JPS62227316A - Blood sampling needle - Google Patents

Blood sampling needle

Info

Publication number
JPS62227316A
JPS62227316A JP61071280A JP7128086A JPS62227316A JP S62227316 A JPS62227316 A JP S62227316A JP 61071280 A JP61071280 A JP 61071280A JP 7128086 A JP7128086 A JP 7128086A JP S62227316 A JPS62227316 A JP S62227316A
Authority
JP
Japan
Prior art keywords
plug
blood collection
blood
puncture
needle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP61071280A
Other languages
Japanese (ja)
Other versions
JPH0256095B2 (en
Inventor
赤池 義明
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Terumo Corp
Original Assignee
Terumo Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Terumo Corp filed Critical Terumo Corp
Priority to JP61071280A priority Critical patent/JPS62227316A/en
Publication of JPS62227316A publication Critical patent/JPS62227316A/en
Publication of JPH0256095B2 publication Critical patent/JPH0256095B2/ja
Granted legal-status Critical Current

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  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は1人体の血液採取等に用いられる採血針に関す
る。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a blood collection needle used for collecting blood from a human body.

[従来の技術] 従来1例えば臨床検査、生化学検査に際に行なう血液採
取には、第7図ないし第8図に示す減圧採血共が用いら
れる。第7図は従来の減圧採血共の使用前の状態を示す
断面図、第8図は同使用時の状態を示す断面図である。
[Prior Art] Conventionally 1, for example, a vacuum blood sampling system shown in FIGS. 7 and 8 is used to collect blood for clinical tests and biochemical tests. FIG. 7 is a cross-sectional view showing a conventional vacuum blood sampling device before use, and FIG. 8 is a cross-sectional view showing the same condition during use.

この減圧採血具10は、第7図に示すように減圧採血管
11と採血針12とを備えてなる採血ホルダー13から
構成される。減圧採血管11は、ガラス材、透明樹脂材
等で形成される管体14のL方間口部に栓体15を取付
けてなり、該管体14の内部を減圧状態としてなる。す
なわち、栓体15は、管体14の内部の減圧状態を維持
し、また後述するように中空針を穿刺可能とすることが
必要とされる。また、栓体15は、穿刺された中空針を
扶去した後において、針孔を閉塞して液密状態を維持す
ることが要求される。この点で従来栓体15には、ゴム
材等を用いることが好適とされていた。
As shown in FIG. 7, this reduced pressure blood collection device 10 is composed of a blood collection holder 13 comprising a reduced pressure blood collection tube 11 and a blood collection needle 12. The reduced pressure blood collection tube 11 has a stopper 15 attached to the L-direction opening of a tube body 14 made of a glass material, a transparent resin material, etc., and the inside of the tube body 14 is brought into a reduced pressure state. That is, the plug body 15 is required to maintain a reduced pressure state inside the tube body 14 and to be able to be punctured with a hollow needle as described later. Further, the plug body 15 is required to close the needle hole and maintain a liquid-tight state after removing the punctured hollow needle. In this respect, it has conventionally been preferable to use a rubber material or the like for the plug body 15.

一方、採血ホルダー13は、下端が開放した筒状のホル
ダ一本体17を有し、その上方先端部に採血針12を取
着してなる。採血針12は、中空の針本体18の一端側
に血管穿刺部19を備えてなり、他端側には上記減圧管
11の栓体15に穿刺される栓体穿刺部20が備えられ
る。針本体18の中間部分にはハブ21が備えられ、該
ハブ21には雄ネジ部22が形成される。採血針12の
ホルダ一本体17に対する取着は、ホルダ一本体17の
上方先端部に形成される酸ネジ部23に上記雄ネジ部2
2を螺合することにより行なわれる。さらにホルダ一本
体17に取着される採血針12の栓体穿刺部20は、鞘
状の被覆カバー24にて被覆される。すなわち、この被
覆カバー24は、軟質ゴム材等の拡縮自在な材質で形成
され、第7図に示す未使用状態で栓体穿刺部20を被覆
+i[能としている。
On the other hand, the blood collection holder 13 has a cylindrical holder main body 17 with an open lower end, and a blood collection needle 12 is attached to the upper tip thereof. The blood collection needle 12 includes a blood vessel puncture section 19 at one end of a hollow needle body 18, and a plug puncture section 20 that is inserted into the plug 15 of the decompression tube 11 at the other end. A hub 21 is provided at the intermediate portion of the needle body 18, and the hub 21 is formed with a male threaded portion 22. The blood collection needle 12 is attached to the holder body 17 by attaching the male threaded portion 2 to the acid threaded portion 23 formed at the upper tip of the holder body 17.
This is done by screwing the two together. Furthermore, the plug piercing portion 20 of the blood collection needle 12 attached to the holder main body 17 is covered with a sheath-like covering cover 24 . That is, the covering cover 24 is made of a material that can be expanded and contracted, such as a soft rubber material, and can cover the plug puncture section 20 in an unused state as shown in FIG.

