METHOD AND APPARATUS FOR RESECTING AND REPLACING AN AORTIC VALVE
Apparatus for resecting a diseased heart valve, the apparatus comprising: a body portion; a first handle and a second handle; a cutting blade; a set of retaining arms; a pass-off tool having a first attachment device configured to selectively engage the first handle attached to the body portion so as to allow placement of the second handle of the body portion adjacent to the diseased heart valve, and a controller tool having a second attachment device at the distal end thereof, the second attachment device configured to selectively engage the second handle attached to the body portion so as to allow positioning of the body portion adjacent to the diseased heart valve, a cutting blade actuator configured to cause the cutting blade to selectively rotate, and a retaining arm actuator configured to selectively position the set of retaining arms from the contracted state to the expanded state.
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The present application is a continuation of U.S. application Ser. No. 11/784,438, filed on Apr. 6, 2007; which is a divisional of U.S. application Ser. No. 10/414,741, filed, on Apr. 16, 2003, now granted as U.S. Pat. No. 7,201,761; which is a continuation-in-part of U.S. application Ser. No. 09/896,259, filed on Jun. 29, 2001, now granted as U.S. Pat. No. 6,769,434; all of which are incorporated by reference herein, in their entirety.
The present application claims priority to the following provisional applications via U.S. application Ser. No. 10/414,741:
U.S. Provisional Patent Application Ser. No. 60/373,042, filed on Apr. 16, 2002; and U.S. Provisional Patent Application Ser. No. 60/425,891, filed on Nov. 13, 2002; all of which are incorporated by reference herein, in their entirety.
FIELD OF THE INVENTIONThis invention relates to apparatus and methods for performing cardiac surgery in general, and more particularly to apparatus and methods for performing cardiac surgery while the heart is beating,
BACKGROUND ARTOf all valvular heart lesions, aortic stenosis carries the worst prognosis. Within one year of diagnosis, approximately half of all patients with critical aortic stenosis have died, and by three years, this figure rises to approximately 80%. Currently, the most prominent and effective treatment for patients with aortic stenosis is aortic valve replacement via open heart surgery. Unfortunately, this procedure is a substantial and invasive undertaking for the patient.
While there have been significant advances in heart valve technology over the past 30 years, there has been little progress in the development of safer and less invasive valve delivery systems. Aortic valve replacement currently requires a sternotomy or thoracotomy, use of cardiopulmonary bypass to arrest the heart and lungs, and a large incision on the aorta. The native valve is resected through this incision and then a prosthetic valve is sutured to the inner surface of the aorta with a multitude of sutures passing only partly into the wall of the aorta. Given the current invasiveness of this procedure and the requirement to utilize cardiopulmonary bypass, aortic valve replacement surgery is associated with a high risk of morbidity and mortality. This is especially true in elderly patients, and in those patients who require concomitant coronary artery bypass grafting. Even when a good surgical result is achieved, virtually all patients require approximately 6 weeks to several months to fully recover from the procedure. In order to decrease these associated risks of aortic valve surgery, many have pursued novel approaches and technologies.
Less invasive approaches to aortic valve surgery have generally followed two paths.
In the 1980's, there was a flurry of interest in percutaneous balloon valvotomy. In this procedure, a cardiologist introduced a catheter through the femoral artery to dilate the patient's aortic valve, thereby relieving the stenosis. Using the technology available at that time, success was limited: the valve area was increased only minimally, and nearly all patients had restenosis within one year.
More recently, surgeons have approached the aortic valve via smaller chest wall incisions. However, these approaches still require cardiopulmonary bypass and cardiac arrest, which themselves entail significant morbidity and a prolonged post-operative recovery.
The ideal minimally invasive approach to the treatment of aortic valve disease requires aortic valve replacement without cardiopulmonary bypass and without cardiac arrest. Such an approach would greatly reduce patient morbidity and mortality and hasten recovery. Unfortunately, although there has been great progress in the treatment of coronary artery disease without cardiopulmonary bypass (e.g., angioplasty, with or without stenting, and “off-pump” coronary artery bypass grafting), similar advances have not yet been realized in heart valve surgery. With an aging population and improved access to advanced diagnostic testing, the incidence and accurate diagnosis of aortic stenosis will continue to increase. The development of a system for “off-pump” aortic valve replacement would be of significant benefit to this increasing patient population.
