IP Library › Granted Patent US 12,059,559
Granted Patent B2
US 12,059,559 · App. 16/950,649 · Granted Aug 13, 2024

Sensors for catheter pumps

Inventors: Paul F. Muller (San Carlos, CA); Keif M. Fitzgerald (San Jose, CA); Richard L. Keenan (Livermore, CA); Veronica J. Neiman (Union City, CA)
Assignee: TC1 LLC
A61M60/857A61M60/13A61M60/174A61M60/216A61M60/411A61M60/554A61M60/808A61M60/816A61M60/825A61M60/827A61M60/867A61B2090/064A61B2090/3966A61M60/148A61M60/211A61M60/414A61M60/577A61M2205/13A61M2205/32A61M2205/3306A61M2205/3334A61M2205/52
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,059,559
App. No.
16/950,649
Filed
Nov 17, 2020
Granted
Aug 13, 2024
Kind
B2
Art Unit
3798
USPC
600/424
Abstract

Sensors for catheter pumps are disclosed herein. The catheter pump can include a catheter assembly comprising a catheter and a cannula coupled to a distal portion of the catheter. The cannula can have a proximal port for permitting the flow of blood therethrough. The catheter assembly can include a sensor to be disposed near the proximal port. A processing unit can be programmed to process a signal detected by the sensor. The processing unit can comprise a computer-readable set of rules to evaluate the signal to determine a position of the cannula relative to an aortic valve of a patient.

Claims (57)

1. A method of pumping blood through a patient, the method comprising:

inserting a catheter pump into the patient, the catheter pump comprising a catheter body, a cannula coupled with the catheter body, an impeller within the cannula, a sensor assembly near the impeller, and a sheath disposed about the catheter body;

providing relative motion between the sheath and the sensor assembly to expose the sensor assembly to the blood;

rotating the impeller; and

measuring a pressure of the blood with the exposed sensor assembly.

2. The method of claim 1 , wherein providing relative motion comprises sliding the sheath proximally relative to the cannula and the sensor assembly.

3. The method of claim 2 , wherein the cannula and impeller expand to deployed configurations upon sliding the sheath proximally.

4. The method of claim 1 , wherein the sensor assembly is disposed proximal the impeller, the method comprising sliding the sheath until a sensor element is exposed through a window of the catheter pump.

5. The method of claim 1 , wherein the sensor assembly is disposed on a wall of the cannula, the method comprising sliding the sheath until a sensor element is exposed to the blood.

6. The method of claim 1 , wherein the sensor assembly is disposed in a central lumen of the catheter pump that extends distal the impeller, the method comprising sliding the sheath until a sensor element is exposed through an opening or window in the central lumen.

7. A method of pumping blood through a patient, the method comprising:

advancing an impeller assembly through a vascular system of the patient to a left ventricle of the patient, the impeller assembly comprising an impeller and a sensor, the sensor configured to measure a pressure of blood flowing through one or more inlets of the impeller assembly;

activating the impeller to pump blood through an aorta of the patient at a flow rate of at least about 2 liters per minute (Lpm); and

maintaining an average pressure of less than about 15 mmHg in the left ventricle of the patient.

8. The method of claim 7 , wherein activating the impeller comprises activating the impeller to pump blood through the aorta at a flow rate of at least about 4 Lpm.

9. The method of claim 7 , wherein activating the impeller comprises activating the impeller to pump blood through the aorta at a flow rate of at least about 5 Lpm.

10. The method of claim 7 , wherein activating the impeller comprises activating the impeller to pump blood through the aorta at a flow rate in a range of about 4 Lpm to about 5.5 Lpm.

11. The method of claim 7 , wherein activating the impeller comprises activating the impeller to pump blood through the aorta in a range of about 4.5 Lpm to about 5.5 Lpm.

12. The method of claim 7 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 10 mmHg in the left ventricle of the patient.

13. The method of claim 12 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 5 mmHg in the left ventricle of the patient.

14. The method of claim 12 , wherein maintaining the average pressure comprises maintaining a pressure in a range of about 2 mmHg to about 8 mmHg.

15. The method of claim 14 , wherein maintaining the pressure comprises maintaining a pressure in a range of about 3 mmHg to about 6 mmHg.

16. The method of claim 15 , wherein maintaining the pressure comprises maintaining a pressure in a range of about 4 mmHg to about 5 mmHg.

17. The method of claim 7 , wherein advancing the impeller assembly comprises advancing a distal portion of the impeller assembly past the aortic valve until the inlet(s) of the cannula are distal the aortic valve by a distance in a range of about 0.5 cm to about 4 cm.

18. The method of claim 17 , wherein advancing the impeller assembly comprises advancing the distal portion of the impeller assembly past the aortic valve until the inlet(s) of the cannula are distal the aortic valve by a distance in a range of about 1.5 cm to about 3 cm.

