PATIENT COMFORT PACK

Abstract

The present invention provides a device and method for delivering thermal therapy about a percutaneous access site while also permitting visual and physical examination of the access site. The device comprises a semi-circumferential shaped housing having a top wall, a bottom wall, and a side wall. The top wall, the bottom wall, and the side wall define a cavity with a fluid tight bladder disposed within the cavity. The semi-circumferential shaped housing has an aperture formed in the housing and a straight edge portion along the circumference of the housing. The device delivers thermal therapy to percutaneous arterial, venous, laparoscopic, and other access procedures sites by allowing visual and physical examination of the access site through the aperture and comfortable placement of the device's straight edge portion against a bend or joint of the patient's body.

Claims

1. A therapeutic thermal device for application about an access site, comprising: a semi-circumferential shaped housing having a top wall, a bottom wall, and a side wall, the top wall, the bottom wall, and the side wall defining a cavity; a fluid tight bladder disposed within the cavity defined by the top wall, the bottom wall, and the side wall; wherein the semi-circumferential shaped housing has an aperture formed in the semi-circumferential housing; and wherein the semi-circumferential shaped housing comprises a straight edge portion along the circumference of the housing.

2. The therapeutic thermal device of claim 1, further comprising on the bottom wall of the housing at least one sterile peel-away paper exposing at least one adhesive point.

3. The therapeutic thermal device of claim 1, wherein the semi-circumferential housing comprises a polyvinyl chloride.

4. The therapeutic thermal device of claim 1, wherein the length of the straight edge portion is 25% of the circumference of the semi-circumferential shaped housing if the housing was a complete circle.

5. The therapeutic thermal device of claim 1, wherein the straight edge portion of the semi-circumferential shaped housing is comprised of three straight edges forming a three-sided substantially rectangular shape.

6. The therapeutic thermal device of claim 1, wherein the fluid tight bladder includes a solution and a separately maintained compartment for an organic or inorganic salt.

7. The therapeutic thermal device of claim 6, wherein the solution is water.

8. The therapeutic thermal device of claim 7, wherein the organic or inorganic salt is selected from the group consisting of ammonium nitrate, calcium ammonium nitrate, potassium nitrate, urea, and ammonium chloride.

9. The therapeutic thermal device of claim 1, wherein the device is placed about an access site exposing the access site for visual and physical examination while also allowing for indirect thermal therapy to the access site.

10. The therapeutic thermal device of claim 1, wherein the straight edge portion is placed at a bend or joint on a body located adjacent to an access site such as the location of the femoral, radial, brachial, pedal and popliteal arteries.

11. The therapeutic thermal device of claim 10, wherein the straight edge portions are tapered accordingly for comfortable and proper placement at a bend or joint on a body located adjacent to an access site such as the location of the femoral, radial, brachial, pedal and popliteal arteries.

12. The therapeutic thermal device of claim 1, wherein the lengths of the sides of the semi-circumferential shaped housing are equal.

13. A method for application of a therapeutic thermal device, comprising the steps of: placing over an access site an aperture formed in a semi-circumferential housing having a top wall, a bottom wall, and a side wall, the top wall, the bottom wall, and the side wall defining a cavity; and orienting a straight edge portion along the circumference of the semi-circumferential housing at a bend or joint on a body located adjacent to an access site such as the location of the femoral, radial, brachial, pedal and popliteal arteries. wherein a fluid tight bladder disposed within the cavity defined by the top wall, the bottom wall, and the side wall includes a solution and a separately maintained compartment for an organic or inorganic salt to provide thermal therapy.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] For a more complete understanding of the present invention, and the advantage thereof, reference is now made to the ensuing descriptions taken in connection with the accompanying drawings briefly described as follows:

[0016] FIG. 1 illustrates a top view of the device according to an embodiment of the invention; and

[0017] FIG. 2 illustrates an alternative top view of the device according to an embodiment of the invention.

