Blood Treatment Device Comprising A Functional Unit For Carrying Out The Blood Treatment And Method For Monitoring The Functionality And/Or The Operating State Of The Functional Unit

Abstract

The invention relates to a blood treatment device comprising an attachment unit 7 for attaching a functional unit 1 intended for single use for carrying out the blood treatment. The blood treatment device according to the invention is characterised by a monitoring unit 8 for monitoring the operability and/or the operating state of the functional unit 1, which functional unit comprises at least one light transmitter 17A, 18A and at least one light receiver 17B, 18B. The light transmitter and light receiver are arranged in the monitoring unit 8 according to the invention on one side of the functional unit 1. The arrangement of the light transmitter and light receiver on the same side has the advantage that the monitoring unit 8 can be integrated into the attachment unit 7 of the blood treatment device without any major structural modifications. The monitoring of the functional unit 1 is based on an optical measurement method in which the light reflected on a part of the functional unit 1 or a part of the attachment unit 7 is detected. A calculation- and evaluation unit 13 is configured such that conclusions can be drawn as to a defective state and/or a certain operating state of the functional unit 1 based on the intensity of the light falling on the functional unit and the light reflected on the functional unit or the attachment unit.

Claims

1. A blood treatment device comprising an attachment unit for attaching a functional unit intended for single use for carrying out the blood treatment and a monitoring unit for monitoring the operability and/or the operating state of the functional unit, characterised in that the monitoring unit comprises at last one light transmitter and at least one light receiver that are arranged such that the light emitted by the light transmitter falls on one side of the functional unit and the light reflected on a part of the functional unit or a part of the attachment unit falls on the light receiver, and the monitoring unit comprises a calculation- and evaluation unit that is configured such that conclusions can be drawn as to a defective state and/or a certain operating state of the functional unit based on the intensity of the light falling on the functional unit and of the light reflected on the functional unit or the attachment unit.

2. The blood treatment device according to claim 1, characterised in that the attachment unit comprises an attachment component and a cover component that are arranged at such a distance from one another that the functional unit can be inserted between the attachment component and the cover component, the light transmitter and the light receiver being provided in or on the cover component.

3. The blood treatment device according to claim 2, characterised in that the attachment component of the attachment unit comprises a contact surface for the functional unit that reflects the light of the light transmitter.

4. The blood treatment device according to claim 3, characterised in that the contact surface of the attachment component comprises a flexible material.

5. The blood treatment device according to claim 2, characterised in that the cover component of the attachment unit is attached to the attachment component so as to be movable between an open position and a closed position.

6. The blood treatment device according to claim 2, characterised in that the cover component of the attachment unit is configured as a clamp component, so that the functional unit can be attached in a clamped manner between the attachment component and the cover component.

7. The blood treatment device according to claim 2, characterised in that the attachment unit comprises a suction unit for creating a vacuum at the attachment component, so that the functional unit can be attached to the attachment component by way of suction power.

8. The blood treatment device according to claim 1, characterised in that the calculation- and evaluation unit of the monitoring unit is configured such that, based on the reduction of the intensity of the light, it can be concluded that a functional unit is attached to the attachment unit.

9. The blood treatment device according to claim 1, characterised in that the calculation- and evaluation unit of the monitoring unit is configured such that, based on the reduction of the intensity of the light, it can be concluded that a chamber or a channel of the functional unit is filled with a fluid, in particular dialysate or substitution fluid.

10. The blood treatment device according to claim 9, characterised in that the calculation- and evaluation unit of the monitoring unit is configured such that a control signal is generated when the calculation- and evaluation unit has detected that the chamber and/or the channel of the functional unit is filled with a fluid, in particular dialysate or substitution fluid, the blood treatment device comprising a control unit that receives the control signal of the calculation- and evaluation unit.

11. The blood treatment device according to claim 9, characterised in that the calculation- and evaluation unit of the monitoring unit is configured such that, based on the reduction of the intensity of the light, it can be concluded that the fluid with which the chamber or the channel is filled contains haemoglobin.

