Medical ventilator systems have long been used to provide ventilatory and supplemental oxygen support to patients. These ventilators typically comprise a source of pressurized oxygen which is fluidly connected to the patient through a conduit or tubing. As each patient may require a different ventilation strategy, modern ventilators can be customized for the particular needs of an individual patient. For example, preterm infants are subject to frequent episodes of spontaneous hypoxia. Accordingly, some ventilators offer a function that allows the user to increase the oxygen concentration by a fixed amount for a fixed period (i.e. a 20% increase in fractional inspired oxygen (FiO2) for two minutes).
Gating User Initiated Increases in Oxygen Concentration During Ventilation
This disclosure describes systems and methods for ventilating a patient. The disclosure describes novel systems and methods for preventing and/or reducing the likelihood of a patient from receiving too much oxygen during a selected limited increase in oxygen concentration for a set period of time.
One aspect of the disclosure relates to a method for operating a ventilator. The method includes:
a) delivering a regular oxygen concentration to a patient during ventilation;
b) receiving a user selection of a limited oxygen concentration increase for a set time period;
c) delivering a selected oxygen concentration above the regular oxygen concentration based on the received user selection;
d) monitoring an oxygen saturation level of blood in the patient during the step of delivering the selected oxygen concentration;
e) determining that the oxygen saturation level of the blood exceeds a predetermined threshold prior to expiration of the set time period for the limited oxygen concentration increase; and
f) delivering an adjusted oxygen concentration to the patient based on the step of determining.
Another aspect of the disclosure relates to a ventilator system that includes a user interface, an Oxygen Increase Option, at least one processor and at least one memory. The Oxygen Increase Option is selectable via the user interface. The Oxygen Increase Option instructs a ventilator system to deliver a selected oxygen concentration above a regular oxygen concentration during ventilation of a patient for a set time period. The memory is communicatively coupled to the at least one processor and contains instructions for operating the ventilator system after receiving a user selection of the Oxygen Increase Option that, when executed by the at least one processor, performs a method. The method includes:
a) monitoring an oxygen saturation level of blood in the patient;
b) determining that the oxygen saturation level of the blood exceeds a predetermined threshold prior to expiration of the set time period; and
c) delivering an adjusted oxygen concentration to the patient based on the step of determining.
An additional aspect of this disclosure relates to a computer-readable medium having computer-executable instructions for performing a method of ventilating a patient with a ventilator. The method includes:
a) repeatedly delivering a regular oxygen concentration to a patient during ventilation;
b) repeatedly receiving a user selection of a limited oxygen concentration increase for a set time period;
c) repeatedly delivering a selected oxygen concentration above the regular oxygen concentration based on the received user selection;
d) repeatedly monitoring an oxygen saturation level of blood in the patient during the step of delivering the selected oxygen concentration;
e) repeatedly determining that the oxygen saturation level of the blood exceeds a predetermined threshold prior to expiration of the set time period for the limited oxygen concentration increase; and
f) repeatedly delivering an adjusted oxygen concentration to the patient based on the step of determining.
Yet another aspect of the disclosure relates to ventilator system. The ventilator system includes means for delivering a regular oxygen concentration to a patient during ventilation; means for receiving a user selection of a limited oxygen concentration increase for a set time period; means for delivering a selected oxygen concentration above the regular oxygen concentration based on the received user selection; means for monitoring an oxygen saturation level of blood in the patient during the step of delivering the selected oxygen concentration; means for determining that the oxygen saturation level of the blood exceeds a predetermined threshold prior to expiration of the set time period for the limited oxygen concentration increase; and means for delivering an adjusted oxygen concentration to the patient based on the step of determining.
These and various other features as well as advantages which characterize the systems and methods described herein will be apparent from a reading of the following detailed description and a review of the associated drawings. Additional features are set forth in the description which follows, and in part will be apparent from the description, or may be learned by practice of the technology. The benefits and features of the technology will be realized and attained by the structure particularly pointed out in the written description and claims hereof as well as the appended drawings.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are intended to provide further explanation of the invention as claimed.
The following drawing figures, which form a part of this application, are illustrative of embodiments of systems and methods described below and are not meant to limit the scope of the invention in any manner.
Although the techniques introduced above and discussed in detail below may be implemented for a variety of medical devices, the present disclosure will discuss the implementation of these techniques in the context of a medical ventilator for use in providing ventilation support to a human patient. A person of skill in the art will understand that the technology described in the context of a medical ventilator for human patients could be adapted for use with other systems such as ventilators for non-human patients and general gas transport systems.
Medical ventilators are used to provide a breathing gas to a patient who may otherwise be unable to breathe sufficiently. In modern medical facilities, pressurized air and oxygen sources are often available from wall outlets. Accordingly, ventilators may provide pressure regulating valves (or regulators) connected to centralized sources of pressurized air and pressurized oxygen. The regulating valves function to regulate flow so that respiratory gas having a desired concentration of oxygen is supplied to the patient at desired pressures and rates. Ventilators capable of operating independently of external sources of pressurized air are also available.
While operating a ventilator, it is desirable to control the percentage of oxygen in the gas supplied by the ventilator to the patient. Further, it is desirable to monitor oxygen saturation level of the blood (SpO2 level) of a patient. Accordingly, medical ventilator systems may be combined with and/or include a system for monitoring the blood oxygen level of a patient, such as an oximeter.
Additionally, as each patient may require a different ventilation strategy, modern ventilators can be customized for the particular needs of an individual patient. For example, ventilation of preterm infants typically requires oxygen concentrations of greater than 21%. Further, preterm infants are subject to frequent episodes of spontaneous hypoxia. Accordingly, some ventilators offer a function that allows the user to increase the oxygen concentration by a fixed amount for a set time period (e.g. a 20% increase in fractional inspired oxygen (FiO2) for two minutes) referred to herein as an “Oxygen Increase Option”. Originally the Oxygen Increase Option was designed to deliver increased oxygen during suctioning of the patient airway. Clinicians, knowing the functionality of the Oxygen Increase Option, began to utilize the Oxygen Increase Option to address the frequent episodes of spontaneous hypoxia of preterm infants. Accordingly, now the use of the Oxygen Increase Option is regularly utilized by clinicians to address the frequent episodes of spontaneous hypoxia of preterm infants.
However, because of the immature development of the lungs and retina, elevated oxygen levels also place preterm infants at greater risk for lung and retinal injury. Many times these predetermined increases in oxygen concentrations for the predetermined amount of time are more than is necessary in order to address a transient occurrence of hypoxemia. Accordingly, the use of the Oxygen Increase Option exposes patients, such as preterm infants, to high levels of oxygen for longer than needed, which places patients at risk for lung, retinal, and other injuries associated with exposure to elevated levels of oxygen.
Accordingly, there is a need for providing increased oxygen for a period of time while preventing a patient from receiving too much oxygen for longer than needed to prevent injury to the patient. The present disclosure describes novel methods and systems for ventilating a patient that monitors the SpO2 level of a patient during an Oxygen Increase Option and automatically reduces the increased oxygen level if the SpO2 level of the patient exceeds a predetermined threshold. In some embodiments, the ventilator additionally automatically reduces the set time period of the Oxygen Increase Option if the SpO2 level of the patient exceeds a predetermined threshold.
Ventilation tubing system 130 (or patient circuit 130) may be a two-limb (shown) or a one-limb circuit for carrying gases to and from the patient 150. In a two-limb embodiment, a fitting, typically referred to as a “wye-fitting” 170, may be provided to couple a patient interface 180 (as shown, an endotracheal tube) to an inspiratory limb 132 and an expiratory limb 134 of the ventilation tubing system 130.
