JPH0622352Y2 - Body fluid treatment circuit member - Google Patents

Body fluid treatment circuit member

Info

Publication number
JPH0622352Y2
JPH0622352Y2 JP1988092528U JP9252888U JPH0622352Y2 JP H0622352 Y2 JPH0622352 Y2 JP H0622352Y2 JP 1988092528 U JP1988092528 U JP 1988092528U JP 9252888 U JP9252888 U JP 9252888U JP H0622352 Y2 JPH0622352 Y2 JP H0622352Y2
Authority
JP
Japan
Prior art keywords
fusion
body fluid
bonding
treatment circuit
fluid treatment
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.)
Expired - Fee Related
Application number
JP1988092528U
Other languages
Japanese (ja)
Other versions
JPH0215152U (en
Inventor
宏臣 筏
雄一 犬飼
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.)
Kawasumi Laboratories Inc
Kuraray Co Ltd
Original Assignee
Kawasumi Laboratories Inc
Kuraray Co Ltd
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 Kawasumi Laboratories Inc, Kuraray Co Ltd filed Critical Kawasumi Laboratories Inc
Priority to JP1988092528U priority Critical patent/JPH0622352Y2/en
Publication of JPH0215152U publication Critical patent/JPH0215152U/ja
Application granted granted Critical
Publication of JPH0622352Y2 publication Critical patent/JPH0622352Y2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【考案の詳細な説明】 [産業上の利用分野] 本考案は、血液透析、血漿交換等の体液処理回路用の圧
力検出器の改良に関するもので特に圧力検出器をコンパ
クト化して、体液の圧力の検出精度を損うことなく、気
泡の残留、体液循環中の血栓の発生を極力抑制して体液
処理に有効な体液処理回路用部材に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention relates to an improvement of a pressure detector for a body fluid treatment circuit such as hemodialysis and plasma exchange. The present invention relates to a body fluid treatment circuit member which is effective for body fluid treatment by suppressing residual bubbles and generation of thrombus during circulation of body fluid without impairing detection accuracy.

[従来の技術] 第13図は、従来の体液処理回路用部材71を使用した減抗
凝固剤透析の方法を示す概略図である。
[Prior Art] FIG. 13 is a schematic diagram showing a conventional anticoagulant dialysis method using a body fluid treatment circuit member 71.

体液処理回路用部材71は、圧力検出部72と体液ロ過部73
から構成され、圧力検出器部72は硬質の外管74中に可と
う性の内管75を液密に収容して構成され、体液ロ過部73
は硬質のドリップチャンバー本体76内にメッシュ状のフ
ィルター77を装填したものである。
The body fluid treatment circuit member 71 includes a pressure detection unit 72 and a body fluid filtration unit 73.
The pressure detector section 72 is configured by liquid-tightly containing a flexible inner tube 75 in a hard outer tube 74, and a body fluid filter section 73.
Is a hard drip chamber body 76 with a mesh filter 77 loaded therein.

図中81は血液透析器で、下流側には、静脈側回路82、上
流側には動脈側回路83が接続されている。静脈側回路82
の途中に、体液処理回路用部材71が装着されている。患
者から導出された血液は、動脈側回路83、血液透析器8
1、体液処理回路用部材71を経て、体液ロ過部材73のフ
ィルター77でロ過されて、静脈側回路82を経て患者へ戻
されていた。
In the figure, 81 is a hemodialyzer, which is connected to a vein side circuit 82 on the downstream side and an arterial side circuit 83 on the upstream side. Vein side circuit 82
A body fluid treatment circuit member 71 is attached in the middle of. Blood drawn from the patient is fed to the arterial circuit 83, hemodialyzer 8
1. After passing through the bodily fluid treatment circuit member 71, it was filtered by the filter 77 of the bodily fluid filtering member 73 and returned to the patient through the vein side circuit 82.

[考案が解決しようとする課題] しかしながら、これらの体液処理回路用部材71は、体液
ロ過部73と圧力検出部72を別々に製造してから接続して
いたので、製造上工程が多く、手間がかかっていたほ
か、さらに個々の形状が大きくならざるを得ないためコ
スト高になっていた。
[Problems to be Solved by the Invention] However, in the body fluid treatment circuit member 71, since the body fluid filtration unit 73 and the pressure detection unit 72 are separately manufactured and then connected, there are many manufacturing steps. In addition to the time-consuming work, the individual shapes have to be larger and the cost is higher.

このように、全体の形状が大きいため体液の充填量も多
くなり、特に透析における血液を使用した場合は、血栓
が生じやすい傾向にあった。体液処理回路用部材71を構
成する材料(血液にとっては異物)と接触する時間が多
くなれば、血栓を生じやすくなるので、接触する時間は
少しでも短縮するほうが望ましい。
As described above, since the whole shape is large, the filling amount of body fluid is large, and particularly when blood is used in dialysis, thrombus tends to occur. If the contact time with the material forming the body fluid treatment circuit member 71 (foreign matter for blood) increases, thrombosis is likely to occur, so it is desirable to shorten the contact time as much as possible.

