WO1996015745A2 - Wound treatment device for attachment to skin - Google Patents
Wound treatment device for attachment to skin Download PDFInfo
- Publication number
- WO1996015745A2 WO1996015745A2 PCT/US1995/015197 US9515197W WO9615745A2 WO 1996015745 A2 WO1996015745 A2 WO 1996015745A2 US 9515197 W US9515197 W US 9515197W WO 9615745 A2 WO9615745 A2 WO 9615745A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- wound treatment
- wound
- treatment device
- plane
- area
- Prior art date
Links
- 206010052428 Wound Diseases 0.000 title claims abstract description 339
- 208000027418 Wounds and injury Diseases 0.000 title claims abstract description 339
- 230000007704 transition Effects 0.000 claims description 64
- 239000006260 foam Substances 0.000 claims description 32
- 239000000463 material Substances 0.000 claims description 25
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- 239000000853 adhesive Substances 0.000 claims description 16
- 230000001070 adhesive effect Effects 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 230000009467 reduction Effects 0.000 claims description 5
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 4
- 230000004044 response Effects 0.000 claims description 3
- 239000003242 anti bacterial agent Substances 0.000 claims description 2
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- 230000003115 biocidal effect Effects 0.000 claims description 2
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- 230000008878 coupling Effects 0.000 claims 3
- 238000010168 coupling process Methods 0.000 claims 3
- 238000005859 coupling reaction Methods 0.000 claims 3
- 230000003213 activating effect Effects 0.000 claims 1
- 239000004599 antimicrobial Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
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- 239000002131 composite material Substances 0.000 description 9
- 238000010276 construction Methods 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 3
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- 238000012546 transfer Methods 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 208000002847 Surgical Wound Diseases 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
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- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
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- 239000012858 resilient material Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 206010040882 skin lesion Diseases 0.000 description 1
- 231100000444 skin lesion Toxicity 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
- A61F7/007—Heating or cooling appliances for medical or therapeutic treatment of the human body characterised by electric heating
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive plasters or dressings
- A61F13/0203—Adhesive plasters or dressings having a fluid handling member
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- A61F15/00—Auxiliary appliances for wound dressings; Dispensing containers for dressings or bandages
- A61F15/008—Appliances for wound protecting, e.g. avoiding contact between wound and bandage
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- A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
- A61F2007/0001—Body part
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- A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
- A61F7/007—Heating or cooling appliances for medical or therapeutic treatment of the human body characterised by electric heating
- A61F2007/0071—Heating or cooling appliances for medical or therapeutic treatment of the human body characterised by electric heating using a resistor, e.g. near the spot to be heated
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- A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
- A61F7/007—Heating or cooling appliances for medical or therapeutic treatment of the human body characterised by electric heating
- A61F2007/0077—Details of power supply
- A61F2007/0078—Details of power supply with a battery
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- A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
- A61F7/02—Compresses or poultices for effecting heating or cooling
- A61F2007/0225—Compresses or poultices for effecting heating or cooling connected to the body or a part thereof
- A61F2007/0226—Compresses or poultices for effecting heating or cooling connected to the body or a part thereof adhesive, self-sticking
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- A61F2013/00187—Wound bandages insulating; warmth or cold applying
- A61F2013/00204—Wound bandages insulating; warmth or cold applying insulating
- A61F2013/00212—Wound bandages insulating; warmth or cold applying insulating infrared absorbing or reflecting
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- A61F13/00—Bandages or dressings; Absorbent pads
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- A61F2013/00731—Plasters means for wound humidity control with absorbing pads
- A61F2013/0074—Plasters means for wound humidity control with absorbing pads containing foams
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- A61F13/00—Bandages or dressings; Absorbent pads
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- A61F2013/00817—Plasters special helping devices handles or handling tabs
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Definitions
- the invention relates to a wound treatment device for covering and in some applications heating skin lesions, surgical wounds and the like.
- the wound treatment device includes a wound cover and optionally a detachable wound heater which provide a non-contact wound treatment volume over the wound area.
- the invention also relates to methods for making and using the wound treatment device.
