Method and apparatus for treating Cheyne-Stokes respiration

• US 7,717,110 B2
• Filed: 09/26/2005
• Issued: 05/18/2010
• Est. Priority Date: 10/01/2004
• Status: Active Grant

• Current Assignee: Philips RS North America LLC (Koninklijke Philips N.V.)
• Original Assignee: RIC INVESTMENTS LLC (Respironics Incorporated)
• Inventors: Kane, Michael T., Siirola, Rochelle, Bann, Susan L., Baloa, Leonardo A., Duff, Winslow K.
• Primary Examiner(s): Douglas; Steven O
• Assistant Examiner(s): MATTER, KRISTEN CLARETTE
• Application Number:
  US11/235,520
• Publication Number:
  US 20060070624A1
• Time in Patent Office: 1,695 Days
• Field of Search: 128/200.24, 128/204.18, 128/204.21, 128/204.22, 128/204.23, 128/204.26, 128/204.29, 128/205.11, 128/204.24, 600/529
• US Class Current: 128/204.21
• CPC Class Codes: A61M 16/0003 Accessories therefor, e.g. sensors, vibrators, negative pressure
• CPC Class Codes: A61M 16/0069 the speed thereof being controlled by respiratory parameters, e.g. by inhalation
• CPC Class Codes: A61M 16/026 specially adapted for predicting, e.g. for determining an information representative of a flow limitation during a ventilation cycle by using a root square technique or a regression analysis
• CPC Class Codes: A61M 16/0883 Circuit type
• CPC Class Codes: A61M 16/101 using an oxygen concentrator
• CPC Class Codes: A61M 2016/0039 in the inspiratory circuit
• CPC Class Codes: A61M 2205/15 Detection of leaks
• CPC Class Codes: A61M 2205/16 with back-up system in case of failure

Abstract

A system and method for delivering a flow of breathing gas to an airway of a patient. A characteristic that varies based on variations of the flow of the breathing gas is monitored and used to determine a Target Flow for the gas delivered to the patient. The Target Flow is set to a level sufficient to treat Cheyne-Stokes respiration or a sleep disordered breathing event. The Target Flow is altered if the patient experiences a sleep disordered breathing event. In a further embodiment, the system determines an apnea detection time (Tapnea) as Tinsp plus a constant, and delivers a machine triggered breath if an amount since the start of inspiration reaches Tapnea. Yet another embodiment monitors the characteristic during an inspiratory phase of a respiratory cycle, and controls the flow of gas during the inspiratory phase of the respiratory cycle based on a result of this comparison.

Claims

1. A system for delivering a flow of breathing gas to an airway of a patient, the apparatus comprising:

a gas flow/pressure generating system that generates a flow of breathing gas;

a patient circuit coupled to the gas flow/pressure generating system and adapted to communicate the flow of breathing gas to an airway of a patient;

monitoring means for monitoring a characteristic that varies based on variations of the flow of the breathing gas;

a controller that determines a Target Flow to be delivered to the patient based on the monitored characteristic, wherein the Target Flow is set to a level sufficient to treat Cheyne-Stokes Respiration (CSR) or a sleep disordered breathing event, wherein the controller determines whether such a patient is experiencing a sleep disordered breathing event, wherein the controller alters the Target Flow based on a determination that such a patient is experiencing a sleep disordered breathing event, wherein the controller determines an Instantaneous Average Inspiratory Flow (Qave(t)) during an inspiratory cycle based on an output of the monitoring means, wherein the controller determines a Maximum Average Inspiratory Flow (Qave(max)) as the maximum value for the Instantaneous Average Inspiratory Flow that occurred during the inspiratory cycle, wherein the controller compares the Qave(max) to the Target Flow, and wherein the controller controls the gas flow/pressure generating system to generate the flow of breathing gas delivered to the patient based on a result of this comparison.

2. The system of claim 1, wherein the gas flow/pressure generating system includes:

a pressure generator adapted to generate a flow of breathing gas; and

a pressure control valve associated with the pressure generator or the patient circuit to control a pressure of the flow of breathing gas delivered to a patient by the patient circuit.

3. The system of claim 1, wherein the controller:

monitors a first amount of time that has elapsed between (a) a transition from an expiratory phase to an inspiratory phase of a respiratory cycle and (b) a transition from the inspiratory phase to an expiratory phase of the respiratory cycle (T_insp);

determines an apnea detection time T_apnea as T_insp+ a constant;

monitors a second amount of time that has elapsed since the transition from the expiratory phase to the inspiratory phase of a respiratory cycle;

compares the second amount of time to T_apnea; and

delivers a machine triggered breath responsive to the second amount of time reaching T_apnea.

