Abstract: Disclosed herein is a combination wound and injury treatment apparatus comprising a tubular body having a first opening, a second opening, a relatively inflexible outer wall having an outer surface and an inner surface.

Abstract: The present invention generally relates to a device for applying a pulsating pressure to a local region of the body and applications thereof. The device may be used to increase the blood flow in a local region of the body, and in preferred embodiments provides a device for regulating the core body temperature of a patient.

Abstract: A hand and wrist restorer and method of use having a cuff which is capable of grasping a portion of the outer skin of a limb and securing the fascia tissue thereunder together with a support which allows a user to provide a distal force upon the limb while rotating or moving the distal portion of the limb whereby a stretch of the fascia tissue occurs.

Abstract: A compression garment assembly comprises a compression garment adapted for placement on a body part in a self-retaining configuration and for removal from the body part. The compression garment has at least one inflatable bladder for applying compression to the body part. A portable controller unit is adapted for fluid connection to the inflatable bladder and is configured for cyclically inflating the bladder. The compression garment and portable controller unit are configured so that the portable controller unit must be disconnected from the compression garment before the compression garment can be removed from the body part. Loss of the portable controller unit by, for example, accidental disposal with the compression garment is thus prevented.

Abstract: This invention provides methods of diagnosing and treating syndromes of reversion to fetal consciousness in a neonate.

Abstract: A device (900) includes a leg engaging section (101) and a foot engaging section (102 intersecting at a heel receiver (103). The leg engaging section and the foot engaging section defining a leg insertion aperture (104). A first compression wrap member (301) and a second compression wrap member (302) extend from the leg engaging section. An inflatable bladder (501) can be disposed along the leg engaging section between the leg insertion aperture and a compressible cushion layer (902). The inflatable bladder can be selectively inflatable through a connection tube (502) exiting the inflatable bladder at a non-orthogonal angle (504) relative to an edge (507) of the inflatable bladder. The leg engaging section can define at least one channel (1002) to permit the connection tube to exit the device.

Abstract: The apparatus comprises an inflatable sleeve 6 to be wrapped around a limb, typically a thigh, of a patient. The sleeve 6 comprises three inflatable chambers 3, 4, 5. Inflation is controlled by a pump 1 so that the distal chamber 3 is inflated first to a low pressure to act as a tourniquet, followed by inflation of the central chamber 4 to a pressure to drive fluid flow upwards, and then inflation of the proximal chamber 5 to a low pressure to act as a tourniquet and deflating both the distal 3 and central 4 chambers to produce a negative pressure gradient down-stream in the limb causing fluid to be drawn up the limb. This cycle is repeated a number of times over a period of two minutes before allowing the limb to rest for two minutes, resulting in increased mean arterial blood flow.

Abstract: A compression garment apparatus includes a compression garment and a pressurizer. The pressurizer intermittently pressurizes a therapeutic bladder on the compression garment and pressurizes a support bladder on the compression garment to enhance the fit of the compression garment and maintain the therapeutic bladder in position with respect to a target compression zone on a body part on which the garment is worn. The support bladder may be selectively pressurized when needed based at least in part on sensed physical characteristics.

Abstract: A compression garment apparatus including a compression garment and a pressurizer. The pressurizer intermittently pressurizes a therapeutic bladder on the compression garment and maintains a baseline pressure in the therapeutic bladder to maintain the therapeutic bladder in position with respect to a target compression zone on a body part on which the garment is worn. The baseline pressure is adjusted in response to sensed physical characteristics.

Abstract: A method of forming a compression device including providing a wicking layer having a perimeter generally corresponding to a perimeter of the device and a surface area comprising the area bounded by the perimeter of the wicking layer. A bladder segment is provided including opposing bladder layers of air-impermeable bladder material defining an inflatable bladder. The bladder segment has a surface area less than the surface area of the wicking layer. An outer layer is provided having openings therein. A portion of the wicking layer is not overlaid by the bladder segment by virtue of the bladder segment having a smaller surface area than the surface area of the wicking layer. The portion of the wicking layer not overlaid by the bladder segment is overlaid by openings in the outer layer. A compression device is also described.

