Device and method for monitoring a patient access, in particular a vascular access in extracorporeal blood treatment

• US 8,180,443 B1
• Filed: 09/08/2007
• Issued: 05/15/2012
• Est. Priority Date: 09/12/2006
• Status: Active Grant

• Current Assignee: Fresenius Medical Care Deutschland GmbH (Fresenius Medical Care AG)
• Original Assignee: Fresenius Medical Care Deutschland GmbH (Fresenius Medical Care AG)
• Inventors: Kleinekofort, Wolfgang, Wüpper, Andreas
• Primary Examiner(s): HOEKSTRA, JEFFREY GERBEN
• Application Number:
  US12/440,951
• Time in Patent Office: 1,711 Days
• Field of Search: 600/300, 600/301, 600/481, 600504-507, 600/547, 600/561, 600/573, 600/576, 600/579
• US Class Current: 600/547
• CPC Class Codes: A61M 1/3653 Interfaces between patient blood circulation and extra-corporal blood circuit
• CPC Class Codes: A61M 1/3656 Monitoring patency or flow at connection sites; Detecting disconnections

Abstract

The present invention relates to a device and a method for monitoring a patient access, in particular a vascular access in extracorporeal blood treatment, in which a patient'"'"'s blood is withdrawn from the patient via an arterial conduit and is returned to the patient via a venous conduit. The blood is conveyed by a blood pump, preferably an occlusive blood pump, such as a roller pump. To monitor the vascular access, the electrical AC voltage and/or the alternating current and/or a derived electrical measured variable that is generated by electrostatic charges during operation of the occlusive peristaltic pump is monitored. If the triboelectric AC voltage generated by the blood pump and/or the alternating current and/or the derived electrical measured variable lies within predetermined limits, this indicates that the vascular access is faulty.

Claims

1. A device for monitoring vascular access during an extracorporeal blood treatment, in which a patient'"'"'s blood is withdrawn from the patient via an arterial tubular conduit comprising an arterial patient connector with an arterial puncture cannula, the patient'"'"'s blood is returned to the patient via a venous tubular conduit comprising a venous patient connector with a venous puncture cannula, and the blood is conveyed by a pump in the arterial tubular conduit or the venous tubular conduit that generates triboelectric charges during operation, the device comprising:

a first contact element adapted to be placed on a patient'"'"'s skin to produce an electrical connection to the patient'"'"'s skin, and a second contact element adapted to be in contact with a fluid flowing in a dialysis fluid circuit or a fluid flowing in a filtrate fluid circuit;

a measurement unit configured to measure at least one of;

an AC voltage, an alternating current, and a derived electrical variable, each resulting only from the triboelectric charges generated by the pump, wherein the AC voltage, the alternating current, or the derived electrical variable is measured between the first contact element and the second contact element; and

an evaluation unit configured to evaluate the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable, wherein when there is a change in an amplitude of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable, this is a first indication of an incorrect vascular access.

2. The device of claim 1, wherein the evaluation unit comprises:

a first comparison unit configured to compare the at least one of;

the amplitude of the measured AC voltage, the amplitude of the measured alternating current, and the amplitude of the measured derived electrical variable, to a respective predetermined limit value,

wherein the change in the amplitude comprises at least one of;

the amplitude of the measured AC voltage, the amplitude of the measured alternating current, and the amplitude of the measured derived electrical variable, being greater than the respective predetermined limit value.

3. The device of claim 2, wherein the comparison unit is configured to compare the amplitude to the respective predetermined limit value at multiple consecutive times,

wherein when the amplitude is greater than the respective predetermined limit value for a predetermined number of measurements at multiple consecutive times, this is a second indication of an incorrect vascular access.

