The application relates generally to ventilators, more particularly, to patient ventilators configured to ventilate patient airways.
Ventilators are machines that provide mechanical ventilation by delivering breathable air into and evacuating it out from patients' lungs. Such ventilators are typically used to deliver breaths to a patient who is physically unable to breathe, or who breathes insufficiently. Ventilators can be computerized microprocessor-controlled machines configured to deliver, in a sequence of ventilation cycles, the necessary volume of breathable air to a patient, a quantity generally referred to as a tidal volume. Although existing ventilators are satisfactory to a certain degree, there always remains room for improvement.
In accordance with a first aspect of the present disclosure, there is provided a ventilator to ventilate an airway of a patient, the ventilator comprising: a conduit having an inlet and an outlet, said outlet being configured to be connected to said airway; a gas delivery element in fluid communication with said inlet of said conduit, said gas delivery element being configured to deliver air in a sequence of ventilation cycles, each ventilation cycle being defined by a corresponding tidal volume to be delivered to said airway via said conduit, each tidal volume corresponding to a difference between a start volume and an end volume of said gas delivery element for that ventilation cycle; a pressure sensor configured to monitor pressure within said conduit; a controller communicatively coupled to said gas delivery element and said pressure sensor, said controller having a processor and a non-transitory memory having stored thereon instructions that when executed by said processor perform the step of reducing said tidal volume between a first ventilation cycle and a successive second ventilation cycle contingent upon said pressure exceeding a pressure threshold in said first ventilation cycle.
In accordance with a second aspect of the present disclosure, there is provided a method of ventilating an airway of a patient, said method comprising: monitoring an airway pressure of said patient; delivering a first ventilation cycle of air to said airway, said first ventilation cycle defined by a first tidal volume and generating pressure variations in said airway; and delivering a second ventilation cycle of air to said airway, said second ventilation cycle subsequent to said first ventilation cycle and defined by a second tidal volume, said second tidal volume being lesser than said first tidal volume contingent upon said airway pressure exceeding an airway pressure threshold during said first ventilation cycle.
In accordance with a third aspect of the present disclosure, there is provided a controller configured for controlling a patient ventilator based on airway pressure monitoring, said controller having a processor and a non-transitory memory having stored thereon instructions that when executed by said processor perform the step of: reducing a tidal volume between a first ventilation cycle and a successive second ventilation cycle contingent upon an airway pressure measurement exceeding a pressure threshold during said first ventilation cycle.
Reference is now made to the accompanying figures in which:
The ventilator 100 has a gas delivery element 116 which is in fluid communication with the fresh air inlet 114a of the conduit 114. It is intended that the gas delivery element 116 is configured to deliver air to the conduit 114, and therefore to the patient's airway 112, in a sequence of ventilation cycles of air. Each ventilation cycle of air is defined by a corresponding tidal volume Vt to be delivered to the airway 112 of the patient via the conduit 114. Each tidal volume Vt corresponds to a difference between a start volume Vs and an end volume Ve of the gas delivery element 114 for the corresponding ventilation cycle.
It is expected that once a given tidal volume Vt of fresh air is delivered to the patient's airway 112, a corresponding volume of used air may be evacuated from the patient's airway 112 via the conduit 114. More specifically, in this embodiment, used air may be channeled from a used air inlet 114c of the conduit 114 towards a used air outlet 114d. As shown in this specific example, the fresh air outlet 114b may coincide with the used air inlet 114c when a valve 118 (e.g., a solenoid valve) is used to determine whether fresh air is to be delivered from the ventilator 120 to the patient's airway 112 in a first air flow direction A or used air is to be evacuated from the patient's airway 112 towards the ventilator 100 in a second air flow B direction opposite to the first air flow direction A.
It is noted that each ventilation cycle generates corresponding pressure variations in the airway. As such, the ventilator 100 is provided with a pressure sensor 120 configured to monitor an airway pressure Paw within the conduit 114, the monitored airway pressure Paw being indicative of a pressure within the patient's airway 112. The pressure sensor 120 is generally provided anywhere within the ventilator 100, provided that is measures the airway pressure Paw as fresh air is delivered to the patient's airway 112. For instance, the pressure sensor 120 may be positioned within the fresh air inlet 114a, within the fresh air outlet 114b, downstream from the conduit 114, or upstream from the conduit 114. In some embodiments, a single pressure sensor may be positioned at the fresh air outlet or at the used air inlet, downstream from the valve thereby monitoring the airway pressure regardless of the position of the valve 118. In some other embodiments, more than one pressure sensor can be provided. For instance, a first pressure sensor may be positioned within the fresh air inlet 114a to monitor the airway pressure Paw as fresh air is delivered to the patient's airway 112 when the valve position is open, and a second pressure sensor may be positioned within the used air outlet 114d to monitor the airway pressure Paw as used air is evacuated from the patient's airway 112 when the valve position is closed. As such, airway pressure Paw may be monitored throughout entire ventilation cycles, during both fresh air delivery and used air evacuation.
