JPH06233813A - Hemocatharsis system - Google Patents

Hemocatharsis system

Info

Publication number
JPH06233813A
JPH06233813A JP5024053A JP2405393A JPH06233813A JP H06233813 A JPH06233813 A JP H06233813A JP 5024053 A JP5024053 A JP 5024053A JP 2405393 A JP2405393 A JP 2405393A JP H06233813 A JPH06233813 A JP H06233813A
Authority
JP
Japan
Prior art keywords
filtrate
pump
blood
container
weight
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.)
Pending
Application number
JP5024053A
Other languages
Japanese (ja)
Inventor
Heihachi Fujii
平八 藤井
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.)
Ube Corp
Original Assignee
Ube Industries 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 Ube Industries Ltd filed Critical Ube Industries Ltd
Priority to JP5024053A priority Critical patent/JPH06233813A/en
Publication of JPH06233813A publication Critical patent/JPH06233813A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a small-sized system easy to handle for performing the gradual body fluid regulation therapy by changing the revolving speed of a filtering pump to adjust the filtrate quantity so that the filtrate quantification unit weight is practically made equal to the set weight. CONSTITUTION:A replenishing fluid container 7, a dialyzing fluid container 8, and a filtrate container 9 are mounted on a filtrate quantification unit 10, the total weight is measured, and it is used for the control index of the revolving speed of a filtering pump 2 as the set value. The venous blood is mixed with an anticoagulant, and the mixture is guided into a homocatharisis device 6 by a pump 5 via a connecting tube 13. The feed of the dialyzing fluid in the dialyzing fluid container 8 is started by a pump 3. The blood guided into the homocatharisis device 6 is dialyzed and filtered by the pump 2, and it is guided into a communicating tube 14 and stored in the filtrate container 9 on the filtrate quantification unit 10. The revolving speed of the pump is controlled by the signal from the filtrate quantification unit 10, and the balance among the replenishing fluid quantity, dialyzing fluid quantity, and filtrate quantity is maintained.

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、静脈より脱血した血液
を血液浄化器に導入し、水分、代謝産物、電解質等を濾
過分離し、生体の腎機能を代行する血液浄化装置に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a blood purifying apparatus which introduces blood removed from a vein into a blood purifier and filters and separates water, metabolites, electrolytes and the like to substitute for the renal function of a living body.

【0002】[0002]

【従来の技術】従来より、血液浄化法として、全血交
換、血漿交換、血液吸着、血液透析、血液濾過、血液透
析濾過、腹膜透析などが広く臨床に応用されている。し
かし、急性腎不全、心疾患に伴う腎機能低下等を発症し
ている患者に対しては、その循環状態の悪化から上記の
ような血液浄化法を適用することが困難なことがある。
そこで生体の腎臓の濾過機能を代行する血液浄化法とし
て、新たに緩徐体液調整治療法が提案されている。この
緩徐体液調整治療法は、上記の重症の患者に適用される
方法であるため、主にICU、CCU等に於ける治療に
用いられている。
2. Description of the Related Art Conventionally, as blood purification methods, whole blood exchange, plasma exchange, blood adsorption, hemodialysis, hemofiltration, hemodiafiltration, peritoneal dialysis and the like have been widely applied clinically. However, it may be difficult to apply the above-mentioned blood purification method to a patient who has developed acute renal failure, decreased renal function associated with heart disease, or the like because of deterioration of the circulatory condition.
Therefore, as a blood purification method that acts as a substitute for the filtration function of the kidney of the living body, a slow body fluid adjustment treatment method has been newly proposed. Since this slow body fluid adjustment treatment method is a method applied to the above-mentioned severely ill patients, it is mainly used for treatment in ICU, CCU and the like.

