The present invention is directed generally to a compression garment for applying compression therapy to a body part of a wearer and more particularly to such a compression garment having a sealable bladder pocket.
Among major concerns for generally immobile persons are medical conditions that form blood clots, such as deep vein thrombosis (DVT), and peripheral edema. Such patients and persons include those undergoing surgery, anesthesia, and extended periods of bed rest. These blood clotting conditions generally occur in the deep veins of the lower extremities and/or pelvis. These veins, such as the iliac, femoral, popliteal, and tibial return deoxygenated blood to the heart. For example, when blood circulation in these veins is retarded due to illness, injury, or inactivity, there is a tendency for blood to accumulate or pool. A static pool of blood may lead to the formation of a blood clot, which can interfere with cardiovascular circulation. More seriously, a fragment of the blood clot can break loose and migrate. A pulmonary embolus can form from the fragment potentially blocking a main pulmonary artery, which may be life threatening. The current invention can also be applied to the treatment of other conditions, such as lymphedema.
Conventional vascular compression systems include a compression garment fluidly connected to a controller for cyclically inflating the compression garment. The cyclical inflation of the compression garment enhances blood circulation and decreases the likelihood of DVT. A system of conduits connects the compression garment to the controller. Newer vascular compression garments have portable controllers that are much smaller and mountable on the compression garment so the patient may move about freely without having to first remove the compression garment or disconnect the compression garment from a controller. These newer compression garments may be worn when a patient is stationary or ambulatory and are believed to enhance patient compliance because of convenience of use.
In general, conventional compression garments are intended for use with a single patient. The garments are discarded after use even through portions of the garments could be reused. Conventional compression garments are constructed with an integrally formed bladder that prevents the bladder from be reused.
In one aspect, a compression garment adapted for applying compression therapy to a selected body part of a patient comprises a selectively inflatable bladder having a hollow interior. The inflatable bladder also includes an inlet connector through which fluid passes when entering the interior to inflate the bladder. The connector is connectable to a fluid supply line in communication with a fluid source for supplying fluid to the bladder. The compression garment also includes a wrap sized and shaped for wrapping around at least a portion of the selected body part. The wrap includes a fastener for fastening the wrap in position when wrapped around the body part and a pocket sized and shaped for receiving the bladder to hold the bladder against the body part when applying compression therapy. The pocket has a main opening sized for passing the bladder therethrough when inserting the bladder in the pocket and removing the bladder from the pocket and a secondary opening separated from the main opening sized, shaped, and positioned with respect to the main opening for permitting the supply line to be operatively connected to the connector when the bladder is positioned in the pocket. The main opening is selectively sealable when closed to hold the bladder in position in the pocket and prevent fluid from entering the pocket through the main opening. The pocket is formed from fluid-impermeable material to shield the bladder from the bodily fluids of the patient.
In another aspect, the present invention is directed to a method of making a garment adapted for holding a bladder on a body part of a patient for imparting compression therapy to the body part. The bladder includes an inflatable chamber and a connector in fluid communication with the inflatable chamber through which the inflatable chamber is inflated. The method comprises disposing inner and outer layers including fluid-impermeable material in stacked relationship and forming a pocket between the inner and outer layers by bonding the inner layer to the outer layer along a boundary defining an outer perimeter of the pocket. First and second segments of the inner layer are maintained free from bonding to the outer layer to define a main opening and a secondary opening between the inner and outer layers providing access to the pocket. The main opening is sized and shaped to permit the bladder to be inserted in the pocket, and the secondary opening is sized and shaped for permitting exposure of the connector on the bladder outside the pocket for connecting a source of pressurized fluid to the chamber for inflating the chamber. The method further comprises applying adhesive to at least one of the inner and outer layers adjacent the main opening and the secondary opening for adhering the inner layer to the outer layer at the respective opening to seal the respective opening to prevent bodily fluid from entering the pocket through the respective opening.
In another aspect, the present invention is directed to a compression garment adapted for applying compression therapy to a selected body part of a patient. The garment includes a selectively inflatable bladder having a hollow interior and an inlet connector through which fluid passes when entering the interior to inflate the bladder. The connector is connectable to a fluid supply line in communication with a fluid source for supplying fluid to the bladder. The garment also includes a wrap sized and shaped for wrapping around at least a portion of the selected body part. The wrap includes a fastener for fastening the wrap in position when wrapped around the body part and a pocket sized and shaped for receiving the bladder to hold the bladder against the body part when applying compression therapy. The pocket has a main opening sized for passing the bladder therethrough when inserting the bladder in the pocket and removing the bladder from the pocket. The main opening is configured for permitting the supply line to be operatively connected to the connector through the main opening when the bladder is positioned in the pocket. The main opening is selectively sealable when closed to hold the bladder in position in the pocket and prevent fluid from entering the pocket through the main opening. The pocket is formed from fluid-impermeable material to shield the bladder from bodily fluids of the patient.
Other features will be in part apparent and in part pointed out hereinafter.
Corresponding reference characters indicate corresponding parts throughout the drawings.
