Oxygen therapy with fluid removal
An apparatus for treating a tissue site includes a dressing, an oxygen source, a valve, and a negative-pressure source. The dressing is configured to be sealed around the tissue site. The oxygen source is fluidly coupled to the dressing and configured to provide a low flow of oxygen. A first port of the valve is fluidly coupled to the dressing and the valve moves between a closed position preventing flow through the valve and an open position permitting flow through the valve. The negative-pressure source is fluidly coupled to a second port of the valve and provides negative pressure to the second port of the valve at a non-therapeutic level. The valve separates the negative-pressure source from the dressing and selectively opens when a positive pressure is applied on an upstream side of the valve.
1. An apparatus for treating a tissue site, the apparatus comprising:
a dressing configured to be sealed around the tissue site;
an oxygen source fluidly coupled to the dressing and configured to provide a low flow of oxygen;
a first valve comprising a first port and a second port, wherein the first port is fluidly coupled to the dressing and the first valve moves between a closed position preventing flow through the first valve and an open position permitting flow through the first valve; and
a negative-pressure source fluidly coupled to the second port of the first valve and providing negative pressure to the second port of the first valve in an operating range of non-therapeutic negative pressure;
wherein the first valve selectively opens if a pressure differential between the first port and the second port is equal to or greater than an opening pressure of the first valve;
a second valve fluidly coupled between the dressing and the oxygen source and configured to release excess pressure in the dressing.
2. The apparatus of claim 1 , wherein the oxygen source provides a continuous flow of oxygen at a rate not greater than 25 milliliters per hour.
3. The apparatus of claim 1 , wherein the oxygen source provides a continuous flow of oxygen at a rate not less than 3 milliliters per hour and not greater than 25 milliliters per hour.
4. The apparatus of claim 1 , wherein the operating range of non-therapeutic negative pressure is from 15 millimeters of mercury to 50 millimeters of mercury.
5. The apparatus of claim 1 , wherein a positive pressure is applied on an upstream side of the first valve.
6. The apparatus of claim 1 , wherein the opening pressure of the first valve is at least 20 millimeters of mercury.
7. The apparatus of claim 1 , further comprising a container disposed in a fluid path between the first valve and the negative-pressure source.
8. The apparatus of claim 1 , wherein the dressing comprises a cover configured to have a leak rate no greater than 5 milliliters per hour.
9. The apparatus of claim 1 , further comprising:
a pressure sensor fluidly coupled to the first valve; and
a controller operatively coupled to the negative-pressure source and to the pressure sensor, the controller configured to operate the negative-pressure source to maintain the negative pressure in the operating range based on a feedback signal from the pressure sensor.
10. The apparatus of claim 1 , wherein the second valve is configured to release pressure in excess of 30 millimeters of mercury.
11. The apparatus of claim 1 , wherein the dressing comprises:
a tissue interface; and
a cover configured to be disposed over the tissue interface.
12. The apparatus of claim 11 , further comprising a sealing layer disposed between the cover and the tissue interface.
13. The apparatus of claim 12 , wherein the sealing layer comprises a material or combination of materials selected from a group consisting of: a silicone gel, a soft silicone, hydrocolloid, hydrogel, polyurethane gel, polyolefin gel, hydrogenated styrenic copolymer gel, a foamed gel, a soft closed cell foam, polyurethane, polyolefin, hydrogenated styrenic copolymers, acrylic adhesives, and light-sensitive or light-deactivated adhesives.
14. The apparatus of claim 1 , wherein the dressing comprises:
a tissue interface;
a hydrophilic filler configured to be disposed over the tissue interface; and
a cover configured to be disposed over the tissue interface.
15. The apparatus of claim 14 , wherein the hydrophilic filler comprises a material selected from a group consisting of open-cell hydrophilic foams and super-absorbent polymers in a form of particulates, fibers, or textiles.
16. The apparatus of claim 14 , wherein the hydrophilic filler comprises an assembly of super absorbent textile between two or more layers of non-woven textile.
17. The apparatus of claim 14 , further comprising a sealing layer disposed between the cover and the hydrophilic filler.
18. The apparatus of claim 17 , wherein the sealing layer comprises a material or combination of materials selected from a group consisting of: a silicone gel, a soft silicone, hydrocolloid, hydrogel, polyurethane gel, polyolefin gel, hydrogenated styrenic copolymer gel, a foamed gel, a soft closed cell foam, polyurethane, polyolefin, hydrogenated styrenic copolymers, acrylic adhesives, and light-sensitive or light-deactivated adhesives.