Pneumatic system 102 may be configured in a variety of ways. In the present example, pneumatic system 102 includes an expiratory module 108 coupled with the expiratory limb 134 and an inspiratory module 104 coupled with the inspiratory limb 132. Compressor 106 or other source(s) of pressurized gases (e.g., air, oxygen, and/or helium) is coupled with inspiratory module 104 and the expiratory module 108 to provide a gas source for ventilatory support via inspiratory limb 132.
The inspiratory module 104 is configured to deliver gases to the patient 150 according to prescribed ventilatory settings. In some embodiments, inspiratory module 104 is configured to provide ventilation according to a breath type or a selected option,
The expiratory module 108 is configured to release gases from the patient's lungs according to prescribed ventilatory settings. Specifically, expiratory module 108 is associated with and/or controls an expiratory valve for releasing gases from the patient 150.
The ventilator 100 may also include one or more sensors 107 communicatively coupled to ventilator 100. The sensors 107 may be located in the pneumatic system 102, ventilation tubing system 130, and/or on the patient 150. The embodiment of
Sensors 107 may communicate with various components of ventilator 100, e.g., pneumatic system 102, other sensors 107, processor 116, oximeter 140, settings module 117, threshold module 118, and/or any other suitable components and/or modules. In one embodiment, sensors 107 generate output and send this output to pneumatic system 102, other sensors 107, processor 116, settings module 117, threshold module 118, oximeter 140, and/or any other suitable components and/or modules. Sensors 107 may employ any suitable sensory or derivative technique for monitoring one or more patient parameters or ventilator parameters associated with the ventilation of a patient 150. Sensors 107 may detect changes in patient parameters indicative of patient triggering, for example. Sensors 107 may be placed in any suitable location, within the ventilatory circuitry or other devices communicatively coupled to the ventilator 100. Further, sensors 107 may be placed in any suitable internal location, such as, within the ventilatory circuitry or within components or modules of ventilator 100. For example, sensors 107 may be coupled to the inspiratory and/or expiratory modules for detecting changes in, for example, circuit pressure and/or flow. In other examples, sensors 107 may be affixed to the ventilatory tubing or may be embedded in the tubing itself. According to some embodiments, sensors 107 may be provided at or near the lungs (or diaphragm) for detecting a pressure in the lungs or on the patient 150 for detecting SpO2. Additionally or alternatively, sensors 107 may be affixed or embedded in or near wye-fitting 170 and/or patient interface 180. Indeed, any sensory device useful for monitoring changes in measurable parameters during ventilatory treatment may be employed in accordance with embodiments described herein.
As should be appreciated, with reference to the Equation of Motion for the lung, ventilatory parameters are highly interrelated and, according to embodiments, may be either directly or indirectly monitored. That is, parameters may be directly monitored by one or more sensors 107, as described above, or may be indirectly monitored or estimated by derivation, such as the Equation of Motion for the lung.
The ventilator 100 may also include a system or module for monitoring the SpO2 of the patient 150. In one embodiment, as illustrated in
The oximeter 140 determines an oxygen gas saturation level of blood in the patient 150 based on the patient readings taken by a sensor 107 during ventilation of patient 150 by the ventilator 100. The oximeter 140 sends the measured oxygen saturation level of the blood of patient 150 to a controller 110, processor 116, threshold module 118, settings module 117, and/or any other suitable component of the ventilator 100.
The pneumatic system 102 may include a variety of other components, including mixing modules, valves, tubing, accumulators, filters, etc. Controller 110 is operatively coupled with pneumatic system 102, signal measurement and acquisition systems, and an operator interface 120 that may enable an operator to interact with the ventilator 100 (e.g., change ventilator settings, select operational modes, view monitored parameters, etc.).
In one embodiment, the operator interface 120 of the ventilator 100 includes a display 122 communicatively coupled to ventilator 100. Display 122 provides various input screens, for receiving clinician input, and various display screens, for presenting useful information to the clinician. In one embodiment, the display 122 is configured to include a graphical user interface (GUI). The GUI may be an interactive display, e.g., a touch-sensitive screen or otherwise, and may provide various windows and elements for receiving input and interface command operations. Alternatively, other suitable means of communication with the ventilator 100 may be provided, for instance by a wheel, keyboard, mouse, or other suitable interactive device. Thus, operator interface 120 may accept commands and input through display 122. For example, the operator may select or input an Oxygen Increase Option via the operator interface 120.
Display 122 may also provide useful information in the form of various ventilatory data regarding the physical condition of a patient 150. The useful information may be derived by the ventilator 100, based on data collected by a processor 116, and the useful information may be displayed to the clinician in the form of graphs, wave representations, pie graphs, text, or other suitable forms of graphic display. For example, patient data may be displayed on the GUI and/or display 122. Additionally or alternatively, patient data may be communicated to a remote monitoring system coupled via any suitable means to the ventilator 100. For example, the display 122 may display the oxygen percentage increase and/or the set time period for the Oxygen Increase Option and/or the activation of an Oxygen Increase Option. In other embodiments, the display 122 may display the SpO2 concentration of the patient 150 during delivery of an Oxygen Increase Option, the early termination of an Oxygen Increase Option, the reduction of a set time period for an Oxygen Increase Option, the reduction of an oxygen increase for an Oxygen Increase Option, and/or a predetermined SpO2 threshold for the threshold module 118.
The Oxygen Increase Option is a button or option provided to the operator that increases the concentration of oxygen delivered to the patient 150 for a set time period. The increase in oxygen concentration and/or the set time period may be selected or input by the operator, may be predetermined based on the ventilator configuration, and/or may be determined by the ventilator 100 based on patient settings and/or ventilator settings. The increased concentration in oxygen from Oxygen Increase Option is also referred to herein as the “selected oxygen concentration.” For example, the Oxygen Increase Option may increase the FiO2 delivered to the patient 150 by about 20% for about two minutes. In other examples, the Oxygen Increase Option may increase the FiO2 delivered to the patient 150 by 15% for one minute. These examples are not meant to be limiting. The Oxygen Increase Option may utilize any suitable increase in oxygen concentration for any suitable time period as would be known by a person of skill in the art.
Controller 110 may include memory 112, one or more processors 116, storage 114, and/or other components of the type commonly found in command and control computing devices. Controller 110 may further include a settings module 117 and/or a threshold module 118 configured to deliver gases to the patient 150 according to prescribed breath types or user selected option, as illustrated in
The memory 112 includes non-transitory, computer-readable storage media that stores software that is executed by the processor 116 and which controls the operation of the ventilator 100. In an embodiment, the memory 112 includes one or more solid-state storage devices such as flash memory chips. In an alternative embodiment, the memory 112 may be mass storage connected to the processor 116 through a mass storage controller (not shown) and a communications bus (not shown). Although the description of computer-readable media contained herein refers to a solid-state storage, it should be appreciated by those skilled in the art that computer-readable storage media can be any available media that can be accessed by the processor 116. That is, computer-readable storage media includes non-transitory, volatile and non-volatile, removable and non-removable media implemented in any method or technology for storage of information such as computer-readable instructions, data structures, program modules or other data. For example, computer-readable storage media includes RAM, ROM, EPROM, EEPROM, flash memory or other solid state memory technology, CD-ROM, DVD, or other optical storage, magnetic cassettes, magnetic tape, magnetic disk storage or other magnetic storage devices, or any other medium which can be used to store the desired information and which can be accessed by the computer.
As illustrated, the ventilator 100 includes a settings module 117. The inspiratory module 104 receives instructions from the settings module 117 for delivering a breath to the patient 150. The settings module 117 may send instructions based on ventilator settings and/or patient parameters. Ventilator settings include any setting selected and or determined by the ventilator 100 and/or input by the operator, such as breath type, ventilation mode, respiration rate, tidal volume and etc. Patient parameters include any measured, monitored, derived, and input patient parameter, such as ideal body weight, height, age, sex, work of breathing, SpO2, heart rate, age, respiration rate, etc. Accordingly, the settings module 117 will change the instructions provided to the inspiratory module 104 based on operator selections and/or inputs. Further, in some embodiments, the expiratory module 108 receives instructions from the settings module 117 for releasing gases from the patient's lungs. For example, if the setting module receives an operator selection or input of an Oxygen Increase Option via the operator interface 120, the settings module 117 will send instructions to the inspiratory module 104 to increase the concentration of oxygen by a predetermined amount for a set time period. As discussed above, the concentration of oxygen delivered during the Oxygen Increase Option is also referred to herein as the selected oxygen concentration.
