Abstract: 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.

Abstract: A sphygmomanometer includes a main body mounted with a pump, a belt, and a cuff structure. The cuff structure having a band shape is disposed facing an inner circumferential surface of the belt in a freely separable manner from the inner circumferential surface of the belt. One end of the cuff structure is attached to the main body. The cuff structure includes a bag-shaped pressure cuff that extends along a circumferential direction of a measurement target site, a bag-shaped sensing cuff that extends in the circumferential direction across an artery passing portion of the measurement target site, and a back plate that is inserted between the pressure cuff and the sensing cuff. A blood pressure is calculated based on a pressure of a pressure transmission fluid contained in the sensing cuff.

Abstract: 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.

Abstract: 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.

Abstract: A thigh compression device and technique to control, time, delay and/or prevent excessive early venous enhancement relative to arterial enhancement and thereby improve and/or enhance MRA images, including peripheral MRA images, is disclosed. In one embodiment, the present invention uses a curved strip of material which is longer on the superior edge and shorter along the inferior edge. When wrapped around the conical shape of the thigh of a subject, for example, a human, the thigh compression device more uniformly conforms to and/or fits around the thigh, providing more even/uniform compression as well as reducing, minimizing and/or eliminating significant movement of the thigh compression device towards the knees of the subject. A snug fit on the thighs may also enable the thigh compression device to be inflated with less fluid, which is faster and less cumbersome for the operator.

Abstract: A connector for an inflatable garment that detects a valid connection with a pump.

Abstract: An inflatable compression device configured to apply a compressive force to a puncture site of a patient's vessel, such as an artery is disclosed. The hemostasis device may comprise a location indicium disposed on an inside surface of an inflatable bladder portion of the device so as to be disposed in close proximity to the skin of the patient to improve alignment of the compression device with the puncture site.

Abstract: A sphygmomanometer includes: a sensing cuff that includes a second sheet disposed to face the pressing member's inner circumferential surface and a first sheet facing the second sheet; a fluid storage control part providing a control of supplying and storing the pressure-transmitting fluid into sensing cuff in a worn state wherein the pressing member and sensing cuff are worn on the wrist; and a blood-pressure calculating part calculating a blood pressure based on a pressure of the pressure-transmitting fluid stored in the sensing cuff. The fluid storage control part supplies fluid in the worn state such that the first and second sheets are in contact with each other in a region corresponding to an ulna, a region corresponding to a radius, and a region corresponding to a tendon while first and second sheets are separated from each other in regions corresponding to two arteries that are radial and ulnar arteries.

Abstract: A blood pressure measurement cuff is a blood pressure measurement cuff to be attached such that it wraps around a measurement site and includes: a curler that is flexible and curves so as to naturally conform to the measurement site; an air bladder containing the curler due to being wrapped around the inner side and outer side of the curler; an inner cloth attached to an outer surface on the measurement site side of the air bladder; and an outer cloth attached to an outer surface on the side opposite to the measurement site of the air bladder.

Abstract: A cuff-type monitoring device, for collecting cardiovascular data relating to an individual user, comprising a control unit housing and a cuff assembly coupled or attached to the control unit housing, the cuff assembly comprising an inner layer, an inflatable bladder, a cuff holder, forming an structural resilient armature of the cuff assembly, an intermediate sheet, an outer band, wherein the cuff assembly is configured, in use, to surround a upper limb of the individual, with the inner layer in contact with the upper limb, wherein control unit housing comprises at least a pump configured to inflate the inflatable bladder, wherein the intermediate sheet is made in an inextensible, i.e. non-stretchable, fabric and there is provided a border joint or seam at least on three sides on a peripheral border of the inflatable bladder, the border joint joining and securing together the inner layer, the inflatable bladder, the intermediate sheet, and the an outer band.

Abstract: A method for manufacturing a blood pressure information measurement apparatus includes the following steps: forming a hole in a flexible resin sheet; inserting a connecting pipe into the hole; overlaying a first end portion and a second end portion of the flexible resin sheet such that an inner side of the first end portion contacts an outer side of the second portion; welding a location at which the first end portion and the second end portion overlap to form a first welded portion, such that the flexible resin sheet forms a tube-shaped body having a first end and a second end; flattening the tube-shaped body; welding the first end and the second to form two second welded portions, such that the tube-shaped body forms a bladder having two long sides and two short sides; and welding portions of the resin sheet which overlap along a first long side to form one or more partial welded portions.