このような構成からなる減圧採血具lOを用いて血液採
取を行なう場合、先ず、採血ホルダー13に備えられる
採血針12の血管穿刺部19を、人体等の血管に穿刺す
る0次に減圧管11を第7図の矢印Aに示すようにホル
ダ一本体17内に挿入する。この時、採血針12の栓体
穿刺部20は、第8図に示すように被覆カバー24.栓
体15を穿刺し、減圧状態とされる管体14の内部に穿
通されることとなる。この際、被清カバー24は、栓体
15とホルダ一本体17との間で蛇腹状に折り畳まれる
こととなる。このようにし、中空の針本体18の他端側
か第8図に示すように管体14の内部に穿通されると、
該管体14の内部の減圧状態により、中空の針本体18
の血管穿刺部19から栓体穿刺部20側に血液を導入す
ることが回部となる。これにより、管体14の内部に血
液を流入し、採血が行なわれることとなる。
When blood is collected using the vacuum blood sampling device IO having such a configuration, first, the blood vessel puncture portion 19 of the blood sampling needle 12 provided in the blood sampling holder 13 is inserted into the blood vessel of the human body, etc. Next, the vacuum tube 11 is inserted into the holder main body 17 as shown by arrow A in FIG. At this time, the plug puncture section 20 of the blood collection needle 12 is inserted into the covering cover 24 as shown in FIG. The plug body 15 is punctured, and the inside of the tube body 14, which is in a reduced pressure state, is penetrated. At this time, the cover 24 to be cleaned is folded into a bellows shape between the plug body 15 and the holder main body 17. In this way, when the other end of the hollow needle body 18 is penetrated into the inside of the tube body 14 as shown in FIG.
Due to the reduced pressure inside the tube body 14, the hollow needle body 18
Introducing blood from the blood vessel puncture part 19 to the plug puncture part 20 side is the turning part. As a result, blood flows into the tube body 14 and blood is collected.

管体14の内部に所定量の血液が採取されると、減圧採
血管11が採血ホルダー13から取外される。取外され
た状態においてそれまで折り畳まれていた被覆カバー2
4は第7図に示すように元の状態に復元されることとな
る。さらに多量の採血を行なう場合、第7図に示すよう
に未使用の減圧採血管11を矢印Aに示すようにホルダ
一本体17内に押入すればよい、採血が完了されると血
管穿刺部19は人体から抜去される。
Once a predetermined amount of blood has been collected inside the tubular body 14, the reduced pressure blood collection tube 11 is removed from the blood collection holder 13. Covering cover 2 that was previously folded in the removed state
4 will be restored to its original state as shown in FIG. If a larger amount of blood is to be collected, as shown in FIG. is removed from the human body.

[発明が解決しようとする問題点] しかしながら、上記従来の減圧採血具10にあっては、
採血時において被覆カバー24が第8図に示すように圧
縮されることとなる。圧縮される被覆カバー24は、一
般にゴム材等の弾性材で形成されるため、減圧採血管1
1に対して矢示B方向の反力を作用することとなる。こ
のため、従来、この種の減圧採血具lOにおいては、採
血中に栓体15から栓体穿刺部20が抜け、採血ホルタ
−13に対して減圧管11が離脱する不具合(いわゆる
キックバック)を生ずることがあった。
[Problems to be Solved by the Invention] However, in the conventional reduced pressure blood sampling device 10,
During blood collection, the covering cover 24 is compressed as shown in FIG. 8. The cover 24 to be compressed is generally made of an elastic material such as rubber, so the reduced pressure blood collection tube 1
1, a reaction force in the direction of arrow B is applied. For this reason, conventionally, in this type of vacuum blood sampling device 10, the problem of the plug puncture part 20 coming off from the plug 15 during blood collection and the vacuum tube 11 coming off from the blood collection holter 13 (so-called kickback) has been avoided. Sometimes it happened.

この種の不具合を防止するため、従来、被覆カバー24
の弾性力を低下させたり、また栓体15に塗布される栓
体穿刺部20の潤滑用の潤滑剤の性能を低下するように
していた。
In order to prevent this kind of malfunction, conventionally, the covering cover 24
In addition, the performance of the lubricant applied to the plug body 15 for lubricating the plug puncture portion 20 is reduced.

