US20230364369A1

US20230364369A1 - Systems and methods for automatic cycling or cycling detection

Info

Publication number: US20230364369A1
Application number: US18/360,010
Authority: US
Inventors: Richard Nakai
Original assignee: Covidien LP
Current assignee: Covidien LP
Priority date: 2018-10-03
Filing date: 2023-07-27
Publication date: 2023-11-16
Also published as: US20200108215A1; US11752287B2

Abstract

Systems and methods for novel ventilation that allows the ventilator to detect a patient intention to cycle exhalation are provided. Further, systems and methods for cycling exhalation based on a muscle pressure are provided.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 16/590,530 filed Oct. 2, 2019, which claims the benefit of U.S. Provisional Application Ser. No. 62/740,740, filed Oct. 3, 2018, the complete disclosures of which are hereby incorporated by reference in their entireties. To the extent appropriate a claim of priority is made to each of the above disclosed applications.

INTRODUCTION

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, several different ventilator modes or settings have been created to provide better ventilation for patients in various different scenarios, such as mandatory ventilation modes and assist control ventilation modes.
It is with respect to this general technical environment that aspects of the present technology disclosed herein have been contemplated. Furthermore, although a general environment has been discussed, it should be understood that the examples described herein should not be limited to the general environment identified herein.

SUMMARY

This summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description section. This summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter.
Aspects of the disclosure relate to providing novel systems and methods for cycling or ending exhalation during mechanical ventilation of a patient. More specifically, this disclosure describes systems and methods for cycling ventilation based on estimated muscle pressure.
In an aspect, a ventilator system is provided. The ventilator system includes at least one sensor, a gas-delivery system configured to deliver ventilation gases to a patient, at least one processor, and at least one memory comprising computer-executable instructions that when executed by the at least one processor cause the ventilator system to perform various operations. The operations include receiving one or more sensor measurements from the at least one sensor during inhalation of the patient and, based on the one or more sensor measurements, estimating a muscle pressure (P_MUS) of the patient during the inhalation of the patient. Based on the estimate of P_MUS, the operations further include determining a P_MUS-based metric and, in response to determining that the P_MUS-based metric meets a cycling threshold, determining a patient intention to cycle. Additionally, the operations include evaluating one or more characteristics of the patient intention to cycle and, when the one or more characteristics of the patient intention to cycle are abnormal, determining a missed cycling effort. In response to the missed cycling effort, the operations include performing an action.
In another aspect, a method of determining a patient intention to cycle is provided. The method includes delivering spontaneous ventilation to a patient and, based on a target setting for the spontaneous ventilation, determining a percent support setting. The method further includes temporarily switching to a proportional assist (PA) breath type and delivering at least one PA breath based on the determined percent support setting. During the at least one PA breath, the method includes receiving one or more sensor measurements from the at least one sensor and, based on the one or more sensor measurements, estimating a muscle pressure (P_MUS) of the patient. In response to determining that the P_MUSmeets a cycling threshold, the method includes determining a patient intention to cycle.
In yet another aspect, a method for detecting a patient intention to cycle during spontaneous ventilation of the patient on a ventilator is provided. The method includes monitoring at least one parameter of the patient receiving spontaneous ventilation based on one or more received non-invasive sensor measurements during inhalation and, based on the one or more received non-invasive sensor measurements, estimating a muscle pressure (P_MUS) of the patient during the inhalation. The method further includes comparing a P_MUS-based metric to a cycling threshold and determining that the P_MUS-based metric meets the cycling threshold to identify a patient intention to cycle. In response to identifying the patient intention to cycle, the method includes evaluating one or more characteristics of the patient intention to cycle and, when the one or more characteristics of the patient intention to cycle are abnormal, determining a missed cycling effort. Additionally, the method includes performing an action in response to the missed cycling effort.
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 disclosure as claimed.
This summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used to limit the scope of the claimed subject matter.

BRIEF DESCRIPTION OF THE DRAWINGS

The following drawing figures, which form a part of this application, are illustrative of aspects of systems and methods described below and are not meant to limit the scope of the disclosure in any manner, which scope shall be based on the claims.

FIG. 1 is a schematic diagram illustrating a ventilator capable of detecting patient exhalation or cycling efforts based on estimated muscle pressure, in accordance with aspects of the disclosure.

FIG. 2 is a flow diagram illustrating a method for cycling detection based on estimated muscle pressure in a spontaneous breath type during ventilation of a patient with a ventilator, in accordance with aspects of the disclosure.

FIG. 3 is a flow diagram illustrating a method for performing process operation 204 of FIG. 2 when the spontaneous breath type is TC, PS or VS and the processed parameter is estimated muscle pressure during ventilation of a patient with a ventilator, in accordance with aspects of the disclosure.

FIG. 4 is a graph illustrating a muscle pressure curve of a volunteer in synchrony with the ventilator and actively exhaling in response to externally imposed breathing resistance.

FIG. 5 is a graph illustrating a missed cycle based on estimated muscle pressure monitoring during a high-percentage support using a proportional assist (PA) breath type of a volunteer, in accordance with aspects of the disclosure.

FIG. 6 illustrates the tidal volume and flow curves for ventilation of the volunteer in FIG. 5 .

FIG. 7 is a graph illustrating P_MUSof an intubated volunteer as measured by an esophageal catheter during a proportional assist (PA) breath type.

FIG. 8 is a graph illustrating P_MUSof an intubated volunteer as measured by a catheter during a high-percentage support, proportional assist (PA) breath type.

