Patent Application
20110046657
The invention pertains to embolic coil introducer catheter locking mechanisms, components and methods of use thereof.
Therapeutic vascular occlusions are used to prevent or treat pathological conditions, such as aneurysms, in situ. Embolic coils are often used to provide such therapeutic vascular occlusions in a variety of situations. Some embolic coils are introduced to the region of interest in a generally straightened condition inside a delivery catheter. The delivery sheath may be advanced to the region of interest, and the embolic coil may then be pushed out the distal end of the delivery catheter using a pusher wire, which may be removably attached to the embolic coil. The embolic coil typically assumes its final, coiled configuration as it is pushed out the distal end of the delivery catheter.
Embodiments of the invention pertain to embolic coil introducer catheter locking mechanisms, as well as related components, systems and methods. In many instances, it may be desirable to lock the relative positions of the catheter to the introducer wire during certain steps of a procedure, and then allow the introducer wire to move relative to the catheter during other steps of a procedure. Embodiments of the invention pertain generally to locking mechanisms of simple construction and easy use. In many cases, no additional steps are needed to use the locking systems of certain embodiments.
In one aspect, embolic coil introducer systems are provided wherein a catheter includes a locking mechanism that provides a friction fit between the catheter and the introducer wire to hold the wire secure relative to the catheter in a first position when no force is applied to the wire and wherein the friction fit may be overcome by the application of a force to the wire to allow the wire to move relative to the catheter.
In a second aspect, the locking mechanism may be configured to automatically hold the wire secure relative to the catheter in a second position after force has been applied to the wire to move the wire relative to the catheter, after the force has then been removed, wherein the locking mechanism may be configured such that the force needed to overcome the friction fit is greater than 0.05 lbs and less than 0.13 lbs.
In a third aspect, the locking mechanism may be distal to the proximal end and in the proximal third of the catheter.
In a fourth aspect, the locking mechanism may be a reduced profile section of the catheter. For example, the locking mechanism may be a section of the catheter having a second inner diameter that is less than the first inner diameter. The catheter may include a stepwise transition between the first inner diameter and the locking mechanism or may include a tapering section between the first inner diameter and the locking mechanism.
In a fifth aspect, the locking mechanism may define a lumen for receiving the wire wherein the cross-sectional shape of the lumen is noncircular, such as a cross-sectional shape that is generally oval. The lumen may be configured to contact the wire along two, three, four, five or more noncontiguous inner surfaces of the locking mechanism, and the noncontiguous inner surfaces of the locking mechanism may have a greater dimension along the direction of the longitudinal axis than in a circumferential direction and may be generally uniformly disposed in a circumferential direction around the locking mechanism.
In a sixth aspect, the locking mechanism may include a first section that provides a friction fit with the wire and a second section that provides a friction fit with the wire separated longitudinally from each other by an intermediate section that does not provide a friction fit with the wire or is otherwise fixed to the wire.
In a seventh aspect, the locking mechanism may be a unitary component of the catheter. For example, the locking mechanism may be formed by crimping the catheter or may be formed from a section of the catheter by applying heat and pressure to that section of the catheter.
In an eighth aspect, the locking mechanism may have only a single configuration such that the locking mechanism components are not movable between a first and a second configuration because there is only a single configuration.
In a further aspect, the system may include a removable element disposed at the proximal end of the catheter to fix the relative longitudinal position of the catheter with the wire, such as a piece of heat shrink tubing, and the removable element may include either a slit and a perforation.
In a further aspect, the locking mechanism may be an insert fixed to the catheter.
In a further aspect, embolic coil introducer systems are provided wherein the catheter may include a non-removable locking mechanism that has essentially the same size and shape in a first position where the catheter is locked to the wire as in a second position where the wire is sliding relative to the catheter. There may be an adhesion bond between the locking mechanism and the wire in the first position, or there may be a friction fit between the locking mechanism and the wire in the first position. There may further be a friction fit between the locking mechanism and the wire in a third position where the wire is static relative to the catheter.
In a further aspect, embolic coil introducer systems are provided wherein the catheter may include a non-removable locking mechanism such that contact between the catheter and the wire fixes the wire in place when less than 0.010 lbs., 0.006 lbs. or 0.003 lbs. of force are applied to the wire.
The above summary is not intended to describe each disclosed embodiment or every implementation of the invention.
All numeric values are herein assumed to be modified by the term “about”, whether or not explicitly indicated. The term “about” generally refers to a range of numbers that one of skill in the art would consider equivalent to the recited value (i.e., having the same function or result). In many instances, the term “about” may be indicative as including numbers that are rounded to the nearest significant figure.
The recitation of numerical ranges by endpoints includes all numbers within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5).
Although some suitable dimensions ranges and/or values pertaining to various components, features and/or specifications are disclosed, one of skill in the art, incited by the present disclosure, would understand desired dimensions, ranges and/or values may deviate from those expressly disclosed.
