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JP5140564B2 - Medical needle - Google Patents
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JP5140564B2 - Medical needle - Google Patents

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JP5140564B2
JP5140564B2 JP2008304841A JP2008304841A JP5140564B2 JP 5140564 B2 JP5140564 B2 JP 5140564B2 JP 2008304841 A JP2008304841 A JP 2008304841A JP 2008304841 A JP2008304841 A JP 2008304841A JP 5140564 B2 JP5140564 B2 JP 5140564B2
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needle
curved
hook
medical needle
notch
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JP2010125173A (en
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誠一 小野
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SB Kawasumi Laboratories Inc
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Description

本発明は、医療用針に関する。   The present invention relates to a medical needle.

皮下埋込式カテーテルアクセスポートに穿刺するための針として、従来、所定角度(例えば90度)に湾曲した湾曲部を有する湾曲針と、パンタグラフのように伸縮する伸縮部と、湾曲針を通過させる通過部を有する板状部材とを備える医療用針が知られている(例えば、特許文献1及び2参照。)。伸縮部の一端は、湾曲針の基端部側に設けられた基部と接続されており、伸縮部の他端は、板状部材と接続されている。   Conventionally, as a needle for puncturing a subcutaneously implantable catheter access port, a curved needle having a curved portion curved at a predetermined angle (for example, 90 degrees), a telescopic portion that expands and contracts like a pantograph, and a curved needle are passed. A medical needle provided with a plate-like member having a passage portion is known (for example, see Patent Documents 1 and 2). One end of the expansion / contraction part is connected to a base part provided on the proximal end side of the curved needle, and the other end of the expansion / contraction part is connected to a plate-like member.

従来の医療用針によれば、上記した伸縮部を備えているため、患者の皮膚(アクセスポート)から湾曲針を抜いたときに、湾曲針(の先端部)を伸縮部によってカバーすることができる。このため、医療用針を使用する者(医療従事者及び患者本人を含む。以下、使用者という。)が誤って使用後の医療用針を自分に刺してしまう事故(いわゆる誤刺)の発生を防止することができる。
また、従来の医療用針によれば、上記した板状部材を備えているため、患者の皮膚から湾曲針を抜く際、板状部材の上面(患者の皮膚に接しない方の面)を上から押さえることにより、比較的スムーズに湾曲針を抜くことができる。
According to the conventional medical needle, since the above-described expansion / contraction part is provided, when the bending needle is pulled out from the patient's skin (access port), the bending needle (the tip part) can be covered by the expansion / contraction part. it can. For this reason, an accident (a so-called false puncture) in which a person who uses a medical needle (including a medical worker and a patient himself / herself, hereinafter referred to as a user) accidentally stabs a medical needle after use by himself / herself Can be prevented.
Moreover, according to the conventional medical needle, since the plate-shaped member described above is provided, when the curved needle is pulled out from the patient's skin, the upper surface of the plate-shaped member (the surface not in contact with the patient's skin) is raised. The curved needle can be pulled out relatively smoothly by pressing from the side.

特開2002−369884号公報JP 2002-369984 A 特開2006−61379号公報JP 2006-61379 A

ところで、患者の皮膚から湾曲針を抜いた後において、伸縮部を伸長させた状態(以下、「伸長状態」ということもある。)のまま維持し続けたいという要望が、近年高まりつつある。なぜなら、使用者の意図しないときに伸縮部の伸長状態が解除されてしまうと、湾曲針の先端部が伸縮部(板状部材)から露出してしまう場合があるからである。湾曲針の先端部が伸縮部(板状部材)から露出してしまうと、誤刺が発生しかねない。   Incidentally, in recent years, there has been an increasing demand for maintaining the stretchable portion in an extended state (hereinafter sometimes referred to as an “extended state”) after the curved needle is removed from the patient's skin. This is because the distal end portion of the curved needle may be exposed from the stretchable portion (plate-like member) if the stretched state of the stretchable portion is released when the user does not intend. If the tip of the curved needle is exposed from the expansion / contraction part (plate-like member), a false puncture may occur.

そこで、本発明は、このような事情に鑑みてなされたもので、患者の皮膚から湾曲針を抜いた後において、伸縮部を伸長状態のまま維持し続けることが可能な医療用針を提供することを目的とする。   Therefore, the present invention has been made in view of such circumstances, and provides a medical needle capable of continuing to maintain the stretchable portion in an expanded state after the curved needle is removed from the patient's skin. For the purpose.

[1]本発明の医療用針は、所定角度に湾曲した湾曲部(14)を有する湾曲針(10)と、前記湾曲針(10)の一部が植設された基部(20)と、前記基部(20)に設けられ、前記湾曲部(14)から前記湾曲針の先端部(16)に沿った第1(z)方向に伸縮可能に構成された伸縮部(30)と、前記伸縮部(30)における前記基部(20)とは反対側に接続配置され、前記湾曲針(10)を通過させる通過部(62)を有する板状部材(60)とを備え、前記伸縮部(30)は、前記伸縮部(30)を最も伸ばしたときの前記第1(z)方向に沿った長さが、前記湾曲針の先端部(16)から前記湾曲部(14)までの長さ以上となるように構成された伸縮部材であり、さらに、パンタグラフ状に伸縮可能であって、前記湾曲針(10)を間にして対向配置された第1伸縮部材(32)及び第2伸縮部材(36)と、前記第1及び第2伸縮部材(32,36)のうち一方側に配置されたフック部(40)と、前記第1及び第2伸縮部材(32,36)のうち他方側に配置され、前記第1及び第2伸縮部材(32,36)が伸長した状態のときに前記フック部(40)が係止される切り欠き部(42)と、前記切り欠き部(42)の近傍に配置され、前記フック部(40)が前記切り欠き部(42)に係止されるときに前記フック部(40)を前記切り欠き部(42)に向けて押さえる機能を有する押さえ部材(46)とを有することを特徴とする。 [1] The medical needle of the present invention includes a curved needle (10) having a curved portion (14) curved at a predetermined angle, a base (20) in which a part of the curved needle (10) is implanted, A telescopic part (30) provided on the base part (20) and configured to be stretchable in the first (z) direction along the distal end part (16) of the curved needle from the curved part (14); A plate-like member (60) that is connected to the opposite side of the base (20) of the part (30) and has a passage part (62) that allows the curved needle (10) to pass therethrough; ), The length along the first (z) direction when the stretchable part (30) is most extended is equal to or longer than the length from the distal end part (16) of the curved needle to the curved part (14). An elastic member configured to be, and further expandable and contractable in a pantograph shape, wherein the curved needle 10) with the first elastic member (32) and the second elastic member (36) arranged opposite to each other, and the hook portion arranged on one side of the first and second elastic members (32, 36). (40) and the hook part (32, 36) disposed on the other side of the first and second elastic members (32, 36), when the first and second elastic members (32, 36) are extended. 40) is disposed in the vicinity of the notch (42) and the notch (42), and the hook (40) is engaged with the notch (42). And a pressing member (46) having a function of pressing the hook portion (40) toward the notch portion (42).

このため、本発明の医療用針によれば、上記したフック部及び切り欠き部を備えているため、第1及び第2伸縮部材を伸長状態にして切り欠き部にフック部を係止することにより、第1及び第2伸縮部材の伸長状態を維持し続けることが可能となる。
したがって、本発明の医療用針は、患者の皮膚から湾曲針を抜いた後において、伸縮部(第1及び第2伸縮部材)を伸長状態のまま維持し続けることが可能な医療用針となる。
For this reason, according to the medical needle of the present invention, since the hook portion and the notch portion described above are provided, the first and second extendable members are extended and the hook portion is locked to the notch portion. Thereby, it becomes possible to continue maintaining the extended state of the first and second elastic members.
Therefore, the medical needle of the present invention is a medical needle capable of maintaining the expansion / contraction portions (first and second expansion / contraction members) in the expanded state after the curved needle is removed from the patient's skin. .

また、本発明の医療用針によれば、上記した押さえ部材を備えているため、フック部と切り欠き部との係合力をさらに高めることが可能となる。このため、第1及び第2伸縮部材の伸長状態を、より強い係合力でもって維持し続けることが可能となる。   In addition, according to the medical needle of the present invention, since the above-described pressing member is provided, the engagement force between the hook portion and the notch portion can be further increased. For this reason, it becomes possible to maintain the expansion | extension state of a 1st and 2nd expansion-contraction member with a stronger engaging force.

また、本発明の医療用針によれば、フック部と切り欠き部と押さえ部材とによる比較的簡易な部材で構成されているため、製造コストがそれほど高くなることもない。   In addition, according to the medical needle of the present invention, the manufacturing cost is not so high because it is constituted by a relatively simple member including a hook portion, a notch portion, and a pressing member.

また、本発明の医療用針によれば、第1及び第2伸縮部材を最も伸ばしたときの第1方向に沿った長さが、湾曲針の先端部から湾曲部までの長さ以上となるように構成されているため、患者の皮膚(アクセスポート)から湾曲針を抜いたときに、湾曲針(の先端部)を伸縮部によってカバーすることができる。このため、使用者による誤刺の発生を防止することができる。   Further, according to the medical needle of the present invention, the length along the first direction when the first and second elastic members are extended to the maximum is equal to or longer than the length from the distal end portion of the bending needle to the bending portion. Thus, when the curved needle is pulled out from the patient's skin (access port), the curved needle (the tip portion thereof) can be covered by the expansion / contraction part. For this reason, generation | occurrence | production of the erroneous stick by a user can be prevented.

[2]上記[1]に記載の医療用針においては、前記切り欠き部(42)は、前記基部(20)側に位置する第1開口端(43)と、前記板状部材(60)側に位置する第2開口端(44)と、前記第1開口端(43)及び前記第2開口端(44)を繋ぐ第3開口端(45)とを有し、前記押さえ部材(46)は、一方端(47)が前記第1開口端(43)近傍位置に接続され、他方端(48)が前記第1開口端(43)から前記第2開口端(44)方向に向けて伸びるツメ状の押さえ部材であって、前記他方端(48)と前記第2開口端(44)との間に所定の空間(P)が形成されるように構成されていることが好ましい。 [2] In the medical needle according to [1], the notch (42) includes a first opening end (43) positioned on the base (20) side and the plate-like member (60). A second opening end (44) positioned on the side, and a third opening end (45) connecting the first opening end (43) and the second opening end (44), and the pressing member (46) The one end (47) is connected to the position near the first opening end (43), and the other end (48) extends from the first opening end (43) toward the second opening end (44). The claw-shaped pressing member is preferably configured such that a predetermined space (P) is formed between the other end (48) and the second opening end (44).

このように構成することにより、ツメ状の押さえ部材の他方端と切り欠き部の第2開口端との間に所定の空間が形成されるため、当該空間が形成されない場合(すなわち、押さえ部材の両端が切り欠き部の開口端近傍位置と接続されている場合)と比べて、スムーズにフック部を切り欠き部に係合させることが可能となる。   By configuring in this way, a predetermined space is formed between the other end of the claw-shaped pressing member and the second opening end of the notch, so that the space is not formed (that is, the pressing member Compared with the case where both ends are connected to positions near the opening end of the notch portion), the hook portion can be smoothly engaged with the notch portion.

