This invention relates to medical coupling and release devices and methods for their assembly and use.
Implants have been used in the treatment of a variety of abnormalities, conditions and diseases, particularly cardiovascular indications such as arterial atherosclerosis and aneurysms. Various mechanisms have been proposed for detachment and release of implants delivered using catheter systems or other endoluminal means. However, there remains a need for mechanisms and methods of delivery of implants, and for their controlled release, that are increasingly precise, reliable, and simple to assemble and use.
Implant delivery devices may be used in treating a variety of endoluminal systems, such as the vascular, urinary or gastrointestinal systems of a patient. These devices are useful for delivery of implants for remediation of vascular system abnormalities and conditions, including arterial aneurisms and arterial atherosclerosis or restenosis, particularly of cardiac arteries. The implant may be of any type, including, without limitation, embolic implants and patent devices, such as stents. These implants may be referred to generally below simply as an implant, regardless of type. The present invention, in its various aspects and embodiments, provides for an implant attachment and release mechanism that permits retention of the implant during precise positioning of the implant and subsequent controlled withdrawal or release of the implant based on the need for its repositioning, or its satisfactory positioning.
Fundamentally, aspects and embodiments of the present invention recognize the use of openings, apertures, penetrations or other surfaces of genus greater than or equal to one (as such structures are referred to in topological terms) to create positively controllable and releasable locking and interlocking relationships advantageous in forming detachable couplings. Other embodiments of aspects of the present invention recognize tensile structures such as loops (or other structures of genus greater than or equal to one) as coupling and detachment mechanisms, which may act as tethers, lashes or other fasteners involving retention based on tension in the detachment mechanism. Although the illustrated embodiments show an example of such a tension loop detachment mechanism coupled to an implant device and releasable from the delivery device, this tensile structure could alternatively be coupled to the delivery device and releasable from the implant. Similarly, although the illustrated embodiment is a flexible structure, which is a structure that is intended to flex during use, and may comprise one or more filamentary elements, part or all of it could also be relatively more rigid in other embodiments of the invention. The flexible filamentary structure can have any flexible structure including without limitation, a shapeless structure, such as a floppy, string-like or spaghetti-like structure having no consistent shape in its elongate dimensions. Moreover, although these tension loops or other tensile structures according to the present invention employ tension to carry out their coupling and retention prior to detachment, and may be in tension when in use, they do not need to be in tension at all times.
In some embodiments of certain aspects of the invention, a first element having an opening (for example, but without limitation, a loop of elongate, flexible material) is provided that is anchored on one device, passes through an opening associated with another device and is retained releasably in position—keeping the two devices attached as long as the retention is positively maintained. Retention can be provided by any number of elements, but in various embodiments retention and engagement may be actuated distally to the point of retention. For endoluminal use inside a patient, a practitioner can thus actuate the retention element from outside the patient, and cause cessation of the retention of the first element having an opening (e.g., the loop) so that the two devices are no longer coupled. In some embodiments, but without limitation, an edge of an orifice in a tubular delivery device serves to maintain a position of a portion of a detachment element having an opening (e.g., a tension loop), relative to a retention member (which may be a pin or similar structure formed by the tip of a wire inserted through a delivery catheter, in certain embodiments). A variety of arrangements can embody this principle regardless of the particular geometries of the components, and which components are attached to which.
The invention, in one embodiment, provides a coupling device for use in delivery of an embolic implant by a delivery tool having a detachment feature. The coupling device comprises a loop structure coupled to the embolic implant, wherein the loop structure is configured to be releasable by the detachment feature. A loop structure, as used herein, includes a structure having an attached or integral elongate element having an aperture or opening. A detachment feature will be understood to include a structure having an attached or integral element actuatable to cause detachment of another structure or element. The detachment feature can be actuatable by the physician using the device upon delivery to release the implant.
In particular embodiments of one aspect of the delivery devices of the invention for use with an implant, the release and detachment of the implant, upon actuation of the detachment mechanism, is immediate or near immediate.
