JPH0340303Y2 - - Google Patents

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Publication number
JPH0340303Y2
JPH0340303Y2 JP5856387U JP5856387U JPH0340303Y2 JP H0340303 Y2 JPH0340303 Y2 JP H0340303Y2 JP 5856387 U JP5856387 U JP 5856387U JP 5856387 U JP5856387 U JP 5856387U JP H0340303 Y2 JPH0340303 Y2 JP H0340303Y2
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Japan
Prior art keywords
conduit
irrigation fluid
patient
amount
liquid
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Expired
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JP5856387U
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Japanese (ja)
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JPS63166249U (en
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Priority to JP5856387U priority Critical patent/JPH0340303Y2/ja
Publication of JPS63166249U publication Critical patent/JPS63166249U/ja
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Description

【考案の詳細な説明】 「産業上の利用分野」 この考案は連続的サイクリツク腹膜透析
(CCPD)や間欠的腹膜透析(IPD)などに適用
することができる腹膜灌流装置に関する。
[Detailed description of the invention] "Field of industrial application" This invention relates to a peritoneal perfusion device that can be applied to continuous cyclic peritoneal dialysis (CCPD), intermittent peritoneal dialysis (IPD), etc.

「従来の技術」 従来のこの種の腹膜灌流装置は例えば特開昭60
−53155号公報に示されている。これを第5図を
参照して簡単に説明する。この例では灌流液源1
1として第1の灌流液が封入されたバツグ12
と、第2の灌流液が封入されたバツグ13とが用
いられ、これらバツグ12,13の各灌流液は弁
14,15をそれぞれ通じて共通の導管16に供
給することができる。その導管16内の灌流液は
給液用ローラポンプ17により導管18を通じて
加温容器19へ供給される。
``Prior art'' A conventional peritoneal perfusion device of this type is, for example, published in Japanese Patent Application Laid-Open No. 1989-1989.
This is shown in Publication No.-53155. This will be briefly explained with reference to FIG. In this example, irrigation fluid source 1
1, a bag 12 containing a first irrigation fluid;
and a bag 13 containing a second irrigation fluid are used, and the irrigation fluid in these bags 12 and 13 can be supplied to a common conduit 16 through valves 14 and 15, respectively. The irrigation fluid in the conduit 16 is supplied to the heating container 19 through the conduit 18 by a roller pump 17 for fluid supply.

加温容器19内に供給された灌流液はほぼ人間
の体温程度に加温される。導管18は分岐され、
弁21を通じて導管22の一端と連結され、導管
22の他端には患者の腹腔に設けたカテーテル
(図示せず)と連結するためのコネクタ23が付
けられている。弁21及び導管22の連結点は弁
24を通じてトラツプ25に連結される。トラツ
プ25内の液は排液用ローラポンプ26により排
液用導管27の一端へ供給される。
The perfusate supplied into the heating container 19 is heated to approximately the human body temperature. Conduit 18 is branched;
It is connected to one end of a conduit 22 through a valve 21, and a connector 23 is attached to the other end of the conduit 22 for connection to a catheter (not shown) provided in the patient's abdominal cavity. The junction of valve 21 and conduit 22 is connected to trap 25 through valve 24. The liquid in the trap 25 is supplied to one end of a drainage conduit 27 by a drainage roller pump 26.

弁21,24を閉じた状態で、弁14、必要に
応じて15も開き、給液用ローラポンプ17を駆
動して、灌流液源11から灌流液が加温容器19
へ所定量送られる。所定温度に処理された加温容
器19からの灌流液は弁21を開き、自然落差に
より導管22を通じて患者の腹腔内へ送られる。
With the valves 21 and 24 closed, the valve 14 and, if necessary, the valve 15 are also opened to drive the fluid supply roller pump 17, so that the irrigation fluid is supplied from the irrigation fluid source 11 to the heating container 19.
A predetermined amount is sent to. Irrigation fluid from the heated container 19, which has been heated to a predetermined temperature, opens the valve 21 and is sent into the abdominal cavity of the patient through the conduit 22 by natural flow.

