Patent Application
20210322711
The present invention relates to a ventilation apparatus for artificial ventilation of a patient, encompassing:
the respiratory gas conduit arrangement comprising at its proximal end a coupling configuration for coupling the respiratory gas conduit arrangement to a patient interface, for instance an endotracheal tube, a larynx mask, or a combination tube, and the like, that transfers respiratory gas between the respiratory gas conduit arrangement and the patient.
A similar ventilation apparatus is known from US 2013/0073013 A1. The known ventilation apparatus uses ambient air as a respiratory gas source, and uses a combination of a fan and a valve to quantitatively modify the flow of a respiratory gas flow in the ventilation apparatus. An evaporator/humidification apparatus is provided in order to humidify the respiratory gas as necessary. The respiratory gas flow flows over a water reservoir present in the evaporator/humidification apparatus and thereby picks up water vapor present above the water level of the water reservoir.
The ventilation apparatus known from US 2013/0073013 A1 further encompasses a heatable respiratory gas conduit arrangement to prevent undesired condensation of moisture out of the respiratory gas by delivering heat to the respiratory gas conduit arrangement.
A flow sensor for ascertaining the respiratory gas flow, a temperature sensor for detecting the temperature of the respiratory gas, and a moisture sensor for detecting the moisture content of the respiratory gas are provided downstream from the humidification apparatus of the known ventilation apparatus but before the heated section of the respiratory gas conduit apparatus begins, i.e. in the region of the distal end of the respiratory gas conduit arrangement. Sensors for detecting the ambient temperature and ambient relative humidity are furthermore provided.
Operating parameters of the ventilation apparatus can be adjusted, by a physician or by care personnel, via an input/output apparatus.
A control apparatus of the known ventilation apparatus controls the ventilation apparatus in a manner that is not further characterized. The control apparatus ascertains, from the detected ambient temperature and the detected ambient relative humidity, from the detected temperature of the respiratory gas flow and the detected moisture content of the respiratory gas flow, and further depending on operating data and design data of the respiratory gas conduit arrangement, a setpoint temperature for operation of the heating system of the respiratory gas conduit arrangement. The setpoint temperature is selected in such a way that the temperature in the respiratory gas conduit arrangement is above the respective dew point temperature. The control apparatus controls the heating system of the respiratory gas conduit arrangement depending on the selected setpoint temperature. According to the disclosure of US 2013/0073013 A1, the dew point temperature is obtained from the available psychrometric data, i.e. from the detected temperature and the detected relative moisture content of the respiratory gas flow.
A ventilation apparatus of the species is known from EP 2 143 459 B1. This too discloses a respiratory gas conduit arrangement having a respiratory gas source and having a fan as a flow modification apparatus. The ventilation apparatus known from EP 2 143 459 B1 likewise comprises an evaporator/humidification apparatus. This too has a water reservoir over which the respiratory gas flow flows during operation, the respiratory gas flow being humidified as it flows over.
That portion of the respiratory gas conduit arrangement of the known ventilation apparatus which extends from the humidification apparatus to the proximal longitudinal end of the respiratory gas conduit arrangement is heatable. In this portion, a flow sensor and a temperature sensor for ascertaining the temperature and the quantitative flow of respiratory gas are arranged in that longitudinal end region of the respiratory gas conduit arrangement which is located closer to the humidification apparatus. A proximal temperature sensor is also arranged at the proximal longitudinal end of the respiratory gas conduit arrangement, at which a patient interface can be attached in order to connect the respiratory gas conduit arrangement to a patient who is to be ventilated.
On a control apparatus of the known ventilation apparatus, an operator can set a desired respiratory gas temperature or a desired moisture level of the respiratory gas supplied by the ventilation apparatus. The control apparatus is data-transferringly connected to the two temperature sensors and to the flow sensor, and thereby obtains their detected values.
Using tables, formulas, or characteristics diagrams stored in a data memory, and in accordance with a required respiratory gas moisture content and a respiratory gas flow and the respiratory gas temperature ascertained via sensors, the control apparatus controls the energy delivery to a heating plate of the humidification apparatus so as thereby to furnish a respiratory gas flow having a desired respiratory gas moisture content and a desired respiratory gas temperature. The required respiratory gas moisture content is either the moisture content set by the operator, or a moisture content previously stored in a data memory.
As is commonly known, delivery to the patient of a respiratory gas flow having a correct degree of humidity is particularly important in artificial ventilation. If the delivered respiratory gas is too dry, the patient becomes dehydrated in the course of artificial ventilation. If the delivered respiratory gas is too moist, water can condense out of the respiratory gas and travel in liquid form into the patient's lungs, where it can interfere with desired metabolic gas exchange.
Even if the water condensed out of the respiratory gas does not travel as far as the patient's lungs, it can condense onto walls of the respiratory gas conduit arrangement and/or of sensors, for example a proximal flow sensor, and can thereby reduce the measurement accuracy of the sensors.
