Surgical correction of female urinary stress incontinence and kit therefor

• US 5,013,292 A
• Filed: 02/24/1989
• Issued: 05/07/1991
• Est. Priority Date: 02/24/1989
• Status: Expired due to Fees

• Current Assignee: R. Laborie Surgical, Ltd.
• Original Assignee: R. Laborie Medical Corporation
• Inventors: Lemay, Claude
• Primary Examiner(s): NOT, DEFINED
• Assistant Examiner(s): NOT, DEFINED
• Application Number:
  US07/315,279
• Time in Patent Office: 802 Days
• Field of Search: 128/830, 128/831, 128/834, 128/839, 128/840, 128/DIG. 25, 600/29, 600/30, 606/144, 606/148, 606/216, 606/222, 606/228-233
• US Class Current: 600/30
• CPC Class Codes: A61B 17/04 for suturing wounds; Holders or packages for needles or suture materials suture materials A61L17/00
• CPC Class Codes: A61B 17/06 Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials puncturing needles A61B17/34; hypodermic needles A61M5/32 ; sewing needles D05B85/00
• CPC Class Codes: A61B 17/062 Needle manipulators
• CPC Class Codes: A61B 2017/00805 Treatment of female stress urinary incontinence
• CPC Class Codes: A61B 50/33 Trays
• CPC Class Codes: A61F 2/0045 Support slings
• CPC Class Codes: Y10S 128/25 Artificial sphincters and devices for controlling urinary incontinence

Abstract

A surgical kit is provided, for a urethropexy procedure, comprising at least one needle (comprising a cannula and a trocar), a pair of implants and a tray for supporting and packaging the needle(s) and implants. The kit is sterilizable. A procedure for urethropexy is disclosed which may be carried out under local anesthesia.

Claims

1. A kit for use in the surgical correction of female urinary stress incontinence comprising:

at least one needle, said needle comprising a cannula and a trocar, said cannula being receivable of said trocar, said trocar being removably disposable within said cannula, said needle being bendable to a desired degree of curvature; and

a pair of implants, each of said implants comprising a head portion and a suture portion, said head portion adapted to rest on the pubic bone, said head protion comprising a substanitally figure eight shaped member of surgical titanium having a central cross bar and said sutrue portion comprising a surgical suture acceptable, substantially non-biodegradable thread having a first end, a second end and a central portion, said central portion being wrapped about said central cross bar with said first and second ends disposed on a single side of said head portion, said first and second ends being guidingly receivable within said cannula.

2. The kit according to claim 1, comprising a pair of said needles.

3. The kit according to claim 1, further comprising a tray for engagingly supporting and packaging said at least one needle and said pair of implants.

4. The kit according to claim 3, wherein said tray is sterilizable.

5. A kit for use in the surgical correction of female urinary stress incontinence comprising:

a pair of implants, each of said implants comprising a head portion and a suture portion, said head portion comprising a substantially figure eight shaped member of surgical titanium having a central cross bar, said suture portion comprising a surgical suture acceptable, substantially non-biodegradable thread having a first end, a second end and a central portion, said central portion being wrapped about said central cross bar with said first and second ends disposed on a single side of said figure eight shaped member;

a pair of needles, each of said needles comprising a cannula and a trocar, said cannula being receivable of said trocar, said trocar being removably disposable within said cannula, each of said needles being bendable to a desired degree of curvature, said cannula, in use, being guidingly receivable of said first end and said second end of said thread;

a tray for supporting and packaging said pair of needles and said pair of implants.

6. The kit according to claim 5, wherein said tray includes holding means for holding said pair of needles and said pair of implants in predetermined positions on said tray.

7. The kit according to claim 6, wherein said holding means comprises a pair of hollow cylinder members supportingly receivable of respective suture portions of said pair of implants therein.

8. The kit according to claim 7, wherein said holding means further comprises a plurality of raised portions formed on said tray, said plurality of raised portions defining a plurality of gaps therebetween, at least a portion of said plurality of gaps being engagingly receivable of respective portions of said pair of hollow cylinder member and said pair of needles.

9. The kit according to claim 5, wherein said tray is sterilizable.

10. The kit according to claim 5, wherein each of said pair of needles is about 150 mm long.

11. The kit according to claim 10, wherein for each of said pair of needles, said cannula has an outside diameter of about 0.80 to 0.95 mm and said trocar has an outside diameter of about 0.60 mm, said trocar being slidable within said cannula.

