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JPH06114103A - Chamber for blood circuit - Google Patents

Chamber for blood circuit

Info

Publication number
JPH06114103A
JPH06114103A JP3240210A JP24021091A JPH06114103A JP H06114103 A JPH06114103 A JP H06114103A JP 3240210 A JP3240210 A JP 3240210A JP 24021091 A JP24021091 A JP 24021091A JP H06114103 A JPH06114103 A JP H06114103A
Authority
JP
Japan
Prior art keywords
blood
chamber
cylindrical body
floating
cap
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
JP3240210A
Other languages
Japanese (ja)
Other versions
JP2519140B2 (en
Inventor
Hisamori Endo
久衛 遠藤
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP3240210A priority Critical patent/JP2519140B2/en
Publication of JPH06114103A publication Critical patent/JPH06114103A/en
Application granted granted Critical
Publication of JP2519140B2 publication Critical patent/JP2519140B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3672Means preventing coagulation
    • A61M1/3673Anticoagulant coating, e.g. Heparin coating
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • A61M1/3627Degassing devices; Buffer reservoirs; Drip chambers; Blood filters

Landscapes

  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • External Artificial Organs (AREA)

Abstract

PURPOSE:To prevent the contact of the blood with the air layer in the upper space within a chamber for a blood circuit and to decrease the usage of the heparin to be injected into the blood by providing a floating cap within the cylindrical body of the chamber for the blood circuit provided with a blood inflow port and blood outflow port in the lower part of the cylindrical body. CONSTITUTION:The floating cap 56 provided freely movably upward and downward within the cylindrical body 43 is constituted by integrally molding a cap plate 57 having a diameter to the extent of forming a spacing in the inside wall of the cylindrical body 43 and a shaft cylinder 58 projecting upward from the central part. A wire 59 supporting the floating cap 56 is hung from the central part of the inside surface of an end plate 52 and is inserted in the shaft cylinder 58 to freely vertically movably hold the floating cap 56. The bottom end of the wire is provided with a stopper 60. The blood 61 admitted into the cylindrical body 43 from below by a pump pressure rises in the space 49 and bypasses the upper part of a partition wall 51. After the blood is filtered by a filter net 90, the blood flows out of the cylindrical body 43 from below. The floating cap 56 keeps floating while moving upward and downward on the liquid level to prevent the contact of the blood 61 with the air layer 64 in the upper space 63.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、人工腎臓用血液回路、
人工肝臓用血液回路、その他の血液回路に使用するチェ
ンバーに関するものである。
BACKGROUND OF THE INVENTION The present invention relates to a blood circuit for artificial kidney,
The present invention relates to a blood circuit for an artificial liver and a chamber used for other blood circuits.

【0002】[0002]

【従来の技術】血液透析時には、血液回路中で血液凝固
が生じないよにヘパリンが注入されているので、患者の
体内にヘパリン化された血液が送り込まれる。そのた
め、透析終了後に患者がけがなどをして出血するような
ことがあると、血液が直ぐに凝固しなくなるので、透析
終了直後に、患者にプロタミンを注入して、血液のヘパ
リン化を解消させる手当がなされている。また近年長期
透析患者の増加に伴い、ヘパリンアレルギーを来す症例
のあることが報告されいる。このような事情から、血液
回路には、ヘパリンの使用量を少なくできるものが要望
されている。
2. Description of the Related Art At the time of hemodialysis, heparin is injected so that blood coagulation does not occur in a blood circuit, so that heparinized blood is sent into the body of a patient. Therefore, if the patient may injure or bleed after dialysis, the blood will not immediately clot, and immediately after dialysis, protamine will be injected into the patient to help heparinize the blood. Has been done. In addition, it has been reported that there have been cases of heparin allergy with the increase in long-term dialysis patients. Under such circumstances, there is a demand for a blood circuit that can reduce the amount of heparin used.