The relative humidity of the respiratory gas is more critical here than its absolute humidity. The absolute humidity indicates the quantity of water dissolved in a reference volume of air. The relative humidity is an indication of how much moisture a predetermined reference volume of air can still accept and, for example, extract from the patient, or of how close the respiratory gas is to its moisture saturation point. When a respiratory gas is almost saturated with moisture, even small changes in the respiratory gas temperature can result in highly undesirable condensation of liquid out of the respiratory gas (also referred to among specialists as “rain out”).
In order to allow the transfer of respiratory gas, from the ventilation apparatus to the particular patient being ventilated, to be adapted in demand-compatible fashion to the patient's needs, the respiratory gas conduit arrangement comprises at its proximal end a coupling configuration for coupling the respiratory gas conduit arrangement to a patient interface that transfers respiratory gas between the respiratory gas conduit arrangement and the patient. A patient interface of this kind can be an endotracheal tube, a larynx mask, or a combination tube, and the like.
Even when the respiratory gas conduit arrangement is heatable in portions or entirely, the patient interface couplable to the respiratory gas conduit arrangement as a rule is not heatable. The temperature of the patient interface and of the respiratory gas flow in the patient interface can therefore fluctuate more than the temperature of the respiratory gas conduit arrangement and of the respiratory gas flow therein.
Regardless of whether the patient interface is a tube or a mask, a portion of the patient interface which directly adjoins the coupling configuration of the respiratory gas conduit arrangement will always be surrounded by ambient air, and can thereby be influenced by the ambient temperature.
Specifically in an extreme emergency transport situation in which an aforementioned ventilation apparatus is used in winter and/or at high elevation in a transport vehicle or transport helicopter, the ambient temperature can be considerably lower than the patient's body temperature and therefore considerably lower than a desired temperature of the respiratory gas flow. Condensation of moisture out of the respiratory gas may therefore occur at or in the patient interface, for example because the temperature at that wall of the patient interface which is cooled by the ambient air has fallen below the dew point temperature of the respiratory gas flow. Because the patient interface is located particularly close to the patient, and in the case of a tracheal tube is in fact introduced into the patient's body, condensation of liquid in the region of the patient interface is particularly hazardous to the patient being ventilated.
Condensation can take place on walls of the patient interface which are greatly cooled by the ambient air. Additionally or alternatively, condensation can take place as fogging directly in the respiratory gas flow.
Not only is the patient interface as a rule unheated; it is as a rule also a single-use or disposable item that is not fitted with sensors. This makes it difficult to recognize and counteract condensation in the patient interface.
The object of the present invention is therefore to refine a ventilation apparatus of the kind recited initially in such a way that it can ventilate a patient in as precise and stable a manner as possible even in extreme external conditions, over a long ventilation period and with correctly humidified respiratory gas, with no condensation in the patient interface.
The present invention achieves this object, on a ventilation apparatus of the kind recited previously, in that in order to avoid undesired condensation of moisture in the respiratory gas flow in the patient interface, the control apparatus is embodied to ascertain, depending on operating parameters of the ventilation apparatus, in particular of the respiratory gas flow, such as temperature, mass flow or volumetric flow, and/or relative humidity, a resultant state of the ventilation situation downstream in an inspiration direction from the coupling configuration, and to modify the operating power level of the evaporation apparatus depending on the ascertained result.
If a resultant state that is critical in terms of condensation in the patient interface is recognized by the control apparatus, the operating power level of the evaporation apparatus is modified, as a rule reduced, and the risk of condensation in the patient interface is thereby decreased or in fact eliminated.
For example, operating parameters of the ventilation apparatus which are relevant for ascertaining the resultant state can encompass the temperature of the respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement, as detected by the proximal temperature sensor and transferred to the control apparatus, and the ambient temperature as detected by the ambient temperature sensor and transferred to the control apparatus. Additionally or alternatively, the magnitude of the respiratory gas flow ascertained by the flow sensor can be utilized in order to ascertain the resultant state. A further relevant operating parameter can be the nature of the patient interface and its design configuration.
The ventilation apparatus therefore preferably comprises a proximal temperature sensor that is embodied and arranged to detect the temperature of the inspiratory respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement.
The ventilation apparatus also preferably comprises an ambient temperature sensor that is embodied to detect the temperature of the environment of the ventilation apparatus.
At least one, preferably empirically ascertained, resultant data correlation can in turn be stored in a data memory that can be queried by the control apparatus, said correlation associating a set of operating parameters of the ventilation apparatus (which can be several or all of the operating parameters recited above) with a resultant parameter that indicates an occurrence of condensation of respiratory gas moisture in the patient interface.
The resultant parameter can be a binary parameter that either can assume a first value that indicates that no condensation is occurring in the patient interface, or can assume a second value that indicates the opposite, namely that condensation is taking place in the patient interface.
Depending on the resultant data correlation stored in the data memory, for example utilizing a modeled mapping (which can be computationally handled analytically or numerically) of the ventilation situation at the interface, the resultant parameter can indicate a probability with which condensation of liquid out of the respiratory gas flow is predicted to take place in the patient interface.
