Endovascular cerebrospinal fluid shunt
10112036 ยท 2018-10-30
Assignee
Inventors
Cpc classification
A61M27/006
HUMAN NECESSITIES
A61M2205/0238
HUMAN NECESSITIES
A61M27/002
HUMAN NECESSITIES
A61F2230/0091
HUMAN NECESSITIES
International classification
Abstract
An endovascular implantable shunt device for draining cerebrospinal fluid from a patient's subarachnoid space includes a shunt having opposed first and second ends, a one-way valve located at the first end of the shunt, a helical tip disposed at the second end, and a hollow passageway extending between the helical tip and one-way valve. The helical tip is constructed to penetrate a patient's sinus wall. Cerebrospinal fluid drains through the helical tip and out through the valve.
Claims
1. A method for draining cerebrospinal fluid from a patient's subarachnoid space, the method comprising the steps of: providing an implantable shunt having opposed first and second ends, a one-way valve located at the first end of the shunt, and a tip disposed at the second end, said tip being constructed to penetrate a sinus wall of the patient, wherein the first and second ends are in fluid communication to enable the cerebrospinal fluid (CSF) to be drained through the tip and out through the valve; endovascularly delivering the shunt to the sinus wall; penetrating the sinus wall and implanting the second end of the shunt in a CSF space of the patient; and draining cerebrospinal fluid from the patient.
2. The method of claim 1, further comprising providing a plurality of apertures to the tip, the plurality of apertures configured to allow cerebrospinal fluid to enter the tip.
3. The method of claim 1, further comprising providing an antithrombic coating on the shunt.
4. The method of claim 1, wherein endovascularly delivering the shunt to the sinus wall includes delivering percutaneously and implanting the shunt into the sinus wall via a delivery catheter.
5. The method of claim 4, wherein endovascularly delivering the shunt to the sinus wall includes delivering percutaneously and implanting the shunt into the sinus wall via a jugular vein.
6. The method of claim 4, wherein endovascularly delivering the shunt to the sinus wall includes delivering percutaneously and implanting the shunt into the sinus wall via a femoral vein.
7. The method of claim 4, wherein endovascularly delivering the shunt to the sinus wall includes delivering the shunt via a sigmoid sinus lumen.
8. The method of claim 4, further comprising positioning the shunt at an end of an internal catheter; and manipulating the internal catheter through the delivery catheter to deliver the shunt to the sinus wall.
9. The method of claim 8, further comprising providing a hollow lumen to the internal catheter.
10. The method of claim 8, further comprising confirming flow of cerebrospinal fluid through the shunt including, after manipulating the internal catheter through the delivery catheter to deliver the shunt to the sinus wall, aspirating the cerebrospinal fluid through the hollow lumen of the internal catheter via the shunt.
11. The method of claim 1, further comprising providing a closed sharpened end to the tip.
12. The method of claim 1, further comprising providing the tip with a formed helix.
13. The method of claim 12, wherein the formed helix has a constant radius.
14. The method of claim 1 further comprising providing a taper to the first end of the shunt.
15. The method of claim 1, further comprising providing a projection between said first and second end of the shunt, wherein said projection extends along a plane perpendicular to a line extending between said first and second ends of said shunt.
16. The method of claim 1, wherein configuring the one-way valve to block liquid from flowing from said first end toward said second end and to permit liquid from flowing from said second end toward said first end.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
(4)
(5)
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
(6) Referring to
(7) A shunt 20 is implanted into a sigmoid sinus wall 16, so that one end communicates with CSF located in the cistern or CSF space 18 around the cerebellum 19. The device of the present invention uses the body's natural disease control mechanisms by delivering the CSF from cistern 18 into sigmoid sinus lumen 12 of the venous system. The venous system of the patient can be accesses either through the femoral or jugular veins (not shown) percutaneously. It should be appreciated that the shunt device of the present invention can be delivered to the sigmoid sinus via other locations.
(8) As shown in
(9) A helical tip 30 is located at second end 24. As will be described further herein, helical tip 30 has a closed sharpened end 31 that is adapted to penetrate sinus wall 16. Tip 30 includes a plurality of apertures 34 through which the CSF enters the tip. A hollow passageway 32 extends from tip 30 and open end 22, such that the CSF fluid entering through apertures 34 can pass through valve 26 and pass from an outlet 36.
(10) Referring to
(11) Delivery catheter 40 includes a second lumen 44 and a shunt delivery port 42. Lumen 44 directs the entire catheter to the correct location with for example, a guide wire, to allow injection of intravenous contrast to visualize the venous lumen. Lumen 44 also supports balloons 46 that can be deployed to occlude venous flow during stunt implantation. Shunt 20 is positioned at an end of an internal catheter 48 that is manipulated through catheter 40 and port 42. To prevent thrombosis within the sigmoid sinus and around the endovascular shunt, shunt 20 can be provided with an antithrombic coating 38
(12) As shown in
(13) Thereafter, delivery catheter 40 can be removed and shunt 20 is implanted as shown in
(14) Thus, the endovascular cerebrospinal fluid shunt of the present invention can be placed into a patient percutaneously via a catheter inserted into the venous system of the body through a needle hole, without the need for open surgery and the skin incisions required with current shunt devices. In some patients, the device can be inserted without general anesthesia, which is not possible with current cerebrospinal fluid shunts. The device also will allow for more physiologic drainage of cerebrospinal fluid since the device is shunting cerebrospinal fluid into the same cerebral venous system that occurs naturally in normal people.
(15) Although the present invention has been described in relation to particular embodiments thereof, many other variations and modifications and other uses will become apparent to those skilled in the art. It is preferred therefore, that the present invention be limited not by the specific disclosure herein, but only by the appended claims.