その灌流液の供給が終わると弁21が閉じられ
て、ほぼ一定時間、例えば1〜2時間、そのまま
とする貯留状態とする。この間に腹膜を通じて老
廃物や水分が腹腔内灌流液に移動する。貯留モー
ドが終了すると排液モードとされ、弁24を開
き、腹腔内の排液は導管22を通りトラツプ25
内へ流出される。トラツプ25内の排液が所定量
に達すると、排液用ローラポンプ26が駆動され
て、トラツプ25内の排液が排液用導管27を通
じて外部に放出される。
When the supply of the perfusate is finished, the valve 21 is closed and the perfusate remains in the reservoir state for a substantially fixed period of time, for example, 1 to 2 hours. During this time, waste products and fluids move through the peritoneum into the intraperitoneal irrigation fluid. When the storage mode is finished, the mode is set to drainage mode, the valve 24 is opened, and the drainage fluid in the abdominal cavity passes through the conduit 22 to the trap 25.
leaked inside. When the drained liquid in the trap 25 reaches a predetermined amount, the drained liquid roller pump 26 is driven, and the drained liquid in the trap 25 is discharged to the outside through the drained liquid conduit 27.

このように従来の腹膜灌流装置においては、灌
流液を加温容器19へ供給するために、ローラポ
ンプ17を用い、また排液にローラポンプ26を
使用し、二つのローラポンプおよび三つの弁を用
いており、構成が複雑になる。
In this way, in the conventional peritoneal perfusion device, the roller pump 17 is used to supply the perfusion fluid to the heating container 19, and the roller pump 26 is used to drain the fluid, and two roller pumps and three valves are used. The configuration is complicated.

更に腹腔への灌流液の注液量の測定を給液用ロ
ーラポンプ17を用いて測定し、排液量を排液用
ローラポンプ26を用いて測定しており、つまり
二つの計量手段で測定しているため、その二つの
ポンプ、これに用いる各チユーブに差があると、
除水量(排液量−注液量)を正しく求めることが
できない。
Furthermore, the amount of irrigation fluid injected into the abdominal cavity is measured using the fluid supply roller pump 17, and the amount of fluid drained is measured using the fluid drainage roller pump 26. In other words, the measurement is performed using two measuring means. Therefore, if there are differences between the two pumps and the tubes used for them,
The amount of water removed (the amount of liquid drained - the amount of liquid injected) cannot be determined correctly.

また従来のものは部品点数が多く、これらを接
続する導管の長さも長く、配管も複雑であり、こ
の点からも高価になり、しかも装置への脱着が面
倒であつた。
In addition, the conventional type has a large number of parts, the length of the conduit connecting these parts is long, and the piping is complicated, which makes it expensive and troublesome to attach and detach from the device.

しかも注入量の誤設定や患者腹腔内に液が大量
に残留していた場合でも設定された注入量を腹腔
内に注入してしまうため、患者の腹腔内の圧力が
異常に高まり患者が危険となる場合もある。また
患者カテーテルと第1導管との接続がはずれた場
合または第1導管およびカテーテルが折れ曲り液
の流れを阻害した場合に検出が遅く危険をまねく
場合がある。
Moreover, even if the injection volume is incorrectly set or a large amount of fluid remains in the patient's abdominal cavity, the set injection volume will be injected into the patient's abdominal cavity, causing abnormal pressure in the patient's abdominal cavity and putting the patient at risk. Sometimes it happens. Further, if the patient catheter and the first conduit become disconnected, or if the first conduit and catheter are bent and obstruct the flow of the liquid, detection may be delayed and may pose a danger.

「問題点を解決するための手段」 この考案によれば、灌流液の患者の腹腔内への
供給は、加温器内に配された灌流液源より患者の
腹腔内圧力を検出する圧力検出手段と注液量設定
手段の両者で制御されるポンプで行なわれる。す
なわち圧力検出手段が、所定値以上の圧力を検出
した場合には注液量が設定値に達していなくて
も、ポンプを停止させ注液を停止させる。
``Means for solving the problem'' According to this invention, the supply of irrigation fluid into the patient's peritoneal cavity is achieved by pressure detection, which detects the patient's intra-abdominal pressure from an irrigation fluid source placed in a warmer. This is carried out using a pump that is controlled by both the means and the liquid injection amount setting means. That is, when the pressure detection means detects a pressure equal to or higher than a predetermined value, the pump is stopped to stop the liquid injection even if the amount of liquid injected has not reached the set value.

