Abstract: An indicating device includes a housing having a longitudinally extending cavity shaped to receive the container and an indicator member disposed in the cavity and having a longitudinally extending wall shaped to surround at least a portion of the container. The indicator member is rotatably mounted within the housing and is rotatable relative thereto about a longitudinal axis. The indicator member includes a driven gear. A drive gear is disposed in the housing and includes a drive portion selectively engaged with the driven gear. An actuator is adapted to move with the container and is selectively engaged with the drive gear.

Abstract: A medical device may include a patient interface for use in a breathing assistance system, an electronic device coupled to the patient interface, and one or more electrical conductors at least partially integrated with the patient interface. The patient interface may include a connection end configured for receiving gas communicated by a gas delivery apparatus, and a patient end configured for insertion into or more breathing passageways of a patient. The one or more electrical conductors at least partially integrated with the patient interface may be capable of facilitating communication of electrical signals between the electronic device and the gas delivery apparatus when the patient interface is communicatively coupled to the gas delivery apparatus.

Abstract: A device for detecting the condition of flow in a respiration system combines the function of a nonreturn valve with the function of flow measurement in a common device. The device includes a valve arrangement (1) with a valve disk (9) and with a valve body (8), wherein the position of a valve disk (9) in relation to a valve seat (11) is detected. An indicator for a flow and a direction of flow (5), (6) is determined from the position of the valve disk (9). The position of the valve disk (9) can be determined inductively, electrically, electromechanically or optically. The flow and direction of flow (5), (6) determined can be used to control the respiration in a medical device.

Abstract: Methods and systems are provided that determine whether a patient is receiving minimal support from a ventilator. In one embodiment, a ventilation system may determine a value of a peak inspiratory pressure (PIP) and a value of a positive end-expiratory pressure (PEEP) of a patient. The ventilation system may determine a pressure differential between the value of PIP and the value of PEEP and compare the pressure differential to a threshold. The ventilation system may determine that the patient is receiving minimal support if the pressure differential is below the threshold. Further, the ventilation system may provide an indication of the detection of minimal support.

Abstract: A breathing apparatus includes components, including, but not limited to, a flow generator, a patient interface, and a delivery conduit. A connector for connecting components of the breathing apparatus includes a male connector, including a recess, extending from a first component, and a female connector, including a lever pivotally connected thereto, extending from a second component. A switch indicates a connection state of the connector. The switch includes a ring provided in an end of the first or second component and the ring includes a projection extending through an aperture in the end of the first or second component. The projection is movable between a first position and a second position to indicate the state of the connector.

Abstract: A vent assembly for use with a mask assembly includes a first vent and a second vent having at least one different flow characteristic wherein the vent assembly can be switched between the first vent and the second vent to alter flow of exhaled gas from a patient.

Abstract: Methods and systems are provided that determine whether a patient is receiving minimal support from a ventilator. In one embodiment, a ventilation system may determine a value of a peak inspiratory pressure (PIP) and a value of a positive end-expiratory pressure (PEEP) of a patient. The ventilation system may determine a pressure differential between the value of PIP and the value of PEEP and compare the pressure differential to a threshold. The ventilation system may determine that the patient is receiving minimal support if the pressure differential is below the threshold. Further, the ventilation system may provide an indication of the detection of minimal support.

Abstract: Methods and systems are provided that determine whether a patient is asynchronous with a ventilator. In certain embodiments, a ventilation system may determine whether a double-triggering event has occurred between the patient and the ventilator. The ventilation system may compare a value of the patient's exhaled tidal volume to a threshold and may determine that a double-triggering event occurred if the patient's exhaled tidal volume is less than or equal to the threshold. The ventilation system may also determine a frequency of the double-triggering events. Further, the ventilation system may provide an indication of a detected double-triggering event and an indication of the frequency of double-triggering events.

