Reduced pressure therapy of the sacral region
First Claim
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1. A device to treat a region of a patient having a skin fold, comprising:
- a multi-lobular base layer comprising a first surface, a second surface, an interior region, and an outer perimeter, wherein each lobular region of the base layer comprises a curve that converges at a central axis of the base layer;
wherein the base layer further comprises a branched conduit system; and
an adhesive conduit located on the base layer, wherein the adhesive conduit encloses an area of the base layer.
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Abstract
Reduced pressure wound therapy is performed on a sacral region of a patient using an adhesive dressing comprising a flexible planar layer and a non-planar fold-sealing region configured to seal to the intergluteal cleft of a patient. The fold-sealing region is located on an outer edge of the adhesive dressing and comprises a tapered configuration.
206 Citations
20 Claims
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1. A device to treat a region of a patient having a skin fold, comprising:
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a multi-lobular base layer comprising a first surface, a second surface, an interior region, and an outer perimeter, wherein each lobular region of the base layer comprises a curve that converges at a central axis of the base layer; wherein the base layer further comprises a branched conduit system; and an adhesive conduit located on the base layer, wherein the adhesive conduit encloses an area of the base layer. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13)
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14. A method of treating a wound having a skin fold, comprising:
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providing a device comprising a multi-lobular base layer comprising a first surface, a second surface, an interior region, and an outer perimeter, wherein each lobular region of the base layer comprises a curve that converges at a central axis of the base layer; and
an adhesive conduit located on the base layer, wherein the adhesive conduit encloses an area of the base layer;placing the device along the skin fold of the wound such that the central axis of the device is aligned with the skin fold; and adhering the device to the wound such that a substantially airtight seal is formed between the wound and the device. - View Dependent Claims (15, 16, 17, 18, 19, 20)
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Specification