Non-invasive measurement of joint translation and range of motion

• US 5,961,474 A
• Filed: 03/20/1998
• Issued: 10/05/1999
• Est. Priority Date: 03/20/1998
• Status: Expired due to Term

• Current Assignee: Arthrex Incorporated
• Original Assignee: Mark T. Reis
• Inventors: Reis, Mark T.
• Primary Examiner(s): HINDENBURG, MAX F
• Application Number:
  US09/045,323
• Time in Patent Office: 564 Days
• Field of Search: 600/587, 600/592, 600/594, 600/595
• US Class Current: 600/595
• CPC Class Codes: A61B 5/1071 measuring angles, e.g. using goniometers A61B5/1123 takes precedence
• CPC Class Codes: A61B 5/4528 Joints A61B5/4533, A61B5/4538 take precedence
• CPC Class Codes: G01B 7/003 for measuring position, not involving coordinate determination coordinate measuring G01B7/004
• CPC Class Codes: G01S 5/0247 Determining attitude

Abstract

Electromagnetic position sensors are placed on the skin of a patient to electronically measure joint translation and range of motion. Non-invasive monitoring is provided during a joint translation examination by placing one position sensor on the skin of the patient to measure the position of a first bone in the vicinity of the joint and another position sensor on the skin of the patient to measure the position of a second bone in the vicinity of the joint. The translation examination is then conducted by the attending physician, and the amount of joint translation is determined objectively by determining the difference in the relative position between the sensors from an initial position for the exam to a clinical end point for the exam. In a glenohumeral translation examination, one sensor is preferably placed on the skin over the scapular spine while the other sensor is preferably placed over the bicipital groove. In a shoulder range of motion examination, the sensor over the bicipital groove is moved to cover the biceps. Again, the range of motion is determined objectively by determining the difference in the relative position between the sensors from an initial position for the exam to a clinical end point for the exam. The invention can be used to objectively monitor translation and range of motion of other joints as well.

Claims

1. In a patient having a first bone and a second bone which are articulated at a joint, a non-invasive method of objectively measuring joint translation at the joint in a clinical setting comprising the steps of

a) placing a first position sensor on the surface of the skin of a patient to measure the position of the first bone in the vicinity of the joint;

b) generating a first position signal in response to the position of the first position sensor;

c) placing a second position sensor on the surface of the skin of the patient to measure the position of the second bone in the vicinity of the joint;

d) generating a second position signal in response to the position of the second position sensor;

e) positioning the first bone and the second bone with respect to each other in a clinical neutral position at the joint and storing the value of the first and second position signals when the first and second bones are positioned in the clinical neutral position;

f) using the stored value of the first and second position signals when the first and second bones are positioned in the clinical neutral position to determine the relative position between the first and second electromagnetic position sensors when the first and second bones are positioned in the clinical neutral position;

g) applying force to move the first bone in the vicinity of the joint with respect to the second bone in the vicinity of the joint to a clinical end point and storing the value of the first and second position signals when the first and second bones are positioned at the clinical end point;

h) using the stored values of the first and second position signals when the first and second bones are positioned at the clinical end point to determine the relative position between the first and second position sensors when the first bone in the vicinity of the joint is positioned at the clinical end point with respect to the second bone in the vicinity of the joint; and

i) determining the translation of the joint by comparing the relative position between the first and second position sensors when the first and second bones are in the clinical neutral position to the relative position between the first and second position sensors when the first bone is positioned at the clinical end point with respect to the second bone.

2. A method of objectively measuring joint translation as recited in claim 1 wherein steps e) through i) are repeated at least three times during an examination.

3. A method of objectively measuring joint translation as recited in claim 1 wherein the first and second position sensors are electromagnetic position sensors and the method further comprises the step of providing a low-level electromagnetic field within a patient examination area and further wherein the first position signal is generated in response to the position of the first electromagnetic position sensor within the low-level electromagnetic field and the second position signal is generated in response to the position of the second electromagnetic position sensor within the low-level electromagnetic field.

29. A method of objectively measuring joint translation as recited in claim 1 further comprising the steps of:

selecting a clinical linear direction of measuring joint translation;

defining an initial relative position vector from the stored values of the first position signal and the second position signal when the first and second bones are positioned in the clinical neutral position;

defining an end point relative position vector from the stored values of the first position signal and the second position signal when the first and second bones are positioned at the clinical end point;

determining a translation vector from the initial relative position vector and the end point relative position vector; and

determining whether force applied to move the first bone with respect to the second bone in the vicinity of the joint is applied in the clinical linear direction by comparing the direction of the translation vector to the selected clinical linear direction.

