WO2012057881A1 - Reduced-pressure systems, dressings, and methods employing a wireless pump - Google Patents

Reduced-pressure systems, dressings, and methods employing a wireless pump Download PDF

Info

Publication number
WO2012057881A1
WO2012057881A1 PCT/US2011/044187 US2011044187W WO2012057881A1 WO 2012057881 A1 WO2012057881 A1 WO 2012057881A1 US 2011044187 W US2011044187 W US 2011044187W WO 2012057881 A1 WO2012057881 A1 WO 2012057881A1
Authority
WO
WIPO (PCT)
Prior art keywords
pressure
pump
reduced
wireless
processor
Prior art date
Application number
PCT/US2011/044187
Other languages
French (fr)
Inventor
Richard Daniel John Coulthard
Christopher Brian Locke
Benjamin Stokes
Original Assignee
Kci Licensing, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kci Licensing, Inc. filed Critical Kci Licensing, Inc.
Priority to CN201180050826.3A priority Critical patent/CN103179930B/en
Priority to EP11738356.2A priority patent/EP2632406B1/en
Priority to AU2011320911A priority patent/AU2011320911B2/en
Priority to CA2814740A priority patent/CA2814740C/en
Priority to JP2013536610A priority patent/JP5843296B2/en
Publication of WO2012057881A1 publication Critical patent/WO2012057881A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/80Suction pumps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/00051Accessories for dressings
    • A61F13/00055Saturation indicators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/02Adhesive bandages or dressings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/05Bandages 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]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/73Suction drainage systems comprising sensors or indicators for physical values
    • A61M1/732Visual indicating means for vacuum pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/90Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
    • A61M1/91Suction aspects of the dressing
    • A61M1/915Constructional details of the pressure distribution manifold
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/90Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
    • A61M1/95Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing with sensors for exudate composition
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/90Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
    • A61M1/96Suction control thereof
    • A61M1/962Suction control thereof having pumping means on the suction site, e.g. miniature pump on dressing or dressing capable of exerting suction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/90Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
    • A61M1/96Suction control thereof
    • A61M1/966Suction control thereof having a pressure sensor on or near the dressing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F2013/00089Wound bandages
    • A61F2013/0017Wound bandages possibility of applying fluid
    • A61F2013/00174Wound bandages possibility of applying fluid possibility of applying pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F2013/00361Plasters
    • A61F2013/00365Plasters use
    • A61F2013/00536Plasters use for draining or irrigating wounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F2013/00361Plasters
    • A61F2013/00902Plasters containing means
    • A61F2013/0094Plasters containing means for sensing physical parameters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/74Suction control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/74Suction control
    • A61M1/75Intermittent or pulsating suction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/90Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
    • A61M1/92Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing with liquid supply means
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/90Negative pressure wound therapy devices, i.e. devices for applying suction to a wound to promote healing, e.g. including a vacuum dressing
    • A61M1/96Suction control thereof
    • A61M1/964Suction control thereof having venting means on or near the dressing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/33Controlling, regulating or measuring
    • A61M2205/3331Pressure; Flow
    • A61M2205/3344Measuring or controlling pressure at the body treatment site
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/35Communication
    • A61M2205/3576Communication with non implanted data transmission devices, e.g. using external transmitter or receiver
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/35Communication
    • A61M2205/3576Communication with non implanted data transmission devices, e.g. using external transmitter or receiver
    • A61M2205/3592Communication with non implanted data transmission devices, e.g. using external transmitter or receiver using telemetric means, e.g. radio or optical transmission
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/60General characteristics of the apparatus with identification means
    • A61M2205/6054Magnetic identification systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49016Antenna or wave energy "plumbing" making
    • Y10T29/49018Antenna or wave energy "plumbing" making with other electrical component

