US 20100280602 A1
A mitral valve annulus reshaping device includes at least a portion that is formed of a biocompatible shape memory alloy SMA having a characteristic temperature, Af, that is preferably below body temperature. The device is constrained in an unstable martensite (UM) state while being introduced through a catheter that passes through the venous system and into the coronary sinus of the heart. The reshaping device is deployed adjacent to the mitral valve annulus of the heart as it is forced from the catheter. When released from the constraint of the catheter, the SMA of the device at least partially converts from the UM state to an austenitic state and attempts to change to a programmed shape that exerts a force on the adjacent tissue and modifies the shape of the annulus. The strain of the SMA can be varied when the device is within the coronary sinus.
1. A device adapted to be inserted into a coronary sinus within a body of a patient, for use in modifying an annulus of a mitral valve of the patient to treat a mitral valve pathology, comprising: (a) a structure having at least a portion thereof comprising a shape memory alloy, said shape memory alloy having a characteristic temperature, Af, selected to be no greater than a normal temperature of a body of a patient in which the device will be used, and having a programmed shape to which the shape memory alloy returns when substantially converted to an austenitic state; and (b) a restraint that mechanically maintains the shape memory alloy in a deformed state while the structure is being inserted info a coronary sinus of a patient, said restraint being controlled to enable the shape memory alloy to return to its austenitic state, causing the shape memory alloy to try to assume its programmed shape with a coronary sinus, said programmed shape being selected and said structure being disposed at a desired orientation within a coronary sinus by the restraint so as to apply a force against a mitral valve to modify an annulus of the mitral valve.
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7. A device adapted to be inserted into a coronary sinus within a body of a patient, for use in modifying an annulus of a mitral valve of the patient to treat a mitral valve pathology, comprising: (a) a venous deliverable component having at least a portion that is formed of a shape memory alloy, said shape memory alloy being selected to have a characteristic temperature, Af, that is no greater than a normal body temperature of a patient with which the device is used, said shape memory alloy being further characterized by being capable of reversibly changing between a martensite state and an austenitic state within a body of a patient, while remaining at substantially a constant temperature, said changes between the martensite state and austenitic state corresponding to a change in shape of the shape memory alloy; and (b) at least a portion of the device comprising a selectively configurable force applying component to apply a force directed against an interior surface of a coronary sinus, causing a modification of an annulus of a mitral valve within a body of a patient.
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This application is a continuation of U.S. application Ser. No. 11/655,710, filed Jan. 18, 2007, now U.S. Pat. No. 7,758,639, which is a continuation of U.S. application Ser. No. 10/359,016, filed Feb. 3, 2003, now U.S. Pat. No. 7,314,485; all of which are incorporated by reference as if fully set forth herein.
All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.
The present invention generally pertains apparatus and a method for treating mitral insufficiency and, more specifically, for treating dilation of the mitral valve annulus of the human heart and concomitant blood leakage, by using force applied with a device formed at least in part of a shape memory alloy that is conditioned to a martensite state before being inserted into a venous system of a patient and advanced into the patient's coronary sinus.
Mitral insufficiency is the inability of the mitral valve to close completely and can occur for several reasons, such as ischemic disease, degenerative disease of the mitral apparatus, rheumatic fever, endocarditis, congenital heart disease, and cardiomyopathy. Because the mitral valve does not close completely, “mitral regurgitation” occurs. Blood thus leaks back through the mitral valve, and the heart becomes less efficient. Over time, the reduced pumping efficiency can cause the heart to become enlarged.
The four major structural components of the mitral valve are the annulus, the two leaflets, the chorda, and the papillary muscles. Any one or all of these components, in different combinations, may be injured or suffer from a congenital defect and cause the insufficiency. Annular dilatation is a major component in the pathology of mitral insufficiency, regardless of its cause. Moreover, many patients experience mitral insufficiency primarily, or only, due to posterior annular dilatation. Annular dilation can occur when the annulus of the anterior leaflet does not dilate because it is anchored to the fibrous skeleton of the base of the heart.
