Evaporative fluid management canister for wound therapy system
A canister for use with a wound therapy system includes first and second compartments configured to receive and contain wound exudate, and an airflow pathway. The airflow pathway includes a planar region positioned between the first compartment and the second compartment, an inlet extending from a first end of the planar region at an obtuse angle relative to the planar region, an outlet at a second end of the planar region.
1 . A canister for use with a wound therapy system, comprising:
first and second compartments configured to receive and contain wound exudate;
an airflow pathway comprising:
a planar region positioned between the first compartment and the second compartment;
an inlet extending from a first end of the planar region at an obtuse angle relative to the planar region; and
an outlet at a second end of the planar region.
2 . The canister of claim 1 , wherein the first compartment is separated from the airflow pathway by a first filter configured to:
allow water molecules to pass from the first compartment to the airflow pathway; and
prevent contaminants from passing from the first compartment to the airflow pathway.
3 . The canister of claim 2 , wherein the first filter comprises a polyether urethane film.
4 . The canister of claim 3 , comprising a rigid structure defining the first and second compartments and formed of a thermoplastic polyurethane resin.
5 . The canister of claim 4 , wherein the rigid structure is ultrasonically welded to the polyether urethane film.
6 . The canister of claim 2 , wherein the first filter comprises a film having a high moisture vapor transmission rate.
7 . The canister of claim 6 , wherein the high moisture vapor transmission rate is in a range between 2000 and 5000 g/m 2 /day.
8 . The canister of claim 1 , wherein the inlet is cylindrical.
9 . The canister of claim 1 , wherein the inlet is formed to match a cross-sectional shape of a fan.
10 . The canister of claim 1 , wherein the inlet widens proximate the planar region to reduce turbulence and back-pressure in the airflow pathway.
11 . The canister of claim 1 , further comprising a curved wall providing a smooth transition from the inlet to the planar region.
12 . The canister of claim 1 , wherein the obtuse angle is in a range between 130 degrees and 150 degrees.
13 . The canister of claim 1 , wherein the inlet has a screw-type form configured to provide rotation of airflow therethrough.
14 . A therapy system, comprising:
a dressing configured to be sealed over a wound site;
a negative pressure source configured to draw a negative pressure at the dressing and cause wound exudate to move out of the dressing;
a canister configured to be placed in fluid communication with the dressing, the canister comprising:
first and second compartments configured to receive and retain the wound exudate from the dressing; and
an airflow pathway comprising:
a planar region positioned between the first compartment and the second compartment;
an inlet extending from a first end of the planar region at an obtuse angle relative to the planar region; and
an outlet at a second end of the planar region; and
an air mover aligned with the inlet and configured to force air through the airflow pathway to facilitate transfer of moisture from the wound exudate out of the first and second components.
15 . The therapy system of claim 14 , comprising a housing, wherein the air mover and the negative pressure source are installed in the housing, and wherein the canister is configured to be selectively and removeably coupled to the housing.
16 . The therapy system of claim 15 , further comprising a battery installed in the housing and configured to power the air mover and the negative pressure source.
17 . The therapy system of claim 14 , further comprising a controller configured to control the air mover to operate in a pulsing pattern.
18 . The therapy system of claim 14 , wherein the first and second compartments are separated from the airflow pathway by a film material configured to:
allow water molecules to pass from the first and second compartments to the airflow pathway; and
prevent contaminants from passing from the first and second compartments to the airflow pathway.
19 . A method of manufacturing a canister for a wound therapy device, comprising:
providing first and second rigid structures formed of a polyurethane resin;
providing first and second filters formed of a polyether urethane film;
ultrasonically welding the first rigid structure to the first filter;
ultrasonically welding the second rigid structure to the second filter; and
ultrasonically welding the first rigid structure to the second rigid structure such that a planar airflow pathway is defined between the first filter and the second filter.
20 . The method of claim 19 , comprising forming the first and second filters such that the first and second filters are configured to allow water molecules to pass across the first and second filters.