CA2471780C - Surgical drape and suction head for wound treatment - Google Patents
Surgical drape and suction head for wound treatment Download PDFInfo
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- CA2471780C CA2471780C CA002471780A CA2471780A CA2471780C CA 2471780 C CA2471780 C CA 2471780C CA 002471780 A CA002471780 A CA 002471780A CA 2471780 A CA2471780 A CA 2471780A CA 2471780 C CA2471780 C CA 2471780C
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Abstract
A suction head for applying suction to a wound area comprises a first face having a substantially planar flange and a connector. The connector is adapted to connect to a suction tube. A second face has a plurality of projections. An aperture is provided from the second face, through the flange and to the connector on the first face. The projections define a plurality of channels that are adapted to facilitate flow of fluids from about the second face toward the aperture.
Description
WO 99/13793 1 , PCT/GB98/02713 Surgical Drape and Suction Head for Wound Treatment This invention relates to surgical drapes and suction heads for wound treatment.
Surgical drapes are widely used in surgical operations for the purpose of reducing infection and facilitating the handling of skin around incisions.
Normally, they are transparent or translucent. Typically, they consist of a flexible, plastics film which is adhesive-coated and which is applied to the area of the operation, prior to making the incision: Surgical drapes are also used for attaching treatment devices to patients after an operation, such as catheters or drainage tubes.
A further, recently developed use is for connecting a suction tube to a wound for the purpose of stimulating healing of the wound. Such use is described in our earlier PCT Applications Nos. WO 96/05873 and WO 97/18007.
Various proposals have been made in the past to design the surgical drape so that handling of the sticky, flexible, plastics film is facilitated. For example, US
Patent No. 5,437,622, describes a surgical drape which is a laminate of three materials.
The first material conYprLsing a transparent, thin plastics film which is adhesive-coated and this is protected with a layer of release-coated paper. The other face of the adhesive-coated film is strengthened with a reinforcing layer of a less flexible, plastics film. Handling bars or strips are attached to the flexible, plastics film at its lateral edges to facilitate handling of the flexible, plastics film after stripping away the protective releasable layer.
Where it is desired to use a surgical drape primarily to attach a device such as a catheter to a wound area after an operation or for long term treatment, it is inconvenient for the surgeon or nurse to have to adapt a standard surgical drape for this purpose. It would be more convenient to have a surgical drape which was suitable without adaptation to accommodate the treatment device.
Surgical drapes are widely used in surgical operations for the purpose of reducing infection and facilitating the handling of skin around incisions.
Normally, they are transparent or translucent. Typically, they consist of a flexible, plastics film which is adhesive-coated and which is applied to the area of the operation, prior to making the incision: Surgical drapes are also used for attaching treatment devices to patients after an operation, such as catheters or drainage tubes.
A further, recently developed use is for connecting a suction tube to a wound for the purpose of stimulating healing of the wound. Such use is described in our earlier PCT Applications Nos. WO 96/05873 and WO 97/18007.
Various proposals have been made in the past to design the surgical drape so that handling of the sticky, flexible, plastics film is facilitated. For example, US
Patent No. 5,437,622, describes a surgical drape which is a laminate of three materials.
The first material conYprLsing a transparent, thin plastics film which is adhesive-coated and this is protected with a layer of release-coated paper. The other face of the adhesive-coated film is strengthened with a reinforcing layer of a less flexible, plastics film. Handling bars or strips are attached to the flexible, plastics film at its lateral edges to facilitate handling of the flexible, plastics film after stripping away the protective releasable layer.
Where it is desired to use a surgical drape primarily to attach a device such as a catheter to a wound area after an operation or for long term treatment, it is inconvenient for the surgeon or nurse to have to adapt a standard surgical drape for this purpose. It would be more convenient to have a surgical drape which was suitable without adaptation to accommodate the treatment device.
2 PCT/GB98/02713 One aspect of the present invention is directed to a solution to this problem.
A second aspect provides a combined surgical drape and suction head for applying suction to a wound area to facilitate application of negative pressure therapy.
According to one aspect of the present invention there is provided a surgical drape which comprises a thim, flexible, adhesive-coated plastics fiim and a strengthening layer applied to the face opposite to the adhesive coating, the strengthening layer being a plastics fil.m which is thicker or less flexible than said adhesive-coated film, and a protective, releasable layer applied to the adhesive coating, the drape having an apertuae through at least the strengthening and adhesive-coated film to permit, in use, access to a wound area, a first edge of the drape having non-adhesive coated handling bars for separating the adhesive-coated film from the protective layer, and wherein the protective layer comprises a separate strip extending parallel to the first edge of the drape, and which protects the adhesive coating in the region of the aperture and carries a flap overlapping the adjacent portion of the protective layer, said flap constituting a handle for facilitating removal of said strip prior to use. Preferably, non-adhesive-coated handling bars are positioned at opposite lateral edges of the drape.
In practice, surgical drapes may be manufactured by laminating an adhesive-coated flexible film, such as a polyurethane fiim, to a protective releasable layer, such as a siliconised paper. A strengthenin.g layer of thicker plastics material, e.g. a polyoiefin such as polyethylene, may be applied to the non-adhesive coated face of the flexible film, so that a three-layer laminate is produced. These laminates are produced in substantial width and may be slit longitudinally to the desired width and then laterally to form drapes of the desired size.