Abstract: 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.

Abstract: The present application discloses a hemostatic device comprising a flexible, adjustable closure device that is adapted to fit the lower leg and foot of patients having a range of anatomical differences in leg and foot shape and size, the hemostatic device further comprising at least one compression element that is adapted to apply targeted pressure to a surgical vascular access site located on the patient's lower leg or foot. In some embodiments, the compression element is moveable such that it may be used to apply pressure to a select one of common arterial access points located on the lower leg or foot.

Abstract: A blood pressure cuff is defined by a first sheet, having an opening, and a second sheet. The second sheet is attached to a bottom of the first sheet to form an interior inflatable portion between the first sheet and the second sheet, with the opening of the first sheet fluidly interconnecting the interior inflatable portion with an exterior of the cuff. The blood pressure cuff is made from a single type of material and can be recycled, biodegradable, or composted.

Abstract: A low-cost contour cuff for surgical tourniquet systems comprises: a sheath containing an inflatable bladder, the sheath having an arcuate shape, an outer surface and a centerline equidistant between first and second side edges; a securing strap non-releasably attached to the outer surface and formed of substantially inextensible material having a shape that is predetermined and substantially flat, wherein the strap includes a bending portion near a first strap end and a fastening portion near a second strap end, and wherein the bending portion is adapted to allow twisting of the bending portion out of the substantially flat shape to facilitate positioning of the fastening portion into any of a plurality of positions in the substantially flat shape; and fastening means for releasably attaching the fastening portion of the securing strap to the outer surface whenever the sheath is curved into a position for surrounding a limb.

Abstract: The invention relates to a device and a method for stopping bleeding at the puncture sites of vessels of patients undergoing an extracorporeal treatment, in particular dialysis. The device has a controller which controls the introduction of fluid into an expandable chamber arranged on a strip-shaped basic element and/or draining from the chamber. The invention also relates to an evaluation unit having at least one sensor for measuring the degree of filling of the chamber. Furthermore, the invention relates to a medical technical treatment unit as an arrangement of a hemodialysis machine and the device.

Abstract: A device for use in preventing stroke is provided. The device may include an expandable member that expands from a non-expanded configuration to an expanded configuration. The expandable member is located at a neck of a patient. An associated method is provided.

Abstract: A hemostatic device can inflate an inflatable portion without using a separate dedicated instrument, can reduce an unpleasant feeling of a wearer, and can prevent a site where bleeding is to be stopped from being unintentionally and unnecessarily compressed. The hemostatic device has a band for being wrapped around a limb, an inflatable portion that is inflated by injecting gas, an injection part that is configured to inject gas into the inflatable portion, and a flow route that permits communication between the inflatable portion and the injection part. The flow route includes a backflow preventer which prevents gas from flowing out to the injection part from the inflatable portion. The injection part is located on the band, and includes holes which penetrate the injection part in a direction intersecting a perpendicular line to a region of the band where the injection part is located.

Abstract: A tourniquet apparatus having an optical tourniquet interface for safe personalization, a safe transfer key and a pressure controller. The optical tourniquet interface communicates with the pressure controller and is operable for contactlessly reading and authenticating a machine-readable instrument symbol associated with a tourniquet cuff if it matches stored instrument authentication data and for contactlessly reading machine-readable personalization data associated with the cuff. The optical tourniquet interface presents a personalization parameter value if the machine-readable instrument symbol has been authenticated. The safe transfer key enables the user to selectively transfer the presented value of the personalization parameter to the pressure controller only if the pressure controller is inoperable. The pressure controller is releasably connectable to the tourniquet cuff and responsive to the transferred value of the personalization parameter.

