JPH09239024A - Blood purifying device - Google Patents

Blood purifying device

Info

Publication number
JPH09239024A
JPH09239024A JP8068984A JP6898496A JPH09239024A JP H09239024 A JPH09239024 A JP H09239024A JP 8068984 A JP8068984 A JP 8068984A JP 6898496 A JP6898496 A JP 6898496A JP H09239024 A JPH09239024 A JP H09239024A
Authority
JP
Japan
Prior art keywords
blood
liquid
dialysate
filtrate
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.)
Granted
Application number
JP8068984A
Other languages
Japanese (ja)
Other versions
JP3928888B2 (en
Inventor
Tomoyuki Wada
朋之 和田
Jun Ishihara
旬 石原
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.)
Asahi Kasei Medical Co Ltd
Original Assignee
Asahi Medical 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 Asahi Medical Co Ltd filed Critical Asahi Medical Co Ltd
Priority to JP06898496A priority Critical patent/JP3928888B2/en
Publication of JPH09239024A publication Critical patent/JPH09239024A/en
Application granted granted Critical
Publication of JP3928888B2 publication Critical patent/JP3928888B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a blood purifying device where an operation is easily executed and also the safety of a patient is secured by automatically measuring and controlling filtration liquid, dialysis liquid and substitution liquid in the device. SOLUTION: A dialysis liquid supply route and a filtration liquid discharging route or a dialysis liquid and dialysis liquid discharging route and a replenish liquid route are respectively provided with a liquid supply pump, a valve, a storage container and weight meters 103 measuring weight and the weight change of the storage container is fed-back so that the flow rate of the liquid supply pump is controlled. Then, when the weight of the storage container becomes a fixed value, the flow rate of the liquid supply pump is controlled and also the valve is opened so as to replenish fresh dialysis liquid and replenish liquid and to abolish filtration liquid.

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、血液浄化装置、特に重
篤な循環器系の合併症を有する腎疾患や多臓器不全等の
救急・集中治療領域での持続緩徐式血液濾過法(以下単
に「CHF」という)並びに持続的血液濾過透析法(以
下単に「CHDF」という)に好適な装置に関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a blood purification device, particularly a continuous slow hemofiltration method in the emergency / intensive care area for renal diseases with severe circulatory complications, multiple organ failure, etc. The present invention relates to a device suitable for continuous hemofiltration and dialysis (hereinafter simply referred to as “CHDF”).

【0002】[0002]

【従来の技術】近年、循環器系の合併症を有する腎疾患
や多臓器不全等の治療にCHFあるいはCHDFの血液
浄化法が効果を上げている。CHFは半透膜を収容した
血液浄化器に血液を流し、膜を介して濾過された液を排
出すると共に置換液を体内に補充することを持続的に緩
徐に施行するものである。また、CHDFはCHFの小
分子量除去能力を改善するために、CHFに加えて濾過
液側に透析液を流して透析効果を得られるようにしたも
のである。これらの治療は、血液浄化器に血液を循環す
る血液ポンプ、血液浄化器から濾過液を排出する濾過液
ポンプ、患者に置換液を補充する補液ポンプ、血液浄化
器に透析液を供給する透析液ポンプ(CHDFの場合の
み)の流量をそれぞれ設定し、体液の変化量(透析液量
+補液量−濾過液量)が目的の量になるように管理して
施行される。
2. Description of the Related Art In recent years, a CHF or CHDF blood purification method has been effective in treating renal diseases having multiple cardiovascular complications and multiple organ failure. CHF is a method in which blood is allowed to flow through a blood purifier containing a semipermeable membrane, the fluid filtered through the membrane is discharged, and replacement fluid is replenished into the body continuously and slowly. In addition, CHDF is a substance in which a dialysate is flowed to the filtrate side in addition to CHF so that a dialysis effect can be obtained in order to improve the ability of CHF to remove small molecules. These treatments include a blood pump that circulates blood through the blood purifier, a filtrate pump that discharges filtrate from the blood purifier, a replacement fluid pump that replenishes the patient with replacement fluid, and a dialysate that supplies dialysate to the blood purifier. The flow rate of the pump (only in the case of CHDF) is set, and the change amount of the body fluid (dialysis fluid amount + replacement fluid amount-filtrate amount) is managed so that the target amount is achieved.