Abstract: A dose counter for use with an inhaler comprising a container for medicament equipped with a reciprocal actuation means to dispense a dose of medicament therefrom, the dose counter comprising: a fixed ratchet member, a trigger member constructed and arranged to undergo reciprocal movement coordinated with the reciprocal movement between the actuation means and the container, said reciprocal movement comprising an outward stroke and a return stroke, a counter member constructed and arranged to undergo a predetermined counting movement each time a dose is dispensed, the counter member being biased towards the ratchet and trigger members and being capable of counting motion in a direction generally orthogonal to the direction of reciprocal movement of the trigger member, the counter member comprising: a first region for interaction with the trigger member which comprises at least one inclined surface which is engaged by the trigger member during its outward stroke causing the counter member to undergo counting m

Abstract: An electronic display device (20) including a display member (21). The display member (21) is permanent so that no energy is required to keep the display unchanged. The display device (20) operates without a battery, the energy required to change the display being created by interaction between two elements, such as by friction or by an impact, thereby creating an electric pulse that is processed by an electronic circuit (25) before being applied to the display member (21) in order to change its display.

Abstract: A medicament dispenser, in particular a metered dose inhaler, which is able to count the number of time the dispenser is activated and then disable the device, which then prevents any additional medicament from being dispensed. Additional embodiments include a medicament dispenser which are adapted to display either the number of activations that have occurred or the number of activations remaining.

Abstract: Tracheal tubes having an integrated calorimetric CO2 indicator are provided. In certain embodiment, the integrated CO2 indicator is selectively sealed from the remainder of the tracheal tube by a removable sterilization barrier. Also provided are CO2 indicators that exhibit long lasting, breath-to-breath dynamic color change and are storage stable. The devices and compositions of the invention find use in a variety of applications, e.g. in emergent intubation of a subject. Also provided are methods of making the devices and compositions, as well as kits that include the devices and/or compositions of the invention.

Abstract: Provided is a method that includes automatically providing air/oxygen at a pre-selected maximum pressure limit, breath volume and respiratory-rate. The pre-selected maximum pressure limit, breath volume, and respiratory-rate are automatically set as a function of a size of a mask coupled to an air/oxygen supply system. Further provided is a ventilator system that includes a ventilator mask, a ventilator supply system, and a mask conduit. The ventilator mask is configured in a size that will fit upon a selected range of sizes of human faces. The ventilator supply system includes an air/oxygen source and an air/oxygen regulator system configured to regulate air/oxygen flow parameters as a function of the size of the mask. The mask conduit is configured to couple the ventilator supply to the ventilator mask.

Abstract: The present invention provides dispensing apparatus for delivering metered doses of product from a pressurized dispensing container comprising: a housing for receiving a pressurized dispensing container; a dose counting mechanism comprising indication means for displaying to a user an indication associated with the number or quantity of doses dispensed from, or the number or quantity of doses remaining in, the received pressurized dispensing container; the dose counting mechanism further comprising an indexing mechanism for advancing the indication means on actuation of the received pressurized dispensing container; wherein the dispensing apparatus comprises an indexing member capable of moving within the housing in sync with the received pressurized dispensing container; wherein on actuation of the received pressurized dispensing container in a normal mode of operation the indexing member is able to interface with the indexing mechanism to apply a force to the indexing mechanism sufficient to incrementally a

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 vent assembly for use with a mask assembly includes a first vent, a second vent and a selector to switch the flow of exhaled gas from a patient between the first and second vents.

Abstract: A blower filter device (1) is provided for a blower filter system (20). The blower filter device (1) has at least one filter (2), a fan wheel (4) arranged in a fan housing (3), a motor (5) for driving the fan wheel (3) as well as a control unit (6) for actuating motor (5) and for processing device-specific parameters of the blower filter device (1). The blower filter device (1) has a housing (13) with a mounting slot (14) for a communication interface module (7). The contact point (15) is arranged in mounting slot (14) for the data-communicating connection of communication interface module (7) to the control unit (6). The blower filter system (20) includes such a blower filter device (1) and, a head piece (21) and a flexible connection hose (22) providing a fluid-communicating connection between the blower filter device (1) and the head piece (21).

Abstract: An anesthesia device supplying a first and second anesthetic in a quantitatively settable, controlled manner. A data processing unit with a corresponding display is set up for determining the current concentrations in the plasma or at the site of action from continuously supplied data on the quantities of the anesthetics administered with a module for a pharmacokinetic compartment model calculation and for storing these concentration values. Concentration data is predicted for at least one point in time in the future. An action module provides a curve of an anesthesia action parameter as a function of the concentrations of the anesthetics. A display module displays a diagram showing the sequence of concentration of the first or second anesthetic, and the predicted concentration.