- the wound treatment device 10 of the present invention has an upper wound covering surface displaced above the patient's skin surface, and an attachment surface lying generally in the plane of the patient's skin. Together these two surfaces define an enclosed non- contact volume over the wound treatment site.
- the wound treatment device 10 may be divided into three separate parts for the purpose of description.
- attachment portion 12 a wound treatment portion 14 and a transition portion 16.
- transition portion 16 a portion of a wound treatment portion
- the attachment portion 12 is used to connect the wound treatment device 10 to the skin of a patient.
- the attachment portion 12 will usually be formed as an annular attachment rim.
- An adhesive will typically be placed on the attachment rim to couple the wound treatment device 10 to the patient.
- the attachment portion 12 lies near the patient's skin and defines a so called first plane.
- the wound treatment portion 14 of the wound treatment device 10 is illustratively an assembly which includes a standoff 15 which rises above the patient's skin surface, and a wound cover 20 which spans the open portion of the standoff 15.
- the standoff 15 helps to define the vertical extent or dimension of the wound treatment device 10 and helps to define the location of a second plane which is used to describe the geometry of the device.
- the wound treatment portion 14 includes a standoff 15 and a wound cover 20 which together define both a wound treatment volume 24 and a wound treatment area 26.
- the wound treatment volume 24 is located over the surface of the wound.
- the atmosphere in this wound treatment volume 24 can be controlled by the wound treatment device 10.
- the wound treatment area 26 is defined on the patient surface 18 under the wound treatment portion 14, and will typically be centered over the lesion or wound.
- the transition portion 16 connects the attachment portion 12 to the wound treatment portion 14. This transition portion 16 improves the comfort and utility of the wound treatment device when the patient moves and stretches the wound treatment device 10. This stretching causes the total projected area of the wound treatment device 10 to increase and the shape of the wound treatment device 10 to change. In practice, the bulk of the patient motion is accommodated by the compliance of the transition portion 16. As a consequence, the transition portion projected area 17 increases.
- the standoff of wound treatment portion 14 rests gently on the patient's skin and it may twist to accommodate patient motion thus producing a device which conforms to the contour of the patient's body. However since the standoff can slide along the patient's skin there is no substantial change in the projected wound treatment area 28 due to patient motion.
- the attachment portion 12 During patient motion the attachment portion 12 remains affixed to the surface of the patient and is easily deformed by body motion because of its relatively small area. Consequently the attachment portion projected area 40 may undergo a slight increase in area as the attachment portion 12 moves with the underlying skin. Throughout this motion the second shaped surface is supported above the patient's skin surface and can be used to support a detachable heater 32 which can heat the wound surface. A switch may also be provided to reduce power supplied to the wound treatment device 10 if the device is crushed in to contact with the wound.
- FIG. 1 is a perspective view of a first embodiment of the wound treatment device
- FIG. 2 is a schematic view of projected areas
- FIG. 3 is a schematic view of projected areas
- FIG. 4 is a perspective view of a detachable heater in combination with a first embodiment of the wound treatment device
- FIG. 5 is an exploded view of the first embodiment of the wound treatment device
- FIG. 6 is an exploded view of the second embodiment of the wound treatment device
- FIG. 7 is a perspective view of a heater system
- FIG. 8 is an electrical schematic of a pressure sensitive switch for a heater system
- FIG. 9A is an exploded view of a pressure sensitive switch incorporated into a wound treatment device
- FIG. 9B is a view of a portion of the pressure sensitive switch
- FIG. 10 is a perspective view of a passive heater embodiment of the wound treatment device
- FIG. 11A is a schematic drawing depicting an alternate geometry for the transition portion
- FIG. 11B is a schematic drawing depicting an alternate geometry for the transition portion
- FIG. 11C is a schematic drawing depicting an alternate geometry for the transition portion
- FIG. 11D is a schematic drawing depicting an alternate geometry for the transition portion
- FIG. 12A is a schematic drawing depicting functional relationships between several elements of the invention
- FIG. 12B is a schematic drawing depicting functional relationships between several elements of the invention
- FIG. 13A is a schematic drawing depicting functional relationships between several elements of the invention.
