Abstract: Methods and apparatus for detecting the occurrence of a potential or actual overpressure during assisted ventilation are described. A blower supplies pressurized gas to a conduit, and in turn to a patient mask for connection with the entrance of a patient's airways. A pressure sensor detects the delivered pressure in the mask, which is provided to a controller. The controller has operation over the blower by way of a servo and motor. The controller determines a relatively longterm average of the pressure signal, and compares it against a threshold value. If the threshold value is approached or exceeded, the controller controls the blower and thus the supplied pressure to the patient. The effect of the control can be to limit or reduce the supplied gas pressure. The relatively longterm average can be of the order of minutes, or taken over ten or more breaths.

Abstract: A system for reducing sound level in a respiratory gas delivery system is described. The system includes an exhaust portion and a sound reducing component that is coupled with the exhaust portion and is configured for absorbing sound. The sound reducing component includes a pathway through which air from within the exhaust portion may move.

Abstract: The present invention provides a system and method for supplying, generating, conserving, and managing oxygen that is ideally suited for use on-board an aircraft for supply of breathable oxygen to passengers and flight crew. The system includes several components that together optimize oxygen utilization while reducing costs from maintenance and added weight of traditional pressurized gaseous cylinders. Components of the system include a pressurized cylinder of oxygen enriched gas or a chemical oxygen generator for rapid use in emergency situations, an on-board oxygen generator (OBOG) of the ceramic oxygen generator (COG) type incorporating solid electrolyte oxygen separation (SEOS) technology, a controller, a pulsed oxygen supplier, a crew/passenger breathing mask, and one or more sensors including sensors that detect inhale/exhale phases and communicate with the controller so that flow of oxygen may be regulated for conservation and to adapt to physiological needs.

Abstract: A usage status notification method and corresponding medication storage device (e.g., mobile medication dispensing cart, medication cabinet, nurse server, etc.) are provided. To generate the usage status notification, the status of one or more components of the medication storage device may be monitored. An in-use notification signal may be generated if it is determined that the medication storage device is in use at a certain point in time (e.g., when a user is logged into the medication storage device). An available notification signal may be generated if it is determined that the medication storage device is available for use at a certain point in time (e.g., when a user is logged out of the medication storage device). Other types of usage status signals may also be provided.

Abstract: This disclosure describes systems and methods for monitoring ventilatory parameters, analyzing ventilatory data associated with those parameters, and providing useful notifications and/or recommendations to clinicians. For example, many clinicians may not easily identify or recognize data patterns and correlations indicative of a fluctuation in resistance during mechanical ventilation of a patient. Furthermore, clinicians may not easily determine potential causes for the fluctuation in resistance and/or steps for mitigating the fluctuation in resistance. According to embodiments, a ventilator may be configured to monitor and evaluate diverse ventilatory parameters to detect fluctuations in resistance and may issue suitable notifications and recommendations to the clinician based on potential causes of the fluctuation, ventilatory and/or patient data, etc.

Abstract: A blower includes a housing including an inlet and an outlet, a stationary component provided to the housing, an impeller positioned between the inlet of the housing and the stationary component, and a motor adapted to drive the impeller. The stationary component includes a tube portion structured to retain and align a pair of bearings that rotatably support a rotor to which the impeller is coupled. The tube portion includes a diameter in a side closest to the impeller that is sufficient size to accommodate adhesive to retain one of the bearings.

Abstract: An indicating device suitable for indicating the number of dosages of a substance that have been dispensed from or remain in a container includes at least one first indicator member incrementally moveable to a plurality of positions and a second indicator member moveable in response to a predetermined number of movements of the at least one first indicator member. The at least one first indicator member includes primary dosage indicia adapted to indicate the number of dosages of substance that have been dispensed from or remain in the container. The second indicator member includes secondary dosage indicia adapted to indicate that less than a minimum predetermined number of dosages of substance remain in the container. In one preferred embodiment, the primary dosage indicia are configured as numerical indicia and the secondary dosage indicia are configured as color indicia.

Abstract: Disclosed is an artificial respiration device for resuscitating a person in a state of cardiac arrest. The device (D2) includes: a tubular element (25), auxiliary channels (29) continuously injecting jets of breathing gas, a deflection element (28) that force the jets of breathing gas to converge inside the tubular element (25), and a local restriction (R2) of the internal cross-section of the tubular element (25).

Abstract: Various embodiments of a connector assembly are provided to removably couple a proximal end of a tracheal tube to components associated with a ventilator or an anesthesiology machine. The disclosed embodiments include a compression fitting, which creates an airtight seal between walls of the tracheal tube and components of the compression fitting, thus allowing air to flow to and from a patient.

