Abstract: A supplemental air diffusion device is shaped and configured to be attached to the body or clothing of a patient below the head and deliver supplemental air toward the mouth and nose of the patient. The supplemental air diffusion device includes a frustroconicoidal air diffusion body that has a smaller inlet opening at an inlet end and an enlarged diffusion opening at a diffusion end. An air inlet stem is integrally attached to the air diffusion body and includes a plurality of ribs and/or recesses for releasably locking a female connector of an air supply hose over the inlet stem. A pair of spaced-apart slits are provided through a flange extending laterally from an outer surface of the air diffusion device. Initially separate accessory patient attachment clamps are looped through the slits and provide for releasable attachment of the air diffusion device to a patient's clothing.

Abstract: A system is provided by applying pressure to a portion of a body of an individual in a chamber having an aperture along a vertical axis for receiving the portion of the body of the individual. A pressure sensor is coupled to the chamber for measuring a pressure inside the chamber. A negative feedback control system, calibrates, adjusts and maintains the pressure inside the chamber.

Abstract: A mask (10) for use with a system for supplying breathable gas pressurized above atmospheric pressure to a human or animal's airways. The mask (10) includes a mask shell (12) which is, in use, in fluid communication with a gas supply conduit and a gas washout vent assembly (20). The gas washout vent assembly (20) includes at least one gas washout orifice (22) extending from a first side of the vent assembly (20) positioned, in use, adjacent the human or animal's face and a second side positioned, in use, adjacent the atmosphere. The cross-sectional area of the orifice (22) at the first side is larger than the cross-sectional area of the orifice (22) at the second side.

Abstract: A method for attaching a removable, washout vent insert to a CPAP mask, the CPAP mask comprised of a rigid plastics shell having an inlet tube, the rigid plastics shell having an opening bounded by a rim, the vent insert being made of a material more flexible than the rigid plastic shell, the vent insert having a plurality of orifices, the vent insert, in a cross-sectional view, having a recess located at its periphery, includes: squeezing the vent insert along its longitudinal axis; aligning the vent insert so it is oriented to match the shape of the opening; inserting the vent insert into the opening; and releasing the vent insert once it is within the opening, the vent insert resiliently expanding to engage the rim of the opening.

Abstract: A guide adapted for facilitating insertion of a medical device into the trachea of a patient is disclosed. The guide includes an integral curved-shaped member having at least a first leg at one end of the guide. The curved-shaped member essentially includes an outside curved side defining a concave groove. A first angle is defined on the first leg configured and dimensioned to allow for at least the first leg to pass through the mouth and into the trachea of the patient. Insertion of the guide into the trachea allows for elevation of the tongue and surrounding soft tissue of the patient thereby forming an air space that allows for passage of a medical device.

Abstract: A probe for medical use comprising a tube (1) and a cuff (3) located around the tube (1) in a region of its external wall, the cuff (3) being inflatable through a conduit (5) arranged at the wall of the tube (1), linking the interior of the tube (1) to the interior of the cuff (3), the inflation and deflation of the cuff (3) being determined by the rhythms of the inspiration and expiration of air, respectively.

Abstract: A full-face cushion comprises a frame and a membrane. The membrane has an aperture into which the wearer's nose is received. The membrane is spaced away from the frame. Respective notches receive the bridge of the wearer's nose. The wearer's nose and lips are received through the aperture into the chamber within the mask body. The seal forming portion thus contacts both the surface of the wearer's nose and a portion of the wearer's face in the region between the bottom lip and the chin, and around the sides and over the bridge of the nose.

Abstract: A delivery device for and method of delivering a substance, the delivery device having an outlet member through which substance is in use delivered in an entraining gas flow, and a substance supply unit for supplying substance to be entrained by an entraining gas flow as one or both of a vapor or a fine aerosol mist, wherein the substance supply unit has a flow channel which is fluidly connected to the outlet member, and a substance supporting element for supporting substance, at least a surface of which is in use disposed in the flow channel.

Abstract: A respiration apparatus and a method for calibrating respiration parameters thereof are provided. A flow measuring reference component arranged behind the inspiratory valve in the ventilator is used as a flow measuring reference sensor for calibrating the flow sensor so that the flow rates of the gas through the flow measuring reference component and the flow sensor to be calibrated are identical or in a corresponding relation. Electrical parameters output from the flow sensor and the flow measuring reference component are respectively acquired and processed to obtain a relation curve of the gas flow rate and the electrical parameter of the flow sensor on the basis of the read gas flow rate and the electrical parameters of the flow sensor. The present invention enables automatic calibration for a flow sensor without using any measuring instrument.

Abstract: A system for providing mechanical ventilation support to a patient and includes a mechanical ventilator. A breathing circuit is pneumatically connected between the mechanical ventilator and a patient connection. An inspiratory check valve is disposed within an inspiratory limb of the breathing circuit. A fresh gas manifold provides fresh gas to the breathing circuit for delivery to the patient. A fresh gas valve is disposed between the fresh gas manifold and the breathing circuit. The fresh gas valve is operable between a first position which directs fresh gas upstream of the inspiratory check valve and a second position that directs fresh gas downstream of the inspiratory check valve. A digital signal processor operates the fresh gas valve selectively between the first position and the second position. A method of ventilating a patient includes introducing a flow of fresh gas into an inspiratory limb of the breathing circuit.