The ventilator 100 has a controller 122 which is communicatively coupled to the gas delivery element 116 and to the pressure sensor 120. Such a communicative coupling may be wired, wireless, or a combination of both depending on the embodiment. As described below, the controller 122 has a processor and a non-transitory memory which has stored thereon instructions that when executed by the processor perform some predetermined steps. More specifically, the controller 122 is configured to reduce the tidal volume Vt1 between a first ventilation cycle and a successive second ventilation cycle contingent upon the monitored airway pressure Paw exceeding a pressure threshold Pthres in the first ventilation cycle (Paw>Pthres).
The controller 122 can be provided as a combination of hardware and software components. The hardware components can be implemented in the form of a computing device 300, an example of which is described with reference to
Referring to
The processor 302 can be, for example, a general-purpose microprocessor or microcontroller, a digital signal processing (DSP) processor, an integrated circuit, a field programmable gate array (FPGA), a reconfigurable processor, a programmable read-only memory (PROM), or any combination thereof.
The memory 304 can include a suitable combination of any type of computer-readable memory that is located either internally or externally such as, for example, random-access memory (RAM), read-only memory (ROM), compact disc read-only memory (CDROM), electro-optical memory, magneto-optical memory, erasable programmable read-only memory (EPROM), and electrically-erasable programmable read-only memory (EEPROM), Ferroelectric RAM (FRAM) or the like. The memory 304 may have stored thereon values such as one or more airway pressure threshold, some tidal volumes, volume increase or decrease increments, a minimal tidal volume, and the like.
Each I/O interface 306 enables the computing device 300 to interconnect with one or more input devices, such as keyboard(s) and mouse(s), or with one or more output devices such as monitor(s), remote network(s). For instance, such input devices can be used as a user interface which can be used to input an initial tidal volume which is to be delivered to the patient's airway. The initial tidal volume, which is often referred to as the first tidal volume herein, can be set by an health professional via the user interface. The initial tidal volume associated with the patient may depend on the patient's characteristics (e.g., height, weight, age, gender), the condition of his/her airway and the like.
Each I/O interface 306 enables the controller 122 to communicate with other components, to exchange data with other components, to access and connect to network resources, to serve applications, and perform other computing applications by connecting to a network (or multiple networks) capable of carrying data including the Internet, Ethernet, plain old telephone service (POTS) line, public switch telephone network (PSTN), integrated services digital network (ISDN), digital subscriber line (DSL), coaxial cable, fiber optics, satellite, mobile, wireless (e.g. Wi-Fi, WiMAX), SS7 signaling network, fixed line, local area network, wide area network, and others, including any combination of these.
The computing device 300 described above is meant to be an example only. Other suitable embodiments of the controller 122 can also be provided, as it will be apparent to the skilled reader.
Referring now to
At step 402, the conduit 114 is connected to the patient's airway 112. This step can be performed by health professional(s) in some embodiments. In some other embodiments, the step 402 can be performed by a suitably programmed robotized machine (not shown).
At step 404, the airway pressure Paw of the patient's airway 112 is monitored. More specifically, the pressure sensor(s) 120 generate(s) airway pressure values Pi over time. The airway pressure values Pi can be communicated to the controller 122 via raw signals, processed signals, raw data, processed data, or any combination thereof. In any case, the controller 122 may receive the airway pressure values Pi measured over time. The airway pressure values Pi can be stored on a local memory system of the controller 122 for later comparison with one or more airway pressure thresholds Pthres in some embodiments. In some other embodiments, the airway pressure values Pi may be compared to the airway pressure threshold(s) Pthres on the go in some embodiments, after which they may be deleted or stored on a memory system.
At step 406, a first ventilation cycle of air is delivered to the patient's airway 112, which generates pressure variations in the airway 112. In step 406, the first ventilation cycle of air is defined by a first tidal volume Vt1. The first tidal volume Vt1 is delivered by moving the gas delivery element 116 from the start position Ps to the end position Pe, thereby delivering a difference between the corresponding start and end volumes Vs ad Ve of the gas delivery element 116.