しかしながら、このような方法を用いる場合、減圧採血
管11を採血ホルダー13から取外した際に、被Yaカ
バー24が元の状態になかなか復元されなかったり、ま
た、栓体穿刺部20の栓体15に対する穿刺抵抗が増大
する等の不具合があった。
However, when such a method is used, when the vacuum blood collection tube 11 is removed from the blood collection holder 13, the Ya cover 24 may not be easily restored to its original state, or the plug 15 of the plug puncture section 20 may There were problems such as increased puncture resistance.

[発明の目的] 本発明は、採血中において圧縮される被覆カバーの反力
により、針本体の栓体穿刺部が減圧採血管の栓体から抜
けることを防止し、円滑かつ安全な採血を行なうことを
目的としている。
[Objective of the Invention] The present invention prevents the plug puncture portion of the needle body from coming off the plug of the vacuum blood collection tube due to the reaction force of the cover that is compressed during blood collection, thereby allowing smooth and safe blood collection. The purpose is to

[問題点を解決するための手段] l二記目的を達成するために、本発明は、中空状の針本
体の中間部分にハブを有し、一端側に血管穿刺部を備え
、他端側に減圧採血管の栓体に穿刺される栓体穿刺部を
備えるとともに、該栓体穿刺部を、該ハブから伸びる鞘
状の拡縮自在な弾性を有する被覆カバーにて被覆してな
る採血針において、」−記栓体穿刺部は、その周上に栓
体に穿刺した状態で該栓体と係合する凹凸部を備えてな
り該栓体と該凹凸部の摩擦抵抗が、該栓体への該栓体穿
刺部の穿刺に伴ない圧縮される該被覆カバーの反発力以
上であることとしでいる。
[Means for Solving the Problems] In order to achieve the second object, the present invention has a hub in the middle part of a hollow needle body, a blood vessel puncture part on one end, and a needle on the other end. A blood collection needle comprising a stopper puncture part that is inserted into a stopper of a vacuum blood collection tube, and the stopper puncture part is covered with a sheath-shaped elastic cover extending from the hub and having expandable and contractible elasticity. , ” - The stopper puncturing part is provided with an uneven part on its circumference that engages with the stopper when the stopper is punctured, and the frictional resistance between the stopper and the uneven part is applied to the stopper. The repulsion force of the cover, which is compressed due to the puncture of the plug puncture portion, shall be greater than or equal to the repulsive force of the cover.

また1本発明における凹凸部は、栓体穿刺部の周上をブ
ラスト加工して形成されるようにしている。
Further, the uneven portion in the present invention is formed by blasting the circumference of the punctured portion of the plug body.

[発明の詳細な説明] 以下、本発明の実施例を図面を参照して説明する。[Detailed description of the invention] Embodiments of the present invention will be described below with reference to the drawings.

第1図は本発明の一実施例に係る採血針を示す正面図、
第1図(A)は第1図のA部を拡大して示す図、第1図
(B)は第1図(A)のB部の表面凹凸状Fgを示す図
、第2図は採血針を用いて形成される減圧採血具の使用
前の状態を示す断面図、第3図は同使用時の状態を示す
断面図、第4図は第2図に示す減圧採血具を用いて人体
の腕から採血する状態を示す斜視図である。第5図は表
面形状測定機で実施例1に係る凹凸部を測定した状態を
示す線図、第6図は表面形状測定機で比較例に係る凹凸
部を測定した状態を示す線図である。
FIG. 1 is a front view showing a blood collection needle according to an embodiment of the present invention;
Figure 1 (A) is an enlarged view of part A in Figure 1, Figure 1 (B) is a diagram showing the surface unevenness Fg of part B in Figure 1 (A), and Figure 2 is blood sampling. A cross-sectional view showing the state before use of the vacuum blood sampling device formed using a needle, FIG. 3 is a cross-sectional view showing the state during use, and FIG. FIG. 2 is a perspective view showing a state in which blood is collected from the arm of a patient. FIG. 5 is a diagram showing the state in which the uneven portion according to Example 1 was measured with a surface shape measuring device, and FIG. 6 is a diagram showing the state in which the uneven portion according to the comparative example was measured with the surface shape measuring device. .