DETAILED DESCRIPTION

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 flow rates. Ventilators capable of operating independently of external sources of pressurized air are also available.
As each patient may require a different ventilation strategy, modern ventilators can be customized for the particular needs of an individual patient. For example, several different ventilator modes, breath types, and/or settings have been created to provide better ventilation for patients in various different scenarios, such as mandatory ventilation modes and assist control ventilation modes. Mandatory ventilation modes provide ventilator-initiated triggering and cycling, whereas assist control modes allow a spontaneously breathing patient to trigger inspiration during ventilation. In a spontaneous mode of ventilation, the ventilator triggers inspiration upon the detection of patient demand or patient effort to inhale and cycles or initiates expiration when a predetermined threshold is met or when a patient demand or effort for exhalation is detected.
The response performance of a medical ventilator to a patient cycle from inhalation into exhalation represents an important characteristic of a medical ventilator. A ventilator's exhalation trigger or cycle response impacts the patient's work of breathing and the overall patient-ventilator synchrony. The exhalation cycle response performance of a ventilator is a function of a patient's expiratory behavior (breathing effort magnitude and timing characteristics) as well as the ventilator's gas delivery dynamics and flow control parameters (actuator response, dead bands, etc.).
Triggering delay time, cycling delay time, and asynchrony index are among key parameters that are used to measure the patient-ventilator synchrony. The asynchrony index is the ratio between the number of asynchronous events and the total respiratory rate. Miss-cycling is also considered as one of the factors that increases the patient-ventilator asynchrony index. Several different factors cause asynchrony events, such as variation in patient's breathing pattern, muscle strength, respiratory mechanics, ventilator performance, and ventilator characteristics.
Traditionally the inspiration is cycled off based on an E_SENSthreshold, which may be a set percentage (normally 25%) of the peak inspiratory flow or a set flow value on many intensive care ventilators. This adjustable value, however, is often not optimal, resulting in patient-ventilator expiratory asynchrony. Expiratory asynchrony has been shown to be a clinical issue in the patients with partial ventilatory support. Under the expiratory asynchrony situation, the termination of the ventilator flow occurs either before or after patients stop their inspiratory efforts. When the termination of the ventilator flow falls behind the end of the patient inspiratory effort (i.e. delayed cycling), the patient recruits his or her expiratory muscles to “fight” against the ventilator flow, which increases expiratory workload, resulting in intrinsic PEEP. When the termination of the ventilator flow occurs before the end of patient inspiratory effort (i.e. premature cycling), the patient inspiratory muscle work continues into or even throughout the ventilator's expiratory phase, thus resulting in inefficient inspiratory muscle work. For PA, TC, PS or VS, to address premature cycling, the percent support setting may be increased or the E_SENSsetting may be decreased (less sensitive). Alternatively, for PA, TC, PS or VS, to address delayed cycling, the percent support setting may be decreased or the E_SENSsetting may be increased (more sensitive). For PS and VS, there is an FAP setting or “rise time %” setting indicating how aggressively the pressure rises. If this setting is too low, then pressure rises sluggishly, which can affect patient support and cycling. This might result in early cycling with the patient continuing to inhale because the pressure rise was not fast enough. In this case, an adjustment could be to increase the “rise time %” setting.
Furthermore, a high lung volume caused by the previous breath with delayed cycling may result in a missed trigger of the subsequent inspiratory effort in patients with Chronic Obstructive Pulmonary Disease (COPD) or with high breathing rates. For patients ventilated with pressure support (PS) ventilation, premature cycling may result in double-triggering or auto-triggering.
Most ventilators in the current market allow the user to select an expiratory cycling setting from a specific range provided by the ventilator. Unlike universal settings such as respiratory rate, PEEP, tidal volume, and pressure support, the expiratory cycling settings are unique to each ventilator. Users who are unfamiliar with a specific ventilator outside their daily use may struggle to properly set the expiratory cycling settings. Moreover, patients need different adjustments when their recovery conditions have changed, or their sedation and pain medications are adjusted. But many clinicians do not adjust the settings optimally to support patient effort.
For example, for triggering the start of exhalation in tube compensated (TC), pressure support (PS) or volume support (VS) ventilation (cycling), the exhalation sensitivity (E_SENS) setting is frequently left at the default value (25%), which can cause asynchrony in some types of patients. For example, with COPD patients, this value can lead to the patient fighting the ventilator trying to exhale. In proportional assist (PA) ventilation, the exhalation sensitivity (E_SENS) setting is also frequently left at a default value (such as 3.0 Lpm), which can cause asynchrony in some types of patients. Further, in proportional assist (PA) ventilation, if the percent support setting is set too high, the patient can be over-supported leading to the patient forcing the exhalation mid-way through inspiration. Having the ventilator identify this over-support condition could give the ventilator the ability to detect the patient fighting the ventilator to exhale, not just in PA, but in PS, VS or TC as well. The exhalation issues contribute to poor synchrony.
Therefore, there is a need to have a smarter, or more intuitive, expiratory cycling method to reduce expiratory asynchrony and optimize the patient-to-ventilator interactions.
Accordingly, the systems and methods described herein provide improved exhalation cycling systems and methods. For example, the improved exhalation cycling systems and methods monitor a P_MUS-based metric to detect patient cycling efforts and/or to determine if the set cycling threshold is appropriate for the patient. Based on this monitoring, the ventilator performs one or more actions. The action may include triggering exhalation, adjusting an exhalation threshold setting, adjusting another ventilator setting, providing a notification, and/or providing a recommendation. For example, the P_MUS-based metric monitoring can be utilized to adjust E_SENSfor PS, PA, TC, and VS breath types to improve ventilator cycling or the percent support setting for PA breath type to improve ventilator-patient synchrony. The improved exhalation cycling systems and methods, in these aspects, are referred to herein as “cycling systems and methods” or “cycling settings.” The cycling setting reduces the occurrence of cycling asynchrony and requires less operator training or knowledge for effective use. While the cycling setting is referred to herein as a cycling setting, it may also be referred to as a cycling mode, supplemental cycling mode, or supplemental mode because the cycling setting is utilized in conjunction with or in addition to any spontaneous mode of ventilation running any suitable breath type (PS, VS, TC, or PA) for a spontaneous mode of ventilation.
In some aspects, the cycling setting improves ventilator synchrony by changing the cycling threshold or recommending a change in cycling threshold based on the monitoring of estimated patient muscle pressure (P_MUS) or a P_MUS-based metric. The P_MUS-based metric may be P_MUS, may be a processed signal of P_MUS, or may represent a shape of the P_MUSwaveform. In other aspects, the cycling setting improves ventilator synchrony by cycling exhalation based on the monitoring of the P_MUS-based metric. As estimated patient muscle pressure is a strong indicator of a patient's effort to exhale, a patient P_MUS-based metric can be utilized to detect cycling or intended cycling and/or to determine if the cycling threshold or pattern is appropriate.
For the purposes of this disclosure, a “breath” refers to a single cycle of inspiration and exhalation delivered with the assistance of a ventilator. The term “breath type” refers to some specific definition or set of rules dictating how the pressure and flow of respiratory gas is controlled by the ventilator during a breath.
A ventilation “mode”, on the other hand, is a set of rules controlling how multiple subsequent breaths should be delivered. Modes may be mandatory, that is controlled by the ventilator, or spontaneous, that is that allow a breath to be delivered or controlled upon detection of a patient's effort to inhale, exhale or both. For example, a simple mandatory mode of ventilation is to deliver one breath of a specified mandatory breath type at a clinician-selected respiratory rate (e.g., one breath every 6 seconds). Until the mode is changed, ventilators will continue to provide breaths of the specified breath type as dictated by the rules defining the mode. For example, breath types may be mandatory mode breath types (that is, the initiation and termination of the breath is made by the ventilator) or spontaneous mode breath types (which refers to breath types in which the breath is initiated and/or terminated by the patient). Examples of breath types utilized in the spontaneous mode of ventilation include proportional assist (PA) breath type (including different versions of PA, such as plus and optimized), tube compensated (TC) breath type, volume support (VS) breath type, pressure support (PS) breath type, and etc. Examples of mandatory breath types include a volume control breath type, a pressure control breath type, and etc.
FIG. 1 illustrates a schematic diagram of an aspect of an exemplary ventilator 100. The exemplary ventilator 100 illustrated in FIG. 1 is connected to a human patient 150. Ventilator 100 includes a pneumatic system 102 (also referred to as a pressure generating system 102) for circulating breathing gases to and from patient 150 via the ventilation tubing system 130, which couples the patient 150 to the pneumatic system 102 via an invasive (e.g., endotracheal tube, as shown) or a non-invasive (e.g., nasal mask) patient interface 180.