A probability value of this kind can additionally or alternatively be produced by the fact that in the context of empirical ascertainment of the data correlation, among the operating parameters relevant to the existing ventilation situation, condensation has taken place only in a portion of the empirically investigated cases involving identical parameters, or by the fact that a data correlation does not exist for all the operating parameter values that describe the existing ventilation situation, for instance because the data correlation is defined in tabular form based on interpolation points. In this case, missing values can be interpolated and/or extrapolated from the values that are present. In the context of a complex multidimensional correlation between operating parameters and a resultant parameter, uncertainties that can occur in the determination of the resultant parameter can appropriately be reproduced or interpreted as a probability.
The control apparatus can thereby, in accordance with the resultant parameter, modify, in particular decrease, the operating power level of the evaporation apparatus in order to avoid impending condensation in the patient interface. In the case of the aforementioned simple binary resultant parameter, for example, the one value can cause a decrease in the operating power level of the evaporation apparatus, but the other value does not. In the case of the above-described resultant parameter in the form of a probability value, i.e. a value between 0 and 1 or between 0% and 100%, it is possible to predetermine a threshold probability value, for instance a probability of 40% or more, of condensation in the patient interface, exceedance of which by the resultant parameter leads to a decrease in the operating power level of the evaporation apparatus by the control apparatus. With or without a threshold probability value, the magnitude of the decrease in the operating power level can depend on the magnitude of the probability with which the resultant parameter forecasts condensation in the patient interface. The dependence of the magnitude of the decrease in the operating power level on the probability value of the resultant parameter can be linear or can be progressive, so that starting from an existing operating power level, the decrease in the operating power level in accordance with the resultant parameter increases with increasing condensation probability more greatly than does the condensation probability.
In a preferred application instance that is easy to handle computationally but is nevertheless highly effective, the resultant state or resultant parameter of the ventilation situation can encompass a resultant temperature of the conduit wall of the patient interface and/or of the respiratory gas flow in the patient interface.
A first advantage of using a resultant temperature to describe the resultant state is on the one hand that, assuming a known design configuration of the patient interface, including the materials used to manufacture the patient interface, and assuming known environmental and operating conditions based on the most recent sensor-detected operating state, for instance in the region of the coupling configuration at the proximal longitudinal end of the respiratory gas conduit arrangement, resultant temperatures downstream in an inspiration direction from the coupling configuration can be calculated with good accuracy based on thermodynamic models. It is thus possible either to calculate a resultant temperature in the patient interface, based on thermodynamic models and proceeding from parameters detected instrumentally, in particular parameters located immediately next to the patient interface, or to read out a resultant temperature based on empirically developed characteristics diagrams based on the aforesaid parameters; or a combination of model prediction and readout from empirical data correlations can be used to ascertain the resultant temperature.
A second advantage of using a resultant temperature to describe the resultant state is that the resultant temperature alone can be sufficient for predicting condensation of liquid out of the respiratory gas flow. If the absolute moisture content of the respiratory gas flow is known, whether by direct measurement or by measuring the relative moisture content and the temperature of the respiratory gas flow, the dew point temperature of the respiratory gas flow is then known or is ascertainable from stored dew-point curves. If the resultant temperature is below the dew point temperature ascertained for the respective respiratory gas flow, condensation—i.e. undesired “rain out”—of moisture in the respiratory gas in the patient interface is preponderantly probable.
The ventilation apparatus preferably comprises a humidity sensor arrangement that is embodied to a detect a resultant humidity value of the inspiratory respiratory gas flow which represents at least a relative moisture content of the inspiratory respiratory gas flow. The humidity sensor arrangement is preferably also embodied to detect the respiratory gas temperature at the detection point of the resultant humidity value, so that the control apparatus can ascertain the absolute moisture level and/or the dew point temperature of the respiratory gas flow at the detection point of the resultant humidity value, for instance on the basis of dew-point data stored in a data memory. Alternatively or additionally, the humidity sensor arrangement can be embodied directly for detection of the absolute moisture content of the respiratory gas constituting the resultant humidity value.
As already indicated above, for prediction of a resultant temperature in the patient interface the ventilation apparatus can comprise a data memory which can be queried by the control apparatus and in which operating parameter values detectable instrumentally by the ventilation apparatus, for instance the ambient temperature, and/or operating parameter values of the respiratory gas flow which are detectable in the respiratory gas conduit arrangement, are associated with resultant temperature values of the conduit wall of the patient interface and/or of the respiratory gas flow. Merely for the sake of completeness and clarity, be it noted that for purposes of the present Application, a value interpolated or extrapolated from instrumentally detected operating parameter values is also considered to be instrumentally detected.
As a result of the data correlation stored in the aforesaid data memory, whether as an empirically ascertained data table or data characteristics diagram, or as an analytical or numerical calculation model, the control apparatus can ascertain the resultant state with good accuracy depending on: the temperature, detected by the proximal temperature sensor, of the respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement; the magnitude of the respiratory gas flow detected by the flow sensor; and the predefined setpoint moisture content of the respiratory gas. The probability of undesired condensation in the patient interface can thus be predicted very quickly, with good accuracy, by way of a manageable number of known or instrumentally detectable parameter values.
Undesired condensation of moisture in the respiratory gas in the patient interface can be predicted particularly accurately when the control apparatus ascertains the resultant state depending on the ambient temperature detected by the ambient temperature sensor. The ambient temperature that acts from outside on at least a portion of the patient interface is a factor that greatly influences the temperature of the respiratory gas flowing in the patient interface, and therefore influences possible condensation in the patient interface.