また、上記のように構成することにより、第1及び第2伸縮部材が伸長状態のときに基部の上方(第1方向に沿った方向)から力が加わった場合に、フック部の端面が第1開口端とぶつかるため、フック部が切り欠き部から外れ難くなる。このときさらに、ツメ状の押さえ部材の他方端が第1開口端から第2開口端方向に向けて伸びるように構成されていることから、フック部が切り欠き部から外れようとするのをさらに抑制することが可能となる。その結果、第1及び第2伸縮部材の伸長状態を、さらに強い係合力でもって維持し続けることが可能となる。   Further, by configuring as described above, when a force is applied from above the base portion (direction along the first direction) when the first and second elastic members are in the extended state, the end surface of the hook portion is Since it collides with one opening end, it becomes difficult for a hook part to come off from a notch part. At this time, since the other end of the claw-shaped pressing member is configured to extend from the first opening end toward the second opening end, the hook portion is further prevented from coming off from the notch portion. It becomes possible to suppress. As a result, the extended state of the first and second elastic members can be maintained with a stronger engagement force.

[3]上記[1]又は[2]に記載の医療用針においては、前記湾曲針における基端部(12)側の部分から前記湾曲部(14)に沿った方向と同一方向を第2(y)方向としたとき、前記フック部(40,50)、前記切り欠き部(42,52)及び前記押さえ部材(46,56)のそれぞれは、前記第1及び第2伸縮部材(32,36)における前記第2(y)方向手前側の面及び前記第2(y)方向奥側の面の両面に配置されていることが好ましい。 [3] In the medical needle according to [1] or [2], the second direction is the same as the direction along the curved portion (14) from the proximal end (12) side portion of the curved needle. In the (y) direction, the hook portions (40, 50), the notches (42, 52), and the pressing members (46, 56) are respectively connected to the first and second elastic members (32, It is preferable that they are disposed on both the second (y) direction front surface and the second (y) direction rear surface in 36).

このように構成することにより、第1及び第2伸縮部材における第2方向手前側及び奥側の両方からフック部と切り欠き部とで係合させ、かつ、押さえ部材で係合力を高めていることから、第1及び第2伸縮部材の伸長状態を、さらに強い係合力でもって維持し続けることが可能となる。   By comprising in this way, it is made to engage by a hook part and a notch part from both the 2nd direction near side and back side in a 1st and 2nd expansion-contraction member, and the engaging force is heightened by the pressing member. Therefore, it is possible to continue to maintain the extended state of the first and second elastic members with a stronger engagement force.

なお、フック部、切り欠き部及び押さえ部材のそれぞれが、第1及び第2伸縮部材における第2方向手前側の面及び第2方向奥側の面の両面に配置されている場合は、(A)第1伸縮部材における第2方向手前側の面及び奥側の面の両方に切り欠き部及び押さえ部材が配置され、第2伸縮部材における第2方向手前側の面及び奥側の面の両方にフック部が配置されていてもよいし、(B)第2伸縮部材における第2方向手前側の面に第1のフック部が配置され、第1伸縮部材における第2方向手前側の面に第1のフック部に対応する第1の切り欠き部及び第1の押さえ部材が配置され、第1伸縮部材における第2方向奥側の面に第2のフック部が配置され、第2伸縮部材における第2方向奥側の面に第2のフック部に対応する第2の切り欠き部及び第2の押さえ部材が配置されていてもよい。   In addition, when each of a hook part, a notch part, and a pressing member is arrange | positioned on both surfaces of the surface of the 1st and 2nd expansion-contraction member in the 2nd direction near side and the 2nd direction back | inner side, (A ) A notch and a pressing member are arranged on both the front surface and the back surface in the second direction of the first elastic member, and both the front surface and the back surface of the second elastic member in the second direction. (B) The first hook portion is disposed on the front surface in the second direction of the second elastic member, and the front surface of the first elastic member is disposed on the front surface in the second direction. A first cutout portion and a first pressing member corresponding to the first hook portion are disposed, a second hook portion is disposed on the back surface in the second direction of the first stretchable member, and a second stretchable member The second notch corresponding to the second hook portion on the back surface in the second direction And the second pressing member may be disposed.

[4]上記[1]〜[3]のいずれかに記載の医療用針においては、前記基部(20)に設けられ、前記基部(20)を中心軸として回動可能に構成された翼部(170)をさらに備え、前記翼部(170)は、前記第1及び第2伸縮部材(32,36)が折り畳まれた状態のときに前記フック部(40,50)が係止される被係止部(175,176)を有し、前記被係止部(175,176)は、前記翼部(170)のうち、前記第1及び第2伸縮部材(32,36)が折り畳まれた状態のときにおける、前記フック部(40,50)の位置に対応する位置に配置され、かつ、前記翼部(170)を回動させることにより前記フック部(40,50)との係合状態を解除可能に構成されていることが好ましい。 [4] In the medical needle according to any one of [1] to [3], the wing portion is provided on the base (20) and is configured to be rotatable about the base (20) as a central axis. (170), and the wing portion (170) is a cover to which the hook portions (40, 50) are locked when the first and second elastic members (32, 36) are folded. The locking portion (175, 176) has the locking portion (175, 176) in which the first and second elastic members (32, 36) of the wing portion (170) are folded. In the state, it is disposed at a position corresponding to the position of the hook part (40, 50) and is engaged with the hook part (40, 50) by rotating the wing part (170). It is preferable that it is comprised so that cancellation | release is possible.

このように構成することにより、第1及び第2伸縮部材が折り畳まれた状態を維持し続けることが可能となる。例えば、患者の皮膚に湾曲針を穿刺した際に、仮に第1及び第2伸縮部材に対して伸長しようとする力(伸縮部が開こうとする力)が発生した場合であっても、本発明の医療用針によれば、被係止部にフック部を係止することによって、そのような伸長しようとする力を抑制することが可能となる。したがって、本発明の医療用針は、患者の皮膚に安定して穿刺可能な医療用針となる。   By comprising in this way, it becomes possible to continue maintaining the state by which the 1st and 2nd expansion-contraction member was folded. For example, even when a force to try to expand the first and second elastic members (force to open the elastic part) is generated when a curved needle is punctured into the patient's skin, According to the medical needle of the invention, it is possible to suppress such a force to extend by locking the hook portion to the locked portion. Therefore, the medical needle of the present invention is a medical needle that can be stably punctured on the skin of a patient.

また、被係止部が、翼部を回動させることによってフック部との係合状態を解除可能に構成されているため、「翼部を摘まむ」という簡単なアクションで被係止部とフック部との係合状態を解除することが可能となる。   In addition, since the locked portion is configured to be able to release the engaged state with the hook portion by rotating the wing portion, the locked portion can be moved with a simple action of “pinch the wing portion”. It is possible to release the engagement state with the hook portion.

[5]上記[1]〜[3]のいずれかに記載の医療用針においては、前記基部(20)に設けられた翼部(70)と、前記伸縮部(30)が折り畳まれた状態で前記翼部(70)及び前記板状部材(60)を押さえるとともに、前記湾曲針(10)を覆う針カバー部材(80)とをさらに備え、前記針カバー部材(80)には、前記第1及び第2伸縮部材(32,36)が折り畳まれた状態のときにおける、前記フック部(40)及び前記押さえ部材(46)のうち少なくとも一方の位置に対応する位置に、所定のクリアランスが設けられていることが好ましい。 [5] In the medical needle according to any one of [1] to [3] above, the wing part (70) provided on the base part (20) and the expandable part (30) are folded. A needle cover member (80) that holds the wing (70) and the plate member (60) and covers the curved needle (10), and the needle cover member (80) includes the first cover member (80). A predetermined clearance is provided at a position corresponding to at least one of the hook portion (40) and the pressing member (46) when the first and second elastic members (32, 36) are folded. It is preferable that

医療用針を使用する前(患者の皮膚に穿刺する前)においては、安全性を確保しつつ、コンパクトな医療用針が求められる。ここで、第1及び第2伸縮部材を折り畳んだ状態とすると、医療用針全体の大きさを小さくすることができる一方、湾曲針(の先端部)を伸縮部によってカバーすることができない。また、第1及び第2伸縮部材を伸ばした状態とすると、湾曲針(の先端部)を第1及び第2伸縮部材によってカバーすることができる一方、医療用針全体の大きさが比較的大きなものとなってしまう。
本発明の医療用針によれば、医療用針を使用する前は、第1及び第2伸縮部材を折り畳んだ状態で針カバー部材内に湾曲針、第1及び第2伸縮部材並びに板状部材などを格納することができるため、第1及び第2伸縮部材を折り畳んだ状態のままで安全性を確保することができる。つまり、本発明の医療用針は、安全性を確保しつつ、コンパクトな医療用針となる。
Before using the medical needle (before puncturing the patient's skin), a compact medical needle is required while ensuring safety. Here, when the first and second elastic members are folded, the size of the entire medical needle can be reduced, while the curved needle (the distal end portion) cannot be covered by the elastic portion. Further, when the first and second extendable members are extended, the curved needle (the tip thereof) can be covered by the first and second extendable members, while the size of the entire medical needle is relatively large. It becomes a thing.
According to the medical needle of the present invention, before using the medical needle, the curved needle, the first and second elastic members, and the plate-like member are folded in the needle cover member in a state where the first and second elastic members are folded. Therefore, safety can be ensured with the first and second elastic members folded. That is, the medical needle of the present invention is a compact medical needle while ensuring safety.

また、針カバー部材に上記した所定のクリアランスが設けられていることにより、針カバー部材内に湾曲針、第1及び第2伸縮部材並びに板状部材などを格納したときに、フック部や押さえ部材が針カバー部材に引っかかってしまうのを防止することができる。
また、上記のように構成することにより、クリアランスを設けた部分以外の針カバー部材の厚みを薄くできるため、針カバー部材も含めた医療用針全体の小型化に寄与することができる。
In addition, since the needle cover member is provided with the predetermined clearance described above, when the curved needle, the first and second extendable members, the plate-like member, and the like are stored in the needle cover member, the hook portion and the pressing member Can be prevented from being caught by the needle cover member.
Moreover, since the thickness of the needle cover member other than the portion provided with the clearance can be reduced by configuring as described above, it is possible to contribute to downsizing of the entire medical needle including the needle cover member.

なお、特許請求の範囲及び本欄(課題を解決するための手段の欄)に記載した各手段の文言下に括弧をもって付加された符号は、特許請求の範囲及び本欄に記載された内容の理解を容易にするために用いられたものであって、特許請求の範囲及び本欄に記載された内容を限定するものではない。   Note that the reference numerals added in parentheses below the wording of each means described in the claims and in this column (the column for means for solving the problem) indicate the contents described in the claims and this column. It is used for easy understanding, and does not limit the contents described in the claims and in this section.

以下、本発明の医療用針について、図に示す実施の形態に基づいて説明する。   Hereinafter, the medical needle of the present invention will be described based on the embodiments shown in the drawings.