Abstract: An abdominal aortic tourniquet having one-piece member for the bladder and cover portions and whose bladder has a triangular cross-sectional shape when inflated that significantly increases the amount of point pressure such that the intended artery is properly occluded. The one-piece bladder/cover design provides for a reduction in cost of materials and provides for a more compact piece as compared to prior designs. The abdominal aortic tourniquet uses a single piece of weldable and gas impermeable fabric that is configured in a novel manner to create a three-dimensional, pneumatic piston while also serving as storage/transport cover, attachment structure, and major component of the belt member.

Abstract: A compression garment having first and second sections includes a stay up device for supporting the compression garment in position on the body. The stay up device is constructed to operatively engage a portion of the body to positively locate the stay up device, and thereby the garment relative to the body.

Abstract: A self-stabilizing pneumatic abdominal aortic tourniquet that utilizes a semi-ridge retaining strap, a ratcheting retaining buckle, and an elastic guide cord on the lower penetrating end of a wedge-shaped bladder. A rigid baseplate is supported by a waist belt having a width identical with the waist belt so that the baseplate provides a stable base for positioning the bladder over a selected area of the patient's abdomen. The air bladder is affixed to the underside of the baseplate, which is initially kept in a deflated condition collapsed against the baseplate, and includes an elastic cord, such as a shock cord, configured to bias the tip of the wedge or “V” shaped bladder in the middle of the baseplate. An air source connected to the air bladder causes inflation and penetration of the lower edge of the bladder into the patient's abdomen thereby causing aorta occlusion.

Abstract: A blood pressure cuff may comprise an alignment component, a sleeve, and a tapered inflatable bladder disposed within the sleeve. The tapered inflatable bladder may have a width that increases as the distance from the alignment component increases, and the tapered inflatable bladder and the alignment component may be configured to position the blood pressure cuff around a limb having a blood vessel and a circumference, such that at a position coincident with the blood vessel, the width of the tapered inflatable bladder is about 40% of the circumference of the limb. A method of using such a blood pressure cuff may comprise placing the alignment component at the position coincident with the blood vessel of the limb, wrapping the cuff around the limb such that the width of the tapered inflatable bladder overlaying the blood vessel is about 40% of the circumference of the limb, and inflating the bladder.

Abstract: A connector for an inflatable garment that detects a valid connection with a pump.

Abstract: A system for diverting emboli within a patient can include a device that detects a presence of emboli in a first blood vessel of a patient. A compression member can be aligned, with a second blood vessel of the patient when a collar supporting the compression member is positioned at, least partially around a portion of the patient. In response to, the detection device, a controller can actuate the compression member, when the presence of emboli is detected, from an unactuated state to an actuated state in which at least a portion of the compression member (i) is closer to the second blood vessel than while in the unactuated state and (ii) compresses and limits blood flow through the second blood vessel.

Abstract: A device to increase intra-pelvic compartment pressure for the controlling of internal hemorrhages is presented. The device controls internal hemorrhaging by supplementing the occlusion effectiveness of a pneumatic tourniquet with a shaped device that increases the overall internal pressure in a human compartment, such as the inguinal area, to assist in the cessation of bleeding in that region. One side of the device includes a flat base that is adapted to be placed against a patient at the targeted body site. The other side has a generally corrugated shape that is sized to receive an inflatable, wedge-shaped bladder from the pneumatic tourniquet. The overall shape of the invention includes a tapered end that corresponds with the inferior angle of the pubic rami and pelvic area generally so that when pressed against the patient by the pneumatic tourniquet bladder a uniform distribution of pressure occurs over the inguinal area.

Abstract: A device to increase intra-abdominal compartment pressure for the controlling of internal hemorrhages is presented. The device controls internal hemorrhaging by supplementing the occlusion effectiveness of a pneumatic tourniquet with a shaped device that increases the overall internal pressure in a human compartment, such as the upper abdomen, to assist in the cessation of bleeding in that region. One side of the device includes a flat base that is adapted to be placed against a patient at the targeted body site. The other side has a generally corrugated shape that is sized to receive an inflatable, wedge-shaped bladder from the pneumatic tourniquet. The overall shape of the invention includes a tapered upper end that corresponds with the inferior angle of the lower ribs in a human torso so that when pressed against the patient by the pneumatic tourniquet bladder a uniform distribution of pressure occurs over the upper abdomen region.