Studies of the natural history of mitral insufficiency have determined that totally asymptomatic patients with severe mitral insufficiency usually progress to severe disability within five years. At present, the preferred treatment for this condition consists of either mitral valve replacement or repair; however, both types of treatment require open heart surgery. Replacement can be performed using either mechanical or biological valves.
Replacement of a mitral valve with a mechanical valve carries the risk of thromboembolism (due to formation of a clot) and requires that an anticoagulant be administered to the patient, with all its potential hazards, whereas a biological prostheses replacement may suffer from limited durability. Another hazard with replacement is the risk of endocarditis (inflammation of the endocardium). These risks and other related complications of valve replacement are greatly diminished if valve repair is carried out, rather than valve replacement.
Mitral valve repair is theoretically possible if a substantially normal anterior leaflet is present. The four basic techniques for repair include: (a) the use of an annuloplasty ring; (b) quadrangular segmental resection of a diseased posterior leaflet; (c) shortening of elongated chorda; and (d) transposition of posterior leaflet chorda to the anterior leaflet.
Annuloplasty rings are employed to achieve a durable reduction of the annular dilatation. Typically, annuloplasty rings are sutured along the posterior mitral leaflet adjacent to the mitral annulus in the left atrium. The installation procedure employed depends upon the specific annuloplasty ring being installed. For example, a Duran ring encircles the valve completely, whereas others types of rings are open towards the anterior leaflet. The ring can either be rigid, as in a Carpentier ring, or flexible, but non-elastic, like the Duran ring or a Cosgrove-Edwards ring.
Effective treatment of mitral insufficiency currently requires open-heart surgery, involving a total cardiopulmonary by-pass, aortic cross-clamping, and temporary cardiac arrest. For certain groups of patients, open-heart surgery and the associated procedures that must be performed are particularly hazardous. It is likely that elderly patients and patients with a poor left ventricular function, renal disease, severe calcification of the aorta, previous cardiac surgery, or other cardiovascular diseases, would particularly benefit from a less invasive approach, even if repair of the mitral valve is incomplete. The current trend towards less invasive coronary artery surgery, without cardiopulmonary by-pass, as well as percutaneous transluminal coronary angioplasty (PTCA) will also call for the development of a less invasive method for repair of the mitral insufficiency that is often associated with PTCA.
To perform typical open surgical procedures in ways that are less invasive will likely require use of technology for storing or transmitting energy so that apparatus for implementing the treatment can be delivered within a limited space, and positioned and released in remote locations in the body. Hydraulic conduits such as those used to inflate balloon catheters, and an electrical current have been employed to actuate devices remotely in the human body. However, one of the most reliable and effective remote actuation methods utilizes self actuating components formed of a shape memory alloy (SMA) that releases stored strain energy at a desired location within the body of a patient.
Materials capable of shape memory are well known. A structural element made of such materials can be deformed from an original, heat-stable configuration to a second, heat-unstable configuration. In the heat-unstable configuration, the element is said to have shape memory because, upon the application of heat alone, the element can be caused to revert, or to attempt to revert, from its deformed configuration to its original, heat-stable configuration. The metal element “remembers” its programmed shape. Programming is accomplished by thermally or mechanically stressing the element, while bending it into a desired shape.
Among certain metallic alloys, the shape memory capability occurs when the alloys undergo a reversible transformation from an austenitic state to a martensite state, with a change in temperature. This transformation is sometimes referred to as a thermo-elastic martensite transformation. An element made from such alloys, for example a hollow sleeve, is easily loaded and deformed from its original configuration to a new configuration if it has been cooled below the temperature at which the alloy is transformed from the austenitic state to the martensite state. The temperature at which this transformation from austenite to martensite begins is usually referred to as Ms (martensite start), and the temperature at which the transformation is complete is Mf (martensite final). When an element that has been thus deformed is warmed to the temperature at which the alloy starts to recover back to an austenite phase, referred to as As, the deformed object will begin to recover to its programmed shape. Assuming that the element is unconstrained, it will assume its programmed shape when it has been fully transformed to an austenitic state (where Af is the temperature at which the recovery is complete).