Definitions

  • the present disclosure relates generally to medical treatment systems and, more particularly, but not by way of limitation, to systems, dressings, and methods that involve wirelessly providing power to a pump that applies reduced pressure to a tissue site.
  • a system for treating a tissue site with reduced pressure includes a reduced-pressure dressing for disposing proximate to the tissue site and a wireless, reduced-pressure pump fluidly coupled to the reduced-pressure dressing.
  • the wireless, reduced-pressure pump includes a Radio Frequency Identification (RFID) antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the processor for receiving power and developing reduced pressure, a first pump-sealing member, a fluid reservoir, and a second pump-sealing member.
  • the first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro- pump is disposed.
  • the system further includes a base unit having a RFID reader.
  • the RFID reader is configured to provide power to the RFID antenna such that the micro-pump is powered.
  • a method of manufacturing a system for treating a tissue site on a patient with reduced pressure includes providing a reduced-pressure dressing for disposing proximate to the tissue site and providing a wireless, reduced-pressure pump.
  • the wireless, reduced-pressure pump includes a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power and developing a reduced pressure, a first pump-sealing member, a fluid reservoir, and a second pump-sealing member.
  • the first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump is disposed.
  • the method may further include providing a reduced-pressure delivery conduit for fluidly coupling the wireless, reduced-pressure pump to the reduced-pressure dressing.
  • the method further includes providing a base unit having a RFID reader.
  • the RFID reader is configured to provide power to the RFID antenna such that the micro-pump is powered.
  • a method for treating a tissue site on a patient with reduced pressure includes placing a reduced-pressure dressing proximate to the tissue site and providing a wireless, reduced-pressure pump.
  • the wireless, reduced- pressure pump includes a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the processor for receiving power and developing reduced pressure, a first pump-sealing member, a fluid reservoir, and a second pump-sealing member.
  • the first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump is disposed.
  • the method further includes fluidly coupling the wireless, reduced-pressure pump to the reduced-pressure dressing, providing a base unit having a RFID reader and a second processor, and activating the base unit whereby the RFID reader and second processor transmit an activation signal to the wireless, reduced- pressure pump to activate the wireless, reduced-pressure pump.
  • a reduced-pressure system for treating a tissue site with reduced pressure includes a reduced-pressure dressing.
  • the reduced- pressure dressing includes a first distribution manifold for placing proximate to the tissue site, an absorbent layer for receiving and retaining fluids from the first distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, and a micro-pump coupled to the first processor for receiving power therefrom and developing reduced pressure.
  • the micro-pump has an inlet and an exhaust outlet.
  • the system also includes a first sealing member for forming a sealed space over the tissue site and the micro-pump, and a vent fluidly coupling the exhaust outlet of the micro-pump to an exterior.
  • the system further includes a base unit that includes a RFID reader. The base unit is operable to supply a pump signal to the reduced-pressure dressing to energize the micro-pump.
  • a method for treating a tissue site on a patient with reduced pressure includes disposing a wireless, reduced-pressure dressing proximate to the tissue site.
  • the wireless, reduced-pressure dressing includes a first distribution manifold for placing proximate to the tissue site, an absorbent layer for receiving and retaining fluids from the first distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump coupled to the first processor for receiving power therefrom and developing reduced pressure.
  • the micro-pump has an inlet and an exhaust outlet, a first sealing member for forming a sealed space over the tissue site and the micro- pump, and a vent fluidly coupling the exhaust outlet of the micro-pump to an exterior.
  • the method further includes providing a base unit comprising a RFID reader.
  • the base unit is operable to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump.
  • the method also includes activating the base unit to deliver the pump signal to the wireless, reduced-pressure dressing.
  • FIGURE 1 is a schematic diagram, with a portion shown in cross section, of an illustrative embodiment of a system for treating a tissue site with reduced pressure;
  • FIGURE 2 is a schematic, exploded, perspective view of an illustrative embodiment of a wireless, reduced-pressure pump used as part of the system of FIGURE 1;
  • FIGURE 3 is a schematic diagram, with a portion shown in cross section, of the system of FIGURE 1 presenting additional aspects and some alternatives;
  • FIGURE 4 is a schematic, partial cross-sectional view of an illustrative embodiment of a wireless, reduced-pressure pump
  • FIGURE 5 is a schematic, cross section of one illustrative embodiment of a micro-pump device for use as part of a system for treating a tissue site with reduced pressure such as in FIGURE 1;
  • FIGURE 6 is a schematic, perspective view of an illustrative embodiment of a wireless, reduced-pressure pump
  • FIGURE 7 is a schematic, cross section of another illustrative embodiment of a wireless, reduced-pressure pump
  • FIGURE 8 is a schematic, perspective view of the wireless, reduced-pressure pump of FIGURE 7;
  • FIGURE 9 is a schematic diagram, with a portion shown in perspective view, of an illustrative embodiment of a reduced-pressure system for treating a tissue site with reduced pressure;
  • FIGURE 10 is a schematic, cross section of the reduced-pressure dressing shown in FIGURE 9 taken along line 10-10;
  • FIGURE 11 is a schematic, exploded, perspective view of the reduced-pressure dressing of FIGURES 9-10;
  • FIGURE 12 is a schematic, cross section of an illustrative embodiment of a system for treating a tissue site with reduced pressure; and [0022]
  • FIGURE 13 is a schematic, exploded, perspective view of another illustrative embodiment of a reduced-pressure dressing.
  • RFID Radio Frequency Identification
  • RFID traditionally uses a RFID tag or label that is on a target and a RFID reader that energizes and reads signals from the RFID tag.
  • RFID tags include an integrated circuit for storing and processing information, a modulator, and demodulator.
  • RFID tags can be passive tags, active RFID tags, and battery-assisted passive tags. Generally, passive tags use no battery and do not transmit information unless they are energized by a RFID reader. Active tags have an on-board battery and can transmit autonomously (i.e., without being energized by a RFID reader).
  • Battery-assisted passive tags typically have a small battery on-board that is activated in the presence of a RFID reader.
  • a microcontroller and sensor may be incorporated into the reduced-pressure dressing.
  • the RFID tag, a microcontroller and sensor allow sensing and optional
  • the RFID tag and microcontroller partially or entirely power a micro-pump.
  • the enhanced RFID technology is a Wireless Identification and Sensing Platform (WISP) device.
  • WISPs involve powering and reading a WISP device, analogous to a RFID tag (or label), with a RFID reader.
  • the WISP device harvests the power from the RFID reader's emitted radio signals and performs sensing functions (and optionally performs computational functions).
  • the WISP device transmits a radio signal with information to the RFID reader.
  • the WISP device receives power from the RFID reader.
  • the WISP device has a tag or antenna that harvests energy and a
  • the WISP device reports data to the RFID reader.
  • the WISP device includes an integrated circuit with power harvesting circuitry, demodulator, modulator, microcontroller, sensors, and may include one or more capacitors for storing energy.
  • a form of WISP technology has been developed by Intel Research Seattle (www. Seattle. intel- research.net/wisp/).
  • RFID devices as used herein also include WISP devices.
  • the system 100 includes a reduced-pressure dressing 106 for disposing proximate to the tissue site 102; a wireless, reduced-pressure pump 108 fluidly coupled to the reduced-pressure dressing 106; and a base unit 110 having a RFID reader 1 12.
  • the wireless, reduced-pressure pump 108 includes a first RFID antenna 1 14 and a micro- pump device 1 16.
  • the RFID reader 1 12 is configured to provide and transmit a pump signal that provides power to the first RFID antenna 1 14.
  • the pump signal received by the first RFID antenna 114 powers the micro-pump device 116.
  • Remotely powering the micro-pump device 116 provides a number of potential benefits. The benefits may include ease of application.
  • the wireless, reduced-pressure pump 108 may be a self-contained, disposable unit. It should be noted that some variation is shown between figures in order to show some of the potential variations in the illustrative system 100.
  • the system 100 may be used with various different types of tissue sites 102.
  • the tissue site 102 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, body cavity or any other tissue.
  • Treatment of the tissue site 102 may include removal of fluids, e.g., exudate or ascites.
  • the wireless, reduced-pressure pump 108 includes the first RFID antenna 114 that is coupled to a first processor 118 by electrical leads 1 19.
  • the first processor 118 is coupled to the micro-pump device 116, or micro-pump, for receiving power.
  • the first processor 1 18 may be incorporated into the micro-pump device 1 16.
  • the first processor 118 and micro-pump device 1 16 may be located within a pump pouch 120.
  • the pump pouch 120 may be formed by coupling a first pump-sealing member 122 to a second pump-sealing member 124.
  • the pump pouch 120 may also be formed by other techniques such as casting the pump pouch 120 from a polymer.
  • At least a portion of the pump pouch 120 comprises a fluid reservoir 126 for receiving and retaining fluids 127 from the tissue site 102.
  • the micro-pump device 1 16 may be a piezoelectric pump, a peristaltic pump, or other small pump that produces reduced pressure with minimal power requirements.
  • the first processor 1 18 is operable to receive a pressure message signal from a pressure sensing device 138.
  • the first processor 118 In response to receiving the pressure message signal, the first processor 118 produces a control signal to activate or deactivate the micro-pump device 116.
  • the pressure sensing device 138 may be a transducer or may be a simple switch that is activated if sufficient reduced pressure is present.
  • the base unit 1 10 includes a second processor 128 coupled to the RFID reader 1 12.
  • a control panel 130 e.g., a user interface
  • a first display 132 e.g., a first display 132
  • a power source 134 e.g., a battery or electrical connection
  • the base unit 110 may include a base housing 136.
  • the second processor 128 and RFID reader 1 12 are configured to transmit a signal 137, e.g., a pump signal or a pressure inquiry signal, to the first RFID antenna 114.
  • the first RFID antenna 1 14 of the reduced-pressure pump 108 is coupled by electrical leads 119 or a wireless coupling to the first processor 118.
  • the first processor 118 is coupled to the micro-pump device 1 16 to provide power and control the micro-pump device 116.
  • a first power source 140 may be included to provide additional power to the first processor 1 18.
  • a pressure sensing device 138 may be coupled to the first processor 118.
  • the pressure sensing device 138 is fluidly coupled to and senses pressure in a pressure sensing lumen 166 (or vent passageway 174 or interface distribution manifold 150).
  • the micro-pump device 1 16 is fluidly coupled to a fluid reservoir 126.
  • the fluid reservoir 126 receives and retains the fluids 127 from a reduced-pressure lumen 164 or from the interface distribution manifold 150.
  • the pump signal transmitted by the base unit 110 is received by the first RFID antenna 114 and energizes the micro-pump device 1 16 to produce reduced pressure.
  • the pressure inquiry signal is transmitted to the first processor 118 of the wireless, reduced- pressure pump 108 by the second processor 128 and RFID reader 1 12.
  • the first processor 1 18 and pressure sensing device 138 of the wireless, reduced-pressure pump 108 transmit a pressure message signal indicative of the pressure experienced at the reduced- pressure dressing 106 to the base unit 110.
  • the second processor 128 is configured to receive the pressure message signal from the wireless, reduced-pressure pump 108 and prepare a control signal.
  • the second processor 128 and RFID reader 1 12 are configured to transmit the control signal to the wireless, reduced-pressure pump 108 to activate or deactivate the micro-pump device 1 16.
  • the first processor 118 is operable to receive a pressure message signal from the pressure sensing device 138 and to produce a control signal to activate or deactivate the micro-pump device 116.
  • the wireless, reduced-pressure pump 108 generates reduced pressure that is delivered to the tissue site 102.
  • the wireless, reduced-pressure pump 108 receives and retains fluids from the tissue site 102.
  • Reduced pressure generally refers to a pressure less than the ambient pressure at a tissue site 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 the 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, unless otherwise indicated, an increase in reduced pressure or vacuum pressure typically refers to a relative reduction in absolute pressure.
  • the wireless, reduced-pressure pump 108 provides the reduced pressure for the system 100.
  • the wireless, reduced-pressure pump 108 may include a first distribution manifold 142, a diverter layer 144, and an absorbent layer 146.
  • a vent 176 is used to fluidly couple an exhaust from the micro-pump device 1 16 to an exterior of the wireless, reduced- pressure pump 108.
  • the first distribution manifold 142 functions to distribute reduced pressure generated by the micro-pump device 1 16.
  • An air/liquid separator 143 e.g., a hydrophobic filter, may be placed between the micro-pump device 1 16 and the first distribution manifold 142 to prevent liquid from entering the micro-pump device 1 16.
  • the absorbent layer 146 functions to receive and retain fluids from the tissue site 102.
  • the absorbent layer 146 may be made from any material capable of absorbing liquid, such as exudate from the tissue site 102.
  • the absorbent layer 146 may be made from super absorbent fibers.
  • the super absorbent fibers may retain or bond to the liquid in conjunction with a physical or chemical change to the fibers.
  • the super absorbent fiber may include the Super Absorbent Fiber (SAF) material from Technical Absorbents, Ltd. of Grimsby, United Kingdom.
  • SAF Super Absorbent Fiber
  • the absorbent layer 146 may be a sheet or mat of fibrous material in which the fibers absorb liquid from the tissue site 102.
  • the structure of the absorbent layer 146 that contains the fibers may be either woven or non-woven.
  • the fibers in the absorbent layer 146 may gel upon contact with the liquid, thereby trapping the liquid.
  • Spaces or voids between the fibers may allow reduced pressure that is applied to the absorbent layer 146 to be transferred within and through the absorbent layer 146.
  • the fiber density of the fibers in the absorbent layer 146 may be approximately 1.4 grams per millimeter.
  • the diverter layer 144 is disposed adjacent to the absorbent layer 146 and the first distribution manifold 142.
  • the diverter layer 144 is formed from a liquid impermeable material but contains a plurality of apertures 145.
  • the plurality of apertures 145 allow reduced pressure from the micro-pump device 116 to be transmitted through the diverter layer 144 at desired locations.
  • the diverter layer 144 helps control the pattern of reduced pressure as applied to the absorbent layer 146.
  • the reduced pressure is distributed to the diverter layer 144 by the first distribution manifold 142.
  • the apertures 145 may be arranged in a pattern for applying the reduced pressure to portions of the absorbent layer 146 to enhance the capability of the absorbent layer 146 to continue transferring reduced pressure to the tissue site 102 as the absorbent layer 146 absorbs more fluid from the tissue site 102.
  • the plurality of apertures 145 may be positioned in a pattern around a peripheral portion of the diverter layer 144 away from the center of the diverter layer 144 such that the reduced pressure is applied to the absorbent layer 146 away from a center region of the absorbent layer 146.
  • the diverter layer 144 acts in conjunction with the first distribution manifold 142 to ensure that the absorption capabilities and absorption efficiency of the absorbent layer 146 are increased relative to an absorbent layer 146 that is not used in conjunction with a diverter layer 144. By providing better distribution of liquid throughout the absorbent layer 146, the diverter layer 144 also increases the effective capacity and treatment time of the wireless, reduced-pressure pump 108.
  • the diverter layer 144 may be made from any material that enhances the reduced pressure transmission and storage capabilities of an adjacent absorbent layer.
  • the diverter layer 144 may be made from a material that is substantially impermeable to liquid and gas and that diverts the reduced pressure to pass through apertures 145.
  • the material from which the diverter layer 144 is made may have a predetermined moisture vapor transfer rate that is consistent with gas permeability.
  • the diverter layer 144 may still include a pattern of apertures for transmitting a greater volume of liquid or gas than that permitted by a gas-permeable material not having apertures. It should be noted, however, that permeability of the diverter layer 144 to gas but not liquid may result in increased transmission of reduced pressure through the dressing while still directing liquid flow around or near the perimeter of the diverter layer 144.
  • the first distribution manifold 142, the diverter layer 144, and the absorbent layer 146 may be disposed within the pump pouch 120.
  • the wireless, reduced-pressure pump 108 may also include the pressure sensing device 138, which is fluidly coupled to the reduced- pressure dressing 106 and in communication with the first processor 118 for sensing pressure.
  • the reduced-pressure conduit 148 delivers fluids from the reduced-pressure dressing 106 to the wireless, reduced-pressure pump 108.
  • the reduced- pressure conduit 148 is disposed directly into the absorbent layer 146.
  • an interface (not shown) fluidly couples the reduced-pressure conduit 148 and the absorbent layer 146.
  • the reduced-pressure dressing 106 is disposed against the tissue site 102.
  • the tissue site 102 may be, for example, the wound 104 through epidermis 156 and into subcutaneous tissue 158 or any other tissue site.
  • the reduced-pressure dressing 106 may be any device for providing reduced pressure to the tissue site 102 and for receiving fluids from the tissue site 102.
  • the reduced-pressure dressing 106 may be formed with a foam member, a structure with a plurality of defined channels, a suction tube, or other device.
  • the reduced-pressure dressing 106 may include the interface distribution manifold 150 for placing proximate to the tissue site 102, a dressing sealing member 152, and a reduced-pressure interface 154.
  • a manifold is a substance or structure that is provided to assist in applying reduced pressure to, delivering fluids to, or removing fluids from a tissue site 102.
  • the interface distribution manifold 150 typically includes a plurality of flow channels or pathways that distribute fluids provided to and removed from the tissue site 102 around the interface distribution manifold 150.
  • the flow channels or pathways are interconnected to improve distribution of fluids provided or removed from the tissue site 102.
  • the interface distribution manifold 150 may be a biocompatible material that is capable of being placed in contact with the tissue site 102 and distributing reduced pressure to the tissue site 102.
  • interface distribution manifolds may include without limitation the following: devices that have structural elements arranged to form flow channels, e.g., cellular foam, open-cell foam, porous tissue collections, liquids, gels, and foams that include, or cure to include, flow channels; foam; gauze; felted mat; or any other material suited to a particular biological application.
  • devices that have structural elements arranged to form flow channels e.g., cellular foam, open-cell foam, porous tissue collections, liquids, gels, and foams that include, or cure to include, flow channels
  • foam gauze; felted mat; or any other material suited to a particular biological application.
  • the interface distribution manifold 150 is a porous foam and includes a plurality of interconnected cells or pores that act as flow channels.
  • the porous foam may be a polyurethane, open-cell, reticulated foam such as GranuFoam® material available from Kinetic Concepts, Incorporated of San Antonio, Texas.
  • the interface distribution manifold 150 may also be used to distribute fluids such as medications, antibacterials, growth factors, and various solutions to the tissue site 102.
  • Other layers may be included in or on the interface distribution manifold 150, such as absorptive materials, wicking materials, hydrophobic materials, and hydrophilic materials.
  • the interface distribution manifold 150 in whole or in part may be constructed from bioresorbable materials that may remain in a patient's body following use of the reduced-pressure dressing 106.
  • 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,
  • the interface distribution manifold 150 may further serve as a scaffold for new cell-growth, or a scaffold material may be used in conjunction with the interface distribution manifold 150 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 interface distribution manifold 150 is covered by a dressing sealing member 152.
  • the dressing sealing member 152 may be any material that provides a fluid seal.
  • a fluid seal is a seal adequate to maintain reduced pressure at a desired site given the particular reduced-pressure source or subsystem involved.
  • the dressing sealing member 152 may, for example, be an impermeable or semi-permeable, elastomeric material.
  • Elastomeric materials have the properties of an elastomer. It generally refers to a polymeric material that has rubber-like properties. More specifically, most elastomers have 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 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.
  • Additional, specific examples of dressing sealing member materials include a silicone drape, 3M Tegaderm® drape, polyurethane (PU) drape such as one available from Avery Dennison Corporation of Pasadena, California.
  • the dressing sealing member 152 forms a sealed space 160 over the tissue site 102, which may or may contain the micro-pump device 116.
  • An attachment device 162 may be used to retain the dressing sealing member 152 against the patient's epidermis 156 or another layer, such as a gasket or additional sealing member.
  • the attachment device 162 may take numerous forms.
  • the attachment device 162 may be a medically acceptable, pressure-sensitive adhesive that extends about a periphery or all of the dressing sealing member 152 or covers at least a potion of the dressing sealing member 152 on a patient-facing side over the epidermis 156.
  • the reduced-pressure interface 154 may be used to provide fluid
  • the reduced pressure may be delivered through the reduced- pressure conduit 148 to the reduced-pressure interface 154 and then to the sealed space 160.
  • the reduced-pressure interface 154 is a T.R.A.C. ® Pad or Sensa T.R.A.C. ® Pad available from KCI of San Antonio, Texas.
  • the reduced-pressure conduit 148 may include the reduced-pressure lumen 164 and the pressure sensing lumen 166 formed as an integral conduit as shown in FIGURE 1 or separately as shown in FIGURE 3.
  • pressure sensing capability may be added to the reduced-pressure dressing 106 to function in addition to or in lieu of pressure sensing device 138.
  • the reduced-pressure dressing 106 may include a second RFID antenna 168, a third processor 170, and a second pressure sensing device 172.
  • the third processor 170 is coupled to the second RFID antenna 168 and to the second pressure sensing device 172.
  • a vent passageway 174 provides fluid communication between the sealed space 160 and the second pressure sensing device 172.
  • the third processor 170 and the second pressure sensing device 172 are operable to receive a pressure inquiry signal from the base unit 1 10 and respond with a pressure message signal indicative of the pressure in the sealed space 160.
  • the wireless, reduced-pressure pump 108 is a wireless and passive (i.e., no battery) device. As such, the wireless, reduced-pressure pump 108 has no source of power other than power delivered through the first RFID antenna 114. In some embodiments, the wireless, reduced-pressure pump 108 may contain a capacitor for storing electrical energy. In another illustrative embodiment, the first power source 140 as shown in FIGURE 3 may be provided to augment the power delivered through the first RFID antenna 114 or to operate the micro-pump device 1 16. The first power source 140 may be recharged by power from the first RFID antenna 114.
  • the micro-pump device 116 may take numerous forms such as a piezoelectric pump, peristaltic pump, or other miniaturized pump. Referring now primarily to FIGURE 5, an illustrative embodiment of a micro-pump device 116 that is suitable for use as an aspect of the wireless, reduced-pressure pump 108 is presented.
  • the micro-pump device 116 includes a cavity 178 that is defined by a first end wall 180, a second end wall 182, and an annular side wall 184.
  • the cavity 178 may be substantially circular in shape, but other shapes are possible, such as elliptical. In one illustrative embodiment, the cavity 178 may hold about 10 ml of fluid or may hold more or less.
  • the cavity 178 is provided with a nodal inlet 186, which may be valved or unvalved.
  • the cavity 178 may also have a valved outlet 190.
  • the first end wall 180 may be a disc 192.
  • an actuator 194 such as a piezoelectric disc, magnetostrictive device, or solenoid actuated device.
  • the actuator 194 is electrically coupled to a drive circuit, which is controlled by the processor.
  • the drive circuit will apply an alternating electrical signal to the actuator 194 to induce an oscillation in the disc 192.
  • the frequency of the oscillation can be adjusted to match the natural frequency of the chamber.
  • the piezoelectric disc may be less than 1 mm in thickness and may be tuned to operate at more than 500 Hz, more than 10 kHz, or even higher than 20 kHz.
  • the actuator 194 may vibrate in a direction substantially perpendicular to the plane of the cavity 178 as shown, thereby generating radial pressure oscillations within the fluid in the cavity 178.
  • One or more micro- pump devices 1 16 may be used in parallel or series.
  • the micro-pump device 1 16 has a fluid in the cavity 178 and has a substantially cylindrical shape that is bounded by the first end wall 180, second end wall 182, and side wall 184. At least two apertures, e.g., inlet 186 and outlet 190, are formed through the walls 180, 182, 184 forming the cavity 178.
  • the cavity 178 has a radius, r, and a height, h, and r/h > 1.2 and h 2 /r > 4 x 10 "10 m.
  • the actuator 194 which is a piezoelectric disc, creates an oscillatory motion of one of the end walls 180, 182 in a direction that is substantially perpendicular to the plane of the first end wall 180 and second end wall 182. Axial oscillations of the end walls 180, 182 drive radial oscillations of fluid pressure in the cavity 178 and allow for pumping that creates reduced pressure.
  • the micro-pump device 116 is like an acoustic pump in that an acoustic resonance is set up within the cavity 178.
  • the inlet 186 is used to pull fluids, and the outlet 190 is coupled to a vent, e.g., the vent 176 in FIGURE 4, to discharge to an exterior. Other micro-pump devices may be used.
  • the micro- pump device 116 may be the type of micro-pump shown in United States Patent Publication 2009/0240185 (application 12/398,904; filed 5 March 2009), entitled, "Dressing and Method for Applying Reduced Pressure To and Collecting And Storing Fluid from a Tissue Site,” which is incorporated herein for all purposes.
  • the reduced-pressure dressing 106 is applied to the tissue site 102.
  • the interface distribution manifold 150 is disposed proximate to the tissue site 102.
  • the interface distribution manifold 150 and the tissue site 102 are covered by the dressing sealing member 152 to create the sealed space 160.
  • the attachment device 162 on the patient- facing side of the dressing sealing member 152 may help provide a fluid seal against a portion of the patient's epidermis 156.
  • the reduced-pressure interface 154 may be applied, such as for example by cutting a small aperture in the dressing sealing member 152 and securing the reduced-pressure interface 154 over or through the aperture, or hole.
  • the wireless, reduced-pressure pump 108 is then provided and fluidly coupled by the reduced-pressure conduit 148 to the reduced-pressure interface 154.
  • the wireless, reduced-pressure pump 108 is positioned such that the first RFID antenna 114 is placed within operating range of the base unit 1 10.
  • the first RFID antenna 114 is placed within a few millimeters of the RFID reader 1 12 of the base unit 1 10.
  • the first RFID antenna 1 14 may be placed as far away as ten meters from the RFID reader 1 12. Any distance within the given range may be readily used.
  • the base unit 110 is then activated by the user.
  • the base unit 110 transmits a pump signal 137 to the wireless, reduced-pressure pump 108.
  • the pump signal is received by the first RFID antenna 1 14, and the energy of the pump signal is delivered to the first processor 1 18.
  • the first processor 118 provides energy to the micro-pump device 116.
  • the micro-pump 1 16 creates reduced pressure that is delivered into the fluid reservoir 126 that is fluidly coupled to the reduced-pressure conduit 148.
  • the reduced pressure is delivered to the reduced-pressure dressing 106 through the reduced-pressure conduit 148. Fluids from the tissue site 102 flow through the interface distribution manifold 150, reduced-pressure interface 154, and reduced-pressure conduit 148 into the fluid reservoir 126.
  • the pressure at the tissue site 102 may be monitored directly or indirectly using a pressure sensing device, such as pressure sensing device 138 of FIGURE 3 or second pressure sensing device 172 of FIGURE 1.
  • a pressure sensing device such as pressure sensing device 138 of FIGURE 3 or second pressure sensing device 172 of FIGURE 1.
  • the second processor 128 and the RFID reader 1 12 of the base unit 110 may, separate from the pump signal or with the pump signal, transmit a pressure inquiry signal to the wireless, reduced- pressure pump 108.
  • the first processor 118 and pressure sensing device 138 may prepare a pressure message signal to communicate a measurement of the pressure at the tissue site. Then, the pressure message signal may be used for further processing by the first processor 1 18 to develop a pump control signal for activating or deactivating the micro-pump 1 16 as may be needed.
  • the first processor 1 18 may transmit the pressure message signal via the first RFID antenna 114 to the RFID reader 1 12. After arriving at the RFID reader 112, the pressure message signal is delivered to the second processor 128. Using the pressure message signal, the second processor 128 may prepare a pump control signal that is transmitted by the RFID reader 1 12 to the wireless, reduced-pressure pump 108 to deactivate or activate the micro-pump 116 as needed.
  • an alarm signal is created by the base unit 110 or by the wireless, reduced-pressure pump 108.
  • the alarm may be a separate audible device, visual alarm, or the micro-pump 116 may function at a different frequency range, e.g., lower, to make an audible noise for the alarm.
  • the reduced-pressure dressing 106 includes the second RFID antenna 168 that is coupled to the third processor 170, which is coupled to the second pressure sensing device 172.
  • the second pressure sensing device 172 experiences the pressure within the sealed space 160 via the vent passageway 174.
  • the base unit 1 10 transmits a pressure inquiry signal to the second RFID antenna 168.
  • the second pressure sensing device 172 and third processor 170 produce a pressure message signal that is transmitted by the second RFID antenna 168 to the base unit 110.
  • the base unit 1 10 then produces a pump control signal that is transmitted to the wireless, reduced- pressure pump 108 to activate or deactivate the micro-pump 1 16.
  • the third processor 170 may evaluate the pressure and prepare a pump control signal as part of a feedback or control loop.
  • the wireless, reduced-pressure pump 108 may be a self-contained, disposable pouch design that may be removably secured to a base unit 1 10 on a pole 196.
  • a pump pouch 120 is formed with a first pump-sealing member 122 and a second pump-sealing member 124.
  • the perimeter of the pump pouch 120 may include a first flange 123 and a second flange 125.
  • the pump pouch 120 may be divided or partitioned into numerous compartments if desired. For example, a compartment (not explicitly shown) may be formed that has the micro-pump 1 16 within the compartment and another compartment may formed that contains the absorbent layer 146.
  • the flanges 123, 125 on the illustrative embodiment of the pump pouch 120 may be formed by welding, bonding or otherwise attaching portions of the first pump-sealing member 122 and second pump-sealing member 124.
  • the first flange 123 may include one or more apertures 129 for receiving one or more posts 198.
  • the posts 198 secure the pump pouch 120 adjacent to the base unit 1 10.
  • the reduced-pressure conduit 148 may enter through an aperture 149 in the second flange 125 that provides a sealed, interference fit or has a coupling that provides a sealed connection. Other connections may be used.
  • the first RFID antenna 1 14 may be placed closest to the base unit 110 such that the first RFID antenna 1 14 is immediately adjacent to RFID reader 112 of the base unit 1 10 as shown best in FIGURE 4.
  • the first RFID antenna 1 14 is positioned two millimeters or one millimeter (1 mm) or less from the RFID reader 1 12.
  • the RFID reader 112 and the first RFID antenna 1 14 may be substantially matched and aligned.
  • the wireless, reduced-pressure pump 108 may be attached to a post 198 with the first RFID antenna 114 facing outward towards a remotely located base unit 1 10 as suggested in FIGURE 1.
  • the base unit 1 10 may be located at a central hub area where the wireless, reduced-pressure pump 108 is monitored and powered using the base unit 1 10, which may be as far away as ten meters or more.
  • the base unit 1 10 may include the control panel 130 and one or more displays 132.
  • the base unit 1 10 may include a base housing or base body 136.
  • the base housing or body 136 may include a shelf portion 199 that may provide physical support to a portion of the wireless, reduced-pressure pump 108 when the wireless, reduced-pressure pump 108 fills with fluids from the tissue site 102.
  • the wireless, reduced-pressure pump 108 shown in FIGURE 6 is shown before use. With the embodiments of FIGURES 4 and 6, when the wireless, reduced- pressure pump 108 has reached its capacity for holding fluids, the micro-pump 1 16 may be deactivated and the user may dispose of the entire wireless, reduced-pressure pump 108.
  • the wireless, reduced-pressure pump 200 may be used as part of a system for treating a tissue site, e.g., the system of FIGURE 1.
  • the wireless, reduced-pressure pump 200 includes a plurality of wall members 202 that form a first chamber 204 and a second chamber 206.
  • One of the plurality of wall members 202 is a partitioning wall 208 that separates the first chamber 204 from the second chamber 206.
  • a micro-pump 210 which is analogous to the micro-pump 116 of the previous figures, may be disposed within the first chamber 204.
  • the micro-pump 116 is configured such that the inlet 212 that receives fluid (or said another way, discharges reduced pressure) is fluidly coupled to the second chamber 206.
  • the micro-pump 210 has an outlet or vent 214 that is fluidly coupled to the first chamber 204.
  • the micro-pump 210 vents positive pressure through outlet or vent 214 into the first chamber 204.
  • a portion of one of the plurality of wall members 202 that forms the first chamber 204 contains an aperture 216.
  • An optional relief valve 218 is coupled to the aperture 216.
  • the relief valve 218 is configured to allow pressure within the first chamber 204 to vent to an exterior of the wireless, reduced-pressure pump 200 when the pressure exceeds a first threshold pressure.
  • At least a portion of the plurality of wall members 202 that make up the second chamber 206 includes an inflatable support member and typically a plurality of inflatable support members 220. While a plurality of inflatable support members 220 are presented, it should be understood that a single inflatable support member may be used create the second chamber 206.
