Surgical kit, closure device, and associated method

• US 20080058710A1
• Filed: 08/10/2007
• Published: 03/06/2008
• Est. Priority Date: 08/15/2006
• Status: Abandoned Application

• Current Assignee: WILK Patent LLC
• Original Assignee: WILK Patent LLC
• Inventors: Wilk, Peter
• Application Number:
  US11/891,621
• Publication Number:
  US 20080058710A1
• Time in Patent Office: Days
• US Class Current: 604/27
• CPC Class Codes: A61B 17/0057 Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect sutures A61B17/04; closing rectum or urethra near body surface A61F2/0009
• CPC Class Codes: A61B 17/12013 for use in minimally invasive surgery, e.g. endoscopic surgery
• CPC Class Codes: A61B 17/3478 Endoscopic needles, e.g. for infusion biopsy needles A61B10/0233; catheters with injection needles A61M25/0067
• CPC Class Codes: A61B 2017/00238 Type of minimally invasive operation A61B2017/00805 takes precedence
• CPC Class Codes: A61B 2017/00287 Bags for minimally invasive surgery
• CPC Class Codes: A61M 29/02 Dilators made of swellable material balloon catheters for angioplasty A61M25/104

Abstract

A surgical device includes a tubular member, a ring made of flexible material, a resilient membrane, and a pusher member. The ring is disposed in a collapsed insertion configuration inside the tubular member and has an expanded configuration surrounding or defining an aperture, the resilient membrane being connected to the ring along an entire circumference thereof so that the membrane is at least coextensive with the aperture, thereby closing or blocking the aperture. The membrane is also disposed in a folded configuration inside the tubular member. The pusher member extends into the tubular member from a proximal end thereof for ejecting the collapsed ring and the folded membrane from a distal end of the tubular member. The ring has internal spring forces or stresses tending to open the ring from the collapsed insertion configuration to the expanded configuration upon an ejection of the ring from the tubular member.

Claims

1. A surgical closure kit comprising:

a body member with at least one elastic membrane attached thereto;

a tubular member, said body member with said membrane being disposed in a collapsed or folded configuration inside said tubular member;

a pusher member insertable into said tubular member for ejecting said body member together with said membrane from said tubular member; and

an at least partially solid membrane deformation element engageable with said membrane and disposable together with said body member and said membrane in a patient for deforming said membrane from a relaxed configuration to an expanded configuration and for maintaining said membrane in said expanded configuration.

2. The surgical closure kit defined in claim 1 wherein said membrane deformation element is taken from a group consisting of a wire, a foam composition, a balloon, and liposuction material.

3. The surgical closure kit defined in claim 1 wherein said body member is a ring and said membrane is a sheet or film member connected at a periphery about an entire circumferential extent of said ring.

4. The surgical closure kit defined in claim 1, further comprising an elongate tubular deployment member for advancing said deformation element inside a patient to a surgical site.

5. A surgical closure kit comprising:

a flexible ring with at least one membrane attached thereto about an entire circumferential extent of said ring;

a tubular member, said ring with said membrane being disposed in a collapsed or folded configuration inside said tubular member, said ring having internal spring forces or stresses tending to open said ring from said collapsed or folded configuration to an expanded configuration upon an ejection of said ring and said membrane from said tubular member;

a pusher member insertable into said tubular member for ejecting said ring together with said membrane from said tubular member; and

a membrane deformation element engageable with said membrane for deforming said membrane from a relaxed configuration substantially coplanar with said expanded configuration of said ring to a mushroom-head configuration substantially displaced from a plane of said expanded configuration of said ring.

6. The surgical closure kit defined in claim 5 wherein said membrane deformation element is taken from a group consisting of a wire, a foam composition, a balloon, and liposuction material.

7. The surgical closure kit defined in claim 6 wherein said membrane deformation element is a wire, said wire being connected at a distal end to said ring.

