Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/90—Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
  • A61M1/98—Containers specifically adapted for negative pressure wound therapy
  • A61M1/982—Containers specifically adapted for negative pressure wound therapy with means for detecting level of collected exudate
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F13/00051—Accessories for dressings
  • A61F13/00055—Saturation indicators
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F13/02—Adhesive bandages or dressings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F13/02—Adhesive bandages or dressings
  • A61F13/0203—Adhesive bandages or dressings with fluid retention members
  • A61F13/0206—Adhesive bandages or dressings with fluid retention members with absorbent fibrous layers, e.g. woven or non-woven absorbent pads or island dressings
• • A—HUMAN NECESSITIES
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  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F13/05—Bandages or dressings; Absorbent pads specially adapted for use with sub-pressure or over-pressure therapy, wound drainage or wound irrigation, e.g. for use with negative-pressure wound therapy [NPWT]
• • A—HUMAN NECESSITIES
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  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/71—Suction drainage systems
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• • A—HUMAN NECESSITIES
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  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
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• • A—HUMAN NECESSITIES
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  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
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  • A61M1/96—Suction control thereof
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• • A—HUMAN NECESSITIES
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  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
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• • A—HUMAN NECESSITIES
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  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
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  • A61M1/98—Containers specifically adapted for negative pressure wound therapy
  • A61M1/984—Containers specifically adapted for negative pressure wound therapy portable on the body
  • A61M1/985—Containers specifically adapted for negative pressure wound therapy portable on the body the dressing itself forming the collection container
• • A—HUMAN NECESSITIES
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  • A61M27/00—Drainage appliance for wounds or the like, i.e. wound drains, implanted drains
• • G—PHYSICS
  • G08—SIGNALLING
  • G08B—SIGNALLING OR CALLING SYSTEMS; ORDER TELEGRAPHS; ALARM SYSTEMS
  • G08B21/00—Alarms responsive to a single specified undesired or abnormal condition and not otherwise provided for
  • G08B21/18—Status alarms
  • G08B21/20—Status alarms responsive to moisture
• • A—HUMAN NECESSITIES
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  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F2013/00089—Wound bandages
  • A61F2013/0017—Wound bandages possibility of applying fluid
  • A61F2013/00174—Wound bandages possibility of applying fluid possibility of applying pressure
• • A—HUMAN NECESSITIES
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  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F2013/00361—Plasters
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  • A61F2013/00412—Plasters use for use with needles, tubes or catheters
  • A61F2013/00421—Plasters use for use with needles, tubes or catheters with double adhesive layer
• • A—HUMAN NECESSITIES
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  • A61F13/00—Bandages or dressings; Absorbent pads
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• • A—HUMAN NECESSITIES
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  • A61F13/00—Bandages or dressings; Absorbent pads
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• • A—HUMAN NECESSITIES
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  • A61F13/00—Bandages or dressings; Absorbent pads
  • A61F2013/00361—Plasters
  • A61F2013/00902—Plasters containing means
  • A61F2013/0094—Plasters containing means for sensing physical parameters
  • A61F2013/00961—Plasters containing means for sensing physical parameters electrical conductivity
• • A—HUMAN NECESSITIES
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  • A61M1/71—Suction drainage systems
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• • A—HUMAN NECESSITIES
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  • A61M1/71—Suction drainage systems
  • A61M1/78—Means for preventing overflow or contamination of the pumping systems
  • A61M1/784—Means for preventing overflow or contamination of the pumping systems by filtering, sterilising or disinfecting the exhaust air, e.g. swellable filter valves
• • A—HUMAN NECESSITIES
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  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/90—Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
  • A61M1/96—Suction control thereof
  • A61M1/962—Suction control thereof having pumping means on the suction site, e.g. miniature pump on dressing or dressing capable of exerting suction
• • A—HUMAN NECESSITIES
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  • A61M2205/6081—Colour codes

Definitions

• the present disclosure relates generally to medical treatment systems and, more particularly, but not by way of limitation, to systems and methods for electrically detecting the presence of exudates in dressings, such as absorbent, reduced-pressure dressings.
• vacuum therapy provides a number of benefits, which may include faster healing and increased formulation of granulation tissue.
• reduced pressure is applied to tissue through a porous pad or other manifold device.
• the porous pad contains cells or pores that are capable of distributing reduced pressure to the tissue and channeling fluids that are drawn from the tissue. Reduced pressure may also be used to remove fluids and for other purposes.
• a dressing for receiving and retaining an ionic fluid includes an absorbent layer for placing in fluid communication with the tissue site and for receiving and retaining the ionic fluids.
• the absorbent layer has a first side and a second, patient-facing side.
• the dressing further includes a sealing member for covering the absorbent layer and a first galvanic cell associated with the absorbent layer.
• the first galvanic cell is configured to produce a voltage when the absorbent layer proximate to the first galvanic cell is substantially saturated with the ionic fluid.
• a system for treating a tissue site on a patient with reduced pressure includes an absorbent layer for placing proximate to the tissue site, a sealing member for covering the dressing and a portion of the patient's epidermis to form a fluid seal, and a reduced-pressure source fluidly coupled to the absorbent layer for providing reduced pressure to the absorbent layer.
• the system further includes a galvanic cell associated with the absorbent layer. The galvanic cell is configured to produce a voltage when the absorbent layer proximate to the galvanic cell is substantially saturated with an ionic fluid.
