USRE50219EExpiredUtility
Method and apparatus for controlling a ventilator
Individually held — no corporate assignee on recordPriority: Nov 21, 2003Filed: Apr 22, 2022Granted: Nov 26, 2024
Est. expiryNov 21, 2023(expired)· nominal 20-yr term from priority
Inventors:Fleur T. Tehrani
A61M 16/0063A61M 16/0051A61M 2230/205A61M 2230/432A61M 2202/0208A61M 2230/435A61M 16/026A61M 16/00
88
PatentIndex Score
1
Cited by
115
References
87
Claims
Abstract
Method and apparatus for controlling a ventilator are described. The invention can be used to control mechanical ventilators as well as respiratory assist devices such as CPAP machines. The apparatus receives input data indicative of patient's oxygen level. A controller determines PEEP, or CPAP, and F IO2 , on the basis of data indicative of the patient's oxygen level. In an alternative embodiment, the apparatus further receives input data indicative of patient's carbon dioxide levels, respiratory elastance and airway resistance, and barometric pressure. The controller further utilizes the said input data to determine the optimal values of tidal volume and breathing frequency for a next breath of the patient, and uses the respiratory elastance and airway resistance data to determine any necessary adjustments in the I:E ratio. The controller also applies safety rules, detects and corrects artifacts, and generates warning signals when needed.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. An apparatus for automatically controlling a ventilator comprising:
first means for processing data indicative of at least a measured oxygen level of a patient, and for providing output data indicative of:
required concentration of oxygen in inspiratory gas of the patient (F IO2 ) and positive end-expiratory pressure (PEEP) for a next breath of the patient;
wherein F IO2 is determined to reduce the difference between the measured oxygen level of the patient and a desired value;
wherein PEEP is determined to keep a ratio of PEEP/F IO2 within a prescribed range and, while keeping the ratio within the prescribed range, to keep the measured oxygen level of the patient above a predefined value; and
second means, operatively coupled to the first means, for providing control signals, based on the output data provided by the first means, to the ventilator; wherein the control signals provided to the ventilator automatically control PEEP, and F IO2 , for a next breath of the patient.
2. The apparatus of claim 1 , wherein the first means comprises a programmable microcomputer.
3. The apparatus of claim 2 , further comprising
an alarm unit; wherein the first means further determines whether there has been an artifact in the measured oxygen levels and replaces and/or corrects the data determined to be based on the artifact; and wherein the second means further provides an alarm control signal to the alarm unit to warn of the artifact in the measured oxygen levels.
4. The apparatus of claim 2 , further comprising
an alarm unit; wherein the first means further determines whether the measured oxygen levels are outside a prescribed range; and wherein the second means further provides an alarm control signal to the alarm unit to warn of the measured oxygen level of the patient being outside a prescribed range.
5. The apparatus of claim 2 , further comprising an analog to digital (A/D) converter connected to an input of the first means for converting analog signals from an oxygen sensor, indicative of the oxygen level of the patient, to digital data.
6. The apparatus of claim 5 , wherein the oxygen sensor is a pulse oximeter measuring arterial hemoglobin oxygen saturation in the patient's blood.
7. The apparatus of claim 2 , wherein data indicative of the lower inflection pressure point on an inspiratory or expiratory pressure volume curve of the patient (LIP) is provided to the first means.
8. The apparatus of claim 7 , wherein the data indicative of LIP is supplied by a monitor operatively coupled to the first means.
9. The apparatus of claim 2 , wherein data indicative of the patient's measured intrinsic positive end-expiratory pressure (PEEPi) is provided to the first means.
10. The apparatus of claim 9 , wherein the data indicative of PEEPi is supplied by a monitor operatively coupled to the first means.
11. The apparatus of claim 2 , wherein the programmable microcomputer further comprises a program means for determining from the input data: the patient's arterial partial pressure of oxygen; the required F IO2 ; the required PEEP; for a next breath of the patient.
12. The apparatus of claim 11 , wherein the program means further determines, from the input data: whether there has been an artifact in the data indicative of the measured oxygen level of the patient, and wherein the program means further replaces and/or corrects the data based on the artifact and generates a warning signal in the event the artifact is determined.