[実施形態1]
図1は、医療用針1の斜視図である。図2は、図1とは異なる方向から見たときの医療用針1の斜視図である。図3は、医療用針1の正面図である。図4は、医療用針1の背面図(医療用針1をチューブ接続部22側から見た図)である。図5は、医療用針1の側面図である。なお、図1〜図5においては、針カバー部材80の図示を省略している。
[Embodiment 1]
FIG. 1 is a perspective view of a medical needle 1. FIG. 2 is a perspective view of the medical needle 1 when viewed from a direction different from that in FIG. FIG. 3 is a front view of the medical needle 1. FIG. 4 is a rear view of the medical needle 1 (a view of the medical needle 1 viewed from the tube connecting portion 22 side). FIG. 5 is a side view of the medical needle 1. Note that the needle cover member 80 is not shown in FIGS.

図6は、第1及び第2伸縮部材32,36が伸縮する様子を説明するために示す図である。図6(a)は第1及び第2伸縮部材32,36を最も折り畳んだ状態のときの医療用針1の正面図であり、図6(e)は第1及び第2伸縮部材32,36を最も伸長させた状態のときの医療用針1の正面図であり、図6(b)〜図6(d)は図6(a)に示す状態から図6(e)に示す状態になるまでの途中経過を示す医療用針1の正面図である。   FIG. 6 is a view for explaining how the first and second elastic members 32 and 36 expand and contract. FIG. 6A is a front view of the medical needle 1 when the first and second elastic members 32 and 36 are most folded, and FIG. 6E is the first and second elastic members 32 and 36. FIG. 6B is a front view of the medical needle 1 in a state where the needle is most extended, and FIGS. 6B to 6D are changed from the state shown in FIG. 6A to the state shown in FIG. It is a front view of the medical needle 1 which shows the middle course until.

図7は、フック部40,50が切り欠き部42,52に係止される様子を説明するために示す図である。なお、図7においては、フック部40,50、切り欠き部42,52及び押さえ部材46,56の部分における、y−x平面での断面を模式的に図示している。   FIG. 7 is a view for explaining a state in which the hook portions 40 and 50 are locked to the cutout portions 42 and 52. In FIG. 7, a cross section in the xy plane is schematically shown in the portions of the hook portions 40 and 50, the cutout portions 42 and 52, and the pressing members 46 and 56.

図8は、フック部40、切り欠き部42及び押さえ部材46を説明するために示す図である。図8(a)は切り欠き部42及び押さえ部材46をy方向に沿って見た部分拡大図であり、図8(b)は切り欠き部42及び押さえ部材46をx方向に沿って見た部分拡大図であり、図8(c)は第1及び第2伸縮部材32,36を伸長状態としたときにおける、フック部40、切り欠き部42及び押さえ部材46をy方向に沿って見た部分拡大図である。   FIG. 8 is a view for explaining the hook portion 40, the cutout portion 42, and the pressing member 46. FIG. 8A is a partially enlarged view of the cutout portion 42 and the pressing member 46 viewed along the y direction, and FIG. 8B is a view of the cutout portion 42 and the pressing member 46 viewed along the x direction. FIG. 8C is a partially enlarged view of the hook portion 40, the cutout portion 42, and the pressing member 46 viewed along the y direction when the first and second elastic members 32, 36 are in the extended state. It is a partial enlarged view.

図9及び図10は、針カバー部材80を説明するために示す図である。図9(a)は針カバー部材80の正面図であり、図9(b)は針カバー部材80の側面図であり、図9(c)は針カバー部材80の上面図であり、図9(d)は針カバー部材80の底面図である。図10(a)は針カバー部材80の斜視図であり、図10(b)は針カバー部材80を装着したときの医療用針1の斜視図である。   9 and 10 are views for explaining the needle cover member 80. 9A is a front view of the needle cover member 80, FIG. 9B is a side view of the needle cover member 80, and FIG. 9C is a top view of the needle cover member 80. (D) is a bottom view of the needle cover member 80. 10A is a perspective view of the needle cover member 80, and FIG. 10B is a perspective view of the medical needle 1 when the needle cover member 80 is attached.

なお、以下の説明においては、互いに直交する3つの方向をそれぞれx方向、y方向、z方向とする。x方向とは「第3方向」のことであり、y方向とは「第2方向」のことであり、z方向とは「第1方向」のことである。x方向は、板状部材60の長辺方向と同一の方向であり、y方向は、板状部材60の短辺方向と同一の方向(または、基部20の長手方向と同一の方向)であり、z方向は、湾曲針10の湾曲部14から先端部16に沿った方向(または、板状部材60における基部20側の面に垂直な方向)である。   In the following description, three directions orthogonal to each other are referred to as an x direction, a y direction, and a z direction, respectively. The x direction is the “third direction”, the y direction is the “second direction”, and the z direction is the “first direction”. The x direction is the same direction as the long side direction of the plate-like member 60, and the y direction is the same direction as the short side direction of the plate-like member 60 (or the same direction as the longitudinal direction of the base portion 20). , Z direction is a direction along the distal end portion 16 from the bending portion 14 of the bending needle 10 (or a direction perpendicular to the surface of the plate-like member 60 on the base portion 20 side).

実施形態1に係る医療用針1は、図1〜図5に示すように、所定角度(例えば90度)に湾曲した湾曲部14を有する湾曲針10と、湾曲針10の一部が植設された基部20と、基部20に設けられ、パンタグラフ状に伸縮可能に構成された伸縮部30と、伸縮部30における基部20とは反対側に接続配置された板状部材60と、基部20に設けられた翼部70と、針カバー部材80(図9及び図10参照。)とを備える。   As shown in FIGS. 1 to 5, the medical needle 1 according to the first embodiment has a curved needle 10 having a curved portion 14 curved at a predetermined angle (for example, 90 degrees), and a part of the curved needle 10 is implanted. The base 20, the expansion / contraction part 30 provided in the base 20 and configured to be expandable and contractable in a pantograph shape, the plate-like member 60 connected to the opposite side of the expansion / contraction part 30 from the base 20, and the base 20 The provided wing | blade part 70 and the needle cover member 80 (refer FIG.9 and FIG.10) are provided.

湾曲針10は、図5に示すように、基端部12と、例えば90度に湾曲した湾曲部14と、患者の皮下に埋め込まれたアクセスポート(後述する図12参照。)に穿刺される先端部16とを有する。基端部12から湾曲部14までは、y方向に平行な直管状であり、湾曲部14から先端部16の手前までは、z方向に平行な直管状である。先端部16は、コアリング(アクセスポートにおけるセプタムの穴あきや削りカスの発生)防止のために若干屈曲した構成となっている。   As shown in FIG. 5, the curved needle 10 is punctured into a proximal end portion 12, a curved portion 14 that is curved at, for example, 90 degrees, and an access port (see FIG. 12 described later) that is implanted under the skin of a patient. And a tip portion 16. From the base end portion 12 to the curved portion 14 is a straight tube parallel to the y direction, and from the curved portion 14 to the front of the distal end portion 16 is a straight tube parallel to the z direction. The distal end portion 16 has a slightly bent configuration for preventing coring (perforation of a septum at the access port and generation of scraps).

基部20は、湾曲針10の基端部12及び湾曲部14を覆うように構成されている。また、基部20は、管状のチューブ接続部22を有し、チューブ接続部22の部分で図示しないチューブに接続可能に構成されている。   The base portion 20 is configured to cover the base end portion 12 and the bending portion 14 of the bending needle 10. The base 20 has a tubular tube connecting portion 22 and is configured to be connectable to a tube (not shown) at the tube connecting portion 22.

伸縮部30は、図3及び図4に示すように、湾曲針10を間にして対向配置された第1伸縮部材32及び第2伸縮部材36と、第2伸縮部材36におけるy方向手前側の面に配置されたフック部40と、第1伸縮部材32におけるy方向手前側の面に配置された切り欠き部42と、切り欠き部42の近傍に配置された押さえ部材46と、第1伸縮部材32におけるy方向奥側の面に配置されたフック部50と、第2伸縮部材36におけるy方向奥側の面に配置された切り欠き部52と、切り欠き部52の近傍に配置された押さえ部材56とを有する。   As shown in FIGS. 3 and 4, the expansion / contraction part 30 includes a first expansion / contraction member 32 and a second expansion / contraction member 36 that are opposed to each other with the bending needle 10 therebetween, and a second expansion / contraction member 36 on the near side in the y direction. A hook portion 40 disposed on the surface, a notch portion 42 disposed on the front surface in the y direction of the first elastic member 32, a pressing member 46 disposed in the vicinity of the notch portion 42, and the first expansion and contraction. The hook portion 50 disposed on the back surface in the y direction of the member 32, the notch portion 52 disposed on the back surface in the y direction of the second elastic member 36, and the vicinity of the notch portion 52. And a pressing member 56.

第1及び第2伸縮部材32,36のそれぞれは、端部が基部20及び板状部材60に接続されており、屈曲部34,38の部分で略「くの字」状に屈曲可能に構成されている(図3及び図4参照。)。また、第1及び第2伸縮部材32,36のそれぞれは、第1及び第2伸縮部材32,36の各端部と基部20及び板状部材60との接続部分においても、屈曲可能に構成されている。このように構成された第1及び第2伸縮部材32,36が湾曲針10を間にして対向配置されているため、図6(a)〜図6(e)に示すように、x方向に沿って広がるように又は狭まるように、パンタグラフ状に伸縮することができる。
また、伸縮部30は、第1及び第2伸縮部材32,36が広がる方向が、後述する板状部材60の長辺方向と同じ方向となるように配置されている。
Each of the first and second elastic members 32, 36 has an end connected to the base 20 and the plate-like member 60, and is configured to be able to be bent in a substantially “<” shape at the bent portions 34, 38. (See FIGS. 3 and 4). In addition, each of the first and second elastic members 32 and 36 is configured to be bendable also at a connection portion between each end of the first and second elastic members 32 and 36 and the base 20 and the plate-like member 60. ing. Since the first and second elastic members 32 and 36 configured in this manner are arranged to face each other with the curved needle 10 therebetween, as shown in FIGS. 6A to 6E, in the x direction. It can be expanded and contracted in a pantograph shape so as to widen or narrow along.
The stretchable portion 30 is arranged so that the direction in which the first and second stretchable members 32 and 36 spread is the same as the long side direction of the plate-like member 60 described later.

第1及び第2伸縮部材32,36は、図6(e)から分かるように、第1及び第2伸縮部材32,36を最も伸ばしたときのz方向に沿った長さが、湾曲針10の先端部16から湾曲部14までの長さ以上となるように構成されている。   As can be seen from FIG. 6 (e), the lengths of the first and second elastic members 32 and 36 along the z direction when the first and second elastic members 32 and 36 are extended to the maximum are the curved needle 10. It is comprised so that it may become more than the length from the front-end | tip part 16 to the curved part 14.

フック部40,50の先端部は、図1及び図2に示すように、鉤状になっている。第1及び第2伸縮部材32,36を伸長状態(図6(e)に示す状態)にすると、図7に示すように、フック部40は切り欠き部42に係止され、フック部50は切り欠き部52に係止されることとなる。   The tip portions of the hook portions 40 and 50 have a hook shape as shown in FIGS. When the first and second elastic members 32 and 36 are in the extended state (the state shown in FIG. 6 (e)), as shown in FIG. 7, the hook part 40 is locked to the notch part 42, and the hook part 50 is It is locked to the notch 52.