• the system may also include a monitoring unit electrically coupled to the galvanic cell for receiving power or voltage from the galvanic cell.
• a method for treating a tissue site includes providing a dressing.
• the dressing includes an absorbent layer for placing in fluid communication with the tissue site and for receiving and retaining ionic fluids.
• the absorbent layer has a first side and a second, patient-facing side.
• the dressing also includes a sealing member for covering the absorbent layer and includes a first galvanic cell associated with the absorbent layer.
• the first galvanic cell is configured to produce a voltage indicative of a full state when the absorbent layer proximate to the first galvanic cell is substantially saturated with the ionic fluid.
• the method also includes deploying the dressing proximate to the tissue site and electrically coupling the first galvanic cell to a monitoring unit.
• a dressing for treating a tissue site on a patient includes an absorbent layer for placing in fluid communication with the tissue site and for receiving and retaining ionic fluids.
• the absorbent layer has a first side and a second, patient-facing side.
• the dressing further includes a sealing member for covering the absorbent layer and a conductive loop fluidly coupled to the absorbent layer.
• the conductive loop has a first terminal, a second terminal, and at least one conductive gap. The conductive gap is sized and configured to be electrically bridged when covered with the ionic fluid.
• a dressing for treating a tissue site on a patient includes an absorbent layer for placing in fluid communication with the tissue site and for receiving and retaining fluids.
• the absorbent layer has a first side and a second, patient-facing side.
• the dressing further includes a dye associated with the absorbent layer. The dye is operable to change colors when becoming wet.
• the dressing also includes a sealing member for covering the absorbent layer and an electrical optical sensor associated with the absorbent layer. The electrical optical sensor is configured to detect a change in color of the dye associated with the absorbent layer and to produce a signal when the change has been sensed.
• a reduced-pressure treatment system includes a treatment manifold for placing in fluid communication with a tissue site and for receiving ionic fluids.
• the treatment manifold has a first side and a second, patient-facing side.
• the reduced-pressure treatment system further includes a sealing member for covering the treatment manifold, an absorbent layer disposed between the sealing member and the treatment manifold, an electronic detection device associated with the absorbent layer for producing an electrical signal indicative of at least a fully saturated state, and a wireless- communication-and-power subsystem.
• the wireless-communication-and-power subsystem includes an antenna, communication, and processing unit associated with the electronic detection device and a remote wireless communication and power unit configured to transmit power to the antenna, communication, and processing unit and to receive a signal therefrom.
• FIGURE 1 is a schematic diagram with a portion shown in cross section of an illustrative embodiment of a reduced-pressure treatment system employing a galvanic cell to electrically sense the presence of exudates;
• FIGURE 2 is a schematic diagram of an illustrative embodiment of galvanic cell on a wound dressing
• FIGURE 3 is a schematic cross section of a portion of an illustrative embodiment of a dressing with a conductive loop
• FIGURE 4A is a schematic top view of an illustrative embodiment of a conductive loop for use with a dressing, such as the dressing in FIGURE 3, showing a plurality of conductive gaps;
• FIGURE 4B is a schematic side view of the conductive loop of FIGURE 4A;
• FIGURE 5 is a schematic diagram of an illustrative embodiment of a circuit for use with the conductive loop of FIGURES 4A-4B;
• FIGURE 6 is a schematic diagram of an illustrative embodiment of a reduced- pressure treatment system that includes a wireless-communication-and-power subsystem.
• tissue site 104 such as a wound 102
• the wound 102 may be centered in a wound bed.
• the wound 102 may be through or involve epidermis 103, dermis 105, and subcutaneous tissue 107.
• the reduced-pressure treatment system 100 may also be used at other tissue sites.
• the tissue site 104 may be the bodily tissue of any human, animal, or other organism, including bone tissue, adipose tissue, muscle tissue, dermal tissue, vascular tissue, connective tissue, cartilage, tendons, ligaments, or any other tissue. Unless otherwise indicated, as used herein, "or" does not require mutual exclusivity.
• the reduced-pressure treatment system 100 includes a treatment manifold 108 and an absorbent layer 115.
• Absorbent in the context of the absorbent layer or absorbent dressing means capable of at least temporarily retaining liquids.
• the reduced- pressure treatment system 100 may include a sealing member 11 1 and a reduced-pressure subsystem 1 13.
• the treatment manifold 108 has a first side 110 and a second, patient-facing side 112.
• the treatment manifold 108 is made from a porous and permeable foam or foam-like material and, more particularly, a reticulated, open-cell polyurethane or polyether foam that allows good permeability of wound fluids while under a reduced pressure.
• foam material that has been used is the VAC ® GranuFoam ® Dressing available from Kinetic Concepts, Inc. (KCI) of San Antonio, Texas.
• the manifold may be any substance or structure that is provided to assist in applying reduced pressure to, delivering fluids to, or removing fluids from the tissue site 104.
• a manifold typically includes a plurality of flow channels or pathways. The plurality of flow channels may be
• treatment manifolds 108 may include, without limitation, devices that have structural elements arranged to form flow channels, cellular foam, such as open-cell foam, porous tissue collections, and liquids, gels, and foams that include or cure to include flow channels.
• the treatment manifold 108 may be constructed from bioresorbable materials that do not have to be removed from a patient's body following use of the dressing 101.
• Suitable bioresorbable materials may include, without limitation, a polymeric blend of polylactic acid (PLA) and polyglycolic acid (PGA).
