FORWARD OSMOSIS MEDICAL AND WOUND CARE DEVICES
20220151835 · 2022-05-19
Inventors
Cpc classification
A61M1/915
HUMAN NECESSITIES
A61M1/69
HUMAN NECESSITIES
A61F13/0206
HUMAN NECESSITIES
A61M1/60
HUMAN NECESSITIES
B01D61/0021
PERFORMING OPERATIONS; TRANSPORTING
A61F13/0213
HUMAN NECESSITIES
A61M2205/7536
HUMAN NECESSITIES
A61M1/98
HUMAN NECESSITIES
A61F13/0223
HUMAN NECESSITIES
B01D61/002
PERFORMING OPERATIONS; TRANSPORTING
A61F13/00063
HUMAN NECESSITIES
B01D61/005
PERFORMING OPERATIONS; TRANSPORTING
A61M1/982
HUMAN NECESSITIES
International classification
A61M1/00
HUMAN NECESSITIES
Abstract
Devices and methods herein remove water from human or animal biological waste fluids using one or more forward osmosis filters. The devices allow for the volume of liquid or semi-liquid waste, including potentially infectious liquid waste, to be filtered to reduce potential exposure of healthcare staff to infectious liquid waste. On a hospital, healthcare staff, or individual patient basis, removing water and concentrating the waste can reduce challenges in management and disposal of the waste. Devices herein use forward osmosis to manage and filter, using one or more suitably sized filter(s), biological fluid exudate from wounds. The devices can be constructed to transport water present in the exudate away from a wound. The wound treatment devices herein not only allow for fluid from wounds to be filtered but also provide structures that can protect wounds from external contaminants, including bacteria and viruses. The wound treatment devices can be incorporated into negative pressure wound therapy systems, if desired.
Claims
1. A wound treatment device comprising: a filter functioning as a forward osmosis filter to remove water from wound drainage fluid, the filter configured to be connectable to at least one chamber or compartment, said chamber for collecting the processed liquid or permeate; at least one osmotic agent to provide the osmotic potential to pull water from the wound drainage fluid through the forward osmosis filter; said osmotic agent located in said chamber and said osmotic agent in contact with the filter; said filter and chamber configured to be a wound dressing and configured to be placed over the wound and secured to the patient.
2. The device of claim 1 further comprising: an absorbent layer or a wicking layer or both between the wound and the forward osmosis filter.
3. The device of claim 1 further comprising: an absorbent layer or a wicking layer or both in said chamber or compartment.
4. The device of claim 1 wherein said chamber or compartment can be removed from the filter and replaced.
5. The device of claim 1 wherein the forward osmosis filter and a second layer of material are secured together to form the chamber.
6. The device of claim 5 wherein the second layer of material provides for a high rate of water vapor transmission.
7. The device of claim 1 further comprising: a port for access to the chamber to add or remove materials from said chamber.
8. The device of claim 1 wherein the wound treatment device is part of a negative pressure wound therapy system.
9. A system for treating and healing wounds comprising: a forward osmosis wound dressing device configured to cover a wound; said wound dressing device configured to transport at least some portion of the water component of the wound fluid exudate away from the wound and out of the wound dressing device via the pressure created by transporting said water through a forward osmosis filter; said wound dressing device configured to be connectable to a secondary collection compartment that collects the filtrate transported out of the wound dressing device.
10. The device of claim 9 wherein at least a portion of said secondary collection compartment material provides for a high rate of water vapor transmission.
11. A negative pressure wound therapy dressing having vacuum access for application of vacuum to the wound; said wound dressing incorporating a forward osmosis membrane to remove water from at least some portion of the wound exudate.
12. The device of claim 11 wherein some portion of the exudate is removed and transported away from the dressing via the vacuum for collection into a container.
13. The device of claim 11 wherein some portion of the water in the filtrate is removed from the wound dressing via transfer as water vapor through a material with a high moisture vapor transmission rate.
14. A device for managing wound exudate fluid comprising: a secondary collection compartment configured to have a connection point connectable to a wound dressing; said secondary collection compartment separated from said wound dressing; said secondary collection compartment configured to store liquid entering the secondary collection compartment via the connection point; said secondary collection compartment located near the patient.
15. The device of claim 14 wherein at least a portion of said secondary collection compartment material provides for a high rate of water vapor transmission.