切り欠き部42は、図8(a)及び図8(b)に示すように、基部20側に位置する第1開口端43と、板状部材60側に位置する第2開口端44と、第1開口端43及び第2開口端44を繋ぐ第3開口端45とを有する。   As shown in FIGS. 8A and 8B, the notch portion 42 includes a first opening end 43 located on the base 20 side, a second opening end 44 located on the plate-like member 60 side, And a third opening end 45 connecting the first opening end 43 and the second opening end 44.

押さえ部材46は、一方端47が第1開口端43近傍位置に接続され、他方端48が第1開口端43から第2開口端44方向に向けて伸びるツメ状の押さえ部材である。言い換えれば、ツメ状の押さえ部材46は、伸縮部30を伸長させたときにツメの先端(他方端48)が板状部材60側に向くように構成されている。押さえ部材46は、他方端48と第2開口端44との間に所定の空間P(図8(b)参照。)が形成されるように構成されている。   The pressing member 46 is a claw-shaped pressing member having one end 47 connected to a position near the first opening end 43 and the other end 48 extending from the first opening end 43 toward the second opening end 44. In other words, the claw-shaped pressing member 46 is configured such that the tip (the other end 48) of the claw is directed toward the plate-shaped member 60 when the telescopic portion 30 is extended. The pressing member 46 is configured such that a predetermined space P (see FIG. 8B) is formed between the other end 48 and the second opening end 44.

押さえ部材46は、フック部40が切り欠き部42に係止されるときにフック部40を切り欠き部42に向けて押さえる機能を有する(図7参照。)。   The pressing member 46 has a function of pressing the hook portion 40 toward the notch portion 42 when the hook portion 40 is locked to the notch portion 42 (see FIG. 7).

なお、フック部40が切り欠き部42に完全に係止された後においては、押さえ部材46は、フック部40と接触していてもよいし、フック部40と接触していなくてもよい。つまり、フック部40が切り欠き部42に完全に係止された後においては、押さえ部材46は、必ずしもフック部40を切り欠き部42に向けて押さえていなくてもよい。   In addition, after the hook part 40 is completely locked to the notch part 42, the pressing member 46 may be in contact with the hook part 40 or may not be in contact with the hook part 40. That is, after the hook portion 40 is completely locked to the notch portion 42, the pressing member 46 does not necessarily hold the hook portion 40 toward the notch portion 42.

切り欠き部52及び押さえ部材56は、上記の切り欠き部42及び押さえ部材46と同様の構成及び機能を有するため、詳細な説明は省略する。   Since the notch 52 and the pressing member 56 have the same configuration and function as the above-described notch 42 and the pressing member 46, detailed description thereof is omitted.

板状部材60は、図1及び図2に示すように、略長方形状の板状部材であり、長方形の四隅の角は丸め処理が施されている。板状部材60は、その長辺がx方向に沿い、短辺がy方向に沿うように配置されている。板状部材60は、略中央部に形成され、湾曲針10を通過させる通過部62を有する。通過部62は、スリット状(切れ込み状)の通過部である。   As shown in FIGS. 1 and 2, the plate-like member 60 is a substantially rectangular plate-like member, and the corners of the four corners of the rectangle are rounded. The plate-like member 60 is arranged such that its long side is along the x direction and its short side is along the y direction. The plate-like member 60 is formed at a substantially central portion and has a passage portion 62 through which the curved needle 10 passes. The passage part 62 is a slit-like (cut-out) passage part.

翼部70は、図1〜図4に示すように、基部20の側方に接続配置された一対の翼部材であって、略矩形状の把持部72,74と、基部20と各把持部72,74との間に配置され、把持部72,74の厚みよりも薄く形成された薄肉部77,78とを有する。把持部72,74は、基部20と薄肉部77,78との接続部分を軸として所定角度回動可能に構成されている(後述する図11(a1)〜図11(c1)及び図11(a2)〜図11(c2)参照。)。薄肉部77,78の厚みが把持部72,74の厚みよりも薄いことから、翼部70を把持する際に、基部20と薄肉部77,78とが干渉してしまうのを抑制することができ、結果として、翼部70を把持しやすくなる。また、薄肉部77,78の厚みが把持部72,74の厚みよりも薄いことから、把持部72,74を回動させやすいという効果もある。   As shown in FIGS. 1 to 4, the wing part 70 is a pair of wing members connected to the side of the base part 20, and includes substantially rectangular gripping parts 72 and 74, the base part 20, and each gripping part. 72 and 74, and thin portions 77 and 78 formed thinner than the grip portions 72 and 74. The grip portions 72 and 74 are configured to be rotatable by a predetermined angle about the connecting portion between the base portion 20 and the thin portions 77 and 78 (FIGS. 11A1 to 11C1 and FIG. a2) to FIG. 11 (c2).) Since the thickness of the thin portions 77 and 78 is thinner than the thickness of the grip portions 72 and 74, it is possible to suppress the interference between the base portion 20 and the thin portions 77 and 78 when gripping the wing portion 70. As a result, the wing part 70 can be easily gripped. Moreover, since the thickness of the thin parts 77 and 78 is thinner than the thickness of the holding parts 72 and 74, there also exists an effect that it is easy to rotate the holding parts 72 and 74.

基部20、伸縮部30、板状部材60及び翼部70は、同一のプラスチック材料(例えば、ポリエチレン、ポリプロピレンなど。)からなり、射出成形することによって形成されている。   The base part 20, the elastic part 30, the plate-like member 60, and the wing part 70 are made of the same plastic material (for example, polyethylene, polypropylene, etc.), and are formed by injection molding.

針カバー部材80は、図9及び図10に示すように、所定の厚みを残して中身がくり抜かれた、正面視略T字状の部材である。針カバー部材80は、伸縮部30を折り畳んだ状態で翼部70、伸縮部30及び板状部材60を格納可能な第1格納部82と、伸縮部30を折り畳んだ状態で湾曲針10(の先端部16)を格納可能な第2格納部84とを有する。第1格納部82の上面には、基部20の位置に対応して切り欠き83が設けられている。伸縮部30を折り畳んだ状態とすると、図10(b)から分かるように、翼部70、伸縮部30及び板状部材60が第1格納部82に格納され、湾曲針10(の先端部16)が第2格納部84に格納される。   As shown in FIGS. 9 and 10, the needle cover member 80 is a member having a substantially T-shape in front view in which the contents are hollowed out while leaving a predetermined thickness. The needle cover member 80 includes a first storage portion 82 that can store the wing portion 70, the expansion / contraction portion 30 and the plate-like member 60 in a state in which the expansion / contraction portion 30 is folded, and the curved needle 10 ( And a second storage portion 84 capable of storing the tip portion 16). A cutout 83 is provided on the upper surface of the first storage portion 82 corresponding to the position of the base portion 20. When the expansion / contraction part 30 is in the folded state, as shown in FIG. 10 (b), the wing part 70, the expansion / contraction part 30 and the plate-like member 60 are stored in the first storage part 82, and the bending needle 10 (the tip part 16 of the curved needle 10). ) Is stored in the second storage unit 84.

また、針カバー部材80には、第1及び第2伸縮部材32,36が折り畳まれた状態(図6(a)に示す状態)のときにおける、フック部40の位置に対応する位置に凸部86が設けられており、フック部50の位置に対応する位置に平面視コの字形状の溝部87が設けられており、押さえ部材46の位置に対応する位置に略四角形状の穴部88が設けられている。これら凸部86、溝部87及び穴部88によって、針カバー部材80とフック部40,50及び押さえ部材46との間に所定のクリアランスが設けられることとなる(図10(b)参照。)。   Further, the needle cover member 80 has a convex portion at a position corresponding to the position of the hook portion 40 when the first and second elastic members 32 and 36 are folded (the state shown in FIG. 6A). 86, a groove portion 87 having a U-shape in plan view is provided at a position corresponding to the position of the hook portion 50, and a substantially square hole 88 is formed at a position corresponding to the position of the pressing member 46. Is provided. A predetermined clearance is provided between the needle cover member 80, the hook portions 40 and 50, and the pressing member 46 by the convex portion 86, the groove portion 87, and the hole portion 88 (see FIG. 10B).

第1格納部82は、図9(a)に示すように、凸部86を設けた部分以外のz方向に沿った厚みT1が、凸部86を設けた部分のz方向に沿った厚みT2よりも薄くなるように構成されている。   As shown in FIG. 9A, the first storage portion 82 has a thickness T1 along the z direction other than the portion where the convex portion 86 is provided, and a thickness T2 along the z direction of the portion where the convex portion 86 is provided. It is comprised so that it may become thinner.

実施形態1に係る医療用針1について、図11〜図13を用いてさらに詳細に説明する。
図11〜図13は、医療用針1を説明するために示す図である。図11(a1)〜図11(e1)は医療用針1を使用したときの各状態を示す正面図であり、図11(a2)〜図11(e2)は図11(a1)〜図11(e1)に示す状態のときの斜視図である。図12(a)は医療用針1を患者の皮膚Sに穿刺したときの様子を模式的に示す図であり、図12(b)は医療用針1を患者の皮膚Sから抜いたときの様子を模式的に示す図である。なお、図12(a)及び図12(b)においては、アクセスポートAPに対する医療用針1の大きさや、患者の皮膚SからアクセスポートAPまでの深さ(距離)などは誇張して図示している。図13(a)は第1及び第2伸縮部材32,36が伸長状態のときに基部20の上方(z方向に沿った方向)から力が加わった場合の、医療用針1の正面図であり、図13(b)は図13(a)の符号Aで示す部分の拡大図である。なお、図13(b)においては、図面を分かりやすくするために、フック部40に斜線を付して図示している。
The medical needle 1 according to Embodiment 1 will be described in more detail with reference to FIGS.
FIGS. 11-13 is a figure shown in order to demonstrate the medical needle 1. FIG. 11 (a1) to 11 (e1) are front views showing respective states when the medical needle 1 is used, and FIGS. 11 (a2) to 11 (e2) are FIGS. 11 (a1) to 11. It is a perspective view at the time of the state shown to (e1). FIG. 12A is a view schematically showing a state where the medical needle 1 is punctured into the patient's skin S, and FIG. 12B is a view when the medical needle 1 is removed from the patient's skin S. It is a figure which shows a mode typically. 12 (a) and 12 (b), the size of the medical needle 1 relative to the access port AP, the depth (distance) from the patient's skin S to the access port AP, and the like are exaggerated. ing. FIG. 13A is a front view of the medical needle 1 when force is applied from above the base portion 20 (direction along the z direction) when the first and second elastic members 32 and 36 are in the extended state. FIG. 13 (b) is an enlarged view of a portion indicated by reference numeral A in FIG. 13 (a). In FIG. 13B, the hook portion 40 is hatched to make the drawing easy to understand.

