Abstract: A device includes a cartridge containing a filter material. An insert extends through at least a portion of the filter material. The insert has gas sample path with an opening to provide a sample of air that is representative of the saturation of the filter material. A return path may be included in the insert to return sampled gas to the filter material. A gas mask contains a gas sensor and coupled to the cartridge, which may be replaced when saturated.

Abstract: A confirmation device. The device includes a housing having a central passageway and a secondary passageway extending from the central passageway. The device also has a negative pressure member in communication with the secondary passageway and an indicator mechanism in fluid communication with the secondary passageway for visually indicating the presence of one or more components within the secondary passageway. The negative pressure member is operable to draw fluid across the indicator mechanism.

Abstract: Various characteristics of a gas flow can be sensed at the end of a respiratory conduit near the patient interface using a sensing module. The sensing module can be removable from the patient end of the respiratory conduit for ease of use and ease of cleaning. The sensor module can transmit sensor data over the same wires used to heat the respiratory conduit.

Abstract: An inhaler for delivery of a medicament by inhalation is disclosed. The inhaler comprises a dispensing mechanism, the dispensing mechanism being configured to dispense a dose of medicament on actuation. The inhaler further comprises a dose counting mechanism comprising a counter and a translating member. The translating member comprises a pawl. The counter comprises a first count wheel, a second count wheel and an intermediate wheel engaged with the second count wheel and in selective engagement with the first count wheel. When the inhaler is fired to dispense a dose of medicament, the dispensing mechanism moves the translating member in a substantially linear direction. The pawl thus rotates the first count wheel, and as the first count wheel rotates, the intermediate wheel is selectively engaged thereby selectively rotating the second count wheel to count the doses of the inhaler.

Abstract: A method of intubating a subject is disclosed. The method comprises inserting an endotracheal tube into the tracheal airway of the subject; inflating a cuff associated with the endotracheal tube within the airway below the vocal cords; measuring a level of at least one measure being indicative of leakage of secretion past the cuff to the lungs; comparing the level of the measure with an optimal level of the measure; and adjusting inflation of the cuff based on the comparison so as to generally minimize leakage of secretion from above the cuff to the lungs, while minimizing pressure associated damages to the airway. The measure(s) can be carbon dioxide concentration, a proxy measure from which such concentration can be inferred, or the level of one or more additives delivered to a subject during intubation.

Abstract: A manual ventilation feedback sensor for use in clinical and training settings is disclosed. Namely, a manual resuscitator device is disclosed that comprises a bag valve mask, a one-way valve, a manual ventilation bag, and a sensing module, wherein the sensing module can comprise a pressure sensor and/or flow transducer. Sensing module may further comprise a controller for processing information from the pressure sensor and/or flow transducer; namely for determining and indicating a ventilation rate. Indicators are provided to guide the user with respect to a target or desired ventilation rate.

Abstract: An interface apparatus identification system for a respiration machine such as, for example, a medical ventilator, includes a detection element which is adapted to communicate with the ventilator, a patient interface assembly including a patient interface apparatus for delivering a flow of gas from the ventilator to an airway of a patient, and a differentiating feature which is incorporated into the patient interface assembly. The patient interface apparatus is selected from a predetermined category such as, for example, a specific make or brand. The differentiating feature is detectable by the detection element to distinguish patient interface apparatus that fall within the predetermined category from those that do not. Operation of the respiration machine in conjunction with the patient interface apparatus is dependent upon detection of the differentiating feature by the detection element. An associated identification method is also disclosed.

Abstract: Embodiments relate generally to low pressure warning devices which may be worn with encapsulated protective suits and hoods by a user and may provide audio and visual alerts. In an embodiment, a low pressure warning device may comprise an earpiece operable to be retained to the ear of a user, wherein the earpiece may comprise a control system operable to sense the pressure inside the encapsulated protective suit or hood and activate the audio and/or visual alerts when necessary. In an embodiment, the low pressure warning device may be equipped with short range wireless communication capabilities.