他方、排液の放出時も、急速に排出しないよう
この圧力検出手段でポンプを比例的に制御する。
またこのポンプの回転数を精算することにより、
注液量、排液量を求め、この値より除水量を算出
する。また、灌流液源を加温する為、加温容器お
よび灌流液源から加温容器への液の流れを制御す
る弁は不要となる。また患者カテーテルと第1導
管との接続がはずれた場合または、第1導管およ
びカテーテルが折れ曲り液の流れを阻害した場合
に即時に検出し警報を発し、動作を停止し、安全
を確保できる。
On the other hand, when discharging waste liquid, the pump is proportionally controlled by this pressure detection means so as not to discharge the liquid too quickly.
Also, by calculating the rotation speed of this pump,
Determine the amount of liquid injected and the amount of drained liquid, and calculate the amount of water removed from these values. Also, since the irrigation fluid source is heated, a heating container and a valve to control the flow of fluid from the irrigation fluid source to the heating container are not required. Furthermore, if the patient catheter and the first conduit are disconnected, or if the first conduit and catheter are bent and obstruct the flow of liquid, it is immediately detected, an alarm is issued, the operation is stopped, and safety can be ensured.

「実施例」 第1〜4図にこの考案の実施例を示す。本体3
1はこの例ではキヤスタにより移動し易いように
されている。
``Example'' Figures 1 to 4 show examples of this invention. Main body 3
1 is made easy to move by casters in this example.

ケース部32内に加温部36が設けられ、その
加温部36内に灌流液源11(第2図参照)が配
されている。加温部36にはヒータ38が設けら
れ、このヒータ38により、空気を介し灌流液源
11を加熱することができる。灌流液源11から
の第1導管41は第1弁39を通じてケース部3
2内を通して外部に導出され、かつその端部に患
者の腹腔のカテーテルに連絡するためのコネクタ
23が接続されている。第1弁39及び第1導管
41の連結点は下方に延長した第2導管42に連
結され、第2導管42の途中に第2弁43が設け
られ、また第2導管42の下端は外部に導出され
て排液容器44内に挿入される。
A heating section 36 is provided within the case portion 32, and an irrigation fluid source 11 (see FIG. 2) is disposed within the heating section 36. A heater 38 is provided in the heating section 36, and the heater 38 can heat the irrigation fluid source 11 via air. A first conduit 41 from the irrigation fluid source 11 is connected to the case portion 3 through a first valve 39.
A connector 23 is connected to the end thereof for communicating with a catheter in the patient's abdominal cavity. The connection point between the first valve 39 and the first conduit 41 is connected to a second conduit 42 extending downward, a second valve 43 is provided in the middle of the second conduit 42, and the lower end of the second conduit 42 is connected to the outside. It is led out and inserted into the drainage container 44.

第1導管41に、圧力検出手段49が設けられ
る。この圧力検出手段49は、第3〜4図に示す
ように腹腔内圧力に応じて変形する軟質容器50
と、軟質容器50の変形量を計測するセンサ51
と、軟質容器50を収納するホルダ52で構成さ
れ、患者の腹腔内圧力は灌流液に非接触で測定さ
れる。
The first conduit 41 is provided with pressure detection means 49 . This pressure detection means 49 includes a soft container 50 that deforms according to intra-abdominal pressure as shown in FIGS. 3 and 4.
and a sensor 51 that measures the amount of deformation of the soft container 50.
and a holder 52 that accommodates a soft container 50, and the intraperitoneal pressure of the patient is measured without contacting the irrigation fluid.

また、圧力検出手段49と、第2導管42の分
岐点との間にはポンプ45が設けられる。そして
このポンプ45は、圧力検出手段49で測定され
る患者の腹腔内圧力に基づいて制御部46を介し
て制御される。
Further, a pump 45 is provided between the pressure detection means 49 and the branch point of the second conduit 42 . The pump 45 is controlled via the control section 46 based on the patient's intra-abdominal pressure measured by the pressure detection means 49.