Many shape memory alloys (SMAs) are known to display stress-induced martensite (SIM) characteristics. When an SMA element exhibiting SIM is stressed at a temperature above Ms (so that the austenitic state is initially stable), but below Md (the maximum temperature at which martensite formation can occur even under stress), it first deforms elastically and then, at a critical stress, begins to transform to a martensite state.
Depending on whether the temperature is above or below As, the behavior of an SMA when the deforming stress is released differs. If the temperature is below As, the thermally induced martensite is stable; but if the temperature is above As, the martensite is unstable, so that the SMA transforms back to austenite and returns (or attempts to return) to its original shape. As used herein, the term “unstable martensite” or (UM) describes a martensite state of an SMA alloy that is at or above the alloy's As temperature. Under certain circumstances, this effect is actually seen in almost all alloys that exhibit a thermo-elastic martensitic transformation, along with the shape memory effect. However, the extent of the temperature range over which UM is observed and the stress and strain ranges for the effect vary greatly with the alloy.
Various proposals have been made to employ shape memory alloys in the medical field. For example, U.S. Pat. No. 3,620,212 to Fannon et al. teaches the use of an SMA intrauterine contraceptive device; U.S. Pat. No. 3,786,806 to Johnson et al. teaches the use of an SMA bone plate; and U.S. Pat. No. 3,890,977 to Wilson teaches the use of an SMA element to bend a catheter or cannula.
These prior art medical SMA devices rely on the property of shape memory to achieve their desired effects, i.e., they rely on the fact that when an SMA element is cooled to its martensitic phase and is subsequently deformed, it will retain its new shape. But when the deformed SMA is warmed to its austenitic phase, the original shape will be recovered. Heating a medical SMA device to activate a recovery to a programmed shape within a patient's body is quite complicated and is generally not practical, because complex and sometimes unreliable heat energy sources are needed to cause the change in state of the metal. In many SMAs, there is a relatively large hysteresis as the alloy is transformed between its austenitic and martensitic states, so that thermal reversing of the state of an SMA element may require a temperature excursion of several tens of degrees Celsius. The use that can be made of SMA medical devices in the body of a human patient is limited because of these factors and because: (a) it is inconvenient to engage in any temperature manipulation of a device in-vivo; and, (b) human tissue cannot be heated or cooled beyond certain relatively narrow limits (approximately 0-60 degrees C. for short periods) without suffering temporary or permanent damage.
It would therefore be desirable to use the advantageous property of shape memory alloys, i.e., their ability to return to a programmed shape after experiencing a relatively substantial deformation, in mitral valve therapy, without requiring the delicacy of alloying control and/or the temperature control of placement or removal needed by thermally activated SMA devices.
Nickel titanium SMA compositions can be tuned with appropriate heat treatments to adjust the Af temperature of the material. Compositions comprising nickel, in about 50 to 60% Ni atomic percent (hereinafter referred to as at. %), using Ti for the remainder of the composition, can have characteristic Af temperatures ranging from 0-100° C. By heat-treating these alloys at or near approximately 500° C., it is possible to precipitate nickel in or out of the Ni—Ti matrix so as to adjust the Af to a specific and desired temperature.
The Af temperature of a SMA can be readily determined. By deforming a cooled SMA sample (comprising stable thermally induced martensite at a temperature well below its Af) from its programmed shape and then increasing its temperature, a distinct temperature can be identified at which the sample has recovered-fully to its programmed shape. It is at this Af temperature that the entire sample has transformed back to an austenite state. The Af temperature of local regions of a component can be adjusted individually and determined in a similar manner, also.
By adjusting the SMA's characteristic Af below body temperature, the alloy will exhibit super-elastic or pseudo-elastic properties at body temperature, allowing it to experience as much as 8% strain and still fully recover. In this application, the SMA is initially austenitic and, under no load, it is not strained. Upon loading the device, the strain developed in the SMA causes it to undergo a phase transformation to UM. Upon unloading, the SMA that is UM will recover to its programmed shape and revert back to an austenitic phase. During loading and unloading, SMA alloys are internally stressed and deliver resistance forces of different magnitudes at the same strain state. The loading curve describes loading (stress) versus strain required to deform an element from its programmed shape while the unloading curve is descriptive of the load (stress) versus strain curve exhibited while the element is recovering to its programmed shape after being loaded, and thus recovering to a zero strain state. The unloading curve can be much lower in magnitude than the loading curve. This bimodal (BM) elastic effect (i.e., the hysteresis between the two curves) can only be accomplished at a constant temperature if the material is conditioned to a state of UM (along the loading curve).