In some embodiments, the ventilator 100 also includes a threshold module 118 as illustrated in
As discussed above, the threshold module 118 only compares the SpO2 of the patient to the predetermined threshold during the set time period of the Operator Increase Option. Accordingly, if the threshold module determines that the set time period for the Oxygen Increase Option expires, the threshold module 118 notifies the settings module 117 of the time period expiration. The settings module 117 based on the received notice of the time period expiration from the threshold module 118, sends instructions to the inspiratory module 104 to reduce the oxygen concentration to the regular (or normal) oxygen concentration, which effectively ends the Oxygen Increase Option.
If the threshold module 118 determines that the patient's SpO2 is below the predetermined threshold, the threshold module 118 continues to the compares the next newly received SpO2 measurement of the patient 150 to the predetermined threshold until the set time period for the Oxygen Increase Option expires or a patient's SpO2 levels exceed the predetermined threshold. If the threshold module 118 determines that the patient's SpO2 is above or exceeds the predetermined threshold, the threshold module 118 determines that the patient 150 is receiving too high a concentration of oxygen and communicates this determination to settings module 117.
The settings module 117, based on the receipt of the threshold violation from the threshold module 118, sends instructions to the inspiratory module 104 to reduce the concentration of oxygen delivered to patient 150. The reduced oxygen concentration delivered to the patient based on the receipt of a threshold violation is also referred to herein as the adjusted oxygen concentration. The adjusted oxygen concentration is an oxygen concentration that is less than the selected oxygen concentration delivered to the patient during an Oxygen Increase Option and is equal or greater than the regular oxygen concentration delivered to the patient prior to the selection of the Oxygen Increase Option. For example, in some embodiments, the settings module 117 reduces the oxygen concentration delivered to the patient 150 to the regular oxygen concentration or the amount delivered to the patient 150 prior to the operator selection or input of the Oxygen Increase Option and effectively ends the Oxygen Increase Option. In other embodiments, the settings module 117 reduces the selected oxygen concentration delivered to the patient 150 by a set percentages or amount, such as by at least 5%, 10%, 30%, or 50% until the set time period of the Oxygen Increase Option expires. Once the setting module 117 receives notice of the time period expiration, the settings module 117 sends instruction to the inspiration module 104 to change the adjusted oxygen concentration to the regular oxygen concentration ending the Oxygen Increase Option. Accordingly, in these embodiments, the ventilator continues the Oxygen Increase Option by delivering the adjusted oxygen concentration until the set time period expires. In further embodiments, the settings module 117 in addition to decreasing the oxygen concentration delivered to the patient 150 also decreases the set time period for the Oxygen Increase Option. For example, the settings module 117 may reduce the set time period by at least 50%, 30%, 20%, 10% or 5%. As known by a person of skill in the art any suitable reduction of the set time period for preventing a patient 150 from receiving too much oxygen during an Oxygen Increase Option may be utilized. Thus, in these embodiments, the ventilator continues the Oxygen Increase Option by delivering the adjusted oxygen concentration until the reduced time period expires.
In some embodiments, the settings module 117 send instructions to the inspiratory module 104 to reduce the oxygen concentration to the new lower level immediately after receiving the threshold violation from the threshold module 118. For example, if the Oxygen Increase Option increased the oxygen percentage by 20%, the settings module 117 will send instructions to the inspiratory module 104 to decrease the amount of oxygen delivered to the patient 150 to the adjusted oxygen concentration immediately after receiving the threshold violation from the threshold module 118. In other embodiments, the settings module 117 sends instruction to the inspiratory module 104 to reduce the oxygen concentration to the new lower level gradually after receiving the threshold violation from the threshold module 118. For example, if the Oxygen Increase Option increased the oxygen percentage by 20%, the settings module 117 will send instructions to the inspiratory module 104 to decrease the amount of oxygen delivered to the patient 150 in increments of 5% every 10 seconds until the amount of oxygen delivered to the patient 150 reaches the adjusted oxygen concentration after receiving the threshold violation from the threshold module 118. Any suitable method or system as known by a person of a skill the art may be utilized to reduce the selected oxygen concentration and/or to reach the adjusted oxygen concentration.
Many times the selected oxygen concentration for the predetermined amount of time from the Oxygen Increase Option is more than is necessary in order to address a transient occurrence of hypoxemia or low oxygen levels in patients. The early termination or reduction of the increase oxygen delivery based on the monitoring of the patient's SpO2 levels provided by ventilator 100 prevents and/or reduces the likelihood of patients, such as infants and preterm infants, from being exposed to high levels of oxygen for longer than needed, which places patients at risk for lung, retinal, and other injuries associated with exposure to elevated levels of oxygen. Accordingly, the ventilator 100 prevents and/or reduces the likelihood that a patient 150 will suffer from lung, retinal, and other injuries associated with exposure to elevated levels of oxygen.
Further, method 200 includes a delivering or normal ventilation operation 204. During the delivering operation 204, the ventilator delivers a regular oxygen concentration to a patient during ventilation. The regular oxygen concentration is based on the normal ongoing ventilation of the patient. In some embodiments, the regular oxygen concentration and other ventilator settings delivered to the patient may be input or selected by the operator or determined by the ventilator based on ventilator settings and/or patient parameters. For example, in some embodiments, the regular oxygen concentration delivered to the patient may be based on the breath type delivered to the patient. In some embodiments, the regular oxygen concentration delivered to the patient is a FiO2 from 10% to 40%.
Also, method 200 includes a receiving operation 206. During the receiving operation 206, the ventilator receives a user selection of a limited oxygen concentration increase for a set time period. For example, the ventilator receives the user selection of a limited oxygen concentration increase for a set time period when an operator selects or inputs an Oxygen Increase Option. The operator may input or select a limited oxygen concentration along with a set time period for the selected oxygen concentration via a user interface, a graphical user interface, a wheel, keyboard, mouse, and/or other suitable interactive device for receiving interface and input command operations. In some embodiments, the operator inputs or selects the amount of oxygen increase and/or the set time period. In alternative embodiments, the amount of oxygen increase and/or the set time period is preconfigured into the ventilator and/or determined by ventilator based on ventilator settings and/or patient parameters and only initiated after operator selection.
Method 200 includes an increased delivering operation 208. In response to the receiving operation 206, an increased delivering operation 208 is performed by the ventilator. During the increased delivering operation 208, the ventilator delivers a selected oxygen concentration above the regular oxygen concentration based on previously received user selections. In some embodiments, the limited oxygen increase is an about 20% increase in oxygen concentration for a set time period of about two minutes. For example, the ventilator may increase the FiO2 delivered to the patient from 30% to 50% for two minutes. This example is not meant to be limiting. The ventilator may increase the delivered oxygen concentration by any suitable amount (e.g., 5%, 10%, 15%, 25%, 30%, 35%, etc.) for any suitable set time period (e.g., 45 seconds, 1 minute 1.5 minutes, 2.5 minutes, etc.) as would be known by a person of skill in the art. In some embodiments, the settings module 117, processor 116, and/or controller 110 send instructions to the pneumatic system 102 and/or inspiratory module 104 for the delivery of the selected oxygen concentration for the set time period.
