Edema is the abnormal accumulation of fluid in connective tissue. Edema typically includes swelling of a user's extremity and results from a combination of passive venous congestion and salt and water retention. Edema may be systemic or localized to a particular region of the body. Edema is sometimes also called dropsy or anasarca. Edema can arise in response to injury or post-operatively, when fluid is released by inflammatory cells and other mechanisms. Edema can also result from the abnormal function or other impairment of the lymph vessels. Fluid accumulation in the tissue of the limbic extremities, for example the ankle or foot, is a physical manifestation associated with a number of different edemic conditions. For example, edema can arise in response to an injury of an extremity, such as an ankle sprain. Edema, particularly that Edema localized in the lower extremities, can be painful and can act to restrict normal circulation, wound healing, injury rehabilitation, and can increase the likelihood of infection.
Prior art devices for treating edema often include the use of a therapy system applied to the ankle or foot to provide a compression for controlling the edema, for example the edema that might arise from either an inversion or eversion sprain or other injury. One such edema-control therapy system is disclosed in U.S. Pat. No. 4,590,932 issued to Wilkerson, incorporated herein by reference in its entirety. The compression applied by the Wilkerson therapy system helps prevent fluid from accumulating to a substantial degree in the area of the trauma and to reverse initial accumulation at that site. This is understood to have a beneficial effect on the patient and the acceleration of the healing process. Other exemplary systems are disclosed in U.S. Pat. No. 5,976,099 issued to Kellogg, incorporated herein by reference in its entirety.
Although the systems described in the art can work, their relatively insensitive compression protocols render them suboptimal. There remains a need for improved systems and methods that reduce edema and reduce the accumulation of fluid and swelling at the sight of a trauma.
The systems and methods described herein, include, among other things, orthopedic appliances and methods of applying therapy to the limb of a patient for the purpose of reducing edema. In one aspect, the invention provides a therapy system that may be fitted over a patient's limb about a joint for the purposes of treating limb injury by reducing or milking edema. In other aspects, the invention provides for systems and methods that may be adapted to provide intermittent massaging of lymph fluid through the lymphatic vessels in a direction toward the heart, which is toward the center of a patient's torso and away from the patient's affected limb.
More particularly, in one aspect, the systems and methods described herein include a brace for applying therapy to a limb. The brace comprises a rigid outer shell, having an inner surface, adapted to be applied over proximal and distal portions of a limb. In certain embodiments, the rigid shell is adapted to be applied over the proximal and distal portions of a leg about at least one joint, e.g., a knee, an ankle, or an elbow. The brace also includes one or more bladder assemblies. A bladder assembly includes one or more inflatable fluid bladders that are attached to the inner surface of the rigid outer shell along a portion of the limb. A plurality of inflatable fluid bladders may be used. In certain embodiments, a proximal bladder assembly is used and includes a plurality of fluid bladders positioned along a proximal portion of the patient's limb. A distal bladder assembly may also be used and includes one or more inflatable fluid bladders positionable along a distal side of the limb. The brace may be configured to have a plurality of proximal bladder assemblies and/or a plurality of distal bladder assemblies, with one or more of such assemblies having a plurality of inflatable fluid bladders.
The one or more inflatable fluid bladders in the proximal and distal bladder assemblies are positioned so as to help facilitate the milking of edema away from the site of an injury. In certain embodiments, the bladders are positioned in the proximal and distal assembly at least partially transverse to each other. An inflatable fluid bladder in the proximal bladder assembly may overlap another inflatable fluid bladder in the proximal bladder assembly. In certain embodiments, each of the plurality of inflatable fluid bladders in the proximal bladder assembly are of different dimensions. An inflatable fluid bladder in the proximal bladder assembly may be positioned inside another inflatable fluid bladder in the proximal bladder assembly. Each of the plurality of inflatable fluid bladders in the proximal bladder assembly may be attached to each other using at least one of gluing, stitching and zipping.
In certain embodiments, a plurality of inflatable fluid bladders in the distal bladder assembly are positioned at least partially transverse to each other. An inflatable fluid bladder in the distal bladder assembly may overlap another inflatable fluid bladder in the distal bladder assembly. In certain embodiments, each of the plurality of inflatable fluid bladders in the distal bladder assembly are of different dimensions. An inflatable fluid bladder in the distal bladder assembly may be positioned inside another inflatable fluid bladder in the distal bladder assembly. Each of the plurality of inflatable fluid bladders in the distal bladder assembly may be attached to each other using at least one of gluing, stitching and zipping.
