SYSTEMS AND METHODS FOR DELIVERING FLUID TO A WOUND THERAPY DRESSING
20210196871 · 2021-07-01
Inventors
- Christopher Brian Locke (Bournemouth, GB)
- Kevin W. Bendele (Oldsmar, FL, US)
- James A. Luckemeyer (San Antonio, TX, US)
Cpc classification
A61M2205/3344
HUMAN NECESSITIES
A61M1/85
HUMAN NECESSITIES
A61M1/73
HUMAN NECESSITIES
A61M1/966
HUMAN NECESSITIES
International classification
Abstract
Systems and methods for delivery of fluid to a wound therapy dressing. In exemplary embodiments, a pressure sensor measures the pressure at the wound therapy dressing and restricts fluid flow to the wound therapy dressing when a predetermined pressure is achieve.
Claims
1. An apparatus for use with a wound dressing, comprising: a controller operatively coupled to a fluid-flow device; wherein the controller is configured to: activate the fluid-flow device to provide fluid to the wound dressing until a predetermined pressure in a range of −10 mmHg to 0 mmHg at the wound dressing is reached.
2. The apparatus of claim 1, wherein the fluid-flow device comprises a valve.
3. The apparatus of claim 2, wherein the valve is a solenoid-actuated pinch valve.
4. The apparatus of claim 1, wherein the fluid-flow device comprises a pump, the pump configured to be activated by the controller.
5. The apparatus of claim 1, wherein the predetermined pressure is indicative of a pressure at the wound dressing.
6. The apparatus of claim 1, wherein the fluid-flow device comprises: a gravity-fed reservoir configured to be fluidly coupled to the wound dressing; and a valve configured to be positioned between the gravity-fed reservoir and the wound dressing; wherein the controller is configured to actuate the valve to restrict fluid flow when the predetermined pressure is reached.
7. The apparatus of claim 1, wherein the fluid-flow device comprises: a reservoir configured to be fluidly coupled to the wound dressing; and a pump configured to be fluidly coupled between the reservoir and the wound dressing; wherein the controller is configured to activate the pump to deliver fluid from the reservoir to the wound dressing until the predetermined pressure is reached.
8. The apparatus of claim 1, wherein the controller is configured to generate an audible signal when the predetermined pressure is reached.
9. The apparatus of claim 1, wherein the controller is configured to generate a visual signal when the predetermined pressure is reached.
10. A non-transitory computer-readable medium comprising executable instructions for performing steps in a method for delivering fluid to a wound dressing, wherein the executable instructions configure a controller to: send a first signal to a fluid-flow device to permit fluid flow to the wound dressing; determine a pressure at the wound dressing based on a signal received from a pressure sensor; and upon the pressure reaching a predetermined pressure, send a second signal to the fluid-flow device to restrict fluid flow to the wound dressing; wherein the predetermined pressure is in a range of −10 mmHg to 0 mmHg.
11. The non-transitory computer-readable medium of claim 10, wherein the executable instructions further configure the controller to: activate a negative-pressure source to create a negative pressure at the wound dressing; and deactivate the negative-pressure source prior to sending the first signal to the fluid-flow device to permit fluid flow to the wound dressing.
12. The non-transitory computer-readable medium of claim 11, wherein the executable instructions further configure the controller to: vent a reservoir to atmosphere after deactivating the negative-pressure source and prior to sending the first signal to the fluid-flow device to permit fluid flow to the wound dressing.
13. A system for providing wound therapy, comprising: a wound dressing in fluid communication with a negative-pressure source and a reservoir; a fluid-flow device fluidly coupled between the reservoir and the wound dressing; and a controller operatively coupled to the negative-pressure source and the fluid-flow device; wherein the controller is configured to activate the fluid-flow device to provide fluid from the reservoir to the wound dressing until a predetermined pressure in a range of −10 mmHg to 0 mmHg at the wound dressing is reached.
14. The system of claim 13, further comprising a pressure sensor configured to be disposed at the wound dressing, the pressure sensor further configured to be operatively coupled to the controller.
15. The system of claim 13, further comprising a vent in fluid communication with an interior of the reservoir and atmosphere, the vent operatively coupled to the controller.
