Abstract: A system for reducing airway obstructions of a patient may include a ventilator, a control unit, a gas delivery circuit with a proximal end in fluid communication with the ventilator and a distal end in fluid communication with a nasal interface, and a nasal interface. The nasal interface may include at least one jet nozzle, and at least one spontaneous respiration sensor in communication with the control unit for detecting a respiration effort pattern and a need for supporting airway patency. The system may be open to ambient. The control unit may determine more than one gas output velocities. The more than one gas output velocities may be synchronized with different parts of a spontaneous breath effort cycle, and a gas output velocity may be determined by a need for supporting airway patency.

Abstract: The present invention provides a system and method for supplying and managing oxygen suited for use on-board an aircraft for providing breathable oxygen to pilots and cockpit crew. Components of the system work together to optimize oxygen utilization while reducing costs from maintenance and added weight of traditional pressurized gaseous cylinders. Components include a rapid oxygen supply for immediate use in emergency situations, an on-board oxygen generator (OBOG), a controller, a pulsed oxygen delivery subsystem that detects inhale/exhale phases and adapts to physiological requirements, and a breathing mask for each pilot and cockpit crew member.

Abstract: A demand regulator (1) for aircraft breathing device (100) comprising: —a respiratory chamber (9) supplied with respiratory gas comprising breathable gas and dilution gas, —a breathable gas supply line (12, 13), —a dilution gas supply line (14, 15), —a first adjusting device (50, 60) of non-electrical type adjusting the pressure in the respiratory chamber (9), and —a second adjusting device (22, 24, 40, 41-49) adjusting the rate of dilution gas in the respiratory gas supplied to the respiratory chamber (9), the second adjusting device comprising a dilution valve (24) disposed in the dilution gas supply line (14, 15), a sensor (41-49) and an electrical control unit (40) adjusting the rate of dilution gas in the respiratory gas by controlling the dilution valve (24).

Abstract: The invention discloses a safety mechanical system by which emergency oxygen is delivered to motor vehicle occupants during an accidental water submersion of the vehicle. The system utilizes an oxygen filled tank located in the trunk, or another concealed area. The tank is connected to a manifold system with an automatic valve. The valve is activated and opened when a series of sensors detects that the vehicle is partially or fully submerged. Upon such detection, the valve is opened and oxygen is delivered through the manifold, then to a series of flexible tubes to a set of drop down masks that automatically deploy from an overhead console in the vehicle's headliner. The drop down assembly is of an adequate length of coiled hose similar to that found on a commercial airliner for oxygen use during sudden decompression. With such an installed system, vehicle occupants are provided with a mask and oxygen until they can be rescued or escape on their own.

Abstract: A gas delivery system including a gas delivery device (100), a control module (200) and a gas delivery mechanism is described. An exemplary gas delivery device includes a valve (107) assembly with a valve and circuit including a memory (134), a processor (122) and a transceiver (120) in communication with the memory. The memory may include gas data such as gas identification, gas expiration and gas concentration. The transceiver on the circuit of the valve assembly may send wireless optical line-of-sight signals to communicate the gas data to a control module. Exemplary gas delivery mechanisms include a ventilator (400) and a breathing circuit (410). Methods of administering gas are also described.

Abstract: A nitric oxide delivery device including a valve assembly, a control module and a gas delivery mechanism is described. An exemplary gas delivery device includes a valve assembly with a valve and circuit including a memory, a processor and a transceiver in communication with the memory. The memory may include gas data such as gas identification, gas expiration and gas concentration. The transceiver on the circuit of the valve assembly may send wireless optical line-of-sight signals to communicate the gas data to a control module. Exemplary gas delivery mechanisms include a ventilator and a breathing circuit. Methods of administering gases containing nitric oxide are also described.

Abstract: The ventilation module (8) regulates the inspiratory pressure (P) according to an inspiratory pressure order (AI). A control module (9) compares the breathed volume at each cycle (VTI) with a minimum volume order (VRImini) and varies the pressure order (AI) in the direction tending to maintain the breathed volume (VTI) just over the minimum (VTImini), but keeping the pressure order (AI) within the interval comprised between the two extreme values (AImini, AImaxi). Utilization to combine the advantages of the pressure mode ventilation with those of the volumetric ventilation.