医療用針1を使用する際には、まず、針カバー部材80が装着された状態の医療用針1(図10(b)参照。)から、針カバー部材80を取り外す。
次に、翼部70の把持部72,74を把持し、把持部72,74が接触するまで翼部70を回動させる(図11(a1)〜図11(c1)及び図11(a2)〜図11(c2)参照。)。
そして、把持部72,74を把持した状態で、患者の皮膚Sの下に埋め込まれたアクセスポートAPの所定部位に湾曲針10を穿刺する(図12(a)参照。)。穿刺後は、必要に応じて、把持部72,74を広げて把持部72,74の上からテープ止めを行う。
When using the medical needle 1, first, the needle cover member 80 is removed from the medical needle 1 (see FIG. 10B) with the needle cover member 80 attached.
Next, the gripping portions 72 and 74 of the wing portion 70 are gripped, and the wing portion 70 is rotated until the gripping portions 72 and 74 come into contact with each other (FIGS. 11A1 to 11C1 and 11A2). To FIG. 11 (c2).)
Then, with the grasping portions 72 and 74 grasped, the curved needle 10 is punctured into a predetermined portion of the access port AP embedded under the skin S of the patient (see FIG. 12A). After puncturing, if necessary, the gripping portions 72 and 74 are spread out and taped from above the gripping portions 72 and 74.

患者の皮膚S(アクセスポートAP)から湾曲針10を抜くときは、テープ止めを行った場合はテープを剥がして、板状部材60を押さえながら把持部72,74を摘まみ上げ、患者の皮膚Sから湾曲針10を引き抜く(図11(d1)、図11(e1)、図11(d2)、図11(e2)及び図12(b)参照。)。この湾曲針10の引き抜き動作とともに、または当該引き抜き動作の直後に、切り欠き部42,52にフック部40,50を係止させる(図8(c)参照。)。   When removing the curved needle 10 from the patient's skin S (access port AP), if the tape is fixed, the tape is peeled off, and the gripping portions 72 and 74 are picked up while holding the plate-like member 60, and the patient's skin. The curved needle 10 is pulled out from S (see FIGS. 11 (d1), 11 (e1), 11 (d2), 11 (e2), and 12 (b)). The hook portions 40 and 50 are engaged with the cutout portions 42 and 52 together with the pulling operation of the bending needle 10 or immediately after the pulling operation (see FIG. 8C).

なお、患者の皮膚S(アクセスポートAP)から湾曲針10を抜く方法としては、上述の方法に限定されない。図示による説明は省略するが、各把持部72,74を第1及び第2伸縮部材32,36に沿わせる(板状部材60側に垂らす)ようにして、第1及び第2伸縮部材32,36と把持部72,74とを一緒に摘まみ上げてもよい。   Note that the method of removing the curved needle 10 from the patient's skin S (access port AP) is not limited to the method described above. Although the description by illustration is omitted, the first and second elastic members 32, 74 are arranged so that the gripping portions 72, 74 are along the first and second elastic members 32, 36 (hanging on the plate-like member 60 side). 36 and the gripping portions 72 and 74 may be picked up together.

実施形態1に係る医療用針1によれば、上記したフック部40,50及び切り欠き部42,52を備えているため、第1及び第2伸縮部材32,36を伸長状態にして切り欠き部42,52にフック部40,50を係止することにより、第1及び第2伸縮部材32,36の伸長状態を維持し続けることが可能となる。
したがって、実施形態1に係る医療用針1は、患者の皮膚から湾曲針を抜いた後において、伸縮部(第1及び第2伸縮部材)を伸長状態のまま維持し続けることが可能な医療用針となる。
According to the medical needle 1 according to the first embodiment, since the hook portions 40 and 50 and the notches 42 and 52 are provided, the first and second elastic members 32 and 36 are in an expanded state and are notched. By locking the hook portions 40, 50 to the portions 42, 52, it is possible to continue to maintain the extended state of the first and second elastic members 32, 36.
Therefore, the medical needle 1 according to the first embodiment is a medical needle capable of maintaining the stretchable parts (first and second stretchable members) in the stretched state after the curved needle is removed from the patient's skin. Become a needle.

また、実施形態1に係る医療用針1によれば、上記した押さえ部材46,56を備えているため、フック部40と切り欠き部42との係合力(及びフック部50と切り欠き部52との係合力)をさらに高めることが可能となる。このため、第1及び第2伸縮部材32,36の伸長状態を、より強い係合力でもって維持し続けることが可能となる。   Further, according to the medical needle 1 according to the first embodiment, since the pressing members 46 and 56 described above are provided, the engagement force between the hook portion 40 and the notch portion 42 (and the hook portion 50 and the notch portion 52). It is possible to further increase the engagement force). For this reason, it becomes possible to maintain the extended state of the 1st and 2nd expansion-contraction members 32 and 36 with a stronger engaging force.

また、実施形態1に係る医療用針1によれば、フック部40,50と切り欠き部42,52と押さえ部材46,56とによる比較的簡易な部材で構成されているため、製造コストがそれほど高くなることもない。   Moreover, according to the medical needle 1 which concerns on Embodiment 1, since it is comprised by the comparatively simple member by the hook parts 40 and 50, the notch parts 42 and 52, and the pressing members 46 and 56, manufacturing cost is low. It won't be so high.

また、実施形態1に係る医療用針1によれば、第1及び第2伸縮部材32,36を最も伸ばしたときのz方向に沿った長さが、湾曲針10の先端部16から湾曲部14までの長さ以上となるように構成されているため、患者の皮膚(アクセスポート)から湾曲針10を抜いたときに、湾曲針10(の先端部16)を伸縮部30によってカバーすることができる(図12(b)参照。)。このため、使用者による誤刺の発生を防止することができる。   Further, according to the medical needle 1 according to the first embodiment, the length along the z direction when the first and second elastic members 32 and 36 are extended to the maximum is from the distal end portion 16 of the bending needle 10 to the bending portion. 14 or more, when the curved needle 10 is pulled out from the patient's skin (access port), the curved needle 10 (tip 16 thereof) is covered by the expansion / contraction part 30. (See FIG. 12B). For this reason, generation | occurrence | production of the erroneous stick by a user can be prevented.

実施形態1に係る医療用針1においては、押さえ部材46(及び押さえ部材56)は、他方端48が第1開口端43から第2開口端44方向に向けて伸びるツメ状の押さえ部材であって、他方端48と第2開口端44との間に所定の空間Pが形成されるように構成されているため、当該空間が形成されない場合(すなわち、押さえ部材の両端が切り欠き部42の開口端近傍位置と接続されている場合)と比べて、スムーズにフック部40,50を切り欠き部42,52に係合させることが可能となる。   In the medical needle 1 according to the first embodiment, the pressing member 46 (and the pressing member 56) is a claw-shaped pressing member whose other end 48 extends from the first opening end 43 toward the second opening end 44. Since the predetermined space P is formed between the other end 48 and the second opening end 44, the space is not formed (that is, both ends of the pressing member are formed on the notch portion 42). The hook portions 40 and 50 can be smoothly engaged with the cutout portions 42 and 52 as compared to the case where the hook portions 40 and 50 are connected to the vicinity of the opening end.

実施形態1に係る医療用針1においては、図13(a)に示すように、第1及び第2伸縮部材32,36が伸長状態のときに基部20の上方(z方向に沿った方向)から力が加わった場合、図13(b)に示すように、フック部40の端面が第1開口端43とぶつかるため、フック部40が切り欠き部42から外れ難くなる。図示による説明は省略するが、フック部50についても同様に、フック部50の端面が切り欠き部52の第1開口端とぶつかるため、フック部50が切り欠き部52から外れ難くなる。さらに、ツメ状の押さえ部材46,56の他方端が、第1開口端から第2開口端方向に向けて伸びるように構成されていることから、フック部40,50が切り欠き部42,52から外れようとするのをさらに抑制することが可能となる。その結果、第1及び第2伸縮部材32,36の伸長状態を、さらに強い係合力でもって維持し続けることが可能となる。   In the medical needle 1 according to the first embodiment, as shown in FIG. 13A, when the first and second elastic members 32 and 36 are in the extended state, the base 20 is above (the direction along the z direction). When the force is applied, the end surface of the hook portion 40 collides with the first opening end 43 as shown in FIG. 13B, so that the hook portion 40 is difficult to come off from the notch portion 42. Although description by illustration is abbreviate | omitted, since the end surface of the hook part 50 collides with the 1st opening end of the notch part 52 similarly, the hook part 50 becomes difficult to remove | deviate from the notch part 52. Further, since the other ends of the claw-shaped pressing members 46 and 56 are configured to extend from the first opening end toward the second opening end, the hook portions 40 and 50 are notched portions 42 and 52. It is possible to further suppress attempts to deviate from the above. As a result, the extended state of the first and second elastic members 32 and 36 can be maintained with a stronger engagement force.

実施形態1に係る医療用針1においては、フック部40,50、切り欠き部42,52及び押さえ部材46,56のそれぞれは、第1及び第2伸縮部材32,36におけるy方向手前側の面及びy方向奥側の面の両面に配置されている。これにより、第1及び第2伸縮部材32,36におけるy方向手前側及び奥側の両方からフック部40,50と切り欠き部42,52とで係合させ、かつ、押さえ部材46,56で係合力を高めていることから、第1及び第2伸縮部材32,36の伸長状態を、さらに強い係合力でもって維持し続けることが可能となる。   In the medical needle 1 according to the first embodiment, the hook portions 40 and 50, the cutout portions 42 and 52, and the pressing members 46 and 56 are respectively located on the front side in the y direction of the first and second elastic members 32 and 36. It arrange | positions on both surfaces of the surface and the surface of the y direction back side. Thus, the hook portions 40 and 50 are engaged with the notches 42 and 52 from both the front side and the back side in the y direction of the first and second elastic members 32 and 36, and the pressing members 46 and 56 are used. Since the engaging force is increased, the extended state of the first and second elastic members 32 and 36 can be maintained with a stronger engaging force.

実施形態1に係る医療用針1においては、上記した翼部70をさらに備えるため、翼部70を把持して湾曲針10の抜き差しを容易に行うことが可能となる。   Since the medical needle 1 according to the first embodiment further includes the wing part 70 described above, the curved needle 10 can be easily inserted and removed by grasping the wing part 70.

実施形態1に係る医療用針1においては、上記した針カバー部材80をさらに備えるため、医療用針1を使用する前は、伸縮部30を折り畳んだ状態で針カバー部材80内に湾曲針10、伸縮部30及び板状部材60などを格納することができる。このため、伸縮部30を折り畳んだ状態のままで安全性を確保することができる。つまり、実施形態1に係る医療用針1は、安全性を確保しつつ、コンパクトな医療用針となる。   Since the medical needle 1 according to the first embodiment further includes the needle cover member 80 described above, the curved needle 10 is placed in the needle cover member 80 in a state where the telescopic portion 30 is folded before the medical needle 1 is used. The telescopic part 30 and the plate-like member 60 can be stored. For this reason, safety | security can be ensured with the expansion-contraction part 30 in the state folded. That is, the medical needle 1 according to the first embodiment is a compact medical needle while ensuring safety.