【0003】従来の人工腎臓用血液回路には、図8に示
すように患者の静脈から血液を抽出して透析装置へ導く
動脈回路1と、透析装置を経て透析された血液を患者の
静脈へ送り込む静脈回路2からなり、動脈チェンバー本
体3と、静脈チェンバー本体4とを、それらに取付けら
れている吊下具5、6によって透析装置、血液ポンプ、
ヘパリン注入機、患者などより上方の位置に吊り下げ、
チェンバー本体3に接続されている血液流入チューブ7
を針11を介して患者の動脈へ接続し、チェンバー本体
3に接続されている血液流出チューブ9をコネクタ12
を介して透析装置の入口へ接続し、チェンバー本体4に
接続されている血液流入チューブ8をコネクタ13を介
して透析装置の出口へ接続し、チェンバー本体4に接続
されている血液流出チューブ10を針14を介して患者
の静脈へ接続するように構成されたものが使用されるて
いる。
In a conventional blood circuit for an artificial kidney, as shown in FIG. 8, an arterial circuit 1 for extracting blood from a patient's vein and guiding it to a dialysis machine, and blood dialyzed through the dialysis machine to the patient's vein. The arterial chamber main body 3 and the venous chamber main body 4 are composed of the feeding venous circuit 2, and the dialysis device, blood pump, and
Suspend above the heparin infusion machine, patient, etc.,
Blood inflow tube 7 connected to chamber body 3
To the patient's artery via a needle 11 and connect the blood outflow tube 9 connected to the chamber body 3 to a connector 12
The blood inflow tube 8 connected to the inlet of the dialyzer via the connector, and the blood inflow tube 8 connected to the chamber body 4 to the outlet of the dialyzer via the connector 13, and the blood outflow tube 10 connected to the chamber body 4. It is used that is configured to connect to a patient's vein via needle 14.

【0004】[0004]

【考案が解決しようとする課題】上記従来の人工腎臓血
液回路において、チェンバー本体3、4の上端に血液流
入チューブ7、8を接続し、チェンバー本体3、4の下
端に血液流出チューブ9、10を接続してなるチェンバ
ーを使用したものには、チェンバー本体3、4内の液面
に対して血液が上方から落下するため、その衝撃で気泡
が発生しやすいという欠点がある。
In the above-mentioned conventional artificial kidney blood circuit, blood inflow tubes 7 and 8 are connected to the upper ends of the chamber bodies 3 and 4, and blood outflow tubes 9 and 10 are connected to the lower ends of the chamber bodies 3 and 4. The one using the chamber connected to the above has a drawback in that blood is likely to be generated due to the impact because blood drops from above against the liquid surface in the chamber main bodies 3 and 4.

【0005】この欠点を解決する考案の一例として、実
公昭58−26655公報に記載されているようにチェ
ンバー本体の下端に血液流入チューブと血液流出チュー
ブとを接続する考案がある。この考案では、血液の流入
口と流出口が液面下に位置するため、チェンバー本体内
での気泡の発生を防止でき、外部から気泡が混入する場
合には、気泡の浮き方向が血液の流入方向に一致するた
め、気泡をチェンバー本体内の上方空間の空気層へ効率
よく排出できる利点がある。その反面、チェンバー本体
内で血液が流入口から流出口へ流動している過程におい
て、血液の液面がチェンバー本体内の上方空間の空気層
に触れて、血液凝固が生じやすいという欠点がある。
As an example of a device for solving this drawback, there is a device for connecting a blood inflow tube and a blood outflow tube to the lower end of a chamber body as described in Japanese Utility Model Publication 58-26655. In this device, since the blood inlet and the blood outlet are located below the liquid surface, it is possible to prevent the generation of bubbles in the chamber body, and when the bubbles are mixed from the outside, the floating direction of the bubbles is the inflow direction of the blood. Since they are aligned in the direction, there is an advantage that bubbles can be efficiently discharged to the air layer in the upper space in the chamber body. On the other hand, in the process of blood flowing from the inflow port to the outflow port in the chamber body, the liquid surface of the blood comes into contact with the air layer in the upper space in the chamber body, and blood coagulation easily occurs.

