Endotracheal Tube for Nerve Monitoring

• US 20160262699A1
• Filed: 08/26/2015
• Published: 09/15/2016
• Est. Priority Date: 03/12/2015
• Status: Abandoned Application

• Current Assignee: Andrew C. Goldstone, Raymond L. Schettino
• Original Assignee: Andrew C. Goldstone, Raymond L. Schettino
• Inventors: Goldstone, Andrew C., Schettino, Raymond L.
• Application Number:
  US14/836,057
• Publication Number:
  US 20160262699A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61B 5/24 Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
• CPC Class Codes: A61B 5/4041 Evaluating nerves condition
• CPC Class Codes: A61B 5/6852 Catheters
• CPC Class Codes: A61M 16/04 Tracheal tubes catheters in general A61M25/00
• CPC Class Codes: A61M 2230/08 Other bio-electrical signals
• CPC Class Codes: A61M 2230/10 Electroencephalographic signals

Abstract

An endotracheal tube for nerve monitoring including one or more ground, reference, or laryngeal-monitoring electrode wires that run in a direction parallel to the central axis of the tube, each such electrode wire having an insulated first wire portion and an uninsulated second wire portion, and further including one or more ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube in a helical, circular, or interposed pattern

Claims

1. A nerve monitoring device comprising:

an endotracheal tube formed from a flexible, non-electrically conducting material and having a distal end, a proximal end, a central axis, and an outer surface;

at least one ground, reference, or laryngeal-monitoring electrode wire including electrically conducting material running in a direction parallel to the central axis at a location between the distal end and the proximal end of the endotracheal tube;

the at least one ground, reference, or laryngeal-monitoring electrode wire having an electrically insulated first wire portion located between the distal end and proximal end of the endotracheal tube and an electrically uninsulated second wire portion located on the outer surface of the endotracheal tube between the first wire portion and the distal end of the endotracheal tube;

the second wire portion comprising means for contacting the laryngeal muscles when the endotracheal tube is placed in the trachea for ventilation; and

at least one ground, reference, or hypoglossal-monitoring electrode wire including electrically conducting material wrapped around the outer surface of the endotracheal tube in a helical or circular pattern.

2. The device of claim 1, wherein the pattern of each of the at least one ground, reference, or hypoglossal-monitoring electrode wire wrapped around the outer surface of the endotracheal tube is helical and begins close to the second wire portion than to the proximal end of the endotracheal tube, wraps over the first wire portion, and terminates closer to the proximal end of the endotracheal tube than to the second wire portion.

3. The device of claim 1, wherein at least two ground, reference, or hypoglossal-monitoring electrode wires are wrapped around the outer surface of the endotracheal tube in a helical or circular pattern.

4. The device of claim 3, wherein the pattern of each of the at least two ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube is helical and is identical and each of the at least two ground, reference, or hypoglossal-monitoring electrode wires having a helical pattern is offset from every other wire having a helical pattern by a longitudinal distance along the endotracheal tube.

5. The device of claim 2, wherein all of the ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube are dedicated to the same purpose.

6. The device of claim 2, wherein not all of the ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube are dedicated to the same purpose.

7. The device of claim 6, wherein the order in which the ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube are wrapped around the outer surface of the endotracheal tube is alternated such that at least one ground, reference, or hypoglossal-monitoring electrode is next to another ground, reference, or hypoglossal-monitoring electrode of a different purpose.

8. The device of claim 1, wherein the first wire portion is coated or embedded within the wall of the endotracheal tube.

9. The device of claim 5, wherein the at least two ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube consist of two ground electrode wires.

10. The device of claim 7, wherein the at least two ground, reference, or hypoglossal-monitoring electrode wires wrapped around the outer surface of the endotracheal tube consist of two ground electrode wires and two hypoglossal-monitoring electrode wires and the ground electrode wires are alternated with the hypoglossal-monitoring wires.

11. The device of claim 1, wherein the at least one ground, reference, or laryngeal-monitoring electrode wire including electrically conducting material running in a direction parallel to the central axis is either a ground or reference electrode wire.

12. The device of claim 1, further comprising an electrical connecting means for attaching at least one of the ground, reference, or laryngeal-monitoring electrode wires to a machine which processes EMG signals.