[課題を解決するための手段] そこで、本考案は体液処理回路用部材のコンパクト化に
重点をおいて体液の圧力検出精度を損うことなく、血液
中の気泡の残留、血栓の発生を極力抑制できる圧力検出
器の改良に検討を重ねた結果、次の考案に到達したので
ある。
[Means for Solving the Problems] Therefore, the present invention focuses on downsizing of the body fluid treatment circuit member and does not impair the pressure detection accuracy of the body fluid to minimize the occurrence of bubbles in the blood and the formation of thrombus. As a result of repeated studies on the improvement of the pressure detector that can be suppressed, the following idea was reached.

すなわち、本考案の請求項1によれば、 体液処理回路に装着される体液処理回路用部材であっ
て、 硬質樹脂製の本体チューブの中間部に体液通路を残して
形成された第1の融着部と、 前記本体チューブの一端部に形成された第2の融着部
と、 該本体チューブの他端部に形成された第3の融着部と、 該第1の融着部と第2の融着部の間の空間部に配置さ
れ、一端部が前記第1の融着部に、他端部が前記第2の
融着部にそれぞれ固定されて圧力検出部を構成する内管
と、 前記第1の融着部と第3の融着部の間の空間部に配置さ
れ、前記第1の融着部または第3の融着部もしくは前記
本体チューブ内側に固定されて体液ロ過部を構成するメ
ッシュフィルターと、 前記第2の融着部に装着された圧力モニターラインと、 前記第2の融着部に装着されて前記第1の融着部と第2
の融着部の間の空間部に通じる体液誘導管と、 前記第3の融着部に装着されて前記第1の融着部と第3
の融着部の間の空間部に通じる体液誘導管と、 を有することを特徴とする。
That is, according to claim 1 of the present invention, a body fluid treatment circuit member to be mounted in a body fluid treatment circuit, wherein the first fusion fluid is formed by leaving a body fluid passage in an intermediate portion of a body tube made of a hard resin. An adhesion part, a second fusion part formed at one end of the body tube, a third fusion part formed at the other end of the body tube, a first fusion part and a first fusion part. An inner pipe which is arranged in a space between two fusion-bonding parts, one end of which is fixed to the first fusion-bonding part and the other end of which is fixed to the second fusion-bonding part to form a pressure detecting part. And a space between the first fusion bonding portion and the third fusion bonding portion, which is fixed inside the first fusion bonding portion or the third fusion bonding portion or the main body tube. A mesh filter forming an excess portion, a pressure monitor line attached to the second fusion-bonding portion, and a pressure monitor line attached to the second fusion-bonding portion The is first fused portion and the second
Body fluid guide tube that communicates with the space between the fusion-bonding parts, and the first fusion-bonding part and the third fusion-bonding part attached to the third fusion-bonding part.
And a bodily fluid guide tube communicating with the space between the fusion-bonded parts of

また本考案の請求項2によれば、 前記第3の融着部に代えて、本体チューブの異なる側の
端部にキャップ部材を固着し、該キャップ部材または第
1の融着部もしくは第2の融着部にメッシュフィルター
を固定したことを特徴とする。
Further, according to claim 2 of the present invention, instead of the third fusion-bonding portion, a cap member is fixed to different end portions of the main body tube, and the cap member or the first fusion-bonding portion or the second fusion-bonding portion is formed. A mesh filter is fixed to the fusion-bonded part of the above.

[作用] 体液処理回路を循環する体液は、一方の体液誘導管から
本体チューブ内に流入し、第1融着部を境にして形成さ
れた圧力検出部と体液ロ過部を短時間で通過して他方の
液体誘導管から流出する。圧力検出部と体液ロ過部は第
1溶着部の体液通路を通って流通する。
[Operation] The body fluid circulating in the body fluid treatment circuit flows into the main body tube from one body fluid guide tube and passes in a short time through the pressure detection unit and the body fluid filtration unit which are formed with the first fusion section as a boundary. And flows out from the other liquid guide tube. The pressure detection unit and the body fluid filtration unit flow through the body fluid passage of the first welding unit.

圧力検出部においては、可とう性内管が、その内部を通
る体液流量に応じて膨張又は収縮し、外管と可とう性内
管との間の空隙部の圧力変動を圧力モニターラインで検
出している。
In the pressure detection part, the flexible inner tube expands or contracts according to the body fluid flow rate passing through it, and the pressure monitor line detects the pressure fluctuation in the gap between the outer tube and the flexible inner tube. is doing.

また体液ロ過部においてはメッシュフィルターにより体
液に含まれる微小異物が除去される。
Further, in the body fluid filtration portion, the fine foreign matter contained in the body fluid is removed by the mesh filter.

[実施例] 第1図(a)は、本考案の体液処理回路用部材の第1実
施例を示す概略図である。第1図(b)は第1図(a)
のA−A断面図を示す。
[Embodiment] FIG. 1 (a) is a schematic view showing a first embodiment of the member for body fluid treatment circuit of the present invention. FIG. 1 (b) is FIG. 1 (a).
A-A sectional drawing of is shown.