16. The system of claim 15, wherein the controller is configured to open the vent to permit fluid communication between the interior of the reservoir and atmosphere prior to activating the fluid-flow device to provide fluid from the reservoir to the wound dressing.
17. The system of claim 16, wherein the controller is configured to deactivate the negative-pressure source prior to activating the fluid-flow device to provide fluid from the reservoir to the wound dressing.
18. The system of claim 13, wherein the fluid-flow device comprises a pump.
19. The system of claim 13, wherein the fluid-flow device comprises a valve.
20. The system of claim 19, wherein the valve comprises a solenoid-actuated pinch valve.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] The following drawings form part of the present specification and are included to further demonstrate certain aspects of exemplary embodiments of the present invention.
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
[0032]
DETAILED DESCRIPTION
[0033] Various features and advantageous details are explained more fully with reference to the non-limiting embodiments that are illustrated in the accompanying drawings and detailed in the following description. Descriptions of well-known starting materials, processing techniques, components, and equipment are omitted so as not to unnecessarily obscure the invention in detail. It should be understood, however, that the detailed description and the specific examples, while indicating embodiments of the invention, are given by way of illustration only, and not by way of limitation. Various substitutions, modifications, additions, and/or rearrangements within the spirit and/or scope of the underlying inventive concept will become apparent to those skilled in the art from this disclosure.
[0034] In the following description, numerous specific details are provided, such as examples of material selections, dimensions, etc., to provide a thorough understanding of the present embodiments. One skilled in the relevant art will recognize, however, that the invention may be practiced without one or more of the specific details, or with other methods, components, materials, and so forth. In other instances, well-known structures, materials, or operations are not shown or described in detail to avoid obscuring aspects of the invention.
[0035]
[0036] Certain embodiments may utilize a gravity fluid flow from fluid supply reservoir 140 to wound dressing 120 without utilizing a pumping device for fluid flow device 150. In such embodiments, fluid flow device 150 may be a valve (e.g., a solenoid-actuated pinch valve) configured to control the flow of fluid between fluid supply reservoir 140 and wound dressing 120. In still other embodiments, negative pressure source 130 may draw fluid into wound dressing 120 from fluid supply reservoir 140, without the aid of gravity feed or a pumping action from fluid flow device 150.
[0037] In particular exemplary embodiments, negative pressure source 130 may comprise a diaphragm vacuum pump. In certain embodiments, system 100 may also comprise a filter or muffler 137 coupled to negative pressure source 130 to reduce the operating noise of negative pressure source 130 and/or filter air exiting negative pressure source 130.
[0038] In certain exemplary embodiments, fluid flow device 150 may comprise a pump, e.g., a peristaltic, centrifugal or other suitable pump. In other exemplary embodiments, fluid flow device may comprise a gravity feed system instead of (or in conjunction with) a pump to deliver fluid to wound dressing 120. In such embodiments, a valve between the gravity feed system and wound dressing 120 can be used to restrict the fluid flow to wound dressing 120 when the predetermined pressure is reached, as explained more fully below.
[0039] In the disclosed embodiment, system 100 also comprises a vent 190 on reservoir 110, and a check valve 180 configured to allow flow in the direction from wound dressing 120 towards negative pressure source 130, and restrict fluid flow in the reverse direction. The exemplary embodiment shown in
[0040]
[0041] During initial operation of system 100 shown in
[0042] Fluid flow device 150 can then be activated to begin fluid delivery to wound dressing 120. In particular embodiments, fluid flow device 150 may be configured to flow approximately 100 ml/minute. As fluid is pumped from fluid flow device 150 to wound dressing 120, the pressure at wound dressing 120 (which can be monitored via pressure sensor 160) will increase. When wound dressing 120 reaches a predetermined pressure, pressure sensor 160 (which may be used to sense both positive and negative pressures) can send a control signal to control device 165 (e.g. a control switch or actuator) to restrict fluid flow from fluid flow device 150 to wound dressing 120. The increase in pressure of wound dressing 120 can be used as an indication that fluid from fluid flow device 150 has sufficiently filled wound dressing 120. By monitoring the pressure of wound dressing 120 with pressure sensor 160, system 100 can reduce the likelihood that wound dressing 120 will be overfilled. This can reduce waste of fluid and leakage of wound dressing associated with overfilling. It is understood that interface circuitry (not shown) may be utilized to generate a sufficiently strong control signal and to implement the control logic.
