a nutrient for the tube feeding method and an administration tube.

参考例1に係る医療用接続具の斜視図である。It is a perspective view of the medical connector which concerns on the reference example 1. FIG. 医療用接続具の使用状態を説明する図である。It is a figure explaining the use condition of a medical connector. 医療用接続具の側面図である。It is a side view of a medical connector. 医療用接続具の正面図である。It is a front view of a medical connector. 図4におけるV−V線断面図である。It is the VV sectional view taken on the line in FIG. 参考例2に係る医療用接続具に投与管を接続した状態を示す斜視図である。It is a perspective view which shows the state which connected the administration tube to the medical connector which concerns on the reference example 2. FIG. 参考例3に係る図6相当図である。FIG. 7 is a diagram corresponding to FIG. 6 according to Reference Example 3. 参考例4に係る図6相当図である。FIG. 7 is a view corresponding to FIG. 6 according to Reference Example 4. 実施形態1に係る医療用接続具の斜視図である。1 is a perspective view of a medical connection tool according to Embodiment 1. FIG. 図9におけるX−X線断面図である。FIG. 10 is a sectional view taken along line XX in FIG. 9. 実施形態1に係る硬質部材の斜視図である。3 is a perspective view of a hard member according to Embodiment 1. FIG. 実施形態1に係る軟質部材及び硬質部材が一体化した状態の側面図である。It is a side view of the state where the soft member and hard member which concern on Embodiment 1 were integrated. 実施形態1に係る容器接続部から容器の出口部を抜く場合を説明する図10相当図である。FIG. 11 is a view corresponding to FIG. 10 for explaining a case where the outlet portion of the container is pulled out from the container connecting portion according to the first embodiment. 実施形態2に係る図9相当図である。FIG. 10 is a diagram corresponding to FIG. 9 according to the second embodiment. 図14におけるXV−XV線断面図である。It is the XV-XV sectional view taken on the line in FIG. 実施形態2に係る図11相当図である。FIG. 12 is a view corresponding to FIG. 11 according to the second embodiment. 実施形態2に係る図12相当図である。FIG. 13 is a view corresponding to FIG. 12 according to the second embodiment.

1 医療用接続具
11 容器接続部
11b 被覆部
13 把持部
13a 平坦面部
14 投与管接続部
15 点滴筒
20、22 突出部
30 骨部
31 延長部
32 隙間
34 アンカー部
A 容器
A2 出口部
B 投与管
DESCRIPTION OF SYMBOLS 1 Medical connector 11 Container connection part 11b Covering part 13 Grasping part 13a Flat surface part 14 Administration pipe connection part 15 Infusion tube 20, 22 Protrusion part 30 Bone part 31 Extension part 32 Crevice 34 Anchor part A Container A2 Outlet part B Administration pipe

Claims (12)

