Adhesive pad and hemostasis system
An adhesive pad for use with a hemostasis device comprising a footplate having a top surface and a receiving device positioned on the footplate, the adhesive pad comprising: (1) a flexible backing layer having a bottom surface, a central portion having an opening, a first side portion, and a second side portion; (2) an adhesive layer applied to the bottom surface of the backing layer; and (3) a release layer removably secured to the adhesive layer. The opening in the central portion of the backing layer is sized to fit the receiving device of the hemostasis device, and the adhesive layer applied to the bottom surface of the first and second side portions of the backing layer is configured to adhere to and extend beyond the top surface of the footplate.
1. A hemostasis system for adhering to a patient's skin and applying a compressive force to a puncture site, the hemostasis system comprising:
(a) a hemostasis device comprising:
a footplate having a top surface and a bottom surface,
a receiving device positioned on the footplate, a plunger positioned within the receiving device and configured to move therethrough and apply a compressive force to the patient's skin at the puncture site, and
a plurality of motion restricting components interposed between the receiving device and the plunger to restrict reverse movement of the plunger through the receiving device; and
(b) an anchoring adhesive pad comprising
a flexible backing layer with a bottom surface, a first side portion, a second side portion, and a central portion;
an adhesive layer on the bottom surface of the backing layer; and
a release liner removably secured to the adhesive layer;
wherein the central portion defines a hole sized to receive the receiving device, and wherein the first side portion and the second side portion of the backing layer overlay and adhere to the top surface of the footplate of the hemostasis device and extend beyond the footplate to the patient's skin.
2. The hemostasis system of claim 1 , wherein the backing layer of the anchoring adhesive pad comprises paper, woven fabric, or non-woven plastic film.
3. The hemostasis system of claim 1 , wherein the backing layer of the anchoring adhesive pad comprises a non-woven plastic film.
4. The hemostasis system of claim 3 , wherein the non-woven plastic film is selected from the group consisting of polyethylene, polypropylene, polyurethane, polyester, poly(ethylene-vinyl acetate), and poly(vinyl chloride).
5. The hemostasis system of claim 1 , wherein the release liner of the anchoring adhesive pad has an opening coincident with the opening in the central portion of the backing layer.
6. The hemostasis system of claim 1 , wherein the release liner of the anchoring adhesive pad comprises a plurality of separate sections.
7. The hemostasis system of claim 1 , wherein the release liner of the anchoring adhesive pad is paper.
8. The hemostasis system of claim 1 , wherein the plunger of the hemostasis device further comprises a compression pad.
9. A method for applying a compressive force to a patient's skin at the site of a puncture site, the method comprising the steps of:
providing an anchoring adhesive pad configured to be received by a hemostasis device comprising a footplate having a top surface and a bottom surface, a receiving device positioned on the footplate, a plunger positioned within the receiving device and configured to move therethrough, and a plurality of motion restricting components interposed between the receiving device and the plunger to restrict reverse movement of the plunger through the receiving device wherein the anchoring adhesive pad comprises a flexible backing layer having a bottom surface, a first side portion, a second side portion, a central portion positioned between the first side portion and the second side portion, defining an opening to receive the receiving device, and an adhesive layer applied to the bottom surface of the flexible backing layer, wherein the first side portion and the second side portion of the backing layer overlay and adhere to the top surface of the footplate of the hemostasis device and extend beyond the footplate to the patient's skin proximal to the puncture site; and
improving securement of the hemostasis device at a puncture site.
10. The method of claim 9 , further comprising improving a compression force of the hemostasis device at the puncture site.
11. A kit comprising:
(a) a hemostasis system comprising:
a hemostasis device comprising a footplate having a top surface and a bottom surface, a receiving device positioned on the footplate, a plunger positioned within the receiving device and configured to move therethrough and apply a compressive force to the patient's skin at the puncture site, and a plurality of motion restricting components interposed between the receiving device and the plunger to restrict reverse movement of the plunger through the receiving device; and
(b) an anchoring adhesive pad comprising
a flexible backing layer with a bottom surface, first side portion, a second side portion, a central portion positioned between the first side portion and the second side portion, defining an opening to receive the receiving device;
an adhesive layer applied to the bottom surface of the backing layer; and
a release liner removably secured to the adhesive layer;
wherein the first side portion and the second side portion of the backing layer overlay and adhere to the top surface of the footplate of the hemostasis device and extend beyond the footplate to the patient's' skin proximal to the puncture site.