A distributed patient monitoring system comprises at least one standalone portable ultrasound imaging unit configured to be fixed to a stable position against the skin on a patient's body and capable of prolonged ultrasound data acquisition, including an ultrasound imaging array, transmit-receive circuitry, a beamformer, backend signal and image processing subsystem, power and communication subsystems, and a monitoring workstation connected to each standalone portable ultrasound imaging unit configured to request and receive ultrasound imaging information from each standalone portable ultrasound imaging unit, and configured to analyze and display acquired ultrasound information.

A hydrogen-containing gas supply system includes one or more hydrogen-containing gas suppliers, one or more acquirers, and a controller. The one or more hydrogen-containing gas suppliers supply a hydrogen-containing gas to one or more areas in a building. The one or more acquirers acquire information indicating that a person is present in the one or more areas. When it is determined that a person is present in a certain area of the one or more areas in accordance with the information acquired by the acquirers, the controller causes at least one of the one or more hydrogen-containing gas suppliers to supply the hydrogen-containing gas to the certain area.

A handheld acupuncture tapping device includes a case that is divided into a head and a handheld part. At least one control button is disposed on the outer surface of the case, and at least one light unit, a vibration unit, a control module, and a contact unit are disposed within the case. The control module is electrically connected to the light unit and the vibration unit for driving the light unit and the vibration unit to generate a light and a vibration signal respectively. Further, the user can control the control module by the control button to adjust the intensity of the light and the waveform, frequency and amplitude of the vibration signal. The contact unit is disposed in front of the light unit and the vibration unit, so that the light and the vibration signal are projected on the contact unit and transmitted to an outside. The user can use the light and the vibration signal generated by the handheld acupuncture tapping device to tap or massage the treatment part.

Methods are disclosed for measuring the size of body parts treated by a compression therapy device. Either the volume or circumference of the body part may be measure. The methods my include evacuating an inflatable compression sleeve to a known pressure, inserting the body part into the compression sleeve, inflating the sleeve to a pre-set condition, and then measuring one or more inflation related parameters. The pre-set conditions may include a predetermined pressure, volume, or size of the inflatable cells comprising the sleeve. The inflation related parameters may include the time to fill the cell to a pre-set pressure, the pressure attained after a pre-set time of inflation, or the measure volume of a cell after a pre-set amount of air is introduced into it. The methods may also include deflating the cells from the known inflation state to a second inflation state and measuring similar parameters.

An ankle exoskeleton device is provided having a lower leg anchor, a foot/ankle anchor, a first actuator and a second actuator. The first actuator includes an upper end disposed at a first anchor point on the right side of the foot/ankle anchor and a lower end disposed at a second anchor point on the right side of the lower leg anchor. The first actuator includes a first biasing mean having a neutral position when the ankle is in a neutral position. The first biasing means provides for compression loading due to ground reaction forces on the foot/ankle anchor to provide a cushioning effect on the ankle as the being takes a step. The second actuator provides for substantially the same elements on the left side of the foot/ankle anchor and the lower leg anchor.

A CPR apparatus includes a chest compression unit and a means for mounting the chest compression unit on a patient. The chest compression unit includes a plunger disposed in a housing. At its one end extending from the housing the plunger has a compression member. The plunger is driven in a reciprocating manner by a reversible electromotor via a mechanism for translating rotational motion to linear motion or by a linear induction electromotor. The chest compression unit includes an electromotor control unit including a microprocessor, a first monitor for monitoring the position of the plunger in respect of the housing and a second monitor for monitoring the position of the plunger in respect of the mechanism for translating rotational motion to linear motion or the rotor of the linear induction electromotor. The monitored positions are communicated to the electromotor control unit. Also disclosed is a corresponding CPR method.

A continuous passive motion apparatus is provided that includes a thigh support (40) connected by a hinge structure (38) to a base plate (36). The plate (36) is itself connected to a base (34). A bladder (54), which inflates to the form of a vertically elongate column, is cyclically inflated and deflated to lift the thigh support (40) in movements about a hinge (46) connecting it to an upper hinge plate (42) of the hinge structure (38). The hinge structure also includes a lower hinge plate (44). A foot support (72) is connected by a cord (68) to the thigh support (40).

A compression garment having one or more flex frames that can be shortened or lengthened to apply or release a compressive force to the limb or other anatomical feature of a user. The compression garment can have a wire made of shape memory material (shape memory alloy). A controller of the compression garment can supply an electrical input to the wire, generating heat that can cause the wire to contract such that the flex frame deflects to a shorter length to apply a compressive force to the limb or other anatomical feature of the user. The one or more flex frames can be contracted in unison or in sequence to direct the flow of bodily fluids in the limb or other anatomical feature of the user.

A cold plasma system and method for treating a region of a biological surface is presented. In one embodiment, the system includes: a housing; an air conduit within the housing; a first electrode configured proximately along the air conduit; a second electrode configured proximately along the air conduit and opposite from the first electrode; and a source of alternating current (AC) electrically connected with the first electrode. The source of alternating current is configured to generate cold plasma in the air conduit.

A compression device for freeing a ring trapped on a digit includes a rigid outer body. The rigid outer body includes a digit cavity extending from a cavity opening at a body proximal end of the body towards a body distal end of the body, a fluid inlet, and a fluid flow path fluidly connecting the fluid inlet to one or more inflation chambers positioned in the digit cavity. The body proximal end includes an upper portion, a lower portion, and two laterally spaced-apart side portions. At least one side portion is distally recessed as compared to the upper and lower portions to accommodate an interdigital fold. At least one flexible bladder lines the digit cavity, each flexible bladder defining at least one wall of one of the one or more inflation chambers.