Abstract: Method and device for diagnosing and/or treating sleep apnea and related sleep disorders, such as snoring and respiratory effort-related arousals, includes an inflatable implement which is applied to the external surface of the chest and/or abdomen (Vest). Pressure is caused to rise to a predetermined positive value. The rate of airflow into and/or out of said Vest is monitored, whereby the Vest Flow is displayed or processed to obtain information about the breathing characteristics of the patient.

Abstract: A compression treatment system is provided that detects the number of and type of garments connected thereto. The system includes a plurality of ports, valves connected thereto and a number of garments having one or more bladders. The bladders are in fluid communication with a fluid source in a pneumatic circuit, to provide compression therapy once a user confirms the number of and type of garments connected to the system for use by a patient. A single pressure sensor communicates with a plurality of detected bladders located in the one or more garments.

Abstract: A pneumatic compression garment comprises a flexible member for placement on a limb of a human body. A bladder in the flexible member defines an inflatable chamber. The bladder has an opening through which the inflatable chamber is inflated. A port mounted on the bladder has an air inlet adapted for communication with a source of pressurized air and an air outlet in communication with the inflatable chamber via the opening in the bladder. Pressurized air is delivered from into the inflatable chamber for inflating the inflatable chamber and thereby applying a compression force to the limb when the flexible member is in place on the limb. Noise attenuating means associated with the bladder opening is provided for reducing noise from air flow through the opening into the inflatable chamber.

Abstract: A compression sleeve includes a wicking layer secured to bladder material defining an inflatable bladder along a seamline. Fibers of the wicking layer extend through the seamline to allow fluid wicked by the wicking layer from the wearer's skin to evaporate to the atmosphere.

Abstract: A compression device for the limb comprising a sleeve adapted to surround the limb, the sleeve comprising an inelastic layer and a cell constructed from an inner part joined to an outer part by one or more side walls so that the cell has a box-like configuration, the inner part being adapted to conform to the shape of the limb when the cell is inflated to provide an even pressure to the limb.

Abstract: A compression device (100) configured to provide compression therapy is provided. The compression device includes a wrap (101) having an outer face (105) defining a proximal edge (106), a distal edge (107), a first side edge (108), and a second side edge (109). The second side edge may include a plurality of attachment tabs (110,111,112). An index line (113) can be disposed on at least one of the plurality of attachment tabs. A measurement scale (114) can be disposed along the outer face. The measurement scale can include longitudinal boundaries (115,116) identifying a range within which the index line should position for the compression device to provide an appropriate fit for compression therapy when the compression device is wrapped about a patient's limb.

Abstract: A heel protector (100) includes a leg engaging section (101) and a foot engaging section (102) intersecting at a heel receiver (103). The leg engaging section (101) and the foot engaging section (102) define a leg insertion aperture (104). The leg engaging section (101) defines at least one aperture (203) disposed in an ankle region (205) to permit a connection tube (1002) extending from an inflatable bladder (901) of a compression device (800) to pass therethrough. The heel protector (100) and compression device (800) work together as a rehabilitation system (1300).

Abstract: A device for use by an individual for sexual pleasure varying in form, i.e. shape, during its use and allowing for the user to select multiple variations of form either discretely or in combination and for these dynamic variations to be controllable simultaneously and interchangeably while being transparent to the normal use of the device, including the ability to insert, withdraw, rotate, and actuate the variable features manually or remotely. According to embodiments of the invention localized and global variations of devices are implemented using fluidics and electromagnetic pumps/valves wherein a fluid is employed such that controlling the pressure of the fluid results in the movement of an element within the device or the expansion/contraction of an element within the device.

Abstract: The present invention is to provide a gas mist pressure bathing cover which is simple in a structure and easy in pressurization.

Abstract: A HFCWO apparatus includes a housing having a port, a therapy system carried by the housing and operable to deliver HFCWO therapy to a patient in accordance with a set of operating parameters, and a memory device couplable to the port for storing at least a portion of the set of operating parameters. The therapy system may be operable in accordance with the portion of the set of operating parameters stored in the memory device. The apparatus may comprise a wireless transmitter carried by the housing and operable to wirelessly transmit data relating to HFCWO therapy to a wireless device, such as a printer, PC, a PDA, and the like.

