OCCLUSIVE MATERIAL REMOVAL DEVICE HAVING SELECTIVELY VARIABLE STIFFNESS

• US 20090163851A1
• Filed: 11/17/2008
• Published: 06/25/2009
• Est. Priority Date: 12/19/2007
• Status: Abandoned Application

• Current Assignee: Arterain Medical, Inc.
• Original Assignee: Arterain Medical, Inc.
• Inventors: Yadav, Sanjay Singh, Holloway, Kenneth A., Al-Jadda, Aadel
• Application Number:
  US12/272,069
• Publication Number:
  US 20090163851A1
• Time in Patent Office: Days
• US Class Current: 604/22
• 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 2017/00539 hydraulically
• CPC Class Codes: A61B 2017/22061 for spreading elements apart
• CPC Class Codes: A61B 2017/22062 to be filled with liquid
• CPC Class Codes: A61B 2017/2217 single wire changing shape to a gripping configuration
• CPC Class Codes: A61B 90/39 Markers, e.g. radio-opaque or breast lesions markers

Abstract

Apparatus and methods for removal of obstructing or occluding material, such as tissue, from within bodily lumens via a minimally invasive approach are disclosed. In one embodiment, an apparatus, such as a medical device, includes an elongate member and a tissue disrupter. The elongate member is configured to be at least partially disposed within a bodily lumen. The tissue disrupter is coupled to a distal end portion of the elongate member. The tissue disrupter is configured to be selectively stiffened and is configured to dislodge a tissue from within the bodily lumen.

Claims

1. An apparatus, comprising:

an elongate member configured to be at least partially disposed within a bodily lumen; and

a tissue disrupter coupled to a distal end portion of the elongate member, the tissue disrupter configured to dislodge a tissue from within the bodily lumen, the tissue disrupter configured to be selectively stiffened.

2. The apparatus of claim 1, wherein the tissue disrupter is configured to be selectively stiffened by increasing a pressure of a fluid within a lumen defined by the tissue disrupter.

3. The apparatus of claim 1, wherein the tissue disrupter defines a lumen configured to contain a fluid, the lumen having a substantially constant volume, the fluid within the lumen having a first pressure when the tissue disrupter has a first stiffness, the fluid within the lumen having a second pressure different from the first pressure when the tissue disrupter has a second stiffness.

4. The apparatus of claim 1, wherein the elongate member is a first elongate member defining a lumen, the apparatus further comprising:

a second elongate member movably disposed within the lumen of the first elongate member, the tissue disrupter configured to be selectively stiffened when the second elongate member is moved with respect to the first elongate member.

5. The apparatus of claim 1, wherein the elongate member is a first elongate member, the apparatus further comprising:

a second elongate member at least partially disposed within a lumen of the first elongate member, a portion of the tissue disrupter disposed about an exterior surface of the second elongate member.

6. The apparatus of claim 1, wherein the tissue disrupter is one of a plurality of tissue disruptors, the plurality of tissue disruptors collectively having a first lateral dimension when the plurality of tissue disruptors is in a first configuration, the plurality of tissue disruptors collectively having a second lateral dimension greater than the first lateral dimension when the plurality of tissue disruptors is in a second configuration, the plurality of tissue disruptors configured to allow passage of a bodily fluid between the plurality of tissue disruptors when the plurality of tissue disruptors is in its second configuration.

7. The apparatus of claim 1, further comprising:

an aspiration shaft defining a lumen, a portion of the elongate member movably disposed within the lumen of the aspiration shaft, an inner surface of the aspiration shaft and an outer surface of the elongate member defining a passageway configured to receive a portion of the tissue.

8. The apparatus of claim 1, wherein the elongate member defines a center line, the tissue disrupter having a first stiffness when in a first configuration and a second stiffness when in a second configuration, the second stiffness different than the first stiffness, a portion of the tissue disrupter configured to move in a direction substantially normal to the center line when the tissue disrupter is moved from its first configuration to its second configuration.

9. The apparatus of claim 1, wherein at least a portion of the elongate member is configured to be selectively stiffened.

10. The apparatus of claim 1, wherein the tissue disrupter is configured to deliver a therapeutic agent into the bodily vessel.

11. The apparatus of claim 1, wherein the tissue disrupter is constructed from a non-metallic material.

12. The apparatus of claim 1, wherein the tissue disrupter includes a fiber defining a lumen, the fiber coupled to a distal end portion of the elongate member such that the lumen of the fiber is fluidically coupled to a lumen defined by the elongate member.

13. The apparatus of claim 1, wherein the tissue disrupter has a first stiffness when in a first configuration and a second stiffness when in a second configuration, the second stiffness different than the first stiffness, the tissue disrupter configured to contact an inner surface of a vessel defining the bodily lumen.

14. The apparatus of claim 1, wherein the tissue disruptor has a length of approximately 1 cm to 600 cm and an internal diameter of approximately 0.006 cm to 0.025 cm.

15. The apparatus of claim 1, wherein the elongate member is a first elongate member, wherein the tissue disruptor is a first tissue disruptor, the apparatus further comprising:

a second elongate member, at least a portion of the second elongate member disposed within the lumen of the first elongate member; and

a second tissue disruptor coupled to the distal end portion of the first elongate member, the tissue disruptor configured to dislodge the tissue from within the bodily lumen,

the first tissue disruptor wrapped about an outer surface of the second elongate member, the first tissue disruptor having a first number of turns about the outer surface of the second elongate member, the second tissue disruptor wrapped about the outer surface of the second elongate member, the second tissue disruptor having a second number of turns about the outer surface of the second elongate member, the second number of turns greater than the first number of turns.