第1図に示す採血針30を用いて形成される減圧採血3
t31は、第2図に示すように減圧採血管32と採血ホ
ルダー33から構成される。減圧採血管32は、透明材
で形成される管体34の上方間「1部に栓体35を取付
けてなり、該管体34の内部を減圧状!6としている。
Vacuum blood collection 3 formed using the blood collection needle 30 shown in FIG.
t31 is composed of a reduced pressure blood collection tube 32 and a blood collection holder 33, as shown in FIG. The reduced pressure blood collection tube 32 is constructed by attaching a stopper 35 to the upper part of a tube body 34 made of a transparent material, so that the inside of the tube body 34 is in a reduced pressure state!6.

管体34の材質としては、ガラス材の他にポリ塩化ビニ
ル、ポリエチレン等の樹脂材が使用可能である。一方、
栓体35は、管体34の内部の減圧状!懲を維持し、ま
た後述するように中空針を穿刺可能とすることが必要と
される。また栓体35は、穿刺された中空側を抜去した
後において、針孔を閉塞して液密状態を維持することが
要求される。このため、該栓体35は、ゴム材等を用い
て形成するようにしている。
As the material for the tube body 34, resin materials such as polyvinyl chloride and polyethylene can be used in addition to glass materials. on the other hand,
The plug body 35 is in the form of a reduced pressure inside the tube body 34! It is necessary to maintain the puncture distance and to be able to insert a hollow needle as described below. Further, the plug body 35 is required to close the needle hole and maintain a liquid-tight state after the punctured hollow side is removed. For this reason, the plug body 35 is made of a rubber material or the like.

採血ホルダー33は、下端が開放した筒状のホルダ一本
体37を有し、該ホルダ一本体37の1−力先端部には
、第1図に示す採血針30が取着される。採血針30は
、中空の針本体38の一端側に面?iτ穿刺部39を備
えてなり、他端側には上記減圧採血管32の栓体35に
穿刺される栓体穿刺部40が備えられる。針本体38の
中間部分にはハブ41が備えられ、該ハブ41には雄ネ
ジ部42が形成される。採血針30のホルダ一本体37
に対する取着は、ホルダ一本体37の上方先端部に形成
される酸ネジ部43に上記雄ネジ部42を螺合すること
により行なわれる。さらにホルダ一本体37に取着され
る採血針30の栓体穿刺部40には、鞘状の被覆カバー
44が被覆される。この被覆カバー44は、拡縮自在な
弾性材で形成される。
The blood collection holder 33 has a cylindrical holder body 37 with an open lower end, and a blood collection needle 30 shown in FIG. 1 is attached to the tip end of the holder body 37. The blood collection needle 30 has a hollow needle body 38 with a surface on one end side. An iτ puncture section 39 is provided, and a stopper puncture section 40 that is inserted into the stopper 35 of the reduced pressure blood collection tube 32 is provided at the other end. A hub 41 is provided at the intermediate portion of the needle body 38, and a male threaded portion 42 is formed on the hub 41. Holder body 37 of blood sampling needle 30
Attachment to the holder body 37 is carried out by screwing the male threaded portion 42 into a threaded threaded portion 43 formed at the upper tip of the holder main body 37. Furthermore, a sheath-like cover 44 covers the plug puncture portion 40 of the blood collection needle 30 attached to the holder main body 37 . This cover 44 is made of an elastic material that can be expanded and contracted.

このようにして、被覆カバー44に被覆される栓体穿刺
部40の先端部周上には、第1図(A)に示すように表
面に凹凸部45が形成される。この凹凸部45は、金属
性の栓体穿刺部4oの外周表面にブラスト加工を施すこ
とにより形成される。ブラスト加工の条件としては、剛
体粒子(アルミナ、炭化ケイ素、ケイ砂、シリコンカー
バイト等)を圧縮空気と共に栓体穿刺部40の外周表面
上に噴射し、衝突させることが最適とされる。
In this way, an uneven portion 45 is formed on the circumference of the distal end portion of the plug puncture portion 40 covered by the covering cover 44, as shown in FIG. 1(A). The uneven portion 45 is formed by blasting the outer peripheral surface of the metallic plug puncture portion 4o. The optimum conditions for blasting are to inject rigid particles (alumina, silicon carbide, silica sand, silicon carbide, etc.) together with compressed air onto the outer circumferential surface of the plug puncture section 40 and cause them to collide.

圧縮空気の圧力は2〜10Kg/cm’、好しくは4〜
8Kg/ cゴが望ましい。
The pressure of compressed air is 2 to 10 Kg/cm', preferably 4 to 10 kg/cm'.
8Kg/c is desirable.

