Sliding connection assembly to facilitate lead stabilization

• US 20040254534A1
• Filed: 06/11/2003
• Published: 12/16/2004
• Est. Priority Date: 06/11/2003
• Status: Abandoned Application

• Current Assignee: St. Jude Medical, Daig Division, Inc.
• Original Assignee: St. Jude Medical, Daig Division, Inc.
• Inventors: Stehr, Richard E., Bjorkman, Bradford A.
• Application Number:
  US10/460,783
• Publication Number:
  US 20040254534A1
• Time in Patent Office: Days
• US Class Current: 604/160
• CPC Class Codes: A61M 2039/062 used with a catheter
• CPC Class Codes: A61M 2039/0633 the seal being a passive seal made of a resilient material with or without an opening
• CPC Class Codes: A61M 2039/064 Slit-valve
• CPC Class Codes: A61M 2039/0646 Duckbill-valve
• CPC Class Codes: A61M 2039/0686 comprising more than one seal
• CPC Class Codes: A61M 39/0606 without means for adjusting the seal opening or pressure A61M39/0693 takes precedence
• CPC Class Codes: A61M 39/1011 Locking means for securing connection; Additional tamper safeties A61M39/16 takes precedence

Abstract

A connection system for connecting a hemostasis valve to a sheath is disclosed. The hemostasis valve has a cannula portion disposed on a distal end and an annular ledge protruding from an outer surface thereof. The sheath has a nipple extending proximally therefrom. The nipple also has an annular ledge disposed on an outer surface thereof and a nipple lumen adapted for receiving the distal end of the cannula portion. A sliding connector defining a connector lumen is disposed about the outer surface of the cannula portion and the outer surface of the nipple when the cannula portion is received in the lumen of the nipple. A connection between the hemostasis valve and the sheath is created by engaging the sliding connector with either or both of the annular ledge on the hemostasis valve and the annular ledge on the nipple.

Claims

1. A connection system for connecting a hemostatis valve to a sheath, the system comprising:

a hemostasis valve having a cannula portion disposed on a distal end and a first ledge protruding from an outer surface of the cannula portion and disposed proximally from the distal end of the cannula portion;

a sheath having a nipple extending proximally therefrom, wherein the nipple further comprises;

a second ledge disposed on an outer surface of the nipple;

a nipple lumen adapted for receiving the distal end of the cannula portion of the hemostasis valve; and

a sliding connector in the form of an annular wall defining a connector lumen and disposed about the outer surface of the cannula portion of the hemostasis valve and the outer surface of the nipple of the sheath when the cannula portion is received in the lumen of the nipple;

wherein

at least one of the cannula portion and the nipple are received in the connector lumen;

the sliding connector slides proximally and distally along an interface between the cannula portion of the hemostasis valve and the nipple of the sheath when the cannula portion is received in the lumen of the nipple; and

the sliding connector further comprises an engagement means for engaging at least one of the first ledge and the second ledge to connect the hemostasis valve and the sheath.

2. The system of claim 1, wherein the sliding connector further comprises an annular lip extending radially inward from the annular wall decreasing the diameter of a portion of the connector lumen for engagement with and retention by at least one of the first ledge and the second ledge to connect the hemostasis valve and the sheath.

3. The system of claim 1, wherein the engagement means comprises an internal threading disposed on the annular wall and the second ledge comprises an external threading for engaging with the internal threading to connect the hemostasis valve and the sheath.

4. The system of claim 1, wherein the engagement means comprises an internal threading disposed on the annular wall and the first ledge comprises an external threading for engaging with the internal threading to connect the hemostasis valve and the sheath.

5. The system of claim 1, wherein the engagement means comprises at least two longitudinally-oriented tabs formed in the annular wall, each of said tabs having a tooth extending radially inward for engaging at least one of the first ledge and the second ledge to connect the hemostasis valve and the sheath.