【0006】そこで、チェンバー本体内で血液の液面に
生理用食塩水を浮かせて、血液がチェンバー本体内の上
方空間の空気層に触れるのを防ぐことも行われている。
この場合には、血液はその比重に個人差があり、その比
重よりも軽い食塩水を使用しないと血液と混じり合って
しまうため、食塩水の調製に手間がかかり、またチェン
バー本体内で血液の液面に食塩水を浮かせるように操作
するのは大変面倒であるなどの欠点がある。本発明は、
上記のような諸欠点を解消しうる血液回路用チェンバー
を提供することを目的とするものである。
Therefore, it is also practiced to float the physiological saline solution on the surface of the blood in the chamber body to prevent the blood from coming into contact with the air layer in the upper space in the chamber body.
In this case, there are individual differences in the specific gravity of the blood, and unless saline that is lighter than that specific gravity is used, it mixes with the blood. There are drawbacks such as it is very troublesome to operate so that the saline solution floats on the liquid surface. The present invention is
It is an object of the present invention to provide a blood circuit chamber capable of eliminating the above-mentioned various drawbacks.

【0007】[0007]

【課題を解決するための手段】上記の目的を達成するた
めに、本発明は、筒状本体の下部に血液流入口と血液流
出口とを設けてなる血液回路用チェンバーにおいて、筒
状本体の内部に、浮蓋を設けることにより構成すること
を特徴とするものである。
To achieve the above object, the present invention provides a blood circuit chamber in which a blood inlet and a blood outlet are provided in a lower portion of a tubular body. It is characterized in that it is configured by providing a floating lid inside.

【0008】[0008]

【作用】上記の構成よりなる血液回路用チェンバーで
は、チェンバー本体内で血液が血液流入口から血液流出
口へ流動している過程において、浮蓋が常に液面に浮上
し続け、液面がチェンバー本体内の上方空間の空気層に
触れるのを防ぐ。なお、外部で血液に気泡が混入して、
チェンバー本体内に流入して来た場合には、その気泡
は、血液の流れに乗って上昇し、浮蓋とチェンバー本体
の間の隙間を通って浮蓋より上の空気層へと排出され
る。
In the chamber for a blood circuit having the above-described structure, in the process in which blood flows from the blood inlet to the blood outlet in the chamber main body, the floating lid always keeps floating on the liquid surface, and the liquid surface is kept in the chamber. Prevents contact with the air space above the body. In addition, when air bubbles are mixed in the blood,
When flowing into the chamber body, the bubbles rise along with the blood flow and are discharged to the air layer above the floating lid through the gap between the floating lid and the chamber body. .

【0009】[0009]

【実施例】以下図1ないし図7にもとづいて本発明の実
施例を説明すると、図1において、15は人工腎臓用血
液回路の動脈回路を示し、これは、動脈チェンバー16
の下端に血液流入口17と、血液流出口18とを設け、
上端に吊り輪19と、レベル調整ライン20と、圧力モ
ニターライン21とを接続し、血液流入口17には、血
液流入チューブ22の一端を接続し、血液流出口18に
は、血液流出チューブ23の一端を接続し、チューブ2
2の他端には、針23を取付けるためのシャント継手2
4を接続し、チューブ23の他端には、透析装置の入口
に接続するためのコネクタ25を接続し、チューブ22
の途中には、血液ポンプによって押圧されるポンプ作用
管26、補液ライン27、ヘパリンライン28、採血及
び混注用ゴム管29をそれぞれ接続してなる。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described below with reference to FIGS. 1 to 7. In FIG. 1, reference numeral 15 represents an arterial circuit of a blood circuit for an artificial kidney, which is an arterial chamber 16.
A blood inlet 17 and a blood outlet 18 at the lower end of
A suspension ring 19, a level adjustment line 20, and a pressure monitor line 21 are connected to the upper end, one end of a blood inflow tube 22 is connected to the blood inflow port 17, and a blood outflow tube 23 is connected to the blood outflow port 18. Connect one end of the tube 2
At the other end of 2, the shunt joint 2 for attaching the needle 23
4 and the connector 25 for connecting to the inlet of the dialysis machine is connected to the other end of the tube 23.
A pump action tube 26 pressed by a blood pump, a replacement fluid line 27, a heparin line 28, and a blood collection and mixed injection rubber tube 29 are connected in the middle of the process.

