CA2247360C - X-ray transmissive transcutaneous stimulating electrode - Google Patents
X-ray transmissive transcutaneous stimulating electrode Download PDFInfo
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- CA2247360C CA2247360C CA002247360A CA2247360A CA2247360C CA 2247360 C CA2247360 C CA 2247360C CA 002247360 A CA002247360 A CA 002247360A CA 2247360 A CA2247360 A CA 2247360A CA 2247360 C CA2247360 C CA 2247360C
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- mat
- electrode member
- electrode
- electrically conductive
- sheet
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09B—DISPOSAL OF SOLID WASTE
- B09B3/00—Destroying solid waste or transforming solid waste into something useful or harmless
- B09B3/0075—Disposal of medical waste
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/046—Specially adapted for shock therapy, e.g. defibrillation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0472—Structure-related aspects
- A61N1/048—Electrodes characterised by a specific connection between lead and electrode
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0472—Structure-related aspects
- A61N1/0492—Patch electrodes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09B—DISPOSAL OF SOLID WASTE
- B09B2101/00—Type of solid waste
- B09B2101/65—Medical waste
- B09B2101/68—Transdermal patches
Abstract
This invention is a disposable transcutaneous electrode (10) comprising a sheet electrode member (21) of electrically conductive carbon filled polymer, an electrically conductive metal/metal coating~
(23) on at least a major portion of the lower side of the electrode member. A pad of electrically conductive gel (25) underlies the metal/metal chloride coating (23).
A current distributing mat (27) conductive adhered to the upper side of the electrode member (See formula I) (21) has a perimeter spaced inwardly of the perimeter of the electrode member (21), and includes an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on upper and lower sides of the web. The electrode member (21) and the current distributing mat (27) are configured to be x-ray transparent and capable of conducting energy at levels sufficient for defibrillation.
(23) on at least a major portion of the lower side of the electrode member. A pad of electrically conductive gel (25) underlies the metal/metal chloride coating (23).
A current distributing mat (27) conductive adhered to the upper side of the electrode member (See formula I) (21) has a perimeter spaced inwardly of the perimeter of the electrode member (21), and includes an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on upper and lower sides of the web. The electrode member (21) and the current distributing mat (27) are configured to be x-ray transparent and capable of conducting energy at levels sufficient for defibrillation.
Description
X-RAY ~RANSMIBSIVE TRANBCUTAHEOUB STIMULATING E'LECTRODB
F ELD OF INVE~ TION
The present application relates to a transcutaneous stimulating or defibrillating electrode, and more particularly to a multi-function defibrillating electrode that is also X-ray transmissive.
~ACKt3ROUND OF L'HS INVENTION
Various X-ray transmissive monitoring electrodes have heretofore been made tc~ facilitate X-ray examination of a patient without requiring removal of the electrodes or significantly impairin~;the X-ray image. Examples of X-ray transmissive monitmring electrodes are disclosed in U.S. patents 4,050,453; 4,257,424; 4,370,984; 4,674,511;
4,685,467; 4,442,315;' 4,539,995; and 5,265,679.
Monitoring electrodes are very small, for example in the order of a few square centimeters and need only carry very low electrical signals in the order of milliamps. In general, such X-ray transmissive monitoring electrodes are not capable of conducting and distributing the high levels of energy requited in transcutaneous stimulation and defibrillation electrodes.
Defibrillation electrodes must be capable of conducting the high energy level required for defibrillation, up to 360 Joules or more, and must also distribute the energy over a relatively large area of the patients~s epidermis to achieve adequate current density distribution within the ventricles. The ANSI/AAMI
presently specify that the minimum active area of individual self-adhesive electrodes used for adult defibrillation and pacing shall be at least 50 square centimeters and that the total area of the two electrodes shall be at least 150 square centimeters.
Some prior defibrillation electrodes such as disclosed in U.S. Patents 4,895,169 and 5,330,526, provide an electrically conductive metal plate having an area to to substantially cover the skin contacting gel pad, for distributing the energy over the area of the pad. Patent 4,748,983 provides an electrode body formed of a porous granular or fibrous carbon impregnated with an electrolytic solution that covers the upper surface of a skin contacting gel pad. Some other stimulations and defibrillation electrodes disclosed in U.S. Patents 4,226,247; 4,239,046; 4,722,354; 5,356,428 and 5,366,497 provide a conductive backing for covering the skin contacting pad and which is formed of expanded metal or 2o metal strands that are woven or formed into an open mesh.
Some of the above patents indicate that the backing is radiolucent or have at least some degree of X-ray transmissivity. In addition, some of the above patents also indicate that the defibrillation electrode disclosed in the patents are combination electrodes that can also function as monitoring electrodes between defibrillation pulses. However, it remains a problem to improve the X-ray transparency of defibrillation electrodes and the ability of the defibrillation electrodes to reliably function as monitoring electrodes promptly after transmission of a defibrillation pulse through the electrode. In addition, problems have been encountered with prior art simulation and def ibrillator electrodes , particularly after application of repeated high level defibrillation or cardiac pacing pulses, with irritation and burning of the patient's skin due to high current density around the perimeter of electrodes.
F ELD OF INVE~ TION
The present application relates to a transcutaneous stimulating or defibrillating electrode, and more particularly to a multi-function defibrillating electrode that is also X-ray transmissive.
~ACKt3ROUND OF L'HS INVENTION
Various X-ray transmissive monitoring electrodes have heretofore been made tc~ facilitate X-ray examination of a patient without requiring removal of the electrodes or significantly impairin~;the X-ray image. Examples of X-ray transmissive monitmring electrodes are disclosed in U.S. patents 4,050,453; 4,257,424; 4,370,984; 4,674,511;
4,685,467; 4,442,315;' 4,539,995; and 5,265,679.
Monitoring electrodes are very small, for example in the order of a few square centimeters and need only carry very low electrical signals in the order of milliamps. In general, such X-ray transmissive monitoring electrodes are not capable of conducting and distributing the high levels of energy requited in transcutaneous stimulation and defibrillation electrodes.
Defibrillation electrodes must be capable of conducting the high energy level required for defibrillation, up to 360 Joules or more, and must also distribute the energy over a relatively large area of the patients~s epidermis to achieve adequate current density distribution within the ventricles. The ANSI/AAMI
presently specify that the minimum active area of individual self-adhesive electrodes used for adult defibrillation and pacing shall be at least 50 square centimeters and that the total area of the two electrodes shall be at least 150 square centimeters.
Some prior defibrillation electrodes such as disclosed in U.S. Patents 4,895,169 and 5,330,526, provide an electrically conductive metal plate having an area to to substantially cover the skin contacting gel pad, for distributing the energy over the area of the pad. Patent 4,748,983 provides an electrode body formed of a porous granular or fibrous carbon impregnated with an electrolytic solution that covers the upper surface of a skin contacting gel pad. Some other stimulations and defibrillation electrodes disclosed in U.S. Patents 4,226,247; 4,239,046; 4,722,354; 5,356,428 and 5,366,497 provide a conductive backing for covering the skin contacting pad and which is formed of expanded metal or 2o metal strands that are woven or formed into an open mesh.
Some of the above patents indicate that the backing is radiolucent or have at least some degree of X-ray transmissivity. In addition, some of the above patents also indicate that the defibrillation electrode disclosed in the patents are combination electrodes that can also function as monitoring electrodes between defibrillation pulses. However, it remains a problem to improve the X-ray transparency of defibrillation electrodes and the ability of the defibrillation electrodes to reliably function as monitoring electrodes promptly after transmission of a defibrillation pulse through the electrode. In addition, problems have been encountered with prior art simulation and def ibrillator electrodes , particularly after application of repeated high level defibrillation or cardiac pacing pulses, with irritation and burning of the patient's skin due to high current density around the perimeter of electrodes.
SiJMMARY OF THE INVENTION
It is an object of the present invention to provide a disposable transcutaneous electrode which is X-ray transparent and capable of conducting energy sufficient for defibrillation, and which has improved current density distribution between the electrode and the skin surface of the patient to efficiently deliver the energy without burning the patient's skin.
Accordingly, the present invention provides a 1o transcutaneous stimulation electrode comprising a sheet electrode member of electrically conductive carbon filled polymer having an electrically conductive metal/metal chloride coating on a lower side of the electrode member, a pad of electrically conductive gel underlying the electrode members and a current distributing mat on the upper surface of the electrode member. The current distributing mat is configured to be electrically conductive along the surface of the mat and transverse to the surface of the mat to transfer and distribute energy between the upper surface of the mat and the upper surface of the sheet electrode member. In one embodiment, the current distributing mat includes an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on the upper and lower sides of the web. In a further embodiment, the current distributing mat includes a conductive metal foil coated with a conductive polymer adhesive on the upper and lower sides of the foil.
The sheet electrode member is electrically conductive 3o and transmits energy from the upper surface to the metal/metal chloride coating on the under surface. The sheet electrode member has an area sufficiently large to achieve adequate current density distribution between the electrode and the skin of the patient and the conductive mat has an area smaller than the area of the electrode member but large enough to distribute the current over an area on the upper side of the electrode. The metal/metal chloride coating on the under side of the electrode is advantageously arranged to have an outer perimeter that is spaced inwardly of the outer perimeter of the electrode member to reduce the current density at the outer perimeter of the electrode member.