13. The apparatus of claim 2 , wherein data corresponding to a set point for arterial partial pressure of oxygen, threshold values for the oxygen level of the patient, and a correction factor for oxygen based on measured blood pH levels of the patient are entered manually and stored in a software program.
14. The apparatus of claim 2 , wherein the first means further processes input data indicative of respiratory elastance, respiratory airway resistance, barometric pressure, and measured carbon dioxide levels of the patient, and based upon the input data, provides digital output data indicative of required ventilation, optimum breathing frequency, and required adjustment in the ratio of inspiration time to expiration time (I:E) for a next breath of the patient, and; wherein the second means further generates additional control signals to the ventilator based on the output data of the first means; wherein the additional control signals to the ventilator control tidal volume and frequency of inhaled gas provided to the patient by the ventilator and effect necessary adjustments in the ratio of I:E for a next breath of the patient.
15. The apparatus of claim 14 , wherein the input data indicative of respiratory elastance and airway resistance of the patient are supplied to the first means by one or more monitors coupled to the first means.
16. The apparatus of claim 14 , wherein the input data indicative of respiratory elastance and airway resistance of the patient are entered manually and stored in a software program.
17. The apparatus of claim 14 , wherein the input data indicative of the measured oxygen level of the patient and the measured carbon dioxide level of the patient are provided to the first means by one or more monitors coupled to the first means.
18. The apparatus of claim 17 , wherein the input data indicative of the measured oxygen level of the patient is provided by a pulse oximeter measuring arterial hemoglobin oxygen saturation of the patient, and the input data indicative of the measured carbon dioxide level of the patient is provided by an exhaled gas analyzer detecting end-tidal partial pressure of carbon dioxide or end-tidal concentration of carbon dioxide in exhaled gas of the patient.
19. The apparatus of claim 17 , wherein, based on data indicative of measured oxygen and carbon dioxide levels of the patient, the first means detects an artifact in the data, discards the data having the artifact, resumes a previous value of the data in a memory, and provides a warning instruction signal; and wherein the second means generates a warning control signal that is supplied to an alarm unit that generates an alarm signal.
20. The apparatus of claim 17 , wherein, based on data indicative of measured carbon dioxide and oxygen levels of the patient, the first means detects a potential pulmonary embolism and produces digital output data indicative of predefined levels of ventilation and breathing frequency and a required adjustment in the I:E ratio, and provides a warning instruction signal; and wherein the second means generates a warning control signal.
21. The apparatus of claim 17 , further comprising program means for determining from the input data: (i) partial pressures of oxygen and carbon dioxide in arterial blood of the patient; (ii) presence of artifact(s) in the data indicative of the measured oxygen and carbon dioxide levels of the patient, and in case of artifact detection, replacing and/or correcting the data and corresponding partial pressure value(s); (iii) net effects of oxygen and carbon dioxide on alveolar ventilation; (iv) total required alveolar ventilation; (v) optimal frequency of breathing; (vi) required ventilation; (vii) required adjustment in the I:E ratio; (viii) required F IO2 ; and (ix) required PEEP; for a next breath of the patient.
22. The apparatus of claim 21 , wherein data corresponding to a set point for arterial partial pressure of oxygen, an adjustment factor for carbon dioxide level of the patient, threshold levels for oxygen level of the patient, and a correction factor for oxygen based on measured blood pH levels of the patient, are entered manually and stored in a software program.
23. The apparatus of claim 14 , wherein the input data indicative of barometric pressure is supplied to the first means by one or more monitors coupled to the first means.
24. The apparatus of claim 14 , wherein the input data indicative of barometric pressure is entered manually and stored in hardware.
25. The apparatus of claim 14 , wherein the input data indicative of barometric pressure is entered manually and stored in a software program.
26. The apparatus of claim 14 , wherein the first means also receives and processes data indicative of the patient's metabolic rate ratio.
27. The apparatus of claim 26 , wherein the data indicative of the patient's metabolic rate ratio is supplied to the first means by a monitor coupled to the first means.