DETAILED DESCRIPTION OF EMBODIMENTS

[0018] Further features and advantages of the invention, as well as the structure and operation of various embodiments of the invention, are described in detail below with reference to the accompanying FIGS. 1-2. Although the invention is described in the context of a cold pack, it is to be understood that the present invention is equally capable of delivering heat therapy to an access site. One of ordinary skill in the art will understand the implementation of therapeutic heat delivery via an exothermic reaction within the device of the present invention.

[0019] Reference throughout this specification to one embodiment, an embodiment, or similar language means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, appearances of the phrases in one embodiment, in an embodiment, and similar language throughout this specification may, but do not necessarily, all refer to the same embodiment.

[0020] Moreover, the described features, structures, or characteristics of the invention may be combined in any suitable manner in one or more embodiments. It will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the spirit and scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents. Reference will now be made in detail to the preferred embodiments of the invention.

[0021] Currently, there are no external, sterile anti-inflammatory medical cold packs capable of treating percutaneous access sites at the femoral, radial, brachial, pedal and popliteal arteries or laparoscopic port access sites after the site has been closed. In addition, there are no cold packs on the market specifically designed to treat the surrounding damaged tissue at the access site while allowing the physician and staff the ability to palpate and visualize the access wound site. The area at and surrounding the access site frequently experiences post procedural complications and post operative pain. For example, these complications may include access site swelling, discomfort, bruising, inflammation and hematoma. Today, there are no sterile cold packs on the market specifically designed to address external arterial access site complications such as hematoma, discomfort, tenderness and swelling and also capable of comfortable placement about the access site.

[0022] The device design and mechanism of the present invention minimizes swelling, pain and discomfort resulting at the access site after a procedure such as laparoscopy or arterial access. In an embodiment of the invention, a sterile semi-circumferential therapeutic cold pack is placed over an access closure site. In an arterial access procedure, the access site may be located at the femoral, radial, brachial, pedal or popliteal artery. The present invention allows the surrounding tissue at the access site to receive direct cryotherapy slowing the inflammatory response and reducing pain. The sterile semi-circumferential therapeutic cold pack includes an aperture. Because the aperture is surrounded by the sterile semi-circumferential therapeutic cold pack, the access site and immediately surrounding tissue also receive indirect cryotherapy. The aperture also allows attending physicians and medical staff to palpitate and visually examine the access site for post procedural complications and post operative pain. As such, placement of the sterile semi-circumferential therapeutic cold pack should be such that the access site is within the aperture to provide visualization, palpitation and indirect cryotherapy.

[0023] In an embodiment, the device may be used at an access site after hemostasis is achieved by either an access closure device or manual hold. The device of the present invention is designed to provide both direct and indirect cyotherapy to an area adjacent to and at an access site. In some embodiments, the direct cryotherapy area extends at least 3.5 cm radially from the access site. In alternative embodiments, the direct cryotherapy area extends radially from the access site a distance sufficient to provide direct cryotherapy to an area known to one of skill in. the art that may be exposed to secondary hypoxic injury and/or other post-procedural complications. The direct cryotherapy area is the area where the device of the present invention is in direct contact with the skin. The device may be made of a flexible rubber/silicone outer shell or the like. The outer shell may be a latex-free thin film based medical grade polymer such as a thermoplastic elastomer copolyester, polyvinyl chloride, or the like.

[0024] In a preferred embodiment, the device is in a semi-circumferential shape. By semi-circumferential, it is meant and intended that the device have a shape as shown in the non-limiting examples of FIGS. 1 and 2. The upper portion of the device is semi-circumferential with the lower portion of the device configured such that there are three substantially straight edges forming three sides of a substantially rectangular shape. An aperture is formed in the upper portion of the device allowing physicians and medical staff to palpitate and visually examine the access site for post procedural complications and post operative pain. Accordingly, the aperture is located in the upper portion of the device to facilitate placement of the aperture directly over the access site. Orientation with the aperture directly over the access site allows for the comfortable placement of the straight edge portions of the device against the groin or other bend or joint adjacent to arterial access sites such as located at the femoral, radial, brachial, pedal or popliteal artery.

