This application generally relates to medical ventilators.
Existing ventilators are expensive and have long lead times to manufacture. Furthermore, many technical limitations with respect to performance, durability, ease of manufacturing, safety and efficiency exist in current ventilator designs. It is necessary or desirable to overcome these and other deficiencies in the art, especially when the public health requires the scaling up of production of sufficient numbers of suitable ventilators to address pandemics as experienced in recent years.
One or more embodiments are directed to a ventilator apparatus, comprising a drive motor acting as a prime mover, receiving energy from a power source and providing a rotational mechanical motor output; a drivetrain, coupled to said drive motor, that receives said rotational mechanical motor output and converts the same into an oscillating linear mechanical movement; an elongated drive shaft, coupled to said drivetrain and driven thereby, the drive shaft further coupled to and powering two fluid pumps including a first (expiratory) fluid pump and a second (inspiratory) fluid pump, said drive shaft disposed in-line with and between said two fluid pumps; wherein said drive shaft translates axially along an axis of the drive shaft according to said oscillating linear mechanical movement of the drivetrain, and wherein said drive shaft forces a linear movement of both of said fluid pumps along said axis; a first fluid pathway that receives an expiratory input volume of fluid into said first (expiratory) fluid pump during a first phase of operation of said apparatus and discharges an expiratory output volume of fluid out of said first (expiratory) fluid pump during a second phase of operation of said apparatus; and a second fluid pathway that receives a breathing gas volume into said second (inspiratory) fluid pump during said first phase of operation of the apparatus and discharges said breathing gas volume during said second phase of operation of the apparatus.
For a fuller understanding of the nature and advantages of the concepts disclosed herein, reference is made to the detailed description of preferred embodiments and the accompanying drawings.
The pistons 120, 220 are driven by a drive motor 150 acting as a prime mover which receives energy from an energy source such as an AC or a DC electric power supply (i.e., utility power outlet and/or battery or similar source). The motor 150 is in mechanical communication with a drive motor assembly 160 acting as a powertrain that takes the rotational motor movement and translates the rotational motion of the motor 150 into a linear motion, in some aspects, oscillating linearly (back and forth) along an axis or direction congruent with a major dimension of the connecting rod or shaft 140.
Piston 220 moves in phase with piston 120, as discussed above, since they are mechanically coupled in series. Therefore, pushing piston 120 from a (first) expanded state to a (second) compressed state causes piston 220 to be pushed from a complementary (first) expanded state to a complementary (second) compressed state. Likewise, pulling or retracting piston 120 from the compressed state to the expanded state causes piston 220 to be pulled/retracted from the compressed state to the expanded state.
A plurality of O-rings 181 is used to form fluid-tight seals in each pump 100, 200. For example, O-rings 181 are disposed on each piston 120, 220 to form a fluid-tight seal around each piston 120, 220. The seal may be resistant to unwanted gas flow by said seal as the seal is seated in a dimensionally-matching aperture and maintains a sufficient pressure on any gap between the seal and the aperture or between the seal and the inner shaft to prevent gas flow between opposing sides of said seal. In addition, one or more O-rings 181 is disposed between the connecting rod 140 and cylinder 130 to form a fluid-tight environment within and between the gas volumes in said cylinders. Additional O-rings 181 can be used to seal the fluid connections into and out of each cylinder 130, 230 as shown.
The ventilator system 10 also includes a common housing 240 that houses the components of the system and a user interface 250 disposed on or in the housing 240. The housing 240 is shown open so that the inner components can be seen in the figure, but the housing can comprise a shell or a multi-part base portion onto which the components are secured and an upper portion or lid that fits over the components to close them off within the housing and to prevent damage or contamination to the components. In some embodiments, all of the housing, or alternatively just the upper lid of the housing may be constructed of a transparent material so the workings of the inner parts can be visible during operation. The base and upper parts of the housing may be glued with epoxy to one another, fused using plastic welding methods, or secured to one another with mechanical fasteners such as screws, optionally with a fluid-resistant gasket sealing leakage of fluids into or out of the housing 240.