Abstract: A human wearable mask includes a skirt for directly contacting a human wearer and a sound conduction component on the skirt. The sound conduction component can provide an alert notification within high-noise environments while allowing ambient sounds to be heard over the conduction speakers. The sound conduction component may be used to reproduce audio for firefighters and other users who need radio communications.

Abstract: Systems and methods are provided for monitoring and evaluating diverse ventilatory parameters to detect an asynchrony and may issue notifications and recommendations suitable for a patient to the clinician when asynchrony, such as an ineffective effort and an auto-trigger, is implicated. The suitable notifications and recommendations may further be provided in a hierarchical format such that the clinician may selectively access summarized and/or detailed information regarding the presence of asynchrony. In more automated systems, recommendations may be automatically implemented.

Abstract: A portable life support apparatus (1102) and particularly a respiratory support apparatus adapted to be easily mounted to a stretcher is disclosed. Prior devices that attach onto a stretcher are heavy and cumbersome and obstruct access to the patient. Accordingly, there is a great need for a portable emergency support device that overcomes the weight, size, positioning, and other portability disadvantages. One aspect relates to a portable life support device including at least one ambient gas inlet (14); a conditioned gas outlet (30); an oxygen concentrator (26,28) fluidly connected between the at least one gas inlet and the gas outlet, and a ventilator (44) fluidly connected downstream from the oxygen concentrator.

Abstract: The present invention relates to a multiple connector device for respiratory circuits with alarm due to disconnection, which comprises a main body which is hollow inside, which is in the form of a cross having four arms which are: an upper vertical tubular arm inside of which is housed a driving element which projects into the interior of the lower vertical arm; a lower vertical arm preferably of a square form, which is partially hollow in the interior thereof for the purpose of housing a segment of the driving element and a control element; a right lateral arm; and a left lateral arm which is a mirror image of the right lateral arm, wherein the driving element is in the form of an arrow that effects an axial movement along the upper vertical arm and the lower vertical arm of the main body and the control element is an electronic board that includes all of the electronic components for operating the multiple connector device and which together with the arrangement of the driving element enable the proper func

Abstract: Indicating fit status of a mask in communication with a respiratory assistance device is disclosed. Upon initiating a therapeutic gas delivery from the respiratory assistance device to the mask, one or more measurements from respective one or more sensors of the respiratory assistance device is received. A leakage value from these measurements is derived, and a mask fit index is assigned. This is based at least upon a correlation of the leakage value to a particular sub-range of predetermined leakage values that corresponds to the mask fit index. The particular sub-range of predetermined leakage values is one among a plurality of sub-ranges, which together comprises an overall mask fit range defined at least by an ideal mask fit region, a loose mask fit region, and a tight mask fit region. A mask fit status based upon the assigned mask fit index is output to an indicator interface.

Abstract: The present invention provides clinical decision support that can be used with non-portable and portable systems when delivering and/or monitoring delivery of a therapeutic gas comprising nitric oxide to a patient. Further, clinical decision support can be used with non-portable and portable systems during delivery and/or monitoring of delivery of therapeutic gas when nebulized drugs may and/or may not be being delivered to a patient (e.g., when nebulizers are delivered upstream in the inspiratory limb of the breathing circuit, into a breathing gas delivery system, etc.).

Abstract: Described are methods for safer nitric oxide delivery, as well as apparatuses for performing these methods. The methods may include detecting the presence or absence of a nasal cannula, and stopping the delivery of nitric oxide or providing an alert if the cannula is disconnected. The methods may also include purging the nasal cannula if it is reconnected after a disconnection or if it is replaced by a new cannula. Other methods pertain to automatic purging of the delivery conduit if the elapsed time between successive deliveries of therapeutic gas exceeds a predetermined period of time.

Abstract: An airway management device is provided that may adjust the inflation level of a cuff associated with an endotracheal tube. The cuff inflation may be adjusted in response to an increase in carbon dioxide levels above the cuff, which may indicate a poor seal of the cuff against the tracheal walls, as well in response to a measured intracuff pressure. By using information about the seal quality of the cuff together with information about the cuff pressure, the inflation of the cuff can be adjusted to minimize cuff inflation pressure while maintaining a high quality tracheal seal.