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: An exhaust assembly (1) adapted for use in a respiratory gas delivery system comprises an exhaust vent, an exhaust gas flow passage, a primary gas flow passage, and a moveable member. The exhaust gas flow passage communicated a flow of exhaust gas from a first end of the exhaust assembly to the exhaust vent. The exhaust vent communicates the exhaust gas from the exhaust gas flow passage to ambient atmosphere. The primary gas flow passage communicates a flow of supply gas from a second end of the exhaust assembly to the first end of the exhaust assembly. The moveable member defines at least a portion of the exhaust gas flow passage and the primary gas flow passage, is operable to isolate the flow of exhaust gas from the flow of supply gas, and is responsive to a pressure differential between the flow of supply gas and the flow of exhaust gas.

Abstract: Disclosed are devices and methods for continuous positive airway pressure (CPAP) devices and related medical devices for treating patients susceptible to respiratory illnesses, including respiratory distress syndrome and sleep apnea. The device and methods employ force gauged CPAP nasal interface devices for these purposes.

Abstract: An oscillating positive expiratory pressure device comprising a housing enclosing at least one chamber, a chamber inlet configured to receive exhaled air into the at least one chamber, and a chamber outlet configured to permit exhaled air to exit the at least one chamber. A channel is positioned in an exhalation flow path between the chamber inlet and the chamber outlet, with the channel being moveably connected to a chamber of the at least one chamber. An air flow regulator is moveable with respect to the channel between a first position, where the flow of air through the channel is restricted and a second position, where the flow of air through the channel is less restricted, the air flow regulator being configured to repeatedly move between the first position and the second position in response to a flow of exhaled air.

Abstract: A system for reducing sound level in a respiratory gas delivery system is described. The system includes a first portion of a breathing circuit tubing and a second portion of the breathing circuit tubing positioned in-line with the first portion, wherein the second portion of the breathing circuit tubing is a sound-reducing tubing.

Abstract: Mask ports 180 for attaching supplemental oxygen tubes 510 or measurement devices to a respiratory mask are downwardly directed and recessed into the base 110 of the mask frame 100. The ports may comprise a pair of downwardly extending tubular spigots 185 each housed in a respective recess 190 in the base 110, with a shallow bridging recess 290 therebetween for receiving a bridging piece 300 of a closure cap 280.

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: 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: There is provided a looped tether to prevent the over-withdrawal of a suction catheter from a connecting fitting in a closed suction catheter respiratory device. The looped tether is made from a single thread or strand that is looped or doubled in length with the two loose ends connected together to produce the loop. The looped tether provides better distribution of the forces at the ends of the device and is relatively simple to assemble. Also provided is a system for preventing the over-withdrawal of a suction catheter from a connecting fitting in a closed suction catheter respiratory device.

Abstract: The present invention comprises a user interface for systems and methods for sedation and analgesia delivery. The user interface receives input from a user of a sedation and analgesia delivery system and relays information regarding the system, the administration of sedation and analgesia, physiological conditions to the user in a context sensitive manner. The information relayed may be displayed to the user on a touch sensitive screen or multi-layer display device. The display may be segregated geographically or may be color coded on the display device where the geographic location and/or color of the displayed information relates further information to the user.

Abstract: An oxygen concentrator and compressor assembly. An oxygen concentrator is disposed in a housing having an upper end. A compressor is disposed in a housing having a lower end. The upper end of the oxygen concentrator housing and the lower end of the compressor housing are configured such that placement of the lower end of the compressor housing on the upper end of the oxygen concentrator housing sets the position of the compressor housing with respect to the oxygen concentrator housing.

Abstract: An nCPAP device for assisting patient breathing includes a generator body forming an inlet, a chamber, and first and second flow circuits. The chamber directs pressurized gas from the inlet to the flow circuits. The flow circuits each include a first and second jets, a flow director and an exhaust conduit. The jets emit a jetstream into the flow director in a direction of a patient side thereof. In some embodiments, the flow director forms a first tapered wall section directing inhaled air toward the patient and a second tapered wall section directing exhaled air toward the exhaust conduit. The generator body requires reduced driving pressures to achieve target CPAP levels and reduces total imposed WOB as compared to conventional designs.

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 respiratory mask assembly for delivering a flow of pressurized breathable gas to a patient includes a structure configured to contact a) at least one point on the patient's forehead, b) two points on the patient's temples, the two temple points being on opposite sides of the patient's face, and c) two points on the patient's cheek, the two cheek points being on opposite sides of the patient's face; a frame, being part of the structure, rigidly connected to other elements of the structure and configured to support a cushion in contact with the patient's face; and a plurality of straps connected to the other elements of the structure and configured to hold the frame against the at least one forehead point, the two temple points, and the two cheek points in a fully constrained manner.

