Abstract: A myofascial tissue release apparatus includes a base portion. At least two side supports are connected to the base portion and positioned substantially opposite to each other, each of the at least two side supports having a terminating upper surface. At least one fully closed cutout portion is formed in an upper part of each of the at least two side supports in a position below the terminating upper surface. At least one substantially cylindrical bar is removably positioned extending between the at least one fully closed cutout portion of each of the at least two side supports, wherein the at least one substantially cylindrical bar is contactable by a user for use with myofascial tissue release of the user. The apparatus can be used to practice various myofascial tissue release techniques.

Abstract: The present disclosure is a handheld apparatus that vaporizes plant-based or synthetic compounds, for the purpose of inhalation, or diffusion into an external environment. More specifically, the disclosure describes a handheld apparatus wherein a laser beam from an internal laser unit heats compounds, such as dried plant, tinctures, resins, or essential oils, to the compound's vaporization temperature for inhalation, or diffusion as part of aromatherapy or other holistic therapeutic treatments.

Abstract: A patient interface, such as a nasal cannula is described. The patient interface has a body portion to be located, in-use upon a face of a user. The body portion has at least one side arm that extends laterally from a central bridge portion to be located about a user's septum region, where each side arm is connected to a resilient, or relatively more rigid, bridge portion element. The interface has at least one, and preferably a pair of, nasal prong(s). The body portion has at least one fluid passageway connected to the nasal prong(s) for supply of a gas to the nare(s) of the user's nose. A cross section of the passageway varies along the length of the body portion to regions of varying flexibility along the body portion. The bridge portion element defines a substantially predetermined spatial relationship for outlet(s) of a gas delivery system supplying gas via each side arm to the outlet(s) from which, for example, the nasal prong(s) may be provided in fluid connection.

Abstract: A steam heating mask having a mask body portion covering a nose and a mouth of a wearer when wearing the mask, a pair of ear hook portions provided at both left and right ends of the mask body portion, and a steam generator on the mask body portion, in which a proportion of an area occupied by the steam generator ranges from 30% to 80% with respect to an area of an entire surface of the mask body portion on a side of the wearer. The steam generator includes a first sheet on a surface of a steam generating portion on the side of the wearer with degree of air permeability being equal to or less than 7,000 sec/100 ml and a second sheet on a surface opposite to the surface of the steam generating portion with a degree of air permeability being greater than 8,000 sec/100 ml.

Abstract: A driving and information transmitting system for an air-filtering protection device includes a filtering mask, an actuating and sensing device mounted on the filtering mask, a power supply device and a connection device. The actuating and sensing device includes at least one sensor, at least one actuating device, a microprocessor, a power controller and a data transceiver. The actuating device is enabled to transfer air to flow toward the sensor. The power supply device transfers an energy to the power controller for enabling the sensor and the actuating device. After monitored information is generated by the sensor and processed into an output data by the microprocessor, the data transceiver receives and transmits the output data to the connection device. After a control command is given by the connection device, the data transceiver receives and transmits the control command to the microprocessor to control the sensor and enable the actuating device.

Abstract: An air-filtering protection device includes a filtering mask and an actuating and sensing device. The filtering mask is for being worn to filter air. The actuating and sensing device is mounted and positioned on the filtering mask and includes at least one sensor, at least one actuating device, a microprocessor, a power controller and a data transceiver. The at least one actuating device is disposed on one side of the at least one sensor and includes at least one guiding channel. The actuating device is enabled to transport air to flow toward the sensor through the guiding channel so as to make the air sensed by the sensor.

Abstract: A mask apparatus for a respiratory treatment can permit delivery of breathable gas to a user. In one example, the mask may employ a frame and cushion to form a seal for both mouth and nose. The frame may be adapted for coupling with a respiratory treatment apparatus so as to permit communication of a pressurized gas from the respiratory treatment apparatus. The cushion, which may be foam, may have a substantially under the nose configuration or over the nose configuration. The mask may have a common plenum chamber for both nose and mouth. The cushion may further define a centrally open lip superior region. The cushion may be adapted to couple with the frame directly or to the frame in conjunction with a cushion support clip. Various features of the cushion may further promote sealing and comfort for the under the nose design.