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 aspect, a fitting, typically referred to as a “wye-fitting” 170, may be provided to couple the patient interface 180 (shown as an endotracheal tube in FIG. 1 ) 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, accumulator and/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 and/or through the inspiratory limb 132 according to prescribed ventilatory settings. The inspiratory module 104 is associated with and/or controls an inspiratory valve for controlling gas delivery to the patient 150 and/or gas delivery through the inspiratory limb 132. In some aspects, inspiratory module 104 is configured to provide ventilation according to various ventilator modes, such as mandatory, spontaneous, and/or assist modes.
The expiratory module 108 is configured to release gases from the patient's lungs according to prescribed ventilatory settings. The expiratory module 108 is associated with and/or controls an expiratory valve for releasing gases from the patient 150. In some aspects, expiratory module 108 is configured to release gas according to various ventilator modes, such as mandatory, spontaneous, and/or assist modes.
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. FIG. 1 illustrates a sensor 107 (e.g., flow sensor, pressure sensor, etc.) in pneumatic system 102.
The ventilator 100 may also include one or more non-invasive sensors 107 communicatively coupled to ventilator 100. Sensors are referred to herein as non-invasive when the sensors are located externally to patient. For example, sensors located in the patient wye 170, in the expiratory module 108, in the inspiratory module 104, or on the patient's finger are all external to the patient and are non-invasive. Sensors are referred to herein as invasive when the sensors are located within the patient or placed inside the patient's body, such as sensors located in an endotracheal tube, near a patient diaphragm, or on an esophageal balloon. While invasive sensors can provide great patient data or measurements, these sensors can often be hard to maintain or keep properly positioned. For example, an esophageal balloon can easily be knocked out of proper position in response to patient movement. Once moved, all of the data recorded from the sensors on the balloon are inaccurate. Further, if condensation or material corrupts the sensor and interferes with accurate measurements, the invasive sensor has to be removed from the body to service and/or clean it. Further, because invasive sensors are located within the patient, they usually require the patient to be sedated or undergo a surgical procedure for implantation or positioning adjustment. As such, invasive sensors are burdensome to the patient, hard to implant, hard to maintain, and hard to keep positioned when compared to non-invasive sensors. The embodiment of FIG. 1 illustrates a sensor 107 in pneumatic system 102.
Sensors 107 may communicate with various components of ventilator 100, e.g., pneumatic system 102, other sensors 107, expiratory module 108, inspiratory module 104, processor 116, controller 110, cycling module 118, and any other suitable components and/or modules. A module as used herein refers to memory, one or more processors, storage, and/or other components of the type commonly found in command and control computing devices. In one aspect, sensors 107 generate output, such as measurements, and send this output to pneumatic system 102, other sensors 107, expiratory module 108, inspiratory module 104, processor 116, controller 110, cycling module 118, and 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 inspiratory or expiratory triggering, for example. Sensors 107 may be placed in any suitable location, e.g., within the ventilatory circuitry or other devices communicatively coupled to the ventilator 100. For example, in some aspects, one or more sensors 107 may be located in an accumulator. 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 module 104 and/or expiratory module 108 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 aspects, sensors 107 may be provided at or near the lungs (or diaphragm) for detecting a pressure in the lungs. Additionally or alternatively, sensors 107 may be affixed or embedded in or near wye-fitting 170 and/or patient interface 180. Any sensory device useful for monitoring changes in measurable parameters during ventilatory treatment may be employed in accordance with aspects described herein. For example, in some aspects, the one or more sensors 107 of the ventilator 100 include an inspiratory flow sensor and an expiratory flow sensor.
As should be appreciated, with reference to the Equation of Motion, ventilatory parameters are highly interrelated and, according to aspects, 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 according to the Equation of Motion or other known relationships from the monitored parameters.
The cycling module 118 monitors a physiological parameter of the patient for each sample period from sensor output from one or more sensors. In some aspects, the sample period as used herein refers to a discrete period of time required to monitor a physiological parameter. In some aspects, the sample period is a computation cycle for the ventilator 100. In some aspects, the sample period is every 5 milliseconds (ms), 10 ms, 15 ms, 20 ms, 25 ms, or 30 ms. This list is exemplary only and is not meant to be limiting. Any suitable sample period for monitoring a physiological parameter of the patient may be utilized by the ventilator 100 as would be understood by a person of skill in the art. In some aspects, the cycling module 118 estimates and/or calculates the physiological parameter for monitoring based on the sensor output from one or more sensors. In other aspects, cycling module 118 determines the physiological parameter for monitoring directly from the sensor output received from the one or more sensors. The physiological parameter may be any suitable physiological parameter for determining a patient initiated cycle as would be known by a person of skill in the art. In some aspects, the physiological parameter is flow rate, net flow, pressure, estimated pressure, estimated flow, other derived signals, and/or etc. This list is exemplary only and is not meant to be limiting.
After determining the physiological parameter, the cycling module 118 may send the physiological parameter to any suitable component and/or module of the ventilator 100, such as the pneumatic system 102, expiratory module 108, inspiratory module 104, processor 116, controller 110, and/or etc. In other aspects, the cycling module 118 receives the physiological parameter measurements from other components of the ventilator, such as a sensor 107, controller 110, and/or processor 116.
The cycling module 118 processes the physiological parameter to detect patient cycling efforts. In some aspects, the cycling module 118 processes the physiological parameter to determine a P_MUSto detect patient cycling efforts. In further aspects, the cycling module 118 processes the physiological parameter to determine a P_MUS-based metric to detect patient cycling efforts.
The cycling module 118 calculates the P_MUSbased on measured flow and/or pressure and based on calculated resistance and/or compliance. During a PA breath type, the ventilator is configured to calculate resistance, compliance, and a P_MUSutilizing non-invasive sensor measurements. Unlike other spontaneous breath types, the PA breath type can calculate compliance and resistance. Knowing compliance and resistance, an estimate of the diaphragmatic muscle pressure can be computed non-invasively. In other spontaneous breath types, an invasive sensor located in an esophageal balloon is needed to measure the diaphragmatic pressure. However, an esophageal balloon can easily become dislodged if the patient moves affecting sensor accuracy, is highly invasive to implant, and/or is uncomfortable for a spontaneously breathing patient. Due to the disruptive nature of the esophageal balloon, the esophageal balloon is rarely utilized during a spontaneous breath type. As such, other spontaneous breath types, such as TC, PS and VS, the ventilator is not configured to calculate resistance, compliance, and/or P_MUSutilizing non-invasive sensor measurements. Accordingly, the cycling module 118 during a spontaneous breath type that is not a PA breath type will temporarily switch from the current breath type into the PA breath type for a predetermined number of breaths, time or measurements in order to calculate resistance and/or compliance and then estimate P_MUSbased on one or more non-invasive sensor measurements.
A PA breath type refers to a type of ventilation in which the ventilator acts as an inspiratory amplifier that provides pressure support based on the patient's effort. Usually, the degree of amplification (the “percent support setting”) during a PA breath type is set by an operator or clinician, for example as a percentage based on the patient's effort. However, during a temporary implementation of the PA breath type, the cycling module 118 determines the percent support setting provided during the temporary PA breath type.
In one implementation of a PA breath type, the ventilator may continuously monitor the patient's instantaneous inspiratory flow and instantaneous net lung volume, which are indicators of the patient's inspiratory effort. These signals, together with ongoing estimates of the patient's lung compliance and lung/airway resistance and the Equation of Motion (Pmus=Pwye−Pend_exp−(Rtube+Rrs)×Q_lung−∫Q_lung ^dt/Crs), allow the ventilator to estimate/calculate a patient effort and derive therefrom a target airway pressure to provide the support that assists the patient's inspiratory muscles to the degree selected by the operator as the percent support setting. In this equation, the patient effort is estimated inspiratory muscle pressure and is negative.
Due to the unique configuration of the PA breath type, the PA breath type is capable of determining a patient respiratory system compliance and/or resistance in an end inspiratory hold of 300 ms or 0.3 seconds, which will usually go unnoticed by a spontaneously breathing patient. In a typical PA breath type, this 300 ms end inspiratory hold is provided intermittently at random. During a temporary PA breath type, the 300 ms end inspiratory hold may be provided in the first, second, third, and/or fourth breath of the temporary PA breath type. Any additional 300 ms holds are provided after a predetermined number of breaths or after a set time period during the temporary PA breath type. In other words, the temporary PA breath type does not provide the 300 ms end inspiratory hold at random but instead at predetermined intervals. As such, the cycling module 118 is able to calculate patient respiratory compliance and patient respiratory system resistance. The cycling module 118 utilizes the following equation to determine patient respiratory system compliance:
C _RAW=(V _LUNG/Pressure_delta).
The cycling module 118 utilizes the following equation to determine patient respiratory system resistance:
R _RAW =R _RAW+ET −R _ET,