Electrical energy is conducted to or from the upper surface of the conductive mat and a medical device. In applications where radio translucency of the wires is also important, the wires are advantageously formed of an X-ray transparent metal coated carbon fiber tow. For applications in which radio translucency of the conductors is not essential, the conductors can be multi-strand metal wires in which the strands can be spread out and bonded to the upper surface of the mat. Alternatively, a reinforced metallic tab or a metallic or conductive plastic post stud may be used for the conductor. It is also contemplated that the electrodes can be used as pad electrodes in which hand held defibrillation paddles are used to transfer current to or from the upper side of the conductor mat.
BRIEF DESCRIPTION OF THE DRI~WINGS
Fig. 1 is a top plan view of the electrode, with certain layers cut away to illustrate details of intermediate layers;
Fig. 2 is an exploded longitudinal sectional view of the electrodes;
Fig. 3 is a bottom plan view of the electrode, with certain layers broken away to illustrate the under side of intermediate layers;
Fig. 4 is a fragmentary sectional view through heated sealing jaws, illustrating flattening of the electric insulation adjacent the end of the conductors;
Fig. 5 is a diagrammatic view illustrating assembly of the conductor between layers of an electrically conductive mat;
Fig. 6 is a diagrammatic view illustrating application of the electrodes to a patient and connection to a defibrillating and ECG apparatus.
Fig. 7 is a top plan view of an electrode modified 5 for use with defibrillating paddles, on a smaller scale than Figs. 1 and 3;
Fig. 8 is a partial top plan view of an alternate embodiment of the electrode utilizing a conductive post stud, with certain layers cut away to illustrate details l0 of the intermediate layers;
Fig. 9 is an exploded longitudinal sectional view of the electrode of Fig. 8; and Fig. 10 is an exploded longitudinal sectional view of an electrode utilizing a conductive tab.
DETAILED DESCRIPTION
An exploded view of a disposable transcutaneous electrode--1t~--erimbodying--the--present invention is illustrated in Fig. 2. In general, the electrode 2o comprises a sheet electrode member 21 of electrically conductive carbon filled polymer; an electrically conductive metal/metal chloride coating 23 (and preferably a silver/silver chloride coating) on at least a major portion of the lower side of the electrode member; a pad of electrically conductive gel 25 underlying the metal/metal chloride coating on the lower side of the electrode member, and a current distributing mat 27 having a lower surface conductively adhered to the upper side of the sheet electrode member, for conducting energy to or from the upper side of the electrode member. The electrode is configured to be X-ray transparent and capable of conducting electrical energy at levels sufficient for defibrillation. As used herein the phrase "X-ray transparent" is defined as the quality of being at least substantially invisible at X-irradiation levels used in routine X-rays of a patient's chest.
It is an object of the present invention to provide a disposable transcutaneous electrode which is X-ray transparent and capable of conducting energy sufficient for defibrillation, and which has improved current density distribution between the electrode and the skin surface of the patient to efficiently deliver the energy without burning the patient's skin.
Accordingly, the present invention provides a 1o transcutaneous stimulation electrode comprising a sheet electrode member of electrically conductive carbon filled polymer having an electrically conductive metal/metal chloride coating on a lower side of the electrode member, a pad of electrically conductive gel underlying the electrode members and a current distributing mat on the upper surface of the electrode member. The current distributing mat is configured to be electrically conductive along the surface of the mat and transverse to the surface of the mat to transfer and distribute energy between the upper surface of the mat and the upper surface of the sheet electrode member. In one embodiment, the current distributing mat includes an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on the upper and lower sides of the web. In a further embodiment, the current distributing mat includes a conductive metal foil coated with a conductive polymer adhesive on the upper and lower sides of the foil.
The sheet electrode member is electrically conductive 3o and transmits energy from the upper surface to the metal/metal chloride coating on the under surface. The sheet electrode member has an area sufficiently large to achieve adequate current density distribution between the electrode and the skin of the patient and the conductive mat has an area smaller than the area of the electrode member but large enough to distribute the current over an area on the upper side of the electrode. The metal/metal chloride coating on the under side of the electrode is advantageously arranged to have an outer perimeter that is spaced inwardly of the outer perimeter of the electrode member to reduce the current density at the outer perimeter of the electrode member.
Electrical energy is conducted to or from the upper surface of the conductive mat and a medical device. In applications where radio translucency of the wires is also important, the wires are advantageously formed of an X-ray transparent metal coated carbon fiber tow. For applications in which radio translucency of the conductors is not essential, the conductors can be multi-strand metal wires in which the strands can be spread out and bonded to the upper surface of the mat. Alternatively, a reinforced metallic tab or a metallic or conductive plastic post stud may be used for the conductor. It is also contemplated that the electrodes can be used as pad electrodes in which hand held defibrillation paddles are used to transfer current to or from the upper side of the conductor mat.
BRIEF DESCRIPTION OF THE DRI~WINGS
Fig. 1 is a top plan view of the electrode, with certain layers cut away to illustrate details of intermediate layers;
Fig. 2 is an exploded longitudinal sectional view of the electrodes;
Fig. 3 is a bottom plan view of the electrode, with certain layers broken away to illustrate the under side of intermediate layers;
Fig. 4 is a fragmentary sectional view through heated sealing jaws, illustrating flattening of the electric insulation adjacent the end of the conductors;
Fig. 5 is a diagrammatic view illustrating assembly of the conductor between layers of an electrically conductive mat;
Fig. 6 is a diagrammatic view illustrating application of the electrodes to a patient and connection to a defibrillating and ECG apparatus.
Fig. 7 is a top plan view of an electrode modified 5 for use with defibrillating paddles, on a smaller scale than Figs. 1 and 3;
Fig. 8 is a partial top plan view of an alternate embodiment of the electrode utilizing a conductive post stud, with certain layers cut away to illustrate details l0 of the intermediate layers;
Fig. 9 is an exploded longitudinal sectional view of the electrode of Fig. 8; and Fig. 10 is an exploded longitudinal sectional view of an electrode utilizing a conductive tab.
DETAILED DESCRIPTION
An exploded view of a disposable transcutaneous electrode--1t~--erimbodying--the--present invention is illustrated in Fig. 2. In general, the electrode 2o comprises a sheet electrode member 21 of electrically conductive carbon filled polymer; an electrically conductive metal/metal chloride coating 23 (and preferably a silver/silver chloride coating) on at least a major portion of the lower side of the electrode member; a pad of electrically conductive gel 25 underlying the metal/metal chloride coating on the lower side of the electrode member, and a current distributing mat 27 having a lower surface conductively adhered to the upper side of the sheet electrode member, for conducting energy to or from the upper side of the electrode member. The electrode is configured to be X-ray transparent and capable of conducting electrical energy at levels sufficient for defibrillation. As used herein the phrase "X-ray transparent" is defined as the quality of being at least substantially invisible at X-irradiation levels used in routine X-rays of a patient's chest.
The gel pad 25 is preferably a skin compatible hydrogel having good ability to retain moisture content and adhesive tack. The gel may, for example, comprise a hydrogel marketed by Ludlow Technical Products division of Ludlow Corporation, under the trademark "Promeon", product number RG73P. It is desirable to laterally confine the gel pad 25 during storage and use, and the gel pad is preferably disposed within an opening 28' in a base frame 28 of X-ray transparent and electrically insulative foam such as .08 to .16 cm thick PE foam, and a removable release carrier sheet 31, for example of PTFE, is attached to the underside of the base frame 28 by a skin compatible adhesive coating 29 on the underside of the base frame.
The carrier sheet underlies the gel pad 25 and covers the latter prior to use. An electrically insulative cover sheet 33 of X-ray transparent and electrically insulative foam such as .08 cm to .16 cm thick PE foam having an adhesive-iayer 3-4,- overlies-the curie-nt-distributing mat 27 and the electrode member 21 and is adhered by the 2o adhesive layer 34 to the upper side of the base frame 28.
The gel pad 25 is of a type that adhesively connects the electrode member to the patient's skin and the adhesive 29 on the underside of the base frame 28 aids in adhering the electrode member to the patient's skin during use.
Alternatively, the frame 28 could be omitted and the adhesive layer on the outer periphery of the cover sheet 33 used to adhere the electrode to the patient's skin.
Means are provided for conducting energy to and from the upper side of the current distributing mat 27 and a 3 o medical device . In the embodiment illustrated in Figs . 1 6, the energy conducting means comprises an electrical conductor 35 having an electrically insulative sheath 36a and a unsheathed end portion 35a that is conductively adhered to the upper side of the current distributing mat 27. The current distributing mat preferably includes a second mat portion 27' arranged to overlie the mat 27 and the unsheathed end portion 35a of the conductor 35.
The carrier sheet underlies the gel pad 25 and covers the latter prior to use. An electrically insulative cover sheet 33 of X-ray transparent and electrically insulative foam such as .08 cm to .16 cm thick PE foam having an adhesive-iayer 3-4,- overlies-the curie-nt-distributing mat 27 and the electrode member 21 and is adhered by the 2o adhesive layer 34 to the upper side of the base frame 28.
The gel pad 25 is of a type that adhesively connects the electrode member to the patient's skin and the adhesive 29 on the underside of the base frame 28 aids in adhering the electrode member to the patient's skin during use.
Alternatively, the frame 28 could be omitted and the adhesive layer on the outer periphery of the cover sheet 33 used to adhere the electrode to the patient's skin.
Means are provided for conducting energy to and from the upper side of the current distributing mat 27 and a 3 o medical device . In the embodiment illustrated in Figs . 1 6, the energy conducting means comprises an electrical conductor 35 having an electrically insulative sheath 36a and a unsheathed end portion 35a that is conductively adhered to the upper side of the current distributing mat 27. The current distributing mat preferably includes a second mat portion 27' arranged to overlie the mat 27 and the unsheathed end portion 35a of the conductor 35.