Abstract: A compression device for the foot comprising: a wrap adapted to surround the foot, the wrap comprising at least two bladders which when inflated conform to the shape of the foot to provide compression, the bladders being positioned on the wrap so that a first bladder focuses compression on the heel of the foot and a second bladder focuses compression on the arch of the foot; a channel attached to each bladder for independently delivering fluid to each bladder; and a controller attached to the channels that generates and independently controls the flow of fluid to the bladders.

Abstract: A compression garment for applying compression therapy to a wearer's body including a compression sleeve having a proximal edge and a distal edge. The sleeve includes at least one bladder. A tube is attached to the bladder. A connector on the tube connects the tube to a source of compressed fluid for inflating the bladder. The distal edge of the compression sleeve has a first portion and a second portion jutting distally from the first portion.

Abstract: A foot cuff that is inflatable to apply compression to the foot to promote blood flow has a bladder formed of two layers of material secured together. An outer layer includes a foot-underlying portion that has a greater thickness and rigidity that an opposing inner layer. The outer layer directs expansion of the bladder upon inflation in the direction of the inner layer and toward the foot for increasing compressive force applied to the foot.

Abstract: A compression garment assembly comprises a compression garment adapted for placement on a body part in a self-retaining configuration and for removal from the body part. The compression garment has at least one inflatable bladder for applying compression to the body part. A portable controller unit is adapted for fluid connection to the inflatable bladder and is configured for cyclically inflating the bladder. The compression garment and portable controller unit are configured so that the portable controller unit must be disconnected from the compression garment before the compression garment can be removed from the body part. Loss of the portable controller unit by, for example, accidental disposal with the compression garment is thus prevented.

Abstract: The subject matter of the invention relates to therapy wraps for the application of compression and/or thermal therapy to a patient. The wraps are formed of at least two layers of material which are sealed together to form at least one cavity between them. The wraps may be used in conjunction with a therapy machine which fills the cavity or cavities of the wraps with fluid such as a gas and/or a liquid. The unique shapes of the wraps are particularly suitable for providing therapy to the human body. The shapes permit the manipulation of the wraps around various portions of the human body such as the shoulder, back and foot.

Abstract: A method of forming a compression sleeve for being wrapped around a leg of a wearer includes securing two layers of flexible material together to at least partially define first and second adjacent flexible sections. The sleeve includes a first inflatable bladder and a second inflatable bladder disposed more proximally than the first inflatable bladder when the sleeve is wrapped around the leg. The method further includes securing a structural component to the sleeve such that the structural component extends generally between the first and second adjacent flexible sections to maintain a spacing between the sleeve sections lengthwise of the leg when the sleeve is wrapped around the leg. The bladder layers are joined together at least at two weld points on opposite sides of the structural component to locate the structural component on the sleeve so as to maintain the spacing of the adjacent sleeve sections.

Abstract: A compression bag having an upper portion for applying a pressure at least to the abdominal area of a patient, and a lower portion for applying a pressure to at least a part of the patient's legs, the bag comprising a back part, a second, front part and a closure means configured for detachably attaching the parts to each other; a separating insert configured for being detachably attached to at least one of the back and front parts of the bag, at least at the lower portion of the bag, to separate between left and right regions of the first and second parts, thereby forming pants in said bag defined by said regions and said insert; and a plurality of inflatable cells in the first and second parts of the bag and in the separating insert, that are sealingly separated from adjacent inflatable cells and configured to be individually inflated and deflated.

Abstract: A reservoir includes a reservoir body portion and a collecting portion. The reservoir body portion having a wall defining an interior volume for containing fluidic media, the reservoir having a first port in the reservoir body portion to be in fluid flow communication with the interior volume, the first port for expelling fluidic media from the interior volume as a plunger is moved within the reservoir. The collecting portion having a wall defining a volume in fluid flow communication with the interior volume, the volume of the collecting portion for collecting gas bubbles in the fluidic media as the fluidic media is expelled through the first port from the interior volume of the reservoir body portion, the reservoir having a second port in the collecting portion to be in fluid flow communication with the volume of the collecting portion, the second port for receiving fluidic media into the reservoir.