Abstract: A hemostatic device has a flexible band that can be wrapped around a hemostasis-requiring site of a limb, a securing portion that secures the band in a state where the band is wrapped around the limb, and an inflation portion that interlocks with the band, and that inflates when a fluid is injected. The inflation portion has a plurality of convex portions in a width direction orthogonal to a longitudinal direction of the band when the inflation portion inflates.

Abstract: A blood pressure cuff includes a first bladder having a width, and a length transverse to the width. The blood pressure cuff also includes a second bladder connected to the first bladder and a port fluidly connected to at least one of the first and second bladders.

Abstract: In an approach, a processor receives classified data, wherein the classified data has been output by a second processor. A processor adjusts a count based on the classified data. A processor determines whether the count is greater than a pre-set threshold, wherein the pre-set threshold is set by a switching module of the processor. Responsive to determining that the count is greater than the pre-set threshold, the processor triggers an alarm of a pre-set alarm length, wherein the pre-set alarm length is set by the switching module of the processor.

Abstract: A blood pressure cuff is defined by a first sheet, having an opening, and a second sheet. The second sheet is attached to a bottom of the first sheet to form an interior inflatable portion between the first sheet and the second sheet, with the opening of the first sheet fluidly interconnecting the interior inflatable portion with an exterior of the cuff. The blood pressure cuff is made from a single type of material and can be recycled, biodegradable, or composted.

Abstract: Disclosed are methods and apparatus for regulating tourniquet cuff pressure based on a personalized tourniquet pressure (PTP) to facilitate safe performance of surgical and medical procedures. The apparatus includes a dual-purpose tourniquet cuff adapted to encircle a region of a patient to provide both a sensor during a first time period and an effector during a second time period. An effector module communicates pneumatically with an inflatable bladder of the cuff for maintaining pressure in the bladder near a PTP during the second time period to safely stop penetration of arterial blood past the cuff. A pulsation sensor that communicates pneumatically with the inflatable bladder during the first time period senses and characterizes pressure pulsations that are indicative of penetration of arterial blood into the region of a patient encircled by the cuff.

Abstract: An abdominal aortic tourniquet having one-piece member for the bladder and cover portions and whose bladder has a triangular cross-sectional shape when inflated that significantly increases the amount of point pressure such that the intended artery is properly occluded. The one-piece bladder/cover design provides for a reduction in cost of materials and provides for a more compact piece as compared to prior designs. The abdominal aortic tourniquet uses a single piece of weldable and gas impermeable fabric that is configured in a novel manner to create a three-dimensional, pneumatic piston while also serving as storage/transport cover, attachment structure, and major component of the belt member.

Abstract: A topical cooling compressive hemostasis wound healing device and methods thereof for affecting a percutaneous access site wound or an acute surgical wound. The device delivers and transports cooling to affect and control vasculature and musculoskeletal motions surrounding the injury site during the blood coagulation, hemostasis, and wound healing phases. The device has a viscoelastic and thermally conductive surface to deliver and transport an adjustable compressive pressure to resist outward blood flow, thus improving patient safety and clinical outcomes. The device is anatomically conforming and treats not only the specific injury site, but also its surrounding anatomical structures together as means to prevent unpredictable delayed hemostasis breach. The device provides comfort to the patient by allowing mobility upon wound healing, thus reducing back pain and strain resulting from being in a constrained position for a prolonged period of time which is known to cause additional medical events.

Abstract: A blood pressure cuff includes an alignment tab, a sleeve, and an inflatable bladder disposed within the sleeve. The inflatable bladder includes a first rectangular section having a first width, a second rectangular section having a second width, wherein the second width is larger than the first width, and a tapered section extending between the first rectangular section and the second rectangular section. The tapered section may be linearly tapered or a curved taper. A length from an edge of the alignment tab to the second end of the first rectangular section adjacent the tapered section is approximately equal to a minimum arm circumference for the blood pressure cuff.

Abstract: A method and apparatus for applying pressure to the abdomen of a patient to facilitate the insertion of a colonoscope is characterized by the use of a tensile compression device in the form of an elastic band which is wrapped around the patient's abdomen and secured in place. The tension of the band is adjusted to apply a desired degree of pressure to the patient's abdomen to reduce loops in the patient's colon so that the colonoscope can be fully inserted into the colon with minimal discomfort to the patient. The ends of the device are connected together when the desired degree of tension is obtained so that constant pressure and support are provided to the patient's colon. Addition pressure can be manually applied simultaneously with the pressure from the tensile device to reduce or eliminate more distal loops in the colon.