After slitting to a desired width, handling bars are normally applied to the adhesive-coated layers at one or both lateral edges to facilitate separation of the film
A second aspect provides a combined surgical drape and suction head for applying suction to a wound area to facilitate application of negative pressure therapy.
According to one aspect of the present invention there is provided a surgical drape which comprises a thim, flexible, adhesive-coated plastics fiim and a strengthening layer applied to the face opposite to the adhesive coating, the strengthening layer being a plastics fil.m which is thicker or less flexible than said adhesive-coated film, and a protective, releasable layer applied to the adhesive coating, the drape having an apertuae through at least the strengthening and adhesive-coated film to permit, in use, access to a wound area, a first edge of the drape having non-adhesive coated handling bars for separating the adhesive-coated film from the protective layer, and wherein the protective layer comprises a separate strip extending parallel to the first edge of the drape, and which protects the adhesive coating in the region of the aperture and carries a flap overlapping the adjacent portion of the protective layer, said flap constituting a handle for facilitating removal of said strip prior to use. Preferably, non-adhesive-coated handling bars are positioned at opposite lateral edges of the drape.
In practice, surgical drapes may be manufactured by laminating an adhesive-coated flexible film, such as a polyurethane fiim, to a protective releasable layer, such as a siliconised paper. A strengthenin.g layer of thicker plastics material, e.g. a polyoiefin such as polyethylene, may be applied to the non-adhesive coated face of the flexible film, so that a three-layer laminate is produced. These laminates are produced in substantial width and may be slit longitudinally to the desired width and then laterally to form drapes of the desired size.
After slitting to a desired width, handling bars are normally applied to the adhesive-coated layers at one or both lateral edges to facilitate separation of the film
3 from the protective, releasable layer. While an aperture could be cut at the desired position through the layers to accommodate a catheter or a device such as those described in our above-mentioned applications, it is difficult to handle the highly pliable and adhesive film after the releasable layer has been stripped off.
Although the strengthening layer does somewhat improve the handling characteristics, this is not a complete answer to the problem. However, the handling characteristics are substantially improved by providing a protective layer which is in at least two portions, one of which is in the form of a strip, e.g. one extending parallel to the lateral edges of the drape, and covering the peripheral area around the aperture through the drape.
By providing a flap on this portion of the releasable layer, it can be stripped off initially so that the drape is first positioned around the device which is to pass through the aperture, and then the remaining part of the protective releasable layer is stripped off to adhere the drape to the patient's skin around the area to be treated.
In a preferred form of the invention in which negative pressure therapy is applied to a wound area, the surgical drape described above is combined with a suction head having a connector piece which is adapted to be connected to a suction tube. Thus, in this embodiment, the suction head can be adhered to the patient's skin in the area of the wound after removing the strip of protective releasable layer, and then the remaining part of the drape affixed to the patient's skin. In this way, the suction head is held firmly in place and, at the same time, seals the suction head to the wound area and prevents leakage of air from atmosphere into the wound area.
The invention also includes a suction head having a design which facilitates the suction of fluid from a wound area.
According to a further feature of the invention, therefore, there is provided a suction head for applying suction to a wound area, said suction head comprising: a first face having a substantially planar flange and a connector, said connector being adapted to connect to a suction tube; a second face having a plurality of projections; an aperture from said second face, through said flange and to said connector on said first face; and wherein said projections define a plurality of channels, said channels being adapted to facilitate flow of fluids from about.said second face toward said aperture.
3a In another broad aspect, then, the present invention relates to a wound therapy combination, said combination comprising: a suction head having a first face, a second face opposite said first face and an opening between said first face and said second face, said opening being adapted for connection to a suction tube; a surgical drape having an aperture coincident said opening, said surgical drape extending over a region, and overlapping beyond the perimeter, of said first face; and wherein said surgical drape comprises a flexible adhesive-coated film adhered to said region of said first face and a release-coated backing extending over said second face and adhered to the overlapping portion of said surgical drape.
In still another broad aspect, then, the present invention relates to a wound therapy combination, comprising: a suction head having a first face; a second face opposite said first face, wherein said second face is comprised of a plurality of projections, said projections defining a plurality of channels for facilitating flow of fluids to an opening in said second face and through said first face, wherein said opening is adapted for connection to a suction tube; and a surgical drape having an aperture coincident said opening, said surgical drape extending over a region, and overlapping beyond the perimeter of said first face, and wherein said surgical drape comprises a flexible adhesive coated film adl,iered to said region of said first face and a release-coated backing extending over said second face and adhered to the overlapping portion of said surgical drape.
In a further broad aspect, then, the present invention relates to a wound dressing for distributing fluid across a wound surface, comprising: a suction head having a first face; a second face opposite said first face; a plurality of projections coincident from said second face, wherein said projections form a contact surface with the wound surface, and wherein a plurality of channels for facilitating flow of fluids are defined between said projections, said channels remaining out of contact with the wound surface; and an aperture in fluid communication with said channels formed by said projections and formed through said first face and said second face.
