The present invention generally relates to a ventilator and ventilator system for assistance with breathing and, more particularly, to an enclosure system and breathing circuit of a ventilator system.
One embodiment of the present invention is directed to a ventilator including a housing having a front panel, and a rear panel opposite the front panel and configured to couple to the front panel, a receptacle coupled to the rear panel of the housing, the receptacle having a recess, a sealing element disposed within the recess, the sealing element having an inlet and an aperture, and a blower having a blower outlet and a blower inlet, the blower inlet coupled to the sealing element such that the blower inlet at least partially abuts the aperture. The receptacle and the sealing element may comprise an airflow pathway configured to allow for flow of air from the inlet of the sealing element into the blower inlet and out of the blower outlet.
In some embodiments, the blower is configured to vent gas when the gas reaches a predetermined amount. The gas may be oxygen, and the predetermined amount may be at least 25%.
In some embodiments, the blower is configured to continuously vent gas to keep the gas at or below a predetermined level. The gas may be oxygen, and the predetermined level may be at least 25%.
In some embodiments, the ventilator further includes a gap between the blower inlet and the receptacle to allow air to flow into blower inlet. The receptacle may be integrally formed with the rear panel of the housing. The receptacle may be coupled to the rear panel of the housing.
In some embodiments, the recess includes a recessed lip and the sealing element is surrounded by the recess lip. The recess may be sized and shaped to receive the sealing element.
In some embodiments, the rear panel of the housing includes a cutout, and the receptacle is disposed within the cutout.
In some embodiments, the aperture of the sealing element is sized and shaped to receive at least a portion of the blower inlet.
In some embodiments, the sealing element is an additively manufactured enclosure.
In some embodiments, the ventilator further includes a securing element coupled to the receptacle, the securing element configured to receive the blower and secure the blower and sealing element within the recess of the receptacle.
In some embodiments, the blower, the sealing element, and the receptacle are coupled together to form a substantially airtight seal.
In some embodiments, the ventilator further includes one or more ports disposed on the housing and a port plate configured to at least partially cover the one or more ports, wherein the port plate is removable from the housing.
In some embodiments, the ventilator further includes one or more ports disposed on the housing and a door configured to at least partially cover the one or more ports, wherein the door is hingedly coupled to the housing and includes at least one of a plug and connection channel.
In some embodiments, the blower outlet and the inlet are coupled to a sensor, the sensor configured to receive air from the blower outlet and direct the air to the inlet.
In some embodiments, the ventilator further includes a breathing circuit coupled to the sealing element, the breathing circuit having an exhale valve configured to open and closed based on air flow generated by the blower.
Another embodiment of the present invention is directed to a ventilator including a housing having a back wall and a cutout disposed on the back wall, a modular fan assembly including a blower having a blower inlet, a sealing element having an aperture, and a receptacle having a recess and disposed within the cutout, the sealing element disposed within the recess of the receptacle and coupled to the blower such that the blower inlet at least partially abuts the aperture, and a securing element coupled to the receptacle, the securing element configured to secure the blower to the sealing element and the receptacle such that a substantially airtight seal is formed between the receptacle, the sealing element, and the blower.
Another embodiment of the present invention is directed to a ventilator including a housing having an inlet, a back wall, and a cutout disposed on the back wall, a modular fan assembly including a blower having a blower inlet and a blower outlet, a sealing element having a sealing aperture and a sealing inlet, and a receptacle having a recess and disposed within the cutout, the sealing element disposed within the recess of the receptacle and coupled to the blower such that the blower inlet at least partially abuts the aperture, and a securing element having a securing aperture and coupled to the receptacle, the securing aperture sized and shaped to receive the blower and the securing element configured to secure the blower to the sealing element and the receptacle. The blower, the sealing element, and the receptacle may comprise an airflow pathway configured to allow for flow of air from the inlet through the receptacle, the sealing aperture, and the blower inlet, and out of the blower outlet. The receptacle, the sealing aperture, and the blower inlet may form a substantially airtight seal.
The following detailed description of embodiments of the ventilator system will be better understood when read in conjunction with the appended drawings of exemplary embodiments. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.
Ventilators have been commonly used to provide treatment to individuals in respiratory distress. For example, ventilators are used in medical and hospital settings to treat individuals who are unable to breath on their own or who receive an inadequate amount of oxygen to their lungs. Current ventilators are bulky and require many wires and large towers located proximate to the patient. These ventilators are not easily portable and do not allow for efficient disassembly if an issue arose. Further, current ventilators may leak air, which can result in inefficiency in delivering gas to the patient, and/or may cause buildup of air or gas (e.g., oxygen) within the blower, which can be potentially dangerous (e.g., fire hazard).
Exemplary embodiments of the present invention provide a ventilator system, generally designated 100. In use, ventilator system 100 may be used to provide assistance with breathing for the treatment of patients in a medical setting, such as the intensive care unit (ICU) of a hospital or a medical clinic. Ventilator system 100 may also be used in other settings such as an ambulance, ambulatory center, in/out-patient centers, nursing homes/long term care facilities, and mobile clinics that can go to a patient directly. In some embodiments, ventilator system 100 is portable to allow for use in different environments. For example, ventilator system 100 may be easily transportable to be used in mobile settings (e.g., an ambulance).
In some embodiments, ventilator system 100 allows for rapid initiation of emergency ventilation to a patient in respiratory distress. Ventilator system 100 may be configured to provide rapid, emergency ventilation to a patient with minimal to no leakage of waste of air. Ventilator system 100 may provide an efficient system for providing ventilation to a patient. As discussed in further detail below, ventilator system 100 may, among other benefits, provide a modular fan assembly that allows for components of the fan assembly to be easily replaced while generating air or gas with minimal to no leakage of air and without causing buildup of air or gas within the fan assembly.
