Abstract: A respirable gas mixture sensor module (10) includes a first sensor (1, 14-1, 14-2) for measuring a gas and a second sensor (18, 18-1, 18-2) for measuring the same gas and apply different principles of measurement. The sensor module (10) is configured to determine a measurement result for the gas taking into account the measurements. As an alternative the sensor module (10) includes a first sensor group (12) including a first sensor (14, 14-1, 14-2) and a second sensor group (16) including a second sensor (18, 18-1, 18-2), each for measuring both a first and a second gas and apply different principles of measurement. The sensor module is configured to determine measurement results for the gases, taking into account the respective measurements of the first and second sensors. A ventilator, a therapy device and a method for measuring a plurality of gases of a respirable gas mixture are also provided.

Abstract: A suction assembly is described. The suction assembly includes a therapy unit with a body that can apply a supplemental therapy to a skin surface. The suction assembly also includes a cup that can be removably connected to the therapy unit and that can interface with a skin surface to define a chamber within the cup. A pump of the therapy unit can reduce a pressure within the chamber to draw the skin surface into the chamber in a cupping therapy. In response to the skin surface being drawn into the chamber, the body can move in a longitudinal direction to maintain contact with the skin surface. A wall of the cup is translucent and the suction assembly is dimensioned to provide a user with a view into the chamber through the wall of the cup that is substantially unobstructed by the housing.

Abstract: A mask for the delivery of a medical gas under positive pressure. The engagement surface is generally circular in shape and is sufficiently rigid that operatively, when a suitable retention force is applied to the mask, an effective seal is produced at the interface of the engagement surface and the surrounding tissue primarily by deformation of the surrounding tissue.

Abstract: The invention relates to a respiratory mask (1) having a mask unit (2) and having an emission device (3) for discharging exhaled gas from the respiratory mask (1). The mask unit (2) comprises a mask body (4) and a connection unit (5) which can be connected to the mask body (4) for connection of a respiratory gas feed line (101). The emission device (3) comprises a plurality of flow channels (6), which are arranged in at least one part of the mask unit (2). Here the emission device (3) comprises at least one flow channel.

Abstract: Provided herein are devices, systems, and methods for providing respiratory therapy to a patient using a nasal cannula comprising a cannula body, first and second inlet tubes, and a nasal prong for the delivery of a flow of breathing gas to the patient. Configured with the cannula is a nebulizer having an aerosol generator positioned to emit aerosolized medicament along a longitudinal axis of the nasal prong. A flow director is configured to direct the flow of breathing gas into the nasal prong such that the breathing gas flows along the longitudinal axis, such that the flow of aerosolized medicament is contained within the flow of breathing gas as it moves along the longitudinal axis of the nasal prong for delivery to the patient.

Abstract: According to the disclosure there is provided an apparatus that assesses chest recoil of a subject during cardio pulmonary resuscitation (CPR) carried out by a rescuer on the subject and provides feedback to the rescuer. This apparatus may include a bio-signal measurement system configured to measure bio-signals of the subject. The apparatus may identify when CPR is required and may provide a CPR start signal to indicate when CPR should be started and this apparatus may identify when CPR is to be ceased. A CPR stop signal may be provided to a rescuer to indicate when CPR should be stopped. The apparatus may include electronic circuits capable of measuring impedance signals of the subject, may include sensors that sense bio-signals, and may include defibrillator shock electronics capable of providing a shock to the subject to restart or reset the heart of the subject.

Abstract: A sex toy with universal connecting structure may include an outer cup body, a sperm collection cup sleeve, an inner cup body, a guide part, a power part, an eccentric wheel transmission assembly and an electric control part, wherein the inner cup body is slidably connected the inside of outer cup body through the guide part, the sperm collection cup sleeve is positioned between the outer cup body and the inner cup body, the cup mouth of the sperm collection cup sleeve is hermetically connected with that of the outer cup body, and the outer cup bottom of the sperm collection cup sleeve is connected with the inner cup bottom of the inner cup body. Since the universal ball head piece matches the universal ball head hole, the inner cup body can rotate along the universal ball head hole while reciprocating along the guide part.