28. The apparatus of claim 26 , wherein the data indicative of the patient's metabolic rate ratio is entered manually and stored in a software program.
29. A method for automatically controlling a ventilator comprising the steps of:
(a) measuring an oxygen level of a patient and providing a data signal indicative of the measured oxygen level; (b) determining: (i) required concentration of oxygen in an inspiratory gas of the patient, F IO2 , based on the data signal indicative of the measured oxygen level of the patient and to reduce the difference between the measured oxygen level of the patient and a desired value; (ii) required positive end-expiratory pressure, PEEP, wherein a ratio of PEEP/F IO2 is maintained within a prescribed range, and to keep the measured oxygen level of the patient above a predefined value; and (c) providing data signals indicative of the required F IO2 and the required PEEP based upon the determining of step (b), for automatically controlling F IO2 and PEEP for a next breath of the patient.
30. The method of claim 29 , wherein step (b) further comprises determining, from the data indicative of the measured oxygen level in (a), whether there has been an artifact in the measured oxygen level, and replacing and/or correcting the data signal in (a) in the event the artifact is determined.
31. The method of claim 29 , wherein the data signal indicative of measured oxygen level of the patient is in analog form and is converted to digital form before the determining of step (b), and wherein the providing of step (c) further comprises converting the data signals from digital to analog form.
32. The method of claim 31 , wherein the measuring of the oxygen level of the patient comprises measuring an arterial hemoglobin oxygen saturation of the patient via pulse oximetry.
33. The method of claim 32 , wherein an arterial partial pressure of oxygen of the patient is derived from the arterial hemoglobin oxygen saturation of the patient measured by the pulse oximeter.
34. The method of claim 33 , wherein the following equation is used to calculate the arterial partial pressure of oxygen (P aO2 ) of the patient from the arterial hemoglobin oxygen saturation data (S pO2 ) measured by pulse oximetry:
P
aO
2
=
-
ln
[
1
-
(
S
pO
2
)
0.5
]
0.046
+
CP
where P aO2 is in mm Hg and CP is a correction parameter which is used to shift P aO2 and CP is based on the patient's measured blood pH level.
35. The method of claim 34 , further comprising:
comparing P aO2 to a minimum acceptable value, and, if P aO2 is found to be less than the minimum acceptable value:
discarding P aO2 and a latest measured S pO2 data;
resuming previous values of P aO2 and S pO2 ; and
generating a warning signal.
36. The method of claim 29 , wherein data corresponding to the lower inflection pressure point on an inspiratory or expiratory pressure volume curve of the patient (LIP) is also provided in step (a), and an initial value for PEEP is set equal to LIP plus 0 to 8 cm H 2 O and the initial value for PEEP is provided in step (b).
37. The method of claim 36 , wherein the data corresponding to LIP is supplied by a monitor.
38. The method of claim 29 , wherein data corresponding to the measured intrinsic PEEP of the patient (PEEPi) is also provided in step (a), and an initial value for PEEP is set between 80% and 100% of PEEPi and the initial value for PEEP is provided in step (b).
39. The method of claim 38 , wherein the data corresponding to PEEPi is supplied by a monitor.
40. The method of claim 29 , wherein an initial value for PEEP is determined by the operator and is manually provided.
41. The method of claim 29 , wherein the required concentration of oxygen in the inspiratory gas of the patient (F IO2 ) is calculated by using a stepwise control scheme and/or by using a proportional-integral-derivative (PID) technique.
42. The method of claim 41 , wherein using a PID technique comprises comparing S pO2 obtained by pulse oximetry to a defined minimum safe value, and wherein using the PID technique continues while S pO2 is greater than the defined minimum safe value.
43. The method of claim 41 , wherein using a PID technique comprises comparing S pO2 obtained by pulse oximetry to a defined minimum safe value, and wherein, if S pO2 is found to be less than or equal to the defined minimum safe value, a stepwise control scheme is followed that comprises the steps of:
raising F IO2 stepwise to avoid hypoxemia, allowing F IO2 to remain high until S pO2 rises to a second threshold value, lowering F IO2 stepwise, comparing S pO2 to a third threshold value, lowering F IO2 stepwise upon S pO2 rising to the third threshold value, comparing S pO2 to a fourth threshold value, returning control to the PID technique upon S pO2 rising to the fourth threshold value.
