Described are nasal cannulas that improve the precision of the delivered dose for nitric oxide therapy by reducing the dilution of nitric oxide. The nasal cannulas may reduce the total volume and potential for retrograde flow during nitric oxide therapy through the design of the specific dimensions of the flow path and/or having check valves in the nitric oxide delivery line and/or having a flapper or umbrella valve dedicated to nitric oxide delivery. The nasal cannulas may also use materials that limit oxygen diffusion through the cannula walls. The nosepiece for these cannulas may be manufactured by a molding technique.

A ventilation gas cooling apparatus is configured in a modular form adapted for selective removable engagement to a ventilator. The apparatus includes a gas inlet port, a gas delivery port, a pressure sensing port, and a thermoelectric cooler. The inlet port is fluidly connectible to a source of therapeutic breathing gas at an external end and is fluidly connectible to an inlet of the ventilator at an internal end. The delivery port is fluidly connectible to a patient circuit at an external end and is fluidly connectable to an outlet of the ventilator at an internal end. The pressure sensing port is fluidly connectible to both a pressure sensing port of the ventilator and to the patient circuit. The apparatus may further include a cooling fluid system operative to circulate either a gas or liquid coolant along at least a portion of a multi-lumen tube integrated into the patient circuit.

A system for measuring the vital parameters of low care patients is described. The system includes a connecting element for a nasal cannula or breathing mask for providing a fluidic connection with the patient and a flow and/or pressure sensor in fluidic connection with the nasal cannula or breathing mask, for sensing, when the nasal cannula or breathing mask is connected to the system, at least a negative pressure signal. The system also includes a processor configured for deriving, directly based on said at least a negative pressure signal, information related to the breathing cycle, and an output means configured for outputting at least one vital parameter of the patient, the outputting comprising outputting information related to the breathing cycle.

A nasal airway passage device that keeps a nasal airway passage open when inserted into both nostrils. The device includes a hollow body having two hollow legs and a transverse segment that has a central opening. A malleable wire is embedded within a wall of the body, that is, embedded in a wall of each of the legs and embedded a wall of the transverse segment. The wire helps to retain the legs in either a straight orientation or a curved orientation. A band may be provided that encircles the legs initially and moves to encircle the transverse segment upon insertion of the legs into the nostrils.

Often when vaporizing herbs like marijuana, the pot gets singed or burned creating smoke; inhaling smoke is unhealthy. An improved vaporizer mode & apparatus allowing a non-burning gas, such as carbon dioxide or nitrogen from small readily-available cartridges, to pass over the heated pot to inhale the herb's vapor instead of air to avoid the risk of the herb being singed or burned which makes smoke amidst the chemical vapor. Without air's oxygen, burning and smoke are just not possible no matter how dry the pot is or how hot the pot gets.

Furthermore, finally, apparatus to facilitate taking a French inhale from an herb vaporizer has been invented! French inhaling is cool, the tobacco or other herb “tastes” and feels more enjoyable (most “flavor” is in the nose) and French inhaling prevents herbal-vapor from “fouling” the user's mouth.

Vapor carried by a non-burning gas may be French inhaled.

A respiratory flow therapy apparatus including a sensing chamber which measures a flow of gases provided to a patient. The sensing chamber can be located after a blower and/or mixer. The sensing chamber can include an ultrasonic transducer, a temperature sensor, a heated temperature sensing element, and/or a gas concentration sensor. A flow path of gases used in conjunction with the sensor system prevents unwanted vorticity in the flow of gases that can create anomalies in measuring flow.

A respiratory information acquisition device used for a PSA type oxygen concentration device that switches and uses multiple adsorption cylinders includes a respiratory information acquisition means of measuring a first pressure of a periodic pressure fluctuation in an oxygen supply path when oxygen is supplied to a patient from the PSA type oxygen concentration device and a second pressure of a periodic pressure fluctuation in the oxygen supply path when oxygen is not supplied to the patient from the PSA type oxygen concentration device, a phase confirmation means of matching phases of the first pressure and the second pressure, and a subtraction processing means of calculating a difference between the first pressure and the second pressure in the condition where the phases are matched.

A nasal cannula includes a distribution conduit running along a virtual distribution path. The distribution path defines a longitudinal direction and has two branch openings. A respective supply conduit branches off from each branch opening. The distribution conduit also has two coupling openings arranged spaced apart from the branch openings. The nasal cannula has a plug via which one of the two coupling openings can be sealed as a closure opening. Another of the two coupling openings is designed as a supply opening. The plug has a flow-directing configuration with an exposed flow-directing surface. In a reference state in which the plug is closing the closure opening, the flow-directing surface is arranged in the distribution conduit in the longitudinal extension region of at least one branch opening and positioned relative to the distribution path to deflect treatment gas flowing in the distribution conduit from the supply opening along the distribution path towards at least one of the branch openings.

Aspects of the present technology comprise a positioning and stabilising structure to hold a seal-forming structure in a therapeutically effective position on a head of a patient. The seal-forming structure may be constructed and arranged to form a seal with a region of the patients face surrounding an entrance to the patients airways for sealed delivery of a flow of air at a therapeutic pressure of at least 4 cmH2O with respect to ambient air pressure throughout the patients respiratory cycle in use. The positioning and stabilising structure may comprise a front hoop arranged to contact, in use, at least a region of the patients head superior to an otobasion superior of the patients head and a rear strap. The positioning and stabilising structure may comprise an adjustment mechanism for adjustment of the front hoop and the rear strap relative to the patients head, the adjustment mechanism being arranged in a single operation to adjust both the front hoop and rear strap to enable the positioning and stabilising structure to fit different size heads.

This disclosure relates to a nasal cannula without nostril prongs. The nasal cannula may be used together with an oxygen delivery system, such as a portable oxygen concentrator, or another type of breathing device such as a continuous positive airway pressure (CPAP) machine. In an example, a nasal cannula includes a tube configured to connect to an oxygen supply, and further includes a fitting configured to connect to the tube. The fitting includes at least one discharge port and does not include nostril prongs.