CONNECTIVE TISSUE REPAIR

Abstract

The invention relates to an implantable prosthetic device, a patch, for the repair of connective tissue in an animal or a human. In one embodiment, a biocompatible repair patch (10) for repair of human or animal tissue is disclosed which comprises a tensile load-bearing component in the form of a pre-formed array (13) of a looped configuration in a desired pattern and having at least one return end, said array being formed of an elongate filamentary material; and a base layer (11) of non-woven fibrous material. The pre-formed array is attached to one surface of the base layer so that the pre-formed array retains its configuration while being handled during surgery. The at least one return end serves to receive a suture or the like to attach the patch to tissue. The fibres of the base layer are entangled with the looped configuration so as to attach the array to the base layer and substantially to maintain the desired pattern.

Description

The present invention relates to an implantable prosthetic device, a patch, for the repair of connective tissue in an animal or a human.

Biological connective tissues are susceptible to tearing, for example when placed under excessive tensile forces. Such tearing is a common problem where a tendon or ligament has been weakened through excessive use as is common to sports professionals. Typical examples include Achilles tendon injuries (at the ankle) and torn rotator cuff at the shoulder.

Example devices for reconstruction of ligaments and tendons are disclosed in GB 2151487, U.S. Pat. No. 5,217,495, US 2004/0078089, U.S. Pat. No. 4,728,329, WO 2006/089267 and WO 2009/109778.

Recent interest in shoulder patches for repair of torn rotator cuff has increased as evidenced by a number of tissue patch products being commercialised by large orthopaedic companies. However, such patches have been largely unsuccessful and have failed due to their lack of strength and the ease with which they are torn by sutures used to attach the patches to surrounding tissue.

Much interest now is focused on patches that are made of synthetic materials and that possess adequate strength for reliable repair of the rotator cuff. Amongst these is the Artelon patch manufactured by Artimplant (Sweden) and marketed by Biomet Inc. and others. Although this patch appears to yield good results, it has some attributes that make it less user friendly. The main difficulties with this patch are: (i) it is stiff and has to be soaked in water for a period of 30 minutes for the user to be able to fold it and introduce it through a cannula into the shoulder joint space for surgeons adopting an arthroscopic surgical approach; (ii) it is difficult to suture through, and (iii) the patch structure does not possess strength that may be required for consistently good results; according to the flyer published by Biomet, distributor of the Artelon patch, the pull out strength of a mattress suture is 82N. This is the higher of the two strength figures published.

There is therefore a continued need for improved connective repair devices that may be conveniently and securely anchored to connective biological tissue.

Accordingly, the invention provides an implantable prosthetic patch that may be secured to connective tissue, such as the rotator cuff at the shoulder joint, using suitable anchorages, typically in the form of sutures, or, where one side of the patch is to be secured to bone, this is typically achieved with a combination of sutures and anchors.

Preferred embodiments of the invention aim to rectify the above mentioned problems or potential problems by being (i) pliable and so, if required, easy to fold or roll without the need for soaking in water; (ii) easy to suture through; and (iii) possesses much greater strength than that of commercially available products.

Structure and Functional Attributes of the Patch

These attributes/advantages are achieved, as the preferred embodiments comprise a group of endless loops, the spatial configuration of which is maintained and stabilised by at least one layer of a material that is attached to the loops. The extremities of the loops provide defined sites to pass sutures through. All tensile loading forces are taken initially by the loops which thereby form a connective bridge between the two biological tissue sites. The main body of the patch is not intended to take substantial tensile load; unlike other patches that have been manufactured from different material with various structures, said patches have eyelets that are reinforced with embroidery to suture through. Alternatively these patches have stitched, applied or embroidered onto them sutures/cords arrayed in different configurations including endless loops, said applied or embroidered features are intended to reinforce the patch to withstand tensile loads. These features however do not make a patch of as great strength as the patch design proposed in this application. Of course it is possible to increase the amount of applied or embroidered features to increase the strength of these other designs, but this would result in too thick and/or stiff device for it to be user friendly in terms of handling during surgery.

