Wound therapy system with conduit blockage detection

1. A wound therapy system comprising:

a canister including a first chamber configured to contain fluid removed from a wound site;

a primary conduit having a first end coupled to the canister and a second end coupled to the wound site;

a pump fluidly coupled to the wound site via the primary conduit and configured to apply negative pressure to the wound site via the primary conduit;

a pressure indicator configured to indicate a negative pressure at the pressure indicator;

a second chamber fluidly isolated from the first chamber, wherein the pressure indicator is located within the second chamber, and wherein the second chamber is configured to controllably leak air into the second chamber at a controlled leak rate; and

a secondary conduit having a first end and a second end, the first end of the secondary conduit fluidly coupled to the pressure indicator and the second chamber, the second end of the secondary conduit coupled to the wound site such that the negative pressure at the wound site is fluidly transmitted to the pressure indicator and the second chamber via the secondary conduit;

wherein a blockage in the primary conduit causes the negative pressure indicated by the pressure indicator to differ from the negative pressure applied by the pump, and wherein the pump is configured to remove the air from the second chamber via the secondary conduit and the primary conduit at an air removal rate greater than the controlled leak rate, causing the negative pressure at the pressure indicator to be substantially equal to the negative pressure applied by the pump before the blockage occurs.

2. The wound therapy system of claim 1 , further comprising a filter located along a wall of the second chamber and configured to controllably leak air into the second chamber.

3. The wound therapy system of claim 1 , further comprising a filter coupled to the first end of the secondary conduit proximate the canister and configured to controllably leak air into the secondary conduit.

4. The wound therapy system of claim 1 , wherein the pressure indicator is configured to physically deform or collapse responsive to the negative pressure at the pressure indicator.

5. The wound therapy system of claim 4 , wherein the pressure indicator comprises a plurality of individual sub-indicators, each of the sub-indicators configured to physically deform or collapse at a different negative pressure such that the negative pressure at the pressure indicator is indicated by which of the sub-indicators are physically deformed or collapsed.

6. The wound therapy system of claim 1 , wherein the pressure indicator is configured to indicate the negative pressure at the pressure indicator relative to a plurality of pressure thresholds.

7. The wound therapy system of claim 6 , wherein the plurality of pressure thresholds comprise at least a low pressure threshold and a high pressure threshold such that the pressure indicator indicates whether the negative pressure at the pressure indicator is:

within a first negative pressure range below the low pressure threshold;

within a second negative pressure range between the low pressure threshold and the high pressure threshold; and

within a third negative pressure range above the high pressure threshold.

8. The wound therapy system of claim 7 , wherein each of the negative pressure ranges corresponds to a different color visible on the pressure indicator such that the pressure indicator indicates:

a first color when the negative pressure at the pressure indicator is within the first negative pressure range;

a second color when the negative pressure at the pressure indicator is within the second negative pressure range; and

a third color when the negative pressure at the pressure indicator is within a third negative pressure range.

9. The wound therapy system of claim 1 , wherein the pressure indicator is an electronic pressure sensor coupled to the first end of the secondary conduit proximate the canister and configured to sense the negative pressure within the secondary conduit.

10. The wound therapy system of claim 9 , wherein the pressure indicator is configured to compare the negative pressure at the pressure indicator to one or more pressure thresholds and generate an alarm based on the negative pressure at the pressure indicator relative to one or more pressure thresholds.

11. The wound therapy system of claim 10 , wherein the pressure indicator comprises a wireless communications interface and is configured to transmit the alarm to an external system or device via the wireless communications interface.

12. A method for detecting a blockage in a wound therapy system, the method comprising:

containing fluid removed from a wound site within a first chamber of a canister;

coupling a first end of a primary conduit to the canister and a second end of the primary conduit to the wound site;

operating a pump fluidly coupled to the wound site via the primary conduit to apply negative pressure to the wound site via the primary conduit;

providing a second chamber fluidly isolated from the first chamber;

locating a pressure indicator within the second chamber;

coupling a first end of a secondary conduit to the pressure indicator and to the second chamber, and a second end of the secondary conduit to the wound site such that the negative pressure at the wound site is fluidly transmitted to the pressure indicator and the second chamber via the secondary conduit;

using the pressure indicator to indicate a negative pressure at the pressure indicator; and

detecting the blockage in response to the negative pressure indicated by the pressure indicator differing from the negative pressure applied by the pump;

wherein air controllably leaks into the second chamber at a controlled leak rate, and wherein operating the pump removes the air from the second chamber via the secondary conduit and the primary conduit at an air removal rate greater than the controlled leak rate, causing the negative pressure at the pressure indicator to be substantially equal to the negative pressure applied by the pump before the blockage occurs.

13. The method of claim 12 , further comprising coupling a filter to the first end of the secondary conduit proximate the canister and controllably leaking the air into the secondary conduit via the filter.

14. The method of claim 12 , wherein the pressure indicator is an electronic pressure sensor coupled to the first end of the secondary conduit proximate the canister that senses the negative pressure within the secondary conduit.

15. The method of claim 14 , further comprising:

comparing the negative pressure at the pressure indicator to one or more pressure thresholds; and

generating an alarm based on the negative pressure at the pressure indicator relative to one or more pressure thresholds.

16. The method of claim 15 , further comprising transmitting the alarm to an external system or device via a wireless communications interface of the pressure indicator.

17. The method of claim 15 , further comprising presenting the alarm to a user via a user interface of the pressure indicator.

18. The method of claim 17 , wherein presenting the alarm to the user comprises at least one of:

presenting the alarm visually via an electronic display of the user interface; or

presenting the alarm aurally via a speaker or sounder of the user interface.

19. A wound therapy system comprising:

a canister including a first chamber configured to contain fluid removed from a wound site;

a primary conduit having a first end coupled to the canister and a second end coupled to the wound site;

a pump fluidly coupled to the wound site via the primary conduit and configured to apply negative pressure to the wound site via the primary conduit;

a pressure indicator configured to indicate a negative pressure at the pressure indicator and to physically deform or collapse responsive to the negative pressure, wherein the pressure indicator comprises a plurality of individual sub-indicators, each of the sub-indicators configured to physically deform or collapse at a different negative pressure such that the negative pressure at the pressure indicator is indicated by which of the sub-indicators are physically deformed or collapsed;

a second chamber fluidly isolated from the first chamber; and

a secondary conduit having a first end and a second end, the first end of the secondary conduit fluidly coupled to the pressure indicator and the second chamber, the second end of the secondary conduit coupled to the wound site such that the negative pressure at the wound site is fluidly transmitted to the pressure indicator and the second chamber via the secondary conduit;

wherein a blockage in the primary conduit causes the negative pressure indicated by the pressure indicator to differ from the negative pressure applied by the pump.