In certain embodiments, one or more inflatable fluid bladders substantially circumferentiates the limb. In certain embodiments, one or more of a plurality of inflatable fluid bladders in at least one of a proximal and distal bladder assemblies substantially circumferentiates the limb.
In certain embodiments, the brace comprises at least one conduit in communication with at least one inflatable fluid bladder for providing fluid. At least one of the plurality of inflatable fluid bladders in at least one of the proximal and distal bladder assemblies may include an inflation port for receiving a conduit. The brace may include or be connected to a fluid source for supplying fluid to at least one of the plurality of inflatable fluid bladders in at least one of the proximal and distal bladder assemblies. In such embodiments, the fluid source includes a fluid reservoir in fluid communication with the brace through at least one of an external and/or internal pump.
In another exemplary embodiment, the systems and methods described herein include an inflatable bladder assembly for applying therapy to a limb. The inflatable bladder assembly is positioned in the vicinity of an anatomical region of a limb and configured to apply pressure to the anatomical region. The bladder assembly includes a first inflatable bladder, a second inflatable bladder that is positioned adjacent to the first inflatable bladder, and a third inflatable bladder that is positioned adjacent to the second inflatable bladder. The first, second and third inflatable bladders are positioned with respect to each other so as to facilitate edema milking. In certain implementations, the bladders are at least partially transverse to each other. In certain embodiments, a substantial portion of the distal end of the bladder assembly includes the first inflatable bladder and a substantial portion of the proximal end of the bladder assembly includes the third inflatable bladder.
In certain embodiments, the first inflatable bladder is smaller than the second inflatable bladder and the second inflatable bladder is smaller than the third inflatable bladder. The first, second and/or third inflatable bladders may be physically coupled such that the second inflatable bladder overlaps a portion of the first inflatable bladder and/or the third inflatable bladder overlaps a portion of the second inflatable bladder. In other embodiments, the first inflatable bladder is positioned inside the second inflatable bladder and/or the second inflatable bladder is positioned inside the third inflatable bladder. At least two of the first, second and third inflatable bladders may be attached to each other using gluing, stitching, zipping or other suitable attachments.
In another aspect, the systems and methods described herein include methods for applying therapy to a limb. The methods generally include applying a multi-chambered bladder assembly about a limb and applying sequential compression and decompression to the limb by inflating and deflating the chambers in a direction from a distal portion of the limb to the proximal portion. In certain implementations the methods comprise applying a proximal bladder assembly on a proximal side of the limb about a joint, applying a distal bladder assembly on a distal side of the limb about a joint and applying compression to a limb by first inflating the proximal bladder assembly and then inflating the distal bladder assembly. The therapy may be applied to at least one of a foot, lower leg, upper leg, arm, wrist, thigh, hand and finger. In certain embodiments, the methods comprise applying at least one of the proximal and distal bladder assemblies to at least one of a lower calf area, a mid-calf area, an upper calf area, a heel region, an ankle region in the area of the maleolus, an Achilles area, a distal metatarsal area, a navicular region, a region proximal to a navicular region and distal to a maleolus region.
In certain embodiments, the methods comprise repeating the application of compression until edema in a patient's limb is reduced to a target level. In certain embodiments, this target level is achieved after a number of cycles of compression are reached, a time limit is reached, a user-selected stopping point is reached, or a therapist selected stopping point is reached.
In certain embodiments, a first bladder assembly is positioned along a patient's limb and has a plurality of inflatable bladders. The first bladder assembly may include three or more inflatable fluid bladders. In such embodiments, inflating the first bladder assembly includes first inflating one or more of the plurality of inflatable bladders in a distal portion of the first bladder assembly and then inflating one or more of the plurality of inflatable bladders in a proximal portion of the bladder assembly.
