Abstract: A face mask (also called full face) for respiratory therapy, in particular for non-invasive mechanical ventilation, has a low value of CO2 rebreathing. The mask includes a shaped shell to cover at least the mouth, the nose and the eyes of a patient when the mask is worn, and includes, on said shaped shell an inlet fitting for the connection to a pipe through which a ventilation apparatus supplies the mask with a mixture of air and oxygen, and an outlet fitting, separate from said inlet fitting, for the discharge of air exhaled by the patient. With this arrangement, the mask allows drastically reducing the phenomenon of carbon dioxide rebreathing, which is very harmful for the patient subjected to ventilation.

Abstract: A massage apparatus providing a pulsed electromagnetic field may comprise: a massage unit which comprises a mount frame provided so as to be movable along the body of a user, and an acupressure module protrudingly provided to the mount frame so as to apply pressure to the body of the user; a pulsed electromagnetic field generator which is provided to the mount frame so as to be independent from the acupressure module, and which generates a pulsed electromagnetic field by means of power applied thereto; and a controller which controls the operation of the acupressure module or the generation of the pulsed electromagnetic field. According to such massage apparatus, a pulsed electromagnetic field may be generated by having the pulsed electromagnetic field generator be provided to the massage unit so as to be separate from the acupressure module or air cells performing a massaging operation.

Abstract: An apparatus for manipulating (in one alternative correcting) the cervical curvature of a user, the apparatus having a top, a bottom, a first end, a second end, a first side and a second side, wherein: proximate the top, a thoracic section for receiving the upper back region of a user, preferably for receiving the thoracic region of the user; proximate the top, a cervical section for receiving the cervical curve region of the user; the cervical section is movable with a traction path in at least one of the following planes vertical, horizontal and combinations thereof; in one alternative, the cervical section is movable in an arc-like motion along the vertical plane.

Abstract: In an example, a ventilator includes a first container and a second container in fluidic communication with each other via a liquid. The second container includes a second container space surrounded by the second container and a second liquid surface. A hydrostatic pressure in the second container space results from a pressure differential defined by a difference between the first liquid surface elevation in the first container and the second liquid surface elevation. The second container space increases in size with an increase in the breathing gas supplied from a gas supply line to the second container space. An inhalation line is configured to open to permit a flow of the breathing gas from an inhalation inlet in the second container space to an inhalation outlet outside of the liquid and outside of the second container and coupled to a patient, causing the second container space to decrease in size.

Abstract: This disclosure describes systems and methods for managing a move of a patient being monitored or treated by a medical system, such as a medical ventilator. The disclosure describes a novel approach for preventing a patient from being moved from a first location to second different location that is connected to a monitoring and/or treatment system, before all of the necessary hoses have been disconnected from the patient. Further, the disclosure describes a novel approach of ensuring that all of the necessary hoses are reconnected to a patient being monitored or treated by a monitoring and/or treatment system after being moved from the first location to the second different location.

Abstract: The principles and embodiments of the present invention relate to methods and systems for safely providing NO to a recipient for inhalation therapy. There are many potential safety issues that may arise from using a reactor cartridge that converts NO2 to NO, including exhaustion of consumable reactants of the cartridge reactor. Accordingly, various embodiments of the present invention provide systems and methods of determining the remaining useful life of a NO2-to-NO reactor cartridge and/or a breakthrough of NO2, and providing an indication of the remaining useful life and/or breakthrough.

Abstract: A breathing device, comprising a mouthpiece forming a breathing channel, to form a connection between a first end and a second end of the mouthpiece; the first end being configured for a user breathing into the mouthpiece through a breathing opening; an at least partly flexible rebreathing air chamber attached to the second end of the mouthpiece, thereby being in fluid connection with the breathing channel; the rebreathing air chamber being formed by at least partly flexible wall section(s), the at least partly flexible rebreathing chamber having at a first wall section, being permeable to gas by a plurality of pores provided in said wall section and/or the mouth piece comprising one or more though going openings.

Abstract: A method of ventilating a patient controls an actuator, in accordance with a prescribed value for a respiratory parameter, to compress an inflatable bag to cause air to flow out of an output valve of the bag. The respiratory parameter may include tidal volume, pressure, volume limit, peak pressure, I:E ratio, inspiratory time, and/or breathing rate of the air flowing through the output valve. The method also senses the pressure flowing through the output valve, and sends a pressure signal to the controller. Additionally, the method senses the flow rate through the output valve, and sends a flow rate signal to the controller. The method also adjusts the compression of the actuator as a function of the flow rate signal and/or the pressure signal to adjust the output tidal volume, pressure, volume limit, peak pressure, I:E ratio, inspiratory time, and/or breathing rate to be in accordance with the prescribed value.

Abstract: A respiration device (1) supports cardio-pulmonary resuscitation (CPR) and a method for operating a respiration device (1) supports cardio-pulmonary resuscitation (CPR). The respiration device (1) has a control and regulation unit (7) in order to actuate an expiratory metering unit (3), and an inspiratory metering unit (2) such that, in a first phase, a current value of pressure is increased relative to a first pre-defined value (16) and such that, in a second phase, the current value of the pressure is reduced relative to the first pre-defined value (16).