Because the effects on the patient can be that much more disadvantageous the farther downstream, i.e. the closer to the patient, the condensation in the respiratory gas in the patient interface takes place, so that liquid in the patient interface becomes a risk, according to an advantageous refinement of the present invention provision is made that the control apparatus ascertains the resultant state for an ascertainment location located closer to the proximal end of the patient interface than to its distal end, the control apparatus preferably ascertaining the resultant state for the proximal end of the patient interface.
Additionally or alternatively, the control apparatus can ascertain the resultant state for a portion of the patient interface which is located between the coupling configuration and the entry point of the patient interface into the body of the patient. The resultant state, in particular the resultant temperature, is then ascertained specifically for that portion of the patient interface which is exposed directly to the influence of the environment and thus of the ambient temperature, which in extreme operating situations can deviate greatly from the desired temperature of the respiratory gas flow.
When an inspiratory conduit portion of the respiratory gas conduit arrangement is heatable by way of a conduit heating arrangement, the control apparatus additionally can modify, in particular can raise, the operating power level of the conduit heating arrangement depending on the ascertainment result. When assessing whether respiratory gas that is briefly slightly too warm, or that contains liquid phase components, is being delivered to the patient, the option of the elevated respiratory gas temperature is to be preferred.
The coupling configuration is preferably embodied at the proximal longitudinal end of a Y-conduit portion of the respiratory gas conduit arrangement, an inspiration hose and an expiration hose being respectively attached to the two distal longitudinal ends of the Y-conduit portion.
The flow sensor can be a distal flow sensor that is received in the operating housing of the ventilation apparatus. Additionally or alternatively, the flow sensor can be a proximal flow sensor that is arranged, preferably replaceably, at the proximal longitudinal end of the respiratory gas conduit arrangement. The proximal flow sensor can be arranged between the coupling configuration and the patient interface. A proximal flow sensor of this kind can offer high measurement accuracy, and can nevertheless be inexpensive, if it is embodied as a differential pressure flowthrough sensor. The proximal flow sensor can be part of the coupling configuration and can itself be embodied for coupling of the patient interface.
The coupling configuration can be embodied on a proximal flow sensor that is provided at the longitudinal end of the respiratory gas conduit arrangement in order to quantitatively detect at least the inspiratory, preferably also the expiratory, respiratory gas flow.
The evaporation apparatus preferably comprises a heating apparatus with which the liquid reservoir is heated and evaporated. The control apparatus is then preferably embodied to decrease the heating output of the heating apparatus when the aforementioned ascertainment result indicates that condensation of liquid in the patient interface is certain or is preponderantly probable, or is above a predefined probability threshold, or that a resultant temperature is above a predefined resultant temperature threshold.
Alternatively or additionally, the evaporation apparatus can be an ultrasonic nebulizer. In such circumstances, the operating power level that is modifiable by the control apparatus depending on the ascertainment result is the operating power level of the ultrasonic nebulizer. The conditions for decreasing the nebulization power level are the conditions recited above for decreasing the heating power level.
Sensor-based ascertainment of an indicated parameter is equivalent, for purposes of the present application, to direct ascertainment of a variable other than the indicated parameter if that other variable represents the indicated parameter on the basis of a known correlation, for instance a calibration correlation.
The terms “moisture (content)” and “humidity” are used synonymously in the present Application.
The empirical ascertainment of data correlations does represent an outlay, since the aforesaid influencing parameters must be varied in controlled fashion in a laboratory in the context of their expected operating value range, and detected in terms of their influence on the target parameter. That outlay needs to be made only once, however, for ventilation apparatuses of identical design. The data correlations thereby ascertained for one design configuration of ventilation apparatuses can then be used for a plurality of ventilation apparatuses of the same design. It is then sufficient to check on a random basis as to whether or not a previously ascertained data correlation is correct for a specific ventilation apparatus.
The flow sensor can then detect the magnitude at least of the inspiratory respiratory gas flow, and the proximal temperature sensor can detect the temperature, in the proximal longitudinal end region of the respiratory gas conduit arrangement, so that humidification of the respiratory gas is effected on the basis of parameters that are as close as possible to the patient.
In order to define a desired ventilation situation, the ventilation apparatus can comprise an input apparatus for inputting at least one setpoint temperature of the respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement and/or for inputting at least one setpoint moisture content of the respiratory gas and/or for inputting at least one setpoint respiratory gas flow. It is also possible for only some of the aforementioned parameters to be inputtable at the input apparatus, while others of the aforementioned parameters can be ascertained on the basis of empirically ascertained data correlations in accordance with the inputted parameters and/or further ones.
In order to simplify the operation of the ventilation apparatus, for example, it can comprise an input apparatus for inputting a setpoint temperature of the respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement, and can furthermore comprise a data memory which can be queried by the control apparatus and in which a (preferably empirically ascertained) correlation between temperature values of the respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement and associated setpoint moisture values of the respiratory gas is stored. All that is then necessary in order for the control apparatus to be capable of determining the associated setpoint moisture content of the respiratory gas is to input the proximal respiratory gas flow temperature.
