Devices and methods for disruption and removal of luminal occlusions

• US 7,618,434 B2
• Filed: 05/12/2004
• Issued: 11/17/2009
• Est. Priority Date: 05/12/2003
• Status: Expired due to Fees

• Current Assignee: University of Florida Research Foundation, Incorporated (State University System of Florida)
• Original Assignee: University of Florida Research Foundation, Incorporated (State University System of Florida)
• Inventors: Santra, Swadeshmukul, Mericle, Robert A., Eskioglu, Eric, Batich, Christopher D., Stanley, Jessie T.
• Primary Examiner(s): Manahan; Todd E
• Assistant Examiner(s): BACHMAN, LINDSEY MICHELE
• Application Number:
  US10/844,737
• Publication Number:
  US 20050033334A1
• Time in Patent Office: 2,015 Days
• Field of Search: 606/113, 606/114, 606/127, 606/159, 606191-200, 604/22, 604104-107
• US Class Current: 606/200
• CPC Class Codes: A61B 17/221 Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions surgical snare instruments A61B17/32056
• CPC Class Codes: A61B 17/320725 with radially expandable cutting or abrading elements A61B17/32075 takes precedence
• CPC Class Codes: A61B 2017/2212 having a closed distal end, e.g. a loop

Abstract

The subject invention pertains to an elastic sheath, device, and methods for disrupting and/or removing occlusive material from lumens, particularly biological lumens, such as the vasculature, ureter, urethra, fallopian tubes, bile duct, intestines, and the like. The subject invention provides for effective disruption and removal of occlusive material, such as a thrombus, from the body lumen with minimal risk of injury to the lumen wall. Advantageously, the invention can be used to achieve a high degree of removal while minimizing the amount of occlusive material that is released into the body lumen. The subject invention further pertains to methods for disrupting and removing occlusive material from a biological lumen. In another aspect, the present invention concerns a device useful as an in vitro model of luminal occlusion and methods for using the device to test the efficacy of devices and methods for treating luminal occlusions.

Claims

1. A method for removal of thrombus material from an intracranial blood vessel of a human subject, using a device having a balloon-activated compartment, said method comprising:

(a) inserting the device into the intracranial blood vessel of the subject, wherein the device comprises a rod, an elastomeric sheath that ensheaths at least a segment of the rod, and an expandable balloon for expanding the elastomeric sheath, wherein the expandable balloon, upon initiation of expansion, provides radial pressure to a portion of the elastomeric sheath, causing an adjacent segment of the elastomeric sheath to be displaced outwardly away from the rod segment, thereby forming the compartment beneath the displaced elastomeric sheath segment, wherein the displaced elastomeric sheath segment comprises a plurality of slits that expand upon expansion of the balloon, and wherein the compartment has a volume that is larger than the space occupied by the expanded balloon;

(b) expanding the balloon;

(c) capturing the thrombus material within the compartment, wherein said capturing of the thrombus material includes;

moving the device within the blood vessel;

bringing the displaced elastomeric sheath segment into contact with the thrombus material; and

causing the thrombus material to pass through a slit of the displaced elastomeric sheath segment;

(d) at least partially collapsing the balloon, thereby collapsing the compartment; and

(e) withdrawing the device from the blood vessel.

2. The method of claim 1, wherein the intracranial blood vessel is an intracranial artery.

3. The method of claim 1, wherein at least one portion of the device is impregnated or coated with a biologically active agent.

4. The method of claim 1, wherein the plurality of slits are longitudinally arranged on the displaced elastomeric sheath segment, and wherein each slit is separated from adjacent slits by a longitudinal band of elastomeric material.

5. The method of claim 4, wherein the longitudinal bands are cross-linked with a plurality of lateral bands that bridge the longitudinal slits, thereby forming a mesh.

6. The method of claim 4, wherein the longitudinal bands make shearing contact with the thrombus material.

7. The method of claim 1, wherein the expandable balloon comprises at least one radially constrained portion and at least one radially unconstrained portion.

8. The method of claim 7, wherein when pressure is applied to the interior of the expandable balloon, the at least one radially unconstrained portion expands to form at least one sphere or spheroid shape.

9. The method of claim 8, wherein the at least one radially constrained portion is constrained with a fiber that is wrapped around the at least one radially constrained portion.

10. The method of claim 8, wherein the compartment is substantially conical in shape.

11. The method of claim 1, wherein the elastomeric sheath comprises a flexible polymer tube.

12. The method of claim 1, wherein the elastomeric sheath comprises a thermoplastic elastomer.

13. The method of claim 1, wherein the elastomeric sheath comprises a flexible polymer selected from the group consisting of silicone, polyurethane, silicone-polyurethane copolymer, and styrene-ethylene-butylene-styrene (copolymer).

14. The method of claim 1, wherein the device is at least partially composed of an imageable material.

15. The method of claim 1, wherein the portion of the elastomeric sheath receiving radial pressure from the balloon has a length that is shorter than the length of the adjacent segment of the elastomeric sheath that is displaced upon expansion of the balloon.

16. The method of claim 1, wherein the volume of the compartment increases with the diameter of the elastomeric sheath segment upon expansion of the balloon.

17. The method of claim 1, wherein the compartment is proximal to the balloon.

18. The method of claim 1, wherein the compartment is distal to the balloon.

19. The method of claim 1, wherein the rod has a distal end and a proximal end, and wherein the compartment has a diameter that decreases toward the proximal end or distal end of the rod.

20. The method of claim 1, wherein the compartment circumferentially surrounds the rod segment.

21. The method of claim 1, wherein the expandable balloon comprises two or more expandable balloons.

22. The method of claim 1, wherein when the balloon is collapsed, the plurality of slits are closed.

23. The method of claim 1, wherein the balloon comprises at least one radially constrained portion and at least one radially unconstrained portion, and wherein the rod segment is ensheathed by the at least one radially constrained portion of the balloon.

24. The method of claim 1, wherein the expandable balloon comprises a single expandable balloon.

25. The method of claim 1, wherein said moving the device within the conduit comprises moving the device in a back-and-forth and/or twisting motion within the blood vessel.

26. The method, according to claim 1, wherein said capturing of the thrombus material consists of:

moving the device within the blood vessel;

bringing the displaced elastomeric sheath segment into contact with the thrombus material; and

causing the thrombus material to pass through a slit of the displaced elastomeric sheath segment.

27. The method, according to claim 1, wherein said capturing of the thrombus material consists essentially of:

moving the device within the blood vessel;

bringing the displaced elastomeric sheath segment into contact with the thrombus material; and

causing the thrombus material to pass through a slit of the displaced elastomeric sheath segment.

28. The method of claim 1, wherein the thrombus material has caused an ischemic thromboembolic stroke in the subject.