このようにして、凹凸部45は、栓体穿刺部40の外周
表面にブラスト加工を施すことにより形成されるが、そ
の他にも栓体穿刺部40の外周表面に次のような処理を
施すことによっても形成可能とされる。その他の加工処
理方法としては、例えばイ)薬品処理;酸(硝酸、硫酸
、fi1酸)や金属塩の水溶液(FeC1+ 、 Cu
C1r 、 CrC:l:+等)等を用いての処理1口
)放゛屯加工、ハ)電解加重、二)研削等がある。
In this way, the uneven portion 45 is formed by blasting the outer circumferential surface of the plug puncture section 40, but the following treatments may also be performed on the outer circumferential surface of the plug puncture section 40. It can also be formed by Other processing methods include, for example, a) chemical treatment; acids (nitric acid, sulfuric acid, fi1 acid) and aqueous solutions of metal salts (FeC1+, Cu
Treatments using C1r, CrC:l:+, etc.) include 1) radiation processing, 3) electrolytic loading, and 2) grinding.

このように形成された凹凸部の大きさは、第1図(B)
で示すTが0.2〜3 p−m程度とされ、好ましくは
0.5〜2ル膳であることが望ましい、また、これらの
凹凸部が表面方向において30pm以下毎に、好ましく
は2部用国以トイηに、さらに好ましくは10ILm以
下毎にあるのが望ましい。
The size of the uneven portion formed in this way is shown in Fig. 1(B).
It is desirable that T shown by 0.2 to 3 pm, preferably 0.5 to 2 pm, and preferably 2 parts for every 30 pm or less of these uneven parts in the surface direction. It is desirable that there be one for every 10 ILm or less, more preferably every 10 ILm or less.

このような構成からなる減圧採血A31を用いて血液採
取を行なう場合、先ず第4図に示すように人体の腕46
に採血ホルタ−33に備えられる抹血側30の血管穿刺
部39を穿刺する。次に減圧採血側32を第2図および
第4図に示すように矢印り方向でホルダ一本体37内に
押入する。この状5Ej、で先ず、栓体穿刺部40が栓
体35に穿刺され、表面に形成される凹凸部45が栓体
35に摺接する状態となる。さらに栓体35に穿刺され
た栓体穿刺部40は、減圧採血管32を矢印り方向に、
押入することで減圧状態とされる管体34の内部に穿通
されることとなる。このようにして、第3図に示すよう
に、中空の針本体38の他端部が管体34の内部に穿通
されると、Irf体34の内部の減圧状態により、中空
の針本体38の血Y穿刺部39から栓体穿刺部40側に
血液を導入することが可能となる。これにより、管体3
4の内部tこ血液を流入し、採血が行なわれることとな
る、 J’: :fn中において、被YOカバー44は第3図
に示tように蛇腹状に折り畳まれ、圧縮されることとな
る。このため、該圧縮される被覆カバー44は、押入さ
れる圧縮管32に対し矢印E方向の反力を作用すること
となる。このように栓体穿刺部40に抜去方向での力が
作用すると、該栓体穿刺部40に形成される凹凸部45
と栓体35の間で摩擦が高まり係合することとなる。こ
れにより、採血中において、栓体35から栓体穿刺部4
0が抜け、採血ホルダー33に対して減圧採血管32が
離脱する不具合(キックパック)を防止することが可能
となる。ここで栓体35と凹凸部45との摩擦抵抗は、
圧縮され、折り畳まれる被覆カバー44の反発力よりも
大きく設定される。
When blood is collected using the reduced pressure blood collection A31 having such a configuration, first, as shown in FIG.
Then, a blood vessel puncture section 39 on the peripheral blood side 30 provided in the blood collection holter 33 is punctured. Next, the reduced pressure blood collection side 32 is pushed into the holder main body 37 in the direction of the arrow as shown in FIGS. 2 and 4. In this state 5Ej, the plug piercing portion 40 first pierces the plug 35, and the uneven portion 45 formed on the surface comes into sliding contact with the plug 35. Furthermore, the stopper puncture part 40 that has been inserted into the stopper 35 moves the reduced pressure blood collection tube 32 in the direction of the arrow.
By pushing it in, the inside of the tube body 34, which is brought into a reduced pressure state, is penetrated. In this way, as shown in FIG. 3, when the other end of the hollow needle body 38 is penetrated into the inside of the tube body 34, the reduced pressure inside the Irf body 34 causes the hollow needle body 38 to open. Blood can be introduced from the blood Y puncturing part 39 to the plug puncturing part 40 side. As a result, the pipe body 3
During the flow of blood into the interior of 4 and blood collection, the YO cover 44 is folded into a bellows shape and compressed as shown in FIG. 3. Become. Therefore, the compressed cover 44 exerts a reaction force in the direction of arrow E on the compressed tube 32 that is pushed into it. When the force in the removal direction acts on the plug puncture part 40 in this way, the uneven part 45 formed on the plug puncture part 40
Friction increases between the plug body 35 and the plug body 35, resulting in engagement. As a result, during blood collection, from the plug body 35 to the plug puncture portion 4.
It is possible to prevent a problem (kick pack) in which the decompression blood collection tube 32 is detached from the blood collection holder 33 due to the zero being removed. Here, the frictional resistance between the plug body 35 and the uneven portion 45 is
The repulsive force is set to be larger than the repulsive force of the covering cover 44 which is compressed and folded.