There are three important challenges to replacing a diseased aortic valve without cardiopulmonary bypass.
The first challenge is to remove the diseased valve without causing stroke or other ischemic events that might result from the liberation of particulate material while removing the diseased valve.
The second challenge is to prevent cardiac failure during removal of the diseased valve. In this respect it must be appreciated that the aortic valve continues to serve a critical function even when it is diseased. However, as the diseased valve is removed, it becomes acutely and severely incompetent, causing the patient to develop heart failure which results in death unless the function of the valve is taken over by another means.
The third challenge is placing a prosthetic valve into the vascular system and affixing it to the wall of the aorta. More particularly, during cardiac rhythm, the aortic and arterial pressures are substantially greater than atmospheric pressure. Therefore, any sizable incision made to the aorta in order to insert a standard valve prosthesis into the arterial system creates the potential for uncontrollable bleeding from the incision site. Furthermore, even if bleeding is successfully controlled, pressures within the aorta may result in weakening of the aorta caused by aortic wall dissection. In addition, large incisions on the aorta also increase the potential for liberating plaque from the aortic wall that can lead to embolic complications.
For these reasons, prior art valve prostheses potentially suitable for off-pump implantation have relied upon relatively flimsy expandable structures to support and secure the valve within the aorta. More particularly, these prosthetic valves are constructed so that they can be compressed to a relatively small dimension suitable for insertion into the arterial system, advanced to the site of the aortic valve, and then expanded against the aortic wall. Unfortunately, however, none of these relatively flimsy valve prostheses have proven adequate to endure the repetitive stresses undergone by the aortic valve over the ten to twenty years typically required.
In addition to the foregoing, the precise placement of such expandable prosthetic valves in the correct sub-coronary position can be extremely challenging, particularly in view of the high pressure, pulsatile blood flow passing through the aorta. Furthermore, expandable prosthetic valves would typically be positioned from a remote artery, which would reduce the ability to precisely control the placement and positioning of the device and therefore would increases the risk of obstructing the coronary arteries. The expandable prosthetic valves are held on the ends of elongate, flexible catheters that are threaded into the aorta, around the aortic arch and then expanded. The pulsatile flow during cardiac rhythm induces a to-and-fro motion of the valve prosthesis relative to the aorta that makes the timing of valve expansion critical for proper placement of the expandable prosthetic valve and hence the survival of the patient.
Finally, many of the challenges discussed in the foregoing section pertaining to aortic valve replacement are also relevant to other procedures in the aortic root such as aortic valve resection, aortic valve decalcification, stem grafting for aortic dissections, etc,
SUMMARY OF THE INVENTIONIt is, therefore, one object of the present invention to enable the passage of a device from the left atrium, through the left ventricle, and into the arterial system.
Further, another object of the present invention is to enable the implantation of a device in the arterial system without cardiopulmonary bypass.
Further, another object of the present invention is to enable the implantation of a prosthetic valve in the arterial system without cardiopulmonary bypass.
Another object of the present invention is to allow the insertion of such a valve while minimizing the risks to the patient posed by large arterial incisions.
And another object of the present invention is to simplify the precise placement of such a valve.
Further, another object of the present invention is to enable the implantation of a device other than a valve, such as but not limited to a valve resection tool, a decalcifying tool, an aortic valve repair tool, or a stented aortic graft, in the arterial system without cardiopulmonary bypass.
Another object of the present invention is to allow the insertion of a device other than a valve, such as but not limited to a valve resection tool, a decalcifying tool, an aortic valve repair tool, or a stented aortic graft, while minimizing the risks to the patient posed by large arterial incisions.
And another object of the present invention is to simplify the precise placement of a device other than a valve, such as but not limited to a valve resection tool, a decalcifying tool, an aortic valve repair tool, or a stented aortic graft.
The present invention relates to a method and apparatus for positioning a device in the arterial system. More specifically, the present invention relates to a method and apparatus for positioning an aortic valve prosthesis in the aorta or aortic outflow tract, with or without cardiopulmonary bypass.
One aspect of the present invention is a method for deploying an aortic valve prosthesis. This valve prosthesis may include any of the known aortic valves including, but not limited to, stented and unstented bioprosthetic valves, stented mechanical valves, and expandable or self-expanding valves, whether biological or artificial.