【0003】[0003]

【発明が解決しようとする課題】通常、濾過液の排出や
置換液の注入には無菌性を保つために、チューブを圧閉
してしごきながら送液する、いわゆるチュービングポン
プが使われる。しかし、チュービングポンプの流量はチ
ューブの物性が疲労や温度によって変化するために一定
の流量を保つことは難しく、通常の使用範囲内での条件
変化に対して5〜10%の誤差をまぬがれない。体液の
変化量を厳密に管理するためには、各ポンプの流量を頻
回に計量して調節する必要がある。この操作は煩雑であ
り、また、誤操作を招きやすいという観点から患者の常
時監視が強いられるなどの問題点がある。これに対して
は図2に示すように、重量計により置換液の注入量や濾
過液の排出量を測定しながら、各ポンプを自動調整する
方法も考案されているが、置換液の補充や濾過液の廃棄
を行なう際、一度治療を停止しなければならず、煩雑な
手順を必要とする。また、誤って治療中に補充や廃棄操
作を行い、大きな誤差を生じるケースもある。加えて、
補充や廃棄操作の頻度を少なくするために、重量計の測
定レンジを広くし、大量の置換液や濾過液を一度に吊せ
るようにすると、測定精度が劣化すると共に振動等によ
る外乱が大きくなり、誤差を招くことになる。本発明は
上記従来技術の問題点を解決するためになされたもの
で、腎疾患や多臓器不全等の治療の際、血液浄化装置の
濾過液、透析液、置換液の流量を自動的に測定し制御す
ることで、操作の容易化を図ると共に患者の安全性を確
保できる装置を提供することを課題とする。
In order to maintain sterility, a so-called tubing pump is used for discharging the filtrate and injecting the replacement liquid, in which the tube is pressure-closed and the solution is fed while being squeezed. However, it is difficult to maintain a constant flow rate of the tubing pump because the physical properties of the tube change due to fatigue and temperature, and an error of 5 to 10% cannot be avoided with respect to changes in conditions within the normal usage range. In order to strictly control the amount of change in body fluid, it is necessary to frequently measure and adjust the flow rate of each pump. This operation is complicated, and there is a problem that the patient is constantly monitored from the viewpoint that it is likely to cause an erroneous operation. On the other hand, as shown in FIG. 2, a method of automatically adjusting each pump while measuring the injection amount of the replacement liquid and the discharge amount of the filtered liquid by a weight scale has been devised. When the filtrate is discarded, the treatment has to be stopped once, which requires a complicated procedure. In addition, there are cases in which replenishment and disposal operations are mistakenly performed during treatment, resulting in a large error. in addition,
In order to reduce the frequency of replenishment and disposal operations, widening the measurement range of the weighing scale so that a large amount of replacement liquid or filtrate can be suspended at one time will deteriorate the measurement accuracy and increase the disturbance due to vibration etc. , Will cause an error. The present invention has been made to solve the above-mentioned problems of the prior art, and automatically measures the flow rates of the filtrate, the dialysate, and the replacement fluid of the blood purification device during the treatment of renal diseases and multiple organ failure. It is an object of the present invention to provide a device capable of facilitating the operation and ensuring the safety of the patient by controlling the operation.

【0004】[0004]

【課題を解決するための手段】患者の血液を半透膜を収
容した血液浄化器に導入して再度患者に戻す血液循環路
と、該血液循環路を介して患者に置換液を補給する補液
路と、該血液浄化器から血液濾過液を排出する濾過液排
出路とから、または、該血液循環路と該補液路と該血液
浄化器に透析液を供給する透析液供給路と該血液浄化器
から血液濾過液及び使用済透析液を排出する濾過液・透
析液排出路からなる、血液濾過、血液透析または血液濾
過透析を行う血液浄化装置において、該透析液供給路と
該濾過液排出路または、該濾過液・透析液排出路と該補
液路にそれぞれ送液ポンプとバルブと貯溜容器と該貯溜
容器の重量を計る重量計を設け、該貯溜容器の重量変化
をフィードバッグすることで該送液ポンプの流量を制御
すると共に、該貯溜容器の重量が一定の値になった時に
該送液ポンプの流量を制御すると共に、該貯溜容器の重
量が一定の値になった時に該バルブを開いて新鮮透析液
及び補液用液の補充及び濾過液の廃棄を行うことを特徴
とする血液浄化装置。
A blood circulation path for introducing blood of a patient into a blood purifier containing a semipermeable membrane and returning it to the patient again, and a replacement fluid for supplying a replacement fluid to the patient via the blood circulation path. And a dialysate supply passage for supplying dialysate to the blood circulation passage, the replacement fluid passage, and the blood purifier, and the blood purification passage, and a filtrate discharge passage for discharging blood filtrate from the blood purifier. In a blood purification device for performing hemofiltration, hemodialysis or hemodiafiltration, which comprises a filtrate / dialysate discharge passage for discharging blood filtrate and used dialysate from a blood vessel, the dialysate supply passage and the filtrate discharge passage Alternatively, by providing a liquid feed pump, a valve, a storage container, and a weight scale for measuring the weight of the storage container in the filtrate / dialysate discharge passage and the replacement fluid passage, respectively, and by feeding back the change in weight of the storage container, While controlling the flow rate of the liquid delivery pump, When the weight of the container reaches a constant value, the flow rate of the liquid feed pump is controlled, and when the weight of the storage container reaches a constant value, the valve is opened to replenish the fresh dialysate and replacement fluid, and A blood purification device characterized in that the filtrate is discarded.