Abstract: A noninvasive of detecting patient-ventilator asynchrony that is easily adaptable to existing ventilator monitoring systems and provides timely and actionable information on the degree of patient asynchrony both during invasive and non-invasive ventilation. Display of, frequency spectra and the use of a measure of spectral organization, such as H1/DC, allows for both manual and automatic adjustment of a ventilators to prevent or correct patient-ventilator asynchrony.

Abstract: Respiratory support and/or controlled mechanical ventilation of a patient are provided. A ventilation apparatus may include a ventilator, a transtracheal prosthesis, and a respiratory relief device. The transtracheal prostheses and ventilation catheter may be arranged such that the patient can breathe freely through the upper airway and/or the tracheal prostheses. Respiratory sensors may measure a breathing rate, lung pressure, airway pressure, or a combination thereof. Pulses of gas may be provided to the patient through the ventilation catheter during inspiration. The pulses may have a first volume while the patient breathes normal and a second volume when the sensors detect a cessation of breathing or reduction in breathing volume. The second volume may be provided at 1-5 times the normal breathing rate, with a volume 25-500% times the first volume, or both.

Abstract: A pressure generating system and method for generating a flow of fluid at a pressure above atmospheric pressure. The system includes a pressure generator and a valve that controls the pressure/flow of gas delivered to the patient. The system monitors energy provided to the valve, a characteristics associated with movement of the valve, a position of the valve, or any combination thereof. In addition, the controller controls an operating speed of the pressure generator such that the valve operates over a majority of the range of positions during use of the pressure support system.

Abstract: Methods relating to the power management of positive airway pressure apparatus using a battery are disclosed herein. The methods, in various aspects, are adapted to prolong the delivery of a positive airway pressurized therapy when the positive airway pressure apparatus is operated under battery power.

Abstract: An electronic anesthesia delivery apparatus for mixing a carrier gas and first and second anesthetic agents comprises a chassis having an electronic vaporizer, the vaporizer having a first anesthetic chamber and a second anesthetic chamber retaining the first anesthetic agent and the second anesthetic agent, a carrier gas input port in flow communication with the first anesthetic chamber and the second anesthetic chamber, a precision orifice and an electronic control valve corresponding to each of the chambers being downstream of the gas input port, each of the chambers having a conduit in flow communication with the carrier gas input port, each of the conduits extending into each of the chambers below an upper level of anesthetic agent, wherein the carrier gas passes through a porous diffuser near an end of the conduit and bubbles through the anesthetic agent, the chamber further comprising an anesthetic gas outlet port, an electronic touchscreen display for controlling carrier gas flow rate to the first ane

Abstract: A respiratory treatment apparatus and method in which a leak is determined by using an averaging window. The window starts at the present time and extends back in time to a point determined according to a current one of progressively detected phase measures of a first respiratory cycle and a corresponding phase measure attributable to a preceding second respiratory cycle. In another aspect, a jamming index indicates whether the leak is rapidly changing. To the extent that jamming is high, the leak estimate used progressively changes from that using sliding breath-window averaging to a more robust and faster responding low-pass filter method, and adjustment of ventilatory support based on measures employing estimated respiratory flow is slowed down or stopped.

Abstract: A ventilator system (100/200/300/400) includes an integrated blower (130/230/330). In one case, the ventilator system includes: an inspiration port (122/222/322) for connection to an inspiratory limb (112/212/312) of a dual-limb patient circuit (110/210/310), and an expiration port (142/242/342) for connection to an expiratory limb (114/214/314) of the dual-limb patient circuit; a gas delivery device (120/220/320) connected to the inspiration port to supply a pressurized flow of gas to the inspiration port to generate a positive pressure; and a blower having an inlet (132/232/332) that is operatively connected to the expiration port and configured to be controlled to selectively supply a negative pressure level between 4 and 120 cmH2O to the expiration port, and an outlet (134/234/334) to exhaust gas received from the expiration port. In another case, the ventilator system includes a blower to generate positive pressure/flow to augment flow for noninvasive ventilation.

