Retractable catheter systems

• US 6,585,705 B1
• Filed: 11/20/2000
• Issued: 07/01/2003
• Est. Priority Date: 01/15/1999
• Status: Expired due to Fees

• Current Assignee: Maginot Catheter Technologies, Inc.
• Original Assignee: Maginot Catheter Technologies, Inc.
• Inventors: Maginot, Thomas J., Maginot, Paul J.
• Primary Examiner(s): Casler, Brian L.
• Assistant Examiner(s): MAYNARD, JENNIFER J
• Application Number:
  US09/716,308
• Time in Patent Office: 953 Days
• Field of Search: 604/28, 604/29, 604/266, 604/93.01, 604/94.01, 604/6-16, 604/164.01, 604/164.02, 604/264, 604/523, 604/510, 604/500, 604/506, 604/508, 604/43, 604/165.01, 604/158, 604/165.02, 604/269, 604/171, 604/174, 604/198, 604/265, 604/164.09, 604/164.08, 604/167.01, 604/167.02, 604/167.03, 604/167.04, 604/167.06, 604/533-535, 205/120.1, 205/121.1, 205/121.2, 205/302
• US Class Current: 604/265
• CPC Class Codes: A61M 1/16 with membranes
• CPC Class Codes: A61M 1/3659 Cannulae pertaining to extracorporeal circulation
• CPC Class Codes: A61M 2025/0293 Catheter, guide wire or the like with means for holding, centering, anchoring or frictionally engaging the device within an artificial lumen, e.g. tube natural lumen, e.g. vessels A61M25/04
• CPC Class Codes: A61M 2025/0681 Systems with catheter and outer tubing, e.g. sheath, sleeve or guide tube
• CPC Class Codes: A61M 25/0194 Tunnelling catheters

Abstract

A catheter system includes a working catheter having a distal working orifice. The catheter systems further includes a guide catheter having a guide lumen and a distal guide orifice. In addition, the catheter system includes a locking mechanism which locks the working catheter relative to the guide catheter in (i) an operative position, and (ii) a stowed position. The catheter system also includes a tissue ingrowth member secured to an outer surface of the guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to the tissue ingrowth member when the tissue ingrowth member remains in contact with the subcutaneous tissue over a period of time. When the working catheter is locked in the operative position, (i) the working catheter extends through the guide lumen of the guide catheter and out of the distal guide orifice of the guide catheter, and (ii) the distal working orifice of the working catheter is positioned outside of the guide catheter. Moreover, when the working catheter is locked in the stowed position, (i) the working catheter extends into the guide lumen of the guide catheter, and (ii) the distal working orifice of the working catheter is positioned within the guide lumen of the guide catheter.

Claims

1. A catheter system, comprising:

a working catheter having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time; and

a distal valve configured to inhibit fluid from advancing through said distal guide orifice and into said guide lumen of said guide catheter,

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned outside of said guide catheter, and

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned within said guide lumen of said guide catheter.

2. The catheter system of claim 1, wherein:

said distal valve is secured to said guide catheter, and

said distal valve is positioned within said guide lumen of said guide catheter.

3. The catheter system of claim 1, wherein:

said guide catheter further includes a proximal guide orifice, and

said distal working orifice of said working catheter is interposed between said proximal guide orifice and said distal valve when said working catheter is locked in said stowed position.

4. A catheter system, comprising:

a working catheter having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time,

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned outside of said guide catheter,

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned within said guide lumen of said guide catheter,

wherein said distal working orifice is positioned on a proximal side of a distal valve of said catheter system when said working catheter is locked in said stowed position, and

wherein said distal working orifice is positioned on a distal side of said distal valve when said working catheter is locked in said operative position.

5. A catheter system, comprising:

a working catheter having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time,

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned outside of said guide catheter,

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned within said guide lumen of said guide catheter,

further comprising a quantity of blood clot dissolving liquid positioned within said guide lumen of said guide catheter when said working catheter is locked in said stowed position, wherein;

said blood clot dissolving liquid contacts said working catheter at said distal working orifice when said working catheter is locked in said stowed position.

6. The catheter system of claim 5, wherein said blood clot dissolving liquid includes urokinase.

7. A catheter system, comprising:

a multi-lumen working catheter having a first distal working orifice and a second distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time,

a distal valve configured to inhibit fluid from advancing through said distal guide orifice and into said guide lumen of said guide catheter

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said first distal working orifice and said second distal working orifice are each positioned outside of said guide catheter, and

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said first distal working orifice and said second distal working orifice are each positioned within said guide lumen of said guide catheter.

8. The catheter system of claim 7, wherein:

said distal valve is secured to said guide catheter, and

said distal valve is positioned within said guide lumen of said guide catheter.

9. A catheter system, comprising:

a multi-lumen working catheter having a first distal working orifice and a second distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time,

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said first distal working orifice and said second distal working orifice are each positioned outside of said guide catheter, and

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said first distal working orifice and said second distal working orifice are each positioned within said guide lumen of said guide catheter,

further comprising a quantity of blood clot dissolving liquid positioned within said guide lumen of said guide catheter when said working catheter is locked in said stowed position, wherein;

said blood clot dissolving liquid contacts said working catheter at each of said first distal working orifice and said second distal working orifice when said working catheter is locked in said stowed position.