12. The blood treatment device according to claim 11, characterised in that the calculation- and evaluation unit of the monitoring unit is configured such that an alarm signal is generated when the calculation- and evaluation unit has detected that the fluid with which the chamber or the channel is filled contains haemoglobin, the blood treatment device comprising an alarm unit that receives the alarm signal of the calculation- and evaluation unit.

13. The arrangement comprising the blood treatment device according to claim 1 and a functional unit intended for single use for carrying out the blood treatment.

14. The arrangement according to claim 13, characterised in that the functional unit comprises a housing body that is permeable to light, in which at least one chamber for receiving a fluid and/or at least one channel for carrying a fluid are formed, the light transmitter and the light receiver being arranged on one side of the housing body such that the light emitted by the light transmitter falls on a chamber and/or a channel of the functional unit that is attached to the attachment unit.

15. The arrangement according to claim 14, characterised in that the housing body of the functional unit comprises a housing part formed having trough-shaped recesses, which housing part is sealed by a flat housing part so as to be impermeable to fluids.

16. The arrangement according to claim 15, characterised in that the flat housing part is a film connected to the housing part formed having trough-shaped recesses.

17. The arrangement according to claim 14, characterised in that the chamber or the channel comprises an opening sealed with a hydrophobic membrane, the light transmitter and the light receiver being arranged such that the light emitted by the light transmitter falls on the hydrophobic membrane of the chamber and the light reflected by the hydrophobic membrane falls on the light receiver.

18. The arrangement according to claim 17, characterised in that the calculation- and evaluation unit of the monitoring unit is configured such that, based on the reduction of the intensity of the light, it can be concluded that the hydrophobic membrane is defective.

19. A method for monitoring the operability and/or the operating state of a functional unit intended for single use, which is attached to an attachment unit of a blood treatment device for carrying out a blood treatment, the functional unit comprising a housing body that is permeable to light, in which a plurality of chambers for receiving a fluid and a plurality of channels for carrying a fluid are formed, and light being emitted from at least one light transmitter on one side of the functional unit and the light reflected on a part of the attachment unit or the functional unit being received by at least one light receiver, characterised in that the operability and/or the operating state of the functional unit is monitored based on the reduction of the intensity of the light, it then being possible to conclude that the functional unit is attached to the attachment unit and/or a chamber or a channel is filled with a fluid, in particular dialysate or substitution fluid, and/or the fluid with which the chamber or the channel is filled contains haemoglobin.

20. The method according to claim 19, characterised in that at least one chamber or at least one channel comprises an opening sealed off with a hydrophobic membrane and that, based on the reduction of the intensity of the light, it can be concluded that the hydrophobic membrane is defective.

Description

[0023] In the following, an embodiment of the invention will be described in detail by reference to the drawings.

[0024] FIG. 1 shows a functional unit for carrying out the blood treatment for a blood treatment device in plan view, and

[0025] FIG. 2 shows the attachment unit together with the functional unit of the blood treatment device as an extremely simplified schematic representation.

[0026] FIG. 1 shows an embodiment of an external functional unit (disposable) for an extracorporeal blood treatment device, in particular a haemodialysis device. The functional unit 1 comprises a flat housing body 2 which consists of a material permeable to light. The housing body 2 may be a transparent plastics body. The functional unit is described in detail in DE 10 2009 018 664 A1, to which reference is explicitly made. The components of the functional unit that are essential to the invention are described below.

[0027] FIG. 1 shows the functional unit 1 in a view from below. The housing body 2 of the functional unit 1 comprises a housing part 2A formed having trough-shaped recesses 23, which housing part is tightly sealed off at the underside with a film 2B (shown only in part) by the formation of a plurality of chambers and channels. During operation of the haemodialysis device, blood or a medicinal fluid, for example dialysate or substitution fluid, is present in the chambers and channels.