6. The system of claim 1, wherein the engagement means comprises at least two teeth disposed upon the annular wall and extending radially inward for engaging at least one of the first ledge and the second ledge to connect the hemostasis valve and the sheath;

and

wherein the annular wall is deformable to allow the at least two teeth to slide past the at least one of the first ledge and the second ledge when connecting the hemostasis valve and the sheath.

7. The system of claim 1, wherein the engagement means comprises at least two teeth disposed upon the annular wall and extending radially inward;

at least one of the first ledge and the second ledge comprises at least two bayonet fittings disposed to engage the at least two teeth, respectively.

8. The system of claim 1, wherein

the sheath is a splittable sheath;

and

the sliding connector has a proximal range of motion such that the sliding connector can be moved to a position entirely about the cannula portion to expose the nipple and allow the splittable sheath to be split.

9. The system of claim 1, wherein

the sheath is a splittable sheath;

the sliding connector has a distal range of motion such that the sliding connector can be moved to a position entirely disengaged from the cannula portion; and

the sliding connector is adapted to be split in half axially in response to radial force imparted by the nipple on an inner surface of the sliding connector defined by the connector lumen as the splittable sheath is split.

10. A hemostasis valve adapted to be releasably connected to a sheath, the hemostatsis valve comprising:

a cannula portion disposed on a distal end;

a ledge protruding from an outer surface of the cannula portion and disposed proximally from the distal end of the cannula portion;

a sliding connector in the form of an annular wall defining a connector lumen and disposed about the outer surface of the cannula portion of the hemostasis valve, wherein the sliding connector slides proximally and distally along the cannula portion; and

wherein the sliding connector further comprises;

a proximal end and a distal end;

an annular lip extending radially inward from the annular wall at the proximal end for engagement with and retention by the ledge; and

an engagement means at the distal end for engaging an opposing mating component of a sheath.

11. The hemostasis valve of claim 10, wherein the engagement means comprises an internal threading disposed on the annular wall.

12. The hemostasis valve of claim 10, wherein the engagement means comprises at least two longitudinally-oriented tabs formed in the annular wall, each of tabs having a tooth extending radially inward for engaging the opposing mating component of the sheath.

13. The system of claim 10, wherein the engagement means comprises at least two teeth disposed upon the annular wall and extending radially inward for engaging the opposing mating component of the sheath.

14. The system of claim 13, wherein the annular wall is deformable to allow the at least two teeth to slide past the opposing mating component of the sheath.

15. A sheath adapted to be releasably connected to a hemostasis valve, the sheath comprising:

a sheath having a nipple extending proximally therefrom, wherein the nipple further comprises;

a ledge disposed on an outer surface of the nipple;

a nipple lumen adapted for receiving a distal end of a cannula portion of a hemostasis valve;

a sliding connector in the form of an annular wall defining a connector lumen and disposed about the outer surface of the nipple, wherein the sliding connector slides proximally and distally along the nipple; and

wherein the sliding connector further comprises;

a proximal end and a distal end;

an annular lip extending radially inward from the annular wall at the distal end for engagement with and retention by the ledge; and

an engagement means at the proximal end for engaging an opposing mating component of a hemostasis valve.

16. The sheath of claim 15, wherein the engagement means comprises an internal threading disposed on the annular wall.

17. The sheath of claim 15, wherein the engagement means comprises at least two longitudinally-oriented tabs formed in the annular wall, each of the tabs having a tooth extending radially inward for engaging the opposing mating component of the hemostasis valve.

18. The system of claim 15, wherein the engagement means comprises at least two teeth disposed upon the annular wall and extending radially inward for engaging the opposing mating component of the hemostasis valve.

19. The system of claim 18, wherein the annular wall is deformable to allow the at least two teeth to slide past the opposing mating component of the hemostasis valve.

20. The system of claim 15, wherein

the sheath is a splittable sheath;

the sliding connector has a distal range of motion such that the sliding connector can be moved to a position entirely disengaged from the hemostasis valve; and

the sliding connector is adapted to be split in half axially in response to radial force imparted by the nipple on an inner surface of the sliding connector defined by the connector lumen as the splittable sheath is split.