16. A device for treating biological waste fluids comprising: a first chamber for inputting at least one biological waste fluid; a filter functioning as a forward osmosis filter to remove water from said biological waste fluid, the filter configured to be connectable to said first chamber; said forward osmosis filter connectable between said first chamber and a second chamber, said second chamber for collecting the processed liquid or filtrate; at least one draw material to provide the osmotic drive to pull water from said first chamber into said second chamber; said draw material located in the second chamber and said draw material in contact with the filter.
17. A system for treating biological waste fluids comprising: at least one chamber for receiving one or more biological waste fluids; a filter in contact with a first chamber; draw material connectable to the filter; said filter functioning as a forward osmosis filter to remove water from the biological waste fluid while keeping bacterial and viral contaminants from passing through the filter.
18. A system for treating biological waste fluids comprising: a forward osmosis filter to convert the waste fluid to reduce the volume of potentially infectious liquid waste and reduce healthcare staff exposure to potentially infectious liquid waste.
19. The system of claim 5 further comprising: chemicals or other materials on the filter material or separate from the filter material and on either side or both sides of the filter material to reduce odor, reduce bacterial or viral load, block or bind or transform specific components present in the biological waste fluid, or absorb left over liquid or the like.
20. A method comprising: providing for an opening into a first chamber for input of biological waste fluid into said first chamber; providing a forward osmosis filter in contact with said first chamber; separating said first chamber from a second chamber with said forward osmosis filter; positioning said forward osmosis filter for contact with at least a portion of the biological waste fluids input into the first chamber; and providing for an outlet for removal of filtrate from the second chamber.
Description
BRIEF DESCRIPTION OF DRAWINGS
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DETAILED DESCRIPTION
[0062]
[0063] The chamber or chambers 134 include draw solute(s) or draw material(s) 140. Exudate from the wound contacts the forward osmosis filter 120 and a portion of the water in the fluid is pulled through the filter into the chamber(s) 134 by forward osmosis leaving other materials from the exudate on the wound side of the filter including bacteria and viruses. Exudate can be considered biological waste fluid. Biological waste fluid as used herein can include, but is not limited to, wound exudate, blood, urine, digestive fluids, digestive output, sputum, cerebral spinal fluid, lymph and the like once removed from the body and no longer needed.
[0064] The second layer 116 extends beyond the seal perimeter 150 and incorporates an adhesive 170 to provide a means for securing the wound dressing 110 to the patient and covering the wound.
[0065] The second layer 116 may be optionally made of a material that provides for moisture vapor transmission through it to reduce the amount of liquid contained in the chamber 134. The water vapor transmission rate (MVTR) is comparable with other commonly used wound care dressings, such as those made of single or multilayer thermoplastic polyurethanes. The MVTR for these materials can be adjusted for the specific application. Higher MVTR materials, including higher MVTR polyurethane, are preferred. For example, a polyurethane film with an active area of 10 cm×10 cm and a MVTR of 3000 g/m.sup.2/24 hours, would allow a nominal 30 g of water vapor to pass through in 24 hours.
[0066] As water vapor leaves the wound dressing through this material, the draw material becomes more concentrated allowing for continued osmotic action. The draw material can pull additional water through the filter membrane which can then pass through the polyurethane film as water vapor and the cycle continues. Preferably, the moisture vapor transmission rate is great enough to keep the chamber 134 from completely filling with water and/or substantially diluting the draw material 140 such that it is no longer effective in pulling water across the membrane 120. At a lower MVTR, chamber 134 may fill up faster. The second layer 116 may be optionally made of stretchable material to allow it to expand and provide for a larger volume inside the chamber 134. This expansion can be measured manually or with electronic sensors to identify the amount of fluid inside the chamber. Alternatively, the second layer 116 can be a rigid or semi rigid material and can be a defined shape, such as a hollow hemisphere. An air vent may be included.
[0067] Other items can be added to the wound dressing 110 such as for reducing odor, reducing bacterial or viral load, blocking or binding or transforming specific components present in the biological fluid, adding or changing color, or absorbing liquid or the like.