44. The method of claim 41 , wherein the difference between a P aO2 set point and the P aO2 of the patient is reduced by using a PID control procedure according to the following equations:
Y 1 (k)=P aO2 (set-point)−P aO2
Y 2 (k)=[Y 1 (k)−Y 1 (k−1)]/T
Y 3 (k)=Y 3 (k−1)+TY 1 (k)
E(k)=αY 1 (k)+βY 3 (k)+γY 2 (k)
G(k)=E(k)+0.21 where Y 1 (k), Y 2 (k), and Y 3 (k) are the proportional, derivative, and integral components of error, respectively, E(k) is an error function, T is a sampling interval, G(k) is the required F IO2 , and parameters α, β, and γ are PID coefficients.
45. The method of claim 41 , wherein the determining of required PEEP of the patient comprises the following procedure:
comparing the PEEP/F IO2 ratio to a defined minimum allowed value, increasing PEEP by a fixed incremental value if the PEEP/F IO2 ratio is lower than the defined minimum allowed value and the time elapsed since the last adjustment in PEEP is longer than or equal to a fixed defined interval T1, comparing the PEEP/F IO2 ratio with a defined maximum allowed value if the PEEP/F IO2 ratio is not less than the defined minimum allowed value, comparing S pO2 with a defined value if the PEEP/F IO2 ratio is less than the defined maximum allowed value, increasing PEEP by a fixed incremental value if S pO2 is less than the defined value and the time elapsed since the last adjustment in PEEP is longer than or equal to T1, if the PEEP/F IO2 ratio is not less than the defined maximum allowed value, comparing the PEEP/F IO2 ratio to a value higher than the defined maximum allowed value, RG, whereby if the PEEP/F IO2 ratio is higher than RG, and the time elapsed since the last adjustment in PEEP is greater than or equal to T1, decreasing PEEP by a fixed incremental amount.
46. An apparatus for automatically controlling a ventilator for a next breath of a patient comprising:
first means for processing input data indicative of at least a measured oxygen level of the patient, and for providing output data indicative of: required concentration of oxygen in inspiratory gas of the patient (F IO2 ) and required positive end-expiratory pressure (PEEP) for a next breath of the patient, wherein F IO2 is determined to reduce the difference between the measured oxygen level of the patient and a desired value; wherein a ratio of PEEP/F IO2 is calculated and PEEP is determined to keep said ratio of PEEP/F IO2 within one prescribed range; wherein PEEP is determined without using a proportional-integral-derivative (PID) control procedure and while PEEP is determined to keep the ratio of PEEP/F IO2 within one prescribed range, PEEP is determined to also keep the measured oxygen level of the patient above a predefined value; and second means, operatively coupled to the first means, for providing control signals, based on the output data provided by the first means, to the ventilator for PEEP and to a mixer regulator, operatively coupled to the ventilator, for F IO2; wherein the control signals automatically control PEEP and F IO2 for a next breath of the patient.
47. The apparatus of claim 46 , wherein the first means comprises a programmable microcomputer.
48. The apparatus of claim 47 , further comprising an alarm unit;
wherein the first means further determines whether there has been an artifact in the measured oxygen level and in response to determining an artifact is present, replaces the measured oxygen level with the artifact with a most recent measured oxygen level without artifact; and wherein the second means further provides an alarm control signal to the alarm unit in response to the determination by the first means that there has been an artifact to warn of an artifact in the current measured oxygen level.
49. The apparatus of claim 47 , further comprising an alarm unit;
wherein the first means further determines whether the measured oxygen level is outside a prescribed range; and wherein the second means further provides an alarm control signal to the alarm unit in response to the determination by the first means that the measured oxygen level is outside the prescribed range to warn of the measured oxygen level of the patient being outside the prescribed range.
50. The apparatus of claim 47 , wherein the input data indicative of at least the measured oxygen level of the patient processed by the first means includes arterial hemoglobin oxygen saturation data measured by a pulse oximeter operatively coupled to the first means.