• the polymeric blend may also include without limitation polycarbonates, polyfumarates, and capralactones.
• the treatment manifold 108 may further serve as a scaffold for new cell-growth, or a scaffold material may be used in conjunction with the treatment manifold 108 to promote cell-growth.
• a scaffold is a substance or structure used to enhance or promote the growth of cells or formation of tissue, such as a three-dimensional porous structure that provides a template for cell growth.
• Illustrative examples of scaffold materials include calcium phosphate, collagen, PLA/PGA, coral hydroxy apatites, carbonates, or processed allograft materials.
• the absorbent layer 1 15 has a first side 1 17 and a second, patient- facing side 119.
• the absorbent layer 115 may be used alone or with the treatment manifold 108 or omitted from the reduced-pressure treatment system 100.
• the absorbent layer 115 may be coupled to the first side of the treatment manifold 108 or merely disposed proximate to the first side of the treatment manifold 108.
• the absorbent layer 115 may be formed with one or more layers including a wicking layer and a storage layer.
• the absorbent layer 115 may be formed from superabsorbent polymers (SAP) of the type often referred to as “hydrogels,” “super-absorbents,” or “hydrocolloids.”
• SAP superabsorbent polymers
• the absorbent layer 115 may also be formed from alginates or cellulose based materials.
• the sealing member 1 11 covers the treatment manifold 108 and absorbent layer 115 and extends past a peripheral edge 114 of the treatment manifold 108 and absorbent layer 115 to form a sealing-member extension 116.
• the sealing-member extension 1 16 has a first side 118 and a second, patient- facing side 120.
• the sealing-member extension 116 may be sealed against the epidermis 103 or against a gasket or drape by a sealing apparatus 124, such as a pressure-sensitive adhesive 126.
• the sealing apparatus 124 may take numerous forms, such as an adhesive sealing tape, or drape tape or strip; double-sided drape tape; pressure- sensitive adhesive 126; paste; hydrocolloid; hydrogel; or other sealing means.
• the tape may be formed of the same material as the sealing member 11 1 with a pre- applied, pressure-sensitive adhesive 126.
• the pressure-sensitive adhesive 126 may be applied on the second, patient-facing side 120 of the sealing-member extension 1 16.
• the pressure-sensitive adhesive 126 provides a substantial fluid seal between the sealing member 11 1 and the epidermis 103, which, as used herein, may also deemed to include a gasket or drape against the epidermis 103.
• removable strips not shown
• a fluid seal is adequate to maintain reduced pressure at a desired site given the particular reduced-pressure source or subsystem involved.
• the sealing member 1 11 may be an elastomeric material or any material or substance that provides a fluid seal.
• Elastomeric means having the properties of an elastomer and generally refers to a polymeric material that has rubber-like properties. More specifically, most elastomers have an ultimate elongations greater than 100% and a significant amount of resilience. The resilience of a material refers to the material's ability to recover from an elastic deformation.
• elastomers may include, but are not limited to, natural rubbers, polyisoprene, styrene butadiene rubber, chloroprene rubber, polybutadiene, nitrile rubber, butyl rubber, ethylene propylene rubber, ethylene propylene diene monomer, chlorosulfonated polyethylene, polysulfide rubber, polyurethane (PU), EVA film, co- polyester, and silicones.
• the sealing member 1 11 may include a silicone drape, 3M Tegaderm® drape, PU drape such as one available from Avery Dennison Corporation of Pasadena, California.
• the reduced-pressure subsystem 113 includes any device or devices that supply reduced pressure to the tissue site 104, and typically, to the treatment manifold 108.
• the reduced-pressure subsystem 113 typically includes a reduced-pressure source 140, which may take many different forms.
• the reduced-pressure source 140 provides reduced pressure as a part of the reduced-pressure treatment system 100.
• Reduced pressure generally refers to a pressure less than the ambient pressure at a tissue site 104 that is being subjected to treatment. In most cases, this reduced pressure will be less than the atmospheric pressure at which the patient is located. Alternatively, the reduced pressure may be less than a hydrostatic pressure at a tissue site. Unless otherwise indicated, values of pressure stated herein are gauge pressures.
• the reduced pressure delivered may be constant or varied (patterned or random) and may be delivered continuously or intermittently. Consistent with the use herein, an increase in reduced pressure or vacuum pressure typically refers to a relative reduction in absolute pressure.
• a portion 146 of the reduced-pressure delivery conduit 144 may have one or more devices, such as a representative device 148.
• the device 148 may be, for example, a fluid reservoir to hold exudates and other fluids removed, a pressure-feedback device, a volume detection system, a blood detection system, an infection detection system, a flow monitoring system, or a temperature monitoring system. Multiple devices 148 may be included. Some of these devices 148 may be integrated with the reduced-pressure source 140.
• the reduced-pressure source 140 may be any device for supplying a reduced pressure, such as a portable therapy unit, a stationary therapy unit, micropump, or other device. While the amount and nature of reduced pressure applied to a tissue site will typically vary according to the application, the reduced pressure will typically be between -5 mm Hg (- 667 Pa) and -500 mm Hg (-66.7 kPa) and more typically between -75 mm Hg (-9.9 kPa) and - 300 mm Hg (-39.9 kPa).
• the reduced pressure developed by reduced-pressure source 140 is delivered through the reduced-pressure delivery conduit 144 to a reduced-pressure interface 150, which may include an elbow port 152.