  • the inflatable support members 220 are in fluid communication with the first chamber 204, such as through a plurality of apertures 222. Thus, the positive pressure within the first chamber 204 fills the plurality of inflatable support members 220. As the plurality of inflatable support members 220 are filled with sufficient fluid, the plurality of inflatable support members 220 gain relative rigidity that provides a structure that helps provide volume to the second chamber 206. Fluids 223 from a tissue site are received through a reduced- pressure conduit 224 into the volume of the second chamber 206.
  • the wireless, reduced- pressure pump 200 which is shown in the shape of a pyramid, may be formed to take other shapes, e.g., a box, a cylinder, or any other shape.
  • the micro-pump 210 may be fully or partially powered by a pump signal delivered to a RFID antenna 226.
  • the RFID antenna 226 is coupled to a first processor 228.
  • the first processor 228 is electrically coupled to the micro-pump 210 by an electrical lead 230, which may be contained in one of the plurality of wall members 202 but is shown separately in FIGURE 7.
  • a floor portion 232 of the plurality of wall members 202 may be contained within a platform member 234.
  • the reduced-pressure conduit 224 is coupled to a reduced-pressure dressing, such as reduced-pressure dressing 106 of FIGURES 1 and 3.
  • a base unit e.g., base unit 1 10 of FIGURE 1
  • the pump signal received by the RFID antenna 226 is delivered to the first processor 228.
  • Power is delivered from the first processor 228 to the micro-pump 210 to energize micro-pump 210.
  • micro-pump 210 is energized, reduced pressure is delivered into the second chamber 206 and positive pressure is delivered to the first chamber 204.
  • a spacer member may cover the inlet 212 to avoid a vapor lock during start up before the inflatable support members 220 fill.
  • the maximum volume is achieved for the second chamber 206. Meanwhile, the reduced pressure in the second chamber 206 is delivered to the reduced-pressure conduit 224. Fluids 223 (including liquids) are introduced into the second chamber 206.
  • a reduced-pressure sensing device e.g., analogous to pressure sensing device 138 in FIGURE 3 may be incorporated into a portion of the second chamber 206 to measure pressure in the second chamber 206.
  • a reduced- pressure sensing device e.g., analogous to pressure sensing device 138 in FIGURE 3 may be included in the reduced-pressure pump 200.
  • the reduced-pressure conduit 224 may also have a pressure sensing lumen that is fluidly coupled to the reduced-pressure sensing device for measuring pressure at a distribution manifold. In both examples, the pressure sensing device is coupled to the first processor 228 to develop a pressure message signal.
  • the pressure message signal may be supplied in response to a pressure inquiry signal from a base unit or self-generated by the first processor 228.
  • the first processor 228 may use the pressure message signal to develop a pump control signal that is delivered to the micro-pump 210.
  • the pressure message signal may be transmitted to the base unit where a processor in the base unit may develop a pump control signal similar to the embodiments previously presented.
  • the wireless, reduced-pressure pumps 108, 200 previously presented have, instead of having RFID antennas, electrical leads or sockets and plugs between the pumps and base.
  • the electrical leads or sockets and plugs may readily plug into one another for communicating power and signals.
  • the reduced-pressure system 300 includes a wireless, reduced-pressure dressing 304 and a base unit 306.
  • the base unit 306 may include a power connector 307.
  • the wireless, reduced- pressure dressing 304 is a self-contained, disposable dressing that receives power and control from the base unit 306.
  • the base unit 306 may be substantially adjacent to the wireless, reduced-pressure dressing 304, e.g., within one or two millimeters, or up to 10 meters or more away or anywhere in between.
  • the micro-pump 316 may be separate from an absorbent layer or absorbent member 310, such that after use, the micro-pump 316 may be readily separated. The micro-pump 316 may then be reconditioned and reused.
  • the wireless, reduced-pressure dressing 304 includes an interface distribution manifold 308 that is placed proximate to the tissue site 302.
  • the wireless, reduced-pressure dressing 304 may also include an absorbent layer 310, a RFID antenna 312, and a first processor 314.
  • the RFID antenna 312 is electrically coupled to the first processor 314.
  • the first processor 314 is electrically coupled to the micro-pump 316.
  • the interface distribution manifold 308, absorbent layer 310, RFID antenna 312, first processor 314, and micro-pump 316 may all be retained in place and secured in a sealed space 318 by one or more sealing members, such as sealing member 320. Additional layers and components may be included in the wireless, reduced-pressure dressing 304.
  • FIGURES 9-11 includes additional layers and components.
  • the additional layers and components may be arranged in different orders.
  • a sealing layer 322 is used to seal the wireless, reduced-pressure dressing 304 around the tissue site 302.
  • the sealing layer 322 is formed with an aperture 323 for providing fluid
  • a first internal distribution manifold 324 is positioned in fluid communication with the interface distribution manifold 308 and the tissue site 302.
  • the absorbent layer 310 is positioned in fluid communication with the first internal distribution manifold 324, the interface distribution manifold 308, and a tissue site 302.
  • a diverter layer 326 is positioned adjacent to the absorbent layer 310.
  • a second internal distribution manifold 328 is positioned in fluid communication with the diverter layer 326.
  • the diverter layer 326 is formed with a plurality of apertures 327 that may take numerous patterns and forms.
  • the diverter layer 326 is shown in this particular illustrative embodiment with a plurality of apertures 327 forming a square pattern. The square pattern has corner apertures that are larger than the other apertures.
  • a liquid-air separator 330 is positioned adjacent to the second internal distribution manifold 328.
  • the micro-pump 316, RFID antenna 312, and first processor 314 may be adjacent to the liquid-air separator 330.
  • a charcoal filter 332 or other odor relieving device may be positioned over an outlet 334 of the micro-pump 316.
  • the sealing member 320 is formed with an aperture 336 that allows the outlet 334 of the micro-pump 316 to exhaust to an exterior of the wireless, reduced-pressure dressing 304.
  • the outlet 334 and aperture 336 together form a vent 338.
  • the micro-pump 316 may be a micro-pump that is small and light enough such that the integrated wireless, reduced-pressure dressing 304 is able to be maintained on the tissue site 302. Furthermore, the size and weight of the micro-pump 316 may be such that the integrated reduced-pressure dressing 304 does not pull or otherwise adversely affect the tissue site 302.
  • the micro-pump 316 may be a disk pump having a piezoelectric actuator similar to that previously described. Reference is also made to the pumps shown in United States Patent Publication 2009/0087323 and United States Patent Publication 2009/0240185, which are hereby incorporated by reference for all purposes.
  • the micro-pump 316 may be a peristaltic pump that is used for pumping a variety of fluids. It should be understood that alternative pump technologies may be utilized and that rotary, linear, or other configurations of pumps may be utilized.
  • the micro-pump 316 creates sufficient reduced pressure to be therapeutic for wound therapy.
  • the micro-pump 316 has sufficient flow, reduced pressure, and operation life characteristics to enable continuous application of reduced pressure treatment.
  • the flow may range between about 5-1000 ml/min and the reduced pressure may range between about -50 and -200 mm Hg (-6.6 to -26.6 kPa). It should be understood that alternative ranges may be utilized depending on the configuration of the integrated, wireless, reduced-pressure dressing 304, size of wound, or type of wound.
  • multiple pumps may be positioned in a single dressing to deliver increased flow rates or vacuum levels as required.
  • the micro-pump 316 is disposed within the dressing to avoid conduits and external canisters for collection of wound exudate.
  • the micro-pump 316 includes the outlet 334 to release air or exhaust out of the reduced-pressure dressing 304. If the outlet 334 is used, the outlet 334 is in fluid communication with, or may be positioned within, the aperture 336 of the sealing member 320. Alternatively, the sealing member 320 may be sealed around an outlet port of the micro-pump 316 such that gas from the micro-pump 316 is able to exhaust directly through the aperture 336.
  • the outlet 334 of the micro-pump 316 is oriented in a direction away from the liquid-air separator 330 (or hydrophobic filter) to avoid adding air to the wireless, reduced-pressure dressing 304.
  • the air exhausts through an aperture 336 in the sealing member 320, which may include a one-way valve. Alternatively, the air or another gas could be exhausted through a gas-permeable portion of the sealing member 320 as long as the ability of the sealing member 320 to maintain reduced pressure is not affected.
  • the piezoelectric actuator associated with the micro-pump 316 may be driven at different frequencies to act as a buzzer or vibrating alert system at times.
  • the alert system may alert a user to an alarm condition.
  • the alarm condition may indicate the presence of a leak in the dressing, a change in reduced pressure as measured by a sensor, that the dressing has absorbed a maximum capacity of liquid as may be indicated by an indicator, or that one or more layers are no longer manifolding reduced pressure efficiently.
  • Control electronics may be physically or functionally incorporated as part of the first processor 314.
  • the control electronics may be utilized to control operation of the micro-pump 316.
  • the control electronics may be analog or digital and be configured with a regulator to regulate speed or duty cycle at which the micro-pump 316 operates.
  • the control electronics may be configured with a controller that receives sense signals from sensors or switches, e.g., a pressure sensing device (see 340 in FIG. 12).
  • the sensors may be disposed throughout the wireless, reduced-pressure dressing 304 to sense parameters, such as pressure, temperature, moisture, chemistry, odor, or any other parameter that may be utilized in managing and controlling the micro-pump 316.
  • the control electronics may include a computer processor or programmable gate array or other control device. It should be understood that the control electronics may include any form of digital or analog components to perform the functions described herein.
  • the control electronics may be or include the first processor 314.
  • the control electronics may be arranged to monitor and provide an alarm for certain conditions, e.g., (i) low pressure, (ii) excessive leak, (iii) level of absorbent layer, and (iv) battery state (if included).
  • the control electronics may include electronics that monitor each of the parameters and generate an alarm signal (e.g., high-pitched beep, vibration, or light) using a speaker, vibrator, or illumination device, such as a light emitting diode (LED).
  • an alarm signal e.g., high-pitched beep, vibration, or light
  • the control electronics may notify a medical professional, patient, or family member that a parameter is outside of a desired range. For example, if a pressure at the tissue site 302 is below a therapeutic level, a continuous tone may be generated.
  • the RFID antenna 312 is utilized to provide electric power to the micro- pump 316 and control electronics.
  • a battery 342 may also be used to provide stored energy to augment power from the RFID antenna 312.
  • the battery 342 may be any size and shape and may be of any material, such as polymer.
  • the battery 342 may provide the entire needed power or a portion thereof.
  • the battery 342 may be recharged by power from the RFID antenna 312.
  • the battery 342 may be configured with a voltage level sensor that is monitored by the control electronics, and the control electronics may provide an alarm when a low power level is detected.
  • the battery 342 may be directly connected to the micro-pump 316.
  • the battery 342 may be connected to the control electronics or processor(s) that use power from the battery 342 to drive the micro- pump 316.
  • the control electronics may provide continuous, modulated power, such as a pulsewidth modulated (PWM) signal, to drive the micro-pump 316.
  • PWM pulsewidth modulated
  • the sealing layer 322 is adhered to or otherwise connected to the sealing member 320 that is used to drape or otherwise cover the components of the reduced-pressure dressing 304.
  • the sealing layer 322 may include a medical-grade adhesive material or other sealing device that is strong enough to form a vacuum seal with epidermis around a wound of a patient.
  • the sealing layer 322 may be a band that has an aperture 323 that is slightly larger than the geometric parameters of the liquid-air separator 330 or other layer so that the sealing member 320 contacts epidermis around the tissue site 302 of the patient.
  • the sealing member 320 is impermeable to fluids, such as air and liquids.
  • the sealing member 320 may be adhered to the diverter layer 326 and the diverter layer 326 adhered to the sealing member 320 to create an upper dressing portion and a lower dressing portion.
  • the upper dressing portion may include the sealing member 320, the micro-pump 316 and related components, the liquid-air separator 330, the second internal distribution manifold 328, and the diverter layer 326.
  • the lower dressing portion may include the absorbent layer 310, the first internal distribution manifold 324, the sealing layer 322, and the interface distribution manifold 308.
  • the wireless, reduced-pressure dressing 304 may be configured to allow replacement of the lower dressing portion once the wireless, reduced-pressure dressing has absorbed a maximum capacity of fluid.
  • the upper dressing portion may be reused after the lower dressing portion is replaced. This allows multiple uses of the micro-pump 316, while disposable portions of the dressing may be replaced.
  • the micro-pump 316, first processor 314, and RFID antenna 312 may be removed from the dressing for reuse and the remaining layers of the dressing replaced.
  • only the absorbent layer 310 may be replaced.
  • only the absorbent layer 310 and the interface distribution manifold 308 may be replaced.
  • the charcoal filter 332 may be utilized in the wireless, reduced-pressure dressing 304 to reduce odors created by the tissue site 302 and dispersed from the wireless, reduced-pressure dressing 304.
  • the charcoal filter 332 may be disposed above a valve or other output vent from the micro-pump 316 to filter exhaust from the micro-pump 316 prior to being released from the integrated reduced-pressure dressing 304. It should be understood that the charcoal filter 332 may be alternatively configured and disposed above or below the micro- pump 316. In another illustrative embodiment, rather than using a charcoal filter, charcoal may be integrated into any or all of the different layers utilized in the integrated reduced- pressure dressing 304.
  • the reduced-pressure system 300 of FIGURES 9-11 is applied by placing the interface distribution manifold 308 proximate to the tissue site 302. Placing the sealing layer 322 over the interface distribution manifold 308 such that the aperture 323 is over the interface distribution manifold 308.
  • the first internal distribution manifold 324 is placed adjacent to the first interface distribution manifold 308 and possibly a portion of the sealing layer 322.
  • the absorbent layer 310 is placed adjacent to the first internal distribution manifold 324.
  • the diverter layer 326 may be placed over all the components thus presented.
  • the second internal distribution manifold 328 may be placed adjacent to a portion of the diverter layer 326 along with the liquid-air separator 330.
  • the micro-pump 316, RFID antenna 312, and first processor 314 may be applied.
  • the components mentioned here may also be pre-assembled as a dressing stack.
  • the sealing member 320 is used to create a seal that forms a sealed space 318.
  • the base unit 306 is used to transmit a pump signal as before to the RFID antenna 312 that is received by the first processor 314 and is used to provide power to the micro-pump 316.
  • the first processor 314 may further include one or more capacitors for holding power or one or more batteries such as a rechargeable battery.
  • the pump signal causes reduced pressure to be developed by the micro-pump 316.
  • the reduced pressure is transmitted to the tissue site 302 to remove fluids or to provide reduced pressure therapy.
  • the fluids removed from the tissue site 302 are transmitted within the reduced-pressure dressing 304 to the absorbent layer 310 where the fluids are retained or substantially retained.
  • a pressure sensing device may be included as part of the wireless, reduced- pressure dressing 304 to provide a pressure message signal to the base unit 306.
  • the reduced-pressure system 300 includes a wireless, reduced-pressure dressing 304 and a base unit 306.
  • the reduced-pressure system 300 in FIGURE 12 is analogous to the system presented in FIGURES 9-1 1, except that the wireless, reduced-pressure dressing 304 includes fewer components and includes the addition of a pressure sensing device 340 that is electrically coupled to the first processor 314.
  • an optional battery 342 is included.
  • the battery 342 may supplement power provided through the RFID antenna 312 or may be used as the primary power source and then recharged by the RFID antenna 312.
  • the RFID antenna 312 receives power from the base unit 306.
  • the sealing member 320 is shown secured to the epidermis 344 by an attachment device 346. Components included in the previous dressing of FIGURES 9-11 have been assigned the same reference numerals and are not necessarily discussed further here.
  • the reduced-pressure system 300 of FIGURE 12 may be used by first applying the interface distribution manifold 308 adjacent to the tissue site 302.
  • the absorbent layer 310 is placed in fluid communication with the interface distribution manifold 308.
  • the liquid-air separator 330 may be placed over the absorbent layer 310.
  • the RFID antenna 312, pressure sensing device 340, first processor 314, micro-pump 316, and battery 342 are disposed on the liquid-air separator 330.
  • only some of the components, such as the micro-pump 316 may be adjacent to the liquid-air separator 330.
  • the sealing member 320 is applied over the tissue site 302 to create a sealed space 318 and to cover all the aforementioned components.
  • the base unit 306 transmits a pump signal or pump activation signal to the reduced-pressure dressing 304 that activates the micro-pump 316.
  • the micro-pump 316 removes air or other fluids from the sealed space 318 and thereby initiates treatment of the tissue site 302 with reduced pressure.
  • the base unit 306 may also transmit a pressure inquiry signal.
  • the RFID antenna 312, the first processor 314, and the pressure sensing device 340 develop a pressure message signal that is transmitted by the RFID antenna to the RFID reader (not explicitly shown) of the base unit 306.
  • the base unit 306 may include a processor (not explicitly shown) that receives the pressure message signal and develops a pump control signal to activate or deactivate the micro-pump 316. If the reduced pressure is in the desired therapy range, the micro-pump 316 may be deactivated. Similarly, if the pressure is too great on an absolute scale, the base unit 306 may transmit a pump signal that activates or continues the micro-pump 316 to produce more reduced pressure. If more than a sufficient elapsed time has passed without the desired pressure being reached, an alarm may be triggered by the base unit 306.
  • the wireless, reduced-pressure dressing 304 may include a galvanic cell (not explicitly shown) to provide a full indication message signal when exudate or other body fluids electrically couple two electrodes. The full indication message signal would be transmitted with the RFID antenna 312 to the base unit 306 indicating that the dressing is full.
  • FIGURE 13 another illustrative embodiment of a reduced-pressure dressing 400 is presented that includes a wireless, reduced-pressure pump 430.
  • the reduced-pressure dressing 400 is shown in an exploded view over a tissue site 402, such as a wound, on a patient 404.
  • the reduced-pressure dressing 400 includes an interface distribution manifold 406, which is disposed proximate the tissue site 402.
  • the interface distribution manifold 406 may be formed from any manifold material, such as a GranuFoam ® material or any other manifold material previously mentioned.
  • the reduced-pressure dressing 400 further includes a lower drape or diverter 408.
  • the lower drape 408 may be a polyethylene material having adhesive on a lower side (tissue-facing side) that adheres to the patient 404 surrounding the tissue site 402 being treated.
  • the lower drape 408 includes apertures or perforations for communicating reduced pressure through the interface distribution manifold 406 to the tissue site 402 and drawing wound fluids (liquids or gases) from the tissue site 402.
  • the lower drape 408 may also include a sealing ring 410 to provide additional adhesive strength to maintain the reduced pressure at a desired therapeutic level.
  • a protective release liner 412 may initially cover the sealing ring 410. The protective release liner 412 is removed from the lower side of the lower drape 408 before the lower drape 408 is positioned on the patient 404.
  • the reduced-pressure dressing 400 includes an absorbent layer 414 that may be a non-woven fabric for absorbing the wound liquids being drawn through the apertures of the lower drape 408.
  • the absorbent layer 414 is sandwiched between two wicking layers 416, 418 that wick and manifold the wound fluid to the absorbent layer 414.
  • the dense side of the wicking layers 416, 418 face away from the absorbent layer 414.
  • the wicking layers 416, 418 sandwich the absorbent layer 414 to form a fluid storage device 420.
  • the reduced-pressure dressing 400 further includes an upper drape 422 that may be a non-porous, occlusive barrier formed of polyethylene.
  • the smooth side of the upper drape 422 faces the upper wicking layer 416.
  • the upper drape 422 includes a aperture or opening 424.
  • the aperture or opening 424 is covered by a hydrophobic filter 426 that separates air from liquid to contain the wound liquids or exudates within the absorbent layer 414.
  • the hydrophobic filter 426 simultaneously permits the flow of gas from the absorbent layer 414 as a result of reduced pressure being applied to the hydrophobic filter 426.
  • the upper drape 422 and the hydrophobic filter 426 comprise a top layer 428 of the reduced- pressure dressing 400 that covers the fluid storage device 420. All the elements of the dressing assembly described above except the release liner 412 may be referred to collectively as the "wound dressing" portion of the reduced-pressure dressing 400.
  • the reduced-pressure dressing 400 further includes the wireless, reduced- pressure pump, or pump portion 430.
  • the pump portion 430 includes a micro-pump assembly 432 positioned on top of the upper drape 422 to provide a reduced pressure for drawing air through the hydrophobic filter 426, the fluid storage device 420, and the interface distribution manifold 406.
  • the micro-pump assembly 432 includes a piezoelectric disc pump 434 that vibrates at a predetermined frequency to generate a desired reduced pressure at the input of the piezoelectric disc pump 434.
  • the piezoelectric disc pump 434 may be analogous to micro- pump 316 of FIGURE 12.
  • the piezoelectric disc pump 434 of the micro-pump assembly 432 may not operate if any liquid drawn from the tissue site 402 into the absorbent layer 414 below the upper drape 422 enters the input port of the piezoelectric disc pump 434.
  • the hydrophobic filter 426 prevents wound liquids or exudates from flowing into the piezoelectric disc pump 434 of the micro-pump assembly 432.
  • the reduced-pressure dressing 400 may also include a spacing ring or ring seal 436 positioned between the hydrophobic filter 426 and the inlet of the piezoelectric disc pump 434 to provide a cavity for air flow to the piezoelectric disc pump 434 of the micro-pump assembly 432.
  • the micro-pump assembly 432 may be sandwiched between a first foam cushion 438 and second foam cushion 440.
  • the micro-pump assembly 432, first cushion 438, and second cushion 440 are sandwiched between an outer ply 442 and an inner ply 444 and form a single composite package that is removably attached to the upper drape 422.
  • the outer ply 442 includes apertures or perforations 446 that provide an exhaust path for the output of the micro-pump assembly 432.
  • the piezoelectric disc pump 434 or other micro-pump may be controlled by a first processor 448 and other control electronics.
  • the piezoelectric disc pump 434 may be powered by a first power unit 450 and a second power unit 452.
  • the power units 450, 452 may be batteries.
  • the first power unit 450 or the second power unit 452 may comprise a RFID antenna that provides power to the first processor 448 and to the piezoelectric disc pump 434.
  • a system for treating a tissue site with reduced pressure includes a reduced-pressure dressing for disposing proximate to the tissue site; and a wireless, reduced-pressure pump fluidly coupled to the reduced-pressure dressing.
  • the wireless, reduced-pressure pump includes a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and a fluid reservoir fluidly coupled to the micro- pump device.
  • the system further includes a base unit having a RFID reader. The RFID reader is configured to provide power to the RFID antenna such that the micro-pump device is powered.
  • the system may further include a first pump-sealing member and a second pump- sealing member.
  • the first pump-sealing member and second pump-sealing member are at least partially coupled to form a pump pouch in which the micro-pump device is disposed.
  • the wireless, reduced-pressure pump may function with no source of power other than the RFID antenna.
  • the wireless, reduced-pressure pump may further comprise a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site.
  • the wireless, reduced-pressure pump may further comprise a pressure sensing device coupled to the first processor.
  • the base unit may comprise a second processor coupled to the RFID reader, and the second processor and RFID reader may be configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced- pressure pump and to receive in response thereto a pressure message signal from the first processor.
  • the wireless, reduced- pressure pump may further comprise a pressure sensing device coupled to the first processor.
  • the base unit may comprise a second processor coupled to the RFID reader.
  • the second processor and RFID reader may be configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor.
  • the first processor and pressure sensing device may be configured to prepare the pressure message signal in response to the pressure inquiry signal.
  • the first processor and RFID antenna may be configured to transmit the pressure message signal.
  • the second processor may be configured to receive the pressure message signal, prepare a control signal.
  • the second processor and RFID may be configured to transmit the control signal to the wireless, reduced-pressure pump to provide a control signal for activating or deactivating the micro-pump device.
  • the wireless, reduced-pressure pump may further comprise a pressure sensing device coupled to the first processor.
  • the pressure sensing device is operable to produce a pressure message signal.
  • the first processor is operable to receive the pressure message signal and to produce a control signal to activate or deactivate the micro-pump device.
  • the system further includes a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site; a first distribution manifold, an absorbent layer, a diverter layer, a pump-sealing member, a second pump-sealing member, wherein the first distribution manifold, the absorbent layer, and the diverter layer are disposed within a pump pouch formed by the a pump-sealing member and a second pump- sealing member; the micro-pump device comprises a piezoelectric pump.
  • the reduced- pressure dressing includes an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and a reduced-reduced pressure interface.
  • the RFID antenna is less than five (5) centimeters from the base unit.
  • a wireless, reduced- pressure pump includes at least one wall member forming a first chamber and a second chamber; a RFID antenna; a first processor coupled to the RFID antenna; and a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure and positive pressure.
  • the micro-pump device has a vent fluidly coupled to the first chamber for exhausting positive pressure thereto and an inlet that is fluidly coupled to the second chamber for delivering reduced pressure thereto.
  • the pump further includes a plurality of inflatable support members fluidly coupled to the first chamber; and a fluid reservoir, wherein the fluid reservoir comprises the second chamber.
  • the pump may further include a first pressure relief valve fluidly coupled to the first chamber.
  • the first pressure relief valve is operable to vent positive pressure above a first threshold pressure.
  • the first chamber and the second chamber may be in the shape of a portion of a pyramid.
  • the pump may function with no source of power other than the RFID antenna.
  • manufacturing a system for treating a tissue site on a patient with reduced pressure includes providing a reduced-pressure dressing for disposing proximate to the tissue site and providing a wireless, reduced-pressure pump.
  • the wireless, reduced-pressure pump includes: a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and a fluid reservoir fluidly coupled to the micro-pump device.
  • the method further includes providing a base unit having a RFID reader.
  • the RFID reader is configured to provide power to the RFID antenna such that the micro-pump device is powered.
  • the method of manufacturing may further include a first pump-sealing member and a second pump-sealing member.
  • the first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed.
  • the method of manufacturing may further include providing a reduced-pressure conduit for fluidly coupling the wireless, reduced- pressure pump to the reduced-pressure dressing.
  • the method of manufacturing may further include providing a pressure sensing device and coupling the pressure sensing device to the reduced-pressure dressing.
  • a method for treating a tissue site on a patient with reduced pressure includes placing a reduced-pressure dressing proximate to the tissue site and providing a wireless, reduced-pressure pump.
  • the wireless, reduced-pressure pump comprises: a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and a fluid reservoir fluidly coupled to the micro-pump device.
  • the method also includes fluidly coupling the wireless, reduced-pressure pump to the reduced- pressure dressing; providing a base unit having a RFID reader and a second processor; and activating the base unit whereby the RFID reader and second processor transmit an activation signal to the wireless, reduced-pressure pump to activate the wireless, reduced-pressure pump.
  • the wireless, reduced-pressure pump may further include a first pump-sealing member and a second pump-sealing member. The first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed. All the power required by the micro-pump device may be delivered by the RFID reader.
  • the method may further include the step of placing the RFID reader within five (5) centimeters of the RFID antenna of the wireless, reduced-pressure pump.
  • the wireless, reduced-pressure pump may have no source of power other than the RFID antenna and the wireless, reduced-pressure pump may further comprise: a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site, a first distribution manifold, an absorbent layer, and a diverter layer.
  • the first distribution manifold, the absorbent layer, and the diverter layer may be disposed within the pump pouch formed by the first pump-sealing member and the second pump-sealing member.
  • the micro-pump device may be a piezoelectric pump.
  • the reduced-pressure dressing may comprise: an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and a reduced-reduced pressure interface.
  • a reduced-pressure system for treating a tissue site with reduced pressure includes a wireless, reduced-pressure dressing that includes: an interface distribution manifold for placing proximate to the tissue site, an absorbent member for receiving and retaining fluids from the interface distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, the micro-pump device having an inlet and an exhaust outlet, a first sealing member for covering the tissue site to form a sealed space, and a vent fluidly coupling the exhaust outlet of the micro-pump device to an exterior.
  • the micro-pump is fluidly coupled to the sealed space for delivering reduced pressure thereto.
  • the system further includes a base unit comprising a RFID reader.
  • the base unit is operable to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump device.
  • the system may further comprise a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor.
  • the first processor and RFID antenna are operable to receive a pressure inquiry signal and to produce a pressure message signal to be transmitted to the base unit.
  • the system may further include a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor.
  • the fist processor and RFID antenna are operable to receive a pressure inquiry signal and produce a pressure message signal to be transmitted to the base unit.
  • the base unit further comprises a second processor.
  • the second processor is operable to receive the pressure message signal and produce a pump control signal.
  • the system may further include a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor, and wherein the first processor is configured to receive a pressure message signal from the first pressure sensor and to produce a control signal for controlling the micro-pump device.
  • the wireless, reduced-pressure pump may function with no source of power other than the RFID antenna.
  • the only reduced pressure supplied to the reduced- pressure dressing may be from the micro-pump device. This system may be assembled such that no conduits or wires are coupled to the wireless, reduced-pressure dressing.
  • a method for treating a tissue site on a patient with reduced pressure includes disposing a wireless, reduced-pressure dressing proximate to the tissue site.
  • the wireless, reduced-pressure dressing includes an interface distribution manifold for placing proximate to the tissue site, an absorbent member for receiving and retaining fluids from the interface distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure and having an inlet and an exhaust outlet, a first sealing member for covering the tissue site and forming a sealed space, and a vent fluidly coupling the exhaust outlet to an exterior.
  • a wireless, reduced- pressure pump the wireless, reduced-pressure pump includes a RFID antenna; a first processor coupled to the RFID antenna; and a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure.
  • the wireless, reduced-pressure pump may further include a fluid reservoir fluidly coupled to the micro- pump device.
  • the wireless, reduced-pressure pump may also further include a first pump- sealing member and a second pump-sealing member, wherein the first pump-sealing member and second pump-sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed.
  • the wireless, reduced-pressure pump may function with no source of power other than the RFID antenna.
  • the wireless, reduced-pressure pump may further include a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site.
  • the pump may further include a pressure sensing device coupled to the first processor and a base unit that comprises a second processor coupled to the RFID reader.
  • the second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor.
  • the wireless, reduced-pressure pump may further include a pressure sensing device coupled to the first processor and a base unit that comprises a second processor coupled to the RFID reader.
  • the second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor.
  • the first processor and pressure sensing device are configured to prepare the pressure message signal in response to the pressure inquiry signal.
  • the first processor and RFID antenna are configured to transmit the pressure message signal.
  • the second processor is configured to receive the pressure message signal, prepare a control signal, and the second processor and RFID are configured to transmit the control signal to the wireless, reduced-pressure pump to provide a control signal for activating or deactivating the micro-pump device.
  • the wireless, reduced-pressure pump may further include a pressure sensing device coupled to the first processor; wherein, the pressure sensing device is operable to produce a pressure message signal, and the first processor is operable to receive the pressure message signal and to produce a control signal to activate or deactivate the micro-pump device.
  • a RFID antenna is used to power a reduced-pressure pump that is fluidly coupled by a conduit to a reduced-pressure dressing.
  • a reduced-pressure dressing incorporates a micro-pump and a RFID antenna that is used to power the micro-pump.
  • Other systems, methods, and devices are presented herein.

