A61H2209/00

PIEZOELECTRIC COMPRESSION STOCKING
20170246073 · 2017-08-31 ·

The present disclosure provides a compression stocking that comprises a tubular fabric body and a piezoelectric material that is incorporated into the tubular fabric body. The piezoelectric material changes shape in response to actuation energy to generate a compressive force. When the compression stocking is placed on a user's leg, the compressive force may compress blood vessels in the user's leg to assist with the return of venous blood.

PATIENT SUPPORT APPARATUS HAVING AN INTEGRATED LIMB COMPRESSION DEVICE

A patient support apparatus includes a frame having a patient support deck. A footboard is removably coupled to the frame. A compression therapy module is located inside the footboard or is mounted to a foot section of the frame. A sleeve port is pneumatically coupled to the compression therapy module and is located on the foot section. The sleeve port is configured for attachment to at least one tube extending from a compression sleeve worn on a limb of a patient. Control circuitry is coupled to the frame and is operable to control functions of the patient support apparatus and to control the compression therapy module. A graphical display screen is coupled to the control circuitry and displays user inputs that are selected to control functions of the patient support apparatus and the compression therapy module.

Sequential compression therapy compliance monitoring systems and methods

A system includes a sequential compression device (SCD) used by a patient as part of a sequential compression therapy (SCT) protocol. The system also includes a computer device that determines whether the SCD is in use in substantially real time in compliance with the protocol. The computer device initiates a notification to a caregiver if noncompliance with the SCT protocol is detected.

Methods for determining the size of body parts as part of compression therapy procedures

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 measured. The methods may 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 pre-determined 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 measured 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.

METHODS AND DEVICES FOR DEEP VEIN THROMBOSIS PREVENTION
20170231852 · 2017-08-17 ·

Portable devices and methods for preventing deep vein thrombosis (DVT) by assuring that the ankle is flexed and extended sufficiently to promote blood flow in the lower leg are disclosed. The device includes an actuator with a free movement mode that allows a patient to move freely between activations or to initiate movement to delay a next automatic activation.

MEDICATED THREAD DRAINAGE THERAPY APPARATUS
20220265476 · 2022-08-25 ·

The present disclosure belongs to the field of treatment devices, and specifically relates to a medicated thread drainage treatment device. The treatment device includes a first treatment unit used for postoperative pain relief and drainage; a second treatment unit used for promoting quick healing of a wound; a third treatment unit used for preventing deep venous thrombosis; and an electropneumatic, negative-pressure, electric stimulation multipurpose therapy apparatus connected with the first treatment unit, the second treatment unit, and the third treatment unit and providing electropneumatic pressure, negative pressure, and electric energy. The present disclosure is used for postoperative quick healing and recovery; promotion of clinical use guidelines will greatly reduce and even eliminate the postoperative complications, particularly postoperative complications of pulmonary embolism, thus saving patients' lives.

SYSTEM, METHOD AND APPARATUS FOR PAIN CONTROL AND HEALING

A device for treating a user includes a housing having apertures. The housing has application areas including a convex top surface, a concave bottom surface, a convex rear surface, convex side surfaces and rounded protrusions extending away from the housing. A vibrational source is located in the housing to produce vibration at the application areas. A switch is in operative communication with the vibrational source to control operation of the vibrational source.

Compression garment apparatus having baseline pressure
09717642 · 2017-08-01 · ·

A compression garment apparatus including a compression garment and a pressurizer. The pressurizer intermittently pressurizes a therapeutic bladder on the compression garment and maintains a baseline pressure in the therapeutic bladder to maintain the therapeutic bladder in position with respect to a target compression zone on a body part on which the garment is worn. The baseline pressure is adjusted in response to sensed physical characteristics.

ACTIVE RECORERY SYSTEM AND METHOD HAVING CAPACITIVE PROXIMITY SENSOR
20170273849 · 2017-09-28 ·

A shoe has a sole having a capacitive sensor and a force actuating mechanism, and a wireless receiver. The capacitive sensor can detect and sense whether or not there is a foot is in the shoe. The force actuating mechanism can operate like a piston in an inactive mode (first position) and active mode (second position), wherein the active mode extends the force actuating mechanism's extending mechanism from first position to second position. The wireless receiver can retrieve any information in regards to geodetic locations from the capacitive sensor based on the capacitance signal.

HEALTH MANAGEMENT SYSTEM

A therapeutic wrap includes a flexible member configured to wrap around an affected area. Actuators are operably coupled to the flexible member. Each actuator is operable between a deployed state and a non-deployed state. A first coupling feature is disposed proximate a first edge on a first surface of the flexible member. A second coupling feature is disposed proximate a second edge on a second surface of the flexible member. The first coupling feature is configured to engage the second coupling feature when the flexible member is wrapped around the affected area and when the flexible member is slidably adjusted relative to the affected area. A retaining feature is coupled to at least one end of the flexible member and configured to retain the flexible member in a selected position on the affected area.