This invention relates to a surgical product. More particularly, this invention relates to a gauze or swab. Still more particularly, this invention relates to an X-ray or radio detectable surgical gauze or swab, including abdominal sponges.
The following references to and descriptions of prior proposals or products are not intended to be, and are not to be construed as, statements or admissions of common general knowledge in the art. In particular, the following prior art discussion does not in relate to what is commonly or well known by the person skilled in the art, but assists in the understanding of the inventive step of the present invention of which the identification of pertinent prior art proposals is but one part.
Surgical cloth materials for dressings, swabs, sponges and the like are traditionally made of woven cotton gauze. Natural fibre cloths comprising a high proportion of cotton are difficult to maintain as sterile and there are high production costs involved in the removal of impurities and contaminants, for example following bleaching.
It has been proposed to make swabs and sponges partly using synthetics such as polyester, and/or blends with wood pulp. Purely synthetic cloths may comprise a range of different types of polymers, copolymers and polymer blends. Suitable materials that may be utilized in medical cloth include alginate, cellulose, urethanes, hydro-gels, hydrocolloids and copolymers of acrylates and acrylamides, amongst many others.
Because X-ray Detectable Sponges and Swabs are primarily used inside body cavities during invasive surgical procedures to soak up blood, it is desirable that gauze, swabs and other medical cloths display properties of low and consistent bioburden and consistent weight. The former aids in maintaining the desired sterility assurance level as prescribed in ISO 11137; the latter helps health professionals in calculating blood loss from the patient.
Predominantly polypropylene-based products have been considered by some research to be unsuitable for surgical applications.
Polypropylene belongs to the family of polyolefins or polyalkenes and is a thermoplastic polymer resin of propylene made from petroleum. Polypropylene is moulded or extruded into many forms, including fibres for suture material, mesh and nonwoven sheets. Although nonwoven polypropylene mesh possesses attractive properties of high absorbency, good bacterial nonadherence, good pliability and moldability for use in surgical packing, the material has generally been considered irritating to touch and medical professionals may tend to avoid its use. Although nonwoven polypropylene materials have been used in the manufacture of products such as sterilisation wraps for sterilising instruments preparatory to surgery, they have not been thought of as suitable for use in the manufacture of surgical gauze or swabs.
Woven swabs and sponges can also suffer from the problem that loose threads, liable to separate from the main body of a swab, can cause contamination or infection. There is therefore a need to provide a product which does not shed loose threads.
Furthermore, a significant systemic problem, in terms of surgical procedure, is the problem of swabs being left in a patient's wound or body cavity following completion of a surgical procedure. Gauze swabs, saturated with fluids such as blood or mucus, are notoriously difficult to distinguish from surrounding human tissue and body fluids, due to the similar consistency and appearance of the used gauze to the surrounding tissue. To prevent medical materials and cloth from being inadvertently left in a patient's body cavity following suturing, a common surgical protocol involves specifically counting each swab on entry and removal from the body cavity or wound. However, despite the best efforts of medical professionals, the inadvertent failure to remove medical materials from a wound or other body cavity continues to be a problem, that may lead to septicaemia and, occasionally, death.
Accordingly, the need persists for effective means of detecting surgical products that are inadvertently left in the body of a patient and preventing this occurrence in the first instance. Therefore, sterile X-ray detectable sponges and swabs are typically supplied in packs of 5 having a determinable weight. Having consistent weight is highly desirable in the manufacturing process because the count of items entering a patient's body (during an operating procedure) is validated by weight of the pack.
An object of the present invention is to ameliorate the aforementioned disadvantages of the prior art or to at least provide a useful alternative thereto.
Accordingly, there is provided a surgical product being a swab or sponge, the surgical product including a single nonwoven sheet made up of multiple layers of a non-woven synthetic material and including an X-ray- or radio-detectable element.
