Lacrimal silicone tube with reduced friction

• US 6,113,567 A
• Filed: 08/13/1998
• Issued: 09/05/2000
• Est. Priority Date: 10/25/1995
• Status: Expired due to Term

• Current Assignee: Bruce B Becker
• Original Assignee: Bruce B Becker
• Inventors: Becker, Bruce B.
• Primary Examiner(s): MCDERMOTT, CORRINE MARIE
• Application Number:
  US09/133,986
• Time in Patent Office: 754 Days
• Field of Search: 604/8-10, 604/28, 604/500, 604/264, 604/265, 604/523, 604/285, 604/289, 604/290, 604/294, 604/175, 604/101, 128/898, 623/11, 623/12, 623/66, 401/49, 427/2.1, 427/2.12, 427/2.24, 427/2.25, 427/2.28, 427/2.3, 427/574, 427/578, 427/579, 427/583, 427/489, 427/491
• US Class Current: 604/8
• CPC Class Codes: A61F 9/00772 Apparatus for restoration of tear ducts
• CPC Class Codes: A61L 31/06 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds A61L31/041 takes precedence
• CPC Class Codes: C08L 83/04 Polysiloxanes

Abstract

Lacrimal tissue inflammation and scarring is minimized when an ostium formed by balloon dacryocystorhinostomy is stented by a silicone member having a stent portion which may be treated to reduce friction between the stent portion and tissue supporting the lacrimal mucosal surface when the silicone member moves due to blinking. The stent portion may be treated by plasma deposition of a vaporized silicone based monomer upon the outer surface of the silicone member which is covalently bonded to the silicone member thereby forming a silicone polymer coating which is very smooth and pit-free. The member has a thin central segment of relatively small outer diameter, a pair of fat segments of relatively large outer diameter at opposite ends thereof, and thin end segments connected to the fat segments. The stent portion is formed from the central segment and the proximate end portions of the fat segments. The member is inserted in the lacrimal system, by threading each end segment from the eye through a respective punctum, a canaliculus, the lacrimal sac and the ostium into the nasal cavity. The member is pulled down the nasal cavity by grasping the thin end segments while pulling the fat segments in the opposite direction less forcefully to stretch and thereby reduce the thickness of the fat segments so that they more easily move through the lacrimal system. After the stent portion is brought into place, the untreated portions of the member are severed.

Claims

1. A lacrimal stent apparatus adapted to be inserted in an ostium formed between a patient'"'"'s lacrimal sac and nasal cavity, said stent apparatus comprising:

an elongated silicone member comprising a central segment having an outer diameter, a pair of non-inflatable middle segments at opposite ends of said central segment, each said middle segment having an outer diameter which is greater than said outer diameter of said central segment, and a pair of end segments at distal ends of the respective middle segments, each said end segment having an outer diameter which is lesser than said outer diameter of said middle segments and having a length which is greater than the length of said central segment, said central segment and the proximate ends of said middle segments forming a stent portion.

2. The lacrimal stent apparatus as defined in claim 1, further including a tapered surface between each of said segments and said middle segments.

3. The lacrimal stent apparatus as defined in claim 1, wherein said silicone member is a tube.

12. The lacrimal stent apparatus as defined in claim 2, wherein said stent portion is treated with a plasma surface treatment.

13. The lacrimal stent apparatus as defined in claim 3, wherein said plasma surface treatment leaves a pit-free polymerized smooth surface.

14. The lacrimal stent apparatus as defined in claim 3, wherein said plasma surface treatment comprises vapor deposition of silicone based monomer which covalently bonds to said portion to form a pit-free polymerized smooth surface.

4. A lacrimal stent apparatus adapted to be inserted in an ostium formed between a patient'"'"'s lacrimal sac and nasal cavity, said stent apparatus comprising:

an elongated silicone member comprising a central segment having an outer diameter, a pair of middle segments at opposite ends of said central segment, each said middle segment having an outer diameter which is greater than said outer diameter of said central segment, and a pair of end segments at distal ends of the respective middle segments, each said end segment having an outer diameter which is lesser than said outer diameter of said middle segments and having a length which is greater than the length of said central segment, said central segment and the proximate ends of said middle segments forming a stent portion, said stent portion being of such length that said stent portion is adapted to extend from said nasal cavity through said ostium, said lacrimal sac, one of the patient'"'"'s canaliculi, and through one of the patient'"'"'s puncta, form a loop over the eye, and extend through the other of the patient'"'"'s puncta, the patient'"'"'s other canaliculus, said lacrimal sac, and said ostium into said nasal cavity, with said central segment positioned in said loop.