In certain embodiments, a second bladder assembly is also used and is positioned distal to the first bladder assembly along a portion of the limb. The distal bladder assembly also includes a plurality of inflatable bladders. The distal bladder assembly may include three or more inflatable fluid bladders. In such embodiments, inflating the distal bladder assembly includes first inflating one or more of the plurality of inflatable bladders in distal portion of the distal bladder assembly and then inflating one or more of the plurality of inflatable bladders in proximal portion of the distal bladder assembly.
In certain embodiments, the methods comprise deflating the proximal bladder assembly after inflating the proximal bladder assembly. In such embodiments, the methods further comprise deflating the proximal bladder assembly during inflating the distal bladder assembly. The methods may also comprise deflating the proximal bladder assembly after inflating the distal bladder assembly.
In certain embodiments, the methods comprise deflating the distal bladder assembly after inflating the distal bladder assembly. In such embodiments, the methods comprise deflating the proximal bladder assembly after deflating the distal bladder assembly. In certain embodiments, the methods comprise first deflating the proximal bladder assembly and then deflating the distal bladder assembly.
In certain embodiments, the methods include first deflating one or more of a plurality of inflatable bladders in a distal portion of a proximal bladder assembly and then deflating one or more of a plurality of inflatable bladders in a proximal portion of a proximal bladder assembly. In certain embodiments, deflating the proximal bladder assembly includes simultaneously deflating substantially all of the plurality of inflatable bladders.
In certain embodiments, the methods include first deflating one or more of a plurality of inflatable bladders in a distal portion of a distal bladder assembly and then deflating one or more of a plurality of inflatable bladders in a proximal portion of a distal bladder assembly. In certain embodiments, deflating the distal bladder assembly includes simultaneously deflating substantially all of the plurality of inflatable bladders.
The following figures depict certain illustrative embodiments of the systems and methods disclosed herein, in which like reference numerals refer to like elements. These depicted embodiments may not be drawn to scale and are to be understood as illustrative of the invention and not as limiting in any way.
The systems and methods described herein will now be described with reference to certain illustrative embodiments. However, the invention is not to be limited to these illustrated embodiments which are provided merely for the purpose of describing the systems and methods of the invention and are not to be understood as limiting in anyway.
As will be seen from the following description, the systems and methods described herein, include, among other things, orthopedic appliances and methods of applying therapy to the limb of a patient for the purpose of reducing edema. In one aspect, the systems include a therapy system that may be fitted over a patient's limb about a joint for the purposes of treating limb injury by reducing or milking edema. In other aspects, the systems and methods may be adapted to provide intermittent massaging of lymph fluid through the lymphatic vessels in a direction toward the heart, which is toward the center of a patient's torso and away from the patient's affected limb.
In certain embodiments, the outer shell 104 is constructed of any suitable rigid material such as plastics, metals or combinations thereof to provide support to the limb while ambulating. The outer shell 104 may be formed from a plurality of separate rigid parts that may be assembled together to form the brace 102. In such embodiments, a person may detach the separate rigid parts of the outer shell 104, slide a limb into the brace 102 and then re-attach the separate rigid parts to secure the brace 102. The person may optionally adjust the straps 110 to tighten or loosen the fit. In other embodiments, the outer shell 104 is formed as a unitary body that is sized and shaped as desired to fit a person's limb. As an example, the outer shell 104 is sized and shaped like a boot to fit a person's leg. In such embodiments, rigid materials are cast in a permanently continuous manner such that at least one of the inner and outer surface of the outer shell 104 is substantially seamless. The rigid outer shell 104 may be formed in other ways without departing from the scope of the invention.
In certain embodiments, the internal inflatable fluid bladders are made of any suitable gas, liquid or gel impermeable material, such as urethane, PVC films, treated nylon, and/or laminates. One or more inflatable fluid bladders may be attached to an inner surface of the outer shell 104 along the length of the brace 102. One embodiment of the brace along with the inflatable fluid bladders is depicted in
The pump 106 may be any pump mechanism capable of inflating and optionally deflating the inflatable bladders, to apply pressure to the person's limb. In certain embodiments, the pump 106 is adapted to operate the plurality of bladders to provide for a massage process that moves the edema away from the lower limb. In such embodiments, the pump 106 may be manually operated, or may be an automatic pump operated by a computer control system so that the bladders are sequentially inflated and deflated. The inflation/deflation sequence may follow a reversed sequence pressure application scheme for massaging a person's limb that is described, in more detail, with reference to
The configuration of bladders in the therapy system 100 allows for milking fluid away from the user's limb. More particularly, the zones and the bladders work in cooperation so that fluid is moved in a manner that pushes fluid first from a proximal part of the limb toward the user's torso, followed by milking the next more distal part of the limb to the already volume-reduced proximal part (e.g., zone 202 first, followed by zone 204, etc.).
