Abstract: A device for maintaining an airway in a patient, the device including a mask having a peripheral portion that forms a seal with the larynx when the mask is positioned in the laryngo pharynx to thereby prevent ingress of extraneous fluids into the larynx; an airway tube connected to or formed with the mask for passing gas to the larynx when the mask is properly inserted into the laryngo pharynx; and one or more elongated members located on the mask, wherein the application of force to the elongated members causes elastic deformation of the device, thereby facilitating insertion of the device into the patient.

Abstract: A non-invasive ventilation system may include an interface. The interface may include at least one gas delivery jet nozzle adapted to be positioned in free space and aligned to directly deliver ventilation gas into an entrance of a nose. The at least one gas delivery jet nozzle may be connected to a pressurized gas supply. The ventilation gas may entrain ambient air to elevate lung pressure, elevate lung volume, decrease the work of breathing or increase airway pressure, and wherein the ventilation gas is delivered in synchrony with phases of breathing. A support for the at least one gas delivery jet nozzle may be provided. A breath sensor may be in close proximity to the entrance of the nose. A patient may spontaneous breathe ambient air through the nose without being impeded by the interface.

Abstract: A ventilator (10) that pressurizes gas from a body of gas to provide a flow of gas to an airway of a subject (14) such that the gas flow mechanically facilitates the respiration of the subject (14). In order to enhance the comfort of the subject (14) during ventilation by the ventilator (10), the ventilator (10) enables the subject (14) to make unsupervised adjustments to one or more of the properties of the gas flow, within predetermined limits.

Abstract: A breathing assistance device includes a patient breathing tube having a leading end in fluid communication with a face mask. A source of air under pressure is connected to a first port formed integrally with a valve in fluid communication with the breathing tube and a nebulizer is connected to a second port formed integrally with the valve. A compartment holding a medicinal compound in liquid fluid form is connected to the nebulizer. A valve actuator has an open position where gaseous fluid and aerosolized medicine from the nebulizer flow to the patient through the breathing tube and a closed position where only gaseous fluid without medication is delivered. Medication can therefore be administered to or withheld from the patient by manipulating the valve actuator. The valve construction enables the patient to exhale against pressure slightly above atmospheric pressure.

Abstract: This disclosure describes systems and methods for providing adaptive base flow scheduling during ventilation of a patient to optimize patient-machine synchrony and accuracy of estimated exhaled as well as inhaled tidal volumes. Further, this disclosure describes systems and methods for providing adaptive inspiratory trigger threshold scheduling during the adaptive base flow scheduling. Further still, this disclosure describes systems and methods for determining an estimated leak flow and adjusting the adaptive base flow scheduling and the adaptive inspiratory trigger threshold scheduling based on the estimated leak flow. Moreover, this disclosure describes systems and methods for determining a change in the estimated leak flow and adjusting the adaptive base flow scheduling and the adaptive inspiratory trigger threshold scheduling based on the change in the estimated leak flow.

Abstract: One embodiment is an improved method for providing a tube for attachment to a medical device such as a catheter that provides for intermittent changes in tube path length as a result of body movement thereby reducing the stress and pain caused by pulling on the device, as well as the optional provision to provide a very low, controlled tension that provides improved stability of the medical device without damage to the surrounding body tissues. In at least one embodiment, there is a decrease in infection risk by the patient. This controlled tension can be applied or removed intermittently by a medical practitioner or the patient. Other embodiments provide for extension in tubal path length while simultaneously providing for intermittent or continuous low tension pull on the catheter. Provision is also made for a continuous smooth fluid path with no moving internal parts.

Abstract: A respiration system includes a patient connection (1), an inspiratory branch (3), an expiratory branch (13), a rebreathing line (99), a reservoir (25), a CO2 absorber (29), a radial compressor respiration drive (33), a fresh gas supply unit (51), an oxygen flushing device (55), connected to the rebreathing line, a pressure sensor (31) and an actuatable control valve (21), arranged in the rebreathing line between a second end (17) of the expiratory branch and the CO2 absorber. The compressor, oxygen flushing device and fresh gas supply unit are arranged in the rebreathing line between the CO2 absorber and a second end (7) of the inspiration branch. The compressor inlet points towards the CO2 absorber and the outlet points towards the second end of the inspiratory branch. The pressure sensor is arranged in the rebreathing line between the compressor and the second end of the inspiratory branch.

Abstract: This disclosure describes systems and methods for providing novel adaptive base flow scheduling during ventilation of a patient to optimize the accuracy of estimated exhaled tidal volume. Further, this disclosure describes systems and methods for providing novel adaptive inspiratory trigger threshold scheduling during the novel adaptive base flow scheduling.

Abstract: A method for administering a gas containing oxygen to a patient. The method includes: measuring an oxygen-dependent physiological parameter in the patient; determining an optimal gas delivery parameter based on the oxygen-dependent physiological parameter; and administering the gas to the patient in accordance with the optimal gas delivery parameter. In some embodiment of the invention, the method also includes monitoring the oxygen-dependent physiological parameter.