Abstract: A gas delivery system including a pressure generator, a pressure sensor, a control valve, and a processor. The pressure generator pressurizes breathable gas for delivery to a patient. The pressure sensor measures a pressure difference between the pressurized breathable gas and atmospheric pressure. The control valve is disposed downstream from the pressure generator and is constructed and arranged to control a flow rate of the pressurized breathable gas. The processor controls the control valve to bring the flow rate of the pressurized breathable gas to substantially zero while the pressure generator is operating and, when the flow rate is substantially zero, determines at least one of atmospheric pressure, an atmospheric air density, or a density correction factor based at least in part on the pressure difference between the pressurized breathable gas and the atmospheric pressure.

Abstract: A method for monitoring patient's breathing action response to changes in a ventilator applied breathing support, where a) a desired target range for a breathing gas indication of O2-consumption for the patient is first determined, after which b) the ventilator applied breathing support is changed, and c) the breathing gas indication of O2-consumption of said patient is measured and d) compared with the desired target range. At least the steps b)-d) are repeated to maintain the measured breathing gas indication of O2-consumption of said patient within the desired target range. A system for monitoring a patient's breathing action is also provided.

Abstract: A method for controlling the transitions between two different pressures supplied by a breathing therapy device using a transition pressure profile for which the basic shape, the magnitude and the duration may be controlled by a user of the device or the user's therapist.

Abstract: The invention is directed to a ventilation control system for controlling the ventilation of a patient. The ventilation control system utilizes a user-friendly user interface for the display of patient data and ventilator status. The user interface includes a graphic representation of a breath cycle that displays the breath cycle currently being ventilated, and is also responsive to changes in ventilation settings to assist the user in evaluation the effect of those changes on the ventilator strategy before the changes are implemented.

Abstract: A ventilation control system for controlling the ventilation of a patient. The ventilation control system utilizes a user-friendly user interface for the display of patient data and ventilator status. The user interface includes a graphic representation of a breath cycle that displays the breath cycle currently being ventilated, and is also responsive to changes in ventilation settings to assist the user in evaluating the effect of those changes on the ventilator strategy before the changes are implemented.

Abstract: A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient, including a breathable air outlet, an outside air inlet, and an pneumatic block module, wherein the pneumatic block module includes: a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage; the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; a casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly, wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet.

Abstract: Systems and methods are provided for providing ventilation to a patient. An air source is configured to provide pressurized air to a patient through a patient circuit according to a ventilation pattern. At least one sensor is configured to monitor a corresponding physiologic property of the patient. A ventilator control system is configured to calculate an alveolar ventilation value from the monitored physiologic property of the patient, determine at least an optimal frequency for the ventilation pattern from the calculated alveolar ventilation value, and update the ventilation pattern according to the determined optimal frequency.

Abstract: The present disclosure relates to a system and method for sampling parametric data provided with a patient monitoring device. A disclosed method includes sampling parametric data associated with a patient and adjusting a sampling interval during the sampling of the parametric data based on a change in a frequency of a periodic physiological event associated with the patient. A disclosed system includes a server computer operative to sample parametric data associated with a patient and to adjust a sampling interval during the sampling of the parametric data based on a change in a frequency of a periodic physiological event associated with the patient.

Abstract: A method for ventilating a patient with a ventilator includes consecutively delivering a plurality of substantially equal volume amounts into a closed ventilator circuit during a ventilator self-test, receiving a pressure measurement for each volume delivery, calculating a change in pressure for each volume delivery, consecutively releasing a plurality of substantially equal volume amounts from the closed ventilator circuit during the ventilator self-test, calculating a change in pressure for each volume release, fitting the calculated change in pressure data for volume delivery and volume release to an inhalation non-linear model equation and an exhalation non-linear model equation, respectively, deriving one or more inhalation tubing compliance compensation coefficients from the inhalation non-linear model equation, and deriving one or more exhalation tubing compliance compensation coefficients from the exhalation non-linear model equation.

Abstract: In accordance with the present invention, there is provided a mask for achieving positive pressure mechanical ventilation (inclusive of CPAP, ventilator support, critical care ventilation, emergency applications), and a method for a operating a ventilation system including such mask. The mask of the present invention includes a piloted exhalation valve that is used to achieve the target pressures/flows to the patient. The pilot for the valve may be pneumatic and driven from the gas supply tubing from the ventilator. The pilot may also be a preset pressure derived in the mask, a separate pneumatic line from the ventilator, or an electro-mechanical control. Additionally, the valve can be implemented with a diaphragm or with a flapper.

