System and method for muscle stimulation and/or impedance measurement to verify proper tube placement
A tubing assembly for use with an electronic catheter guidance systems is provided and includes a catheter and a stimulation electrode assembly, and an electrical connection for delivering a stimulation waveform to the stimulation electrode assembly. The catheter extends in a longitudinal direction and has a proximal end and a distal end that define a lumen therebetween. Further, the catheter is configured for placement within a patient's digestive tract. The stimulation electrode assembly is configured to deliver an electrical stimulation to tissue. A catheter guidance system and method for accurately placing a catheter in the digestive tract are also provided.
1. A tubing assembly comprising:
a catheter having a proximal end and a distal end and extending in a longitudinal direction, wherein the proximal end and the distal end define a lumen therebetween, and wherein the catheter is configured for placement within a digestive tract of a patient including an esophagus;
a stimulation electrode assembly, wherein the stimulation electrode assembly is configured to deliver an electrical stimulation waveform to tissue at a voltage of from about 1.01volts to about 100 volts and a noise signal over a frequency range, wherein the tissue comprises muscle or cartilage;
a recording electrode assembly, wherein the recording electrode assembly monitors for electrical activity elicited by the tissue in response to the noise signal and communicates the electrical activity elicited by the tissue to a processor in real-time, wherein the processor is configured to:
determine if the electrical activity elicited by the tissue is in the form of one or more evoked potentials or corresponds with an impedance signature for the tissue over the frequency range,
determine whether the catheter is positioned in the esophagus based, at least in part, on the one or more evoked potentials or the determined impedance signature, and
generate an alert in response to determining that the catheter is not positioned in the esophagus; and
an electrical connection for delivering the electrical stimulation waveform and noise signal to the stimulation electrode assembly.
2. The tubing assembly of claim 1 , wherein the stimulation electrode assembly comprises an anode and a cathode, wherein the anode and the cathode are disposed on an outer wall of the distal end of the catheter.
3. The tubing assembly of claim 1 , wherein the stimulation electrode assembly comprises a first electrode disposed on an outer wall of the catheter and a second electrode configured for placement on a surface of skin.
4. The tubing assembly of claim 1 , wherein the recording electrode assembly comprises an active recording electrode, an inactive recording electrode, and a reference electrode.
5. The tubing assembly of claim 4 , wherein the active recording electrode, the inactive recording electrode, and the reference electrode are disposed on an outer wall of the distal end of the catheter.
6. The tubing assembly of claim 4 , wherein the active recording electrode, the inactive recording electrode, and the reference electrode are configured for placement on a surface of skin.
7. The tubing assembly of claim 1 , wherein the stimulation electrode assembly is configured for a wired connection or a wireless connection to the processor.
8. The tubing assembly of claim 7 , wherein the wired connection comprises a wire or a printed conduit.
9. The tubing assembly of claim 1 , wherein the electrical stimulation waveform is a square-wave pulsed waveform.
10. A catheter guidance system configured for placement within a digestive tract of a patient including an esophagus, the catheter guidance system comprising:
(a) a processor;
(b) a power source;
(c) a stimulator; and
(d) a tubing assembly comprising:
a catheter having a proximal end and a distal end and extending in a longitudinal direction, wherein the proximal end and the distal end define a lumen therebetween;
a stimulation electrode assembly, wherein the stimulation electrode assembly is configured to deliver an electrical stimulation waveform to tissue at a voltage of from about 1.01 volts to about 100 volts and a noise signal over a frequency range, wherein the tissue comprises muscle or cartilage; and
a recording electrode assembly, wherein the recording electrode assembly monitors for electrical activity elicited by the tissue in response to the noise signal and communicates the electrical activity elicited by the tissue to the processor in real time, the processor being configured to:
determine if the electrical activity elicited by the tissue is in the form of one or more evoked potentials or corresponds with an impedance signature for the tissue over the frequency range,
determine whether the catheter is positioned in the esophagus, based, at least in part, on the one or more evoked potentials or the determined impedance signature, and
generate an alert in response to determining that (a) the catheter is not placed in the esophagus, or (b) the catheter is correctly placed in a digestive tract of a patient.
11. The catheter guidance system of claim 10 , further comprising a display device, wherein the display device is coupled to the processor and displays a graph of the electrical activity elicited by the tissue and communicated to the processor by the recording electrode assembly.
12. The catheter guidance system of claim 10 , further comprising a memory device storing instructions which, when executed by the processor, cause the processor to (i) interpret the electrical activity elicited by the tissue and communicated by the recording electrode assembly and (ii) cause the catheter guidance system to alert the user as to correct placement of the catheter in the digestive tract of the patient or alert the user as to incorrect placement of the catheter in the respiratory tract of the patient based on the interpretation of the electrical activity elicited by the tissue.
13. The catheter guidance system of claim 10 , wherein the stimulation electrode assembly comprises an anode and a cathode, wherein the anode and the cathode are disposed on an outer wall of the distal end of the catheter.
14. The catheter guidance system of claim 10 , wherein the stimulation electrode assembly comprises a first electrode disposed on an outer wall of the catheter and a second electrode configured for placement on a surface of skin.
15. The catheter guidance system of claim 10 , wherein the recording electrode assembly comprises an active recording electrode, an inactive recording electrode, and a reference electrode.
16. The catheter guidance system of claim 15 , wherein the active recording electrode, the inactive recording electrode, and the reference electrode are disposed on an outer wall of the distal end of the catheter.
17. The catheter guidance system of claim 15 , wherein the active recording electrode, the inactive recording electrode, and the reference electrode are configured for placement on a surface of skin.