As illustrated, method 200 includes a monitoring operation 210. During the increased delivering operation 208, the monitoring operation is performed by the ventilator. As part of the monitoring operation 210, the ventilator monitors an oxygen saturation level of blood in the patient during the delivery of the selected oxygen concentration. The monitoring operation 210 uses various sensors to monitor one or more parameters of the patient, e.g., SpO2. The sensors may include any suitable sensing device as known by a person of skill in the art for monitoring the SpO2 of a patient. In some embodiments, the sensors are part of a ventilator and/or an oximeter. In some embodiments, the ventilator during monitoring operation 210 monitors the SpO2 levels of the patient periodically or continuously during the set time period of the delivery of the increase oxygen concentration. For example, the ventilator during the monitoring operation 210 may monitor the SpO2 every computational cycle (e.g., 2 milliseconds, 5 milliseconds, 10 milliseconds, etc.). In other embodiments, the ventilator during the monitoring operation 210 may monitor SpO2 after a predetermined amount of time or a predetermined event, such as set number of breaths.
In some embodiments, method 200 includes a time determination operation 212. During the time determination operation 212, the ventilator determines if the set time period for the limited oxygen concentration increase has expired. If the time period has expired, then the limited oxygen concentration increase has ended causing the ventilator to deliver the amount of oxygen delivered prior to the step of receiving a user selection of the limited oxygen concentration increase or the regular oxygen concentration. If the ventilator during the time determination operation 212 determines that the set time period for the limited oxygen concentration has expired, the ventilator selects to perform delivering operation 204. If the ventilator during the time determination operation 212 determines that the set time period for the limited oxygen concentration has not expired, the ventilator selects to perform threshold determination operation 214.
Method 200 includes a threshold determination operation 214. During the threshold determination operation 214, the ventilator determines if the oxygen saturation level of the blood of the patient exceeds a predetermined threshold. If the ventilator during the threshold determination operation 214 determines that the oxygen saturation level of the blood of the patient exceeds a predetermined threshold, the ventilator selects to perform adjusted delivering operation 216. If the ventilator during the threshold determination operation 214 determines that the oxygen saturation level of the blood of the patient does not exceed a predetermined threshold, the ventilator selects to perform monitoring operation 210.
The predetermined threshold may be input or selected by an operator, set during ventilator configuration, and/or determined by the ventilator based on ventilator settings and/or patient parameters, In some embodiments, the predetermined threshold is a SpO2 level, a percent increase in SpO2, a percent increase in SpO2 in a certain amount of time, or a set increase in slope of SpO2. This list is not meant to be limiting. Any predetermined threshold for preventing a patient from receiving too much oxygen for an extended period of time as know by a person of skill in the art may be utilized, For example, the predetermined threshold may be a SpO2 percentage of 90% or 95%. In another example, the predetermined threshold is a 20% increase in SpO2 in a 20 second time frame. In some embodiments, the predetermined threshold may be based on a patient parameter, such as disease state, body surface area, height, weight, age, ideal or predicted body weight, and/or gender.
The monitor operation 210, the time determination operation 212, and the threshold determination operation 214 are all performed by the ventilator during the increased delivering operation 208. Further, the monitor operation 210, the time determination operation 212, and/or the threshold determination operation 214 may be performed by the ventilator continuously, periodically, after a set time period, every computational cycle (e.g., 2 milliseconds, 5 milliseconds, 10 milliseconds, etc.), or based on a predetermined event, such as set number of breaths during the increase delivering operation 208.
Further, method 200 includes an adjusted delivering operation 216. During the adjusted delivering operation 216, the ventilator delivers an adjusted oxygen concentration to the patient. The adjusted oxygen concentration is an oxygen concentration that is less than the selected oxygen concentration and equal to or greater than the regular oxygen concentration delivered before the ventilator received the user selection of a limited oxygen concentration increase for a set time period. For example, in some embodiments, if the ventilator determines that the SpO2 level of the patient is above the predetermined threshold, the ventilator during the adjusted delivering operation 216 delivers the regular oxygen concentration or the oxygen concentration delivered to the patient prior to the increased delivering operation 208. In these embodiments, the ventilator during the adjusted delivery option 208 ends the increased delivery operation 208. In an alternative example, if the ventilator determines that the SpO2 level of the patient exceeds the predetermined threshold, the ventilator during the adjusted delivering operation 216 decreases the selected oxygen concentration by a set percentage, such as 5%, 10%, 15%, 25%, 50%, 75%, 85%, etc. In other embodiments, the adjusted oxygen concentration reduces the selected oxygen concentration by at least 5%, by at least 10%, by at least 30%, and/or by at least 50%.
In some embodiments, the amount the selected oxygen concentration is reduced may be based on a patient parameter, such as disease state, body surface area, height, weight, age, ideal or predicted body weight, and/or gender. In other embodiments, the ventilator during the reduced delivering operation 216 reduces the selected oxygen concentration immediately to the adjusted oxygen concentration. In alternative embodiments, the ventilator during the reduced delivering operation 216 reduces the selected oxygen concentration gradually until the adjusted oxygen concentration is met, such as in increments of 5%.
If the adjusted oxygen concentration is not equivalent to the regular oxygen concentration, the ventilator during the reduced delivering operation 216 delivers the adjusted oxygen concentration until the set time period expires. Accordingly, in some embodiments, the ventilator during the reduced delivering operation 216 also reduces the set time period. For example, the ventilator during the reduced delivering operation 216 may reduce the set time period by at least 10%, 15%, 30%, 50%, 70%, 75%, 80%, and etc. After the expiration of the set time period and/or the expiration of the reduced time period during the reduced delivering operation 216, the ventilator performs delivering operation 204.
In further embodiments, method 200 includes a display operation (not shown). The ventilator during the display operation displays or illustrates any relevant or beneficial ventilator and/or patient information to the operator and/or patient. For example, the ventilator during the display operation may display at least one of a SpO2 concentration of the patient during delivery of the selected oxygen concentration, the early termination of the selected oxygen concentration, the reduction of a set time period for the selected oxygen concentration, the adjusted oxygen concentration, and/or a predetermined SpO2 threshold. This list is exemplary only and is not meant to be limiting of the invention.
In some embodiments, a microprocessor-based ventilator that accesses a computer-readable medium having computer-executable instructions for performing the method of ventilating a patient with a medical ventilator is disclosed. This method includes repeatedly performing the steps disclosed in method 200 above and/or as illustrated in
In some embodiments, the ventilator system includes: means for delivering a regular oxygen concentration to a patient during ventilation; means for receiving a user selection of a limited oxygen concentration increase for a set time period; means for delivering a selected oxygen concentration above the regular oxygen concentration based on the received user selection; means for monitoring an oxygen saturation level of blood in the patient during the step of delivering the selected oxygen concentration; means for determining that the oxygen saturation level of the blood exceeds a predetermined threshold prior to expiration of the set time period for the limited oxygen concentration increase; and means for delivering an adjusted oxygen concentration to the patient based on the step of determining
The bottom waveform on the graph in
Each of the dashed and dotted vertical lines show when the SpO2 level of the patient increased above 95% due to a manual elevation of the oxygen concentration, prior to the two minutes elapsing. During the 4 hour time period, the oxygen concentration was increased 21 times, and in 13 of those, the selected oxygen concentration caused the SpO2 level of the patient to rise above 95%. Accordingly, the patient received too much oxygen 13 times as a result of the manual elevation of oxygen concentration showing the need for systems and methods for preventing and/or reducing the likelihood of a patient from receiving too much oxygen during a selected limited increase in oxygen concentration for a set period of time.