Abstract: A compression device for providing compression treatment to a limb of a wearer includes a compression garment positionable on the limb of the wearer. The garment includes an inflatable bladder for providing compression treatment to the limb. A controller is adapted for fluidly connecting to the inflatable bladder and configured for inflating and deflating the bladder during a compression cycle. The controller has an exhaust port positioned to direct exhaust fluid through the bladder so exhaust fluid flows over the limb of the wearer to cool the limb.

Abstract: A compression garment including a bladder having a reduced inflatable volume. Connector elements positioned inside an inflatable chamber of the bladder limit expansion of the bladder for limiting a fluid volume required for fully inflating or expanding the bladder. A controller inflates and deflates the inflatable chamber for imparting compression therapy on a body part on which the garment is worn. The reduced inflation volume of the inflatable chamber reduces the demand on a pump of the controller.

Abstract: A method of forming a compression sleeve for being wrapped around a leg of a wearer includes securing two layers of flexible material together to at least partially define first and second adjacent flexible sections. The securing of the two layers of flexible material includes securing two bladder layers together to define a first inflatable bladder and a second inflatable bladder disposed more proximally than the first inflatable bladder when the sleeve is wrapped around the leg. The first bladder forms at least a part of the first flexible sleeve section and the second bladder forms at least a part of the second flexible sleeve section. The method further includes securing a structural component to the sleeve such that the structural component extends generally between the first and second adjacent flexible sections to maintain a spacing between the sleeve sections lengthwise of the leg when the sleeve is wrapped around the leg.

Abstract: A two layer compression garment measuring system that displays a pressure indicia when the garment is stretched, wherein the pressure indicia is displayed by moving from a position under an opaque layer of material (at low or no pressure) to a position under a window or transparent or translucent layer of material (at higher pressure). When the indicia can be seen by an observer through the window or transparent or translucent layer, then the higher pressure has been reached. The viewed indicia optionally displays the pressure level. In various optional designs, the location of attachment between the two spaced-apart locations is adjustable, or the length of the upper layer is adjustable such that the attachment location can be aligned with the indicia. A design having a free ended upper layer is also included.

Abstract: A compression sleeve for being wrapped around a leg of a wearer includes adjacent flexible sleeve sections. At least one of the sleeve sections has an air bladder therein adapted to inflate for compressing a portion of the leg. A structural component is secured to the sleeve and extends generally between the flexible sleeve sections to maintain a spacing of the adjacent sleeve sections lengthwise of the leg when the sleeve is wrapped around the leg. Bladder layers are joined together to form the air bladder. The bladder is joined together at least at two weld points on opposite sides of the structural component to locate the structural component on the sleeve so as to maintain the spacing of the adjacent sleeve sections.

Abstract: An extended term resuscitation system includes a plurality of inflatable cuffs adapted to extend around separate portions of the anatomy of a patient (i.e. the chest, abdomen and legs) for enhancing the circulation when inflated/deflated periodically. A primary low-pressure-high-volume air compressor is in fluid communication with each of the cuffs through individual air handlers. The air handlers are formed with an inflation and a deflation diaphragm valve which, under the control of an electronic timer and a pneumatic circuit, connect the respective cuff to the output of the compressor for inflation or to the atmosphere for deflation. A secondary air compressor provides air under suitable pressure to the pneumatic circuit for the control of the diaphragm valves. As an option the operator may change the cyclical rate and cuff pressure. A ventilator provides oxygen to the patient in selected volumes or on demand.

Abstract: A connector for attaching at least one flexible tube to a fluid passage of another object includes a body and at least one connector port on the body. At least one tube port projects from the body and is adapted for fluid communication with the connector port. A portion of the body at least partially surrounds the tube port and defines an interior space containing at least a portion of the tube port. The tube port is sized and shaped for being received in an end of the flexible tube to establish fluid communication with the flexible tube. A tube retainer is at least partially disposed in the interior space defined by the portion of the body and has an engaging portion disposed in relation to the tube port to restrain the flexible tube from lateral movement with respect to the tube port.