体液処理回路用部材1は、例えば硬質ポリ塩化ビニル等
からなるチューブ状本体2の中間部に、体液通路3を残
して融着部4が形成され、該融着部4を隔てて、圧力検
出部5と体液ロ過部6が形成されている。
In the body fluid treatment circuit member 1, a fused portion 4 is formed in an intermediate portion of a tubular body 2 made of, for example, hard polyvinyl chloride, leaving a body fluid passageway 3, and the fusion portion 4 is separated to detect pressure. A part 5 and a body fluid filtration part 6 are formed.

圧力検出部5は、内部に例えば、軟質のポリ塩化ビニル
等からなる肉薄の可とう性の内管7が配置され、該可と
う性内管7の両端部は、本体2と共に高周波溶着により
形成される融着部4、8により固定されている。
The pressure detecting portion 5 has therein a thin flexible inner tube 7 made of, for example, soft polyvinyl chloride, and both ends of the flexible inner tube 7 are formed by high frequency welding together with the main body 2. It is fixed by the fused portions 4 and 8.

体液ロ過部6は、例えばポリエステル、ポリアミド等か
らなるメッシュフィルター若しくはこれらの表面に水に
対する後退接触角が45度以下の親水性高分子(例えば
ヒドロキシエチルメタクリレート、ヒドロキシプロピル
メタクリレート、メトキシエチルアクリレート、エトキ
シエチルアクリレート、ジアセトンアクリルアミドの重
合体等が好適である)をコーティングしたメッシュフィ
ルター又は硬質のポリ塩化ビニルからなり、リング部と
メッシュ部を一体に成形したフィルター(以下「フィル
ター9」と略記する)が配置され該フィルター9の開口
端部15は本体2と共に高周波溶着により形成される融着
部4により固定されている。
The body fluid filtration part 6 is, for example, a mesh filter made of polyester, polyamide, or the like, or a hydrophilic polymer having a receding contact angle with water of 45 degrees or less on the surface thereof (eg, hydroxyethyl methacrylate, hydroxypropyl methacrylate, methoxyethyl acrylate, ethoxy). A mesh filter coated with ethyl acrylate, a polymer of diacetone acrylamide, or the like) or a filter made of hard polyvinyl chloride and integrally formed with a ring portion and a mesh portion (hereinafter abbreviated as "filter 9") And the open end portion 15 of the filter 9 is fixed together with the main body 2 by the fusion bonding portion 4 formed by high frequency welding.

さらに本体2の上端部には血液流出管10、下端部には血
液流入管11が高周波溶着により融着部8、12に固定され
ている。
Further, a blood outflow pipe 10 is fixed to the upper end of the main body 2, and a blood inflow pipe 11 is fixed to the lower end of the main body 2 to the fusion-bonded portions 8 and 12 by high frequency welding.

図中13は脱気ライン、14は圧力モニターラインで高周波
溶着により形成される融着部8により固定されている。
脱気ライン13は、融着部4又は8のどちらに固定しても
良い。なお、第1図において、融着部4が第1の融着
部、融着部4が第2の融着部、融着部12が第3の融着部
となる。
In the figure, 13 is a deaeration line, and 14 is a pressure monitor line, which are fixed by a fusion-bonding portion 8 formed by high-frequency welding.
The degassing line 13 may be fixed to either the fusion bonding section 4 or 8. In FIG. 1, the fusion-bonding portion 4 is the first fusion-bonding portion, the fusion-bonding portion 4 is the second fusion-bonding portion, and the fusion-bonding portion 12 is the third fusion-bonding portion.

第1図(a)の体液処理回路用部材1のその他の実施例
として次の態様が考えられる。
The following modes are conceivable as other examples of the body fluid treatment circuit member 1 of FIG. 1 (a).

すなわち、第2図の体液処理回路部材1aは、体液ロ過
部6aに配置した帽冠状のフィルタ9aの開口端部15a
の円周面を本体2aの内壁に高周波溶着により固定した
ものである。
That is, the body fluid treatment circuit member 1a shown in FIG. 2 has the open end portion 15a of the cap-shaped filter 9a arranged in the body fluid filtration portion 6a.
The circumferential surface of is fixed to the inner wall of the main body 2a by high frequency welding.

第3図の体液処理回路用部材1bは、圧力検出部5bと
体液ロ過部6bのお互いに対向する角度が90度となる
ように形成した例である。すなわち、この例では本体中
間部の融着部4と、体液ロ過部6b側の端部融着部12の
融着面が、本体の軸心に対して互いにねじれ方向となる
ように形成されている。このねじれ角は任意である。な
お、圧力検出部5b側の端部融着部8の融着面は中間融
着部4と同方向に形成されている。
The body fluid treatment circuit member 1b of FIG. 3 is an example in which the pressure detecting portion 5b and the body fluid filtering portion 6b are formed so that the opposing angles thereof are 90 degrees. That is, in this example, the fusion-bonding portion 4 in the middle portion of the main body and the fusion-bonding surface of the end fusion-bonding portion 12 on the body fluid filtration portion 6b side are formed so as to be twisted with respect to the axis of the main body. ing. This twist angle is arbitrary. The fusion-bonding surface of the end fusion-bonding portion 8 on the pressure detecting portion 5b side is formed in the same direction as the intermediate fusion-bonding portion 4.