13. The device of claim 1, further comprising a self-contained indicator connected to at least one of the ground, reference, laryngeal-monitoring, or hypoglossal-monitoring electrode wires, wherein the self-contained indicator produces at least one of a sound or a light upon receiving certain electrical signals.

14. The device of claim 13, wherein the self-contained indicator includes at least one of an amplifier, a filter, and a processor.

27. The device of claim 1, wherein the electrical connecting means is a universal jack.

15. A nerve monitoring device comprising:

an endotracheal tube formed from a flexible, non-electrically conducting material and having a distal end, a proximal end, a central axis, and an outer surface;

at least one ground, reference, or laryngeal-monitoring electrode wire including electrically conducting material running in a direction parallel to the central axis at a location between the distal end and the proximal end of the endotracheal tube;

the at least one electrode wire having an electrically insulated first wire portion located between the distal end and proximal end of the endotracheal tube and an electrically uninsulated second wire portion located on the outer surface of the endotracheal tube between the first wire portion and the distal end of the endotracheal tube; and

the second laryngeal monitoring wire portion comprising means for contacting the laryngeal muscles when the endotracheal tube is placed in the trachea for ventilation;

a first primary electrode wire including electrically conducting material connected to a first set of branch electrode wires including electrically conducting material and a second primary electrode wire including electrically conducting material connected to a second set of branch electrode wires including electrically conducting material, wherein the first set of branch electrode wires and the second set of branch electrode wires are interposed with one another.

16. The device of claim 15, wherein the first primary electrode wire and the second primary electrode wire run parallel to one another and to the central axis of the endotracheal tube from a location on the tube closer to the second wire portion than to the proximal end of the endotracheal tube, over the first wire portion, and to a location closer to the proximal end of the endotracheal tube than to the second wire portion.

17. The device of claim 16, wherein the first primary electrode wire and the first set of branch electrode wires have the same purpose of ground, reference, or hypoglossal-monitoring as each other, and the second primary electrode wire and second set of branch electrode wires have the same purpose of ground, reference, or hypoglossal-monitoring as each other.

18. The device of claim 17, wherein the first set of branch electrode wires run in a first annular direction around a portion of the circumference of the endotracheal tube and the second set of branch electrode wires run in a second annular direction that is opposite the first annular direction around a portion of the circumference of the endotracheal tube.

19. The device of claim 18, wherein the length of each branch electrode wire of the first set of branch electrode wires and the second set of branch electrode wires is less than the longer annular distance between the first primary electrode wire and the second primary electrode wire.

20. The device of claim 19, wherein each branch electrode wire of the first set of branch electrode wires and the second set of branch electrode wires is parallel to every other branch electrode wire of the first set of branch electrode wires and the second set of branch electrode wires.

21. The device of claim 17, wherein the first primary electrode wire and first set of branch electrode wires have the same purpose as the second primary electrode wire and second set of branch electrode wires.

22. The device of claim 17, wherein the first primary electrode wire and first set of branch electrode wires have a different purpose than the second primary electrode wire and second set of branch electrode wires.

23. The device of claim 19, wherein the first primary electrode wire and first set of branch electrode wires are ground wires and the second primary electrode wire and second set of branch electrode wires are hypoglossal-monitoring wires.

24. The device of claim 15, wherein the first wire portion is coated or embedded within the wall of the endotracheal tube.

25. The device of claim 15, wherein the at least one ground, reference, or laryngeal-monitoring electrode wire including electrically conducting material running in a direction parallel to the central axis is either a ground or reference electrode wire.

26. The device of claim 15, further comprising an electrical connecting means for attaching at least one of the ground, reference, or laryngeal-monitoring electrode wires to a machine which processes EMG signals.

28. The device of claim 26, wherein the electrical connecting means is a universal jack.

31. The device of claim 15, further comprising a self-contained indicator connected to at least one of the ground, reference, laryngeal-monitoring, first primary, or second primary electrode wires, wherein the self-contained indicator produces at least one of a sound or a light upon receiving certain electrical signals.

32. The device of claim 31, wherein the self-contained indicator includes at least one of an amplifier, a filter, and a processor.