In order to avoid undesired condensation of liquid onto the walls of the respiratory gas conduit arrangement, at least one inspiratory conduit portion of the respiratory gas conduit arrangement can comprise a conduit heating apparatus. The inspiratory conduit portion can be heated with this conduit heating apparatus. It is thereby possible to prevent the temperature of a wall of the inspiratory conduit portion from falling below the dew point temperature of the respiratory gas flowing in the conduit portion. The control apparatus can then be embodied to control the operating power level of the conduit heating apparatus depending on a predefined setpoint temperature of the respiratory gas flow in the proximal longitudinal end region of the respiratory gas conduit arrangement. The control apparatus can furthermore take the detected ambient temperature into account when ascertaining the energy or power level to be delivered to the conduit heating apparatus. This considerably simplifies the control loop for heating the conduit portion, since as a rule the respiratory gas conduit arrangement is contacted on its outer side by ambient air at ambient temperature. Undesired temperature fluctuations on the heated wall of the inspiratory conduit portion can be avoided if the ambient temperature is taken into account when heating the conduit portion. The temperature of the heated conduit portion can thereby be maintained more consistently.
The respiratory gas source arrangement, constituting a respiratory gas source, can comprise an intake opening through which ambient air, or gas from a predetermined gas reservoir, can be taken in. Additionally or alternatively, the respiratory gas source arrangement can comprise a gas reservoir as a respiratory gas source, for example a reservoir container or a connecting configuration for attachment of a supply conduit that connects the ventilation apparatus to a locally installed gas reservoir, as is often the case in hospitals. In order to furnish the capability of mixing different gases to yield a respiratory gas, the respiratory gas source arrangement can comprise a plurality of individual respiratory gas sources such as those recited above. The different gases to be mixed can be at different temperatures, and/or can have different moisture contents, as a result of expansion and how they are furnished. In order to ensure that the humidity sensor arrangement detects the moisture content of the respiratory gas actually delivered to the patient, the humidity sensor arrangement is preferably arranged downstream, in an inspiration direction of the respiratory gas flow, from the respiratory gas source arrangement. For the reasons recited, it is particularly preferred that no further respiratory gas constituent be added, downstream from the humidification apparatus in an inspiration direction, to the respiratory gas emerging from the humidification apparatus.
The control apparatus can be signal-transferringly connected to the evaporation apparatus in order to detect and control the energy or the power level delivered to the evaporation apparatus. Additionally or alternatively, the control apparatus can be signal-transferringly connected to an energy supply of the evaporation apparatus. For example, the control apparatus can be embodied to directly detect an electrical current delivered to the evaporation apparatus, and the electrical voltage applied in that context. If embodiment of the control apparatus for the direct detection of energy, in particular electrical energy, implies too great an outlay, the control apparatus can be signal-transferringly connected to at least one energy sensor that is embodied to detect an energy delivered to the evaporation apparatus. The energy and/or power level currently being delivered to the evaporation apparatus can be ascertainable by the control apparatus from signals that are transferred to the control apparatus via the signal-transferring connection. The ascertainment of energy and that of power level differ only in that the power level represents a detection of energy over time.
The present invention will be explained in further detail below with reference to the appended drawings, in which:
In
Ventilation apparatus 10 comprises a housing 14 in which an intake opening 15 is embodied and in which a flow modification apparatus 16 and a control device 18 (not visible from outside because of the opaque housing material) are received. Intake opening 15 allows flow modification apparatus 16 to take in ambient air from external environment U of the ventilation apparatus and, after purification known per se by means of filters, to deliver it as respiratory gas to patient 12. Intake opening 15 is therefore a respiratory gas source arrangement for purposes of the present Application.
An ambient temperature sensor 17, which measures the temperature of the air of environment U and transfers it to sensor apparatus 18, is located in intake opening 15.
Flow modification apparatus 16 is constructed in a manner known per se and can comprise a pump, a compressor, a fan 52, a pressure vessel, a reduction valve 54 (see
Control device 18 is usually implemented as a computer or microprocessor. It encompasses a data memory, labeled 19 in
Ventilation apparatus 10 comprises an input apparatus 24, which in the example depicted in
Ventilation apparatus 10 can comprise an output device 28, in the example depicted a display screen, for outputting data to the therapist providing care.
For artificial ventilation, patient 12 is connected to ventilation apparatus 10, more precisely to flow modification apparatus 16 in housing 14, via a respiratory gas conduit arrangement 30. Patient 12 is intubated for that purpose by means of an endotracheal tube constituting a patient interface 31. A proximal longitudinal end 31a of patient interface 31 delivers inspiratory respiratory gas flow AF into the lungs of patient 12. The expiratory respiratory gas flow also flows through proximal longitudinal end 31a into the respiratory gas conduit arrangement.
A distal longitudinal end 31b of patient interface 31 is embodied for connection to respiratory gas conduit arrangement 30. From location 31c, downstream in an inspiration direction to proximal longitudinal end 31a, the patient interface is surrounded by the body of patient 12. This means conversely that from its distal longitudinal end 31b to location 31c, patient interface 31 is exposed to external environment U and is in (predominantly convective) thermally transferring communication therewith.
