Peri-orbital trauma monitor and ocular pressure / peri-orbital edema monitor for non-ophthalmic surgery

• US 20060135864A1
• Filed: 11/23/2005
• Published: 06/22/2006
• Est. Priority Date: 11/24/2004
• Status: Abandoned Application

• Current Assignee: Christian P. Valcke, Westerlund L. Erik
• Original Assignee: Christian P. Valcke, Westerlund L. Erik
• Inventors: Valcke, Christian P., Westerlund, L. Erik
• Application Number:
  US11/286,312
• Publication Number:
  US 20060135864A1
• Time in Patent Office: Days
• US Class Current: 600/398
• CPC Class Codes: A61B 2562/0247 Pressure sensors
• CPC Class Codes: A61B 3/16 for measuring intraocular pressure, e.g. tonometers
• CPC Class Codes: A61B 5/103 Detecting, measuring or recording devices for testing the shape, pattern, colour, size or movement of the body or parts thereof, for diagnostic purposes A61B5/08 takes precedence; measuring aids for tailors A41H1/00; measuring instruments specially adapted for dentistry A61C19/04
• CPC Class Codes: A61B 5/6821 Eye

Abstract

An ocular pressure monitoring system includes a plurality of transducer assemblies that measure externally applied force(s) and/or peri-orbital edema from peri-orbital tissue areas associated with one or both of a patient'"'"'s eyes. Each of the transducer assemblies has at least one external force transducer and/or one edema transducer, and at least one mounting that is shaped to secure the transducer(s) to at least one peripheral peri-orbital tissue area. A microprocessor is connected to the transducers by leads or telemetrically. A display unit is in communication with the microprocessor for displaying data representative of peri-orbital edema.

Claims

1. A method of monitoring a patient'"'"'s eyes during a surgical procedure comprising:

applying a first pressure sensor to a first eye of the patient, wherein the pressure sensor is applied to a peripheral superior eyelid, an inferior eyelid, or other peri-orbital tissue such that forces directed at the patient'"'"'s anterior peri-orbital tissue are detected; and

transmitting a first set of data representative of the detected forces to a display; and

monitoring the display during the surgical procedure.

2. The method of claim 1, further including the step of placing the patient in a prone position prior to performing the surgical procedure.

3. The method of claim 1, further comprising:

applying a second pressure sensor to a second eye of the patient, wherein the second pressure sensor is applied to a superior eyelid, an inferior eyelid, or other peri-orbital tissue such that forces directed at the patient'"'"'s anterior peri-orbital tissue are detected; and

transmitting a second set of data representative of the detected forces to the display; and

monitoring the display during the surgical procedure.

4. The method of claim 3, further comprising comparing the first set of data to the second set of data during the surgical procedure to assess the risk of peri-orbital visual compromise.

5. A peri-orbital trauma monitoring system comprising:

a pressure sensor capable of measuring external applied loads to peripheral anterior peri-orbital tissue;

a microprocessor that is capable of processing information received from the sensor;

communication means between the sensor and microprocessor;

a display in communication with the microprocessor;

a sensor mount that is shaped to attach the sensor to peri-orbital tissue.

6. The peri-orbital trauma monitoring system of claim 5, wherein the pressure sensor comprises one or more transducers that measure non-averaged point specific gradients of applied external forces.

7. The peri-orbital trauma monitoring system of claim 5, wherein the pressure sensor comprises an array of transducers that are arranged in a predetermined pattern to measure an array of forces, wherein the predetermined pattern includes at least one transducer adjacent to each of the superior eyelid and inferior eyelid.

8. The peri-orbital trauma monitoring transducer system of claim 7, wherein the array of transducers measures one or more dimensional parameters and the microprocessor processes data received from the array and provides an output that characterizes the forces measured by the array and thereby provides a relative risk of peri-operative visual compromise as a result of the applied external forces.

9. The peri-orbital trauma monitoring system of claim 8, wherein the one or more dimensional parameters comprise magnitude, direction, and rate of change of force.

10. The peri-orbital trauma monitoring system of claim 5, wherein the means for communication between the sensor and microprocessor comprises a telemetric signal and electronics for generating and receiving said signal.

11. The peri-orbital trauma monitoring system of claim 5, wherein the means for communication between the sensor and microprocessor comprises one or more leads connecting the sensor and microprocessor.

12. The peri-orbital trauma monitoring system of claim 5, wherein the sensor is adapted to be mounted away from the eye at the periphery of an eye orbit to measure external force as a measure of non-ocular peri-orbital tissue pressure.