Abstract: A device for use with an inhaler spacer to improve compliance with a medicament dosage regime. The device comprises a display, detection means for detecting indications of successful inhalations by a patient using an inhaler spacer and a memory storing computer readable instructions. The computer readable instructions are configured to present at least one incentive graphic on said display, and to update the incentive graphic in response to detection of an indication of a successful inhalation by the detection means.

Abstract: A sensor 40 that detects a chemical such as an organic vapor. The sensor 40 includes a film that has a film body 58 that includes a detection layer 48 and that is responsive to the presence of a chemical by providing a color change. The film also includes an occluding layer 54 that has a first major surface 59 and that is bound to the film body 58 but is inert to the detection layer 48 to preclude the occluding layer 54 and the chemical from causing a color change in the film body 58 in an area 42 normal to the first major surface 59 of the occluding layer 54. A sensor having this construction can provide a distinctly visible image on the sensor, which may be helpful in evaluating the remaining life of a filter cartridge.

Abstract: A coupling for use in a system (2) for communicating a flow of gas from a pressure generating device (4) to an airway of a patient includes a first portion (16, 16?, 16?) adapted to be coupled in fluid communication with the pressure generating device and a second portion (10) selectively coupled to the first portion. The second portion is adapted to be coupled in fluid communication with the airway of the patient. At least one of the first portion and the second portion includes an illuminated portion (18, 20), the illuminated portion being adapted to be visible to a patient when the first and second portions are uncoupled and adapted to be not visible to a user when the first and second portions are coupled. The illuminated portion assists a user in locating and recoupling the first and second portions of the coupling in a darkened room.

Abstract: A method is provided for detecting the presence of an anomaly within an observed physical signal. The observed signal includes an addition of a physical disturbance signal and a reference signal. The anomaly is relative to a change in the behavior of the reference signal compared with a first tolerance value. Such a method includes: determining a time span having at least one moment of interest; detecting the presence of the anomaly within the observed physical signal during the time span by conducting a hypothesis test using the first tolerance value, a first rate of tolerated false alarms, and data obtained from processing the observed signal.

Abstract: A mask for patient ventilation comprises a frame portion, a retention portion, and a connector portion. The frame portion is for surrounding a respiratory opening of a patient. The retention portion is for maintaining positive pressure between the frame portion and the patient. The connector portion is for connecting delivery tubes to the mask. The connector portion is configured such that the connector only couples with compatible components.

Abstract: A device for monitoring gases present in a breathing mask. A gas sensing element carried by the breathing mask senses the partial pressure of a gas present in the breathing mask and outputs signals corresponding to the sensed gas partial pressure. The gas sensing element may comprise a gas-sensing material configured to emit, in response to light excitation, an optical signal at an intensity corresponding to the partial pressure of a sensed gas.

Abstract: Systems, methods, and devices for an end of service life indicator for a respirator are described herein. For example, a device can include a cartridge containing a filter material and an insert extending through at least a portion of the filter material having a first path with a first opening to provide a sample of air that is representative of a saturation of the filter material and a second path with a second opening configured to provide a filtered sample of the air throughout a service life of the cartridge.

Abstract: A breathing assistance apparatus is configured with features that improve serviceability of the apparatus. The apparatus can include animations to provide instruction regarding correcting easily-identified fault conditions and to provide instruction regarding routine maintenance routines. The apparatus also can be configured with top level control menus that are obscured in a manner to limit manipulation of the top level control elements by unauthorized users.

Abstract: The present disclosure provides a method of issuing an alert for optimizing interaction between a patient and a ventilatory system. The method includes ventilating a patient using a ventilatory system and retrieving one or more of current ventilatory settings, collected ventilatory data, and patient data. The method also includes detecting corruption of interaction between a patient and the ventilatory system, determining one or more root causes of the corruption, and determining and displaying a recommendation for resolving the corruption based on the one or more root causes.