【0005】[0005]

【実施例】次に本発明装置の一実施例を図面にて説明す
る。図1は本発明装置でCHDFを実施する場合の構成
を示すフロー図である。血液ポンプ4により患者から取
り出された血液は採血ライン17を通り、濾過膜Mを収
容した血液浄化器16に導入され、返血ライン18から
再度患者に戻るように血液循環路を形成している。ま
た、返血ライン18には補液ライン24が接続されてお
り補液ポンプ7で置換液を患者に注入できる。一方、血
液浄化器16の濾過膜Mで濾過された血液成分は、濾過
液ライン20に設けられた濾過液ポンプ6により排出さ
れる。更に、透析液ポンプ5により、透析液供給ライン
19から血液浄化器16に透析液を供給し、濾過液と共
に濾過液ポンプ6で排出されるようになっている。ここ
で、補液ポンプの流量をQC (ml/h)、濾過液ポン
プの流量をQF (ml/h)、透析液ポンプの流量をQ
D (ml/h)とすると、患者の体液量の変化dV(m
l/h)は、dV=QD +QC −QFで表される。通
常、患者は腎機能低下により尿量減少を来して水分過剰
になっている場合が多く、dVを負の値にして水分を除
去(以下単に「除水」という)するように設定するた
め、治療中の総体液変化量は除水量と呼ばれ管理され
る。除水量は正確に管理されなければならないが、治療
時間が長いために、QD 、QC 、QF の僅かな誤差が大
きな除水量誤差を生む。例えば、QD =500ml/
h、QC =400ml/h、QF =1,000ml/h
で20時間の治療を行った場合、除水量は2,000m
lとなるが、各ポンプが±5%の誤差を持っているとす
ると、除水誤差は(±25±20±50)×20=±
1,900mlとなり、目的とした除水量に対してはほ
ぼ±100%の誤差を持つことになる。そこで、本発明
装置ではQD 、QC 、QF を実測して各ポンプをフィー
ドバック制御することで除水量の精度を向上している。
BRIEF DESCRIPTION OF THE DRAWINGS FIG. FIG. 1 is a flow chart showing the configuration when CHDF is implemented in the device of the present invention. Blood taken from the patient by the blood pump 4 passes through the blood sampling line 17, is introduced into the blood purifier 16 containing the filtration membrane M, and forms a blood circulation path so as to return to the patient again from the blood returning line 18. . A replacement fluid line 24 is connected to the blood return line 18 so that the replacement fluid can be injected into the patient by the replacement fluid pump 7. On the other hand, the blood component filtered by the filter membrane M of the blood purifier 16 is discharged by the filtrate pump 6 provided in the filtrate line 20. Further, the dialysate pump 5 supplies the dialysate from the dialysate supply line 19 to the blood purifier 16, and the dialysate pump 6 discharges the dialysate together with the filtrate. Here, the flow rate of the replacement fluid pump is Q C (ml / h), the flow rate of the filtrate pump is Q F (ml / h), and the flow rate of the dialysate pump is Q
Assuming D (ml / h), the change in the body fluid volume of the patient dV (m
1 / h) is represented by dV = Q D + Q C −Q F. Usually, patients often have decreased urine output due to decreased renal function and become overhydrated, so that dV is set to a negative value to remove water (hereinafter simply referred to as “water removal”). The amount of change in total body fluid during treatment is called water removal amount and is managed. The amount of water removed must be controlled accurately, but due to the long treatment time, a slight error in Q D , Q C , and Q F causes a large amount of water removed error. For example, Q D = 500 ml /
h, Q C = 400 ml / h, Q F = 1,000 ml / h
If treated for 20 hours, the amount of water removed is 2,000m
However, if each pump has an error of ± 5%, the water removal error is (± 25 ± 20 ± 50) × 20 = ±
It will be 1,900 ml, and will have an error of approximately ± 100% with respect to the desired amount of water removed. Therefore, in the device of the present invention, the precision of the amount of water removed is improved by measuring Q D , Q C , and Q F and performing feedback control of each pump.

