Valving slit construction and cooperating assembly for penetrating the same

• US 4,447,237 A
• Filed: 05/07/1982
• Issued: 05/08/1984
• Est. Priority Date: 05/07/1982
• Status: Expired due to Term

• Current Assignee: Dow, Inc., Research Against Cancer Incorporated
• Original Assignee: Dow Corning Corporation (Dow, Inc.), Research Against Cancer Incorporated
• Inventors: Frisch, Eldon E., Parks, Leon C.
• Primary Examiner(s): Rosenbaum, C. Fred
• Assistant Examiner(s): Lester, Michelle N.
• Application Number:
  US06/376,002
• Time in Patent Office: 732 Days
• Field of Search: 128/1 R, 128/399, 128/400-402, 128/DIG. 26, 604/4, 604/8, 604/175, 604/9, 604/256, 251/150, 141/19, 141/287, 141/329, 141/330, 141/382-386
• US Class Current: 604/175
• CPC Class Codes: A61M 1/3623 Means for actively controlling temperature of blood
• CPC Class Codes: A61M 1/3655 Arterio-venous shunts or fistulae

Abstract

An improvement in the implantable shunt device of the type disclosed in U.S. Pat. No. 4,181,132 wherein each valving slit within the elastomeric body of the shunt is formed by a flattened sleeve of woven vascular prosthesis material presenting opposed interior surfaces interengaged when the valving slit is in a closed condition and spaced apart when the valving slit is in an open condition. The opposed surfaces of the sleeve are formed by a material having a coefficient of friction with respect to the material of the cannula insertable therethrough less than that of the elastomeric material of the body. A separate yieldable bias operable in addition to the bias provided by the elastomeric material of the body is provided for yieldably biasing the opposed surfaces of the flattened sleeve into sealed relation when in the closed interengaged condition and into sealed relation to the exterior periphery of the portion of the cannula extending therethrough when in the open spaced apart condition. The additional bias is provided by filling under pressure opposed cavities in the elastomeric body with a yieldable material so located with respect to the flattened sleeve as to transmit the pressure thereof as the additional bias of the opposed surfaces into sealed relation when in the closed interengaged condition and into sealed relation with the exterior periphery of the cannula when in the open spaced apart condition.

Claims

1. In an implant for use with an apparatus providing an extracorporeal blood flow path extending from a blood withdrawing cannula cooperable with said implant to a blood returning cannula cooperable with said implant, said implant comprising a body of elastomeric material having means therein defining an arterial passage, a spaced venous passage, and a bypass conduit extending from one end of said arterial passage to one end of said venous passage, arterial inlet means for connecting said arterial passage in communicating relation with the interior of an artery, venous outlet means for connecting said venous passage in communicating relation with the interior of a vein, outlet valving slit means in said elastomeric body movable between (1) a closed condition so that blood flowing from said arterial inlet means through said arterial passage will pass therefrom through said bypass conduit into said venous passage and out of said venous outlet means and (2) an open condition in sealing relation with the exterior periphery of the portion of a blood withdrawing cannula extending therethrough so that blood flowing from said arterial outlet means through said arterial passage will flow through said blood withdrawing cannula and said bypass conduit and inlet valving slit means in said elastomeric body movable between (1) a closed condition so that blood flowing from said bypass conduit will pass therefrom into said venous passage and out of said venous outlet means, and (2) an open condition in sealing relation with the exterior periphery of the portion of a blood returning cannula extending therethrough so that said venous passage will receive blood flowing both from said blood returning cannula and said bypass conduit, the improvement which comprises each valving slit means comprising:

flattened sleeve means of vascular prosthesis material within said elastomeric body presenting opposed interior surfaces interengaged when said valving slit means is in said closed condition and spaced apart when said valving slit means is in said open condition, and

means operable in addition to the bias provided by the elastomeric material of said body for yieldably biasing the opposed surfaces of said flattened sleeve means into sealed relation when in said closed interengaged condition and into sealed relation to the exterior periphery of the portion of the cannula extending therethrough when in said open spaced apart condition, said additional biasing means including cavity means having a yieldable material under pressure therein so located with respect to said flattened sleeve means as to transmit the pressure thereof as the additional bias of the opposed surfaces into sealed relation when in said closed interengaged condition and into sealed relation with the exterior periphery of the cannula when in said open spaced apart condition.

2. The improvement as claimed in claim 1 wherein said elastomeric body is manufactured from a cured silicone elastomer and the yieldable material within said cavity means is selected from the group consisting of a cured silicone elastomer, a polydiorganosiloxane fluid which is substantially impermeable to the silicone elastomer body and vegetable oils.

3. The improvement as claimed in claim 2 wherein said cavity means includes opposed cavities.

4. The improvement as claimed in claim 1, 2 or 3 wherein said yieldable material is a cured silicone elastomer.

5. The improvement as claimed in claim 1, 2 or 3 wherein said yieldable material is initially in a form capable of being injected into said cavity means under a sufficient amount of pressure to seal against a pressure of at least 300 mm Hg from the blood.

6. The improvement as claimed in claim 1, 2 or 3 wherein the material of said flattened sleeve means is woven polyester.

23. The improvement as claimed in claim 1, 2 or 3 wherein said opposed surfaces of said sleeve means are formed by a material having a coefficient of friction with respect to the material of the cannula less than that of said elastomeric material.