In operation, the therapy system 100 depicted in
The inflatable fluid bladders may be constructed of two sheets of flexible plastic sealed around their perimeter to make a gas impermeable packet. In certain optional embodiments, the bladders 318 and 320 may be formed from a single sheet of flexible plastic material folded over onto itself and sealed along the open edge. In such embodiments, the bladders 318 and 320 are formed and sealed in a single step. The bladders 318 and 320 may be sealed by RF heat sealing or standard heatsealing techniques. In certain embodiments, Polyvinyl chloride films and polyurethane films are suitable for use in the inflatable fluid bladders. In certain optional embodiments, the bladders 318 and 320 include a layer of foam, including open cell or closed cell foam disposed therein. The layer of foam may be larger than the typical space between the patient's ankle and corresponding shell portion of the outer shell when the foam is in its fully expanded state.
In certain optional embodiments, one or more bladders 318 and 320 are disposed on the inner surface of the foam liner 312 such that they are closer to the person's limb than the foam liner 312 and outer shell 302. In such embodiments, a layer of fabric is attached to the one or more of the bladders 318 and 320. The layer of fabric may be selected based, at least in part, on its tactile and/or ventilation and/or therapeutic and/or washability properties. The layer of fabric may include a proportion of Nylon to facilitate bonding to one or more bladders 318 and 320.
Referring to
During operation, the pump 106 inflates one or more inflatable bladders in distal portion of proximal bladder assemblies 702, 704 and 706 then inflates one or more inflatable bladders in a proximal portion of proximal bladder assemblies 702, 704 and 706. Similarly, during operation, the pump 106 inflates one or more inflatable bladders in a distal portion of distal bladder assemblies 706 and 708 then inflates one or more inflatable bladders in a proximal portion distal bladder assemblies 706 and 708. The bladders are sequentially activated so that in each bladder assembly, the bladder most distal is activated first, and the other bladders are subsequently activated such that fluid is moved from the distal most portion of the zone in a proximal direction away from the zone. Bladder assembly 708 may be positioned on top of and adjacent to the upper part of the person's foot providing pressure from the most distal section of the person's leg. In certain embodiments of the four-zone system, an exemplary sequence of inflation begins by inflating bladder 711a in bladder assembly 702 and concludes by inflating bladder 714c in bladder assembly 708 as follows:
In certain embodiments, the methods comprise repeating the step of inflating one or more bladders and thereby applying compression to the limb until a desired target level is reached. The target level may include at least one of a number of cycles of compression, a time limit, a user-selected stopping point and a therapist selected stopping point. Other suitable target levels may be used without departing from the scope of the invention.
A series of deflation steps may also be included to allow the brace to optimally move fluid away from the affected limb. To this end the brace is adapted to sequentially deflate the bladders within the zones to optimize the flow of fluid away from the limb. The deflation sequences are programmed to deflate a zone at or near the same time the zone just distal begins to inflate. For example, bladder 702 begins to deflate as bladder 704 begins to fill, such that the fluid pressure decreases in bladder 702 to receive the fluid flowing from bladder 704 as a result of the filling and pressurizing of bladder 704. In an exemplary implementation, the inflation sequence identified above would include deflation steps as follows:
In certain embodiments, one or more of the bladders in the proximal bladder assemblies 702, 704 and 706 are deflated after inflation, and while inflating one or more of the bladders in the distal bladder assemblies 706 and 708. In alternative embodiments, one or more of the bladders in the proximal bladder assemblies 702, 704 and 706 are deflated after inflating one or more of the bladders in the distal bladder assemblies 706 and 708. One or more of the bladders in the distal bladder assemblies 706 and 708 may be deflated after inflation. In certain embodiments, one or more of the bladders in the proximal bladder assemblies 702, 704 and 706 are deflated after deflating one or more of the bladders in the distal bladder assemblies 706 and 708. In certain embodiments, deflating the proximal bladder assembly 702, 704 and 706 and/or the distal bladder assemblies 706 and 708 includes simultaneously deflating substantially all of the plurality of inflatable bladders. The bladders in the bladder assemblies 702, 704, 706 and 708 may be inflated and/or deflated in any sequence so as to move edema towards the user's torso.
