Internally powered CSF pump systems and methods

• US 7,025,742 B2
• Filed: 08/05/2003
• Issued: 04/11/2006
• Est. Priority Date: 07/11/1996
• Status: Expired due to Fees

• Current Assignee: Integra Lifesciences Corporation (Integra LifeSciences Holdings Corporation)
• Original Assignee: Integra Lifesciences Corporation (Integra LifeSciences Holdings Corporation)
• Inventors: Rubenstein, Edward, Vargas, Jaime S., Saul, Tom A., Levinthal, Elliott C., Karshmer, David L.
• Primary Examiner(s): Bianco, Patricia
• Application Number:
  US10/635,807
• Publication Number:
  US 20040030279A1
• Time in Patent Office: 980 Days
• Field of Search: 604 8- 10, 604/264, 604/523, 604/537, 604/540, 604/541
• US Class Current: 604/9
• CPC Class Codes: A61M 27/006 Cerebrospinal drainage; Accessories therefor, e.g. valves
• CPC Class Codes: A61M 60/882 Devices powered by the patient, e.g. skeletal muscle powered devices

Abstract

A method treats a patient for adult-onset dementia of the Alzheimer'"'"'s type by removing a portion of the patient'"'"'s cerebrospinal fluid, preferably (although not necessarily) by transporting the fluid to another portion of the patient'"'"'s body. An apparatus for removing cerebrospinal fluid includes (1) a conduit with a first opening and a second opening, the first opening of the conduit being disposed in fluid communication with a space within a patient'"'"'s subarachnoid space, the second opening being disposed in fluid communication with another portion of the patient'"'"'s body; and (2) a flow rate control device attached to the conduit.

Claims

1. An implantable system for draining cerebrospinal fluid (CSF), said system comprising:

a conduit having a first opening and a second opening, the first opening of the conduit being adapted to be disposed in fluid communication with a space with a patient'"'"'s CSF space and the second opening being adapted to be disposed in fluid communication with a drainage location in another portion of the patients body;

a pump coupled to the conduit to induce flow from the CSF space to the drainage location;

an implantable battery connectable to power the pump; and

a recirculation loop and a valve in the recirculation loop, wherein the valve selectively directs flow to the drainage end of the conduit or to an inlet of the pump.

2. A system as in claim 1, further comprising a pressure transducer connected to the valve.

3. An implanted system for draining cerebrospinal fluid (CSF), said system comprising:

a conduit having a first opening and a second opening, the first opening of the conduit being adapted to be disposed in fluid communication with a space within a patient'"'"'s CSF space and the second opening being adapted to be disposed in fluid communication with a drainage location in another portion of the patients body;

a pump of a type selected from the group consisting of diaphragm pumps, piston pumps, rotor pumps, peristaltic pumps, and screw pumps coupled to the conduit to induce flow from the CSF space to the drainage location; and

an implantable battery connectable to power the pump, and a

recirculation loop and a valve in the recirculation loop, wherein the valve selectively directs flow to the drainage end of the conduit or to an inlet of the pump.

4. A system as in claim 3, further comprising a pressure transducer connected to the valve.

5. An implantable system for draining cerebrospinal fluid (CSF), said system comprising:

a conduit having a first opening and a second opening, the first opening of the conduit being adapted to be disposed in fluid communication with a space within a patient'"'"'s CSF space and the second opening being adapted to be disposed in fluid communication with a drainage location in another portion of the patients body;

a pump coupled to the conduit to induce flow from the CSF space to the drainage location;

an implantable power source connectable to power the pump; and

a recirculation loop and a valve in the recirculation loop, wherein the valve selectively directs flow to the drainage end of the conduit or to an inlet of the pump.

6. A system as in claim 5, wherein the conduit comprises:

a ventricular catheter having a proximal end and a distal end adapted for implantation into the CSF space; and

a peritoneal catheter having a proximal end and a distal end adapted for implantation into the drainage location in the patient'"'"'s peritoneum, wherein the pump is connected to receive CSF from the ventricular catheter and deliver CSF to the peritoneal catheter.

7. A system as in claim 6, wherein the ventricular catheter has a length in the range from 10 cm to 50 cm and a lumen having a diameter in the range from 0.1 mm to 2 mm.

8. A system as in claim 5, wherein the pump is of a type selected from the group consisting of diaphragm pumps, piston pumps, rotor pumps, peristaltic pumps, and screw pumps.

9. A system as in claim 5, wherein the power source is a battery.

10. A system as in claim 5, wherein the pump is adapted to be operated on demand.

11. A system as in claim 5, wherein the pump is programmed to operate on a schedule.

12. A system as in claim 5, wherein the pump comprises a hermetically scaled pump drive.

13. A system as in claim 5, further comprising a pressure transducer connected to the valve.

14. A system as in claim 6, wherein the peritoneal catheter has a length in the range from 25 cm to 125 cm and a lumen having a diameter in the range from 0.1 mm to 2 mm.