LOW MASS DENSITY SURGICAL IMPLANT AND METHODS OF USE

• US 20130289341A1
• Filed: 06/21/2013
• Published: 10/31/2013
• Est. Priority Date: 03/30/2001
• Status: Active Grant

• Current Assignee: Coloplast A/S
• Original Assignee: Coloplast A/S
• Inventors: Browning, James
• Granted Patent: US 8,603,120 B2
• Time in Patent Office: Days
• US Class Current: 600/37
• CPC Class Codes: A61F 2/0036 implantable A61F2/0018 takes precedence
• CPC Class Codes: A61F 2/0063 Implantable repair or support meshes, e.g. hernia meshes
• CPC Class Codes: A61F 2002/0068 having a special mesh pattern
• CPC Class Codes: A61F 2002/0072 Delivery tools therefor
• CPC Class Codes: A61F 2002/0081 directly machined on the prosthetic surface, e.g. holes, grooves A61F2/30771 takes precedence
• CPC Class Codes: A61F 2002/0086 for preferentially controlling or promoting the growth of specific types of cells or tissues of bone tissue onto implantable joints A61F2002/3093
• CPC Class Codes: A61F 2250/0071 breakable or frangible

Abstract

A surgical implant adapted to treat a prolapse in a patient is provided. The implant comprises a knitted mesh having a mass density of less than 25 g/m². The knitted mesh includes at least one biocompatible polypropylene filament and openings. The implant is configured to be implanted in a region of the prolapse, wherein the prolapse is selected from the group consisting of urethrocoele prolapse, cystocoele prolapse, vault prolapse, uterine prolapse, enterocoele prolapse, and rectocoele prolapse. Methods of using a surgical implant are also provided.

Claims

1. A surgical implant adapted to treat a prolapse in a patient, the surgical implant comprising:

a knitted mesh having a mass density of less than 25 g/m², wherein the knitted mesh comprises;

at least one biocompatible monofilament formed from polypropylene and having a diameter of from about 0.02 mm to 0.15 mm; and

openings formed between the at least one monofilament to allow blood to pass through the knitted mesh or to allow fibroblast throughgrowth,

wherein the openings include at least one of pores having a diameter of from about 50 μ

m to 200 μ

m and major spaces having a width of from about 1 mm to 10 mm,

wherein the implant is non-absorbable and is configured to be implanted in a region of the prolapse, wherein the prolapse is selected from the group consisting of urethrocoele prolapse, cystocoele prolapse, vault prolapse, uterine prolapse, enterocoele prolapse, and rectocoele prolapse, and

wherein the knitted mesh is configured to be secured in place to treat the prolapse.

2. The implant of claim 1, wherein the at least one monofilament has a diameter of from about 0.08 mm to 0.1 mm.

3. The implant of claim 1, wherein the implant has a width of from about 1 cm to 10 cm.

4. The implant of claim 1, wherein the knitted mesh is a warp knitted mesh.

5. The implant of claim 1, wherein the openings include major spaces formed by spaced apart strands.

6. The implant of claim 5, wherein the openings further include pores formed within the strands.

7. The implant of claim 5, wherein the strands have a diameter of from about 150 μ

m to 600 μ

m.

8. A surgical implant adapted to treat a prolapse in a patient, the surgical implant comprising:

a knitted mesh having a mass density of less than 25 g/m², wherein the mesh comprises;

at least one biocompatible polypropylene filament and having a diameter of from about 0.02 mm to 0.15 mm; and

openings formed in the knitted mesh to allow blood to pass through the knitted mesh or allow fibroblast throughgrowth,

wherein the openings include at least one of pores having a diameter of from about 50 μ

m to 200 μ

m and major spaces having a width of from about 1 mm to 10 mm,

wherein the implant is configured to be implanted in a region of the prolapse, wherein the prolapse is selected from the group consisting of urethrocoele prolapse, cystocoele prolapse, vault prolapse, uterine prolapse, enterocoele prolapse, and rectocoele prolapse, and

wherein the knitted mesh is configured to be secured in place to treat the prolapse.

9. The implant of claim 8, wherein the at least one filament is a monofilament.

10. The implant of claim 8, wherein the implant is non-absorbable.

11. The implant of claim 8, wherein the at least one filament forms strands and wherein the pores are formed between the at least one filament and within the strands.

12. The implant of claim 11, wherein the implant is configured to be attached to a vaginal wall.

13. A method for treating a vaginal prolapse in a patient, the method comprising:

accessing the vaginal prolapse, wherein the prolapse is selected from the group consisting of urethrocoele prolapse, cystocoele prolapse, vault prolapse, uterine prolapse, enterocoele prolapse, and rectocoele prolapse;

inserting an implant into a patient, the implant comprising;

a knitted mesh having a mass density of less than 25 g/m², wherein the mesh comprises;

at least one biocompatible monofilament formed from polypropylene and having a diameter of from about 0.02 mm to 0.15 mm; and

openings formed in the mesh to allow at least one of blood to pass through the mesh and fibroblast throughgrowth,

wherein the openings formed between the monofilaments include at least one of pores having a diameter of from about 50 μ

m to 200 μ

m and major spaces having a width of from about 1 mm to 10 mm; and

securing the knitted mesh in place such that the implant supports the pelvic floor of the patient.

14. The method of claim 13, wherein securing the knitted mesh in place includes securing the knitted mesh in place with sutures.

15. The method of claim 13, wherein inserting the implant includes inserting a non-absorbable implant.

16. The method of claim 13, wherein the knitted mesh is a warp knitted mesh.

17. The method of claim 13, wherein securing the knitted mesh in place comprises securing the knitted mesh in place such that the implant supports a vaginal wall of the patient.

18. The method of claim 13, wherein accessing the vaginal prolapse comprises accessing the vaginal prolapse through a minimally invasive surgical procedure.

19. The method claim 13, wherein the at least one monofilament forms strands and wherein the knitted mesh comprise pores formed within the strands and major spaces formed between adjacent strands.

20. The method of claim 19, wherein the strands have a diameter of from about 150 μ

m to 600 μ

m.