4. A non-invasive system for objectively measuring joint translation in a joint of a patient comprising:

an electromagnetic transmitter that produces a magnetic field in an examination area;

a first electromagnetic position sensor that generates a first position signal in response to the position of the first electromagnetic position sensor in the magnetic field, where the first electromagnetic position sensor is configured for placement on the surface of the skin of the patient over a first bone in the vicinity of the joint;

a second electromagnetic position sensor that generates a second position signal in response to the position of the second electromagnetic position sensor in the magnetic field, wherein the second electromagnetic position sensor is part of a sensor assembly that includes means for mounting the second sensor on the surface of the skin of the patient over a second bone in the vicinity of the joint; and

a programmed computer that receives the first and second position signals, the programmed computer including means for objectively determining joint translation of the joint when the patient undergoes a joint translation examination with the first electromagnetic position signal placed on the surface of the skin of the patient over the first bone in the vicinity of the joint and the second electromagnetic position sensor placed on the surface of the skin of the patient over the second bone in the vicinity of the joint.

5. A system as recited in claim 4 further comprising a screen display which includes an image of the first bone at least in the vicinity of the joint and an image of the second bone at least in the vicinity of the joint, wherein the image of the first bone moves relative to the image of the second bone in proportion to the movement of the first electromagnetic position sensor with respect to the second electromagnetic position sensor.

6. A system as recited in claim 4 wherein the first electromagnetic position sensor is part of a sensor assembly that includes a cutaneous mount for the sensor assembly.

7. A system as recited in claim 4 wherein the second electromagnetic position sensor is part of a sensor assembly that includes a contoured outer surface that facilitates the gripping of the sensor assembly in the fingers of a physician performing the joint translation examination.

8. A non-invasive method of objectively measuring glenohumeral translation in a patient in a clinical setting comprising the steps of:

a) placing a scapula position sensor on the surface of the skin of a patient over the patient'"'"'s scapula;

b) generating a scapula position signal in response to the position of the scapular position sensor;

c) placing a humeral head position sensor on the surface of the skin of the patient at a location corresponding to the humeral head of the patient;

d) generating a humeral head position signal in response to the position of the humeral head position sensor;

e) centering the humeral head within a glenoid of the scapula, and storing the values of the scapula position signal and the humeral head position signal when the humeral head is centered within the glenoid of the scapula;

f) using the stored values of the scapula position signal and the humeral head position signal to determine the relative position between the scapula position sensor and the humeral head position sensor when the humeral head is centered within the glenoid of the scapula;

g) applying force to move the humeral head with respect to the glenoid of the scapula to a clinical end point, and storing the values of the scapula position signal and the humeral head position signal when the humeral head is positioned at the clinical end point with respect to the glenoid of the scapula;

h) using the stored values of the scapula position signal and the humeral head position signal to determine the relative position between the scapula position sensor and the humeral head position sensor when the humeral head of the patient is positioned at the clinical end point with respect to the glenoid of the scapula;

i) determining glenohumeral translation by comparing the relative distance between the scapula position sensor and the humeral head position sensor when the humeral head is centered in the glenoid to the relative distance between the scapular position sensor and the humeral head position sensor when the humeral head is positioned at the clinical end point with respect to the glenoid.

9. A method of objectively measuring glenohumeral translation as recited in claim 8 wherein the scapular position sensor and the humeral head position sensors are electromagnetic position sensors and the method further comprises the step of providing a low-level electromagnetic field within a patient examination area and further wherein the scapula position signal is generated in response to the position of the scapula scapular position sensor within the low-level electromagnetic field and the humeral head position signal is generated in response to the position of the humeral head position sensor within the low-level electromagnetic field.

10. A method of objectively measuring glenohumeral translation as recited in claim 8 wherein steps e) through i) are repeated at least three times.

11. A method as recited in claim 8 wherein the humeral head position sensor is placed on the surface of the skin of the patient over an anterior portion of the humeral head.

12. A method as recited in claim 8 wherein the humeral head position sensor is placed on the surface of the skin of the patient over a posterior portion of the humeral head of the patient.

13. A method as recited in claim 8 wherein the humeral head position sensor is placed on the surface of the skin of the patient over the bicipital groove at the anterior of the patient'"'"'s shoulder.

14. A method as recited in claim 8 wherein the scapula position sensor is placed on the surface of the skin over the acromion portion of the scapula.

15. A method as recited in claim 8 wherein the scapula position sensor is placed on the surface of the skin over the spine of the scapula.

16. A method as recited in claim 8 wherein the scapula position sensor is temporarily adhered directly on to the surface of the skin of the patient when the scapular position sensor is placed on the skin over the patient'"'"'s scapula using a cutaneous mount.

17. A method as recited in claim 8 wherein the humeral head position sensor is held in a hand of a person applying force to move the humeral head with respect to the scapula.

18. A method as recited in claim 8 further comprising the step of:

placing the patient in an upright position;

wherein force is applied to move the humeral head of the patient with respect to the scapula of the patient by grasping the scapular spine and the clavicle of the patient with a first hand, grasping the humeral head of the patient with a second hand, and moving the humeral head within the glenoid of the scapula either anteriorly or posteriorly to a clinical end point.

