System and methods for the treatment of wounds with dressing having closed cells
In one example embodiment, a system for treating a tissue site is disclosed that may comprise a manifold including a non-porous film having a plurality of closed cells defined by a sealed region perforated with apertures extending through the sealed region, wherein the manifold is adapted to contact the tissue site. The system may further comprise a cover adapted to provide a fluid seal between a therapeutic environment including the manifold proximate one side of the cover and a local external environment on the other side of the cover. In one embodiment, the plurality of closed cells is adapted to form distal channels with the cover and the apertures are adapted to provide fluid communication between the distal channels and the tissue site. The system may further comprise a negative-pressure source fluidly coupled to the therapeutic environment and adapted to provide negative pressure through the distal channels and the apertures to the tissue site. In another example embodiment, a method for treating a tissue site is disclosed comprising positioning a manifold including a non-porous film having a plurality of closed cells defined by a sealed region perforated with apertures extending through the seals to contact the tissue site. The method may further comprise covering the manifold and the tissue site with a drape to provide a fluid seal between a therapeutic environment including the manifold proximate one side of the drape and a local external environment the other side of the drape. The method may further comprise providing negative pressure from a negative-pressure source coupled to the therapeutic environment wherein the negative pressure is applied through the distal channels and the apertures to the tissue site.
1. A system for treating a tissue site, comprising:
a manifold including a non-porous film having a plurality of closed cells containing fluid, passageways fluidly coupling at least two of the closed cells together to form a closed chamber, apertures disposed in the film between the closed cells and extending through the film to allow fluid flow between a first side and a second side of the manifold, and surface features on at least an outer surface of at least some of the closed cells;
a cover adapted to provide a fluid seal between a therapeutic environment including the tissue site and the manifold on one side of the cover and a local external environment on the other side of the cover; and
a negative-pressure source fluidly coupled to the therapeutic environment and adapted to provide negative pressure through distal channels formed between the manifold and the cover and the apertures to the tissue site.
2. The system of claim 1 , wherein the film further comprises at least one non-leaking tear path configured to facilitate tearing the manifold into separate components.
3. The system of claim 2 , wherein the film further comprises two sheets of polymeric film, and wherein the at least one non-leaking tear path is formed by perforations in at least one of the two sheets of polymeric film.
4. The system of claim 1 , wherein the film further comprises non-leaking tear paths defining multiple regions of the film wherein the smallest region has an area greater than 20 cm 2 .
5. The system of claim 1 , wherein the surface features include ridges and grooves.
6. The system of claim 1 , wherein the surface features are embossed on film.
7. The system of claim 1 , wherein the surface features have a depth or height in the range of about 0.4 mm to about 1.5 mm.
8. The system of claim 1 , wherein the non-porous film comprises two sheets of polymeric film having inner surfaces sealed to each other to form a sealed region.
9. The system of claim 8 , wherein the plurality of closed cells are formed in a first one of the two sheets of polymeric film.
10. The system of claim 9 , wherein the closed cells have a volumetric shape that is any one of a hemispherical, conical, cylindrical, or geodesic shape.
11. The system of claim 9 , further comprising nodes projecting outwardly from a second one of the two sheets of polymeric film and adapted to form proximal channels between the seals and the tissue site in fluid communication with the apertures.
12. The system of claim 9 , further comprising a grid projecting outwardly from a second one of the two sheets of polymeric film and adapted to form proximal channels between the seals and the tissue site in fluid communication with the apertures.
13. The system of claim 8 , wherein the plurality of closed cells are formed in both of the two sheets of polymeric film.
14. The system of claim 13 , wherein the closed cells have a volumetric shape that is any one of a hemispherical, conical, cylindrical, or geodesic shape.
15. The system of claim 13 , wherein the closed cells have a volumetric shape that is generally hemispherical and coincide with each other on both sheets to form a generally spherical shape.
16. The system of claim 13 , wherein distal channels are formed between the closed cells of a first one of the two sheets of polymeric film and wherein proximal channels are formed between the closed cells of a second one of the two sheets of polymeric film in fluid communication with the distal channels through the apertures.
17. The system of claim 16 , further comprising nodes projecting outwardly from the closed cells of the second one of the two sheets of polymeric film adjacent the proximal channels.
18. The system of claim 13 , further comprising a grid projecting outwardly from the closed cells of the second one of the two sheets of polymeric film adjacent the proximal channels.