Abstract: There is provided an actuation counter comprising a driver feature having one or more driver elements, which driver feature is arranged for drivable movement in response to an actuation; and a count member including one or more drive receipt elements arranged thereon for receipt of drive from said one or more driver elements of the driver feature for drivable movement of the count member. The driver feature includes one or more brake elements arranged to selectively interact with the count member to prevent overrun thereof when registering a count of an actuation. The actuation is suitably arranged for use with a drug dispenser device.

Abstract: Transmitter and receiver devices and related methods are provided for monitoring air supplies and optionally directions of a group of divers. A transmitter device includes an acoustic transmitter, and may have a housing with two nonconcentric generally cylindrical portions of different diameters. The transmitter device may send brief sonic data packets comprising pressure, identification and error checking portions encoded with an on/off modulation scheme. A receiver device decodes sonic packets received from a transmitter device, and may include a plurality of acoustic transducers for determining a direction of a transmitter device. Both the transmitter and receiver devices may be compact, low cost and have long battery life.

Abstract: A ventilator provides breathing support to a patient in an EMG controlled mode, and has an input that receives an EMG signal representative of breathing activity from the patient and a control unit for controlling the ventilation in dependence of said EMG signal. The ventilator has a registration unit that registers the actual breathing support provided from the ventilator to the patient, and the control unit determines if there is asynchrony between the EMG signal and the breathing activity and, in case of asynchrony, causes a switch from EMG controlled ventilation to a second ventilation mode not dependent on the EMG signal. If synchrony is detected the ventilator can return to EMG controlled ventilation.

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 system and method of providing bi-level CPAP therapy is provided that incorporates an infrared carbon-dioxide sensor to determine whether a patient is inhaling or exhaling. Patient exhalation causes the infrared light to be absorbed, while patient inhalation reduces the presence of carbon-dioxide causes little or no absorption of carbon-dioxide. The level of carbon-dioxide in an associated patient breathing interface is monitored for thresholds that trigger higher CPAP pressure upon inhalation and lower CPAP pressure upon exhalation.

Abstract: A system for performing simultaneous ventilation and resuscitation of a patient includes an oxygen source, at least one inspiration control valve, a breathing apparatus, at least one expiration control valve, at least one indicator, and at least one timer. The breathing apparatus is configured to form an air seal with at least a portion of the patient's respiratory tract such that a gas including oxygen can flow from the oxygen source to the lungs. The at least one expiration control valve being configured to selectively actuate an exhalation valve. The at least one indicator for indicating when a rescuer should perform a chest compression. The at least one timer for synchronizing actuation of the at least one inspiration control valve, the at least one expiration control valve, and the indicator, thereby enabling continuous compressions to be provided to the patient while the patient undergoes inspiration and expiration.

Abstract: Methods and devices to determine rate of particle production and the size range for the particles produced for an individual are described herein. The device (10) contains a mouthpiece (12), a filter (14), a low resistance one-way valve (16), a particle counter (20) and a computer (30). Optionally, the device also contains a gas flow meter (22). The data obtained using the device can be used to determine if a formulation for reducing particle exhalation should be administered to an individual.

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 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 medical air tubing and anti-mismatch fluid distribution system is provided for preventing the inadvertent connection of a feed line to an incorrect source of fluid. The fluid distribution system includes an adapter that is connected permanently to the fluid supply and has an outlet end that is compatible with a coupling member on the feed line. The coupling member on the feed line is compatible with the adapter but is not compatible with the other coupling member of the second fluid supply. A feed line assembly includes a feed line with a connector fixed to a first end and a nebulizer or other medical device fixed to a second end to form a one piece, integrally formed unit. The second fluid supply can include an adapter that is different from the first adapter so that the coupling members of the feed lines are compatible only with the appropriate adapter for the desired fluid source.

Abstract: A method for displaying ventilator data at a remote device. The method includes accessing ventilator data of a ventilator associated with a patient, by a remote device; and displaying the ventilator data, at the remote device.