第4図に体液処理回路用部材1cは、これを体液処理回
路に取り付けたとき、圧力検出部5cが本体2cの上部
に位置し、体液ロ過部6cが下部に位置するように構成
したものである。圧力モニターライン14cは、融着部12c
に固定され、フィルター9cは、開口端部15cを本体2
cと共に高周波溶着により形成される融着部8cにより
固定される。他方、可とう性内管7cは、両端部を本体
2と共に高周波溶着により形成される融着部4c,12c
により固定されている。なお、第4図において、融着部
4cが第1の融着部、融着部12cが第2の融着部、融着
部8cが第3の融着部である。
In FIG. 4, the body fluid treatment circuit member 1c is configured such that, when the body fluid treatment circuit member 1c is attached to the body fluid treatment circuit, the pressure detection portion 5c is located above the main body 2c and the body fluid filtration portion 6c is located below. Is. The pressure monitor line 14c is connected to the fused portion 12c.
The filter 9c is fixed to the main body 2 with the open end 15c.
It is fixed by the fusion-bonding part 8c formed by high frequency welding together with c. On the other hand, the flexible inner tube 7c has fused portions 4c and 12c formed by high frequency welding together with the main body 2 at both ends.
It is fixed by. In FIG. 4, the fused portion 4c is the first fused portion, the fused portion 12c is the second fused portion, and the fused portion 8c is the third fused portion.

第5図の体液処理回路用部材1dは、体液ロ過部6d内
に配置したフィルター9dの開口端部15dの円周面を本
体2dが内壁に高周波溶着により固定したものである。
The body fluid treatment circuit member 1d shown in FIG. 5 is constructed by fixing the circumferential surface of the open end portion 15d of the filter 9d arranged in the body fluid filtration portion 6d to the inner wall of the main body 2d by high frequency welding.

第6図の体液処理回路用部材1eは、圧力検出部5eと
体液ロ過部6eのお互いに対向する角度が90度となる
ように形成したものである。すなわち第4図と比較し
て、本体中間部の融着部4cと、圧力検出部5e側の端
部融着部12cの融着面が本体の軸心に対して互いにね
じれ方向となるように形成されている。このねじれ角は
任意である。
The body fluid treatment circuit member 1e of FIG. 6 is formed such that the pressure detecting portion 5e and the body fluid filtering portion 6e face each other at an angle of 90 degrees. That is, as compared with FIG. 4, the fusion-bonding surfaces of the fusion-bonding portion 4c at the intermediate portion of the main body and the end-fusion-bonding portion 12c on the pressure detecting portion 5e side are twisted with respect to the axial center of the main body. Has been formed. This twist angle is arbitrary.

第7図は、本考案体液処理回路用部材の第2実施例を示
す概略図である。体液処理回路用部材21は、例えば硬質
のポリ塩化ビニル等からなる本体22内に体液通路23を
残して融着部24が形成され、該融着部24を隔てて、圧力
検出部25と体液ロ過部26が形成されている。
FIG. 7 is a schematic view showing a second embodiment of the member for body fluid treatment circuit according to the present invention. The body fluid treatment circuit member 21 includes a body 22 made of, for example, hard polyvinyl chloride, and a body fluid passage 23 left in the body 22 to form a fusion portion 24. The fusion portion 24 is separated from the pressure detection portion 25 and the body fluid. A filter portion 26 is formed.

圧力検出部25は、内部に例えば軟質のポリ塩化ビニル等
からなる肉薄の可とう性の内管27が配置され、該可とう
性の内管27の両端部は本体22と共に高周波溶着により形
成される融着部24、32により固定されている。
The pressure detection unit 25 has a thin flexible inner tube 27 made of, for example, soft polyvinyl chloride, arranged inside, and both ends of the flexible inner tube 27 are formed by high frequency welding together with the main body 22. It is fixed by the fusion-bonding portions 24 and 32.

体液ロ過部26は、フィルター29が内部に配置され、該フ
ィルター29の開口端部35は、本体22と共に高周波溶着に
より形成される融着部24により固定されている。
A filter 29 is disposed inside the bodily fluid filtration part 26, and an open end 35 of the filter 29 is fixed together with the body 22 by a fusion part 24 formed by high frequency welding.

さらに本体22の下端部には、血液流出管30、圧力モニタ
ーライン34が高周波溶着により融着部32より固定してい
る。他方上端部には、体液流入管31と脱気ライン33の接
続管36を一体に成形したトラップキャップ37が装着され
ている。なお、第7図において、融着部24が第1の融着
部、融着部が第2の融着部である。
Further, a blood outflow pipe 30 and a pressure monitor line 34 are fixed to the lower end portion of the main body 22 by a high frequency welding from the fusion bonding portion 32. On the other upper end, a trap cap 37, which is integrally formed with a body fluid inflow pipe 31 and a connection pipe 36 of the degassing line 33, is attached. In FIG. 7, the fusion-bonding portion 24 is the first fusion-bonding portion, and the fusion-bonding portion is the second fusion-bonding portion.