Ventilation conduit arrangement 30 comprises an inspiration hose 32 through which fresh respiratory gas can be directed from flow modification apparatus 16 into the lungs of patient 12. Inspiration hose 32 can be interrupted, and can comprise a first inspiration hose 34 and a second inspiration hose 36 between which a humidification apparatus 38, for controlled humidification and optionally also temperature control of the inspiratory respiratory gas delivered to patient 12, can be provided. Humidification apparatus 38 can be connected to an external liquid reservoir 40 by way of which water for humidification, or also a medication e.g. to inhibit inflammation or to dilate the airways, can be delivered to humidification apparatus 38. When the present ventilation apparatus 10 is used as an anesthesia ventilation apparatus, it is thereby possible to deliver volatile anesthetics to patient 12 in controlled fashion via ventilation apparatus 10. Humidification apparatus 38 ensures that the fresh respiratory gas is conveyed to patient 12 with a predetermined moisture content, optionally with addition of a medication aerosol, and at a predetermined temperature.
In the present example, second inspiration hose 36 is electrically heatable by a conduit heating apparatus 37. Conduit heating apparatus 37 can be controlled by control apparatus 18 for operation. Unlike what was said above, first inspiration hose 34 can also be heatable, and/or the at least one hose 34 and/or 36 can be heatable by a conduit heating apparatus 37 that is other than electric, for instance by having a heat exchange medium flow around it.
Respiratory gas conduit arrangement 30 further comprises, in addition to the aforementioned inspiration valve 20 and expiration valve 22, an expiration hose 42 by way of which metabolized respiratory gas is expelled from the lungs of patient 12 into external environment U.
At distal longitudinal end 30b of respiratory gas conduit arrangement 30, inspiration hose 32 is coupled to inspiration valve 20, and expiration hose 42 to expiration valve 22. Preferably only one of the two valves is respectively open simultaneously for passage of a gas flow. Actuation control of valves 20 and 22 is likewise accomplished by control device 18.
During a ventilation cycle, firstly expiration valve 22 is closed and inspiration valve 20 is opened for the duration of the inspiration phase, so that fresh inspiratory respiratory gas can be directed from housing 14 to patient 12. A flow of fresh respiratory gas is produced by flow modification arrangement 16 by controlled elevation of the pressure of the respiratory gas. As a result of the pressure elevation, the fresh respiratory gas flows into the lungs of patient 12 where it expands the body region in the vicinity of the lungs, i.e. in particular the thorax, against the individual elasticity of the body parts near the lungs. The gas pressure in the interior of the lungs of patient 12 also rises as a result.
At the end of the inspiration phase, inspiration valve 20 is closed and expiration valve 22 is opened. The expiration phase begins. Because the gas pressure of the respiratory gas present in the lungs of patient 12 has been elevated until the end of the inspiration phase, said gas flows into external environment U after expiration valve 22 is opened, while the gas pressure in the lungs of patient 12 decreases as the flow continues. When the gas pressure in lungs 12 reaches a positive end expiration pressure (PEEP) that is set on ventilation apparatus 10, i.e. a pressure slightly higher than atmospheric pressure, the expiration phase is terminated with the closing of expiration valve 22, and is followed by a further ventilation cycle.
The so-called ventilation tidal volume, i.e. the volume of respiratory gas for each breath, is delivered to patient 12 during the inspiration phase. The ventilation tidal volume multiplied by the number of ventilation cycles per minute, i.e. multiplied by the ventilation frequency, equals the volume per minute of artificial ventilation being performed in the present case.
Ventilation apparatus 10, in particular control device 18, is preferably embodied to repeatedly update or ascertain, during ventilation operation, ventilation operating parameters that characterize the ventilation operation of ventilation apparatus 10, in order to ensure that ventilation operation is coordinated as optimally as possible, at every point in time, with patient 12 who is respectively to be ventilated. Particularly advantageously, the determination of one or several ventilation operation parameters is made at the ventilation frequency, so that ventilation operating parameters that are current, and are thus optimally adapted to patient 12, can be furnished for each ventilation cycle.
Ventilation apparatus 10 can be data-transferringly connected for that purpose to one or several sensors that monitor the status of the patient and/or the operation of ventilation apparatus 10. A proximal flow sensor 44, which quantitatively detects the respiratory gas flow existing in respiratory gas conduit arrangement 30, is mentioned in
More precisely, in the preferred exemplifying embodiment respiratory gas conduit arrangement 30 comprises at its proximal longitudinal end region 30a a separately embodied Y-conduit portion 47, which is connected at its distal end region to second inspiration hose 36 and to expiration hose 42, and is connected at its proximal end region to proximal flow sensor 44.
Proximal flow sensor 44 comprises at its proximal end region a coupling configuration 44a with which patient interface 31, which could also be a mask rather than a tube, is couplable to proximal flow sensor 44 and consequently to respiratory gas conduit arrangement 30.
Second inspiration hose 36 comprises, at its proximal longitudinal end region, a proximal temperature sensor 48 that measures the temperature of respiratory gas flow AF in second inspiration hose 36 as close as possible to patient 12, and transfers it to control apparatus 18.