Abstract: An inhalation device for delivering doses of medicament to a user comprising: —a canister (5), said canister being adapted to accommodate the medicament to be dispensed to a user, and —a counter (15) which is connected to the canister (5). According to the invention —the canister (5) is adapted to receive the counter (15) on a base end (6a), —the counter and/or the canister further having contact parts (18, 20) for their attachment having means for increasing the friction and thereby allowing the counter to fixedly be attached onto the canister in a range of different positions in the lengthwise direction, —the counter further being adapted to during the process to assemble the counter to the canister, be urged onto the canister until the length of the counter and canister together is within a predefined tolerance of a predefined length.

Abstract: This disclosure describes systems and methods for monitoring and evaluating ventilatory parameters, analyzing ventilatory data associated with those parameters, and providing useful notifications and/or recommendations to clinicians. Modern ventilators monitor, evaluate, and graphically represent a myriad of ventilatory parameters. However, many clinicians may not easily identify or recognize data patterns and correlations indicative of certain patient conditions, changes in patient condition, and/or effectiveness of ventilatory treatment. Further, clinicians may not readily determine appropriate ventilatory adjustments that may address certain patient conditions and/or the effectiveness of ventilatory treatment. Specifically, clinicians may not readily detect or recognize the presence of Auto-PEEP during various types of pressure ventilation.

Abstract: This disclosure describes systems and methods for monitoring and evaluating ventilatory parameters, analyzing ventilatory data associated with those parameters, and providing useful notifications and/or recommendations to clinicians. Modern ventilators monitor, evaluate, and graphically represent a myriad of ventilatory parameters. However, many clinicians may not easily identify or recognize data patterns and correlations indicative of certain patient conditions, changes in patient condition, and/or effectiveness of ventilatory treatment. Further, clinicians may not readily determine appropriate ventilatory adjustments that may address certain patient conditions and/or the effectiveness of ventilatory treatment. Specifically, clinicians may not readily detect or recognize the presence of Auto-PEEP during various types of pressure ventilation of a patient exhibiting an obstructive component.

Abstract: This disclosure describes systems and methods for monitoring and evaluating ventilatory parameters, analyzing those parameters and providing useful notifications and recommendations to clinicians. That is, modern ventilators monitor, evaluate, and graphically represent multiple ventilatory parameters. However, many clinicians may not easily recognize data patterns and correlations indicative of certain patient conditions, changes in patient condition, and/or effectiveness of ventilatory treatment. Further, clinicians may not readily determine appropriate ventilatory adjustments that may address certain patient conditions and/or the effectiveness of ventilatory treatment. Specifically, clinicians may not readily detect or recognize the presence of Auto-PEEP during volume ventilation of a non-triggering patient exhibiting an obstructive component.

Abstract: This disclosure describes systems and methods for monitoring and evaluating ventilatory parameters, analyzing those parameters and providing useful notifications and recommendations to clinicians. That is, modern ventilators monitor, evaluate, and graphically represent multiple ventilatory parameters. However, many clinicians may not easily recognize data patterns and correlations indicative of certain patient conditions, changes in patient condition, and/or effectiveness of ventilatory treatment. Further, clinicians may not readily determine appropriate ventilatory adjustments that may address certain patient conditions and/or the effectiveness of ventilatory treatment. Specifically, clinicians may not readily detect or recognize the presence of Auto-PEEP during volume ventilation of a triggering patient exhibiting an obstructive component.

Abstract: A patient interface device that includes a support member sized and configured to span at least a portion of a patient's face while remaining below the patient's eyes responsive to the patient interface device being donned by such a patient and a sealing assembly operatively coupled to the support member such that the support member is moveable relative to the support member. The support member defines a gas carrying conduit adapted to carry a flow of gas to the sealing assembly. The support member is a single-piece unitary member and includes a conduit coupling portion adapted to be coupled to a patient circuit.

Abstract: A dose counter (100) for counting the number of doses of fluid or powder that have been dispensed or that remain to be dispensed from a fluid dispenser device (200), said counter including a first rotary counter element forming a units wheel, and a second rotary counter element forming a tens wheel, said first and second counter elements co-operating with each other to define and to display, in a viewing window (151), said number of doses, said first counter element co-operating with an actuator member that is adapted to cause said first counter element to turn each time said actuator member is actuated, said counter including a base body that incorporates a pivot pin for said first and second counter elements and an opening, said counter possibly being pre-assembled in said base body so as to form a pre-assembled counter unit.