Should the monitored airway pressure Paaw does not exceed a predetermined airway pressure threshold Pthres, step 406 may be repeated any given number of times to suitably ventilate the patient's airway 112.
At step 408, contingent upon the airway pressure Paw exceeding an airway pressure threshold Pthres during step 406, a second ventilation cycle of air is delivered to the patient's airway 112 subsequent to the delivery of the first ventilation cycle. In step 408, the second ventilation cycle of air is defined by a second tidal volume Vt2 which is lesser than the first tidal volume Vt1, i.e., Vt2<Vt1. By delivering a lesser volume of air to the patient's airway 112 during one or more consecutive ventilation cycles of air, it is expected that the monitored airway pressure Paw may eventually stop rising, and/or ultimately decrease back under the airway pressure threshold Pthres.
In some embodiments, the gas delivery element 116 may be interrupted during the first ventilation cycle of air in response to the airway pressure Paw exceeding the airway pressure threshold Pthres. For instance, as soon as the controller 122 monitors that the airway pressure threshold Pthres is produced, air delivery may be immediately interrupted to avoid damaging the patient's airway 112. In such circumstances, air evacuation of that ventilation cycle may be performed, after which the patient's airway 112 may be ventilated using either a regular or a modified ventilation cycle of air. It is noted that this step is only optional, as a given ventilation cycle of air may be completed even though the airway pressure threshold Pthres is produced during the given ventilation cycle of air.
In some embodiments, the second tidal volume Vt2 may be maintained for a given number of subsequent ventilation cycles once the airway pressure threshold Pthres has been produced. For instance, in an embodiment where the airway pressure threshold Pthres is met during a first ventilation cycle of air, the subsequent, second ventilation cycle of air may be set to deliver the reduced, second tidal volume Vt2. The reduced, second tidal volume Vt2 may be delivered during a third ventilation cycle of air subsequent to the second ventilation of air; during a fourth ventilation cycle of air subsequent to the third ventilation of air, and so forth.
In some embodiments, the second tidal volume Vt2 may be further reduced between the second ventilation cycle and a successive third ventilation cycle upon determining that the airway pressure threshold Pthres is met again during the second ventilation of air. For instance, if the airway pressure threshold Pthres is met again during the second ventilation cycle of air, the second tidal volume Vt2 may be reduced to a third tidal volume Vt3 being lesser than the second tidal volume Vt2, i.e., Vt3<Vt2. As such, the third tidal volume Vt3 may be delivered to the patient's airway 112 during the third ventilation cycle of air. It is noted that the tidal volume Vt to be delivered should not be reduced below a given minimal tidal volume Vtmin which is generally associated to a corresponding patient.
In some embodiments, as soon as the monitored airway pressure Paw goes below the airway pressure threshold Pthres during a given ventilation cycle, the tidal volume Vt to be delivered during a subsequent ventilation cycle may be increased.
In some embodiments, the controller 122 may be configured for incrementally reduce a tidal volume Vt of a preceding ventilation cycle upon determining that the monitored airway pressure Paw meet the airway pressure threshold Pthres. The tidal volume Vt1 may be reduced by increment ΔV1, from a first tidal volume Vt1 to a second tidal volume Vt2 where Vt2=Vt1−ΔVt1, from a second tidal volume Vt2 to a third tidal volume Vt3 where Vt3=Vt2−ΔVt1, and so forth. It is expected that the tidal volume Vt to be delivered may be reduced until a minimal tidal volume Vtmin is reached. For instance, in embodiments where Vt3<Vtmin, the tidal volume Vt to be delivered may never reach the third tidal volume Vt3 as it would be below the minimal tidal volume Vtmin.
When the monitored airway pressure Paw goes back below the airway pressure threshold Pthres, the controller 122 may be configured for incrementally increase a tidal volume Vt of a preceding ventilation cycle, until the initial, first tidal volume Vt1 is reached. The tidal volume Vt may be increased by increment ΔVt2, from a fifth tidal volume Vt5 to a fourth tidal volume Vt4 where Vt5=Vt4+ΔVt2, from the fourth tidal volume Vt4 to a third tidal volume Vt3 where Vt4=Vt3+ΔVt2, and so forth, until the initial, first tidal volume Vt1 is reached. In some embodiments, increments ΔVt1 and ΔVt2 are similar to one another. In some other embodiments, increments ΔVt1 and ΔVt2 may be different from one another.