- where:
- R_RAWis patient respiratory system resistance;
- R_RAW+ETis the combined resistance of the patient respiratory system and the endotracheal tube/tracheostomy tube resistance; and
- R_ETis endotracheal tube/tracheostomy tube resistance.
- R_RAW+ETis the difference in lung pressure and wye pressure divided by the estimated lung flow. The lung pressure may be based upon the lung pressure at the beginning of exhalation minus exhaled volume times the elastance. Wye pressure is estimated as the measured pressure within the ventilator breathing system (VBS) at the circuit wye, which is compensated for breathing circuit limb resistance.

During the temporary PA breath type, the cycling module 118 calculates patient respiratory resistance and/or compliance based on non-invasive sensor output. The cycling module 118 provides the temporary PA breath type for at least one breath. In some aspects, the cycling module 118 provides the temporary PA breath type for at least three breaths. In some aspects, the cycling module 118 provides the temporary PA breath type until a predetermined number of patient respiratory compliance and/or resistance measurements or calculations have been made by the ventilator 100. In some aspects, the cycling module 118 provides the temporary PA breath type until at least two or three patient respiratory compliance and/or resistance measurements have been made by the ventilator 100. In other aspects, the cycling module 118 provides the temporary PA breath type until at least one, two, three, four, or five patient respiratory compliance and/or resistance measurements have been made by the ventilator 100. The predetermined number of patient respiratory compliance and/or resistance measurements can be completed in 1 breath, 2 breaths, 3 breaths, 5 breaths, 7 breaths, 8 breaths, 10 breaths, 12 breaths, 15 breaths, 20 breaths, 25 breaths or 30 breaths. In other aspects, a predetermined number of patient respiratory compliance and/or resistance measurements can be completed by the cycling module 118 in 4 to 12 breaths.
After the temporary PA breath type has been completed (e.g., the predetermined number of patient respiratory compliance and/or resistance measurements have been made by the ventilator 100), the cycling module 118 switches the ventilation of the patient back to the previously utilized spontaneous breath type (TC, PS or VS).
After the return to the previously utilized spontaneous breath type, the cycling module 118 monitors respiratory data of the patient, such as the non-invasive sensor output. In some aspects, the cycling module 118 calculates a P_MUSof the patient during the spontaneous breath type utilizing the respiratory system compliance and/or the respiratory system resistance calculated during the temporary PA breath type, and the current respiratory data measured after the return to TC, VS or PS breath type.
The cycling module 118 measures the P_MUSrepeatedly throughout a breath. In some aspects, the cycling module 118 measures P_MUSevery servo cycle, such as every 2 milliseconds, 5 millisecond, or 10 milliseconds. The servo cycle is a fixed, periodic amount of time during which sensor data from sensors 107 are sampled, control calculations are made by the processor 116 or controller 110 of the ventilator 100, and new valve or actuator commands are issued. In some aspects, the sensors 107 send output or measurements every servo cycle. The cycling module 118 communicates the P_MUSto other modules, such as the controller 110, the pneumatic system 102, and/or the display 122.
During ventilation with a spontaneous breath type other than the PA breath type, when the P_MUS-based metric is utilized to determine cycling, the cycling module 118 determines when to perform the temporary switch into the PA breath type by monitoring input to determine the occurrence of one or more conditions. In some aspects, the cycling module 118 monitors the measurements from the non-invasive sensors. In other aspects, the cycling module 118 monitors other received ventilator data or calculations to determine the occurrence of the condition.
In some aspects, the condition may be any event that is indicative of a change in patient respiratory system compliance and/or patient respiratory system resistance, such as a predetermined pressure differential, volume differential, a tidal volume differential, a specific flow waveform shape, a specific volume waveform shape, a specific pressure waveform shape, a predetermined change in pressure, a predetermined change in flow, a predetermined change in tidal volume and/or etc. For example, the condition may be a change in non-invasively monitored flow, pressure, and/or of volume of at least 25%. In other aspects, the condition is an expiration of a set period or predetermined number of breaths, since the last temporary PA breath type switch or since the start of the last temporary PA breath type. For example, the condition may be the expiration of 30, 60, 90, or 120 minutes or the occurrence of 400, 300, or 200 breaths since the last temporary switch into the PA breath type or the start of the last temporary PA breath type. In other examples, the cycling module 118 monitors for the following condition to occur: 1) expiration of 1 hour since the last temporary PA breath type; or 2) a 25% change in one of non-invasively measured pressure, flow, or tidal volume during the spontaneous breath type that is not a PA breath type. If the breath type was just initialized, the conditions discussed above may be monitored from the start of ventilation or the start of the breath type instead of since the last temporary switch into the PA breath type or the start of the last temporary PA breath type. If the cycling module 118 detects a condition, the cycling module 118 of the controller 110 determines a percent support setting and sends instructions to the pressure generating system 102 to provide a short temporary switch into a PA breath type utilizing the determined percent support setting.
In some aspects, the cycling module 118 determines a percent support setting for the temporary PA breath by utilizing a predetermined or preset percent support setting. In other aspects, the cycling module 118 determines a percent support setting based on a target setting for the spontaneous breath type that is not the PA breath type. For example, if the target pressure for the PS breath type is 10 cm H₂O, then the cycling module 118 will determine a percent supporting setting for the temporary PA breath to achieve approximately the same pressure level. In another example, if the target volume for a VS breath type is 400 ml, then the cycling module 118 will determine a percent support setting for the temporary PA breath to achieve approximately the same volume level. In other aspects, the percent setting is determined by the cycling module 118 based on outputs from the non-invasive sensor. For example, if inspiratory pressure measurement is 9.8 cm H₂O from inspiratory pressure sensor, then the cycling module 118 will determine a percent support setting for the temporary PA breath to achieve approximately the same pressure level. In further aspects, the cycling module 118 may utilize additional ventilator parameters or inputs to the target setting and/or the outputs from the non-invasive sensor to determine a percent support setting for the temporary PA breath, such as mask type, patient circuit diameter, and etc.
The cycling module 118 may compare the P_MUS-based metric to a cycling threshold to form a comparison. If the P_MUS-based metric meets the cycling threshold based on the comparison, the cycling module 118 determines that the patient is making an effort to end inhalation and start exhalation. If the P_MUS-based metric does not meet the cycling threshold based on the comparison, the cycling module 118 determines that the patient is not making an effort to end inhalation and start exhalation. In response to determining that the patient is not making an effort to end inhalation and start exhalation, the cycling module 118 continues to the monitor the P_MUS-based metric and compare it to the cycling threshold. The cycling threshold may be dynamic and/or dependent on the magnitude of P_MUS-based metric.