第7図の体液処理回路用部材21のその他の実施例として
次の態様が考えられる。
The following modes are conceivable as other examples of the body fluid treatment circuit member 21 of FIG.

すなわち第8図の体液処理回路用部材21aは、体液ロ過
部26a内に配置したフィルター29aの開口端部35aの円周
面を本体22aの内壁に高周波溶着により固定したもので
ある。
That is, the body fluid treatment circuit member 21a shown in FIG. 8 has the circumferential surface of the open end portion 35a of the filter 29a arranged in the body fluid filtration portion 26a fixed to the inner wall of the main body 22a by high frequency welding.

第9図の体液処理回路用部材21bは、体液ロ過部材26b内
に配置したフィルター29bの開口端部35bを本体22bと共
に、高周波溶着により体液通路39を残して形成した融着
部38により固定したものである。なお、第9図におい
て、融着部38が第2の融着部である。
In the body fluid treatment circuit member 21b of FIG. 9, the open end portion 35b of the filter 29b arranged in the body fluid filter member 26b is fixed together with the main body 22b by the fusion portion 38 formed by the high frequency welding leaving the body fluid passage 39. It was done. In addition, in FIG. 9, the fused portion 38 is the second fused portion.

次に本考案の体液処理回路用部材1を、血液透析に使用
した場合の実施例について説明する。第10図は通常の透
析における使用例で、第11図は減抗凝固剤透析での使用
例である。
Next, an example in which the body fluid treatment circuit member 1 of the present invention is used for hemodialysis will be described. FIG. 10 shows an example of use in normal dialysis, and FIG. 11 shows an example of use in reduced anticoagulant dialysis.

第10図において、41は血液透析器で血液透析器41の上流
側には血液導入口44を介して動脈側回路42、下流側には
血液導出口45を介して静脈側回路43が装着されている。
In FIG. 10, reference numeral 41 denotes a hemodialyzer, on the upstream side of the hemodialyzer 41, an arterial circuit 42 is attached via a blood inlet 44, and on the downstream side a vein circuit 43 is attached via a blood outlet 45. ing.

静脈側回路43の途中には、体液処理回路用部材1が装着
されている。
The body fluid treatment circuit member 1 is attached in the middle of the vein side circuit 43.

透析液は、血液透析器41の下部入口46から入り上部出口
47へ流出するように還流される。
The dialysate enters from the lower inlet 46 of the hemodialyzer 41 and the upper outlet.
It is refluxed so as to flow to 47.

血液透析器41、動脈側回路42、静脈側回路43内に生理食
塩水をプライミングして、中の気泡を追い出した後、シ
ャント48、49を介して動脈側回路42と静脈側回路43を患
者に接続した後血液ポンプ50を駆動させて血液を動脈側
回路42を経て血液透析器41へ導入し、透析液と接触させ
て老廃物(低分子量の有害物質)を除去して、浄化した
血液を静脈側回路43、体液処理回路用部材1を経て患者
に返還する。
After priming physiological saline into the hemodialyzer 41, the arterial circuit 42, and the venous circuit 43 to expel air bubbles therein, the arterial circuit 42 and the venous circuit 43 are connected to the patient via the shunts 48 and 49. After connecting to the blood, the blood pump 50 is driven to introduce blood into the hemodialyzer 41 through the arterial circuit 42, and the blood is brought into contact with dialysate to remove waste products (hazardous substances of low molecular weight) and purified blood. Is returned to the patient via the vein side circuit 43 and the body fluid treatment circuit member 1.

静脈側回路43を経て体液処理回路用部材1内に導入され
た血液は、圧力検出部5の可とう性内管7aを通り体液
通路3、フィルター9を通って体液流出管10を経て静脈
側回路43へ流出される。
The blood introduced into the body fluid treatment circuit member 1 through the vein side circuit 43 passes through the flexible inner tube 7a of the pressure detection unit 5, the body fluid passage 3, the filter 9 and the body fluid outflow tube 10 to the vein side. Spilled to circuit 43.

透析中に血液中に圧力変動が生じた場合には肉薄に形成
された可とう性内管7が敏感に膨張、収縮を行うから圧
力モニターライン14を介して圧力計51へ伝えられるので
すばやく知ることができる。
If a pressure fluctuation occurs in the blood during dialysis, the thin flexible inner tube 7 is sensitively expanded and contracted, so that the pressure can be transmitted to the pressure gauge 51 via the pressure monitor line 14, so that it can be quickly known. be able to.