Referring to
In practice, ventilator 102 may output air, and breathing circuit 200 may provide a controlled pathway for the air to flow from ventilator 102 to patient interface 300. For example, breathing circuit 200 may include a tube (e.g., breathing tube) with one or more valves to control the flow of air from ventilator 102 to patient interface 300. Patient interface 300 may include a device (e.g., mask or nasal cannula) coupled to a patient to provide the air from ventilator 102 via breathing circuit 200.
Ventilator 102 may serve as the control hub or control system of ventilator system 100. Ventilator 102 may be configured to provide mechanical ventilation to a patient under respiratory failure through breathing circuit 200. Ventilator 102 may provide the necessary gas flow or airflow, which may be directed through breathing circuit 200 to patient interface 300, which is coupled to the face of a patient (e.g., the mouth and/or nose of the patient). Ventilator 102 may include blower 104, control system 106 and power supply 108. Breathing circuit 200 may include tube 202 which may be coupled to ventilator 102 at first end 204 and coupled to patient interface 300 at second end 206. Patient interface 300 may be a device that is secured to the face of a patient. For example, patient interface 300 may be a bag valve mask, respirator, or an endotracheal (ET) tube used for intubation.
In some embodiments, ventilator 102 is used to provide assistance to a patient in respiratory distress. Ventilator 102 may be a pump, pneumatic system, or any other type of device configured to provide air to a patient and/or assist a patient with respiration. Ventilator 102 may be configured to provide different modes of ventilation to a patient. For example, ventilator 102 may be configured to provide assist-control ventilation, volume-controlled ventilation, pressure support, pressure-controlled ventilation, pressure regulated volume control, positive end expiatory pressure, synchronized intermittent-mandatory ventilation, and/or manual ventilation. Ventilator 102 may be used instead of a bag valve device, an emergency transport ventilator, or any other modes or devices for providing ventilation to a patient.
Referring to
In some embodiments, housing 132 is lightweight to allow for easy portability of ventilator 102. For example, housing 132 may be comprised a lightweight yet durable material to allow for easy transportation of ventilator 102 while still providing protection for the internal components of ventilator 102. In some embodiments, housing 132 is comprised of one or more of acrylonitrile butadiene styrene (ABS), polyoxymethylene (POM), aliphatic polyamides (PPA), polycarbonate (PC), polyphenylsulfone (PPSU), polyetherimide (PEI), and polypropylene (PP). Housing 132 may be comprised of a lightweight, but durable material to allow for repeated use in harsh environments while still providing portability. For example, housing 132 may be comprised of ABS to provide portability and ensure that the components disposed within housing 132 remain secured and undamaged during use and/or transportation. In some embodiments, housing 132 of ventilator 102 is substantially rectangular shaped to allow for easy storage. However, housing 132 may be square, circular, triangle, octagonal, or any other shape desired. In some embodiments, housing 132 includes sidewalls 130. In a preferred embodiment, housing 132 includes four sidewalls 130 to define a substantially rectangular shape of ventilator 102. In some embodiments, housing 132 has rounded corners and beveled edges to allow for a more ergonomic shape and to prevent injury to a user.
Referring to
Housing 132 may include cutout 120 disposed on top surface 122 of housing 132. Cutout 120 may be sized and shaped to receive user interface 124. User interface 124 may be a display device, which may be disposed within cutout 120 and may be configured to receive input from a user. For example, user interface 124 may be a liquid crystal display (LCD), a light emitting diode (LED) display, an organic LED display, or any other type of display. In some embodiments, user interface 124 is a graphical user interface. For example, user interface 124 may be a touch screen configured to receive inputs from a user and transmits the inputs to control system 106. Further, user interface 124 may be used to display information about a patient using ventilator 102. For example, user interface 124 may provide (e.g., display) an indication of the respiratory status of a patient coupled to ventilator 102 via patient interface 300. In some embodiments, user interface 124 may display various settings, parameters, and/or functionalities of the components disposed within ventilator 102. For example, user interface 124 may display the peak inspiratory pressure (PIP), tidal volume (TV), respiratory rate (RR), positive end expiratory pressure (PEEP), inspiratory to expiatory ratio (I:E ratio), ventilation mode, peak flow, and sensitivity. User interface 124 may be coupled to control system 106 and may be configured to control various components of ventilator system 100. For example, a user may interact with user interface 124 to change parameters of blower 104. In some embodiments, user interface 124 is configured to display instructions to the user. For example, user interface 124 may provide instructions to a user for correcting an error to ventilator 102. In some embodiments, user interface 124 is configured to display a video or graphics to a user to instruct them on how to fix or address an error associated with ventilator 102.
In some embodiments, a user interacts with user interface 124 to change various modes and/or parameters of ventilator 102. For example, user interface 124 may provide an option for adjusting the PEEP, the PIP, the tidal volume, the I:E ratio, or other parameters. In some embodiments, ventilator 102 includes beacon or indicator 134 to provide a status of ventilator system 100. Indicator 134 may provide the status of ventilator system 100 and/or ventilator 102. For example, indicator 134 may indicate whether ventilator 102 is damaged, inoperable, and/or functionally properly. Indicator 134 may be an LED, and control system 106 may transmit a status to indicator 134 causing indicator 134 to illuminate a specific color and/or flash at a specific frequency. However, indicator 134 may be a transmitter configured to transmit an outgoing signal. In some embodiments, indicator 134 is configured to continuously transmit an outgoing signal regarding the status of ventilator 102. For example, indicator 134 may be configured to continuously transmit a signal without being requested to transmit a signal. Indicator 134 may transmit a signal indicating all components of ventilator 102 are functioning correctly.