• the reduced-pressure interface 150 is a T.R.A.C. ® Pad or Sensa T.R.A.C. ® Pad available from KCI of San Antonio, Texas.
• the reduced-pressure interface 150 allows the reduced pressure to be delivered through the sealing member 11 1 to the treatment manifold 108, as well as to a sealed treatment space 154, in which the treatment manifold 108 is located.
• the reduced- pressure interface 150 extends through the sealing member 11 1 and into the treatment manifold 108.
• the reduced-pressure interface 150 delivers reduced pressure to the absorbent layer 1 15 and the absorbent layer 115 delivers the reduced pressure to the treatment manifold 108.
• the reduced-pressure treatment system 100 may be used without the reduced- pressure interface 150.
• the reduced-pressure delivery conduit 144 may be disposed through an aperture in the sealing member 1 11 and into the absorbent layer 1 15.
• the reduced-pressure delivery conduit 144 may be placed under an edge of the sealing member 1 11 and into the absorbent 1 15 or the treatment manifold 108 and sealed.
• the reduced-pressure delivery conduit 144 may be sealed using, for example, a drape tape.
• An electronic detection device 159 is used to determine when the absorbent layer 115 is at least substantially saturated.
• the absorbent layer 1 15 becomes substantially saturated when the absorbent layer 115 fills with a liquid or when the area near the electronic detection device 159 becomes wet from the position of the dressing.
• one or more galvanic cells e.g., a first galvanic cell 160, may be associated with the absorbent layer 115 to assess the presence of an ionic fluid, e.g., exudate.
• the electronic detection device 159 is typically placed such that the electronic device 159 contacts the absorbent layer 1 15 at locations where liquid will gather as the absorbent layer 115 becomes saturated.
• the electronic detection device 159 may be located on the sealing member 1 11 or within the absorbent material of the absorbent layer 115. Where the electronic detection devices 159 are mounted on the sealing member 1 11, electrical contact can be made to the sensing hardware directly through apertures in the sealing member 11 1. When wires or the direct contact method is used, the wires or components extend through the sealing member 11 1. The wires or components are sealed with respect to the sealing member 11 1 where the wires or components pass through the sealing member 11 1 in order to maintain the integrity of the reduced pressure, i.e., to maintain a fluid seal.
• the first galvanic cell 160 produces a small current when the absorbent layer 115 proximate to the first galvanic cell 160 is substantially saturated with the ionic fluid.
• the first galvanic cell 160 will be located at a location that will experience the ionic fluid last as the absorbent layer 1 15 receives fluids from the tissue site 104 or the treatment manifold 108, and thereby functions as a full indicator for the absorbent layer 1 15. In other words, when the absorbent layer 115 is saturated, the first galvanic cell 16 produces a signal indicative of the same.
• the first galvanic cell 160 includes a first electrode 162 that is electrically coupled to a first electrical lead 164.
• the first galvanic cell 160 also includes a second electrode 166 that is spaced from the first electrode 162 and that is electrically coupled to a second electrical lead 168.
• the first electrode 162 and second electrode 166 are formed from different conducting materials suitable for use with a galvanic cell.
• the first electrode 162 is copper (Cu) and the second electrode 166 is tin (Sn).
• the first electrode 162 is copper (Cu) and the second electrode 166 is zinc (Zn).
• the first electrode 162 is nickel (Ni) and the second electrode 166 is aluminum (Al).
• the first electrode 162 is nickel (Ni) and the second electrode 166 is aluminum (Al).
• any combination of materials on an electrochemical potential chart may be used, e.g., any combination of two of the following: F, CI, Pt, Hg, Ag, I, Cu, Pb, Ni, Fe, Zn, Al, Na, Ca, K, or Li.
• the selected combination of metals should be dissimilar. Alloys will impact the exact voltage measured. Some combinations of metals on the list of metals would not be practical if elementally pure, such as Li, K and others.
• a monitoring unit 170 is electrically coupled to the first electrical lead 164 and the second electrical lead 168 and is configured to detect voltage, current, or power generated by the first galvanic cell 160. As shown in FIGURE 2, the voltage across 272 could be presented to a differential amplifier, or used in a single ended fashion with one end of 272 grounded and the other end presented to an operational voltage amplifier (OP AMP).
• the monitoring unit 170 includes a circuit for measuring the power or voltage produced, e.g., a comparator circuit. When the ionic fluid substantially saturates the absorbent layer 115 proximate to the first and second electrodes 162, 166, the ionic fluid functions as a salt bridge between the two electrodes 162, 166 and current is produced.
• the monitoring unit 170 may include a visual or an audible alarm that signals when a threshold power or current has been reached. The alarm, or dressing full signal, signifies that the dressing 101 is full, and more specifically, that the absorbent layer 1 15 is full.
• the treatment manifold 108 is deployed proximate to the tissue site 104, e.g., in the wound bed on the wound 102, with a portion near a wound edge 109.
• the absorbent layer 1 15 is placed proximate to the treatment manifold 108 (if not already attached) to receive ionic fluids.
• the first galvanic cell 160 is applied to the absorbent layer 1 15.
• the sealing member 11 1 is placed over the tissue site 104 and the treatment manifold 108 and at least partially against epidermis 103 (or gasket or drape) to form a fluid seal and to form the sealed treatment space 154. If not already installed, the reduced-pressure interface 150 is installed.