血液中のマイクロアグリゲート又は体外循環回路中の微
小ゴミ等が含まれていてもフィルター9により阻止され
るので患者の体内に入る恐れがない。さらに微小な気泡
が本体2内に混入しても、脱気ライン13より容易に除去
することができる。
Even if microaggregates in the blood or minute dusts in the extracorporeal circulation circuit are contained, they are blocked by the filter 9 and do not enter the patient's body. Even if minute bubbles are mixed in the main body 2, they can be easily removed from the degassing line 13.

体液処理回路用部材1内に密に充填した生理食塩液を順
に、下部から上部に亘って血液で置換した後血液を常に
体液処理回路用部材1内に密に充填した状態で、血液の
還流を行うため血液が空気と接触することがなく、血栓
が生じる恐れがない。
The physiological saline, which is densely filled in the body fluid treatment circuit member 1, is sequentially replaced with blood from the lower part to the upper portion, and then blood is constantly filled in the body fluid treatment circuit member 1 and the blood is refluxed. Since blood does not come into contact with air, there is no risk of blood clots.

さらに、血栓の生じにくい要因としでロ過部材6を通過
する血液の流体圧によるフィルター9の膨らみが小さ
く、血液はフィルター9の中央部を経てすみやかに通過
するので、実質的に圧力検出部5内に滞留する時間が短
いことが考えられる。
Further, the swelling of the filter 9 due to the fluid pressure of the blood passing through the filter member 6 is small as a factor that makes it difficult for the thrombus to occur, and the blood quickly passes through the central portion of the filter 9, so that the pressure detecting unit 5 is substantially provided. It is conceivable that the time to stay inside is short.

第11図において、41aは血液透析器で、血液透析器41aの
下流側には、血液導出口45aを介して静脈側回路43a、上
流側には血液導入口44aを介して動脈側回路42aが接続さ
れている。
In FIG. 11, reference numeral 41a is a hemodialyzer, and a downstream side of the hemodialyzer 41a has a vein side circuit 43a via a blood outlet 45a and an upstream side has an arterial side circuit 42a via a blood inlet 44a. It is connected.

静脈側回路43aの途中には、体液処理回路用部材1が装
着されている。
The body fluid treatment circuit member 1 is attached in the middle of the vein side circuit 43a.

透析液は、血液透析器41aの上部流入口46aから入り下部
出口47aへ流出するように環流される。
The dialysate is refluxed so as to enter from the upper inlet port 46a of the hemodialyzer 41a and flow out to the lower outlet port 47a.

血液透析器41a、動脈側回路42a、静脈側回路43a内に生
理食塩液をプライミングして、中の気泡を、追い出した
後、シャント48a、49aを介して動脈側回路42a、静脈側回
路43aを患者に接続した後、血液ポンプ50aを作動させて
血液を上流の動脈側回路42aを経て血液透析器41aへ導入
し、透析液と接触させて老廃物(低分子量の有害物質)
を除去して浄化した血液を下流の静脈側回路43a、体液
処理回路用部材1を経て患者に返還する。
Hemodialyzer 41a, arterial side circuit 42a, venous side circuit 43a prime saline solution, after expelling the bubbles in, shunts 48a, 49a arterial side circuit 42a, venous side circuit 43a through After connecting to the patient, the blood pump 50a is operated to introduce blood into the hemodialyzer 41a through the upstream arterial circuit 42a and contact with the dialysate to generate waste products (low molecular weight harmful substances).
The blood that has been removed and purified is returned to the patient via the downstream venous circuit 43a and the body fluid treatment circuit member 1.

静脈側回路43aを経て、体液処理回路用部材1内に導入
された血液は、前述と同様に処理され、血液中のマイク
ロアグリゲート又は体外循環回路中の微小ゴミ、気泡の
除去、圧力変動の検出も同様に行われ、さらに血栓が生
じない点も同様であった。最後に本考案の体液処理回路
用部材の製造方法の一例について第1図(a)の体液処
理回路用部材1の場合について説明する(第12図参
照)。
The blood introduced into the body fluid treatment circuit member 1 via the vein side circuit 43a is treated in the same manner as described above, and the microaggregates in the blood or the removal of fine dust and bubbles in the extracorporeal circulation circuit, the pressure fluctuation The detection was performed in the same manner, and the same was true in that thrombus did not occur. Finally, an example of the method for manufacturing the body fluid treatment circuit member of the present invention will be described for the case of the body fluid treatment circuit member 1 of FIG. 1 (a) (see FIG. 12).

図中55a 55bは金型でお互いに対称に形成されている。
該金型55aは基本的に3つの挟持部56a、57a、58aから構成
されており、該挟持部56a、57a、58aは金型全体に一体成
形又はセパレート式に装着されており、それぞれには、
血液流入管11等の挟持溝59a、60a、61a、62a、63aが形成さ
れている。
In the figure, 55a and 55b are molds and are formed symmetrically with each other.
The mold 55a is basically composed of three holding parts 56a, 57a, 58a, and the holding parts 56a, 57a, 58a are integrally or separately mounted on the entire mold, and each of them is attached to the mold. ,
Clamping grooves 59a, 60a, 61a, 62a, 63a of the blood inflow pipe 11 and the like are formed.