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: Various embodiments of a tracheal tube having a flexible membrane disposed therein for separation of a ventilation lumen of the tracheal tube into multiple channels are provided. The flexible membrane is configured to divide a main ventilation lumen of the tracheal tube into an inspiration channel and an expiration channel. In some embodiments, a volume of the inspiration channel is substantially equal to a volume of the expiration channel.

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: Prior approaches have delivered 17O2 to a subject by inhalation, but the relationship between local signal changes and metabolism has been complicated by H217O created in non-cerebral tissues. During a brief pulse of 17O2 inhalation, this arterial input function for H217O is negligible due to convective transport delays. Additional delays in the arterial input function due to restricted diffusion of water makes pulsed inhalation of 17O2 even more effective. Accordingly, ventilator system are provided to deliver 17O2 as a brief pulse to a subject. Subsequent MR imaging demonstrates delayed appearance of H217O in the cerebral ventricles, suggesting that the arterial input function of H217O is delayed by restricted water diffusion in addition to convective transit delays. Delivery as a brief pulse therefore offers significant advantages in relating MR signal changes directly to metabolism.

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: 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: An assembly for modifying airflow into a nasopharyngeal airway or trachea of a patient. A valve assembly having an inlet and an outlet attaches to a traditional airflow generator. A valve seal within the assembly is operable by a solenoid and is adapted to cycle in response to a programmable controller circuit wherein upon activation of both the airflow generator and the controller circuit, pressurized air from the airflow generator continuously enters the inlet but passes out of the outlet of the assembly only when the solenoid causes the valve seal to retract and to at least partially unblock the outlet such that the pressurized air is converted into a single, repeatable burst exiting the outlet thereby modifying the traditional airflow.

Abstract: A CPAP device includes a flow generator including an outlet, a humidifier including an inlet, and an adaptor connector between the outlet of the flow generator and the inlet of the humidifier. The connector includes a flexible and conformable sealing portion that is movable to accommodate misalignment.

Abstract: A respirator (1) and a mount for a respirator are provided including a mounting device for a cylinder (2), preferably an oxygen cylinder. The mounting device forms an upper housing half (4) and a lower housing half (3) of the respirator (1) and includes at least one grip (6), which makes transportation of the respirator (1) possible. The upper housing half (4) and lower housing half (3) are provided with a connection mechanism (5), which connects the upper housing half (4) and the lower housing half (3).

Abstract: An oscillating positive respiratory pressure apparatus and a method of performing oscillating positive respiratory pressure therapy. The apparatus includes a housing having an interior chamber, a chamber inlet, a chamber outlet, an exhalation flow path defined between the inlet and the outlet, and a restrictor member rotatably mounted within the interior chamber. The restrictor member has an axis of rotation that is substantially perpendicular to the flow path at the inlet, and includes at least one blocking segment. Rotation of the restrictor member moves the at least one blocking segment between an open position and a closed position. Respiratory pressure at the chamber inlet oscillates between a minimum when the at least one blocking segment is in the open position and a maximum when the at least one blocking segment is in the closed position. By exhaling into the apparatus, oscillating positive expiratory pressure therapy is administered.

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: A flow regulation vent includes a fixed portion adapted to engage a gas supply conduit and a spring force biased movable portion connected by a hinge to the fixed portion and flowingly connected to the pressurized gas supply. The fixed portion includes a gas flow orifice. The movable portion is pivotably movable between 1) a relaxed position, wherein at a specified minimum operating pressure, the movable portion is pivoted by the spring force away from the fixed portion to a position to establish a first gas washout flow area between the movable portion and the gas flow orifice; and 2) a fully pressurized position, wherein at a specified maximum operating pressure, the pressurized gas offsets the spring force to pivot the movable portion to a position adjacent the fixed portion to establish a minimum gas washout flow area between the movable portion and the gas flow orifice.

Abstract: A nasal cannula adapter. The nasal cannula adapter includes a chamber having cannula clips, and a connector having an opening and a connector lumen in communication with the chamber and the opening. Systems for administering a gas to a patient comprise the nasal cannula adapter, a nasal cannula, and an airway device. Methods for administering a gas to a patient comprise administering a gas through a nasal cannula operably connected to the nasal cannula adapter operably connected to an airway device inserted into the airway of the patient.

