IP Library Granted Patent US 8,486,104
Granted Patent B2
US 8,486,104 · App. 12/966,311 · Granted Jul 16, 2013

Mechanical clot treatment device with distal filter

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Quick Facts
Patent No.
US 8,486,104
App. No.
12/966,311
Granted
Jul 16, 2013
Kind
B2
Abstract

This is a surgical device usually delivered through an intravascular catheter. It may be used in several ways. It may, for instance, be used to open a clear passageway adjacent thrombus to allow both blood and medication to bypass the clot. It may be used to pierce and to remove thrombus. These thrombus are often found in tortuous vasculature. The device includes several sections. The device has a core element, typically a core wire. Placed around the distal end of the core element is a collapsible but preferably self expanding proximal cage assembly and a distal filter, preferably a self-expanding cage assembly or other filter component. The various portions of those components are preferably radio-opaque. The proximal end of the proximal cage is typically is affixed to an actuator in such a way as to allow expansion of the cage after deployment. The proximal cage assembly may be used for collecting emboli or for displacing them to allow blood flow to resume, either with or without concurrent clot-dissolving drug treatment. The distal sector, whether a self-expanding cage or fan, is placed distally of the thrombus to collect portions of the thrombus which may loosen during the treatment or removal procedure.

Claims (33)

1. An embolism treatment device, comprising:

an elongated core wire having a proximal section, a distal section, and a distal coil tip;

a proximal cage assembly rotatably disposed on the distal section of the elongated core wire;

a distal cage assembly rotatably disposed on the distal section of the elongated core wire distal the proximal cage assembly;

a separation member disposed between the proximal cage assembly and the distal cage assembly; and

an actuator element located proximal of the proximal cage assembly, the actuator element axially movable along the elongated core wire such that when the actuator element is in a first position, the proximal and distal cage assemblies are each in a collapsed configuration, and when the actuator element is in a second position, the proximal and distal cage assemblies are each in an expanded configuration;

wherein the proximal cage assembly and the distal cage assembly are each self-collapsing.

2. The embolism treatment device of claim 1 , wherein the proximal cage assembly has a substantially open interior in the expanded configuration.

3. The embolism treatment device of claim 1 , wherein the distal cage assembly has a substantially open interior in the expanded configuration.

4. The embolism treatment device of claim 1 , wherein the distal cage assembly includes a tubular liner.

5. The embolism treatment device of claim 4 , wherein the tubular liner moves independently of the actuator element.

6. The embolism treatment device of claim 4 , wherein a distal-most end of the distal cage assembly is fixed to the tubular liner.

7. The embolism treatment device of claim 1 , wherein the elongated core wire includes a braid member disposed on and adhered to the elongated core wire.

8. The embolism treatment device of claim 1 , wherein at least one of the proximal cage assembly and the distal cage assembly comprises a woven braid of wires that are each tightly wrapped with radiopaque wire.

9. A method of treating an embolism, the method comprising:

obtaining an embolism treatment device comprising:

an elongated core wire;

a proximal cage assembly rotatably disposed on the elongated core wire;

a distal cage assembly rotatably disposed on the elongated core wire distal the proximal cage assembly;

a separation member disposed between the proximal cage assembly and the distal cage assembly; and

an actuator element located proximal of the proximal cage assembly, the actuator element axially movable along the elongated core wire such that when the actuator element is in a first position, the proximal and distal cage assemblies are each in a collapsed configuration, and when the actuator element is in a second position, the proximal and distal cage assemblies are each in an expanded configuration;

inserting the embolism treatment device in the collapsed configuration into a blood vessel containing a clot having a proximal end and a distal end;

positioning the embolism treatment device within the vessel such that the distal cage assembly is disposed distal the clot distal end and the proximal cage assembly overlaps the clot proximal end and the clot distal end;

expanding the proximal cage assembly and the distal cage assembly such that the proximal cage assembly displaces at least a portion of the clot and blood flows through a lumen of the proximal cage assembly;

capturing fragments of the clot that break loose when the clot is displaced by the proximal cage assembly with the distal cage assembly; and

removing the fragments captured by the distal cage assembly from the blood vessel.

10. The method of claim 9 , wherein the step of removing the fragments captured by the distal cage assembly further comprises introducing thrombolytics into the blood vessel to dissolve the fragments while the embolic treatment device prevents downstream movement of the clot.

11. The method of claim 9 , wherein the step of removing the fragments captured by the distal cage assembly further comprises:

collapsing the proximal cage assembly and the distal cage assembly; and

removing the embolism treatment device and the captured fragments from the blood vessel.

12. The method of claim 9 , wherein the elongated core wire includes a braid member disposed on and adhered to the elongated core wire.

13. The method of claim 9 , wherein at least one of the proximal cage assembly and the distal cage assembly comprises a woven braid of wires that are each tightly wrapped with radiopaque wire.

14. The method of claim 9 , wherein the proximal cage assembly and the distal cage assembly are each self-collapsing.

Assignments (7)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 7, 2020
From: STRYKER EUROPEAN HOLDINGS I, LLC
To: STRYKER EUROPEAN HOLDINGS III, LLC
Reel/Frame 052861/0001 →
CHANGE OF NAME Recorded Jun 7, 2020
From: STRYKER EUROPEAN HOLDINGS III, LLC
To: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
Reel/Frame 052860/0716 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT LISTED SERIAL NOS. 09/905,670 AND 07/092,079 PREVIOUSLY RECORDED AT REEL: 037153 FRAME: 0241. ASSIGNOR(S) HEREBY CONFIRMS THE NUNC PRO TUNC ASSIGNMENT EFFECTIVE DATE 9/29/2014. Recorded Mar 8, 2016
From: STRYKER MEDTECH LIMITED
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 038043/0011 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT SERIAL # 09/905,670 AND 07/092,079 PREVIOUSLY RECORDED AT REEL: 037153 FRAME: 0034. ASSIGNOR(S) HEREBY CONFIRMS THE NUNC PRO TUNC ASSIGNMENT. Recorded Mar 8, 2016
From: STRYKER NV OPERATIONS LIMITED
To: STRYKER MEDTECH LIMITED
Reel/Frame 038039/0001 →
NUNC PRO TUNC ASSIGNMENT Recorded Nov 23, 2015
From: STRYKER NV OPERATIONS LIMITED
To: STRYKER MEDTECH LIMITED
Reel/Frame 037153/0034 →
NUNC PRO TUNC ASSIGNMENT Recorded Nov 23, 2015
From: STRYKER MEDTECH LIMITED
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 037153/0241 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2011
From: TARGET THERAPEUTICS, INC.
To: STRYKER CORPORATION; STRYKER NV OPERATIONS LIMITED
Reel/Frame 026018/0677 →