51. The apparatus of claim 47 , wherein data indicative of a lower inflection pressure point on an inspiratory or expiratory pressure volume curve of the patient (LIP) is provided to the first means.
52. The apparatus of claim 51 , wherein the data indicative of LIP is supplied by a monitor operatively coupled to the first means.
53. The apparatus of claim 47 , wherein data indicative of the patient's measured intrinsic positive end-expiratory pressure (PEEPi) is provided to the first means.
54. The apparatus of claim 53 , wherein the data indicative of PEEPi is supplied by a monitor operatively coupled to the first means.
55. The apparatus of claim 47 , wherein the programmable microcomputer further comprises a program means for determining from the input data:
a patient's arterial partial pressure of oxygen; the required F IO2 ; and the required PEEP
for a next breath of the patient.
56. The apparatus of claim 55 , wherein the program means further determines, from the input data:
whether there has been an artifact in the measured oxygen level of the patient, and wherein the program means, in response to determining an artifact is present, further replaces the measured oxygen level with the artifact with a most recent measured oxygen level without artifact, and the apparatus further comprising alarm means for generating a warning signal in the event the artifact is determined to be present.
57. The apparatus of claim 47 , wherein data corresponding to a set point for arterial partial pressure of oxygen, threshold values for arterial hemoglobin oxygen saturation level of the patient, and a correction factor for arterial partial pressure of oxygen based on measured blood pH levels of the patient are entered manually and stored in a software program.
58. The apparatus of claim 47 , wherein input data indicative of at least a measured oxygen level of the patient which is processed by the first means further includes input data indicative of respiratory elastance, respiratory airway resistance, barometric pressure, and measured carbon dioxide level of the patient, and based upon the input data, the first means provides digital output data indicative of required ventilation, optimum breathing frequency, and required adjustment in the ratio of inspiration time to expiration time (I:E) for a next breath of the patient;
wherein the second means further generates additional control signals to the ventilator based on the digital output data of the first means; and wherein the additional control signals to the ventilator control tidal volume and frequency of inhaled gas provided to the patient by the ventilator and effect necessary adjustments in the ratio of I:E for a next breath of the patient.
59. The apparatus of claim 58 , wherein the input data indicative of respiratory elastance and airway resistance of the patient are supplied to the first means by one or more monitors coupled to the first means.
60. The apparatus of claim 58 , wherein the input data indicative of respiratory elastance and airway resistance of the patient are entered manually and stored in a software program.
61. The apparatus of claim 58 , wherein the input data indicative of the measured oxygen level of the patient and the measured carbon dioxide level of the patient are provided to the first means by one or more monitors coupled to the first means.
62. The apparatus of claim 61 , wherein the input data indicative of the measured oxygen level of the patient is provided by a pulse oximeter measuring arterial hemoglobin oxygen saturation of the patient, and the input data indicative of the measured carbon dioxide level of the patient is provided by an exhaled gas analyzer detecting end-tidal partial pressure of carbon dioxide or end-tidal concentration of carbon dioxide in exhaled gas of the patient.
63. The apparatus of claim 61 , wherein, based on the input data indicative of the measured oxygen level and the measured carbon dioxide level of the patient, the first means detects an artifact in the input data indicative of the measured oxygen level and/or the measured carbon dioxide level of the patient, discards the input data indicative of the measured oxygen level and/or the measured carbon dioxide level of the patient having the artifact, and resumes a value of data indicative of the most recent measured oxygen level without artifact and/or the most recent measured carbon dioxide level without artifact stored in a memory; and wherein the second means generates a warning control signal that is supplied to an alarm unit that generates an alarm signal.
64. The apparatus of claim 61 , wherein, based on the input data indicative of the measured carbon dioxide level and the measured oxygen level of the patient, the first means detects a potential pulmonary embolism and produces digital output data indicative of predefined levels of ventilation and breathing frequency and a required adjustment in the I:E ratio, and provides a warning instruction signal; and wherein the second means generates a warning control signal in response to the warning instruction signal provided by the first means.