7. A valve assembly for providing exterior access to a pressurized blood system comprising

a body of elastomeric material,

flattened sleeve means of vascular prosthesis material within said elastomeric body biased into a closed condition for sealingly containing the pressurized blood in communication therewith and movable into a seal maintaining open condition in response to the insertion of an exterior access member therethrough, said flattened sleeve means having opposed interior surfaces interengaged when said valving slit means is in said closed condition and spaced apart when said valving slit means is in said open condition, and

means operable in addition to the bias provided by the elastomeric material of said body for yieldably biasing the opposed surfaces of said flattened sleeve means into sealed relation when in said closed interengaged condition and into sealed relation to the exterior periphery of the portion of the access member extending therethrough when in said open spaced apart condition, said additional biasing means including cavity means within said elastomeric body having a yieldable material under pressure therein so located with respect to said flattened sleeve means as to transmit the pressure thereof as the additional bias of the opposed surfaces into sealed relation when in said closed interengaged condition and into sealed relation with the exterior periphery of the access member when in said open spaced apart condition.

8. A valve assembly as claimed in claim 7 wherein said elastomeric body is manufactured from a cured silicone elastomer and the yieldable material within said cavity means is selected from the group consisting of a cured silicone elastomer, a polydiorganosiloxane fluid which is substantially impermeable to the silicone elastomer body and vegetable oils.

9. A valve assembly as claimed in claim 8 wherein said cavity means includes opposed cavities.

10. A valve assembly as claimed in claim 7, 8 or 9 wherein said yieldable material is a cured silicone elastomer.

11. A valve assembly as claimed in claim 7, 8 or 9 wherein said yieldable material is initially in a form capable of being injected into said cavity means under a sufficient amount of pressure to seal against a pressure of at least 300 mm Hg from the blood.

12. A valve assembly as claimed in claim 7, 8 or 9 wherein the material of said flattened sleeve means is woven polyester.

24. Apparatus as claimed in claim 7, 8 or 9 wherein said opposed surfaces of said sleeve means are formed by a material having a coefficient of friction with respect to the material of the cannula less than that of said elastomeric material.

13. Apparatus for medical use in a pressurized fluid system associated with a living body comprising

insertable fluid engaging means for exterior insertion into communication with the pressurized fluid and

a valve assembly biased into a closed condition for sealingly containing the pressurized fluid in communication therewith and movable into a seal maintaining open condition in response to the insertion of said insertable fluid engaging means therethrough,

said valve assembly including a body of elastomeric material having flattened sleeve means therein;

defining a slit presenting opposed surfaces interengaged when said valve assembly is in said closed condition and spaced apart when said valve assembly is in said open condition, said insertable fluid engaging means having a tapered end construction suitable for gradually moving said opposed surfaces from said closed interengaged condition into said open spaced apart condition in response to the insertion of said insertable fluid engaging means therethrough, said insertable fluid engaging means including an exterior periphery configured to be biasingly engaged in sealing relation by said opposed surfaces when the latter are in said open spaced apart condition,

said valve assembly further including means operable in addition to the bias provided by the elastomeric material of said body for yieldably biasing said opposed surfaces into sealed relation when in said closed interengaged condition and into sealed relation to the exterior periphery of said insertable fluid engaging means when in said open spaced apart condition, said additional biasing means including cavity means having a yieldable material under pressure therein so located with respect to said flattened sleeve means as to transmit the pressure thereof as the additional bias of the opposed surfaces into sealed relation when in said closed interengaged condition and into sealed relation with the exterior periphery of said insertable fluid engaging means when in said open spaced apart condition.

14. Apparatus as defined in claim 13 wherein the fluid of said fluid system is blood and wherein said flattened sleeve means is made of woven vascular prosthesis material having a coefficient of friction with respect to the material forming the exterior periphery of said insertable fluid engaging means which is less than that of said elastomeric material.

15. Apparatus as defined in claim 14 wherein said body of elastomeric material is mounted within an extracorporeal end of a percutaneous cannula and said insertable fluid engaging means comprises a trocar cooperable with said cannula.

16. Apparatus as defined in claim 14 wherein said body of elastomeric material constitutes a subcutaneous implant and said insertable fluid engaging means comprises a percutaneous cannula and trocar assembly, said trocar providing said tapered end construction, said cannula providing said exterior periphery, said exterior periphery having a biconvex lens-shaped cross-sectional configuration.

17. Apparatus as defined in claim 16 wherein said exterior periphery includes an initial portion of substantially constant cross-sectional configuration dimensions and a shorter final portion which gradually increases in cross-sectional configuration dimensions in a direction toward the extracorporeal end of said cannula.

18. Apparatus as claimed in claim 13, 14, 15, 16 or 17 wherein said elastomeric body is manufactured from a cured silicone elastomer and the yieldable material within said cavity means is selected from the group consisting of a cured silicone elastomer, a polydiorganosiloxane fluid which is substantially impermeable to the silicone elastomer body and vegetable oils.

19. Apparatus as claimed in claim 13, 14, 15, 16 or 17 wherein said cavity means includes opposed cavities.

20. Apparatus as claimed in claim 13, 14, 15, 16 or 17 wherein said yieldable material is a cured silicone elastomer.

21. Apparatus as claimed in claim 13, 14, 15, 16 or 17 wherein said yieldable material is initially in a form capable of being injected into said cavity means under a sufficient amount of pressure to seal against a pressure of at least 300 mm Hg from the fluid system.

22. Apparatus as claimed in claim 13, 14, 15, 16 or 17 wherein the material of said flattened sleeve means is polyester.