Abstract: Massage mechanisms of a massage machine individually include a pair of left and right treatment members provided along a height direction of the massage machine. A first massage mechanism is disposed on a relatively upper side, and a second massage mechanism is disposed on a relatively lower side. A control means that controls operations of the first and second massage mechanisms. The control means controls advancing/retreating drive portions such that the treatment members of the first massage mechanism and the treatment members of the second massage mechanism advance or retreat at speeds different from each other such as with a time lag.

Abstract: A nasal pillow system for treating sleep apnea is disclosed that may include a nasal pillow. The pillow has a cavity wall that defines a cavity, and two nasal interface structures connected to and extending away from the cavity wall. The nasal interface structures are in fluid communication with the cavity. Each nasal interface structure includes a conical nasal interface, a cylindrical trunk structure connected to conical nasal interface, and an annular relief pocket connected to the cylindrical trunk structure and to the cavity wall. The connection between the annular relief pocket and the cavity wall defines substantially a plane, and a first portion of the annular relief pocket extends away from the plane while a second portion extends towards the plane.

Abstract: A powered air-purifying respirator (PAPR). The PAPR comprises an air pump comprising an electric motor, an eccentric venturi communicatively coupled to an air channel of the air pump, wherein the eccentric venturi comprises a first sensor port and a second sensor port, a differential air pressure sensor mechanically coupled to the first sensor port and the second sensor port, and a controller that is communicatively coupled to an electrical output of the differential air pressure sensor and to the electric motor, wherein the controller is configured to control the speed of the electric motor to maintain a predefined rate of flow of purified air based on the electrical output of the differential air pressure sensor.

Abstract: A method for the management of secretions in an intubated patient by means of an endotracheal tube to which an inflatable cuff is externally associated, includes the steps of inflating the inflatable cuff for isolating the broncho-pulmonary zone of the patient from the external environment, generating a succession of overpressures inside the endotracheal tube in order to induce breathing in the patient, and a step of deflating the inflatable cuff during the generation of one of the overpressures in order to permit a drainage of the secretions generated by the patient along the trachea towards the outside.

Abstract: A system selectively delivers either breath-synchronized, flow-targeted ventilation (BSFTV) or closed-system positive pressure ventilation (CSPPV) to augment respiration of a patient with a standard tracheal tube. A removable adaptor has a cap that can be removably attached to the proximal connector of the tracheal tube in BSFTV mode, and an inner cannula that extends within the tracheal tube to effectively divide it into two lumens. The adaptor includes a ventilator connector for removably engaging a ventilator hose to deliver air/oxygen through the adaptor and one lumen of the tracheal tube with a flow rate varying over each respiratory cycle in a predetermined waveform synchronized with the patient's respiratory cycle to augment the patient's spontaneous respiration. The adaptor also includes a port allowing the spontaneously-breathing patient to freely inhale and exhale in open exchange with the atmosphere through the other lumen.

Abstract: A near-patient humidification system provides vapor to a respiratory breathing circuit. The system includes an expiratory gas conduit and an inspiratory gas conduit. A patient coupling member is provided for coupling the expiratory and inspiratory gas conduits to a patient interface. A vapor injection unit is located at least partially within the housing of the patient coupling member. The vapor injection unit heats a supply of fluid into vapor and injects the vapor into the inspiratory gas passage of the patient coupling member at a vapor injection location for providing moisture to the inspiratory gas flow. A method of simultaneously and independently controlling the temperature and humidity of inspiratory gas in a respiratory breathing circuit is performed by injecting vapor having a temperature determined as a function of measured temperatures and measured humidities of the breathing gas at different locations along the breathing circuit.