The electrode member 21 is formed of a thin flexible sheet of electrically conductive polymer film such as graphite filled polyvinyl chloride film preferably having a thickness of the order of two to four mils. An example of carbon filled polymer which can be used is thin carbon filled PvC available from Burkhardt/Freeman, Holyoke, Mass., under the trademark "Conduction."
The carbon filled sheet electrode member is X-ray transparent and the coating 23 of metal/metal chloride is applied in a layer or layers to the lower face of the electrode member as by silk screening or by flexographic printing. If the coating 23 is silver/silver chloride , it is preferably less than ten microns in thickness, which is sufficient to provide good electrical conductivity without impairing the X-ray transparency of the electrode member. A carbon filled PvC material with silver/silver chloride coating on the underside suitable for use as an electrode member is available from Prime Label And Screen, Inc., New Berlin, Wisconsin. Alternatively, the metal/metal chloride coating can comprise a single layer, chloride-coated metallic foil coated with a conductive acrylic adhesive. The metallic foil may comprise silver, tin, copper, nickel, gold, aluminum, platinum, chromium, cadmium, pladmium, zinc, antimony, or indium covered with an adhesive such as the Arclad 8001 bonding tape or Arclad EC2 adhesive described below.
The electrode member 2I has a surface area dimensioned to distribute energy over an area of the patient's epidermis to achieve proper current density 3o distribution within the ventricles of the patient's heart.
The ANSI standards for the size of defibrillation electrodes published by AAMI presently recommends that the minimum active area of individual self-adhesive electrodes used for adult defibrillation and pacing shall be at least 50 cm2 and that the total area of two electrodes used in defibrillation shall be at least 150 cm2. The electrode member 21 has an area of at least 50 cm2 and preferably about 80 cm2 or more so that a pair of the electrodes used for defibrillation can be of the same size. 15 cm2 is the minimum electrode area recommended for pediatric transthoracic use and the area of the electrode member 21 of the present invention for pediatric use can be made correspondingly smaller.
The carbon filled polymer electrode 21 is conductive in the plane of the electrode and transverse to the plane electrode and the metal/metal chloride coating on the under side of the electrode member is also conductive in the plane of the coating and transverse to the plane of the coating. The carbon filled polymer electrode member has a surface resistance substantially higher than the surface resistance of the metal/metal chloride coating and it has been found that the carbon filled polymer electrode member with a silver/silver chloride coating is not alone capable for transmitting and distributing the high levels of energy encountered--in-de~i.brillation beer-the entire surface of the electrode member.
In the preferred embodiment, the current distributing mat 27 is configured to have electrical conductivity in the of the mat and transverse to the plane of the mat and a higher current carrying capacity than the sheet electrode member. The current distributing mat includes a non-woven open mesh metallized carbon fiber web having an electrically conductive carbon impregnated pressure sensitive adhesive composition on the upper and lower sides of the web. The web of the current distribution mat is thin and preferably less than five mills in thickness and is comprised of semi-metallic fibers such as carbon fibers which are metal plated or coated before or after being formed into a web with a metal coating that is 35$
to 40~ by weight of the metal plated carbon fiber web.
The semi-metallic carbon fibers are X-ray transparent before plating or coating and the metal plating or coating of the fibers of the web is sufficiently think for example less than ten microns in thickness, and such that the thin open-mesh web formed of the metal plated fibers remains X-ray transparent. The electrically conductive pressure sensitive adhesive that is applied to opposite sides of the web is loaded with sufficient carbon or graphite for good electrical conductivity and such that the composite web and adhesive provide a mat that is electrically conductive in the plane of the mat and transverse to the plane of the mat. An example of a conductive double face pressure sensitive tape with a conductive carrier which l0 can be used for the mat is a thin pressure sensitive bonding tape available from Adhesives Research, Inc., Glen Rock, Pa. under the trademark "Arclad," product No. 8001.
This tape comprises a non-woven open mesh mat or carrier formed of metal coated carbon filaments having a metal coating of a few microns, for example five or six microns in thickness, and such that the metal coated mat is X-ray transparent. The electrically conductive pressure sensitive adhesive comprises a pressure sensitive adhesive impregnated with carbon or graphite for conductivity.
U.S. Patent No. 5,082,595 assigned to Adhesive Research, Inc. discloses a method of making such a double faced pressure sensitive adhesive tape with conductivity in X, Y and Z axes.
Alternatively, the current distributing mat 27 may comprise a solid metallic foil or fine screen mesh covered with a conductive polymer adhesive for attaching the mat to the sheet electrode 21. The foil is on the order of 0.001-0.002 inches thick and suitable metals include copper or tin. Other metals may be used, such as gold, silver, nickel, aluminum, platinum, chromium, cadmium, pladmium, zinc, antimony, and indium. However, the cost of certain of these metals could make their use unlikely.
If the monitoring aspects of the electrode are important, the foil should comprise a metal halide. (Of course, the use of metal foils for the current distributing mat adversely affects the x-ray transmissivity of the electrode.) Suitable adhesives include the Arclad 8001 bonding tape described above. EC2 adhesive by Adhesive Research can also be used.
Published literature indicates that, when a metal plate electrode having an electrolytic gel coating on its 5 underside, is placed on the skin and used to delivery current, the current density is very much higher under the perimeter of the electrode than under the center. A
similar problem occurs at the energy accepting electrode of a set of such defibrillation electrodes. The mat 27 is 1o arranged to distribute current over a central area of the electrode member 21 and has an outer perimeter 27p spaced inwardly of the perimeter 21p of the electrode member.
The mat is sized to distribute the current more uniformly over the central portion of the electrode member to inhibit arcing through the central portion of the electrode member, and is spaced inwardly from the perimeter of the electrode member to avoid conveying high current levels to the outer periphery of the electrode member. For example, with an electrode member having an area of about 80 cma, a mat area of about 25 cm2 has been found sufficient to distribute the energy of defibrillation pulses over a sufficiently large area to overcome arcing through the electrode member.
The metal/metal chloride coating an be applied to the entire under side of the electrode member. However, in order to reduce the possibility of skin irritation at the periphery of the electrode member, the outer perimeter of the metal/metal chloride coating 23 is preferably spaced inwardly from the perimeter 21p of the electrode member 3 0 and outwardly of the perimeter 2 7p of the conductive mat .
The metal/metal chloride coating is preferably formed in two layers each of a few microns in thickness with one layer designated 23' having an outer perimeter 23p' spaced inwardly of the perimeter 21p of the electrode member and a second layer 23" having an outer perimeter 23p~~ spaced inwardly from the perimeter 23p' and outwardly of the perimeter 27p of the current distributing mat 27. The layers 23', 23" are applied in successive layers on the electrode member 21 to allow a first layer to dry before applying the second. The layer 23" is preferably applied first with layer 23' underlying the layer 23". The dual layers provide higher electrical conductivity in the are where the metal/metal chloride layers overlap, with the conductivity stepping down in the single layer and decreasing to the conductivity of the carbon filled polymer of the electrode member 21 in the area outwardly of the metal/metal chloride coating. The area where the layers overlap, which corresponds to the area of coating 23' , is preferably made substantially equal to the minimum active electrode area prescribed by ANSI/AAMI. For example, the layers 23' and 23" can each have a thickness of about 3 to 5 microns, with a combined thickness in the area of overlap of about six to ten microns. In addition, the outer perimeter of the layers 23' and 23" are advantageously serrated or undulated, for example as shown in Figs. 1 and 3. This arrangement further decreases the current density by increasing the effective perimeter of the electrode member and minimized the likelihood of skin burns or irritation.
In the embodiment of Figs . 1-5 , electrical conductors 35 are provided to conduct current to or from the electrode member. In some applications it is desirable that the conductors also be X-ray transparent. X-ray transparent conductors are preferably formed of metallized carbon fiber tows with an insulating sheath formed of an X-ray transparent material. The carbon fiber tows are preferably of a size having between 3, 000 to 12, 000 fibers and metal plated with a metal coating that is about 20~ to 50~ by weight of the metal plated carbon fiber tow. The higher weights plating on the larger size tows provides improved current carrying capacity for repeated defibrillation pulses. Standard carbon fiber tows are made from a polyacrylonitrile precursor and are referred to as pan base carbon fiber and are commercially available from Amoco Performance Products, Inc., Atlanta, GA. In general, the carbon fiber tows are made by procedures described in U.S. Patent 3,677,705 by heating polymeric fiber, e.g. acrylonitrile polymers or copolymers tin two stages, one to remove volatiles and carbonize and the other to convert amorphous carbon into crystal and carbon.
During such procedures, the carbon changes from amorphous to single crystal and then orients into fibrous carbon.
The fibrous carbon has a fiber diameter in the range of about 5 to 8 microns and the number of fibers in the tow can vary in a wide range from a few hundred to many thousand. The carbon fiber tows can be metal plated or coated by vacuum deposition for example as disclosed in U.S. Patent 4,132,828; by vapor deposition for example as disclosed in U.S. Patent 3,733,213; by electroplating such as disclosed in U.S. Patent 4,661,403; or by chemical vapor deposition such as by thermo decomposition of nickel carbonyl gas.
In general, tinplated pan base carbon fiber tows have a low density and are X-ray transparent as compared to metal wires of comparable size. Pan base carbon fiber tows have a longitudinal electrical resistance that is very high and longitudinal thermal conductivity that is very low as compared to metal wires of comparable size.