A device made from an SMA alloy can be manipulated from one performance level to another simply by varying the load applied to the device, thereby changing its level of stored strain energy. The bimodal (BM) effect between the curves enables a medical device to be assisted, using force, to a different equilibrium condition as the device bears on soft tissue. A medical device made from this family of SMAs can be deployed from a delivery system (allowing it to partially recover towards a programmed shape along its unloading curve) to achieve a balanced, low force condition in a patient's body. Using hydraulic, pneumatic, electrical, heat energy, or mechanical force, the device can be assisted to further displace tissue, by adjusting the load along the unloading curve, to approach a zero strain state. As the assisting force is removed, an elastic recoil of the tissue will displace the device in a reverse direction, towards a slightly more deformed shape, thus causing the alloy to resist bending more effectively by forcing it to the loading curve (i.e., to a stiffer condition). This bimodal (BM) effect acts as a one-way ratchet with minimal moving parts and thus enables effective and reliable adjustment of load bearing elements in the human body to achieve a desired effect on adjacent tissue.
UM can be stress induced in SMAs by imparting sufficient stress to transform an SMA element from an austenite to a UM state. This type of UM is referred to as strain induced. Also, SMA elements can be cooled to form stable, thermally induced martensite. The SMA element can then be easily deformed to a new shape, constrained in the new shape, and then warmed to a temperature above the Af temperature of the SMA to create a UM state. There are also combinations of these conditioning techniques that will accomplish the same UM condition. These conditioning methods inevitably create a condition of stored strain energy sufficient to enable self-actuation and adjustment of medical devices remotely placed in a patient's body.
An SMA element with an Af temperature adjusted above body temperature will remain in a state of stable martensite in the human body if unconstrained. At body temperature, an SMA element in this condition will not recover to an original programmed shape upon loading and unload. If sufficiently loaded, its shape will be altered and it will remain in the new shape. In this bending process, SMA comprising primarily nickel and titanium, as described above, work hardens at a high rate, which increases the alloy's effective stiffness and strength. A device that is self-actuating must avoid these problems if it is to be practical for use in modifying the annulus of a mitral valve to correct mitral valve leakage. Accordingly, such a device should be formed using an SMA that is super-elastic at body temperatures, so that when unloaded, the device will recover to its programmed shape when unloaded within the body of a patient.
The present invention takes advantage of the coronary sinus being adjacent to the mitral annulus, and the properties of SMAs that are conditioned to a state of UM. Using the present invention, mitral valve repair can be carried out using catheter-guided techniques to deploy a device within the coronary sinus, so that the device self actuates when released from a constraint.
According to the present invention, a device for treatment of mitral insufficiency is sized so as to be capable of insertion into the coronary sinus and is formed at least in part of an SMA having two states. In a first state, the device has a shape adaptable to fit the shape of the coronary sinus, but when allowed to transform to the second state, the device assumes a second shape that enables a force to be applied to modify the mitral valve annulus in a way that reduces mitral valve regurgitation. The transformation from the first shape to the second shape is facilitated at least partially by utilizing the release of strain energy as the device or a portion thereof is unconstrained and allowed to change from a state of UM to a lower strain condition. Thus, the device may change to an austenite state upon being unloaded. UM is generally induced at strain levels above about 1.0%, and more typically, at strain levels above about 1.5%.
As used herein, the term “coronary sinus” is meant to refer to not only the coronary sinus itself, but in addition, to encompass the venous system associated with the coronary sinus, including the great cardiac vein, the coronary sinus, the junction between the cardiac vein and the coronary sinus, and the right atrium of the human heart. The present invention is intended to be delivered into the coronary sinus, because the coronary sinus is advantageously located adjacent to the mitral valve of the human heart and in a location to which the device can be maneuvered through peripheral vasculature, using common or custom catheter-based instruments, without the need for an open chest operation.