As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
The following detailed description should be read with reference to the drawings in which similar elements in different drawings are numbered the same. The detailed description and the drawings, which are not necessarily to scale, depict illustrative embodiments and are not intended to limit the scope of the invention. The illustrative embodiments depicted are intended only as exemplary. Selected features of any illustrative embodiment may be incorporated into an additional embodiment unless clearly stated to the contrary.
Embolic coil delivery systems and detachable embolic coils are described, for example, in U.S. Patent Pub. No. 2008/0221554 to O'Connor et al., filed on Feb. 12, 2008; U.S. Pat. No. 5,304,195 to Twyford, Jr. et al.; U.S. Pat. No. 5,895,385 to Guglielmi et al.; and U.S. Patent Pub. No. 2007/0141099 to Buiser et al., filed on Dec. 19, 2005; all of which are incorporated herein by reference.
Catheter 112 includes toward its proximal end a locking mechanism 114. In this embodiment, locking mechanism 114 is a narrowed section of catheter 112. Catheter 112 gradually reduces in size to the locking mechanism. Locking mechanism 114 is sized to contact wire 111 and hold wire 111 in place. Such contact may be, for example, a friction fit which applies force to the wire to hold it in place. The locking mechanism may be sized so that a particular amount of force applied to the wire may overcome the effect of the contact to allow the wire slide relative to the catheter. The amount of force needed to overcome the locking mechanism may be in the range of about 0.001-0.030 lbs, about 0.002-0.020 lbs, about 0.003-0.012 lbs, about 0.003-0.009 lbs, or about 0.004-0.007 lbs. The amount of force needed to overcome the locking the mechanism is preferably sufficient to prevent the inadvertent release of the wire from the catheter yet not so great as to prevent an operator from manually overcoming the locking mechanism.
As the locking mechanism 114 needs no direct interaction with the operator to work, it may be placed along a substantial portion of the length of the catheter. When the embolic coil delivery system 100 is loaded with the embolic coil 110 and the introducer wire 111, the distal end of the introducer wire, proximal to any end fitting 132, defines the distal most preferable position for the locking mechanism. In this position, the locking mechanism may also act as a proximal stop for end fitting 132. As shown in
In the embodiment of
Embolic coil introducer systems including locking mechanisms as described above are not limited to systems where the introducer wire has a circular cross section. The introducer wire 111 may have, for example, and oblong cross-section. In such a case, the locking mechanism would define a corresponding lumen. The lumen may have been oblong cross-sectional shape as well or it may define several noncontiguous contact surfaces between the locking mechanism and the wire.
Locking mechanisms 114 may be produced by pressing or crimping that sheath to the wire with a pair of heated crimp pliers melting a section of the sheath to produce intimate contact with the wire. The cross-section of the crimped sheath is determined by the design shape of the crimping section of the pliers, with the purpose of producing sufficient adhesion and/or friction force between the sheath and the wire as a way to secure the sheath onto the wire. The adhesion or friction force is determined by factors including the contact area, the shape of the cross-section of the crimped sheath, and the temperature and crimp force applied to the heated pliers. The temperature of the heated pliers is preferably high enough to ensure the crimped section of the sheath is melted. The crimping section of the pliers may have any appropriate shape, including but not limited to a star or an oval shape. In another method of manufacture, the locking mechanism section of the catheter may be produced by extruding a narrower section of the catheter. Other appropriate methods of manufacture may be used as well.
In use, an embolic coil introducer system 110 may be provided having an introducer wire 111 and an embolic coil 110 loaded therein. The system may be advanced as desired within a body lumen, while the locking mechanism 114 retains the relative positions of the catheter and introducer wire. When the desired location is reached, the physician may advance the wire relative to the catheter, without doing anything to the locking mechanism to deploy embolic coil by applying an appropriate degree of force to the wire. When the physician stops applying force to the wire, the force provided by the locking mechanism keeps the wire from moving within the catheter. Typically, the distal end of the introducer wire is advanced out of the distal end of the catheter to release embolic coil. Once the embolic coil is released, the introducer wire may be withdrawn back into the catheter, and the system may be withdrawn from the patient's body. This example of use is intended to show that the locking mechanism of the embodiments described can be used within embolic coil introducer systems without the time or complication of additional steps in the procedure.
Various embodiments of the invention have now been described in detail. Since changes, alterations and additions to the above described embodiments may be made without departing from the nature, spirit or scope of the invention, the invention is not to be limited to the embodiments described above, but rather the scope of the invention is defined only by the appended claims. For example, while the invention is described with respect to embolic coil introducer systems, the invention may be used in any catheter system where releasable fixing of an elongate interior member to the catheter is desirable.
This application claims the benefit of U.S. Provisional Application Ser. No. 61/235,397, filed Aug. 20, 2009, the entire disclosure of which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61235397 | Aug 2009 | US |
