Abstract: Systems and methods for a manually operable volume-adjustable ventilation device. In some embodiments, the device includes a reservoir with an inlet mechanism, an outlet mechanism, and a volume adjuster configured to move a volume adjustment limit of the reservoir and change an expressed maximum volume of the reservoir. The reservoir may have a body comprising a plurality of movable walls defining an enclosed volume. The walls of the reservoir may be movable such that movement expresses the volume adjustment limit of the reservoir. In addition, the walls may be operably connected by movable structures such that two adjacent walls are be configured to rotate around substantially orthogonal axes with respect to each other when the reservoir moves from an uncompressed to a compressed state. Methods of ventilating a patient that involve the manually operable volume-adjustable ventilation device are also disclosed.

Abstract: The improved hydraulic system utilizes a secondary hydraulic force control circuit that changes the gripping force on the load independently of movement of the clamp arms.

Abstract: Embodiments relate to devices, systems and methods of assisting blood flow return to the heart from a limb. The device comprising a wearable garment (115) and a compression apparatus (110) embedded in the garment (115) for applying an external compression according to a compression sequence to a muscle of a limb of a user based on real-time measurements regarding a cardiac cycle having a diastolic phase and systolic of the user and real-time measurements of muscle activity. The compression sequence is synchronized to comment when both the local blood flow at the limb is in the diastolic phase and the muscle is in a non-contracted state.

Abstract: Arterial compression methods and apparatus may include high-frequency pulse waveforms applied to one or more cuffs on a limb. Additionally or alternatively, they may include high inflation rate configurations, such as may be used to more quickly inflate a cuff on a limb. They may also include inflating a cuff on a limb using a plurality of inflation pulses.

Abstract: A method for automatically configuring a medical device with user-specific configuration data includes determining, by a first medical device, that the first medical device is being placed into service to provide medical therapy to a patient, wherein the first medical device is a replacement medical device for a second medical device that was previously placed into service to provide medical therapy to the patient in accordance with user-specific configuration data stored on the second medical device, communicating, by the first medical device, data indicative of the first medical device being placed into service, after communicating the data indicative of the first medical device being placed into service, obtaining, by the first medical device, the user-specific configuration data stored on the second medical device, and configuring, by the first medical device, the first medical device to provide therapy in accordance with the obtained user-specific configuration data.

Abstract: A fluid source comprises a connector assembly for connecting a fluid supply device to either a first therapy device or to a second therapy device. A controller automatically provides a first configuration of a user interface associated with a first therapy when a supply connector is operatively coupled to the first therapy device and provides a second configuration of the user interface associated with a second therapy, different than the first configuration, when the supply connector is operatively coupled to the second therapy device. A hanger assembly is provided to hang the fluid source on different support structures. The fluid source also comprises a housing with a watershed region to shed liquid away from the user interface.

Abstract: A therapeutic garment for treatment of over-shunting headaches and method for use of the same are disclosed. In one embodiment, the therapeutic garment includes a waistband and an abdominal portion that extends from the waistband to encircle the abdomen and hips from the groin to the costal margin of a person wearing the therapeutic garment. A binder portion is partially coincident to the abdominal portion. The binder portion includes a pressure subassembly including a network of interconnected channels having an inflation valve accessible from an exterior of the abdominal portion. The pressure assembly, when selectively inflated, provides a qualified degree of compression to distend an epidural venous plexus of the person wearing the therapeutic garment. The therapeutic garment may further be fashioned into a brief, a tank top, or include leg extensions.

Abstract: A system and a method for managing patient therapy protocols are disclosed. The system includes a patient support apparatus for supporting a patient, a first input device for use by a first caregiver, a second input device coupled for use by a second caregiver, a location system for determining a location of the first caregiver, and a therapy management system. The therapy management system receives a location of the first caregiver and a selection of a patient therapy protocol, which includes a location requirement. The therapy management system then determines whether the first caregiver location input signal satisfies the location requirement before initiating the selected patient therapy protocol or notifying the second caregiver if the location of the first caregiver does not satisfy the location requirement.

Abstract: The present invention provides a tourniquet apparatus that can be inflated hands-free. The tourniquet apparatus includes a sleeve and a pressurizing device to provide pressurized air to inflate the sleeve as required. In the tourniquet apparatus, the pressurizing device includes a pedal that is foot-operated and can be used to regulate the flow of pressurized air therein.

Abstract: A method for therapeutically affecting the circulation of blood in a person in combination with or with medication to treat a medical condition includes the steps of administering a composition for treating a circulatory condition, providing a source of high pressure air in fluid communication with a plurality of air pressure actuated valves, each of the valves mounted on, and in fluid communication with, an inflatable bladder disposed within a cuff removably attached about at least one of the feet, calves, thighs, buttocks of the person; providing a source of low pressure aft in fluid communication with the plurality of valves, wherein a constant pressure is exerted against said valves; and controlling inflation of the bladders in a predetermined sequence, magnitude of inflation pressure and period of time during a cardiac cycle of the person and as a function of the person's physiological reaction to said composition.