In some embodiments, indicator 134 continuously transmits a signal until an error occurs, which interrupts the signal transmission resulting in indicator 134 no longer transmitting a signal. A user may check a receiver to determine whether indicator 134 is transmitting a signal and whether an error has occurred based on the transmission ceasing. In other embodiments, indicator 134 is configured to transmit a first signal when ventilator 102 is functioning correctly without significant errors and is configured to transmit a second signal when an error occurs. The first signal may be different than the second signal. Indicator 134 may transmit a signal wirelessly via radio frequency, Wi-Fi, cellular signal, Bluetooth, near field communication, or any other type of wireless modality.
In some embodiments, housing 132 may further include indicator 133. Indicator 133 may indicate the status of ventilator 102 and may be used to provide alerts to the user regarding an alarm condition. For example, indicator 133 being green in color may indicate normal operation of ventilator 102. However, indicator 133 flashing amber, red, yellow, or orange may indicate a malfunction or error with ventilator 102. In some embodiments, the degree of flashing of indicator 133 indicates the severity of the error. Indicator 133 may also indicate the battery status associated with power supply 108. For example, indicator 133 being green may indicate that the battery of ventilator 102 is fully charged. Indicator 133 being other colors, such as red, orange, yellow, amber, and/or flashing may indicate a malfunction or power level of the battery.
Ventilator 102 may include one or more buttons that control ventilator system 100. For example, ventilator 102 may include buttons 126 and 128, which control the power status and functions of ventilator 102. In some embodiments, button 126 is a power button (e.g., ON/OFF button) to control the power status of ventilator 102. For example, a user may press button 126 to power on ventilator 102. Button 128 may be a manual breath button, which delivers a single breath at a predetermined tidal volume to a patient. In some embodiments, button 128 may need to be pressed for a predetermined amount of time before ventilator 102 delivers a single breath to the patient.
Referring to
Referring to
Enclosure 114 may be sized and shaped to receive blower 104. In some embodiments, enclosure 114 is comprised of two halves that surround blower 104. However, enclosure 114 may be a unitary piece. For example, enclosure 114 may be configured to receive blower 104 such that blower 104 is disposed within enclosure 114. Enclosure 114 may be disposed within housing 132 such that when blower 104 is disclosed within enclosure 114, enclosure 114 is disposed within housing 132. Enclosure 114 being a unitary piece and configured to secure blower 104 within housing 132 allows for the reduction of components and material needed to manufacture ventilator system 100. Enclosure 114 may include inflow 169, which may pull air into blower 104 such that the air is received by blower 104.
In some embodiments, enclosure 114 is received by receptacle 159. Receptacle 159 may be sized and shaped to receive enclosure 114. In some embodiments, receptacle 159 is integrally formed with rear panel 131 of housing 132. For example, receptacle 159 may be integrally formed with rear panel 131 such that back wall 164 is the back wall of receptacle 159. However, receptacle 159 may be a separate component from back wall 164 and housing 132. Receptacle 159 may include recess 160. Enclosure 114 may be configured to be disposed within recess 160 of receptacle 159. Receptacle 159 may be integrally formed with housing 132 and enclosure 114 and recess 160 may assist in aligning blower 104 within housing 132 such that calibration and adjustment of the position of blower 104 is not required.
In some embodiments, blower 104 is disposed within enclosure 114, which is disposed within recess 160. However, enclosure 114 may be disposed within front panel 129. Blower 104 and enclosure 114 may be secured within recess 160 to create a substantially airtight seal around enclosure 114 and blower 104. For example, blower 104 may be disposed within enclosure 114, which is disposed within recess 160, and enclosure 114 may be configured to create an airtight seal with back wall 164 and recess lip 162 of recess 160 to allow air to flow from enclosure inlet 166 to blower inlet 172. In some embodiments, air flows from enclosure inlet 166 to blower inlet 172 without substantially leaking into housing 132 or buildup due to recess 160 creating an airtight seal around enclosure 114 and enclosure 114 creating an airtight tight seal around blower 104 thereby allowing air to flow easily into blower inlet 172. In some embodiments, the airtight seal around enclosure 114 and blower 104 results in less than 1% of air or gas leaking out of blower 104 and/or enclosure 114 into the rest of ventilator 102. However, the airtight seal around enclosure 114 and blower 104 may result in air or gas leakage of approximately 0.01% to approximately 5%, approximately 0.1% to approximately 4%, approximately 1% to approximately 3%, less than 5%, less than 4%, less than 3%, less than 2%, less than 1%, less than 0.5%, less than 0.1%, or less than 0.01%.
Referring to
In some embodiments, enclosure 114 may be additively manufactured. For example, enclosure 114 may be 3D printed. In alternative embodiments, enclosure 114 may be manufactured using a CNC machine or via injection molding. In some embodiments, enclosure 114 is comprised of Polycarbonate. However, enclosure 114 may be comprised of acrylonitrile butadiene styrene (ABS), polyoxymethylene (POM), aliphatic polyamides (PPA), polyphenylsulfone (PPSU), polyetherimide (PEI), or polypropylene (PP). In practice, use of enclosure 114 reduces the cost of the device as it decreases the amounts of components necessary, allowing for high-volume manufacturing. In some embodiments, enclosure 114 enables the precise location of all or portions of blower 104 within ventilator 102.
Referring to
Referring to
In some embodiments, a portion of housing 132 comprises the back wall of enclosure 114. For example, housing 132 may comprise a portion of enclosure 114 such that housing 132 and enclosure 114 create a pathway for air flow from blower 104. Housing 132 and enclosure 114 may be configured to create a pneumatic/airflow pathway allowing for air to flow through ventilator 102.
