Apparatus and methods are described for use with a portion of plant material that includes at least one active ingredient. A vaporizing unit includes a heating element configured to heat the plant material, and a sensor configured to detect an indication of airflow rate through the vaporizing unit. Control circuitry is configured to receive an indication of the airflow rate through the vaporizing unit, and, in response thereto, to determine a smoking profile that is desired by the user. The control circuitry drives the heating element to vaporize the active ingredient of the plant material by heating the plant material according to the determined smoking profile. The control circuitry dynamically updates the smoking profile in response to changes in airflow rate over the course of a smoking session. Other applications are also described.

A system and method for dermal spraying includes a portable, hand - held dermal application device with one or more disposable cartridges that spray a dermal formulation onto the skin, the disposable cartridge having a nozzle that can be activated by placing the cartridge into the spray device.

A system and method for dermal spraying includes a portable, hand - held dermal application device with one or more disposable cartridges that spray a dermal formulation onto the skin, the disposable cartridge having a nozzle that can be activated by placing the cartridge into the spray device.

A bubble machine designed to illicit a zen and calm environment for the user. The machine includes a square frame mirroring that of a picture frame with a hollow center. Positioned within the hollow center of the frame is an acrylic envelope which is a hollow unit that houses a closed loop. Water is also found within the acrylic envelope. The closed loop is positioned within the acrylic envelope at its outer edge. An air pump is connected to the closed loop suppling a stream of air. The steel loop has a plurality of holes allowing air to escape producing a bubble effect. In addition to the bubbles, a string of LED is positioned outside the acrylic envelope, sitting beneath the envelope, that changes color while in use adding to the calming effect.

Systems and methods for generating nitric oxide are disclosed. A nitric oxide (NO) generation system includes at least one pair of electrodes configured to generate a product gas containing NO from a flow of a reactant gas; and a controller configured to regulate the amount of nitric oxide in the product gas produced by the at least one pair of electrodes by utilizing duty cycle values of plasma pulses selected from a plurality of discrete duty cycles to produce a target rate of NO production based on an average of discrete production rates associated with each of the plurality of discrete duty cycles.

An insufflation apparatus and methods for using same are disclosed. The apparatus is equipped with an interactive system for administering reproducible intratracheal aerosols in a consistent automated manner. The insufflation system is useful, in particular for use with experimental animals, including mice and rats and also for treating small animals via the pulmonary route in veterinary medicinal practice.

Methods and apparatus infer or indicate sleep stage(s) of a patient from a respiratory flow rate signal of the patient. The method may include applying a plurality of detection pathways to a signal representing a respiratory flow rate of the patient, wherein each detection pathway is configured to generate start events and end events indicating start times and end times of episodes respectively of a corresponding sleep stage, wherein each start event and each end event has a priority; and combining the start events and end events based on their priorities to produce an indication of the sleep stage of the patient. The apparatus may include a sensor configured to generate a signal representing a property of a flow of air within a patient interface; and a processor configured to implement a method of inferring a sleep stage of the patient from the signal.

A patient support apparatus comprises a support structure, an articulation system, and a headboard assembly. The support structure comprises a head end, a foot end, a base, and a patient support deck to support a patient between the head end and the foot end. The patient support deck comprises a first section and a second section capable of articulating relative to the first section. The articulation system articulates the second section relative to the first section. The headboard assembly is coupled to the second section to be arranged adjacent to a head of the patient lying on the patient support deck. At least a portion of the headboard assembly articulates with the second section when the second section articulates relative to the first section. The headboard assembly comprises one or more environment controls operable to alter an environment of the patient on the patient support deck.

A negative pressure wound therapy system can include a reduced pressure wound therapy device and a wound therapy monitoring device configured to emit an indication when it detects that at least one parameter associated with the provision of negative pressure wound therapy is outside an operational range. The wound therapy monitoring device can operate in a low power mode in which the at least one parameter is periodically monitored. The reduced pressure wound therapy device can be configured to detect the indication and selectively generate an alarm. In some cases, the wound therapy monitoring device can be disposed in a wound or in a fluidic connector connecting the reduced pressure wound therapy device to the wound.

In one embodiment, there is provided an inlet for a humidification chamber for use in a medical humidification system, the inlet comprising an inlet end configured to receive gases flow from a gases source, an outlet end configured to introduce the gases flow to the inside of the humidification chamber, and at least one wall defining, at least in part, a passageway between the inlet end and the outlet end for conveying gases therebetween. The outlet end of the inlet is configured to terminate in the humidification chamber or at a wall of the humidification chamber, and the passageway is configured to guide the gases flow such that the center of the gases flow at the inlet end and at the outlet end are substantially aligned along a common axis or the outlet end defines a profile of the passageway thereat that has a width and a height, a ratio of the width to height being between about 1:20 and 1:5.