Reduced pressure treatment system having blockage clearing and dual-zone pressure protection capabilities
A method of treating a tissue site is provided. The method includes applying a reduced pressure to a tissue site with a reduced pressure source. A source pressure is monitored at the reduced pressure source, and a differential pressure is determined between the source pressure and the desired tissue site pressure. If a blockage is present between the reduced pressure source and the tissue site, the differential pressure is limited to a first maximum differential pressure. If no blockage is present between the reduced pressure source and the tissue site, the differential pressure is limited to a second maximum differential pressure.
1. Apparatus for detecting a blockage between a tissue site and a reduced-pressure source fluidly connected to the tissue site, comprising:
a sensing device configured to sense a source pressure (SP) corresponding to pressure provided by the reduced-pressure source and a tissue site pressure (TSP) corresponding to pressure at the tissue site; and
a processor coupled to the sensing device and configured to receive the source pressure (SP) and the tissue site pressure (TSP), the processor having a first input adapted to be set to a target pressure (TP) desired for therapy at the tissue site and a second input adapted to be set to a first maximum differential pressure (DP 1 ) above the target pressure (TP), the processor being configured to
monitor a differential pressure (DP) being the difference between the source pressure (SP) and the target pressure (TP),
determine if the differential pressure (DP) is greater than or equal to the first maximum differential pressure (DP 1 ) when the tissue site pressure (TSP) is less than the target pressure (TP), and
determine whether a change in the source pressure (SP) results in a blockage between the tissue site and the reduced-pressure source.
2. The apparatus according to claim 1 , wherein the processor is configured further to determine whether the change in the source pressure (SP) results in a directionally corresponding change in the tissue site pressure (TSP).
3. The apparatus according to claim 1 , wherein the processor is further configured to indicate a blockage is present if (i) the tissue-site pressure (TSP) is less than the target pressure (TP), (ii) the differential pressure (DP) is greater than or equal to the first maximum differential pressure (DP 1 ), and (iii) a change in the source pressure (SP) does not result in a directionally corresponding change in the tissue-site pressure (TSP).
4. The apparatus according to claim 3 , wherein the first maximum differential pressure (DP 1 ) is less than or equal to about 50 mm Hg.
5. The apparatus according to claim 3 , wherein the processor further comprises an alarm device to alert a user of the presence of a blockage between the reduced pressure source and the tissue site.
6. The apparatus according to claim 1 , wherein the processor is further configured to indicate a blockage is not present if (i) the tissue-site pressure (TSP) is less than the target pressure (TP), (ii) the differential pressure (DP) is greater than or equal to the first maximum differential pressure (DP 1 ), and (iii) a change in the source pressure (SP) does result in a directionally corresponding change in the tissue-site pressure (TSP) confirming no blockage between the reduced pressure source and the tissue site.
7. The apparatus according to claim 6 , wherein the first maximum differential pressure (DP 1 ) is less than or equal to about 50 mm Hg.
8. The apparatus according to claim 1 , wherein the processor is further configured to prevent the source pressure (SP) from increasing further if (i) the tissue-site pressure (TSP) is less than the target pressure (TP), (ii) the differential pressure (DP) is greater than or equal to the first maximum differential pressure (DP 1 ), and (iii) a change in the source pressure (SP) does not result in a directionally corresponding change in the tissue-site pressure (TSP) indicating a blockage between the reduced-pressure source and the tissue site.
9. The apparatus according to claim 8 , wherein the first maximum differential pressure (DP 1 ) is less than or equal to about 50 mm Hg.
10. The apparatus according to claim 8 , wherein the processor further comprises an alarm device to alert a user of the presence of a blockage between the reduced pressure source and the tissue site.
11. The apparatus according to claim 1 , wherein the processor is further configured to allow the source pressure (SP) to increase further if (i) the tissue-site pressure (TSP) is less than the target pressure (TP), (ii) the differential pressure (DP) is greater than or equal to the first maximum differential pressure (DP 1 ), and (iii) a change in the source pressure (SP) does result in a directionally corresponding change in the tissue-site pressure (TSP) indicating no blockage between the reduced pressure source and the tissue site.
12. The apparatus according to claim 11 , wherein the first maximum differential pressure (DP 1 ) is less than or equal to about 50 mm Hg.
13. The apparatus according to claim 1 , wherein the processor further comprises a third input adapted to be set as a second maximum differential pressure (DP 2 ) greater than the target pressure (TP).
14. The apparatus according to claim 13 , wherein the second maximum differential pressure (DP 2 ) is greater than the first maximum differential pressure (DP 1 ).
15. The apparatus according to claim 13 , wherein the first maximum differential pressure (DP 1 ) is less than or equal to about 50 mm Hg.
16. The apparatus according to claim 13 , wherein the second maximum differential pressure is less than or equal to about 100 mm Hg.
17. The apparatus according to claim 13 , wherein the processor is further configured to prevent the source pressure (SP) from increasing further if the differential pressure (DP) is greater than or equal to the second maximum differential pressure (DP 2 ).
18. The apparatus according to claim 13 , wherein the processor further comprises an alarm device to alert a user that the differential pressure (DP) is greater than or equal to the second maximum differential pressure (DP 2 ).
19. The apparatus according to claim 1 , wherein the apparatus further includes a second sensing device.
20. The apparatus according to claim 19 , further comprising a canister fluidly connected between the tissue site and the reduced pressure source, and wherein the second sensing device measures the source pressure (SP) at the canister corresponding to pressure provided by the reduced-pressure source.