A patch of the present design comprising five loops, when subjected to tensile load that is equally distributed on these loops, would fail at a load in excess of 800N.

According to a first aspect of the invention there is provided a biocompatible repair patch for repair of human or animal tissue and comprising:

a tensile load-bearing component in the form of a pre-formed array of a looped configuration in a desired pattern and having at least one return end, said array being formed of an elongate filamentary material; anda base layer of non-woven fibrous material;in which:(a) the pre-formed array is attached to one surface of the base layer so that the pre-formed array retains its configuration while being handled during surgery;(b) the at least one return end serves to receive a suture or the like to attach the patch to tissue; and(c) the fibres of the base layer are entangled with the looped configuration so as to attach the array to the base layer and substantially to maintain the desired pattern.

According to a further aspect of the invention there is provided a biocompatible patch to aid repair of human or animal tissue and comprising:

a tensile load-bearing component in the form of a pre-formed array of a looped configuration in a desired pattern so as to have at least one return end to receive a suture or the like to attach the patch to tissue, said array being formed of elongate filamentary material;a base layer to which the pre-formed array is attached so as substantially to maintain the desired pattern; anda further layer overlying the pre-formed array.

According to still further aspect of the invention, there is provided a method of manufacture of a biocompatible repair patch for repair of human or animal tissue and comprising:

pre-forming a tensile load-bearing array of a looped configuration in a desired pattern so as to have at least one return end for receiving a suture or the like to attach the patch to tissue, said array being formed of elongate filamentary material; andattaching the pre-formed array to a surface of a base layer of non-woven fibrous material by entanglement of the fibres of the base layer with the looped configuration to maintain the desired pattern.

Further preferred features are set out in the dependent claims.

Optionally, the patch is square or rectangular. As will be appreciated any shape is suitable including hexagonal, circular, oval, diamond, or trapezium shaped.

According to a preferred embodiment of the present invention there is provided a biocompatible composite tissue repair patch for the repair of tissue of an animal or human, the patch comprising: a group of accurately dimensioned preformed loops in a prescribed configuration so the patch suits a specific application, the spatial configuration of said loops is maintained, for, example by sandwiching the loops between two layers of materials, said layers (carrier materials) can be films that are adhered to both sides of the loops and to each other in the spaces between the loops.

Alternatively the loops may be retained in position by hydroentangling them with the fibres of one or two layers of non-woven webs, said webs are made of numerous filaments and said webs are loosely formed for ease of hydroentanglement with the loops. The group of loops may be sandwiched between two layers of loosely structured non-woven webs the filaments of which are hydroentangled to each other and to the loops thus retaining their preformed configuration.

The loops are substantially coplanar and can be formed individually and so are separate from each other, or are formed with a single yarn that is wound in different patterns or routes to form the loops. Preferably, the loops are continuous (or endless) loops so that when they are sutured through they are capable of transmitting tension without unravelling. The terms ‘continuous loops’ and ‘endless loops’ refer to multifilamentous loops in which the filaments do not end at the region of any one of the loops or if ends are present these are incorporated in the body of the loops to appear seemingly endless, with the filament ends held by the frictional contact with neighbouring filaments of the loop.

Optionally, the elongate loops can take any directions relative to each other. Accordingly the axis of each loop, relative to the axes of other loops of the device can be parallel, transverse or angled relative to one another and so may intersect at right angles or at an acute or obtuse angle.

Optionally, the loops extend across the surface of the carrier material within a perimeter of the patch. Alternatively, the loops extend across the surface of the carrier material beyond the perimeter of the patch and thus the respective ends of at least some of the loops extended beyond a perimeter of the layer.

In this specification and claims, the term “looped configuration” of the pre-formed array is intended to be interpreted widely, and includes any suitable loop-type configuration having at least one return end which is at least part circular and which is joined to the further parts of the configuration.

Any desired pre-formed array may be provided, including wavy, sinusoidal, serpentine, and parallel run configurations, and/or combinations thereof.