19. A method as recited in claim 8 further comprising the step of:

lying the patient in a supine position;

wherein force is applied to move the humeral head of the patient with respect to the glenoidal of the patient by grasping the humeral head of the patient and moving the humeral head relative to the glenoid to a clinical end point as the patient remains in the supine position.

20. A method as recited in claim 8 further comprising the steps of:

selecting a clinical linear direction of measuring glenohumeral translation;

defining an initial relative position vector from the stored values of the scapula position signal and the humeral head position signal when the humeral head is centered within the glenoid of the scapula;

defining an end point relative position signal from the stored values of the scapula position signal and the humeral head position signal when the humeral head is positioned at the clinical end point with respect to the glenoid of the scapula;

determining a translation vector from the initial relative position vector and the end point relative position vector;

determining whether force applied to move the humeral head with respect to the glenoid is applied in the clinical linear direction by comparing the direction of the translation vector to the clinical linear direction.

21. In a patient having a first bone and a second bone articulated at a joint, a non-invasive method of objectively measuring range of motion of the joint in a clinical setting comprising the steps of:

a) placing a first position sensor on the surface of the skin of the patient to measure the position of the first bone in the vicinity of the joint;

b) generating a first position signal in response to the position of the first position sensor;

c) placing a second position sensor on the surface of the skin of the patient to measure the position of the second bone;

d) generating a second position signal in response to the position of the second position sensor;

e) placing the second bone at an initial position and storing the value of the first and second position signals when the second bone is in the initial position;

f) actively or passively moving the second bone through a clinical range of motion examination to a clinical end point and storing the value of the first and second position signals when the second bone is positioned at the clinical end point; and

g) objectively determining the range of motion of the joint by comparing the relative position of the first and second position sensors when the second bone of the patient is in the initial position to the relative position of the first and second sensors when the second bone of the patient is positioned at the range of motion clinical end point.

22. A method of objectively measuring range of motion as recited in claim 21 wherein the second position sensor is placed on the surface of the skin of the patient over the second bone of the patient at a location away from the joint.

23. A method of objectively measuring range of motion as recited in claim 21 wherein the first and second position sensors are electromagnetic position sensors and the method further comprises the step of providing a low-level electromagnetic field within a patient examination area;

and further wherein the first position signal is generated in response to the position of the first electromagnetic position sensor in the electromagnetic field and the second position signal is generated in response to the position of the second electromagnetic position sensor within the electromagnetic field.

24. A method of objectively measuring range of motion as recited in claim 21 wherein steps e) through g) are repeated at least three times.

25. A method of objectively measuring range of motion as recited in claim 21 further comprising the steps of:

selecting a clinical range of motion plane;

defining an initial relative position vector from the stored values of the first and second position signals when the second bone is in the initial position;

defining an end point relative position vector from the stored values of the first and second position signals when the second bone is positioned at the clinical end point;

determining a range of motion vector from the initial relative position vector and the end point relative position vector; and

determining whether the second bone has been moved during the clinical range of motion examination within the selected clinical range of motion plane by comparing the direction of the range of motion vector to the clinical range of motion plane.

26. For use with a patient having a first bone and a second bone which are articulated at a joint, a non-invasive electromagnetic monitoring system for objectively measuring range of motion of the joint comprising:

an electromagnetic transmitter that produces a magnetic field in an examination area;

a first electromagnetic position sensor that generates a first position signal in response to the position of the first electromagnetic position sensor in the magnetic field, wherein the first electromagnetic position sensor is configured for placement on the surface of the skin of the patient over the second bone articulated at the joint;

a second electromagnetic position sensor that generates a second position signal in response to the position of the second electromagnetic position sensor in the magnetic field, wherein the second electromagnetic position sensor is configured for placement on the surface of the skin of the patient over the second bone articulated at the joint; and

a programmed computer that receives the first and second position signals, the programmed computer including means for objectively determining joint range of motion when the patient undergoes a range of motion examination with the first electromagnetic position sensor placed on the surface of the skin of the patient over the first bone in the vicinity of the joint and the second electromagnetic position sensor placed on the surface of the skin of the patient over the second bone.

27. A system as recited in claim 26 further comprising a screen display including an image of the first bone at least in the vicinity of the joint and an image of the second bone at least in the vicinity of the joint, wherein the image of the first bone moves relative to the image of the second bone on the screen display in proportion to the movement of the first electromagnetic position sensor relative to the second electromagnetic position sensor.

28. A system as recited in claim 26 wherein the first electromagnetic position sensor is part of a first sensor assembly that includes a cutaneous mount for the first sensor assembly and the second electromagnetic position sensor is part of a second sensor assembly that includes a cutaneous mount for the second sensor assembly.