Resorbable device for reconstructing rotator cuffs

Abstract

A device for the reconstruction of the rotator cuff including a flat element having at least two opposite ends and adapted to be connected to at least one of the damaged tendons of the rotator cuff of a patient at the ends; the flat element being entirely made of biodegradable and resorbable material.

Claims

1. A wedge-shaped biodegradable and resorbable device for a reconstruction of a rotator cuff, the device comprising: a flat element having two opposite ends adapted to be connected to at least one damaged tendon of the rotator cuff of a patient, wherein the flat element is entirely made of biodegradable and resorbable material, wherein the flat element is a triangular-shaped flat element having a rounded end at a vertex located at a first end of the two opposite ends and a base with two other vertices at a second end of the two opposite ends, wherein the flat element comprises fixing areas located at the two opposite ends of the flat element adapted to be employed for fixing, through resorbable suture, the flat element to the at least one damaged tendon, wherein the flat element is made of homopolymer PGA fiber fabric which continuously extends across the entire surface of the flat element such that there is an absence of a hole, wherein the homopolymer PGA fiber fabric is a warp knitted fabric having a thickness between 0.4 mm to 0.45 mm, and wherein the biodegradable and resorbable material is completely decomposed in a span of one month following implantation.

2. The device according to claim 1, further comprising resorbable suture, wherein the triangular-shaped flat element has an isosceles triangle form in plan view having the rounded end at the vertex located at a first end of the two opposite ends and a base with two other vertices defining acute angles with respective pointed ends at a second end of the two opposite ends, wherein the flat element comprises three said fixing areas attachable by suturing with respective resorbable suture, the three fixing areas located at the rounded vertex and two other vertices, respectively of the triangular-shaped flat element.

3. The device according to claim 1, wherein the flat element is made of fabric with a thread having a density between 50 and 200 denier.

4. The device according to claim 1, wherein the opposite ends of the triangular-shaped flat element include an upper end defined by the vertex of the triangular-shaped flat element and a lower end defined by the two vertices of the triangular-shaped flat element.

5. The device according to claim 4, wherein the flat element comprises three said fixing areas to allow the suturing, through resorbable suture, of the three fixing areas to the at least one damaged tendon, the three fixing areas located at the rounded vertex and two other vertices, respectively, of the triangular-shaped flat element.

6. The device according to claim 1, wherein the flat element is made of textured fabric.

7. The device according to claim 5, wherein the triangular-shaped flat element has an isosceles triangle form in plan view.

8. The device according to claim 7, wherein the isosceles triangle form has equal length sides extending from the vertex located at the first end.

9. The device according to claim 2, wherein the fabric has a weft defining interstitial space less than 200 m with the weft having a thickness between 0.1 mm and 2 mm.

10. The device according to claim 1, wherein the wherein the fabric has a weft defining interstitial space of about 160 m and having a weft thickness between 0.1 mm and 2 mm, and wherein the device comprises fixing areas located at the two opposite ends of the flat element adapted to be employed for fixing, through resorbable suture, the flat element to the at least one tendon.

11. The device according to claim 1, wherein the triangular-shaped flat element is a triangular-shaped element having an upper rounded vertex located at an upper end of the triangular-shaped element and two vertices located at a lower end of the triangular-shaped element.

12. The device according to claim 11, wherein the flat element is made of PGA fiber fabric having a thickness between 0.4 mm to 0.45 mm, wherein the triangular-shaped flat element has an isosceles triangle form in plan view, wherein the fabric has a weft defining interstitial space which is less than 200 m with the weft having a thickness between 0.1 mm and 2 mm, and wherein the device comprises fixing areas located at the two opposite ends of the flat element adapted to be employed for fixing, through resorbable suture, the flat element to the at least one tendon.

13. The device according to claim 1, wherein the PGA fiber fabric is textured and made with a thread having a density between 50 and 200 denier.

14. The device according to claim 8, wherein the flat element comprises three said fixing areas to allow the suturing, through resorbable suture, of the three fixing areas to the at least one damaged tendon, the three fixing areas located at the rounded vertex and two other vertices, respectively, of the triangular-shaped flat element.