The return ends may be generally semi-circular, or completely circular, or just closed e.g. of elliptical shape under tensile load, if additional tensile strength is required for securement of suture(s) to the patch and to tissue.

Also, in this specification, the looped configuration in the pre-formed array is formed of any suitable “elongate filamentary material”, and this term is intended to include monofilaments, multifilaments, and twisted yarns, and made of natural or synthetic materials. The array may be formed of a single length of elongate material, or from more than one element.

Materials and Rationale for their Choice

All components of said patches are made of biocompatible materials.

The loops are made of yarn comprising continuous filaments; said yarns are loose and possess between 30 to 100 twists per metre. Preferably, said continuous filaments possess a diameter in the range 20 to 50 microns. The above yarn material is selected in preference to sutures or cord because these latter alternatives have tight structures that do not allow the entanglement of filaments of the non-woven layers as does the loose structure of the yarn mentioned above. Further the yarn would form of strong loops of smaller bulk than that if loops were made of cords or sutures, which would be weaker.

Optionally, when one layer is of a non-woven material formed from randomly oriented filaments, the filaments of the layer are entangled with the filaments of the loops to retain their spatial configuration and dimensions in a stable manner. Preferably, the fibres or filaments of the layer are entangled with the filaments of the loops by hydroentanglement. This process is advantageous for use with the present invention in preference to an alternative needle punching attachment process. In particular, the barbed needles used in this latter process would cause disruption of the loop configurations and possible damage, which could weaken the loops strength. On the other hand the process of hydroentanglement causes no such disruption or damage to the loops or their strength.

Where the device comprises two layers formed from non-woven webs, the fibres of the webs are orientated randomly and loosely arranged, and the two webs are attached to each other, to, and through the loops, via the hydroentanglement process.

Optionally, non-woven material is bioabsorbable or permanent (non-bioabsorbable). Optionally, the non-woven material comprises silk and is bioabsorbable.

Method of Manufacturing

One method of manufacturing such a patch is described as follows:

The patch is formed by winding a number of continuous loops around pins fixed on a porous plate in patterns to result in prescribed loop configurations that suit the various specific applications. A sheet of loosely formed non-woven material is placed on top of the plate before the loops are wound in the desired/prescribed manner on top of that sheet of material. Another sheet of non-woven material is placed on top of the formed loops and the filaments forming said sheet are mechanically entangled with those forming the first sheet and with the yarns forming the loops. The entanglement is achieved with tiny water jets—a process known as hydroentanglement.

The non-woven components of a patch can occupy part of the area of the patch so that the loop ends project beyond the body of the patch thus defining clearly the locations for suturing. The number of loop ends for suturing, and their positions can be easily controlled during the manufacturing process. The strength of the patch in different directions can be controlled by the number of throws in the different loops. The handling properties could also be improved by replacing one of the non-woven layers with a woven layer, which may be a loosely woven layer, or just by including an additional such layer within the assembly of the patch. A loosely woven layer may be one which has a relatively low weave density. This may be advantageous during attachment of the woven layer to another component of the patch, particularly by (hydro)entanglement. The additional layer may be provided between two non-woven layers, or may be attached to one of the non-woven layers. For example, the woven layer may be attached to an external facing surface of the base layer, or to an external facing surface of the further layer which overlies the pre-formed array. The woven layer may be attached to the non-woven layer(s) by any of the methods disclosed herein, but in particular it may be attached by a hydroentanglement process. To this end, it may be desirable to provide the woven layer with a relatively open weave, so as not to hamper the entanglement process. This may also promote the in-growth of tissue. It may be preferred to hydroentangle all of the components of the patch together at the same time.

In the foregoing description of the manufacturing process the non-woven, or woven material will easily be penetrated by the various pins. However, when manufacturing a patch in which the array of preformed loops is trapped between two films that are adhered together, these latter will have perforations that correspond to the pins on the plate. The manufacturing process will comprise placing one such perforated film on the plate, with the adhesive side of the film pointing away from the plate. The array of loops is then wound around the pins in the desired form. A second layer of perforated film is place onto the plate with the adhesive side facing towards the first film. Pressure is then applied so the two films adhere to the preformed array of loops and to each other through the spaces between the loops.