16. The apparatus of claim 1, wherein the elongate member is a first elongate member, wherein the tissue disruptor is a first tissue disruptor, the apparatus further comprising:

a second elongate member, at least a portion of the second elongate member disposed within the lumen of the first elongate member; and

a second tissue disruptor coupled to the distal end portion of the first elongate member, the tissue disruptor configured to dislodge the tissue from within the bodily lumen,

each of the first tissue disruptor and the second tissue disruptor having a first configuration and a second configuration, the first tissue disruptor having a lateral dimension when the first tissue disruptor is in its second configuration, the second tissue disruptor having a lateral dimension greater than the lateral dimension of the first tissue disruptor when the second tissue disruptor is in its second configuration.

17. An apparatus, comprising:

an elongate assembly configured to be disposed within a bodily lumen, the elongate assembly including a first shaft and a second shaft, the first shaft defining a first lumen and a second lumen, a portion of the second shaft being movably disposed within the first lumen of the first shaft; and

a fiber having a proximal end portion and a distal end portion and defining a lumen, the proximal end portion of the fiber coupled to a distal end portion of the first shaft such that the lumen of the fiber is in fluid communication with the second lumen of the first shaft, the distal end portion of the fiber coupled to a distal end portion of the second shaft.

18. The apparatus of claim 17, wherein the fiber is configured to be selectively stiffened.

19. The apparatus of claim 17, wherein the lumen of the fiber is configured to contain a fluid, the lumen of the fiber having a substantially constant volume, the fluid within the lumen of the fiber having a first pressure when the fiber is in a first configuration, the fluid within the lumen of the fiber having a second pressure different than the first pressure when the fiber is in a second configuration.

20. The apparatus of claim 17, wherein the second shaft is configured to move within the first lumen of the first shaft to move a portion of the fiber in a radial direction relative to at least one of the first shaft and the second shaft.

21. The apparatus of claim 17, wherein the elongate assembly includes a third shaft, a portion of the first shaft disposed within a lumen defined by the third shaft, an inner surface of the third shaft and an outer surface of the first shaft collectively defining a suction passageway configured to receive a bodily material.

22. The apparatus of claim 17, further comprising:

a valve coupled to a proximal end portion of the elongate assembly, the valve configured to selectively control a fluid pressure within the second lumen of the first shaft.

23. The apparatus of claim 17, wherein the fiber is constructed from a substantially non-compliant material.

24. The apparatus of claim 17, wherein the fiber is constructed from a non-metallic material.

25. The apparatus of claim 17, wherein the fiber has a first stiffness when in a first configuration and a second stiffness when in a second configuration, the second stiffness different than the first stiffness, the fiber is configured to contact a wall of the bodily lumen when the fiber is in the second configuration.

26. The apparatus of claim 17, wherein:

the distal end portion of the second shaft includes a dilator; and

the fiber is a first fiber from a plurality of fibers, a distal end portion of each fiber from the plurality of fibers being coupled to the dilator.

27. A method, comprising:

inserting a distal end portion of an elongate assembly into a bodily lumen, the elongate assembly including a tissue disrupter;

increasing a stiffness of the tissue disrupter; and

dislodging a portion of a tissue from within the bodily lumen by engaging the tissue disrupter with the tissue.

28. The method of claim 27, wherein the increasing includes conveying a fluid into a lumen defined by the tissue disruptor.

29. The method of claim 27, wherein the increasing includes selectively increasing a pressure of a fluid within a lumen defined by the tissue disruptor.

30. The method of claim 27, wherein the increasing includes selectively increasing a pressure of a fluid within a lumen defined by the tissue disrupter while maintaining a volume of the tissue disrupter at a substantially constant value.

31. The method of claim 27, wherein:

the elongate assembly includes an elongate shaft; and

the increasing includes rotating a distal end portion of the tissue disrupter with respect to the elongate shaft.

32. The method of claim 27, further comprising:

inflating an expandable member coupled to the distal end portion of the elongate assembly within the bodily lumen to substantially prevent flow of a bodily fluid therethrough.

33. The method of claim 27, wherein the elongate assembly includes an elongate shaft, further comprising:

moving a distal end portion of the tissue disruptor in a proximal direction with respect to the elongate shaft, a portion of the tissue disruptor moving in a radial direction towards a wall of the bodily lumen when the distal end portion of the tissue disrupter moves in the proximal direction with respect to the elongate shaft such that the portion of the tissue disruptor contacts the tissue within the bodily lumen.

34. The method of claim 27, wherein the dislodging includes moving a portion of the elongate assembly in a first direction within the bodily lumen and a second direction within the bodily lumen different than the first direction.

35. The method of claim 27, further comprising:

capturing a portion of the tissue with the tissue disruptor; and

withdrawing the tissue disruptor and captured tissue from the bodily lumen.

36. The method of claim 27, further comprising:

aspirating, after the dislodging, the portion of the tissue through a passageway defined by an outer surface of an elongate shaft of the elongate assembly and an inner surface of an aspiration shaft disposed about a portion of the elongate shaft.

37. The method of claim 27, further comprising:

conveying a therapeutic agent into the bodily lumen via the tissue disrupter.

38. A method, comprising:

inserting a portion of a medical device into a bodily lumen about a guidewire disposed within the bodily lumen; and

dislodging at least a portion of a bodily tissue from within the bodily lumen when the guidewire remains in the bodily lumen.

39. The method of claim 38, further comprising:

moving a tissue disruptor of the medical device with respect to the guidewire from a first position within the bodily lumen to a second position within the bodily lumen, the moving be in at least one of a translation direction or a rotational direction.

40. The method of claim 38, further comprising:

moving a tissue disrupter of the medical device from a first configuration to a second configuration while the guidewire remains within the bodily lumen, the tissue disrupter configured to dislodge the portion of the bodily tissue.