【0010】図1において、30は人工腎臓用血液回路
の静脈回路を示し、これは、静脈チェンバー31の下端
に血液流入口32と、血液流出口33とを設け、上端に
吊り輪34と、レベル調整ライン35と、圧力モニター
ライン36とを接続し、血液流入口32には、血液流入
チューブ37の一端を接続し、血液流出口33には、血
液流出チューブ38の一端を接続し、チューブ37の他
端には、透析装置の出口に接続するためのコネクタ39
を接続し、チューブ38の他端には、針40を取付ける
ためのシャント継手41を接続し、チューブ38の途中
には、採血及び混注用ゴム管42を接続してなる。
In FIG. 1, reference numeral 30 denotes a venous circuit of a blood circuit for an artificial kidney, which is provided with a blood inlet 32 and a blood outlet 33 at a lower end of a vein chamber 31 and a hanging ring 34 at an upper end. The level adjustment line 35 and the pressure monitor line 36 are connected to each other, one end of a blood inflow tube 37 is connected to the blood inflow port 32, and one end of a blood outflow tube 38 is connected to the blood outflow port 33. At the other end of 37 is a connector 39 for connecting to the outlet of the dialysis machine.
, A shunt joint 41 for attaching the needle 40 is connected to the other end of the tube 38, and a blood collection and mixed injection rubber tube 42 is connected in the middle of the tube 38.

【0011】図2及び図3には、動脈チェンバー16
と、静脈チェンバー31の一実施例が示してあり、その
説明をすると、43は筒状本体、44は筒状本体43の
下端を液密に遮閉する端板で、その外面には、血液流入
口45と、血液流出口46を設けて、血液流入チューブ
47と、血液流出チューブ48をそれぞれ接続し、端板
44の内面には、筒状本体43内の下端から適当な高さ
に至る空間を、血液流入口45と連通する空間49と、
血液流出口46と連通する空間50とに区分する隔壁5
1を設けてある。89は血液流出口46と連通するよう
に端板44の内面から突出するように設けた血液排出パ
イプ、90はこの血液排出パイプ89に被せた濾過網9
0で、筒状本体43を動脈チェンバー16の筒状本体と
して使用する場合には、血液排出パイプ89と濾過網9
0を省くこともある。52は筒状本体43の上端を液密
に遮閉する端板で、外面には、レベル調整ライン20、
35の接続口53と、圧力モニターライン21、36の
接続口54とを設けるとともに、吊り輪55を接続して
ある。56は筒状本体43内に昇降自在に設けた浮蓋
で、これは、シリコン、テフロンなど抗凝固性の材質を
用いて、筒状本体43の内壁との間に隙間を形成する程
度の径を有する蓋板57と、その中心部から上向きに突
出する軸筒58とを一体成形してなる。59は浮蓋56
を支持する針金で、端板52の内面中心部から吊り下
げ、軸筒58に挿通して、浮蓋56を昇降自在に支持
し、下端には、浮蓋56を受け止めるストッパー60を
設けてある。
2 and 3, the arterial chamber 16 is shown.
An example of the vein chamber 31 is shown. The description will be made with reference to 43. The reference numeral 43 denotes a tubular body, 44 denotes an end plate for liquid-tightly closing the lower end of the tubular body 43, and the outer surface of An inflow port 45 and a blood outflow port 46 are provided to connect a blood inflow tube 47 and a blood outflow tube 48, respectively, and the inner surface of the end plate 44 reaches an appropriate height from the lower end of the tubular main body 43. A space 49 communicating the space with the blood inlet 45,
Partition wall 5 which is divided into a space 50 communicating with the blood outlet 46
1 is provided. Reference numeral 89 is a blood discharge pipe provided so as to project from the inner surface of the end plate 44 so as to communicate with the blood outlet 46, and 90 is a filter net 9 covering the blood discharge pipe 89.
0, when the tubular body 43 is used as the tubular body of the arterial chamber 16, the blood drainage pipe 89 and the filter mesh 9 are used.
Sometimes 0 is omitted. Reference numeral 52 is an end plate that liquid-tightly closes the upper end of the cylindrical main body 43, and the level adjustment line 20,
A connection port 53 of 35 and a connection port 54 of the pressure monitor lines 21 and 36 are provided, and a suspension ring 55 is connected. Reference numeral 56 denotes a floating lid provided in the cylindrical main body 43 so as to be able to move up and down. The floating lid 56 is made of an anticoagulant material such as silicon or Teflon, and has a diameter such that a gap is formed between the inner wall of the cylindrical main body 43. A lid plate 57 having a groove and a shaft cylinder 58 projecting upward from its center are integrally formed. 59 is a floating lid 56
A wire for supporting the floating plate 56 is hung from the center of the inner surface of the end plate 52 and inserted into the shaft cylinder 58 to support the floating lid 56 so that the floating lid 56 can move up and down. A stopper 60 for receiving the floating lid 56 is provided at the lower end. .