According to a third aspect of the present invention there is provided a kit of parts for the repair of tissue of an animal or human comprising:

• • a biocompatible patch/as described above and
  • an introducer tool having retaining means positioned towards a distal end of an elongate shaft, the retaining means capable of retaining the in a folded or rolled configuration to introduce through a cannula into a patient's joint during an implantation procedure where the surgery is to performed arthroscopically.

According to a fourth aspect of the present invention there is provided a method of tissue repair of an animal or human comprising:

• • securing a first side of a biocompatible patch as described above to a first tissue site using anchorage cord/suture, and
  • securing a second side of the patch to a second tissue repair site using anchorage cord such that the is secured in position to bridge the first and second tissue sites;
  • wherein the anchorage cord/suture at the first and second tissue sites passes through at least one of the same loops at respective first and second ends of the loops.

A specific implementation of the present invention will now be described by way of example only and with reference to the accompanying drawings in which:

FIG. 1 is a plan view of an implantable prosthetic device for the repair of connective tissue having a preformed array of separately looped configuration extending over a base layer of a non-woven material;

FIG. 2 is a plan view of another example of the patch according to the invention, in which the array of looped configuration is formed from one or more single length of elongate filamentary material, attached to and extended over the base layer (the loops here are interconnected);

FIG. 3 is a plan view of an embodiment of the repair patch of FIG. 2 in which the loop ends extend across the patch within the perimeter of the patch;

FIG. 4 is a plan view of a further embodiment of the reinforced repair patch of FIG. 1 in which the loop ends extend beyond a perimeter of the patch;

FIG. 4 a is a perspective view showing the repair patch of FIG. 4 after it has been removed from the pins which define the configuration of the loops;

FIG. 5 is an exploded view illustrating part of an assembly process for the construction of a patch in FIGS. 3 and 4;

FIG. 6 is plan view of a sheet of a base layer (non-woven material or adhesive film) retaining preformed arrays formed from a continuous yarn or filament;

FIGS. 7 a & b show perspective views of an introducer tool useable to assist with implantation of a patch in FIGS. 1 to 4a at a tissue repair site in a rolled or folded configuration according to a specific implementation of the present invention;

FIG. 8 illustrates a cannula for introducing a patch of FIGS. 1 to 4 rolled around an introducer tool of FIG. 7a & b according to a specific implementation of the present invention.

Referring to FIGS. 1 to 4a, one embodiment of the present invention provides a composite tissue repair patch having at least one base layer of a non-woven fibrous material, such as a felt-like material formed from randomly arranged fibres. A tensile load-bearing component is attached to the base layer, and comprises a pre-formed array of a looped configuration in a desired pattern. The array is formed of an elongate filamentous material, and has at least one return end. In the description of the following examples, the array of looped configurations is formed in any desired pattern using an elongate element such as yarn comprising continuous monofilaments, and will be referred to hereinafter as a “cord”.

The array of loops is formed by winding the cord around and back on itself on one surface of the non-woven layer to form substantially planar elongate loops that are considered to be ‘endless’ as described earlier. The single piece of looped cord is arranged so as to provide a plurality of elongate loops extending across of the surface of the layer and towards or beyond the perimeter of the layer. The respective pair of ends of each loop (the return ends) therefore provide attachment regions to receive tissue or anchorage attachment means such as medical sutures and the like which are threaded through and within the two opposite ends of the same loop and connect the patch to the soft tissue to be repaired. According to specific implementations, the tensile strength of the loops may be reinforced by overlaying the cord in multiple passes or throws. According to further embodiments the ends of the loops extend beyond a perimeter of the layer so as to overhang the layer and present exposed loop end regions to receive the anchorage medical cord/suture.