In one aspect, the bladders, such as the bladders used with the brace shown in
In one exemplary implementation, the bladders 810a-c of
A plurality of bladder assemblies, such as assembly 800, can be configured in an inflation system, with a separate bladder assembly being positioned along the limb in operational contact with one or more anatomical regions corresponding to zones near bladder assemblies 702, 704, 706 and 708 of
The encapsulated configuration shown in
In exemplary methods of operation, the bladders of the assemblies 800, 900, 1000, 1100 and/or 1200 may be inflated and/or deflated at selected cycles to cause the movement of fluid away from the limb and toward the torso, in the direction of arrow 920. In one such implementation, in a first step, bladder “a” (810a, 902a, 1002a, 1104a, or 1204a) is inflated, which compresses the limb in the region covered by bladder “a” and pushes fluid in that region away from the region. In a second step, bladder “b” (810b, 902b, 1002b, 1104b, or 1204b) is inflated and bladder “a” is optionally deflated. In this step, bladder “b” compresses the region under bladder “b” to push the fluid received from the compression of bladder “a” toward the torso and to hinder the fluid that was pushed during the first step from flowing back into the region of bladder “a.” In a third step, bladder “c” (810c, 902c, 1002c, 1104c, or 1204c) is inflated and bladder “b” is optionally deflated, further pushing the fluid toward the torso and impeding the fluid from flowing back into the region covered by bladder “a” and bladder “b.”
The exemplary assemblies 900, 1000, 1100 and 1200 are described above as being applied to a particular zone of the user's limb. In alternative implementations, an inflation system is provided that includes plurality of inflation assemblies similar to those described, with each individual inflation assembly being configured to be applied at a different anatomical zone along the limb, such as the zones shown in
As noted above, the inflation systems may be configured to provide compression and decompression massage to the regions of one or more limbs of a patient to provide enhanced circulation and for causing fluid to flow toward the patient's torso. In certain representative embodiments, the compression pressures that may be selected for upper and/or lower pressure limits, as applicable, may be selected from those set forth in U.S. Utility application Ser. No. 10/389,449 (Berish, et al.), the entire contents of which is incorporated herein by reference in its entirety. Other exemplary pressure levels and other applications are those set forth in U.S. Pat. No. 6,463,934, U.S. Pat. No. 6,592,534, and U.S. Pat. No. 5,588,955, the entire contents of each of which are incorporated herein by reference in their entirety. In certain exemplary implementations, the pressure applied by inflating any particular inflation cell used with an inflation assembly is between about 20 to about 50 mm Hg. In certain exemplary applications, the pressure applied during inflation of an inflation cell is greater than about 50 mm Hg, even greater than about 70 mm Hg, or even greater than about 100 mm Hg. In certain applications, the pressure of an inflation cell is less than about 50 mm Hg, or even less than about 30 mm Hg, or even less than about 20 mm Hg.
In certain applications, the inflation systems described above include one or more pumps that may be assembled with the inflation assembly (such as through a direct fixation of the pump with the inflation system) or may be housed separately and connected to the inflation system through one or more tubes or other conduits. In certain applications, a particular inflation assembly is provided with a plurality of pumps, with each pump provided in a manner that is configured to independently inflate and deflate its respective particular cell within the inflation system. In certain embodiments, the inflation assembly is provided with a separate pump independently operable for inflating each inflation cell within the inflation system. By providing for a separate and independent inflation of any particular cell within the system, the inflation assembly is configured to provide variable pressures within each region, within each zone, or within any combination thereof. In certain exemplary applications, the patient and/or the attendant healthcare provider can inflate any particular cell at any particular time to any desired level of pressurization.
In other embodiments, the cycles of this inflation and deflation of the cells can also be established through the independent inflation and deflation of the particular cells within the inflation assembly. Moreover, the patient and/or the healthcare provider can provide variable levels of pressure within each particular inflation region within each particular zone in the inflation system. In another implementation, the pressure levels within a particular cell could be pre-set to a particular desired level, which could vary from one cell to another within a particular inflation assembly, and the inflation system configured to inflate and/or deflate each particular cell as desired to achieve a particular inflation and deflation sequence.