• the reduced-pressure delivery conduit 144 is fluidly coupled to the reduced-pressure interface 150 and the reduced-pressure source 140 whereby reduced pressure may be provided to the treatment manifold 108.
• the reduced-pressure source 140 may be activated to begin the delivery of reduced pressure to the treatment manifold 108 in the sealed treatment space 154.
• the reduced pressure delivered will extract exudates into the treatment manifold 108.
• the exudates are absorbed, at least in part, from the treatment manifold 108 by the absorbent layer 1 15 and eventually will substantially saturate the absorbent layer 115.
• the saturated absorbent layer 1 15 functions as a salt bridge and the first galvanic cell 160 provides a current flow that may be detected and used to sound an alarm or produce a signal indicating that the absorbent layer 1 15 is full.
• FIGURE 1 While the illustrative embodiment of FIGURE 1 is shown with reduced pressure applied and with a treatment manifold 108, it should be understood that in other embodiments, the absorbent layer 1 15 may be placed directly proximate to a tissue site.
• a reduced-pressure source may not be used to attract exudates or other ionic fluids, but rather a wicking layer may be used with the absorbent layer 115 to attract fluids.
• a plurality of galvanic cells may be used to provide progressive feedback on the state of fill of the absorbent layer 1 15. The plurality of galvanic cells may be located in geometrically significant areas where liquids are expected to collect. The positions could also be chosen to indicate the progress of the liquid through the dressing 101 so that an estimation of remaining capacity may be calculated.
• the system 200 includes a dressing 201 and an electronic detection device 159.
• the electronic detection device 159 may include a first galvanic cell 260.
• the first galvanic cell 260 includes a first electrode 262 electrically coupled to a first electrical lead 264.
• the first galvanic cell 260 includes a second electrode 266 electrically coupled to a second electrical lead 268.
• the first and second electrodes 262, 266 may be coupled to a base 263, or stabilizing platform.
• a power-using device, e.g., a resistor 272 may be electrically coupled between the first electrical lead 264 and the second electrical lead 268.
• a voltage may be measured between the electrical leads 264, 268 by a monitoring unit 270.
• the voltage between the electrodes 262, 266 will rise above a threshold value as the absorbent layer 1 15 becomes saturated proximate to the electrodes 262, 266.
• the longitudinal length of the base 263 is 20 mm
• the width is 10 mm
• the electrodes are 8 mm by 8 mm.
• the monitoring unit 270 may produce an analog signal indicative of the voltage and that signal may be delivered by a third lead 274 to an analog-to-digital converter 276.
• a digital signal may then be delivered by a fourth lead 278 to a microprocessor unit 280.
• the microprocessor unit 280 may monitor and manipulate the signal as desired. Upon determining that a threshold value has been reached, the microprocessor unit 280 may provide a signal to an alarm 282 (visual or audible) or to another unit.
• the reduced-pressure system 300 includes an electronic detection device 359.
• the electronic detection device 359 may include one or more conductive loops, e.g., a first conductive loop 384, a second conductive loop 386, and a third conductive loop 388. It should be understood that the "conductive loops" are selectively conductive or only conductive at times when the circuit is completed as is described herein.
• the dressing 301 may include a treatment manifold 308 having a first side 310 and a second side 312.
• the dressing 301 includes an absorbent layer 315, which has a first side 317 and a second, patient-facing side 319.
• the system 300 excludes the treatment manifold 308, and the second, patient-facing side 319 of the absorbent layer 315 is placed adjacent to the tissue site 304.
• the treatment manifold 308 is placed proximate to the tissue site 304.
• the tissue site is a wound 302 that extends through epidermis 303, through dermis 305 and into subcutaneous tissue 307.
• a sealing member 31 1 is placed over the absorbent layer 315 and optionally (if included) over the treatment manifold 308 to form a sealed space 354.
• the conductive loops 384, 386, 388 are disposed under the sealing member 31 1 and proximate to the absorbent layer 315.
• the conductive loops 384, 386, 388 are in the sealed space 354.
• a reduced-pressure source 340 is covered by the sealing member 31 1 and provides reduced pressure in the sealed space 354.
• the sealing member 311 includes an aperture 323 to allow the reduced-pressure source 340 to vent.
• the reduced-pressure source 340 may be a micro pump, a diaphragm pump, disc pump, piezoelectric pump, or other small pump.
• the reduced-pressure source is built into the dressing 301.
• a layer 343 may be included to help distribute reduced pressure or prevent fluids from entering the reduced-pressure source 340. It should be understood that other sources of reduced pressure may be utilized and in other embodiments may be excluded altogether.
• the reduced-pressure source 340 may utilize a connecting member 341 to fluidly couple the reduced-pressure source 340 to the absorbent layer 315.
• the connecting member 341 may extend through the absorbent layer 315 and directly couple the reduced-pressure source 340 to the treatment manifold 308.
• the dressing 301 receives exudates or other ionic fluid from the tissue site 304 and stores the exudate in the absorbent layer 315.
• the absorbent layer 315 may have a wicking layer to help pull exudate from the treatment manifold 308.
• the absorbent layer 315 When the absorbent layer 315 becomes fully saturated, the absorbent layer 315 will no longer hold additional exudate. Accordingly, the patient or healthcare provider will want to be alerted when the absorbent layer 315 is saturated.
• the conductive loops 384, 386, 388 (with speaker or visual alert or the another alert device) provide such an alert.