Referring to FIG. 1, a composite repair patch 10 comprises a layer 11 of a non-woven filamentous material. According to the specific implementation, layer 11 is substantially planar and generally rectangular as defined by the patch perimeter 12. However, according to further specific embodiments, layer 11 may have any substantially planar shape such as a circle, oval, generally triangular, a trapezium or any polygonal shape.

At one face of the non-woven filamentous layer 11 is attached array of loops pre-formed from an elongate cord 13 comprising continuous multifilaments. The looped cord 13 extends over discrete regions of the face of layer 11 across the patch length, width, or diameter, within the patch perimeter 12. According to the embodiment of FIG. 1, four loops extend lengthwise over layer 11 and four loops extend widthways across layer 11. One or more return end of each loop can be used to define an attachment region configured to receive sutures or other medical anchorage cord to attach patch 10 to body tissue. In the embodiment of FIG. 1, the array is formed from more than one length of cord. The number of loops forming the array can be varied in any direction to suit a particular application.

FIG. 2 illustrates a further embodiment of the composite repair patch 20 having an array preformed by a single length of filamentous material (cord 21) wound in a different pattern and attached to base layer 22 also of non-woven filamentous material.

FIG. 5 is an exploded view illustrating a stage in the assembly process of a patch designated generally by reference 30, where the patch comprises a dual layer structure, namely base layer 31, a pre-formed array 32 of looped configuration in a desired pattern determined by the path followed by cord 33, and a second layer 34. According to this embodiment, the elongate cord 33 is attached to an inner (or upward) facing surface 35 of layer 31. The second layer 34 is of the same fibrous material as base layer 31 and having the same inner facing surface 36 which is overlaid onto the first layer 31 so as to sandwich the elongate cord 33 between opposed surfaces 35 & 36. The external facing surfaces 37 of each layer 31 & 34 thereby form the outer surfaces of the patch 30.

According to further embodiments, the material of upper layer 34 may be different to that of the non-woven attachment layer 31. In particular, second layer 34 may comprise a woven textile, or a filamentous based material having a looped or woven configuration. The second layer 34 may also comprise a plastics film formed from a suitable polymer. A downward facing surface 36 of the polymer film may comprise an adhesive for attachment to the opposed upward facing surface 35 of lower layer 31. The second layer 34 may alternatively be attached to the inner facing surface 35 of the lower layer 31 by a heat-sealing process, by selection of an appropriate material forming the second layer. Where upper layer 34 is formed from a non-woven fibrous based material, the density of the material of layer 34 may be the same or greater than that of the first layer 31. Where the two layers 31, 34 are non-woven, they may be attached to sandwich the cord therebetween by entanglement of the respective fibres of each layer 31, 34. The preferred technique for attachment of cord 33 to surface 35 of layer 31 is hydrojet entanglement whereby the filaments of the cord 33 are mechanically entangled with the fibres or filaments of layer 31 using very fine jets of water discharged at high pressure through a porous plate (not shown) on which the three components (31, 32, 34) of the patch are laid. The plate has projecting pins arranged according to the required pattern of the array (32) and engaged by the cord 33 to pre-form the looped configuration of the array 32.

According to one method of manufacture of a single layer patch (having single layer 31 and cord 33 attached thereto in a desired manner), and referring to FIG. 3, patch 10 is formed by winding cord 13 (formed from a plurality of continuous filaments) around pins 14 fixed on a common porous plate (not shown). The layer 12 of non-woven material is placed on top of the formed loops 13 and the layer 12 is then mechanically entangled around the various sides of the groups of loops of cord 13 using the water jet entanglement as described. The process provides a composite patch 10 that is reinforced with strong loops of cord (e.g. yarn) 13. FIG. 3 shows patch 10 with the pre-formed array (13) attached within the perimeter 16 of the base layer 12, whereas FIG. 4 shows patch 10a with the preformed array (13a) extending partly outside the perimeter 16a of the base layer 12a.

Where the patch 30 (FIG. 5) is formed as a dual layer structure with the cord 33 positioned intermediate between the two layers 31, 34, the fibres of each of the layers are also entangled together via the same hydroentanglement process that attaches the cord 33 to the first layer 31. The resulting patch 30 is therefore a fully connected, integrated and unitary structure via entanglement of the respective constituent fibres on the micron scale.