According to another aspect of the present invention, a method of altering the shape of the mitral valve annulus includes the steps of inserting a device at least partially comprising an SMA constrained in a state of UM, into the coronary sinus, and releasing the constraint to allow the device to recover towards a previously programmed shape and lower strain state. In yet another aspect of the invention, a force is applied to the device while it is positioned in the coronary sinus so as to adjust the intrinsic stiffness and shape of the device and thereby alter the shape of the coronary sinus to modify the shape of the mitral valve annulus.
Preferably, the device is formed from an SMA that has been treated so that it is super-elastic within the body of a patient. The super-elastic properties are employed by the device in its change of configuration between constrained and relaxed states. An appropriate treatment can involve a combination of cold working (for example by swaging, drawing or, in particular, by mandrel expansion) and heat treatment at a temperature that is less than the recrystallization temperature of the alloy while the device is constrained in the configuration resulting from the cold work. A plurality of the cold work and heat treatment steps can be used. The device can then be deformed towards the configuration of its first shape in its constrained first state, the deformation being recoverable and substantially elastic. In this way, deformations of up to 8% strain can be imparted and recovered substantially elastically.
Alloys from which the device can be made include Ni—Ti based alloys, especially Ni—Ti binary alloys, such as those in which the nickel content is at least about 50% at. %, and preferably, at least about 50.5 at. %. The nickel content will usefully be less than about 54 at. %, and preferably, less than about 52 at. %. The device may be produced from other Ni—Ti based alloys, including alloys with ternary and quaternary additions. Examples of other elements that can be incorporated as additions to the alloy include Fe, Co, Cr, Al, Cu, and V. Other elements can be present in amounts up to about 10 at. %, and preferably, up to about 5 at. %.
In still another aspect of the present invention, a device is defined for treatment of mitral insufficiency. The device has an elongate body with dimensions selected so that the device can readily be inserted into the coronary sinus and at least in part is formed of a material having two states, including a first state in which the device has a shape that is adaptable to fit the shape of the coronary sinus, and a second state in which the device is transformed from the said first state to assume a shape having either a reduced radius of curvature or an increased radius of curvature. The radius of curvature of the coronary sinus is thus modified by the device, as well as the radius of the circumference of the mitral valve annulus, when the elongate body is positioned in or through the coronary sinus. The distal and proximal ends of the device, and points in between, apply localized forces on the mitral annulus at one or more discrete locations.
The transformation from the first to the second state is facilitated through the use of SMA constrained in a UM state, utilizing the release of strain energy as the device or portion thereof is unconstrained and allowed to transform from UM to a lower strain condition (and in at least one embodiment, to transform to stable austenite) upon unloading. The constraining element can be a typical catheter, e.g., of the type commonly used to deliver devices such as arterial stents.
An optimal method to use the above-described device includes deploying the device and then assisting it into a more optimal shape using a drawstring (tether) or other element, to vary the length of the device along one side and thereby cause a curvature enhancement of the device. This mechanical assistance will alter the stiffness and enhance performance of the device by utilizing the BM effect of UM, as described above.
In another embodiment, the device includes one or more stents that are formed of SMA alloy having UM properties for self-deployment and adjustment. In this embodiment, the device may further include wires and/or spring elements for shortening the distance between the stent sections using UM properties. The stent sections may be actuated by force provided by balloon devices or they may be self-actuated by the transformation from UM, as described above. Stent radial stiffness and wire tension performance is adjustable using mechanical or balloon devices to enable a new stiffness condition using the BM effect of UM. The devices could optionally include dedicated anchor structures that apply a low expansive force against the wall of the coronary sinus.
In one preferred embodiment, the present invention is directed to an assembly that includes a tubular delivery device in which the mitral annulus shaping device is disposed and constrained, prior to insertion into a patient's body through a catheter. The constraint imparts a strain in excess of 1.5% on a region of the mitral valve annulus reshaping device so that it is UM at normal body temperature.