[0025] In an alternative embodiment as illustrated in the figures of U.S. Provisional Patent Application No. 62/119,896 incorporated herein by this reference, the device includes a singular straight edge portion along the circumference of the semi-circumferential shape. In this alternative embodiment, the length of the singular straight edge portion of the device is approximately one-quarter (25%) of the circumference of a complete circle with a given diameter. For example, if the device was a complete circle with a diameter of 10 cm, then the circumference of the circle would be 31.4 cm (c=d, where c=circumference and d=diameter of a circle). One-quarter of the circumference would then be 7.9 cm. Therefore, the straight edge would have a length of approximately 8 cm. In alternative embodiments, the length of the straight edge portion is between 5% and 30% of the circumference of the device if the device was a complete circle. The straight edge portion facilitates placement of the device adjacent to a patient's inner groin or any location on the body where a bend or joint may be located adjacent to an access site such as the location of the femoral, radial, brachial, pedal and popliteal arteries.

[0026] FIG. 1 illustrates a top view of the device 100 according to an embodiment of the present invention. The outer shell of the device includes a top wall 110, a side wall 120, and a bottom wall (not shown) forming a fluid digit cavity. An aperture 130, located in the upper portion of the device 100 of the semi-circumferential shape, exposes the access site for visual and physical examination while also allowing for indirect cryotherapy. The lower portion of the device 100 includes three substantially straight edges, 140a, 140b, and 140c, continuous with the semi-circumferential upper portion of the device. The three substantially straight edges, 140a, 140b, and 140c, allow for the comfortable placement of the therapeutic thermal device against the inner groin or any location on the body where a bend or joint may be located adjacent to an access site such as the location of the femoral, radial, brachial, pedal and popliteal arteries. The three substantially straight edges, 140a, 140b, and 140c, combine to form a substantially rectangular shape defining the bottom portion of the device 100. The straight edges, 140a and 140c, are at a slight tapered configuration to allow for correct and comfortable placement against the inner groin. This slight tapered configuration aligns with the angle formed in the groin region where the leg meets the groin. In other embodiments, the straight edges, 140a, 140b, and 140c, may be configured to adapt to the area adjacent to an access site such as at the bend or joint at the location of the femoral, radial, brachial, pedal and popliteal arteries. Once the access site is placed within the aperture 130, the device may be correctly oriented for comfortable placement against a bend or joint adjacent to an access site.

[0027] FIG. 2 illustrates an alternative top view of the device 200 according to an embodiment of the invention. In a preferred embodiment, the dimensions of the device 200 are equal along the periphery of the device as shown in FIGS. 2 at 210a and 210b. The specific lengths of the periphery of the device are configured to accommodate the specific end use of the device. For example, the dimensions will be dictated by the location of the access site i.e., at the femoral, radial, brachial, pedal and popliteal arteries. Moreover, the dimensions of the device are dependent upon the thermal qualities of the reactive chemicals used in the device to produce heat or cold therapy. In this preferred embodiment. the side wall 220 of the device is at least 1 inch in height. It is to be understood that the specific height of the side wall 220 may vary depending on the thermal qualities of the reactive chemicals used in the device to produce heat or cold therapy. For example, the height of the side wall 220 may vary depending upon the choice of reactive chemicals used to produce endothermic or exothermic reactions. The choice of solution and dry chemicals may dictate the specific amounts needed to achieve an appropriate heat of reaction (H) necessary to produce the desired therapeutic thermal effect. In this preferred embodiment, the aperture 230 has a diameter of at least 38 millimeters to allow visual and physical examination of the access site. It is to be understood that the diameter of the aperture 230 will vary dependent upon the end use of the device. For example, if the end use of the device is for use with an access site that requires a larger or smaller viewing and examination area, then the aperture may be larger or smaller to accommodate that particular end use.