【0006】まず、透析液流量QD の制御について説明
する。透析液貯溜部14に溜められた透析液は透析液補
充ライン21に設けられたバルブ8を開けることにより
落差で計量バッグ11に送られる。重量計1は計量バッ
グ11の重さを測定し、制御装置25にデータを送る。
制御装置25は計量バッグ11の重さが一定の値以上に
なったことを検知してバルブ8を閉じ、計量バッグ11
への透析液の流れを止め、この状態を初期状態とする。
透析液ポンプ5は、予め設定された流量に応じた回転数
でモーターを駆動することで透析液を血液浄化器16へ
送り始める。制御装置25は、重量計1のデータを常に
監視し、単位時間当たりの重量変化から透析液の実流量
を計算するが、この実流量と設定流量の間に差があれば
モーターの回転数を自動的に調整し、設定流量と実流量
が等しくなるように制御する。やがて計量バッグ11の
中の透析液の残りが少なくなり、重量が一定の値を下回
れば、制御装置25は再度バルブ8を開き計量バッグ1
1に透析液を充填し、初期状態に戻す。バルブ8が開い
ている間、透析液ポンプ5は直前の回転数を保持する
が、初期状態に戻れば再度制御が始まる。以上を繰り返
すことによって透析液流量は精度良く設定流量を保つこ
とができる。なお、バルブ8が開いている間は透析液ポ
ンプは制御されないが、制御している時間よりはるかに
短く、ポンプの流量特性が急激に変化することはないた
めに、大きな誤差にはならない。
First, the control of the dialysate flow rate Q D will be described. The dialysate stored in the dialysate reservoir 14 is sent to the measuring bag 11 by dropping the valve 8 provided in the dialysate replenishing line 21. The weighing scale 1 measures the weight of the weighing bag 11 and sends data to the control device 25.
The control device 25 detects that the weight of the weighing bag 11 exceeds a certain value, closes the valve 8, and
Stop the flow of dialysate to the cell and set this state as the initial state.
The dialysate pump 5 starts to send the dialysate to the blood purifier 16 by driving the motor at a rotation speed according to a preset flow rate. The controller 25 constantly monitors the data of the weighing scale 1 and calculates the actual flow rate of the dialysate from the weight change per unit time. If there is a difference between this actual flow rate and the set flow rate, the number of rotations of the motor is changed. Automatically adjust and control so that the set flow rate and the actual flow rate are equal. When the amount of dialysate remaining in the measuring bag 11 is reduced and the weight falls below a certain value, the control device 25 opens the valve 8 again and the measuring bag 1
Fill 1 with dialysate and return to the initial state. While the valve 8 is open, the dialysate pump 5 retains the immediately preceding rotation speed, but the control starts again when the dialysate pump 5 returns to the initial state. By repeating the above, the dialysate flow rate can be accurately maintained at the set flow rate. Although the dialysate pump is not controlled while the valve 8 is open, it is much shorter than the control time, and the flow rate characteristic of the pump does not change abruptly, so it does not cause a large error.

