Reduced-pressure wound dressings

1. A reduced-pressure system for treating a tissue site having a linear wound, the reduced-pressure system comprising:

a dressing bolster formed from a medical bolster material, the dressing bolster for placing on a patient's epidermis and sized to overlay the linear wound;

a reduced-pressure source;

a first reduced-pressure interface fluidly coupled to the dressing bolster and the reduced-pressure source, the first reduced-pressure interface for delivering reduced pressure to the dressing bolster;

a reduced-pressure delivery conduit for fluidly coupling the reduced-pressure source and the first reduced-pressure interface; and

a second reduced-pressure interface fluidly coupled to the dressing bolster, the second reduced-pressure interface comprising a molded elastomer having an aperture sized to receive a subcutaneous delivery conduit and generate a compressive force against an outer circumference of the subcutaneous delivery conduit; and

an over-drape disposed between the dressing bolster and the second reduced-pressure interface and configured to provide a fluid seal over the dressing bolster and a portion of the patient's epidermis;

wherein the second reduced-pressure interface is configured to reinforce the over-drape to maintain the fluid seal around the tissue site when the over-drape is breached by the subcutaneous delivery conduit.

2. The reduced-pressure system of claim 1 , further comprising a pre-formed pathway for routing the subcutaneous delivery conduit through the dressing bolster and the over-drape.

3. The reduced-pressure system of claim 1 , wherein the second reduced-pressure interface comprises a nipple with an aperture having an interior diameter D 1 , wherein the subcutaneous delivery conduit has an external diameter D 2 , and wherein D 1 <D 2 whereby the fluid seal is formed.

4. The reduced-pressure system of claim 1 , wherein the dressing bolster has a first surface and a second, inward facing surface for deploying over the patient's epidermis and substantially sized to overlay the linear wound; and further comprising:

an inner layer having a first surface and a second, inward-facing surface, and formed within a treatment-area aperture, and wherein the first surface of the inner layer is coupled at least in part to the second surface of the dressing bolster, wherein the inner layer is pre-cut to receive the subcutaneous delivery conduit.

5. The reduced-pressure system of claim 1 , wherein the second reduced-pressure interface further comprises one or more o-rings.

6. The reduced-pressure system of claim 1 , wherein the tissue site is a first tissue site, the reduced-pressure delivery conduit is a first reduced-pressure delivery conduit and the reduced-pressure system further comprises:

a manifold delivery tube having a passageway and a distal end, the distal end configured to be inserted into the subcutaneous delivery conduit and placed adjacent a second tissue site;

a flowable material deliverable through the manifold delivery tube to the second tissue site such that the flowable material is capable of filling a void adjacent the second tissue site to create a manifold having a plurality of flow channels in fluid communication with the second tissue site; and

a second reduced-pressure delivery conduit capable of fluid communication with the plurality of flow channels of the manifold.

7. The reduced-pressure system of claim 6 , wherein the manifold delivery tube and the second reduced-pressure delivery conduit are the same tube.

8. The reduced-pressure system of claim 6 , wherein the manifold is bioresorbable.

9. The reduced-pressure system of claim 1 , wherein:

the subcutaneous delivery conduit comprises a first conduit segment and a second conduit segment; and

the second reduced-pressure interface further comprises an intermediate conduit segment disposed through the aperture that is sized and configured to:

receive an end portion of the first conduit segment;

receive an end portion of the second conduit segment; and

maintain a fluid coupling between the first conduit segment and the second conduit segment.

10. The reduced-pressure system of claim 1 , wherein the molded elastomer is a plastic cylindrical part is sized to transfer a force equal to an amount of force required to puncture the over-drape with the subcutaneous delivery conduit.

11. A wound dressing assembly for treating a tissue site, the wound dressing assembly comprising:

a dressing bolster having a first surface and a second, inward facing surface for deploying over a patient's epidermis;

a first reduced-pressure interface fluidly coupled to the dressing bolster and operable to receive a reduced-pressure supply conduit;

an inner layer having a first surface and a second, inward-facing surface, formed within a treatment-area aperture, and wherein the first surface of the inner layer is coupled at least in part to the second surface of the dressing bolster; and

a second reduced-pressure interface fluidly coupled to the dressing bolster, wherein the second reduced-pressure interface comprises:

an interface body comprising a molded elastomer formed with an aperture sized to receive a subcutaneous delivery conduit and to form a fluid seal therewith; and

an over-drape disposed between the dressing bolster and the second reduced-pressure interface and configured to provide a fluid seal over the dressing bolster and a portion of the patient's epidermis;

wherein the second reduced-pressure interface is configured to reinforce the over-drape to maintain the fluid seal around the tissue site when the over-drape is breached by the subcutaneous delivery conduit.

