Percutaneous catheter directed intravascular occlusion device

Patent metadata

Field	Value
Publication number	US-9743918-B2
Application number	US-23505908-A
Country	US
Kind code	B2
Filing date	Sep 22, 2008
Priority date	Jan 18, 2008
Publication date	Aug 29, 2017
Grant date	Aug 29, 2017

Abstract

Embodiments of the present invention provide medical devices and methods for occluding a target site are provided. For example, the medical device may include a tubular member having proximal and distal ends and at least one plane of occlusion. The at least one plane of occlusion may be configured to substantially occlude the patent ductus arteriosus in less than about 1 minute. In addition or alternatively, the tubular member may consist of a single layer of material and be configured to be constrained within a catheter having an outer diameter of less than about 4 French for percutaneous delivery to the patent ductus arteriosus.

First claim

That which is claimed:

1. A medical device for occluding a patent ductus arteriosus between an aorta and a pulmonary artery, the medical device comprising:
only one layer of braided fabric;
wherein the only one layer of braided fabric forms a tubular member having proximal and distal ends;
wherein the tubular member comprises a proximal disk-shaped portion at the proximal end and a distal disk-shaped portion at the distal end and a geometrical-shaped portion disposed therebetween, each of the proximal and distal disk-shaped portions having a maximum cross-sectional dimension larger than the geometrical shaped portion, the proximal disk-shaped portion having a maximum diameter at a distal end thereof and the distal disk-shaped portion having a maximum diameter at a proximal end thereof;
wherein the tubular member further comprises a transition segment coupled to either of the proximal or distal disk-shaped portions and the geometrical-shaped portion, the transition segment having a maximum cross-sectional dimension smaller than both the proximal and distal disk-shaped portions and the geometrical shaped portion, wherein each of the proximal disk-shaped portion maximum diameter and the distal disk-shaped portion maximum diameter extend inwardly to overlap the respective transition segment; and
wherein the only one layer of braided fabric is configured to be constrained within a catheter having an outer diameter of about 5 French or smaller for percutaneous delivery to the patent ductus arteriosus.

2. The medical device of claim 1 , further comprising a pair of transition segments, each transition segment coupled to one of the proximal or distal disk-shaped portions and the geometrical shaped portion and having a maximum cross-sectional dimension smaller than both the proximal and distal disk-shaped portions and the geometrical shaped portion.

3. The medical device of claim 1 , wherein the only one layer of braided fabric comprises a plurality of braided metal strands.

4. The medical device of claim 3 , wherein the metal strands comprise a material selected from the group consisting of stainless steel, nickel based, cobalt based, nickel-titanium, shape memory, and super-elastic materials.

5. The medical device of claim 1 , wherein the tubular member is configured to be constrained within a catheter having an outer diameter of about 4 French or smaller for percutaneous delivery.

6. The medical device of claim 1 , wherein the tubular member comprises at least one plane of occlusion configured to substantially occlude the patent ductus arteriosus in less than or equal to 1 minute from the time the tubular member is deployed in the patent ductus arteriosus to a time wherein contrast media injected on one side of the tubular member in the aorta does not flow through the tubular member to the other side of the tubular member in the pulmonary artery.

7. A delivery system for delivering a medical device for occluding a patent ductus arteriosus, the delivery system comprising:
a delivery device coupled to the medical device according to claim 1 ; and
a catheter configured to overlie the delivery device and constrain the medical device therein, wherein the medical device is configured to be deployed from the catheter, and wherein the delivery device and catheter are configured to be delivered bi-directionally to the patent ductus arteriosus either transarterially or transvenously and to deploy the medical device at least partially within the patent ductus arteriosus.

8. The delivery system of claim 7 , wherein the medical device comprises a plurality of planes of occlusion configured to be positioned outside of the patent ductus arteriosus and a plurality of planes of occlusion configured to be positioned within a cavity defined by the patent ductus arteriosus.

9. The delivery system of claim 7 , wherein the catheter has an outer diameter of about 5 French.

10. The delivery system of claim 7 , wherein the catheter has an outer diameter of about 4 French or smaller.

11. The delivery system of claim 7 , wherein the delivery device and catheter are configured to be delivered to the patent ductus arteriosus over a guidewire.

12. The delivery system of claim 7 , wherein the catheter is axially displaceable relative to the delivery device such that the medical device is configured to be deployed from the catheter in response to displacement of the catheter with respect to the delivery device.

13. A method for occluding a patent ductus arteriosus, the method comprising:
providing a medical device according to claim 1 ;
constraining the medical device from a preset expanded configuration to a reduced configuration;
positioning the constrained medical device in a catheter, the catheter and device configured to be delivered bi-directionally, either transarterially or transvenously;
delivering the medical device to the patent ductus arteriosus either transarterially or transvenously; and
deploying the medical device from the catheter at least partially within the patent ductus arteriosus such that the tubular member returns to the preset expanded configuration.

14. The method of claim 13 , wherein the medical device comprises a plurality of planes of occlusion, and wherein deploying comprises deploying the medical device such that at least one plane of occlusion is positioned outside the patent ductus arteriosus and at least one plane of occlusion is positioned within a cavity defined within the patent ductus arteriosus.

15. The method of claim 13 , wherein deploying comprises detaching a delivery system positioned within the catheter and coupled to the medical device.

16. The method of claim 13 , wherein delivering comprises delivering the medical device over a guide wire.

17. The method of claim 13 , further comprising imaging the patent ductus arteriosus using at least one of two-dimensional intracardiac echocardiography, angiography, magnetic resonance imaging, transesphogeal echocardiograpy, or Doppler color flow mapping.

18. The method of claim 13 , further comprising verifying occlusion of the patent ductus arteriosus by injecting a radiopaque contrast media through the catheter and into the aorta downstream of the deployed medical device and observing with angiography whether contrast enters the cavity defined by the patent ductus arteriosus and further whether any contrast within the cavity is stagnant.

Assignees

• Amplatz Kurt
• Gu Xiaoping
• Oslund John C
• St Jude Medical Cardiology Div Inc

Inventors

• Amplatz Kurt
• Gu Xiaoping
• Oslund John C

Classifications

• A61B2017/00606

  Implements H-shaped in cross-section, i.e. with occluders on both sides of the opening · CPC title

• A61B2017/00575

  for closure at remote site, e.g. closing atrial septum defects · CPC title

• A61B2017/00592

  Elastic or resilient implements · CPC title

• A61B17/0057 Primary

  Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect (sutures A61B17/04; closing rectum or urethra near body surface A61F2/0009) · CPC title

• A61B2017/00911

  for fields applied by a magnetic resonance imaging system · CPC title