In response to determining that the patient is making an effort to end inhalation and start exhalation, the cycling module 118 performs one or more actions. The one or more actions may include cycling, providing a notification, providing a recommendation, determining cycling synchrony, displaying a detected cycling effort, recommending a parameter change, and/or automatically changing a parameter.
In some aspects, the one or more actions may include sending a command to end inspiration and begin exhalation. In these aspects, the spontaneous breath types may be adjusted to cycle in response meeting a P_MUS-based metric threshold instead of based on E_SENS(such as a percent of peak flow or a set flow value in Lpm) in PS, VS, TC or PA. In these aspects, the ventilator effectively identifies the end of patient inspiratory effort and determines the optimal time to trigger the expiratory phase. Based on this approach, cycling to the expiratory phase will be variable based on patient effort and will not be purely dependent upon exhaled flow. The cycling module 118 minimizes the patient-to-ventilator asynchrony and provides a feature that is easy to use by the clinician since the clinician does not have to set an E_SENSas a primary cycling mechanism.
The one or more actions may include determining if exhalation was provided by the breath type within an interval of time of the detected cycling effort. In these aspects, cycling is still controlled by E_SENSin PS, VS, TC and PA and can be influenced by the percent support setting in PA and the rise-time setting in PS or VS. As such, the cycling module 118 determines if the detected cycling effort occurred within a predetermined amount of time of the cycling effort delivered by the spontaneous breath type. In some aspects, the interval of time may be about 300 ms. If the detected effort is not within the interval of time from the delivered exhalation, the cycling module 118 determines asynchronous cycling. In response to determining asynchronous cycling, the cycling module 118 may provide a notification (such as a notification of an asynchronous cycling), provide a recommendation (such as a recommendation to adjust E_SENSfor a VS, PS, TC or PA breath type or percent support setting for PA breath type), automatically adjust a ventilator setting (such as automatically adjust E_SENSfor a VS, PS, TC or PA breath type or percent support setting for PA breath type).
In other aspects, the one or more actions may include displaying the detected cycling effort. In some aspects, the detected cycling effort may be displayed on a waveform. In other aspects, a prompt may indicate that a cycling effort was detected and/or missed. In further aspects, the one or more actions may include providing, such as displaying, a recommendation to change a percent support setting in PA, an E_SENSsetting in PS, VS, TC or PA, or a rise-time setting in PS or VS, as discussed above. For example, if the detected cycling effort happened before exhalation was delivered, the cycling module 118 may recommend increasing the E_SENSsetting or decreasing the percent support setting. If the detected cycling effort happened after exhalation was delivered, the cycling module 118 may recommend decreasing the E_SENSsetting or increasing the percent support setting. In further aspects, the one or more actions may include automatically changing a percent support setting in PA, an E_SENSsetting in PS, VS, TC or PA, or a rise-time setting in PS or VS. For example, if the detected cycling effort happened before exhalation was delivered, the cycling module 118 may automatically increase the E_SENSsetting or decrease the percent support setting. For example, if the detected cycling effort happened after exhalation was delivered, the cycling module 118 may automatically decrease the E_SENSsetting or increase the percent support setting.
The cycling module 118 ends inspiration by sending instructions and/or a command to a pneumatic system 102, an expiratory module 108, an inspiratory module 104, a processor 116, and/or a controller 110. The instructions and/or commands cause the one or more ventilator components and/or modules to change the delivered flow and/or pressure and to adjust the valves as needed to end inspiration and start exhalation.
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 (e.g., sensor(s) 107), 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 some aspects, the operator interface 120 of the ventilator 100 includes a display 122 communicatively coupled to ventilator 100. Display 122 may provide various input screens, for receiving clinician input, and various display screens, for presenting useful information to the clinician. In aspects, 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.
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. In some aspects, the display 122 illustrates a physiological parameter, a graph or waveform of the physiological parameter, a graph or waveform of P_MUS, a detected patient cycle effort, an exhalation sensitivity, a cycle type, a recommendation, a notification, and/or any other information known, received, or stored by the ventilator 100.
In some aspects, controller 110 includes 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 the cycling module 118 as illustrated in FIG. 1 . In alternative aspects, the cycling module 118 is located in other components of the ventilator 100, such as in the pressure generating system 102 (also known as the pneumatic system 102) or inspiratory module 104.
The memory 112 includes non-transitory, computer-readable storage media that stores and/or encodes software (or computer readable instructions) that is executed by the processor 116 and which controls the operation of the ventilator 100. In an aspect, the memory 112 includes one or more solid-state storage devices such as flash memory chips. In an alternative aspect, 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.
FIG. 2 illustrates an example of a method 200 for cycling from inspiration to exhalation during ventilation of a patient on a ventilator. In some aspects, method 200 cycles to exhalation based on the monitoring of a P_MUS-based metric. As such, method 200 provides spontaneous ventilation utilizing a cycling setting. Method 200 begins at the start of spontaneous ventilation utilizing a cycling setting. As discussed above, method 200 can detect a patient's attempt to exhale. In other aspects, method 200 improves ventilator synchrony by detecting patient efforts to exhale and/or by changing or recommending setting changes to improve cycling.
As illustrated, method 200 includes a monitor operation 202, a process operation 204, a compare operation 206, a threshold decision operation 208, and an action operation 214. In some aspects, method 200 also includes an optional timing operation 210 and/or an optional missed cycling determination operation 212.
During the monitor operation 202, the ventilator monitors a physiological parameter based on one or more sensor measurements for each sample period in a first set of sample periods during inspiration. In some aspects, the ventilator during the monitor operation 202 monitors flow, pressure, and/or other derived signals, such as a P_MUS-based metric. Sensors suitable for this detection may include any suitable sensing device as known by a person of skill in the art for a ventilator, such as an inspiratory flow sensor, inspiratory pressure sensor, an exhalation flow sensor, an exhalation pressure sensor, and/or exhalation auxiliary pressure sensor. In further aspects, the one or more sensor measurements are from one or more non-invasive sensors. In further aspects, the ventilator during the monitor operation 202 is delivering inhalation.
During the process operation 204, the ventilator processes the one or more received sensor measurements of the physiological patient parameter. In some aspects, the ventilator processes the received sensor measurements of the physiological parameter by calculating a P_MUSor a P_MUS-based metric based on the received sensor measurements. Accordingly, the one or more processed parameters include P_MUSor a P_MUS-based metric.