3b In yet another broad aspect, then, the present invention relates to a method for securing a substantially planar, flanged suction head to a wound site, said method comprising the steps of: providing a surgical drape, said surgical drape comprising: a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head; a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film; and a second releasable protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film; releasing said first protective layer from said adhesive-coated plastic film; adhering said surgical drape to the substantially planar, flanged suction head;
releasing said second protective layer from said adhesive-coated plastic film; and applying the substantially planar, flanged suction head to the wound site -by means of said adhesive coated plastic film exposed by release of said second protective layer.
In still another broad aspect, then, the present invention relates to a method for securing a suction device to a wound site, said method comprising the steps of: applying a layer of open-celled polymer foam to the wound site; applying a suction head to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and hermetically sealing said suction head and said foam within a region about the wound site with a surgical drape, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
In a further broad aspect, then, the present invention relates to a method for preparing a substantially planar, flanged suction head for application to a wound site, said method comprising the steps of: providing a surgical drape, said surgical drape comprising: a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head; a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film; and a second releasable 3c protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film; releasing said first protective layer from said adhesive-coated plastic film; adhering said surgical drape to the substantially planar, flanged suction head; releasing said second protective layer from said adhesive-coated plastic film; whereby said substantially planar, flanged suction head is prepared for application to the wound site.
In a still further broad aspect, then, the present invention relates to a method for preparing a suction device to be hermetically sealed to a wound site, said method comprising the steps of: providing a suction head for application to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and applying a surgical drape about said suction head for subsequent application in the region of said wound site, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
Preferably, the suction head described above is combined with a surgical drape, the drape comprising a thin, flexible, adhesive-coated plastics film, and the tubular connector piece extends through an opening in the plastics film with the adhesive coating adhered to said first face of the flange portion.
Although the strengthening layer does somewhat improve the handling characteristics, this is not a complete answer to the problem. However, the handling characteristics are substantially improved by providing a protective layer which is in at least two portions, one of which is in the form of a strip, e.g. one extending parallel to the lateral edges of the drape, and covering the peripheral area around the aperture through the drape.
By providing a flap on this portion of the releasable layer, it can be stripped off initially so that the drape is first positioned around the device which is to pass through the aperture, and then the remaining part of the protective releasable layer is stripped off to adhere the drape to the patient's skin around the area to be treated.
In a preferred form of the invention in which negative pressure therapy is applied to a wound area, the surgical drape described above is combined with a suction head having a connector piece which is adapted to be connected to a suction tube. Thus, in this embodiment, the suction head can be adhered to the patient's skin in the area of the wound after removing the strip of protective releasable layer, and then the remaining part of the drape affixed to the patient's skin. In this way, the suction head is held firmly in place and, at the same time, seals the suction head to the wound area and prevents leakage of air from atmosphere into the wound area.
The invention also includes a suction head having a design which facilitates the suction of fluid from a wound area.
According to a further feature of the invention, therefore, there is provided a suction head for applying suction to a wound area, said suction head comprising: a first face having a substantially planar flange and a connector, said connector being adapted to connect to a suction tube; a second face having a plurality of projections; an aperture from said second face, through said flange and to said connector on said first face; and wherein said projections define a plurality of channels, said channels being adapted to facilitate flow of fluids from about.said second face toward said aperture.
3a In another broad aspect, then, the present invention relates to a wound therapy combination, said combination comprising: a suction head having a first face, a second face opposite said first face and an opening between said first face and said second face, said opening being adapted for connection to a suction tube; a surgical drape having an aperture coincident said opening, said surgical drape extending over a region, and overlapping beyond the perimeter, of said first face; and wherein said surgical drape comprises a flexible adhesive-coated film adhered to said region of said first face and a release-coated backing extending over said second face and adhered to the overlapping portion of said surgical drape.
In still another broad aspect, then, the present invention relates to a wound therapy combination, comprising: a suction head having a first face; a second face opposite said first face, wherein said second face is comprised of a plurality of projections, said projections defining a plurality of channels for facilitating flow of fluids to an opening in said second face and through said first face, wherein said opening is adapted for connection to a suction tube; and a surgical drape having an aperture coincident said opening, said surgical drape extending over a region, and overlapping beyond the perimeter of said first face, and wherein said surgical drape comprises a flexible adhesive coated film adl,iered to said region of said first face and a release-coated backing extending over said second face and adhered to the overlapping portion of said surgical drape.
In a further broad aspect, then, the present invention relates to a wound dressing for distributing fluid across a wound surface, comprising: a suction head having a first face; a second face opposite said first face; a plurality of projections coincident from said second face, wherein said projections form a contact surface with the wound surface, and wherein a plurality of channels for facilitating flow of fluids are defined between said projections, said channels remaining out of contact with the wound surface; and an aperture in fluid communication with said channels formed by said projections and formed through said first face and said second face.
3b In yet another broad aspect, then, the present invention relates to a method for securing a substantially planar, flanged suction head to a wound site, said method comprising the steps of: providing a surgical drape, said surgical drape comprising: a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head; a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film; and a second releasable protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film; releasing said first protective layer from said adhesive-coated plastic film; adhering said surgical drape to the substantially planar, flanged suction head;
releasing said second protective layer from said adhesive-coated plastic film; and applying the substantially planar, flanged suction head to the wound site -by means of said adhesive coated plastic film exposed by release of said second protective layer.