Another feature of embodiments of certain aspects of the delivery devices of the invention for use with an implant, is that once positioned in the target lumen, the implant is stably maintained in that location during the actuation of the detachment mechanism by the practitioner, causing release and detachment of the implant. In other words, the actuation of the release and detachment mechanism in no way, or only minimally, disturbs the implant and its precise positioning. This is stability of the implant after positioning is achieved because the delivery device does not recoil on actuation and subsequent detachment and release, thereby leaving the implant undisturbed in the original placement position.
In an embodiment of one of its aspects, the invention provides an engagement and detachment mechanism for a delivery device used for placement of an embolic or other implant in the patient. The implant has an associated releasable engagement feature, the releasable engagement feature having an aperture. The delivery device has an associated surface having at least one aperture adapted for receiving the engagement feature and at least a subset of its aperture, permitting positive control of engagement or detachment of the implant.
In an embodiment of another aspect, the invention provides a coupling and detachment device for use in delivery of an implant by a delivery tool having an associated actuatable detachment feature, the coupling and detachment device comprising a loop structure coupled to an implant and being configured to be coupled to the detachment feature of the delivery tool and released from the delivery tool upon actuation of the detachment feature.
An embodiment of another aspect of the invention provides a detachment mechanism for use in endoluminal placement of an implant by a delivery device, in which the implant is coupled to a releasable engagement structure provided with an opening, the detachment mechanism comprising: a surface coupled to the delivery device having at least one penetration adapted for receipt and controlled release of a portion of the engagement structure that includes the at least one opening.
In yet another embodiment of one of its aspects, the invention provides a mechanism for release of an embolic implant from a delivery device comprising: (i) a first element having an opening and associated with the embolic implant; (ii) a second element having an opening and associated with the delivery device; and (iii) a retaining member retractably passing through at least one of the openings of the first and the second elements.
In another embodiment of one of its aspects, the invention provides a detachment device for an endoluminal implant comprising a loop, in which a capability to maintain tension in the loop prevents detachment and a cessation of the capability to maintain tension in the loop permits detachment.
Another embodiment of an aspect of the invention provides a detachment apparatus for controlled release of an implant using a delivery device, at least one of the implant and delivery device having an associated surface defining a first aperture and having an associated retaining member. The detachment apparatus comprises an engagement member coupled to a first one of the implant and the delivery device and also comprises a second aperture. The second one of the implant and delivery device includes the associated surface defining the first aperture. The engagement member is adapted to pass through the first aperture to releasably engage the retaining member. The engagement member can be a structure that includes a loop or other aperture, and the retaining member can be a structure having an attached or integral element that in one position prevents detachment, and in another position permits detachment and release.
In one embodiment of another aspect, the invention provides a detachment apparatus for an implant delivery device, the apparatus being adapted for use in releasably engaging a detachment structure. The detachment structure is coupled to the implant and is provided with an aperture. The detachment apparatus comprises: (i) a retaining member adapted to engage the aperture of the detachment structure coupled to the implant, when the retaining member is in a first position, and to disengage the aperture of the detachment structure when the retaining member is in a second position; and (ii) a constraining member positioned relative to the retaining member for at least partially maintaining a spatial relationship between the detachment structure and the retaining member. The detachment apparatus can include a loop or a retainer or both. The constraining member can be a structure having an attached or integral element that limits the degrees of freedom of motion of another element. For instance, in one example, the constraining member can be an edge of an opening or aperture (through which the detachment structure may be positioned while retained) such as an opening in a wall of a tubular element.
In yet another embodiment of one of its aspects, the invention provides a method for assembling a detachment mechanism for an endoluminal implant for placement by a delivery device, the method comprising the steps of: (i) providing a detachable engagement structure having a first opening and adapted to pass through an opening associated with the delivery device; and (ii) coupling the detachable engagement structure to the implant.
In another embodiment of one of its aspects, the invention provides a method for assembling a detachment mechanism for an endoluminal implant for placement by a delivery device, the method comprising the steps of: (i) providing a loop structure configured to maintain attachment of the implant to the delivery device when placed tension, and to detach the implant from the delivery device upon cessation of a capability to maintain tension; and (ii) coupling the loop structure to at least one of the implant and the delivery device.
In another embodiment of one of its aspects, the invention provides a method for assembling an endoluminal implant delivery and detachment system comprising the steps of: (i) providing an implant having a tension loop releasable detachment component; (ii) providing a delivery device having a tension loop releasable retention component; and (iii) coupling the tension loop releasable detachment component to the tension loop releasable retention component.