Abstract: A headgear assembly for retaining a respiratory mask on a user's face includes arrangements or components that allow for variation in a size of the headgear assembly. In some configurations, the headgear assembly includes one or more hubs, each of which are configured to connect a top and rear strap together. The size of the headgear assembly can be determined by the size or configuration of the hub. In other configurations, the headgear assembly comprises one or more spacer elements within one or more straps of the headgear. The size of the headgear assembly can be determined by the size of the spacer element or a relative position between the strap and the spacer element.

Abstract: A cushion for use in providing a regimen of respiratory therapy to a patient includes a base that defines a main cavity therein an aperture for receiving a flow of breathing gas. A pair of nasal pillows each extend from the base, each having a cone-shaped head that tapers inward and upward from a base portion, that extends directly from the base, to a top opening. Each head is formed to engage an inner portion of a nare of the patient. Each head defines a passage extending between the main cavity and the top opening for further conveying the flow of breathing gas from the main cavity to a nasal passage of the patient. Each base portion includes an inner edge positioned near the center of the cushion that merges with the hollow base and an opposite outer edge spaced upward from an outer surface of the hollow base.

Abstract: A headgear portion or assembly for use in combination with a breathing apparatus in some configurations is at least substantially inelastic and is three dimensional in shape. The headgear portion or assembly can comprise a plastic core and a textile casing. The headgear, or part thereof, may also have integrally moulded labels, connectors, adjustment mechanisms and/or grips.

Abstract: Some embodiments of the invention relate to a system for delivering to a subject at least one pre-determined amount of THC, the system comprising: a memory which stores a scheduled regimen for delivery of THC to the subject, the scheduled regimen defining: a maximal amount of THC to be delivered, the amount being 0.75 mg THC or less, and a time period within which that amount is delivered, the time period being 2 hours or longer; a decision module which decides, according to the scheduled regimen, if a delivery should take place; and an inhaler device for delivering THC to the subject, the inhaler device comprising a controller which carries out delivery of THC based on the decision made by the decision module.

Abstract: A nasal patient interface arrangement is for transporting breathing gas from a pressurized gas supply to a patient. The arrangement provides a first bidirectional gas passage in contact with ambient air and receives nasally expired air. The arrangement includes an inspiratory air conduit connecting to a pneumatic unit. The arrangement also includes a nose adapter for bidirectional gas transport. The nose adapter is connected to a nose of the patient. The arrangement further includes a valve arrangement controlling the passage of gas through the first bidirectional gas passage. The arrangement provides a second bidirectional gas passage which is connected to the inspiratory air conduct, the nose adapter, and the first gas passage. The valve arrangement is substantially enclosed in the first bidirectional gas passage.

Abstract: A ventilation device includes a mechanical ventilator (10), respiratory sensors (30, 32) configured to acquire measurements of respiratory variables including at least measurements of airway pressure and airway flow, and an electronic processor (14) programmed to perform a ventilation method including: operating the mechanical ventilator to provide mechanical ventilation controlled using measurements acquired by the respiratory sensors; performing a pause maneuver comprising closing at least one of an inhalation valve (38) and an exhalation valve (40) for a pause interval and estimating a respiratory mechanics index from one or more respiratory system parameters estimated from measurements acquired by the respiratory sensors during or after the pause interval; and triggering a pause maneuver in response to detecting a change in the estimated respiratory mechanics index.