Abstract: A compression garment for applying compression to a part of a wearer's body includes a flexible member, an inflatable bladder defining an inflatable chamber, and a port for communication between a source of pressurized air and the inflatable chamber. The garment also incorporates noise attenuation. The noise attenuation can include noise attenuating members on an air impingement surface of the inflatable bladder.

Abstract: A compression device for the foot comprising: a wrap adapted to surround the foot, the wrap comprising at least two bladders which when inflated conform to the shape of the foot to provide compression, the bladders being positioned on the wrap so that a first bladder focuses compression on the heel of the foot and a second bladder focuses compression on the arch of the foot; a channel attached to each bladder for independently delivering fluid to each bladder; and a controller attached to the channels that generates and independently controls the flow of fluid to the bladders.

Abstract: A compression device includes an inflatable member and a frame member extending along substantially an entirety of the perimeter edge margin of the inflatable member. The frame member imparts rigidity to the inflatable member so that rigidity of the inflatable member at the perimeter edge margin is greater than the rigidity of the inflatable member inside the perimeter edge margin.

Abstract: A therapeutic compression device for applying compression force to a patient. The device is constructed of multiple layers, at least two of which are fluid-tight. At least two fluid-tight layers define a fluid-tight chamber that has a smaller surface area than the overall device. Fluid supplied to the fluid-tight chamber causes compressive force to be exerted on a patient. Preferably at least one layer is a fluid permeable material. An additional layer of fluid permeable material may be also be added to ensure a fluid permeable barrier exists between the fluid-tight chamber and a patient.

Abstract: Apparatuses for reducing migraine headache pain comprising head-contacting expanses of compressible material having pressure-versus-deflection characteristics possessing plateau conditions defined by ranges of compressive material deflections associated throughout with substantially constant material compression produced by an applied, material-compressing pressure which is slightly less than that pressure which, when applied to the anatomy, occludes anatomical, venous-return blood flow, and shells substantially surrounding, and contacting, the compressible-material expanses, appropriately sized, and operable, with the apparatuses in place on a wearers' heads, to place the compressible material in the expanse in its characteristic “plateau” condition of compression, wherein such compression, at every location, is a non-adjustable value dependent entirely upon the fit-spacing at that location between a wearer's head and the inside of the shell.

Abstract: An apparatus and method for treatment of patients suffering from lymphedema. The apparatus includes a multiple chamber sleeve positioned in a wrap around fashion on a body extremity to be treated. The chambers are sequentially inflated and maintained so until all chambers are inflated and then all the chambers are simultaneously deflated except the proximal end chamber to move edema fluids out of the afflicted area. The apparatus includes the capability of applying interferential therapy either alone or in combination with compression therapy. Advantageously, the sleeve chambers capture pressurized air when applied thereto, at designated locations, so as to form air pockets that can selectively apply isolated points of pressure, and in combination with the application of electrical current to a patient's affected area, provide effective lymphedema therapy without disrupting normal vascular and lymphatic functioning.

Abstract: The invention to provide a carbon dioxide mist pressure bath system which is possible to cause the carbon dioxide mist to be absorbed efficiently through the skin and mucous membrane of the human living-body. The system comprises a carbon dioxide supply means 11; a liquid supply means 21; a carbon dioxide mist generating means 31 for pulverizing and dissolving carbon dioxide and the liquid to generate the carbon dioxide mist; a living-body cover member 41 for covering the skin and mucous membrane of the living-body and formed with a space of sealing inside the carbon dioxide mist generated by the carbon dioxide mist generating means 31; a liquid circulation means 61 for again supplying a liquid collected in the carbon dioxide mist generating means 31 into the carbon dioxide mist generating means; and a pressurization means 81 for pressurizing the inside of the living-body cover member 41.