Referring now to the drawings, and in particular to
The compression garment includes a wrap, generally indicated by the reference number 20, and a selectively inflatable bladder, generally indicated by the reference number 22. The wrap 20 is sized and shaped for wrapping around at least a portion of the limb. The wrap 20 includes a pocket, generally indicated by the reference number 26, which is sized and shaped for receiving the bladder 22 to hold the bladder against the limb. The wrap may be formed using various materials. For example, the wrap may be formed using various layers of non-woven material such as polyester. In some embodiments, the wrap is formed using fluid-impermeable material for reasons which will become apparent. Other types of materials may be used without departing from the scope of the present invention.
The wrap 20 includes one or more fasteners 24 for securing the wrap in position when wrapped around the limb. For example, as shown in
The bladder 22 may be formed by joining sheets of fluid-impermeable material such as PVC in face to face relation. For example, the bladder 22 may be made using pliable PVC material having a thickness in a range from about 0.002 inches to about 0.020 inches. In one embodiment, the material may be 0.006 inches thick. The sheets may be joined by radiofrequency welding, heat welding, ultrasonic welding, or using other types of mechanical or chemical bonding processes. For example, the bladder illustrated in
The bladder 22 and pocket 26 are configured so the bladder may be inserted and removed from the pocket. This arrangement allows the bladder 22 to be interchangeable with other wraps and vice versa. For example, a bladder chosen for use may be selected from a variety of differently configured bladders based on the desired type of compression therapy. A single bladder may be reused in two, three, or more wraps for the same or multiple patients. Moreover, the bladders may be used in differently configured wraps. For example, a wrap may have multiple pockets, each for holding one or more bladders.
Referring again to
As viewed in
The pocket 26 may be formed in a variety of ways. For example, as illustrated in
The pocket 26 is desirably constructed to shield the bladder 22 from bodily fluids and other potential sources of contamination. In other words, the pocket 26 encapsulates the bladder 22 to prevent external fluids from contacting the bladder. The pocket 26 may be formed from fluid-impermeable material to shield the bladder. For example, the cover 20c and main body 20d of the wrap 20 may comprise a fluid-impermeable non-woven material such as a PVA/polyester laminate. In addition, the main and secondary openings 50, 52 are selectively sealable when closed to hold the bladder 22 in position in the pocket 26 and prevent fluid from entering the pocket through the openings. The main and secondary openings 50, 52 may be sealed using adhesive. Various types of adhesives may be used, such as polyacrylate based adhesives (e.g., hot melt and solvent types) and polyolefin based adhesives. The adhesive may be applied by spraying, by extruding, or by applying an adhesive film adhesive. In some embodiments, adhesive may be provided on the wrap 20 adjacent the openings 50, 52 and covered with film strips 60a, 60b as shown in
To use the compression garment 10, a health care provider administers compression therapy to a body part by selecting a wrap and bladder configured for the desired type of compression therapy. For example, the bladder 22 is inserted in the pocket 26 of the wrap 20 through the main opening 50. The connector 34 is accessible through the secondary opening 52 for connecting the connector in fluid communication with a fluid source for inflating the hollow interior 30 (e.g., one or more of the chambers 30a, 30b, 30c). For example, the fluid line from the fluid supply may be inserted through the secondary opening 52 and connected to the connector 34. The main and secondary openings 50, 52 are closed and sealed to shield the bladder 22 from bodily fluid by removing the film strips 60a, 60b to expose the adhesive provided on the wrap 20 adjacent the openings. The compression garment 10 is applied to the selected body part of the patient. For example, the garment 10 may be wrapped around a limb to be treated and fastened in place using a conventional method. Fluid pressure in the hollow interior 30 is increased to exert a compressive force on the body part. At the end of the compression therapy, the bladder 22 may be removed from the pocket 26 through the main opening 50 by releasing the adhesive seal.
The sealed configuration of the pocket 26 shields the bladder 22 from bodily fluids and/or other potential contaminants sufficiently that the bladder 22 may be reused in another wrap 20 for the same patient or a different patient. Because the bladder 22 is shielded during use, the bladder 22 desirably requires less cleaning or sterilization (e.g., minimal or none) than if the bladder 22 were used in an unsealed pocket. The reusable nature of the bladder 22 decreases the cost associated with compression therapy, and the sealable bladder pocket 26 reduces the potential of spreading disease if the bladder 22 is reused.
As shown in
As is now apparent, in this embodiment only the main opening 250 needs to be sealed after inserting the bladder 222 in the pocket 226 to prevent bodily fluid from entering the pocket during use. As described above, the secondary opening 252 is pre-sealed against the port 265 during manufacture to prevent bodily fluid from entering the pocket 226 through the secondary opening.
When introducing elements of the present invention or the preferred embodiments(s) thereof, the articles “a,” “an,” “the,” and “said” are intended to mean that there are one or more of the elements. The terms “comprising,” “including,” and “having” are intended to be inclusive and mean that there may be additional elements other than the listed elements.
In view of the above, it will be seen that the several objects of the invention are achieved and other advantageous results attained.
As various changes could be made in the above constructions, products, and methods without departing from the scope of the invention, it is intended that all matter contained in the above description and shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
This application is a continuation of U.S. Ser. No. 13/248,390, filed Sep. 29, 2011, the entire content of which is incorporated herein by reference.
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Number | Date | Country | |
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20160374891 A1 | Dec 2016 | US |
Number | Date | Country | |
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Parent | 13248390 | Sep 2011 | US |
Child | 15192655 | US |