Referring to
In some embodiments, sealing element 186 is coupled to receptacle 182 and blower 180. For example, sealing element 186 and blower 180 may be coupled to receptacle 182 such that blower 180 and sealing element 186 are at least partially disposed within recess 177. Sealing element 186 may include inlet portion 187, which may couple to inlet 118. In some embodiments, inlet portion 187 is coupled to inlet 118 via inlet adapter 188. In some embodiments, inlet adapter 188 is a modular component of fan assembly 175 and is configured to be easily swapped out and replaced. However, inlet adapter 188 may alternatively be integrally formed with inlet portion 187.
Sealing element 186 may be coupled to blower 180. Sealing element 186 may include sealing aperture 192. In some embodiments, sealing element 186 is coupled to blower inlet 189. Sealing element 186 may be coupled to blower 180 such that a portion or all of blower inlet 189 abuts or is disposed within sealing aperture 192. Sealing element 186 may assist with forming an airtight seal between blower inlet 189 and receptacle 182. Sealing element 186 forming an airtight seal may allow air to enter ventilator 102 via inlet 118 and travel through receptacle 182 and into blower inlet 189 of blower 180 via sealing aperture 192. In some embodiments,
Blower 180 may be substantially the same as blower 104, but blower 180 may include heatsink 181. Heatsink 181 may be configured to dissipate heat generated by blower 180 and/or fan assembly 175. Incoming air (e.g., air entering blower 180 via blower inlet 189) may be pushed/forced out by blower 180 through blower outlet 194. Blower 180 may be secured to sealing element 186, which is secured to receptacle 182, via securing element 184. Securing element 184 may include securing aperture 197 and blower 180 may be received by securing element 184 such that blower 180 is disposed within securing aperture 197. Securing element 184 may couple to receptacle 182.
In some embodiments, securing element 184 is coupled to receptacle 182 such that blower 180 and sealing element 186 are disposed between securing element 184 and receptacle 182. Blower 180 and sealing element 186 being disposed between securing element 184 and receptacle 182 allows for a tight seal between blower 180, sealing element 186, and receptacle 182. For example, blower 180 may be coupled to sealing element 186, then blower 180 and sealing element 186 may be disposed with receptacle 182. Securing element 184 may be placed on blower 180 and coupled to receptacle 182. Tightening and securing of securing element 184 to receptacle 182 results in compression of blower 180 and sealing element 186 against receptacle 182 to create an airtight seal between blower 180, sealing element 186, and receptacle 182. Forming an airtight seal between blower 180, sealing element 186, and receptacle 182 maximizes the amount of air the is able to travel from inlet 118 to outlet 116.
In some embodiments, when blower 180 and sealing element 186 are disposed within receptacle 182, gasket 183 may be received by sealing aperture 192. For example, disposing sealing element 186 within receptacle 182 may result in aligning gasket 183 within sealing aperture 192 such that gasket 183 is at least partially disposed within sealing aperture 192. In some embodiments, gasket 183 may be disposed around the circumference of sealing aperture 192 to secure sealing element 186 in place within receptacle 182. Gasket 183 being disposed around the circumference of sealing aperture 192 prevent air from leaking out of receptacle 182 and sealing element 186 and maximizing the air entering blower inlet 189. In some embodiments, sealing element 186 includes a plurality of apertures disposed proximate blower inlet 189 when sealing element 186 is coupled to blower 180. The plurality of apertures may allow air flow from sealing element 186 and into blower inlet 189. For example, air may flow from inlet 118 through inlet portion 187 and out of the plurality of apertures such that the air can then flow into blower inlet 189.
In some embodiments, blower outlet 194 is coupled to outlet adapter 185. Outlet adapter 185 may be an S-shaped tube coupling blower 180 to outlet 116. In some embodiments, outlet adapter 185 is comprised of silicone. Outlet adapter 185 may integrally formed with blower outlet 194 or may be removably coupled to blower outlet 194. Inlet adapter 188 and outlet adapter 185 may assist in fan assembly 175 being modular. For example, damage to or obstruction of inlet adapter 188 and/or outlet adapter 185 may not require disassembly of fan assembly 175. This is because fan assembly 175 is modular thereby allowing inlet adapter 188 and/or outlet adapter 185 to be easily replaced without having to remove the entirety of fan assembly 175 from ventilator 102.
Similar to
In some embodiments, air or gas may flow from inlet 118 into sealing element 186. The air or gas may flow into interior space 179 formed between receptacle 182 and blower inlet 189. In some embodiments, interior space 179 is the area within sealing aperture 192. Blower 180 being disposed within sealing element 186, which is disposed within receptacle 182, creates an airtight seal between blower inlet 189 and receptacle 182. This allows air to flow from inlet portion 187, through interior space 179, and into blower inlet 189 with minimal to no leakage of air.
In some embodiments, ventilator 102 is configured to allow a small amount of air to leak to prevent accumulation of air within enclosure 114. For example, due to fire hazard concerns, enclosure 114 may prevent the buildup of air/gas within enclosure 114 by allowing a small amount of air/gas within enclosure 114 to leak out. In some embodiments, ventilator 102 may be configured to limit the amount of oxygen accumulated within enclosure 114 and/or housing 132. For example, enclosure 114 may include a sensor to measure the percentage of oxygen within enclosure 114 and/or housing 132 and may vent out the oxygen when above a pre-determined amount. For example, blower 104 of ventilator 102 may be configured to vent or leak out air/oxygen when the sensor determines that there is more than 15%, 20%, 25%, 30%, 35%, 40%, 45%, or 50% oxygen within enclosure 114 and/or housing 132. In some embodiments, ventilator 102 is configured to continuously vent or leak out air/oxygen to keep the amount of oxygen within enclosure 114 and/or housing 132 at or below 15%, 20%, 25%, 30%, 35%, 40%, 45%, or 50%.