【0007】補液流量QC は透析液流量QD と同様に制
御される。即ち、置換液貯溜部15に溜められた置換液
は置換液補充ライン22に設けられたバルブ10を開け
ることにより落差で計量バッグ13に送られる。重量計
3は計量バッグ13の重さを測定し、制御装置25にデ
ータを送る。制御装置25は計量バッグ13の重さが一
定の値以上になったことを検知してバルブ10を閉じ、
計量バッグ13への置換液の流れを止め、この状態を初
期状態とする。補液ポンプ7は、予め設定された流量に
応じた回転数でモーターを駆動することで置換液を補液
ライン24、返血ライン18を介して患者へ注入し始め
る。制御装置25は、重量計3のデータを常に監視し、
単位時間当たりの重量変化から置換液の実流量を計算す
るが、この実流量と設定流量の間に差があればモーター
の回転数を自動的に調整し、設定流量と実流量が等しく
なるように制御する。やがて計量バッグ13の中の置換
液の残りが少なくなり、重量が一定の値を下回れば、制
御装置25は再度バルブ10を開き計量バッグ13に置
換液を充填し、初期状態に戻す。バルブ10が開いてい
る間、補液ポンプ7は直前の回転数を保持するが、初期
状態に戻れば再度制御が始まる。
The replacement fluid flow rate Q C is controlled similarly to the dialysate flow rate Q D. That is, the replacement liquid stored in the replacement liquid storage portion 15 is sent to the measuring bag 13 by a drop by opening the valve 10 provided in the replacement liquid replenishing line 22. The weighing scale 3 measures the weight of the weighing bag 13 and sends data to the control device 25. The control device 25 detects that the weight of the weighing bag 13 exceeds a certain value and closes the valve 10,
The flow of the replacement liquid to the measuring bag 13 is stopped, and this state is set as the initial state. The replacement fluid pump 7 starts to inject the replacement solution into the patient through the replacement fluid line 24 and the blood return line 18 by driving the motor at a rotation speed according to a preset flow rate. The control device 25 constantly monitors the data of the weighing scale 3,
The actual flow rate of the replacement liquid is calculated from the weight change per unit time, but if there is a difference between this actual flow rate and the set flow rate, the motor speed is automatically adjusted so that the set flow rate and the actual flow rate become equal. To control. Eventually, when the amount of the replacement liquid remaining in the measuring bag 13 decreases and the weight falls below a certain value, the control device 25 opens the valve 10 again to fill the measuring bag 13 with the replacement liquid and restore the initial state. While the valve 10 is open, the replacement fluid pump 7 retains the rotation speed immediately before, but the control is started again when it returns to the initial state.

【0008】濾過液流量QF は以下の通り制御装置25
で制御される。濾過液ポンプ6は予め設定された流量に
応じた回転数でモーターを駆動することで濾過液を計量
バッグ12に送り始める。この時バルブ9は閉じられて
おり、重量計2によって検出された計量バッグ12の重
量変化は濾過液の実流量となる。この実流量が設定流量
と等しくなるようにモーターの回転数を制御する。やが
て計量バッグ12が充満し重量が一定の値を上回ればバ
ルブ9を開けて計量バッグ12中の濾液を廃液ライン2
3から廃棄する。この時濾過液ポンプ6は直前の回転数
を保持するが、計量バッグ12の重量が一定の値を下回
って濾過液の廃棄が終了するとバルブ9が閉じられ、再
度同様の回転数制御が始まる。以上によって各ポンプは
高い流量精度を維持することができ、その結果、除水量
の誤差を少なく管理できる。また、本実施例によると置
換液や透析液の補充や濾過液の廃棄は、重量測定に直接
影響しないため、治療を停止することなく任意に行なえ
る。更に、各重量計の測定レンジは各計量バッグの容量
の範囲でよく測定精度を高く保てると共に外乱も少なく
なる。
The filtrate flow rate Q F is as follows:
Is controlled by The filtrate pump 6 starts to send the filtrate to the measuring bag 12 by driving the motor at a rotation speed according to a preset flow rate. At this time, the valve 9 is closed, and the weight change of the weighing bag 12 detected by the weight scale 2 becomes the actual flow rate of the filtrate. The rotation speed of the motor is controlled so that this actual flow rate becomes equal to the set flow rate. Eventually, if the weighing bag 12 is full and the weight exceeds a certain value, the valve 9 is opened to remove the filtrate in the weighing bag 12 from the waste liquid line 2
Discard from 3. At this time, the filtrate pump 6 holds the immediately preceding rotation speed, but when the weight of the measuring bag 12 falls below a certain value and the disposal of the filtrate is completed, the valve 9 is closed and the same rotation speed control is started again. With the above, each pump can maintain a high flow rate accuracy, and as a result, an error in the amount of water removed can be controlled to be small. Further, according to the present embodiment, the replacement liquid and the dialysate supplement and the discard of the filtrate do not directly affect the weight measurement, and thus can be arbitrarily performed without stopping the treatment. Furthermore, the measuring range of each weighing scale is well within the range of the capacity of each weighing bag, and the measuring accuracy can be kept high and the disturbance is reduced.

【0009】[0009]

【発明の効果】以上説明したように、本発明によれば透
析液流量、補液流量、濾過液流量を自動的に高い精度で
制御でき、スタッフによる頻回な計量及び調節作業を必
要とせずに安全に患者の体液量管理を行いながら治療が
できる。
As described above, according to the present invention, the dialysate flow rate, the replacement fluid flow rate, and the filtrate flow rate can be automatically controlled with high accuracy, and frequent measurement and adjustment work by staff is not required. Treatment can be performed while safely managing the body fluid volume of the patient.

