An intravenous (IV) therapy system to facilitate the insertion of a catheter or another suitable IV device into a patient may include a band made of flexible material to be secured around a limb of a patient. The IV therapy system may include a window formed through the band to provide access to the patient's body. The IV therapy system may include a tourniquet formed within the band to selectively apply a pressure against the patient's body. The IV therapy system may include a blood vessel indicator to indicate where the catheter or other suitable IV device is to be inserted.

Radial artery compression devices with an inflatable chamber and a substantially rigid frame are disclosed. The inflatable chamber of the radial artery compression devices can be inflated and then deflated according to a predetermined protocol. Some substantially rigid frames can form a wall of the inflatable chamber. Some substantially rigid frames can include indicia to facilitate positioning of the inflatable chamber relative to a puncture site of a patient.

An aspect of the present invention is a consciousness disorder mitigation apparatus, including: a first estimation unit configured to estimate body fluid volume information, the body fluid volume information being information on a body fluid volume present in a head of a user; a second estimation unit configured to estimate oxygen supply volume information, the oxygen supply volume information being information on an oxygen supply volume representing an amount of oxygen in a brain of the user; a pressurization unit configured to be attached to the user and to apply a pressure corresponding to an estimation result of the first estimation unit and an estimation result of the second estimation unit; and an oxygen supply unit configured to supply oxygen to the user based on the estimation result of the second estimation unit.

An automated emergency pneumatic tourniquet system including multiple interchangeable tourniquet cuffs, each having an inflatable bladder and an indicator tag designating the type of cuff, preferred pressure of application, and other data. A detachable controller reads the indicator tag and inflates the bladder to a predetermined pressure, which can be modified once applied. The detachable controller may be used to inflate multiple cuffs individually and monitor the amount the pressure applied by the cuffs. It also allows for periodic reperfusion for reducing and/or preventing ischemia. The cuff is held in place on a limb using a manual tightening mechanism independent of the bladder and controller.

A system comprising: a wearable element designed to be worn on a body region of a subject; an array of sensors arranged at specified locations, attached to the wearable element; and a detection module in communication with each of the sensors in the array and configured to determine a parameter indicative of an injury to the body region, based on the signal. The parameter indicative of an injury to the body region may include at least in part, on at least one of: (i) an impact event associated with said subject calculated from the signal, (ii) a location of each of the at least one of the sensors relative to the body region, and a timing of the generating in the signal generated by the at least one sensor.

The present invention relates to a device for treating an aneurysm of a human or mammal patient, wherein the aneurysm may self expand, leading to the aneurysm bursting with high risk for death of the human or mammal patient. The device is provided with an implantable member to be placed in connection with the outside of a blood vessel having the aneurysm, and to exercise a pressure on the outside of the blood vessel having the aneurysm, a measuring device or sensor for measuring or sensing an expansion of the aneurysm, and a monitoring system for monitoring the expansion of the aneurysm based on a signal received from the measuring device or sensor.

An inflatable belt 100 for use in a BFR system with an outer belt material 102 hermetically sealed to an inner belt material 101 along a perimeter, thereby forming at least one inflatable chamber 103, the inflatable chamber having an input port 104 for accepting a gas into the chamber, the inflatable belt further comprising a first fastening means 110 in communication with the outer belt material, for attaching to a second fastening means 111 in communication with the outer belt material, thereby locking a circumference of the inflatable belt when wrapped around a user's limb, the inflatable belt providing sufficient volume and compliance so as to reduce spikes in pressure and thereby improve comfort and safety of the inflatable belt for use in restriction of blood flow for muscle development.

Disclosed are devices, systems, and methods of a wearable compression control system for actively controlling an applied pressure against an extremity to restrict blood flow along the extremity of a user performing an exercise or undergoing a therapy. In some embodiments, the system can include an inflatable band that extends circumferentially around the extremity. The inflatable band can include a bladder having an expandable inner volume for receiving fluid to cause the inflatable band to increase in thickness and increase an applied pressure against the extremity. The system can further include a controller that releasably couples to the inflatable band and includes a processor having a programmed pressure range. The processor can be configured to actively maintain the applied pressure within the programmed pressure range throughout the user performing the exercise or the user undergoing the therapy.

An automatic tourniquet apparatus comprises a tourniquet cuff, a pressure transducer, a user interface, a patient hazard shield and a pressure regulator. The pressure transducer produces a cuff pressure signal. The user interface produces a reference pressure signal. The patient hazard shield is responsive to the cuff pressure signal and the reference pressure signal, and operable during a regulation time period to produce a patient hazard signal if, in one implementation, a current level of pressure in the tourniquet cuff is greater than the reference level of pressure by at least a predetermined overpressure limit. The pressure regulator is responsive to the patient hazard signal, and has a pressurizing element for increasing pressure in the cuff and a depressurizing element for decreasing pressure in the cuff. The pressurizing element is configured to be non-responsive if the patient hazard signal is produced.

Methods and apparatus for increasing cerebral blood flow for improving the flow of blood to the brain during and/or following an ischaemic stroke. The apparatus includes a plurality of inflatable cuffs to be positioned, in use, around a respective limb of a patient. Once inflated, the cuffs exert a pressure upon the limb to reduce blood flow to the limb below the point at which the cuff is positioned. Reducing blood flow to the limbs causes an increase in blood flow to the brain, and will therefore improve stroke outcomes. The apparatus includes a control module for controlling inflation and deflation of each cuff. The control module detects, measures and monitors cerebral blood flow and uses these measurements to control inflation and deflation of each cuff such that cerebral blood flow is maintained above a baseline level during treatment of the patient.