Abstract: A massage tool includes a rod having a proximal end and a distal end, and a body follower having a proximal side and a distal side. The proximal end is configured for attachment to a reciprocating shaft of a reciprocating motor. The reciprocating shaft has a stroke axis and a stroke length, and the distal end of the rod is configured to rotatably attach to the proximal side of the body follower by means of a rotating joint defining a center of rotation. The distal side of the body follower may include a body contact area having a maximum length at least three times greater than a minimum distance from the center of rotation of the rotating joint to the body contact area.

Abstract: Devices and methods for treating carpal tunnel syndrome or DeQuervain's syndrome. The device may include a resting portion for receiving a user's forearm, first and second contact portions configured to contact the user's forearm, and a stretching mechanism configured to apply opposing forces to the first contact portion and the second contact portion to stretch the user's underlying tissue. 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.

Abstract: This disclosure describes systems and methods for providing a high pressure controlled proportional assist ventilation breath type during ventilation of a patient. The disclosure describes a novel breath type that reduces ventilator support (or a percent support setting) based on the occurrence of a predetermined number of high pressure alarms.

Abstract: An integrated oxygen supply device that is configured to generate oxygen continuously and release the oxygen non-continuously is provided. In some embodiments, the oxygen generated by the integrated oxygen supply device is stored in a porous material with the integrated oxygen supply device. The delivery of the oxygen produced by integrated oxygen supply device to a patient, in those embodiments, is controlled. In some embodiments, the control of the delivering oxygen is according one or more breathing patterns. The breathing pattern(s) may or may not be a current breathing pattern of the patient. For example, in one embodiment, the breathing pattern is a predetermined breathing pattern with a specified inspiration period followed by a specified expiration period.

Abstract: A patient interface device includes a frame member and a cushion having a main body, a sealing portion, and first and second posts extending from the main body. The frame member defines a first orifice and a second orifice. The first post of the cushion is rotatably received within the first orifice and the second post is rotatably received within the second orifice in a manner that permits the cushion to rotate relative to the frame member.

Abstract: Systems and methods for producing nitric oxide (NO) to be used in medical applications are provided. In some embodiments, systems and methods are provided for a NO generator that is capable of generating a desired concentration of NO to be provided to a respiratory system for inhalation by a patient.

Abstract: This disclosure describes systems and methods for providing novel adaptive base flow scheduling during ventilation of a patient to optimize the accuracy of estimated exhaled tidal volume. Further, this disclosure describes systems and methods for providing novel adaptive inspiratory trigger threshold scheduling during the novel adaptive base flow scheduling.

Abstract: An electrically heated aerosol-generating device includes a main housing having a cavity, a closure body engageable with the main housing to enclose a cartridge in the cavity, and a heater assembly. The heater assembly includes an elongate piercing assembly configured to extend into the open-ended passage of the cartridge and one or more electric heaters. The piercing assembly has a first hollow shaft portion connected to the main housing and a second hollow shaft portion connected to the closure body. The first and second hollow shaft portions have first and second piercing surfaces configured to breakthrough first and second frangible seals when the cartridge is enclosed in the cavity.

Abstract: A fluid control device includes a case including an internal space that is partitioned by a partition wall into an air blowing chamber and a control chamber. A dividing wall is disposed inside the air blowing chamber to partition an internal space of the air blowing chamber into a first air blowing chamber and a second air blowing chamber. A fan unit is housed in the second air blowing chamber. A differential pressure sensor senses a differential pressure between a pressure inside the first air blowing chamber and a pressure inside the second air blowing chamber. A controller controls a fan based on the sensed differential pressure.

Abstract: A system for delivering oxygen comprises an oxygen source; a ventilator operatively connected to the oxygen source to receive a supply of oxygen therefrom; a valve having a) an open position in which the ventilator receives the supply of oxygen from the oxygen source and b) a closed position in which the ventilator is not in fluid communication with the oxygen source; a sensor configured to measure breath flow information for the patient; and a computer system to: determine a volume of gas delivered to the patient during a breath cycle of the patient and an inspiratory volume of gas delivered to the patient during an inspiration phase of the breath cycle by using the breath flow information; and provide input to the valve based on the determined volumes, the provided input causing a movement of the valve between the open and the closed positions.

Abstract: A patient interface assembly includes a flexible cushion configured to sealingly engage the patient's nares and a frame with a pair of flexible extending members that extend laterally from opposite sides of the frame. The frame and the flexible cushion together form a chamber. The patient interface assembly also includes a positioning and stabilising structure configured to maintain the flexible cushion in engagement with the patient's nares. The positioning and stabilizing structure has a pair of headgear straps. Each headgear strap is connected to a respective one of the flexible extending members. The flexible extending members do not form an airflow path for the breathable gas. The headgear straps have a multi-layered structure, at least one layer being made of fabric and at least one layer being made of plastic. In addition, the at least one plastic layer is a rigidizer that adds rigidity to the respective headgear strap.