In one embodiment of a particular aspect, the invention provides a method for delivering an endoluminal implant by a delivery and detachment system. The system includes a detachable engagement structure having a first opening and is adapted to pass through an opening associated with the delivery device to be retained by an actuatable retaining member. The detachable engagement structure is coupled to the implant. The method includes the following steps: (i) positioning the implant; and (ii) actuating the retaining member to cease retaining and to release the engagement structure; thereby detaching the implant. In one embodiment the detachment of the implant occurs immediately upon actuation of the retaining member.
In one embodiment of another particular aspect, the invention provides a method for sensing the positioning and release of an endoluminal implant from a delivery and detachment system. The system includes a detachable engagement structure having a first opening and adapted to pass through an opening associated with the delivery device, and the detachable engagement structure being coupled to the implant. The method includes the following steps: (i) sensing the position of each of the engagement structure and the implant prior to detachment of the engagement structure; (ii) sensing the position of each of the engagement structure and the implant after detachment of the engagement structure; and (iii) determining that the position of the implant is separated from the position of the engagement structure after detachment of the engagement structure. In one embodiment the sensing includes sensing of a radiopaque marker on the implant and a radiopaque marker on the engagement structure. In another embodiment a detectable marker is located on or near an engagement structure, such as the distal tip of a delivery catheter or pusher tube, and also on a functional wire (for instance, a wire that functions as a retaining member). Actuation of the retaining member causes a change in position of the retaining member relative to the distal tips of a delivery catheter, and/or the pusher tube. This change in relative positions of the markers can be sensed and may be visualized, for instance by fluoroscopy, demonstrating that the detachment and release has occurred.
In an embodiment of another particular aspect, the invention provides a coupling and detachment device for use in delivery of an implant by a delivery tool. The delivery tool has an associated actuatable detachment feature, and the coupling and detachment device includes a flexible loop structure coupled to the implant. The flexible loop structure is configured to be coupled to the detachment feature of the delivery tool and released from the delivery tool upon actuation of the detachment feature.
In another embodiment of another particular aspect, the invention provides a mechanism for release of an implant from a delivery device. The mechanism includes a flexible first element having an opening and associated with the implant; a second element that has an opening and is associated with the delivery device; and a retaining member retractably passing through at least one of the openings of the first and the second elements.
The invention can be more readily understood with reference to the following embodiments and the examples depicted in the figures, which are not to scale.
In its various embodiments and aspects, the present invention makes possible detachable coupling mechanisms for endoluminal and other medical delivery that maintain reliable closure, are simple of structure and assembly, and that permit positive control and detachment or disengagement of the delivered implant or other object from the delivery device.
As used in this specification, terms like loop, opening, pass-through, aperture, orifice or hole generally refer to topological surfaces of genus one or greater than one, the genus of a topological surface being the maximum number of cuts along closed simple curves that can be made without separating a section of the surface. Thus, a solid sphere or block has a topological genus of zero, since any cut along a closed curve of its surface separates the enclosed area of the surface. A hollow cylinder has a topological genus of one, since one cut along a closed curve in its surface in the direction of the cylindrical axis opens the walls of the cylinder, but does not separate any area of its surface. In a classic example, a doughnut and a coffee mug with a handle are both examples of structures of genus one. Similarly, surfaces of higher genus number encompass openings of that higher number.
The term “detachment,” such as when the term is used in conjunction “mechanism,” “means,” “device,” or other label, is used to refer at least to an ability to decouple, but is not intended to exclude structures that can be both decoupled in one action, and separately detached, or be released in a subsequent step.
In particular aspects and embodiments, the present invention provides coupling by a non-friction penetration interlock of an element of an implant and an element of a delivery device. As used herein the term “non-friction interlock” denotes an interlock that does not particularly require friction between the interlocking components for proper function, at least as compared with other forces, though it will be understood that the interlock may not necessarily be altogether friction-free. In some instances, tension loop structures according to the present invention may be embodiments of non-friction interlock detachment mechanisms of the present invention.