Abstract: A hemostatic device is provided to stop bleeding at a puncture site on the wrist of a patient, the device comprising a transparent flexible band to be wrapped at the site where the bleeding is to be stopped, a curved frame having an inner peripheral side and possessing a first curved portion in its first half and a second curved portion in its second half, a first balloon provided on the inner peripheral side in the first half of the curved frame and a second balloon provided on the inner peripheral side in the second half of the curved frame, the first balloon being larger than the second balloon. The bleeding from radial artery is stopped by compressing the radial artery at the puncture site using inflation of the first balloon and radial artery flow is increased by compression of ipsilateral ulnar artery using inflation of the second balloon.

Abstract: A tourniquet cuff includes a first sheet, a second sheet, and a seal joining the first sheet and second sheet to form an inflatable bladder. A securing strap is attached to the cuff. The cuff encircles the limb so that the bladder overlaps upon itself. A stiffener fits inside the bladder and sized to extend substantially the length of the bladder but not the entire bladder length, and to fit completely within the seal. A tubular port is connected to the bladder for directing gas into the bladder from a tourniquet instrument to which the port may be releasably connected, and a cuff marking weld is located on an outer surface of the cuff, having a shape selected to form a symbol or indicia that is visible to a user.

Abstract: A junctional and truncal tourniquet and hip-girdling pelvic sling device for maintaining a desired amount of tension surrounding a person's hips and pelvis to securely support and stabilize a pelvis that has been fractured and to secure a pressure applying device with a preferred amount of tension so that blood vessel-occluding pressure can be applied to stem hemorrhaging. The device may be wrapped around a patient's torso and may include inflatable pressure application bladders useful to occlude blood vessels proximal to an injury on a limb. A stabilizing support device may carry an inflatable pressure application bladder and a separate and removable pressure-concentrating member. An auxiliary strap may be connected to the stabilizing support device and used to keep the junctional and truncal tourniquet and the inflatable pressure application bladder in place on a patient's torso.

Abstract: A hemostatic device is provided to stop bleeding at a puncture site on the wrist of a patient, the device comprising a transparent flexible band to be wrapped at the site where the bleeding is to be stopped, a curved frame having an inner peripheral side and possessing a first curved portion in its first half and a second curved portion in its second half, a first balloon provided on the inner peripheral side in the first half of the curved frame and a second balloon provided on the inner peripheral side in the second half of the curved frame, the first balloon being larger than the second balloon. The bleeding from radial artery is stopped by compressing the radial artery at the puncture site using inflation of the first balloon and radial artery flow is increased by compression of ipsilateral ulnar artery using inflation of the second balloon.

Abstract: Preferably, an intravenous assist device includes at least, a pneumatic tourniquet portion, a pneumatic barrier having a first side contactingly adjacent the pneumatic barrier, a tissue compression portion contactingly adjacent a second side of said pneumatic barrier, and a pneumatic gate in fluid communication with each the pneumatic tourniquet portion and the tissue compression portion. The pneumatic gate promotes an inflation of the tissue compression portion only after full inflation of the pneumatic tourniquet forms a tourniquet. The pneumatic gate is formed between the pneumatic tourniquet portion and the tissue compression portion by an aperture only.

Abstract: An abdominal aortic tourniquet having one-piece member for the bladder and cover portions and whose bladder has a triangular cross-sectional shape when inflated that significantly increases the amount of point pressure such that the intended artery is properly occluded. The one-piece bladder/cover design provides for a reduction in cost of materials and provides for a more compact piece as compared to prior designs. The abdominal aortic tourniquet uses a single piece of weldable and gas impermeable fabric that is configured in a novel manner to create a three-dimensional, pneumatic piston while also serving as storage/transport cover, attachment structure, and major component of the belt member.