【0003】[0003]

【本発明の解決すべき課題】しかしながら、ICU、C
CU等に入室する患者は、前記のように合併症を持つ者
が多いため、それらの患者への治療は単一の手段では行
い得ず、患者のベッドサイドには多くの治療器具が設置
されることとなり、このため、ICU、CCU等で使用
される治療器具には、性能が優れていることはもとよ
り、可能な限り小型であること、取り扱いが容易である
ことなどが要求される。
However, ICU, C
As many patients who enter the CU etc. have complications as described above, it is not possible to treat them with a single means, and many treatment devices are installed at the bedside of the patient. For this reason, therapeutic instruments used in ICU, CCU, etc. are required to have not only excellent performance but also be as small as possible and easy to handle.

【0004】しかしながら、従来、ICU、CCU等で
の緩徐体液調整治療法の実施に於いては、血液ポンプ、
濾液ポンプ、薬剤注入ポンプなどを単体で使用していた
ため、ベッドサイドの空間の多くがこれらの機器で占め
られることとなり、医師等が治療のため自由に行動し得
ない状況となっている。
However, in the conventional practice of the slow body fluid adjustment therapy in ICU, CCU, etc., a blood pump,
Since the filtrate pump, the drug infusion pump, etc. were used alone, most of the bedside space was occupied by these devices, and doctors etc. could not act freely for treatment.

【0005】更に、緩徐体液調整治療法では、血液浄化
器により濾過された濾液量に応じて、補液(輸液)を行
う必要があり、濾液量が変動する場合、それに連動して
補液量を調整しなければならず、それでなくても繁忙な
治療現場に於いて、それに携わる人々に更なる負担を強
いることとなる。又、この種の治療機器に一般に用いら
れているローラーポンプは、ポンプ回転数は一定であっ
ても、濾液側の圧力の変動により、例えば、設定値を越
えて圧力が高くなれば、ポンプチューブが通常より膨ら
むことにより濾液量が増加する現象がみられ、この濾液
量の変動は検出することが困難であるため、濾液量と補
液量との均衡が崩れ、治療上重大な問題を引き起こす危
険性がある。
Further, in the slow body fluid adjusting treatment method, it is necessary to perform replacement fluid (infusion) according to the amount of filtrate filtered by the blood purifier, and when the amount of filtrate fluctuates, the amount of replacement fluid is adjusted in conjunction with it. Even if it is not done, it will impose a further burden on those involved in a busy treatment site. In addition, a roller pump that is generally used in this type of treatment device has a pump tube that has a constant pump rotation speed, but if the pressure exceeds a set value due to fluctuations in the pressure on the filtrate side, the pump tube There is a phenomenon that the amount of filtrate increases due to swelling than usual, and it is difficult to detect this fluctuation in the amount of filtrate, so the balance between the amount of filtrate and the replacement fluid becomes unbalanced, which may cause a serious therapeutic problem. There is a nature.

【0006】[0006]

【本発明の解決すべき課題】本発明の血液浄化装置は、
緩徐体液調整治療法を実施するための、小型、且つ、取
り扱いが容易な装置である。即ち、本発明は、静脈より
採血し、静脈に返血する血液静脈間循環系内に、少なく
とも採血ポンプ、血液浄化器、濾過ポンプ及び濾液定量
器を備え、濾液定量器によって補液容器、透析液容器及
び濾液容器の重量を測定、設定し、補液及び透析液を設
定流量で供給しつつ、濾液定量器重量が設定重量と実質
的に同一重量となるよう、濾過ポンプの回転数を変動す
ることにより、濾液量を調整することを特徴とする血液
浄化装置に関する。
The blood purification device of the present invention comprises:
It is a small-sized and easy-to-use device for performing a slow body fluid adjustment treatment method. That is, the present invention collects blood from a vein and returns to the vein in the blood-venous circulation system, at least a blood sampling pump, a blood purifier, a filtration pump and a filtrate quantifier, and a replacement fluid container and a dialysate by the filtrate quantifier. Measuring and setting the weight of the container and the filtrate container, supplying the replacement fluid and the dialysate at the set flow rate, and changing the rotation speed of the filtration pump so that the weight of the filtrate meter is substantially the same as the set weight. The present invention relates to a blood purification device characterized in that the amount of filtrate is adjusted.