In another particular embodiment, the present invention provides a delivery system (also referred to as a delivery device) for an implant, such as a vascular occlusion device, the implant having a proximal end and a distal end, the distal end having a engagement element coupled to it, comprising: (i) an introducer component having a longitudinally extending lumen or cannula and proximal and distal ends; (ii) a pusher component slideable within the introducer component, the pusher component having a distal end positioned adjacent to the distal end of the implant; and (iii) a core component having a distal end and extending through the pusher component and parallel to the implant so that the distal end of the core component contacts the engagement element, thereby applying a tensile force to the implant.
The invention, in one embodiment of its aspects, provides for a tension loop detachment mechanism, which can act as a tether, lash or other fastener providing retention based on tension in the detachment mechanism. Although the embodiments illustrated in the drawings show the tension loop detachment mechanism coupled to the implant device and releasable from the delivery device, it will be understood that alternative embodiments are within the scope of the present invention. For instance, in another embodiment of one aspect, the tension loop detachment mechanism can be coupled to the delivery device and releasable from the implant. Similarly, although the illustrated embodiments relate to a flexible structure comprising one or more filamentary elements, part or all of the tension loop detachment mechanism can be relatively more rigid in other embodiments of the invention.
Pusher member 55 is advanced distally to expel implant 45 through the microcatheter. In the event that implant 45 is incorrectly placed, pusher member 55 is retracted proximally to reinsert implant 45 into the microcatheter, during which loop member 62 may be under a tensile load while maintaining implant 45 attached to the delivery device. This controlled delivery or retraction of implant 45 into the target lumen can be repeated until the desired positioning of implant 45 is achieved. When implant 45 is appropriately positioned wire, 70 is rotated causing disengagement of wire 70 from threading 66 and permitting wire 70 to be retracted. Wire 70 is retracted sufficiently to withdraw its distal end 75 beyond lateral opening 60 as shown in
Distal end pusher member 50 and the distal end 75 of wire 70, in certain embodiments, may each comprise a marker radiopaque material, such as platinum, to assist an practitioner during delivery. When distal end pusher member 50 and distal end 75 of wire 70 are in the engaged position, the radiopaque markers will be visible as a single spot under fluoroscopy; however, when distal end pusher member 50 and distal end 75 of wire 70 disengage, and release the loop member 62 from the implant 45, the separation of the markers will be visible as two separate spots under fluoroscopy indicating release of the implant 45.
Implant 105 is released, in an embodiment of the invention, by rotation and withdrawal of wire 70 in a proximal direction to a position such that protrusion 120 of distal end 75 is withdrawn beyond lateral opening 60 and no longer penetrates loop member 62. Loop member 62 is no longer restrained by wire 70 and is free to pass through lateral opening 60 releasing implant 105 from any attachment to the delivery device as shown in
Implant 105 is released, essentially as before, by rotation and withdrawal of wire 70 in a proximal direction to a position such that angled or deformable flexible, pivotable or otherwise radially moveable protrusion 120 of distal end 75 is withdrawn from opening 153 and and no longer penetrates loop member 62. Loop member 62 is no longer restrained by wire 70 and is free to pass through opening 157 in distal face 150, detaching and releasing implant 105 as shown in
In a further embodiment openings 153 and 157 in distal face 150 of distal end member 50 are shaped such that opening 153 is axially located in distal face 150 to receive distal end protrusion 120 without any angular deformation. In this embodiment, opening 157 is an elongate channel confined to an off-center location as shown in
One or more of the following components can be provided with a marker for sensing and visualization during placement, deployment and detachment of the implant from the delivery device: the distal tip 14 of the delivery catheter, the proximal tip 11 of the pusher tube 2, the distal tip 12 of internal core wire 3, can each carry a marker for visualization, such as a radiopaque marker, for monitoring its location by fluoroscopy.
The distal tip 14 of the delivery catheter is guided by the practitioner to the desired location. Once accurately positioned, the implant is deployed as shown in
In a particular embodiment, the control wire or other selective protrusion for engaging an element having an opening or aperture, is reciprocally threaded and mated with the threading on an inside wall of the end piece of the pusher tube or other engagement element as described above. In this embodiment, the control wire passes through the lumen of a hypotube (the needle tube of a hypodermic needle) and through the male portion of a luer lock fitting attached to the hypotube 72 as shown in
In another embodiment of the invention, a delivery system further includes an interlocking wire, also referred to as a control wire, having a distal end extending longitudinally into a pusher member. The occlusion device has an engagement/release element at its proximal end, and the distal end of the pusher component has an opening through which the release element extends. The distal end of the interlocking wire is releasably held within the distal end of the pusher member, and the distal end of the interlocking wire releasably engages the release element so that the distal end of the pusher component releasably engages the proximal end of the occlusion device.