5. A lacrimal stent apparatus as defined in claim 4, wherein said stent portion having a surface which is treated to reduce friction between said stent portion and tissue when said stent portion moves during blinking, whereby lacrimal tissue inflammation and scarring is minimized.

6. The lacrimal stent apparatus as defined in claim 5, wherein said stent portion is treated with a plasma surface treatment.

7. The lacrimal stent apparatus as defined in claim 6, wherein said plasma surface treatment leaves a pit-free polymerized smooth surface.

8. The lacrimal stent apparatus as defined in claim 6, wherein said plasma surface treatment comprises vapor deposition of silicone based monomer which covalently bonds to said stent portion to form a pit-free polymerized smooth surface.

9. The lacrimal stent apparatus as defined in claim 4, further including a tapered surface between each of said end segments and said middle segments.

10. The lacrimal stent apparatus as defined in claim 4, wherein said silicone member is a tube.

16. The method as defined in claim 8, wherein said stent has a surface which is treated to reduce friction between said stent and tissue when said stent moves during blinking.

17. The method as defined in claim 8, wherein said threading step further includes threading the other end of said silicone member through a second punctum and canaliculus from the patient'"'"'s eye, into and through the lacrimal sac and the ostium, and into the nasal cavity;

and

wherein said cutting off step comprises cutting off both ends of said silicone member after said ends emerge from the ostium into the nasal cavity to leave said stent therein.

18. The method as defined in claim 10, wherein said pulling step comprises pulling both said end segments down the nasal cavity by grasping said end segments while pulling less forcefully on said middle segments in the opposite direction to stretch and effectively reduce the diameter of said middle segments allowing said silicone member to be pulled into position and then grasping said middle segments in the nasal cavity and pulling said stent into position extending from nasal cavity through the ostium, the lacrimal sac, one of the canaliculi, one of the puncta, the other of the puncta, the other of the canaliculi, the lacrimal sac, and the ostium back to the nasal cavity.

19. The method as defined in claim 8, wherein said silicone member is a tube.

11. A lacrimal stent apparatus adapted to be inserted in an ostium formed between a patient'"'"'s lacrimal sac and nasal cavity, said stent apparatus comprising:

an elongated silicone member comprising a central segment having an outer diameter, a pair of middle segments at opposite ends of said central segment, each said middle segment having an outer diameter which is greater than said outer diameter of said central segment, and a pair of end segments at distal ends of the respective middle segments, each said end segment having an outer diameter which is lesser than said outer diameter of said middle segments and having a length which is greater than the length of said central segment, said central segment and the proximate ends of said middle segments forming a stent portion, said stent portion having a surface which is treated to reduce friction between said stent portion and tissue when said stent portion moves during blinking, whereby lacrimal tissue inflammation and scarring is minimized.

15. A method of inserting a silicone stent in an ostium between a patient'"'"'s lacrimal sac and nasal cavity, comprising the steps of:

providing an elongated silicone member having a central segment having an outer diameter, a pair of middle segments at opposite ends of said central segment, each said middle segment having an outer diameter which is greater than said outer diameter of said central segment, and a pair of end segments at distal ends of the respective middle segments, each said end segment having an outer diameter which is lesser than said outer diameter of said middle segments and having a length which is greater than the length of said central segment, said central segment and the proximate ends of said middle segments forming said silicone stent;

threading an end of said silicone member through a punctum and canaliculus from the patient'"'"'s eye, into and through said lacrimal sac and the ostium, and into the nasal cavity;

grasping said silicone member within the nasal cavity;

pulling said silicone member down the nasal cavity and out a nostril to position said silicone stent in the punctum, canaliculus, lacrimal sac and ostium; and

cutting off the remaining portions of said silicone member to leave only said silicone stent in the punctum, canaliculus, lacrimal sac, and the ostium, extending into the nasal cavity.