Abstract: A method and apparatus for determining suitable settings for a servo-ventilator to be used during sleep. Respiratory characteristics of a patient are measured during an awake learning period. With these measured characteristics, a target ventilation setting may be calculated by alternative methods. The calculated setting may then be used for enforcing a minimum ventilation during a treatment period where ventilatory support is provided with a servo-controlled ventilator.

Abstract: The invention relates to a respiratory gas supply circuit for an aircraft carrying passengers, comprising a pressurized source of respiratory gas (R1, R2) and a supply line (2, 3), said circuit further comprising on said supply line a regulating device (12, 30) for controlling the supply in respiratory gas to said passengers, wherein said regulating device further comprises an electro-valve (12) controlled by a pulse width modulation signal provided by an electronic unit (20).

Abstract: A dose counter for a metered dose inhaler includes a force sensor, an electronic controller, a memory for storing data indicative of a remaining number of doses and an electronic display device coupled to the controller for displaying the remaining number of doses. The dose counter is attached or integrated into a base of a canister containing medicament such that force applied to the base of the canister is registered by the force sensor, the controller being configured to measure force applied to the dose counter when depressing the canister and being responsive to measured force to decrement the remaining number of doses stored in the memory and shown on the display device.

Abstract: An MIE apparatus has a blower, a direction valve, an oscillator, and a mask hose connector. The blower is connected to the direction valve, which is connected to the oscillator, which is connected to the hose connector. During insufflation, a direction valve connects exhaust of a blower to an oscillator, causing positive pressure at the hose connector. During exsufflation, the direction valve connects the blower intake to the oscillator, causing negative pressure at the hose connector. The oscillator is a butterfly valve with a 360° rotating disc. During insufflation, the disc is fixed to steadily modulate the airflow. During exsufflation, the oscillator is inactive or in flutter mode. When inactive, the disc is fixed to allow maximum air flow. In flutter mode, the disc continuously rotates so that the air flow rapidly alternates between maximum and minimum.

Abstract: The disclosure describes a novel approach for displaying information on a ventilator system. The disclosure describes a novel respiratory system including a primary display and system status display. Further, the disclosure describes a novel method for displaying ventilator information.

Abstract: Lung ventilator (14) and/or anaesthesia machine with a blender for mixing a pressurised medical gas, e.g. oxygen, with air drawn in by a blower (1), comprising a gas line (10) for the medical gas, and an air line (11), which open into a common breathing gas line (12), whereby the opening of the gas line (10) into the common gas line (12) is downstream of the blower (1) and in the gas line (10) a regulating valve (8) is provided for variable adjustment of the gas flow and in the common breathing gas line (12) a regulating valve (4) is provided for dosing the breathing gas, and whereby in the breathing gas line (12) a flow sensor (3) is provided for measuring the breathing gas flow and in the gas line (10) a flow sensor (9) is provided for measuring the gas flow.

Abstract: Systems, methods, and/or apparatuses for acclimatizing a user to positive airway pressure (PAP) therapy are provided. Generally, a sub-therapeutic treatment pressure is provided initially. It may be ramped up to a full treatment pressure over the course of one or more therapy sessions. The pressure level may be ramped up based on, for example, sleep state, sleep phase, patient compliance with types of treatment (e.g. bilevel vs. CPAP, etc.), clinician input (either at the site, remotely, via pre-programmed smartcards, etc.), etc. Such techniques may be used alone or in combination.

Abstract: A device and a process for controlling a respirator with inclusion of an oxygen saturation value (34) for compensating a device-dependent time response (15), a physiological time response (16) and a measuring method-dependent time response (17) are described. The device-dependent time response (15), the physiological time response (16) and the measuring method-dependent time response (17) are determined in a continuous sequence and a run time of a change in the oxygen concentration from the metering means (9) in the respirator to the patient (4) is determined and taken into account in regulating the oxygen concentration.

Abstract: This disclosure describes systems and methods for purging narrow diameter sensor tubing, occasionally referred to as “sensor lines,” in a ventilation system. The disclosure describes a novel approach in which a series of short, periodic releases of pressurized gas through the sensor tubes are used to clear any blockages due to condensation or patient secretions.