Carbon fiber tows also exhibit anisotropic electrical conductivity which presents a problem when making electrical connection to other devices. The addition of the metal coating on the carbon fiber tows converts the 'conduction from anisotropic to isotropic, thereby 3o alleviating the problem. Since the density of the carbon fiber tows is very low as compared to the density of the metal coating, a metal coating of 30~ to 40~ by weight of the metal plated carbon fiber tow is very thin and is X-ray transparent. The metal coating is preferably nickel which provides good electrical conductivity and corrosion resistance at moderate costs, but other metal such as copper or silver or gold could be used alone or in combination with the nickel coating.
The unsheathed end portion 35a of the conductor is spread or fanned out as shown in Figs . 1 and 3 and pressed against the upper side of the conductive mat 27 to electrically connect the conductor to the mat and through the mat to the electrode member 21. In order to assure good conductivity and sealing of the fibers, the mat preferably includes a second section 27' arranged to l0 overlie the unsheathed end portion of the conductor.
Conveniently, the sections 27 and 27' of the mat can be formed in one piece and folded over so that they are interconnected at one end as shown in Fig. 5 In order to minimize the likelihood of pulling the conductors relative to the mat, the sheath 36 is preferably heat softened and flattened against the conductors 35 as by heated jaws 51 as shown in Fig. 4, prior to attachment of the conductor to -the -conductive-mat-.-- The--sheath- is- preferably -flattened over a length indicated at 36a sufficient to extend outwardly beyond the perimeter of the electrode 21 but inwardly of the perimeter of the cover, to minimize displacement of the gel pad. In electrode applications where x-ray transparency of the conductors is nor required, the conductors can be formed of metal, preferably multi-stand conductors which can be spread out, to increase the contact area between the conductor and the conductive mat. When metal conductors are used, the electrode remains X-ray transparent, and only the metal wires and to a lesser extent the sheath, show up on the X-rays. Further, if the conductive mat is a metal foil, the conductor may be attached to the conductive mat by solder.
Alternatively, as illustrated in Figs. 8 and 9, the energy conducting means may comprise a conductive post stud connector 135 and conductive washer 135a, conductively adhered to the current distributing mat 27.
Such a conductor permits cost-effective use of the electrode with certain defibrillators currently on the market. The post stud connector 135 and washer 135a may be made of a conductive metal ( such as nickel-plated brass or stainless steel) or a conductive plastic. The conductive plastic may be ABS plastic resin, nylon 12, or Carillon polymer crystal resin manufactured by Shell Oil, loaded with 25-40~ nickelized carbon fibers. After being molded into the post stud and washer, the conductive plastic may be silver-coated (by, e.g., electrolysis) to further enhance its conductivity.
to The current distributing mat preferably includes a second mat portion 27' arranged to overlie the mat 27.
Conveniently, the sections 27 and 27' can be formed in one piece and folded over so that they are interconnected to one end. Further, section 27' of the conductive mat includes a centrally located hole through which the post stud connector 135 protrudes. To provide added resistance to the post stud 135 being pulled through the conductive mat 27 and cover sheet 33 and to help distribute current, a reinforcement sheet 135b of a Tyvek or Mylar polyester 2o sheet material laminated to a flexible tin or other metal foil 135c is secured to the washer 135a by a locking ring 135d.
In a further alternative, the energy conducting means may comprise a metallic conductive tab 235, as illustrated in Fig. 10. The conductive tab 235 is made of metal foil, preferably tin, and extends from the central portion of the electrode 10 to outside the periphery of the base frame 28 to permit connection of the tab to a further conductor (not shown) that connects to a defibrillator.
3o As with the embodiment of Figs. 8 and 9, the current distributing mat 27, 27' is of one piece with section 27' overlying the mat 27 to encase the end of the conductive tab 235. In order to provide the conductive tab 235 with increased tensile strength, the bottom side of the tab 235 is laminated with spun-bonded polyester fiber mat 235a ( such as Remay fiber made by DuPont ) . The reinforcing mat 235a is bonded to the conductive tab 235 with a non-conductive rubber-based or acrylic adhesive.
Alternatively, a polyester coating material (such as Fastclear made by Fasson Avery) can be used for the reinforcing mat 235a. The reinforcing mat 235a extends 5 from the outer portion of the conductive tab 235 to just inside the current distributing mat 27, 27' so as to not interfere with the conduction of energy from the conductive tab 235 to the mat 27, 27' . A two-part locking ring ( not shown ) may be used to more positively secure the l0 conductive tab 235 to the mat 27, 27'.
The electrode construction including the carbon filled polymer electrode member with the metal/metal chloride coating on the underside and the conductive mat having a metallized carbon fiber web and pressure 15 sensitive adhesive on the upper and lower sides of the web, not only provides an electrode that is X-ray transparent and capable of transmitting energy at levels sufficient --~a~--d-efibriiiation,--but which--also--has--a recovery time after delivery of a defibrillation pulse that meets or exceeds the AAMI/ANSI standards for pre-gelled ECG disposable electrodes. Thus, the electrodes can function as combination defibrillation electrodes and ECG electrodes. Since the electrodes are X-ray transparent, they can be positioned on the patient at any of the customary positions used for defibrillation without adversely affecting X-rays of the patient's chest in areas underlying the electrodes. As diagrammatically shown in Fig. 6, the energy delivery and energy accepting electrodes 10, 10' are connected through conductors 35, 3 0 35 ' to a polarized connector 5 0 to lead conductors 51, 51 ' connected to a combination defibrillator and ECG monitor 52. Further, electrodes configured in the manner described above are also capable of conducting AC energy at levels sufficient for use as current receiving or ground electrodes in electrosurgery.
The energy delivering and energy accepting electrodes 10 and 10' can also be used with defibrillation paddles.
As shown in Fig. 7, an electrode 10" is configured the same as that previously described in connection with electrode 10, but the conductor 35 is omitted. The insulating cover sheet 33' is provided with an opening 33"
in an area overlying the conductive mat, such that a defibrillation paddle can contact the mat. A removable cover sheet 36 is provided to cover the opening 33' prior to use of the electrode.
The electrode construction also provides more uniform to current distribution over the electrode area than that achieved by prior electrodes using metal plates or metal wire mesh. The surface resistance (X, Y resistance) and the volume resistance (Z resistance) was measured using a pair of stainless steel blocks with the dimensions 1.0"x1.0"x0.5" and an ohmmeter. For measuring surface resistance the blocks were placed on the 3"xl" material with 1.0" between them. For measuring volume resistance, a piece of the layer or layers being tested was placed between the blocks so as to be sandwiched by them.
The surface resistance (X, Y resistance) of the conductive mat 27 is much lower than the surface resistance of the electrode member 21. The measured surface resistance of the electrode member (without an Ag/Agcl coat) was in a range of about 200 to 250 ohms/sq.
in. for electrode members of about two mils in thickness and in a range of about 75 to 100 ohms/sq. in. for electrode members of about four mils in thickness, and the surface resistance varied in those ranges with the texture of the surface and the contact pressure between the blocks 3o and the electrode member. The surface resistance of the conductive mat 27 was in a range of about 3 to 6 ohms/sq.
in.
The surface resistance of the underside of the electrode member with the Ag/Agcl coating is lower than without the coating, and the surface resistance decreases as the thickness of the Ag/Agcl coating is increased. For example, the surface resistance of the electrode member having a single Ag/Agcl coating of about 3 to 4 microns, such as layer 23' is about 185 ohms/sq. in. and the electrode member having a thicker coating of about 9 or 10 microns has a surface resistance less than one ohm. The thickness of a coating in the area where the coating 23' and 23" overlap, is preferably in the range of about 8 to microns in thickness.
The resistance measured perpendicular to the surface is herein referred to the volume resistance or "Z"
10 resistance. The volume resistance of the conductive mat 27 is about one or two ohms/sq. in. and the volume resistance of the other layers is lower, generally less than one ohmm per square inch. The overall volume resistance of the electrode, measured from the top of conductive mat 27' to the underside center of Ag/AgCl coating 23' on the bottom of the electrode member, is only about one to three ohms/sq. in.
The DC resistance of the gel layer decreases rapidly with increasing current density and an ohmmeter cannot be used to indicate the resistance offered to defibrillation current. However, the volume or Z axis resistance of the gel is very low at the current density encountered in defibrillation.
The carbon filled sheet electrode member is X-ray transparent and the coating 23 of metal/metal chloride is applied in a layer or layers to the lower face of the electrode member as by silk screening or by flexographic printing. If the coating 23 is silver/silver chloride , it is preferably less than ten microns in thickness, which is sufficient to provide good electrical conductivity without impairing the X-ray transparency of the electrode member. A carbon filled PvC material with silver/silver chloride coating on the underside suitable for use as an electrode member is available from Prime Label And Screen, Inc., New Berlin, Wisconsin. Alternatively, the metal/metal chloride coating can comprise a single layer, chloride-coated metallic foil coated with a conductive acrylic adhesive. The metallic foil may comprise silver, tin, copper, nickel, gold, aluminum, platinum, chromium, cadmium, pladmium, zinc, antimony, or indium covered with an adhesive such as the Arclad 8001 bonding tape or Arclad EC2 adhesive described below.
The electrode member 2I has a surface area dimensioned to distribute energy over an area of the patient's epidermis to achieve proper current density 3o distribution within the ventricles of the patient's heart.