[0028] In FIG. 1, one of the chambers is denoted by reference sign 3 and one of the channels is denoted by reference sign 4. Blood is present in the chamber 3 during operation of the dialysis device. The channel 4 is a channel in which substitution fluid flows during operation of the dialysis device. Moreover, the functional unit 1 comprises a hydrophobic filter 5 which has a hydrophobic membrane 5A (merely indicated in FIG. 1). Furthermore, the functional unit 1 also has a valve arrangement (not shown in more detail in FIG. 1) having a plurality of valves via which the fluid connections between the individual chambers and channels can be established.

[0029] The blood and the medical fluids are supplied and led away by means of hose lines (not shown) which are connected to connectors 6A to 6D of the housing body 2. The hose lines (not shown) are, together with further components (which are not shown) where appropriate, a part of the functional unit 1.

[0030] FIG. 2 shows as an extremely simplified schematic representation the part of the housing 24 of the blood treatment device where an attachment unit 7 for attaching the functional unit 1 is located. FIG. 2 only shows the components of the functional unit 1 and the attachment unit 7 that are essential to the invention. A monitoring unit 8 for monitoring the operability and/or the operating state of the functional unit is also shown in FIG. 2.

[0031] The functional unit 1 is inserted into the attachment unit 7. FIG. 2 shows a cross-section of the functional unit 1. In the sectional view, the substitution fluid channel 4 and the hydrophobic filter 5 comprising the hydrophobic membrane 5A can be seen. The rest of the chambers and channels are not shown for the sake of clarity.

[0032] The hydrophobic filter 5 comprises a chamber 5B in the housing body 2, which has an opening 5C on the upper surface. The opening 5C of the chamber 5B is tightly sealed by the hydrophobic membrane 5A. Above the hydrophobic membrane 5C, the housing body 2 is formed as a support structure so that the hydrophobic membrane is fixed in the housing body. During operation of the haemodialysis device, for example in single-needle mode, the chamber 5B of the hydrophobic filter 5 is filled with blood.

[0033] The attachment unit 7 of the blood treatment device comprises an attachment component 9 on the machine side, which is formed as a housing open on one side for receiving the functional unit 1.

[0034] For carrying out the blood treatment, the functional unit 1 is inserted into the attachment component 9, the lower surface of the functional unit 1 abutting a contact surface 10 of the attachment component 9. The attachment unit 7 comprises a suction unit 11 which creates a vacuum at the contact surface 10 so that the functional unit 1 is sucked in at the contact surface 10.

[0035] Moreover, the attachment unit 7 comprises a cover component 12 which is attached to the attachment component 9 such that it can pivot about an axis 12A. The cover component 12 is opened for inserting the functional unit and closed for the operation of the blood treatment device.

[0036] The monitoring unit 8 for monitoring the operability and/or the operating state of the functional unit 1 will be described in the following.

[0037] The monitoring unit 8 comprises a calculation- and evaluation unit 13 which may also be a component of the central control unit 14 of the blood treatment device. The calculation- and evaluation unit 13 is connected to the central control unit 14 via a data line 15, so that calculation- and evaluation unit 13 can receive signals which signalise the operating state of the blood treatment device. An alarm unit 16 is connected to the calculation- and evaluation unit 13 via a data line 17. Furthermore, the monitoring unit 8 comprises a first transmitting- and receiving unit 17 and a second transmitting- and receiving unit 18 which transmit and receive light.

[0038] The first and second transmitting- and receiving units 17, 18 each comprise a light transmitter 17A, 18A and a light receiver 17B, 18B. The light transmitter and the light receiver may be light-emitting diodes (LEDs). The light-emitting diodes of the light transmitter preferably transmit light having a wavelength corresponding to the absorption peak of haemoglobin. The effect of this is that the monitoring unit 8 has maximum sensitivity for detecting blood.

[0039] Light transmitter and light receiver 17A, 17B of the first transmitting- and receiving unit 17 is arranged on the cover component 12 of the attachment unit 7 above the substitution fluid channel 4, while the light transmitter and light receiver 18A, 18B of the second transmitting- and receiving unit 18 is arranged above the hydrophobic membrane 5A of the hydrophobic filter 5 in the cover component 12.