It is noted that the difference between the first and second tidal volumes Vt1 and Vt2 may depend on a difference between the monitored airway pressure Paw, e.g., its maximal value Paw,max throughout a current ventilation cycle, and the airway pressure threshold Pthres. For instance, the more the monitored airway pressure Paw exceeds the airway pressure threshold Pthres, the more the tidal volume Vt to be delivered in a subsequent ventilation cycle may be reduced.
It is noted that the controller may be configured to generate alarm(s) whenever the airway pressure threshold Pthres is produced. Moreover, the alarm(s) may remain activate as long as the tidal volume Vt to be delivered is below the initial, first tidal volume Vt1. The alarm(s) may be displayed on a user interface, be transmitted over a network, and/or be stored for later consultation, depending on the embodiment.
Steps 404, 406 and 408 and some of the optional steps described above are schematically shown in
In some embodiments, the reduced, second tidal volume Vt2 can be maintained between said second ventilation cycle and one or more successive ventilation cycles when the airway pressure Paw still exceeds the pressure threshold Pthres in the second ventilation cycle. Referring now to
In the embodiment illustrated in
In some embodiments, the tidal volume Vt can be reduced in an incremental manner until a given minimal tidal volume Vtmin is reached. For example, in the example shown in
The ventilator 800 has a gas delivery element 816 which is in fluid communication with the fresh air inlet 814a of the conduit 814. As shown, the gas delivery element 816 is configured to deliver air in a sequence of ventilation cycles as described above. The gas delivery element 816 has a cylinder 830 within which a piston 824 moves. By moving the piston 824 from a start position to an end position, a corresponding tidal volume Vt can be delivered to the patient's airway 812. In this specific example, the gas delivery element 816 has an actuator 832, e.g., an electrical linear actuator 834, which is mechanically coupled to the piston 824, and sealed relative to the cylinder 830. The actuator 832 can move the piston 824 in a sequence of back and forth at different axial positions based on an electrical signal.
Referring back to
A controller 822, in this example provided in the form of a computer, is also provided. As shown, the controller 822 and the pressure sensor 820 are communicatively coupled to one another via wired connections 842. The signal(s) and/or data generated by the pressure sensor 820 in real time are communicated to the controller 822 which may locally or remotely process, compare and/or store them as they are received. The controller 822 is also communicatively coupled to the gas delivery unit 816 via a wired connection 842 to control the actuator, for instance.
As discussed above, depending on whether the instantaneous pressure value exceeds a given airway pressure threshold, which may be stored on a memory of the controller, the gas delivery unit 816 is configured to reduce a tidal volume Vt to be delivered to the patient's airway 812, in order to avoid unnecessary and potentially damaging pressure buildup within the patient's airway 812.
The ventilator 800 draws fresh air from the surrounding environment 844, which may be filtered using a fresh air filter 846. As shown, an oxygen source 848 may be used to increase the oxygen content of the surrounding fresh air that is drawn by the ventilator 800. As such, when the piston 824 from the gas delivery element 816 is pulled backward, fresh air from the surrounding environment 844, and also oxygenated by the oxygen source 848, may be drawn within the ventilator 800, and more specifically within a given portion of the cylinder 830, ready to be delivered into the patient's airway 812 by pushing the piston 824 in an opposite direction towards the conduit 814. A first check valve 850 upstream from the gas delivery unit 816 may be used to control entry of fresh air within the ventilator 800. A second check valve 852 downstream from the gas delivery unit 826 may be used to prevent air from reaching the gas delivery unit 816 once it has been breathed or otherwise used by the patient's airway 812. A solenoid valve 854 may be provided downstream from the conduit 814, and more specifically downstream from the used air outlet 814d of the Y-piece conduit. The solenoid valve 854 may be operated to be either closed, thereby favoring a fresh air flow between the gas delivery unit 816 and the patient's airway 812, or open, thereby favoring a used air flow between the patient's airway 812 and a remainder of the ventilator 800 or ultimately the surrounding environment 844, where used air is to be evacuated. An enlarged view of the solenoid valve 854 is shown in
Referring back to
The embodiments described in this document provide non-limiting examples of possible implementations of the present technology. Upon review of the present disclosure, a person of ordinary skill in the art will recognize that changes may be made to the embodiments described herein without departing from the scope of the present technology. Further modifications could be implemented by a person of ordinary skill in the art in view of the present disclosure, which modifications would be within the scope of the present technology.
Number | Date | Country | |
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63055940 | Jul 2020 | US |