- FIG. 13B is a schematic drawing depicting functional relationships between several elements of the invention.
- FIG. 14A is a schematic drawing depicting functional relationships between several elements of the invention.
- FIG. 14B is a schematic drawing depicting functional relationships between several elements of the invention.
- FIG. 15 is a perspective view of an alternate version of the wound treatment device;
- FIG. 16 is a perspective view of an alternate version of the wound treatment device
- FIG. 17A is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 17B is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 17C is a perspective view of an alternate version of the wound treatment device
- FIG. 18 is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 19A is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 19B is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 20A is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 20B is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 21A is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 21B is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 22A is a perspective view of an alternate version of the wound treatment device with a heater
- FIG. 22B is a perspective view of an alternate version of the wound treatment device with a heater.
- FIG. 1 is a perspective view of the wound treatment device 10 applied to a patient's skin surface 18.
- a coordinate system 11 is depicted on the patient's skin surface 18 and it defines X,Y and Z directions.
- the attachment portion 12 is formed as an planar rim or flange. This element is attached to the patient's skin with an adhesive and it lies in a first XY plane.
- the transition portion 16 is integrally formed with the attachment portion 12.
- the transition portion 16 rises vertically from the skin surface in the Z direction to connect to the wound treatment portion 14.
- the wound treatment portion 14 has a transparent planar wound cover 20 which allows one to see the wound treatment area 28.
- the wound cover 20 is supported above the first XY plane by a foam ring standoff 15.
- the planar wound cover 20 lies in a second XY plane that is vertically displaced along the Z-axis by the foam ring standoff 15 from the first XY plane.
- the wound cover 20 and foam ring standoff 15 together form the wound treatment portion 14.
- the region over the wound treatment area 28 is called the wound treatment volume 24.
- FIG. 2 and FIG. 3 should be considered together.
- FIG. 2 and FIG. 3 are top views of the wound treatment device 10 of FIG. 1 with the various portions of the wound treatment device 10 projected onto the first XY plane.
- FIG. 2 the wound covering is shown in a relaxed and un-stretched state having a nominal total projected area 27.
- the projected wound treatment area 28 is shown at the center of the wound treatment device 10.
- the outline of the foam ring standoff 15 may be seen as the Crosshatch area bounded by exterior perimeter 25 of the foam ring standoff 15, and the interior perimeter 26 of the foam ring standoff 15.
- the transition portion projected area 17 is shown in the figure bounded by the inner periphery 23 of the attachment portion 12, and the interior perimeter 26 of the foam ring standoff 15.
- the attachment portion projected area 40 is shown as the cross hatched area bounded by the outer periphery 22 and the inner periphery 23 of the attachment portion 12.
- FIG. 3 shows the wound treatment device 10 stretched along the X-axis by patient motion.
- the overall or total projected area 27 of the wound treatment device 10 has increased.
- the attachment portion projected area 40 has increased slightly as the attachment portion moves with the underlying skin.
- the projected wound enclosure area 28 is essentially unchanged in area since in this embodiment the foam ring standoff 15 is free move against the skin.
- the largest percentage area change occurs in the transition portion projected area 17.
- the transition portion is compliant and pays out material permitting the majority of the total projected area 27 increase to be accommodated primarily by the transition portion projected area 17.
- FIG. 4 shows a detachable heater 32 positioned for insertion into a pocket formed by pocket cover 21.
- Pocket cover 21 is bonded to the wound cover 20 and is sized to retain the heater 32.
- the foam ring standoff 15 and wound cover 20 serve to stabilize the shape of the wound treatment device while the transition portion accommodates patient motion. Consequently the heater is reliably and comfortably positioned above the wound surface.
- FIG. 5 is an exploded view of the first embodiment of the wound treatment device 10.
- the attachment portion 12 and transition portion membrane 36 are formed as a unitary composite shell 38.
- the composite shell may be vacuum formed from closed cell polyolefin foams such as Volara-6AS, which is a polyethylene material as sold by Illbruck Inc. of Mpls MN. It should be apparent that many other materials may be substituted within the scope of the invention.