【0007】上記の濾液量を調整するとの意味は、濾液
定量器の重量が設定値から増減するに伴い濾液量を増減
させるということであり、実質的には、補液及び透析液
の供給量と平衡する濾液量という意味である。
The meaning of adjusting the amount of filtrate is to increase or decrease the amount of filtrate as the weight of the filtrate meter increases or decreases from the set value. It means the amount of filtrate to be equilibrated.

【0008】[0008]

【発明の構成】本発明の血液浄化装置は、緩徐体液調整
治療法を実施するための各種ポンプ類及び多重の安全機
構が一体に装備されているため、非常に小型であって、
ベッドサイドの狭い空間に設置しても、特に医療活動の
障害になることはない。
The blood purification apparatus of the present invention is extremely small in size because it is integrally equipped with various pumps and multiple safety mechanisms for carrying out the slow body fluid adjustment treatment method.
Even if it is installed in a narrow space at the bedside, it does not particularly interfere with medical activities.

【0009】本発明の血液浄化装置は、予め設定された
濾液定量器の重量設定値に従い、濾液定量器から送られ
る信号によって、濾過ポンプの回転数を調整することに
より濾液量を制御している。本発明では供給され減量す
る補液及び透析液と、増加する濾液量との重量の平衡に
よって濾過ポンプの回転数を制御しているため、回転数
が一定であっても濾液量が変動し得るというローラーポ
ンプの欠点に影響されることもなく、濾液量と補液量と
の均衡が崩れるという危険な事態を招致する恐れがな
い。又、従来のように濾液量をバッチ式に測定するので
はなく、連続的に定量し、送られる信号によって適時に
ポンプの回転数が制御されるため、正確な濾液量が得ら
れ、緩徐体液調整治療法を実施するための煩雑な操作が
軽減され、安全性が向上すると共に他の治療手段も容易
に実施できる。
In the blood purification apparatus of the present invention, the amount of filtrate is controlled by adjusting the rotation speed of the filtration pump according to the preset weight setting value of the filtrate quantifier and the signal sent from the filtrate quantifier. . In the present invention, since the rotation speed of the filtration pump is controlled by the weight balance between the supplied replacement fluid and dialysate and the increased filtrate quantity, the filtrate quantity may vary even if the rotation speed is constant. It is not affected by the defects of the roller pump, and there is no fear of causing a dangerous situation in which the balance between the filtrate amount and the replacement liquid amount is lost. Further, instead of measuring the amount of filtrate in a batch manner as in the conventional method, the number of revolutions of the pump is controlled in a timely manner by the signal sent continuously, and an accurate amount of filtrate can be obtained. The complicated operation for carrying out the adjusted treatment method is reduced, the safety is improved, and other treatment means can be easily carried out.

【0010】以下に、本発明の一実施例を図面に従って
詳しく説明する。
An embodiment of the present invention will be described below in detail with reference to the drawings.

【実施例】図1は、本発明に係る血液浄化装置の血液の
流れを概略的に示したものである。血液体外循環に先立
って、先ず、濾液定量器10上に補液容器7、透析液容
器8(当初は容器は補液及び透析液で満たされている)
及び濾液容器9を載せ、その全重量を測定し、その重量
を設定値として濾過ポンプ2の回転数の制御指標とし、
以下の運転を開始する。静脈血が、ポンプ1によって連
結管11の先端の穿刺針により脱血され、ポンプ5によ
り連結管12を経て導入される抗凝固剤と混合され、連
結管13を経て血液浄化器6に導入される。同時に、ポ
ンプ4によって補液容器7中の補液の供給が開始され、
ポンプ3によって透析液容器8中の透析液の供給が開始
される。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS FIG. 1 schematically shows the flow of blood in a blood purification apparatus according to the present invention. Prior to extracorporeal blood circulation, first, a replacement fluid container 7 and a dialysate container 8 are placed on the filtrate quantification device 10 (the containers are initially filled with the replacement fluid and the dialysate).
And the filtrate container 9 is placed, the total weight thereof is measured, and the weight is set as a set value to be a control index of the rotation speed of the filtration pump 2,
Start the following operations. The venous blood is removed by the puncture needle at the tip of the connecting tube 11 by the pump 1, mixed with the anticoagulant introduced through the connecting tube 12 by the pump 5, and introduced into the blood purifier 6 through the connecting tube 13. It At the same time, the supply of the replacement fluid in the replacement fluid container 7 is started by the pump 4,
The pump 3 starts the supply of dialysate in the dialysate container 8.