[0043] As previously mentioned, in certain embodiments, fluid flow device 150 may be a valve (e.g., a solenoid-actuated pinch valve) that restricts fluid flow from fluid supply reservoir 140 or a pump that is activated to provide fluid flow. The operation of fluid flow device 150 (e.g., the position of a valve or the activation/deactivation of a pump) may be automatically altered when a predetermined pressure is reached at wound dressing 120. In exemplary embodiments, the predetermined pressure of wound dressing 120 at which the operation of fluid flow device 150 is altered may be approximately 1.0 mm Hg (gauge pressure as measured by pressure indicator 160). In specific embodiments the predetermined pressure may be −10 and 10 mm Hg, including −10, −9, −8, −7, −6, −5, −4, −3, −2, −1, 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 mm Hg, or any values between.
[0044] In other embodiments a user may monitor pressure sensor 160 and manually control operation of fluid flow device 150 when wound dressing 120 reaches the predetermined pressure. For example, a user may deactivate fluid flow device 150 by manipulating a control switch or restrict fluid flow from fluid flow device 150 by closing a valve.
[0045] When wound dressing 120 is sufficiently filled with fluid, the user may continue with the desired fluid instillation and vacuum therapy treatments. Exemplary embodiments can be used for each instillation cycle, which may offer advantages for wound dressings on articulated joints (e.g., knee) where the wound or dressing volume could be influenced by the patient's body position. In certain embodiments utilizing a foam dressing, the dressing volume can change over time in part due to compression-set of the foam. For example, the volume of the foam may be reduced over time as the foam is subjected to pressure. This change in volume occupied by the foam can affect the volume of fluid needed to fill wound dressing 120. Such volume changes can be accommodated by exemplary embodiments, which utilize pressure readings to indicate when the wound dressing has received a sufficient volume of liquid.
[0046] It is understood that the features shown
[0047] Referring now to
[0048] As shown in
[0049] Referring now to
[0050] In certain embodiments, system 100 may comprise an audible or visual pressure indicator 123 at the dressing or elsewhere in the negative pressure path (e.g., a Prevena™ dressing type available from Kinetic Concepts, Inc., San Antonio, Tex. U.S.A. has a visual indicator that retracts when the dressing is below a pressure setpoint and extends when the dressing is above the pressure setpoint) that the predetermined pressure has been reached and that wound dressing 120 contains a sufficient volume of fluid 125. At this stage, the user may proceed with the desired fluid instillation and vacuum therapy treatments.
[0051] The schematic flow chart diagrams that follow are generally set forth as logical flow chart diagrams. As such, the depicted order and labeled steps are indicative of one embodiment of the presented method. Other steps and methods may be conceived that are equivalent in function, logic, or effect to one or more steps, or portions thereof, of the illustrated method. Additionally, the format and symbols employed are provided to explain the logical steps of the method and are understood not to limit the scope of the method. Although various arrow types and line types may be employed in the flow chart diagrams, they are understood not to limit the scope of the corresponding method. Indeed, some arrows or other connectors may be used to indicate only the logical flow of the method. For instance, an arrow may indicate a waiting or monitoring period of unspecified duration between enumerated steps of the depicted method. Additionally, the order in which a particular method occurs may or may not strictly adhere to the order of the corresponding steps shown.
[0052] Referring now to
[0053] In this exemplary embodiment, step 210 comprises activating the negative pressure source to create negative pressure on the wound dressing. Step 220 comprises de-activating the negative pressure source and maintaining negative pressure on the wound dressing. Step 230 comprises activating the fluid flow device to begin fluid flow to the wound dressing, in this embodiment. Step 240 comprises monitoring the wound dressing pressure with the pressure sensor and determining when the predetermined wound dressing pressure is reached. In this embodiment, step 250 comprises sending a control signal from the pressure sensor to the control device to stop the fluid flow from the fluid flow device.
[0054] All of the methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the apparatus and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. In addition, modifications may be made to the disclosed apparatus, and components may be eliminated or substituted for the components described herein, where the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope, and concept of the invention as defined by the appended claims.