Preferably, there is provided a surgical product and a method of making same comprising the combination of the overlaying of multiple layers of non-woven material, preferably alternately oriented in machine and cross directions, and having an X-ray or radio detectable element, preferably barium sulphate coated thread or ribbon, preferably aligned in both machine and cross directions, and preferably crossing along their respective lengths.
Preferably, the surgical product is wholly or predominantly made from wood pulp and polyester spun bonded layers of non-woven material, the single sheet folded over one or more times. For example, a 10×10 cm sheet may be folded once to form a rectangular swab and twice or more to form a sponge. In UK, Australia and in NZ, if the folded surgical product is also stitched together, it is generally referred to as a “sponge”, and if it is simply folded without stitching the folder layers, it is referred to as a swab. Typical swabs are 100 mm×100 mm and 100 mm×150 mm, 4-ply-16-ply. For example, a 100 mm×100 mm 4-ply swab is made from a 200 mm×200 mm sheet. A “sponge” is usually made from a 250 mm×250 mm sheet. The range of products that are used for packing include 125 mm×1 m rolls and may be referred to as “X-ray Detectable Packing Gauze”. Such packaging products may be provided in rolls having widths between 10 mm to 125 mm, and preferably widths of 12.5 mm to 100 mm, and in lengths of 1 m to 2 m.
Optionally, one or more sheets of the same or a different material may be sandwiched within the folded laminated sheet. Preferably, a single sheet of the same material is sandwiched within the folded sheet.
Preferably, the sheet is wholly or predominantly made from wood pulp/polyester fibres. The material constituting such products is generally characterised by good physical strength, a high body fluid absorption capacity and hypo-allergenic properties. The surgical cloth product also advantageously retains its integrity when wet so that loose fibres or particles thereof are not easily separated from the main body of the product when used as a swab or sponge or as packing/spacing material during a surgical procedure.
The surgical cloth product fibres may be impregnated with agents to improve and modify the properties of the material. Advantageously, however, and in a particularly preferred aspect of the invention, the surgical cloth product may be sterilised by ethylene oxide or irradiation after they are counted and packed.
The surgical cloth product may be made from one or more (bided sheets with X-ray detectable thread or tape embedded or attached by means of heat bonding. The X-ray detectable thread or tape is usually made from a barium sulphate and polymer composite. The thread or tape may be coloured a dark colour, such as blue or black, for identification against the typically light-coloured background (such as white) of the surgical cloth product. The folded sheets may be bonded one layer one to another. Bonding may be effected by arrangements of suitable means, such as ultrasonic bonding, bonding using heat, stitching or by the use of adhesives. The bonding may be achieved by continuous sealing. Alternatively, the bonding may be achieved by spot sealing. In its simplified form, surgical cloth product may simply be folded without any bonding or stitching.
The surgical product may come in a variety of sizes and shapes. Preferably, the surgical product is rectangular in shape. The layers of material may be joined one to another by stitching around the edges. In a particularly preferred embodiment, the material is a synthetic, non-woven polypropylene fibre material.
In a particularly preferred form of the invention, the surgical cloth product may be in the form of a sponge, in particular an abdominal sponge for assisting in the cleaning out of wounds and as packing against body tissues during a surgical procedure.
The surgical product may be provided in a range of sizes. The surgical product may be square shaped. Sizes may range from 10 cm square through to 50 cm square whereby different sizes suit different applications. The nonwoven sheet may be folded once and stitched or otherwise bonded as set out above. In one embodiment, the primary nonwoven sheet is folded about a secondary separate single sheet, stitched and then folded again, to form a sponge which may be unfolded to act as a swab, this giving versatility to the product.
The product may be stitched or otherwise bonded in any chosen pattern but preferably is stitched in a Z or X pattern or simply folded without any stitching or bonding.
The X-ray- or radio-detectable element may comprise an X-ray opaque material made from barium sulphate held together by an inert polymer. The X-ray opaque material may be in the form of a wire, thread, ribbon, scam or bead interposed across, through or between the spun bonded fibres, the laminate layers or the sheet layers. Preferably, the element is in the form of a thread that is hydroentangled with one or more of the spun bonded layers. Even more preferably, the element is a thread hydroentangled with a secondary separate single sheet which is then enclosed when the primary nonwoven sheet is folded about it.