A user interface 250 is electrically coupled to the processor based controller 180 which may be constructed on a printed circuit board (PCB) or other electronic integrated circuit to receive one or more input signals from the user interface 250 to set one or more parameters, settings, and/or operating modes (collectively, settings) of the ventilator. A ribbon connector or printed circuit lines can connect the user interface panel 250 with the internal processor circuits and other electrical components on electrical controller 180. Examples the settings that can be set with the user interface 250 include (1) ventilation operating mode (e.g., volume control with PEEP, pressure control with PEEP, pressure support, and/or another ventilation operating mode), (2) the patient's tidal volume, (3) the positive inhalation pressure set point (e.g., when operating in pressure-control mode), (4) the purified oxygen concentration and flow rate, (5) oxygen concentration in patient's inhalation gas, (6) expiratory flow rate, (7) respiratory rate, (8), I:E ratio, and/or (9) breath pause length. Examples of these and/or other settings are illustrated in
When piston 220 transitions from the compressed state to the expanded state, a negative pressure is formed in cylinder 230 to receive air and purified oxygen from one-way or check valves 301 and 302, respectively. Thus, cylinders 130, 230 respectively store exhaled gas and oxygen-enriched gas-to-be-inhaled in the next breath concurrently when the respective pistons 120, 220 transition from the compressed state to the expanded state. The valves 301, 302, and 304 close when pistons 120, 220 reach the respective positions corresponding to the expanded state.
When expiratory piston 120 transitions from the expanded state to the compressed state, a positive pressure is formed in cylinder 130 to force the exhaled gas out of cylinder 130 (e.g., into the atmosphere) via output line 410. Fluid communication between cylinder 130 and output line 410 is controlled by a one-way valve 305 that only allows fluid to flow out of the cylinder 130. When piston 220 transitions from the expanded state to the compressed state, a positive pressure is formed in cylinder 230 to force the oxygen-enriched gas-to-be-inhaled into the inhalation line 310 for patient inhalation. Thus, cylinders 130, 230 respectively discharge exhaled gas and oxygen-enriched gas-to-be-inhaled in the next breath concurrently when the respective pistons 120, 220 transition from the expanded state to the compressed state.
The inhalation line 310 can be fluidly coupled to a humidifier to increase the water-vapor content of the oxygen-enriched gas-to-be-inhaled. In some embodiments, a humidifier can be integrated into the ventilator system 10.
In volume-control mode, the processor-based controller 180 determines the position of the pistons 120, 220 to transition from the expanded state to the compressed state based on the patient's tidal volume, which is received by the controller 180 as a user input via user interface 250. The controller 180 can have a user input or can be pre-programmed with the diameters of the cylinders 130, 230 which the controller 180 can use to determine the position of the pistons 120, 220 to form the set-point tidal volume in each cylinder 130, 230 (e.g., the displacement of each piston 120, 220 equals the set-point tidal volume). In one example, each cylinder 130, 230 has approximately a 4-inch diameter. Other diameters of cylinders 130, 230 can also be provided. The position of the pistons 120, 220 can be determined by the number of rotations of motor 150, which can be stored in the memory of controller 180 as a look-up table, a formula, or other relationship. Fully compressing piston 220 therefore results in the delivery of the tidal volume set point to the patient (e.g., via inhalation line 310).
The frequency that the controller 180 transitions the pistons 120, 220 between the compressed state and the expanded state corresponds to the respiratory rate, which is an input setting in user interface 250. Additional input settings that can be used by the controller 180 include the inspiratory-rate-to-expiratory-rate ratio (or I:E ratio) and any pause between inspiration (inhalation) and expiration (exhalation). The controller can determine the expiratory flow rate using the inputs of respiratory rate, I:E ratio, and optionally the breath pause length. The expiratory flow rate corresponds to the speed that the pistons 120, 220 transition (e.g., retract) from the expanded state to the compressed state, which the controller 180 can determine based on the diameter of the cylinders 130, 230. The speed of the pistons 120, 220 can be controlled by adjusting the rotational speed of motor 150, which can be stored in the memory of controller 180 as a look-up table, a formula, or other relationship.