Referring to
In some embodiments, ventilator 102 includes exhaust conduit 156. Exhaust conduit 156 may be disposed on or within blower 104 and may be configured to provide a pathway for air/exhaust to exit blower 104 thereby preventing buildup of air within blower 104 and preventing overheating of blower 104. In some embodiments, ventilator 102 includes exhaust manifold 158, which includes exhaust inlet 161 and exhaust outlet 163. Exhaust manifold 158 may be communicatively coupled to exhaust conduit 156 and may be configured to provide a pathway for air to exit ventilator 102. Air may flow through exhaust manifold 158 to exhaust port 165, which is configured to provide a pathway for air to flow outside of ventilator 102.
Referring to
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Valve 195 may be coupled to outlet adapter 185 and inlet adapter 188. Valve 195 may further be coupled to control line port 136. Valve 195 may be a solenoid valve. However, valve 195 may be a valve such as a solenoid valve, rotary valve, a linear valve, a plug valve, or a ball valve. In some embodiments, connector 198 provides air from outlet adapter 185 to control line 616 via valve 195. For example, valve 195 may be coupled to control line port 136 via an air tube, which is in communication with control line 616. As discussed in further detail below, valve 195 being coupled to control line 616 may control exhale valve 208. For example, valve 195 is opened, air flows from outlet adapter 185 through control line 616. The resulting force from the air flow results in exhale valve 208 closing and remaining closed. In some embodiments, the pressure of air within control line 616 builds up. In order to relieve the built up pressure of air in control line 616, valve 195 may allow air to flow into inlet adapter 188 via connector 191. The air flowing into inlet adapter 188 may alleviate the pressure built up in control line 616. In some embodiments, valve 195 is configured to allow air to flow from control line 616 to inlet adapter 188 to prevent build up of air pressure within control line 616.
Outlet adapter 185 may also include connector 199. Connector 199 may couple outlet adapter 185 to sensor 196 via an air tube. Connector 199 may be an elbow joint configured to couple outlet adapter 185 to sensor 196. However, connector 199 may be a valve such as a solenoid valve, rotary valve, a linear valve, a plug valve, or a ball valve. In some embodiments, sensor 196 is an gas sensor. For example, sensor 196 may be an oxygen sensor configured to measure the amount of oxygen of the air or gas within through outlet adapter 185. Sensor 196 may be a galvanic oxygen sensor, an ultrasonic oxygen sensor, or any other type of oxygen sensor. In some embodiments, sensor 193 and sensor 196 are different sensors. For example, sensor 193 may be a pressure sensor and sensor 196 may be a gas sensor. In some embodiments, connector 198 only couples outlet adapter 185 to sensor 196, and sensor 196 may be both a gas and pressure sensor
In some embodiments, sensor 196 is also coupled to inlet adapter 188. For example, sensor 196 may be coupled to inlet adapter at connector 191 via an air tube. Air or gas may flow from outlet adapter 185 to sensor 196 then to inlet adapter 188. For example, inlet adapter 188 may also be coupled to sensor 196 via an air tube. Air or gas from outlet adapter 185 may flow to sensor 196 and then may be discharged to inlet adapter 188. In some embodiment, sensor 196 is configured to receive air from outlet adapter 185 via connector 199, determine the concentration of a certain gas in the air from outlet adapter 185, and then direct the air to inlet adapter 188 via connector 191. In practice, sensor 196 may be configured to measure air or gas from outlet adapter 185 and discharge the air or gas to inlet adapter 188. For example, air may flow from outlet adapter 185 through connector 199 to sensor 196. Sensor 196 may measure a concentration (e.g., oxygen) within the air then direct the air to inlet adapter 188 via connector 191 to ensure that air is not wasted when it flows from outlet adapter 185 to sensor 196. This configuration increases efficiency of ventilator 102 as no air is wasted during sampling and measuring of gas concentration via sensor 196.
In some embodiments, each of outlet adapter 185 and inlet adapter 188 are coupled to valve 195. Valve 195 may be configured to control the flow of air to and from outlet adapter 185 and inlet adapter 188. For example, valve 195 may be coupled to connector 198 of outlet adapter 185 and/or connector 191 of inlet adapter 188 to control the flow of air in and out of outlet adapter 185 and/or inlet adapter 188.
In some embodiments, connector 198, connector 191, valve 195 and sensor 193 assist fan assembly 175 and ventilator 102 in preventing buildup of air or gas (e.g., oxygen). For example, connector 198, connector 191, valve 195, and sensor 193 may be configured to monitor the pressure and control the path of air throughout fan assembly 175 to prevent leakage of air. Further, connector 198, connector 191, valve 195 and sensor 193 may assist in maximizing the efficiency of ventilator 102 by allow air from outlet adapter 185 that is sent for testing/monitoring (e.g., via sensor 196) to be recirculated back to inlet adapter 188 to be used by blower 180 and outputted to the patient via outlet 116.
Referring to
In some embodiments, writing device 113 is disposed within ventilator 102. However, writing device 113 may be disposed outside of ventilator 102 and may be an external device. Writing device 113 may be disposed within, on, or outside of ventilator 102 and may wirelessly communicate with transmitting device 117. In some embodiments, writing device 113 is configured to wirelessly write information to transmitting devices 117. Writing device 113 may be coupled to control system 106 and may be stored anywhere within ventilator 102. Writing device 113 may further be coupled to memory 115, which may be coupled to control system 106.