In still another broad aspect, then, the present invention relates to a method for securing a suction device to a wound site, said method comprising the steps of: applying a layer of open-celled polymer foam to the wound site; applying a suction head to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and hermetically sealing said suction head and said foam within a region about the wound site with a surgical drape, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
In a further broad aspect, then, the present invention relates to a method for preparing a substantially planar, flanged suction head for application to a wound site, said method comprising the steps of: providing a surgical drape, said surgical drape comprising: a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head; a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film; and a second releasable 3c protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film; releasing said first protective layer from said adhesive-coated plastic film; adhering said surgical drape to the substantially planar, flanged suction head; releasing said second protective layer from said adhesive-coated plastic film; whereby said substantially planar, flanged suction head is prepared for application to the wound site.
In a still further broad aspect, then, the present invention relates to a method for preparing a suction device to be hermetically sealed to a wound site, said method comprising the steps of: providing a suction head for application to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and applying a surgical drape about said suction head for subsequent application in the region of said wound site, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
Preferably, the suction head described above is combined with a surgical drape, the drape comprising a thin, flexible, adhesive-coated plastics film, and the tubular connector piece extends through an opening in the plastics film with the adhesive coating adhered to said first face of the flange portion.
4 Preferably, the suction head is used in conjunction with an open-celled foam pad so that one surface of the foam pad is placed in contact with a wound area and the suction head applied to the other surface of the foam pad. In the case of deep wounds the foam may be shaped and placed so that it is packed into the wound cavity as described in our above cited PCT applications. According to another technique, which is particularly applicable to superficial wounds, the foam pad may be a relatively thin pad which is placed over the wound. The suction head is placed in contact with the open face of the foam pad and the drape applied over the suction liead to fix the assembly to the patient's skin.
Various types of open celled foams can be used as described in our above cited PCT
applications. The foam may be a polyurethane foam but polyvinyl acetate (pva) foams are preferred, especially when used as a pad which is placed over the wound. These are to some extent hydrophilic, which seems to exhibit beneficial comfort properties when applied to the skin. Wound healing is stimulated by maintenance of moist conditions in the wound area, and this is facilitated by using a hydrophilic foam.
Further features and advantages of the present invention will be apparent from the following description and accompanying drawings, of non-limited examples in accordance with the invention.
Referring to the accompanying drawings:-Figure 1 represents a conventional design of surgical drape;
Figure 2 represents a variation in the design of the handling bars at one end of the drape shown in Figure 1;
Figure 3 is a view similar to Figure I of a surgical drape in accordance with the invention;
Figure 4 is a plan view of the surgical drape shown in Figure 3;
Figure 5 is a plan view from beneath of a suction head in accordance with the invention; and Figure 6 is a side elevation of the suction head shown in Figure 5;
Figure 7 is a view similar to Figure 6 but shows the suction head secured to a skin surface with the drape and with a foam pad located between the head and the skin surface.
Figure 8 is a perspective view of the drape with a central strip portion of the protective sheet in the course of being removed, and Figures 9(a)-9(c) illustrate the steps of affixing the dressing assembly to a wound area on a patient's leg and attachment to a negative pressure assembly.
Referring to Figures 1 and 2 of the accompanying drawings, a conventional laminate for use as a surgical drape comprises a thin, flexible, transparent plastics film I which is adhesive-coated on one face 2, normaIIy with a high-tack pressure-sensitive adhesive, and is protected with a releasable layer 3. The thin plastics fiim is conveniently of polyurethane because it transmits moisture: Layer 3 is normally considerably thicker than film 1 and is coated on the surface adjacent to the adhesive with a releasable material such as a silicone to facilitate stripping away from the adhesive-coated film.
In order to facffitate removal of the adhesive-coated film prior to use of the device, handling bars 4 are bonded at each end to the adhesive-coated film 1.
Thus, by holding one of the bars 4, the protective layer 3 can be stripped off and the adhesive face applied to the skin of the patient. To facilitate handling of the thin, flexible film 1, a strengthening plastics fihn 5 is frequently applied to the free face of the plastics film 1. This is generally also transparent or translucent. Film 5 is preferably not bonded with adhesive to film 1, but may remain in contact by reason of electrostatic forces or because of close contact between the two conforming surfaces of filxu I and film 5.
Usually, the surgeon or nurse will wish to strip off the protective layer 5 after the film I has been correctly placed on the patient's skin, and this can be facilitated by making partial cuts 6 through the films 1 and 5, so that as the handling bar 4 is drawn upwards from the patient's skin, the adhesive film I remains adhered to the patient, while the partial cuts 6 causes separation of the flexible film from the strengthening film S. Strengthening bars 7 may be provided to hold the lateral edges of the strengthening filmm 5 and film 1 together with their main parts.
An alternative arrangement is shown in Figure 2, in which the strengthening film 5 is provided with a separate overlapping handling bar 14, to facilitate its removal from the flexible fshn 1.
Further details of the make-up and manufacture of surgical drapes are given in US Patent No. 5,437,622 and European Patent Application No. 4161865 and the prior art referred to therein, the disclosure of which is incorporated herein.
Referring to Figure 3 and 4, the surgical drape of this invention comprises .a protective outer film 20, laminated to a thin, flexible film 21. The flexible film 21 includes an adhesive-coated layer which is protected with a release-coated sheet materia124. Lateral edges of the flexible film 21 are provided with handling bars 23.