- the foam ring standoff 15 may be die cut from foam sheeting of a reticulated polyurethane foam. The absorbency of the foam as well as its mechanical properties can be tailored to the particular wound treatment application. For example, the foam standoff may be impregnated with a medicament such as an antibiotic; antifungal; or antimicrobial material.
- the wound cover 20 and wound pocket 21 may be made from a thin film of polyethylene.
- the composite shell should be sufficiently self supporting so that when the wound treatment device 10 is removed from its release liner the wound treatment portion 14 is held up or supported by the shaped flexion joint of the transition portion membrane 36, and some effort is required to evert the composite shell and turn it inside out. This behavior defines the self supporting feature which causes the foam ring standoff 15 to lie gently against the skin even when the wound treatment device 10 is upside down. For larger wound coverings it may be desirable to apply a tacky adhesive to the patient contact surface of the standoff.
- FIG. 6 is an exploded view of the second embodiment of the wound treatment device 10.
- the attachment portion 12 and transition portion membrane 36 are formed as a unitary composite shell 38.
- the wound treatment volume is formed by a serrated cup standoff 34.
- This member made be made from a more rigid polymeric material such as polyethylene or the like.
- the serrations typified by serration 44 permit the serrated cup to flex and accommodate patient motion.
- This embodiment shows a release liner 42 coupled to the attachment portion 12 of the composite shell 38 with an adhesive 46.
- the pocket cover 21 is bonded to the composite shell 38.
- FIG. 7 depicts a power supply to permit the ambulatory use of the heated versions of the wound treatment device.
- a collection of battery cells may be wired together to form the power supply 48 which may be conveniently attached to a belt 49.
- a suitable cable 50 may be used to conduct power to the heater 32.
- FIG. 8 shows a schematic representation of a touch switch which may be incorporated directly into the detachable heater 32.
- the heater 32 includes a continuous resistive heating coil 51.
- a conductive membrane 52 is arranged near the coil 51 so that it may "short out” segments or portions of the coil 51. In use power to the coil is completely turned off by pressure applied to the entire touch sensor 53.
- FIG. 9A shows an exploded version of the heater 32 which incorporates a touch switch of the type described schematically in FIG. 8.
- the switch cover 45 has a conductive membrane which is located over the conductive pattern of the heating coil 51. It is held in position with an adhesive band 54.
- FIG. 9B shows the underside of the switch cover 45 showing a number of discrete insulation bumps typified by bump 47 which serve to space and support the conductive membrane 52 above the heating coil pattern 51. Pressure supplied to the switch cover inactivates the heater coil 51.
- FIG. 10 shows a an accessory device 55 or cover.
- the accessory device may take the form of a passive heater with a reflective surface facing the wound.
- the accessory device may also take the form of a mapping grid where a grid work of lines is positioned on a transparent card to permit tacking of the wound healing process.
- FIG. 11A through FIG. 11D should be considered together.
- These drawings facilitate a description of connection structures of the invention and represent several alternative connection geometries.
- the transition portion pays out stored material to increase the projected area of the transition portion.
- Each of these drawings represents a mechanical schematic cross section of a wound treatment device 10 in the XZ plane. In each figure the wound covering is in the relaxed state.
- FIG. 11A shows a schematic view of a ring standoff 15 extending from a first plane 56 to a second plane 58.
- the transition portion 16 has a transition portion membrane 60 which is coupled to the attachment portion 12 by a first flexible connection 62 formed at the intersection of the attachment portion 12 and the transition portion 16.
- the transition portion membrane 60 is connected to the treatment portion at a second flexible connection 64 which is formed at the intersection of the transition portion 16 and the wound treatment portion 14.
- the wound treatment portion 14 is generally a cylindrical cup shaped structure defining a wound treatment area on the patient skin surface.
- the minimum interconnection distance 66 is depicted as a dashed line extending from the first flexible connection 62 to the second flexible connection 64.
- the length of this minimum interconnection distance 66 can be used to characterize the "length" of the transition portion membrane 60.
- the length of the transition portion 16 between the first flexible connection 62 and the second flexible connection 64 is greater than the length of the straight line drawn between these points. This relationship is true for many embodiments of the wound treatment device when they are in the relaxed or unstressed position.