Merely for the sake of completeness, be it noted that ventilation apparatus 10 according to the present invention can constitute a mobile ventilation apparatus 10 and can be received on a rollable frame 50.
Flow modification apparatus 16 encompasses a fan 52 and a reduction valve 54 located downstream therefrom in an inspiration direction. It is also possible for only fan 52 to be provided. For operation, control apparatus 18 can apply control to fan 52 and to reduction valve 54 via respective leads 56 and 58.
Fan 52 can take in ambient air from external environment U through intake opening 15. Additionally or alternatively, gas, for instance pure oxygen, from a reservoir vessel 62 can be used via a valve 60 as a respiratory gas or can be mixed into the ambient air that is taken in. In the exemplifying embodiment depicted, intake opening 15 and reservoir vessel 62 therefore together constitute a respiratory gas source arrangement.
The ambient air that is taken in is purified in ventilation apparatus 10, in filters that are not depicted, in a manner known per se.
Inspiration valve 20, which is controllable by control apparatus 18 via a lead 64 for opening and closing, is located downstream in an inspiration direction from flow modification apparatus.
Farther downstream in an inspiration direction, inspiration valve 20 is followed by first inspiration hose 34.
Upstream in an inspiration direction from humidification apparatus 38 in the narrower sense, ventilation apparatus 10 encompasses a humidity sensor arrangement 66 that, in the economically preferred instance depicted, encompasses a sensor 68 for ascertaining the relative humidity of inspiratory respiratory gas flow AF and a temperature sensor 70 for ascertaining the respiratory gas temperature in the region in which humidity is detected by sensor 68. Alternatively, humidity sensor arrangement 66 could encompass only a sensor for detecting the absolute moisture content of the respiratory gas, but for cost reasons this is not preferred.
Humidity sensor arrangement 66 detects, along with the relative moisture content and the temperature of the respiratory gas upstream from humidification apparatus 38, the relative moisture content and the temperature of the respiratory gas after respiratory gas sources 15 and 62 but before humidification measures are taken by ventilation apparatus 10. Humidity sensor arrangement 66 can be arranged in the housing, shown in
The detected values of sensors 68 and 70 are transferrable via leads 78 and 80 to control apparatus 18.
From the detected values thereby obtained for the relative moisture content and the temperature of the respiratory gas before reaching humidification apparatus 38, control apparatus 18 can ascertain the absolute moisture content of the respiratory gas and compare it to a desired setpoint moisture content of the respiratory gas.
The setpoint moisture content of the respiratory gas can be obtained, for example, from a data correlation, stored in data memory 19, of signals of proximal temperature sensor 48, and optionally also of the proximal respiratory gas flow detected by proximal flow sensor 44. Alternatively, a desired setpoint moisture content of the respiratory gas can also be inputted manually via input apparatus 24.
Proceeding from the setpoint moisture content of the respiratory gas, and also depending on the signals of proximal temperature sensor 48 (which are transferred via a lead 82 to control apparatus 18), of humidity sensor arrangement 66, and of proximal flow sensor 44, control apparatus 18 ascertains an operating power level that is to be delivered to evaporation apparatus 76 in the form of a heating plate. Control apparatus 18 applies control via a lead 84 to an energy supply 86 of evaporation apparatus 76 in accordance with the ascertained operating power level. By way of lead 84, control apparatus 18 receives information regarding the operating power level delivered to evaporation apparatus 76, for example in the form of the voltage applied to evaporation apparatus 76 and the current intensity flowing to it. Energy supply apparatus 86 can deliver a variable power level to evaporation apparatus 76, for example by pulse width modulation. In a context of pulse width modulation, the voltage applied to evaporation apparatus 76 is a time-averaged voltage.
Liquid is evaporated from liquid reservoir 74 by evaporation apparatus 76, and is entrained by respiratory gas flow AF that flows over liquid reservoir 74.
In order to account for heat losses from evaporation apparatus 76 to environment U, control apparatus 18 ascertains the energy to be delivered per unit time to evaporation apparatus 76 via energy supply apparatus 86 additionally in consideration of the ambient temperature ascertained by ambient temperature sensor 17.
In order to ascertain the operating power level to be delivered to evaporation apparatus 76 depending on the setpoint moisture content of the respiratory gas, and further depending on the proximal respiratory gas temperature, the absolute moisture content detected indirectly by humidity sensor arrangement 66, the proximal respiratory gas flow detected by proximal flow sensor, and further depending on the ambient temperature, a corresponding data correlation, which was determined previously in the laboratory for a ventilation apparatus 10 of identical design by parameter variation under controlled conditions, is stored in data memory 19.
It is therefore to be assumed that as a result of the operation of evaporation apparatus 76, controlled by control apparatus 18 in accordance with the parameters recited, inspiratory respiratory gas flow AF leaves humidification apparatus 38 with the setpoint moisture content. The inspiratory respiratory gas flow then enters second inspiration hose 36, which can be heated by conduit heating apparatus 37. The operation of conduit heating apparatus 37 is controllable by control apparatus 18 by means of a lead 88, in accordance with the temperature detected by proximal temperature sensor 48, in such a way that the proximal respiratory gas temperature detected by proximal temperature sensor 48 is above the dew point temperature of the humidified inspiratory respiratory gas flow AF.
