Gas inflation/evacuation system incorporating a multiple element valved guidewire assembly having an occlusive device

• US 7,615,031 B2
• Filed: 09/01/2005
• Issued: 11/10/2009
• Est. Priority Date: 09/01/2005
• Status: Expired due to Fees

• Current Assignee: Boston Scientific Limited (Boston Scientific Corporation)
• Original Assignee: Medrad Incorporated (Bayer AG)
• Inventors: Bonnette, Michael J., Prather, Richard R., Thor, Eric J.
• Primary Examiner(s): Lucchesi; Nicholas D
• Assistant Examiner(s): KOHARSKI, CHRISTOPHER
• Application Number:
  US11/217,546
• Publication Number:
  US 20070060881A1
• Time in Patent Office: 1,531 Days
• Field of Search: 604/533, 604/96.01, 604/97.01, 604/97.02, 604/97.03, 604/98.01, 604/99.01, 604/99.02, 604/99.03, 604/99.04, 604/110.01, 604/100.03, 604/102.03, 604/103.04, 604/103.06, 604/103.01, 604/107, 604/912, 604/914, 604/915, 604/528, 606/192, 606/194, 606/198
• US Class Current: 604/99.01
• CPC Class Codes: A61M 25/10182 Injector syringes
• CPC Class Codes: A61M 25/10185 Valves
• CPC Class Codes: A61M 25/10187 Indicators for the level of inflation or deflation

Abstract

A gas inflation/evacuation system incorporating a multiple element valved guidewire assembly having an occlusive device for use in thrombectomy or other vascular procedures includes a multiple element valved guidewire assembly having an occlusive balloon removably and sealingly connectible to an included manifold assembly where a guidewire tube defines a lumen for inflation or deflation of the occlusive balloon. A first syringe for evacuating the lumen and a second syringe for introducing a biocompatible gas into the lumen to inflate the occlusive balloon that is in fluid communication with the lumen a plurality of times are included. A sealing valve arrangement selectively seals the proximal portion of the guidewire tube to control inflated or deflated states of the occlusive balloon.

Claims

1. A gas inflation/evacuation system comprising:

a. a multiple element valved guidewire assembly for enabling guidance and use of various intravascular devices, the multiple element valved guidewire assembly including;

i. a guidewire tube having a proximal end and a distal end and defining a lumen therein, the guidewire tube being flexible and having an occlusive balloon near the distal end thereof and defining in a wall thereat at least one orifice in communication with the occlusive balloon to permit inflation and evacuation thereof;

ii. a seal fixed internally within the proximal end of the guidewire tube;

the seal defining an opening therein, and

iii. a sealing rod and a support extension extending distally therefrom, the sealing rod having a cross section larger than that of the support extension, the support extension and the sealing rod being slidable within the lumen of the guidewire tube and within the opening of the seal disposed in the proximal end of the guidewire tube to form a flow valve thereat such that the flow valve is in (A) an open position when the sealing rod is slid proximally relative to and away from the opening and (B) in a closed position when the sealing rod is slid distally into the opening wherein the exterior surface of the sealing rod forms a sealed fit therein;

b. a manifold assembly removably connectible to the multiple element valved guidewire assembly, the manifold assembly having a manifold body inclusive of a manifold, a first branch and a second branch such that;

i. the manifold defines a main passageway wherein a hemostatic valve is sealingly disposed at each end thereof, the main passageway for permitting the proximal end of the guidewire tube to be removably inserted therein through the hemostatic valve at one end with the sealing rod thereof protruding from the hemostatic valve at the other end such that the flow valve is located within the main passageway between the hemostatic valves;

ii. the first branch defines an inflation/evacuation passageway in communication with the main passageway; and

iii. the second branch defines a pressure monitor passageway in communication with the main passageway, the pressure monitor passageway being adapted to enable a pressure gauge to be removably connectible thereto for monitoring pressure within the manifold assembly and, when the flow valve is situated in the main passageway and placed in the open position therein, within the guidewire tube and the occlusive balloon near the distal end thereof;

c. an evacuation syringe being adapted for cooperation with the first branch of the manifold assembly for selectively withdrawing a biocompatible gas from the multiple element valved guidewire assembly so as to selectively evacuate the occlusive balloon a plurality of times; and

,

d. an inflation syringe being adapted for cooperation with the first branch of the manifold assembly for selectively introducing a biocompatible gas under pressure into the multiple element valved guidewire assembly so as to selectively inflate the occlusive balloon a plurality of times.