During the compare operation 206, the ventilator compares the one or more processed parameters to a cycling threshold. For example, the P_MUS-based metric is compared to a cycling threshold. In other aspects, the cycling threshold for the P_MUS-based metric may be a dynamic function of its magnitude.
Next, during threshold decision operation 208, the ventilator determines if the one or more processed parameters meet a cycling threshold based on the comparison of the one or more processed parameters to the cycling threshold performed during operation 206. In some aspects, the ventilator during threshold decision operation 208 determines a patient intention to cycle based on the comparison of a P_MUS-based metric to a cycling threshold. For example, the ventilator may determine based on a shape of the P_MUScurve a patient intention to cycle. Alternatively, the ventilator may compare one or more measured parameters to an E_SENSsetting to determine a patient intention to cycle. In other aspects, the ventilator during threshold decision operation 208 determines if a patient intends to cycle based on the comparison of a P_MUS-based metric to a cycling threshold and scores or grades the asynchrony based on the comparison. An example of a score or grade of asynchrony includes an asynchrony index.
If a patient intention to cycle is detected, the method progresses to cycling operation 216. Additionally, if a patient intention to cycle is detected, an optional evaluation of cycling characteristics may be performed at evaluation operation 210. Alternatively, if a patient intention to cycle is not detected, the method may return to monitor operation 202.
At optional evaluation operation 210, if the ventilator during threshold decision operation 208 determines or detects that a threshold has been met, then the ventilator may evaluate one or more cycling conditions associated with the patient intention to cycle. For instance, the ventilator may evaluate the shape of the P_MUScurve. Additionally or alternatively, the ventilator may evaluate a timing of the ventilator cycling versus a timing of the patient intention to cycle. For instance, at evaluation operation 210, the ventilator may evaluate the shape of the P_MUScurve to determine whether the curve is normal or abnormal. In other aspects, at evaluation operation 210, the ventilator may evaluate a timing of the detected patient intention to cycle to a timing of the cycling delivered by the ventilator. Based on the evaluation, the ventilator may determine whether characteristics of the patient intention to cycle are normal or abnormal. In aspects, when the P_MUScurve is abnormal or the timing of the patient intention to cycle is abnormal, a percent support setting, a rise-time setting, or an E_SENSsetting may be inappropriate.
At decision operation 212, the ventilator determines or detects if characteristics of the detected patient intention to cycle are normal or abnormal. For instance, if the shape of the P_MUScurve is indicative of the patient actively exhaling (see e.g., FIG. 5 ), the P_MUScurve may be identified as “abnormal.” Additionally or alternatively, if the timing of the patient intention to cycle falls outside of a timing threshold, the timing may be identified as “abnormal.” In aspects, timing of ventilator cycling may be abnormal when the timing of ventilator cycling is too early (before the patient intention to cycle) or too late (after the patient intention to cycle). In some aspects, the timing of the ventilator cycling may be compared to a patient neural inspiratory time (e.g., a P_MUS-based characteristic) to determine whether characteristics of the patient intention to cycle are abnormal. If the ventilator determines or detects during decision operation 212 that the characteristics of the patient intention to cycle (e.g., the P_MUScurve, the timing, or the like) are not abnormal, the ventilator may return to monitor operation 202. If the ventilator determines or detects during decision operation 212 that the characteristics of the patient intention to cycle (e.g., the P_MUScurve, the timing, or the like) are not abnormal, the ventilator is in synchrony with the patient exhalation demand. Alternatively, if the ventilator determines or detects during decision operation 212 that the characteristics of the patient intention to cycle (e.g., the P_MUScurve, the timing, or the like) are abnormal, the ventilator may progress to optional action operation 214. If the ventilator determines or detects during decision operation 212 that the characteristics of the patient intention to cycle (e.g., the P_MUScurve, the timing, or the like) are abnormal, the ventilator is not in synchrony with the patient exhalation demand.
At optional action operation 214, the ventilator may performs an action. In some aspects, the action is performed in response to detection that characteristics of a patient intention to cycle are abnormal at decision operation 208. In these aspects, the action may be one or more of: a notification of a missed cycling effort, display of a missed cycling effort, a recommendation to change a ventilator setting (e.g., a percent support setting or an E_SENSsetting), an automatic change of a ventilator setting, and/or notification of an automatic change of ventilator setting. In some aspects, the ventilator may recommend or automatically change percent support setting or an E_SENSsetting during a PA, TC, VS or PS breath type. In other aspects, the ventilator may additionally or alternatively recommend or automatically change a rise-time setting during a VS or PS breath type.
In some aspects, where the processed parameter is a P_MUS-based metric and the set breath type is TC, PS or VS, the process operation 204 includes several additional steps to determine the P_MUS-based metric as illustrated in FIG. 3 . For example, in these aspects, the process operation 204 may include a determination operation 302, a support setting operation 304, a switch operation 306, an analyze operation 308, a respiratory mechanics estimation operation 310, and a return operation 312.
FIG. 3 is a flow diagram illustrating a method for performing process operation 204 of FIG. 2 when the spontaneous breath type is TC, PS or VS and the processed parameter is a P_MUS-based metric during ventilation of a patient with a ventilator, in accordance with aspects of the disclosure.
At determination operation 302, the ventilator determines if a condition occurred. In some aspects, the ventilator during determination operation 302 monitors non-invasive sensor output to determine if the condition has occurred. In other aspects, the ventilator during determination operation 302 monitors the number of delivered breaths or the passage of time to determine if a condition has occurred. If the ventilator determines that the condition occurred at determination operation 302, the ventilator selects to perform support setting operation 304. If the ventilator determines that the condition did not occur during determination operation 302, the ventilator selects to continue to monitor the non-invasive sensor output during determination operation 302. The condition may be the expiration of a predetermined amount of time, the delivery of a predetermined number of breaths, and/or a change in one or more monitored parameters that indicates that a change in patient respiratory system compliance and/or resistance has occurred. In some aspects, the condition is a change in monitored pressure, monitored tidal volume, or monitored flow of at least 25%. In other aspects, the condition is expiration of 1 hour from the last use of a temporary PA breath type without a change in monitored pressure, monitored tidal volume, monitored flow by a specific value (such as 3 Lpm), or monitored flow of at least 25% since the last temporary PA breath type. In further aspects, the condition is the delivery of 200 breaths from the last use of the temporary PA breath type without a change in monitored pressure, monitored tidal volume, monitored flow by a specific value (such as 3 Lpm), or monitored flow of at least 25% since the last temporary PA breath type.