Landscapes

  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Anesthesiology (AREA)
  • Hematology (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
  • External Artificial Organs (AREA)
  • Infusion, Injection, And Reservoir Apparatuses (AREA)
  • Measuring And Recording Apparatus For Diagnosis (AREA)

Abstract

Systems, methods, and dressings for providing reduced pressure to a tissue site on a patient are presented that involve wirelessly providing power to a reduced-pressure pump. In one instance, a RFID antenna is used to power a reduced-pressure pump that is fluidly coupled by a conduit to a reduced-pressure dressing. In another instance, a reduced-pressure dressing incorporates a micro-pump and a RFID antenna that is used to power the micro-pump. Other systems, methods, and devices are presented.

Description

TITLE OF THE INVENTION
REDUCED-PRESSURE SYSTEMS, DRESSINGS, AND METHODS EMPLOYING A
WIRELESS PUMP
RELATED APPLICATION [0001] The present invention claims the benefit, under 35 USC § 119(e), of the filing of U.S. Provisional Patent Application serial number 61/407, 194, entitled "System and Methods For Electrically Detecting The Presence of Exudate In Reduced-Pressure Dressings," filed 27 October 2010, which is incorporated herein by reference for all purposes
[VAC.0975PRO1]; U.S. Provisional Patent Application serial number 61/418,730, entitled "Systems and Methods for Electrically Detecting the Presence of Exudate in Dressings," filed 1 December 2010, which is incorporated herein by reference for all purposes
[VAC.0975PRO2]; U.S. Provisional Patent Application serial number 61/445,383, entitled "Interactive, Wireless Reduced-Pressure Dressings, Methods, and Systems," filed 22 February 2011, which is incorporated herein by reference for all purposes [VAC.0999PRO]; and U.S. Provisional Patent Application serial number 61/445,338, entitled "Reduced-Pressure Systems, Dressings, and Methods Employing a Wireless Pump," filed 22 February 201 1, which is incorporated herein by reference for all purposes [VAC.1000PRO].
FIELD
[0002] The present disclosure relates generally to medical treatment systems and, more particularly, but not by way of limitation, to systems, dressings, and methods that involve wirelessly providing power to a pump that applies reduced pressure to a tissue site.
BACKGROUND
[0003] Clinical studies and practice have shown that providing a reduced pressure in proximity to a tissue site augments and accelerates the growth of new tissue at the tissue site. The applications of this phenomenon are numerous, but application of reduced pressure has been particularly successful in treating wounds. This treatment (frequently referred to in the medical community as "negative pressure wound therapy," "reduced pressure therapy," or "vacuum therapy") provides a number of benefits, which may include faster healing and increased formulation of granulation tissue. Typically, when applied to open wounds, reduced pressure is applied to tissue through a porous pad or other manifold device. The porous pad distributes reduced pressure to the tissue and channels fluids that are drawn from the tissue. Reduced pressure may also be used to remove fluids from a body cavity, such as an abdominal cavity.
SUMMARY
[0004] According to an illustrative embodiment, a system for treating a tissue site with reduced pressure includes a reduced-pressure dressing for disposing proximate to the tissue site and a wireless, reduced-pressure pump fluidly coupled to the reduced-pressure dressing. The wireless, reduced-pressure pump includes a Radio Frequency Identification (RFID) antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the processor for receiving power and developing reduced pressure, a first pump-sealing member, a fluid reservoir, and a second pump-sealing member. The first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro- pump is disposed. The system further includes a base unit having a RFID reader. The RFID reader is configured to provide power to the RFID antenna such that the micro-pump is powered.
[0005] According to another illustrative embodiment, a method of manufacturing a system for treating a tissue site on a patient with reduced pressure includes providing a reduced-pressure dressing for disposing proximate to the tissue site and providing a wireless, reduced-pressure pump. The wireless, reduced-pressure pump includes a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power and developing a reduced pressure, a first pump-sealing member, a fluid reservoir, and a second pump-sealing member. The first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump is disposed. The method may further include providing a reduced-pressure delivery conduit for fluidly coupling the wireless, reduced-pressure pump to the reduced-pressure dressing. The method further includes providing a base unit having a RFID reader. The RFID reader is configured to provide power to the RFID antenna such that the micro-pump is powered.
[0006] According to another illustrative embodiment, a method for treating a tissue site on a patient with reduced pressure includes placing a reduced-pressure dressing proximate to the tissue site and providing a wireless, reduced-pressure pump. The wireless, reduced- pressure pump includes a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the processor for receiving power and developing reduced pressure, a first pump-sealing member, a fluid reservoir, and a second pump-sealing member. The first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump is disposed. The method further includes fluidly coupling the wireless, reduced-pressure pump to the reduced-pressure dressing, providing a base unit having a RFID reader and a second processor, and activating the base unit whereby the RFID reader and second processor transmit an activation signal to the wireless, reduced- pressure pump to activate the wireless, reduced-pressure pump.
[0007] According to another illustrative embodiment, a reduced-pressure system for treating a tissue site with reduced pressure includes a reduced-pressure dressing. The reduced- pressure dressing includes a first distribution manifold for placing proximate to the tissue site, an absorbent layer for receiving and retaining fluids from the first distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, and a micro-pump coupled to the first processor for receiving power therefrom and developing reduced pressure. The micro-pump has an inlet and an exhaust outlet. The system also includes a first sealing member for forming a sealed space over the tissue site and the micro-pump, and a vent fluidly coupling the exhaust outlet of the micro-pump to an exterior. The system further includes a base unit that includes a RFID reader. The base unit is operable to supply a pump signal to the reduced-pressure dressing to energize the micro-pump.
[0008] According to another illustrative embodiment, a method for treating a tissue site on a patient with reduced pressure includes disposing a wireless, reduced-pressure dressing proximate to the tissue site. The wireless, reduced-pressure dressing includes a first distribution manifold for placing proximate to the tissue site, an absorbent layer for receiving and retaining fluids from the first distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump coupled to the first processor for receiving power therefrom and developing reduced pressure. The micro-pump has an inlet and an exhaust outlet, a first sealing member for forming a sealed space over the tissue site and the micro- pump, and a vent fluidly coupling the exhaust outlet of the micro-pump to an exterior. The method further includes providing a base unit comprising a RFID reader. The base unit is operable to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump. The method also includes activating the base unit to deliver the pump signal to the wireless, reduced-pressure dressing.
[0009] Other features and advantages of the illustrative embodiments will become apparent with reference to the drawings and detailed description that follow. BRIEF DESCRIPTION OF THE DRAWINGS
[0010] FIGURE 1 is a schematic diagram, with a portion shown in cross section, of an illustrative embodiment of a system for treating a tissue site with reduced pressure;
[0011] FIGURE 2 is a schematic, exploded, perspective view of an illustrative embodiment of a wireless, reduced-pressure pump used as part of the system of FIGURE 1;
[0012] FIGURE 3 is a schematic diagram, with a portion shown in cross section, of the system of FIGURE 1 presenting additional aspects and some alternatives;
[0013] FIGURE 4 is a schematic, partial cross-sectional view of an illustrative embodiment of a wireless, reduced-pressure pump;
[0014] FIGURE 5 is a schematic, cross section of one illustrative embodiment of a micro-pump device for use as part of a system for treating a tissue site with reduced pressure such as in FIGURE 1;
[0015] FIGURE 6 is a schematic, perspective view of an illustrative embodiment of a wireless, reduced-pressure pump;
[0016] FIGURE 7 is a schematic, cross section of another illustrative embodiment of a wireless, reduced-pressure pump;
[0017] FIGURE 8 is a schematic, perspective view of the wireless, reduced-pressure pump of FIGURE 7;
[0018] FIGURE 9 is a schematic diagram, with a portion shown in perspective view, of an illustrative embodiment of a reduced-pressure system for treating a tissue site with reduced pressure;
[0019] FIGURE 10 is a schematic, cross section of the reduced-pressure dressing shown in FIGURE 9 taken along line 10-10;
[0020] FIGURE 11 is a schematic, exploded, perspective view of the reduced-pressure dressing of FIGURES 9-10;
[0021] FIGURE 12 is a schematic, cross section of an illustrative embodiment of a system for treating a tissue site with reduced pressure; and [0022] FIGURE 13 is a schematic, exploded, perspective view of another illustrative embodiment of a reduced-pressure dressing.
DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
[0023] In the following detailed description of the illustrative, non-limiting embodiments, reference is made to the accompanying drawings that form a part hereof. These illustrative embodiments are described in sufficient detail to enable those skilled in the art to practice the invention, and it is understood that other embodiments may be utilized and that logical structural, mechanical, electrical, and chemical changes may be made without departing from the spirit or scope of the invention. To avoid detail not necessary to enable those skilled in the art to practice the embodiments described herein, the description may omit certain information known to those skilled in the art. The following detailed description is not to be taken in a limiting sense, and the scope of the illustrative embodiments is defined only by the appended claims.
[0024] The illustrative embodiments herein involve using Radio Frequency
Identification (RFID) or an enhanced type of Radio Frequency Identification (RFID) technology to energize a micro-pump device in a reduced-pressure dressing. RFID traditionally uses a RFID tag or label that is on a target and a RFID reader that energizes and reads signals from the RFID tag. One common example is a toll tag. Most RFID tags include an integrated circuit for storing and processing information, a modulator, and demodulator. RFID tags can be passive tags, active RFID tags, and battery-assisted passive tags. Generally, passive tags use no battery and do not transmit information unless they are energized by a RFID reader. Active tags have an on-board battery and can transmit autonomously (i.e., without being energized by a RFID reader). Battery-assisted passive tags typically have a small battery on-board that is activated in the presence of a RFID reader. To enhance the RFID tag, a microcontroller and sensor may be incorporated into the reduced-pressure dressing. The RFID tag, a microcontroller and sensor allow sensing and optional
computational functions. Moreover, the RFID tag and microcontroller partially or entirely power a micro-pump.
[0025] In one illustrative embodiment, the enhanced RFID technology is a Wireless Identification and Sensing Platform (WISP) device. WISPs involve powering and reading a WISP device, analogous to a RFID tag (or label), with a RFID reader. The WISP device harvests the power from the RFID reader's emitted radio signals and performs sensing functions (and optionally performs computational functions). The WISP device transmits a radio signal with information to the RFID reader. The WISP device receives power from the RFID reader. The WISP device has a tag or antenna that harvests energy and a
microcontroller (or processor) that can perform a variety of tasks, such as sampling sensors. The WISP device reports data to the RFID reader. In one illustrative embodiment, the WISP device includes an integrated circuit with power harvesting circuitry, demodulator, modulator, microcontroller, sensors, and may include one or more capacitors for storing energy. A form of WISP technology has been developed by Intel Research Seattle (www. Seattle. intel- research.net/wisp/). RFID devices as used herein also include WISP devices.
[0026] Referring now to the drawings and initially to FIGURES 1-5, an illustrative embodiment of a system 100 for treating a tissue site 102, e.g., a wound 104 or a cavity, with reduced pressure is presented. The system 100 includes a reduced-pressure dressing 106 for disposing proximate to the tissue site 102; a wireless, reduced-pressure pump 108 fluidly coupled to the reduced-pressure dressing 106; and a base unit 110 having a RFID reader 1 12. The wireless, reduced-pressure pump 108 includes a first RFID antenna 1 14 and a micro- pump device 1 16. The RFID reader 1 12 is configured to provide and transmit a pump signal that provides power to the first RFID antenna 1 14. The pump signal received by the first RFID antenna 114 powers the micro-pump device 116. Remotely powering the micro-pump device 116 provides a number of potential benefits. The benefits may include ease of application. In addition, the wireless, reduced-pressure pump 108 may be a self-contained, disposable unit. It should be noted that some variation is shown between figures in order to show some of the potential variations in the illustrative system 100.
[0027] The system 100 may be used with various different types of tissue sites 102. The tissue site 102 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, body cavity or any other tissue. Treatment of the tissue site 102 may include removal of fluids, e.g., exudate or ascites.
[0028] The wireless, reduced-pressure pump 108 includes the first RFID antenna 114 that is coupled to a first processor 118 by electrical leads 1 19. The first processor 118 is coupled to the micro-pump device 116, or micro-pump, for receiving power. The first processor 1 18 may be incorporated into the micro-pump device 1 16. The first processor 118 and micro-pump device 1 16 may be located within a pump pouch 120.
[0029] The pump pouch 120 may be formed by coupling a first pump-sealing member 122 to a second pump-sealing member 124. The pump pouch 120 may also be formed by other techniques such as casting the pump pouch 120 from a polymer. At least a portion of the pump pouch 120 comprises a fluid reservoir 126 for receiving and retaining fluids 127 from the tissue site 102. The micro-pump device 1 16 may be a piezoelectric pump, a peristaltic pump, or other small pump that produces reduced pressure with minimal power requirements. The first processor 1 18 is operable to receive a pressure message signal from a pressure sensing device 138. In response to receiving the pressure message signal, the first processor 118 produces a control signal to activate or deactivate the micro-pump device 116. The pressure sensing device 138 may be a transducer or may be a simple switch that is activated if sufficient reduced pressure is present.
[0030] Referring primarily to FIGURE 3, the base unit 1 10 includes a second processor 128 coupled to the RFID reader 1 12. A control panel 130 (e.g., a user interface), a first display 132 and a power source 134 (e.g., a battery or electrical connection) may also be coupled to the second processor 128. The base unit 110 may include a base housing 136. The second processor 128 and RFID reader 1 12 are configured to transmit a signal 137, e.g., a pump signal or a pressure inquiry signal, to the first RFID antenna 114.
[0031] The first RFID antenna 1 14 of the reduced-pressure pump 108 is coupled by electrical leads 119 or a wireless coupling to the first processor 118. The first processor 118 is coupled to the micro-pump device 1 16 to provide power and control the micro-pump device 116. A first power source 140 may be included to provide additional power to the first processor 1 18. A pressure sensing device 138 may be coupled to the first processor 118. The pressure sensing device 138 is fluidly coupled to and senses pressure in a pressure sensing lumen 166 (or vent passageway 174 or interface distribution manifold 150). The micro-pump device 1 16 is fluidly coupled to a fluid reservoir 126. The fluid reservoir 126 receives and retains the fluids 127 from a reduced-pressure lumen 164 or from the interface distribution manifold 150.
[0032] The pump signal transmitted by the base unit 110 is received by the first RFID antenna 114 and energizes the micro-pump device 1 16 to produce reduced pressure. The pressure inquiry signal is transmitted to the first processor 118 of the wireless, reduced- pressure pump 108 by the second processor 128 and RFID reader 1 12. In response, the first processor 1 18 and pressure sensing device 138 of the wireless, reduced-pressure pump 108 transmit a pressure message signal indicative of the pressure experienced at the reduced- pressure dressing 106 to the base unit 110.
[0033] The second processor 128 is configured to receive the pressure message signal from the wireless, reduced-pressure pump 108 and prepare a control signal. The second processor 128 and RFID reader 1 12 are configured to transmit the control signal to the wireless, reduced-pressure pump 108 to activate or deactivate the micro-pump device 1 16. In another illustrative embodiment, as previously mentioned, the first processor 118 is operable to receive a pressure message signal from the pressure sensing device 138 and to produce a control signal to activate or deactivate the micro-pump device 116.
[0034] Referring now primarily to FIGURES 2 and 4, the wireless, reduced-pressure pump 108 generates reduced pressure that is delivered to the tissue site 102. The wireless, reduced-pressure pump 108 receives and retains fluids from the tissue site 102. Reduced pressure generally refers to a pressure less than the ambient pressure at a tissue site 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 the 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, unless otherwise indicated, an increase in reduced pressure or vacuum pressure typically refers to a relative reduction in absolute pressure.
[0035] The wireless, reduced-pressure pump 108 provides the reduced pressure for the system 100. The wireless, reduced-pressure pump 108 may include a first distribution manifold 142, a diverter layer 144, and an absorbent layer 146. A vent 176 is used to fluidly couple an exhaust from the micro-pump device 1 16 to an exterior of the wireless, reduced- pressure pump 108. The first distribution manifold 142 functions to distribute reduced pressure generated by the micro-pump device 1 16. An air/liquid separator 143, e.g., a hydrophobic filter, may be placed between the micro-pump device 1 16 and the first distribution manifold 142 to prevent liquid from entering the micro-pump device 1 16. The absorbent layer 146 functions to receive and retain fluids from the tissue site 102. The absorbent layer 146 may be made from any material capable of absorbing liquid, such as exudate from the tissue site 102.
[0036] The absorbent layer 146 may be made from super absorbent fibers. The super absorbent fibers may retain or bond to the liquid in conjunction with a physical or chemical change to the fibers. In one non-limiting example, the super absorbent fiber may include the Super Absorbent Fiber (SAF) material from Technical Absorbents, Ltd. of Grimsby, United Kingdom. The absorbent layer 146 may be a sheet or mat of fibrous material in which the fibers absorb liquid from the tissue site 102. The structure of the absorbent layer 146 that contains the fibers may be either woven or non-woven. The fibers in the absorbent layer 146 may gel upon contact with the liquid, thereby trapping the liquid. Spaces or voids between the fibers may allow reduced pressure that is applied to the absorbent layer 146 to be transferred within and through the absorbent layer 146. In one illustrative embodiment, the fiber density of the fibers in the absorbent layer 146 may be approximately 1.4 grams per millimeter.
[0037] The diverter layer 144 is disposed adjacent to the absorbent layer 146 and the first distribution manifold 142. The diverter layer 144 is formed from a liquid impermeable material but contains a plurality of apertures 145. The plurality of apertures 145 allow reduced pressure from the micro-pump device 116 to be transmitted through the diverter layer 144 at desired locations. The diverter layer 144 helps control the pattern of reduced pressure as applied to the absorbent layer 146. The reduced pressure is distributed to the diverter layer 144 by the first distribution manifold 142. The apertures 145 may be arranged in a pattern for applying the reduced pressure to portions of the absorbent layer 146 to enhance the capability of the absorbent layer 146 to continue transferring reduced pressure to the tissue site 102 as the absorbent layer 146 absorbs more fluid from the tissue site 102.
[0038] The plurality of apertures 145 may be positioned in a pattern around a peripheral portion of the diverter layer 144 away from the center of the diverter layer 144 such that the reduced pressure is applied to the absorbent layer 146 away from a center region of the absorbent layer 146. The diverter layer 144 acts in conjunction with the first distribution manifold 142 to ensure that the absorption capabilities and absorption efficiency of the absorbent layer 146 are increased relative to an absorbent layer 146 that is not used in conjunction with a diverter layer 144. By providing better distribution of liquid throughout the absorbent layer 146, the diverter layer 144 also increases the effective capacity and treatment time of the wireless, reduced-pressure pump 108. [0039] The diverter layer 144 may be made from any material that enhances the reduced pressure transmission and storage capabilities of an adjacent absorbent layer. For example, the diverter layer 144 may be made from a material that is substantially impermeable to liquid and gas and that diverts the reduced pressure to pass through apertures 145.
Alternatively or in addition, the material from which the diverter layer 144 is made may have a predetermined moisture vapor transfer rate that is consistent with gas permeability. In either example, the diverter layer 144 may still include a pattern of apertures for transmitting a greater volume of liquid or gas than that permitted by a gas-permeable material not having apertures. It should be noted, however, that permeability of the diverter layer 144 to gas but not liquid may result in increased transmission of reduced pressure through the dressing while still directing liquid flow around or near the perimeter of the diverter layer 144.
[0040] The first distribution manifold 142, the diverter layer 144, and the absorbent layer 146 may be disposed within the pump pouch 120. The wireless, reduced-pressure pump 108 may also include the pressure sensing device 138, which is fluidly coupled to the reduced- pressure dressing 106 and in communication with the first processor 118 for sensing pressure. The reduced-pressure conduit 148 delivers fluids from the reduced-pressure dressing 106 to the wireless, reduced-pressure pump 108. In one illustrative embodiment, the reduced- pressure conduit 148 is disposed directly into the absorbent layer 146. In another illustrative embodiment, an interface (not shown) fluidly couples the reduced-pressure conduit 148 and the absorbent layer 146.
[0041] Referring now primarily to FIGURES 1 and 3, the reduced-pressure dressing 106 is disposed against the tissue site 102. The tissue site 102 may be, for example, the wound 104 through epidermis 156 and into subcutaneous tissue 158 or any other tissue site. The reduced-pressure dressing 106 may be any device for providing reduced pressure to the tissue site 102 and for receiving fluids from the tissue site 102. For example, the reduced-pressure dressing 106 may be formed with a foam member, a structure with a plurality of defined channels, a suction tube, or other device. In one illustrative embodiment, the reduced-pressure dressing 106 may include the interface distribution manifold 150 for placing proximate to the tissue site 102, a dressing sealing member 152, and a reduced-pressure interface 154.
[0042] A manifold is a substance or structure that is provided to assist in applying reduced pressure to, delivering fluids to, or removing fluids from a tissue site 102. The interface distribution manifold 150 typically includes a plurality of flow channels or pathways that distribute fluids provided to and removed from the tissue site 102 around the interface distribution manifold 150. In one illustrative embodiment, the flow channels or pathways are interconnected to improve distribution of fluids provided or removed from the tissue site 102. The interface distribution manifold 150 may be a biocompatible material that is capable of being placed in contact with the tissue site 102 and distributing reduced pressure to the tissue site 102. Examples of interface distribution manifolds may include without limitation the following: devices that have structural elements arranged to form flow channels, e.g., cellular foam, open-cell foam, porous tissue collections, liquids, gels, and foams that include, or cure to include, flow channels; foam; gauze; felted mat; or any other material suited to a particular biological application.
[0043] In one embodiment, the interface distribution manifold 150 is a porous foam and includes a plurality of interconnected cells or pores that act as flow channels. The porous foam may be a polyurethane, open-cell, reticulated foam such as GranuFoam® material available from Kinetic Concepts, Incorporated of San Antonio, Texas. In some situations, the interface distribution manifold 150 may also be used to distribute fluids such as medications, antibacterials, growth factors, and various solutions to the tissue site 102. Other layers may be included in or on the interface distribution manifold 150, such as absorptive materials, wicking materials, hydrophobic materials, and hydrophilic materials.
[0044] In one illustrative embodiment, the interface distribution manifold 150 in whole or in part may be constructed from bioresorbable materials that may remain in a patient's body following use of the reduced-pressure dressing 106. 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 interface distribution manifold 150 may further serve as a scaffold for new cell-growth, or a scaffold material may be used in conjunction with the interface distribution manifold 150 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.
[0045] The interface distribution manifold 150 is covered by a dressing sealing member 152. The dressing sealing member 152 may be any material that provides a fluid seal. A fluid seal is a seal adequate to maintain reduced pressure at a desired site given the particular reduced-pressure source or subsystem involved. The dressing sealing member 152 may, for example, be an impermeable or semi-permeable, elastomeric material. Elastomeric materials have the properties of an elastomer. It generally refers to a polymeric material that has rubber-like properties. More specifically, most elastomers have 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. Examples of elastomers 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. Additional, specific examples of dressing sealing member materials include a silicone drape, 3M Tegaderm® drape, polyurethane (PU) drape such as one available from Avery Dennison Corporation of Pasadena, California. The dressing sealing member 152 forms a sealed space 160 over the tissue site 102, which may or may contain the micro-pump device 116.
[0046] An attachment device 162 may be used to retain the dressing sealing member 152 against the patient's epidermis 156 or another layer, such as a gasket or additional sealing member. The attachment device 162 may take numerous forms. For example, the attachment device 162 may be a medically acceptable, pressure-sensitive adhesive that extends about a periphery or all of the dressing sealing member 152 or covers at least a potion of the dressing sealing member 152 on a patient-facing side over the epidermis 156.
[0047] The reduced-pressure interface 154 may be used to provide fluid
communication between the reduced-pressure conduit 148 and the sealed space 160 of the reduced-pressure dressing 106. The reduced pressure may be delivered through the reduced- pressure conduit 148 to the reduced-pressure interface 154 and then to the sealed space 160. In one illustrative embodiment, the reduced-pressure interface 154 is a T.R.A.C.® Pad or Sensa T.R.A.C.® Pad available from KCI of San Antonio, Texas. The reduced-pressure conduit 148 may include the reduced-pressure lumen 164 and the pressure sensing lumen 166 formed as an integral conduit as shown in FIGURE 1 or separately as shown in FIGURE 3.
[0048] In one illustrative embodiment shown in FIGURE 1, pressure sensing capability may be added to the reduced-pressure dressing 106 to function in addition to or in lieu of pressure sensing device 138. The reduced-pressure dressing 106 may include a second RFID antenna 168, a third processor 170, and a second pressure sensing device 172. The third processor 170 is coupled to the second RFID antenna 168 and to the second pressure sensing device 172. A vent passageway 174 provides fluid communication between the sealed space 160 and the second pressure sensing device 172. The third processor 170 and the second pressure sensing device 172 are operable to receive a pressure inquiry signal from the base unit 1 10 and respond with a pressure message signal indicative of the pressure in the sealed space 160.
[0049] In one illustrative embodiment, the wireless, reduced-pressure pump 108 is a wireless and passive (i.e., no battery) device. As such, the wireless, reduced-pressure pump 108 has no source of power other than power delivered through the first RFID antenna 114. In some embodiments, the wireless, reduced-pressure pump 108 may contain a capacitor for storing electrical energy. In another illustrative embodiment, the first power source 140 as shown in FIGURE 3 may be provided to augment the power delivered through the first RFID antenna 114 or to operate the micro-pump device 1 16. The first power source 140 may be recharged by power from the first RFID antenna 114.
[0050] The micro-pump device 116 may take numerous forms such as a piezoelectric pump, peristaltic pump, or other miniaturized pump. Referring now primarily to FIGURE 5, an illustrative embodiment of a micro-pump device 116 that is suitable for use as an aspect of the wireless, reduced-pressure pump 108 is presented. The micro-pump device 116 includes a cavity 178 that is defined by a first end wall 180, a second end wall 182, and an annular side wall 184. The cavity 178 may be substantially circular in shape, but other shapes are possible, such as elliptical. In one illustrative embodiment, the cavity 178 may hold about 10 ml of fluid or may hold more or less.
[0051] The cavity 178 is provided with a nodal inlet 186, which may be valved or unvalved. The cavity 178 may also have a valved outlet 190. The first end wall 180 may be a disc 192. On the disc 192 is an actuator 194, such as a piezoelectric disc, magnetostrictive device, or solenoid actuated device. The actuator 194 is electrically coupled to a drive circuit, which is controlled by the processor. The drive circuit will apply an alternating electrical signal to the actuator 194 to induce an oscillation in the disc 192. The frequency of the oscillation can be adjusted to match the natural frequency of the chamber. The piezoelectric disc may be less than 1 mm in thickness and may be tuned to operate at more than 500 Hz, more than 10 kHz, or even higher than 20 kHz. Upon activation, the actuator 194 may vibrate in a direction substantially perpendicular to the plane of the cavity 178 as shown, thereby generating radial pressure oscillations within the fluid in the cavity 178. One or more micro- pump devices 1 16 may be used in parallel or series.
[0052] In one illustrative embodiment, the micro-pump device 1 16 has a fluid in the cavity 178 and has a substantially cylindrical shape that is bounded by the first end wall 180, second end wall 182, and side wall 184. At least two apertures, e.g., inlet 186 and outlet 190, are formed through the walls 180, 182, 184 forming the cavity 178. The cavity 178 has a radius, r, and a height, h, and r/h > 1.2 and h2/r > 4 x 10"10 m. The actuator 194, which is a piezoelectric disc, creates an oscillatory motion of one of the end walls 180, 182 in a direction that is substantially perpendicular to the plane of the first end wall 180 and second end wall 182. Axial oscillations of the end walls 180, 182 drive radial oscillations of fluid pressure in the cavity 178 and allow for pumping that creates reduced pressure. The micro-pump device 116 is like an acoustic pump in that an acoustic resonance is set up within the cavity 178. The inlet 186 is used to pull fluids, and the outlet 190 is coupled to a vent, e.g., the vent 176 in FIGURE 4, to discharge to an exterior. Other micro-pump devices may be used. The micro- pump device 116 may be the type of micro-pump shown in United States Patent Publication 2009/0240185 (application 12/398,904; filed 5 March 2009), entitled, "Dressing and Method for Applying Reduced Pressure To and Collecting And Storing Fluid from a Tissue Site," which is incorporated herein for all purposes.
[0053] Referring now primarily to FIGURES 1-3, according to one illustrative embodiment, in operating the system 100, the reduced-pressure dressing 106 is applied to the tissue site 102. In particular, the interface distribution manifold 150 is disposed proximate to the tissue site 102. Then the interface distribution manifold 150 and the tissue site 102 are covered by the dressing sealing member 152 to create the sealed space 160. The attachment device 162 on the patient- facing side of the dressing sealing member 152 may help provide a fluid seal against a portion of the patient's epidermis 156. If not already installed, the reduced-pressure interface 154 may be applied, such as for example by cutting a small aperture in the dressing sealing member 152 and securing the reduced-pressure interface 154 over or through the aperture, or hole.
[0054] The wireless, reduced-pressure pump 108 is then provided and fluidly coupled by the reduced-pressure conduit 148 to the reduced-pressure interface 154. The wireless, reduced-pressure pump 108 is positioned such that the first RFID antenna 114 is placed within operating range of the base unit 1 10. In one illustrative embodiment, the first RFID antenna 114 is placed within a few millimeters of the RFID reader 1 12 of the base unit 1 10. In another illustrative embodiment, the first RFID antenna 1 14 may be placed as far away as ten meters from the RFID reader 1 12. Any distance within the given range may be readily used.
[0055] The base unit 110 is then activated by the user. The base unit 110 transmits a pump signal 137 to the wireless, reduced-pressure pump 108. The pump signal is received by the first RFID antenna 1 14, and the energy of the pump signal is delivered to the first processor 1 18. The first processor 118 provides energy to the micro-pump device 116. The micro-pump 1 16 creates reduced pressure that is delivered into the fluid reservoir 126 that is fluidly coupled to the reduced-pressure conduit 148. Thus, the reduced pressure is delivered to the reduced-pressure dressing 106 through the reduced-pressure conduit 148. Fluids from the tissue site 102 flow through the interface distribution manifold 150, reduced-pressure interface 154, and reduced-pressure conduit 148 into the fluid reservoir 126.
[0056] The pressure at the tissue site 102 may be monitored directly or indirectly using a pressure sensing device, such as pressure sensing device 138 of FIGURE 3 or second pressure sensing device 172 of FIGURE 1. In the first illustrative example, the second processor 128 and the RFID reader 1 12 of the base unit 110 may, separate from the pump signal or with the pump signal, transmit a pressure inquiry signal to the wireless, reduced- pressure pump 108. In response to the pressure inquiry signal, the first processor 118 and pressure sensing device 138 may prepare a pressure message signal to communicate a measurement of the pressure at the tissue site. Then, the pressure message signal may be used for further processing by the first processor 1 18 to develop a pump control signal for activating or deactivating the micro-pump 1 16 as may be needed. Alternatively or in addition, the first processor 1 18 may transmit the pressure message signal via the first RFID antenna 114 to the RFID reader 1 12. After arriving at the RFID reader 112, the pressure message signal is delivered to the second processor 128. Using the pressure message signal, the second processor 128 may prepare a pump control signal that is transmitted by the RFID reader 1 12 to the wireless, reduced-pressure pump 108 to deactivate or activate the micro-pump 116 as needed.
[0057] If, after providing an adequate interval, the pressure remains outside of a desired operating range, an alarm signal is created by the base unit 110 or by the wireless, reduced-pressure pump 108. The alarm may be a separate audible device, visual alarm, or the micro-pump 116 may function at a different frequency range, e.g., lower, to make an audible noise for the alarm.
[0058] With the second illustrative approach, the reduced-pressure dressing 106 includes the second RFID antenna 168 that is coupled to the third processor 170, which is coupled to the second pressure sensing device 172. The second pressure sensing device 172 experiences the pressure within the sealed space 160 via the vent passageway 174. The base unit 1 10 transmits a pressure inquiry signal to the second RFID antenna 168. In response, the second pressure sensing device 172 and third processor 170 produce a pressure message signal that is transmitted by the second RFID antenna 168 to the base unit 110. As before, the base unit 1 10 then produces a pump control signal that is transmitted to the wireless, reduced- pressure pump 108 to activate or deactivate the micro-pump 1 16. Alternatively, the third processor 170 may evaluate the pressure and prepare a pump control signal as part of a feedback or control loop.
[0059] Referring now primarily to FIGURES 4 and 6, an illustrative embodiment of a wireless, reduced-pressure pump 108 is presented. In this illustrative embodiment, the wireless, reduced-pressure pump 108 may be a self-contained, disposable pouch design that may be removably secured to a base unit 1 10 on a pole 196. As previously presented, a pump pouch 120 is formed with a first pump-sealing member 122 and a second pump-sealing member 124. The perimeter of the pump pouch 120 may include a first flange 123 and a second flange 125. The pump pouch 120 may be divided or partitioned into numerous compartments if desired. For example, a compartment (not explicitly shown) may be formed that has the micro-pump 1 16 within the compartment and another compartment may formed that contains the absorbent layer 146.
[0060] The flanges 123, 125 on the illustrative embodiment of the pump pouch 120 may be formed by welding, bonding or otherwise attaching portions of the first pump-sealing member 122 and second pump-sealing member 124. The first flange 123 may include one or more apertures 129 for receiving one or more posts 198. The posts 198 secure the pump pouch 120 adjacent to the base unit 1 10. The reduced-pressure conduit 148 may enter through an aperture 149 in the second flange 125 that provides a sealed, interference fit or has a coupling that provides a sealed connection. Other connections may be used.
[0061] The first RFID antenna 1 14 may be placed closest to the base unit 110 such that the first RFID antenna 1 14 is immediately adjacent to RFID reader 112 of the base unit 1 10 as shown best in FIGURE 4. In one non-limiting example, the first RFID antenna 1 14 is positioned two millimeters or one millimeter (1 mm) or less from the RFID reader 1 12. The RFID reader 112 and the first RFID antenna 1 14 may be substantially matched and aligned. In another illustrative embodiment, the wireless, reduced-pressure pump 108 may be attached to a post 198 with the first RFID antenna 114 facing outward towards a remotely located base unit 1 10 as suggested in FIGURE 1. For example, the base unit 1 10 may be located at a central hub area where the wireless, reduced-pressure pump 108 is monitored and powered using the base unit 1 10, which may be as far away as ten meters or more.
[0062] Referring now primarily to FIGURE 6, the base unit 1 10 may include the control panel 130 and one or more displays 132. The base unit 1 10 may include a base housing or base body 136. The base housing or body 136 may include a shelf portion 199 that may provide physical support to a portion of the wireless, reduced-pressure pump 108 when the wireless, reduced-pressure pump 108 fills with fluids from the tissue site 102. In this regard, it should be noted that the wireless, reduced-pressure pump 108 shown in FIGURE 6 is shown before use. With the embodiments of FIGURES 4 and 6, when the wireless, reduced- pressure pump 108 has reached its capacity for holding fluids, the micro-pump 1 16 may be deactivated and the user may dispose of the entire wireless, reduced-pressure pump 108.
[0063] Referring now primarily to FIGURES 7 and 8, another illustrative embodiment of a wireless, reduced-pressure pump 200 is presented. The wireless, reduced-pressure pump 200 may be used as part of a system for treating a tissue site, e.g., the system of FIGURE 1.
The wireless, reduced-pressure pump 200 includes a plurality of wall members 202 that form a first chamber 204 and a second chamber 206. One of the plurality of wall members 202 is a partitioning wall 208 that separates the first chamber 204 from the second chamber 206. A micro-pump 210, which is analogous to the micro-pump 116 of the previous figures, may be disposed within the first chamber 204. The micro-pump 116 is configured such that the inlet 212 that receives fluid (or said another way, discharges reduced pressure) is fluidly coupled to the second chamber 206. The micro-pump 210 has an outlet or vent 214 that is fluidly coupled to the first chamber 204. The micro-pump 210 vents positive pressure through outlet or vent 214 into the first chamber 204.
[0064] A portion of one of the plurality of wall members 202 that forms the first chamber 204 contains an aperture 216. An optional relief valve 218 is coupled to the aperture 216. The relief valve 218 is configured to allow pressure within the first chamber 204 to vent to an exterior of the wireless, reduced-pressure pump 200 when the pressure exceeds a first threshold pressure. At least a portion of the plurality of wall members 202 that make up the second chamber 206 includes an inflatable support member and typically a plurality of inflatable support members 220. While a plurality of inflatable support members 220 are presented, it should be understood that a single inflatable support member may be used create the second chamber 206.
