BREATH SENSING WITH REMOTE PRESSURE SENSOR
Devices and methods are provided herein for sensing and monitoring of patient breathing during high flow respiratory therapy. A nasal cannula having a sensing lumen and remotely-located pressure sensor is provided herein for breath sensing that provides an accurate and clear signal while high flow rates of breathing gas are delivered from the nasal cannula. Condensation can be removed from the sensing lumen by applying a constant, pulsatile, or burst flow of purge gas. The breath sensing apparatus can be integrated in a respiratory system with a breathing gas source or can be packaged as a separate device capable of adapting to a variety of systems.
1 . A nasal cannula for breath sensing of a patient being provided high flow respiratory therapy, the nasal cannula comprising:
a cannula body having a first connector configured to receive a first flow of breathing gas and a second connector configured to receive a second flow of breathing gas;
a first nasal prong configured to deliver the first flow of breathing gas to a nare of the patient;
a second nasal prong configured to deliver the second flow of breathing gas to a nare of the patient;
a first sensing lumen having a first sensing tip positioned along the first nasal prong such that, during patient inspiration and expiration, gas flows over the first sensing tip to create a pressure change within the first sensing lumen; and
a first pressure sensor configured to detect a first pressure in the first sensing lumen, the first pressure sensor being positioned at a proximal end of the first sensing lumen opposite the first sensing tip.
2 . The nasal cannula of claim 1 , further comprising:
a second sensing lumen having a second sensing tip positioned along the second nasal prong such that, during patient inspiration and expiration, gas flows over the second sensing tip to create a second pressure change within the second sensing lumen; and
a second pressure sensor configured to detect a second pressure in the second sensing lumen and positioned at a proximal end of the second sensing lumen opposite the second sensing tip.
3 . The nasal cannula of claim 1 , wherein the first sensing lumen comprises:
a housing mounted on the cannula body, and
a tube configured to enable fluid communication between the first sensing tip and the pressure sensor, wherein the tube is in fluid communication with the pressure sensor at the proximal end of the first sensing lumen,
wherein the housing is fluidically connected to the tubing.
4 . The nasal cannula of claim 3 , wherein the tube has a length between about 5 mm and about 3 m.
5 . The nasal cannula of claim 3 , wherein the tube has an internal diameter between about 0.25 mm and about 2.5 mm.
6 . The nasal cannula of claim 3 , wherein a control gas flows from a flow generator through at least a portion of the tube in a direction from the proximal end to the sensing tip.
7 . The nasal cannula of claim 6 , wherein the control gas collides with patient breath at a boundary region adjacent to the first sensing tip.
8 . The nasal cannula of claim 6 , wherein the control gas is delivered intermittently as a bolus flow.
9 . The nasal cannula of claim 6 , wherein the control gas has a flow rate between about 0.1 mL/min and about 10 mL/min.
10 . The nasal cannula of claim 6 , wherein the flow generator is one of a fan, a syringe pump, a blower, a compressor, a bellows, or a wall air source.
11 . The nasal cannula of claim 6 , wherein the nasal cannula is configured with the control gas so as to purge condensation from the first sensing lumen.
12 . The nasal cannula of claim 6 , wherein the sensing lumen comprises a tee joint positioned along the tube and configured to convey the control gas into the tube from the flow generator.
13 . The nasal cannula of claim 1 , further comprising a temperature sensor configured to measure a breath temperature.
14 . The nasal cannula of claim 1 , wherein the detected first pressure indicates a difference between an internal pressure within the first sensing lumen and ambient pressure of the surrounding environment.
15 . The nasal cannula of claim 14 , wherein the difference is at least about 1 Pa to at least about 5 Pa.
16 . The nasal cannula of claim 1 , wherein the first pressure sensor is configured to output a pressure signal indicative of the detected first sensing lumen pressure.
17 . The nasal cannula of claim 1 , wherein the first sensing tip is angled relative to a longitudinal axis of the first sensing lumen.
18 . The nasal cannula of claim 17 , wherein the first sensing tip comprises a tip face at an angle other than 90 degrees relative to the longitudinal axis.
19 . The nasal cannula of claim 18 , wherein the angle is between about 30 degrees and about 60 degrees.
20 . The nasal cannula of claim 19 , wherein the angle is about 45 degrees.
21 . The nasal cannula of claim 18 , wherein the tip face has rounded, beveled, or chamfered edges.
22 . The nasal cannula of claim 1 , wherein the sensing tip is positioned on an exterior surface of the first nasal prong.
23 . The nasal cannula of claim 22 , wherein the sensing tip is positioned on a dorsal side of the exterior surface of the first nasal prong.
24 . The nasal cannula of claim 22 , wherein the sensing tip is positioned proximally to a prong tip of the first nasal prong.
25 . The nasal cannula of claim 1 , wherein the sensing tip is positioned on the nasal cannula such that the sensing tip resides within the nare of the patient while the cannula is in use.
26 . The nasal cannula of claim 1 , wherein the sensing tip has an internal diameter between about 0.25 mm and 2.5 mm.
27 . The nasal cannula of claim 1 , wherein the first nasal prong has an internal diameter of about 1.0 to about 4.0 mm.
28 - 85 . (canceled)