Abstract: An inhaler (1) for delivery of a powder-form inhalation formulation from a blister strip (2) with a plurality of blister pockets (3) is proposed. A tape is used for numbering.

Abstract: The gases temperature supplied to a patient when the patient is undergoing treatment such as oxygen therapy or positive pressure treatment for conditions such as Obstructive Sleep Apnea (OSA) or Chronic Obstructive Pulmonary Disease (COPD) is often measured for safety and to enable controlling of the humidity delivered to the patient. The invention disclosed is related to measurement of properties, particularly temperature (thermister 23), of gases flowing through a heated tube (3), supplying gases to a patient, which utilises the heating wire (21, 28) within the tube.

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 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: Systems and methods for synchronizing machine-induced expiratory airflow of a subject with user-induced expiratory airflow include an indicator time at which a user should initiate treatment to aid airway clearance of the subject. Such treatment may include compressing the stomach area of the subject. At the indicator time, a user responds to an indication, e.g. an audible sound, by initiating treatment in accordance with a therapeutic regimen.

Abstract: Feedback information is provided to a subject regarding reception of pressure support therapy, and/or other respiratory support therapy. The feedback information may indicate compliance to a respiratory therapy regimen. The feedback information is provided to the subject by transmitting the feedback information through a communication network to a client device associated with the subject. The feedback information may include a characterization of the therapy received by the subject with respect to a usage goal.

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: 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: An assembly structured to inflate a retaining or pressure cuff associated with an artificial airway tube such as an endotracheal and/or tracheotomy tube and concurrently monitor pressure therein including a casing having an interior pressure chamber. A pump assembly is movably connected to the casing and structured to force fluid flow to the retaining cuff through said pressure chamber. An indicator member is disposed within the casing, is visually accessible through casing window, and is variably positionable dependent on and indicative of existing pressure within the retaining cuff. The existing pressure within the pressure chamber is substantially equivalent to that within the retaining cuff thereby facilitating the variable position of the indicator member to indicate pressure within the cuff. A junction is disposed between the casing and an inflation lumen to the restraining cuff and is structured to allow disconnection between the casing and the lumen but prevent reconnection thereto.

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: 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: Inhaler device (10) comprising an actuator body (20) and an inhaler canister assembly (70), the inhaler canister assembly (70) is comprised of a canister (30) with a metering valve at a valve end and a dose counter unit (60) attached to a base end thereof. Further, the inhaler canister assembly (70) comprises first position ensuring means (110, 230), the actuator body comprises second position ensuring means (120,210), wherein the first and second position ensuring means being complementary mating means, and the first and second position ensuring means being so arranged that the inhaler device (10) cannot be fired, nor the counter unit (60) count unless the first and second position ensuring means are in a mating relationship. There is also provided an inhaler canister assembly (70) and an actuator body (20).

Abstract: This invention relates to a breath indicator that is receivable by a part of a breathing assistance apparatus that supplies gas to a patient. The indicator comprises an elongate body having a gas sampling end and an attachment end. The attachment end is adapted to attach to a part of a breathing assistance apparatus and for locating the gas sampling end. The gas sampling end is to be located in a region where gas from the patient is to be exhaled. The gas sampling end being in communication with a sensor comprising a detector material changeable between a first visual indicator state relating to an inhalation phase of the patient, and a second visual indicator state relating to an exhalation phase of the patient. The detector material is capable of changing between the visual indicator states at a sufficient rate to substantially correspond with the inhalation and exhalation phases of the patient.

Abstract: This application discloses a dose counter device of the type for use on an aerosol dispensing assembly having an aerosol container and an actuator. The dose counter device is used for indicating the release of a dose of aerosol medication caused by the application of a force, in an axial direction, on the aerosol dispensing assembly. The dose counter device has a cap, a slider and a first counter ring. The cap is moved in a first direction along an axis of the container, which causes movement of the slider in a first linear direction laterally, relative to the axis of the container, as a function of the movement of the cap in the first direction. The first counter ring is rotated through a first arc in a first circumferential direction about the axis of the container, as a function of the movement of the slider in the first linear direction.