Abstract: A percussive pulsing therapy device configured for delivering pulsating or intermittent airflow to a patient device, such as a patient vest. The percussive pulsed air device may have an airflow generator for controlling amplitude of the percussive pulsed air and a pulse frequency control module for controlling frequency of the percussive pulsed air. In some embodiments, the pulse frequency control module may have a rotatable fan blade, such as a circular fan blade having one or more cutout portions. In some embodiments, the rotating fan blade may have one or more channels configured to redirect percussive pulsed air. Moreover, a percussive pulsed air device of the present disclosure may have a dampening element flowably coupled to an inlet of the pulse frequency control module. In some embodiments, at least one inlets of the pulse frequency control module may be arranged on a different airflow plane than one or more outlets.

Abstract: A detection system for patient therapy devices is provided. A controller is coupled to the detection system. The controller determines a desired operational parameter based on the type of patient therapy device detected.

Abstract: A DVT and temperature therapy system. A temperature therapy blanket includes a fluid bladder for delivering hot and/or cold therapy to a patient. The temperature therapy blanket may also include an air bladder for providing compression. The DVT system functions independently of the temperature therapy. This Abstract is provided to comply with rules requiring an Abstract that allows a searcher or other reader to quickly ascertain subject matter of the technical disclosure. This Abstract is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims. 37 CFR 1.72(b).

Abstract: A dermatologic hair-regrowth-inhibiting apparatus is disclosed which is cordless and sufficiently compact as to be hand-held. A self-contained housing is configured for gripping by a person's hand for cordless manipulation in a hair-regrowth-inhibiting procedure. A light source and electrical circuit are contained within the housing. The circuit includes one or more batteries for energizing the light source to produce output light pulses. A light path within the housing includes an aperture through which eye-safe light pulses are propagated out of the housing having properties sufficient for at least temporary hair-regrowth inhibition. A diffuser is disposed along the light path to reduce the integrated radiance to an eye-safe level.

Abstract: A cordless, hand-held dermatologic hair-regrowth-inhibiting apparatus may include: a self-contained housing configured for gripping by a person's hand for cordless manipulation in a hair-regrowth-inhibiting procedure; a light source comprising one or more diode laser bars within the housing; a direct drive electrical circuit within the housing comprising one or more batteries for energizing the light source to produce output light pulses, wherein the electrical circuit does not include any storage capacitors that energize the light source by capacitor discharge; and a light path within the housing including an aperture through which the output light pulses are propagated out of the housing having properties sufficient for at least temporary hair-regrowth inhibition.

Abstract: A compression device controller for use with a compression garment includes a pressurized fluid source (e.g., a pump), a manifold in fluid communication with the pressurized fluid source, a pressure sensor in communication with the manifold, at least two bladder ports, and at least two two-way valves. The pressure sensor is arranged to measure a signal representative of pressure in the manifold. Each bladder port is connectable in fluid communication to a respective inflatable bladder of the compression garment. Each two-way valve is in fluid communication with the manifold and with a respective bladder port. Each two-way valve is actuatable to control fluid communication between the manifold and the respective bladder port.

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: Apparatus and methods are provided to control a device, such as a light emitting dermatologic or cosmetic treatment device, and ensure that the device is in contact with skin while also determining the pigmentation level of skin. One or more light sources contact the skin and one or more detectors measure spectral remission from the skin. The obtained remission measurements are compared with known skin spectral remission values, and calibration allows measurements of absolute remission to be converted to fractional remission values. Skin pigmentation levels are compared to known base-line levels to determine and control appropriate treatment parameters. A temperature sensor allows correction for temperature variations. The apparatus may or may not be incorporated into the treatment device.

Abstract: A compression garment includes a plurality of inflatable bladders, a valve body, an inlet, an exhaust, and a rotary valve. The plurality of inflatable bladders is positionable around a limb of a wearer. The manifold defines a plurality of bladder ports, each bladder port in fluid communication with a respective inflatable bladder. The inlet defines an inlet port, and the exhaust defines an exhaust port. The rotary valve is in fluid communication with the inlet port, the exhaust port, and the plurality of bladder ports. Rotation of the valve in a first direction controls fluid communication between the inlet port and the plurality of bladder ports, and rotation of the valve in a second direction, opposite the first direction, controls fluid communication between the exhaust port and the plurality of bladder ports.