In some embodiments, transmitting device 117 is stored within ventilator 102 and is communicatively coupled to control system 106. However, transmitting device 117 may be disposed on or near housing 132 of ventilator 102 and may be configured to wirelessly communicate with control system 106. For example, transmitting device 117 may be coupled to the exterior surface of housing 132 and may wirelessly receive information from control system 106. Transmitting device 117 may be a storage device configured to wirelessly transmit information, such as a wireless transmitting device. For example, transmitting device 117 may include one or more of an RFID chip/tag, a near-field communication chip, a Bluetooth transmitter, a digital barcode, or a Wi-Fi module. In some embodiments, transmitting device 117 only transmits information upon request. However, transmitting device 117 may be configured to transmit information automatically and/or autonomously without intervention by a user or external device. Transmitting device 117 may be configured for low-power consumption and may be configured to receive power only from an external source. However, transmitting device 117 may be powered by power supply 108 or its own power supply.
Control system 106 may receive information associated with, for example, the status of ventilator system 100 and store the information in memory 115 or directly to transmitting device 117. Writing device 113 may access memory 115 and may write the information stored within memory 115 to transmitting device 117. In some embodiments, memory 115 includes transmitting device 117. Memory 115 may include, for example, random access memory (RAM), a hard disk drive and/or a removable storage drive, such as a floppy disk drive, a magnetic tape drive, an optical disk drive, or a wireless device, such as an RFID tag. Memory 115 may include other similar means for allowing computer programs or other instructions to be loaded into ventilator system 100. For example, memory 115 may include a removable memory chip (such as an EPROM, or PROM, or flash memory) and associated socket, and other removable storage units and interfaces which allow software and data to be transferred from a removable storage unit to ventilator system 100. In some embodiments, memory 115 is a non-volatile memory. In some embodiments, memory 115 is configured for low-power consumption or configured to receive power only from an external source.
In some embodiment, control system 106 is coupled to power supply 108, which may be configured provide power to the various components of ventilator system 100. For example, control system 106 may be configured to route power from power supply 108 to motor 110 of blower 104. Power supply 108 may be disposed within ventilator 102. Power supply 108 may include one or more of an internal rechargeable battery, a removable rechargeable battery, and a removable non-rechargeable battery. As shown in
In some embodiments, ventilator system 100 is configured to administer a status check or a self-test to ensure that all components are working properly and that there are not any malfunctions. In some embodiments, control system 106 is configured to test the various components of ventilator system 100 to determine the functional status of, for example, blower 104, power supply 108, writing device 113, memory 115, transmitting device 117, and control system 106, in addition to reporting the operational status of ventilator system 100. For example, control system 106 may be configured to receive information from memory 115 regarding any corrupted cores, from blower 104 regarding an occlusion of fan 112, from outlet 116 or inlet 118 regarding occlusions, from power supply 108 regarding improper voltages, or any other information necessary to ensure that ventilator 102 is functioning properly.
In some embodiments, ventilator 102 of ventilator system 100 is configured to administer a status check, store the results of the status check, and then power down. In some embodiments, ventilator 102 is configured to perform a self-test while ventilator 102 is in storage or otherwise not in active use (e.g., in a powered down state). The results of the status check may be stored on memory 115, which may be configured to transmit the results without receiving power from ventilator 102. For example, ventilator 102 may power on, administer a status check, store the results of the status check on transmitting device 117 and/or memory 115, and then power down. Transmitting device 117 may be configured to transmit the results only when interrogated by an external source. The external source may be a receiving or reading device that provides power to transmitting device 117 enabling transmitting device 117 to transmit the results. This allows ventilator 102 to conserve power as it does not need to power on to transmit the results of the status check and enables ventilator 102 to provide results at any time upon interrogation by a user.
In some embodiments, ventilator 102 includes inlet 118 and outlet 116. Inlet 118 may be disposed on one of sidewalls 130 of housing 132 and allow for air to flow from the external environment (ambient air) or an air source, such as a reservoir of gas (02), to blower 104. For example, blower 104 may be configured to pull in air from inlet 118 and push the air out through outlet 116. In some embodiments, ventilator 102 relies on blower 104 to provide air and does not require compressed air to operate. In some embodiments, blower 104 is coupled to outlet 116, which is disposed on an outer periphery of housing 132. For example, outlet 116 may be disposed on sidewall 130 of housing 132. Outlet 116 may be cylindrical in shape and hollow. In some embodiments, outlet 116 couples blower 104 to breathing circuit 200 to patient interface 300. For example, outlet 116 may be configured to allow air to flow from blower 104 of ventilator 102 through breathing circuit 200 to patient interface 300. In some embodiments, outlet 116 is a valve that may open or close to control the airflow from blower 104 to breathing circuit 200. In some embodiments, blower 104 includes blower inlet 172. Blower inlet 172 may be in communication with inlet 118 and may be configured to pull air into blower 104, which is then pushed out of blower 104 at a higher flow rate by fan 112.
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In some embodiments, breathing circuit 200 does not include an active control or anti-asphyxiation valve that are traditionally used to prevent/reduce asphyxiation in the patient. In traditional ventilators, asphyxiation valves are used when there is device failure, and the patient needs to breathe spontaneously by allowing gas from the external atmosphere into the breathing circuit. Further, traditional ventilators utilize an anti-asphyxiation/check valve to maintain PEEP, while allowing the patient to breathe spontaneously if the device fails or set incorrectly. In practice, breathing circuit 200 allows ventilator system 100 to maintain pressure with positive pressure from blower 104, instead of a valve. In some embodiments, ventilator system 100 maintains PEEP by driving motor 110 of blower 104 on exhalation. Breathing circuit 200 may be configured to not utilize an anti-asphyxiation/check valve by including a non-obstructed pathway between the patient and an air source. This allows the patient to breathe even when there is failure to ventilator system 100. Breathing circuit 200 allows for a clear path for the patient to inhale and inspire ambient air without obstructions even when motor 110 and/or blower 104 fails.