Abstract: The invention relates to a device for the automated determination of the PEEP of a patient. Said device comprises sensors and a suitable electronic system for determining a pressure-volume characteristic curve during a P/V maneuver. The electronic system is designed in such a way as to generate, specifically in terms of breathing pressure, the difference between “lung volume during exhalation (Vdef)” and “lung volume during inhalation (Vinf)”, and to determine the maximum value of said difference. The breathing pressure is then determined, for which the volume difference has a value defined in relation to the maximum value of the volume difference. The device calculates a PEEP value on the basis of said determined breathing pressure value.

Abstract: A cockpit oxygen supply device includes at least one oxygen mask which is conductively connectable to an oxygen tank, wherein at least one throughput measurement device is arranged in the flow path of the device. A breathing activity of the pilot and/or an undesired outflow from the mask may be recognized with the help of an evaluation device.

Abstract: An apparatus for supplying a respiratory gas to a patient within the scope of the diagnosis and/or the treatment of sleep-related breathing disorders includes an electronic signal processing device for generating a pressure control signal on the basis of indicative signals relating to the breathing activity and/or the physiological state of a person. The signal processing device comprises a signal inputting device and an extraction device for generating data field entries according to predefined signal analysis procedures. A pressure signal generator is provided for generating the pressure control signal, taking into account determined data field entries which are at least selected by the extraction device.

Abstract: A portable ventilator uses a ROOTS-type blower as a compressor to reduce both the size and power consumption of the ventilator. Various functional aspects of the ventilator are delegated to multiple subassemblies having dedicated controllers and software that interact with a ventilator processor to provide user interface functions, exhalation control and flow control servos, and monitoring of patient status. The ventilator overcomes noise problems through the use of noise reducing pressure compensating orifices on the ROOTS-type blower housing and multiple baffling chambers. The ventilator is configured with a highly portable form factor, and may be used as a stand-alone device or as a docked device having a docking cradle with enhanced interface and monitoring capabilities.

Abstract: A high flow therapy system including a microprocessor, a heating element a non-sealing respiratory interface and a sensor is disclosed. The heating element is disposed in electrical communication with the microprocessor and is capable of heating a liquid to create a gas. The non-sealing respiratory interface is configured to deliver the gas to a patient. The sensor is disposed in electrical communication with the microprocessor and is configured to measure pressure in an upper airway of the patient.

Abstract: A method for ventilating a patient with a ventilator includes receiving a target pressure input for a breathing phase, receiving at least one oscillation parameter, imposing an oscillatory waveform on the target pressure, the oscillatory waveform having characteristics defined by the at least one oscillation parameter and configured to oscillate substantially about the target pressure for at least a portion of the breathing phase, and delivering an amount of flow sufficient to achieve an oscillatory target pressure based on the imposed oscillatory waveform.

Abstract: An apparatus for producing gas for use in medical applications. The apparatus includes a compressed gas unit having at least one container of compressed gas and a solenoid valve. An adjustable pressure regulator communicably connected to the gas container, separate and distinct from the solenoid valve, is adjusted to control the pressure of the gas provided from the container to the solenoid valve. An electrical power source is connected to the solenoid valve. A pressure activated electronic switch connected to the power source is responsive to a selected amount of voluntary fingertip, pressure for opening the solenoid valve to transmit the gas therethrough to a conduit, which further transmits the gas to a destination for use or storage.

Abstract: A method for relating to each other cardiovascular and sleep disordered breathing conditions of a patient. The patient's heart rate and/or detailed echocardiogram data is monitored and recorded continuously or periodically together with sleep disordered breathing information on similar time scales. Changes in the patient's heart rate associated with changes in sleep disordered breathing can then be observed. More specifically, positive airway pressure at therapeutic levels for treatment of sleep disordered breathing is applied while events associated with the treatment of the patient's sleep disordered breathing are detected and recorded. At the same time, information concerning the cardiovascular condition of the patient is stored and the stored information concerning the cardiovascular condition of the patient and the recorded events associated with the treatment of the patient's sleep disordered breathing are related to each other.

Abstract: Methods and systems for delivering a pharmaceutical gas to a patient. The methods and systems provide a known desired quantity of the pharmaceutical gas to the patient independent of the respiratory pattern of the patient over a plurality of breaths every nth breath, where n is greater than or equal to 1. The pharmaceutical gases include CO and NO, both of which are provided as a concentration in a carrier gas. The gas control system determines the delivery of the pharmaceutical gas to the patient to result in the known desired quantity (e.g. in molecules, milligrams or other quantified units) of the pharmaceutical gas being delivered. Upon completion of that known desired quantity of pharmaceutical gas over a plurality of breaths, the system can either terminate, continue, activate and alarm, etc.