【0011】抗凝固剤としては、体外循環に使用できる
ものであれば何れでもよく、例えば、クエン酸(AC
D、CPD等)、ヘパリン、プロスタグランジン、メシ
ル酸ガベキサート等が使用される。これらは穿刺部又は
その下流側の血液ラインに設けられた分岐部等から持続
投与器或いは点滴で投与すればよい。
Any anticoagulant may be used as long as it can be used for extracorporeal circulation. For example, citric acid (AC
D, CPD, etc.), heparin, prostaglandin, gabexate mesylate and the like are used. These may be administered by a continuous administration device or a drip from a puncture portion or a branch portion provided in the blood line on the downstream side.

【0012】血液浄化器6に導入された血液は、ポンプ
2により透析、濾過され、血液中の低分子物質を含む水
が連結管14に導入され、濾液定量器10上の濾液容器
9内に収容される。濾液定量器10は、重量を測定でき
る機器であればよく、ストレインゲージ型の電気信号が
取り出せる秤等を使用することができる。感度、精度も
それほど高いものでなくてもよく、例えば、ストレイン
ゲージであれば感度1g程度のものであれば充分使用で
きる。一方、血液浄化器6内の濃縮血液は、連結管15
を経て静脈内に返血される。
The blood introduced into the blood purifier 6 is dialyzed and filtered by the pump 2, water containing low molecular weight substances in the blood is introduced into the connecting pipe 14, and the water is introduced into the filtrate container 9 on the filtrate meter 10. Be accommodated. The filtrate quantification device 10 may be any device that can measure the weight, and a strain gauge type balance or the like that can take out an electric signal can be used. The sensitivity and accuracy may not be so high. For example, a strain gauge having a sensitivity of about 1 g can be used sufficiently. On the other hand, the concentrated blood in the blood purifier 6 is connected to the connecting pipe 15
The blood is returned to the vein.

【0013】血液浄化器としては、中空糸膜を濾過材と
する中空糸膜モジュールが好適である。中空糸膜モジュ
ールに用いられる中空糸膜としては、限外濾過膜が好ま
しい。限外濾過膜としては有孔であれ、無孔であれ血漿
蛋白の漏洩が少ないか、或いは皆無であって、水分を除
去できる膜であればよい。中空糸膜を構成する材料は特
に制限されないが、セルロース系、ポリスルホン系、ポ
リアミド系、ポリアクリロニトリル系、ポリ(エチレン
−ビニルアルコール)系、ポリメチルメタアクリレート
系、ポリカーボネート系の材料が挙げられる。又、有孔
の膜で限外濾過性能を有する膜であれば、既述の材料に
加えてポリオレフィン[ポリエチレン、ポリプロピレ
ン、ポリ(4−メチル−ペンテン−1)等]或いはガラ
ス、セラミックス、カーボン等の無機材料も挙げられ
る。中空糸膜の外径は特に制限されるものではないが、
一般的には10〜1000ミクロン程度のものが好まし
い。
As a blood purifier, a hollow fiber membrane module using a hollow fiber membrane as a filtering material is suitable. An ultrafiltration membrane is preferable as the hollow fiber membrane used in the hollow fiber membrane module. The ultrafiltration membrane may be perforated or non-perforated as long as it has little or no leakage of plasma proteins and can remove water. The material forming the hollow fiber membrane is not particularly limited, and examples thereof include cellulose-based, polysulfone-based, polyamide-based, polyacrylonitrile-based, poly (ethylene-vinyl alcohol) -based, polymethylmethacrylate-based, and polycarbonate-based materials. In addition to the above-mentioned materials, polyolefin [polyethylene, polypropylene, poly (4-methyl-pentene-1), etc.], glass, ceramics, carbon, etc. may be used as long as it is a porous film having ultrafiltration performance. Inorganic materials can also be used. The outer diameter of the hollow fiber membrane is not particularly limited,
Generally, those having a size of about 10 to 1000 μm are preferable.