In some embodiments, exhale valve 208 is controlled by control system 106 to control the exhalation of the patient. In another embodiment, exhale valve 208 is controlled based on the exhalation of the patient. In yet another embodiment, exhale valve 208 is controlled by both control system 106 and the exhalation of the patient. Exhale valve 208 may be configured to allow for a specific respiration rate but may be opened by the exhalation of the patient as well. For example, for a respiration rate of 12 (one breath every five seconds), exhale valve 208 may open every five seconds and may also open more than every five seconds if the patient is breathing at different rate.
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In practice, on inhalation, ventilator system 100 may be configured such that valve 610 is opened, resulting in exhale valve 208 closing such that no gas/air leaves ventilator system 100 via exhale valve 208. On exhalation, valve 610 may be closed, allowing exhale valve 208 to be opened since no positive pressure is being exerted on exhale valve 610 and the gas exhaled by the patient may be vented into the atmosphere. In some embodiments, PEEP is maintained after exhalation by driving motor 110 at a lower speed to prevent backflow into ventilator system 100, which would cause CO2 rebreathing. In some embodiments, the patient exhalation passes through a breathing filter so that internal components and atmosphere are protected from potential microbial contamination, dust, dirt and other particulate.
In some embodiments, ventilator system 100 is configured to allow the patient to breathe during failure of ventilator system 100 by using blower 104 and valve 610, as discussed above. In this configuration, if there is a fault that results in critical failure of ventilator system 100 and motor 110/blower 104 stops, exhale valve 208 may be opened. Opening of exhale valve 208 during failure allows the patient to freely be able to breathe. If exhale valve 208 is stuck closed or there is an issue with control system 106, the patient will still be able to breathe through breathing circuit 200 since there is no check valve between the patient's airway and inlet 118 preventing backflow. If there is a failure that causes motor 110 and/or fan 112 to get stuck in an active position (inhale state), exhalation would still be possible because exhale valve 208 has a maximum pressure limit that the patient would be able to overcome through their force of breathing. In some embodiments, fan 112 may be a non-occlusive fan configured to allow air flow even when motor 110 and/or fan 112 becomes stuck or fails. In some embodiments, ventilator system 100 includes a blow-off/check valve configured to release pressure within breathing circuit 200 when a pre-determined pressure is reached.
In some embodiments, ventilator system 100 determines inspiratory pressure using pressure line 618 that is connected to breathing circuit 200 near the patient. The pressure reading of pressure sensor 606 at pressure line 618 may be used to determine the measured PIP (max inspiratory pressure per breath cycle), PEEP, and to generate pressure graphs. In some embodiments, a flow meter external to ventilator 102 may determine airflow and may be connected to ventilator 102 via It is connected to the device using a flow line. The data from the flow meter may be used to measure flow into and out of the patient, and thus to calculate Tidal Volume and other patient monitoring parameters such as minute volume amongst other things. In some embodiments, ventilator system 100 includes a pressure sensor to determine the atmospheric pressure and is configured to calibrate delivery of air to the patient via breathing circuit 200 accordingly.
In some embodiments, ventilator system 100 may be configured to obtain a differential pressure reading at differential pressure sensor 604. The differential pressure reading may be used to measure flow. Since flow is proportional to the pressure drop of a gas/liquid moving over a resistance in a pipe, ventilator 102 can determine the air flow to and from the patient. With some intentional resistance in breathing circuit 200, and a differential pressure measurement from one side of the resistance to the other (and proper calibration), ventilator 102 can determine the flow in breathing circuit 200. In some embodiments, ventilator system 100 includes differential pressure line 615, which provides air to patient sensor 612, which may be a pressure sensor.
In some embodiments, breathing circuit 200 includes flow sensor 210, which may be disposed on or within tube 202. Flow sensor 210 may be configured to sense the flow of air within breathing circuit 200. For example, flow sensor 210 may detect the rate and amount of air flowing through tube 202. In some embodiment, flow sensor 210 is coupled to control system 106 to provide feedback to ventilator system 100. For example, flow sensor 210 may provide information to control system 106, which may change the parameters of blower 104 based on the information.
Breathing circuit 200 may further include patient filter 212, which may be disposed proximate second end 206 of tube 202. For example, patient filter 212 may be disposed on or within tube 202 proximate second 206 and adjacent to patient interface 300. Patient filter 212 may be configured to filter out particles within air. For example, patient filter 212 may filter out particles and airborne viruses to protect the patient using ventilator system 100.
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Inlet 118 may include cover or door 121 disposed over inlet 118. Cover 121 may be configured to allow inlet 118 to be connected to air/gas source, such as an oxygen source. Inlet 118 may also include cover 121 to prevent connection of the wrong connector to inlet 118. For example, inlet 118 may include a specialized cover configured to allow only for reservoirs of only certain gases or fluids to flow into inlet 118. In some embodiments, cover 121 prevents inadvertent connection of breathing circuit 200 to the wrong connection. In some embodiments, a user would have to actively remove cover 121 from inlet 118 to allow connection of an air/gas source to inlet 118. Cover 121 may be coupled to port plate 119. For example, cover 121 may be hingedly coupled to port plate 119 to allow for covering of inlet 118. In some embodiments, cover 121 may allow ambient air to flow into inlet 118 without removing cover 121 from inlet 118. In some embodiments, cover 121 includes special markings to indicate the sources of air/gas that can be coupled to inlet 118. In some embodiments, a special tool is required to remove cover 121 from inlet 118 to prevent inadvertent connection to inlet 118. In some embodiments, cover 121 includes a sensor to only allow removal from inlet 118 when certain gases are detected. Cover 121 may also be configured to prevent debris from entering inlet 118.