The ANSI standards for the size of defibrillation electrodes published by AAMI presently recommends that the minimum active area of individual self-adhesive electrodes used for adult defibrillation and pacing shall be at least 50 cm2 and that the total area of two electrodes used in defibrillation shall be at least 150 cm2. The electrode member 21 has an area of at least 50 cm2 and preferably about 80 cm2 or more so that a pair of the electrodes used for defibrillation can be of the same size. 15 cm2 is the minimum electrode area recommended for pediatric transthoracic use and the area of the electrode member 21 of the present invention for pediatric use can be made correspondingly smaller.
The carbon filled polymer electrode 21 is conductive in the plane of the electrode and transverse to the plane electrode and the metal/metal chloride coating on the under side of the electrode member is also conductive in the plane of the coating and transverse to the plane of the coating. The carbon filled polymer electrode member has a surface resistance substantially higher than the surface resistance of the metal/metal chloride coating and it has been found that the carbon filled polymer electrode member with a silver/silver chloride coating is not alone capable for transmitting and distributing the high levels of energy encountered--in-de~i.brillation beer-the entire surface of the electrode member.
In the preferred embodiment, the current distributing mat 27 is configured to have electrical conductivity in the of the mat and transverse to the plane of the mat and a higher current carrying capacity than the sheet electrode member. The current distributing mat includes a non-woven open mesh metallized carbon fiber web having an electrically conductive carbon impregnated pressure sensitive adhesive composition on the upper and lower sides of the web. The web of the current distribution mat is thin and preferably less than five mills in thickness and is comprised of semi-metallic fibers such as carbon fibers which are metal plated or coated before or after being formed into a web with a metal coating that is 35$
to 40~ by weight of the metal plated carbon fiber web.
The semi-metallic carbon fibers are X-ray transparent before plating or coating and the metal plating or coating of the fibers of the web is sufficiently think for example less than ten microns in thickness, and such that the thin open-mesh web formed of the metal plated fibers remains X-ray transparent. The electrically conductive pressure sensitive adhesive that is applied to opposite sides of the web is loaded with sufficient carbon or graphite for good electrical conductivity and such that the composite web and adhesive provide a mat that is electrically conductive in the plane of the mat and transverse to the plane of the mat. An example of a conductive double face pressure sensitive tape with a conductive carrier which l0 can be used for the mat is a thin pressure sensitive bonding tape available from Adhesives Research, Inc., Glen Rock, Pa. under the trademark "Arclad," product No. 8001.
This tape comprises a non-woven open mesh mat or carrier formed of metal coated carbon filaments having a metal coating of a few microns, for example five or six microns in thickness, and such that the metal coated mat is X-ray transparent. The electrically conductive pressure sensitive adhesive comprises a pressure sensitive adhesive impregnated with carbon or graphite for conductivity.
U.S. Patent No. 5,082,595 assigned to Adhesive Research, Inc. discloses a method of making such a double faced pressure sensitive adhesive tape with conductivity in X, Y and Z axes.
Alternatively, the current distributing mat 27 may comprise a solid metallic foil or fine screen mesh covered with a conductive polymer adhesive for attaching the mat to the sheet electrode 21. The foil is on the order of 0.001-0.002 inches thick and suitable metals include copper or tin. Other metals may be used, such as gold, silver, nickel, aluminum, platinum, chromium, cadmium, pladmium, zinc, antimony, and indium. However, the cost of certain of these metals could make their use unlikely.
If the monitoring aspects of the electrode are important, the foil should comprise a metal halide. (Of course, the use of metal foils for the current distributing mat adversely affects the x-ray transmissivity of the electrode.) Suitable adhesives include the Arclad 8001 bonding tape described above. EC2 adhesive by Adhesive Research can also be used.
Published literature indicates that, when a metal plate electrode having an electrolytic gel coating on its 5 underside, is placed on the skin and used to delivery current, the current density is very much higher under the perimeter of the electrode than under the center. A
similar problem occurs at the energy accepting electrode of a set of such defibrillation electrodes. The mat 27 is 1o arranged to distribute current over a central area of the electrode member 21 and has an outer perimeter 27p spaced inwardly of the perimeter 21p of the electrode member.
The mat is sized to distribute the current more uniformly over the central portion of the electrode member to inhibit arcing through the central portion of the electrode member, and is spaced inwardly from the perimeter of the electrode member to avoid conveying high current levels to the outer periphery of the electrode member. For example, with an electrode member having an area of about 80 cma, a mat area of about 25 cm2 has been found sufficient to distribute the energy of defibrillation pulses over a sufficiently large area to overcome arcing through the electrode member.
The metal/metal chloride coating an be applied to the entire under side of the electrode member. However, in order to reduce the possibility of skin irritation at the periphery of the electrode member, the outer perimeter of the metal/metal chloride coating 23 is preferably spaced inwardly from the perimeter 21p of the electrode member 3 0 and outwardly of the perimeter 2 7p of the conductive mat .
The metal/metal chloride coating is preferably formed in two layers each of a few microns in thickness with one layer designated 23' having an outer perimeter 23p' spaced inwardly of the perimeter 21p of the electrode member and a second layer 23" having an outer perimeter 23p~~ spaced inwardly from the perimeter 23p' and outwardly of the perimeter 27p of the current distributing mat 27. The layers 23', 23" are applied in successive layers on the electrode member 21 to allow a first layer to dry before applying the second. The layer 23" is preferably applied first with layer 23' underlying the layer 23". The dual layers provide higher electrical conductivity in the are where the metal/metal chloride layers overlap, with the conductivity stepping down in the single layer and decreasing to the conductivity of the carbon filled polymer of the electrode member 21 in the area outwardly of the metal/metal chloride coating. The area where the layers overlap, which corresponds to the area of coating 23' , is preferably made substantially equal to the minimum active electrode area prescribed by ANSI/AAMI. For example, the layers 23' and 23" can each have a thickness of about 3 to 5 microns, with a combined thickness in the area of overlap of about six to ten microns. In addition, the outer perimeter of the layers 23' and 23" are advantageously serrated or undulated, for example as shown in Figs. 1 and 3. This arrangement further decreases the current density by increasing the effective perimeter of the electrode member and minimized the likelihood of skin burns or irritation.
In the embodiment of Figs . 1-5 , electrical conductors 35 are provided to conduct current to or from the electrode member. In some applications it is desirable that the conductors also be X-ray transparent. X-ray transparent conductors are preferably formed of metallized carbon fiber tows with an insulating sheath formed of an X-ray transparent material. The carbon fiber tows are preferably of a size having between 3, 000 to 12, 000 fibers and metal plated with a metal coating that is about 20~ to 50~ by weight of the metal plated carbon fiber tow. The higher weights plating on the larger size tows provides improved current carrying capacity for repeated defibrillation pulses. Standard carbon fiber tows are made from a polyacrylonitrile precursor and are referred to as pan base carbon fiber and are commercially available from Amoco Performance Products, Inc., Atlanta, GA. In general, the carbon fiber tows are made by procedures described in U.S. Patent 3,677,705 by heating polymeric fiber, e.g. acrylonitrile polymers or copolymers tin two stages, one to remove volatiles and carbonize and the other to convert amorphous carbon into crystal and carbon.
During such procedures, the carbon changes from amorphous to single crystal and then orients into fibrous carbon.
The fibrous carbon has a fiber diameter in the range of about 5 to 8 microns and the number of fibers in the tow can vary in a wide range from a few hundred to many thousand. The carbon fiber tows can be metal plated or coated by vacuum deposition for example as disclosed in U.S. Patent 4,132,828; by vapor deposition for example as disclosed in U.S. Patent 3,733,213; by electroplating such as disclosed in U.S. Patent 4,661,403; or by chemical vapor deposition such as by thermo decomposition of nickel carbonyl gas.
In general, tinplated pan base carbon fiber tows have a low density and are X-ray transparent as compared to metal wires of comparable size. Pan base carbon fiber tows have a longitudinal electrical resistance that is very high and longitudinal thermal conductivity that is very low as compared to metal wires of comparable size.
Carbon fiber tows also exhibit anisotropic electrical conductivity which presents a problem when making electrical connection to other devices. The addition of the metal coating on the carbon fiber tows converts the 'conduction from anisotropic to isotropic, thereby 3o alleviating the problem. Since the density of the carbon fiber tows is very low as compared to the density of the metal coating, a metal coating of 30~ to 40~ by weight of the metal plated carbon fiber tow is very thin and is X-ray transparent. The metal coating is preferably nickel which provides good electrical conductivity and corrosion resistance at moderate costs, but other metal such as copper or silver or gold could be used alone or in combination with the nickel coating.
The unsheathed end portion 35a of the conductor is spread or fanned out as shown in Figs . 1 and 3 and pressed against the upper side of the conductive mat 27 to electrically connect the conductor to the mat and through the mat to the electrode member 21. In order to assure good conductivity and sealing of the fibers, the mat preferably includes a second section 27' arranged to l0 overlie the unsheathed end portion of the conductor.
Conveniently, the sections 27 and 27' of the mat can be formed in one piece and folded over so that they are interconnected at one end as shown in Fig. 5 In order to minimize the likelihood of pulling the conductors relative to the mat, the sheath 36 is preferably heat softened and flattened against the conductors 35 as by heated jaws 51 as shown in Fig. 4, prior to attachment of the conductor to -the -conductive-mat-.-- The--sheath- is- preferably -flattened over a length indicated at 36a sufficient to extend outwardly beyond the perimeter of the electrode 21 but inwardly of the perimeter of the cover, to minimize displacement of the gel pad. In electrode applications where x-ray transparency of the conductors is nor required, the conductors can be formed of metal, preferably multi-stand conductors which can be spread out, to increase the contact area between the conductor and the conductive mat. When metal conductors are used, the electrode remains X-ray transparent, and only the metal wires and to a lesser extent the sheath, show up on the X-rays. Further, if the conductive mat is a metal foil, the conductor may be attached to the conductive mat by solder.
