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.

A system is disclosed which includes a walking assistance robot for assisting a smooth start of a user's action after standing up from a chair. A system according to an aspect of the present disclosure includes a walking assistance robot and an automatic elevation chair that moves a seating surface where a user sits. The automatic elevation chair detects a consciousness level of the user and transmits consciousness level information on the detected consciousness level of the user to the walking assistance robot via the network. The walking assistance robot, including a body and a rotor that moves the walking assistance robot, receives the consciousness level information via the network and controls resistance force to rotation of the rotor based on the received consciousness level information.

A portable medical device having improved ECG trace display and reporting. Embodiments implement features to ameliorate artifacts created by virtue of attempting to eliminate compression artifacts due to mechanical compression devices. Other embodiments additionally implement features to seek to detect the occurrence of ROSC while chest compressions are ongoing.

An apparatus for minimally-invasive, including non-invasive, prevention and/or treatment of hydrocephalus and method for use of the same are disclosed. In one embodiment of the apparatus, a housing is sized for superjacent contact with a skull having a fontanel. Within the housing, a compartment includes a pressure applicator, such as a fluid-filled bladder, under the control of a pressure regulator. The pressure applicator is configured to selectively apply an external pressure to the fontanel. The compartment includes a pressure sensor configured to measure intracranial pulse pressure of the fontanel. Further, in one embodiment, the apparatus can cause pulse pressure modulation by adjusting the intracranial pulse pressure via the pressure applicator. This enables a non-invasive measurement of the pulse pressure and modulation thereof in infants, for example.

The present invention relates to a movement-dependent stabilisation support system (100) for stabilising a moving body (200), which comprises a plurality of sensors (110), a plurality of actuators (120) and a control unit (130). The plurality of sensors (110) continuously detects movement parameters of the body (200), on which basis the control unit (130) determines whether there is an instability of the body (200). If it is determined that there is an instability, the control unit (130) selects a stabilisation strategy, according to which the actuators (120) are controlled. When controlled, the actuators (120) attached to the body (200) stiffen and limit the freedom of movement of the body (200), such that a movement in the direction of the imminent unstable state is prevented or suppressed. In this way, the body (200) is supported in its stabilisation and an imminent fall is prevented.

A method and related systems for treating and/or preventing spasticity in a patient using negative pressure therapy. The negative pressure therapy may include intermittent application of negative pressure to a limb or portion of a body, such as alternating between periods of negative pressure and ambient pressure. The negative pressure therapy may be applied on a regular basis for a predetermined period, such that an effective amount of negative pressure for treating spasticity and other symptoms of neurogenerative diseases is administered. The negative pressure therapy may be applied to cause intermittent activation of the venous arterial reflex in the body for a sustained period, such that symptoms of neurogenerative diseases are alleviated or prevented.

A Multi-function Pelvic Trigger Point Massage Wand is a handheld device for the treatment of pelvic pain and pain/discomfort caused by related urinary and sexual dysfunctions. The device provides an adjustable combination of heat, vibration, electric stimulation, electromyography, photoplethysmography pulse oximetry, and biofeedback, depending on the treatment regimen desired. A metal sensor band around the release-end of the wand conducts electromyography and electrical stimulation. Photodiode sensors are coupled with green and infrared LEDs to calculate the users heart rate and blood flow. A sensor for biofeedback measurement assigns data produced from electrical stimulation sensors, electromyography sensors, photodiode sensors and the biofeedback/pressure measuring function to a smart device with operating software created specifically for the pelvic trigger point wand. The information output is collected and analyzed to show the results of different treatment techniques.

A feedback device for an acute care provider includes: at least one motion sensor; a haptic output component for providing feedback having a varying haptic pattern to the acute care provider regarding performance of a resuscitation activity; and a controller. The controller can be configured to receive and process a signal representative of performance of the resuscitation activity from the at least one motion sensor, compare the acute care provider's performance of the resuscitation activity to a target performance of the resuscitation activity, and cause the haptic output component to provide haptic feedback to the acute care provider by changing the haptic pattern based, at least in part, on the signal from the at least one motion sensor and the comparison of the acute care provider's performance to the target performance of the resuscitation activity. The device can be adapted to be wrist-worn by the acute care provider.

Various embodiments of systems, devices, components, and methods for providing external therapeutic vibration stimulation to a patient are disclosed and described. Therapeutic vibration stimulation is provided to at least one location on or adjacent to a patient's skin (such as through clothing or a layer disposed next to the patient's skin), and is configured to trigger or induce resonance or high amplitude oscillations in a cardiovascular system of the patient. Inducing such resonance can aid in training autonomic reflexes and improve their functioning.

An exemplary method of identifying a source of chest compressions administered during cardiopulmonary resuscitation (CPR) includes receiving, at a processor, signals indicative of pressure exerted during the chest compressions from at least one sensor communicatively coupled to the processor and disposed at a location on the victim's chest away from an indicated compression point for manual chest compressions, generating a compression waveform based on the received signals, detecting compression waveform features representative of the chest compressions based on the compression waveform, comparing the detected compression waveform features to a pre-determined criterion to discriminate between chest compressions from an automated compression device and manual chest compressions, determining whether the chest compressions are from the automated compression device or the manual chest compressions based on the comparison, and generating an output based on whether the chest compressions are determined to be from the automated compression device or the manual chest compressions.