[0068] Additional layers can be added to the wound dressing 110 including, but not limited to, a non-adherent layer (not shown) placed against the wound, an absorbent or wicking layer 160 between the wound and forward osmosis filter, an absorbent or wicking layer between the forward osmosis filter and the second layer (not shown), an oxygen permeable layer to allow oxygen transport to the wound (not shown), and/or a wound filling layer (not shown), for example. For NPWT, a vacuum distribution layer (not shown) may be employed. The vacuum distribution layer may include a more open structure, for example, an open cell foam. Even in non-NPWT wound dressings, this type of open layer may enhance distribution of oxygen to the wound to promote wound healing. One or more of the layers may be multi-functional. Multiple layers can be used for any of the additional layers. The absorbent layers are fluid holding layers and may be hydrophilic or hydrophobic material.
[0069] In
[0070] In
[0071] Measurement examples include, but are not limited to, fullness of the chamber and salinity. The chamber can be emptied via a vacuum pump, such as a peristaltic pump, attached to the chamber(s) 234. Emptying can be done automatically.
[0072]
[0073] As shown in
[0074] The secondary collection compartment 390 can contain one or more absorbent layers or wicking layers (not shown). This secondary collection compartment 390 can be connected to the wound dressing chamber by an extended passageway, such as tubing, allowing for positioning the secondary collection compartment 390 in a location separate from the wound, for example, attached to the patient's belt. Connection 368 allows for opening, removal, or replacement of either wound dressing 310 or secondary collection compartment 390. The secondary collection compartment 390 may also be useful in wound drainage systems that do not use a forward osmosis filter.
[0075]
[0076] Vacuum from the NPWT pump is applied to the wound and water in the exudate is pulled through the forward osmosis filter 420 by osmotic agents (not shown) and is captured between the forward osmosis filter 420 and the second layer 416. Other layers and materials can be incorporated as previously described. Foam or gauze 460 are commonly used in filling the wound in traditional NPWT.
[0077] Alternatively, forward osmosis can work in combination with a cannister collection system where some exudate can be sucked into the pump tubing. This provides a dual action for managing exudate. This may allow for a small size cannister or other collection device, for example a small bag with foam sealed inside, to be used and may extend the life of the wound dressing.
[0078]
[0079] The outlet 560 from the second compartment 534 is located on the second sheet side 514A of the bag 510 and allows the water that passes through the filter 520 from the first chamber 532 to the second chamber 534 to be emptied from the collection bag 510. The outlet 560 can allow for single, periodic, or continual emptying of the second chamber 534. The outlet 60 in this embodiment has a mechanical valve 562 that preferably allows for one-way flow out of the bag 510. Other mechanical or electromechanical approaches for opening the outlet 560 can be used and can even include automated activation of the valve 562 based on a set volume.
[0080] The second chamber includes the draw solute(s) 40 which can be added during or post-manufacture of the device. A separate opening 542 can be included on the second sheet side 514A of the bag 510 to provide access for adding draw material(s) 540. Other items can be added into the chambers of the bag such as for reducing odor, reducing bacterial or viral load, blocking or binding or transforming specific components present in the biological waste fluid, or absorbing left over liquid or the like.
[0081] In alternative embodiments (not shown), the container can be a rigid container or a combination of rigid and flexible materials. The container can have multiple inputs. The outlet port can attach to tubing to allow transfer of the water, and other materials in the water, to a selected location for disposal such as a sink or toilet.
[0082] As filtrate volume is increased in the second compartment, especially if the compartment is rigid or otherwise constrained, pressure created by the increase in filtrate volume within the compartment can be harnessed to open the outlet valve to expel a portion of the filtrate. In another embodiment (not shown) the inlet port is connected to tubing with a suction cannister port connection on it to allow transfer of collected fluid from the cannister. The tubing can be put into a peristaltic pump to drive the collected fluid from the suction cannister port into the fluid collection bag.
[0083] In yet another embodiment (not shown), no outlet is provided or an outlet is created post-manufacture, for example by piercing the container with a spiked connector.
[0084] In yet another embodiment (not shown) a forward osmosis device is used for larger volumes or even bulk collections of biological waste fluids, potentially from different sources. It is of larger scale than the forward osmosis device described.
[0085] In
[0086] A portion of water in the filtrate can be vaporized by adding heat or by other methods to keep the draw solution concentrated. Advantageously, this can reduce the amount of draw material required and associated need for refilling of draw material while reducing the amount of fluid that is otherwise stored and possibly emptied from the second chamber 634.
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[0088] While various aspects and exemplary embodiments have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and exemplary embodiments disclosed herein are for the purposes of illustration and are not intended to be limiting.