Abstract: A patient interface for delivering breathable gas to a patient includes a nasal prong assembly including a pair of nasal prongs structured to sealingly communicate with nasal passages of a patient's nose in use and headgear to maintain the nasal prong assembly in a desired position on the patient's face. The headgear includes side straps and rigidizers provided to respective side straps. Each rigidizer includes a first end portion that provides a connector structured to engage a respective end of the nasal prong assembly and an inwardly curved protrusion in the form of a cheek support that curves inwardly of the connector. The cheek support is adapted to follow the contour of the patient's cheek and guide a respective end portion of the side strap into engagement with the patient's cheek to provide a stable cheek support.

Abstract: Disclosed is a suction device. The suction device includes a sensor unit which measures a breathing condition of a patient, a tube unit which is inserted into a bronchus of the patient in order to suck foreign material generated in the bronchus of the patient, when the values measured by the sensor unit exceeds a predetermined reference value, and a control unit which controls to drive the tube unit based on the measured value received from the sensor unit. According to the present invention, there is provided the suction device which is automatically operated by directly determining whether foreign material is generated in the bronchus of the patient.

Abstract: Ventilator associated pneumonia (VAP) may be prevented in a patient, or its occurrence reduced in a population of patients, by using an anti-VAP device or an anti-VAP material such as an anti-VAP mouthpiece that absorbs secretions. By reducing the problem of bacterial-containing secretions that otherwise build up in the airway of, and elsewhere in, the intubated patient, VAP can be prevented from occurring in intubated patients, such as patients intubated with an endotracheal tube (ETT) or a nasogastric tube. Anti-VAP mouthpieces also are useable in non-intubated patients to maintain oral hygiene.

Abstract: Devices and methods are provided to conduct fluid away from or deliver fluid to an area of a treatment site of a patient's body. In one example, a catheter includes a fluid exchange portion and a member attached to the fluid exchange portion for biasing fluid flow at the treatment site.

Abstract: An inner type tracheostomy tube has an outer tube and an inner cannula. The outer tube has an airway tube, an inflatable cuff and an inflating tube. The inner cannula is connected to the outer tube and has an inner tube, a disk segment, a connecting mount and a connector. The connecting mount is soft and bendable, is securely mounted around the disk segment and has a bottom end, a top end and a flange coat. The bottom end is securely mounted around the disk segment and has an inner surface and an air gap formed between the inner surface of the bottom end of the connecting mount and the disk segment. The connector is securely mounted around the top end of the connecting mount and has a bottom end and a flange formed around the bottom end of the connector and enclosed by the flange coat.

Abstract: Constrained fluid delivery devices are described that deliver fluid to an anatomical region of a mammal in a controlled release manner where the device comprises an elongate body defining a lumen throughout a portion thereof, a distal end interiorly positionable adjacent the anatomical region of the mammal and a proximal end in communication with an exterior of the mammal. The device also includes a delivery member and one or more withdrawal members. Also provided herein are methods and kits incorporating the fluid delivery device.

Abstract: Devices for intranasally delivering therapeutic gases to a patient. The devices may include a measurement chamber, a combination pressure regulators and a sequencing mechanism that controls valves associated with the pressure regulators. When implemented in a hand-held dispenser, the hand-held dispenser may reliably deliver consistent doses of gas regardless of the unknown state and pressure of the therapeutic gas in the measurement chamber.

Abstract: Tracheal tube systems may include first and second tubes and an inflatable balloon. The first tube may be flexible and hollow and have first and second open ends. The inflatable balloon may be affixed to and circumferentially surround a portion of the first tube. The inflatable balloon may include an indentation sized and positioned to accommodate a portion of a second tube positioned therein, when the inflatable balloon is inflated. The second tube may be hollow and have a multiplicity of holes along a sidewall not in contact with the balloon. The second tube may be configured to be coupled to a suction device that creates a negative pressure in the second tube. When the tracheal tube system is inserted in a patient's trachea, the negative pressure in the second tube may act to remove, or suction out, fluids and other matter from the trachea.

Abstract: A double counterlung for the breathing circuit of a diver has regulators (41, 51) for automatic addition and venting of breathing gas. Also disclosed is a weighted hinged plate (3) for a double counterlung, to reduce breathing effort when the diver is horizontal. Other improvements to the breathing circuit are described including use of a two stage compressor (151, 155), and single actuator valves for back-up circuits.

Abstract: The present disclosure relates to a method for entraining in an airflow a medicament powder contained in a cavity having a cavity opening. Large airflow vortices are provided, for instance, by use of an obstacle in a flow passage, The airflow with large vortices is arranged to by-pass the cavity opening, thereby generating an eddy in the cavity which contributes to entraining the powder in said airflow. The present disclosure also relates to a medical dispenser, for instance an inhaler, in which the method may be performed.

Abstract: Devices and methods are provided to conduct fluid away from or deliver fluid to an area of a treatment site of a patient's body. In one aspect of the invention, a catheter includes a terminal end with a fluid exchange portion. The terminal end may further include a diffuser. The terminal end may further include a barrier.