8. The surgical closure kit defined in claim 6 wherein said membrane deformation element is a foam composition, further comprising a balloon for temporarily deforming said membrane to facilitate a filling of the deformed membrane with said foam composition.

9. The surgical closure kit defined in claim 6 wherein said membrane deformation element is liposuction material harvested from a patient in which said ring and membrane are implanted.

10. The surgical closure kit defined in claim 5 wherein said ring is provided with at least one pressure sensor for measuring mucosal pressure upon installation of said ring and expansion or deformation of said membrane.

11. The surgical closure kit defined in claim 5 wherein at least one of said ring and said membrane is provided with a growth factor taken from the group consisting of angiogenesis factors, mucosal implants, mucosal stimulation factors, gene therapy factors, and ox fascia.

12. A surgical device comprising:

a tubular member;

a ring made of flexible material, said ring being disposed in a collapsed insertion configuration inside said tubular member, said ring having an expanded configuration surrounding or defining an aperture;

at least one resilient membrane connected to said ring along an entire circumference thereof so that said membrane is at least coextensive with said aperture, thereby closing or blocking said aperture, said membrane being disposed in a folded configuration inside said tubular member; and

a pusher member extending into said tubular member from a proximal end thereof for ejecting the collapsed ring and the folded membrane from a distal end of said tubular member, said ring having internal spring forces or stresses tending to open said ring from said collapsed insertion configuration to said expanded configuration upon an ejection of said ring from said tubular member.

13. The surgical device defined in claim 12 wherein said ring is provided with at least one pressure sensor for measuring mucosal pressure upon installation of said ring and expansion or deformation of said membrane.

14. The surgical closure kit defined in claim 12 wherein at least one of said ring and said membrane is provided with a growth factor taken from the group consisting of angiogenesis factors, mucosal implants, mucosal stimulation factors, gene therapy factors, and ox fascia.

15. A surgical closure method comprising:

inserting a distal end of a tubular member into a patient;

thereafter ejecting from a distal end of said tubular member a flexible ring with at least one membrane attached thereto about an entire circumferential extent of said ring;

upon ejecting of said ring and said membrane, expanding or unfolding said ring from a collapsed or folded configuration to an expanded substantially planar configuration;

positioning the expanded ring against a wall of an internal organ of the patient about a hole in the organ wall so that the membrane covers the hole; and

pressing said membrane to deform said membrane from a relaxed configuration substantially coplanar with said expanded configuration of said ring to a mushroom-head configuration substantially displaced from a plane of said expanded configuration of said ring, thereby sandwiching, between said ring and the deformed membrane, a portion of the organ wall about the hole, closing and sealing the hole.

16. The method defined in claim 15 wherein the pressing of the membrane includes inserting a deformation element into the patient and placing said deformation element in contact with said membrane.

17. The method defined in claim 16 wherein said deformation element is a wire, the inserting of said deformation element including bending said wire multiple times.

18. The method defined in claim 16 wherein said membrane deformation element is a foam composition, further comprising inserting a foam ejector into the patient and dispensing said foam from a distal end of said foam ejector against said membrane.

19. The method defined in claim 16 wherein said membrane deformation element is liposuction material harvested from a patient in which said ring and membrane are implanted, further comprising inserting an ejector instrument into the patient and dispensing said foam from a distal end of said ejector instrument against said membrane.

20. The method defined in claim 15 wherein said ring is provided with at least one pressure sensor, further comprising operating said sensor to measure mucosal pressure upon installation of the expanded ring and expansion or deformation of said membrane.

21. The method defined in claim 15 wherein at least one of said ring and said membrane is provided with a growth factor taken from the group consisting of angiogenesis factors, mucosal implants, mucosal stimulation factors, gene therapy factors, and ox fascia.

22. A surgical device comprising an implantable body having at least one surface disposable in contact with internal tissues of a patient upon implantation of said body, at least part of said body being provided with a growth factor taken from the group consisting of angiogenesis factors, mucosal implants, mucosal stimulation factors, gene therapy factors, and ox fascia.