12. The wound dressing assembly of claim 11 , wherein dressing bolster and inner layer are at least partially pre-cut to allow the subcutaneous delivery conduit to pass from the treatment-area aperture to the second reduced-pressure interface.

13. The wound dressing assembly of claim 11 , wherein the second reduced-pressure interface further comprises a pliable over-drape and one or more o-rings.

14. A method of treating a tissue site, the method comprising:

applying a wound dressing assembly to the tissue site, wherein the wound dressing assembly comprises:

a dressing bolster formed from a medical bolster material shaped for placing on a patient's epidermis and substantially sized to overlay the tissue site,

a first reduced-pressure interface fluidly coupled to the dressing bolster for delivering reduced-pressure to the dressing bolster, and

a second reduced-pressure interface fluidly coupled to the dressing bolster, the second reduced-pressure interface comprising a molded elastomer having an aperture sized to receive a conduit and generate a compressive force against an outer circumference of the conduit; and

an over-drape disposed between the dressing bolster and the second reduced-pressure interface and configured to provide a fluid seal over the dressing bolster and a portion of the patient's epidermis,

wherein the second reduced-pressure interface is configured to reinforce the over-drape to maintain the fluid seal around the tissue site when the over-drape is breached by the subcutaneous delivery conduit;

fluidly coupling a reduced-pressure delivery conduit to a reduced-pressure source and the first reduced-pressure interface;

delivering reduced pressure to the reduced-pressure delivery conduit;

fluidly coupling a subcutaneous delivery conduit to the second interface; and

and delivering reduced pressure to the subcutaneous delivery conduit.

15. The method of treating a tissue site of claim 14 , wherein the dressing bolster is pre-cut to receive the subcutaneous delivery conduit.

16. The method of treating a tissue site of claim 14 , wherein the tissue site is a first tissue site and further comprising:

coupling a manifold delivery tube to the second reduced-pressure interface, the manifold delivery tube having a passageway and a distal end, the distal end configured to be inserted into the subcutaneous delivery conduit;

delivering a flowable bioresorbable material through the manifold delivery tube to the second tissue site such that the flowable bioresorbable material is capable of filling a void adjacent the second tissue site to create a manifold having a plurality of flow channels in fluid communication with the second tissue site;

coupling a reduced-pressure delivery conduit to the second reduced-pressure interface, the reduced-pressure delivery conduit capable of fluid communication with the plurality of flow channels of the manifold; and

applying reduced pressure to the second tissue site.

17. The method of treating a tissue site of claim 16 , wherein the manifold delivery tube and the reduced-pressure delivery conduit are the same tube.

18. A method of manufacturing a wound dressing assembly for treating subcutaneous tissue, the method of manufacturing comprising the steps of:

providing a dressing bolster formed from a medical bolster material, the dressing bolster for placing on a patient's epidermis;

providing a reduced-pressure source;

providing a first reduced-pressure interface for delivering reduced pressure to the dressing bolster;

providing a second reduced-pressure interface for fluidly coupling to the dressing bolster configured to receive a subcutaneous delivery conduit and to form a fluid seal therebetween; and

providing an over-drape for disposing between the dressing bolster and the second reduced-pressure interface and configured to provide a fluid seal over the dressing bolster and a portion of the patient's epidermis;

wherein the second reduced-pressure interface comprises a molded elastomer having an aperture sized to receive a conduit and generate a radial compressive force against the conduit, and wherein the second reduced-pressure interface is configured to reinforce the over-drape to maintain the fluid seal around the tissue site when the over-drape is breached by the subcutaneous delivery conduit.

19. The method of manufacturing a wound dressing assembly of claim 18 , wherein the second reduced-pressure interface further comprises a preformed pathway for routing the subcutaneous delivery conduit through the dressing bolster.

20. The method of manufacturing a wound dressing assembly of claim 18 , wherein the dressing bolster has a first surface and a second surface for deploying over the patient's epidermis; and further comprising:

providing an inner layer having a first surface and a second surface formed with a treatment-area aperture,

wherein the first surface of the inner layer is coupled at least in part to the second surface of the dressing bolster, and

wherein the inner layer is pre-cut to receive the subcutaneous delivery conduit.