19. The system of claim 1 , wherein the non-porous film comprises three sheets of polymeric film including two outer sheets and one internal sheet having surfaces sealed to each other to form a sealed region.
20. The system of claim 19 , wherein the plurality of closed cells are formed in one of the two outer sheets of polymeric film.
21. The system of claim 19 , wherein the plurality of closed cells are formed in both of the two outer sheets of polymeric film.
22. The system of claim 21 , wherein the closed cells have a volumetric shape that is generally hemispherical and coincide with each other on the two outer sheets to form a generally spherical shape divided by the inner sheet.
23. The system of claim 1 , further comprising a processor operatively coupled to the negative-pressure source to provide a target pressure to the therapeutic environment in a pressure control mode.
24. The system of claim 23 , wherein the pressure control mode is a continuous pressure mode.
25. The system of claim 23 , wherein the pressure control mode is an intermittent pressure mode.
26. The system of claim 1 , further comprising a processor operatively coupled to the negative-pressure source to provide a variable target pressure to the therapeutic environment in a dynamic pressure mode.
27. The system of claim 1 , further comprising a positive-pressure source fluidly coupled to the therapeutic environment and adapted to deliver a solution through the apertures to the tissue site.
28. The system of claim 27 , further comprising a processor operatively coupled to the positive-pressure source to provide the solution to the therapeutic environment in a predetermined dosage.
29. The system of claim 27 , further comprising a processor operatively coupled to the positive-pressure source to provide the solution to the therapeutic environment for a predetermined time.
30. The system of claim 27 , further comprising a processor operatively coupled to the positive-pressure source to provide the solution to the therapeutic environment at a predetermined rate over time.
31. The system of claim 27 , further comprising a processor operatively coupled to the negative-pressure source and the positive-pressure source to provide negative pressure to the therapeutic environment prior to providing the solution to the therapeutic environment.
32. The system of claim 27 , further comprising a processor operatively coupled to the negative-pressure source and the positive-pressure source to provide negative pressure to the therapeutic environment while providing the solution to the therapeutic environment.
33. The system of claim 1 , wherein the plurality of closed cells are generally hemispherical and have a diameter between about 0.5 mm and 10 mm.
34. The system of claim 1 , wherein the plurality of closed cells are generally hemispherical and have a pitch between about 1.5 mm and 15 mm.
35. The system of claim 1 , wherein the non-porous film comprises two sheets of polymeric film having inner surfaces sealed to each other to form a sealed region having a thickness between about 10 μm and 1000 μm.
36. The system of claim 1 , wherein the closed cells are formed in a pattern of rows and columns.
37. The system of claim 36 , further comprising passageways fluidly coupling the closed cells in at least one of the rows to form a closed chamber.
38. The system of claim 36 , wherein the rows are formed in a nested pattern.
39. The system of claim 36 , wherein the rows are formed in an in-line pattern.
40. The system of claim 36 , wherein the closed cells have a generally spherical shape.
41. The system of claim 1 , wherein the closed cells have a generally spherical shape.
42. The system of claim 1 , wherein the closed cells have a geodesic shape.
43. A method for treating a tissue site, comprising:
positioning a manifold including a non-porous film having a plurality of closed cells and apertures extending through the film, at least two of the closed cells being fluidly coupled by passageways to form a closed chamber, the closed cells and apertures defining fluid flow paths;
covering the manifold and the tissue site with a drape to provide a fluid seal between a therapeutic environment including the manifold on one side of the drape and a local external environment the other side of the drape; and
providing negative pressure from a negative-pressure source coupled to the therapeutic environment wherein the negative pressure is applied to the tissue site through the fluid flow paths.
44. The method of claim 43 wherein the positioning step includes placing the manifold on a surface wound.
45. The method of claim 43 , further comprising delivering a solution from a solution source fluidly coupled to the therapeutic environment wherein the solution is applied through the apertures to the tissue site.
46. The method of claim 43 , further providing a target pressure from the negative-pressure source to the therapeutic environment in a pressure control mode.
47. The method of claim 46 , wherein the pressure control mode is a continuous pressure mode.
48. The method of claim 46 , wherein the pressure control mode is an intermittent pressure mode.
49. The method of claim 43 , further providing a variable target pressure from the negative-pressure source to the therapeutic environment in a dynamic pressure mode.