65. The apparatus of claim 61 , wherein the first means comprises a first control program means for determining from the input data:
(i) partial pressures of oxygen and carbon dioxide in arterial blood of the patient; (ii) presence of artifact(s) in the input data indicative of the measured oxygen level and/or carbon dioxide level of the patient, and in case of artifact detection, replacing the input data indicative of the measured oxygen level and/or carbon dioxide level of the patient with the artifact and corresponding partial pressure value with data indicative of most recent measured oxygen level without an artifact and/or the measured carbon dioxide level without artifact and corresponding partial pressure value(s); (iii) net effects of oxygen and carbon dioxide on alveolar ventilation; (iv) total required alveolar ventilation; (v) the optimal frequency of breathing; (vi) the required ventilation; and (vii) the required adjustment in the I:E ratio for a next breath of the patient; and a second control program means for determining: (i) the required F IO2 ; and (ii) the required PEEP for a next breath of the patient.
66. The apparatus of claim 65 , wherein data corresponding to a set point for the arterial partial pressure of oxygen, an adjustment factor for the measured carbon dioxide level of the patient, threshold levels for arterial hemoglobin oxygen saturation level of the patient, and a correction factor for the arterial partial pressure of oxygen based on measured blood pH levels of the patient are entered manually and stored in a software program.
67. The apparatus of claim 58 , wherein the input data indicative of barometric pressure is supplied to the first means by one or more monitors coupled to the first means.
68. The apparatus of claim 58 , wherein the input data indicative of barometric pressure is entered manually and stored in hardware.
69. The apparatus of claim 58 , wherein the input data indicative of barometric pressure is entered manually and stored in a software program.
70. The apparatus of claim 58 , wherein the first means also receives and processes data indicative of the patient's metabolic rate ratio.
71. The apparatus of claim 70 , wherein the data indicative of the patient's metabolic rate ratio is entered manually and stored in a software program.
72. A method for automatically controlling a ventilator for a next breath of a patient comprising the steps of:
(a) measuring an oxygen level of the patient and providing a data signal indicative of the measured oxygen level; (b) determining for a next breath of the patient: (i) required concentration of oxygen in an inspiratory gas of the patient, F IO2 , based on the data signal indicative of the measured oxygen level of the patient, to reduce the difference between the measured oxygen level of the patient and a desired value; and (ii) required positive end expiratory pressure, PEEP, wherein a ratio of PEEP/F IO2 is calculated and PEEP is determined to keep said ratio of PEEP/F IO2 within one prescribed range, wherein PEEP is determined without using a proportional-integral-derivative (PID) control procedure, and while PEEP is determined to keep the ratio of PEEP/F IO2 within one prescribed range, PEEP is determined to also keep the measured oxygen level of the patient above a predefined value; and (c) providing data signals indicative of the required F IO2 and the required PEEP, based upon the determining of step (b), for automatically controlling F IO2 and PEEP for a next breath of the patient.
73. The method of claim 72 , wherein step (b) further comprises determining, from the data signal indicative of the measured oxygen level in step (a), whether there has been an artifact in the measured oxygen level, and, in the event an artifact is determined, replacing the measured oxygen level with the artifact with a most recent measured oxygen level without artifact.
74. The method of claim 72 , wherein the measuring of the oxygen level of the patient comprises measuring an arterial hemoglobin oxygen saturation of the patient via pulse oximetry.
75. The method of claim 74 , wherein an arterial partial pressure of oxygen of the patient is derived from the arterial hemoglobin oxygen saturation of the patient (S pO2 ) measured by a pulse oximeter.
76. The method of claim 75 , wherein the following equation is used to calculate the arterial partial pressure of oxygen (P aO2 ) of the patient from the arterial hemoglobin oxygen saturation data (S pO2 ) measured by pulse oximetry:
P
aO
2
=
-
ln
[
1
-
(
S
pO
2
)
0.5
]
0.046
+
CP
where P aO2 is in mm Hg and CP is a correction parameter which is used to shift P aO2 and CP is based on a measured blood pH level of the patient.
