Method and apparatus for changing the concentration of a target gas at the blood compartment of a patient's lung during artificial ventilation

• US 20070089741A1
• Filed: 10/20/2006
• Published: 04/26/2007
• Est. Priority Date: 04/23/2004
• Status: Abandoned Application

• Current Assignee: Christoph Manegold, Gerardo Tusman, Stephan Bohm
• Original Assignee: Christoph Manegold, Gerardo Tusman, Stephan Bohm
• Inventors: Bohm, Stephan, Tusman, Gerardo, Manegold, Christoph
• Application Number:
  US11/583,952
• Publication Number:
  US 20070089741A1
• Time in Patent Office: Days
• US Class Current: 128/203.120
• CPC Class Codes: A61M 16/01 specially adapted for anaesthetising A61M16/104, A61M16/18 take precedence
• CPC Class Codes: A61M 16/08 Bellows; Connecting tubes having means for taking samples G01N1/22; Water traps; Patient circuits
• CPC Class Codes: A61M 2016/1035 the anaesthetic agent concentration
• CPC Class Codes: A61M 2230/437 the anaesthetic agent concentration

Abstract

The invention refers to a method and apparatus for changing the concentration of a target gas at the blood compartment of a patient'"'"'s lung from an actual target gas concentration to a desired target gas concentration during artificial ventilation with an inspiratory gas composition by a respirator being controlled via a set of ventilation parameters. In order to decrease the negative effects of general anaesthesia during artificial ventilation even further, the method according to the invention comprises the following steps: a) ventilating the lung in a first ventilation stage, and b) ventilating the lung in a second ventilation stage in which alveolar recruitment is promoted.

Claims

1. Method for changing the concentration of a target gas at the blood compartment of a patient'"'"'s lung from an actual target gas concentration to a desired target gas concentration during artificial ventilation with an inspiratory gas composition by a respirator being controlled via a set of ventilation parameters, by varying

the fraction of the target gas supplied to the inspiratory gas composition, and/or

the fraction of the re-breathed gas supplied to the inspiratory gas composition, and/or

the set of ventilation parameters being responsible for the ventilated lung volume,

wherein

a) the lung is ventilated in a first ventilation stage by setting a fraction of target gas, a fraction of re-breathed gas and a set of ventilation parameters, wherein said setting results in the actual target gas concentration, and

b) the lung is ventilated in a second ventilation stage in which at least once

the set of ventilation parameters is varied for yielding an increased ventilated lung volume compared to the first ventilation stage and

on the basis of the increased ventilated lung volume the fraction of target gas and/or the fraction of re-breathed gas is varied such that the target gas concentration is changed towards the desired target gas concentration.

2. Method according to claim 1, wherein the lung is ventilated in a third ventilation stage by setting a fraction of target gas, a fraction of re-breathed gas and a set of ventilation parameters, wherein the set of ventilation parameters yields a decreased ventilated lung volume compared to the second ventilation stage and wherein said setting results in the desired target gas concentration.

3. Method according to claim 1, wherein the target gas is an anaesthetic agent.

4. Method according to claim 3, wherein during a wash-in process of anaesthesia the target gas supplied in the first ventilation stage is an anaesthetic agent corresponding to a state of shallow or no general anaesthesia and the target gas supplied in the second ventilation stage is an anaesthetic agent corresponding to a state of deeper general anaesthesia.

5. Method according to claim 3, wherein during a wash-out process of anaesthesia the target gas supplied in the first ventilation stage is an anaesthetic agent corresponding to a state of deeper general anaesthesia and the target gas supplied in the second ventilation stage is an anaesthetic agent corresponding to a state of shallow or no general anaesthesia.

6. Method according to claim 1, wherein the set of ventilation parameters of the first ventilation stage is based on a first peak inspiratory pressure and a first positive end-expiratory pressure.

7. Method according to claim 1, wherein the set of ventilation parameters of the second ventilation stage is based on a time-varying second peak inspiratory pressure above the first peak inspiratory pressure and a time-varying second positive end-expiratory pressure above the first positive end-expiratory pressure.

8. Method according to claim 2, wherein the set of ventilation parameters of the third ventilation stage is based on a third peak inspiratory pressure, which is lower than the maximum of the time-varying second peak inspiratory pressure and a third positive end-expiratory pressure, which is lower or equal to the maximum of the time-varying second positive end-expiratory pressure.

9. Apparatus for changing the concentration of a target gas at the blood compartment of a patient'"'"'s lung from an actual target gas concentration to a desired target gas concentration during artificial ventilation with an inspiratory gas composition by a respirator being controlled via a set of ventilation parameters, comprising

target gas varying means for varying the fraction of the target gas supplied to the inspiratory gas composition,

re-breathed gas varying means for varying the fraction of the re-breathed gas supplied to the inspiratory gas composition,

parameter varying means for varying the ventilation parameters being responsible for the ventilated lung volume, and

controlling means for controlling the target gas varying means, the re-breathed gas varying means and the parameter varying means such that

a) the lung is ventilated in a first ventilation stage by setting a fraction of target gas, a fraction of re-breathed gas and a set of ventilation parameters, wherein said setting results in the actual target gas concentration, and

b) the lung is ventilated in a second ventilation stage in which at least once

the set of ventilation parameters is varied for yielding an increased ventilated lung volume compared to the first ventilation stage and

on the basis of the increased ventilated lung volume the fraction of target gas and/or the fraction of re-breathed gas is varied such that the target gas concentration is changed towards the desired target gas concentration.

10. Apparatus according to claim 9, wherein the lung is ventilated in a third ventilation stage by setting a fraction of target gas, a fraction of re-breathed gas and a set of ventilation parameters, wherein the set of ventilation parameters yields a decreased ventilated lung volume compared to the second ventilation stage and wherein said setting results in the desired target gas concentration.

11. Apparatus according to claim 9, wherein the target gas is an anaesthetic agent.

12. Apparatus according to claim 11, wherein during a wash-in process of anaesthesia the target gas supplied in the first ventilation stage is an anaesthetic agent corresponding to a state of shallow or no general anaesthesia and the target gas supplied in the second ventilation stage is an anaesthetic agent corresponding to a state of deeper general anaesthesia.

13. Apparatus according to claim 11, wherein during a wash-out process of anaesthesia the target gas supplied in the first ventilation stage is an anaesthetic agent corresponding to a state of deeper general anaesthesia and the target gas supplied in the second ventilation stage is an anaesthetic agent corresponding to a state of shallow or no general anaesthesia.

14. Apparatus according to claim 9, wherein the set of ventilation parameters of the first ventilation stage is based on a first peak inspiratory pressure and a first positive end-expiratory pressure.

15. Apparatus according to claim 9, wherein the set of ventilation parameters of the second ventilation stage is based on a time-varying second peak inspiratory pressure above the first peak inspiratory pressure and a time-varying second positive end-expiratory pressure above the first positive end-expiratory pressure.

16. Apparatus according to claim 10, wherein the set of ventilation parameters of the third ventilation stage is based on a third peak inspiratory pressure, which is lower than the maximum of the time-varying second peak inspiratory pressure and a third positive end-expiratory pressure, which is lower or equal to the maximum of the time-varying second positive end-expiratory pressure.