Those skilled in the art will recognize that the methods and systems of the present disclosure may be implemented in many manners and as such are not to be limited by the foregoing exemplary embodiments and examples. In other words, functional elements being performed by a single or multiple components, in various combinations of hardware and software or firmware, and individual functions, can be distributed among software applications at either the client or server level or both. In this regard, any number of the features of the different embodiments described herein may be combined into single or multiple embodiments, and alternate embodiments having fewer than or more than all of the features herein described are possible. Functionality may also be, in whole or in part, distributed among multiple components, in manners now known or to become known. Thus, myriad software/hardware/firmware combinations are possible in achieving the functions, features, interfaces and preferences described herein. Moreover, the scope of the present disclosure covers conventionally known manners for carrying out the described features and functions and interfaces, and those variations and modifications that may be made to the hardware or software firmware components described herein as would be understood by those skilled in the art now and hereafter.
Numerous other changes may be made which will readily suggest themselves to those skilled in the art and which are encompassed in the spirit of the disclosure and as defined in the appended claims. While various embodiments have been described for purposes of this disclosure, various changes and modifications may be made which are well within the scope of the present invention. Numerous other changes may be made which will readily suggest themselves to those skilled in the art and which are encompassed in the spirit of the disclosure and as defined in the claims.
Number | Name | Date | Kind |
---|---|---|---|
269929 | Hanlon | Jan 1883 | A |
3805780 | Cramer et al. | Apr 1974 | A |
3941124 | Rodewald et al. | Mar 1976 | A |
4056098 | Michel et al. | Nov 1977 | A |
4141354 | Ismach | Feb 1979 | A |
4211221 | Schwanbom et al. | Jul 1980 | A |
4211239 | Raemer et al. | Jul 1980 | A |
4305388 | Brisson | Dec 1981 | A |
4340044 | Levy et al. | Jul 1982 | A |
4592349 | Bird | Jun 1986 | A |
4651729 | Rae | Mar 1987 | A |
4752089 | Carter | Jun 1988 | A |
4889116 | Taube | Dec 1989 | A |
4921642 | LaTorraca | May 1990 | A |
4939647 | Clough et al. | Jul 1990 | A |
4954799 | Kumar | Sep 1990 | A |
4971052 | Edwards | Nov 1990 | A |
4986268 | Tehrani | Jan 1991 | A |
5007420 | Bird | Apr 1991 | A |
5020516 | Biondi et al. | Jun 1991 | A |
5057822 | Hoffman | Oct 1991 | A |
5072737 | Goulding | Dec 1991 | A |
5092326 | Winn et al. | Mar 1992 | A |
5094235 | Westenskow et al. | Mar 1992 | A |
5116088 | Bird | May 1992 | A |
5150291 | Cummings et al. | Sep 1992 | A |
5161525 | Kimm et al. | Nov 1992 | A |
5237987 | Anderson et al. | Aug 1993 | A |
5271389 | Isaza et al. | Dec 1993 | A |
5279549 | Ranford | Jan 1994 | A |
5299568 | Forare et al. | Apr 1994 | A |
5301921 | Kumar | Apr 1994 | A |
5315989 | Tobia | May 1994 | A |
5319540 | Isaza et al. | Jun 1994 | A |
5325861 | Goulding | Jul 1994 | A |
5333606 | Schneider et al. | Aug 1994 | A |
5339807 | Carter | Aug 1994 | A |
5343857 | Schneider et al. | Sep 1994 | A |
5351522 | Lura | Oct 1994 | A |
5357946 | Kee et al. | Oct 1994 | A |
5365922 | Raemer | Nov 1994 | A |
5368019 | LaTorraca | Nov 1994 | A |
5377671 | Biondi et al. | Jan 1995 | A |
5383449 | Forare et al. | Jan 1995 | A |
5385142 | Brady et al. | Jan 1995 | A |
5388575 | Taube | Feb 1995 | A |
5390666 | Kimm et al. | Feb 1995 | A |
5398682 | Lynn | Mar 1995 | A |
5401135 | Stoen et al. | Mar 1995 | A |
5402796 | Packer et al. | Apr 1995 | A |
5407174 | Kumar | Apr 1995 | A |
5413110 | Cummings et al. | May 1995 | A |
5429123 | Shaffer et al. | Jul 1995 | A |
5437272 | Fuhrman | Aug 1995 | A |
5438980 | Phillips | Aug 1995 | A |
5443075 | Holscher | Aug 1995 | A |
5452714 | Anderson et al. | Sep 1995 | A |
5503147 | Bertheau | Apr 1996 | A |
5513631 | McWilliams | May 1996 | A |
5517983 | Deighan et al. | May 1996 | A |
5520071 | Jones | May 1996 | A |
5524615 | Power | Jun 1996 | A |
5531221 | Power | Jul 1996 | A |
5535738 | Estes et al. | Jul 1996 | A |
5540220 | Gropper et al. | Jul 1996 | A |
5542415 | Brady | Aug 1996 | A |
5544674 | Kelly | Aug 1996 | A |
5549106 | Gruenke et al. | Aug 1996 | A |
5551419 | Froehlich et al. | Sep 1996 | A |
5596984 | O'Mahony et al. | Jan 1997 | A |
5605151 | Lynn | Feb 1997 | A |
5623923 | Bertheau et al. | Apr 1997 | A |
5630411 | Holscher | May 1997 | A |
5632270 | O'Mahony et al. | May 1997 | A |
5645048 | Brodsky et al. | Jul 1997 | A |
5660171 | Kimm et al. | Aug 1997 | A |
5664560 | Merrick et al. | Sep 1997 | A |
5664562 | Bourdon | Sep 1997 | A |
5664563 | Schroeder et al. | Sep 1997 | A |
5671767 | Kelly | Sep 1997 | A |
5672041 | Ringdahl et al. | Sep 1997 | A |
5673689 | Power | Oct 1997 | A |
5692497 | Schnitzer et al. | Dec 1997 | A |
5694926 | DeVries et al. | Dec 1997 | A |
5715812 | Deighan et al. | Feb 1998 | A |
5752509 | Lachmann et al. | May 1998 | A |
5762480 | Adahan | Jun 1998 | A |
5771884 | Yarnall et al. | Jun 1998 | A |
5791339 | Winter | Aug 1998 | A |
5794986 | Gansel et al. | Aug 1998 | A |
5813399 | Isaza et al. | Sep 1998 | A |
5826575 | Lall | Oct 1998 | A |
5829441 | Kidd et al. | Nov 1998 | A |
5862802 | Bird | Jan 1999 | A |
5864938 | Gansel et al. | Feb 1999 | A |
5865168 | Isaza | Feb 1999 | A |