Abstract: A system for monitoring the use of a home-based medical apparatus providing medical therapy to a patient incorporates communication technology to permit communication from the operated component of the medical apparatus via a cellular network to a Cloud storage site. The operated medical apparatus can report any operational function to the Cloud storage site, which can be accessed by appropriate medical professionals or caregivers by contacting the Cloud storage site through a cellular network. If the medical apparatus is properly configured, the medical professional could change certain operational functions of the medical apparatus through the Cloud by communicating with the medical apparatus directly. Alternatively, a medical caregiver can visit the home-based patient to modify the operation of the medical apparatus. By limiting the number of visits needed to maintain proper operation of the medical apparatus, a medical caregiver can provide services to a larger number of patients.

Abstract: The present invention relates to a deep pressure therapy system. The system comprises an inflatable component and a shell component. The inflatable component can be removably attached to the shell component to form a wearable assembly. The inflatable component is shaped to conform to a portion of a body of an individual, and comprises an inflatable bladder having an inlet port and an outlet port for passage of a fluid. The bladder comprises a plurality of depressions which are generally evenly-distributed over a portion of the bladder. In some embodiments, the depressions are circular welds. In some embodiments, the depressions are three-dimensional welds. The bladder may additionally comprise weld strips. The shell component may comprise one or more stretchable strips which are expandable as safety feature.

Abstract: The present invention generally relates to a device for applying a pulsating pressure to a local region of the body and applications thereof. The device may be used to increase the blood flow in a local region of the body, and in preferred embodiments provides a device for regulating the core body temperature of a patient.

Abstract: A pneumatic compression garment comprises a flexible member for placement on a limb of a human body. A bladder in the flexible member defines an inflatable chamber. The bladder has an opening through which the inflatable chamber is inflated. A port mounted on the bladder has an air inlet adapted for communication with a source of pressurized air and an air outlet in communication with the inflatable chamber via the opening in the bladder. Pressurized air is delivered from into the inflatable chamber for inflating the inflatable chamber and thereby applying a compression force to the limb when the flexible member is in place on the limb. Noise attenuating means associated with the bladder opening is provided for reducing noise from air flow through the opening into the inflatable chamber.

Abstract: A negative/positive pressure, thermal energy therapy device is described in this application. The present invention uses a conventional negative pressure, thermal energy device and/or an alternative embodiment thereof and adds a significant modification. The modification is that positive pressure, not just ambient pressure, is at least occasionally applied to the patient's body contained in the negative pressure, thermal energy device.

Abstract: An therapy system is operable to deliver a plurality of respiratory therapies to the patient and has an assessment system operable to assess the efficacy of at least one of the respiratory therapies. The therapy system may be operable to deliver any one or more of the following therapies: a positive expiratory pressure (PEP) therapy, a nebulizer therapy, an intermittent positive pressure breathing (IPPB) therapy, a cough assist therapy, a suction therapy, a bronchial dilator therapy, and the like. The assessment system may comprise any one or more of the following devices: a flow meter, a spirometer, an electronic stethoscope, a tympanic thermometer, a pulse oximeter, a respiration rate monitor, and the like.

Abstract: A therapeutic compression device for applying compression force to a patient. The device is constructed of multiple layers, at least two of which are fluid-tight. At least two fluid-tight layers define a fluid-tight chamber that has a smaller surface area than the overall device. Fluid supplied to the fluid-tight chamber causes compressive force to be exerted on a patient. Preferably at least one layer is a fluid permeable material. An additional layer of fluid permeable material may be also be added to ensure a fluid permeable barrier exists between the fluid-tight chamber and a patient.

Abstract: A device to compress the limb of a living being includes a user interface, a programmable logic controller, a power source, a source of fluidic pressure, valves with ports in fluidic connection with the source of fluidic pressure, other valves, and a first and second inflatable bladders, wherein the programmable logic controller is programmed to cause the repeating sequence of inflating the first inflatable bladder by manipulating the ports of the valves, after a first preset period of time, deflating the first inflatable bladder and allowing the pressure within the first inflatable bladder to inflate partially the second inflatable bladder by manipulating the ports of the valves. The source of fluidic pressure can be a self-contained pump, a connection to fluidic pressure in a health care facility, or a pressurized canister. The power source can be a battery. The device may extend the life of the power source.