• the plurality of conductive loops 384, 386, and 388 are added to the absorbent layer 315 to help provide an indication of the fullness of the absorbent layer 315.
• the first conductive loop 384 includes a first terminal 385 and a second terminal 387.
• the first terminal 385 is coupled by a first electrical lead 389 to a monitoring unit 370 that includes a first LED 371, a second LED 373, and a third LED 375.
• the second terminal 387 is coupled by a second electrical lead 397 to the monitoring unit 370.
• the monitoring unit 370 includes circuitry that provides power to the conductive loops 384, 386, and 388.
• the conductive loops 384, 386, 388 contain conductive gaps 399 that are electrically bridged when sufficient exudate reaches the conductive loops 384, 386, 388. Sufficient exudate reaches the conductive loops at least when liquid saturates the absorbent layer 315 in the area of the conductive loop involved as will be explained further below.
• the second conductive loop 386 has a first terminal 390 and a second terminal 391. The first terminal 390 and the second terminal 391 of the second conductive loop 386 are electrically coupled by leads 393 and 394 to the monitoring unit 370 and are particularly associated with second LED 373.
• the third conductive loop 388 includes leads 395 and 396 that are electrically coupled to the monitoring unit 370 and are associated with third LED 375.
• FIGURES 4A and 4B show the first conductive loop 384, which is
• the first conductive loop 384 contains a conductive path 398 formed with one or more conductive gaps 399.
• the conductive path 398 may be mounted on a base 379.
• an electrical insulation layer (not explicitly shown) may cover the conductive path 398 and have apertures only at the conductive gaps 399. It will be appreciated that as an ionic fluid surrounds and covers the conductive path 398, the ionic fluid will electrically couple the conductive gaps 399. In other words, the ionic fluid serves as an electrical bridge for the conductive gap 399 and allows the conductive path 398 to carry a current. When the current is carried sufficiently, the monitoring unit 370 provides a signal, such as first LED 371.
• the other conductive loops 386, 388 are analogous. It should be understood that while three conductive loops 384, 386, and 388 are shown, any number of conductive loops may be used. Multiple conductive loops may be used to assess saturation of the dressing 301 at different locations and provide an escalating scale of fullness for the dressing 301.
• the detection circuit 400 may be included in the monitoring unit 370.
• the detection unit 400 may be configured to power an LED 402 in response to a current flowing through the first terminal 385 and the second terminal 387 indicating exudate in the dressing 301 as sensed by a completed conduction or conductive path.
• the detection circuit 400 may, for example, provide a conductive loop that supplies a voltage from a battery 401 to the LED 402 in response to activation by a small current passing between the first terminal 385 and the second terminal 387.
• the detection circuit 400 may utilize at least two capacitors 404 and 406 to respond to the current through the first terminal 385 and the second terminal 387.
• a number of resistors 408, 410, 412, 414, 416, 418, and 420 in the detection circuit 400 generate voltage differentials that function with the capacitors 404 and 406 to drive a NPN transistor 422 and a PNP transistor 424 to activate the LED 402.
• a completed conductive path across the first terminal 385 and second terminal 387 allows current through the resistor 408 to bypass the capacitor 404.
• Current flows through the resistor 410 to the base of the NPN transistor 422, rather than through the higher resistance path provided by resistor 412.
• the current entering the base of the NPN transistor 422 amplifies the current allowed to flow into the NPN transistor 422 through the resistors 414 and 416.
• the NPN transistor 422 is "on" when the base is pulled high by the input signal through the resistor 410 relative to the emitter output.
• the PNP transistor 424 is "on" when the base receiving current through the resistor 414 is pulled low relative to the emitter. As a result, the current through the base of the NPN transistor 422 activates the PNP transistor 424 to amplify current to the collector supplying current to the resistor 418 and the LED 402. As a result, the NPN transistor 422 and the PNP transistor 424 are only activated to supply a current lighting the LED 402 in response to the first terminal 385 and the second terminal 387 completing a closed circuit or conductive path.
• the detection circuit 400 may also include an output 426 that functions as a terminal.
• the output 426 may communicate a signal received through the resistor 420 indicating that the PNP transistor 424 has been activated thereby supplying current through the LED 402.
• the output 426 may communicate with a recording or logging device that records the point at which the conduction path was created between the first terminal 385 and the second terminal 387. This information or data may be utilized to track the presence of a threshold level of exudate in the dressing 301.
• the detection circuit 400 When the exudate within the dressing is insufficient to complete the conduction path between terminals 385 and 387, the detection circuit 400 is inactive. The DC current passing through the resistor 408 from the battery 401 is blocked by the capacitor 404. As a result, neither the NPN transistor 422 nor the PNP transistor 424 is activated to supply current to the LED 402.
• the detection circuit 400 may be replaced by other current detection circuits.
• the resistance, capacitance, and other characteristics of the detection circuit 400 may vary based on the sensitivity of the readings across the first terminal 385 and the second terminal 387 and the power requirements of the LED 402.
• the LED 402 may be replaced by a visual or digital indicator that, based on the level of current passing through the resistor 418 to the indicator, indicates the amount or type of exudate within the dressing 301.
• the indicator may be an analog or digital element specifically calibrated to provide audible, visual, or tactile feedback to one or more users.
• a capacitive senor may be located on an exterior of the dressing, e.g., on the sealing member 11 1 above where electrode 162 is shown in FIGURE 1.