5868133 | DeVries et al. | Feb 1999 | A |
5881717 | Isaza | Mar 1999 | A |
5881722 | DeVries et al. | Mar 1999 | A |
5881723 | Wallace et al. | Mar 1999 | A |
5884623 | Winter | Mar 1999 | A |
5891023 | Lynn | Apr 1999 | A |
5909731 | O'Mahony et al. | Jun 1999 | A |
5915379 | Wallace et al. | Jun 1999 | A |
5915380 | Wallace et al. | Jun 1999 | A |
5915382 | Power | Jun 1999 | A |
5918597 | Jones et al. | Jul 1999 | A |
5921238 | Bourdon | Jul 1999 | A |
5925831 | Storsved | Jul 1999 | A |
5931160 | Gilmore et al. | Aug 1999 | A |
5934274 | Merrick et al. | Aug 1999 | A |
6013619 | Cochrane et al. | Jan 2000 | A |
6024089 | Wallace et al. | Feb 2000 | A |
6041780 | Richard et al. | Mar 2000 | A |
6047860 | Sanders | Apr 2000 | A |
6076523 | Jones et al. | Jun 2000 | A |
6089105 | Ricciardelli | Jul 2000 | A |
6116240 | Merrick et al. | Sep 2000 | A |
6116464 | Sanders | Sep 2000 | A |
6123073 | Schlawin et al. | Sep 2000 | A |
6123074 | Hete et al. | Sep 2000 | A |
6135106 | Dirks et al. | Oct 2000 | A |
6142150 | O'Mahoney | Nov 2000 | A |
6148814 | Clemmer et al. | Nov 2000 | A |
6158432 | Biondi et al. | Dec 2000 | A |
6158434 | Lugtigheid et al. | Dec 2000 | A |
6161539 | Winter | Dec 2000 | A |
6220245 | Takabayashi et al. | Apr 2001 | B1 |
6223064 | Lynn et al. | Apr 2001 | B1 |
6269812 | Wallace et al. | Aug 2001 | B1 |
6273444 | Power | Aug 2001 | B1 |
6283119 | Bourdon | Sep 2001 | B1 |
6305373 | Wallace et al. | Oct 2001 | B1 |
6321748 | O'Mahoney | Nov 2001 | B1 |
6325785 | Babkes et al. | Dec 2001 | B1 |
6342039 | Lynn et al. | Jan 2002 | B1 |
6357438 | Hansen | Mar 2002 | B1 |
6358215 | Ricciardelli | Mar 2002 | B1 |
6360745 | Wallace et al. | Mar 2002 | B1 |
6369838 | Wallace et al. | Apr 2002 | B1 |
6371114 | Schmidt et al. | Apr 2002 | B1 |
6390091 | Banner et al. | May 2002 | B1 |
6412483 | Jones et al. | Jul 2002 | B1 |
6439229 | Du et al. | Aug 2002 | B1 |
6463930 | Biondi et al. | Oct 2002 | B2 |
6467478 | Merrick et al. | Oct 2002 | B1 |
6512938 | Claure et al. | Jan 2003 | B2 |
6526970 | DeVries et al. | Mar 2003 | B2 |
6532958 | Buan et al. | Mar 2003 | B1 |
6532959 | Berthon-Jones | Mar 2003 | B1 |
6532960 | Yurko | Mar 2003 | B1 |
6533730 | Strom | Mar 2003 | B2 |
6536429 | Pavlov et al. | Mar 2003 | B1 |
6543449 | Woodring et al. | Apr 2003 | B1 |
6546930 | Emerson et al. | Apr 2003 | B1 |
6553991 | Isaza | Apr 2003 | B1 |
6557553 | Borrello | May 2003 | B1 |
6561187 | Schmidt et al. | May 2003 | B2 |
6571795 | Bourdon | Jun 2003 | B2 |
6584973 | Biondi et al. | Jul 2003 | B1 |
6609016 | Lynn | Aug 2003 | B1 |
6622726 | Du | Sep 2003 | B1 |
6640806 | Yurko | Nov 2003 | B2 |
6644310 | Delache et al. | Nov 2003 | B1 |
6644312 | Berthon-Jones et al. | Nov 2003 | B2 |
6659962 | Ricciardelli | Dec 2003 | B2 |
6668824 | Isaza et al. | Dec 2003 | B1 |
6668829 | Biondi et al. | Dec 2003 | B2 |
6671529 | Claure et al. | Dec 2003 | B2 |
6675801 | Wallace et al. | Jan 2004 | B2 |
6688307 | Berthon-Jones | Feb 2004 | B2 |
6718974 | Moberg | Apr 2004 | B1 |
6718975 | Blomberg | Apr 2004 | B2 |
6723055 | Hoffman | Apr 2004 | B2 |
6725447 | Gilman et al. | Apr 2004 | B1 |
6739337 | Isaza | May 2004 | B2 |
6745764 | Hickle | Jun 2004 | B2 |
6748252 | Lynn et al. | Jun 2004 | B2 |
6752151 | Hill | Jun 2004 | B2 |
6758216 | Berthon-Jones et al. | Jul 2004 | B1 |
6760608 | Lynn | Jul 2004 | B2 |
6761165 | Strickland, Jr. | Jul 2004 | B2 |
6761167 | Nadjafizadeh et al. | Jul 2004 | B1 |
6761168 | Nadjafizadeh et al. | Jul 2004 | B1 |
6796305 | Banner et al. | Sep 2004 | B1 |
6807965 | Hickle | Oct 2004 | B1 |
6814074 | Nadjafizadeh et al. | Nov 2004 | B1 |
6820618 | Banner et al. | Nov 2004 | B2 |
6830048 | Wruck et al. | Dec 2004 | B2 |
6837242 | Younes | Jan 2005 | B2 |
6839753 | Biondi et al. | Jan 2005 | B2 |
6866040 | Bourdon | Mar 2005 | B1 |
6868346 | Larson et al. | Mar 2005 | B2 |
6871645 | Wartman et al. | Mar 2005 | B2 |
6877511 | DeVries et al. | Apr 2005 | B2 |
6895963 | Martin et al. | May 2005 | B1 |
6938619 | Hickle | Sep 2005 | B1 |
6960854 | Nadjafizadeh et al. | Nov 2005 | B2 |
6986347 | Hickle | Jan 2006 | B2 |
7008380 | Rees et al. | Mar 2006 | B1 |
7017574 | Biondi et al. | Mar 2006 | B2 |
7036504 | Wallace et al. | May 2006 | B2 |
7066173 | Banner et al. | Jun 2006 | B2 |
7077131 | Hansen | Jul 2006 | B2 |
7081095 | Lynn et al. | Jul 2006 | B2 |
RE39225 | Isaza et al. | Aug 2006 | E |
7089936 | Madaus et al. | Aug 2006 | B2 |
7089937 | Berthon-Jones et al. | Aug 2006 | B2 |
7092757 | Larson et al. | Aug 2006 | B2 |
7100609 | Berthon-Jones et al. | Sep 2006 | B2 |
7117438 | Wallace et al. | Oct 2006 | B2 |
7152598 | Morris et al. | Dec 2006 | B2 |
7152604 | Hickle et al. | Dec 2006 | B2 |
7210478 | Banner et al. | May 2007 | B2 |
7222623 | DeVries et al. | May 2007 | B2 |
7229430 | Hickle et al. | Jun 2007 | B2 |
7267122 | Hill | Sep 2007 | B2 |
7270126 | Wallace et al. | Sep 2007 | B2 |
7275540 | Bolam et al. | Oct 2007 | B2 |
7296573 | Estes et al. | Nov 2007 | B2 |
7297119 | Westbrook et al. | Nov 2007 | B2 |
7308894 | Hickle | Dec 2007 | B2 |
7316231 | Hickle | Jan 2008 | B2 |
7331343 | Schmidt et al. | Feb 2008 | B2 |
7334578 | Biondi et al. | Feb 2008 | B2 |
7337778 | Martin et al. | Mar 2008 | B2 |
7353824 | Forsyth et al. | Apr 2008 | B1 |
7369757 | Farbarik | May 2008 | B2 |
7370650 | Nadjafizadeh et al. | May 2008 | B2 |
7398115 | Lynn | Jul 2008 | B2 |
7406870 | Seto | Aug 2008 | B2 |
7428902 | Du et al. | Sep 2008 | B2 |
7448381 | Sasaki et al. | Nov 2008 | B2 |
7455583 | Taya | Nov 2008 | B2 |
7460959 | Jafari | Dec 2008 | B2 |
7472702 | Beck et al. | Jan 2009 | B2 |
7487773 | Li | Feb 2009 | B2 |