As noted, one or more pumps may be applied to inflate and deflate the bladders used in the particular inflation systems described herein. Each of the bladders described and shown in the Figures or otherwise implicated by this disclosure can be configured to receive a pump through a conduit tube or other mechanism whereby the bladder is configured with an inflation port to receive a tube from a pump or other inflation source. As noted, each bladder used in a particular inflation assembly may be separately configured to receive a pump through an interface, or the bladders may be configured to be inflatable and deflatable through a single inflation port that runs through each of them and connects to a single inflation source. As multiple inflation ports and assemblies are used, one or more pumps may be used to inflate and deflate the bladders, and the inflation may be configured through the use of a single or multiple inflation ports adapted to connect to one or more inflation sources.
The above described applications are representative of exemplary embodiments of the systems and methods described herein and are not to be understood as limiting in any way. The embodiments depicted in the figures are shown as applying to treatment of edema in a patient's lower leg; however, the invention may be readily adapted for use in treating edema in any extremity of a patient (e.g., patient's foot, lower leg, upper leg, arm, wrist, thigh, hand or finger). The embodiments described above could be adapted to provide an inflation assembly to any number of anatomical zones along a limb, and optionally configured to provide inflation bladders for operation upon any number of regions within each particular zone. For example, an inflation assembly may be provided that provides a plurality of inflation bladders in a region adjacent to an upper limb, and another plurality of bladders applied to a region adjacent to a lower zone on a limb. In certain exemplary configurations, an inflation system is provided with a plurality of inflation bladders arranged in a plurality of bladder series, with one or more series applied to one limb while one or more other series is applied to a second or other limb more limbs. In certain exemplary configurations, an inflation assembly is provided that includes inflation bladders for application to at least two or more anatomical zones along a limb, and such that each zone has one or more inflation bladders applied to one or more particular regions within each zone. Other adaptations, modifications and supplements to the systems and methods described herein may also be employed without department from the scope of the invention and such adaptations, modifications and supplements will be understood to fall within the scope of the invention.
In certain adaptations, an inflation bladder assembly such as those described above are configured for use in a computer-controlled bracing system.
In one embodiment, during operation, the brace of system 1300 is applied to the limb and the pump 1312 supplies or removes air to and from the inflatable fluid bladders within the brace. The flow of air is modulated through a software based system. Alternatively, a manually operated valve may be connected along the length of the tubing 1310 to control the flow of air and allow the flow to be stopped when a desired pressure is reached by manually closing the valve.
During operation, the circulation of fluid in the brace causes the expansion and contraction of the inflatable fluid bladders. The rigid support system 1306 helps maintain the structural integrity of the brace of system 1300 during the expansion and contraction of the inflatable fluid bladders.
The massage process described herein for controlling a pump may be programmed and executed on a conventional data processing platform such as an IBM PC-compatible computer running the Windows operating systems, a SUN workstation running a UNIX operating system or another equivalent personal computer or workstation. Alternatively, the data processing system may comprise a dedicated processing system that includes an embedded programmable data processing unit. For example, the data processing system may comprise a single board computer system that has been integrated into a system for performing micro-array analysis.
The massage process described herein for controlling a pump may also be realized as a software component operating on a conventional data processing system such as a UNIX workstation. In such an embodiment, the process may be implemented as a computer program written in any of several languages well-known to those of ordinary skill in the art, such as (but not limited to) C, C++, FORTRAN, Java or BASIC. The process may also be executed on commonly available clusters of processors, such as Western Scientific Linux clusters, which are able to allow parallel execution of all or some of the steps in the present process.
As noted above, the order in which the steps of the present method are performed is purely illustrative in nature. The steps can be performed in any order or in parallel, unless otherwise indicated by the present disclosure.