Abstract: A powered air purifying respirator (PAPR) that alerts when remaining battery time is below a predefined threshold. The powered air purifying respirator comprises an electric motor mechanically coupled to a blower, a battery coupled to the electric motor, an alarm device, and an electronic controller. The electronic controller determines a second battery time remaining value and actuates the alarm device when the second battery time remaining value is less than a predefined threshold, wherein the controller determines the second battery time remaining value based on indexing into a look-up table of values with a first battery time remaining value and a battery voltage.

Abstract: A method, system and computer-readable medium are provided for determining compliance with one or more patient care rules and protocols, the method including the steps of sending infusion information from a pump to a processor pertaining to one or more drugs provided to a patient, sending ventilation information from a ventilator to the processor pertaining to ventilation provided to the patient and determining, with the processor, a variation between actual care of the patient and a set of rules and protocols associated with care of the patient at least in part based on the infusion information and the ventilation information.

Abstract: A system for controlling and monitoring flow in a cuffed endotracheal tube device is disclosed. The system comprises: a connector panel having at least three connectors adapted for establishing fluid communication with proximal ends of at least a first fluid line, a second fluid line and a cuff inflation line of the endotracheal tube device. The system can further comprise a processing unit and a control unit, wherein the processing unit is configured to instruct the control unit to execute various operations, including at least a rinsing procedure, a suctioning procedure, a cuff inflation procedure, a leak detection procedure and a venting procedure, and to select any of the first and the second fluid lines for any of the rinsing, suctioning, leak detection and venting procedures. In some embodiments, the system exploits the cuff as sensor to sense pulmonary data.

Abstract: An apparatus assesses a condition of a patient. The apparatus may contain a patient interface for communicating a treatment generated by a respiratory treatment apparatus to the respiratory system of a patient. The apparatus may also include a sensing module containing one or more electrochemical sensors to sense chemicals in exhaled breath in real time, or over an extended period of time. The apparatus may also include one or more collectors to accumulate a breath condensate over an extended period of time. The sample collectors may contain an absorbent material, and may also be adapted for replacement within a sensing module. The absorbent material may also include a preservative for preserving a chemical component of the breath, such as an analyte of the exhaled breath. The technology may provide treatment recommendations based on the detected condition of the breath condensate or the chemical components thereof.

Abstract: This disclosure describes systems and methods for providing novel back-up ventilation that allows the patient to trigger or initiate the delivery of breath. Further, this disclosure describes systems and methods for triggering ventilation when base flow is unknown or undeterminable by the ventilator.

Abstract: A carbon dioxide sensor for use in a respiratory therapy system. The carbon dioxide sensor determines whether a patient interface is fluidly coupled to a patient.

Abstract: A heads-up display has a display panel which displays information related to a partial pressure of oxygen in a breathing gas. The display panel comprises a first indicia, a second indicia, a third indicia, and a fourth indicia. The first indicia and the fourth indicia respectively indicate a near hyperoxic condition and a near hypoxic condition. The second indicia and the third indicia together indicate the partial pressure of oxygen in the breathing gas.

Abstract: An method and system for supplemental gas delivery that enables the identification of a need of therapeutic attention for patient receiving the supplemental gas (20) by detecting an onset of an exacerbation of a medical condition. Such a detection is performed by detecting audible events using a microphone (60) that is in fluid communication with a cannula (28) that is used to communicate the supplemental gas (20) with the airways of the patient (8). The audible event may be, for instance, a cough in the patient. A change in the relative frequency of coughs in the patient may be identified by the routines as being indicative of an onset of an exacerbation.

Abstract: The invention relates to a breathing mask, in particular for human beings, comprising a flexible mask body designed to fit over a mouth and nose on a user's face, at least one sealing lip for a gas-proof fit on the user's face, comprising at least one inhalation valve penetrating the mask body, a filter material assigned to the inhalation valve and an exhalation valve penetrating the mask body. It is intended that a manually actuable test valve is arranged downstream of the exhalation valve and designed to provide a gas passage from the exhalation valve to the surroundings in its normal state and to close said passage in its actuated state.