7509957 | Duquette et al. | Mar 2009 | B2 |
7520279 | Berthon-Jones | Apr 2009 | B2 |
7527054 | Misholi | May 2009 | B2 |
7565905 | Hickle | Jul 2009 | B2 |
7654802 | Crawford, Jr. et al. | Feb 2010 | B2 |
7668579 | Lynn | Feb 2010 | B2 |
7694677 | Tang | Apr 2010 | B2 |
7717113 | Andrieux | May 2010 | B2 |
D618356 | Ross | Jun 2010 | S |
7758503 | Lynn et al. | Jul 2010 | B2 |
7784461 | Figueiredo et al. | Aug 2010 | B2 |
7802571 | Tehrani | Sep 2010 | B2 |
7814906 | Moretti | Oct 2010 | B2 |
7823588 | Hansen | Nov 2010 | B2 |
7855716 | McCreary et al. | Dec 2010 | B2 |
D632796 | Ross et al. | Feb 2011 | S |
D632797 | Ross et al. | Feb 2011 | S |
7891354 | Farbarik | Feb 2011 | B2 |
7893560 | Carter | Feb 2011 | B2 |
D638852 | Skidmore et al. | May 2011 | S |
7984714 | Hausmann et al. | Jul 2011 | B2 |
D643535 | Ross et al. | Aug 2011 | S |
7992557 | Nadjafizadeh et al. | Aug 2011 | B2 |
8001967 | Wallace et al. | Aug 2011 | B2 |
D645158 | Sanchez et al. | Sep 2011 | S |
8021310 | Sanborn et al. | Sep 2011 | B2 |
D649157 | Skidmore et al. | Nov 2011 | S |
D652521 | Ross et al. | Jan 2012 | S |
D652936 | Ross et al. | Jan 2012 | S |
D653749 | Winter et al. | Feb 2012 | S |
8113062 | Graboi et al. | Feb 2012 | B2 |
D655405 | Winter et al. | Mar 2012 | S |
D655809 | Winter et al. | Mar 2012 | S |
D656237 | Sanchez et al. | Mar 2012 | S |
8181648 | Perine et al. | May 2012 | B2 |
8210173 | Vandine | Jul 2012 | B2 |
8210174 | Farbarik | Jul 2012 | B2 |
8240684 | Ross et al. | Aug 2012 | B2 |
8267085 | Jafari et al. | Sep 2012 | B2 |
8272379 | Jafari et al. | Sep 2012 | B2 |
8272380 | Jafari et al. | Sep 2012 | B2 |
8302600 | Andrieux et al. | Nov 2012 | B2 |
8302602 | Andrieux et al. | Nov 2012 | B2 |
20020185126 | Krebs | Dec 2002 | A1 |
20030209242 | Hickle | Nov 2003 | A1 |
20030217747 | Hickle et al. | Nov 2003 | A1 |
20050039748 | Andrieux | Feb 2005 | A1 |
20050070477 | Cochrane | Mar 2005 | A1 |
20050112325 | Hickle | May 2005 | A1 |
20050139212 | Bourdon | Jun 2005 | A1 |
20050150494 | DeVries et al. | Jul 2005 | A1 |
20050172965 | Thulin | Aug 2005 | A1 |
20050188083 | Biondi et al. | Aug 2005 | A1 |
20050247311 | Vacchiano et al. | Nov 2005 | A1 |
20060112959 | Mechlenburg et al. | Jun 2006 | A1 |
20060155206 | Lynn | Jul 2006 | A1 |
20060155207 | Lynn et al. | Jul 2006 | A1 |
20060161071 | Lynn et al. | Jul 2006 | A1 |
20060189880 | Lynn et al. | Aug 2006 | A1 |
20060195041 | Lynn et al. | Aug 2006 | A1 |
20060235324 | Lynn | Oct 2006 | A1 |
20060241708 | Boute | Oct 2006 | A1 |
20060264762 | Starr | Nov 2006 | A1 |
20060266355 | Misholi | Nov 2006 | A1 |
20060272642 | Chalvignac | Dec 2006 | A1 |
20060286038 | Rairkar et al. | Dec 2006 | A1 |
20070000494 | Banner et al. | Jan 2007 | A1 |
20070017515 | Wallace et al. | Jan 2007 | A1 |
20070027375 | Melker et al. | Feb 2007 | A1 |
20070028921 | Banner et al. | Feb 2007 | A1 |
20070044805 | Wedler et al. | Mar 2007 | A1 |
20070072541 | Daniels II, et al. | Mar 2007 | A1 |
20070077200 | Baker | Apr 2007 | A1 |
20070093721 | Lynn et al. | Apr 2007 | A1 |
20070095347 | Lampotang et al. | May 2007 | A1 |
20070107728 | Ricciardelli et al. | May 2007 | A1 |
20070129647 | Lynn | Jun 2007 | A1 |
20070142716 | Biondi | Jun 2007 | A1 |
20070144521 | DeVries et al. | Jun 2007 | A1 |
20070149860 | Lynn et al. | Jun 2007 | A1 |
20070157931 | Parker et al. | Jul 2007 | A1 |
20070163579 | Li et al. | Jul 2007 | A1 |
20070191697 | Lynn et al. | Aug 2007 | A1 |
20070215154 | Borrello | Sep 2007 | A1 |
20070227537 | Bemister et al. | Oct 2007 | A1 |
20070272241 | Sanborn et al. | Nov 2007 | A1 |
20070277823 | Al-Ali et al. | Dec 2007 | A1 |
20070284361 | Nadjafizadeh et al. | Dec 2007 | A1 |
20080000479 | Elaz et al. | Jan 2008 | A1 |
20080053441 | Gottlib et al. | Mar 2008 | A1 |
20080066752 | Baker et al. | Mar 2008 | A1 |
20080066753 | Martin et al. | Mar 2008 | A1 |
20080072896 | Setzer et al. | Mar 2008 | A1 |
20080072902 | Setzer et al. | Mar 2008 | A1 |
20080078390 | Milne et al. | Apr 2008 | A1 |
20080081974 | Pav | Apr 2008 | A1 |
20080083644 | Janbakhsh et al. | Apr 2008 | A1 |
20080092894 | Nicolazzi et al. | Apr 2008 | A1 |
20080097234 | Nicolazzi et al. | Apr 2008 | A1 |
20080110461 | Mulqueeny et al. | May 2008 | A1 |
20080119753 | Ricciardelli et al. | May 2008 | A1 |
20080178880 | Christopher et al. | Jul 2008 | A1 |
20080178882 | Christopher et al. | Jul 2008 | A1 |
20080200775 | Lynn | Aug 2008 | A1 |
20080200819 | Lynn et al. | Aug 2008 | A1 |
20080236582 | Tehrani | Oct 2008 | A1 |
20080251079 | Richey | Oct 2008 | A1 |
20080314385 | Brunner et al. | Dec 2008 | A1 |
20090165795 | Nadjafizadeh et al. | Jul 2009 | A1 |
20090171176 | Andersohn | Jul 2009 | A1 |
20090171226 | Campbell et al. | Jul 2009 | A1 |
20090205661 | Stephenson et al. | Aug 2009 | A1 |
20090205663 | Vandine et al. | Aug 2009 | A1 |
20090241952 | Nicolazzi et al. | Oct 2009 | A1 |
20090241953 | Vandine et al. | Oct 2009 | A1 |
20090241956 | Baker, Jr. et al. | Oct 2009 | A1 |
20090241957 | Baker, Jr. | Oct 2009 | A1 |
20090241958 | Baker, Jr. | Oct 2009 | A1 |
20090241962 | Jafari et al. | Oct 2009 | A1 |
20090247891 | Wood | Oct 2009 | A1 |
20090301486 | Masic | Dec 2009 | A1 |
20090301487 | Masic | Dec 2009 | A1 |
20090301490 | Masic | Dec 2009 | A1 |
20090301491 | Masic et al. | Dec 2009 | A1 |
20100006098 | McGinnis et al. | Jan 2010 | A1 |
20100011307 | Desfossez et al. | Jan 2010 | A1 |
20100024820 | Bourdon | Feb 2010 | A1 |
20100051026 | Graboi | Mar 2010 | A1 |
20100051029 | Jafari et al. | Mar 2010 | A1 |
20100069761 | Karst et al. | Mar 2010 | A1 |
20100071689 | Thiessen | Mar 2010 | A1 |
