Interspinous process spacer diagnostic balloon catheter and methods of use

• US 8,317,831 B2
• Filed: 01/13/2010
• Issued: 11/27/2012
• Est. Priority Date: 01/13/2010
• Status: Active Grant

• Current Assignee: Medtronic Europe SARL (Medtronic Plc)
• Original Assignee: Kyphon SARL (Medtronic Plc)
• Inventors: Auyoung, Bryan J., Osorio, Reynaldo A.
• Primary Examiner(s): Truong, Kevin T
• Assistant Examiner(s): BECCIA, CHRISTOPHER J
• Application Number:
  US12/686,617
• Publication Number:
  US 20110172596A1
• Time in Patent Office: 1,049 Days
• Field of Search: 600206-208, 606/90, 606/102, 606191-192, 606247-249, 606/915, 623 1711- 1716
• US Class Current: 606/249
• CPC Class Codes: A61B 17/7065 Devices with changeable shape, e.g. collapsible or having retractable arms to aid implantation; Tools therefor
• CPC Class Codes: A61B 2017/0256 for the spine
• CPC Class Codes: A61M 2025/1072 having balloons with two or more compartments

Abstract

An interspinous process spacer diagnostic balloon catheter and method. The balloon catheter has a main expandable member, a distal expandable member and a proximal expandable member that all can be expanded from a collapsed configuration to an expanded configuration and then collapsed again to a collapsed configuration. The device can be used to determine whether a particular patient is a candidate for implantation of an interspinous process spacer to treat the symptoms of lumbar spinal stenosis and the size of such a spacer if indicated.

Claims

1. An interspinous process spacer diagnostic balloon catheter, comprising:

an elongate member;

a main expandable member connected to a distal portion of the elongate member and configured for disposal between adjacent spinous processes, the main expandable member comprises a height equal to a distance between adjacent spinous processes and a width substantially equal to the width of a typical spinous process;

a distal expandable member connected to a distal portion of the elongate member adjacent to a distal end of the main expandable member and configured for disposal on a distal side of adjacent spinous processes;

a proximal expandable member connected to a distal portion of the elongate member adjacent to a proximal end of the main expandable member and configured for disposal adjacent spinous processes on an opposite side of the distal expandable member; and

a plurality of lumens disposed in the elongate member in communication with one or more of the main expandable member, the distal expandable member and the proximal expandable member,

wherein the proximal and distal expandable members each have a height that is greater than the distance between adjacent spinous processes and greater than the height of the main expandable member,

wherein the distal expandable member and the proximal expandable member are configured to lock the diagnostic balloon catheter in place.

2. The catheter of claim 1 wherein the main expandable member is formed from a relatively non-compliant material.

3. The catheter of claim 1 wherein the distal expandable member and the proximal expandable member are formed from a relatively compliant material.

4. The catheter of claim 2 wherein the distal expandable member and the proximal expandable member are formed from a relatively compliant material.

5. The catheter of claim 4 wherein the main expandable material is formed from a three layer material having a middle layer, an inner layer and an outer layer.

6. The catheter of claim 5 wherein the middle layer is a relatively non-compliant material.

7. The catheter of claim 6 wherein the inner layer and the outer layer are a relatively compliant material.

8. The catheter of claim 1 wherein the lumens are coaxial.

9. The catheter of claim 1 wherein the elongate member defines at least two lumens extending therein wherein one lumen is in fluid communication with the distal expandable member and the proximal expandable member and one lumen is in fluid communication with the main expandable member.

10. The catheter of claim 9 wherein the two lumens extend coaxially in the elongate member.

11. The catheter of claim 1 wherein the elongate member defines one lumen extending therein wherein the one lumen is in fluid communication with the distal expandable member, the main expandable member and the proximal expandable member.

12. The catheter of claim 11 wherein the lumen extends coaxially in the elongate member.

13. The catheter of claim 1 wherein the elongate member defines at least three lumens extending therein wherein one lumen is in fluid communication with the distal expandable member, one lumen is in fluid communication with the main expandable member and one lumen is in fluid communication with the proximal expandable member.

14. A method of diagnosing a spinal disorder of a patient, comprising:

unilaterally inserting an expandable member while in a closed orientation into an interspinous space between adjacent spinous processes of the patient, with the expandable member in a closed configuration;

inflating expanding the expandable member to a first expanded diameter size;

thereafter, identifying whether the patient experiences pain relief when the expandable member is expanded to the first expanded size and disposed in the interspinous space diameter;

thereafter, deflating the expandable member to collapse collapsing the expandable member to a size smaller than the first expanded size;

thereafter, removing the expandable member from the interspinous space;

thereafter, implanting an interspinous process spacer into the Interspinous space, the spacer selected based on whether the patient experiences pain relief when the expandable member is expanded to the first expanded size patient.

15. The method of claim 14 further comprising expanding the expandable member to a second expanded size after identifying whether the patient experiences pain relief when the expandable member is expanded to the first size, and prior to the removing the expandable member.

16. The method of claim 14 wherein the expandable member is a central portion of a diagnostic spacer, and wherein the diagnostic spacer further comprises a distal balloon section and a proximal balloon section disposed on opposing lateral sides of the central portion, the method further comprising:

after the inserting and prior to the identifying, expanding at least one of the proximal and distal balloon sections by inflation thereof.

17. The method of claim 16 wherein the expanding the at least one of the proximal and distal balloon sections occurs prior to the inflating of the expandable member.

18. The method of claim 14 wherein the expandable member is a central portion of a diagnostic spacer, and wherein the diagnostic spacer further comprises a distal balloon section and a proximal balloon section disposed on opposing lateral sides of the central portion, the method further comprising:

after the inserting and prior to the identifying, expanding both the proximal and distal balloon sections by inflation thereof independently of the inflating of the expandable section.

19. The method of claim 14 wherein identifying whether the patient experiences pain relief comprises receiving feedback from the patient after the patient has become ambulatory with the first expandable member expanded to the first size.

20. The method of claim 14 further comprising selecting the interspinous process spacer based on both the first expanded size and whether the patient experiences pain relief with the expandable member expanded to the first size.