Thus far, the design is essentially the same as that shown in Figures 1 and 2.
The drape of the present invention differs from the drape shown in Figures 1 and 2 in that an aperture 25 is cut through the strengthening layer 20 and through the flexible layer 21. The other difference compared with the prior art drapes is that the protective releasable layer is formed in at least two sections.
In the embodiments shown in Figures 3 and 4, the central portion of the releasable layer comprises a strip 26, having flaps 27 which overlap the remaining outboard portions of the releasable layer. The purpose of this is to enable the central strip 26 to be removed first, without disturbing the remaining portions of the releasable layer. The drape can then be fitted around the wound area and, if desired, a suction device or other treatment device passed through the aperture 25 and secured to the patient's skin with the peripheral areas of exposed adhesive-coated film.
An example of a device for applying suction to the wound area is illustrated in Figures 5, 6 and 7.
Referring to these Figures, the suction head comprises a flange portion 30 having a tapered edge 31, and a profile which may be of any desired shape but is generally rounded at its edges. On the face of the flange 30 intended for contact with the patient's skin or a foam pad are formed a series of projections 32 which are distributed over the surface of the flange apart from the peripheral edge portion 31.
The purpose of these projections is to provide fluid channels 33 facilitating the flow of fluids from any point of the flange to a central point 34, from which it is intended to apply suction. The suction head includes a connector 35, located above the aperture 34, having a tubular end 36 adapted for receiving and connecting a catheter.
The tubular end may have an outwardly tapered portion to facilitate feeding a catheter into the connector. The upper surface 37 of the suction head has a substantially smooth surface.
SUBSTITUTE SHEET (RULE 26) WO 99/13793 $ PCT/GB98/02713 In use, the connector portion 35 is sized so that it extends through the aperture 25 in the surgical drape shown in Figures 3 and. 4, with the adhesive surface around the aperture bonded to the smooth surface 37 of the flange 30. The suction head may be packaged in this condition with the surgical drape so that in use, the strip 26 is removed by pulling on the handles 27 thus exposing the adhesive surface in the vicinity of and surrounding the suction head. The suction head can then fixed in the desired position on the patient's wound and then the remaining portion of the protective film removed to fix the drape to the patient. The flange 30 of the suction head may be somewhat oval as shown in Figure 5, and have dimensions as indicated in this Figure, i.e. a longer dimension of about 95mm and a short dimension of about 70mm.
Alternatively, the flange may be oircular and be smaller in plan view. For example, the diameter of a circular suction head may be from about 30 to 50mm in diameter, e.g. about 40mm It has been found that the suction head flange should not overlap the area of the wound. Thus, in the case of smaller wounds a smaller suction head is indicated.
Figure 7 shows the suction head attached to a wound area 71 of a patient 70.
The suction head is pressed into firm contact with a flexible, open==celled foam 73, which is itself pressed into contact with the wound area 71. The suction head and foam pad are pressed into contact with the wound area by a surgical drape 20 having an adhesive surface 74. The adhesive surface is bonded to the patient's skin outside the periphery of the foam pad and suction head. it is also bonded to upper surface 37 of the suction head. An aperture is formed in the drape to permit the connector portion 35 to extend upwardly through the drape. In order to avert the danger of incorrect catheter tubes being fitted to the connector 35, the latter may have a customised cross-section or internal projection such as a rib or key which co-operates with a corresponding slot or key way in the catheter. lAlternatively, the catheter may WO 99/13793 9 PCTlGB98/02713 be moulded with a projection or longitudinal rib which co-operates with a corresponding slot or key way in the aperture of the connector 35.
The foam pad may be packaged in a plastic pouch, sterilised by gamma irradiation and supplied in the same box or in other paclcing units as the suction head and drape.
Figures 8 and 9(a)-(b) illustrate the way in which the drape/suction head combination is fitted to a wound on a patient's skin. In Figure 8, a backing sheet 101 having a release coated surface is removed in the first step from the adhesive face 102 of the drape to expose the face of the connector 30. A pad 103 of foam is positioned over the wound area and the drape placed over the foam paid, the drape being adhered to the skin above and below the pad (Figure 9a). The lateral protective strips and 105 are removed in turn from the drape and the assembly adhered to the skin (Figures 9(b) and 9(c). Finally, the spout 36 is connected to a tube 106 which is then connected to a source of suction, e.g. a pump as described in our above PCT
application, in order to apply negative pressure to the wound. The suction b.ead and drape assembly is shown in Figure 8, with the smooth surface 37 adhered to the drape, is conveniently packaged in an easily openable plastic bag or pouch, and sterilised for immediate use.
Various types of open celled foams can be used as described in our above cited PCT
applications. The foam may be a polyurethane foam but polyvinyl acetate (pva) foams are preferred, especially when used as a pad which is placed over the wound. These are to some extent hydrophilic, which seems to exhibit beneficial comfort properties when applied to the skin. Wound healing is stimulated by maintenance of moist conditions in the wound area, and this is facilitated by using a hydrophilic foam.
Further features and advantages of the present invention will be apparent from the following description and accompanying drawings, of non-limited examples in accordance with the invention.