20100071692 | Porges | Mar 2010 | A1 |
20100071695 | Thiessen | Mar 2010 | A1 |
20100071696 | Jafari | Mar 2010 | A1 |
20100071697 | Jafari et al. | Mar 2010 | A1 |
20100078017 | Andrieux et al. | Apr 2010 | A1 |
20100078026 | Andrieux et al. | Apr 2010 | A1 |
20100081119 | Jafari et al. | Apr 2010 | A1 |
20100081955 | Wood, Jr. et al. | Apr 2010 | A1 |
20100139660 | Adahan | Jun 2010 | A1 |
20100147303 | Jafari et al. | Jun 2010 | A1 |
20100186742 | Sherman et al. | Jul 2010 | A1 |
20100186744 | Andrieux | Jul 2010 | A1 |
20100218765 | Jafari et al. | Sep 2010 | A1 |
20100218766 | Milne | Sep 2010 | A1 |
20100218767 | Jafari et al. | Sep 2010 | A1 |
20100236555 | Jafari et al. | Sep 2010 | A1 |
20100242961 | Mougel et al. | Sep 2010 | A1 |
20100282259 | Figueiredo et al. | Nov 2010 | A1 |
20100288283 | Campbell et al. | Nov 2010 | A1 |
20100292544 | Sherman et al. | Nov 2010 | A1 |
20100300446 | Nicolazzi et al. | Dec 2010 | A1 |
20100331639 | O'Reilly | Dec 2010 | A1 |
20110011400 | Gentner et al. | Jan 2011 | A1 |
20110023878 | Thiessen | Feb 2011 | A1 |
20110023879 | Vandine et al. | Feb 2011 | A1 |
20110023880 | Thiessen | Feb 2011 | A1 |
20110023881 | Thiessen | Feb 2011 | A1 |
20110029910 | Thiessen | Feb 2011 | A1 |
20110041849 | Chen et al. | Feb 2011 | A1 |
20110041850 | Vandine et al. | Feb 2011 | A1 |
20110126829 | Carter et al. | Jun 2011 | A1 |
20110126832 | Winter et al. | Jun 2011 | A1 |
20110126834 | Winter et al. | Jun 2011 | A1 |
20110126835 | Winter et al. | Jun 2011 | A1 |
20110126836 | Winter et al. | Jun 2011 | A1 |
20110126837 | Winter et al. | Jun 2011 | A1 |
20110128008 | Carter | Jun 2011 | A1 |
20110132361 | Sanchez | Jun 2011 | A1 |
20110132362 | Sanchez | Jun 2011 | A1 |
20110132364 | Ogilvie et al. | Jun 2011 | A1 |
20110132365 | Patel et al. | Jun 2011 | A1 |
20110132366 | Ogilvie et al. | Jun 2011 | A1 |
20110132367 | Patel | Jun 2011 | A1 |
20110132368 | Sanchez et al. | Jun 2011 | A1 |
20110132369 | Sanchez | Jun 2011 | A1 |
20110132371 | Sanchez et al. | Jun 2011 | A1 |
20110133936 | Sanchez et al. | Jun 2011 | A1 |
20110138308 | Palmer et al. | Jun 2011 | A1 |
20110138309 | Skidmore et al. | Jun 2011 | A1 |
20110138311 | Palmer | Jun 2011 | A1 |
20110138315 | Vandine et al. | Jun 2011 | A1 |
20110138323 | Skidmore et al. | Jun 2011 | A1 |
20110146681 | Jafari et al. | Jun 2011 | A1 |
20110146683 | Jafari et al. | Jun 2011 | A1 |
20110154241 | Skidmore et al. | Jun 2011 | A1 |
20110175728 | Baker, Jr. | Jul 2011 | A1 |
20110196251 | Jourdain et al. | Aug 2011 | A1 |
20110209702 | Vuong et al. | Sep 2011 | A1 |
20110209704 | Jafari et al. | Sep 2011 | A1 |
20110209707 | Terhark | Sep 2011 | A1 |
20110213215 | Doyle et al. | Sep 2011 | A1 |
20110230780 | Sanborn et al. | Sep 2011 | A1 |
20110249006 | Wallace et al. | Oct 2011 | A1 |
20110259330 | Jafari et al. | Oct 2011 | A1 |
20110259332 | Sanchez et al. | Oct 2011 | A1 |
20110259333 | Sanchez et al. | Oct 2011 | A1 |
20110265024 | Leone et al. | Oct 2011 | A1 |
20110271960 | Milne et al. | Nov 2011 | A1 |
20110273299 | Milne et al. | Nov 2011 | A1 |
20120000467 | Milne et al. | Jan 2012 | A1 |
20120000468 | Milne et al. | Jan 2012 | A1 |
20120000469 | Milne et al. | Jan 2012 | A1 |
20120000470 | Milne et al. | Jan 2012 | A1 |
20120029317 | Doyle et al. | Feb 2012 | A1 |
20120030611 | Skidmore | Feb 2012 | A1 |
20120060841 | Crawford, Jr. et al. | Mar 2012 | A1 |
20120071729 | Doyle et al. | Mar 2012 | A1 |
20120090611 | Graboi et al. | Apr 2012 | A1 |
20120096381 | Milne et al. | Apr 2012 | A1 |
20120133519 | Milne et al. | May 2012 | A1 |
20120136222 | Doyle et al. | May 2012 | A1 |
20120137249 | Milne et al. | May 2012 | A1 |
20120137250 | Milne et al. | May 2012 | A1 |
20120167885 | Masic et al. | Jul 2012 | A1 |
20120185792 | Kimm et al. | Jul 2012 | A1 |
20120197578 | Vig et al. | Aug 2012 | A1 |
20120197580 | Vij et al. | Aug 2012 | A1 |
20120216809 | Milne et al. | Aug 2012 | A1 |
20120216810 | Jafari et al. | Aug 2012 | A1 |
20120216811 | Kimm et al. | Aug 2012 | A1 |
20120226444 | Milne et al. | Sep 2012 | A1 |
20120247471 | Masic et al. | Oct 2012 | A1 |
20120272960 | Milne | Nov 2012 | A1 |
20120272961 | Masic et al. | Nov 2012 | A1 |
20120272962 | Doyle et al. | Nov 2012 | A1 |
20120304995 | Kauc | Dec 2012 | A1 |
20130000644 | Thiessen | Jan 2013 | A1 |
20130006133 | Doyle et al. | Jan 2013 | A1 |
20130006134 | Doyle et al. | Jan 2013 | A1 |
20130025596 | Jafari et al. | Jan 2013 | A1 |
20130025597 | Doyle et al. | Jan 2013 | A1 |
20130053717 | Vandine et al. | Feb 2013 | A1 |
Number | Date | Country |
---|---|---|
WO2004000114 | Dec 2003 | WO |
WO2006121372 | Nov 2006 | WO |
WO2007085110 | Aug 2007 | WO |
WO2007145948 | Dec 2007 | WO |
Entry |
---|
7200 Series Ventilator, Options, and Accessories: Operator's Manual. Nellcor Puritan Bennett, Part No. 22300 A, Sep. 1990, pp. 1-196. |
7200 Ventilatory System: Addendum/Errata. Nellcor Puritan Bennett, Part No. 4-023576-00, Rev. A, Apr. 1988, pp. 1-32. |
800 Operator's and Technical Reference Manual. Series Ventilator System, Nellcor Puritan Bennett, Part No. 4-070088-00, Rev. L, Aug. 2010, pp. 1-476. |
840 Operator's and Technical Reference Manual. Ventilator System, Nellcor Puritan Bennett, Part No. 4-075609-00, Rev. G, Oct. 2006, pp. 1-424. |
Claure, Nelson, MSc., PhD. et al., Graph from “Automated Adjustment of Inspired Oxygen in Preterm Infants with Frequent Fluctuations in Oxygenation: A Pilot Clinical Trial”, The Journal of Pediatrics, 2009; 155: pp. 640-645 (1 page). |
Number | Date | Country | |
---|---|---|---|
20130104896 A1 | May 2013 | US |