19. The method of claim 7 further comprising:

monitoring the pressure in the left ventricle of the patient based at least in part on a signal representative of the pressure; and

moving the impeller assembly relative to the aortic valve of the patient to substantially smooth out spikes in the signal.

20. The method of claim 7 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 135% of the normal human average ventricular pressure.

21. The method of claim 20 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 125% of the normal human average ventricular pressure.

22. The method of claim 21 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 115% of the normal human average ventricular pressure.

23. The method of claim 22 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 105% of the normal human average ventricular pressure.

24. The method of claim 7 , wherein the sensor is positioned near the one or more inlets of the impeller assembly.

25. The method of claim 7 , wherein the sensor is positioned near a proximal portion of the impeller.

26. A catheter pump comprising:

an impeller assembly comprising an impeller and one or more inlets; and

a sensor configured to measure a pressure of blood flowing through the inlet(s) of the impeller assembly,

wherein the impeller assembly is configured such that the inlet(s) can be positioned in a left ventricle of the patient during a treatment procedure, the impeller assembly also configured to pump blood into an aorta of the patient at a flow rate of at least about 2 liters per minute (Lpm) and to maintain an average pressure of less than about 15 mmHg in the left ventricle of the patient.

27. The catheter pump of claim 26 , further comprising a processing unit programmed to process a signal detected by the sensor, the processing unit comprising a computer-readable set of rules to evaluate the signal to determine a pressure of blood in the left ventricle of the patient.

28. The catheter pump of claim 26 , wherein the impeller assembly is configured to pump blood through the aorta at a flow rate of at least about 4 Lpm.

29. The catheter pump of claim 26 , wherein the impeller assembly is configured to pump blood through the aorta at a flow rate in a range of about 4 Lpm to about 5.5 Lpm.

30. The catheter pump of claim 29 , wherein the impeller assembly is configured to pump blood through the aorta in a range of about 4.5 Lpm to about 5.5 Lpm.

31. The catheter pump of claim 26 , wherein the impeller assembly is configured to maintain an average pressure of less than about 10 mmHg in the left ventricle of the patient.

32. The catheter pump of 24 , wherein the impeller assembly is configured to maintain a pressure in a range of about 2 mmHg to about 8 mmHg.

33. The catheter pump of claim 32 , wherein the impeller assembly is configured to maintain a pressure in a range of about 3 mmHg to about 6 mmHg.

34. The catheter pump of claim 33 , wherein the impeller assembly is configured to maintain a pressure in a range of about 4 mmHg to about 5 mmHg.

35. The catheter pump of claim 26 , wherein the sensor is positioned near the inlet(s) of the impeller assembly.

36. The catheter pump of claim 26 , wherein the sensor is positioned near a proximal portion of the impeller.

37. A method of pumping blood through a patient, the method comprising:

advancing an impeller assembly through a vascular system of the patient to a left ventricle of the patient, the impeller assembly comprising an impeller and a sensor configured to measure a pressure of blood flowing through one or more inlets of the impeller assembly;

activating the impeller to pump blood through an aorta of the patient at a flow rate of at least about 2 liters per minute (Lpm); and

maintaining an average pressure in the left ventricle of the patient of less than about 135% of the normal human average ventricular pressure.

38. The method of claim 37 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 125% of the normal human average ventricular pressure.

39. The method of claim 38 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 115% of the normal human average ventricular pressure.

40. The method of claim 39 , wherein maintaining the average pressure comprises maintaining an average pressure of less than about 105% of the normal human average ventricular pressure.

41. The method of claim 37 , wherein the sensor is positioned near the one or more inlets of the impeller assembly.

42. The method of claim 37 , wherein the sensor is positioned near a proximal portion of the impeller.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2020
From: MULLER, PAUL F.; FITZGERALD, KEIF M.; KEENAN, RICHARD L.; NEIMAN, VERONICA J.
To: THORATEC CORPORATION
Reel/Frame 054395/0192 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2020
From: THORATEC CORPORATION
To: THORATEC LLC
Reel/Frame 054452/0444 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2020
From: THORATEC LLC
To: TC1 LLC
Reel/Frame 054452/0481 →
Continuity (4)
Continuation 16020674 · Jun 27, 2018
Division 14687493 · Apr 15, 2015
Provisional Application 61979920 · Apr 15, 2014
Related Publication 20210069392A1 · Mar 11, 2021
Cited By (31)
US 12,201,823 US 12,222,267 US 12,257,424 US 12,263,333 US 12,310,708 US 12,311,160 US 12,324,906 US 12,377,256 US 12,383,727 US 12,390,633 US 12,403,296 US 12,447,327 US 12,465,744 US 12,478,267 US 12,478,775 US 12,478,776 US 12,491,357 US 12,502,524 US 12,508,418 US 12,515,036 US 12,523,228 US 12,569,671 US 12,576,263 US 12,589,237 US 12,589,238 US 12,599,749 US 12,667,714 US 12,702,816 US 12,702,821 US 12,728,255 US 12,741,135