4. The system of claim 3, where the constant is adjusted by the controller based on whether such a patient has experienced a sleep disordered breathing event.

5. The system of claim 1, wherein the controller monitors the characteristic during an inspiratory phase of a respiratory cycle, and controls the gas flow/pressure generating system during the inspiratory phase of the respiratory cycle based on a result of this comparison.

6. The system for claim 1, wherein the controller (1) increases a pressure of the flow of breathing gas provided by the gas flow/pressure generating system responsive to the controller determining that the Target Flow will not be met, and (2) does not increase the pressure of the flow of breathing gas responsive to the controller determining that the Target Flow will be exceeded.

7. The system of claim 1, wherein the controller determines a characteristic associated with patient respiration, and detects CSR by comparing the characteristic to a CSR template.

8. The system of claim 1, further comprising an oxygen saturation monitor adapted to output a signal indicative of an oxygen saturation of such a patient, and wherein the controller determines whether such a patient is experiencing CSR based, at least in part, on an output of the oxygen saturation monitor.

9. The method of claim 1, further comprising monitoring an oxygen of such a patient, and wherein determining whether such a patient is experiencing a sleep disordered breathing event is accomplished based, at least in part, on the oxygen saturation of such a patient.

10. A method of delivering pressurized breathing gas to an airway of a patient, the method comprising the steps of:

delivering a flow of gas to the airway of the patient from a source of breathing gas via a patient circuit;

monitoring a characteristic that varies based on variations of the flow of the breathing gas;

determining a Target Flow to be delivered to the patient based on the monitored characteristic, wherein the Target Flow is set to a level sufficient to treat Cheyne-Stokes respiration or a sleep disordered breathing event;

determining whether such a patient is experiencing a sleep disordered breathing event;

altering the Target Flow based on a determination that such a patient is experiencing a sleep disordered breathing event; and

controlling the flow of breathing gas based on the Target Flow by determining an Instantaneous Average Inspiratory Flow (Qave(t)) during an inspiratory cycle based on the monitored characteristic, and then by determining a Maximum Average Inspiratory Flow (Qave(max)) as the maximum value for the Instantaneous Average Inspiratory Flow that occurred during the inspiratory cycle, and comparing the Qave(max) to the Target Flow, and delivering the flow of gas based on a result of this comparison.

11. The method of claim 10, wherein delivering a flow of gas includes generating a flow of breathing gas via a pressure generator and controlling a pressure of the flow of gas via (1) a pressure control valve associated with the pressure generator or the patient circuit, (2) controlling an operating speed of the pressure generator, or (3) a combination of both (1) and (2).

12. The method of claim 10, further comprising:

monitoring a first amount of time that has elapsed between (a) a transition from an expiratory phase to an inspiratory phase of a respiratory cycle and (b) a transition from the inspiratory phase to an expiratory phase of the respiratory cycle (T_insp);

determining an apnea detection time T_apnea as T_insp+ a constant;

monitoring a second amount of time that has elapsed since the transition from the expiratory phase to the inspiratory phase of a respiratory cycle;

comparing the second amount of time to T_apnea; and

delivering a machine triggered breath responsive to the second amount of time reaching T_apnea.

13. The method of claim 12, further comprising:

determining whether such a patient has experienced a sleep disordered breathing event; and

adjusting the constant based on whether such a patient has experienced a sleep disordered breathing event.

14. The method of claim 10, further comprising:

monitoring the characteristic during an inspiratory phase of a respiratory cycle; and

controlling the flow of gas during the inspiratory phase of the respiratory cycle based on a result of this comparison.

15. The method of claim 14, wherein controlling the flow of gas includes:

increasing a pressure of the flow of breathing gas provided by the gas flow/pressure generating system responsive a determination that the Target Flow will not be met; and

preventing an increase in the pressure of the flow of breathing gas responsive to a determination that the Target Flow will be exceeded.

16. The method of claim 10, wherein determining whether such a patient is experiencing a sleep disordered breathing event includes:

determining a respiratory characteristic associated with patient respiration based on the characteristic; and

detecting CSR by comparing the respiratory characteristic to a CSR template.