INTRA-VAGINAL SENSOR TO MEASURE PELVIC FLOOR LOADING

• US 20100222708A1
• Filed: 12/21/2009
• Published: 09/02/2010
• Est. Priority Date: 12/19/2008
• Status: Abandoned Application

• Current Assignee: University of Utah Research Foundation (State of Utah)
• Original Assignee: University of Utah Research Foundation (State of Utah)
• Inventors: Johnson, Paul, Rosenbluth, Evan, Nygaard, Ingrid, Hitchcock, Robert
• Application Number:
  US12/643,438
• Publication Number:
  US 20100222708A1
• Time in Patent Office: Days
• US Class Current: 600/591
• CPC Class Codes: A61B 5/036 by means introduced into body tracts A61B5/032 and A61B5/035 take precedence
• CPC Class Codes: A61B 5/07 Endoradiosondes
• CPC Class Codes: A61B 5/1076 for measuring dimensions inside body cavities, e.g. using catheters A61B3/1005 takes precedence

Abstract

Devices and methods are provided for measuring pressure in a non-fluid-filled area of a patient'"'"'s body. The device includes a capsule having an outer wall and a base surface that define an inner cavity, which retains fluid. The outer wall of the capsule can be made of a flexible material. The device also has a pressure sensor that measures external pressure placed on the outer wall of the capsule. Methods of use include providing the device, positioning the device in the non-fluid-filled area, and measuring pressure within the non-fluid-filled area. The pressure measurement is compared with a predetermined pressure threshold, and a treatment regimen is generated based on the differences between the measured pressure and the predetermined pressure threshold.

Claims

1. A device for measuring pressure therein an area of a patient, comprising:

a capsule having an outer wall and a base surface, wherein the outer wall and the base surface cooperate to define an inner cavity configured to retain a fluid, and wherein at least a portion of the outer wall of the capsule comprises a flexible material; and

a pressure sensor configured to measure intra-capsular pressure that may be induced by any external pressure or force placed on the outer wall of the capsule.

2. The device of claim 1, wherein the capsule is configured to be positioned therein a non-fluid-filled area of the patient and measure pressure therein the non-fluid-filled area.

3. The device of claim 1, wherein the pressure sensor is positioned therein the inner cavity of the capsule.

4. The device of claim 3, wherein the pressure sensor is configured for wireless communication with an external data acquisition device.

5. The device of claim 1, wherein the flexible material is an elastomeric material.

6. The device of claim 5, wherein the elastomeric material is silicone elastomer.

7. The device of claim 1, wherein the capsule comprises a substantially hemi-spherical distal end portion, an opposing proximal end portion, and a substantially cylindrical body portion extending therebetween the proximal end portion and the distal end portion.

8. The device of claim 7, wherein a diameter of the substantially cylindrical body portion is between about 0.5 centimeters and 1.5 centimeters.

9. The device of claim 8, wherein the diameter of the substantially cylindrical body portion is about 1.2 centimeters.

10. The device of claim 7, wherein the capsule has a longitudinal axis that extends between the proximal end portion and the distal end portion, and wherein the capsule has a length taken along the longitudinal axis of between about 2 centimeters and about 3 centimeters.

11. The device of claim 10, wherein the length of the capsule is about 3 centimeters.

12. The device of claim 1, further comprising a tether member comprising a lumen having a distal end in communication with the pressure sensor and an opposing proximal end in communication with an atmospheric pressure source.

13. The device of claim 12, wherein the tether member further comprises means for providing wired communication from the pressure sensor to an external data acquisition device.

14. The device of claim 1, wherein the fluid comprises silicone gel.

15. A method for measuring intra-vaginal pressure of a patient, comprising:

providing a device for measuring the intra-vaginal pressure of the patient, comprising;

a capsule having an outer wall and a base surface, wherein the outer wall and the base surface cooperate to define an inner cavity configured to retain a fluid, and wherein at least a portion of the outer wall of the capsule comprises a flexible material; and

a pressure sensor configured to measure pressure placed on the outer wall of the capsule;

positioning the device therein a vagina of the patient above the pelvic floor of the patient; and

taking at least one pressure measurement based on the pressure placed on the outer wall of the capsule by the vagina of the patient.

16. The method of claim 15, wherein taking at least one pressure measurement comprises taking at least one pressure measurement while the patient performs at least one activity.

17. The method of claim 16, wherein the at least one activity comprises at least one of:

sitting, standing, walking, running, jumping, coughing, sneezing, performing a Valsalva maneuver, squatting, or lifting weights.

18. The method of claim 17, further comprising determining if the at least one pressure measurement differs from a predetermined pressure threshold for the at least one activity.

19. The method of claim 18, further comprising generating a treatment regimen based on the determined differences between the at least one pressure measurement and the predetermined pressure threshold for the at least one activity.

20. The method of claim 15, wherein the capsule comprises a substantially hemi-spherical distal end portion, an opposing proximal end portion, and a substantially cylindrical body portion extending therebetween the proximal end portion and the distal end portion, and wherein positioning the device therein the vagina of the patient comprises inserting the device therein the vagina such that the distal end portion of the capsule is proximate a cervix of the patient.

21. The method of claim 20, wherein the device further comprises a tether member operably connected to the proximal end portion of the capsule, wherein the tether member is configured for removal of the device from the vagina of the patient.

22. The method of claim 15, further comprising transmitting the at least one pressure measurement wirelessly to an external data acquisition device.

23. A method for measuring pressure therein a non-fluid-filled area of a patient, comprising:

providing a device for measuring the pressure therein the non-fluid-filled area of the patient, comprising;

a capsule having an outer wall and a base surface, wherein the outer wall and the base surface cooperate to define an inner cavity configured to retain a fluid, and wherein at least a portion of the outer wall of the capsule comprises a flexible material; and

a pressure sensor configured to measure pressure placed on the outer wall of the capsule;

positioning the device therein the non-fluid-filled area of the patient; and

taking at least one pressure measurement based on the pressure placed on the outer wall of the capsule by the non-fluid-filled area of the patient.

24. The method of claim 23, further comprising determining if the at least one pressure measurement differs from a predetermined pressure threshold.

25. The method of claim 24, further comprising generating a treatment regimen based on the determined difference between the at least one pressure measurement and the predetermined pressure threshold.

26. A device for measuring pressure therein a non-fluid-filled area of a patient, comprising:

a capsule having an outer wall and a base surface, wherein the outer wall and the base surface cooperate to define an inner cavity configured to retain a fluid, and wherein at least a portion of the outer wall of the capsule comprises a flexible material; and

a pressure sensor configured to measure external pressure placed on the outer wall of the capsule.