Alternatively, as illustrated in Figs. 8 and 9, the energy conducting means may comprise a conductive post stud connector 135 and conductive washer 135a, conductively adhered to the current distributing mat 27.
Such a conductor permits cost-effective use of the electrode with certain defibrillators currently on the market. The post stud connector 135 and washer 135a may be made of a conductive metal ( such as nickel-plated brass or stainless steel) or a conductive plastic. The conductive plastic may be ABS plastic resin, nylon 12, or Carillon polymer crystal resin manufactured by Shell Oil, loaded with 25-40~ nickelized carbon fibers. After being molded into the post stud and washer, the conductive plastic may be silver-coated (by, e.g., electrolysis) to further enhance its conductivity.
to The current distributing mat preferably includes a second mat portion 27' arranged to overlie the mat 27.
Conveniently, the sections 27 and 27' can be formed in one piece and folded over so that they are interconnected to one end. Further, section 27' of the conductive mat includes a centrally located hole through which the post stud connector 135 protrudes. To provide added resistance to the post stud 135 being pulled through the conductive mat 27 and cover sheet 33 and to help distribute current, a reinforcement sheet 135b of a Tyvek or Mylar polyester 2o sheet material laminated to a flexible tin or other metal foil 135c is secured to the washer 135a by a locking ring 135d.
In a further alternative, the energy conducting means may comprise a metallic conductive tab 235, as illustrated in Fig. 10. The conductive tab 235 is made of metal foil, preferably tin, and extends from the central portion of the electrode 10 to outside the periphery of the base frame 28 to permit connection of the tab to a further conductor (not shown) that connects to a defibrillator.
3o As with the embodiment of Figs. 8 and 9, the current distributing mat 27, 27' is of one piece with section 27' overlying the mat 27 to encase the end of the conductive tab 235. In order to provide the conductive tab 235 with increased tensile strength, the bottom side of the tab 235 is laminated with spun-bonded polyester fiber mat 235a ( such as Remay fiber made by DuPont ) . The reinforcing mat 235a is bonded to the conductive tab 235 with a non-conductive rubber-based or acrylic adhesive.
Alternatively, a polyester coating material (such as Fastclear made by Fasson Avery) can be used for the reinforcing mat 235a. The reinforcing mat 235a extends 5 from the outer portion of the conductive tab 235 to just inside the current distributing mat 27, 27' so as to not interfere with the conduction of energy from the conductive tab 235 to the mat 27, 27' . A two-part locking ring ( not shown ) may be used to more positively secure the l0 conductive tab 235 to the mat 27, 27'.
The electrode construction including the carbon filled polymer electrode member with the metal/metal chloride coating on the underside and the conductive mat having a metallized carbon fiber web and pressure 15 sensitive adhesive on the upper and lower sides of the web, not only provides an electrode that is X-ray transparent and capable of transmitting energy at levels sufficient --~a~--d-efibriiiation,--but which--also--has--a recovery time after delivery of a defibrillation pulse that meets or exceeds the AAMI/ANSI standards for pre-gelled ECG disposable electrodes. Thus, the electrodes can function as combination defibrillation electrodes and ECG electrodes. Since the electrodes are X-ray transparent, they can be positioned on the patient at any of the customary positions used for defibrillation without adversely affecting X-rays of the patient's chest in areas underlying the electrodes. As diagrammatically shown in Fig. 6, the energy delivery and energy accepting electrodes 10, 10' are connected through conductors 35, 3 0 35 ' to a polarized connector 5 0 to lead conductors 51, 51 ' connected to a combination defibrillator and ECG monitor 52. Further, electrodes configured in the manner described above are also capable of conducting AC energy at levels sufficient for use as current receiving or ground electrodes in electrosurgery.
The energy delivering and energy accepting electrodes 10 and 10' can also be used with defibrillation paddles.
As shown in Fig. 7, an electrode 10" is configured the same as that previously described in connection with electrode 10, but the conductor 35 is omitted. The insulating cover sheet 33' is provided with an opening 33"
in an area overlying the conductive mat, such that a defibrillation paddle can contact the mat. A removable cover sheet 36 is provided to cover the opening 33' prior to use of the electrode.
The electrode construction also provides more uniform to current distribution over the electrode area than that achieved by prior electrodes using metal plates or metal wire mesh. The surface resistance (X, Y resistance) and the volume resistance (Z resistance) was measured using a pair of stainless steel blocks with the dimensions 1.0"x1.0"x0.5" and an ohmmeter. For measuring surface resistance the blocks were placed on the 3"xl" material with 1.0" between them. For measuring volume resistance, a piece of the layer or layers being tested was placed between the blocks so as to be sandwiched by them.
The surface resistance (X, Y resistance) of the conductive mat 27 is much lower than the surface resistance of the electrode member 21. The measured surface resistance of the electrode member (without an Ag/Agcl coat) was in a range of about 200 to 250 ohms/sq.
in. for electrode members of about two mils in thickness and in a range of about 75 to 100 ohms/sq. in. for electrode members of about four mils in thickness, and the surface resistance varied in those ranges with the texture of the surface and the contact pressure between the blocks 3o and the electrode member. The surface resistance of the conductive mat 27 was in a range of about 3 to 6 ohms/sq.
in.
The surface resistance of the underside of the electrode member with the Ag/Agcl coating is lower than without the coating, and the surface resistance decreases as the thickness of the Ag/Agcl coating is increased. For example, the surface resistance of the electrode member having a single Ag/Agcl coating of about 3 to 4 microns, such as layer 23' is about 185 ohms/sq. in. and the electrode member having a thicker coating of about 9 or 10 microns has a surface resistance less than one ohm. The thickness of a coating in the area where the coating 23' and 23" overlap, is preferably in the range of about 8 to microns in thickness.
The resistance measured perpendicular to the surface is herein referred to the volume resistance or "Z"
10 resistance. The volume resistance of the conductive mat 27 is about one or two ohms/sq. in. and the volume resistance of the other layers is lower, generally less than one ohmm per square inch. The overall volume resistance of the electrode, measured from the top of conductive mat 27' to the underside center of Ag/AgCl coating 23' on the bottom of the electrode member, is only about one to three ohms/sq. in.
The DC resistance of the gel layer decreases rapidly with increasing current density and an ohmmeter cannot be used to indicate the resistance offered to defibrillation current. However, the volume or Z axis resistance of the gel is very low at the current density encountered in defibrillation.
Claims (52)
1. A disposable transcutaneous electrode comprising, a sheet electrode member of electrically conductive polymer having upper and lower sides and an outer perimeter, an electrically conductive silver/silver chloride coating on at least a major portion of the lower side of the electrode member, a pad of electrically conductive gel having an upper surface underlying the silver/silver chloride coating on the lower side of the electrode, a removable carrier sheet on a lower surface of the pad for covering the latter prior to use, a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the electrode member, the mat including an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having the lower surface conductively adhered to the upper side of the sheet electrode member, means for conducting defibrillating energy to or from the upper side of the mat and a medical device, the sheet electrode member and the current distributing mat being configured to be X-ray transparent and capable of conducting energy at levels sufficient for defibrillation.
2. An electrode according to Claim 1 wherein the means for conducting defibrillation energy comprises an electrical conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively adhered to the mat.
3. An electrode according to Claim I wherein the electrical resistance of the mat in directions paralleling the surface of the mat is less than the electrical resistance of the sheet electrode member in directions paralleling the upper side of the sheet electrode member.
4. An electrode according to Claim 1 wherein the silver/silver chloride coating has an outer edge spaced inwardly of the outer perimeter of the sheet electrode.
5. An electrode according to Claim 1 wherein the silver/silver chloride coating includes first and second layers, the first layer having an outer edge spaced inwardly of the outer perimeter of the sheet electrode member and the second layer having an outer edge spaced inwardly of the outer edge of the first layer.
6. A disposable transcutaneous electrode comprising, a sheet electrode member of electrically conductive carbon filled polymer having upper and lower sides and an outer perimeter, an electrically conductive silver/silver chloride coating on at least a major portion of the lower side of the electrode member, a pad of electrically conductive gel having an upper surface underlying the silver/silver chloride coating on the lower side of the electrode member, a removable carrier sheet on a lower surface of the pad for covering the latter prior to use, a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the electrode member, the mat including an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having the lower surface conductively adhered to the upper side of the sheet electrode member, an electrical conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively adhered to the mat for conducting defibrillating energy to or from the upper side of the mat and a medical device, the sheet electrode member and the current distributing mat being configured to be X-ray transparent and capable of conducting energy sufficient for defibrillation.
7. An electrode according to Claim 6 including a second mat having a metallized carbon fiber web and electrically conductive pressure sensitive adhesive composition on upper and lower sides, the end portion of the conductor being adhered to the upper side of the first-mentioned mat and the lower side of the second mat overlying and adhered to the end portion of the conductor and at least a portion of the upper side of the first-mentioned mat.
8. An electrode according to Claim 7 wherein said conductor comprises an X-ray transparent metal coated carbon fiber tow.
9. An electrode according to Claim 8 wherein the metal coating on the carbon fiber tow is about 20% to 50%
by weight of the metal coated fiber tow.
by weight of the metal coated fiber tow.