In the interlocking wire embodiment of the non-friction releasable interlock mechanism of the invention, the wire can be of any suitable material. The wire can be any substantially flexible wire having no memory set, such as a metallic wire, for instance, a NiTinol or stainless steel wire, although a hard polymer material can also be used. The interlocking wire may be of any suitable length. NiTinol may be particularly suitable because of its super-elastic properties and its ability to return to a straight conformation and not take on a set even after navigating through a tortuous path, such as may be found in vasculature. In one embodiment the interlocking wire is a NiTinol wire of from about 180 to about 220 cm in length. The interlocking wire may include a distal ground portion with a serial stepwise reduction in diameter to provide a gradual decrease in stiffness from the stiffer proximal end to the softer, more flexible distal tip. In one embodiment the serial stepwise reduction in diameter extends from about 30 cm to about 50 cm from the distal tip.
In a particular embodiment, the interlocking wire has a diameter of between about 0.014 inch and about 0.016 inch at the proximal end and has one or more stepwise reductions in diameter along its length. For example, the outside diameters at the stepwise reductions may be to about 0.010 inch in a first step, to about 0.007 inch in a second step, to about 0.005 inch in a third step, and finally to about 0.003 inch or even to about 0.002 inch at the distal tip. In one embodiment, the proximal end of the wire passes through a hypotube. The hypotube can be fitted with a luer lock that can be used to attach the hypotube to any other device, such as a side arm for receiving the control wire or other selective protrusion, or a syringe for flushing the hypotube and connected intralumenal space with a physiologically compatible fluid to reduce friction between elements of the delivery device as described above.
In certain embodiments of a delivery system of the invention, the releasable engagement element can include at least one loop. The loop can be formed from any material, including flexible materials, such as a suture material. When suture material is used, it can be formed from any flexible biocompatible material, such as for instance, a monofilament or multifilament surgical suture material, a microbraided wire, or a flexible polymer material microbraided with a platinum wire. In a preferred embodiment, the loop is formed from a 7.0 or 9.0 gauge surgical suture material (from Genzyme Medical, Boston, Mass., or from Ethicon, Somerville, N.J.).
In certain other embodiments of a delivery system of the invention, the engagement element includes a tensioning element that is restrained in a first coupled position and released in a second position. The tensioning element can be under tension in the first coupled position. In one embodiment, the tensioning element is formed into at least one loop. In another embodiment, the tensioning element is formed into a loop that is penetrated by a restraining element such as a mandrel, a control wire (also referred to as an interlocking wire), pin or other structure capable of forming an interlock with the engagement element.
In another embodiment the invention provides a mechanism for detaching an implant from a delivery device, the implant having a proximal end and a coupling component at its proximal end, comprising: (i) an engagement element coupled at a distal end of the delivery device, the engagement element having a first, engaged position and a second, disengaged position; and (ii) an energy transfer component coupled to the engagement element at a distal portion of the component to actuate the engagement element. The engagement element, when actuated, engages the coupling component of the implant when in the first position and releases the coupling component when in the second position.
In another embodiment of a mechanism of the invention, the coupling component of the implant comprises a flexible structure. In another embodiment of a mechanism of the invention, the flexible structure comprises at least one opening through which an embodiment of one aspect of the engagement element of the delivery device may pass when in the first, engaged position. In another embodiment of a mechanism of the invention, the flexible structure comprises a loop.
In another embodiment of a mechanism of the invention, the engagement element comprises a structure that moves, along an axis, from the first position to the second position. In a particular embodiment, the engagement element comprises a substantially rigid element, such as for instance a metallic wire. The metallic wire can comprise one or more metal components, such as an alloy, for instance, in one embodiment, the metallic wire engagement element comprises NiTinol.