The method of the present invention may be performed in either hardware, software, or any combination thereof, as those terms are currently known in the art. In particular, the present method may be carried out by software, firmware, or microcode operating on a computer or computers of any type. Additionally, software for performing the systems and methods may comprise computer instructions in any form (e.g., source code, object code, interpreted code, etc.) stored in any computer-readable medium (e.g., ROM, RAM, magnetic media, punched tape or card, compact disc (CD) in any form, DVD, etc.). Furthermore, such software may also be in the form of a computer data signal embodied in a carrier wave, such as that found within the well-known Web pages transferred among devices connected to the Internet. Accordingly, the systems are not limited to any particular platform, unless specifically stated otherwise in the present disclosure.
The computer terminal may include any computer system having a microprocessor, a memory and a microcontroller. The memory typically includes a main memory and a read only memory. The memory may also include mass storage components having, for example, various disk drives, tape drives, etc. The mass storage may include one or more magnetic disk or tape drives or optical disk drives, for storing data and instructions for use by the microprocessor. The memory may also include one or more drives for various portable media, such as a floppy disk, a compact disc read only memory (CD-ROM), or an integrated circuit non-volatile memory adapter ( i.e. PC-MCIA adapter) to input and output data and code to and from microprocessor. The memory may also include dynamic random access memory (DRAM) and high-speed cache memory.
Hardware components typically used to build the process module 106 may include programmable logic devices, programmable logic controllers, logic gates and flip flops or relays. Hardware implementation typically requires a register to store states, a block of combinational logic which determines the test conditions of transition rules, and a second block of combinational logic that determines the responses of transition rules. An FSM may be created and implemented using software tools including, but not limited to, the AT&T FSM Library™ provided by AT&T Labs, New Jersey, U.S.A. An FSM may also be created and implemented using software languages including, but not limited to, C, C++, JAVA, SCXML (State Chart XML). Interactive software modules may also be included in the computer that may assist users with pump control.
In certain embodiments, the pump is controlled by hand, such that a person may control the flow of air into the inflatable fluid bladders.
During operation, the pump 1418 is shown to be hand squeezed to go from an open state 1414 in
In one embodiment, the pump 1418 includes a rectangular body portion to which is attached a strap having a VELCRO™ strip thereon. The pump 1418 may be folded about its center and the VELCRO™ strap wrapped around the open end of the pump to have a mating contact with a second VELCRO™ strip on the obverse side of the pump. The pump 1418 may be formed from air impervious resilient material such as plastic. The pump may include layers of rigid material and/or layers of foam material. Other types of pumps may be used for supplying pressurized fluids without departing from the scope of the invention.
In one embodiment, the brace 1600 is slid over the arm 1608 of an individual such that the notch is aligned with the elbow joint and the brace is snugly fit. An alternate embodiment for the elbow could be similar to brace 100 or 300 configured as a separate rigid brace. Fluid is introduced into the inflatable fluid bladders 1620 through the fluid port 1606. In certain embodiments, the temperature of the fluid is regulated at a particular value or range. For example, the fluid can be regulated to maintain a temperature below room temperature and close to freezing temperatures to provide cold therapy to the location of the joint. The fluid can also be regulated to maintain a temperature above room temperature and to provide heat therapy to the location of the joint. The fluid fills the inflatable fluid bladder and thereby causes it to expand. The expanding inflatable fluid bladder compresses the region of joint to stabilize the joint, while the temperature regulated fluid may also provide thermal therapy.
In certain optional embodiments, the brace includes a support system having rigid members and a hinge near a joint for controlling movement of the limb about the joint. The hinge may be lockable to prevent hyper-extension of the elbow. Prior to the application of the brace 1600 on the elbow, the hinge may be in an unlocked state such that the rigid members can pivot freely about the hinge. Once the brace 1600 is secured to the elbow, the hinge may be locked to allow the rigid members to pivot about the hinge within a certain desired range.
Those skilled in the art will know or be able to ascertain using no more than routine experimentation, many equivalents to the embodiments and practices described herein. Accordingly, it will be understood that the systems and methods are not to be limited to the embodiments disclosed herein, but are to be understood from the following claims, which are to be interpreted as broadly as allowed under the law. All references cited herein are expressly incorporated by reference in their entirety.
This application claims priority to and the benefit of U.S. Provisional Patent Application Ser. No. 60/751,091, filed on Dec. 15, 2005 and entitled “Edema Flow with Reversed Sequence Pressure Application,” the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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60751091 | Dec 2005 | US |