Spinal motion measurement device

• US 8,721,566 B2
• Filed: 11/12/2010
• Issued: 05/13/2014
• Est. Priority Date: 11/12/2010
• Status: Expired due to Fees

• Current Assignee: Hart Garner, Robert A. Connor
• Original Assignee: Hart Garner, Robert A. Connor
• Inventors: Connor, Robert A., Garner, Hart
• Primary Examiner(s): Towa, Rene
• Assistant Examiner(s): ABOUELELA, MAY A
• Application Number:
  US12/927,348
• Publication Number:
  US 20120123301A1
• Time in Patent Office: 1,278 Days
• Field of Search: 600/587, 600/594, 600/595, 606/53, 606/54, 606/57, 606/251, 606/252, 606/279, 606/257, 606/246, 606/258, 623/23.47
• US Class Current: 600/587
• CPC Class Codes: A61B 17/70 Spinal positioners or stabilisers ; Bone stabilisers comprising fluid filler in an implant
• CPC Class Codes: A61B 5/1121 Determining geometric values, e.g. centre of rotation or angular range of movement
• CPC Class Codes: A61B 5/4528 Joints A61B5/4533, A61B5/4538 take precedence
• CPC Class Codes: A61B 5/6878 Bone

Abstract

This invention is a minimally-invasive device, including bone-moving members and motion-measuring members, that can help surgeons to obtain objective, quantitative information concerning spinal flexion, extension, lateral bending, decompression, compression and torsion in order to select the best therapy for each patient. The prior art does not offer surgeons the opportunity to objectively and independently measure each of these movements. As a result, currently there is tremendous variation concerning which therapies are selected for which conditions. It is very unlikely that quality is being optimized and costs are being best managed with such high variation in practice patterns. This variation may be greatly reduced by the availability of objective information concerning spinal motion from this device. In this manner, this device can help surgeons to select the optimal therapy, to improve the quality of care, and to reduce the risk and expense of unnecessary spinal procedures and hardware.

Claims

1. A first bone-moving member which has a longitudinal axis, wherein the distal portion of this longitudinal axis is configured to be inserted into a first spinal vertebra, wherein the proximal portion of this longitudinal axis is configured to protrude out from the skin of a person'"'"'s back, one or more actuators to apply force to at least two longitudinally-separated locations along the proximal portion of the longitudinal axis of this bone-moving member;

and wherein this application of force is active and not just passive resistance of force that comes from natural muscle movement;

wherein the one or more actuators are electric, hydraulic or pneumatic actuators;

a second bone-moving member which has a longitudinal axis, wherein the distal portion of this longitudinal axis is configured to be inserted into a second spinal vertebra, wherein the proximal portion of this longitudinal axis is configured to protrude out from the skin of a person'"'"'s back, wherein the one or more actuators apply force to at least two longitudinally-separated locations along the proximal portion of the longitudinal axis of this bone-moving member;

wherein this application of force is active and not just passive resistance of force that comes from natural muscle movement;

wherein movement of a least one of the first and second bone-moving members causes vertebral movement of the first and second spinal vertebrae relative to each other;

wherein this vertebral movement is selected from one, or a combination, of the movements in the group consisting of flexion, extension, lateral bending, decompression, compression, and torsion;

wherein an amount of flexion or extension can be adjusted independently of an amount of decompression or compression; and

wherein an amount of decompression or compression can be adjusted independently of an amount of flexion or extension;

one or more bone movement measuring members that measure movement of the first and second spinal vertebrae relative to each other in response to the active application of force to the first and/or second bone-moving members; and

one or more movement analyzing members that analyze movement of the first and second spinal vertebrae relative to each other, wherein the results of this analysis are used to help select a therapy.

2. The device in claim 1 wherein amounts of flexion, extension, or lateral bending are defined as follows:

an amount of flexion is the degree of a linear angle formed by the intersection of the lateral cross-sectional planes of two vertebrae, wherein the vertex of this angle is anterior to the center of the vertebrae;

an amount of extension is the degree of a linear angle formed by the intersection of the lateral cross-sectional planes of two vertebrae, wherein the vertex of this angle is posterior to the center of the vertebrae; and

an amount of lateral bending is the degree of a linear angle formed by the intersection of the lateral cross-sectional planes of two vertebrae, wherein the vertex of this angle is to the right or left of the center of the vertebrae.

3. The device in claim 1 wherein amounts of decompression or compression are defined as follows:

decompression is movement that increases the average distance between all points in the lateral cross-sections of two vertebrae; and

compression is movement that decreases the average distance between all points in the lateral cross-sections of two vertebrae.

4. The device in claim 1 wherein analysis of flexion, extension, lateral bending, decompression, compression, and/or torsion is used to determine the extent to which vertebrae should be stabilized by application of stabilization procedures and/or devices.

5. A first bone-moving member which has a longitudinal axis, wherein the distal portion of this longitudinal axis is configured to be inserted into a first spinal vertebra, wherein the proximal portion of this longitudinal axis is configured to protrude out from the skin of a person'"'"'s back, one or more actuators to apply force to at least two longitudinally-separated locations along the proximal portion of the longitudinal axis of this bone-moving member;

and wherein this application of force is active and not just passive resistance of force that comes from natural muscle movement;

wherein the one or more actuators are electric, hydraulic or pneumatic actuators;

a second bone-moving member which has a longitudinal axis, wherein the distal portion of this longitudinal axis is configured to be inserted into a second spinal vertebra, wherein the proximal portion of this longitudinal axis is configured to protrude out from the skin of a person'"'"'s back, wherein the one or more actuators apply force to at least two longitudinally-separated locations along the proximal portion of the longitudinal axis of this bone-moving member;

wherein this application of force is active and not just passive resistance of force that comes from natural muscle movement;

wherein movement of a least one of the first and second bone-moving members causes vertebral movement of the first and second spinal vertebrae relative to each other;

wherein this vertebral movement is selected from one, or a combination, of the movements in the group consisting of flexion, extension, lateral bending, decompression, compression, and torsion;

wherein an amount of flexion or extension can be adjusted independently of an amount of decompression or compression; and

wherein an amount of decompression or compression can be adjusted independently of an amount of flexion or extension;

one or more bone movement measuring members that measure movement of the first and second spinal vertebrae relative to each other in response to the active application of force to the first and/or second bone-moving members; and

one or more movement analyzing members that analyze movement of the first and second spinal vertebrae relative to each other, wherein the results of this analysis are used to help select a therapy.

6. The device in claim 5 wherein the bone-moving members cause spinal vertebrae to move in flexion, extension, lateral bending, decompression, compression, or torsion.

7. The device in claim 5 wherein analysis of flexion, extension, lateral bending, decompression, compression, and/or torsion is used to determine the extent to which vertebrae should be stabilized by application of stabilization procedures and/or devices.