To achieve the desired oxygen concentration in the patient's inhalation gas, the controller 180 can calculate the required purified oxygen flow rate based on the calculated piston 120, 220 retraction speed, the diameter of the cylinders 130, 230, and the purified oxygen concentration. The required purified oxygen flow rate can be displayed on the user interface 250 with instructions for a nurse or other health care professional to set accordingly (e.g., by adjusting a valve in the hospital oxygen line). Alternatively, the valve 302 can be adjusted by the controller 180 (e.g., based on a pressure sensor in the purified oxygen intake line) to achieve the required purified oxygen flow rate.
Each one-way valve 301-305 can be a check valve, a solenoid valve, or another one-way valve. When the one-way valves 301-305 are check valves, the one-way valves 301-305 open and close automatically in response to the relative pressure differential across the respective valve. When the one-way valves 301-305 are solenoid valves, the one-way valves 301-305 open and close in response to electrical control signals sent from the controller 180. Each one-way valve 301-305 has a normally-closed position and an open position. The default for each valve 301-305 is the normally closed-position, and each valve 301-305 opens only in response to a minimum pressure differential across the valve (e.g., in a check valve) or in response to a control signal (e.g., in a solenoid valve).
The ventilator 10 includes pressure sensors that are in electrical communication with the controller 180. For example, a PEEP pressure sensor 420 is located in, or in fluid communication with, the exhalation line 400 to sense the pressure in the exhalation line 400. The controller 180 controls the expansion of piston 120 so that a minimum positive end-expiratory pressure (PEEP) remains in the patient's lungs at the end of the exhalation cycle. The PEEP can be set via the user interface 250 (e.g., a graphical user interface or other interface) on the ventilator 10. Examples of PEEP set points include the range of 3 cm H2O to 5 cm H2O, but higher or lower PEEP set points can be used. In operation, the controller 180 stops the rotation of motor 150 to stop pistons 120, 220 from further transitioning to the expanded state (e.g., to the left in
A positive pressure sensor 430 and a negative pressure sensor 440 are located in, or in fluid communication with, the inhalation line 310 to sense the positive and negative pressure, respectively, in the inhalation line 310. The controller 180 controls the compression of piston 220 so that positive inhalation pressure in the inhalation line 310, measured by positive pressure sensor 430, is less than or equal to a positive inhalation pressure set point. The positive inhalation pressure set point can be set via the user interface 250 (e.g., a graphical user interface or other interface) on the ventilator 10. In operation, when the ventilator 10 operates in pressure-control mode, the controller 180 stops the rotation of motor 150 to stop pistons 120, 220 from further transitioning to the compressed state (e.g., to the right in
When the ventilator 10 operates in volume-control mode, the controller 180 uses the positive pressure sensor 430 to generate an alarm when the positive inhalation pressure reaches or exceeds a maximum or peak positive inhalation pressure. The controller 180 does not use the positive inhalation pressure set point in volume-control mode. Otherwise, in volume-control mode, the piston 220 is fully compressed to deliver the entire volume of the oxygen-enriched gas mixture to the patient.
When the ventilator 10 operates in pressure-support mode (e.g., when the patient can initiate a breath, such as when the patient is weaning off ventilator-assisted respiration), the controller 180 uses the negative inhalation pressure sensed by negative pressure sensor 440 as a trigger to determine when the patient has initiated a breath. The trigger causes the controller 180 to begin the inspiration or inhalation cycle by starting the rotation of motor 150 to transition the pistons 120, 220 from the expanded state to the compressed state. The controller 180 does not use the negative inhalation pressure in pressure-control mode or volume-control mode.
As can be seen, a technical advantage of the disclosed ventilator is that it can be manufactured quickly and inexpensively without sacrificing functionality. In addition, the disclosed ventilator is re-usable even with patients that may have infectious diseases such as COVID-19 or other respiratory ailments.
This disclosure should not be considered limited to the particular embodiments described above. Various modifications, equivalent processes, as well as numerous structures to which the technology may be applicable, will be apparent to those skilled in the art to which the technology is directed upon review of this disclosure.
This application claims priority to U.S. Provisional Application No. 63/139,025, bearing the present title, filed on Jan. 19, 2021, which is hereby incorporated by reference.
Number | Date | Country | |
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63139025 | Jan 2021 | US |