10. An electrode according to Claim 8 wherein the tow of carbon fibers has greater than six thousand fibers.
11. An electrode according to Claim 6 wherein said conductor comprises an X-ray transparent nickel plated carbon fiber tow.
12. An electrode according to Claim 6 wherein said conductor comprises a multiple strand metallic conductor.
13. An electrode according to Claim 6 wherein the sheath is formed of a thermoplastic material and the sheath is best softened and flattened to a thickness less than the normal thickness of the sheath along a length contiguous to the unsheathed end portion.
14. A set of disposable transcutaneous electrode including an energy delivering electrode and an energy accepting electrode, each electrode comprising, a sheet electrode member of electrically conductive carbon filled polymer having upper and lower sides and an outer perimeter, an electrically conductive silver/silver chloride coating on at least a major portion of the lower side of the electrode member, a pad of electrically conductive gel having an upper surface underlying the silver/silver chloride coating on the lower side of the electrode member, a removable carrier sheet on a lower surface of the pad for covering the latter prior to use, a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the electrode member, the mat including an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having the lower surface conductively adhered to the upper side of the sheet electrode member, an electrically conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively adhered to the mat for conducting defibrillating energy to or from the upper side of the mat and a medical device, the sheet electrode member and the current distributing mat being configured to be X-ray transparent and capable for conducting energy sufficient for defibrillation, and a cover member of electrical insulating material attached to the upper sheet electrode and mat.
15. An electrode set according to Claim 14 wherein each electrode includes a second mat having a metallized carbon fiber web and electrical resistance of the mat in directions paralleling the surface of the mat is less than the electrical resistance of the sheet electrode member in directions paralleling the upper side of the sheet electrode member.
16. An electrode set according to Claim 14 wherein the silver/silver chloride coating on each electrode has an outer edge spaced inwardly of the outer perimeter of the sheet electrode member.
17. An electrode set according to Claim 14 wherein the silver/silver chloride coating on each electrode includes first and second layers, the first layer having an outer edge spaced inwardly of the outer perimeter of the sheet electrode member and the second layer having an outer edge spaced inwardly of the outer edge of the first layer.
18. An electrode set according to Claim 14 wherein the electrical conductor associated with each electrode comprises an X-ray transparent metal coated carbon fiber tow.
19. An electrode set according to Claim 18 wherein the metal coating on the carbon fiber tow is at least 30%
by weight of the metal coated carbon fiber tow.
by weight of the metal coated carbon fiber tow.
20. An electrode set according to Claim 19 wherein tow of carbon fibers has greater than six thousand fibers.
21. An electrode set according to Claim 14 wherein the electrical conductor associated with each electrode comprises an X-ray transparent nickel plated carbon fiber tow.
22. An electrode set according to Claim 14 wherein the electrical conductor associated with each electrode comprises a multiple strand metallic conductor.
23. A disposable transcutaneous energy accepting electrode comprising, a sheet electrode member of electrically conductive carbon filled polymer having upper and lower sides and an outer perimeter, an electrically conductive silver/silver chloride coating on at least a major portion of the lower side of the electrode member, a pad of electrically conductive gel having an upper surface underlying the silver/silver chloride coating on the lower side of the electrode member, a removable carrier sheet on a lower surface of the pad for covering the latter prior to use, a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the electrode member, the mat including an open mesh metallized carbon fiber web having a carbon impregnated pressure sensitive adhesive composition on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having the lower surface conductively adhered to the upper side of the sheet electrode member, an electrical conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively adhered to the mat for conducting defibrillating energy to or from the upper side of the mat, the sheet electrode member and the current distributing mat being configured to be X-ray transparent and capable of conducting energy at levels sufficient for use as an energy receiving electrode in defibrillation and electro-surgery.
24. A disposable transcutaneous electrode comprising, a sheet electrode member of electrically conductive polymer having upper and lower sides and an outer perimeter, an electrically conductive metallic layer conductively affixed to at least a major portion of the lower side of the electrode member, the electrode member having a surface electrical resistance, measured in directions paralleling the upper and lower sides, higher than the surface electrical resistance of the metallic layer, a pad of electrically conductive gel having an upper surface underlying the metallic layer on the lower side of the electrode member, a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the electrode member, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having surface electrical resistance, measured in directions paralleling the surfaces of the mat, less than the surface electrical resistance of the sheet electrode member, the mat having the lower surface conductively affixed to the upper side of the sheet electrode member, and means for conducting defibrillating energy to or from the mat and a medical device, the sheet electrode member and the current distributing mat being configured to be capable of conducting energy at levels sufficient for deffibrillation.
25. A disposable transcutaneous electrode comprising, a sheet electrode member of electrically conductive carbon filled polymer material having upper and lower sides and an outer perimeter, an electrically conductive metal/metal chloride coating on at least a major portion of the lower side of the electrode member, a pad of electrically conductive gel having an upper surface underlying the metal/metal chloride coating on the lower side of the electrode member, a pad of electrically conductive gel having an upper surface underlying the metal/metal chloride coating on the lower side of the electrode member, a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the sheet electrode member, the mat including a metallized carbon fiber web having a carbon impregnated electrically conductive pressure sensitive adhesive composition on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having surface electrical resistance, measured in directions paralleling the surfaces of the mat, less than the surface electrical resistance of the sheet electrode member measured in directions paralleling the sides of the sheet electrode member, the mat having the lower surface conductively adhered to the upper side of the sheet electrode member, an electrical conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively adhered to the mat for conducting defibrillating energy to or from the upper side of the mat and a medical device, the sheet electrode member and the current distributing mat being configured to be X-ray translucent and capable of conducting energy sufficient for defibrillation.
26. A disposable transcutaneous electrode comprising:
(a) a sheet electrode member of electrically conductive polymer material having upper and lower sides and an outer perimeter;
(b) means for conducting and distributing energy from a medical device to an area of the sheet electrode member less than an area defined by the outer perimeter of the sheet electrode member, the means for conducting and distributing the energy being conductively affixed to the upper side of the sheet electrode member;
(c) an electrically conductive metallic layer conductively affixed to a least a major portion of the lower side of the sheet electrode member, the sheet electrode member having a surface electrical resistance, measured in directions paralleling the upper and lower sides, higher than the surface electrical resistance of the metallic layer, the electrically conductive metallic layer having a region of high conductivity in a central region located inwardly from the outer perimeter of the sheet electrode member and a region of low conductivity in an encircling region surrounding the central region and adjacent the outer perimeter of the sheet electrode member; and (d) a pad of electrically conductive gel having an upper surface underlying the metallic layer, the pad conducting the energy from the sheet electrode member to a patient on which the electrode is disposed.
(a) a sheet electrode member of electrically conductive polymer material having upper and lower sides and an outer perimeter;
(b) means for conducting and distributing energy from a medical device to an area of the sheet electrode member less than an area defined by the outer perimeter of the sheet electrode member, the means for conducting and distributing the energy being conductively affixed to the upper side of the sheet electrode member;
(c) an electrically conductive metallic layer conductively affixed to a least a major portion of the lower side of the sheet electrode member, the sheet electrode member having a surface electrical resistance, measured in directions paralleling the upper and lower sides, higher than the surface electrical resistance of the metallic layer, the electrically conductive metallic layer having a region of high conductivity in a central region located inwardly from the outer perimeter of the sheet electrode member and a region of low conductivity in an encircling region surrounding the central region and adjacent the outer perimeter of the sheet electrode member; and (d) a pad of electrically conductive gel having an upper surface underlying the metallic layer, the pad conducting the energy from the sheet electrode member to a patient on which the electrode is disposed.
27. The disposable transcutaneous electrode of Claim 26, wherein the electrically conductive metallic layer comprises a first layer and a second layer, the first layer being conductively disposed against the sheet electrode member and having a perimeter that is spaced inwardly from the outer perimeter of the sheet electrode member, the second layer overlapping the first layer and being conductively disposed against the first layer and the sheet electrode member and having a perimeter that is spaced outwardly from the perimeter of the first layer and inwardly from the outer perimeter of the sheet electrode member.
28. The disposable transcutaneous electrode of Claim 27, wherein the perimeter of the first layer is serrated.
29. The disposable transcutaneous electrode of Claim 27, wherein the perimeter of the second layer is serrated.
30. The disposable transcutaneous electrode of Claim 27, wherein the electrically conductive metallic layer is a metal/metal chloride coating.
31. The disposable transcutaneous electrode of Claim 27, wherein the electrically conductive metallic layer is a silver/silver chloride coating.
32. The disposable transcutaneous electrode of Claim 26 wherein the means for conducting and distributing energy from a medical device comprises:
(a) a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the sheet electrode member, the mat having the lower surface conductively affixed to the upper side of the sheet electrode member, and (b) an electrical conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively affixed to the mat for conducting energy to or from the upper surface of the mat and the medical device.
(a) a current distributing mat having upper and lower surfaces and an outer perimeter spaced inwardly of the outer perimeter of the sheet electrode member, the mat having the lower surface conductively affixed to the upper side of the sheet electrode member, and (b) an electrical conductor sheathed in an electrical insulating material and having an unsheathed end portion conductively affixed to the mat for conducting energy to or from the upper surface of the mat and the medical device.
33. The disposable transcutaneous electrode of Claim 32, wherein the current distributing mat, the sheet electrode member, and the metallic layer are substantially translucent to x-rays.