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: The proposed method and devices provide for an effective improvement of the blood flow in the vessels of a human's extremities due to generation of an ante-grade pressure wave of blood synchronized with phases of the cardiac cycle with the help of compression impulses. The devices provide an improved accuracy of the time and amplitude characteristics of the compression impulses and functioning in modes of generation both the ante-grade wave and external counter-pulsation.

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 therapeutic garment includes at least one first expandable bladder configured to underlie a wearer's left shoulder blade, at least one second expandable bladder configured to underlie the wearer's right shoulder blade, and an actuator configured to alternatingly (a) expand the at least one first expandable bladder from a collapsed state to an expanded state such that the wearer's torso is rolled in a rightward direction and (b) expand the at least one second expandable bladder from a collapsed state to an expanded state such that the wearer's torso is rolled in a leftward direction.

Abstract: An integrated tourniquet system enables the user to establish with suitable warnings, and with timely user confirmation, individualized maximum pressure levels in the cuff that may be above normal maximum pressure levels. Also provided is a rapid and accurate method of testing for leakage in the cuff and connectors. The system is adapted for communication to remote devices for receiving and providing information relating to the pressure levels, tests, etc.

Abstract: The present invention relates to a massage device, and provides a palm massager comprising a plurality of air bags corresponding to each part of the palm, an air pump, a plurality of electromagnetic valves for controlling the air charging and air discharging of the plurality of air bags, a main control module and a plurality of load driving modules.

Abstract: A system and method for rejuvenating skin through ablation using a handheld device (200) having a removable treatment component (213) with an abrasive material on one surface of the component which surface is on a portion of the treatment component (213) configured to conform to a skin surface. The system further includes application of other elements to facilitate skin recovery and rejuvenation processes.

Abstract: A mobile compression integument for applying controllable scrolling or intermittent sequential forces, such as compression forces, to the body and limbs of a user comprises an elongated fabric body sized to encircle a limb of a user, one or more shape-changing elements carried by the fabric body and configured to apply a compression pressure to the limb through the fabric body upon changing shape in response to a stimulus, and a micro-processor based controller for selectively actuating the one or more shape-changing elements to reduce the effective diameter of the integument encircling the limb, to thereby apply pressure to the limb.

Abstract: A device for compressive treatment of a body part includes a compression member, adapted to at least partly encircle the body part, and an actuation unit, arranged to tighten the compression member to provide a compressive force to the body part. Methods are provided for its therapeutic, cosmetic and non-therapeutic use and operation.

Abstract: A patient support for supporting a patient includes an inflatable mattress defining a support surface and a pneumatic system for inflating the inflatable mattress. The pneumatic system includes a pressurized reservoir for holding pressurized air and selectively releases pressurized air from the reservoir to the mattress.

Abstract: An electronic device (100) includes a component portion (101) and a strap (102). The strap defines an air chamber (402) therein having a corresponding volume. A driver (403) is disposed in the component portion at a first port (404) between the component portion and the strap. A frequency detector (405) is disposed in the component portion at a second port (406) between the component portion and the strap. A control circuit (407) is operable with the driver and the frequency detector and is configured to determine a peak of a resonant frequency over a frequency range in the air chamber with the frequency detector that are a function of the corresponding volume and are responsive to signals produced by the driver, correlate the frequency of pressure variations determined with a user input, and perform an operation based upon the user input.

Abstract: Apparatus, systems, and methods are sized and configured to effectively and efficiently augment the flow of fluid within body vessels, not only during conditions in which a patient is bedbound and immobile, but also in conditions when the individual is out of bed, and completely mobile and ambulatory.

Abstract: Apparatus, systems, and methods are sized and configured to effectively and efficiently augment the flow of fluid within body vessels, not only during conditions in which a patient is bedbound and immobile, but also in conditions when the individual is out of bed, and completely mobile and ambulatory.

Abstract: Apparatus, systems, and methods are sized and configured to effectively and efficiently augment the flow of fluid within body vessels, not only during conditions in which a patient is bedbound and immobile, but also in conditions when the individual is out of bed, and completely mobile and ambulatory.

Abstract: Apparatus, systems, and methods are sized and configured to effectively and efficiently augment the flow of fluid within body vessels, not only during conditions in which a patient is bedbound and immobile, but also in conditions when the individual is out of bed, and completely mobile and ambulatory.

Abstract: A support surface system provides alternating pressure therapy and low air loss therapy simultaneously using a single pump. The system includes a plurality of cells. Each cell has a foam-filled lower chamber and an upper chamber. Fluid communication between the lower and upper chambers is controlled by a normally closed valve that opens if the pressure within the lower chamber exceeds a predetermined threshold pressure. Pressurized air is alternatingly supplied to the lower chambers of a first subset of cells and the lower chambers of a second subset of cells, thereby providing alternating pressure therapy. When the pressure in the lower chamber exceeds the threshold, the valve opens to allow air from the lower chamber to flow into the upper chamber. Air is expelled from the upper chamber through perforations therein, to remove moisture and humidity and possibly reducing the temperature of the micro-climate beneath a patient.