In one aspect of the invention, there is provided a method of inserting a prosthesis or device from a lower pressure region into a higher pressure region of the cardiovascular system comprising the steps of: making an opening in a wall of a lower pressure region of the cardiovascular system; advancing the prosthesis or device through the opening and into the lower pressure region; and advancing the prosthesis or device through a natural barrier between the lower pressure region and the higher pressure region.
In another aspect of the invention, there is provided a method of inserting a prosthesis or device into a vessel within the arterial system comprising the steps of: making an opening in a wall of a low pressure region of the heart; advancing the prosthesis or device through the opening and into the low pressure region; advancing the prosthesis or device through a natural barrier between the low pressure region and the left ventricle; and advancing the prosthesis or device from the left ventricle into the arterial system and the vessel.
And in another aspect of the invention, there is provided a method of inserting a prosthesis or device into a vessel within the arterial system comprising the steps of: making an opening in a wall of the left atrium; advancing the prosthesis or device through the opening and into the left atrium; advancing the prosthesis or device through the mitral valve and into the left ventricle; and advancing the prosthesis or device from the left ventricle into the arterial system and the vessel.
And in another aspect of the present invention, there is provided a method for positioning a device in the arterial system comprising the steps of: making a first opening leading to the left atrium; passing a valve prosthesis through the first opening and into a cardiac chamber of the left side of the heart using a first manipulation instrument; making a second opening in the arterial system and advancing one end of a second manipulation instrument through the second opening and into the aforementioned cardiac chamber; securing the second manipulation instrument to the valve prosthesis; and then using the second manipulation instrument to retract at least some portion of the valve prosthesis out of the aforementioned cardiac chamber.
An alternative method for positioning a device in the arterial system comprises the steps of: making an opening leading to the left atrium; passing a valve prosthesis through the opening and into a cardiac chamber of the left side of the heart using an articulating manipulation instrument; using the articulating manipulation instrument to guide the valve prosthesis into the arterial cardiac chamber; releasing the valve prosthesis into a desired position; and then retracting at least a portion of the articulating manipulation instrument out of the aforementioned cardiac chamber and left atrium.
The pressure of blood flowing through the left atrium is very low, peaking at a few inches of water during the cardiac cycle. This pressure is a small fraction of that found within the arterial system and thus permits insertion of a conventional valve prosthesis through a relatively large opening formed in the wall of the left atrium without the risk of uncontrollable bleeding. In this respect it will be appreciated that various methods are known to those skilled in the art for controlling bleeding from an incision into the left atrium. The left atrium also rarely suffers from atherosclerotic plaque formation or calcification, thus minimizing the risk of embolic debris during such incision.
Another aspect of the present invention is the use of a prosthesis holding apparatus for releasably holding the valve prosthesis during manipulation to its implant site. The prosthesis holding apparatus may be secured to the prosthetic valve at any suitable location(s) through the use of any of a variety of approaches including, but not limited to, suture loops, barbs, hooks, grasping jaws, opposing magnetic poles, friction fits and the like. The prosthesis holding apparatus is configured to provide first and second manipulation mounts for engagement by the aforementioned first and second manipulation instruments, respectively, whereby the prosthetic valve can be delivered to its implant site. This construction is highly advantageous in that it permits the valve prosthesis to be passed easily and reliably from the first manipulation instrument to the second manipulation instrument within the vascular system.
In an alternative preferred embodiment, the prosthetic holding apparatus is attached on the ventricular side of the prosthesis. The aforementioned first manipulation instrument would articulate at or near the prosthetic valve to facilitate manipulation of the prosthesis holding apparatus (and hence the prosthesis itself) through the smallest possible incision site, then through the left atrium, the mitral valve and within the heart to align and position the prosthesis within the aortic annulus or left ventricular outflow track. In this alternative embodiment, there is no need for the aforementioned second manipulation instrument or the second manipulation mount.
In addition, if the prosthesis holding apparatus is attached on the aortic side of the prosthesis, the manipulation instrument may articulate and may be introduced into the arterial system, brought across the mitral valve into the left atrium, out the left atrium to pick up the prosthesis holding apparatus (and hence the prosthesis) and then retracted back to position the prosthesis directly into the aortic annulus without the need for another manipulation instrument.