Cord 33 is a multifilament cord in which the filaments are twisted together only lightly or moderately so as to provide a composite yarn having a ‘loose’ structure. Accordingly, the individual filaments are capable of independent movement as part of the composite yarn strand so as to allow mechanical entanglement with the fibres of the layer 31. In particular, yarn 33 may comprise 30 to 100 twists per metre and preferably around 50 twists per metre. Each filament may comprise a diameter in the range 20 to 50 microns. In one implementation, the yarn is formed from between 70 and 100 monofilaments.

Referring to FIG. 4, the looped cord 13a extends over the face of layer 12 across the length, width, or diameter, such that the loop ends extend beyond the perimeter 13a such that in the finished patch the loop ends overhang or project from the perimeter. That is, during the assembly process, layer 31 of FIG. 5 is positioned within the set of pins 14a around which the yarn is wound to form the loops. FIG. 4a illustrates the patch 10a after it has been removed from the group of pins 14a defining the configuration of the loops. The loop ends 15 project beyond the perimeter of the patch 10, and may be of length varying between perhaps 4 mm to 15 mm, to suit the purposes of different applications. The loops may be dimensioned so that they project further beyond the perimeter of the patch, if desired. It may be desired to anchor the patch 10a to tissue in the form of a bone (not shown) in which a narrow channel has been prepared to receive the loop ends 15. Such narrow channels can be straight or circular; the former shape can be prepared with an oscillating saw blade, the latter with a hollow thin-walled reamer. In use, the loop ends would be pushed down into the annular channel with a suitable instrument, and, over time, tissue-in growth through the loops would anchor the patch 10a to the bone. Forming longer loops may facilitate the process of locating the loop ends in the said channels.

Referring to FIG. 6, the present composite patch may be produced in numbers, using a large porous plate accommodating groups of pins, each group being for winding an array of endless groups for one of the patches described. A larger sheet of the non-woven layer 61 will be pushed onto the plate, and will be penetrated by the pins. Thereafter this sheet supports a plurality of regions or groups 62 of loops of cord 63, each group 62 being suitable to be cut from the larger sheet 61. Each group 62 may comprise the same or a different arrangement of looped cord 63 so as to provide different geometries and configurations of patch 60. The groups 62 of loops are connected together by a traversing yarn between regions 63. Accordingly, an array of repair patches is formed using the same yarn (which is comprised of a group of continuous monofilaments typically of a diameter of 20-50 microns) on the single non-woven layer 64 following a clockwise path 65, 66, 67, 68 and 69. Each patch region 70 may then be cut from the larger sheet using a punch or similar.

As will be appreciated, the single layer arrangement shown in FIG. 6 may comprise a further layer so as to form the dual layer structure described with reference to FIG. 5.

It is also possible to replace one of the non-woven layers with a loosely woven layer such as the layer 38 shown in FIG. 5, or to provide an additional such layer 38, to improve the handling characteristics of the patch. Said loosely woven layer may be combined with one non-woven layer or sandwiched between two non-woven layers. For example, the woven layer 38 may be attached to external facing surface 37 of the base layer 31 (which may be a bottom or lower surface), and/or to external facing surface 37 of layer 34 (which may be an upper or outer surface).

The present composite patch is suitable for laparoscopic, arthroscopic, thoracoscopic or other keyhole surgery techniques. Referring to FIGS. 7a,b and 8, a suitable delivery tool 40 comprises a handle being one end of an elongate shaft 41. Releasable attachment members in the form of two elongate parallel prongs 43 extend from a distal end 42 of shaft 41. Referring to FIG. 7a, a patch 45 is inserted between prongs 43 and then rolled over and about prongs 43 by rotation of shaft 41 with the fingers and thumb. In this rolled configuration the patch 45 and the distal end of introducer tool 40 are suitable for passage within a delivery cannula 46 (see FIG. 8) inserted through an incision 47 and having its distal end positioned at a repair site. Once the rolled patch 45 is delivered to the repair site via cannula 46, shaft 41 is rotated in the opposite direction so as to unfold patch 45 at the shaft distal end. A surgeon may then secure the respective sides of the patch in position conveniently as the patch is capable of being delivered and unfolded in a controlled manner precisely at the desired location in vivo.