[0065] The inflatable support members 220 are in fluid communication with the first chamber 204, such as through a plurality of apertures 222. Thus, the positive pressure within the first chamber 204 fills the plurality of inflatable support members 220. As the plurality of inflatable support members 220 are filled with sufficient fluid, the plurality of inflatable support members 220 gain relative rigidity that provides a structure that helps provide volume to the second chamber 206. Fluids 223 from a tissue site are received through a reduced- pressure conduit 224 into the volume of the second chamber 206. The wireless, reduced- pressure pump 200, which is shown in the shape of a pyramid, may be formed to take other shapes, e.g., a box, a cylinder, or any other shape.
[0066] As with the previous illustrative embodiments, the micro-pump 210 may be fully or partially powered by a pump signal delivered to a RFID antenna 226. The RFID antenna 226 is coupled to a first processor 228. The first processor 228 is electrically coupled to the micro-pump 210 by an electrical lead 230, which may be contained in one of the plurality of wall members 202 but is shown separately in FIGURE 7. As shown in FIGURE 8, a floor portion 232 of the plurality of wall members 202 may be contained within a platform member 234.
[0067] Referring now primarily to FIGURES 7 and 8, in operation according to one illustrative embodiment, the reduced-pressure conduit 224 is coupled to a reduced-pressure dressing, such as reduced-pressure dressing 106 of FIGURES 1 and 3. A base unit, e.g., base unit 1 10 of FIGURE 1, is used to transmit a pump signal or a pump activation signal to the RFID antenna 226 of the wireless, reduced-pressure pump 200. The pump signal received by the RFID antenna 226 is delivered to the first processor 228. Power is delivered from the first processor 228 to the micro-pump 210 to energize micro-pump 210. As the micro-pump 210 is energized, reduced pressure is delivered into the second chamber 206 and positive pressure is delivered to the first chamber 204. As pressure builds in the first chamber 204, the pressure fills the plurality of inflatable support members 220 such that the wireless, reduced-pressure pump 200 changes from a deflated state to an inflated state. A spacer member (not shown) may cover the inlet 212 to avoid a vapor lock during start up before the inflatable support members 220 fill.
[0068] Once the inflatable support members 220 are inflated, the maximum volume is achieved for the second chamber 206. Meanwhile, the reduced pressure in the second chamber 206 is delivered to the reduced-pressure conduit 224. Fluids 223 (including liquids) are introduced into the second chamber 206.
[0069] While not explicitly shown, it should be understood that a reduced-pressure sensing device, e.g., analogous to pressure sensing device 138 in FIGURE 3, may be incorporated into a portion of the second chamber 206 to measure pressure in the second chamber 206. Again, while not explicitly shown, it should be understood that a reduced- pressure sensing device, e.g., analogous to pressure sensing device 138 in FIGURE 3, may be included in the reduced-pressure pump 200. The reduced-pressure conduit 224 may also have a pressure sensing lumen that is fluidly coupled to the reduced-pressure sensing device for measuring pressure at a distribution manifold. In both examples, the pressure sensing device is coupled to the first processor 228 to develop a pressure message signal. The pressure message signal may be supplied in response to a pressure inquiry signal from a base unit or self-generated by the first processor 228. The first processor 228 may use the pressure message signal to develop a pump control signal that is delivered to the micro-pump 210. Alternatively, the pressure message signal may be transmitted to the base unit where a processor in the base unit may develop a pump control signal similar to the embodiments previously presented.
[0070] In an alternative embodiment, the wireless, reduced-pressure pumps 108, 200 previously presented have, instead of having RFID antennas, electrical leads or sockets and plugs between the pumps and base. The electrical leads or sockets and plugs may readily plug into one another for communicating power and signals.
[0071] Referring now primarily to FIGURES 9-11, an illustrative embodiment of a reduced-pressure system 300 for treating a tissue site 302 with reduced pressure is presented. The reduced-pressure system 300 includes a wireless, reduced-pressure dressing 304 and a base unit 306. The base unit 306 may include a power connector 307. The wireless, reduced- pressure dressing 304 is a self-contained, disposable dressing that receives power and control from the base unit 306. The base unit 306 may be substantially adjacent to the wireless, reduced-pressure dressing 304, e.g., within one or two millimeters, or up to 10 meters or more away or anywhere in between. In one embodiment, the micro-pump 316 may be separate from an absorbent layer or absorbent member 310, such that after use, the micro-pump 316 may be readily separated. The micro-pump 316 may then be reconditioned and reused.
[0072] The wireless, reduced-pressure dressing 304 includes an interface distribution manifold 308 that is placed proximate to the tissue site 302. The wireless, reduced-pressure dressing 304 may also include an absorbent layer 310, a RFID antenna 312, and a first processor 314. The RFID antenna 312 is electrically coupled to the first processor 314. The first processor 314 is electrically coupled to the micro-pump 316. The interface distribution manifold 308, absorbent layer 310, RFID antenna 312, first processor 314, and micro-pump 316 may all be retained in place and secured in a sealed space 318 by one or more sealing members, such as sealing member 320. Additional layers and components may be included in the wireless, reduced-pressure dressing 304.
[0073] The illustrative embodiment of FIGURES 9-11 includes additional layers and components. The additional layers and components may be arranged in different orders. A sealing layer 322 is used to seal the wireless, reduced-pressure dressing 304 around the tissue site 302. The sealing layer 322 is formed with an aperture 323 for providing fluid
communication to the interface distribution manifold 308. A first internal distribution manifold 324 is positioned in fluid communication with the interface distribution manifold 308 and the tissue site 302. The absorbent layer 310 is positioned in fluid communication with the first internal distribution manifold 324, the interface distribution manifold 308, and a tissue site 302. A diverter layer 326 is positioned adjacent to the absorbent layer 310. A second internal distribution manifold 328 is positioned in fluid communication with the diverter layer 326. The diverter layer 326 is formed with a plurality of apertures 327 that may take numerous patterns and forms. The diverter layer 326 is shown in this particular illustrative embodiment with a plurality of apertures 327 forming a square pattern. The square pattern has corner apertures that are larger than the other apertures. A liquid-air separator 330 is positioned adjacent to the second internal distribution manifold 328.
[0074] The micro-pump 316, RFID antenna 312, and first processor 314 may be adjacent to the liquid-air separator 330. A charcoal filter 332 or other odor relieving device may be positioned over an outlet 334 of the micro-pump 316. The sealing member 320 is formed with an aperture 336 that allows the outlet 334 of the micro-pump 316 to exhaust to an exterior of the wireless, reduced-pressure dressing 304. The outlet 334 and aperture 336 together form a vent 338.
[0075] The micro-pump 316 may be a micro-pump that is small and light enough such that the integrated wireless, reduced-pressure dressing 304 is able to be maintained on the tissue site 302. Furthermore, the size and weight of the micro-pump 316 may be such that the integrated reduced-pressure dressing 304 does not pull or otherwise adversely affect the tissue site 302. In one illustrative embodiment, the micro-pump 316 may be a disk pump having a piezoelectric actuator similar to that previously described. Reference is also made to the pumps shown in United States Patent Publication 2009/0087323 and United States Patent Publication 2009/0240185, which are hereby incorporated by reference for all purposes. In an alternative embodiment, the micro-pump 316 may be a peristaltic pump that is used for pumping a variety of fluids. It should be understood that alternative pump technologies may be utilized and that rotary, linear, or other configurations of pumps may be utilized.
[0076] The micro-pump 316 creates sufficient reduced pressure to be therapeutic for wound therapy. In one illustrative embodiment, the micro-pump 316 has sufficient flow, reduced pressure, and operation life characteristics to enable continuous application of reduced pressure treatment. The flow may range between about 5-1000 ml/min and the reduced pressure may range between about -50 and -200 mm Hg (-6.6 to -26.6 kPa). It should be understood that alternative ranges may be utilized depending on the configuration of the integrated, wireless, reduced-pressure dressing 304, size of wound, or type of wound. In one illustrative embodiment, multiple pumps may be positioned in a single dressing to deliver increased flow rates or vacuum levels as required.
[0077] The micro-pump 316 is disposed within the dressing to avoid conduits and external canisters for collection of wound exudate. The micro-pump 316 includes the outlet 334 to release air or exhaust out of the reduced-pressure dressing 304. If the outlet 334 is used, the outlet 334 is in fluid communication with, or may be positioned within, the aperture 336 of the sealing member 320. Alternatively, the sealing member 320 may be sealed around an outlet port of the micro-pump 316 such that gas from the micro-pump 316 is able to exhaust directly through the aperture 336. In the illustrative embodiment in FIGURES 9-11, the outlet 334 of the micro-pump 316 is oriented in a direction away from the liquid-air separator 330 (or hydrophobic filter) to avoid adding air to the wireless, reduced-pressure dressing 304. The air exhausts through an aperture 336 in the sealing member 320, which may include a one-way valve. Alternatively, the air or another gas could be exhausted through a gas-permeable portion of the sealing member 320 as long as the ability of the sealing member 320 to maintain reduced pressure is not affected.
[0078] When the micro-pump 316 is a piezoelectric pump, the piezoelectric actuator associated with the micro-pump 316 may be driven at different frequencies to act as a buzzer or vibrating alert system at times. The alert system may alert a user to an alarm condition. For example, the alarm condition may indicate the presence of a leak in the dressing, a change in reduced pressure as measured by a sensor, that the dressing has absorbed a maximum capacity of liquid as may be indicated by an indicator, or that one or more layers are no longer manifolding reduced pressure efficiently.
[0079] Control electronics may be physically or functionally incorporated as part of the first processor 314. The control electronics may be utilized to control operation of the micro-pump 316. The control electronics may be analog or digital and be configured with a regulator to regulate speed or duty cycle at which the micro-pump 316 operates. Furthermore, the control electronics may be configured with a controller that receives sense signals from sensors or switches, e.g., a pressure sensing device (see 340 in FIG. 12). The sensors may be disposed throughout the wireless, reduced-pressure dressing 304 to sense parameters, such as pressure, temperature, moisture, chemistry, odor, or any other parameter that may be utilized in managing and controlling the micro-pump 316. The control electronics may include a computer processor or programmable gate array or other control device. It should be understood that the control electronics may include any form of digital or analog components to perform the functions described herein. The control electronics may be or include the first processor 314.
[0080] The control electronics may be arranged to monitor and provide an alarm for certain conditions, e.g., (i) low pressure, (ii) excessive leak, (iii) level of absorbent layer, and (iv) battery state (if included). Accordingly, the control electronics may include electronics that monitor each of the parameters and generate an alarm signal (e.g., high-pitched beep, vibration, or light) using a speaker, vibrator, or illumination device, such as a light emitting diode (LED). Thus, the control electronics may notify a medical professional, patient, or family member that a parameter is outside of a desired range. For example, if a pressure at the tissue site 302 is below a therapeutic level, a continuous tone may be generated. As another example, if the absorbent layer 310 is saturated, then continuous beeps may be generated. If the battery drops below a certain voltage level, then a different audible frequency may be generated or an LED may be activated. A variety of different alarm signals may be established to notify a medical professional to take a particular action.
[0081] The RFID antenna 312 is utilized to provide electric power to the micro- pump 316 and control electronics. A battery 342 may also be used to provide stored energy to augment power from the RFID antenna 312. The battery 342 may be any size and shape and may be of any material, such as polymer. The battery 342 may provide the entire needed power or a portion thereof. The battery 342 may be recharged by power from the RFID antenna 312.
[0082] In one illustrative embodiment, the battery 342 may be configured with a voltage level sensor that is monitored by the control electronics, and the control electronics may provide an alarm when a low power level is detected. The battery 342 may be directly connected to the micro-pump 316. Alternatively, the battery 342 may be connected to the control electronics or processor(s) that use power from the battery 342 to drive the micro- pump 316. The control electronics may provide continuous, modulated power, such as a pulsewidth modulated (PWM) signal, to drive the micro-pump 316.
[0083] The sealing layer 322 is adhered to or otherwise connected to the sealing member 320 that is used to drape or otherwise cover the components of the reduced-pressure dressing 304. The sealing layer 322 may include a medical-grade adhesive material or other sealing device that is strong enough to form a vacuum seal with epidermis around a wound of a patient. The sealing layer 322 may be a band that has an aperture 323 that is slightly larger than the geometric parameters of the liquid-air separator 330 or other layer so that the sealing member 320 contacts epidermis around the tissue site 302 of the patient. The sealing member 320 is impermeable to fluids, such as air and liquids.
[0084] In another illustrative embodiment, the sealing member 320 may be adhered to the diverter layer 326 and the diverter layer 326 adhered to the sealing member 320 to create an upper dressing portion and a lower dressing portion. The upper dressing portion may include the sealing member 320, the micro-pump 316 and related components, the liquid-air separator 330, the second internal distribution manifold 328, and the diverter layer 326. The lower dressing portion may include the absorbent layer 310, the first internal distribution manifold 324, the sealing layer 322, and the interface distribution manifold 308. The wireless, reduced-pressure dressing 304 may be configured to allow replacement of the lower dressing portion once the wireless, reduced-pressure dressing has absorbed a maximum capacity of fluid. The upper dressing portion may be reused after the lower dressing portion is replaced. This allows multiple uses of the micro-pump 316, while disposable portions of the dressing may be replaced. In another illustrative embodiment, the micro-pump 316, first processor 314, and RFID antenna 312 may be removed from the dressing for reuse and the remaining layers of the dressing replaced. In still another illustrative embodiment, only the absorbent layer 310 may be replaced. In yet another illustrative embodiment, only the absorbent layer 310 and the interface distribution manifold 308 may be replaced.
[0085] The charcoal filter 332 may be utilized in the wireless, reduced-pressure dressing 304 to reduce odors created by the tissue site 302 and dispersed from the wireless, reduced-pressure dressing 304. The charcoal filter 332 may be disposed above a valve or other output vent from the micro-pump 316 to filter exhaust from the micro-pump 316 prior to being released from the integrated reduced-pressure dressing 304. It should be understood that the charcoal filter 332 may be alternatively configured and disposed above or below the micro- pump 316. In another illustrative embodiment, rather than using a charcoal filter, charcoal may be integrated into any or all of the different layers utilized in the integrated reduced- pressure dressing 304.
[0086] According to one illustrative embodiment, in operation, the reduced-pressure system 300 of FIGURES 9-11, is applied by placing the interface distribution manifold 308 proximate to the tissue site 302. Placing the sealing layer 322 over the interface distribution manifold 308 such that the aperture 323 is over the interface distribution manifold 308. The first internal distribution manifold 324 is placed adjacent to the first interface distribution manifold 308 and possibly a portion of the sealing layer 322. The absorbent layer 310 is placed adjacent to the first internal distribution manifold 324. The diverter layer 326 may be placed over all the components thus presented. Then the second internal distribution manifold 328 may be placed adjacent to a portion of the diverter layer 326 along with the liquid-air separator 330. The micro-pump 316, RFID antenna 312, and first processor 314 may be applied. The components mentioned here may also be pre-assembled as a dressing stack.
[0087] The sealing member 320 is used to create a seal that forms a sealed space 318. The base unit 306 is used to transmit a pump signal as before to the RFID antenna 312 that is received by the first processor 314 and is used to provide power to the micro-pump 316. The first processor 314 may further include one or more capacitors for holding power or one or more batteries such as a rechargeable battery. The pump signal causes reduced pressure to be developed by the micro-pump 316. The reduced pressure is transmitted to the tissue site 302 to remove fluids or to provide reduced pressure therapy. The fluids removed from the tissue site 302 are transmitted within the reduced-pressure dressing 304 to the absorbent layer 310 where the fluids are retained or substantially retained. As will be described in connection with FIGURE 12, a pressure sensing device may be included as part of the wireless, reduced- pressure dressing 304 to provide a pressure message signal to the base unit 306.
[0088] Referring now primarily to FIGURE 12, another illustrative embodiment of a reduced-pressure system 300 is presented. As before, the reduced-pressure system 300 includes a wireless, reduced-pressure dressing 304 and a base unit 306. The reduced-pressure system 300 in FIGURE 12 is analogous to the system presented in FIGURES 9-1 1, except that the wireless, reduced-pressure dressing 304 includes fewer components and includes the addition of a pressure sensing device 340 that is electrically coupled to the first processor 314. In addition, an optional battery 342 is included. The battery 342 may supplement power provided through the RFID antenna 312 or may be used as the primary power source and then recharged by the RFID antenna 312. The RFID antenna 312 receives power from the base unit 306. The sealing member 320 is shown secured to the epidermis 344 by an attachment device 346. Components included in the previous dressing of FIGURES 9-11 have been assigned the same reference numerals and are not necessarily discussed further here.
[0089] According to an illustrative embodiment, in operation, the reduced-pressure system 300 of FIGURE 12 may be used by first applying the interface distribution manifold 308 adjacent to the tissue site 302. The absorbent layer 310 is placed in fluid communication with the interface distribution manifold 308. The liquid-air separator 330 may be placed over the absorbent layer 310. Then the RFID antenna 312, pressure sensing device 340, first processor 314, micro-pump 316, and battery 342 are disposed on the liquid-air separator 330. Alternatively, only some of the components, such as the micro-pump 316, may be adjacent to the liquid-air separator 330. The sealing member 320 is applied over the tissue site 302 to create a sealed space 318 and to cover all the aforementioned components. The previously mentioned components may be entirely or partially preassembled. The base unit 306 transmits a pump signal or pump activation signal to the reduced-pressure dressing 304 that activates the micro-pump 316. The micro-pump 316 removes air or other fluids from the sealed space 318 and thereby initiates treatment of the tissue site 302 with reduced pressure. [0090] In addition to providing the pump activation signal or pump signal from the base unit 306 to the RFID antenna 312, the base unit 306 may also transmit a pressure inquiry signal. Upon receiving the pressure inquiry signal, the RFID antenna 312, the first processor 314, and the pressure sensing device 340 develop a pressure message signal that is transmitted by the RFID antenna to the RFID reader (not explicitly shown) of the base unit 306. The base unit 306 may include a processor (not explicitly shown) that receives the pressure message signal and develops a pump control signal to activate or deactivate the micro-pump 316. If the reduced pressure is in the desired therapy range, the micro-pump 316 may be deactivated. Similarly, if the pressure is too great on an absolute scale, the base unit 306 may transmit a pump signal that activates or continues the micro-pump 316 to produce more reduced pressure. If more than a sufficient elapsed time has passed without the desired pressure being reached, an alarm may be triggered by the base unit 306. The wireless, reduced-pressure dressing 304 may include a galvanic cell (not explicitly shown) to provide a full indication message signal when exudate or other body fluids electrically couple two electrodes. The full indication message signal would be transmitted with the RFID antenna 312 to the base unit 306 indicating that the dressing is full.
[0091] Referring now primarily to FIGURE 13, another illustrative embodiment of a reduced-pressure dressing 400 is presented that includes a wireless, reduced-pressure pump 430. The reduced-pressure dressing 400 is shown in an exploded view over a tissue site 402, such as a wound, on a patient 404. The reduced-pressure dressing 400 includes an interface distribution manifold 406, which is disposed proximate the tissue site 402. The interface distribution manifold 406 may be formed from any manifold material, such as a GranuFoam® material or any other manifold material previously mentioned.
[0092] The reduced-pressure dressing 400 further includes a lower drape or diverter 408. The lower drape 408 may be a polyethylene material having adhesive on a lower side (tissue-facing side) that adheres to the patient 404 surrounding the tissue site 402 being treated. The lower drape 408 includes apertures or perforations for communicating reduced pressure through the interface distribution manifold 406 to the tissue site 402 and drawing wound fluids (liquids or gases) from the tissue site 402. The lower drape 408 may also include a sealing ring 410 to provide additional adhesive strength to maintain the reduced pressure at a desired therapeutic level. A protective release liner 412 may initially cover the sealing ring 410. The protective release liner 412 is removed from the lower side of the lower drape 408 before the lower drape 408 is positioned on the patient 404.
[0093] The reduced-pressure dressing 400 includes an absorbent layer 414 that may be a non-woven fabric for absorbing the wound liquids being drawn through the apertures of the lower drape 408. The absorbent layer 414 is sandwiched between two wicking layers 416, 418 that wick and manifold the wound fluid to the absorbent layer 414. The dense side of the wicking layers 416, 418 face away from the absorbent layer 414. The wicking layers 416, 418 sandwich the absorbent layer 414 to form a fluid storage device 420.
[0094] The reduced-pressure dressing 400 further includes an upper drape 422 that may be a non-porous, occlusive barrier formed of polyethylene. The smooth side of the upper drape 422 faces the upper wicking layer 416. The upper drape 422 includes a aperture or opening 424. The aperture or opening 424 is covered by a hydrophobic filter 426 that separates air from liquid to contain the wound liquids or exudates within the absorbent layer 414. The hydrophobic filter 426 simultaneously permits the flow of gas from the absorbent layer 414 as a result of reduced pressure being applied to the hydrophobic filter 426. The upper drape 422 and the hydrophobic filter 426 comprise a top layer 428 of the reduced- pressure dressing 400 that covers the fluid storage device 420. All the elements of the dressing assembly described above except the release liner 412 may be referred to collectively as the "wound dressing" portion of the reduced-pressure dressing 400.
[0095] The reduced-pressure dressing 400 further includes the wireless, reduced- pressure pump, or pump portion 430. The pump portion 430 includes a micro-pump assembly 432 positioned on top of the upper drape 422 to provide a reduced pressure for drawing air through the hydrophobic filter 426, the fluid storage device 420, and the interface distribution manifold 406. The micro-pump assembly 432 includes a piezoelectric disc pump 434 that vibrates at a predetermined frequency to generate a desired reduced pressure at the input of the piezoelectric disc pump 434. The piezoelectric disc pump 434 may be analogous to micro- pump 316 of FIGURE 12. The piezoelectric disc pump 434 of the micro-pump assembly 432 may not operate if any liquid drawn from the tissue site 402 into the absorbent layer 414 below the upper drape 422 enters the input port of the piezoelectric disc pump 434. The hydrophobic filter 426 prevents wound liquids or exudates from flowing into the piezoelectric disc pump 434 of the micro-pump assembly 432. [0096] The reduced-pressure dressing 400 may also include a spacing ring or ring seal 436 positioned between the hydrophobic filter 426 and the inlet of the piezoelectric disc pump 434 to provide a cavity for air flow to the piezoelectric disc pump 434 of the micro-pump assembly 432. The micro-pump assembly 432 may be sandwiched between a first foam cushion 438 and second foam cushion 440. The micro-pump assembly 432, first cushion 438, and second cushion 440 are sandwiched between an outer ply 442 and an inner ply 444 and form a single composite package that is removably attached to the upper drape 422. The outer ply 442 includes apertures or perforations 446 that provide an exhaust path for the output of the micro-pump assembly 432.
[0097] The piezoelectric disc pump 434 or other micro-pump may be controlled by a first processor 448 and other control electronics. The piezoelectric disc pump 434 may be powered by a first power unit 450 and a second power unit 452. The power units 450, 452 may be batteries. In another illustrative, embodiment, the first power unit 450 or the second power unit 452 may comprise a RFID antenna that provides power to the first processor 448 and to the piezoelectric disc pump 434.
[0098] According to an embodiment, a system for treating a tissue site with reduced pressure includes a reduced-pressure dressing for disposing proximate to the tissue site; and a wireless, reduced-pressure pump fluidly coupled to the reduced-pressure dressing. The wireless, reduced-pressure pump includes a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and a fluid reservoir fluidly coupled to the micro- pump device. The system further includes a base unit having a RFID reader. The RFID reader is configured to provide power to the RFID antenna such that the micro-pump device is powered. The system may further include a first pump-sealing member and a second pump- sealing member. The first pump-sealing member and second pump-sealing member are at least partially coupled to form a pump pouch in which the micro-pump device is disposed. The wireless, reduced-pressure pump may function with no source of power other than the RFID antenna. The wireless, reduced-pressure pump may further comprise a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site. The wireless, reduced-pressure pump may further comprise a pressure sensing device coupled to the first processor. The base unit may comprise a second processor coupled to the RFID reader, and the second processor and RFID reader may be configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced- pressure pump and to receive in response thereto a pressure message signal from the first processor.
[0099] With respect to the system of the preceding paragraph, the wireless, reduced- pressure pump may further comprise a pressure sensing device coupled to the first processor. The base unit may comprise a second processor coupled to the RFID reader. The second processor and RFID reader may be configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor. The first processor and pressure sensing device may be configured to prepare the pressure message signal in response to the pressure inquiry signal. The first processor and RFID antenna may be configured to transmit the pressure message signal. And, the second processor may be configured to receive the pressure message signal, prepare a control signal. The second processor and RFID may be configured to transmit the control signal to the wireless, reduced-pressure pump to provide a control signal for activating or deactivating the micro-pump device.
[00100] With respect to the system of the preceding paragraphs, the wireless, reduced-pressure pump may further comprise a pressure sensing device coupled to the first processor. The pressure sensing device is operable to produce a pressure message signal. The first processor is operable to receive the pressure message signal and to produce a control signal to activate or deactivate the micro-pump device.
[00101] In another embodiment of the system of the preceding paragraphs, the system further includes a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site; a first distribution manifold, an absorbent layer, a diverter layer, a pump-sealing member, a second pump-sealing member, wherein the first distribution manifold, the absorbent layer, and the diverter layer are disposed within a pump pouch formed by the a pump-sealing member and a second pump- sealing member; the micro-pump device comprises a piezoelectric pump. The reduced- pressure dressing includes an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and a reduced-reduced pressure interface. In one embodiment, the RFID antenna is less than five (5) centimeters from the base unit.
[00102] According to another illustrative embodiment, a wireless, reduced- pressure pump includes at least one wall member forming a first chamber and a second chamber; a RFID antenna; a first processor coupled to the RFID antenna; and a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure and positive pressure. The micro-pump device has a vent fluidly coupled to the first chamber for exhausting positive pressure thereto and an inlet that is fluidly coupled to the second chamber for delivering reduced pressure thereto. The pump further includes a plurality of inflatable support members fluidly coupled to the first chamber; and a fluid reservoir, wherein the fluid reservoir comprises the second chamber. The pump may further include a first pressure relief valve fluidly coupled to the first chamber. The first pressure relief valve is operable to vent positive pressure above a first threshold pressure. The first chamber and the second chamber may be in the shape of a portion of a pyramid. The pump may function with no source of power other than the RFID antenna.
[00103] According to another illustrative embodiment, a method of
manufacturing a system for treating a tissue site on a patient with reduced pressure includes providing a reduced-pressure dressing for disposing proximate to the tissue site and providing a wireless, reduced-pressure pump. The wireless, reduced-pressure pump includes: a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and a fluid reservoir fluidly coupled to the micro-pump device. The method further includes providing a base unit having a RFID reader. The RFID reader is configured to provide power to the RFID antenna such that the micro-pump device is powered. The method of manufacturing may further include a first pump-sealing member and a second pump-sealing member. The first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed. The method of manufacturing may further include providing a reduced-pressure conduit for fluidly coupling the wireless, reduced- pressure pump to the reduced-pressure dressing. The method of manufacturing may further include providing a pressure sensing device and coupling the pressure sensing device to the reduced-pressure dressing.
[00104] According to another illustrative embodiment, a method for treating a tissue site on a patient with reduced pressure includes placing a reduced-pressure dressing proximate to the tissue site and providing a wireless, reduced-pressure pump. The wireless, reduced-pressure pump comprises: a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and a fluid reservoir fluidly coupled to the micro-pump device. The method also includes fluidly coupling the wireless, reduced-pressure pump to the reduced- pressure dressing; providing a base unit having a RFID reader and a second processor; and activating the base unit whereby the RFID reader and second processor transmit an activation signal to the wireless, reduced-pressure pump to activate the wireless, reduced-pressure pump. The wireless, reduced-pressure pump may further include a first pump-sealing member and a second pump-sealing member. The first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed. All the power required by the micro-pump device may be delivered by the RFID reader. The method may further include the step of placing the RFID reader within five (5) centimeters of the RFID antenna of the wireless, reduced-pressure pump.
[00105] With respect to the method of the preceding paragraph, the wireless, reduced-pressure pump may have no source of power other than the RFID antenna and the wireless, reduced-pressure pump may further comprise: a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site, a first distribution manifold, an absorbent layer, and a diverter layer. The first distribution manifold, the absorbent layer, and the diverter layer may be disposed within the pump pouch formed by the first pump-sealing member and the second pump-sealing member. The micro-pump device may be a piezoelectric pump. The reduced-pressure dressing may comprise: an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and a reduced-reduced pressure interface.
[00106] According to another illustrative embodiment, a reduced-pressure system for treating a tissue site with reduced pressure includes a wireless, reduced-pressure dressing that includes: an interface distribution manifold for placing proximate to the tissue site, an absorbent member for receiving and retaining fluids from the interface distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, the micro-pump device having an inlet and an exhaust outlet, a first sealing member for covering the tissue site to form a sealed space, and a vent fluidly coupling the exhaust outlet of the micro-pump device to an exterior. The micro-pump is fluidly coupled to the sealed space for delivering reduced pressure thereto. The system further includes a base unit comprising a RFID reader. The base unit is operable to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump device. The system may further comprise a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor. The first processor and RFID antenna are operable to receive a pressure inquiry signal and to produce a pressure message signal to be transmitted to the base unit.
[00107] In another embodiment of he system of the preceding paragraphs, the system may further include a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor. The fist processor and RFID antenna are operable to receive a pressure inquiry signal and produce a pressure message signal to be transmitted to the base unit. The base unit further comprises a second processor. The second processor is operable to receive the pressure message signal and produce a pump control signal.
[00108] In another embodiment of he system of the preceding paragraphs, the system may further include a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor, and wherein the first processor is configured to receive a pressure message signal from the first pressure sensor and to produce a control signal for controlling the micro-pump device. In another embodiment of he system of the preceding paragraphs, the wireless, reduced-pressure pump may function with no source of power other than the RFID antenna. In addition, the only reduced pressure supplied to the reduced- pressure dressing may be from the micro-pump device. This system may be assembled such that no conduits or wires are coupled to the wireless, reduced-pressure dressing.
[00109] According to another illustrative embodiment, a method for treating a tissue site on a patient with reduced pressure includes disposing a wireless, reduced-pressure dressing proximate to the tissue site. The wireless, reduced-pressure dressing includes an interface distribution manifold for placing proximate to the tissue site, an absorbent member for receiving and retaining fluids from the interface distribution manifold, a RFID antenna, a first processor coupled to the RFID antenna, a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure and having an inlet and an exhaust outlet, a first sealing member for covering the tissue site and forming a sealed space, and a vent fluidly coupling the exhaust outlet to an exterior. The method further includes providing a base unit comprising a RFID reader, wherein the base unit is configured to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump device; and activating the base unit to deliver the pump signal to the wireless, reduced- pressure dressing. [00110] According to another illustrative embodiment, a wireless, reduced- pressure pump, the wireless, reduced-pressure pump includes a RFID antenna; a first processor coupled to the RFID antenna; and a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure. The wireless, reduced-pressure pump may further include a fluid reservoir fluidly coupled to the micro- pump device. The wireless, reduced-pressure pump may also further include a first pump- sealing member and a second pump-sealing member, wherein the first pump-sealing member and second pump-sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed. The wireless, reduced-pressure pump may function with no source of power other than the RFID antenna. The wireless, reduced-pressure pump may further include a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site.
[00111] With respect to the wireless, reduced-pressure pump of preceding paragraph, the pump may further include a pressure sensing device coupled to the first processor and a base unit that comprises a second processor coupled to the RFID reader. The second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor.
[00112] With respect to the wireless, reduced-pressure pump of the preceding paragraphs, the wireless, reduced-pressure pump may further include a pressure sensing device coupled to the first processor and a base unit that comprises a second processor coupled to the RFID reader. The second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor. The first processor and pressure sensing device are configured to prepare the pressure message signal in response to the pressure inquiry signal. The first processor and RFID antenna are configured to transmit the pressure message signal. The second processor is configured to receive the pressure message signal, prepare a control signal, and the second processor and RFID are configured to transmit the control signal to the wireless, reduced-pressure pump to provide a control signal for activating or deactivating the micro-pump device. The wireless, reduced-pressure pump may further include a pressure sensing device coupled to the first processor; wherein, the pressure sensing device is operable to produce a pressure message signal, and the first processor is operable to receive the pressure message signal and to produce a control signal to activate or deactivate the micro-pump device.
[00113] In general terms, systems, methods, and dressings for providing reduced pressure to a tissue site on a patient are presented that involve wirelessly providing power to a reduced-pressure pump. In one instance, a RFID antenna is used to power a reduced-pressure pump that is fluidly coupled by a conduit to a reduced-pressure dressing. In another instance, a reduced-pressure dressing incorporates a micro-pump and a RFID antenna that is used to power the micro-pump. Other systems, methods, and devices are presented herein.
[00114] Although the present invention and its advantages have been disclosed in the context of certain illustrative, non-limiting embodiments, it should be understood that various changes, substitutions, permutations, and alterations can be made without departing from the scope of the invention as defined by the appended claims. It will be appreciated that any feature that is described in connection to any one embodiment may also be applicable to any other embodiment.
[00115] It will be understood that the benefits and advantages described above may relate to one embodiment or may relate to several embodiments. It will further be understood that reference to "an" item refers to one or more of those items.
[0100] The steps of the methods described herein may be carried out in any suitable order, or simultaneously where appropriate. [0101] Where appropriate, aspects of any of the embodiments described above may be combined with aspects of any of the other embodiments described to form further examples having comparable or different properties and addressing the same or different problems.
[0102] It will be understood that the above description of preferred embodiments is given by way of example only and that various modifications may be made by those skilled in the art. The above specification, examples and data provide a complete description of the structure and use of exemplary embodiments of the invention. Although various embodiments of the invention have been described above with a certain degree of particularity, or with reference to one or more individual embodiments, those skilled in the art could make numerous alterations to the disclosed embodiments without departing from the scope of the claims.