Abstract: A laryngeal mask insertable into a patient, an airway tube of the laryngeal mask having a bore extending from a proximal to a distal end of the airway tube, a connector provided at the proximal end of the airway tube, the connector comprising a connector body with a longitudinal bore, at least two wall portions extending longitudinally from a first continuous wall to a second continuous wall, and two parallel and opposite longitudinal wall cut-away portions intermediate the at least two wall portions, the length of the longitudinal wall cut-away portions being greater than the length of the first continuous wall.

Abstract: The present invention provides a method for reducing condensed humidifying agent in a humidification system by pulsing a delivery of humidifying agent into a respiratory circuit. During a non-pulsed interval, gas flowing through the respiratory circuit will evaporate the condensed humidifying agent present in the respiratory circuit. The present invention also provides a method and apparatus for delivering humidified gas to a patient, wherein the delivery avoids the problems associated with a stationary water humidifier. In the method, the delivery of humidifying agent is precisely controlled to deliver a flow of humidifying agent to a volume of gas.

Abstract: An inhaler device (1) contains, or is capable of accepting, a plurality of doses of a medicament to be dispensed from the inhaler (1). To ameliorate the problem of double dosing from the inhaler (1), the device further comprises prevention means (26, 28, 40) for preventing, at least temporarily, the dispensing of a dose of medicament, and detection means (32) for detecting the inhalation of a previously dispensed dose of medicament. When the detection means (32) detects the inhalation of the previously dispensed dose of medicament, it releases the prevention means (26, 28, 40), allowing the device to dispense a further dose of medicament. The detection means (32) may be a pressure sensor, and the prevention means (26, 28, 40) may operate by causing a disengagement of an actuation mechanism.

Abstract: A breathing circuit system for supplying a breathable gas from a breathable gas supply system to a patient interface. The system comprises a heated conduit, comprising a hose and a hose heating system associated with the hose, and a plurality of adapter elements. The hose heating system is provided for operating within a first predetermined voltage range. A controller is associated with the breathing circuit and provides voltage within a second predetermined voltage range. Each adapter element comprises at least one electric component provided for adjusting the voltage supplied by the controller from a second range to the first range.

Abstract: Described are systems and methods for compensating long term sensitivity drift of catalytic type electrochemical gas sensors used in systems for delivering therapeutic nitric oxide (NO) gas to a patient by compensating for drift that may be specific to the sensors atypical use in systems for delivering therapeutic nitric oxide gas to a patient. In at least some instances, the long term sensitivity drift of catalytic type electrochemical gas sensors can be addressed using calibration schedules, which can factor in the absolute change in set dose of NO being delivered to the patient that can drive one or more baseline calibrations. The calibration schedules can be used reduce the amount of times the sensor goes offline. Systems and methods described may factor in in actions occurring at the delivery system and/or aspects of the surrounding environment, prior to performing a baseline calibration, and may postpone the calibration and/or rejected using the sensor's output for the calibration.

Abstract: Various embodiments of tracheal tube assemblies disclosed herein may include a tubular body having an open distal end for ventilating a patient and a cuff disposed around the tubular body above the open distal end. The cuff may be adapted to be inflated to seal the cuff against a wall of a trachea of the patient. The cuff may include a first portion that spaces the tubular body a first distance from the tracheal wall when inflated and a second portion that spaces the tubular body a second distance from the tracheal wall when inflated. The second distance may be greater than the first distance.

Abstract: A process for automatic control of a respirator changes between two phases of respiration by checking a detected respiratory breathing activity signal for a threshold criterion. If the threshold criterion is met, a changeover is made.

Abstract: A respiration appliance (10), system (40), and method (62, 72, 86) for supporting the airway of a subject (12) as the subject (12) breaths. The flow of gas from the lungs of the subject (12) during exhalation is leveraged to provide support to the airway. In particular, a body (14) that encloses one or more external orifices of the subject (12) provides a resistance differential between inhaled gas flows and exhaled gas flows that supports the subject's airway.

Abstract: A respiration appliance (10), system (40), and method (62, 72, 86) for supporting the airway of a subject (12) as the subject (12) breaths. The flow of gas from the lungs of the subject (12) during exhalation is leveraged to provide support to the airway. In particular, a body (14) that encloses one or more external orifices of the subject (12) provides a resistance differential between inhaled gas flows and exhaled gas flows that supports the subject's airway.

Abstract: A fluid dispenser device having a dispenser member, such as a pump or a valve, that is mounted on a fluid reservoir and that is actuated by a dispenser head that includes a spray orifice. The device further having a visual indicator that is movable between an indicating position and a non-indicating position, the visual indicator being moved into their non-indicating position at the start of each actuation of the dispenser member, and being moved from the non-indicating position towards the indicating position by the fluid, while it is being dispensed.

Abstract: According to various embodiments, methods and systems for determining pressure in an inflatable cuff of a tracheal tube may employ pressure transducers associated with a cuff inflation line or a pilot balloon assembly. The pressure transducers may be implemented to provide continuous or intermittent cuff pressure. Also provided are tracheal tubes with adapters or other devices that incorporate pressure transducers. The tracheal tubes may facilitate wireless cuff pressure monitoring.