血液流入管11等を本体2に融着するには次の様にして行
う。鉄、ステンレス、黄銅、ジュラルミン等の導電性材
料からなる金属棒64、65、66、67にそれぞれ血液流通管68
を装着して、これらを可とう性内管7、フィルター9と
共に本体2の中に配置して、前記金型55a、55bの血液流
入管11等の挟持溝59a、60a、61a、62a、63aと位置合せを行
う。
The fusion of the blood inflow pipe 11 and the like to the main body 2 is performed as follows. Blood circulation tubes 68 are attached to metal rods 64, 65, 66 and 67 made of a conductive material such as iron, stainless steel, brass and duralumin.
And the flexible inner tube 7 and the filter 9 together with the flexible inner tube 7 and the filter 9 are placed in the main body 2, and the clamping grooves 59a, 60a, 61a, 62a, 63a of the blood inflow tube 11 of the molds 55a, 55b are attached. And align.

しかる後、本体2を金型55a、55bより上下方向から押し
つぶしながら、金型55a、55b→金属棒64、65、66、67の
順序で通電を行うと、挟持部56a、57a、58aと接触した本
体2、血液流入管11等が溶融して融着される。
After that, when the main body 2 is crushed from the molds 55a and 55b from above and below while the molds 55a and 55b are energized in the order of the metal rods 64, 65, 66 and 67, they come into contact with the sandwiching parts 56a, 57a and 58a. The main body 2, the blood inflow pipe 11 and the like are melted and fused.

[考案の効果] 上述した本考案によれば以下のような効果を得ることが
できる。
[Effects of the Invention] According to the present invention described above, the following effects can be obtained.

圧力検出部と体液ロ過部とを一体化するにあたり、両
者を第1の溶着部により隔てたので、圧力検出部と体液
ロ過部は独立して機能し、相互に影響を及ぼすことがな
いので、圧力検出を均一かつ安定して行うことができ
る。
In integrating the pressure detection unit and the body fluid filtration unit, since they are separated by the first welding unit, the pressure detection unit and the body fluid filtration unit function independently and do not affect each other. Therefore, pressure detection can be performed uniformly and stably.

圧力検出部と体液ロ過部が同一の本体チューブに一体
的に成形され、本体チューブと融着部の共通化ないし一
体化を図ることにより、これら圧力検出部材と体液ロ過
部材のコンパクト化を図ることができる。また構成部材
の使用原料を低減ることもでき、製造工程も削減するこ
とができるため、安価に量産することができる。さら
に、全体がコンパクト化されることで、圧力検出部と体
液ロ過部の体液通過時間(滞留時間)が短縮し、これら
圧力検出部と体液ロ過部の構成材料(異物)と接触する
時間が短くなるため、血栓の発生が低減する。
The pressure detection part and the body fluid filtration part are integrally molded in the same main body tube, and by making the main body tube and the fusion part common or integrated, these pressure detection member and body fluid filtration member can be made compact. Can be planned. Further, since the raw materials used for the constituent members can be reduced and the manufacturing process can be reduced, mass production can be carried out at low cost. Furthermore, by making the whole compact, the body fluid passage time (residence time) between the pressure detection unit and the body fluid filtration unit is shortened, and the time for contact with the constituent materials (foreign matter) of these pressure detection unit and body fluid filtration unit As a result, the occurrence of thrombus is reduced.

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

第1図(a)は、本考案の体液処理回路用部材の第1実
施例を示す概略図、第1図(b)は第1図(a)のA−
A断面図、第2図から第6図は第1図のその他の実施例
を示す概略図、第7図は本考案の体液処理回路用部材の
第2実施例を示す概略図、第8図及び第9図は第7図の
その他の実施例を示す概略図、第10図及び第11図は、本
考案の体液処理回路用部材の使用例を示す概略図、第12
図は本考案の体液処理回路用部材の製造方法を示す概略
図である。第13図は従来の体液処理回路用部材及びその
使用例を示す概略図である。 図中、1、21は体液処理回路用部材、2、22は本体、
3、23、39は体液通路、4、8、12、24、32、38は融着部、
5、25は圧力検出部、6、26は体液ロ過部、7、27
は可とう性内管、9、29はフィルター、10、30は血液流
出管、11、31は血液流入管、13、33は脱気ライン、14、34
は圧力モニターライン、15、35は開口端部、37はトラッ
プキャップを示す。
FIG. 1 (a) is a schematic view showing a first embodiment of a member for body fluid treatment circuit of the present invention, and FIG. 1 (b) is an A- line in FIG. 1 (a).
Sectional view A, FIGS. 2 to 6 are schematic views showing another embodiment of FIG. 1, FIG. 7 is a schematic view showing a second embodiment of the body fluid treatment circuit member of the present invention, and FIG. FIG. 9 and FIG. 9 are schematic views showing another embodiment of FIG. 7, FIG. 10 and FIG. 11 are schematic views showing an example of use of the body fluid treatment circuit member of the present invention, and FIG.
The drawings are schematic views showing a method for manufacturing a body fluid treatment circuit member of the present invention. FIG. 13 is a schematic view showing a conventional body fluid treatment circuit member and an example of its use. In the figure, 1 and 21 are members for body fluid treatment circuit, 2 and 22 are main bodies,
3, 23, 39 are body fluid passages, 4, 8, 12, 24, 32, 38 are fusion-bonded parts,
5, 25 are pressure detecting parts, 6, 26 are body fluid filtration parts, 7, 27
Is a flexible inner tube, 9 and 29 are filters, 10 and 30 are blood outflow tubes, 11 and 31 are blood inflow tubes, 13 and 33 are deaeration lines, and 14 and 34
Is a pressure monitor line, 15 and 35 are open ends, and 37 is a trap cap.