15. The device according to claim 1, wherein the flat element is made of the PGA fiber warp knitted fabric having the thickness between 0.4 mm to 0.45 mm, wherein the PGA fiber fabric has a weft defining interstitial space which is less than 200 m with the weft having a thickness between 0.1 mm and 2 mm, wherein the PGA fiber fabric extends continuously across the entire surface of the flat element such that there is an absence of a hole, wherein the triangular-shaped flat element has an isosceles triangle form in plan view, wherein the triangular-shaped flat has an upper rounded vertex located at an upper end of the triangular-shaped element and two vertices located at a lower end of the triangular-shaped element, wherein the isosceles triangle form has equal length sides extending from the rounded vertex located at the upper end, and wherein the flat element comprises three fixing areas of said PGA fiber fabric for suturing, through resorbable suture, of the three fixing areas to the at least one damaged tendon, the three fixing are respectively located at the rounded vertex at the upper end of the flat element and two other vertices, respectively, of the triangular-shaped flat element at the opposite lower end of the flat element.

Description

(1) Further characteristics and advantages of the present invention will be clearer from the exemplifying and therefore non-limiting description of a preferred but not exclusive embodiment of a device for the reconstruction of the rotator cuff, as illustrated in the enclosed drawings in which:

(2) FIG. 1 is a schematic plan view of a device for the reconstruction of the rotator cuff.

(3) With reference to the enclosed drawing, reference number 1 overall indicates a device for the reconstruction of the rotator cuff in accordance with the present invention.

(4) The device 1 comprises a flat element 2, which has at least one first 2a and one second 2b end that are opposite each other.

(5) The flat element 2, during use, is fixed by means of resorbable suture to the damaged muscle-tendon tissue of the rotator cuff.

(6) The flat element 2 has a substantially wedge-shaped form. In other words, the flat element 2 has a substantially triangular form in plan view. In particular, the flat element 2 has the form of an isosceles triangle.

(7) The vertex at the equivalent sides is rounded.

(8) The vertex at the equivalent sides defines the first end 2a of the flat element 2.

(9) The portion of flat element 2 at the base side opposite the vertex instead defines the second end 2b.

(10) In accordance with the present invention, the flat element 2 of the device 1 is made of biodegradable and resorbable material. Advantageously, the flat element 2 of the device 1 is completely made of biodegradable and resorbable material.

(11) Preferably, the flat element 2 of the device 1 is made of a PGA fiber fabric (polyglycolide or polyglycolic acid), preferably homopolymer. PGA is a highly biocompatible and resorbable polymer. In detail, the resorption time of PGA is approximately one month.

(12) Advantageously, the use of PGA fibers in making the fabric of the flat element 2 allows the formation of muscle-tendon tissue during the device 1 resorption phase.

(13) In other words, the flat element 2 is completely decomposed in the span of one month, without leaving any trace. Simultaneously, it facilitates the development of the muscle-tendon tissue.

(14) In addition, once the device 1 is inserted, the fabric of the flat element 2 is soaked with blood and in particular with plasma, which allows the antibiotic drugs to be effective on the device itself.

(15) The fabric of the flat element 2 can be obtained by weaving the PGA thread in various ways, giving rise to a knitted fabric, a woven fabric or a non-woven fabric.

(16) Preferably, the fabric is a knitted fabric, still more preferably a warp knitted fabric.

(17) In such case, the fabric has a rougher surface capable of assuming a net configuration with sufficiently small meshes.

(18) In detail, its weft is such that its interstitial space is less than 200 m, preferably around 160 m, corresponding to an average area of the holes equal to approximately 0.02 mm.sup.2. This ensures impermeability to urine, preventing leaks.

(19) In addition, the fabric is preferably textured, in a manner so as to confer still greater surface roughness thereto.

(20) Still merely by way of example, the fabric has a thickness substantially comprised between 0.3 mm and 0.6 mm, more preferably comprised between 0.4 mm and 0.53 mm, still more preferably being substantially 0.45 mm.

(21) The device 1 has fixing areas 3 placed at the ends 2a, 2b of the flat element 2 for fixing, through resorbable suture, the flat element 2 to the damaged muscle-tendon tissue.

(22) In particular, the fixing areas 3 are arranged at the vertices of the flat element 2.

(23) The invention attains the aforesaid object.

(24) Indeed, the resorption of the device during convalescence does not leave any residue in the articulation of the patient. Therefore, upon completed healing, the articulation remains completely free, without causing any irritation or impediment for the patient.