実施形態1に係る医療用針1においては、針カバー部材80には、上記した凸部86、溝部87及び穴部88が形成されている。すなわち、針カバー部材80とフック部40,50及び押さえ部材46との間に所定のクリアランスが設けられているため、針カバー部材80内に湾曲針10、第1及び第2伸縮部材32,36並びに板状部材60などを格納したときに、フック部40,50や押さえ部材46が針カバー部材80に引っかかってしまうのを防止することができる。
また、上述したように、凸部86を設けた部分以外の針カバー部材80の厚みを薄くできるため(図9(a)に示すように「T1<T2)」に設定されているため)、針カバー部材80も含めた医療用針1全体の小型化に寄与することができる。
In the medical needle 1 according to the first embodiment, the needle cover member 80 is formed with the convex portion 86, the groove portion 87, and the hole portion 88 described above. That is, since a predetermined clearance is provided between the needle cover member 80 and the hook portions 40, 50 and the pressing member 46, the curved needle 10, the first and second extendable members 32, 36 are provided in the needle cover member 80. In addition, when the plate-like member 60 and the like are stored, the hook portions 40 and 50 and the pressing member 46 can be prevented from being caught by the needle cover member 80.
Further, as described above, since the thickness of the needle cover member 80 other than the portion where the convex portion 86 is provided can be reduced (because it is set to “T1 <T2” as shown in FIG. 9A), This can contribute to the miniaturization of the entire medical needle 1 including the needle cover member 80.

[実施形態2]
図14は、実施形態2に係る医療用針2を説明するために示す図である。図14(a)は医療用針2の正面図であり、図14(b)は図14(a)のA−A断面図である。なお、図14においては、針カバー部材80の図示を省略している。また、図14において、図1〜図5と同一の部材については同一の符号を付し、詳細な説明は省略する。
[Embodiment 2]
FIG. 14 is a view for explaining the medical needle 2 according to the second embodiment. 14 (a) is a front view of the medical needle 2, and FIG. 14 (b) is a cross-sectional view taken along the line AA in FIG. 14 (a). In FIG. 14, the needle cover member 80 is not shown. Moreover, in FIG. 14, the same code | symbol is attached | subjected about the member same as FIGS. 1-5, and detailed description is abbreviate | omitted.

実施形態2に係る医療用針2は、基本的には実施形態1に係る医療用針1と良く似た構成を有するが、翼部の構成が実施形態1に係る医療用針1とは異なる。   The medical needle 2 according to the second embodiment basically has a configuration similar to that of the medical needle 1 according to the first embodiment, but the configuration of the wings is different from that of the medical needle 1 according to the first embodiment. .

すなわち、実施形態2に係る医療用針2においては、図14に示すように、翼部として、被係止部175,176(被係止部176のみ図14(a)及び図14(b)に図示。)を有する翼部170を備えている。   That is, in the medical needle 2 according to the second embodiment, as shown in FIG. 14, the locked portions 175 and 176 (only the locked portion 176 are shown in FIGS. 14A and 14B) as wing portions. And a wing portion 170 having a shape shown in FIG.

翼部170は、略矩形状の把持部172,174と、基部20と各把持部172.174との間に配置され、把持部172,174の厚みよりも薄く形成された薄肉部177,178と、各把持部172,174の端面の一部に配置された被係止部175,176とを有する。把持部172,174及び薄肉部177,178は、実施形態1で説明した把持部72,74及び薄肉部77,78と同様の構成であるため、詳細な説明は省略する。   The wing portion 170 is disposed between the grip portions 172 and 174 having a substantially rectangular shape, and between the base portion 20 and the grip portions 172.174, and the thin portions 177 and 178 formed thinner than the thickness of the grip portions 172 and 174. And locked portions 175 and 176 disposed on part of the end surfaces of the gripping portions 172 and 174. Since the gripping portions 172 and 174 and the thin portions 177 and 178 have the same configuration as the gripping portions 72 and 74 and the thin portions 77 and 78 described in the first embodiment, detailed description thereof is omitted.

被係止部175,176は、第1及び第2伸縮部材32,36が折り畳まれた状態のときにおける、フック部40,50の位置に対応する位置に配置されている。また、被係止部175,176は、第1及び第2伸縮部材32,36が折り畳まれた状態のときにフック部40,50が係止される機能と、翼部70(把持部172,174)を回動させたときにフック部40,50との係合状態が解除される機能とを有する。   The locked portions 175 and 176 are disposed at positions corresponding to the positions of the hook portions 40 and 50 when the first and second elastic members 32 and 36 are folded. The locked portions 175 and 176 have a function of locking the hook portions 40 and 50 when the first and second elastic members 32 and 36 are folded, and the wing portion 70 (the gripping portion 172 and 172). 174) has a function of releasing the engaged state with the hook portions 40 and 50 when the lever 174 is rotated.

このように、実施形態2に係る医療用針2は、実施形態1に係る医療用針1とは翼部の構成が異なるが、実施形態1に係る医療用針1の場合と同様に、上記したフック部40,50及び切り欠き部42,52を備えているため、第1及び第2伸縮部材32,36を伸長状態にして切り欠き部42,52にフック部40,50を係止することにより、第1及び第2伸縮部材32,36の伸長状態を維持し続けることが可能となる。
したがって、実施形態2に係る医療用針2は、患者の皮膚から湾曲針を抜いた後において、伸縮部(第1及び第2伸縮部材)を伸長状態のまま維持し続けることが可能な医療用針となる。
As described above, the medical needle 2 according to the second embodiment is different from the medical needle 1 according to the first embodiment in the configuration of the wings, but as in the case of the medical needle 1 according to the first embodiment, Since the hook portions 40 and 50 and the cutout portions 42 and 52 are provided, the first and second elastic members 32 and 36 are extended and the hook portions 40 and 50 are locked to the cutout portions 42 and 52. As a result, it is possible to continue to maintain the extended state of the first and second elastic members 32 and 36.
Therefore, the medical needle 2 according to the second embodiment is a medical needle that can continue to maintain the stretchable portions (first and second stretchable members) in the stretched state after removing the curved needle from the patient's skin. Become a needle.

実施形態2に係る医療用針2においては、上記した被係止部175,176を有する翼部170を備えているため、第1及び第2伸縮部材32,36が折り畳まれた状態を維持し続けることが可能となる。例えば、患者の皮膚に湾曲針10を穿刺した際に、仮に第1及び第2伸縮部材32,36に対して伸長しようとする力(伸縮部が開こうとする力)が発生した場合であっても、実施形態2に係る医療用針2によれば、被係止部175,176にフック部40,50を係止することによって、そのような伸長しようとする力を抑制することが可能となる。したがって、実施形態2に係る医療用針2は、患者の皮膚に安定して穿刺可能な医療用針となる。   Since the medical needle 2 according to the second embodiment includes the wing part 170 having the above-described locked parts 175 and 176, the first and second elastic members 32 and 36 are maintained in a folded state. It is possible to continue. For example, when the curved needle 10 is punctured into the patient's skin, there is a case in which a force to expand the first and second elastic members 32 and 36 (force to open the expansion / contraction part) is generated. However, according to the medical needle 2 according to the second embodiment, the hooking portions 40 and 50 are locked to the locked portions 175 and 176, so that it is possible to suppress such a force to extend. It becomes. Therefore, the medical needle 2 according to the second embodiment is a medical needle that can be stably punctured on the skin of the patient.

また、被係止部175,176が、翼部170を回動させることによってフック部40,50との係合状態を解除可能に構成されているため、「翼部170を摘まむ」という簡単なアクションで被係止部175,176とフック部40,50との係合状態を解除することが可能となる。   In addition, since the locked portions 175 and 176 are configured to be able to release the engaged state with the hook portions 40 and 50 by rotating the wing portion 170, it is easy to “pick the wing portion 170”. It is possible to release the engaged state between the locked portions 175 and 176 and the hook portions 40 and 50 with a simple action.

実施形態2に係る医療用針2は、翼部の構成が異なる点以外では、実施形態1に係る医療用針1と同様の構成を有するため、実施形態1に係る医療用針1が有する効果のうち該当する効果をそのまま有する。   The medical needle 2 according to the second embodiment has the same configuration as that of the medical needle 1 according to the first embodiment except that the configuration of the wings is different. Therefore, the effect of the medical needle 1 according to the first embodiment is provided. Of the relevant effects.

以上、本発明の医療用針を上記の各実施形態に基づいて説明したが、本発明は上記の各実施形態に限定されるものではなく、その要旨を逸脱しない範囲において種々の態様において実施することが可能であり、例えば次のような変形も可能である。   As mentioned above, although the medical needle of this invention was demonstrated based on said each embodiment, this invention is not limited to each said embodiment, In the range which does not deviate from the summary, it implements in a various aspect. For example, the following modifications are possible.

(1)上記各実施形態においては、ツメ状の押さえ部材46,56が、伸縮部30を伸長させたときにツメの先端が板状部材60側に向くように構成されている場合を例示して説明したが、本発明はこれに限定されるものではなく、伸縮部30を伸長させたときにツメの先端が基部20側に向くように構成されていてもよい。また、上記各実施形態においては、押さえ部材として、他方端48が切り欠き部42の第2開口端44に接続されていない、いわゆるツメ状の押さえ部材を例示して説明したが、本発明はこれに限定されるものではなく、押さえ部材の両端が切り欠き部の第1又は第2開口端近傍位置に接続された構成からなる押さえ部材であってもよい。 (1) In each of the above embodiments, the case where the claw-shaped pressing members 46 and 56 are configured such that the tips of the claw are directed toward the plate-shaped member 60 when the telescopic portion 30 is extended is illustrated. However, the present invention is not limited to this, and it may be configured such that the tip of the claw is directed toward the base 20 when the stretchable portion 30 is extended. In each of the above embodiments, as the pressing member, a so-called claw-shaped pressing member in which the other end 48 is not connected to the second opening end 44 of the notch 42 has been described as an example. It is not limited to this, The pressing member which consists of a structure where the both ends of the pressing member were connected to the 1st or 2nd opening end vicinity position of a notch part may be sufficient.

(2)上記各実施形態においては、切り欠き部42,52の切り欠き形状が、図1及び図8(b)から分かるように、略コの字形状である場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、U字状や台形状など、フック部が係止可能な形状であれば、どのような切り欠き形状であってもよい。また、フック部の形状についても、切り欠き部の切り欠き形状に応じて適宜変更することが可能である。 (2) In each of the above-described embodiments, the case where the notch shapes of the notch portions 42 and 52 are substantially U-shaped as illustrated in FIG. 1 and FIG. However, the present invention is not limited to this. For example, any cutout shape may be used as long as the hook portion can be locked, such as a U shape or a trapezoidal shape. Also, the shape of the hook portion can be appropriately changed according to the notch shape of the notch portion.