According to further embodiments, a sleeve or sheath (not shown) may be positioned to surround patch 45 in the rolled or folded configuration with this sheath being configured to be withdrawn or cut from patch 45 so that it may unfold in vivo in the desired way.

According to a further embodiment, and referring to FIG. 5, the patch does not utilise any non-woven fibrous structure, but instead each layer 31,34 comprises a polymer sheet of film having an adhesive extending fully or partially over the surface 35, 36. Accordingly, by pressing adhesive backed surfaces 35, 36 together, both layers 31, 34 adhere strongly to one another and sandwich elongate cord 33 therebetween. The looped configuration of cord 33 is therefore retained by the adhesive present on at least one or both opposed adhesive surfaces 35, 36. Alternatively and as described above, a heat-sealing process may be employed. According to the further embodiment, the polymer layers 31, 34 may be formed from a bioabsorbable or non-bioabsorbable material.

Importantly, cord 33 and the material of layer 31, 34 is biocompatible. According to the specific embodiments, cord 33 is non-bioabsorbable and is formed from a polyester. According to certain embodiments, layers 31, 34 and/or yarn 33 are bioabsorbable or permanent (non-bioabsorbable) being effectively scaffolds to encourage tissue ingrowth around looped cord 33.

According to one embodiment, layers 31, 34 and/or yarn 31 are bioabsorbable and comprise silk or a silk based material. According to further specific embodiments, layer 31 may comprise a woven configuration formed from a multifilament yarn being the same or a different yarn to that of the elongate cord 33.

Claims

1. A biocompatible repair patch for repair of human or animal tissue and comprising: a tensile load-bearing component in the form of a pre-formed array of a looped configuration in a desired pattern and having at least one return end, said array being formed of an elongate filamentary material; anda base layer of non-woven fibrous material; in which:(a) the pre-formed array is attached to one surface of the base layer so that the pre-formed array retains its configuration while being handled during surgery;(b) the at least one return end serves to receive a suture or the like to attach the patch to tissue; and(c) the fibres of the base layer are entangled with the looped configuration so as to attach the array to the base layer and substantially to maintain the desired pattern.

2. A patch according to claim 1, in which the fibres of the base layer are entangled by a process of hydroentanglement with the looped configuration.

3. A patch according to claim 1 or 2, in which a further layer is attached to the pre-formed array.

4. A patch according to claim 3, in which the further layer is a non-woven fibrous layer.

5. A patch according to claim 4, in which the further layer is attached to the pre-formed array by hydroentanglement of the fibres of the further layer with the looped configuration.

6. A patch according to claim 1, comprising at least one woven layer.

7. A patch as claimed in claim 6, in which a woven layer is attached to the pre-formed array, and in which a further non-woven layer is attached to the woven layer so that the woven layer is effectively sandwiched between the non-woven layers.

8. A patch as claimed in claim 6, in which a woven layer is attached to an external facing surface of the base layer.

9. A patch as claimed in claim 6, in which the patch comprises a further non-woven layer attached to the pre-formed array, and in which a woven layer is attached to an external facing surface of the further non-woven layer.

10. A patch as claimed in claim 5, in which the layers and the pre-formed array are entangled by a process of hydroentanglement.

11. A biocompatible patch to aid repair of human or animal tissue and comprising: a tensile load-bearing component in the form of a pre-formed array of a looped configuration in a desired pattern so as to have at least one return end to receive a suture or the like to attach the patch to tissue, said array being formed of elongate filamentary material;a base layer to which the pre-formed array is attached so as substantially to maintain the desired pattern; anda further layer overlying the pre-formed array.