• the capacitive sensor has a sensing profile that measures capacitance at a location that fills last. When liquids reach the location that corresponds with the sensing profile, the capacitance of the portion of the dressing associated with the capacitive sensor changes within the dressing as seen by the fill sensor. As a result, the capacitance sensor produces a signal indicating that the dressing is saturated.
• a dye is placed in the absorbent layer, e.g., absorbent layer 315, that provides a change visual appearance (or optical properties) upon becoming wet.
• the visual indication may be a change in contrast, change in color, change in brightness, a change in reflectivity or other visual cue.
• the change in visual appearance may be a change perceptible to a human eye or only to a device, e.g., an electrical photo detector.
• the electrical photo detector may detect more subtle changes in visual appearance.
• the electrical photo detector is attached proximate to the sealing member 31 1 and can optically detect the change in contrast and produce a signal indicative of the change.
• the dye may be placed in the treatment manifold, e.g., manifold 108.
• metal capacitance plates are put within or near the absorbent layer, e.g., absorbent layer 315, having defined space between plates.
• the capacitance changes as the ionic fluid fills the space between the plates.
• the change in capacitance is measured and the change is noted when the ionic fluid fills the space between the plates.
• the reduced-pressure treatment system 500 includes a wound dressing 501 that may include a manifold 508 and an absorbent layer 515.
• An electronic detection device 559 is associated with the absorbent layer 515 and is configured to electronically determine when the absorbent layer (or some portion thereof) is substantially saturated.
• the electronic detection device 559 may be, for example, a galvanic cell or a conductive loop with conductive gaps or other means of electronically determining when the absorbent layer 515 is substantially saturated.
• the wireless-communication-and-power subsystem 571 may provide power to the electronic detection device 559 and may wirelessly receive information related to the status of the absorbent layer 515 as produced by the electronic detection device 559.
• the wireless-communication-and-power subsystem 571 may include a wireless-communication-and-power-transmission unit 572, which is on a base station 573, and an antenna-communication-and-processing unit 574.
• the wireless-communication- and-power subsystem 571 is analogous to a Radio-Frequency Identification Device (RFID). Power is transmitted by a wireless signal 575 from the wireless-communication-and-power- transmission unit 572 to the antenna-communication-and-processing unit 574 from where the power is provided by coupling 576 to the electronic detection device 559.
• RFID Radio-Frequency Identification Device
• the power provided to the electronic detection device 559 may augment power already developed, e.g., by a galvanic cell, or provide all the power, e.g., for a resistive circuit.
• the electronic detection device 559 is configured to determine if the absorbent layer 515 is saturated or possibly to what extent liquid exists within the absorbent layer 515 and to produce a signal with the relevant information.
• the signal may be delivered by coupling 576 to the antenna-communication-and-processing unit 574 from where a wireless signal 575 carries the information to the wireless-communication-and-power-transmission unit 572.
• the wireless-communication-and-power-transmission unit 572 may further process the signal for display or use by other systems monitoring or controlling the reduced-pressure treatment system 500. As such, with this embodiment, no direct electronic connection is required between a monitoring device and the electronic detection device 559. Accordingly, less power may be needed and comfort may be enhanced.
• the systems 100, 200, 300, 500 presented allow for the saturation of the absorbent layer, e.g., 115, 215, 315, 515 to be determined using an electrical device. Because a visual determination or a tactile inspection is not required, the electrical signal may be used to set off an alarm or otherwise signal the user or healthcare provider that the dressing is saturated and should be changed. Moreover, by arranging the components, intermediate indications of the percentage full may be provided. It should be understood that the output signal also enables easy interface with an electronic controller or circuit in an analog or digital system.
• the systems and methods for receiving an ionic fluid may be analogous to the systems and methods previously presented, but the system may not utilize an absorbent layer, e.g., absorbent layer 115 in the reduced-pressure treatment system 100 may be omitted.
• the electrodes are fluidly coupled to a portion of a dressing that will be exposed to liquids last as the liquids build up in the dressing.
• the dressings of FIGURES 1-4B may be used without reduced pressure, but may use wicking from the absorbent layer and may include additional wicking layers. In this embodiment, a completed circuit would indicate saturation of the dressing and signal a needed change.
• a dressing for receiving an ionic fluid includes an absorbent layer for placing in fluid communication with the tissue site and for receiving and at least temporarily retaining ionic fluids.
• the absorbent layer has a first side and a second, patient-facing side.
• the dressing further includes a sealing member for covering the absorbent layer and a first galvanic cell associated with the absorbent layer and configured to produce a voltage when the absorbent layer proximate to the first galvanic cell is substantially saturated with the ionic fluid.
• the galvanic cell typically includes a first electrode and a second electrode, the first electrode and second electrode in fluid
• the first electrode comprises copper and the second electrode comprises tin.
• the first electrode comprises copper and the second electrode comprises tin, and wherein the ionic fluid comprises exudate from a patient.
• the first electrode comprises copper and the second electrode comprises zinc.
• the dressing further includes a plurality of galvanic cells associated with the absorbent layer and configured to provide power proportional to the saturation of the absorbent layer of the dressing.
• the dressing may further include a wireless-communication-and-power subsystem.