(3)上記各実施形態においては、第1伸縮部材32におけるy方向手前側の面に切り欠き部42及び押さえ部材46が配置され、第2伸縮部材36におけるy方向手前側の面にフック部40が配置され、第1伸縮部材32におけるy方向奥側の面にフック部50が配置され、第2伸縮部材36におけるy方向奥側の面に切り欠き部52及び押さえ部材56が配置された場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、第1伸縮部材32におけるy方向手前側の面及び奥側の面の両方に切り欠き部及び押さえ部材が配置され、第2伸縮部材36におけるy方向手前側の面及び奥側の面の両方にフック部が配置されていてもよい。 (3) In each of the above embodiments, the notch portion 42 and the pressing member 46 are disposed on the front surface in the y direction of the first elastic member 32, and the hook portion is disposed on the front surface of the second elastic member 36 in the y direction. 40 is disposed, the hook portion 50 is disposed on the back surface of the first elastic member 32 in the y direction, and the notch portion 52 and the pressing member 56 are disposed on the back surface of the second elastic member 36 in the y direction. Although the case has been described by way of example, the present invention is not limited to this. For example, the notch portion and the pressing member are arranged on both the front surface and the back surface in the y direction of the first elastic member 32, and the front surface and the back surface of the second elastic member 36 on the front surface in the y direction. The hook part may be arrange | positioned at both.

(4)上記各実施形態においては、第1及び第2伸縮部材32,36における屈曲部34,38よりも板状部材60に近い位置に、フック部40,50、切り欠き部42,52及び押さえ部材46,56が配置されている場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、第1及び第2伸縮部材32,36における屈曲部34,38近傍位置又は屈曲部34,38よりも基部20に近い位置に、フック部、切り欠き部及び押さえ部材がそれぞれ配置されていてもよい。 (4) In each of the above embodiments, the hook portions 40, 50, the cutout portions 42, 52, and the hook portions 40, 50 are located closer to the plate member 60 than the bent portions 34, 38 in the first and second elastic members 32, 36. Although the case where the pressing members 46 and 56 are disposed has been described as an example, the present invention is not limited to this. For example, the hook part, the notch part, and the pressing member are arranged at positions near the bent parts 34, 38 in the first and second elastic members 32, 36 or closer to the base part 20 than the bent parts 34, 38, respectively. Also good.

(5)上記各実施形態においては、第1及び第2伸縮部材32,36におけるy方向手前側の面及び奥側の面の両方に、フック部、切り欠き部及び押さえ部材が1組ずつ配置されている場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、第1及び第2伸縮部材32,36におけるy方向手前側の面及び奥側の面のいずれか一方にのみ、フック部、切り欠き部及び押さえ部材が1組配置されていてもよいし、第1及び第2伸縮部材32,36におけるy方向手前側の面及び奥側の面のいずれか一方にのみ、フック部、切り欠き部及び押さえ部材が複数組配置されていてもよいし、第1及び第2伸縮部材32,36におけるy方向手前側の面及び奥側の面の両方に、フック部、切り欠き部及び押さえ部材が複数組配置されていてもよい。 (5) In each of the above-described embodiments, one set of hook portion, notch portion, and pressing member is disposed on both the front and back surfaces in the y direction of the first and second elastic members 32, 36. However, the present invention is not limited to this. For example, one set of the hook portion, the notch portion, and the pressing member may be disposed on only one of the front surface and the rear surface in the first and second elastic members 32, 36. In addition, a plurality of sets of hook portions, notch portions, and pressing members may be arranged on only one of the front surface and the back surface in the y direction of the first and second elastic members 32, 36, A plurality of sets of hook portions, notch portions, and pressing members may be disposed on both the front surface and the back surface in the y direction of the first and second elastic members 32 and 36.

(6)上記各実施形態においては、針カバー部材とフック部40,50及び押さえ部材46との間に所定のクリアランスを設けるために、凸部86、溝部87及び穴部88が設けられた針カバー部材80を例示して説明したが、本発明はこれに限定されるものではない。針カバー部材とフック部40,50及び押さえ部材46との間に所定のクリアランスを設けることが可能であれば、他の形状・構成からなる針カバー部材を用いてもよい。また、凸部86、溝部87及び穴部88についても、上記した形状に限定されるものではない。 (6) In each of the embodiments described above, a needle having a convex portion 86, a groove portion 87, and a hole portion 88 in order to provide a predetermined clearance between the needle cover member and the hook portions 40, 50 and the pressing member 46. Although the cover member 80 has been exemplified and described, the present invention is not limited to this. As long as a predetermined clearance can be provided between the needle cover member and the hook portions 40 and 50 and the pressing member 46, a needle cover member having another shape and configuration may be used. Further, the convex portions 86, the groove portions 87, and the hole portions 88 are not limited to the shapes described above.

(7)上記実施形態2においては、図14から分かるように、把持部172,174の端面の一部に被係止部175,176が設けられている場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、把持部172,174の端面全体に被係止部が設けられていてもよい。 (7) In the second embodiment, as can be seen from FIG. 14, the case where the locked portions 175 and 176 are provided on part of the end surfaces of the grip portions 172 and 174 has been described as an example. The invention is not limited to this. For example, the locked portion may be provided on the entire end surface of the grip portions 172 and 174.

(8)上記各実施形態においては、板状部材が略長方形状である場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、楕円形状や丸形状の板状部材であってもよいし、三角形状や正方形状の板状部材であってもよいし、5角形以上の多角形状の板状部材であってもよい。 (8) In each of the above embodiments, the case where the plate-like member is substantially rectangular has been described as an example, but the present invention is not limited to this. For example, an elliptical or round plate-shaped member may be used, a triangular or square plate-shaped member may be used, and a pentagonal or more polygonal plate-shaped member may be used.

(9)上記各実施形態においては、板状部材60に形成される通過部62が、スリット状(切れ込み状)のものである場合を例示して説明したが、本発明はこれに限定されるものではない。通過部としては、例えば、湾曲針10が通過する位置(板状部材の略中央部)に形成された穴(丸穴や角穴)であってもよい。 (9) In each of the above embodiments, the case where the passage portion 62 formed on the plate-like member 60 is slit-shaped (notched) has been described as an example, but the present invention is limited to this. It is not a thing. As a passage part, the hole (round hole or square hole) formed in the position (substantially center part of a plate-shaped member) where the curved needle 10 passes may be sufficient, for example.

(10)上記各実施形態においては、基部20、伸縮部30、板状部材60及び翼部70,170が一体成形されている場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、これら各部材を個別に作成した後、各部材を接合してもよい。 (10) In each of the above embodiments, the case where the base portion 20, the stretchable portion 30, the plate-like member 60, and the wing portions 70 and 170 are integrally formed has been described, but the present invention is limited to this. It is not a thing. For example, these members may be created individually and then joined.

(11)上記各実施形態においては、基部20、伸縮部30、板状部材60及び翼部70,170が同一のプラスチック材料(例えば、ポリエチレン、ポリプロピレンなど。)からなる場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、部材ごとで異なるプラスチック材料を用いてもよいし、プラスチック材料以外の材料でこれら部材を形成してもよい。 (11) In each of the above embodiments, the case where the base portion 20, the stretchable portion 30, the plate member 60, and the wing portions 70 and 170 are made of the same plastic material (for example, polyethylene, polypropylene, etc.) has been described as an example. However, the present invention is not limited to this. For example, different plastic materials may be used for each member, or these members may be formed of a material other than the plastic material.

(12)上記各実施形態においては、湾曲針10の湾曲部14が90度湾曲している場合を例示して説明したが、本発明はこれに限定されるものではない。90度未満又は90度を超える角度で湾曲した湾曲針を備える医療用針についても本発明を適用可能である。 (12) In each of the above embodiments, the case where the bending portion 14 of the bending needle 10 is bent 90 degrees has been described as an example, but the present invention is not limited to this. The present invention can also be applied to a medical needle including a curved needle that is curved at an angle of less than 90 degrees or greater than 90 degrees.

(13)上記各実施形態においては、翼部70,170が、基部20の側方に接続配置された一対の翼部材である場合を例示して説明したが、本発明はこれに限定されるものではなく、例えば、基部20の上方に1つの翼部材がz方向に沿って伸びるように配置されていてもよい。また、上記各実施形態においては、略矩形状の把持部72,74,172,174を有する翼部70,170を例示して説明したが、本発明はこれに限定されるものではなく、略矩形状とは異なる形状(例えば丸形状など)の把持部を有する翼部であってもよい。 (13) In each of the above embodiments, the case where the wing portions 70 and 170 are a pair of wing members connected to the side of the base portion 20 has been described as an example, but the present invention is limited to this. For example, one wing member may be arranged above the base 20 so as to extend along the z direction. In each of the above embodiments, the wing portions 70 and 170 having the substantially rectangular gripping portions 72, 74, 172, and 174 have been described as examples. However, the present invention is not limited to this, and the The wing | blade part which has a holding part of the shape (for example, round shape etc.) different from rectangular shape may be sufficient.

(14)上記各実施形態においては、伸縮部30を折り畳んだときに第1及び第2伸縮部材32,36の広がる方向と板状部材60の長辺方向とが同じx方向で揃えられ、翼部70,170の把持部72,74,172,174がx方向に伸びる場合を例示して説明したが、本発明はこれに限定されるものではない。例えば、第1及び第2伸縮部材の広がる方向と板状部材の長辺方向とが同じx方向で揃えられ、翼部の把持部がy方向に伸びるように構成されていてもよい。または、第1及び第2伸縮部材の広がる方向と板状部材の長辺方向とが同じy方向で揃えられ、翼部の把持部がy方向に伸びるように構成されていてもよい。
なお、後者の場合、すなわち、第1及び第2伸縮部材の広がる方向と、板状部材の長辺方向と、翼部の把持部が伸びる方向とが、基部20の長手方向であるy方向と同じ向きに揃えられているときには、医療用針全体のx方向の幅を比較的小さくすることができるため、例えば、医療用針を2つ以上並べて配置したいときに、各医療用針と繋がる各チューブの導出方向を一方向に揃えた状態で医療用針を配置することが可能となる。
(14) In each of the above embodiments, the direction in which the first and second elastic members 32 and 36 spread and the long side direction of the plate-like member 60 are aligned in the same x direction when the elastic part 30 is folded, and the blade Although the case where the grip portions 72, 74, 172, and 174 of the portions 70 and 170 extend in the x direction has been described as an example, the present invention is not limited to this. For example, the spreading direction of the first and second elastic members and the long side direction of the plate-like member may be aligned in the same x direction, and the grip portion of the wing portion may be configured to extend in the y direction. Alternatively, the extending direction of the first and second elastic members and the long side direction of the plate-like member may be aligned in the same y direction, and the grip portion of the wing portion may be configured to extend in the y direction.
In the latter case, that is, the direction in which the first and second expandable members spread, the long side direction of the plate-like member, and the direction in which the gripping portion of the wing portion extends is the y direction, which is the longitudinal direction of the base portion 20. When the medical needles are aligned in the same direction, the width of the entire medical needle in the x direction can be made relatively small. For example, when two or more medical needles are arranged side by side, The medical needle can be arranged in a state where the tube outlet direction is aligned in one direction.