Abstract: A respiratory therapy device including a housing and an interrupter valve assembly. The housing is sized for handling by a patient and defines a patient breathing passage extending from a patient end and through which a patient inhales and exhales air. The interrupter valve assembly is carried by the housing and includes a control port, a valve body, and a drive mechanism. Expiratory airflow is released from the patient breathing passage through the control port. The valve body is sized to at least partially obstruct fluid flow through the control port. The drive mechanism moves the valve body relative to the control port in response to the expiratory airflow such that the valve body repeatedly transitions between a position of maximum obstruction and a position of minimum obstruction relative to the control port to create an oscillatory positive expiratory pressure effect.

Abstract: A continuous positive airway pressure system features a housing forming an airway chamber, and an air pressure inlet and an air pressure outlet. The housing further defines internally a pair of tapered air jets, and a pair of tapered air receivers. The air receivers are located downstream of the air supply jets and disposed coaxially with respective ones of the air supply jets. Each receiver has a taper in an opposite direction to the direction of the taper of the air supply jets. A pair of nasal prongs is located downstream of the air receiving jets.

Abstract: Method and apparatus for the treatment of cardiac failure, Cheyne Stokes breathing or central sleep apnea are disclosed. A subject is provided with ventilatory support, for example positive pressure ventilatory support using a blower and mask. Respiratory airflow is determined. From the respiratory airflow are derived a measure of instantaneous ventilation (for example half the absolute value of the respiratory airflow) and a measure of longterm average ventilation (for example the instantaneous ventilation low pass filtered with a 100 second time constant). A target ventilation is taken as 95% of the longterm average ventilation. The instantaneous ventilation is fed as the input signal to a clipped integral controller, with the target ventilation as the reference signal. The output of the controller determines the degree of ventilatory support. Clipping is typically to between half and double the degree of support that would do all the respiratory work.

Abstract: A monitoring device for monitoring a therapy device, for example, an anesthesia device or a respirator, is provided by which an alarm device for triggering an alarm when the value drops beyond a warning limit (4) is automatically activated when a determined therapy parameter drops beyond this warning limit (4). The warning limit (4) is set automatically in this case. In addition, a therapy device monitored by the monitoring device and especially an anesthesia device as well as a respirator are provided. A process for triggering an alarm as well as a process for treating a patient is also provided.

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: 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: The present invention provides a vent assembly suitable for use with a respiratory mask of the type used in CPAP treatment. In one embodiment the vent is made of a thin air permeable membrane. Generally, the membrane is thinner than 0.5 mm. The membrane can be made of a hydrophobic material such as polytetrafluoroethylene (PTFE). The membrane can also be fabricated from expanded PTFE. The expanded PTFE membrane is mounted on a polypropylene scrim. The pores of the membrane have a reference pore size of 10 to 15 microns. In an alternative embodiment, the vent assembly includes a vent constructed from stainless steel. In another embodiment the membrane has a superficial cross-sectional area of approximately 500 mm2. In another embodiment the vent assembly comprises a membrane attached to a vent frame, the vent assembly forming an insert which can be removeably attached to a mask frame.

Abstract: A respiratory therapy device including a housing, a flow diverter structure, a high frequency pressure port (HF port), and an entrainment port. The housing defines a primary passageway having a patient interface side. The flow diverter structure is in fluid communication with the primary passageway and is characterized by the absence of a venturi tube. The HF port is configured for fluid connection to a source of oscillatory gas flow, and is fluidly associated with the flow diverter structure. The entrainment port is openable to ambient air, and is fluidly associated with the flow diverter structure. With this construction, the device is configured such that flow characteristics of gas flow from an external source are altered upon interacting with the flow diverter structure to create a pressure drop for drawing in ambient air through the entrainment port in delivering a percussive pressure therapy to the patient side.

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 respiratory therapy device has both a standard positive expiratory pressure (PEP) device and an oscillatory PEP device packaged together. A manually operable member is movable to select which of the standard and oscillatory PEP device is placed in communication with a patient's airway. A nebulizer connector may also be provided for connection of a nebulizer.

Abstract: An airway management apparatus for engagement with a catheter for oxygenation of a patient includes a main body having a major axis, a first port extending in a proximal direction along the major axis, a second port, and a third port extending in a distal direction along the major axis. The third port comprises a connector for engagement with a proximal end of the catheter. The connector may have a plurality of radially compressible members extending in a distal direction, and circumferentially aligned to receive the catheter proximal end. An axially movable member is positioned to selectively compress the compressible members around the catheter proximal end to form a locking engagement, and to release the compressible members. A wire guide is insertable into the trachea through the first and third ports, and the catheter.

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.