2. The gas inflation/evacuation system of claim 1, wherein the guidewire tube is made of braided polyimide;

a flexible tip is located distal to the occlusive balloon; and

, the seal comprises a flexible compliant material.

3. The gas inflation/evacuation system of claim 1, wherein the evacuation syringe includes a plunger, a check valve, a connector and a needle.

4. The gas inflation/evacuation system claim 3, wherein the needle of the evacuation syringe is blunt.

5. The gas inflation/evacuation system of claim 1, wherein at least one of the evacuation syringe and the inflation syringe includes a plunger, a check valve, and a needle.

6. The gas inflation/evacuation system of claim 5, wherein the needle is blunt.

7. The gas inflation/evacuation system of claim 1, wherein the hemostatic valves each include a hemostatic nut threadably connectible to the manifold body and snappingly engageable to the manifold body.

8. The gas inflation/evacuation system of claim 7, wherein the hemostatic valves are each self-sealing hemostatic valves, each being compressible and sealingly expandable.

9. The gas inflation/evacuation system of claim 8, wherein the hemostatic valves are formed of silicone material.

10. The gas inflation/evacuation system of claim 9, wherein the hemostatic valves are symmetrically fashioned and include mirror-like planar and circular-shaped faces having opposing radiused recessed surfaces increasingly thinner in a direction toward the center.

11. The gas inflation/evacuation system of claim 10, wherein the hemostatic valves each have a plurality of slits.

12. The gas inflation/evacuation system of claim 11, wherein the plurality of slits of the hemostatic valves extend outwardly in radial fashion from the center of the hemostatic valve thereby creating boundaries and defining lobes.

13. The gas inflation/evacuation system of claim 12, wherein the hemostatic valves have plural lobes defined by boundaries corresponding to slits, such that adjacent lobes have mutual contact along a slit and thereby effect a seal from side-to-side, thereby effecting a self-sealing hemostatic valve relationship to be formed on the manifold.

14. The gas inflation/evacuation system of claim 13, wherein the hemostatic valves each have three slits.

15. The gas inflation/evacuation system of claim 14, wherein the hemostatic valves are each self-sealing hemostatic valves, which can be modified in sealing properties by the hemostatic nut associated therewith.

16. The gas inflation/evacuation system of claim 1, wherein the occlusive balloon may be inflated or deflated when the flow valve is open and is maintained when the flow valve is closed.

17. The gas inflation/evacuation system of claim 1, wherein the occlusive balloon is formed of a material selected from polymer or rubber.

18. The gas inflation/evacuation system of claim 17, wherein the occlusive balloon has been prestretched to render expansion relatively linear with pressure.

19. The gas inflation/evacuation system of claim 1, wherein the distal end of the multiple element valved guidewire assembly is visible under fluoroscopy.

20. The gas inflation/evacuation system of claim 19, wherein the occlusive balloon is two-layer balloon with a fluoroscopy visible liquid employed between layers of the two-layer balloon.