[0028] The bottom wall (not shown) is identical to the top wall 110 of FIG. 1 but includes at least one sterile-unitary peel away paper that exposes at least one adhesive point. The at least one sterile-unitary peel away paper exposes at least one adhesive point. The at least one adhesive point temporarily adheres the device to the skin such that the aperture exposes the access site and the bottom wall rests on the area adjacent to the access site. The adhesives used in the device may be any adhesive appropriate for contacting a patient's skin known to one of skill in the art. In an embodiment of the device, the adhesive is a medical grade adhesive glue similar to self sticking bandages. The adhesive may be a breathable polymer based pressure sensitive adhesive including a slight liquid carrier that will facilitate bonding with a patient's skin.

[0029] The device as described herein is a cryotherapy device capable of absorbing heat. As such, the device includes a fluid tight inner bladder (not shown) disposed between the top wall 110 and the bottom wall (not shown) of FIG. 1. In an embodiment of the invention, the inner bladder includes water and either an organic or inorganic salt maintained separately from the water. To initiate an endothermic reaction, the salt is dissolved in the water. This process is known in the art and used in many commercially available instant cold packs. Typically, dry chemicals are maintained in a small bag within the inner bladder containing an aqueous solution. The small bag is manually manipulated or crushed thereby causing the dry chemicals to be released from the bag and dissolved in the surrounding solution. The salts used in the reaction may be any salt, including but not limited to ammonium nitrate, calcium ammonium nitrate, potassium nitrate, urea, ammonium chloride, or the like. It is to be understood that the particular salt and solution used in the endothermic reaction have a heat of reaction (H) known to those of skill in the art capable of providing cryotherapy to a patient in a post procedure setting.

[0030] In an embodiment of the invention, the placement of the aperture in the device is off center such that the inner bladder is of a sufficient size to accommodate an endothermic reaction with a heat of reaction capable of providing at least 25-30 minutes of cryotherapy. In alternative embodiments, the aperture in the device may be oriented at a location on the device dependent on the size of the inner bladder required to produce an endothermic reaction with a heat of reaction capable of providing cryotherapy for a length of time given the particular end use of the therapy. For example, cryotherapy for lengths of time greater or less than 30 minutes would require an inner bladder that is larger or smaller to accommodate the chemicals needed to create an endothermic reaction for that particular period of time.

[0031] In alternative embodiments, the device is a heat therapy device capable of delivering heat to an area at an access site. Those of skill in the art understand the implementation of this embodiment within the device of the present invention. For example, a supersaturated solution of sodium acetate may be used whereby activation of the exothermic reaction occurs by creating a nucleation site for the crystallization of sodium acetate thereby releasing heat.

[0032] The specific sterile design of the present invention addresses patient and physician requests to minimize swelling from hematoma, discomfort, tenderness and swelling at an arterial access site, while still allowing for visualization and palpitation. The device addresses multi-physician specialties, while satisfying an unmet patient need. Percutaneous arterial, venous, laparoscopic, and other access procedures are addressed through the use of this device.

[0033] The above description of the disclosed embodiments, and that provided in the accompanying documents, is provided to enable any person skilled in the art to make or use the invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles described herein, and in the accompanying documents, can be applied to other embodiments without departing from the spirit or scope of the invention. Thus, it is to be understood that the description and drawings presented herein, and presented in the accompanying documents, represent particular aspects and embodiments of the invention and are therefore representative examples of the subject matter that is broadly contemplated by the present invention. It is further understood that the scope of the present invention fully encompasses other embodiments that are, or may become, obvious to those skilled in the art and that the scope of the present invention is accordingly not limited by the descriptions presented herein, or by the descriptions presented in the accompanying documents.