Interspinous process spacer diagnostic parallel balloon catheter and methods of use

• US 8,147,526 B2
• Filed: 02/26/2010
• Issued: 04/03/2012
• Est. Priority Date: 02/26/2010
• Status: Active Grant

• Current Assignee: Medtronic Europe SARL (Medtronic Plc)
• Original Assignee: Kyphon SARL (Medtronic Plc)
• Inventors: Auyoung, Bryan J.
• Primary Examiner(s): Robert, Eduardo C
• Assistant Examiner(s): HOFFMAN, MARY C
• Application Number:
  US12/714,173
• Publication Number:
  US 20110213301A1
• Time in Patent Office: 767 Days
• Field of Search: 60410101-10203, 604/96.01, 606191-192, 606/915, 606247-249, 606/90, 606/102, 600206-208
• US Class Current: 606/279
• 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 2017/00557 inflatable A61B2017/22051 takes precedence
• CPC Class Codes: A61B 2017/0256 for the spine
• CPC Class Codes: A61M 25/1029 Production methods of the balloon members, e.g. blow-moulding, extruding, deposition or by wrapping a plurality of layers of balloon material around a mandril

Abstract

An interspinous process spacer diagnostic parallel balloon catheter and method. The balloon catheter has a plurality of maim expandable members disposed one inside another, a distal expandable member and a proximal expandable member that all can be expanded from a collapsed configuration to an expanded configuration and than 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. A spinal surgery method using a device having an elongate member, a first main expandable member connected to a distal portion of the elongate member, a second main expandable member disposed in the first expandable member, a distal expandable member connected to the distal portion of the elongate member adjacent to a distal end of the first main expandable member, and a proximal expandable member connected to the distal portion of the elongate member adjacent to a proximal end of the first main expandable member;

the method comprising;

inserting the distal portion of the device into the patient;

expanding one of the distal expandable member or the proximal expandable member;

determining whether the distal portion of the device is properly located;

thereafter, deflating one of the distal expandable member or the proximal expandable member;

repositioning the distal portion of the device;

inflating the proximal expandable member and the distal expandable member;

inflating the second main expandable member with a first volume of fluid;

identifying whether the patient experiences pain relief while the second main expandable member is expanded with the first volume of fluid;

after the identifying step, collapsing the second main expandable member, the proximal expandable member and the distal expandable member and removing the device from the patient.

2. The method of claim 1 further comprising implanting an interspinous process spacer into the patient based on the size of the first expandable member or the second expandable member.

3. The method of claim 1 further comprising inflating the first expandable member and identifying whether the patient experiences pain relief when the first main expandable member is expanded with a second volume of fluid.

4. The method of claim 3 wherein the second expandable member is collapsed prior to inflating the first expandable member.

5. The method of claim 3 wherein the second expandable member is ruptured during inflation of the first expandable member.

6. The method of claim 1 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.

7. The method of claim 1 further comprising noting the first volume of fluid and correlating the first volume with a diameter of the second main expandable member.

8. The method of claim 1 further comprising implanting an interspinous process spacer into the patient based on the diameter of the second main expandable member.