【0012】この実施例では、ポンプ圧により血液流入
チューブ47を通って筒状本体43内へ下から流入した
血液61は、空間49内を上昇し、隔壁51の上方を迂
回して、濾過網90で濾過された後、血液排出パイプ8
9内に流入し、筒状本体43の下から血液流出チューブ
48を通って流出する。その過程で、浮蓋56が液面6
2にその変位に応じて昇降しながら浮上し続けて、血液
61が筒状本体43内の上方空間63の空気層64に触
れるのを防ぐ。なお、筒状本体43内に流入した血液6
1に気泡が混入して来る場合は、その気泡が血液61の
上昇流によって筒状本体43の上方へ運ばれ、血液61
が隔壁51の上方を迂回する過程で、上記気泡の全てが
筒状本体43の内壁と浮蓋56の間の隙間を通過し、空
気層64内へ排出されるので、筒状本体43から流出す
る血液61に上記気泡が混入することはない。
In this embodiment, the blood 61 flowing from below into the tubular main body 43 through the blood inflow tube 47 by the pump pressure rises in the space 49 and bypasses the upper part of the partition wall 51 to bypass the filter mesh. Blood drain pipe 8 after being filtered at 90
9 and flows out from below the tubular body 43 through the blood outflow tube 48. In the process, the floating lid 56 moves to the liquid surface 6
2 keeps ascending and descending according to the displacement and continues to float to prevent the blood 61 from touching the air layer 64 in the upper space 63 in the tubular body 43. The blood 6 that has flowed into the tubular body 43
When air bubbles are mixed in 1, the air bubbles are carried to the upper side of the cylindrical main body 43 by the ascending flow of the blood 61, and the blood 61
In the process of bypassing above the partition wall 51, all of the bubbles pass through the gap between the inner wall of the tubular body 43 and the floating lid 56 and are discharged into the air layer 64, so that they flow out from the tubular body 43. The bubbles do not mix with the blood 61 to be discharged.

【0013】上記実施例では、隔壁51を、図2に示す
ように下端部を厚くし、上端に至るにつれて徐々に薄く
なるように成形することもあり、また上下両端で同一の
厚さを有するように成形することもある。また隔壁51
の両側面を平面に成形することもあり、凹面に成形する
ここともある。また隔壁51は、図3に示すようにその
両側縁65、66と筒状本体43の内壁の間に隙間6
7、68を有するように成形し、あるいは両側縁65、
66のどちらか一方と筒状本体43の内壁の間に隙間6
7又は68を有するように成形して、透析終了後、筒状
本体43内に残留する血液61を患者の身体に返血する
際に、筒状本体43を少し傾けるだけで空間49内の血
液61を空間50内へ容易に回収できるように構成する
こともあり、隙間67、68を省いて、隔壁51の両側
縁65、66を筒状本体43の内壁に密着させるように
成形することもある。また血液流入口45と血液流出口
46は、それらの内側の口縁に血液61が残留するのを
防ぐため、図2に示すようにテーパー69、70を付し
て成形することもある。また血液流入口45の口径を血
液流出口46の口径よりも小さく成形し、血液61の流
入速度を速くするとともに、流出速度を遅くして、流入
血液中に気泡が混入した場合、それを筒状本体43内の
空気層64へ送り込みやすくすることもある。
In the above embodiment, the partition wall 51 may be formed such that the lower end portion is thicker and gradually becomes thinner toward the upper end as shown in FIG. 2, and the upper and lower ends have the same thickness. It may be molded as follows. Also, the partition wall 51
Both side surfaces may be formed into a flat surface or may be formed into a concave surface. Further, as shown in FIG. 3, the partition wall 51 has a gap 6 between both side edges 65, 66 and the inner wall of the cylindrical main body 43.
7, 68, or both side edges 65,
A gap 6 is formed between either one of the 66 and the inner wall of the tubular main body 43.
7 or 68, and when blood 61 remaining in the tubular body 43 is returned to the patient's body after dialysis is completed, the blood in the space 49 can be simply tilted. 61 may be configured to be easily recovered in the space 50, or the side walls 65 and 66 of the partition wall 51 may be formed so as to be in close contact with the inner wall of the cylindrical main body 43 by omitting the gaps 67 and 68. is there. The blood inflow port 45 and the blood outflow port 46 may be formed with tapers 69 and 70 as shown in FIG. 2 in order to prevent the blood 61 from remaining on the inner edges thereof. Further, the diameter of the blood inflow port 45 is formed smaller than that of the blood outflow port 46 to increase the inflow speed of the blood 61 and decrease the outflow speed, and when bubbles are mixed in the inflow blood, the In some cases, it may be easier to send the air to the air layer 64 in the body 43.