The X-ray opaque material may alternatively be particulate. In the latter case, the X-ray opaque material may be sprayed onto the fibres or may be otherwise impregnated by emersion, by brush application, injection or spraying. Preferably, the X-ray opaque material is in the form of filament having sufficient flexibility to bend with the fibres during use.
The X-ray- or radio-detectable element is advantageously not susceptible to separation from the surgical cloth product in use, preferably by hydroentanglement with, or bonding to, the surgical cloth fibres.
The X-ray opaque material may comprise a range of suitable materials having large atomic particles adapted to display good X-ray-detectable properties. For example, barium salts such as barium sulphate are particularly preferred.
The X-ray detectable elements may be added by planting or spraying them into the fibre web or into the surface of the fibre web or by heating them into the surface of the surgical cloth product. The X-ray detectable element is preferably barium sulphate thread. The X-ray detectable element may optionally include barium phosphate. The barium phosphate component may be in the form of a coating applied to a synthetic thread, such as polypropylene extruded thread. The X-ray detectable element may be heated onto the surface of the non-woven cloth, for example by hot heating, hot pressing or ultrasonic wave treatment.
A sheet of the surgical cloth may comprise two, four or more layers. The surgical product may be in the form of an abdominal sponge. The abdominal sponge can be made with three layers of fabric. In such cases, the edges of the respective layers are preferably stitched or welded as described herein. The surgical product may be in the form of a swab. The swab may have the plan dimensions 100 mm×100 mm. The swab may be made by folding a 200 mm×200 mm fabric twice.
Each layer of non-woven web or fabric may be separately manufactured by an extrusion process in which fibres or filaments are deposited on a forming surface in a so-called Machine Direction (MD) corresponding to the direction of travel of the extrusion machine. Each layer is preferably made from non-woven spun bonded material. Cross fibres are simultaneously laid perpendicular to the MD in a cross-direction (CD). The strength of the resulting fabric or web layer in the MD is considerably stronger than in the CD. The present Applicants have found that by overlaying multiple layers of fabric in alternating perpendicular orientation, relative to one another, then the resulting multi-layered sheet is extremely strong in both MD and CD of the first layer. Preferably sheets of non-woven material comprise four or more layers of non-woven fabric alternatively layered in MD and CD directions. Preferably, the layers rut joined, preferably ultrasonically or by stitching, at the sheet's periphery to secure the layers in overlaid relationship relative to one another. The stitching or welding may be continuous, may be intermittent and spaced, or may be extended only along one or more edges and not other sides of the sheet.
Preferably the X-ray detectable element is in the form of a strip or ribbon oriented in the MD, although the X-ray detectable element may be alternatively or additionally oriented in the CD. By alternatively layering layers in the MD and CD, the X-ray elements cross paths. This arrangement provides an improved visual clue to users of the presence of the X-ray element, because of the distinguishable opaque line extending in two different directions. It also informs the user, notably theatre stair, of the MD of a particular layer and also improves the X-ray detectability of the product in the unfortunate event that it is inadvertently left in a patient post-surgery.
The radio-detectable element may be a passive inductor chip trapped in the tangled fibres of the surgical product. The inductor chip is thus detectable by an RF device that avoids the further use of X-ray and the deleterious affects such use may have on patients and medical staff. The inductor chip may comprise peripheral nodules, hooks, notches, apertures or other surface features with which the fibres of the surgical product material may mesh, for example by hydraulic entanglement.