- the vertical distance between the first plane 56 and the second plane 58 represents a minimum value for the minimum interconnection distance 66.
- the first flexible connection 62 forms a first perimeter 61 and a second perimeter 63. In the embodiment depicted in FIG. 11A the first perimeter 61 is larger than the second perimeter 63.
- FIG. 11B is a mechanical schematic diagram which represents a cross section of another embodiment of the wound treatment device 10 with an alternate connection geometry.
- the wound cover 20 extends radially beyond the wound treatment volume 24 so that the second perimeter 68 is greater than the first perimeter 71.
- This generates a reflex transition portion 74 construction which may be adopted to increase the "length" and amount of material in the reflex transition portion 74.
- FIG. 11C shows a construction where the first perimeter 76 and the second perimeter 78 have approximately the same value and are both concentric with the axis 90. This construction can produce an undulated transition portion 77. Once again the length of the undulated transition portion 77 exceeds the length of the line 65 between the first perimeter 78 and the second perimeter 76.
- FIG. 11D shows a hemispheric shell 70 as the wound treatment portion 14.
- the second perimeter 80 is a single attachment point generally concentric with the axis 90.
- the first perimeter 81 has a length which greatly exceeds the second perimeter 80 length.
- This construction forms a hemispheric transition portion 79 which has a length which exceeds the linear distance between the second perimeter 80 and the first perimeter 81 along the line 85.
- the transition portion from a resilient material which is generally self-supporting, yet sufficiently flexible so that it acts as a compliant hinge mechanism. This flexibility prevents the transfer of shearing force from the wound treatment portion 14 to the attachment portion 12 of the wound treatment device 10 and visa versa.
- the transition portion of the wound treatment device 10 forms a shaped flexion joint or formed expansion joint which stores "material” in a pleat, convolution or bellows or the like.
- This type of structure provides a means for expanding the size of the transition portion to minimize the transfer of forces from the attachment portion 12 to the wound treatment portion 14.
- FIG. 12A through FIG. 14B should be considered together.
- the standoff structure reduces in height to result in the increased transition portion area during the stretching of the wound treatment device.
- FIG. 12A shows a part of a wound treatment device having a foam ring standoff 15 which is shown in the unstressed or relaxed state. In this instance the transition portion projected area 17 is proportional to dimension 88.
- FIG. 12B the wound treatment device has been stretched and the height of the foam ring standoff 15 is reduced in the Z direction which has increased the transition portion projected area as represented by dimension 91.
- FIG. 13A shows a part of a wound treatment device having a serrated cup standoff 34 which is shown in the unstressed or relaxed state. In this instance the transition portion projected area 17 is proportional to dimension 98.
- FIG. 13B the wound treatment device has been stretched and the height of the serrated cup standoff 34 is reduced in the Z direction.
- FIG. 14A shows a part of a wound treatment device having a foam ring standoff 15 which is shown in the unstressed or relaxed state. However in this construction the attachment portion 12 and transition portion membrane 96 lie entirely in the first plane 56. In this instance the transition portion projected area 17 is proportional to dimension 94.
- FIG. 14B the wound treatment device has been stretched and the height of the foam ring standoff 15 is reduced in the Z direction. This height reduction which has increased • the transition portion projected area is represented by dimension 92.
- FIG. 15 shows a version of the wound treatment device 10 which includes a dome shaped or hemispheric wound cover 19. At least a portion of this device lies in the second XY plane 58.
- FIG. 16 shows a version of the wound treatment device 10 which includes a releasable and resealable wound cover 20.
- the wound cover 20 may have a tab 29 located at the periphery of the wound cover 20.
- a reusable adhesive 30 may be applied to the periphery of the wound cover 20 as well to allow the cover to be releasable attached to the standoff 15 structure or composite shell 38.
- FIG. 17A shows a releasable wound cover incorporating a heater pocket cover 21.
- the resealable wound cover 20 and pocket cover 21 forms a space for the heater 32.
- FIG. 17B shows that one advantage of the resealable and removable construction is that the opening for the heater may be shifted without removing or repositioning the wound treatment device 10.