(15)上記各実施形態においては、基部として、チューブ接続部22を有する基部20を例示して説明したが、本発明はこれに限定されるものではなく、例えば、チューブ接続部が省略された基部(チューブ接続部を有しない基部)を備えていてもよい。この場合は、例えば、湾曲針10の基端部12を基部から露出させ、基端部12とチューブとを直接接続すればよい。 (15) In each of the above-described embodiments, the base 20 having the tube connecting portion 22 is exemplified and described as the base, but the present invention is not limited to this, and for example, the tube connecting portion is omitted. You may provide the base (base which does not have a tube connection part). In this case, for example, the base end portion 12 of the curved needle 10 may be exposed from the base portion, and the base end portion 12 and the tube may be directly connected.

医療用針1の斜視図。1 is a perspective view of a medical needle 1. FIG. 図1とは異なる方向から見たときの医療用針1の斜視図。FIG. 3 is a perspective view of the medical needle 1 when viewed from a direction different from that in FIG. 1. 医療用針1の正面図。1 is a front view of a medical needle 1. FIG. 医療用針1の背面図。The rear view of the medical needle 1. FIG. 医療用針1の側面図。The side view of the medical needle 1. FIG. 第1及び第2伸縮部材32,36が伸縮する様子を説明するために示す図。The figure shown in order to demonstrate a mode that the 1st and 2nd expansion-contraction members 32 and 36 expand and contract. フック部40,50が切り欠き部42,52に係止される様子を説明するために示す図。The figure shown in order to demonstrate a mode that the hook parts 40 and 50 are latched by the notch parts 42 and 52. FIG. フック部40、切り欠き部42及び押さえ部材46を説明するために示す図。The figure shown in order to demonstrate the hook part 40, the notch part 42, and the pressing member 46. FIG. 針カバー部材80を説明するために示す図。The figure shown in order to demonstrate the needle cover member 80. FIG. 針カバー部材80を説明するために示す図。The figure shown in order to demonstrate the needle cover member 80. FIG. 医療用針1を説明するために示す図。The figure shown in order to demonstrate the medical needle 1. FIG. 医療用針1を説明するために示す図。The figure shown in order to demonstrate the medical needle 1. FIG. 医療用針1を説明するために示す図。The figure shown in order to demonstrate the medical needle 1. FIG. 実施形態2に係る医療用針2を説明するために示す図。The figure shown in order to demonstrate the medical needle 2 which concerns on Embodiment 2. FIG.

符号の説明Explanation of symbols

1,2 医療用針
10 湾曲針
12 湾曲針の基端部
14 湾曲部
16 湾曲針の先端部
20 基部
22 チューブ接続部
30 伸縮部
32 第1伸縮部材
34,38 屈曲部
36 第2伸縮部材
40,50 フック部
42,52 切り欠き部
43 第1開口端
44 第2開口端
45 第3開口端
46,56 押さえ部材
47 (押さえ部材の)一方端
48 (押さえ部材の)他方端
60 板状部材
62 通過部
70,170 翼部
72,74,172,174 把持部
77,78,177,178 薄肉部
80 針カバー部材
82 第1格納部
83 (第1格納部の)切り欠き
84 第2格納部
86 凸部
87 溝部
88 穴部
175,176 被係止部
AP アクセスポート
S 患者の皮膚
T1 凸部を設けた部分以外のz方向に沿った厚み
T2 凸部を設けた部分のz方向に沿った厚み
DESCRIPTION OF SYMBOLS 1, 2 Medical needle 10 Curved needle 12 Curved needle base end part 14 Curved part 16 Curved needle distal end part 20 Base part 22 Tube connecting part 30 Stretchable part 32 First stretchable member 34, 38 Bent part 36 Second stretchable member 40 , 50 Hook parts 42, 52 Notch part 43 First opening end 44 Second opening end 45 Third opening end 46, 56 Pressing member 47 (pressing member) one end 48 (pressing member) other end 60 Plate-like member 62 Passing part 70, 170 Wing part 72, 74, 172, 174 Grasping part 77, 78, 177, 178 Thin part 80 Needle cover member 82 First storing part 83 Notch 84 (first storing part) Second storing part 86 Convex part 87 Groove part 88 Hole part 175,176 Locked part AP Access port S Patient's skin T1 Thickness T2 along the z direction other than the part provided with the convex part Along the z direction of the part provided with the convex part Thickness

Claims (5)

所定角度に湾曲した湾曲部(14)を有する湾曲針(10)と、
前記湾曲針(10)の一部が植設された基部(20)と、
前記基部(20)に設けられ、前記湾曲部(14)から前記湾曲針の先端部(16)に沿った第1(z)方向に伸縮可能に構成された伸縮部(30)と、
前記伸縮部(30)における前記基部(20)とは反対側に接続配置され、前記湾曲針(10)を通過させる通過部(62)を有する板状部材(60)とを備え、
前記伸縮部(30)は、
前記伸縮部(30)を最も伸ばしたときの前記第1(z)方向に沿った長さが、前記湾曲針の先端部(16)から前記湾曲部(14)までの長さ以上となるように構成された伸縮部材であり、さらに、
パンタグラフ状に伸縮可能であって、前記湾曲針(10)を間にして対向配置された第1伸縮部材(32)及び第2伸縮部材(36)と、
前記第1及び第2伸縮部材(32,36)のうち一方側に配置されたフック部(40)と、
前記第1及び第2伸縮部材(32,36)のうち他方側に配置され、前記第1及び第2伸縮部材(32,36)が伸長した状態のときに前記フック部(40)が係止される切り欠き部(42)と、
前記切り欠き部(42)の近傍に配置され、前記フック部(40)が前記切り欠き部(42)に係止されるときに前記フック部(40)を前記切り欠き部(42)に向けて押さえる機能を有する押さえ部材(46)とを有することを特徴とする医療用針(1)。
A curved needle (10) having a curved portion (14) curved at a predetermined angle;
A base (20) in which a part of the curved needle (10) is implanted;
An extendable portion (30) provided on the base portion (20) and configured to be extendable in the first (z) direction along the distal end portion (16) of the curved needle from the curved portion (14);
A plate-like member (60) having a passage portion (62) that is connected and arranged on the opposite side to the base portion (20) in the stretchable portion (30) and allows the curved needle (10) to pass therethrough,
The stretchable part (30)
The length along the first (z) direction when the stretchable part (30) is most extended is equal to or longer than the length from the distal end part (16) of the curved needle to the curved part (14). It is an elastic member configured to,
A first expandable member (32) and a second expandable member (36) that are expandable and contractable in a pantograph shape and are opposed to each other with the curved needle (10) interposed therebetween;
A hook portion (40) disposed on one side of the first and second elastic members (32, 36);
Arranged on the other side of the first and second elastic members (32, 36), the hook portion (40) is locked when the first and second elastic members (32, 36) are extended. A notch (42) to be made;
It is arranged in the vicinity of the notch (42), and when the hook (40) is locked to the notch (42), the hook (40) is directed to the notch (42). A medical needle (1) having a pressing member (46) having a function of pressing and holding.
請求項1に記載の医療用針において、
前記切り欠き部(42)は、前記基部(20)側に位置する第1開口端(43)と、前記板状部材(60)側に位置する第2開口端(44)と、前記第1開口端(43)及び前記第2開口端(44)を繋ぐ第3開口端(45)とを有し、
前記押さえ部材(46)は、一方端(47)が前記第1開口端(43)近傍位置に接続され、他方端(48)が前記第1開口端(43)から前記第2開口端(44)方向に向けて伸びるツメ状の押さえ部材であって、前記他方端(48)と前記第2開口端(44)との間に所定の空間(P)が形成されるように構成されていることを特徴とする医療用針(1)。
The medical needle according to claim 1, wherein
The notch (42) includes a first opening end (43) located on the base (20) side, a second opening end (44) located on the plate-like member (60) side, and the first An open end (43) and a third open end (45) connecting the second open end (44);
The pressing member (46) has one end (47) connected to a position near the first opening end (43) and the other end (48) from the first opening end (43) to the second opening end (44). ) Is a claw-shaped pressing member extending in the direction, and is configured such that a predetermined space (P) is formed between the other end (48) and the second opening end (44). A medical needle (1) characterized by the above.
請求項1又は2に記載の医療用針において、
前記湾曲針における基端部(12)側の部分から前記湾曲部(14)に沿った方向と同一方向を第2(y)方向としたとき、
前記フック部(40,50)、前記切り欠き部(42,52)及び前記押さえ部材(46,56)のそれぞれは、前記第1及び第2伸縮部材(32,36)における前記第2(y)方向手前側の面及び前記第2(y)方向奥側の面の両面に配置されていることを特徴とする医療用針(1)。
The medical needle according to claim 1 or 2,
When the same direction as the direction along the curved portion (14) from the proximal end (12) side portion of the curved needle is the second (y) direction,
The hook part (40, 50), the notch part (42, 52), and the pressing member (46, 56) are respectively connected to the second (y) in the first and second elastic members (32, 36). ) The medical needle (1), which is disposed on both the front surface and the back surface in the second (y) direction.
請求項1〜3のいずれかに記載の医療用針において、
前記基部(20)に設けられ、前記基部(20)を中心軸として回動可能に構成された翼部(170)をさらに備え、
前記翼部(170)は、前記第1及び第2伸縮部材(32,36)が折り畳まれた状態のときに前記フック部(40,50)が係止される被係止部(175,176)を有し、
前記被係止部(175,176)は、
前記翼部(170)のうち、前記第1及び第2伸縮部材(32,36)が折り畳まれた状態のときにおける、前記フック部(40,50)の位置に対応する位置に配置され、かつ、
前記翼部(170)を回動させることにより前記フック部(40,50)との係合状態を解除可能に構成されていることを特徴とする医療用針(2)。
The medical needle according to any one of claims 1 to 3,
A wing (170) provided on the base (20) and configured to be rotatable about the base (20) as a central axis;
The wing portion (170) is a locked portion (175, 176) to which the hook portion (40, 50) is locked when the first and second elastic members (32, 36) are folded. )
The locked portion (175, 176) is
Among the wing parts (170), the first and second elastic members (32, 36) are arranged at positions corresponding to the positions of the hook parts (40, 50) when folded. ,
The medical needle (2) configured to be able to release the engaged state with the hook portion (40, 50) by rotating the wing portion (170).
請求項1〜3のいずれかに記載の医療用針において、
前記基部(20)に設けられた翼部(70)と、
前記伸縮部(30)が折り畳まれた状態で前記翼部(70)及び前記板状部材(60)を押さえるとともに、前記湾曲針(10)を覆う針カバー部材(80)とをさらに備え、
前記針カバー部材(80)には、前記第1及び第2伸縮部材(32,36)が折り畳まれた状態のときにおける、前記フック部(40)及び前記押さえ部材(46)のうち少なくとも一方の位置に対応する位置に、所定のクリアランスが設けられていることを特徴とする医療用針(1)。
The medical needle according to any one of claims 1 to 3,
A wing (70) provided in the base (20);
A needle cover member (80) covering the curved needle (10) while pressing the wing portion (70) and the plate member (60) in a state where the stretchable portion (30) is folded;
The needle cover member (80) has at least one of the hook portion (40) and the pressing member (46) when the first and second elastic members (32, 36) are folded. A medical needle (1), wherein a predetermined clearance is provided at a position corresponding to the position.
JP2008304841A 2008-11-28 2008-11-28 Medical needle Expired - Fee Related JP5140564B2 (en)

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