10. The catheter system of claim 9, wherein said blood clot dissolving liquid includes urokinase.

11. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said conduit relative to said guide catheter in (i) an operative position, and (ii) a stowed position;

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time; and

a distal valve configured to inhibit fluid from advancing through said distal guide orifice and into said guide lumen of said guide catheter,

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is locked in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is locked in said stowed position.

12. The catheter system of claim 11, wherein:

said distal valve is secured to said guide catheter, and

said distal valve is positioned within said guide lumen of said guide catheter.

13. The catheter system of claim 11, wherein:

said guide catheter further includes a proximal guide orifice, and

said distal working orifice of said conduit is interposed between said proximal guide orifice and said distal valve when said conduit is locked in said stowed position.

14. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said conduit relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time;

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is locked in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is locked in said stowed position,

wherein said distal working orifice is positioned on a proximal side of a distal valve of said catheter system when said conduit is locked in said stowed position, and

wherein said distal working orifice is positioned on a distal side of said distal valve when said conduit is locked in said operative position.

15. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said conduit relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time;

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is locked in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is locked in said stowed position,

further comprising a quantity of blood clot dissolving liquid positioned within said guide lumen of said guide catheter when said conduit is locked in said stowed position, wherein;

said blood clot dissolving liquid contacts said conduit at said distal working orifice when said conduit is locked in said stowed position.

16. The catheter system of claim 15, wherein said blood clot dissolving liquid includes urokinase.

17. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice, said conduit being positionable relative to said guide catheter in (i) an operative position, and (ii) a stowed position;

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time; and

a distal valve configured to inhibit fluid from advancing through said distal guide orifice and into said guide lumen of said guide catheter,

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is positioned in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is positioned in said stowed position.

18. The catheter system of claim 17, wherein:

said distal valve is secured to said guide catheter, and

said distal valve is positioned within said guide lumen of said guide catheter.

19. The catheter system of claim 17, wherein:

said guide catheter further includes a proximal guide orifice, and

said distal working orifice of said conduit is interposed between said proximal guide orifice and said distal valve when said conduit is positioned in said stowed position.

20. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice, said conduit being positionable relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time;

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is positioned in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is positioned in said stowed position,

wherein said distal working orifice is positioned on a proximal side of a distal valve of said catheter system when said conduit is positioned in said stowed position, and

wherein said distal working orifice is positioned on a distal side of said distal valve when said conduit is positioned in said operative position.

21. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice, said conduit being positionable relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time;

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is positioned in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is positioned in said stowed position,

further comprising a quantity of blood clot dissolving liquid positioned within said guide lumen of said guide catheter when said conduit is positioned in said stowed position, wherein;

said blood clot dissolving liquid contacts said conduit at said distal working orifice when said conduit is positioned in said stowed position.

22. The catheter system of claim 21, wherein said blood clot dissolving liquid includes urokinase.

23. A catheter system, comprising:

a working catheter having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time,

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned outside of said guide catheter,

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said distal working orifice of said working catheter is positioned within said guide lumen of said guide catheter,

further comprising a quantity of heparin solution positioned within said guide lumen of said guide catheter when said working catheter is locked in said stowed position, wherein;

said heparin solution contacts said working catheter at said distal working orifice when said working catheter is locked in said stowed position.

24. A catheter system, comprising:

a multi-lumen working catheter having a first distal working orifice and a second distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said working catheter relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time,

wherein when said working catheter is locked in said operative position, (i) said working catheter extends through said guide lumen of said guide catheter and out of said distal guide orifice of said guide catheter, and (ii) said first distal working orifice and said second distal working orifice are each positioned outside of said guide catheter, and

wherein when said working catheter is locked in said stowed position, (i) said working catheter extends into said guide lumen of said guide catheter, and (ii) said first distal working orifice and said second distal working orifice are each positioned within said guide lumen of said guide catheter,

further comprising a quantity of heparin solution positioned within said guide lumen of said guide catheter when said working catheter is locked in said stowed position, wherein;

said heparin solution contacts said working catheter at each of said first distal working orifice and said second distal working orifice when said working catheter is locked in said stowed position.

25. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice;

a locking mechanism which locks said conduit relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time;

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is locked in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is locked in said stowed position,

further comprising a quantity of heparin solution positioned within said guide lumen of said guide catheter when said conduit is locked in said stowed position, wherein;

said heparin solution contacts said conduit at said distal working orifice when said conduit is locked in said stowed position.

26. A catheter system, comprising:

a conduit having a distal working orifice;

a guide catheter having a guide lumen and a distal guide orifice, said conduit being positionable relative to said guide catheter in (i) an operative position, and (ii) a stowed position; and

a tissue ingrowth member secured to an outer surface of said guide catheter and configured to facilitate fibrous tissue growth therein, whereby subcutaneous tissue of a body becomes affixed to said tissue ingrowth member when said tissue ingrowth member remains in contact with said subcutaneous tissue over a period of time;

wherein said distal working orifice of said conduit is positioned outside of said guide catheter when said conduit is positioned in said operative position, and

wherein said distal working orifice of said conduit is positioned within said guide lumen of said guide catheter when said conduit is positioned in said stowed position,

further comprising a quantity of heparin solution positioned within said guide lumen of said guide catheter when said conduit is positioned in said stowed position, wherein;

said heparin solution contacts said conduit at said distal working orifice when said conduit is positioned in said stowed position.