管体34の内部に所定量の血液が採取されると、減圧採
血管32が採血ホルダー33から取外される。減圧採血
管32を取外した状態において、それまで折り畳まれて
いた被覆カバー44は第2図に示す元の状態に復元され
ることとなる。
Once a predetermined amount of blood has been collected inside the tubular body 34, the reduced pressure blood collection tube 32 is removed from the blood collection holder 33. When the vacuum blood collection tube 32 is removed, the covering cover 44, which has been folded up to that point, is restored to its original state as shown in FIG.

さらに多量の採血を行なう場合、第2図および第4図に
示すように未使用の減圧採血管32を矢印りに−示すよ
うにホルダ一本体37内に押入すればよい、採血が完了
されると血管穿刺部39は、腕46から取外される。
If a larger amount of blood is to be collected, as shown in FIGS. 2 and 4, the unused vacuum blood collection tube 32 can be pushed into the holder main body 37 as shown by the arrow, and the blood collection is completed. and the vascular puncture section 39 is removed from the arm 46.

このように1−記実施例に係る血管穿刺30によれば、
栓体穿刺部40を栓体35に穿刺して採血を行なう際、
凹凸部45が栓体35に対してWI接し、保合すること
となり、この係合力が圧縮状j島にある被覆力/<−4
4の反力に対抗作用することとなる。これにより、栓体
穿刺部40が栓体35から抜tすることが防1ヒされ、
円滑かつ安全な採血を行なうことが可f蔚となる。
As described above, according to the blood vessel puncture 30 according to the first embodiment,
When puncturing the plug body 35 with the plug body puncture part 40 to collect blood,
The uneven portion 45 comes into WI contact with the plug body 35 and is secured, and this engagement force is the covering force in the compressed j island /<-4
This will counteract the reaction force of 4. This prevents the plug puncture part 40 from being pulled out from the plug 35,
It becomes possible to perform blood sampling smoothly and safely.

ここで栓体穿刺部40に対し凹凸部45を形成した具体
例を以下のように示す。
Here, a specific example in which the concavo-convex portion 45 is formed on the plug puncture portion 40 will be shown below.

[実施例1] 次の条件のブラスト加工により凹凸部の形成を行なった
[Example 1] The uneven portions were formed by blasting under the following conditions.

針本体:チル七社製21Gマルチプル採血針加I−条件
:ブラスト加工 1)剛 体 粒 子:モ均粒径25鉢アルミナ粒子2)
ブラスト装置:  I:OMGO社製マイクロプラスタ
ーMe−1o。
Needle body: 21G multiple blood collection needle manufactured by Chill Shichisha I-Conditions: Blasting 1) Rigid particles: Average particle size 25 pot alumina particles 2)
Blasting device: I: Microplaster Me-1o manufactured by OMGO.

3)条  件   :エア圧 5kg/  cゴカッテ
ィングスピード 80″ 4)凹凸部の形成範囲:形成長さL−ニアーm周形成固
定領域→全周 [実施例2] 周形成領域を1/2周にした以外は実施例1と同様に行
なった。
3) Conditions: Air pressure 5kg/c Cutting speed 80'' 4) Formation range of uneven parts: Shape growth L-Near m Circumference formation fixed area → Full circumference [Example 2] 1/2 circumference of the circumference formation area The same procedure as in Example 1 was carried out except that .

[実施例3] 形成長さLを51にした以外は実施例1と同様に行なっ
た。
[Example 3] The same procedure as in Example 1 was carried out except that the shape growth length L was set to 51.

し実施例4] 形成長さLを5畷曽にし、周形成領域を172周にした
以外は実施例1と同様に行なった。
Example 4] The same procedure as in Example 1 was carried out except that the shape growth length L was set to 5 turns and the circumference forming area was set to 172 turns.