Claims (2)

【実用新案登録請求の範囲】[Scope of utility model registration request] 【請求項1】体液処理回路に装着される体液処理回路用
部材であって、 硬質樹脂製の本体チューブの中間部に体液通路を残して
形成された第1の融着部と、 前記本体チューブの一端部に形成された第2の融着部
と、 該本体チューブの他端部に形成された第3の融着部と、 該第1の融着部と第2の融着部の間の空間部に配置さ
れ、一端部が前記第1の融着部に、他端部が前記第2の
融着部にそれぞれ固定されて圧力検出部を構成する内管
と、 前記第1の融着部と第3の融着部の間の空間部に配置さ
れ、前記第1の融着部または第3の融着部もしくは前記
本体チューブ内側に固定されて体液ロ過部を構成するメ
ッシュフィルターと、 前記第2の融着部に装着された圧力モニターラインと、 前記第2の融着部に装着されて前記第1の融着部と第2
の融着部の間の空間部に通じる体液誘導管と、 前記第3の融着部に装着されて前記第1の融着部と第3
の融着部の間の空間部に通じる体液誘導管と、 を有することを特徴とする体液処理回路用部材。
1. A body fluid treatment circuit member to be mounted in a body fluid treatment circuit, comprising: a first fusion-bonding portion formed by leaving a body fluid passage in an intermediate portion of a body tube made of hard resin; A second fusion-bonding part formed at one end of the body tube, a third fusion-bonding part formed at the other end of the body tube, and a space between the first fusion-bonding part and the second fusion-bonding part. An inner tube that is disposed in a space portion of the first end, is fixed to the first fusion-bonding portion at one end, and is fixed to the second fusion-bonding portion at the other end to form a pressure detection unit; A mesh filter that is arranged in a space between the attachment part and the third fusion part and is fixed to the inside of the first fusion part, the third fusion part, or the main body tube to form a body fluid filtration part. A pressure monitor line attached to the second fusing part, and a pressure monitor line attached to the second fusing part and the first fusing part Two
Body fluid guide tube that communicates with the space between the fusion-bonding parts, and the first fusion-bonding part and the third fusion-bonding part attached to the third fusion-bonding part.
A bodily fluid guide tube communicating with a space between the fusion-bonded parts of the bodily fluid treatment circuit member.
【請求項2】前記第3の融着部に代えて、本体チューブ
の異なる側の端部にキャップ部材を固着し、該キャップ
部材または第1の融着部もしくは第2の融着部にメッシ
ュフィルターを固定したことを特徴とする請求項1に記
載の体液処理回路用部材。
2. A cap member is fixed to different end portions of the main body tube in place of the third fusion-bonding portion, and the cap member or the first fusion-bonding portion or the second fusion-bonding portion is meshed. The body fluid treatment circuit member according to claim 1, wherein a filter is fixed.
JP1988092528U 1988-07-14 1988-07-14 Body fluid treatment circuit member Expired - Fee Related JPH0622352Y2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1988092528U JPH0622352Y2 (en) 1988-07-14 1988-07-14 Body fluid treatment circuit member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1988092528U JPH0622352Y2 (en) 1988-07-14 1988-07-14 Body fluid treatment circuit member

Publications (2)

Publication Number Publication Date
JPH0215152U JPH0215152U (en) 1990-01-30
JPH0622352Y2 true JPH0622352Y2 (en) 1994-06-15

Family

ID=31316963

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1988092528U Expired - Fee Related JPH0622352Y2 (en) 1988-07-14 1988-07-14 Body fluid treatment circuit member

Country Status (1)

Country Link
JP (1) JPH0622352Y2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9171857B2 (en) 2000-08-14 2015-10-27 Sandisk 3D Llc Dense arrays and charge storage devices

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5019943U (en) * 1973-06-23 1975-03-06

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6223488U (en) * 1985-07-26 1987-02-13
JPH041948Y2 (en) * 1986-06-20 1992-01-23

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9171857B2 (en) 2000-08-14 2015-10-27 Sandisk 3D Llc Dense arrays and charge storage devices
US9559110B2 (en) 2000-08-14 2017-01-31 Sandisk Technologies Llc Dense arrays and charge storage devices

Also Published As

Publication number Publication date
JPH0215152U (en) 1990-01-30

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