12. The kit according to claim 10, wherein each of said pair of needles is provided with a predetermined curvature.

13. The kit according to claim 12, wherein said predetermined curvature has a radius of curvature of about 102 mm.

14. The kit according to claim 5, wherein said head portion is encased within a coating of medical grade polymer.

15. The kit according to claim 14, wherein said polymer is a silicone.

16. A saddle for supporting a neck portion of the female urethra comprising

a substantially rectangular, planar abase, said base having an upper surface, a lower surface and four corners;

a pair of arms protruding upwardly and outwardly from a central portion of said upper surface of said base, said arms being integrally formed with said base and forming a substantially V-shaped notch therewith;

a reinforcing element attached to said lower surface of said base and substantially coextensive therewith;

means defining an aperture in each of the four corners of said base, each said aperture passing through said base and said reinforcing element.

17. The saddle according to claim 16, wherein said reinforcing element is formed of medical grade polyester.

18. The saddle according to claim 17, wherein said polyester is polyethylene terephthalate.

19. The saddle according to claim 17, wherein said base is formed of medical grade silicone rubber.

20. A method for surgically correcting female urinary stress incontinence comprising the steps of

(1) providing a pair of implants, each of said implants comprising a head portion and a suture portion, said head portion adapted to rest on the symphysis pubis, said suture portion comprising a surgical suture acceptable, substantially non-biodegradable thread connected to said head portion, said thread having a first end and a second end disposed on a single side of said head portion;

(2) providing at least one needle, said at least one needle comprising a cannula and a trocar, said cannula being receivable of said trocar, said trocar being removably disposable within said cannula, said at least one needle being bendable to a desired degree of curvature, said first and second ends of said thread being guidingly receivable within said cannula;

(3) incising only the vaginal mucosa with an incision about 1 cm in length at the urethro-vesical junction;

(4) introducing said needle at the right distal extremity of said vaginal incision and non-traumatizingly guiding said needle along the symphysis pubis to a first point about 3 cm to the right of a median line at the superior border of the symphysis pubis and passing said needle through the skin at this first point;

(5) incising the skin with a cutaneous incision about 0.5 cm in length at said first point;

(6) removing said trocar from said needle while leaving the cannula in place;

(7) introducing the first end of said thread from one of said pair of implants into said cannula until it protrudes into the vagina;

(8) withdrawing said cannula through the vagina;

(9) introducing said needle at the right distal extremity of said vaginal incision and non-traumatizingly guiding said needle along the symphysis pubis to said incision of step (5);

(10) removing said trocar from said needle while leaving the cannula in place;

(11) introducing the second end of said thread from said one of said pair of implants into said cannula until it protrudes into the vagina;

(12) withdrawing said cannula through the vagina;

(13) introducing said needle a the left distal extremity of said vaginal incision and non-traumatizingly guiding said needle along the symphysis pubis to a second point about 3 cm to the left of a median line at the superior border of the symphysis pubis and passing said needle through the skin at this second point;

(14) incising the skin with a cutaneous incision about 0.5 cm in length at said second point;

(15) removing said trocar from said needle while leaving the cannula in place;

(16) introducing the first end of said thread from the other of said pair of implants into said cannula until it protrudes into the vagina;

(17) withdrawing said cannula through the vagina;

(18) introducing said needle at the left distal extremity of said vaginal incision and non-traumatizingly guiding said needle along the symphysis pubis to said incision of step (14);

(19) removing said trocar from said needle while leaving the canula in place;

(20) introducing the second end of said thread from the other of said pair of implants into said cannula until it protrudes into the vagina;

(21) withdrawing said cannula through the vagina;

(22) burying each of said implants under the skin over the symphysis pubis;

(23) adjusting the urethro-vesical angle to a desired position;

(24) tying the ends of said threads from the right side to respective ends of said threads from the left side to hold the desired urethro-vesical angle.

21. The method according to claim 20, wherein, prior to step (3), an anesthetically-effective amount of a local anesthetic is injected at the urethro-vesical junction;

and anesthetically-effective amounts of a local anesthetic are injected at a point about 3 cm to the right of the median line at the superior border of the symphysis pubis to a depth of about 4-5 cm and at a point about 3 cm to the left of the median line at the superior border of the symphysis pubis to a depth of about 4-5 cm.