これらの実施例1〜4ごとに20本ずつに゛)いてキッ
クバックの試験を行なった。結果を表1に示す、なお、
比較例として無処理のチル七社製21Gマルチ針を用い
た。
A kickback test was conducted using 20 pieces for each of Examples 1 to 4. The results are shown in Table 1.
As a comparative example, an untreated 21G multi-needle manufactured by Chill Shichisha was used.

また、実施例1の凹凸部を表面形状測定機(小板研究所
MODEL 5E−3A)で4一定すると第5図のよう
であった。また、比較例の表面は第6図のようであった
Further, when the uneven portions of Example 1 were measured using a surface profile measuring machine (Koita Research Institute MODEL 5E-3A) at a constant value of 4, the results were as shown in FIG. Moreover, the surface of the comparative example was as shown in FIG.

表  1 この表から凹凸部45の形成範囲を形成長さし= 5m
m以」二でかつ周形成領域半周以上とすれば。
Table 1 From this table, the formation range of the uneven portion 45 is determined by the shape growth scale = 5 m
m or more and the circumference forming area is half the circumference or more.

キックパックをほとんど防止できることがわかる。It can be seen that most kick packs can be prevented.

[発明の効果] 以にのように1本発明は、中空状の針本体の中間部分に
ハブを有し、一端側に血管穿刺部を備え、他端側に減圧
採血管の栓体に穿刺される栓体穿刺部を備えるとともに
、該栓体穿刺部を、該ハブから伸びる鞘状の拡縮自在な
弾性を有する被稜カバーにて被覆してなる採血針におい
て、上記栓体穿刺部は、その周上に栓体に穿刺した状態
で該栓体と係合する凹凸部を備えてなり、該栓体と該凹
凸部の摩擦抵抗が、該栓体への該栓体穿刺部の穿刺に伴
ない圧縮される該被覆カバーの反発力以上であることと
したため、採血中において圧縮される被覆カバーの反力
により、針本体の栓体穿刺部が減圧採血管の栓体から抜
けることを防止し、円滑かつ安全な採血を行なうことが
できるという効果がある。
[Effects of the Invention] As described above, the present invention has a hub in the middle part of a hollow needle body, a blood vessel puncture part on one end, and a blood vessel puncture part on the other end for puncturing the stopper of a vacuum blood collection tube. In a blood collection needle comprising a plug puncturing part, the plug puncturing part is covered with a sheath-like elastic ridged cover extending from the hub, the plug puncturing part comprising: It has an uneven part on its circumference that engages with the stopper when the stopper is punctured, and the frictional resistance between the stopper and the uneven part prevents the puncture part of the stopper from puncturing the stopper. The repulsive force of the cover, which is compressed during blood collection, is set to be greater than or equal to the repulsive force of the cover, which is compressed during blood collection, to prevent the punctured part of the needle body from coming off the stopper of the vacuum blood collection tube. This has the effect of allowing smooth and safe blood sampling.

また1本発明における凹凸部は、栓体穿刺部の周トをブ
ラスト加工して形成されることとしたため、該凹凸部の
形成を容易に行なうことができる。
Furthermore, since the uneven portion in the present invention is formed by blasting the circumference of the punctured portion of the plug, the uneven portion can be easily formed.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の一実施例に係る採血針を示す正面図、
第1図(A)は第1図のA部を拡大して示す図、第1図
(B)は第1図(A)のB部の表面凹凸状態を示す図、
第2図は採血針書を用いて形成される減圧採血具の使用
前の状態を示す断面図、第3図は同使用時の状態を示す
断面図、第4図は第2図に示す減圧採血具を用いて人体
の腕から採血する状態を示す斜視図である。第5図は表
面形状測定機で実施例1に係る凹凸部を測定した状!E
;を示す線図、第6図は表面形状測定機で比較例に係る
凹凸部を測定した状態を示す線図、第7図は従来の減圧
採血共の使用前の状態を示す断面図、第8図は同使用時
の状態を示す断面図である30・・・採血針、31・・
・減圧採血具、32・・・減圧採血管、33・・・採血
ホルダー、35・・・栓体、38・・・針本体、39・
・・血管穿刺部、40・・・栓体穿刺部。 44・・・被覆カバー、45・・・凹凸部。
FIG. 1 is a front view showing a blood collection needle according to an embodiment of the present invention;
FIG. 1(A) is an enlarged view of part A in FIG. 1, FIG. 1(B) is a diagram showing the surface unevenness of part B in FIG. 1(A),
Figure 2 is a cross-sectional view showing the vacuum blood sampling device formed using a blood sampling needle before use, Figure 3 is a cross-sectional view showing the same state during use, and Figure 4 is the reduced pressure shown in Figure 2. FIG. 2 is a perspective view showing a state in which blood is collected from an arm of a human body using a blood collection tool. Figure 5 shows the unevenness of Example 1 measured using a surface profile measuring machine! E
; FIG. 6 is a diagram showing the state in which the unevenness according to the comparative example was measured with a surface profile measuring machine; FIG. 7 is a cross-sectional view showing the state before use of the conventional vacuum blood sampling; Figure 8 is a cross-sectional view showing the state in use. 30...Blood collection needle, 31...
- Decompression blood collection device, 32... Decompression blood collection tube, 33... Blood collection holder, 35... Stopper, 38... Needle body, 39.
... Blood vessel puncture section, 40... Plug body puncture section. 44... Covering cover, 45... Uneven part.

