Bioactive aneurysm closure device assembly and kit

Surgery – Means for introducing or removing material from body for... – Treating material introduced into or removed from body...

Reexamination Certificate

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C604S104000, C606S032000

Reexamination Certificate

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06663607

ABSTRACT:

FIELD OF THE INVENTION
This invention is an implantable medical device assembly for use in surgical procedures. It is most preferably an implantable structure having stenting properties but only partially coated with or partially associated with a material causing an angiogenic response. One variation of the invention is an artificial occlusion kit having the inventive implantable stenting structure situatable and vaso-occlusive devices. The inventive implantable stenting structure is typically situated so to prevent migration of artificial occlusion devices or implants from an occlusion site, such as an aneurysm, and into an adjacent body space, such as a blood vessel.
BACKGROUND OF THE INVENTION
Different implantable medical devices have been developed for treating various ailments associated with body lumens, such as ailments of body vessel walls or other lumenal walls. One category of implantable medical device that has been developed for artificial occlusion of body spaces is the category of “artificial occlusion devices.” Although artificial occlusion devices are useful in occluding body spaces, other applications include the occlusion of body lumens. Examples of lumens that have been identified as candidates for treatment with artificial occlusion devices include, for example, the vas deferens or the fallopian tubes. Most commonly, however, artificial occlusion devices have been disclosed for medical treatment of the vascular lumens and aneurysms in the walls of such vessels. This treatment is commonly referred to as “artificial vaso-occlusion.”
Artificial Vaso-Occlusion
Artificial vaso-occlusion is a medical treatment that has involved techniques such as the delivery of various occlusive agents including solidifying suspensions, thrombogenic fluids, solublized polymeric compositions, or emboli such as hog hair or suspensions of metal particles. Delivery of such agents or emboli normally causes a thrombogenic or other occlusive tissue response. Recent advancements in artificial occlusion of vessels and aneurysms have included the delivery and implantation of metal coils. Implantable metal coils that are useful as artificial occlusion devices in vascular lumens or aneurysms are herein referred to as “vaso-occlusion coils.”
Vaso-occlusion coils generally are constructed of a wire, usually made of a coils may be delivered through microcatheters such as the type disclosed in U.S. Pat. No. 4,739,768, to Engelson. The microcatheter commonly tracks a guide wire to a point just proximal of or within the desired site for occlusion. After removal of the guide wire, the coil is advanced through the microcatheter and out the distal end hole so to at least partially fill the selected space and create an occlusion.
Once a vaso-occlusion coil is implanted at a desired site, occlusion results either from the space-filling mechanism inherent in the coil itself, or from a cellular response to the coil such as a thrombus formation, or both. The space-filling mechanism of the vaso-occlusion coil may be either based upon a predetermined secondary geometry, or may be based upon random flow characteristics of the coil as it is expelled from a delivery sheath lumen.
Various commercially available vaso-occlusion coils have a secondary shape which dictates (at least in part) a space-filling occlusion mechanism. Such a secondary shape may include a secondary helical structure which involves the primary coil helix being itself wound into a second helix. In addition to the space-filling feature, another benefit to having a secondary coil shape is that it may allow the coil readily to anchor itself against the walls of a delivery site. For example, a vaso-occlusion coil having a secondary shape may be ejected from a sheath lumen where it was constrained in a stretched condition to have a first outer diameter equal to the sheath lumen inner diameter. When ejected, the coil passively expands to its secondary shape, often having a larger, second outer diameter to aid in space-filling the body cavity or lumen. This may be an expansion to the coil's relaxed, unrestrained memory state—or at least until the coil encounters a vessel wall against which it exerts a force to complete the anchoring process.
One example of a type of vaso-occlusion coil having a pre-determined secondary shape is described in U.S. Pat. No. 4,994,069, to Ritchart et al. Ritchart et al describes a vaso-occlusive wire having a memory imparted thereto by heating the wire at about 800° F. for 24 hours after it is shaped. This memory is effective to return the wire from a stretched, linear condition (in which shape it is advanced through a catheter) to a space-filling relaxed condition as the wire is released from the catheter. The diameter of the secondary shape may be approximately equal to or even larger than the vessel in which it is deployed.
In addition to vaso-occlusion coils having pre-determined secondary shapes that dictate in part their space-filling mechanism, other vaso-occlusion coils have been disclosed that take on random shapes when expelled from a delivery catheter. One such type of vaso-occlusive coil is often referred to as the “liquid coil.” An example of such a vaso-occlusive coil which takes on a random occlusive shape when delivered into a body space is shown in U.S. Pat. No. 5,718,711, issued Feb. 17, 1998, to Berenstein et al. This patent describes very soft, flexible coils which are flow-injectable through the delivery catheter using, e.g., a saline solution.
In addition to the various types of space-filling mechanisms and geometries of vaso-occlusion coils, other particularized features of coil designs, such as mechanisms for delivering vaso-occlusion coils through delivery catheters and implanting them in a desired occlusion site, have also been described. Examples of categories of vaso-occlusion coils based upon their delivery mechanisms include pushable coils, mechanically detachable coils, and electrolytically detachable coils.
One example of the type of vaso-occlusion coil referred to as the “pushable coil” is disclosed in U.S. Pat. No. 4,994,069 to Ritchart et al., introduced above. Pushable coils are commonly provided in a cartridge and are pushed or “plunged” from the cartridge into a delivery catheter lumen. A pusher rod advances the pushable coil through and out of the delivery catheter lumen and into the site for occlusion.
In contrast to pushable coils, mechanically detachable vaso-occlusion coils are integrated with a pusher rod and mechanically detached from the pusher after exiting a delivery catheter. Examples of such mechanically detachable vaso-occlusion coils are provided in U.S. Pat. No. 5,261,916 to Engelson, or U.S. Pat. No. 5,250,071 to Palermo.
Further in contrast to the mechanically detachable type of vaso-occlusion coil, the electrolytically detachable type is also integrated with a pusher rod, but is detached from the pusher by applying a direct current that dissolves a sacrificial link between the pusher and the coil. Examples of such electrolytically detachable vaso-occlusion coils are disclosed in U.S. Pat. No. 5,122,136 to Guglielmi et al, and U.S. Pat. No. 5,354,295 also to Guglielmi, et al.
Improvements for enhancing the thrombogenic or other occlusive tissue response to metal coils have also been disclosed. For example, vaso-occlusion coils having vaso-occlusive fibers attached thereto have been described (see for example, U.S. Pat. No. 5,226,911 to Chee et al.).
Vaso-Occlusion Coils in Aneurysms
A wide variety of clinical abnormalities in body lumens may be treated with artificial occlusion methods. For example, artificial occlusion methods have been disclosed for treating feeder vessels into tumors, arterio-venous malformations, fistulas, and aneurysms of vessel walls. Among arterial abnormalities, aneurysms present particular medical risk due to the dangers of potential rupture of the thinned wall inherent in an aneurysm. Occlusion of aneurysms with vaso-occlusion coils without occluding the adjacent artery is a desirable method of reducing such risk.
In one disclose

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