In another embodiment of a mechanism of the invention, the delivery device comprises at least one of the group consisting of a wire and a sheath, the axis is parallel to the longitudinal axis of the delivery device, and the energy transfer component comprises at least one of the wire and the sheath. The sheath (interchangeably referred herein to as a pusher tube) can comprise any suitable sheath material, such as a hypotube. In a particular embodiment, the hypotube can comprise a thermoplastic polymer, such as for instance a PEEK (polyetheretherketone) polymer, or any other thermoplastic polymer of similar desirable physical and chemical properties. The desirable physical and chemical properties of PEEK include its high performance metal-like rigidity and resistance to wear and corrosion. In one embodiment, the distal tip of the pusher tube has an end piece, also referred to herein as an end cap or tip. In one embodiment the end piece comprises a metal, which can be a radiopaque metal such as platinum. In a particular embodiment the platinum end piece is about 1-2 mm in length and includes a threaded inside wall. The threaded inside wall can have from about 2 to about 5 rotations, and in a particular embodiment can be formed by a platinum wire coil affixed to the inside wall. The platinum wire coil can be slightly open to permit mating by a platinum wire coil of slightly smaller diameter. The platinum wire coil of slightly smaller diameter can be affixed to the engagement element as a reciprocal thread for mating with the thread of the inside wall of the end piece. In a first position, the threaded of the inside wall of the end piece is mated with the wire coil affixed to the engagement element and is locked in place. In a second position, achieved after rotating a sufficient number of turns, the threaded of the inside wall of the end piece is free from the wire coil affixed to the engagement element. In this position, the engagement element is no longer constrained by the end piece from sliding within the pusher tube. The engagement element is thereby released and can be withdrawn from the pusher tube.
In other embodiments, the end piece mating with the engagement element can include both non-frictional and frictional fastening mechanisms, including snap-lock, lock and key, a bayonet coupling, clasp, or other mechanism, rather than mated threads on the end piece inside wall and the engagement element as described above.
In another embodiment of a mechanism of the invention, the delivery device comprises a sheath and the energy transfer component comprises a wire, and the engagement element transitions between the first position and the second position as a result of a relative rotation of the wire engagement element with respect to the delivery device sheath.
In another embodiment of a mechanism of the invention, the engagement element comprises a distal portion of the wire, the coupling component of the implant comprises a loop structure, and, in the first position of the engagement element, the loop structure is stably retained about a distal portion of the wire and, in the second position of the engagement element, the loop structure is released over a free distal end of the wire.
In another embodiment of a mechanism of the invention, the distal portion of the wire has threads that engage mating threads coupled to the sheath, the delivery device comprises a distal portion having a side wall with an aperture through which the loop structure passes and is held in place when the engagement element is in the first position, and when the engagement element is in the second position, the distal end of the wire is proximal of the aperture, releasing the loop structure and allowing it to exit through the aperture.
In another embodiment of a mechanism of the invention, the control wire or other actuatable engagement element of the delivery device is operable by a practitioner.
Other objects, advantages and embodiments of the various aspects of the present invention will be apparent to those who are skilled in the field of the invention and are within the scope of the appended claims. For example, but without limitation, structural or functional elements might be rearranged, or method steps reordered, consistent with the present invention. Similarly, principles according to the present invention, and systems and methods that embody them, could be applied to other examples, which, even if not specifically described here in detail, would nevertheless be within the scope of the appended claims.
This application is a continuation-in-part of co-pending U.S. Ser. No. 11/______ entitled “Aneurysm Treatment Devices and Methods” filed Sep. 15, 2005 which is a continuation-in-part of co-pending U.S. Ser. No. 11/111,487, filed Apr. 21, 2005, which in turn is a continuation-in-part of co-pending U.S. Ser. No. 10/998,357, filed Nov. 26, 2004, all of which are are incorporated herein by reference in their entireties. This application is also a continuation-in-part of each of the above-identified co-pending U.S. Ser. Nos. 11/111,487 and 10/998,357.
Number | Date | Country | |
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Parent | 11229044 | Sep 2005 | US |
Child | 11264402 | Oct 2005 | US |
Parent | 11111487 | Apr 2005 | US |
Child | 11229044 | Sep 2005 | US |
Parent | 10998357 | Nov 2004 | US |
Child | 11111487 | Apr 2005 | US |