Still another aspect of the present invention is directed to a construction in which a mitral annulus shaping device can be constrained in a strained configuration for delivery into the coronary sinus within a hollow member, such as a catheter. A suitable catheter might be formed, for example, from a polymeric material that constrains the mitral annulus shaping device while disposed in the catheter, and which facilitates discharge of the mitral valve annulus reshaping device from the catheter.
The mitral valve annulus reshaping device can be discharged from the delivery device either by advancing the mitral annulus shaping device forward with respect to the delivery device, or by withdrawing the delivery device from the site at which the mitral annulus shaping device is being deployed.
The configuration of the delivery device is selected so that it can properly contain the mitral valve annulus reshaping device and withstand the elastic forces exerted by the device prior to discharge from the delivery device. Preferably, the delivery device has a minimum wall thickness necessary to satisfy these criteria. A constraint provided according to the present invention has the advantage of being thin-walled and flexible in bending, while also having sufficient radial stiffness to be able to withstand the forces exerted by the mitral annulus shaping device as it attempts to recover, even when these forces are applied over a long period of time, at temperatures above body temperature.
Preferably, the mitral valve annulus reshaping assembly includes means for facilitating release of the mitral valve annulus reshaping device from within the delivery device. For example, one of the contacting surfaces of the shaping device and the delivery device can be coated with a material that reduces friction effects between those surfaces.
The foregoing aspects and many of the attendant advantages of this invention will become more readily appreciated as the same becomes better understood by reference to the following detailed description, when taken in conjunction with the accompanying drawings, wherein:
To understand the present invention, it is necessary to understand austenite to martensite transformations that occur in a SMA and understand how SMA can be used advantageously in the coronary sinus for modifying the mitral valve annulus. After discussing these concepts, the disclosure will turn to specific devices, methods and assemblies of the present invention.
The key difference between the material properties of the SMAs shown in
UM can be produced in an SMA having an Af temperature set below body temperature by freezing the alloy to a temperature well below its Af temperature (so that it behaves like the material shown in
Moreover, by applying an external force to assist the mitral valve reshaping device to even further displace the surrounding coronary sinus tissue, the material stiffness of the SMA comprising the device can be adjusted and enhanced. For example, by assisting the SMA of the device to a lower strain state, such as a point F, the device can be stiffened using stored energy arising from the elasticity of the deformed tissue. As the assisting load is removed, the elastic recoil of the tissue will push the reshaping device towards a higher strain state, i.e., towards or beyond point G. The slope between F and G represents the new modulus of rigidity of this mitral valve annulus reshaping device. As the SMA in the device is allowed to relax to a lower strain state, its strain level will move onto the lower plateau curve. As the SMA is forced to a higher strain state, the strain level will move to the upper plateau curve. Therefore, by forcing the device to a higher or lower strain state, a mitral valve annulus reshaping device can be advantageously adjusted to a required stiffness to reshape the mitral valve annulus as needed to reduce mitral valve regurgitation. The ability to reversibly change between the austenitic and martensite states after the device has been deployed in the body of the patient provides greater flexibility and control of a mitral valve annulus modification using the present invention.
It will be understood that each of the embodiments discussed below can be implemented using SMA produced in accord with the preceding discussion. At least a portion of the SMA may be in an austenitic state when introduced into the body of a patient and then changed, at least partially, to a martensite state. Preferably, however, the SMA comprising the device will be constrained and introduced into the patient's body as UM. The UM state of the device can be achieved using any of the approaches discussed above.
Various known techniques can be employed for inserting a catheter into the coronary sinus through a venous incision to enable deployment of a mitral valve annulus device in accord with the present invention. For example, it is contemplated that the mitral valve annulus reshaping device can be constrained within a catheter in preparation for insertion within the coronary sinus, and the catheter can then be guided into the coronary sinus, using a guide wire or other appropriate means. Once thus in place, the reshaping device can either be pushed from the catheter, or the catheter can be pulled back, leaving the device in a desired position within the coronary sinus.