21. A gas inflation/evacuation system comprising:

(a) a guidewire assembly for enabling guidance and use of various intravascular devices, the guidewire assembly including;

(i) a guidewire tube having a proximal end and a distal end and defining a lumen therein, the guidewire tube being flexible and having an occlusive balloon near the distal end thereof and defining in a wall thereat at least one orifice in communication with the occlusive balloon to permit inflation and evacuation thereof;

(ii) a seal fixed internally within the proximal end of the guidewire tube;

the seal defining an opening therein, and

(iii) a sealing rod and a support extension extending distally therefrom, the sealing rod having a cross section larger than that of the support extension, the support extension and the sealing rod being slidable within the lumen of the guidewire tube and within the opening of the seal disposed in the proximal end thereof to form a flow valve thereat such that the flow valve is in (A) an open position when the sealing rod is slid proximally relative to and away from the opening and (B) in a closed position when the sealing rod is slid distally into the opening wherein the exterior surface of the sealing rod forms a sealed fit therein; and

(b) a manifold assembly removably operable with the guidewire assembly, the manifold assembly having a manifold body inclusive of a manifold, a first branch and a second branch such that;

(i) the manifold defines a main passageway wherein a hemostatic valve is sealingly disposed at each end thereof, the main passageway for permitting the proximal end of the guidewire tube to be removably inserted therein through the hemostatic valve at one end with the sealing rod thereof protruding from the hemostatic valve at the other end such that the flow valve is located within the main passageway between the hemostatic valves;

(ii) the first branch defines an inflation/evacuation passageway in communication with the main passageway, the first branch being adapted for cooperation with (A) an evacuation syringe for selectively withdrawing a biocompatible gas from the guidewire assembly so as to selectively evacuate the occlusive balloon a plurality of times via the flow valve when in the open position and (B) an inflation syringe for selectively introducing a biocompatible gas under pressure into the guidewire assembly so as to selectively inflate the occlusive balloon a plurality of times via the flow valve when in the open position, the pressure within the occlusive balloon being maintainable when the flow valve is in the closed position; and

(iii) the second branch defining a pressure monitor passageway in communication with the main passageway, the pressure monitor passageway being adapted to enable a pressure gauge to be removably connectible thereto for monitoring pressure within the manifold assembly and, when the flow valve is situated in the main passageway and placed in the open position therein, within the guidewire tube and the occlusive balloon near the distal end thereof.

22. The gas inflation/evacuation system of claim 21 wherein the manifold assembly further includes an intermediate positionable valve threadingly engaged to an end of the first branch through which the evacuation syringe and the inflation syringe are selectively enabled to communicate with the inflation/evacuation passageway of the manifold assembly.

23. A manifold assembly of a gas inflation/evacuation system for use with a intravascular device, the intravascular device having a flow valve incorporated therein near a proximal end thereof and an occlusive balloon near a distal end thereof, the manifold assembly comprising:

(a) at least two hemostatic valves; and

(b) a manifold body inclusive of a manifold, a first branch and a second branch such that (I) the manifold defines a main passageway wherein one of the hemostatic valves is sealingly disposed at each end thereof, the main passageway for permitting the proximal end of the intravascular device to be removably inserted therein through the hemostatic valve at one end with the proximal end protruding from the hemostatic valve at the other end such that the flow valve is located within the main passageway between the hemostatic valves;

(II) the first branch defines an inflation/evacuation passageway in communication with the main passageway, the first branch being adapted for cooperation with (A) an evacuation syringe for selectively withdrawing a biocompatible gas from the intravascular device so as to selectively evacuate the occlusive balloon a plurality of times via the flow valve when in an open position and (B) an inflation syringe for selectively introducing a biocompatible gas under pressure into the intravascular device so as to selectively inflate the occlusive balloon a plurality of times via the flow valve when in the open position, the pressure within the occlusive balloon being maintainable when the flow valve is in the closed position; and

(III) the second branch defines a pressure monitor passageway in communication with the main passageway, the pressure monitor passageway being adapted to enable a pressure gauge to be removably connectible thereto for monitoring pressure within the manifold assembly and, when the flow valve is situated in the main passageway and placed in the open position therein, within the intravascular device and the occlusive balloon near the distal end thereof.

24. The manifold assembly of claim 23 further including an intermediate positionable valve threadingly engaged to an end of the first branch through which the evacuation syringe and the inflation syringe are selectively enabled to communicate with the inflation/evacuation passageway of the manifold assembly.