すなわち腹腔内圧力は20mmHg程度が正常とさ
れているので、例えば腹腔内圧力の上限値を30mm
Hgに設定し、圧力検出手段49が30mmHg以上の
圧力を検出した場合には、注液量が設定値に達し
ていなくてもポンプ45を停止させ、注液を停止
させる。なお腹腔内圧力が20〜30mmHgの間、注
液速度を徐々に減少させるようにしてもよい。
In other words, the normal intra-abdominal pressure is around 20 mmHg, so for example, the upper limit of intra-abdominal pressure should be set to 30 mm.
Hg, and when the pressure detection means 49 detects a pressure of 30 mmHg or more, the pump 45 is stopped and the injection of liquid is stopped even if the amount of liquid injected has not reached the set value. The injection rate may be gradually decreased while the intra-abdominal pressure is between 20 and 30 mmHg.

他方排液の放出時も、急速に排出しないように
圧力検出手段49でポンプ45を比例的に制御す
る。また、ポンプ45の正逆方向への回転数の精
算から各々注液量及び排液量を求め、この値から
除水量を算出する。
On the other hand, when discharging the waste liquid, the pump 45 is proportionally controlled by the pressure detection means 49 so as not to discharge the liquid rapidly. In addition, the amount of liquid injected and the amount of liquid drained are determined by calculating the number of rotations of the pump 45 in the forward and reverse directions, and the amount of water removed is calculated from these values.

この圧力検出手段49の実施例として第3図に
示したものは、センサ51に差動トランス53を
用いた例で、軟質容器50の変位はプランジヤ5
4、コア53aを介して差動トランス53で検出
される。第4図には、同様に変位を反射板55と
発受光器56で光学的に検出する圧力検出手段4
9を例示する。
The embodiment of the pressure detection means 49 shown in FIG. 3 is an example in which a differential transformer 53 is used as the sensor 51, and the displacement of the soft container 50 is
4. Detected by the differential transformer 53 via the core 53a. FIG. 4 shows a pressure detection means 4 that optically detects displacement using a reflection plate 55 and a light emitting/receiving device 56.
9 is illustrated.

第2図に示す通り、制御部46がケース32に
設けられ、制御部46に対し、キー操作部47及
び表示部48が接続され、キー操作部47を設定
キー47aにより注液量を設定することができ、
その設定注液量は表示部48の表示面48aに表
示される。また、キー操作部47の他の制御キー
47bの操作により、弁39,43に対する順次
制御が行なわれポンプ45による注液、排液の各
流量測定値が注液量表示面48b、排液量表示面
48cにそれぞれ表示され、また除水量が演算さ
れて除水量表示面48dに表示される。キー操作
部47のキー、表示部48の各表示面48a〜4
8dはケース部32の操作表示パネル57に設け
られている。
As shown in FIG. 2, a control unit 46 is provided in the case 32, a key operation unit 47 and a display unit 48 are connected to the control unit 46, and the injection amount is set using a setting key 47a. It is possible,
The set injection amount is displayed on the display surface 48a of the display section 48. Further, by operating the other control key 47b of the key operation unit 47, the valves 39 and 43 are sequentially controlled, and each flow rate measurement value of liquid injection and drainage by the pump 45 is displayed on the liquid injection amount display screen 48b, and the amount of liquid drained. They are each displayed on the display surface 48c, and the amount of water removed is calculated and displayed on the water removal amount display surface 48d. Keys on the key operation section 47 and display surfaces 48a to 4 on the display section 48
8d is provided on the operation display panel 57 of the case portion 32.

灌流液バツグ12は常時は密封され、スパイク
で突き刺すことにより開くことができる出口ポー
トを下部に有するものが好ましい。これらのバツ
グ、腹腔カテーテルへの接続、排液への導管を含
むすべての導管は、排液を除いて全て閉鎖的に接
続され感染が防止されている。導管34,41,
42などは合成樹脂材のチユーブであり、弁3
9,43はそのチユーブを押し潰すことにより、
流路を閉じることができる。
Preferably, the irrigation fluid bag 12 is normally sealed and has an exit port at the bottom that can be opened by piercing with a spike. All conduits, including these bags, connections to the peritoneal catheter, and conduits to drainage, are all connected in a closed manner to prevent infection, except for drainage. Conduit 34, 41,
42 is a synthetic resin tube, and valve 3
9,43 by crushing the tube,
The channel can be closed.

注液モードでは第1弁39を開くと、加温部に
よりあらかじめ37°Cに加温された灌流液源11の
灌流液をポンプ45により第1導管41を通して
患者の腹腔内へ供給する。
In the fluid injection mode, when the first valve 39 is opened, the pump 45 supplies the irrigation fluid from the irrigation fluid source 11, which has been preheated to 37° C. by the heating unit, into the patient's abdominal cavity through the first conduit 41.