Claims

CLAIMS We claim:
Claim 1. A system for treating a tissue site with reduced pressure, the system
comprising:
a reduced-pressure dressing for disposing proximate to the tissue site;
a wireless, reduced-pressure pump fluidly coupled to the reduced-pressure dressing, the wireless, reduced-pressure pump comprising:
a RFID antenna,
a first processor coupled to the RFID antenna,
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and
a fluid reservoir fluidly coupled to the micro-pump device; a base unit having a RFID reader; and
wherein the RFID reader is configured to provide power to the RFID antenna such that the micro-pump device is powered.
Claim 2. The system of claim 1, further comprising a first pump-sealing member and a second pump-sealing member, wherein the first pump-sealing member and second pump- sealing member are at least partially coupled to form a pump pouch in which the micro- pump device is disposed.
Claim 3. The system of claim 1 or claim 2, wherein the wireless, reduced-pressure pump has no source of power other than the RFID antenna.
Claim 4. The system of claim 1 or claim 2 or claim 3, wherein the wireless, reduced- pressure pump further comprises a pressure sensing device fluidly coupled to the reduced- pressure dressing and to the first processor for sensing pressure at the tissue site.
Claim 5. The system of claim 1 or claim 2 or claim 3, wherein
the wireless, reduced-pressure pump further comprises a pressure sensing device coupled to the first processor,
the base unit comprises a second processor coupled to the RFID reader, and the second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor.
Claim 6. The system of claim 1 or claim 2 or claim 3, wherein
the wireless, reduced-pressure pump further comprises a pressure sensing device coupled to the first processor,
the base unit comprises a second processor coupled to the RFID reader, the second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor,
the first processor and pressure sensing device are configured to prepare the pressure message signal in response to the pressure inquiry signal, the first processor and RFID antenna are configured to transmit the pressure message signal, and
the second processor is configured to receive the pressure message signal, prepare a control signal, and the second processor and RFID are configured to transmit the control signal to the wireless, reduced- pressure pump to provide a control signal for activating or deactivating the micro-pump device.
Claim 7. The system of claim 1 or claim 2 or claim 3, wherein
the wireless, reduced-pressure pump further comprises a pressure sensing device coupled to the first processor,
the pressure sensing device is operable to produce a pressure message signal, and
the first processor is operable to receive the pressure message signal and to produce a control signal to activate or deactivate the micro-pump device.
Claim 8. The system of claim 1, further comprising:
a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site;
a first distribution manifold,
an absorbent layer,
a diverter layer,
a pump-sealing member,
a second pump-sealing member,
wherein the first distribution manifold, the absorbent layer, and the diverter layer are disposed within a pump pouch formed by the a pump-sealing member and a second pump-sealing member;
the micro-pump device comprises a piezoelectric pump;
the reduced-pressure dressing comprising:
an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and
a reduced-reduced pressure interface; and
wherein the RFID antenna is less than five (5) centimeters from the base unit.
Claim 9. A wireless, reduced-pressure pump comprising:
at least one wall member forming a first chamber and a second chamber;
a RFID antenna;
a first processor coupled to the RFID antenna;
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure and positive pressure;
wherein the micro-pump device has a vent fluidly coupled to the first chamber for exhausting positive pressure thereto and an inlet that is fluidly coupled to the second chamber for delivering reduced pressure thereto;
a plurality of inflatable support members fluidly coupled to the first chamber; and a fluid reservoir, wherein the fluid reservoir comprises the second chamber.
Claim 10. The wireless, reduced-pressure pump of claim 9, further comprising a first pressure relief valve fluidly coupled to the first chamber, the first pressure relief valve is operable to vent positive pressure above a first threshold pressure.
Claim 1 1. The wireless, reduced-pressure pump of claim 9 or claim 10, wherein the first chamber and the second chamber are in the shape of a portion of a pyramid.
Claim 12. The wireless, reduced-pressure pump of claim 9 or any of claims 10-1 1, wherein the wireless, reduced-pressure pump has no source of power other than the RFID antenna.
Claim 13. A method of manufacturing a system for treating a tissue site on a patient with reduced pressure, the method comprising:
providing a reduced-pressure dressing for disposing proximate to the tissue site; providing a wireless, reduced-pressure pump, the wireless, reduced-pressure pump comprising:
a RFID antenna,
a first processor coupled to the RFID antenna,
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and
a fluid reservoir fluidly coupled to the micro-pump device; providing a base unit having a RFID reader; and
wherein the RFID reader is configured to provide power to the RFID antenna such that the micro-pump device is powered.
Claim 14. The method of manufacturing of claim 13, further comprising a first pump- sealing member and a second pump-sealing member, wherein the first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed.
Claim 15. The method of manufacturing of claim 13, further comprising providing a reduced-pressure conduit for fluidly coupling the wireless, reduced-pressure pump to the reduced-pressure dressing.
Claim 16. The method of manufacturing of claim 13, further comprising providing a pressure sensing device and coupling the pressure sensing device to the reduced-pressure dressing.
Claim 17. A method for treating a tissue site on a patient with reduced pressure, the method comprising:
placing a reduced-pressure dressing proximate to the tissue site;
providing a wireless, reduced-pressure pump, wherein the wireless, reduced- pressure pump comprises:
a RFID antenna,
a first processor coupled to the RFID antenna,
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, and
a fluid reservoir fluidly coupled to the micro-pump device; fluidly coupling the wireless, reduced-pressure pump to the reduced-pressure dressing;
providing a base unit having a RFID reader and a second processor; and activating the base unit whereby the RFID reader and second processor transmit an activation signal to the wireless, reduced-pressure pump to activate the wireless, reduced-pressure pump.
Claim 18. The method of claim 17, wherein the wireless, reduced-pressure pump further comprises:
a first pump-sealing member; and
a second pump-sealing member, wherein the first pump-sealing member and second pump sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed.
Claim 19. The method of claim 17 or claim 18, wherein all the power required by the micro-pump device is delivered by the RFID reader.
Claim 20. The method of claim 17 or any of claims 18-19, further comprising the step of placing the RFID reader within five (5) centimeters of the RFID antenna of the wireless, reduced-pressure pump.
Claim 21. The method of claim 18,
wherein the wireless, reduced-pressure pump has no source of power other than the
RFID antenna;
the wireless, reduced-pressure pump further comprises:
a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site, a first distribution manifold,
an absorbent layer,
a diverter layer,
wherein the first distribution manifold, the absorbent layer, and the diverter layer are disposed within the pump pouch formed by the first pump- sealing member and the second pump-sealing member, and the micro-pump device comprises a piezoelectric pump; and the reduced-pressure dressing comprises:
an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and
a reduced-reduced pressure interface.
Claim 22. A reduced-pressure system for treating a tissue site with reduced pressure, the reduced-pressure system comprising:
a wireless, reduced-pressure dressing comprising:
an interface distribution manifold for placing proximate to the tissue site, an absorbent member for receiving and retaining fluids from the interface distribution manifold,
a RFID antenna,
a first processor coupled to the RFID antenna,
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure, the micro-pump device having an inlet and an exhaust outlet,
a first sealing member for covering the tissue site to form a sealed space, and a vent fluidly coupling the exhaust outlet of the micro-pump device to an exterior;
wherein the micro-pump is fluidly coupled to the sealed space for delivering reduced pressure thereto; and
a base unit comprising a RFID reader, wherein the base unit is operable to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump device.
Claim 23. The system of claim 22, further comprising a first pressure sensor on the wireless, reduced-pressure dressing that is coupled to the first processor, the fist processor and RFID antenna are operable to receive a pressure inquiry signal and to produce a pressure message signal to be transmitted to the base unit.
Claim 24. The system of claim 22, further comprising a first pressure sensor on the
wireless, reduced-pressure dressing that is coupled to the first processor, the fist processor and RFID antenna are operable to receive a pressure inquiry signal and produce a pressure message signal to be transmitted to the base unit, wherein the base unit further comprises a second processor, the second processor is operable to receive the pressure message signal and produce a pump control signal.
Claim 25. The system of claim 22, further comprising a first pressure sensor on the
wireless, reduced-pressure dressing that is coupled to the first processor, and wherein the first processor is configured to receive a pressure message signal from the first pressure sensor and to produce a control signal for controlling the micro-pump device.
Claim 26. The system of claim 22, wherein the wireless, reduced-pressure pump has no source of power other than the RFID antenna and wherein the only reduced pressure supplied to the reduced-pressure dressing is from the micro-pump device.
Claim 27. The system of claim 22 or claims 23-26, wherein no conduits or wires are coupled to the wireless, reduced-pressure dressing.
Claim 28. A method for treating a tissue site on a patient with reduced pressure, the method comprising:
disposing a wireless, reduced-pressure dressing proximate to the tissue site, the wireless, reduced-pressure dressing comprising:
an interface distribution manifold for placing proximate to the tissue site, an absorbent member for receiving and retaining fluids from the interface distribution manifold,
a RFID antenna,
a first processor coupled to the RFID antenna,
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure and having an inlet and an exhaust outlet,
a first sealing member for covering the tissue site and forming a sealed space, and
a vent fluidly coupling the exhaust outlet to an exterior;
providing a base unit comprising a RFID reader, wherein the base unit is configured to supply a pump signal to the wireless, reduced-pressure dressing to energize the micro-pump device; and
activating the base unit to deliver the pump signal to the wireless, reduced-pressure dressing.
Claim 29. A wireless, reduced-pressure pump, the wireless, reduced-pressure pump comprising:
a RFID antenna;
a first processor coupled to the RFID antenna; and
a micro-pump device coupled to the first processor for receiving power therefrom and developing reduced pressure.
Claim 30. The wireless, reduced-pressure pump of claim 29, further comprising a fluid reservoir fluidly coupled to the micro-pump device.
Claim 31. The wireless, reduced-pressure pump of claim 29 or claim 30, further
comprising:
a first pump-sealing member; and
a second pump-sealing member, wherein the first pump-sealing member and second pump-sealing are at least partially coupled to form a pump pouch in which the micro-pump device is disposed.
Claim 32. The wireless, reduced-pressure pump of claim 29 or claim 30 or claim 31, wherein the wireless, reduced-pressure pump has no source of power other than the RFID antenna.
Claim 33. The wireless, reduced-pressure pump of claim 29 or any of claims 30-32, wherein the wireless, reduced-pressure pump further comprises a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site.
Claim 34. The wireless, reduced-pressure pump of claim 29 or any of claims 30-32, wherein the wireless, reduced-pressure pump further comprises a pressure sensing device coupled to the first processor;
further comprising a base unit that comprises a second processor coupled to the
RFID reader; and
wherein the second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor.
Claim 35. The wireless, reduced-pressure pump of claim 29 or any of claims 30-32,
wherein the wireless, reduced-pressure pump further comprises a pressure sensing device coupled to the first processor,
further comprising a base unit that comprises a second processor coupled to the
RFID reader,
the second processor and RFID reader are configured to transmit a pressure inquiry signal to the first processor of the wireless, reduced-pressure pump and to receive in response thereto a pressure message signal from the first processor,
the first processor and pressure sensing device are configured to prepare the
pressure message signal in response to the pressure inquiry signal, the first processor and RFID antenna are configured to transmit the pressure
message signal, and
the second processor is configured to receive the pressure message signal, prepare a control signal, and the second processor and RFID are configured to transmit the control signal to the wireless, reduced-pressure pump to provide a control signal for activating or deactivating the micro-pump device.
Claim 36. The wireless, reduced-pressure pump of claim 29 or any of claims 30-32,
wherein:
the wireless, reduced-pressure pump further comprises a pressure sensing device coupled to the first processor,
the pressure sensing device is operable to produce a pressure message signal, and the first processor is operable to receive the pressure message signal and to produce a control signal to activate or deactivate the micro-pump device.
Claim 37. The wireless, reduced-pressure pump of claim 29 or any of claims 30-32, wherein the wireless, reduced-pressure pump further comprises:
at least one wall member forming a first chamber and a second chamber, wherein the micro-pump device has a vent fluidly coupled to the first chamber for delivering positive pressure thereto and an inlet fluidly coupled to the second chamber for delivering reduced pressure thereto,
a first pressure relief valve fluidly coupled to the first chamber, the first pressure relief valve is operable to vent positive pressure above a first threshold pressure,
a plurality of inflatable support members fluidly coupled to the first chamber, and wherein the fluid reservoir comprises the second chamber.
Claim 38. The wireless, reduced-pressure pump of claim 29 or claim 30, wherein the wireless, reduced-pressure pump further comprises:
a first chamber and a second chamber in the shape of a portion of a pyramid;
wherein the micro-pump device has a vent fluidly coupled to the first chamber; a first pressure relief valve fluidly coupled to the first chamber that is operable to vent positive pressure above a first threshold pressure;
a plurality of inflatable support members fluidly coupled to the first chamber; and wherein the fluid reservoir comprises the second chamber.
Claim 39. The wireless, reduced-pressure pump of claim 29 or claim 30, wherein:
the wireless, reduced-pressure pump has no source of power other than the RFID antenna;
the wireless, reduced-pressure pump further comprises:
a pressure sensing device fluidly coupled to the reduced-pressure dressing and to the first processor for sensing pressure at the tissue site, a first distribution manifold,
an absorbent layer,
a diverter layer, and
wherein the first distribution manifold, the absorbent layer, and the diverter layer are disposed within the pump pouch formed by the first pump- sealing member and the second pump-sealing member; the micro-pump device comprises a piezoelectric pump;
the reduced-pressure dressing comprises:
an interface distribution manifold for placing proximate to the tissue site, a dressing sealing member, and
a reduced-reduced pressure interface;
the RFID antenna is less than about five (5) centimeters from the base unit; and a reduced-pressure conduit fluidly couples a reduced-pressure interface to the wireless, reduced-pressure pump.
PCT/US2011/044187 2010-10-27 2011-07-15 Reduced-pressure systems, dressings, and methods employing a wireless pump WO2012057881A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CN201180050826.3A CN103179930B (en) 2010-10-27 2011-07-15 Reduced-pressure systems, dressings, and methods employing a wireless pump
EP11738356.2A EP2632406B1 (en) 2010-10-27 2011-07-15 Reduced-pressure systems, dressings, and methods employing a wireless pump
AU2011320911A AU2011320911B2 (en) 2010-10-27 2011-07-15 Reduced-pressure systems, dressings, and methods employing a wireless pump
CA2814740A CA2814740C (en) 2010-10-27 2011-07-15 Reduced-pressure systems, dressings, and methods employing a wireless pump
JP2013536610A JP5843296B2 (en) 2010-10-27 2011-07-15 Pressure reducing system, dressing and method using wireless pump