Referring to the accompanying drawings:-Figure 1 represents a conventional design of surgical drape;
Figure 2 represents a variation in the design of the handling bars at one end of the drape shown in Figure 1;
Figure 3 is a view similar to Figure I of a surgical drape in accordance with the invention;
Figure 4 is a plan view of the surgical drape shown in Figure 3;
Figure 5 is a plan view from beneath of a suction head in accordance with the invention; and Figure 6 is a side elevation of the suction head shown in Figure 5;
Figure 7 is a view similar to Figure 6 but shows the suction head secured to a skin surface with the drape and with a foam pad located between the head and the skin surface.
Figure 8 is a perspective view of the drape with a central strip portion of the protective sheet in the course of being removed, and Figures 9(a)-9(c) illustrate the steps of affixing the dressing assembly to a wound area on a patient's leg and attachment to a negative pressure assembly.
Referring to Figures 1 and 2 of the accompanying drawings, a conventional laminate for use as a surgical drape comprises a thin, flexible, transparent plastics film I which is adhesive-coated on one face 2, normaIIy with a high-tack pressure-sensitive adhesive, and is protected with a releasable layer 3. The thin plastics fiim is conveniently of polyurethane because it transmits moisture: Layer 3 is normally considerably thicker than film 1 and is coated on the surface adjacent to the adhesive with a releasable material such as a silicone to facilitate stripping away from the adhesive-coated film.
In order to facffitate removal of the adhesive-coated film prior to use of the device, handling bars 4 are bonded at each end to the adhesive-coated film 1.
Thus, by holding one of the bars 4, the protective layer 3 can be stripped off and the adhesive face applied to the skin of the patient. To facilitate handling of the thin, flexible film 1, a strengthening plastics fihn 5 is frequently applied to the free face of the plastics film 1. This is generally also transparent or translucent. Film 5 is preferably not bonded with adhesive to film 1, but may remain in contact by reason of electrostatic forces or because of close contact between the two conforming surfaces of filxu I and film 5.
Usually, the surgeon or nurse will wish to strip off the protective layer 5 after the film I has been correctly placed on the patient's skin, and this can be facilitated by making partial cuts 6 through the films 1 and 5, so that as the handling bar 4 is drawn upwards from the patient's skin, the adhesive film I remains adhered to the patient, while the partial cuts 6 causes separation of the flexible film from the strengthening film S. Strengthening bars 7 may be provided to hold the lateral edges of the strengthening filmm 5 and film 1 together with their main parts.
An alternative arrangement is shown in Figure 2, in which the strengthening film 5 is provided with a separate overlapping handling bar 14, to facilitate its removal from the flexible fshn 1.
Further details of the make-up and manufacture of surgical drapes are given in US Patent No. 5,437,622 and European Patent Application No. 4161865 and the prior art referred to therein, the disclosure of which is incorporated herein.
Referring to Figure 3 and 4, the surgical drape of this invention comprises .a protective outer film 20, laminated to a thin, flexible film 21. The flexible film 21 includes an adhesive-coated layer which is protected with a release-coated sheet materia124. Lateral edges of the flexible film 21 are provided with handling bars 23.
Thus far, the design is essentially the same as that shown in Figures 1 and 2.
The drape of the present invention differs from the drape shown in Figures 1 and 2 in that an aperture 25 is cut through the strengthening layer 20 and through the flexible layer 21. The other difference compared with the prior art drapes is that the protective releasable layer is formed in at least two sections.
In the embodiments shown in Figures 3 and 4, the central portion of the releasable layer comprises a strip 26, having flaps 27 which overlap the remaining outboard portions of the releasable layer. The purpose of this is to enable the central strip 26 to be removed first, without disturbing the remaining portions of the releasable layer. The drape can then be fitted around the wound area and, if desired, a suction device or other treatment device passed through the aperture 25 and secured to the patient's skin with the peripheral areas of exposed adhesive-coated film.
An example of a device for applying suction to the wound area is illustrated in Figures 5, 6 and 7.
Referring to these Figures, the suction head comprises a flange portion 30 having a tapered edge 31, and a profile which may be of any desired shape but is generally rounded at its edges. On the face of the flange 30 intended for contact with the patient's skin or a foam pad are formed a series of projections 32 which are distributed over the surface of the flange apart from the peripheral edge portion 31.
The purpose of these projections is to provide fluid channels 33 facilitating the flow of fluids from any point of the flange to a central point 34, from which it is intended to apply suction. The suction head includes a connector 35, located above the aperture 34, having a tubular end 36 adapted for receiving and connecting a catheter.
The tubular end may have an outwardly tapered portion to facilitate feeding a catheter into the connector. The upper surface 37 of the suction head has a substantially smooth surface.
SUBSTITUTE SHEET (RULE 26) WO 99/13793 $ PCT/GB98/02713 In use, the connector portion 35 is sized so that it extends through the aperture 25 in the surgical drape shown in Figures 3 and. 4, with the adhesive surface around the aperture bonded to the smooth surface 37 of the flange 30. The suction head may be packaged in this condition with the surgical drape so that in use, the strip 26 is removed by pulling on the handles 27 thus exposing the adhesive surface in the vicinity of and surrounding the suction head. The suction head can then fixed in the desired position on the patient's wound and then the remaining portion of the protective film removed to fix the drape to the patient. The flange 30 of the suction head may be somewhat oval as shown in Figure 5, and have dimensions as indicated in this Figure, i.e. a longer dimension of about 95mm and a short dimension of about 70mm.