【0014】体外循環系内に於いて本発明の装置は、各
ポンプ、特に、ポンプ2の回転数、採血ライン及び血液
浄化器の濾過側等の圧力、濾液定量器からの設定重量か
らの偏差を示す信号、気泡検知器内の気泡の有無等の情
報を各々電気信号により検出し、交流/直流変換器によ
り、交流/直流変換された信号がコンピューターに取り
込まれ、各々の状態が監視されるようになっている。
In the extracorporeal circulatory system, the apparatus of the present invention is designed so that each pump, in particular, the number of revolutions of the pump 2, the pressure of the blood collecting line and the filtration side of the blood purifier, and the deviation from the set weight from the filtrate metering device. Signal, and information such as the presence / absence of bubbles in the bubble detector are detected by electric signals, and the AC / DC converter converts the AC / DC converted signals into a computer to monitor each state. It is like this.

【0015】ポンプ3、4は初期に設定された回転数で
回転するが、濾液定量器10の重量が予め設定された重
量に満たない場合には、表示器に濾液定量器10の重量
が予め設定された重量より低いことが表示され、ポンプ
2の回転数が増加する。このように濾液定量器10から
の信号によりポンプの回転数が制御され、補液、透析液
量と濾液量との平衡が保たれる。ポンプ2、ポンプ3及
びポンプ4は通常設定回転数で運転され、系内の補液、
透析液及び血液の総量はほぼ一定に保たれる。しかし、
上記の平衡が崩れ、濾液定量器10の重量が減少した場
合は、その重量を初期設定値に保ため、ポンプ2の回転
数が徐々に増加され、血液浄化器6の濾過側の負圧が徐
々に増大する。又、この負圧は中空糸膜の性能低下に伴
っても増大していくが、本発明の装置では、安全を見込
んだうえで負圧が200mmHgに達した時点で、その旨警
報が表示される。その場合は、装置上何らかのトラブル
が発生したか或いは中空糸膜モジュールの性能低下、劣
化等による使用限界が考えられるため、装置の点検或い
は部品の取り替えが必要となる。
The pumps 3 and 4 rotate at the initially set number of revolutions, but when the weight of the filtrate quantitative meter 10 is less than the preset weight, the weight of the filtrate quantitative meter 10 is previously indicated on the display. It is displayed that the weight is lower than the set weight, and the rotation speed of the pump 2 increases. In this way, the number of revolutions of the pump is controlled by the signal from the filtrate quantifier 10, and the amount of the replacement fluid and the dialysate and the amount of the filtrate are balanced. Pump 2, pump 3 and pump 4 are normally operated at the set rotational speed,
The total volume of dialysate and blood remains approximately constant. But,
When the above-mentioned equilibrium is lost and the weight of the filtrate quantifier 10 decreases, the rotation speed of the pump 2 is gradually increased to maintain the weight at the initial set value, and the negative pressure on the filtration side of the blood purifier 6 is reduced. Gradually increase. This negative pressure also increases as the performance of the hollow fiber membrane deteriorates. However, in the device of the present invention, when the negative pressure reaches 200 mmHg in consideration of safety, an alarm to that effect is displayed. It In that case, some trouble may occur in the device, or there may be a limit in use due to performance degradation or deterioration of the hollow fiber membrane module, so that the device must be inspected or parts replaced.