34. The disposable transcutaneous electrode of Claim 33, wherein the sheet electrode member is carbon filled.
35. The disposable transcutaneous electrode of Claim 32, wherein the current distributing mat includes a metallized carbon fiber web having an electrically conductive adhesive on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having surface electrical resistance, measured in directions paralleling the surfaces of the mat, less than the surface electrical resistance of the sheet electrode member.
36. The disposable transcutaneous electrode of Claim 35, wherein sheet electrode member and the current distributing mat are configured to be capable of conducting energy at level sufficient for defibrillation.
37. The disposable transcutaneous electrode of Claim 26, further comprising a removable carrier sheet on a lower surface of the pad for covering the pad prior to use.
38. A disposable transcutaneous electrode comprising:
(a) a sheet electrode member of electrically conductive polymer material having upper and lower sides and an outer perimeter;
(b) a current distributing mat for conducting and distributing energy from a medical device to an area of the sheet electrode member less than an area defined by the outer perimeter of the sheet electrode member, the mat being conductively affixed to the upper side of the sheet electrode member;
(c) an electrically conductive metallic layer conductively affixed to a least a major portion of the lower side of the sheet electrode member, the sheet electrode member having a surface electrical resistance, measured in directions paralleling the upper and lower sides, higher than the surface electrical resistance of the metallic layer, the electrically conductive metallic layer having a region of high conductivity in a central region located inwardly from the outer perimeter of the sheet electrode member and a region of low conductivity in an encircling region surrounding the central region and adjacent the outer perimeter of the sheet electrode member; and (d) a pad of electrically conductive gel having an upper surface underlying the metallic layer, the pad conducting the energy from the sheet electrode member to a patient on which the electrode is disposed.
(a) a sheet electrode member of electrically conductive polymer material having upper and lower sides and an outer perimeter;
(b) a current distributing mat for conducting and distributing energy from a medical device to an area of the sheet electrode member less than an area defined by the outer perimeter of the sheet electrode member, the mat being conductively affixed to the upper side of the sheet electrode member;
(c) an electrically conductive metallic layer conductively affixed to a least a major portion of the lower side of the sheet electrode member, the sheet electrode member having a surface electrical resistance, measured in directions paralleling the upper and lower sides, higher than the surface electrical resistance of the metallic layer, the electrically conductive metallic layer having a region of high conductivity in a central region located inwardly from the outer perimeter of the sheet electrode member and a region of low conductivity in an encircling region surrounding the central region and adjacent the outer perimeter of the sheet electrode member; and (d) a pad of electrically conductive gel having an upper surface underlying the metallic layer, the pad conducting the energy from the sheet electrode member to a patient on which the electrode is disposed.
39. The disposable transcutaneous electrode of Claim 38, wherein the electrically conductive metallic layer comprises a first layer and a second layer, the first layer being conductively disposed against the sheet electrode member and having a perimeter that is spaced inwardly from the outer perimeter of the sheet electrode member, the second layer overlapping the first layer and being conductively disposed against the first layer and the sheet electrode member and having a perimeter that is spaced outwardly from the perimeter of the first layer and inwardly from the outer perimeter of the sheet electrode member.
40. The disposable transcutaneous electrode of Claim 39, wherein the perimeter of the first layer is undulated.
41. The disposable transcutaneous electrode of Claim 39, wherein the perimeter of the second layer is undulated.
42. The disposable transcutaneous electrode of Claim 39, wherein the electrically conductive metallic layer is a metal/metal chloride coating.
43. The disposable transcutaneous electrode of Claim 39, wherein the electrically conductive metallic layer is a silver/silver chloride coating.
44. The disposable transcutaneous electrode of Claim 38, wherein the current distributing mat comprises:
(a) upper and lower surfaces with an outer perimeter spaced inwardly of the outer perimeter of the sheet electrode member, the mat having the lower surface conductively affixed to the upper side of the sheet electrode member, and (b) an electrical conductor and having an end portion conductively of fixed to the mat for conducting energy to or from the mat and the medical device.
(a) upper and lower surfaces with an outer perimeter spaced inwardly of the outer perimeter of the sheet electrode member, the mat having the lower surface conductively affixed to the upper side of the sheet electrode member, and (b) an electrical conductor and having an end portion conductively of fixed to the mat for conducting energy to or from the mat and the medical device.
45. The disposable transcutaneous electrode of Claim 35, wherein the current distributing mat, the sheet electrode member, and the metallic layer are substantially translucent to x-rays.
46. The disposable transcutaneous electrode of Claim 45, wherein the sheet electrode member is carbon filled.
47. The disposable transcutaneous electrode of Claim 44, wherein the current distributing mat comprises a metallized carbon fiber web having an electrically conductive adhesive on upper and lower sides of the web, the mat being configured to be electrically conductive along the surfaces of the mat and transverse to the surfaces of the mat, the mat having surface electrical resistance, measured in directions paralleling the surfaces of the mat, less than the surface electrical resistance of the sheet electrode member.
48. The disposable transcutaneous electrode of Claim 44 wherein the current distributing mat comprises a metal foil coated with a conductive polymer adhesive.
49. The disposable transcutaneous electrode of Claim 47 wherein the metal comprising the foil is selected from the group consisting of coppery tin, silver, gold, nickel, aluminum, platinum, chromium, cadmium, pladmium, zinc, antimony, and indium.
50. The disposable transcutaneous electrode of Claim 47 wherein the electrical conductor is affixed to the current distributing mat by solder.
51. The disposable transcutaneous electrode of Claim 44 wherein the electrical conductor comprises a conductive metal tab.
52. The disposable transcutaneous electrode of Claim 44 wherein the electrical conductor comprises a conductive post stud.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/569,567 US5571165A (en) | 1995-12-08 | 1995-12-08 | X-ray transmissive transcutaneous stimulating electrode |
| US08/569,567 | 1995-12-08 | ||
| US08/739,586 | 1996-10-30 | ||
| US08/739,586 US5733324A (en) | 1995-12-08 | 1996-10-30 | X-ray transmissive transcutaneous stimulating electrode |
| PCT/US1996/019312 WO1997021465A1 (en) | 1995-12-08 | 1996-12-05 | X-ray transmissive transcutaneous stimulating electrode |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2247360A1 CA2247360A1 (en) | 1997-06-19 |
| CA2247360C true CA2247360C (en) | 2004-02-24 |
Family
ID=27075087
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002247360A Expired - Lifetime CA2247360C (en) | 1995-12-08 | 1996-12-05 | X-ray transmissive transcutaneous stimulating electrode |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5733324A (en) |
| EP (3) | EP0778046B1 (en) |
| JP (1) | JP4493737B2 (en) |
| AT (3) | ATE517654T1 (en) |
| AU (1) | AU1146197A (en) |
| CA (1) | CA2247360C (en) |
| DE (2) | DE69633489T2 (en) |
| ES (2) | ES2322898T3 (en) |
| WO (1) | WO1997021465A1 (en) |
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- 1996-10-30 US US08/739,586 patent/US5733324A/en not_active Expired - Lifetime
- 1996-12-03 AT AT04004134T patent/ATE517654T1/en not_active IP Right Cessation
- 1996-12-03 EP EP96119390A patent/EP0778046B1/en not_active Expired - Lifetime
- 1996-12-03 EP EP04004135A patent/EP1424094B1/en not_active Expired - Lifetime
- 1996-12-03 AT AT96119390T patent/ATE277668T1/en active
- 1996-12-03 EP EP04004134A patent/EP1421971B1/en not_active Expired - Lifetime
- 1996-12-03 ES ES04004135T patent/ES2322898T3/en not_active Expired - Lifetime
- 1996-12-03 DE DE69633489T patent/DE69633489T2/en not_active Expired - Lifetime
- 1996-12-03 ES ES96119390T patent/ES2230556T3/en not_active Expired - Lifetime
- 1996-12-03 AT AT04004135T patent/ATE422939T1/en not_active IP Right Cessation
- 1996-12-03 DE DE69637841T patent/DE69637841D1/en not_active Expired - Lifetime
- 1996-12-05 AU AU11461/97A patent/AU1146197A/en not_active Abandoned
- 1996-12-05 CA CA002247360A patent/CA2247360C/en not_active Expired - Lifetime
- 1996-12-05 WO PCT/US1996/019312 patent/WO1997021465A1/en active Search and Examination
- 1996-12-06 JP JP34041996A patent/JP4493737B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU1146197A (en) | 1997-07-03 |
| JPH09276240A (en) | 1997-10-28 |
| ES2322898T3 (en) | 2009-07-01 |
| EP0778046B1 (en) | 2004-09-29 |
| CA2247360A1 (en) | 1997-06-19 |
| EP0778046A2 (en) | 1997-06-11 |
| EP1421971A3 (en) | 2004-10-13 |
| EP1424094A1 (en) | 2004-06-02 |
| EP1421971B1 (en) | 2011-07-27 |
| ATE422939T1 (en) | 2009-03-15 |
| DE69637841D1 (en) | 2009-04-02 |
| ATE517654T1 (en) | 2011-08-15 |
| EP1424094B1 (en) | 2009-02-18 |
| US5733324A (en) | 1998-03-31 |
| JP4493737B2 (en) | 2010-06-30 |
| EP0778046A3 (en) | 1999-05-19 |
| EP1421971A2 (en) | 2004-05-26 |
| ATE277668T1 (en) | 2004-10-15 |
| DE69633489T2 (en) | 2005-11-10 |
| DE69633489D1 (en) | 2004-11-04 |
| WO1997021465A1 (en) | 1997-06-19 |
| ES2230556T3 (en) | 2005-05-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKEX | Expiry |
Effective date: 20161205 |