In some embodiments, port plate 119 includes a testing cap configured to allow for the testing of airflow and pneumatic system 104 of ventilator 102. The testing cap may be configured to disposed over port plate 119 and allow air coming from outlet 116 of fan 112 to flow through the testing cap into a pressure sensor disposed on port plate 119 or the testing cap. For example, the testing cap may include a recess that allows air to flow form outlet 116 to the pressure sensor to determine the pressure of air provided by pneumatic system 104. The recess of the testing cap may allow for air to be channeled from outlet 116 to the pressure sensor, which may be disposed on port plate 119. For example, the testing cap may allow for testing of pneumatic system 104 when ventilator 102 is in storage. The testing cap may be configured to ensure the integrity of pressure sensors of ventilator 102 in addition to providing additional protection to port plate 119 and outlet 116. In some embodiments, the recess of testing cap allows air to flow from outlet 116 to other sensors disposed on port plate 119 and/or within the testing cap. The testing cap may be hingedly coupled to port plate 119 or housing 132 and may be configured to be completely removable from ventilator 102.
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In some embodiments, blower 104 is ramped up to test the functionality of blower 104 via pressure sensor 608. For example, by ramping up blower 104 and blocking outputs of pressure line 618, control line 616, and exhale line 619, pressure is built up via connection line 617, thereby allowing pressure sensor 608 to receive a pressure reading. In some embodiments, blower 104 includes a tachometer configured to provide RPM (revolutions per minute) data. In some embodiments, the RPM data is correlated with pressure readings, such that a specific RPM equates to a specific pressure reading at pressure sensor 608. In other words, a pressure reading at pressure sensor 608 may be dependent on the RPM data provided by the tachometer. For example, pressure sensor 608 may output a pressure value based on the RPM data provided by the tachometer. Given a mismatch in the expected pressure based on the RPM data and the pressure reading at pressure sensor 608, an error may have occurred in ventilator system 100, such as blower 104 or with pressure sensor 608.
In some embodiments, the functionality of each of pressure sensor 608, pressure sensor 606, and differential pressure sensor 604 are tested by ramping up blower 104. For example, by ramping up blower 104, having valve 610 open, and outlet valve 620 closed, air may travel from blower 104 to pressure sensor 608 and through valve 310 and connection line 617 to pressure sensor 606 and differential pressure sensor 604. Each of pressure sensor 608, pressure sensor 606, and differential pressure sensor 604 may provide the same pressure reading when valve 610 is opened, outlet valve 620 is closed, and connection line 617 is an opened state. In some embodiments, the pressure reading at pressure sensor 608 and pressure sensor 606 is dependent on the RPM data provided the tachometer disposed within blower 104.
In some embodiments, ventilator system 100 is configured to test the functionality of valve 610. For example, ventilator system 100 may open valve 610 and vent out and release the air within blower 104 to the atmosphere, which should result in the pressure reading at pressure sensor 608 to decrease since the pressure is no longer built up. Ventilator system 100 may close valve 610, which thereby blocks the air path to exhale valve 208 via control line 616. Closing valve 610 results in the pressure reading at pressure sensor 608 increasing and the pressure reading at pressure sensor 606 decreasing to, for example, atmospheric pressure. In some embodiments, the pressure reading at pressure sensor 606 is substantially the same as the pressure reading at pressure sensor 608, which confirms that both pressure sensor 606 and pressure sensor 608 are operating correctly. In some embodiments, opening valve 610 results in the venting of air to atmosphere, which results in a decrease in the pressure reading at pressure sensor 606. In some embodiments, opening valve 610 allows for pressure line 618 to connect with control line 616 via connection line 617, which allows ventilator system 100 to assess pressure sensor 606 and differential pressure sensor 604.
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It will be appreciated by those skilled in the art that changes could be made to the exemplary embodiments shown and described above without departing from the broad inventive concepts thereof. It is understood, therefore, that this invention is not limited to the exemplary embodiments shown and described, but it is intended to cover modifications within the spirit and scope of the present invention as defined by the claims. For example, specific features of the exemplary embodiments may or may not be part of the claimed invention and various features of the disclosed embodiments may be combined. Unless specifically set forth herein, the terms “a”, “an” and “the” are not limited to one element but instead should be read as meaning “at least one”.
It is to be understood that at least some of the figures and descriptions of the invention have been simplified to focus on elements that are relevant for a clear understanding of the invention, while eliminating, for purposes of clarity, other elements that those of ordinary skill in the art will appreciate may also comprise a portion of the invention. However, because such elements are well known in the art, and because they do not necessarily facilitate a better understanding of the invention, a description of such elements is not provided herein.
Further, to the extent that the methods of the present invention do not rely on the particular order of steps set forth herein, the particular order of the steps should not be construed as limitation on the claims. Any claims directed to the methods of the present invention should not be limited to the performance of their steps in the order written, and one skilled in the art can readily appreciate that the steps may be varied and still remain within the spirit and scope of the present invention.
Filing Document | Filing Date | Country | Kind |
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PCT/US22/17146 | 2/21/2022 | WO |
Number | Date | Country | |
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20240131283 A1 | Apr 2024 | US |
Number | Date | Country | |
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63151913 | Feb 2021 | US |