この時圧力検出手段49により、腹腔内圧力が
30mmHg以上にならないようにポンプ45を制御
しながら注液する。もし腹腔内圧力が30mmHgを
超えれば第1弁39を閉じポンプ45を停止し警
報を発する。腹腔内圧力が30mmHg以下であれば、
ポンプ45の回転数に基づいて注液量を測定し、
設定注液量に達した時第1弁39を閉じポンプ4
5を停止させる。
At this time, the pressure detection means 49 detects the intra-abdominal pressure.
The liquid is injected while controlling the pump 45 so as not to exceed 30 mmHg. If the intra-abdominal pressure exceeds 30 mmHg, the first valve 39 is closed, the pump 45 is stopped, and an alarm is issued. If the intra-abdominal pressure is below 30mmHg,
Measuring the amount of liquid injected based on the rotation speed of the pump 45,
When the set injection amount is reached, the first valve 39 is closed and the pump 4
Stop 5.

またこの注液量は制御部46に記憶され、かつ
表示面48bに表示される。
Further, this injection amount is stored in the control unit 46 and displayed on the display surface 48b.

貯留モード 患者の腹腔内に灌流液を定められた時間貯留す
る。
Reservoir mode Retains the perfusate within the patient's abdominal cavity for a predetermined period of time.

排液モード 第2弁43を開き、患者の腹腔内より第1導管
41を通じて、ポンプ45により排液する。この
時圧力検出手段49により腹腔内圧力を10mmHg
以下にしないようにポンプ45の回転を制御す
る。なおこの時ポンプ45は注液モード時とは反
対方向に回転させる。
Drainage Mode The second valve 43 is opened, and the pump 45 drains fluid from the patient's abdominal cavity through the first conduit 41. At this time, the pressure detection means 49 detects intra-abdominal pressure of 10 mmHg.
The rotation of the pump 45 is controlled so as not to cause the following. At this time, the pump 45 is rotated in the opposite direction to that in the liquid injection mode.

排液量はポンプ45の回転数に基づいて計測
し、その排液量を制御部46に記憶し、表示面4
8cに表示する。制御部46は「排液量−注入液
量=除水量」を計算し、この除水量を表示面48
dに表示する。
The amount of drained liquid is measured based on the rotation speed of the pump 45, and the amount of drained liquid is stored in the control unit 46 and displayed on the display screen 4.
Displayed on 8c. The control unit 46 calculates "amount of drained fluid - amount of injected fluid = amount of water removed" and displays this amount of water removed on the display screen 48.
Display on d.

この注液モード、貯留モード、排液モードを1
サイクルとし、これを設定されたサイクル数繰り
返す。なお排液モードは排液速度が所定値以下に
なると停止する。
This liquid injection mode, storage mode, and liquid drainage mode are set to 1.
This is repeated for the set number of cycles. Note that the liquid draining mode is stopped when the liquid draining speed becomes equal to or less than a predetermined value.

「考案の効果」 以上述べたようにこの考案によれば、液の移送
は患者の腹腔内圧力を監視しながら行なわれ安全
性が高い。またチユーブ接続の異常をも即時に検
出できる為この面でも安全性が高まる。
"Effects of the Device" As described above, according to this device, the fluid is transferred while monitoring the patient's intra-abdominal pressure, resulting in high safety. Furthermore, since abnormalities in tube connections can be detected immediately, safety is increased in this aspect as well.

また複数のポンプを用いず、弁も3ケから2ケ
になるため、安価に構成でき、かつ故障も少な
い。第1導管41内の液の移動をポンプ45で測
定し、つまり注液量も、排液量も同一のポンプで
測定するため、それだけ正確に除水量を求めるこ
とができる。また、部品点数が少なく、接続導管
の長さも短かく、その装着、取外しが容易であ
り、可動部がないから故障し難く、しかも安価な
ものとすることができる。
Furthermore, since multiple pumps are not used and the number of valves is reduced from three to two, it can be constructed at low cost and has fewer failures. Since the movement of the liquid in the first conduit 41 is measured by the pump 45, that is, the amount of liquid injected and the amount of liquid drained are also measured by the same pump, the amount of water removed can be determined more accurately. In addition, the number of parts is small, the length of the connecting conduit is short, it is easy to install and remove, and since there are no moving parts, it is difficult to break down and can be made at low cost.