【0016】[0016]

【発明の効果】本発明の血液浄化装置では、採血量を一
定とし、補液容器、透析液容器及び濾液容器を同一の濾
液定量器に載置し、補液及び透析液を設定流量で供給し
つつ、濾液定量器の初期の重量を保つことにより、濾液
量と補液、透析液量との均衡が常に保たれ、治療上重大
な問題を引き起こす恐れがない。
According to the blood purification apparatus of the present invention, the amount of blood collected is constant, the replacement fluid container, the dialysate container and the filtrate container are placed on the same filtrate meter, and the replacement fluid and the dialysate are supplied at the set flow rate. By maintaining the initial weight of the filtrate quantitative meter, the balance between the filtrate amount and the replacement fluid and dialysate fluid is always maintained, and there is no fear of causing a serious problem in treatment.

【0017】次に、本発明の血液浄化器を用いた具体的
な実施結果を説明する。 実施例1 容量10リットルの円筒形のガラス容器にヘマトクリッ
ト値37%の牛血を入れ、この中に穿針部を浸漬して、
図1に示した血液回路によって血液を循環させた。先
ず、濾液定量器上に補液容器、透析液容器(何れも規定
量の液が充填されている)及び濾液容器を静置し、その
全重量を測定したところ5.54kgであり、これを設
定重量とした。次いで、ポンプ1によって100ミリリ
ットル/分の速度で血液を流すと共に、ポンプ4によっ
て補液を500ミリリットル/時間、ポンプ3によって
透析液を1000ミリリットル/時間の速度で供給し
た。ポンプ2によって血液浄化器を通過する血液中から
1500ミリリットル/時間の速度で水分等を濾過しな
がら2日間運転を続けたが(この間に補液容器及び透析
液容器を24回取り替え、同時に濾液容器中の濾液を廃
棄し、濾液定量器の重量を測定したが略同じであっ
た)、この間、濾液定量器の重量は5.50〜5.57
kgの範囲でほぼ一定であった。血液浄化器入口側の圧
力は運転開始1日後には50〜58mmHg、2日後には2
00mmHgとなり、警報が発せられた。そこで装置全体を
点検したが特に不具合はなかったため、血液浄化器の中
空糸膜モジュールを取り替え、当初と同様の条件で運転
を再開した。このように、本発明の血液浄化装置によれ
ば、濾液量が予め設定された一定量に保たれるため、補
液量との均衡も保たれ、治療上重大な問題を引き起こす
ことがない。
Next, the concrete results of implementation using the blood purifier of the present invention will be described. Example 1 Bovine blood having a hematocrit value of 37% was placed in a cylindrical glass container having a volume of 10 liters, and a perforating needle portion was immersed therein,
Blood was circulated by the blood circuit shown in FIG. First, a replacement fluid container, a dialysate container (each of which is filled with a prescribed amount of liquid) and a filtrate container were allowed to stand on the filtrate quantifier, and the total weight thereof was measured to be 5.54 kg, which was set. Weight and weight. Then, blood was flown by the pump 1 at a rate of 100 ml / min, a replacement fluid was supplied by the pump 4 at a rate of 500 ml / hour, and a dialysate was supplied by a pump 3 at a rate of 1000 ml / hour. The pump 2 continued operation for 2 days while filtering water and the like from the blood passing through the blood purifier at a rate of 1500 ml / hour (during which the replacement fluid container and the dialysate fluid container were replaced 24 times, and at the same time in the filtrate fluid container). The filtrate was discarded, and the weight of the filtrate meter was measured, but it was almost the same.) During this period, the weight of the filtrate meter was 5.50 to 5.57.
It was almost constant in the kg range. The pressure on the inlet side of the blood purifier is 50 to 58 mmHg one day after the start of operation and two after two days.
It became 00 mmHg and an alarm was issued. Therefore, the entire device was inspected, but there was no particular problem, so the hollow fiber membrane module of the blood purifier was replaced, and operation was restarted under the same conditions as at the beginning. As described above, according to the blood purification device of the present invention, since the amount of filtrate is kept at a preset constant amount, a balance with the amount of replacement fluid is kept, and a serious problem in treatment is not caused.