13. The peri-orbital trauma monitoring system of claim 12, wherein the microprocessor provides an output representative of peri-orbital tissue pressure as a measure of transmitted ocular pressure and optic nerve pressure.

14. The peri-orbital trauma monitoring system of claim 5, wherein the sensor measures external force as a measure of non-ocular peri-orbital tissue pressure and the microprocessor provides an output representative of peri-orbital tissue pressure as a measure of transmitted ocular pressure and optic nerve pressure.

15. A method of assessing ocular pressure comprising:

providing an ocular pressure monitoring system;

using the ocular pressure monitoring system to monitor peri-orbital edema during prone positioning of a patient; and

performing a surgical procedure while monitoring peri-orbital edema.

16. The method of claim 15, wherein the ocular pressure monitoring system comprises:

a first transducer mounted in a material mounting that attaches to peri-orbital tissue of a first eye of a patient;

a second transducer mounted in a material mounting that attaches to peri-orbital tissue of a second eye of a patient; and

a microprocessor that is in communication with the first and second transducers, wherein said microprocessor processes data received from the transducers; and

a display that displays the data.

17. The method of claim 16, wherein the peri-orbital tissue of the first eye and second eye comprises the superior eyelid and inferior eyelid respectively of each of said first and second eyes.

18. The method of claim 15, further including the step of placing the patient in a prone position prior to performing the surgical procedure.

19. An ocular pressure monitoring system comprising:

a plurality of transducer assemblies that measure peri-orbital edema from peri-orbital tissue areas associated with one or both of a patient'"'"'s eyes, each of said transducer assemblies comprising at least one pressure transducer and at least one mounting that is shaped to secure the transducer to at least one peripheral peri-orbital tissue area;

a plurality of leads wherein each of the leads is attached to one of the transducers;

a microprocessor connected to the transducers by the leads; and

a display unit in communication with the microprocessor for displaying data representative of peri-orbital edema.

20. The ocular pressure monitoring system of claim 19, wherein the transducers measure change in tissue surface length using optical, mechanical, electrical, or chemical means.

21. The ocular pressure monitoring system of claim 19, wherein the transducers measure change in tissue surface length using measured change in the electrical resistivity of a conductive polymer matrix.

22. The ocular pressure monitoring system of claim 19, wherein the display unit provides visible, audible, or tactile indicators to monitoring personnel.

23. The ocular pressure monitoring system of claim 19, wherein the mountings comprise a shape, adhesive pattern, and material property that supports the eye against anterior translation during prone positioning.

24. The ocular pressure monitoring system of claim 19, wherein the transducers measure non-averaged point specific gradients of applied external forces on the peri-orbital tissue areas.

25. The ocular pressure monitoring system of claim 19, wherein the force sensor comprises an array of transducers that are arranged in a predetermined pattern to measure an array of forces, wherein the predetermined pattern includes at least one transducer adjacent to each of a superior eyelid and an inferior eyelid of each eye.

26. The ocular pressure monitoring system of claim 25, wherein each of the array of transducers measures one or more dimensional parameters and the microprocessor processes data received from the array and provides an output that characterizes the forces measured by the array, thereby providing a relative risk of peri-operative visual compromise as a result of the applied external forces.

27. The ocular pressure monitoring system of claim 26, wherein the one or more dimensional parameters comprise magnitude, direction, and rate of change of force.

28. The ocular pressure monitoring system of claim 19, wherein at least one of the mountings has an oval shape comprising a superior mounting region adapted for attachment to a portion of a superior eyelid and an inferior mounting region adapted for attachment to an inferior eyelid, wherein a central cut-out portion separates the superior mounting region from the inferior mounting region and exposes a substantial portion of the superior eyelid.

29. The ocular pressure monitoring system of claim 19, wherein at least one of the mountings comprises:

a first arm with a proximal end and a distal end, the first arm adapted for attachment to a superior eyelid and sized to cover substantially all of the superior eyelid; and

a second arm with a proximal end and a distal end, the second arm adapted for attachment to an inferior eyelid,

wherein the two arms are connected at their proximal ends but not their distal ends, and wherein the two arms have a length that extends laterally of the eye to cover an osseous orbital rim of the eye.

30. The ocular pressure monitoring system of claim 19, wherein there are two transducer assemblies each with its own mounting, and wherein each of the two mountings has a shape that is different from the other such that the two transducers measure a different peri-orbital region.