The invention features methods and devices for controlling bleeding from blood vessels that may be damaged as a result of trauma or impact with an object, such as a bullet or shrapnel. The device may be wearable by a user and include one or more components, such as wound sealant and multiple inflatable balloons/bladders. The device may be integrated into a garment, e.g., a vest, jacket, trousers, or full body suit. Once triggered (automatically or manually), the device may be used to deliver wound sealant to a wound site and/or pressure to the wound site by selective inflation of one or more balloons over exsanguinating blood vessels that may be damaged, thereby stopping or minimizing the bleeding. Alternatively, or in addition, the device may be used to stabilize a wounded wearer for, e.g., transportation purposes, or to provide buoyancy. Devices of the invention may also be used as a blood pressure monitor, as a massaging device, and as a breast pump. Devices and methods of the invention may also be used for repairing or stabilizing machines, such as vehicles (e.g., automobiles and boats).

A tourniquet apparatus comprises a cuff, a user interface, a controller, a protocol hazard key and a protocol safety interlock. The cuff encircles the patient's limb and applies a level of pressure. The UI presents a protocol symbol from a plurality of protocol symbols wherein each protocol symbol is indicative of a corresponding safety protocol. The controller is responsive to stored pressure levels and stored times specified by the safety protocol, after any adjustments by the user, and operable during the stored protocol time period for maintaining the level of pressure applied by the cuff to the individual patient near the plurality of stored pressure levels at the plurality of stored times. The protocol hazard key is actuatable to end the stored protocol time period while the controller is operable. The protocol safety interlock prevents selection of a second protocol symbol while the controller is operable.

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.

A wearable device comprises a tourniquet. The tourniquet comprises an inflatable chamber and is configured to occlude blood flow in an artery of a wearer. The wearable device comprises a compressed gas source. The wearable device comprises a valve. The valve comprises a valve input in fluid communication with the compressed gas source, and a valve output in fluid communication with the inflatable chamber. The wearable device comprises at least one fixed pressure regulator. Each fixed pressure regulator comprises a regulator output in direct fluid communication with the valve input, and a regulator input in direct fluid communication with the compressed gas source. Each fixed pressure regulator is configured to receive at least one compressed gas from the compressed gas source and regulate a pressure of the at least one compressed gas delivered to the valve. The wearable device comprises a switch. The switch is configured to operate the valve.

A device for treating a vascular aneurysm of a human or mammal patient, comprising an implantable member adapted to hold fluid, the implantable member being adapted to be placed against an outside of a blood vessel having the aneurysm, exercise a pressure on the aneurysm to prevent or reduce an expansion of the aneurysm, follow an outer contour of the aneurysm, and provide a pressure that is equal or less than the diastolic blood pressure of the human or mammal patient.

Provided is a method of determining a hemostatic pressure in a tourniquet includes: driving a limb occlusion pressure (LOP) sensor, which measures a pulse signal of a subject, at a first brightness (S1); checking whether the LOP sensor and a main body are connected to each other (S2); providing a first hemostatic pressure from the main body to the tourniquet (S3); checking, on the basis of a result value of the LOP sensor, whether a pulse of the subject is detected (S4); and, when, on the basis of the result value of the LOP sensor, the pulse of the subject is determined as “not detected,” providing a hemostatic pressure, which is obtained by increasing the current hemostatic pressure by a safe hemostatic pressure, from the main body to the tourniquet (S7).

A personalized tourniquet cuff assembly comprises a sterile tourniquet cuff, a machine-readable instrument symbol, machine-readable personalization data and a sterile connector. The instrument symbol identifies a predetermined first type of tourniquet instrument from a plurality of types of tourniquet instruments, and is adapted for contactless reading by an optical tourniquet interface of the first type of tourniquet instrument. The personalization data represents a value of a personalization parameter for safe operation of the tourniquet cuff with the first type of tourniquet instrument and is adapted for contactless reading by the optical tourniquet interface. The connector is adapted for releasably connecting the tourniquet cuff to the first type of tourniquet instrument. The instrument symbol and the personalization data are carried at a location enabling contactless reading thereof only if the assembly is positioned within a predetermined range of distances and range of orientations relative to the optical tourniquet interface.

A modular wound treatment system includes a central modular hub having a modular connection for one or more pneumatically-actuated, modular components, such as a pneumatically-actuated soft robotic gripper component configured to curve and at least partially encircle the wound when actuated and thereby apply direct pressure to the wound, and a pneumatically-actuated tourniquet component configured to apply pressure proximal to the wound to limit the flow of arterial blood to the wound. The system also includes a pressurized gas supply in pneumatic communication with the modular connection, sensors for measuring the amount of pressure being applied by the pneumatically-actuated, modular components, a display for providing system information, and a controller for controlling the system. Methods of treating a wounded subject using the system are also provided.

A pneumatic physiotherapy apparatus with optimized compression, including a wrap and a controller. The wrap includes an outer wrap and an inner airbag set; the controller can be fixedly connected to, detachably connected to, or separately connected to the outer wrap; the inner airbag set includes the first airbag and the second airbag that are interconnected and overlapped; the controller contains an inflating motor and an integrated control board that are electrically connected. The inflating motor that is controlled by the integrated control board inflates the second airbag first and then the first airbag to achieve the overlapped compression between the second airbag and the first airbag. Therefore, the user can use the pneumatic physiotherapy apparatus with optimized compression to promote blood flow, improve blood circulation, prevent deep vein thrombosis and other diseases, and improve user experience in the treatment areas.

A pressure controller for a fluidic bladder has in sequence a pump, a first fluid line, a supply pressure sensor, a second fluid line, a bladder having an inlet coupled to the second fluid line, a bladder outlet coupled to a third fluid line of substantially equal length to the second fluid line, a return pressure sensor, and a fourth fluid line coupled to the return pressure sensor and returning fluid from the pump to the reservoir. A pressure estimate is formed by averaging the supply pressure and return pressure. The pressure controller receives a setpoint pressure as a command and data over a wireless channel, and computes a head pressure offset by turning the pump off and measuring the supply and return pressures.