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

第1図はこの考案による腹膜灌流装置の一例を
示す見取図、第2図は第1図の装置の系統図、第
3図、及び第4図はそれぞれ異なるセンサを用い
た圧力検出手段の一例を示す図、第5図は従来の
装置の系統図である。 11……灌流液源、39……第1弁、41……
第1導管、42……第2導管、43……第2弁、
45……ポンプ、49……圧力検出手段。
FIG. 1 is a sketch showing an example of a peritoneal perfusion device according to this invention, FIG. 2 is a system diagram of the device shown in FIG. 1, and FIGS. 3 and 4 each show an example of pressure detection means using different sensors. The figure shown in FIG. 5 is a system diagram of a conventional device. 11... Irrigation fluid source, 39... First valve, 41...
First conduit, 42... Second conduit, 43... Second valve,
45...Pump, 49...Pressure detection means.

Claims (1)

【実用新案登録請求の範囲】 灌流液を供給する灌流液源と、その灌流液源を
加温する加温器と、 その灌流液源と患者の腹腔カテーテルとを連結
する第1導管と、 その第1導管に分岐連結された第2導管と、 上記第1導管の上記灌流液源と上記第2導管の
分岐点との間に設けられ、上記加温容器から患者
腹腔への灌流液の供給、遮断を制御する第1弁
と、 上記第2導管に設けられ上記患者腹腔からの排
液の排出、遮断を制御する第2弁と、 上記第2導管の分岐点と上記カテーテルとの間
に設けられ患者の腹腔内圧力を検出する圧力検出
手段と、この圧力検出手段と上記第2導管の分岐
点との間に設けられ、圧力検出手段で検出された
圧力に基づいて、その流量が制御されるポンプと
を具備する腹腔灌流装置。
[Scope of Claim for Utility Model Registration] An irrigation fluid source that supplies irrigation fluid, a warmer that warms the irrigation fluid source, a first conduit that connects the irrigation fluid source and a patient's peritoneal catheter; a second conduit that is branched and connected to the first conduit; and a second conduit provided between the irrigation fluid source of the first conduit and a branch point of the second conduit, for supplying irrigation fluid from the heating container to the patient's abdominal cavity. , a first valve that controls blocking, a second valve provided in the second conduit that controls draining and blocking of drainage from the patient's peritoneal cavity, and between a branch point of the second conduit and the catheter. a pressure detection means for detecting the intra-abdominal pressure of the patient; and a pressure detection means provided between the pressure detection means and the branch point of the second conduit, the flow rate of which is controlled based on the pressure detected by the pressure detection means. A peritoneal perfusion device comprising:
JP5856387U 1987-04-16 1987-04-16 Expired JPH0340303Y2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5856387U JPH0340303Y2 (en) 1987-04-16 1987-04-16

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5856387U JPH0340303Y2 (en) 1987-04-16 1987-04-16

Publications (2)

Publication Number Publication Date
JPS63166249U JPS63166249U (en) 1988-10-28
JPH0340303Y2 true JPH0340303Y2 (en) 1991-08-23

Family

ID=30889251

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5856387U Expired JPH0340303Y2 (en) 1987-04-16 1987-04-16

Country Status (1)

Country Link
JP (1) JPH0340303Y2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003533243A (en) * 2000-02-10 2003-11-11 バクスター・インターナショナル・インコーポレイテッド Method and apparatus for monitoring and controlling peritoneal dialysis treatment

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2684807A1 (en) * 2007-04-05 2008-10-16 Velomedix, Inc. Automated therapy system and method
DE102008031662A1 (en) * 2008-07-04 2010-01-07 Fresenius Medical Care Deutschland Gmbh Device for peritoneal dialysis
WO2012006625A2 (en) 2010-07-09 2012-01-12 Velomedix, Inc. Method and apparatus for pressure measurement

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003533243A (en) * 2000-02-10 2003-11-11 バクスター・インターナショナル・インコーポレイテッド Method and apparatus for monitoring and controlling peritoneal dialysis treatment

Also Published As

Publication number Publication date
JPS63166249U (en) 1988-10-28

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