Abstract: A wearable stimulation device includes a wearable member, a stimulation unit, and a driver. The stimulation unit is secured to the wearable member. The stimulation unit includes an immovable end, a stimulation end, and a power element. The power element is connected between the immovable end and the stimulation end for driving the stimulation end to reciprocate relative to the immovable end. The driver is in signal connection with the power element. The driver is configured to output a vibration signal to the power element for the stimulation end to have a stroke of between 8.8 mm and 10.8 mm, a thrust of between 5.6 N and 7.6 N and a reciprocating frequency of between 180 Hz and 220 Hz, thereby stimulating the deep muscles of the abdomen or waist of a human body without affecting the superficial muscles.

Abstract: A process (10), with a computer program, a device (30) and a ventilation system (40) detect a leak in a patient gas module, which suctions and analyzes a continuous sample gas stream from a ventilated patient (20), in a ventilation system for ventilating a patient (20). The process includes a determination (12) of a first time curve of a carbon dioxide concentration in a breathing gas mixture of the patient (20) and the determination (14) of a second time curve of a concentration of another gas in the breathing gas mixture, which gas is different from carbon dioxide. The process (10) further includes a determination (16) of a statistical similarity indicator between the first time curve and the second time curve and the detection (18) of the leak based on the similarity indicator.

Abstract: The present disclosure pertains to a system and method for facilitating pressure support therapy, mechanical inexsufflation therapy, and suctioning therapy for a subject. The system and method described herein offer a novel combination of mechanical inexsufflation with suctioning from a vacuum system. The invasive nature of current closed suctioning systems poses many potential risks, such as tissue trauma, less optimum secretion clearance at the peripheral airway, and lung decruitment. The system and method described herein provide a non-invasive method of suctioning with a suctioning volume measurement and a monitoring alarm to ensure a baseline lung volume and a positive end expiratory pressure (PEEP) level are maintained. This non-invasive method of suctioning is provided together with mechanical inexsufflation and pressure support therapy.

Abstract: A respiratory assistance apparatus includes a conduit connecting a flow generator and an outlet. The conduit includes a venture formation. The apparatus further includes an oxygen inlet in fluid communication or selective fluid communication with an oxygen outlet. The oxygen outlet is directed into the conduit and toward a mouth of the venture formation. The flow generator provides a flow path for air to enter the conduit when the flow generator is not operating.

Abstract: Presented is a chiropractic adjustment and soft tissue mobilization tool. The tool includes a flat bottom section, and a spine adjustment section. The spine adjustment section includes two raised supports aligned substantially parallel, and a spine accommodating area formed along and between the length of the two raised supports for supporting an intended vertebrae portion of a patient's spine during chiropractic adjustment. The spine adjustment section further transitions to form a protruding edge adapted for performing soft tissue mobilization. The protruding edge further protrudes upwardly and rolls off to form a planar raised surface parallel to the flat bottom. Each side of the spine adjustment section features a recessed area formed thereof to allow a provider to hold the tool with the provider's fingertips and to aid in collection and re-dispersal of lotion applied during soft tissue mobilization procedure.

Abstract: A system for automated adjustment of a pressure set by a ventilation device, in particular a positive and-expiratory pressure and/or a maximum airway pressure, the system comprising a pressure detection arrangement for detecting a transpulmonary pressure at the end of an expiration phase and/or for detecting a transpulmonary pressure at the end of an inspiration phase, and a device for automated adjustment of the pressure set by the ventilation device on the basis of the transpulmonary pressure detected at the end of the expiration phase and/or the transpulmonary pressure detected at the end of the inspiration phase.

Abstract: Wearable devices and methods for preventing and treating carpal tunnel syndrome or DeQuervain's syndrome. The wearable device may include a wrist contact portion for receiving a user's forearm, a stretching mechanism configured to apply opposing forces to a first contact portion and a second contact portion to stretch the user's underlying tissue, the first and second contact portions configured to contact the user's forearm, and one or more straps configured to adjust the compressive force being applied to the user's forearm by the first and second contact portions. The first contact portion may be configured to apply a compressive force to the user's forearm at a first location. The second contact portion may be configured to apply a compressive force to the user's forearm at a second location different than the first location.