Adjustable flow rate glaucoma shunt and method of using same

• US 5,626,558 A
• Filed: 05/05/1995
• Issued: 05/06/1997
• Est. Priority Date: 05/05/1995
• Status: Expired due to Fees

• Current Assignee: John Suson
• Original Assignee: John Suson
• Inventors: Suson, John
• Primary Examiner(s): Weiss, John G.
• Assistant Examiner(s): Cho, David J.
• Application Number:
  US08/435,037
• Time in Patent Office: 732 Days
• Field of Search: 604/289, 604/294, 604/8-9
• US Class Current: 604/8
• CPC Class Codes: A61F 9/00781 Apparatus for modifying intraocular pressure, e.g. for glaucoma treatment drainage implants in general A61M27/002

Abstract

An adjustable flow rate implantable shunt device for use in treating glaucoma is provided. The device comprises a tubular member having a first sealed end and an open second end which are joined by a wall. The first end is inserted into the anterior portion of the eye for receipt of aqueous humor, and the second end is fastened to the sclera of the eye. The first end of the shunt device is sealed when implanted, so that flow of aqueous humor through the device immediately after implantation is prevented. After a sufficient post-implantation period such that a fibrous capsule has formed around the shunt device, at least one perforation is made along the segment of the wall of the tubular member which is located within the anterior portion of the eye to allow aqueous humor to flow through and out of the device, thereby lowering intraocular pressure within the eye. The flow rate of aqueous humor through the device can be adjusted periodically by placing additional perforations along the portion of the tubular member located within the anterior chamber of the eye. The perforations are conveniently made using a laser.

Claims

1. An adjustable flow rate implant device for draining aqueous humor from an eye, comprising:

a hollow tubular member having a first and second end, the first end being sealed and having a size and shape to allow the first end to be inserted in anterior portion of an eye, the second end being open, and the first and second ends being connected by a wall, and wherein the flow rate of aqueous humor from the device may be adjusted after implantation by providing the portion of the wall of the tubular member located within the anterior portion of the eye with at least one opening to allow a sufficient flow rate of aqueous humor from the eye into the first end of and through the tubular member to the exterior of the implant device, to relieve damaging intraocular pressure, wherein at least one portion of the wall connecting the first and second ends of the tubular member is thinner than the remaining portion of the wall.

2. The device of claim 1, wherein the device further comprises an episcleral plate, the plate being mounted adjacent to the second end.

3. The device of claim 1, wherein the wall of the tubular member is provided with at least one perforation prior to implantation to allow the flow of aqueous humor through the device, wherein the flow of aqueous humor through the device from the perforation in the wall of the tubular member is insufficient to relieve damaging intraocular pressure within the eye.

4. The device of claim 1, wherein the tubular member is made of pigmented silicone.

5. An adjustable flow rate implant device for draining aqueous humor from an eye, comprising:

a hollow tubular member having a first end and a second end, the first end being open, and the tubular member having a size and shape to allow one end to be inserted into an anterior chamber of an eye, the second end being open, and the first and second ends being connected by a wall;

a reservoir for receipt of aqueous humor passing through the tubular member having a single opening therein, through which the second end of the tubular member is inserted, with the junction of the reservoir and tubular member being sealed so that the only opening of the implant device is the open first end of the tubular member.

6. The device of claim 5, wherein the reservoir has at least one perforation that is made prior to implantation to allow the flow of aqueous humor through the device, wherein the flow of aqueous humor through the device from the perforation is insufficient to relieve damaging intraocular pressure.

7. The device of claim 5, wherein the reservoir is made of pigmented silicone.