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

【図1】本発明装置の1実施例の構成を示すフロー図で
ある。
FIG. 1 is a flowchart showing the configuration of an embodiment of the device of the present invention.

【図2】従来装置の1例の構成を示すフロー図である。FIG. 2 is a flowchart showing the configuration of an example of a conventional device.

【符号の説明】[Explanation of symbols]

1、2、3 重量計 4 血液ポンプ 5 透析液ポンプ 6 濾過液ポンプ 7 補液ポンプ 8、9、10 バルブ 11、12、13 計量バッグ 14 透析液貯溜部 15 置換液貯溜部 16 血液浄化器 17 採血ライン 18 返血ライン 19 透析液供給ライン 20 濾過液ライン 21 透析液補充ライン 22 置換液補充ライン 23 廃液ライン 24 補液ライン 25 制御装置 26 濾過液貯溜部 1, 2, 3 Weight scale 4 Blood pump 5 Dialysis fluid pump 6 Filtration fluid pump 7 Replacement fluid pump 8, 9, 10 Valves 11, 12, 13 Measuring bag 14 Dialysis fluid storage portion 15 Replacement fluid storage portion 16 Blood purification device 17 Blood sampling Line 18 Blood return line 19 Dialysate supply line 20 Filtrate line 21 Dialysate replenishment line 22 Replacement fluid replenishment line 23 Waste fluid line 24 Replacement fluid line 25 Controller 26 Filtrate reservoir

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 患者の血液を半透膜を収容した血液浄化
器に導入して再度患者に戻す血液循環路と、該血液循環
路を介して患者に置換液を補給する補液路と、該血液浄
化器から血液濾過液を排出する濾過液排出路とから、ま
たは、該血液循環路と該補液路と該血液浄化器に透析液
を供給する透析液供給路と該血液浄化器から血液濾過液
及び使用済透析液を排出する濾過液・透析液排出路から
なる、血液濾過、血液透析または血液濾過透析を行う血
液浄化装置において、該透析液供給路と該濾過液排出路
または、該濾過液・透析液排出路と該補液路にそれぞれ
送液ポンプとバルブと貯溜容器と該貯溜容器の重量を計
る重量計を設け、該貯溜容器の重量変化をフィードバッ
グすることで該送液ポンプの流量を制御すると共に、該
貯溜容器の重量が一定の値になった時に該送液ポンプの
流量を制御すると共に、該貯溜容器の重量が一定の値に
なった時に該バルブを開いて新鮮透析液及び補液用液の
補充及び濾過液の廃棄を行うことを特徴とする血液浄化
装置。
1. A blood circulation path for introducing blood of a patient into a blood purifier containing a semipermeable membrane and returning it to the patient again, and a replacement fluid path for supplying a replacement fluid to the patient via the blood circulation path, Blood filtration from a filtrate discharge passage for discharging blood filtrate from the blood purifier, or from the blood circulation passage, the replacement fluid passage, and a dialysate supply passage for supplying dialysate to the blood purifier and the blood purifier. In a blood purification apparatus for performing hemofiltration, hemodialysis or hemodiafiltration, which comprises a filtrate and a dialysate discharge path for discharging a liquid and a used dialysate, the dialysate supply path and the filtrate discharge path or the filtration The liquid / dialysate discharge passage and the replacement fluid passage are provided with a liquid feed pump, a valve, a storage container, and a weighing scale for measuring the weight of the storage container, and a feed bag is provided to measure the weight change of the storage container. The flow rate is controlled and the weight of the storage container is When the weight of the reservoir reaches a constant value, the valve is opened to control the flow rate of the liquid delivery pump when the value reaches a constant value, and the fresh dialysate and replacement fluid are replenished and the filtrate is discarded. A blood purification device characterized by performing.
JP06898496A 1996-03-01 1996-03-01 Blood purification equipment Expired - Lifetime JP3928888B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06898496A JP3928888B2 (en) 1996-03-01 1996-03-01 Blood purification equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06898496A JP3928888B2 (en) 1996-03-01 1996-03-01 Blood purification equipment

Publications (2)

Publication Number Publication Date
JPH09239024A true JPH09239024A (en) 1997-09-16
JP3928888B2 JP3928888B2 (en) 2007-06-13

Family

ID=13389447

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3928888B2 (en)

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CN111526900A (en) * 2017-10-31 2020-08-11 耐斯特基尼公司 Automatic extracorporeal blood treatment device
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