Abstract: A medical ventilator (100, 200) including a first user interface (114) having a touch-sensitive display having a display area; and at least one controller (104) which determines whether a second user interface (122, 222) having a touch-sensitive display is coupled to the medical ventilator, enables the first user interface when it is determined that the second user interface is not coupled to the medical ventilator, and enables the second user interface when it is determined that the second user interface is coupled to the medical ventilator.

Abstract: A healthy gas generating system for generating healthy gas for inhalation by a user includes an electrolysis device, a gas mixing device, and a backfire barrier. The electrolysis device electrolyzes water to generate a gas with hydrogen. The gas mixing device includes a mixer and a vibrator for mixing the combination gas with an atomized gas to produce the healthy gas. The backfire barrier is configured on the output of the gas mixing device or the gas passage of receiving the combination gas to avoid the backflow of the gas.

Abstract: A powered air-purifying respirator (PAPR). The PAPR comprises an air pump comprising an electric motor, an eccentric venturi communicatively coupled to an air channel of the air pump, wherein the eccentric venturi comprises a first sensor port and a second sensor port, a differential air pressure sensor mechanically coupled to the first sensor port and the second sensor port, and a controller that is communicatively coupled to an electrical output of the differential air pressure sensor and to the electric motor, wherein the controller is configured to control the speed of the electric motor to maintain a predefined rate of flow of purified air based on the electrical output of the differential air pressure sensor.

Abstract: The electronically regulated temperature compression device is a brace that applies pressure to an appendage. The electronically regulated temperature compression device applies heat therapy and cooling therapy to the appendage. The temperature of the selected therapy is electronically regulated and controlled. The electronically regulated temperature compression device uses a refrigerant-based heat exchange mechanism during the therapy process. The electronically regulated temperature compression device comprises a composite textile, plurality of fasteners, and a controller. The plurality of fasteners attaches the composite textile to the appendage of the patient. The plurality of fasteners controls the pressure applied by the composite textile to the appendage. The composite textile is a temperature controlled textile used to generate a heat exchange between the electronically regulated temperature compression device and the appendage.

Abstract: A compliance monitoring module for an inhaler comprising: a miniature pressure sensor, a sensor port of said sensor being configured to be pneumatically coupled to a flow channel of said inhaler through which a user can inhale; a processor configured to: receive data from a sensing element of the pressure sensor; receive data from a mode sensor configured to detect when the inhaler changes from an inactive mode to an active mode; and based on said data from said pressure sensor sensing element and said data from said mode sensor, compile a compliance report; and a transmitter configured to issue said compliance report.

Abstract: A system (1) for ventilating patients includes a gas passage unit (2), which has a first inlet opening (6) with a fluid-communicating connection to a pressurized gas source (12, 13) and an outlet opening (9) connected to the first inlet opening (6) in a manner. A patient interface (3), for ventilation, includes an interface inlet opening (10). A gas line element (4) has a fluid-communicating connection to the outlet opening (9) and to the interface inlet opening (10). A controllable pressure change element (5) is provided between the first inlet opening (6) and the interface inlet opening (10). A second inlet opening (8) has a fluid-communicating connection to the gas line element (4). A control unit (7) controls the controllable pressure change element (5). A device or a system (1), which provides fully adequate ventilation with high performance with minimal expenditure for hardware, is provided.

Abstract: A device for generating a condensation aerosol includes (a) vaporization chamber having an upstream first inlet and a downstream outlet; (b) a heater element in the vaporization chamber between the upstream first inlet and the downstream outlet; (c) an airflow path in fluid communication with the vaporization chamber, wherein the airflow path comprises a second inlet configured to permit a substantially laminar flow of air into the airflow path, wherein the second inlet is downstream of the heater element; and (d) the device having components or apparatus on or in the device for changing air flow in the vaporization chamber. Changing the air flow in the vaporization chamber may be used to change the particle size of a condensation aerosol produced in the vaporization chamber, and/or to change the amount of visible vapor emitted from the device.