At support setting operation 304 the ventilator determines a percent support setting for a temporary PA breath type. In some aspects, at support setting operation 304, the ventilator utilizes a predetermined support setting. In other aspects, at support setting operation 304 the ventilator selects a support setting based on at least one of a target setting from the spontaneous TC, PS or VS breath type or the non-invasively measured respiratory data collected during the TC, PS or VS spontaneous breath type. In further aspects, the ventilator during support setting operation 304 determines other settings for the temporary PA breath type. For example, a PEEP level for the temporary PA breath type may be set based on a PEEP level utilized in the spontaneous TC, PS or VS breath type.
Next, switch operation 306 is performed by the ventilator. At switch operation 306 the ventilator automatically and temporarily switches from the TC, PS or VS spontaneous breath type into a temporary PA breath type for at least one breath utilizing the determined or calculated percent support setting. In some aspects, at switch operation 306 the ventilator automatically and temporarily switches from the spontaneous TC, PS or VS breath type into the temporary PA breath type for at least three breaths utilizing the determined or calculated percent support setting. The temporary PA breath type is performed for at least one breath, at least two breaths, or at least three breaths. In some aspects, the temporary PA breath type is delivered by the ventilator during switch operation 306 until at least one patient respiratory system compliance and/or resistance measurement has been obtained. In some aspects, the temporary PA breath type is delivered by the ventilator during switch operation 306 until at least two different patient respiratory system compliance and/or resistance measurements have been obtained. In some aspects, the temporary PA breath type is delivered by the ventilator during the switch operation 306 until 5, 4, 3, or 2 patient respiratory system compliance and/or resistance measurements have been obtained. As such, the ventilator may deliver ventilation utilizing the temporary PA breath type for at most 4 breaths, 8 breaths, 10 breaths, 12 breaths, 15 breaths, 20 breaths, 30 breaths, 40 breaths, or 50 breaths.
The ventilator during the PA collect and analyze operation 308, collects and analyzes the non-invasively measured respiratory data during the temporary PA breath type. Next, a respiratory mechanics estimation operation 310 is performed by the ventilator. During the respiratory mechanics estimation operation 310, the ventilator calculates or estimates the patient respiratory system compliance and/or resistance based on the non-invasively measured respiratory data taken during the temporary PA breath type during the PA collect and analyze operation 308. If multiple patient respiratory system compliance and/or resistance measurements are taken by the ventilator during respiratory mechanics estimation operation 310, the ventilator determines a compliance measurement and/or a resistance measurement based on these multiple measurements. For example, if multiple patient respiratory system compliance measurements are taken, the ventilator may average the measurements or select the middle or last obtained measurement to be utilized as the temporary PA breath type calculated compliance measurement for use during process operation 204.
At return operation 312 the ventilator switches from the temporary PA breath type back to the previously utilized spontaneous TC, PS or VS breath type. As discussed above, the ventilator returns to the spontaneous TC, VS or PS breath type after a predetermined number of patient respiratory system compliance or resistance measurements have been obtained during the temporary PA breath type, after a predetermined number of breaths, or after a predetermined amount of time.
FIG. 4 is a graph illustrating a P_MUScurve of a volunteer in response to additional externally applied resistance. In this example, P_MUSends coincident with cycling at 402 as indicated by the synchronicity with the ventilator phase signal. Upon application of external resistance of 10 (R=10), P_MUSof the volunteer is elevated during exhalation, as shown by the upward slope of the P_MUScurve at 404. In this case, active exhalation is indicated.
FIG. 5 is a graph illustrating a missed cycle during ventilation of a volunteer in the laboratory with a ventilator based on P_MUSmonitoring, in accordance with aspects of the disclosure. In this example, the volunteer is being ventilated in a PA breath type with a plateau breath. The PA support setting was set to 95% to force the over-support condition and the volunteer was ventilated. In this case, the volunteer was intentionally over-supported. As shown by FIG. 5 , the P_MUSshape pushed to positive pressure (as shown by reference circle 502), which indicates that the patient was actively exhaling in response to the over-support. The ventilator did not deliver exhalation until about a 1.5 seconds later, which is outside of a time interval of 300 ms. As such, in this example, the ventilator detects a missed exhalation attempt. Accordingly, the ventilator may perform an action in response to this determination, such as display a missed cycle, indicate that the percent support setting is set too high, recommend lowering the percent support setting, and/or automatically lower the percent support setting to eliminate over-support. Additionally or alternatively, the ventilator indicate that the E_SENSsetting is too low, may recommend increasing the E_SENSsetting, or may automatically increase the E_SENSsetting to improve cycling synchrony.
FIG. 6 illustrates the tidal volume and flow curves for ventilation of the volunteer in FIG. 5 . At just after time of 37 s, the flow waveform peaks in response to the volunteer pushing back against the ventilator's over-support, that is, actively exhaling to avoid over-delivery. This peak is in synchrony with the pressure waveform peak of FIG. 5 . The volume waveform shows the high inspired volume (nearly 1800 mL) in response to this self-truncated breath.
FIG. 7 is a graph illustrating P_MUSof an intubated volunteer as measured by an esophageal catheter during a PA breath type. In this example, the inverted P_MUSshape 702 is due to the sign of the catheter pressures. This waveform shows the relationship between the ventilator pressure at the patient connection port or “wye” and the measured P_MUScurve or the difference between the gastric and esophageal pressures that cross the diaphragm muscle (lower large dashed line). In this case, there is late ventilator triggering that might have been created by a trigger sensitivity that was too high. However, the cycling was reasonably synchronous with the end of the P_MUSeffort. This demonstrates good cycling synchrony.
FIG. 8 is a graph illustrating P_MUSof an intubated volunteer as measured by an esophageal catheter during high-percentage support. In this example, percent support is set to 80% and the patient appears to be pushing against the ventilator due to the rise in gastric pressure at 802. For comparison, see the flat gastric curve at 704 in FIG. 7 . Additionally, there is a late rise in Pwye at 804 and an early reversal of P_MUSat 806 indicating that the volunteer is actively exhaling in the middle of the inspiratory phase. The P_MUScurve also shows a flat push 808 at the end of inhalation to a lower pressure than at the start of the inhalation. Based on the indications associated with over-support illustrated by FIG. 8 , the ventilator may indicate that the percent support setting is set too high, may recommend lowering the percent support setting, and/or may automatically lower the percent support setting to eliminate over-support. Additionally or alternatively, the ventilator indicate that the E_SENSsetting is too low, may recommend increasing the E_SENSsetting, or may automatically increase the E_SENSsetting to improve cycling synchrony.
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 aspects 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 aspects described herein may be combined into single or multiple aspects, and alternate aspects 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 aspects have been described for purposes of this disclosure, various changes and modifications may be made which are well within the scope of the disclosure. 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.