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US40719410P 2010-10-27 2010-10-27
US61/407,194 2010-10-27
US41873010P 2010-12-01 2010-12-01
US61/418,730 2010-12-01
US201161445338P 2011-02-22 2011-02-22
US201161445383P 2011-02-22 2011-02-22
US61/445,338 2011-02-22
US61/445,383 2011-02-22

Publications (1)

Publication Number Publication Date
WO2012057881A1 true WO2012057881A1 (en) 2012-05-03

Family

ID=45994285

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US2011/044189 WO2012057882A1 (en) 2010-10-27 2011-07-15 Interactive, wireless reduced-pressure dressings, methods, and systems
PCT/US2011/044187 WO2012057881A1 (en) 2010-10-27 2011-07-15 Reduced-pressure systems, dressings, and methods employing a wireless pump

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PCT/US2011/044189 WO2012057882A1 (en) 2010-10-27 2011-07-15 Interactive, wireless reduced-pressure dressings, methods, and systems

Country Status (8)

Country Link
US (3) US20120109034A1 (en)
EP (2) EP2632406B1 (en)
JP (2) JP2014500739A (en)
CN (2) CN103179929A (en)
AU (2) AU2011320911B2 (en)
CA (2) CA2814742A1 (en)
TW (2) TW201217021A (en)
WO (2) WO2012057882A1 (en)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013149078A1 (en) * 2012-03-28 2013-10-03 Kci Licensing, Inc. Reduced-pressure systems, dressings, and methods facilitating separation of electronic and clinical component parts
WO2014004701A1 (en) * 2012-06-28 2014-01-03 Kci Licensing, Inc. Wound connection pad with rfid and integrated strain gauge pressure sensor
WO2014066057A1 (en) * 2012-10-25 2014-05-01 Kci Licensing, Inc. Wound connection pad with pneumatic connection confirmation ability
WO2016107775A3 (en) * 2014-12-29 2016-08-25 Smith & Nephew Plc Negative pressure wound therapy apparatus and method of operating the apparatus
WO2017142874A3 (en) * 2016-02-16 2017-10-12 Insera Therapeutics, Inc. Aspiration devices and anchored flow diverting devices
WO2017186771A1 (en) * 2016-04-26 2017-11-02 Smith & Nephew Plc Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component
US9833251B2 (en) 2013-03-15 2017-12-05 Insera Therapeutics, Inc. Variably bulbous vascular treatment devices
US9901435B2 (en) 2013-03-15 2018-02-27 Insera Therapeutics, Inc. Longitudinally variable vascular treatment devices
WO2018064077A3 (en) * 2016-09-29 2018-05-11 Smith & Nephew, Inc. Construction and protection of components in negative pressure wound therapy systems
WO2018108724A1 (en) * 2016-12-12 2018-06-21 Smith & Nephew Plc Pressure wound therapy status indication via external device
WO2018108784A1 (en) * 2016-12-12 2018-06-21 Smith & Nephew Plc Wound dressing
EP3473218A1 (en) * 2017-10-23 2019-04-24 KCI Licensing, Inc. Area management of tissue sites on articulating joints
USD847866S1 (en) 2018-01-22 2019-05-07 Insera Therapeutics, Inc. Pump
WO2020139475A3 (en) * 2018-12-26 2020-08-20 Kci Licensing, Inc. Piezoelectric pump adapter for negative-pressure therapy
US10779993B2 (en) 2016-05-09 2020-09-22 Convatec Technologies Inc. Negative pressure wound dressing management system
EP3174570B1 (en) * 2014-07-31 2021-03-17 Smith & Nephew, Inc Inventory management and location tracking of medical devices
US11266774B2 (en) 2016-07-08 2022-03-08 Convatec Technologies Inc. Fluid collection apparatus
US11452808B2 (en) 2016-07-08 2022-09-27 Convatec Technologies Inc. Fluid flow sensing
US11554206B2 (en) 2018-02-01 2023-01-17 Kci Licensing, Inc. Negative pressure wound therapy device using a vacuum generating pump providing audible therapy feedback
US11596554B2 (en) 2016-07-08 2023-03-07 Convatec Technologies Inc. Flexible negative pressure system
US11707564B2 (en) 2017-11-01 2023-07-25 Smith & Nephew Plc Safe operation of integrated negative pressure wound treatment apparatuses
US11974903B2 (en) 2017-03-07 2024-05-07 Smith & Nephew, Inc. Reduced pressure therapy systems and methods including an antenna
US12121420B2 (en) 2022-03-02 2024-10-22 Smith & Nephew Plc Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component

Families Citing this family (115)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2604623C (en) 2006-09-28 2018-10-30 Tyco Healthcare Group Lp Portable wound therapy system
CA2705896C (en) 2007-11-21 2019-01-08 Smith & Nephew Plc Wound dressing
BRPI0906095A2 (en) 2008-03-05 2016-06-21 Kci Licensing Inc reduced pressure dressing to apply a reduced pressure treatment to a tissue site, method for collecting fluid in a bandage positioned at a tissue site and a reduced pressure dressing adapted to deliver a reduced pressure to a tissue site.
US8814842B2 (en) 2010-03-16 2014-08-26 Kci Licensing, Inc. Delivery-and-fluid-storage bridges for use with reduced-pressure systems
US9265665B2 (en) * 2010-07-19 2016-02-23 Kci Licensing, Inc. Inflatable off-loading wound dressing assemblies, systems, and methods
GB201015656D0 (en) 2010-09-20 2010-10-27 Smith & Nephew Pressure control apparatus
AU2011316599B2 (en) 2010-10-12 2018-09-20 Smith & Nephew, Inc. Medical device
US9084845B2 (en) 2011-11-02 2015-07-21 Smith & Nephew Plc Reduced pressure therapy apparatuses and methods of using same
EP3005997B1 (en) 2011-12-16 2024-06-26 Solventum Intellectual Properties Company Releasable medical drapes
US10940047B2 (en) 2011-12-16 2021-03-09 Kci Licensing, Inc. Sealing systems and methods employing a hybrid switchable drape
EP2812577B1 (en) * 2012-02-10 2017-09-06 KCI Licensing, Inc. Systems and methods for monitoring a disc pump system using rfid
EP3708196A1 (en) 2012-03-12 2020-09-16 Smith & Nephew PLC Reduced pressure apparatus and methods
US9024751B2 (en) * 2012-04-12 2015-05-05 Elwha Llc Dormant to active appurtenances for reporting information regarding wound dressings
US9084530B2 (en) * 2012-04-12 2015-07-21 Elwha Llc Computational methods and systems for reporting information regarding appurtenances to wound dressings
US10265219B2 (en) * 2012-04-12 2019-04-23 Elwha Llc Wound dressing monitoring systems including appurtenances for wound dressings
US10158928B2 (en) 2012-04-12 2018-12-18 Elwha Llc Appurtenances for reporting information regarding wound dressings
US10130518B2 (en) * 2012-04-12 2018-11-20 Elwha Llc Appurtenances including sensors for reporting information regarding wound dressings
WO2013155199A1 (en) * 2012-04-12 2013-10-17 Elwha Llc Computational methods and systems for reporting information regarding appurtenances to wound dressings
US10226212B2 (en) * 2012-04-12 2019-03-12 Elwha Llc Appurtenances to cavity wound dressings
US9427505B2 (en) 2012-05-15 2016-08-30 Smith & Nephew Plc Negative pressure wound therapy apparatus
MX2014014266A (en) 2012-05-22 2015-06-23 Smith & Nephew Apparatuses and methods for wound therapy.
KR20150085837A (en) 2012-11-16 2015-07-24 케이씨아이 라이센싱 인코포레이티드 Medical drafe with pattern adhesive layers and method of manufacturing same
EP3081199B1 (en) * 2013-01-03 2019-10-30 KCI Licensing, Inc. Moisture absorbing seal
MX2015011812A (en) 2013-03-14 2016-07-05 Smith & Nephew Inc Systems and methods for applying reduced pressure therapy.
US9737649B2 (en) 2013-03-14 2017-08-22 Smith & Nephew, Inc. Systems and methods for applying reduced pressure therapy
EP3052156B1 (en) * 2013-10-02 2020-12-23 3M Innovative Properties Company Diposable reduced-pressure therapy system with electronic feedback
WO2015065742A1 (en) 2013-10-28 2015-05-07 Kci Licensing, Inc. Hybrid sealing tape
EP3257486B1 (en) 2013-10-30 2019-06-05 KCI Licensing, Inc. Condensate absorbing and dissipating system
EP3744361B1 (en) 2013-10-30 2024-07-24 Solventum Intellectual Properties Company Absorbent conduit and system
EP3173054B1 (en) 2013-10-30 2018-04-25 KCI Licensing, Inc. Dressing with diffrentially sized perforations
US9956120B2 (en) 2013-10-30 2018-05-01 Kci Licensing, Inc. Dressing with sealing and retention interface
US11026844B2 (en) * 2014-03-03 2021-06-08 Kci Licensing, Inc. Low profile flexible pressure transmission conduit
EP3151795B1 (en) 2014-06-05 2017-09-27 KCI Licensing, Inc. Dressing with fluid acquisition and distribution characteristics
US10031582B2 (en) 2014-06-05 2018-07-24 Immersion Corporation Systems and methods for induced electrostatic haptic effects
WO2016006457A1 (en) * 2014-07-07 2016-01-14 株式会社村田製作所 Negative-pressure closure therapy device
WO2016008154A1 (en) * 2014-07-18 2016-01-21 科际精密股份有限公司 Negative pressure wound therapy apparatus
US9770369B2 (en) 2014-08-08 2017-09-26 Neogenix, Llc Wound care devices, apparatus, and treatment methods
AU2015370583B2 (en) 2014-12-22 2020-08-20 Smith & Nephew Plc Negative pressure wound therapy apparatus and methods
CN107530531B (en) 2015-04-27 2021-07-13 史密夫及内修公开有限公司 Pressure reducing device
EP3294245B1 (en) 2015-05-08 2019-09-04 KCI Licensing, Inc. Low acuity dressing with integral pump
EP3117807A1 (en) * 2015-07-16 2017-01-18 Carag AG Multifunctional wound treatment dressing
PE20180755A1 (en) 2015-07-29 2018-05-03 Innovative Therapies Inc WOUND THERAPY DEVICE PRESSURE MONITORING AND CONTROL SYSTEM
US9922525B2 (en) * 2015-08-14 2018-03-20 Gregory J. Hummer Monitoring system for use with mobile communication device
EP3344205B1 (en) 2015-09-01 2020-09-30 KCI Licensing, Inc. Dressing with increased apposition force
EP3349807B1 (en) 2015-09-17 2021-02-24 3M Innovative Properties Company Hybrid silicone and acrylic adhesive cover for use with wound treatment
EP3360063A1 (en) 2015-10-07 2018-08-15 Smith & Nephew, Inc Systems and methods for applying reduced pressure therapy
EP3389525B1 (en) * 2015-12-14 2022-02-02 Buffalo Filter LLC Method and apparatus for attachment and evacuation
US9928696B2 (en) 2015-12-30 2018-03-27 Immersion Corporation Externally-activated haptic devices and systems
JP6911043B2 (en) 2016-03-07 2021-07-28 スミス アンド ネフュー ピーエルシーSmith & Nephew Public Limited Company Wound healing devices and methods in which the negative pressure source is integrated within the wound dressing
US11311231B2 (en) * 2016-03-29 2022-04-26 Walgreen Health Solutions, Llc Dressing assembly
US11305047B2 (en) 2016-05-03 2022-04-19 Smith & Nephew Plc Systems and methods for driving negative pressure sources in negative pressure therapy systems
US11096831B2 (en) 2016-05-03 2021-08-24 Smith & Nephew Plc Negative pressure wound therapy device activation and control
CA3038206A1 (en) 2016-05-03 2017-11-09 Smith & Nephew Plc Optimizing power transfer to negative pressure sources in negative pressure therapy systems
WO2017195038A1 (en) 2016-05-13 2017-11-16 Smith & Nephew Plc Sensor enabled wound monitoring and therapy apparatus
US11602461B2 (en) 2016-05-13 2023-03-14 Smith & Nephew, Inc. Automatic wound coupling detection in negative pressure wound therapy systems
CA3034789A1 (en) 2016-08-25 2018-03-01 Smith & Nephew Plc Absorbent negative pressure wound therapy dressing
US11096832B2 (en) * 2016-09-27 2021-08-24 Smith & Nephew Plc Wound closure devices with dissolvable portions
GB201811494D0 (en) * 2018-07-13 2018-08-29 Smith & Nephew Inter-device communications and device control in wound therapy systems
EP3519001A1 (en) 2016-09-30 2019-08-07 Smith & Nephew PLC Negative pressure wound treatment apparatuses and methods with integrated electronics
TWI629072B (en) * 2017-01-13 2018-07-11 廈門聖慈醫療器材有限公司 Suction disc
CA3053299A1 (en) 2017-02-15 2018-08-23 Smith & Nephew Pte. Limited Negative pressure wound therapy apparatuses and methods for using the same
WO2018156730A1 (en) * 2017-02-22 2018-08-30 Cornell University Mechanical vacuum dressing for mechanically managing, protecting and suctioning small incisional wounds
WO2018162613A1 (en) 2017-03-08 2018-09-13 Smith & Nephew Plc Negative pressure wound therapy device control in presence of fault condition
WO2018162736A1 (en) 2017-03-09 2018-09-13 Smith & Nephew Plc Wound dressing, patch member and method of sensing one or more wound parameters
US11324424B2 (en) 2017-03-09 2022-05-10 Smith & Nephew Plc Apparatus and method for imaging blood in a target region of tissue
US11883262B2 (en) 2017-04-11 2024-01-30 Smith & Nephew Plc Component positioning and stress relief for sensor enabled wound dressings
AU2018265052B2 (en) 2017-05-09 2023-08-31 Smith & Nephew Plc Redundant controls for negative pressure wound therapy systems
WO2018210693A1 (en) 2017-05-15 2018-11-22 Smith & Nephew Plc Negative pressure wound therapy system using eulerian video magnification
EP3635732A1 (en) 2017-05-15 2020-04-15 Smith & Nephew plc Wound analysis device and method
WO2018229008A1 (en) * 2017-06-14 2018-12-20 Smith & Nephew Plc Negative pressure wound therapy apparatus
DE202018006806U1 (en) 2017-06-15 2023-01-30 Chiaro Technology Limited breast pump system
EP3641627B1 (en) 2017-06-23 2023-05-31 Smith & Nephew PLC Positioning of sensors for sensor enabled wound monitoring or therapy
US11712508B2 (en) 2017-07-10 2023-08-01 Smith & Nephew, Inc. Systems and methods for directly interacting with communications module of wound therapy apparatus
GB201809007D0 (en) 2018-06-01 2018-07-18 Smith & Nephew Restriction of sensor-monitored region for sensor-enabled wound dressings
GB201804502D0 (en) 2018-03-21 2018-05-02 Smith & Nephew Biocompatible encapsulation and component stress relief for sensor enabled negative pressure wound therapy dressings
CN111093726B (en) 2017-08-10 2023-11-17 史密夫及内修公开有限公司 Sensor positioning for performing wound monitoring or treatment of sensors
GB201804971D0 (en) 2018-03-28 2018-05-09 Smith & Nephew Electrostatic discharge protection for sensors in wound therapy
GB201718870D0 (en) 2017-11-15 2017-12-27 Smith & Nephew Inc Sensor enabled wound therapy dressings and systems
EP3681376A1 (en) 2017-09-10 2020-07-22 Smith & Nephew PLC Systems and methods for inspection of encapsulation and components in sensor equipped wound dressings
US11701265B2 (en) 2017-09-13 2023-07-18 Smith & Nephew Plc Negative pressure wound treatment apparatuses and methods with integrated electronics
GB201718070D0 (en) 2017-11-01 2017-12-13 Smith & Nephew Negative pressure wound treatment apparatuses and methods with integrated electronics
GB201718859D0 (en) 2017-11-15 2017-12-27 Smith & Nephew Sensor positioning for sensor enabled wound therapy dressings and systems
EP3687380A1 (en) 2017-09-27 2020-08-05 Smith & Nephew plc Ph sensing for sensor enabled negative pressure wound monitoring and therapy apparatuses
EP3687396A1 (en) 2017-09-28 2020-08-05 Smith & Nephew plc Neurostimulation and monitoring using sensor enabled wound monitoring and therapy apparatus
GB201718072D0 (en) 2017-11-01 2017-12-13 Smith & Nephew Negative pressure wound treatment apparatuses and methods with integrated electronics
EP3703632B1 (en) 2017-11-01 2024-04-03 Smith & Nephew plc Negative pressure wound treatment apparatuses and methods with integrated electronics
JP2021502845A (en) 2017-11-15 2021-02-04 スミス アンド ネフュー ピーエルシーSmith & Nephew Public Limited Company Integrated sensor-enabled wound monitoring and / or treatment coverings and systems
US11839527B2 (en) 2017-12-06 2023-12-12 Cornell University Manually-operated negative pressure wound therapy (NPWT) bandage with improved pump efficiency, automatic pressure indicator and automatic pressure limiter
GB201813282D0 (en) * 2018-08-15 2018-09-26 Smith & Nephew System for medical device activation and opertion
EP3735278A1 (en) * 2018-01-02 2020-11-11 KCI Licensing, Inc. Negative pressure wound therapy device with silent piezoelectric pump
US10624794B2 (en) 2018-02-12 2020-04-21 Healyx Labs, Inc. Negative pressure wound therapy systems, devices, and methods
GB201804347D0 (en) 2018-03-19 2018-05-02 Smith & Nephew Inc Securing control of settings of negative pressure wound therapy apparatuses and methods for using the same
GB201805584D0 (en) * 2018-04-05 2018-05-23 Smith & Nephew Negative pressure wound treatment apparatuses and methods with integrated electronics
GB201806988D0 (en) 2018-04-30 2018-06-13 Quintanar Felix Clarence Power source charging for negative pressure wound therapy apparatus
EP3787704A1 (en) 2018-04-30 2021-03-10 Smith & Nephew Asia Pacific Pte Limited Systems and methods for controlling dual mode negative pressure wound therapy apparatus
GB201808438D0 (en) 2018-05-23 2018-07-11 Smith & Nephew Systems and methods for determining blockages in a negative pressure wound therapy system
WO2020005577A1 (en) * 2018-06-28 2020-01-02 Kci Licensing, Inc. Distributed negative pressure wound therapy system incorporating an absorbent dressing and piezo-electric pump
EP3849401A1 (en) 2018-09-12 2021-07-21 Smith & Nephew plc Device, apparatus and method of determining skin perfusion pressure
USD898925S1 (en) 2018-09-13 2020-10-13 Smith & Nephew Plc Medical dressing
GB201820668D0 (en) 2018-12-19 2019-01-30 Smith & Nephew Inc Systems and methods for delivering prescribed wound therapy
GB201820927D0 (en) 2018-12-21 2019-02-06 Smith & Nephew Wound therapy systems and methods with supercapacitors
US12082997B2 (en) * 2019-01-29 2024-09-10 Kci Licensing, Inc. Removable and replaceable dressing interface for a negative-pressure therapy system
GB2614490B (en) 2019-03-18 2023-12-06 Smith & Nephew Design rules for sensor integrated substrates
GB201903778D0 (en) * 2019-03-20 2019-05-01 Smith & Nephew Exhaust blockage detection for negative pressure wound treatment apparatuses
GB201903774D0 (en) 2019-03-20 2019-05-01 Smith & Nephew Negative pressure wound treatment apparatuses and methods with integrated electronics
WO2020197759A1 (en) * 2019-03-25 2020-10-01 Kci Licensing, Inc. Systems and methods for sensing ph of fluids on wound tissue interface
KR102238777B1 (en) * 2019-04-02 2021-04-09 한국광기술원 Wearable wound treatment device
GB201907716D0 (en) 2019-05-31 2019-07-17 Smith & Nephew Systems and methods for extending operational time of negative pressure wound treatment apparatuses
US11484640B2 (en) 2019-07-03 2022-11-01 T.J.Smith And Nephew, Limited Negative pressure wound therapy dressing recognition, wound status detection, and therapy adjustment
GB201914443D0 (en) 2019-10-07 2019-11-20 Smith & Nephew Sensor enabled negative pressure wound monitoring apparatus with different impedances inks
US11878104B2 (en) * 2020-02-20 2024-01-23 Convatec Limited Wound dressing and a wound therapy apparatus
GB202002339D0 (en) * 2020-02-20 2020-04-08 Convatec Ltd A wound dressing and a wound therapy apparatus
GB202004395D0 (en) 2020-03-26 2020-05-13 Chiaro Technology Ltd Lima
US20240024565A1 (en) * 2020-10-05 2024-01-25 T.J.Smith And Nephew,Limited Temperature monitoring and control for negative pressure wound therapy systems
WO2023227975A1 (en) * 2022-05-24 2023-11-30 3M Innovative Properties Company Modular negative pressure wound therapy systems

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020032508A (en) * 2002-04-16 2002-05-03 주식회사 코스모지놈 An adhesive infusion pump contoled by wireless remote control
WO2008051924A2 (en) * 2006-10-23 2008-05-02 Abbott Diabetes Care, Inc. Flexible patch for fluid delivery and monitoring body analytes
US20090087323A1 (en) 2005-04-22 2009-04-02 David Mark Blakey Pump
US20090227969A1 (en) * 2008-03-05 2009-09-10 Jonathan Paul Jaeb Dressing and method for applying reduced pressure to and collecting and storing fluid from a tissue site