Alternatively, the flange may be oircular and be smaller in plan view. For example, the diameter of a circular suction head may be from about 30 to 50mm in diameter, e.g. about 40mm It has been found that the suction head flange should not overlap the area of the wound. Thus, in the case of smaller wounds a smaller suction head is indicated.
Figure 7 shows the suction head attached to a wound area 71 of a patient 70.
The suction head is pressed into firm contact with a flexible, open==celled foam 73, which is itself pressed into contact with the wound area 71. The suction head and foam pad are pressed into contact with the wound area by a surgical drape 20 having an adhesive surface 74. The adhesive surface is bonded to the patient's skin outside the periphery of the foam pad and suction head. it is also bonded to upper surface 37 of the suction head. An aperture is formed in the drape to permit the connector portion 35 to extend upwardly through the drape. In order to avert the danger of incorrect catheter tubes being fitted to the connector 35, the latter may have a customised cross-section or internal projection such as a rib or key which co-operates with a corresponding slot or key way in the catheter. lAlternatively, the catheter may WO 99/13793 9 PCTlGB98/02713 be moulded with a projection or longitudinal rib which co-operates with a corresponding slot or key way in the aperture of the connector 35.
The foam pad may be packaged in a plastic pouch, sterilised by gamma irradiation and supplied in the same box or in other paclcing units as the suction head and drape.
Figures 8 and 9(a)-(b) illustrate the way in which the drape/suction head combination is fitted to a wound on a patient's skin. In Figure 8, a backing sheet 101 having a release coated surface is removed in the first step from the adhesive face 102 of the drape to expose the face of the connector 30. A pad 103 of foam is positioned over the wound area and the drape placed over the foam paid, the drape being adhered to the skin above and below the pad (Figure 9a). The lateral protective strips and 105 are removed in turn from the drape and the assembly adhered to the skin (Figures 9(b) and 9(c). Finally, the spout 36 is connected to a tube 106 which is then connected to a source of suction, e.g. a pump as described in our above PCT
application, in order to apply negative pressure to the wound. The suction b.ead and drape assembly is shown in Figure 8, with the smooth surface 37 adhered to the drape, is conveniently packaged in an easily openable plastic bag or pouch, and sterilised for immediate use.
Claims (19)
OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method for securing a substantially planar, flanged suction head to a wound site, said method comprising the steps of:
providing a surgical drape, said surgical drape comprising:
a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head;
a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film;
and a second releasable protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film;
releasing said first protective layer from said adhesive-coated plastic film;
adhering said surgical drape to the substantially planar, flanged suction head;
releasing said second protective layer from said adhesive-coated plastic film;
and applying the substantially planar, flanged suction head to the wound site -by means of said adhesive coated plastic film exposed by release of said second protective layer.
providing a surgical drape, said surgical drape comprising:
a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head;
a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film;
and a second releasable protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film;
releasing said first protective layer from said adhesive-coated plastic film;
adhering said surgical drape to the substantially planar, flanged suction head;
releasing said second protective layer from said adhesive-coated plastic film;
and applying the substantially planar, flanged suction head to the wound site -by means of said adhesive coated plastic film exposed by release of said second protective layer.
2. The method as recited in claim 1, wherein said surgical drape further comprises a plastic strengthening film over said adhesive-coated plastic film, said strengthening film being less flexible than said adhesive-coated plastic film and being adapted to rigidify said adhesive-coated plastic film.
3. The method as recited in claim 2, wherein said strengthening film is of substantially the same cross section as said adhesive-coated plastic film.
4. The method as recited in claim 2, wherein said strengthening film is disassociated from said adhesive-coated plastic film.
5. A method for securing a suction device to a wound site, said method comprising the steps of:
applying a layer of open-celled polymer foam to the wound site;
applying a suction head to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and hermetically sealing said suction head and said foam within a region about the wound site with a surgical drape, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
applying a layer of open-celled polymer foam to the wound site;
applying a suction head to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and hermetically sealing said suction head and said foam within a region about the wound site with a surgical drape, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
6. The method as recited in claim 5, wherein said foam comprises a hydrophilic foam.
7. The method as recited in claim 6, wherein said hydrophilic foam comprises a polyvinyl acetate (PVA) foam.
8. The method as recited in claim 5, wherein said second face comprises a plurality of projections, said projections defining a plurality of channels for facilitating flow of fluids to said opening.
9. The method as recited in claim 5, wherein said strengthening film is adapted to rigidify said adhesive-coated plastic film.