Abstract: A system for controlling medical devices, wherein this system can comprise a device having at least one wireless or cellular based communication module. The module can be in the form of a GPRS module associated with a SIM card, or a CDMA module. The SIM card can be adapted such that it contains additional memory for storing a program for controlling the device or the system. Multiple cellular communication modules can also be installed in this system. Additional communication modules such as wireless modules including but not limited to Bluetooth, IRDA, RF, or any other wireless module can also be incorporated into the system. Wired modules can also be used, for example these wired modules can be RS-232 modules, USB, Serial adapters, phone and fax modem.

Abstract: Methods and apparatus for determining leak and respiratory airflow are disclosed. A pressure sensor (34) and a differential pressure sensor (32) have connection with a pneumotach (24) to derive instantaneous mask pressure and airflow respectively. A microcontroller (38) estimates a non-linear conductance of any leak path occurring at a mask (12) as being the low pass filtered instantaneous airflow divided by the low pass filtered square root of the instantaneous pressure. The instantaneous leak flow is then the conductance multiplied by the square root of the instantaneous pressure, and the respiratory airflow is calculated as being the instantaneous airflow minus the instantaneous leak flow. The time constants for the low pass filtering performed by the microcontroller (38) can be dynamically adjusted dependent upon sudden changes in the instantaneous leak flow.

Abstract: The invention relates to a portable vacuum connector device 100. The connector device can be attached to various surfaces such as surfaces of CT scanner or other medical equipment by means of vacuum cups or connectors 102. The vacuum connector device 100 has a connection structure 101 such as a rail to which a portable medical device can be attached via its connection feature 202, e.g. a hook. Accordingly, the connector device 100 makes may make it easier to let the portable medical device follow the patient as the patient is moved from location to location. An air pressure sensor 104 is provided for monitoring the vacuum level and for enabling generation of an alarm via an external monitoring device such as the portable medical device 201.

Abstract: A lighting device for a respiratory humidifier (1) is provided, the humidifier comprising a liquid container (3) with a bottom plate and a housing (2) with a heating plate (8), wherein the heating plate (8) can be heated for heating the liquid in the liquid container (3), and wherein the bottom plate can be brought into contact with the heating plate (8), wherein the housing (2) comprises a light source (20) and a light exit portion (22), and the liquid container (3) comprises a light entrance portion (21), wherein the light proceeding from the light source (20) proceeds in a lighting direction through the light exit portion (22) and the light entrance portion (21) and thus arrives in the liquid container (3).

Abstract: The present disclosure relates to a method and a system for quantifying timing discrepancies between inspiratory effort and ventilatory assist. A trigger error is determined by comparing a start time of neural inspiration with a start time of the ventilatory assist. A cycling-off error is determined by comparing an end time of the neural inspiration with an end time of the ventilatory assist. The ventilatory assist is synchronized when the trigger error is lower than a first threshold and the cycling-off error is lower than a second threshold. The ventilatory assist may also be characterized in terms of early or late trigger and of early or late cycling-off. A trigger of a ventilator may be adjusted according to the trigger error and a cycling-off of a ventilator may be adjusted according to the cycling-off error.

Abstract: A pressure regulating syringe comprises a barrel assembly terminating with a tubular tip positionable in fluid communication with a fluid chamber, a plunger that is manually and axially displaceable within a barrel of the barrel assembly, a pressure sensor mounted onto the plunger adjacent to its distal end, for generating one or more electrical signals representative of a change in pressure within the fluid chamber, circuitry housed within the plunger for processing the generated signals, and a display mounted on the plunger for displaying an output indicative of the processed signals. The output is changeable upon axial displacement of the plunger when the tubular tip is positioned in fluid communication with the fluid chamber, which is for example a cuff surrounding a medical tube. Fluid is delivered by manually manipulating a fluid delivery element in response to the displayed output until a desired fluid delivery operation is performed.

Abstract: A closed circuit breathing apparatus (2) and a method of operating the same, the method comprising: determining whether a sufficient amount of replenishing gas is being supplied to a breathing circuit (4); sensing pressure within the breathing circuit (4) using a pressure sensor (6); generating a pressure signal representative of the sensed pressure; determining whether the pressure signal is representative of breathing; and generating an alert if it is determined that both an insufficient amount of replenishing gas, such as oxygen, is being supplied to the breathing circuit (4) and that the pressure signal is representative of breathing.