[0040] The light transmitter 17A and light receiver 17B of the first transmitting- and receiving unit 17 are arranged such that all of the light of the light transmitter 17A is reflected on the contact surface 10 of the attachment component 9 and hits the light receiver 17B. In a preferred embodiment, the contact surface 10 of the attachment component 9 is covered with a flexible material, for example a plastics mat 10A, which the functional unit 1 abuts. The plastics mat 10A is designed such that the light rays are reflected. For instance, the flexible material may be provided with a reflective coating.

[0041] The light transmitter 18A and light receiver 18B of the second transmitting- and receiving unit 18 are arranged above the hydrophobic filter 5 in such a manner that the rays from the light transmitter 18A are reflected by the hydrophobic membrane 5A and hit the light receiver 18B.

[0042] The calculation- and evaluation unit 13 receives the signals of the light transmitter and light receiver 17A, 17B; 18A, 18B via data lines 19, 20, 21, 22. The calculation- and evaluation unit 13 is configured such that conclusions can be drawn as to a defective operating state and/or a certain operating state of the functional unit based on a reduction of the intensity of the reflected light; in particular it can be concluded that there has been a leakage of blood. The calculation- and evaluation unit 13 may detect a leakage of blood for example on the basis of a measurement based on Lambert's law. Such optical measurement methods can be found in the prior art.

[0043] If, when the functional unit 1 is defective, blood ends up in the substitution fluid, the light of the light transmitter 17A is absorbed by the haemoglobin in the substitution fluid so that the intensity of the light is reduced. If the calculation- and evaluation unit 13 has detected such a malfunction, the calculation- and evaluation unit 13 generates an alarm signal which is received by the alarm unit 16 via the data line 17. Furthermore, the calculation- and evaluation unit 13 generates a control signal which is received by the central control unit 14 of the blood treatment device via the data line 15, so that the control unit 15 can make an intervention in the machine control.

[0044] If the hydrophobic membrane 5A of the hydrophobic filter 5 is defective, blood seeps into the membrane so that the membrane is stained red. Thus, the intensity of the reflected light received by the light receiver 18B changes, and therefore the calculation- and evaluation unit 13 once again generates an alarm signal and a control signal for the alarm unit 16 and the control unit 14. The monitoring unit 8 therefore allows the monitoring of all regions of the functional unit where leakages can occur. For this purpose, the monitoring unit may also comprise further transmitting- and receiving units.

[0045] In addition to operability, the monitoring unit 8 also monitors the operating state of the functional unit. If the functional unit 1 comprising the transparent housing body 2 is inserted into the attachment unit 7, the intensity of the reflected light changes. On the basis of the signal level of the light receiver 17B for example of the first transmitting- and receiving unit 17, the calculation- and evaluation unit 13 detects whether the functional unit is inserted by comparing the measured signal level with a predetermined reference level. This reference level can be set by means of calibration measurements and stored in a memory of the calculation- and evaluation unit 13.

[0046] Furthermore, the calculation- and evaluation unit 13 can detect whether the substitution fluid channel 4 is filled with substitution fluid. The filling of the substitution fluid channel with substitution fluid once again results in the light being absorbed. For the measurement, a further reference level can be set which is stored in the memory of the calculation- and evaluation unit 13. It is also possible to detect the fill level when corresponding reference levels are set.

[0047] The monitoring unit 8 can be tested and/or calibrated by means of the signal sequence when the functional unit 1 is inserted, sucked in and filled. For this purpose, the calculation- and evaluation unit 13 can receive the control signals of the central control unit 14, which signalise the operating state of the blood treatment device.

[0048] In a particularly preferred embodiment, the safety of the blood treatment is improved by the different operating states of the blood treatment device being compared in the calculation- and evaluation unit 13 with the operating state of the functional unit 1. Thus, a plausibility test can take place. For example, it can be monitored by means of the calculation- and evaluation unit 13 whether the control unit 14 can initiate the blood treatment, which is only supposed to happen when the functional unit 1 is positioned in the attachment unit 7. The control unit 14 only activates the blood treatment device when it has received the corresponding control signal from the calculation- and evaluation unit 13, said control signal signalising that the functional unit has been properly inserted in the attachment unit.