Claims (2)

【特許請求の範囲】[Claims] (1)中空状の針本体の中間部分にハブを有し、一端側
に血管穿刺部を備え、他端側に減圧採血管の栓体に穿刺
される栓体穿刺部を備えるとともに、該栓体穿刺部を、
該ハブから伸びる鞘状の拡縮自在な弾性を有する被覆カ
バーにて被覆してなる採血針において、上記栓体穿刺部
は、その周上に栓体に穿刺した状態で該栓体と係合する
凹凸部を備えてなり、該栓体と該凹凸部の摩擦抵抗が、
該栓体への該栓体穿刺部の穿刺に伴ない圧縮される該被
覆カバーの反発力以上であることを特徴とする採血針。
(1) It has a hub in the middle part of the hollow needle body, has a blood vessel puncture part on one end side, has a plug puncture part to be punctured into the stopper of a vacuum blood collection tube on the other end, and body puncture site,
In the blood collection needle covered with a sheath-like elastic covering cover extending from the hub and having elasticity that can be expanded and contracted, the plug piercing part engages with the plug while piercing the plug on its circumference. It is provided with an uneven part, and the frictional resistance between the plug body and the uneven part is
A blood collection needle characterized in that the repulsion force is greater than the repulsive force of the cover that is compressed as the plug body is punctured by the plug body piercing portion.
(2)上記凹凸部は、栓体穿刺部の周上をブラスト加工
して形成されてなる特許請求の範囲第1項に記載の採血
針。
(2) The blood collection needle according to claim 1, wherein the uneven portion is formed by blasting the circumference of the plug puncture portion.
JP61071280A 1986-03-31 1986-03-31 Blood sampling needle Granted JPS62227316A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61071280A JPS62227316A (en) 1986-03-31 1986-03-31 Blood sampling needle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61071280A JPS62227316A (en) 1986-03-31 1986-03-31 Blood sampling needle

Publications (2)

Publication Number Publication Date
JPS62227316A true JPS62227316A (en) 1987-10-06
JPH0256095B2 JPH0256095B2 (en) 1990-11-29

Family

ID=13456140

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61071280A Granted JPS62227316A (en) 1986-03-31 1986-03-31 Blood sampling needle

Country Status (1)

Country Link
JP (1) JPS62227316A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11169359A (en) * 1997-10-07 1999-06-29 Sekisui Chem Co Ltd Vacuum blood drawing needle
WO2000076401A1 (en) 1997-12-19 2000-12-21 Sekisui Chemical Co.,Ltd. Vacuum sample collecting tube and method of collecting sample under vacuum
US7726498B2 (en) 2003-07-18 2010-06-01 Sekisui Chemical Co., Ltd. Hermetically sealed container and vacuum test substance-collecting container

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005342100A (en) * 2004-06-01 2005-12-15 Techno Medica Co Ltd Blood-collecting holder with blood-collecting needle for vacuum blood-collecting tube
EP2327434A4 (en) * 2008-09-10 2014-08-06 Terumo Corp Medical device

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11169359A (en) * 1997-10-07 1999-06-29 Sekisui Chem Co Ltd Vacuum blood drawing needle
WO2000076401A1 (en) 1997-12-19 2000-12-21 Sekisui Chemical Co.,Ltd. Vacuum sample collecting tube and method of collecting sample under vacuum
US7726498B2 (en) 2003-07-18 2010-06-01 Sekisui Chemical Co., Ltd. Hermetically sealed container and vacuum test substance-collecting container

Also Published As

Publication number Publication date
JPH0256095B2 (en) 1990-11-29

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