Abstract: A device for compressive treatment of a body part includes a compression member, adapted to at least partly encircle the body part, and an actuation unit, arranged to tighten the compression member to provide a compressive force to the body part. The actuation unit includes an active material actuator. There is also disclosed a system comprising such a device and methods for its therapeutic, cosmetic and non-therapeutic use and operation.

Abstract: An anesthesia machine having an automatic scavenger system is disclosed herein. The anesthesia machine includes a scavenger hose configured to direct the transfer of an exhaled anesthetic agent from a patient, and a valve operatively connected to the scavenger hose. The valve is configured to selectively control the transmission of the exhaled anesthetic agent through the scavenger hose. The anesthesia machine also includes a switch operatively connected to the valve and to a controller. The switch is configured to link an operational status of the anesthesia machine with a position of the valve.

Abstract: The invention relates to an inhaler component for forming a vapor-air mixture and/or condensation aerosol by vaporising a liquid material and optionally condensing the vapor formed, including: a heating element for vaporising a portion of the liquid material; a wick for automatically supplying the liquid material to the heating element, wherein the wick comprises at least two end sections arranged apart from each other; a first capillary gap for automatically supplying the liquid material to the wick, wherein a first end section of the wick projects into the first capillary gap. In order that the heating element can be supplied more quickly and more reliably with the liquid material, a second capillary gap is provided, which receives therein the second end section of the wick.

Abstract: An inhalation nebulizer includes an aerosol generator that can be removed from the inhalation therapy device or inserted therein, and a control device that sends a control signal to the aerosol generator. The aerosol generator has a characterization device containing information about the aerosol generator, that can be determined by an identification device of the inhalation therapy device, in order to influence the operation of the inhalation therapy device.

Abstract: A method for selecting a device adapted to treat disordered breathing includes determining a number of characteristics associated with at least a portion of the airway of a patient, comparing each of at least some of the number of characteristics to a corresponding threshold, and selecting such a device in response to the comparison. An alternative method for selecting a device adapted to treat disordered breathing includes delivering a flow of breathing gas to the airway of a patient, determining a minimum effective therapeutic pressure associated with such patient, and selecting, relative to the minimum effective therapeutic pressure, an oral appliance or one of a number of patient interface devices.

Abstract: A liquid trap cup and a liquid trap assembly using the same are provided. The liquid trap cup comprises a hollow cup tube with a upper portion and a lower portion, a piston element with a top portion and a tail portion and a liquid discharge structure, in which the piston element is arranged airtight in the lower portion and is movable between a start point and an end point of the lower portion so as to control the opening and the closing of the liquid discharge structure. The liquid trap assembly includes the liquid trap cup and a multi-necked adapter tube with an expanded-plate structure, in which expanded-plate structure can be tightly sealed with the liquid trap. The liquid trap assembly is useful to a breathing system.

Abstract: The present invention relates generally to the field of ventilators, and, more specifically, to a ventilator system that addresses respiratory distress due to the onset of an epidemic or pandemic disease state. In particular, the present invention is a ventilator system that can be manufactured quickly with minimal skill requirements and employed rapidly in response to epidemic respiratory disease conditions.

Abstract: A tracheal tube apparatus includes a cannula having first and second ends. An inflatable cuff is formed on the cannula between the first and second ends. A conduit extends from the cuff for introducing an inflating fluid into the cuff when it is desired to inflate the cuff and removing inflating fluid from the cuff when it is desired to deflate the cuff. A gauge for indicating the inflation pressure of the cuff is coupled in the conduit.

Abstract: An adaptor for delivering an aerosolized active agent to a patient with concomitant positive pressure ventilation includes an aerosol flow channel having an aerosol inlet port and a patient interface port, and defining an aerosol flow path from the aerosol inlet port to and through the patient interface port; and a ventilation gas flow channel in fluid communication with the aerosol flow channel and having a gas inlet port and a gas outlet port, and defining a ventilation gas flow path from the gas inlet port to and through the gas outlet port, wherein the ventilation gas flow path is at least partially offset from the aerosol flow path and at least partially encircles the aerosol flow path. Systems and methods for delivering an aerosolized active agent to a patient with concomitant positive pressure ventilation incorporate the adaptor.

Abstract: In one aspect, a system for delivering nitric oxide to a patient can include a first gas source including nitrogen dioxide mixed in air or oxygen, a second gas source supplying compressed air, a ventilator coupled to the first and second gas sources, where the ventilator can be resistant to nitrogen dioxide, and where the ventilator provides a gas flow having a proper amount of nitrogen dioxide, one or more conversion devices operably coupled to the ventilator, where the conversion devices covert nitrogen dioxide into nitric oxide, and a patient interface operably coupled to the conversion devices, where the patient interface delivers nitric oxide to the patient.