Family Cites Families (148)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1355846A (en) 1920-02-06 1920-10-19 David A Rannells Medical appliance
US2547758A (en) 1949-01-05 1951-04-03 Wilmer B Keeling Instrument for treating the male urethra
US2632443A (en) 1949-04-18 1953-03-24 Eleanor P Lesher Surgical dressing
GB692578A (en) 1949-09-13 1953-06-10 Minnesota Mining & Mfg Improvements in or relating to drape sheets for surgical use
US2682873A (en) 1952-07-30 1954-07-06 Johnson & Johnson General purpose protective dressing
NL189176B (en) 1956-07-13 1900-01-01 Hisamitsu Pharmaceutical Co PLASTER BASED ON A SYNTHETIC RUBBER.
US2969057A (en) 1957-11-04 1961-01-24 Brady Co W H Nematodic swab
US3066672A (en) 1960-09-27 1962-12-04 Jr William H Crosby Method and apparatus for serial sampling of intestinal juice
US3367332A (en) 1965-08-27 1968-02-06 Gen Electric Product and process for establishing a sterile area of skin
US3520300A (en) 1967-03-15 1970-07-14 Amp Inc Surgical sponge and suction device
US3568675A (en) 1968-08-30 1971-03-09 Clyde B Harvey Fistula and penetrating wound dressing
US3682180A (en) 1970-06-08 1972-08-08 Coilform Co Inc Drain clip for surgical drain
BE789293Q (en) 1970-12-07 1973-01-15 Parke Davis & Co MEDICO-SURGICAL DRESSING FOR BURNS AND SIMILAR LESIONS
US3826254A (en) 1973-02-26 1974-07-30 Verco Ind Needle or catheter retaining appliance
DE2527706A1 (en) 1975-06-21 1976-12-30 Hanfried Dr Med Weigand DEVICE FOR THE INTRODUCTION OF CONTRAST AGENTS INTO AN ARTIFICIAL INTESTINAL OUTLET
DE2640413C3 (en) 1976-09-08 1980-03-27 Richard Wolf Gmbh, 7134 Knittlingen Catheter monitor
NL7710909A (en) 1976-10-08 1978-04-11 Smith & Nephew COMPOSITE STRAPS.
GB1562244A (en) 1976-11-11 1980-03-05 Lock P M Wound dressing materials
US4080970A (en) 1976-11-17 1978-03-28 Miller Thomas J Post-operative combination dressing and internal drain tube with external shield and tube connector
US4139004A (en) 1977-02-17 1979-02-13 Gonzalez Jr Harry Bandage apparatus for treating burns
US4184510A (en) 1977-03-15 1980-01-22 Fibra-Sonics, Inc. Valued device for controlling vacuum in surgery
US4165748A (en) 1977-11-07 1979-08-28 Johnson Melissa C Catheter tube holder
US4245637A (en) 1978-07-10 1981-01-20 Nichols Robert L Shutoff valve sleeve
SE414994B (en) 1978-11-28 1980-09-01 Landstingens Inkopscentral VENKATETERFORBAND
DE2953373A1 (en) 1978-12-06 1981-01-08 P Svedman Device for treating tissues,for example skin
US4266545A (en) 1979-04-06 1981-05-12 Moss James P Portable suction device for collecting fluids from a closed wound
US4284079A (en) 1979-06-28 1981-08-18 Adair Edwin Lloyd Method for applying a male incontinence device
US4261363A (en) 1979-11-09 1981-04-14 C. R. Bard, Inc. Retention clips for body fluid drains
US4569348A (en) 1980-02-22 1986-02-11 Velcro Usa Inc. Catheter tube holder strap
EP0035583B1 (en) 1980-03-11 1985-08-14 Schmid, Eduard, Dr.Dr.med. Skin graft pressure bandage
US4297995A (en) 1980-06-03 1981-11-03 Key Pharmaceuticals, Inc. Bandage containing attachment post
US4333468A (en) 1980-08-18 1982-06-08 Geist Robert W Mesentery tube holder apparatus
US4465485A (en) 1981-03-06 1984-08-14 Becton, Dickinson And Company Suction canister with unitary shut-off valve and filter features
US4392853A (en) 1981-03-16 1983-07-12 Rudolph Muto Sterile assembly for protecting and fastening an indwelling device
US4373519A (en) 1981-06-26 1983-02-15 Minnesota Mining And Manufacturing Company Composite wound dressing
US4392858A (en) 1981-07-16 1983-07-12 Sherwood Medical Company Wound drainage device
US4419097A (en) 1981-07-31 1983-12-06 Rexar Industries, Inc. Attachment for catheter tube
AU550575B2 (en) 1981-08-07 1986-03-27 Richard Christian Wright Wound drainage device
SE429197B (en) 1981-10-14 1983-08-22 Frese Nielsen SAR TREATMENT DEVICE
DE3146266A1 (en) 1981-11-21 1983-06-01 B. Braun Melsungen Ag, 3508 Melsungen COMBINED DEVICE FOR A MEDICAL SUCTION DRAINAGE
US4551139A (en) 1982-02-08 1985-11-05 Marion Laboratories, Inc. Method and apparatus for burn wound treatment
US4475909A (en) 1982-05-06 1984-10-09 Eisenberg Melvin I Male urinary device and method for applying the device
DE3361779D1 (en) 1982-07-06 1986-02-20 Dow Corning Medical-surgical dressing and a process for the production thereof
NZ206837A (en) 1983-01-27 1986-08-08 Johnson & Johnson Prod Inc Thin film adhesive dressing:backing material in three sections
US4548202A (en) 1983-06-20 1985-10-22 Ethicon, Inc. Mesh tissue fasteners
US4540412A (en) 1983-07-14 1985-09-10 The Kendall Company Device for moist heat therapy
US4543100A (en) 1983-11-01 1985-09-24 Brodsky Stuart A Catheter and drain tube retainer
US4525374A (en) 1984-02-27 1985-06-25 Manresa, Inc. Treating hydrophobic filters to render them hydrophilic
GB2157958A (en) 1984-05-03 1985-11-06 Ernest Edward Austen Bedding Ball game net support
US4897081A (en) 1984-05-25 1990-01-30 Thermedics Inc. Percutaneous access device
US5215522A (en) 1984-07-23 1993-06-01 Ballard Medical Products Single use medical aspirating device and method
GB8419745D0 (en) 1984-08-02 1984-09-05 Smith & Nephew Ass Wound dressing
US4872450A (en) 1984-08-17 1989-10-10 Austad Eric D Wound dressing and method of forming same
US4655754A (en) 1984-11-09 1987-04-07 Stryker Corporation Vacuum wound drainage system and lipids baffle therefor
US4826494A (en) 1984-11-09 1989-05-02 Stryker Corporation Vacuum wound drainage system
US4605399A (en) 1984-12-04 1986-08-12 Complex, Inc. Transdermal infusion device
US5037397A (en) 1985-05-03 1991-08-06 Medical Distributors, Inc. Universal clamp
US4640688A (en) 1985-08-23 1987-02-03 Mentor Corporation Urine collection catheter
US4710165A (en) 1985-09-16 1987-12-01 Mcneil Charles B Wearable, variable rate suction/collection device
US4758220A (en) 1985-09-26 1988-07-19 Alcon Laboratories, Inc. Surgical cassette proximity sensing and latching apparatus
US4733659A (en) 1986-01-17 1988-03-29 Seton Company Foam bandage
WO1987004626A1 (en) 1986-01-31 1987-08-13 Osmond, Roger, L., W. Suction system for wound and gastro-intestinal drainage
US4838883A (en) 1986-03-07 1989-06-13 Nissho Corporation Urine-collecting device
JPS62281965A (en) 1986-05-29 1987-12-07 テルモ株式会社 Catheter and catheter fixing member
GB8621884D0 (en) 1986-09-11 1986-10-15 Bard Ltd Catheter applicator
GB2195255B (en) 1986-09-30 1991-05-01 Vacutec Uk Limited Apparatus for vacuum treatment of an epidermal surface
US4743232A (en) 1986-10-06 1988-05-10 The Clinipad Corporation Package assembly for plastic film bandage
DE3634569A1 (en) 1986-10-10 1988-04-21 Sachse Hans E CONDOM CATHETER, A URINE TUBE CATHETER FOR PREVENTING RISING INFECTIONS
JPS63135179A (en) 1986-11-26 1988-06-07 立花 俊郎 Subcataneous drug administration set
GB8628564D0 (en) 1986-11-28 1987-01-07 Smiths Industries Plc Anti-foaming agent suction apparatus
GB8706116D0 (en) 1987-03-14 1987-04-15 Smith & Nephew Ass Adhesive dressings
US4787888A (en) 1987-06-01 1988-11-29 University Of Connecticut Disposable piezoelectric polymer bandage for percutaneous delivery of drugs and method for such percutaneous delivery (a)
US4863449A (en) 1987-07-06 1989-09-05 Hollister Incorporated Adhesive-lined elastic condom cathether
US5176663A (en) 1987-12-02 1993-01-05 Pal Svedman Dressing having pad with compressibility limiting elements
US4906240A (en) 1988-02-01 1990-03-06 Matrix Medica, Inc. Adhesive-faced porous absorbent sheet and method of making same
US4985019A (en) 1988-03-11 1991-01-15 Michelson Gary K X-ray marker
GB8812803D0 (en) 1988-05-28 1988-06-29 Smiths Industries Plc Medico-surgical containers
US4919654A (en) 1988-08-03 1990-04-24 Kalt Medical Corporation IV clamp with membrane
US5000741A (en) 1988-08-22 1991-03-19 Kalt Medical Corporation Transparent tracheostomy tube dressing
DE69017479T2 (en) 1989-01-16 1995-07-13 Roussel Uclaf Azabicyclohepten derivatives and their salts, processes for their preparation, their use as medicaments and preparations containing them.
GB8906100D0 (en) 1989-03-16 1989-04-26 Smith & Nephew Laminates
US5261893A (en) 1989-04-03 1993-11-16 Zamierowski David S Fastening system and method
US5100396A (en) 1989-04-03 1992-03-31 Zamierowski David S Fluidic connection system and method
US5527293A (en) 1989-04-03 1996-06-18 Kinetic Concepts, Inc. Fastening system and method
US4969880A (en) 1989-04-03 1990-11-13 Zamierowski David S Wound dressing and treatment method
US5358494A (en) 1989-07-11 1994-10-25 Svedman Paul Irrigation dressing
JP2719671B2 (en) 1989-07-11 1998-02-25 日本ゼオン株式会社 Wound dressing
US5232453A (en) 1989-07-14 1993-08-03 E. R. Squibb & Sons, Inc. Catheter holder
GB2235877A (en) 1989-09-18 1991-03-20 Antonio Talluri Closed wound suction apparatus
US5134994A (en) 1990-02-12 1992-08-04 Say Sam L Field aspirator in a soft pack with externally mounted container
US5092858A (en) 1990-03-20 1992-03-03 Becton, Dickinson And Company Liquid gelling agent distributor device
US5149331A (en) 1991-05-03 1992-09-22 Ariel Ferdman Method and device for wound closure
US5278100A (en) 1991-11-08 1994-01-11 Micron Technology, Inc. Chemical vapor deposition technique for depositing titanium silicide on semiconductor wafers
US5636643A (en) 1991-11-14 1997-06-10 Wake Forest University Wound treatment employing reduced pressure
US5645081A (en) 1991-11-14 1997-07-08 Wake Forest University Method of treating tissue damage and apparatus for same
US5279550A (en) 1991-12-19 1994-01-18 Gish Biomedical, Inc. Orthopedic autotransfusion system
US5167613A (en) 1992-03-23 1992-12-01 The Kendall Company Composite vented wound dressing
FR2690617B1 (en) 1992-04-29 1994-06-24 Cbh Textile TRANSPARENT ADHESIVE DRESSING.
DE4306478A1 (en) 1993-03-02 1994-09-08 Wolfgang Dr Wagner Drainage device, in particular pleural drainage device, and drainage method
US6241747B1 (en) 1993-05-03 2001-06-05 Quill Medical, Inc. Barbed Bodily tissue connector
US5342376A (en) 1993-05-03 1994-08-30 Dermagraphics, Inc. Inserting device for a barbed tissue connector
US5344415A (en) 1993-06-15 1994-09-06 Deroyal Industries, Inc. Sterile system for dressing vascular access site
US5437651A (en) 1993-09-01 1995-08-01 Research Medical, Inc. Medical suction apparatus
US5549584A (en) 1994-02-14 1996-08-27 The Kendall Company Apparatus for removing fluid from a wound
US5607388A (en) 1994-06-16 1997-03-04 Hercules Incorporated Multi-purpose wound dressing
US5556375A (en) 1994-06-16 1996-09-17 Hercules Incorporated Wound dressing having a fenestrated base layer
US5664270A (en) 1994-07-19 1997-09-09 Kinetic Concepts, Inc. Patient interface system
ES2223977T3 (en) 1994-08-22 2005-03-01 Kci Licensing, Inc. CONTAINER.
US8280682B2 (en) * 2000-12-15 2012-10-02 Tvipr, Llc Device for monitoring movement of shipped goods
DE29504378U1 (en) 1995-03-15 1995-09-14 MTG Medizinisch, technische Gerätebau GmbH, 66299 Friedrichsthal Electronically controlled low-vacuum pump for chest and wound drainage
GB9523253D0 (en) 1995-11-14 1996-01-17 Mediscus Prod Ltd Portable wound treatment apparatus
US6135116A (en) 1997-07-28 2000-10-24 Kci Licensing, Inc. Therapeutic method for treating ulcers
GB9719520D0 (en) 1997-09-12 1997-11-19 Kci Medical Ltd Surgical drape and suction heads for wound treatment
AU755496B2 (en) 1997-09-12 2002-12-12 Kci Licensing, Inc. Surgical drape and suction head for wound treatment
US6071267A (en) 1998-02-06 2000-06-06 Kinetic Concepts, Inc. Medical patient fluid management interface system and method
US6488643B1 (en) 1998-10-08 2002-12-03 Kci Licensing, Inc. Wound healing foot wrap
US6287316B1 (en) 1999-03-26 2001-09-11 Ethicon, Inc. Knitted surgical mesh
US7799004B2 (en) 2001-03-05 2010-09-21 Kci Licensing, Inc. Negative pressure wound treatment apparatus and infection identification system and method
US6856821B2 (en) 2000-05-26 2005-02-15 Kci Licensing, Inc. System for combined transcutaneous blood gas monitoring and vacuum assisted wound closure
US6991643B2 (en) 2000-12-20 2006-01-31 Usgi Medical Inc. Multi-barbed device for retaining tissue in apposition and methods of use
AU4176101A (en) 2000-02-24 2001-09-03 Venetec Int Inc Universal catheter anchoring system
US6540705B2 (en) 2001-02-22 2003-04-01 Core Products International, Inc. Ankle brace providing upper and lower ankle adjustment
EP1343112A1 (en) * 2002-03-08 2003-09-10 EndoArt S.A. Implantable device
US20040073177A1 (en) * 2002-05-16 2004-04-15 Scott Laboratories, Inc. Kits of medical supplies for sedation and analgesia
EP2650028B1 (en) * 2002-05-31 2017-08-09 KCI Medical Resources Wound treatment apparatus
DE20213196U1 (en) * 2002-08-28 2004-01-15 Campus Micro Technologies Gmbh Device for measuring and monitoring local pressure loads acting on the human body
US7976519B2 (en) 2002-12-31 2011-07-12 Kci Licensing, Inc. Externally-applied patient interface system and method
GB0408492D0 (en) * 2004-04-16 2004-05-19 Univ Strathclyde Performance measurement of wound dressings
US7191013B1 (en) 2004-11-08 2007-03-13 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Hand held device for wireless powering and interrogation of biomems sensors and actuators
WO2007002154A2 (en) * 2005-06-21 2007-01-04 Medrad, Inc. Medical fluid injection and inflation system
CN101257875A (en) * 2005-09-06 2008-09-03 泰科保健集团有限合伙公司 Self contained wound dressing with micropump
WO2007030647A2 (en) * 2005-09-07 2007-03-15 Hydranautics Reverse osmosis filtration devices with rfid tag-powered flow and conductivity meters
AU2006287461A1 (en) * 2005-09-07 2007-03-15 Tyco Healthcare Group L.P. Self contained wound dressing apparatus
US8083710B2 (en) * 2006-03-09 2011-12-27 The Invention Science Fund I, Llc Acoustically controlled substance delivery device
JP5076167B2 (en) * 2005-11-09 2012-11-21 ザ インベンション サイエンス ファンド アイ,エルエルシー Osmotic pump with remotely controlled osmotic pressure generation
US7779625B2 (en) * 2006-05-11 2010-08-24 Kalypto Medical, Inc. Device and method for wound therapy
US20080041401A1 (en) * 2006-08-15 2008-02-21 Casola Robert P Computer adjusted pressure wound care devices, systems & methods
CA2604623C (en) * 2006-09-28 2018-10-30 Tyco Healthcare Group Lp Portable wound therapy system
DK2242522T3 (en) 2008-01-08 2012-06-18 Bluesky Medical Group Inc Wound treatment with uninterrupted variable pressure and methods for controlling it
WO2009093116A1 (en) * 2008-01-25 2009-07-30 The University Of Cape Town Wound dressing system and method
KR100916616B1 (en) * 2008-02-27 2009-09-14 인하대학교 산학협력단 Medical treatment bandage made with cellulose-chitosan composit film, RFID sensor and biosensor, and Method thereof
US8449508B2 (en) * 2008-03-05 2013-05-28 Kci Licensing, Inc. Dressing and method for applying reduced pressure to and collecting and storing fluid from a tissue site
AU2009223037A1 (en) * 2008-03-12 2009-09-17 Smith & Nephew Plc Negative pressure dressing and method of using same
US20090240218A1 (en) * 2008-03-20 2009-09-24 Tyco Healthcare Group Lp Wound Therapy System
JP2011516167A (en) * 2008-04-04 2011-05-26 スリーエム イノベイティブ プロパティズ カンパニー Wound dressing with micropump
US20100022990A1 (en) * 2008-07-25 2010-01-28 Boehringer Technologies, L.P. Pump system for negative pressure wound therapy and improvements thereon
US8486032B2 (en) * 2008-12-24 2013-07-16 Kci Licensing, Inc. Reduced-pressure treatment systems and methods employing debridement mechanisms
US8377018B2 (en) * 2009-12-23 2013-02-19 Kci Licensing, Inc. Reduced-pressure, multi-orientation, liquid-collection canister

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020032508A (en) * 2002-04-16 2002-05-03 주식회사 코스모지놈 An adhesive infusion pump contoled by wireless remote control
US20090087323A1 (en) 2005-04-22 2009-04-02 David Mark Blakey Pump
WO2008051924A2 (en) * 2006-10-23 2008-05-02 Abbott Diabetes Care, Inc. Flexible patch for fluid delivery and monitoring body analytes
US20090227969A1 (en) * 2008-03-05 2009-09-10 Jonathan Paul Jaeb Dressing and method for applying reduced pressure to and collecting and storing fluid from a tissue site
US20090240185A1 (en) 2008-03-05 2009-09-24 Jonathan Paul Jaeb Dressing and method for applying reduced pressure to and collecting and storing fluid from a tissue site

Cited By (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10286129B2 (en) 2012-03-28 2019-05-14 Kci Licensing, Inc. Reduced-pressure systems, dressings, and methods facilitating separation of electronic and clinical component parts
WO2013149078A1 (en) * 2012-03-28 2013-10-03 Kci Licensing, Inc. Reduced-pressure systems, dressings, and methods facilitating separation of electronic and clinical component parts
US10086117B2 (en) 2012-06-28 2018-10-02 Kci Licensing, Inc. Wound connection pad with RFID and integrated strain gauge pressure sensor
WO2014004701A1 (en) * 2012-06-28 2014-01-03 Kci Licensing, Inc. Wound connection pad with rfid and integrated strain gauge pressure sensor
EP3597227A1 (en) * 2012-06-28 2020-01-22 KCI Licensing, Inc. Wound connection pad with rfid and integrated strain gauge pressure sensor
CN104602719A (en) * 2012-06-28 2015-05-06 凯希特许有限公司 Wound connection pad with RFID and integrated strain gauge pressure sensor
AU2013280335B2 (en) * 2012-06-28 2017-06-29 Kci Licensing, Inc. Wound connection pad with RFID and integrated strain gauge pressure sensor
US10773000B2 (en) 2012-10-25 2020-09-15 Kci Licensing, Inc. Wound connection pad with pneumatic connection confirmation ability
EP3964244A1 (en) * 2012-10-25 2022-03-09 3M Innovative Properties Co. Wound connection pad with pneumatic connection confirmation ability
WO2014066057A1 (en) * 2012-10-25 2014-05-01 Kci Licensing, Inc. Wound connection pad with pneumatic connection confirmation ability
CN104853785A (en) * 2012-10-25 2015-08-19 凯希特许有限公司 Wound connection pad with pneumatic connection confirmation ability
US9744278B2 (en) 2012-10-25 2017-08-29 Kci Licensing, Inc. Wound connection pad with pneumatic connection confirmation ability
AU2013335084B2 (en) * 2012-10-25 2018-04-26 Kci Licensing, Inc. Wound connection pad with pneumatic connection confirmation ability
US10251739B2 (en) 2013-03-15 2019-04-09 Insera Therapeutics, Inc. Thrombus aspiration using an operator-selectable suction pattern
US11298144B2 (en) 2013-03-15 2022-04-12 Insera Therapeutics, Inc. Thrombus aspiration facilitation systems
US9901435B2 (en) 2013-03-15 2018-02-27 Insera Therapeutics, Inc. Longitudinally variable vascular treatment devices
US10342655B2 (en) 2013-03-15 2019-07-09 Insera Therapeutics, Inc. Methods of treating a thrombus in an artery using cyclical aspiration patterns
US10463468B2 (en) 2013-03-15 2019-11-05 Insera Therapeutics, Inc. Thrombus aspiration with different intensity levels
US10335260B2 (en) 2013-03-15 2019-07-02 Insera Therapeutics, Inc. Methods of treating a thrombus in a vein using cyclical aspiration patterns
US9833251B2 (en) 2013-03-15 2017-12-05 Insera Therapeutics, Inc. Variably bulbous vascular treatment devices
US10751159B2 (en) 2013-07-29 2020-08-25 Insera Therapeutics, Inc. Systems for aspirating thrombus during neurosurgical procedures
US10390926B2 (en) 2013-07-29 2019-08-27 Insera Therapeutics, Inc. Aspiration devices and methods
EP3174570B1 (en) * 2014-07-31 2021-03-17 Smith & Nephew, Inc Inventory management and location tracking of medical devices
WO2016107775A3 (en) * 2014-12-29 2016-08-25 Smith & Nephew Plc Negative pressure wound therapy apparatus and method of operating the apparatus
US10828403B2 (en) 2014-12-29 2020-11-10 Smith & Nephew Plc Negative pressure wound therapy apparatus and methods for operating the apparatus
EP3656408A1 (en) * 2014-12-29 2020-05-27 Smith & Nephew plc Negative pressure wound therapy apparatus and methods for operating the apparatus
CN108697423A (en) * 2016-02-16 2018-10-23 伊瑟拉医疗公司 The part flow arrangement of suction unit and anchoring
EP3416568A4 (en) * 2016-02-16 2019-10-16 Insera Therapeutics, Inc. Aspiration devices and anchored flow diverting devices
WO2017142874A3 (en) * 2016-02-16 2017-10-12 Insera Therapeutics, Inc. Aspiration devices and anchored flow diverting devices
US11285047B2 (en) 2016-04-26 2022-03-29 Smith & Nephew Plc Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component
AU2017256692B2 (en) * 2016-04-26 2022-03-03 Smith & Nephew Plc Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component
WO2017186771A1 (en) * 2016-04-26 2017-11-02 Smith & Nephew Plc Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component
US10779993B2 (en) 2016-05-09 2020-09-22 Convatec Technologies Inc. Negative pressure wound dressing management system
US11266774B2 (en) 2016-07-08 2022-03-08 Convatec Technologies Inc. Fluid collection apparatus
US11452808B2 (en) 2016-07-08 2022-09-27 Convatec Technologies Inc. Fluid flow sensing
US11596554B2 (en) 2016-07-08 2023-03-07 Convatec Technologies Inc. Flexible negative pressure system
US11369730B2 (en) 2016-09-29 2022-06-28 Smith & Nephew, Inc. Construction and protection of components in negative pressure wound therapy systems
WO2018064077A3 (en) * 2016-09-29 2018-05-11 Smith & Nephew, Inc. Construction and protection of components in negative pressure wound therapy systems
WO2018108784A1 (en) * 2016-12-12 2018-06-21 Smith & Nephew Plc Wound dressing
US12005181B2 (en) 2016-12-12 2024-06-11 Smith & Nephew Plc Pressure wound therapy status indication via external device
US11806217B2 (en) 2016-12-12 2023-11-07 Smith & Nephew Plc Wound dressing
AU2017375560B2 (en) * 2016-12-12 2023-07-06 Smith & Nephew Plc Pressure wound therapy status indication via external device
WO2018108724A1 (en) * 2016-12-12 2018-06-21 Smith & Nephew Plc Pressure wound therapy status indication via external device
US11974903B2 (en) 2017-03-07 2024-05-07 Smith & Nephew, Inc. Reduced pressure therapy systems and methods including an antenna
WO2019083872A1 (en) * 2017-10-23 2019-05-02 Kci Licensing, Inc. Area management of tissue sites on articulating joints
EP3473218A1 (en) * 2017-10-23 2019-04-24 KCI Licensing, Inc. Area management of tissue sites on articulating joints
WO2019083979A1 (en) * 2017-10-23 2019-05-02 Kci Licensing, Inc. Area management of tissue sites on articulating joints
EP3936094A1 (en) * 2017-10-23 2022-01-12 3M Innovative Properties Co. Area management of tissue sites on articulating joints
US11707564B2 (en) 2017-11-01 2023-07-25 Smith & Nephew Plc Safe operation of integrated negative pressure wound treatment apparatuses
USD847866S1 (en) 2018-01-22 2019-05-07 Insera Therapeutics, Inc. Pump
USD847865S1 (en) 2018-01-22 2019-05-07 Insera Therapeutics, Inc. Pump
USD896847S1 (en) 2018-01-22 2020-09-22 Insera Therapeutics, Inc. Pump
USD847864S1 (en) 2018-01-22 2019-05-07 Insera Therapeutics, Inc. Pump
USD850490S1 (en) 2018-01-22 2019-06-04 Insera Therapeutics, Inc Pump
US11554206B2 (en) 2018-02-01 2023-01-17 Kci Licensing, Inc. Negative pressure wound therapy device using a vacuum generating pump providing audible therapy feedback
WO2020139475A3 (en) * 2018-12-26 2020-08-20 Kci Licensing, Inc. Piezoelectric pump adapter for negative-pressure therapy
US12121420B2 (en) 2022-03-02 2024-10-22 Smith & Nephew Plc Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component

Also Published As

Publication number Publication date
TW201217020A (en) 2012-05-01
JP2013545519A (en) 2013-12-26
US20120109034A1 (en) 2012-05-03
US20140039426A1 (en) 2014-02-06
JP2014500739A (en) 2014-01-16
US8579872B2 (en) 2013-11-12
CA2814740A1 (en) 2012-05-03
US9265867B2 (en) 2016-02-23
AU2011320911A1 (en) 2013-04-18
CN103179930A (en) 2013-06-26
CA2814742A1 (en) 2012-05-03
EP2632406A1 (en) 2013-09-04
EP2632406B1 (en) 2016-11-23
CA2814740C (en) 2018-02-20
TW201217021A (en) 2012-05-01
US20120109083A1 (en) 2012-05-03
EP2632407B1 (en) 2017-08-23
JP5843296B2 (en) 2016-01-13
WO2012057882A1 (en) 2012-05-03
AU2011320911B2 (en) 2016-05-26
EP2632407A1 (en) 2013-09-04
CN103179929A (en) 2013-06-26
AU2011320912A1 (en) 2013-04-18
CN103179930B (en) 2014-12-24
AU2011320912B2 (en) 2016-11-10

Similar Documents

Publication Publication Date Title
US9265867B2 (en) Reduced-pressure systems, dressings, and methods employing a wireless pump
EP3318228B1 (en) Inflatable off-loading wound dressing assemblies, systems, and methods
US8449508B2 (en) Dressing and method for applying reduced pressure to and collecting and storing fluid from a tissue site
EP2249761B1 (en) Dressing for applying reduced pressure to and collecting and storing fluid from a tissue site
AU2013237989B2 (en) Reduced-pressure systems, dressings, and methods facilitating separation of electronic and clinical component parts
AU2014277788B2 (en) Dressing and method for applying reduced pressure to and collecting and storing fluid from a tissue site

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 11738356

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2814740

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 2011320911

Country of ref document: AU

Date of ref document: 20110715

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2013536610

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

REEP Request for entry into the european phase

Ref document number: 2011738356

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2011738356

Country of ref document: EP