Claims

What is claimed is:

1. A ventilator system comprising:

at least one sensor;

a gas-delivery system configured to deliver ventilation gases to a patient;

at least one processor; and

at least one memory comprising computer-executable instructions that when executed by the at least one processor cause the ventilator system to:

receive one or more sensor measurements from the at least one sensor during inhalation of the patient;

based on the one or more sensor measurements, estimate a physiological parameter of the patient during the inhalation of the patient;

in response to determining that the physiological parameter meets a cycling threshold, determine a patient intention to cycle from inhalation to exhalation;

evaluate one or more characteristics of the patient intention to cycle from inhalation to exhalation;

when the one or more characteristics of the patient intention to cycle from inhalation to exhalation are abnormal, determine a missed cycling effort; and

perform an action in response to the missed cycling effort.

2. The ventilator system of claim 1, wherein ventilation is delivered to the patient based on one of: a volume support (VS) breath type, a pressure support (PS) breath type, or a tube compensated (TC) breath type.

3. The ventilator system of claim 2, wherein the computer-executable instructions further causing the ventilator system to:

temporarily switch to a proportional assist (PA) breath type; and

while delivering the temporary PA breath type, receive the one or more sensor measurements from the at least one sensor during the inhalation of the patient.

4. The ventilator system of claim 3, wherein the computer-executable instructions further causing the ventilator system to:

estimate a respiratory mechanics parameter based on the one or more sensor measurements received while delivering the temporary PA breath type; and

based on the estimated respiratory mechanics parameter, estimate the physiological parameter of the patient during the inhalation of the patient.

5. The ventilator system of claim 4, wherein the estimated respiratory mechanics parameter is at least one of: a resistance or a compliance of the patient.

6. The ventilator system of claim 2, wherein the computer-executable instructions further causing the ventilator system to:

determine a percent support setting based on one of a pressure support setting or a volume support setting.

7. The ventilator system of claim 1, wherein the physiological parameter is an estimate of a muscle pressure (P_MUS).

8. The ventilator system of claim 1, wherein the computer-executable instructions further causing the ventilator system to determine a percent support setting based on one of a pressure support setting or a volume support setting.

9. The ventilator system of claim 8, wherein the computer-executable instructions further causing the ventilator system to:

temporarily switch to a proportional assist (PA) breath type; and

deliver at least one breath based on the determined percent support setting.

10. The ventilator system of claim 1, wherein the action is at least one of displaying a notification or automatically adjusting a target setting for spontaneous ventilation.

11. A ventilator system comprising:

at least one sensor;

a gas-delivery system configured to deliver ventilation gases to a patient;

at least one processor; and

based on the one or more sensor measurements, estimate a muscle pressure (P_MUS) of the patient during the inhalation of the patient;

determine a P_MUS-based metric based on the estimate of P_MUS; and

in response to determining that the P_MUS-based metric meets a cycling threshold, determine a patient intent to cycle from inhalation to exhalation.

12. The ventilator system of claim 11, wherein the computer-executable instructions further causing the ventilator system to:

in response to determining the patient intent to cycle, compare a timing of the patient intent to cycle to a timing of exhalation delivery by the ventilator system; and

when the timing of the patient intent to cycle exceeds a timing threshold, determine a missed cycling effort.

13. The ventilator system of claim 12, wherein the computer-executable instructions further causing the ventilator system to:

in response to the missed cycling effort, perform at least one of: displaying a notification or automatically adjusting a target setting for spontaneous ventilation.

14. The ventilator system of claim 11, wherein the computer-executable instructions further causing the ventilator system to:

in response to determining that the P_MUS-based metric meets a cycling threshold, cycle from inhalation to exhalation.

15. The ventilator system of claim 11, wherein ventilation is delivered based on one of: a volume support (VS) breath type, a pressure support (PS) breath type, or a tube compensated (TC) breath type.

16. A method for detecting a patient intention to cycle during spontaneous ventilation of a patient on a ventilator, comprising:

receiving one or more sensor measurements from at least one sensor during inhalation of the patient;

based on the one or more sensor measurements, estimating a physiological parameter of the patient during the inhalation of the patient;

in response to determining that the physiological parameter meets a cycling threshold, determining a patient intention to cycle from inhalation to exhalation;

evaluating one or more characteristics of the patient intention to cycle from inhalation to exhalation;

when the one or more characteristics of the patient intention to cycle from inhalation to exhalation are abnormal, determining a missed cycling effort; and

perform an action in response to the missed cycling effort.

17. The method of claim 16, wherein the action is one of displaying a notification or automatically adjusting a target setting for spontaneous ventilation.

18. The method of claim 16, wherein the physiological parameter is an estimate of a muscle pressure (P_MUS).

19. The method of claim 16, wherein ventilation is delivered based on one of: a volume support (VS) breath type, a pressure support (PS) breath type, or a tube compensated (TC) breath type.

20. The method of claim 16, further comprising:

temporarily switching to a proportional assist (PA) breath type; and

while delivering the temporary PA breath type, receiving the one or more sensor measurements from the at least one sensor during the inhalation of the patient.