Abstract: A multiple stage variable speed blower for Continuous Positive Airway Pressure (CPAP) ventilation of patients includes two impellers in the gas flow path that cooperatively pressurize gas to desired pressure and flow characteristics. Thus, the multiple stage blower can provide faster pressure response and desired flow characteristics over a narrower range of motor speeds, resulting in greater reliability and less acoustic noise.

Abstract: CPAP treatment apparatus is disclosed having a controllable flow generator (34, 38, 40) operable to produce breathable gas at a treatment pressure elevated above atmosphere to a patient by a delivery tube (32) coupled to a mask (30) having connection with a patient's airway. A sensor (44, 50, 56, 58) generates a signal representative of patient respiratory flow, that is provided to a controller (54, 62, 64). The controller (54, 62, 64) is operable to determine the occurrence of an apnea from a reduction in respiratory airflow below a threshold, and if an apnea has occurred, to determine the duration of the apnea and to cause the flow generator (34, 38) to increase the treatment pressure. In one preferred form the increase in pressure is zero if the treatment pressure before the apnea exceeds a pressure threshold.

Abstract: The invention relates to an ink cartridge for an ink jet printer. The ink cartridge comprises a cartridge body and a detection mechanism for detecting the ink cartridge and residual quantity of ink, wherein the cartridge body comprises an ink tank for storing ink, an ink outlet for supplying ink to a printing head of the printer and an air inlet, the ink tank comprises a first ink chamber and a second ink chamber, a first negative pressure mechanism and a second negative pressure mechanism are arranged between the first ink chamber and the second cavity, the first negative pressure mechanism and the second negative pressure mechanism cooperatively control the ink inside the first ink chamber to be consumed preferentially than the ink inside the second ink chamber, and the second negative pressure mechanism generates negative pressure when a certain quantity of ink inside the ink tank is used for printing.

Abstract: The disclosure describes a novel approach for displaying information on a ventilator system. The disclosure describes a novel respiratory system including a removable primary display and system status display. Further, the disclosure describes a novel method for displaying ventilator information and a novel method for controlling a ventilator system.

Abstract: A humidification system is provided for a respiratory system is provided with a controller having two processors that monitor the operation of each other and of heating elements in the respiratory system to provide CPU redundancy and heating element control. Each heating element is provided with two control paths, for example a relay and a triac connected in series with the heating element and a power supply. Each heater element has one control path connected to a first one of the processors and at least one heating element has at least one control path connected to a second one of the controllers. A hardware watchdog monitors the operation of the first processor, and can be triggered by a signal from the second processor, in response to which it can disable all heating elements.

Abstract: A flow generator for delivering breathable gas to a patient includes a processor coupled with operation sensors and a user interface. The processor is programmed to generate at least one of time-based or event-based messages relating to at least one of flow generator operation, flow generator service, flow generator use, patient health, peripheral devices and services, patient treatment, and reminders. Time-based messages are generated at predetermined time intervals based on either time of use or elapsed time. The event-based messages are generated based on signals from the operation sensors. The user interface is configured to deliver the messages to at least one of a display, a flow generator service provider, the patient and a physician. By this system, operation of the flow generator is facilitated and enhanced.

Abstract: A mask system for treating sleep disordered breathing, comprising headgear, a shell/cushion including a channel adjacent a front aperture, a frame, an elbow including at least one undercut on a proximal end, a retaining ring including a rear flange adapted to be retainably insertable in the channel of the shell/cushion, and a front flange adapted to retainably engage with the at least one undercut of the elbow.

Abstract: Ventilation systems are provided. In one aspect, a ventilation system includes system includes a ventilation device that is configured to provide breathable air or gas mixture to a patient according to certain operating parameters, a memory that includes instructions, and a processor. The processor is configured to execute the instructions to receive, over a network, at least one of patient data, order data, configuration data, user data, or rules or protocols, and provide a modification of operating parameters of the ventilation device based on the received patient data, order data, configuration data, user data, or rules or protocols. Methods and machine-readable media are also provided.