【0014】図4及び図5には、動脈チェンバー16と
静脈チェンバー31の別の実施例が示してあり、この実
施例は、前記実施例における隔壁51の代わりに血液の
濾過性能に優れた二重濾過器を設け、それ以外の部分
は、前記実施例と同様に構成するものであるから、二重
濾過器に関連する構成について説明すると、71は端板
44の内面から直立するように固定した二重濾過器で、
これは、上枠板72と下枠板73の両端を縦枠板74、
75でそれぞれ結合し、これらの枠板によって囲まれた
空間を左右の個室76、77に仕切る仕切壁78を設
け、下枠板73のうち仕切壁78の両側部分には、血液
流入口45と個室76に連通する通孔79と、血液流出
口46と個室77に連通する通孔80を設け、各個室7
6、77には、開口部81、82を設け、この各開口部
81、82には、濾過網83、84を張設してなる。8
5は端板44の内面において、血液流入口45及び血液
流出口46を取り囲み、かつ下枠板73を嵌合しうる形
状に成形した溝で、この溝85に下枠板73を嵌合固定
することにより、二重濾過器71を端板44の内面から
直立させてある。
4 and 5 show another embodiment of the arterial chamber 16 and the venous chamber 31. In this embodiment, instead of the partition wall 51 in the above-mentioned embodiment, a superior blood filtering performance is obtained. Since a double filter is provided and the other parts are configured in the same manner as in the above-described embodiment, the configuration related to the double filter will be described. 71 is fixed so as to stand upright from the inner surface of the end plate 44. With a double filter
This is because both ends of the upper frame plate 72 and the lower frame plate 73 are vertical frame plates 74,
A partition wall 78 is provided for partitioning the space enclosed by these frame plates into left and right individual chambers 76, 77, respectively, at both sides of the partition wall 78 of the lower frame plate 73. A through hole 79 that communicates with the individual chamber 76 and a through hole 80 that communicates with the blood outlet 46 and the individual chamber 77 are provided.
6, 77 are provided with openings 81, 82, and filtration meshes 83, 84 are stretched over the openings 81, 82, respectively. 8
Reference numeral 5 denotes a groove formed on the inner surface of the end plate 44 so as to surround the blood inlet 45 and the blood outlet 46 and to which the lower frame plate 73 can be fitted. The lower frame plate 73 is fixedly fitted in the groove 85. By doing so, the double filter 71 is erected from the inner surface of the end plate 44.

【0015】この実施例では、血液61は、血液流入チ
ューブ47、血液流入口45、通孔79、個室76、濾
過網83の順に通過し、濾過網83によって濾過され
て、筒状本体43内へ流入し、その液面62に浮蓋56
が浮上する。上記のように筒状本体43内へ流入した血
液61は、濾過網84で再度濾過された後、個室77、
通孔79、血液流出口46、血液流出チューブ48の順
に通過し、筒状本体43外へ流出する。
In this embodiment, the blood 61 passes through the blood inflow tube 47, the blood inflow port 45, the through hole 79, the private chamber 76, and the filter net 83 in this order, and is filtered by the filter net 83 to be stored in the tubular body 43. Flow into the liquid surface 62 and the floating lid 56
Emerges. The blood 61 that has flowed into the tubular main body 43 as described above is filtered again by the filter net 84, and then the private chamber 77,
It passes through the through hole 79, the blood outlet 46, and the blood outflow tube 48 in this order, and flows out of the cylindrical main body 43.