- FIG. 17C shows a wedge shaped wound treatment device 10.
- a line 31 in the XY plane 11 of the attachment portion 12 intersects with a line 33 which lies across the top of the standoff 15. These tow lines may meet a point 35 in space as seen in the drawing.
- FIG. 18 shows a an alternate method of attaching the planar heater 32 to the wound cover 20.
- the heater has a hook or loop material 37 attached to the edge of the heater 32 and the complimentary loop or hook material 39 is attached tot he composite shell 38.
- the wound cover need not be accessible to reorient the heater 32. It should be appreciated that an adhesive may be used to attach the heater as well.
- FIG. 19A is a perspective view of an alternate version of the wound treatment device with a heater.
- the heater 83 is dome shaped to conform to the shape of the wound cover 84.
- complimentary loop and hook material 37 and 39 may be used for releasable attachment to the wound treatment device.
- FIG. 19B is a perspective view of an alternate version of the wound treatment device with a heater attached to the wound treatment device with an adhesive or the like.
- a resistive heater grid is formed in the cover to generate heat in response to electrical energy applied trough leads 50.
- FIG. 20A is a perspective view of an alternate version of the wound treatment device with a dome shaped heater 86.
- the heater 86 has a collection of independent parallel connected resistive loops typified by loop 87. In use the resistance of the loop is selected to ensure that the radiated heat is uniform as measured at the wound surface.
- FIG. 20B is a perspective view of an alternate version of the wound treatment device with a dome shaped heater 86 attached to the wound treatment device 10.
- FIG. 21A is a perspective view of an alternate version of the wound treatment device with a dome shaped heater 89.
- a heater wire is coiled to provide the heater element.
- FIG. 21B is a perspective view of an alternate version of the wound treatment device with a dome shaped heater 89. In use the coil spacing indicated by dimension
- 87 can be adjusted to provide uniform heating of the wound area.
- FIG. 22A is a perspective view of a wound treatment device 10 having two complimentary pockets shown as pocket 97 and pocket 95 which cooperate with tab 83 and tab 75 formed on the heater 32.
- FIG. 22B is a perspective view which shows tab 75 and tab 83 inserted into the complimentary pockets 95 and pocket 97 to position and retain a planar heater structure.
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE69533989T DE69533989T2 (en) | 1994-11-21 | 1995-11-21 | WOUND TREATMENT DEVICE FOR FASTENING TO THE SKIN |
EP95940794A EP0793467B1 (en) | 1994-11-21 | 1995-11-21 | Wound treatment device for attachment to skin |
AT95940794T ATE288244T1 (en) | 1994-11-21 | 1995-11-21 | WOUND TREATMENT DEVICE TO BE ATTACHED TO THE SKIN |
JP51705496A JP3918158B2 (en) | 1994-11-21 | 1995-11-21 | Trauma treatment tool for skin application |
US08/836,066 US6013097A (en) | 1994-11-21 | 1995-11-21 | Wound treatment device for attachment to skin |
CA002204159A CA2204159C (en) | 1994-11-21 | 1995-11-21 | Wound treatment device for attachment to skin |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/342,741 US5817145A (en) | 1994-11-21 | 1994-11-21 | Wound treatment device |
US08/342,741 | 1994-11-21 |
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US08/342,741 Continuation-In-Part US5817145A (en) | 1994-11-21 | 1994-11-21 | Wound treatment device |
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Application Number | Title | Priority Date | Filing Date |
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US09/428,952 Continuation US6293917B1 (en) | 1994-11-21 | 1999-11-04 | Wound treatment device for attachment to skin |
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WO1996015745A2 true WO1996015745A2 (en) | 1996-05-30 |