Abstract: Bleeding from blood vessels located in difficult-to-compress regions of the body (especially the abdomen, pelvic or groin region) is controlled by the use of a portable, small-footprint belt-like device that contains multiple inflatable bladders. The inflatable bladders are selectively positioned and inflated over exsanguinating blood vessels, thereby exerting pressure to stop the bleeding. The device may also be used to provide perfusion support in low flow disease states such as hemorrhagic shock and cardiac arrest.

Abstract: A blood pressure sleeve includes a first sheet having a top side and a bottom side and a second sheet having a top surface and a bottom surface. The second sheet is attached to the first sheet and defines an inflatable portion, the first and second sheets each having a fluid impermeable surface. The inflatable portion includes an opening sized for receiving a port that interconnects the exterior of the sleeve with the interior of the inflatable portion and in which the first sheet includes a slotted portion opposite the port and aligned therewith to receive the port when the sleeve is wrapped about the limb of a patient, and in which at least a portion of the wrapped cuff is treated to reduce frictional effects.

Abstract: A portable pneumatic abdominal aortic tourniquet for occlusion of the abdominal descending aorta to restrict blood supply to a non-compressible arterial hemorrhage in or below the inguinal region is presented. The tourniquet includes an adjustable waist strap for securing it around the abdomen of a patient and a windlass rod connected to the waist strap to selectively tighten the strap as needed to tightly secure it to patient. A directed air bladder is mounted to the waist strap having a generally “V” shaped construction and is expanded for exerting directed pressure against the abdomen. Upon inflation of the air bladder and adjustment of the windlass, occlusion or restriction of blood flow through the abdominal descending aorta will occur which will achieve cessation of hemorrhage in or below the inguinal area or achieve other therapeutic effects like elevated blood pressure to enhance CPR or blood flow control to the lower extremities.

Abstract: A tourniquet hazard suppressor suppresses an action initiated by a user of a surgical tourniquet system having a touchscreen user interface if implementation of that action by the system may be hazardous to a surgical patient.

Abstract: Disclosed is a method and apparatus for regulating tourniquet cuff pressure based on a personalized tourniquet pressure (PTP) to facilitate safe performance of a surgical procedure. The apparatus includes a dual-purpose tourniquet cuff adapted to encircle a region of a patient limb to provide both a sensor during a pre-surgical time period and an effector during a surgical time period. An effector module communicates pneumatically with an inflatable bladder of the cuff for maintaining pressure in the bladder near a PTP during the surgical time period to safely stop penetration of arterial blood past the cuff. A pulsation sensor that communicates pneumatically with the inflatable bladder during the pre-surgical time period senses and characterizes pressure pulsations that are indicative of penetration of arterial blood into the region of the limb encircled by the cuff.

Abstract: A pre-fabricated pneumatic tourniquet apparatus and related methods are provided. The tourniquet is easy to apply, ensures consistent and even circumferential pressure, is light weight, provides standard life saving operation, and can be utilized in any setting or situation. The pneumatic tourniquet apparatus is comprised of a bladder, a reservoir chassis, a retaining cover, a receiver and a slider. The bladder is elongated in shaped—long enough to wrap around most human limbs.

Abstract: A method and device for reducing the damaging effects of radiant energy, blast, or concussive events includes applying pressure to at least one jugular vein to reduce the egress of blood from the cranial cavity during or before the incidence of the imparting event. Reducing blood outflow from the cranial cavity increases intracranial volume and/or pressure of the cerebrospinal fluid to reduce the risk of traumatic brain injury and injuries to the spinal column. Reducing blood outflow further increases the intracranial pressure and volume, and thereby increases the pressure and volume of the cochlear fluid, the vitreous humor and the cerebrospinal fluid to thereby reduce the risk of injury to the inner ear, internal structure of the eye and of the spinal column.

Abstract: Tissue compression devices having pressure indicators and methods of using the same. The tissue compression devices provide feedback to a user with respect to the pressure being applied to selected tissue at a selected location such as a radial artery to assist the user in applying the desired amount of pressure to the tissue (such as the pressure needed to achieve hemostasis at an access site). The pressure indication may be provided by a ring indicator that moves between two configurations (e.g., a concave configuration and a convex configuration), a bellow chamber in a housing, a bladder located below a bladder window, etc.