【0016】本発明は、上記各実施例に限定されるもの
ではなく、人工肝臓用血液回路、その他の血液回路のチ
ェンバーとしても実施しうる。また浮蓋56は、抗凝固
性の材質以外の各種材質で成形することもある。また浮
蓋56は、針金59で昇降自在に支持する代わりに、端
板52から吊り下げた糸を浮蓋56に挿通し、あるいは
浮蓋56に結び付けることにより昇降自在に支持するこ
ともあり、あるいは何ら支持部で支持することなく、単
に筒状本体内へ昇降自在に差し入れるともあり、あるい
は図6に示すように筒状本体43にその上方部分の内壁
を拡径した拡径部86を設け、この拡径部86に浮蓋5
6を嵌合させて、浮蓋56を昇降自在に支持することも
あり、あるいは図7に示すように筒状本体43の上方部
分の内面に垂直なガイドレール87、87を設け、この
ガイドレール87、87に浮蓋56に設けた係合凹部8
8、88又は係合孔を係合させて、浮蓋56を昇降自在
に支持することもあり、その他各種の手段により昇降自
在に支持することもある。
The present invention is not limited to the above-mentioned embodiments, but may be implemented as a blood circuit for an artificial liver or a chamber for other blood circuits. The floating lid 56 may be formed of various materials other than the anticoagulant material. Further, the floating lid 56 may be supported so as to be able to move up and down by inserting a thread suspended from the end plate 52 into the floating lid 56 or by tying it to the floating lid 56, instead of supporting the floating lid 56 so as to be able to move up and down. Alternatively, it may be simply inserted vertically into the tubular body without being supported by any supporting portion, or as shown in FIG. 6, the tubular body 43 may be provided with an enlarged diameter portion 86 in which the inner wall of the upper portion is enlarged. The floating lid 5 is provided on the expanded diameter portion 86.
6 may be fitted to support the floating lid 56 so as to be able to move up and down, or as shown in FIG. 7, guide rails 87, 87 that are perpendicular to the inner surface of the upper portion of the cylindrical main body 43 are provided. 87, 87 engaging recesses 8 provided on the floating lid 56
The floating lid 56 may be supported so as to be able to move up and down by engaging with 8, 88 or the engaging holes, or may be supported so as to be able to move up and down by various other means.

【0017】[0017]

【発明の効果】本発明は、叙上のように構成したから、
筒状本体内で下方の血液流入口から流入し、下方の血液
流出口に向かって流動する血液の液面に浮蓋が常に浮上
して、血液が筒状本体内の上方空間の空気層に触れるの
を防ぐため、使用上の手間はかからず、血液を筒状本体
内で空気層に触れさせることなく流すことができる。し
かも、筒状本体内での気泡の発生を防ぐことができ、ま
た外部から気泡が血液に混入して来る場合には、その気
泡の全てを血液の上昇流によって液面へ運び、筒状本体
の内壁と浮蓋の間の隙間から空気層へ排出できる。その
ため、血液回路の使用中に、チェンバー本体内で血液凝
固を生じるおそれは殆どなくなり、したがって従来の血
液回路用チェンバーに比し、ヘパリンの使用量を極端に
減らすことができ、ヘパリンアレルギーの発生を防止で
きる血液回路用チェンバーを提供することができる。
Since the present invention is constructed as described above,
The floating lid always floats on the surface of the blood flowing from the lower blood inlet into the tubular body and flowing toward the lower blood outlet, so that the blood is deposited in the air space in the upper space inside the tubular body. In order to prevent the touch, it is easy to use and the blood can flow in the tubular body without touching the air layer. Moreover, it is possible to prevent the formation of bubbles in the tubular body, and when bubbles come into the blood from the outside, carry all of the bubbles to the liquid surface by the upward flow of blood, and It can be discharged to the air layer through the gap between the inner wall of the and the floating lid. Therefore, there is almost no risk of blood coagulation in the chamber body during use of the blood circuit, and therefore, compared to the conventional blood circuit chamber, the amount of heparin used can be extremely reduced, and the occurrence of heparin allergy can be prevented. A blood circuit chamber that can be prevented can be provided.

