An example of a system for providing patient care guidance to a caregiver based on ultrasound detection of blood flow includes a defibrillator including an electrode assembly and an output device, a portable computing device communicatively coupled to the defibrillator and including an output device, a Doppler shift waveform evaluation engine disposed at the defibrillator and/or the portable computing device, and a wearable ultrasound blood flow sensor configured to couple to a patient and the defibrillator and/or the portable computing device and to generate data signals representing a Doppler shift waveform. The engine is configured to receive the data signals representing the waveform, generate caregiver instructions according to a cardiac arrest protocol, analyze the waveform based on the received data signals, identify heart-induced blood flow based on the waveform analysis, and generate and provide caregiver instructions according to a non-cardiac arrest protocol based on the identified heart-induced blood flow.

A flexible anchor member comprising a member for placement about a body part; at least one substantially inextensible textile element circumscribing the member and secured to itself or the member; and a force transfer coupler coupling a portion of the at least one substantially inextensible textile element to an actuator such that the substantially inextensible textile element constricts about the member for a duration of an applied force. Another flexible anchor member comprising an outer member including a substantially inextensible textile material configured for directing a force applied by an actuator to act upon all or a portion of the body part; an inner member for positioning between the body part and the outer member, a first surface of the inner member configured for frictionally engaging the body part or intervening clothing; and at least one coupler for coupling the outer member and the inner member.

A method for performing cardiopulmonary resuscitation (CPR) includes elevating the heart of an individual to a first height relative to a lower body of the individual. The lower body may be in a substantially horizontal plane. The method may also include elevating the head of the individual to a second height relative to the lower body of the individual. The second height may be greater than the first height. The method may further include performing one or more of a type of CPR or a type of intrathoracic pressure regulation while elevating the heart and the head. The first height and the second height may be determined based on one or both of the type of CPR or the type of intrathoracic pressure regulation.

A system that assists acupuncture based on the physiological signals of the human body. Physiological signals comprise respiratory signals, electrocardiographic signals, electrical skin signals, electroencephalograph signal, blood flow signals, pulse wave signals and/or signals derived from above signals. The acupuncture treatment process comprises the following: controlling the actuator of the automatic acupuncture device through physiological signals to start, to stop acupuncture treatment or to perform acupuncture techniques such as twisting or lifting-thrusting. It also provides an automatic acupuncture system to assist acupuncture based on Chinese Medicine Body Clock information.

A pressure application relating to a garment that includes at least one active part for applying pressure to at least one body part of a subject and the active part includes at least one bladder fillable with a fluid so as to obtain a homogeneous positive pressure applied to the whole of the corresponding at least one body part of the subject, the pressure application garment also including for the or each active part, at least one interface pressure sensor, a control unit, and a driving module wherein the pressure application garment further includes at least one sheet of a fabric made of at least three superimposed layers.

Systems, and methods relate to a medical device receiving a treatment parameter operating point within a first operating region defined by a first set of operating points for which automatic incremental adjustment of a parameter in the current operation is permitted. In an illustrative example, incremental adjustment may use artificial intelligence based on patient feedback and sensor measurement of outcomes. Some exemplary devices may receive a request to alter the current treatment parameter operating point to a second treatment parameter operating point outside the first operating region and in a second operating region in a known safe operation zone, bounded by a known unsafe zone unavailable to the user. In the second operating region, some examples may restrict the step size of incremental adjustments requested by the user. Data may be collected for cloud-based analysis, for example, to facilitate discovery of more effective treatment protocols.

The invention relates to an adult choke pleasure enhancement adjustable pressure cuff device. Participants can engage in solo autoerotic asphyxiation (AEA) without accidentally suffocating to death. The adjustable cuff is inflatable and sized to encompass a participant's neck and has a timed safety release function. The participant can apply the device at default setting to fit snugly, but not impede blood flow. The participant can inflate the device to the desired level of pressure that would remain at that setting at participant's discretion. They can control what happens and for how long, as long as the participant is not incapacitated. However, if at any time, the controls/settings are not engaged by the participant, the device would automatically default to zero pressure after a set time. The use of the device therefore allows a participant to safely engage in solo AEA without risking injury or death.

A sleep assessment system includes a blood flow measurement unit and a assessment unit. The blood flow measurement unit acquires first information related to the blood flow of the user. The assessment unit determines the sleep stage of the user based on the first biological information.

A method includes disposing a plurality of actuators about a subject, each actuator being configured to generate a respective vibration signal, each vibration signal applying a normal force to the subject, and controlling the plurality of actuators such that the respective vibration signal of each actuator of the plurality has a respective vibration characteristic. Each actuator is oriented such that the respective vibration signal propagates along a longitudinal axis of the subject for stimulation of the subject remote from the plurality of actuators.

A system for generating stimulations in relation to medicines, and meridians, organs and tissues of a human body includes a control device, a pulse examining device and a stimulation device. Based on a pulsation signal obtained from a user, the stimulation device obtains a meridian-related spectrum. Based on operation input to the control device, the stimulation device obtains an organ-tissue-related spectrum and a medication-related spectrum. The stimulation device obtains a stimulation spectrum by making a linear combination of these spectrums, and stimulates a sensory system of the user based on the stimulation spectrum.