IP Library Granted Patent US 8,192,367
Granted Patent B2
US 8,192,367 · App. 12/024,937 · Granted Jun 5, 2012

Method and apparatus for monitoring respiration

Assignee: Laerdal Medical AS
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Quick Facts
Patent No.
US 8,192,367
App. No.
12/024,937
Granted
Jun 5, 2012
Kind
B2
Abstract

A device for monitoring respiration comprises a duct, a flow restricting element in the duct, and a pressure sensor arranged in the duct. The pressure sensor measures a pressure drop across the flow restricting element as a pressure difference between a pressure at a location in the duct on a first side of the flow restricting element and a substantially constant pressure on a second side of the flow restricting element opposite the first side.

Claims (26)

1. A system for monitoring respiration, comprising:

a duct configured to allow a fluid to flow therethrough;

a flow restricting element in the duct, the flow restricting element having a flow resistance, the flow restricting element shaped symmetrically with respect to an axis perpendicular to a direction of flow such that, in operation, velocity of the fluid is substantially equal upstream and downstream of the flow restricting element;

a single pressure sensor arranged in the duct proximate a patient end of the flow restricting element, the single pressure sensor configured to measure a pressure of the fluid at a single location;

an outlet valve coupled to an end of the duct opposite the patient end, the outlet valve having a flow resistance, the outlet valve configured to allow the fluid to exit the duct to a substantially constant pressure; and

a processing unit coupled to the single pressure sensor, the processing unit being configured to determine a flow rate based on the pressure measurement of the fluid from the single pressure sensor relative to the substantially constant pressure and based on the flow resistance of the flow restricting element and the flow resistance of the outlet valve.

2. The system of claim 1 wherein the duct is connected to a respiration device.

3. The system of claim 2 wherein the respiration device comprises one of a respiratory mask, a tracheal tube, and a bellow.

4. The system of claim 1 wherein the duct is integrated in a respiration device.

5. The system of claim 4 wherein the respiration device comprises one of a respiratory mask, a tracheal tube, and a bellow.

6. The system of claim 1 wherein the pressure sensor comprises an absolute pressure sensor.

7. The system of claim 1 wherein the substantially constant pressure is ambient pressure.

8. The system of claim 1 wherein the outlet valve comprises a one-way valve.

9. The system of claim 1 , further comprising a user interface for providing information regarding the respiration to a user.

10. The system of claim 1 wherein the processing unit is operable to calculate flow values from a linear relationship between pressure drop and flow.

11. The system of claim 1 wherein the processing unit is operable to calculate respired volume by integrating the flow rate over time.

12. The system of claim 1 wherein the processing unit is operable to calculate a pressure difference between the single pressure measurement and the substantially constant pressure, the processing unit being further operable to calculate an expired volume based on a linear relationship between the expired volume and the pressure difference.

13. A method of determining a flow rate during respiration, comprising:

allowing a fluid to flow through a duct, the duct including a restriction in the duct, the restriction being shaped symmetrically with respect to an axis perpendicular to a direction of flow such that, in operation, velocity of the fluid is substantially equal upstream and downstream of the restriction, and the duct with the restriction having a flow resistance;

measuring a single pressure of the fluid proximate a patient end of the restriction;

allowing the fluid to exit the duct through an outlet valve to a substantially constant pressure, the outlet valve having a flow resistance; and

determining the flow rate based on the single pressure measurement relative to the substantially constant pressure and the respective flow resistances of the restriction and the outlet valve.

14. The method of claim 13 , further comprising determining at least one of volume flow and mass flow of the fluid by integrating the measured flow rate over time.

15. The method of claim 13 wherein the substantially constant pressure is ambient pressure.

16. The method of claim 13 wherein determining the flow rate through the duct comprises determining a total resistance of the flow resistance through the restriction and the flow rate through the outlet valve in series to obtain total flow resistance, and determining a relative pressure difference between the measured pressure and the substantially constant pressure.

17. The method of claim 13 wherein determining the flow rate further comprises calculating a pressure difference between the single pressure measurement and the substantially constant pressure, and calculating an expired volume based on a linear relationship between the expired volume and the pressure difference.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2008
From: MYKLEBUST, HELGE; EILEVSTJONN, JOAR; NYSAETHER, JON
To: LAERDAL MEDICAL AS
Reel/Frame 020824/0071 →
Priority Claims (1)
GB 0702078.7 · Feb 2, 2007 · national
Continuity (2)
Provisional Application 60887819 · Feb 2, 2007
Related Publication 20080214948A1 · Sep 4, 2008