Once handle 48 has fully engaged and been locked onto control knob 44, the mitral valve annulus reshaping device should have been advanced to a point just within the distal end of catheter 40. Control knob 44 is then rotated in engagement with the threads on the outside of the cartridge, to advance the mitral valve annulus reshaping device from the constraint of catheter 40, into the coronary sinus of the patient. Thus, control knob 44 controls the advancement and deployment of a mitral valve annulus reshaping device within the coronary sinus. A release knob 50 is employed for uncoupling pusher cable 46 from the device after it has been fully deployed within the coronary sinus and adjusted as desired by the medical personnel using-the assembly. Once the mitral valve annulus reshaping device is fully disposed within the coronary sinus, catheter 40 is withdrawn from the patient's body.
While the mitral valve annulus reshaping device remains constrained within catheter 40, the shape memory alloy comprising the reshaping device at least partially remains as UM. The shape memory alloy comprising the device has a characteristic temperature, Af, that is below or equal the normal body temperature of the patient. Accordingly, the SMA is in a super-elastic state, and the device can readily be delivered into the coronary sinus through catheter 40 while constrained in the UM state. Because the SMA of the device is super-elastic, the device is readily deformed to a size that fits within the catheter and can be advanced into the coronary sinus. The interior surface of the distal portion of catheter 40 or the exterior surface of the mitral valve annulus reshaping device can be coated with a friction reducing material, such as a lubricating material or the catheter provided with a low friction lining material to facilitate deployment of the device from the distal end of the catheter.
The SMA comprising the mitral valve annulus reshaping device 60 at least partially converts from UM to its austenitic state once released from the constraint of the catheter as is illustrated in
Alternatively, the SMA of the device can be modified to have less stiffness. The reduced radius of curvature of the annulus in
As shown in
Prior to deploying and releasing the constraint on proximal anchor 110, the user will apply tension to a tether line 112. The tether line forms a double loop around and through the distal and proximal ends of helical coil spring 102. The tensile load resulting from the application of a tensile load on the tether line will cause straight wire sections 104 and 106 and helical coil spring 102 to form UM. The proximally applied tension in the tether line pulls the distal anchor, straight wire section 104, and tissue distal to the helical coil spring in the proximal direction. The helical coil spring will thus be assisted to relax to its tightly wound programmed shape, which is therefore at a lower strain state. Upon release of the tension produced by the tether line, elastic tissue recoil and internal heart pressure will load the previously relaxed helical coil spring and transform the spring stiffness to a higher level. Thus, by applying tensile load to the tether line, the reshaping device spring stiffness and length are adjusted to an appropriate level required to reshape adjacent tissue and the mitral valve annulus, and thereby reduce mitral valve regurgitation. Also, the tension applied to tether line 112 determines the force applied against the adjacent tissue to modify the shape annulus 32, before the final disposition of proximal anchor 110 is determined.
Yet another embodiment of the present invention is shown in
A tether 146 passes through loop 144, and both ends of the tether extend outside the patient's body through the venous system within the catheter (not shown), enabling medical personnel to apply tension to the tether after the distal end of arched leaf spring 140 has been deployed within the coronary sinus and anchored by loop 142. Using tether 146, it is possible to applying loading tension to arched leaf spring 140, thereby adjusting the stiffness of the arched leaf spring and the relative force applied by the device against the adjacent tissue and mitral valve annulus, prior to releasing loop 144 from the constraint of the catheter. The applied tension tends to straighten arched leaf spring 140, so that it has a greater radius of curvature, R′, as shown in
Each of the embodiments disclosed above illustrates how SMA and its super-elasticity can be applied in modifying the shape of the annulus and thereby correcting defects in a mitral valve within the body of a patient. The characteristics of the SMA comprising each of these embodiments, as illustrated in
Although the present invention has been described in connection with the preferred form of practicing it, those of ordinary skill in the art will understand that many modifications can be made thereto within the scope of the claims that follow. Accordingly, it is not intended that the scope of the invention in any way be limited by the above description, but instead be determined entirely by reference to the claims that follow.