Abstract: This disclosure describes systems and methods for providing novel back-up ventilation that allows the patient to trigger or initiate the delivery of a breath. Further, this disclosure describes systems and methods for triggering ventilation when exhalation flow and/or exhalation pressure is unknown or unreliable by the ventilator.

Abstract: This disclosure describes systems and methods for providing novel back-up ventilation that allows the patient to trigger or initiate the delivery of breath. Further, this disclosure describes systems and methods for triggering ventilation when base flow and/or inspiratory flow is unknown or indeterminable by the ventilator.

Abstract: A respiratory mask body defining a breathable air zone for a wearer and having a shut-off valve is provided. In an exemplary embodiment, the mask body includes one or more inlet ports configured to receive one or more breathing air source components. The shut-off valve is operable between a closed position and an open position, and when in a closed position the shut-off valve prevents fluid communication between the one or more inlet ports and the breathable air zone and the shut-off valve returns to an open position in the absence of an applied force.

Abstract: A filter system includes a housing, a filter medium disposed within the housing and a optical analyte sensor also disposed within the housing in fluid communication with the filter medium. The optical analyte sensor includes a detection medium that changes at least one of its optical characteristics in response to an analyte. The filter system further includes an optical reader having at least one light source and at least one detector. The optical reader is attached to the housing such that at least a portion of light emitted by at least one light source is reflected from the optical analyte sensor and captured by at least one detector.

Abstract: Gas-pressure-based testing, in some embodiments, features a self-leak-testing module (120) that includes an internal sensor and is configured for measuring, using the sensor, gas leakage (179, 180) from a set of walls that defines respective gas passageways that both exist within the module and are incident to the gas pressure measured. One or more walls of the set may extend outside the module. The module can be configured for deciding, based on a result of the measuring, whether a magnitude of the leakage exceeds a predetermined threshold. A source for applying the pressure may be internal (138) or external (104, 132, 135). Gas pressure based pattern recognition can be used to identify, optionally during treatment and in real time, one or more leak sites responsible for the leakage. The module is implementable as a ventilation monitoring module that measures differential flow of a breathing circuit, the testing serving to prevent cross-contamination of patients.

Abstract: A PAP system for delivering breathable gas to a patient includes a flow generator to generate a supply of breathable gas to be delivered to the patient; a humidifier including a heating plate to vaporize water and deliver water vapor to humidify the supply of breathable gas; a heated tube configured to heat and deliver the humidified supply of breathable gas to the patient; a power supply configured to supply power to the heating plate and the heated tube; and a controller configured to control the power supply to prevent overheating of the heating plate and the heated tube.

Abstract: A respiratory circuit apparatus and circuit are provided. The circuit includes: an adapter having a plurality of connectors of two or more different internal or outer diameters; and a pressure release valve configured to emanate sound if a pressure of a gas received at the pressure release valve is greater than or equal to an activation pressure of the pressure release valve. The pressure release valve can have a first end of a body portion coupled with one of the plurality of connectors of the adapter. The pressure release valve can be coupled inline in the respiratory circuit via the adapter and in close proximity to a patient location.

Abstract: A speaking valve includes a hollow body configured to be secured to a connector of a tracheostomy system disposed in a patient. The speaking valve further includes a cap that houses a valve member, which enables the speaking valve to act as a one-way check valve. The valve member, hollow body, or other components of the valve may include a material that undergoes a chemical changed when exposed to moisture, i.e., a hydrosensitive material. Particularly, the hydrosensitive material may exhibit a color change when exposed to moisture. As such, the hydrosensitive material may be useful in providing a visual indication of the saturation and/or moisture level of the speaking valve.

Abstract: The invention discloses devices and methods for identifying a diver in distress and initiating a rescue response. Specifically, embodiments of the present invention allow for identification of a diver who is not breathing properly and in response giving local stimuli to allow the diver to response. Should he/she not respond, the instant invention will initiate steps to bring the diver back to the water surface and alert others as to his/her need of assistance.