The dew point temperature can be ascertained, proceeding from the assumption that the respiratory gas exhibits the setpoint moisture content after passing through humidification apparatus 38, based on the proximal respiratory gas temperature detected by proximal temperature sensor 48 and further based on a dew point temperature curve stored in data memory 19. What is obtained from the dew point temperature curve is thus a setpoint temperature above which the temperature at proximal temperature sensor 48 should remain, preferably in fact should remain with a certain safety margin.
Storage of a dew point temperature curve in data memory 19 does not necessarily mean storage of a continuously differentiable curve. It is sufficient to store a dew point temperature curve that is approximated by a sufficient number of interpolation points, for example as a table. It is also possible to store, for the dew point temperature, an approximate mathematical function with which a dew point temperature can be ascertained based on a known absolute moisture content or on a known value pair of a relative moisture content and an associated temperature.
One problem in terms of properly supplying the patient with respiratory gas that is sufficiently humidified, but not over-humidified, is patient interface 31. Patient interface 31 is not heatable as second inspiration hose 36 is, nor is it equipped with any sensors that might detect the ventilation state in patient interface 31. The reason for this is the usual nature of patient interface 31 as a disposable or single-use interface.
Specifically when ambient temperatures are very low, for instance in emergency situations, at the least the portion exposed to external environment U, between distal longitudinal end 31b of patient interface 31 and the entry of patient interface 31 into patient 12 at location 31c, is therefore greatly influenced by the ambient temperature. In this portion, patient interface 31 can be so severely cooled by the ambient temperature that an undesirable “rain out” occurs in patient interface 31. This undesired condensation of liquid out of inspiratory respiratory gas flow AF as a rule will occur most readily on the conduit wall of patient interface 31 which is cooled by ambient air. It is also not to be excluded, however, that respiratory gas flow AF in patient interface 31 cools to such an extent, under the influence of the ambient temperature, that fogging occurs in respiratory gas flow AF.
In order to avoid such undesired condensation of liquid in patient interface 31, control apparatus 18 is embodied to ascertain, on the basis of operating parameters of the ventilation apparatus which are transferred to it by the available sensors and in particular based on inspiratory respiratory gas flow AF, a resultant state, produced under the influence of the ambient temperature, of the ventilation situation in patient interface 31 downstream in an inspiration direction from coupling configuration 44a, and to determine on the basis of that ascertained resultant state whether condensation in patient interface 31 is to be expected.
For that purpose, either empirically ascertained data correlations or an analytically or numerically solvable equation system, constituting a model description of the thermal state of patient interface 31 during operation depending on operating data of ventilation apparatus 10 and its environment U, can be stored in data memory 19.
In a particularly simple and rapidly ascertainable calculation model, the resultant state of patient interface 31 is a resultant temperature of patient interface 31 which is ascertainable, for example, based on the proximal respiratory gas temperature at temperature sensor 48, in further consideration of the design configuration of patient interface 31 including the materials used therein, and in consideration of the ambient temperature measured by ambient temperature sensor 17. The inspiratory respiratory gas flow AF detected by proximal flow sensor 44, and if desired even an expiratory respiratory gas flow likewise detected by proximal flow sensor 44, can also be utilized in order to ascertain the resultant temperature.
Control apparatus 18, to which the dew point temperature of inspiratory respiratory gas flow AF is already available by way of the above-described control of ventilation apparatus 10, can thus assume that a risk of condensation in patient interface 31 is immediately imminent if a resultant temperature of patient interface 31 at a point located upstream in an inspiration direction from distal longitudinal end 31b (said temperature being ascertained based on an empirically ascertained data correlation and/or based on a thermodynamic model) falls below the dew point temperature. For the safety of the patient, what is utilized is preferably not the dew point temperature directly, but rather a threshold temperature that is a dew point temperature raised by a predetermined safety margin.
For the instance in which control apparatus 18 ascertains in this manner that condensation is definitely, or with a preponderant probability, or with more than a predetermined limit probability, occurring in patient interface 31, control apparatus 18 is embodied to decrease the operating power level delivered to evaporation apparatus 76. The amount by which the operating power level of evaporation apparatus 76 is decreased can be selected to be greater, the greater the condensation risk based on the ascertainment result, for example the greater the degree to which the resultant temperature of patient interface 31 quantitatively exceeds the threshold temperature or even the dew point temperature.
In addition, control apparatus 18 can also increase the operating power level of conduit heating arrangement 37 in order to increase the temperature of inspiratory respiratory gas flow AF on the way to proximal longitudinal end 30a of respiratory gas conduit arrangement 30. But because the present control apparatus 18 is intended to be able to prevent condensation of respiratory gas in patient interface 31 even for inspiration hoses that are not heatable, the decrease in the operating power level of evaporation apparatus 76 is implemented in all cases.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2018 214 557.1 | Aug 2018 | DE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2019/072729 | 8/26/2019 | WO | 00 |