Abstract: The present invention provides an air massage device for a bed. The air massage device includes at least one air wave generator disposed on the bed. The air wave generator includes a shell, a permanent magnet disposed in the shell, a coil electromagnet movably disposed in the shell and a membrane attached to the coil electromagnet. When the coil electromagnet is powered by an alternating current, the coil electromagnet moves reciprocatingly relative to the permanent magnet along with the membrane so that the membrane generates an air wave which is adapted to massage people on the bed.

Abstract: A portable micro air pump includes a body, an air output port and a quick-disconnect air tube connector. The body is hand-sized, and has a user control and information panel with a power on/off button switch and a button switch for choosing which type of therapy garment is to be utilized, limb or foot. Status lights within the information panel show on/off and battery status, the therapy garment selected and alarm states of which the user needs to be aware. Within the body are an air compressor with an air output tube, a battery power source, and an electronic circuit board. The electronic circuit board has functional subunits including: a controller, a timer, a memory, an input/output interface, a pressure sensor, a status light driver and a power control driver.

Abstract: A portable article for administrating therapy to a user includes a device positioned along the area of the body requiring therapy. At least one power pod is associated with the device and the power pod simultaneously applies a firs force component perpendicular to the user's body surface and a second force component parallel to the user's body surface. An illustrative embodiment is a vest worn by the user during therapy.

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 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: A single system may provide to a patient: temperature change, remote ischemic conditioning, and sometimes both concurrently. The system may include a patient unit that includes an inflatable bladder, and a duct having a cavity. The patient unit is intended to be applied around a patient's limb. A temperature subsystem can force a flow of a first fluid through the cavity so that the first fluid can exchange heat with the patient's limb. The pressure subsystem may force a fluid into the bladder, to establish pressure against the limb. A controller may control both the temperature subsystem and the pressure subsystem, so as to control the treatment received by the patient.

Abstract: The invention provides a compression device for the limb of a mobile patient. The device includes an inflatable sleeve adapted to surround the limb; a conduit attached to the sleeve for delivering fluid to the sleeve; and a portable, wearable controller attached to the conduit that generates and controls the flow of fluid in the device.

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 device is disclosed for generating controlled pneumatic pressure to a human body to achieve mucus clearance from the pulmonary system. Controlled pneumatic pressure consisting of individual vibratory pressure and constrictive pressure variations are generated and applied to the thorax to promote mucus clearance. The vibratory pressure variation is channeled to a pressure receiver secured to the upper thorax of the body, and the constrictive pressure variation is channeled to a pressure receiver secured to the lower thorax of the body. The vibratory pressure variation serves to loosen the mucus, while the constrictive pressure variation provides the motive force that promotes mucus expulsion from the pulmonary system.

Abstract: A method for therapeutically affecting the circulation of blood in a person in combination with or with medication to treat a medical condition includes the steps of administering a composition for treating a circulatory condition, providing a source of high pressure air in fluid communication with a plurality of air pressure actuated valves, each of the valves mounted on, and in fluid communication with, an inflatable bladder disposed within a cuff removably attached about at least one of the feet, calves, thighs, buttocks of the person; providing a source of low pressure air in fluid communication with said plurality of valves, wherein a constant pressure is exerted against said valves; and controlling inflation of said bladders in a predetermined sequence, magnitude of inflation pressure and period of time during a cardiac cycle of the person and as a function of said person's physiological reaction to said composition.

Abstract: A high frequency chest wall oscillation (HFCWO) therapy system includes an inflatable garment, an air pulse generator operable to produce oscillating pressure pulses that are communicated to the inflatable garment, at least one hose to interconnect the air pulse generator with the inflatable garment and to communicate the oscillatory pressure pulses from the air pulse generator to the inflatable garment. The air pulse generator is sized, shaped, and configured so as to occupy a volume no greater than about 1,200 in.3 and to weigh no more than about 17 lbs.

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: 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 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.

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: Methods and systems are disclosed for determining patient compliance for using a compression therapy device. The systems may include a compression therapy sleeve and a controller having a non-transitory memory device. During a therapy session, the controller may record in the memory device operational therapy data obtained from sensors associated with the controller and/or sleeve. The controller may calculate a compliance metric based in part on the therapy data. The controller may then communicate the data or metric to one or more recipients. The methods may include allowing the patient to transfer a removable memory device from the controller to a personal computer, and uploading the therapy data or metric stored on it to a recipient website. Alternative methods may include the patient receiving the metric from the controller at the end of the therapy session, and then providing the metric to a recipient by phone.