77. The method of claim 76 , further comprising: comparing P aO2 to a minimum acceptable value, and, if P aO2 is found to be less than the minimum acceptable value, discarding the P aO2 found to be less than the minimum acceptable value and a latest measured S pO2 data corresponding thereto; resuming a most recent value of P aO2 found to be equal to or greater than the minimum acceptable value and corresponding value of S pO2 ; and generating, by a signal generator, a warning signal.
78. The method of claim 72 , wherein data corresponding to the lower inflection pressure point on an inspiratory or expiratory pressure volume curve of the patient (LIP) is also provided in step (a), and an initial value for PEEP is set equal to LIP plus 0 to 8 cm H 2 O and the initial value for PEEP is provided in step (b).
79. The method of claim 78 , wherein the data corresponding to LIP is supplied by a monitor.
80. The method of claim 72 , wherein data corresponding to a measured intrinsic PEEP of the patient (PEEPi) is also provided in step (a), and an initial value for PEEP is set between 80% and 85% of PEEPi and the initial value for PEEP is provided in step (b).
81. The method of claim 80 , wherein the data corresponding to PEEPi is supplied by a monitor.
82. The method of claim 72 , wherein an initial value for PEEP is determined by the operator and is manually provided.
83. The method of claim 72 , wherein the required concentration of oxygen in the inspiratory gas of the patient (F IO2 ) in step (b)(i) is calculated by using a stepwise control scheme and/or by using a proportional-integral-derivative (PID) control procedure.
84. The method of claim 83 , wherein using the PID control procedure comprises comparing S pO2 obtained by pulse oximetry to a defined minimum safe value, and wherein using the PID control procedure continues while S pO2 is greater than the defined minimum safe value.
85. The method of claim 83 , wherein using the PID control procedure comprises comparing S pO2 obtained by pulse oximetry to a defined minimum safe value, and wherein, if S pO2 is found to be less than or equal to the defined minimum safe value, the stepwise control scheme is followed and comprises the steps of:
raising F IO2 stepwise to avoid hypoxemia, allowing F IO2 to remain high until S pO2 rises to a second threshold value, lowering F IO2 stepwise, comparing S pO2 to a third threshold value, lowering F IO2 stepwise upon S pO2 rising to the third threshold value, comparing S pO2 to a fourth threshold value, returning control to the PID control procedure upon S pO2 rising to the fourth threshold value.
86. The method of claim 83 , wherein the difference between a P aO2 set point and a P aO2 of the patient is reduced by using the PID control procedure according to the following equations:
Y 1 (K)=P aO2 (set-point)−P aO2
Y 2 (K)=[Y 1 (K)−Y 1 (K−1)]/T
Y 3 (K)=Y 3 (K−1)+TY 1 (K)
E(K)=αY 1 (K)+βY 3 (K)+γY 2 (K)
G(K)=E(K)+0.21 where Y 1 (k), Y 2 (k), and Y 3 (k) are the proportional, derivative, and integral components of error, respectively, E(k) is an error function, T is a sampling interval, G(k) is the required F IO2 , and parameters α, β, and γ are PID coefficients.
87. The method of claim 83 , wherein the determining of required PEEP of the patient comprises the following procedure:
comparing the PEEP/F IO2 ratio to a defined minimum allowed value, increasing PEEP by a fixed incremental value if the PEEP/F IO2 ratio is lower than the defined minimum allowed value and a time elapsed since the last adjustment in PEEP is longer than or equal to a fixed defined interval T1, comparing the PEEP/F IO2 ratio with a defined maximum allowed value if the PEEP/F IO2 ratio is not less than the defined minimum allowed value, comparing S pO2 with a defined value if the PEEP/F IO2 ratio is less than the defined maximum allowed value, increasing PEEP by a fixed incremental value if S pO2 is less than the defined value and the time elapsed since the last adjustment in PEEP is longer than or equal to T1, if the PEEP/F IO2 ratio is not less than the defined maximum allowed value, comparing the PEEP/F IO2 ratio to a value higher than the defined maximum allowed value, RG, whereby if the PEEP/F IO2 ratio is higher than RG, and the time elapsed since the last adjustment in PEEP is greater than or equal to T1, decreasing PEEP by a fixed incremental amount.Join the waitlist — get patent alerts
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