【0018】[0018]

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

【図1】本発明の血液浄化装置の回路図である。FIG. 1 is a circuit diagram of a blood purification device of the present invention.

【符号の説明】[Explanation of symbols]

1 脱血ポルプ 2 濾過ポンプ 3 透析液ポンプ 4 補液ポンプ 5 抗凝固剤注入ポンプ 6 血液浄化器 7 補液容器 8 透析液容器 9 濾液容器 10 濾液定量器 11 第1の連結管 12 第2の連結管 13 第3の連結管 14 第4の連結管 15 第5の連結管 1 Blood Removal Pump 2 Filtration Pump 3 Dialysis Fluid Pump 4 Replacement Fluid Pump 5 Anticoagulant Injection Pump 6 Blood Purifier 7 Replacement Fluid Container 8 Dialysis Fluid Container 9 Filtrate Container 10 Filtrate Quantitator 11 First Connection Pipe 12 Second Connection Pipe 13 Third Connection Pipe 14 Fourth Connection Pipe 15 Fifth Connection Pipe

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】静脈より採血し、静脈に返血する血液静脈
間循環系内に、少なくとも採血ポンプ、血液浄化器、濾
過ポンプ及び濾液定量器を備え、濾液定量器によって補
液容器、透析液容器及び濾液容器の重量を測定、設定
し、補液及び透析液を設定流量で供給しつつ、濾液定量
器重量が設定重量と実質的に同一重量となるよう、濾過
ポンプの回転数を変動することにより、濾液量を調整す
ることを特徴とする血液浄化装置。
1. A blood intervenous circulation system for collecting blood from a vein and returning the blood to the vein, which is provided with at least a blood collection pump, a blood purifier, a filtration pump and a filtrate quantifier, and a filtrate quantifier for a replacement fluid container and a dialysate container. By measuring and setting the weight of the filtrate container and supplying the replacement fluid and the dialysate at the set flow rate, by changing the rotation speed of the filtration pump so that the weight of the filtrate quantitative meter becomes substantially the same as the set weight. A blood purification device characterized by adjusting the amount of filtrate.
JP5024053A 1993-02-12 1993-02-12 Hemocatharsis system Pending JPH06233813A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5024053A JPH06233813A (en) 1993-02-12 1993-02-12 Hemocatharsis system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5024053A JPH06233813A (en) 1993-02-12 1993-02-12 Hemocatharsis system

Publications (1)

Publication Number Publication Date
JPH06233813A true JPH06233813A (en) 1994-08-23

Family

ID=12127726

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5024053A Pending JPH06233813A (en) 1993-02-12 1993-02-12 Hemocatharsis system

Country Status (1)

Country Link
JP (1) JPH06233813A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007236923A (en) * 2006-02-07 2007-09-20 Jms Co Ltd Blood purification circuit
JP2007236924A (en) * 2006-02-07 2007-09-20 Jms Co Ltd Blood purification apparatus
US9011678B2 (en) 2006-02-07 2015-04-21 Jms Co., Ltd. Blood purification apparatus and blood purification circuit
JP2017086198A (en) * 2015-11-04 2017-05-25 ニプロ株式会社 Blood purifying device
JP2017148152A (en) * 2016-02-23 2017-08-31 ニプロ株式会社 Blood purifier

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007236923A (en) * 2006-02-07 2007-09-20 Jms Co Ltd Blood purification circuit
JP2007236924A (en) * 2006-02-07 2007-09-20 Jms Co Ltd Blood purification apparatus
US9011678B2 (en) 2006-02-07 2015-04-21 Jms Co., Ltd. Blood purification apparatus and blood purification circuit
JP2017086198A (en) * 2015-11-04 2017-05-25 ニプロ株式会社 Blood purifying device
JP2017148152A (en) * 2016-02-23 2017-08-31 ニプロ株式会社 Blood purifier

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