4. The device of claim 1, further comprising:

a sensor configured to measure a frequency of a rotor of the pump;

wherein the evaluation unit further comprises;

a second comparison unit configured to determine a frequency of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable; and

configured to compare the measured frequency of the rotor of the pump to the at least one of;

the frequency of the measured AC voltage, the frequency of the measured alternating current, and the frequency of the measured derived electrical variable,

wherein when the frequency of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable correlates with the frequency of the rotor, this is a third indication of an incorrect vascular access.

5. The device of claim 4, further comprising:

an alarm that is activated when there is at least one of;

the first indication, the second indication, and the third indication of an incorrect vascular access.

6. The device of claim 1, wherein the pump is an occlusive peristaltic pump.

7. The device of claim 1, wherein the measurement unit is configured to measure the derived electrical variable, and the derived electrical variable is a resistance.

8. A blood treatment device comprising:

at least one of;

a dialysis fluid circuit comprising a dialyzer divided by a semi-permeable membrane into a blood chamber and a dialysis fluid chamber, and a filtrate fluid circuit comprising a membrane filter divided by a semi-permeable membrane into a blood chamber and a filtrate chamber;

an extracorporeal blood circuit comprising;

an arterial blood conduit connected to an inlet of the blood chamber and to an arterial puncture cannula for a vascular access, and

a venous blood conduit connected to an outlet of the blood chamber and to a venous blood cannula for the vascular access; and

the device for monitoring vascular access of claim 1.

9. The blood treatment device of claim 8, further comprising:

a dialysis fluid preparation device,

wherein the second contact element is in contact with the dialysis fluid in the dialysis fluid preparation device.

10. A method for monitoring the vascular access during an extracorporeal blood treatment, in which a patient'"'"'s blood is withdrawn from the patient via an arterial tubular conduit comprising an arterial patient connector with an arterial puncture cannula, and the patient'"'"'s blood is returned to the patient via a venous tubular conduit comprising a venous patient connector with a venous puncture cannula, the method comprising:

conveying the blood in the arterial conduit or the venous conduit by a pump;

generating triboelectric charges by operation of the pump;

placing a first contact element on a patient'"'"'s skin to produce an electrical connection to the patient'"'"'s skin;

contacting a second contact element with a fluid flowing in a dialysis fluid circuit or a fluid flowing in a filtrate fluid circuit;

measuring at least one of the following;

an AC voltage, an alternating current, and a derived electrical variable, each resulting only from the triboelectric charges generated by the pump, wherein the AC voltage, the alternating current, or the derived electrical variable is measured between the first contact element and the second contact element;

evaluating the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable; and

determining there is a first indication of an incorrect vascular access when there is a change in an amplitude of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable.

11. The method of claim 10, further comprising:

comparing the amplitude of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable, to a respective predetermined limit value; and

wherein the change in the amplitude comprises at least one of;

the amplitude of the measured AC voltage, the amplitude of the measured alternating current, and the amplitude of the measured derived electrical variable being greater than the respective predetermined limit value.

12. The method of claim 11, further comprising:

comparing the amplitude at multiple consecutive times; and

determining there is a second indication of an incorrect vascular access if the amplitude is greater than the respective predetermined limit value for a predetermined number of measurements at multiple consecutive times.

13. The method of claim 10, further comprising:

determining a frequency of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable;

comparing the frequency of a rotor of the pump to the at least one of;

the frequency of the measured AC voltage, the frequency of the measured alternating current, and the frequency of the measured derived electrical variable; and

determining there is a third indication of an incorrect vascular access if the frequency of the at least one of;

the measured AC voltage, the measured alternating current, and the measured derived electrical variable correlates to the frequency of the rotor.

14. The method of claim 13, further comprising:

activating an alarm following at least one of;

the first indication, the second indication, and the third indication of an incorrect vascular access.

15. The method of claim 13, further comprising:

activating an alarm following the first indication, the second indication, and the third indication of an incorrect vascular access.

16. The method of claim 10, further comprising measuring the derived electrical variable, wherein the derived electrical variable is a resistance.

17. The method of claim 10, wherein the pump is an occlusive peristaltic pump.