The present application discloses devices and methods for monitoring the performance of a hemostasis device during a hemostatic procedure.

This application discloses embodiments for a device contemplated for use by combat medics and first responders for rapid treatment of Zone 2 penetrating neck injuries. The device incorporates a support arm and an occlusion arm featuring an occluding head which is applied to the wound. In certain embodiments, the support arm is in the form of a detachable neck support which attaches to a laryngoscope blade.

A multifunctional pill box carrying pouch is revealed. The pill box carrying pouch includes at least one pill box, at least one pouch, and at least two long ties. The pill box is a rigid rectangular box while the two long ties form a single longer tie. The respective long ties are detachably connected to the pouch by the two second connecting members. The pill box carrying pouch has a limb-carrying mode and a waist-carrying mode. Users can select the limb-carrying mode of the pill box carrying pouch when user's limb is injured and a support for the limb is required. By the two long ties arranged adjacent to each other and tightened around an arm or a leg of the human body, the pill box carrying pouch is closely attached to the wound on the limb for supporting wounded area or for hemostasis.

A radial artery sheath assembly includes a cuff that is wearable around a patient's wrist and a receiver is integrated into the cuff. The cuff is inflatable to compress an incision in the patient's wrist to achieve homeostasis for stopping bleeding. A ring is removably attachable to the cuff and a radial sheath is extendable through the ring to retain the radial sheath in the incision in the user's wrist when the ring is attached to the cuff. The ring is inflatable for compressing the radial sheath in the ring to inhibit the radial sheath from being removed from the incision. A lock is coupled to the ring and the lock releasably engages the receiver in the cuff for attaching the ring to the cuff.

We report a method of treating an epileptic seizure in a patient, comprising: detecting said epileptic seizure, based on body data from said patient; and reducing a flow of blood to a brain of said patient in response to said detected seizure; wherein said reducing is effected by: increasing the parasympathetic input to said patient's heart, such as by electrically stimulating a parasympathetic nervous structure, applying cooling energy to a sympathetic nervous structure, or administering a cholinergic or a sympatho-blocking agent to said patient. We also report a medical device system configured to implement the method. We also report a non-transitory computer readable program storage unit encoded with instructions that, when executed by a computer, perform the method.

A hemostatic device includes a main body belt to be wound around at least a part of a patient's hand/wrist, and a pressing member positionable at a puncture site of the patient's hand to compress the puncture site. The main body belt includes a distal region, and a proximal region farther from the patient's fingertip than the distal region. The distal region includes an anchor portion having a space portion configured to receive the patient's finger and open at opposite ends to receive the patient's finger while the fingertip protrudes distally beyond the anchor portion. The pressing member allows the puncture site to be viewed from outside while the pressing member is at the puncture site, and is fixed to the distal region at a position spaced from the insertion port on an inner surface of the main body belt at which the insertion port is provided.

An adhesive pad for use with a hemostasis device comprising a footplate having a top surface and a receiving device positioned on the footplate, the adhesive pad comprising: (1) a flexible backing layer having a bottom surface, a central portion having an opening, a first side portion, and a second side portion; (2) an adhesive layer applied to the bottom surface of the backing layer; and (3) a release layer removably secured to the adhesive layer. The opening in the central portion of the backing layer is sized to fit the receiving device of the hemostasis device, and the adhesive layer applied to the bottom surface of the first and second side portions of the backing layer is configured to adhere to and extend beyond the top surface of the footplate.

An adhesive pad for use with a hemostasis device comprising a footplate having a top surface and a receiving device positioned on the footplate, the adhesive pad comprising: (1) a flexible backing layer having a bottom surface, a central portion having an opening, a first side portion, and a second side portion; (2) an adhesive layer applied to the bottom surface of the backing layer; and (3) a release layer removably secured to the adhesive layer. The opening in the central portion of the backing layer is sized to fit the receiving device of the hemostasis device, and the adhesive layer applied to the bottom surface of the first and second side portions of the backing layer is configured to adhere to and extend beyond the top surface of the footplate.

A fistula bandage comprising a bandage and an adjustment device for adjusting a tension of the bandage, where the adjustment device comprises: a first engagement portion connected to a first end of the bandage; and a second engagement portion connected to a second end of the bandage; wherein the second engagement portion comprises: a base having a first sliding slot and connected to the second end of the bandage; a moving member slidingly engaged with the base and connected to the first engagement portion; a driving mechanism supported on the base and driving the moving member to slide in a first direction relative to the base; and a stopping mechanism connected to the driving mechanism. The driving mechanism drives the first engagement portion to move relative to the second engagement portion, thereby achieving the purpose of adjusting the tension of the bandage.

A non-pneumatic tourniquet including a tourniquet ring configured to resiliently constrict around a body part of a subject. The tourniquet ring defines a plurality of openings. A handle moves the tourniquet ring onto the body part and includes a first strap having a first end secured to the tourniquet ring at one of the openings and a second end secured to the tourniquet ring at one of the openings. A second strap has a first end secured to the tourniquet ring at one of the openings and a second end secured to the tourniquet ring at one of the openings.