Abstract: A system for transferring solutions from a first cartridge into a second cartridge comprises a cartridge holder, a plunger driver, and a cartridge connector. The cartridge connector carries a transfer needle and an exhaust needle. The cartridge holder positions the first cartridge against the cartridge connector so that the transfer needle penetrates the first cartridge septum. The second cartridge is removably inserted into another end of the cartridge connector so that both the transfer needle and the exhaust needle penetrate the second cartridge septum. The plunger driver is disposed to advance a plunger on the first cartridge to transfer solution from the first cartridge into the second cartridge thus displacing solution from the second cartridge through the exhaust needle. The cartridge connector includes a sealed interior waste chamber for receiving the solution from the second cartridge.

Abstract: A method of operating a ventilator or pressure support system that automatically determines a timed back up rate for the patient based on the patient's spontaneous breathing patterns. The aggressiveness of the determined rate increases as the patient takes less spontaneous breaths. Also, a method wherein one or more mechanisms are used to determine whether a machine breath should be issued. Each mechanism consists of a basic timing element coupled with one or more logical permits. Both the timing element and each of the one or more logical permits must be satisfied to allow the timing mechanism to trigger a machine breath.

Abstract: The function of a respiration system, with a patient port (1) with connected inspiration branch (3) and expiration branch, is checked. A rebreathing line (9) connects the inspiration branch to the expiration branch. A reservoir (25) is connected to a reservoir port (27) in the rebreathing line. An actuatable control valve (29) is provided in the rebreathing line between the expiration branch and the reservoir port. A pressure sensor (33) is connected to the rebreathing line. A control unit (39) is connected to the control valve and to pressure sensor. The process includes closing the control valve for a preset inspiration time and opening it for a preset expiration time. The value sent by the pressure sensor is detected with the control valve opened during the expiration time and compared with a preset first threshold valve. An error message is generated when the value sent exceeds the first threshold value.

Abstract: A system for reducing airway obstructions of a patient may include a ventilator, a control unit, a gas delivery circuit with a proximal end in fluid communication with the ventilator and a distal end in fluid communication with a nasal interface, and a nasal interface. The nasal interface may include at least one jet nozzle, and at least one spontaneous respiration sensor in communication with the control unit for detecting a respiration effort pattern and a need for supporting airway patency. The system may be open to ambient. The control unit may determine more than one gas output velocities. The more than one gas output velocities may be synchronized with different parts of a spontaneous breath effort cycle, and a gas output velocity may be determined by a need for supporting airway patency.

Abstract: An arrangement and method for guiding expired gas flow in a breathing circuit through a housing assembly for removing an undesired gas component is disclosed herein, The housing assembly includes a first port and a second port, one of the ports receiving the flow and another discharging the flow. The arrangement includes a gas routing device in flow communication with the breathing circuit and the housing assembly. The routing device is provided with at least two different route options. According to a first option the gas is guided to the first port and through the housing assembly to the second port and to the gas routing device for guiding for the inspiration. According to a second option the gas is guided to the second port and through the housing assembly to the first port and to the gas routing device for guiding for the inspiration.

Abstract: A first source of medical gas has a generally cylindrical male outlet with a cylindrical bore and a threaded outer cylindrical surface. A flexible cylindrical elastomeric medical gas tubing has an input end with a bushing making a flush abutment with the male outlet at the output orifice. An output end attaches to any of a plurality of medical gas utilizing devices, but preferably with a dampening disperser held in position in the space in the vicinity of a patient's nose and mouth. An annular flange of the input end bushing resides within a central cylindrical bored out region extending through the first end and nearly to the second end of a rotatable connector forming an interior surface of a connector with threads coupling with the threads of the male outlet. The second end is an annular abutment against the annular flange holding the input end tubing bushing against the outlet source and providing an airtight coupling. A gripping means is on the exterior surface of the connector.

Abstract: A fan unit which in use forms part of a gases supply unit, the gases supply unit suitable for use as part of a system for providing heated humidified gases to a user, the fan unit having a casing that has an inlet aperture and an outlet passage, the outlet passage including an exit aperture, the fan unit also including a fan which is located inside the casing and which is adapted for connection to a motor to drive rotation of the fan in use, the fan drawing gases into the casing via the inlet aperture, and forcing these gases out of the casing via the outlet passage as a gases stream, the outlet passage further including at least one bypass vent hole independent of the exit aperture and arranged at an angle to the path of the gases stream through the outlet passage.

Abstract: A sensor support arm, adapted for use with a breathing mask such that the arm is extendable underneath a sealing surface of a breathing mask is disclosed. The arm is adaptable at one end for fixing on to equipment worn by a user, having a sensor disposed at an opposing end positionable in the interior of a breathing mask. The arm has lead connections necessary for the sensor extending along the arm. The arm has a greater width than thickness and comprises a flexible material such that it is flexible about both longitudinal and transverse axes. The arm is provided with a substantially planar side. A breathing mask having a freely self-supporting sensor arm is also disclosed.

Abstract: An information display and control device of an air purifying respirator comprises: a blower motor; a pulse width modulation drive unit controlling rotation of the blower motor; a temperature sensor; an air flow sensor; an oxygen sensor; a voltage detection unit for a battery; a differential pressure sensor detecting a differential pressure value of a filter; a switch input unit for a user to input predetermined temperature, air flow, and oxygen amount and operation commands; a controller executing a diagnostic mode, calibrating the oxygen sensor, calculating a detected value of the voltage detection unit to determine whether the voltage is low, comparing the detected value of the differential pressure sensor with a reference to determine whether the filter is absent or clogged, and comparing the detected value of the oxygen sensor with a reference to determine whether oxygen is insufficient or excessive; and an alarm output unit outputting an alarm.