System and methods for providing respiratory therapy include predetermined and/or automatically determined perturbations of levels of pressure, flow, and/or other gas parameters integrated and/or combined (Start with a supplied pressurized flow of breathable gas for a subject. The perturbations are intended to improve secretion management through intra-pulmonary percussive ventilation integrated with ventilation therapy.

Devices disclosed herein relate to humidification systems for making humidified ventilator air. The humidification system provides an elongated air path that increases both the surface area and time for air-water interaction, and thus increases efficiency of humidification. The humidification system also enables even distribution of heat and inhibition of bacterial growth within the system, thus improves comfort and safety for patients receiving respiratory therapy. Device disclosed herein also relates to tubing for delivering humidified ventilator air. The tubing includes an air passage and a heat blanket that envelops and warms up the air passage. The tubing thus prevents or decreases water condensation and loss of humidity of humidified air.

A compact wearable inhaler, vaporizer and/or atomizer is addressed by the wearable multifunctional inhaler, vaporizer and smartwatch of the present invention. In the best mode, the invention includes a housing with a chamber having at least port; a lid adapted to engage the housing and open the chamber in a first position and close the chamber in a second position; a source of inhalant mounted within the housing for sourcing inhalant into the chamber via the ports; and an mechanism coupled to the housing for wearing the device. The source of inhalant may be a vaporizer, pipe, inhaler or atomizer.

A medical tube comprises a tail to connect an embedded wire to an electrical component. The tail may comprise a flattened portion and an exposed portion to facilitate attachment of the medical tube to an electrical component. The tail may comprise a second flattened portion. One or more wires, such as a heater wire or a sensor wire, may be embedded in the medical tube. The medical tube may comprise a connector that comprises a printed circuit board to which the one or more wires is attached. The connector may comprise features to support the printed circuit board, aid in assembly of the one or more wires to the connector, and protect electrical components against liquid ingress.

A humidifier and humidity sensor is disclosed for use with a breathing assistance apparatus. The humidity sensor preferably includes means to sense absolute humidity, relative humidity and/or temperature at both the patient end and humidifier end. The humidifier may also include provision to both control independently the humidity and temperature of the gases. Further, a chamber manifold is disclosed to facilitate easy connection of the humidifier to various outlets, inlets and sensors. A heated conduit is described which provides a more effective temperature profile along its length.

The gases temperature supplied to a patient when the patient is undergoing treatment such as oxygen therapy or positive pressure treatment for conditions such as Obstructive Sleep Apnea (OSA) or Chronic Obstructive Pulmonary Disease (COPD) is often measured for safety and to enable controlling of the humidity delivered to the patient. The invention disclosed is related to measurement of properties, particularly temperature (thermister 23), of gases flowing through a heated tube (3), supplying gases to a patient, which utilises the heating wire (21, 28) within the tube.

A method of estimating respiratory demand of a patient being administered flow therapy comprising: administering a gas flow rate to the patient through both nostrils using a flow therapy apparatus with a patient interface for each nostril, measuring a parameter associated with that nostril, the parameter being one or more of: respiratory demand of that nostril, indicative of respiratory demand of that nostril, or a parameter from which respiratory demand of that nostril can be derived, determining respiratory demand (or parameter indicative of respiratory demand) for the patient from the nostril parameter for each nostril.

A pressurized flow of breathable gas is delivered to the airway of a subject in accordance with a therapy regimen. One or more fluid parameters of the pressurized flow of breathable gas are adjusted based on the therapy regimen. The therapy regimen dictates that such adjustments be made based on the respiratory state of the subject. Transitions in respiratory state are identified without relying on measurement or estimation of flow at or near the airway of subject. Transitions in respiratory state are identified based on changes in the first time derivative of flow at or near the airway of the subject. In one embodiment, an effort parameter is determined that approximates the second time derivative of flow. Based on comparisons of the effort parameter to a dynamic threshold, transitions in respiratory state are identified.

Hyperbaric chamber control system and apparatus and related methods. A system for controlling, measuring, and reporting hyperbaric chamber sessions using the partial pressure of oxygen as the lead variable. Air is gently flushed from the bottom of the chamber, upwards, and a nostril-level oxygen pickup measures oxygen concentration in the chamber. Chamber pressure and oxygen concentration values are used to calculate the partial pressure of oxygen, and the session time is adjusted so that a subject treatment accurately reflects prescribed treatment.

Introduced are methods and systems for: gathering human biological signals, such as heart rate, respiration rate, or temperature; analyzing the gathered human biological signals; and controlling a vibrating pillow strip based on the analysis.