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

【図1】図1は本発明に係る血液回路用チェンバーが組
み込まれた人工腎臓用血液回路の説明図である。
FIG. 1 is an explanatory view of a blood circuit for artificial kidney in which a chamber for blood circuit according to the present invention is incorporated.

【図2】図2は本発明に係る血液回路用チェンバーの一
例を示す断面図である。
FIG. 2 is a sectional view showing an example of a blood circuit chamber according to the present invention.

【図3】図3は図2のA−A線断面図である。3 is a cross-sectional view taken along the line AA of FIG.

【図4】図4は本発明に係る血液回路用チェンバーの別
の例を示す断面図である。
FIG. 4 is a cross-sectional view showing another example of the blood circuit chamber according to the present invention.

【図5】図5は図4のB−B線断面図である。5 is a sectional view taken along line BB of FIG.

【図6】図6は浮蓋の支持部の変更例を説明する図であ
る。
FIG. 6 is a diagram illustrating a modified example of a support portion of a floating lid.

【図7】図7は浮蓋の支持部のさらに別の変更例を説明
する図である。
FIG. 7 is a diagram illustrating still another modification of the support portion of the floating lid.

【図8】図8は従来の血液回路用チェンバーが組み込ま
れた人工腎臓用血液回路の説明図である。
FIG. 8 is an explanatory diagram of a blood circuit for an artificial kidney in which a conventional blood circuit chamber is incorporated.

【符号の説明】[Explanation of symbols]

43…筒状本体、45…血液流入口、46…血液流出
口、56…浮蓋。
43 ... Cylindrical body, 45 ... Blood inlet, 46 ... Blood outlet, 56 ... Float.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 筒状本体の下部に血液流入口と血液流出
口とを設けてなる血液回路用チェンバーにおいて、筒状
本体の内部に、浮蓋を設けることを特徴とする血液回路
用チェンバー。
1. A blood circuit chamber in which a blood inlet and a blood outlet are provided in a lower portion of a tubular body, wherein a floating lid is provided inside the tubular body.
【請求項2】 筒状本体の内部に、浮蓋を昇降自在に支
持する支持部を設けてなる請求項1記載の血液回路用チ
ェンバー。
2. The blood circuit chamber according to claim 1, wherein a support portion that supports the floating lid so as to be able to move up and down is provided inside the tubular main body.
JP3240210A 1991-08-28 1991-08-28 Blood circuit chamber Expired - Lifetime JP2519140B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3240210A JP2519140B2 (en) 1991-08-28 1991-08-28 Blood circuit chamber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3240210A JP2519140B2 (en) 1991-08-28 1991-08-28 Blood circuit chamber

Publications (2)

Publication Number Publication Date
JPH06114103A true JPH06114103A (en) 1994-04-26
JP2519140B2 JP2519140B2 (en) 1996-07-31

Family

ID=17056094

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3240210A Expired - Lifetime JP2519140B2 (en) 1991-08-28 1991-08-28 Blood circuit chamber

Country Status (1)

Country Link
JP (1) JP2519140B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999066972A1 (en) * 1998-06-25 1999-12-29 Edwards Lifesciences Corporation Chamber for extracorporeal circuit
EP1053760A3 (en) * 1999-05-21 2001-08-16 Medtronic, Inc. Fully constrained soft shell reservoir
JP2005211513A (en) * 2004-01-30 2005-08-11 Terumo Corp In vitro circulating device
JP2008036327A (en) * 2006-08-10 2008-02-21 Sophia Kai Miyata Naika Iin Drip chamber for pressure monitoring

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999066972A1 (en) * 1998-06-25 1999-12-29 Edwards Lifesciences Corporation Chamber for extracorporeal circuit
EP1053760A3 (en) * 1999-05-21 2001-08-16 Medtronic, Inc. Fully constrained soft shell reservoir
JP2005211513A (en) * 2004-01-30 2005-08-11 Terumo Corp In vitro circulating device
JP2008036327A (en) * 2006-08-10 2008-02-21 Sophia Kai Miyata Naika Iin Drip chamber for pressure monitoring

Also Published As

Publication number Publication date
JP2519140B2 (en) 1996-07-31

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