Airway system with carbon dioxide sensor for determining tracheal cuff inflation and technique for using the same
View Patent ↗An airway management device is provided that may adjust the inflation level of a cuff associated with an endotracheal tube. The cuff inflation may be adjusted in response to an increase in carbon dioxide levels above the cuff, which may indicate a poor seal of the cuff against the tracheal walls, as well in response to a measured intracuff pressure. By using information about the seal quality of the cuff together with information about the cuff pressure, the inflation of the cuff can be adjusted to minimize cuff inflation pressure while maintaining a high quality tracheal seal.
1. A system comprising:
an endotracheal tube having a proximal end and a distal end configured to inserted into a patient's airway;
an inflatable cuff disposed about the distal end of the endotracheal tube, wherein the inflatable cuff is configured to form a seal with a wall of the patient's airway;
a carbon dioxide sensor configured to produce an output related to carbon dioxide concentration at a location in the patient's airway proximal to the inflatable cuff;
a cuff pressure sensor configured to produce an output, wherein the output comprises a direct measurement of an intracuff pressure of the inflatable cuff;
a cuff pressure regulator configured to change the inflation of the cuff based at least in part on the output from the carbon dioxide sensor and the output from the cuff pressure sensor;
a controller operatively coupled to the cuff pressure regulator and configured to determine whether the inflatable cuff is properly inflated and whether the inflatable cuff properly placed in the patient's airway based at least in part upon the output from the carbon dioxide sensor and the output from the cuff pressure sensor, wherein the controller is configured to:
cause the cuff pressure regulator to add air to the inflatable cuff in response to a determination that the intracuff pressure is less than a predetermined low pressure threshold;
cause the cuff pressure regulator to add air to the inflatable cuff in response to a determination that the intracuff pressure does not violate a threshold and the carbon dioxide concentration is greater than a predetermined carbon dioxide threshold;
cause the cuff pressure regulator to remove air from the inflatable cuff in response to a determination that the intarcuff pressure is greater than a predetermined high pressure threshold and the carbon dioxide concentration is less than the predetermined carbon dioxide threshold; and
trigger an alarm that is triggered if in response to a determination that the inflatable cuff is misplaced in the patient's airway, wherein the controller is configured to determine that the inflatable cuff is misplaced in response to a determination that the intracuff pressure is above the predetermined high pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold; and
an information element disposed on the endotracheal tube, wherein the information element comprises stored data related to the inflatable cuff, the predetermined high pressure threshold, and the predetermined carbon dioxide threshold.
2. The system of claim 1 , wherein the predetermined carbon dioxide threshold is about 2 mm Hg and the predetermined low pressure threshold is about 20 cm H 2 O.
3. The system of claim 1 , wherein the controller is configured to trigger comprising an alarm that is triggered if the intracuff pressure is below the predetermined low pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold.
4. The system of claim 1 , wherein the predetermined carbon dioxide threshold is about 2 mm Hg and the predetermined high pressure threshold is about 25 cm H 2 O.
5. The system of claim 1 , comprising a ventilator to which the endotracheal tube is operatively connected.
6. The system of claim 5 , wherein the ventilator is operatively connected to an inflation line of the cuff to allow the cuff to be inflated.
7. The system of claim 1 , wherein the carbon dioxide sensor comprises a chemical indicator, an electrochemical transducer, a non-optical transducer, an optical transducer, or a quantum-restricted element.
8. The system of claim 1 , wherein the carbon dioxide sensor is disposed on the endotracheal tube.
9. The system of claim 1 , wherein the endotracheal tube comprises a suction lumen adapted to delivery airway gases to a distally located carbon dioxide sensor.
10. The system of claim 1 , wherein the cuff pressure sensor comprises a manometer.
11. A method comprising the steps of:
receiving a direct measurement of the intracuff pressure of an inflatable cuff disposed about a distal end of an endotracheal tube inserted in a patient's airway, wherein the inflatable cuff is configured to form a seal with a wall of the patient's airway;
receiving an output related to a carbon dioxide concentration of the patient's airway at a location proximal to the inflatable cuff;
receiving information relating to a predetermined high pressure threshold and a predetermined carbon dioxide threshold from an information element disposed on the endotracheal tube;
determining that the inflatable cuff is misplaced in the patient's airway in response to a determination that the intracuff pressure is above the predetermined high pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold; and
triggering an alarm in response to the determination that the inflatable cuff is misplaced if the intracuff pressure is above the predetermined high pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold.
12. The method of claim 11 , comprising providing instructions to add more air to the cuff if the intracuff pressure falls below a predetermined low pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold.
13. The method of claim 11 , comprising providing instructions to remove air from the cuff if the intracuff pressure is above a predetermined high pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold.
14. The method of claim 11 , wherein the predetermined high pressure threshold is about 25 cm H 2 O.
15. A medical device programmed with instructions for:
receiving a direct measurement of the intracuff pressure of an inflatable cuff disposed about a distal end of an endotracheal tube inserted in the patient's airway, wherein the inflatable cuff is configured to form a seal with the wall of the patient's airway;
receiving an output related to the carbon dioxide concentration of the patient's airway at a location proximal to the inflatable cuff;
receiving information relating to a predetermined high pressure threshold and a predetermined carbon dioxide threshold from an information element disposed on the endotracheal tube;
providing instructions for adding more air to the inflatable cuff in response to a determination that the intracuff pressure is less than a predetermined low pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold;
providing instructions for adding more air to the inflatable cuff in response to a determination that the intracuff pressure is less than the predetermined high pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold;
providing instructions to remove air from the inflatable cuff in response to a determination that the intracuff pressure is greater than the predetermined high pressure threshold and the carbon dioxide concentration in the airway is less than the predetermined carbon dioxide threshold; and
triggering an alarm in response to a determination that the inflatable cuff is misplaced in the patient's airway, wherein determining that the inflatable cuff is misplaced in the airway comprises determining that the intracuff pressure is above the predetermined high pressure threshold and the carbon dioxide concentration in the airway is greater than the predetermined carbon dioxide threshold.
16. The device of claim 15 , comprising receiving an input related to the patient's clinical condition, wherein the patient's clinical condition is used to select the predetermined high pressure threshold.
17. The device of claim 16 , wherein the predetermined high pressure threshold is about 30 cm H 2 O when the patient's clinical condition is chronic obstructive pulmonary disease.