12. A patch according to claim 11, in which the base layer and the further layer are adhesively secured together.

13. A patch according to claim 1, in which the pre-formed array has more than one return end.

14. A patch according to claim 13, in which the return ends are located within the perimeter of the base layer.

15. A patch according to claim 13, in which at least one return end is located outside the perimeter of the base layer.

16. A medical repair kit comprising a patch according to claim 1, in combination with an introducer tool having attachment members around which the patch can be folded prior to insertion into a patient.

17. A method of manufacture of a biocompatible repair patch for repair of human or animal tissue and comprising: pre-forming a tensile load-bearing array of a looped configuration in a desired pattern so as to have at least one return end for receiving a suture or the like to attach the patch to tissue, said array being formed of elongate filamentary material; andattaching the pre-formed array to a surface of a base layer of non-woven fibrous material by entanglement of the fibres of the base layer with the looped configuration to maintain the desired pattern.

18. A method according to claim 17, in which the fibres of the base layer are entangled with the looped configuration by a process of hydroentanglement.

19. A method according to claim 17, in which the pre-formed array is formed by winding the elongate material of the array at least partly around pins fixed onto a plate in an arrangement that results in the desired pattern of the array.

20. A method according to claim 19, in which the plate is provided with jets which operate to inject water through the base layer in order to entangle its fibres with the looped configuration.

21. A patch according to claim 1, in which the filaments of the array are loose and comprise between 30 to 70 twists per metre.

22. A patch according to claim 1, in which a diameter of the filaments of the array is in the range 20 to 50 microns.

23. A patch according to claim 1, in which at least the base layer is bioabsorbable.

24. A patch according to claim 23, in which bioabsorbable silk forms the base layer.

25. A medical repair kit according to claim 16, including a cannula capable of being at least partially inserted at a tissue repair site and having a size and/or diameter that is sufficient to allow the distal end of the introducer tool and the patch in the folded or rolled configuration to pass internally through the cannula from a proximal to a distal end.

26. A method of tissue repair of an animal or human comprising: securing a first side of a biocompatible patch to a first tissue site using anchorage cord, the patch comprising: at least one layer of a non-woven material having a first surface;a filamentous elongate cord attached to the first surface, the cord arranged in loops extending over the surface wherein respective ends of the loops define attachment regions capable of receiving anchorage cord to attach the patch to the tissue;wherein the fibres of the layer are entangled with the filaments of the cord to attach the layer to the cord and maintain the position of the loops over the layer surface; andsecuring a second side of the patch to a second tissue repair site using anchorage cord such that the patch is secured in position to bridge the first and second tissue sites;wherein the anchorage cord at the first and second tissue sites passes through at least one of the same loops at respective first and second ends.

27. A method of tissue repair of an animal or human comprising: positioning a distal end of a cannula at a tissue repair site;introducing a patch in a folded or rolled configuration to the repair site by passing the patch through the cannula from a proximal end to the distal end using an introducer tool, the patch comprising: at least one layer of a non-woven material having a first surface;a filamentous elongate cord attached to the first surface, the cord arranged in loops extending over the surface wherein respective ends of the loops define attachment regions capable of receiving anchorage cord to attach the patch to the tissue;wherein the fibres of the layer are entangled with the filaments of the cord to attach the layer to the cord and maintain the position of the loops over the layer surface;securing a first side of a biocompatible patch to a first tissue site using anchorage cord; andsecuring a second side of the patch to a second tissue repair site using anchorage cord such that the patch is secured in position to bridge the first and second tissue repair sites;wherein the anchorage cord at the first and second tissue repair sites passes through at least one of the same loops at respective first and second ends.

28. A medical repair kit comprising a patch according claim 15, in combination with an introducer tool having attachment members around which the patch can be folded prior to insertion into a patient.

29. A medical repair kit according to claim 28, including a cannula capable of being at least partially inserted at a tissue repair site and having a size and/or diameter that is sufficient to allow the distal end of the introducer tool and the patch in the folded or rolled configuration to pass internally through the cannula from a proximal to a distal end.