WO1996015745A3 WO1996015745A3 (en) | 1996-08-08 |
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PCT/US1995/015197 WO1996015745A2 (en) | 1994-11-21 | 1995-11-21 | Wound treatment device for attachment to skin |
Country Status (7)
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US (8) | US5817145A (en) |
EP (2) | EP0982015B1 (en) |
JP (1) | JP3918158B2 (en) |
AT (2) | ATE337767T1 (en) |
CA (1) | CA2204159C (en) |
DE (2) | DE69533989T2 (en) |
WO (1) | WO1996015745A2 (en) |
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- 1995-11-21 EP EP99121265A patent/EP0982015B1/en not_active Expired - Lifetime
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US6419651B1 (en) | 1992-06-19 | 2002-07-16 | Augustine Medical, Inc. | Normothermic heater covering |
US6217535B1 (en) | 1992-06-19 | 2001-04-17 | Augustine Medical, Inc. | Normothermic heater wound covering |
US6213966B1 (en) | 1992-06-19 | 2001-04-10 | Augustine Medical, Inc. | Normothermic tissue heating wound covering |
US6605051B2 (en) | 1992-06-19 | 2003-08-12 | Augustine Medical, Inc. | Near hyperthermic tissue treatment |
US6465708B1 (en) * | 1992-06-19 | 2002-10-15 | Augustine Medical, Inc. | Covering |
US6423018B1 (en) | 1992-06-19 | 2002-07-23 | Augustine Medical, Inc. | Normothermic tissue heating wound covering |
US5954680A (en) * | 1992-06-19 | 1999-09-21 | Augustine Medical, Inc. | Near hyperthermic heater wound covering |
US5961480A (en) * | 1992-06-19 | 1999-10-05 | Augustine Medical, Inc. | Wound covering |
US6840915B2 (en) | 1992-06-19 | 2005-01-11 | Arizant Healthcare Inc. | Normothermic tissue treatment |
US6921374B2 (en) | 1992-06-19 | 2005-07-26 | Arizant Healthcare Inc. | Tissue treatment by normothermic heating |
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US6406448B1 (en) | 1992-06-19 | 2002-06-18 | Augustine Medical, Inc. | Normothermic heater covering for tissue treatment |
US5986163A (en) * | 1992-06-19 | 1999-11-16 | Augustine Medical, Inc. | Normothermic heater wound covering |
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US6241697B1 (en) * | 1992-06-19 | 2001-06-05 | Augustine Medical, Inc. | Wound covering |
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US6071254A (en) * | 1992-06-19 | 2000-06-06 | Augustine Medical, Inc. | Near hyperthermic heater wound covering |
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US6407307B1 (en) | 1993-06-18 | 2002-06-18 | Augustine Medical, Inc. | Near hyperthermic heater covering |
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WO1998046178A1 (en) | 1997-04-11 | 1998-10-22 | Augustine Medical, Inc. | Flexible non-contact wound treatment device with a single joint |
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US10076318B2 (en) | 2008-07-18 | 2018-09-18 | Wake Forest University Health Sciences | Apparatus and method for cardiac tissue modulation by topical application of vacuum to minimize cell death and damage |
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Also Published As
Publication number | Publication date |
---|---|
US20030023286A1 (en) | 2003-01-30 |
DE69535208D1 (en) | 2006-10-12 |
EP0793467B1 (en) | 2005-02-02 |
WO1996015745A3 (en) | 1996-08-08 |
EP0982015B1 (en) | 2006-08-30 |
US20020026133A1 (en) | 2002-02-28 |
US6013097A (en) | 2000-01-11 |
EP0982015A3 (en) | 2000-03-15 |
US6248084B1 (en) | 2001-06-19 |
US6468295B2 (en) | 2002-10-22 |
US6010527A (en) | 2000-01-04 |
CA2204159A1 (en) | 1996-05-30 |
ATE337767T1 (en) | 2006-09-15 |
US6293917B1 (en) | 2001-09-25 |
DE69535208T2 (en) | 2007-08-23 |
EP0982015A2 (en) | 2000-03-01 |
US5817145A (en) | 1998-10-06 |
EP0793467A1 (en) | 1997-09-10 |
DE69533989D1 (en) | 2005-03-10 |
JP3918158B2 (en) | 2007-05-23 |
JPH10509886A (en) | 1998-09-29 |
US7122046B2 (en) | 2006-10-17 |
CA2204159C (en) | 2002-01-22 |
ATE288244T1 (en) | 2005-02-15 |
US20010018602A1 (en) | 2001-08-30 |
DE69533989T2 (en) | 2006-02-02 |
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