10. A method for preparing a substantially planar, flanged suction head for application to a wound site, said method comprising the steps of:
providing a surgical drape, said surgical drape comprising:
a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head;
a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film;
and a second releasable protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film;
releasing said first protective layer from said adhesive-coated plastic film;
adhering said surgical drape to the substantially planar, flanged suction head;
releasing said second protective layer from said adhesive-coated plastic film;
whereby said substantially planar, flanged suction head is prepared for application to the wound site.
providing a surgical drape, said surgical drape comprising:
a flexible adhesive-coated plastic film, said adhesive-coated plastic film having a cross sectional area greater than that of the flanged suction head;
a first releasable protective layer, said first protective layer being of substantially the same cross section as the flanged suction head and being adapted to cover the central portion of the adhesive coating of said adhesive-coated plastic film;
and a second releasable protective layer, said second protective layer having a cross sectional area substantially the difference of said adhesive-coated plastic film and said first protective layer and being adapted to cover the non-central portions of the adhesive coating of said adhesive-coated plastic film;
releasing said first protective layer from said adhesive-coated plastic film;
adhering said surgical drape to the substantially planar, flanged suction head;
releasing said second protective layer from said adhesive-coated plastic film;
whereby said substantially planar, flanged suction head is prepared for application to the wound site.
11. The method as recited in claim 10, wherein said surgical drape further comprises a plastic strengthening film over said adhesive-coated plastic film, said strengthening film being less flexible than said adhesive-coated plastic film and being adapted to rigidify said adhesive-coated plastic film.
12. The method as recited in claim 11, wherein said strengthening film is of substantially the same cross section as said adhesive-coated plastic film.
13. The method as recited in claim 11, wherein said strengthening film is disassociated from said adhesive-coated plastic film.
14. A method for preparing a suction device to be hermetically sealed to a wound site, said method comprising the steps of:
providing a suction head for application to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and applying a surgical drape about said suction head for subsequent application in the region of said wound site, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
providing a suction head for application to the wound site, said suction head comprising a first face, a second face and an opening between said first face and said second face; and applying a surgical drape about said suction head for subsequent application in the region of said wound site, said surgical drape comprising a flexible adhesive-coated plastic film and a plastic strengthening layer, said strengthening layer being thicker and less flexible than said adhesive-coated plastic film and being applied to the side of said adhesive-coated plastic film opposite the adhesive coating.
15. The method of claim 14, further comprising providing a layer of open-celled polymer foam for application to said wound site between said suction head and said wound site.
16. The method as recited in claim 15, wherein said foam comprises a hydrophilic foam.
17. The method as recited in claim 16, wherein said hydrophilic foam comprises a polyvinyl acetate (PVA) foam.
18. The method as recited in claim 14 or 15, wherein said second face comprises a plurality of projections, said projections defining a plurality of channels for facilitating flow of fluids to said opening.
19. The method as recited in claim 14 or 15, wherein said strengthening film is adapted to rigidify said adhesive-coated plastic film.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9719520.0 | 1997-09-12 | ||
| GBGB9719520.0A GB9719520D0 (en) | 1997-09-12 | 1997-09-12 | Surgical drape and suction heads for wound treatment |
| CA002303085A CA2303085C (en) | 1997-09-12 | 1998-09-09 | Surgical drape and suction head for wound treatment |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002303085A Division CA2303085C (en) | 1997-09-12 | 1998-09-09 | Surgical drape and suction head for wound treatment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2471780A1 CA2471780A1 (en) | 1999-03-25 |
| CA2471780C true CA2471780C (en) | 2008-01-29 |
Family
ID=32870047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002471780A Expired - Lifetime CA2471780C (en) | 1997-09-12 | 1998-09-09 | Surgical drape and suction head for wound treatment |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2471780C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9452248B2 (en) | 2003-10-28 | 2016-09-27 | Smith & Nephew Plc | Wound cleansing apparatus in-situ |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7846141B2 (en) | 2002-09-03 | 2010-12-07 | Bluesky Medical Group Incorporated | Reduced pressure treatment system |
| GB0224986D0 (en) | 2002-10-28 | 2002-12-04 | Smith & Nephew | Apparatus |
| US7128735B2 (en) | 2004-01-02 | 2006-10-31 | Richard Scott Weston | Reduced pressure wound treatment appliance |
| US8100887B2 (en) | 2004-03-09 | 2012-01-24 | Bluesky Medical Group Incorporated | Enclosure-based reduced pressure treatment system |
| US8062272B2 (en) | 2004-05-21 | 2011-11-22 | Bluesky Medical Group Incorporated | Flexible reduced pressure treatment appliance |
| US7776028B2 (en) | 2004-04-05 | 2010-08-17 | Bluesky Medical Group Incorporated | Adjustable overlay reduced pressure wound treatment system |
| US7909805B2 (en) | 2004-04-05 | 2011-03-22 | Bluesky Medical Group Incorporated | Flexible reduced pressure treatment appliance |
| US7708724B2 (en) | 2004-04-05 | 2010-05-04 | Blue Sky Medical Group Incorporated | Reduced pressure wound cupping treatment system |
| US10058642B2 (en) | 2004-04-05 | 2018-08-28 | Bluesky Medical Group Incorporated | Reduced pressure treatment system |
| US7998125B2 (en) | 2004-05-21 | 2011-08-16 | Bluesky Medical Group Incorporated | Hypobaric chamber treatment system |
| GB0712735D0 (en) | 2006-07-26 | 2007-08-08 | Smith & Nephew | Dressing |
-
1998
- 1998-09-09 CA CA002471780A patent/CA2471780C/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9452248B2 (en) | 2003-10-28 | 2016-09-27 | Smith & Nephew Plc | Wound cleansing apparatus in-situ |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2471780A1 (en) | 1999-03-25 |
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