Because the product of the present invention presents an external surface comprising non-woven synthetic material, the present invention provides a surgical product capable of having a lower bacterial content compared to cotton or other non-synthetics. The material is easier to be sterilised than prior art materials, contains less contaminants because there is no need to bleach the material compared to, for example, cotton gauze and the chosen materials are particularly suitable to manufacture in a closed and controlled environment. The non-woven synthetic materials do not need stitching like traditional gauze, although stitching may be used for aesthetic reasons and to give the product a better feel. Finally, the non-woven synthetic materials contemplated according to the present invention maintain good integrity so that loose threads, particles or fibres do not disassociate from the main body of the surgical product under normal use, therefore improves healing time for patients. The more consistent weight helps in mounting during manufacturing and also make blood loss calculation more accurate.
The invention may be better understood from the following non-limiting description of so preferred embodiments, in which:
a-2f are schematic side sectional views of various embodiments made according to the invention;
Preferred features of the present invention will now be described with particular reference to the accompanying drawings. However, it is to be understood that the features illustrated in and described with reference to the drawings are not to be construed as limiting on the scope of the invention.
Referring to
In an alternative arrangement conveniently shown in
In another arrangement, the inductor chip 60b may be unmodified from the standard planar plate type design having no specific edge or surface entangling features and may instead be trapped in a capsule 70 possessing the peripheral features 62, 63 suitable for entanglement with the fibres of the swab or sponge 10.
In still another arrangement, the RF chip 60c as shown in
With reference to
In particular, in
In
d shows a variation on the embodiment shown in
Referring to
With respect to
It is note worthy that the embodiment shown in
Accordingly, the double layer of sheet 82 provides a pair of layers 82a, b made of non woven wood based and surgical grade polymeric material that is highly absorbent and resistant to bacterial adherence, whilst maintaining good tactile and aesthetic properties, as well as the capacity for high absorption of bodily fluids.
The X-ray detection thread 50 is inculcated into the first spun bond layer 82a by hydraulic bonding subsequent to the formation of the single sheet of swab 82 and subsequent to the folding over of the single sheet and the optional stitching 14 together thereof.
Once the thread 50 is hydroentangled into the fibres 22, the swab, sponge or pad 81-86 is subjected to sterilising radiation or steaming in an autoclave to achieve sterilisation and they are then stacked and packaged in a plastic sealed envelope in a closed and sterile environment.
In use, the packaged product 10, 81-86 is removed under sterile conditions, for example in surgery, and utilized as a gauze, pad, sponge or swab during, for example, a surgical procedure.
Turning to
In still another embodiment shown in
Moreover, although stitching may be optionally provided for primarily aesthetic, rather than functional purposes, it will be appreciated that stitching may also achieve functional differences, such as improved strength and resistance to disassociation of loosely adhered-to layers.
In
As a skilled person will appreciate, the sheet 30 is much stronger in the MD, relative to the CD. However, it is customary to overlay multiple sheets in the same alignment direction, that is all overlaid sheets are aligned in, for example, the MD.
Counter to the traditional approach of aligning multiple overlaid sheets in the same direction, as shown in
In the embodiment shown in
As shown in
Not all layers of the surgical product 40 may include an X-ray detectable element 50,52. One, two or more of a multiple of layers may include the X-ray detectable element 50,52.
Throughout the specification and claims the word “comprise” and its derivatives are intended to have an inclusive rather than exclusive meaning unless the contrary is expressly stated or the context requires otherwise. That is, the word “comprise” and its derivatives will be taken to indicate the inclusion of not only the listed components, steps or features that it directly references, but also other components, steps or features not specifically listed, unless the contrary is expressly stated or the context requires otherwise.
Orientational terms used in the specification and claims such as vertical, horizontal, top, bottom, upper and lower are to be interpreted as relational and are based on the premise that the component, item, article, apparatus, device or instrument will usually be considered in a particular orientation, typically with the first half of layer 22, or the spaced layer 92a, uppermost.
It will be appreciated by those skilled in the art that many modifications and variations may be made to the methods of the invention described herein without departing from the spirit and scope of the invention.
Number | Date | Country | Kind |
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2009903602 | Aug 2009 | AU | national |
2009905964 | Dec 2009 | AU | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/AU2010/000974 | 8/3/2010 | WO | 00 | 6/11/2012 |