液状物を収容する容器から突出するように設けられた出口部と、上記液状物を生体に導く投与管との間に配置され、上記出口部及び上記投与管を接続する医療用接続具において、
上記投与管の上流端部が接続される投与管接続部と、
上記容器の出口部が挿入された状態で接続される筒状をなし、挿入された状態にある上記出口部の外周面形状に対応して拡径するように変形する柔軟性を有する容器接続部と、
上記容器接続部の投与管接続部側に設けられ、該容器接続部よりも硬く構成された把持部とを備え、
上記容器接続部の周壁には、該容器接続部よりも硬く構成されて中心線方向に延びる骨部が埋め込まれ
上記把持部は、上記出口部が挿入される側へ向けて上記容器接続部を外側から覆うように延びる延長部を有し、
上記延長部と上記容器接続部との間には、隙間が設けられ、
上記延長部の先端部は、上記容器接続部における上記出口部が挿入される側の端部よりも上記投与管接続部側に位置付けられていることを特徴とする医療用接続具。
In a medical connector that is disposed between an outlet portion provided so as to protrude from a container that stores a liquid substance and an administration tube that guides the liquid substance to a living body, and connects the outlet portion and the administration tube.
An administration tube connection to which an upstream end of the administration tube is connected;
A container connecting portion that has a cylindrical shape that is connected in a state where the outlet portion of the container is inserted, and has a flexibility that deforms so as to expand the diameter corresponding to the outer peripheral surface shape of the outlet portion in the inserted state. When,
Provided on the administration tube connection part side of the container connection part, and comprises a gripping part configured to be harder than the container connection part,
The peripheral wall of the container connecting portion is embedded with a bone portion configured to be harder than the container connecting portion and extending in the center line direction ,
The gripping portion has an extension that extends to cover the container connection portion from the outside toward the side where the outlet portion is inserted,
A gap is provided between the extension part and the container connection part,
The medical connector according to claim 1, wherein a distal end portion of the extension portion is positioned closer to the administration tube connection portion side than an end portion of the container connection portion on the side where the outlet portion is inserted .
請求項1に記載の医療用接続具において、
投与管の上流端部と投与管接続部との間に配置される点滴筒を備えており、
上記投与管接続部は、上記点滴筒を介して上記投与管の上流端部と接続され、
上記点滴筒は把持部に固定されていることを特徴とする医療用接続具。
The medical connector according to claim 1, wherein
A drip tube disposed between the upstream end of the administration tube and the administration tube connection,
The administration tube connection is connected to the upstream end of the administration tube via the infusion tube,
A medical connector characterized in that the drip tube is fixed to a gripping part.
請求項1または2に記載の医療用接続具において、
把持部の外周面には、平坦面部が設けられていることを特徴とする医療用接続具。
The medical connector according to claim 1 or 2,
A medical connector characterized in that a flat surface portion is provided on the outer peripheral surface of the grip portion.
請求項1から3のいずれか1つに記載の医療用接続具において、
把持部の外周面には、突出部が設けられていることを特徴とする医療用接続具。
The medical connector according to any one of claims 1 to 3,
A medical connector characterized in that a protrusion is provided on the outer peripheral surface of the grip portion.
請求項1から4のいずれか1つに記載の医療用接続具において、
把持部と投与管接続部とが一体であることを特徴とする医療用接続具。
The medical connector according to any one of claims 1 to 4,
A medical connector, wherein the gripping part and the administration tube connecting part are integrated.
請求項1から5のいずれか1つに記載の医療用接続具において、
容器接続部と投与管接続部とが一体であることを特徴とする医療用接続具。
The medical connector according to any one of claims 1 to 5,
A medical connector, wherein the container connecting portion and the administration tube connecting portion are integrated.
請求項1から6のいずれか1つに記載の医療用接続具において、
把持部は筒状に形成され、
容器接続部には、上記把持部の内周面を覆う筒状の被覆部が一体成形されていることを特徴とする医療用接続具。
The medical connector according to any one of claims 1 to 6,
The gripping part is formed in a cylindrical shape,
A medical connector, wherein the container connecting portion is integrally formed with a cylindrical covering portion that covers the inner peripheral surface of the gripping portion.
請求項7に記載の医療用接続具において、
容器接続部の被覆部の内周面は平滑面で構成されていることを特徴とする医療用接続具。
The medical connector according to claim 7, wherein
A medical connector characterized in that the inner peripheral surface of the covering portion of the container connecting portion is a smooth surface.
請求項7に記載の医療用接続具において、
把持部の内周面には、被覆部の厚みに対応した段部が形成され、該段部内に被覆部が位置していることを特徴とする医療用接続具。
The medical connector according to claim 7, wherein
A medical connector, wherein a step portion corresponding to the thickness of the covering portion is formed on the inner peripheral surface of the grip portion, and the covering portion is located in the step portion.
請求項1から9のいずれか1つに記載の医療用接続具において、
容器接続部には、把持部の外周面に固着した固着部が設けられていることを特徴とする医療用接続具。
The medical connector according to any one of claims 1 to 9,
The medical connector, wherein the container connecting portion is provided with a fixing portion fixed to the outer peripheral surface of the gripping portion.
請求項1に記載の医療用接続具において、
骨部の長手方向に直交する方向の断面積は、容器の出口部が挿入される側に近づくほど小さくなるように設定されていることを特徴とする医療用接続具。
The medical connector according to claim 1, wherein
A medical connector, wherein a cross-sectional area in a direction orthogonal to a longitudinal direction of a bone part is set so as to become smaller toward a side where an outlet part of a container is inserted.
請求項1から1のいずれか1つに記載の医療用接続具において、
把持部と容器接続部とは別部材で構成され、該容器接続部には、該把持部に係合するアンカー部が設けられていることを特徴とする医療用接続具。
The medical connector according to any one of claims 1 to 11,
A medical connector, wherein the gripping portion and the container connecting portion are formed of different members, and the container connecting portion is provided with an anchor portion that engages with the gripping portion.
JP2006279203A 2006-10-12 2006-10-12 Medical connector Expired - Fee Related JP5125051B2 (en)

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