• a system for treating a tissue site on a patient with reduced pressure includes: an absorbent layer for placing proximate to the tissue site; a sealing member for covering the dressing and a portion of the patient's epidermis to form a fluid seal; a reduced-pressure source fluidly coupled to the absorbent layer for providing reduced pressure to the absorbent layer; a galvanic cell associated with the absorbent layer, wherein the galvanic cell is configured to produce power when the absorbent layer proximate to the galvanic cell is substantially saturated with an ionic fluid; and a monitoring unit electrically coupled to the galvanic cell for receiving power from the galvanic cell.
• the monitoring unit may be a comparator circuit or an analog-to-digital converter coupled to a microprocessor.
• the microprocessor is configured to develop an alarm signal when the power reaches a power threshold value.
• a method for treating a tissue site includes providing a dressing, wherein the dressing comprises: an absorbent layer for placing in fluid communication with the tissue site.
• the absorbent layer is for receiving and retaining ionic fluids.
• the absorbent layer has a first side and a second, patient-facing side.
• the dressing also includes a sealing member for covering the first side of the absorbent layer and a first galvanic cell associated with the absorbent layer and configured to produce a voltage indicative of a full state when the absorbent layer proximate to the first galvanic cell is substantially saturated with the ionic fluid.
• the method also includes deploying the dressing proximate to the tissue site; electrically coupling the first galvanic cell to a monitoring unit, wherein the monitoring unit is configured to produce a dressing-full signal when receiving the voltage indicative of a full state from the first galvanic cell; and providing reduced pressure to the dressing until the monitoring unit provides the dressing-full signal.
• the dressing may further comprise a plurality of galvanic cells associated with the absorbent layer and configured to provide voltage proportional to the saturation of the absorbent layer of the dressing.
• a dressing for treating a tissue site on a patient includes an absorbent layer for placing in fluid communication with the tissue site, the absorbent layer for receiving and retaining ionic fluids, the absorbent layer having a first side and a second, patient-facing side; a sealing member for covering the absorbent layer; and a conductive loop fluidly coupled to the absorbent layer and having a first terminal, a second terminal, and at least one conductive gap, wherein the conductive gap is sized and configured to be electrically bridged when covered with the ionic fluid.
• a dressing for treating a tissue site on a patient includes: an absorbent layer for placing in fluid communication with the tissue site, the absorbent layer for receiving and retaining fluids, the absorbent layer having a first side and a second, patient-facing side; a dye associated with the absorbent layer, wherein the dye is operable to change optical properties when becoming wet; a sealing member for covering the first side of the absorbent layer; and an electrical optical sensor associated with the absorbent layer and configured to detect a change in optical properties of the dye and to produce an electrical signal when the change has been sensed.
• a dressing for receiving an ionic fluid comprising: a treatment manifold for placing in fluid communication with the tissue site and for receiving ionic fluids, the treatment manifold having a first side and a second, patient- facing side; a sealing member for covering the first side of the treatment manifold; and a first galvanic cell associated with the treatment manifold and configured to produce a voltage when the treatment manifold proximate to the first galvanic cell is substantially saturated with the ionic fluid.
• s reduced-pressure treatment system includes: a treatment manifold for placing in fluid communication with a tissue site and for receiving ionic fluids, the treatment manifold having a first side and a second, patient- facing side; a sealing member for covering the first side of the treatment manifold; an absorbent layer disposed between the sealing member and the treatment manifold; an electronic detection device associated with the absorbent layer for producing an electrical signal indicative of at least a fully saturated state; and a wireless-communication-and-power subsystem comprising: an antenna, communication, and processing unit associated with the electronic detection device, and a remote wireless communication and power unit configured to transmit power to the antenna, communication, and processing unit and to receive a signal therefrom.
• a dressing for treating a tissue site includes: a tissue dressing member for location adjacent to the tissue being treated; and at least one liquid sensor for detecting the presence of liquid at a location on or in the tissue dressing member.
• the dressing member may include a treatment manifold.
• the dressing member may include an absorbent member.
• the dressing may further include a sealing member for covering the tissue dressing member.
• the at least one liquid sensor may be a galvanic cell.
• the least one liquid sensor may be a selectively conductive loop; the loop may be a conductive material having spaces which may be bridged by an ionic liquid contacting the surface of the loop thereby electrically completing the loop.
• the optical properties of the tissue dressing member may be configured to change upon absorption of a liquid, and the sensor may an optical sensor for detecting that change.
• the optical property may be color.
• a plurality of sensors may be included in the dressing.
• a least one sensor is located on the surface of the tissue dressing.
• at least one sensor is located within the tissue dressing.
• the sensor may be located on the outside of a sealing member covering the tissue dressing member.
• a pump may be located within the dressing for applying a reduced pressure to the tissue site.
• a wound treatment system that includes a dressing according to any of the preceding descriptions and a monitoring device electrically connected to the at least one liquid sensor and configured to provide an indication of detection of liquid by the at least one liquid sensor.
• a galvanic cell is used as an electronic detection device.
• the galvanic cell is placed in the dressing and produces voltage when the dressing is substantially saturated.
• the dressing is a reduced-pressure, absorbent dressing.
• each of the sensor types may be utilized with each of the pump types (external to the dressing, internal to the dressing, or without any pump).
• the various sensor types may be used in any number of combination of types as required.

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• 2011
  • 2011-07-14 US US13/183,280 patent/US9265665B2/en not_active Expired - Fee Related
  • 2011-07-14 US US13/183,245 patent/US8795257B2/en active Active
  • 2011-07-15 EP EP11738357.0A patent/EP2595589B1/en not_active Not-in-force
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