In another form of the present invention, there is provided an apparatus for resetting a diseased heart valve, the apparatus comprising:
a first frame member and a second frame member configured in opposition to one another;
a cutting edge configured on the first frame member;
an adjustable connector positionably joining the first frame member to the second frame member, the adjustable connector configured to selectively position the first frame member and the second frame member between a first position and a second position, wherein the first frame member and the second frame member are positioned apart from one another in the first position so as to allow at least a portion of the diseased heart valve therebetween, and the first frame member and the second frame member are positioned together in the second position so as to cut the at least a portion of the diseased heart valve therebetween with the cutting blade so as to resect the diseased heart valve;
an actuator configured in operable connection to the adjustable connector, the actuator configurable to selectively position the adjustable connector between the first position and the second position; and
a first screen portion and a second screen portion disposed on the first frame portion and the second frame portion, respectively, the first screen portion and the second screen portion configured to allow blood flow through first frame member and second frame member and to contain the at least a portion of the diseased heart valve between the first frame member and the second frame member.
In another form of the present invention, there is provided a method of resecting diseased heart valve, the method comprising:
providing apparatus for resecting the diseased heart valve, the apparatus comprising:
a first frame member and a second frame member configured in opposition to one another;
a cutting edge configured on the first frame member;
an adjustable connector positionably joining the first frame member to the second frame member, the adjustable connector configured to selectively position the first frame member and the second frame member between a first position and a second position, wherein the first frame member and the second frame member are positioned apart from one another in the first position so as to allow at least a portion of the diseased heart valve therebetween, and the first frame member and the second frame member are positioned together in the second position so as to cut the at least a portion of the diseased heart valve therebetween with the cutting blade so as to resect the diseased heart valve;
an actuator configured in operable connection to the adjustable connector, the actuator configurable to selectively position the adjustable connector between the first position and the second position; and
a first screen portion and a second screen portion disposed on the first frame portion and the second frame portion, respectively, the first screen portion and the second screen portion configured to allow blood flow through first frame member and second frame member and to contain the at least a portion of the diseased heart valve between the first frame member and the second frame member;
positioning the first frame member and the second frame member on opposed sides of the diseased heart valve, with the first frame member and the second frame member in the first position;
closing the first frame member and the second frame member from the first position to the second position by manipulating the actuator in operable connection to the adjustable connector so as to move the cutting edge through the at least a portion of the diseased heart valve; and
removing from a patient the first frame member and the second frame member closed together in the second position, with the at least a portion of the diseased heart valve therebetween.
In another form of the present invention, there is provided a method of resecting a diseased heart valve, the method comprising:
positioning a first frame member and a second frame member on opposed sides of the diseased heart valve, with the first frame member and the second frame member positioned apart from one another;
dosing the first frame member and the second frame member toward one another so as to pass a cutting edge disposed on the first frame member through at least a portion of the diseased heart valve; and
removing from the patient the first frame member and the second frame member closed together, with the at least a portion of the diseased heart valve therebetween.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a power shaver having a proximal end and a distal end, the power shaver defining a longitudinal axis from the proximal end to the distal end, and a cutting element disposed adjacent to the distal end of the power shaver; and
a power shaver guide having a first end and a second end in opposition to one another, the power shaver guide defining a first opening extending into the first end, the first opening defining a first axis from the first end of the power shaver guide to the second end of the power shaver guide, the first opening configured to receive a portion of the power shaver therein, the power shaver guide having a given width from the first opening to an outer surface in a direction perpendicular to the first axis, the given width of the power shaver guide configured to prevent the wall of a cardiovascular structure from being cut by the power shaver disposed within the first opening and to permit the power shaver to be placed within the diseased valve.
In another form of the present invention, there is provided a method for resecting a diseased heart valve comprising:
providing apparatus for resecting the diseased heart valve, the apparatus comprising:
a power shaver having a proximal end and a distal end, the power shaver defining a longitudinal axis from the proximal end to the distal end, and a cutting element disposed adjacent to the distal end of the power shaver; and
a power shaver guide having a first end and a second end in opposition to one another, the power shaver guide defining a first opening extending into the first end, the first opening defining a first axis from the first end of the power shaver guide to the second end of the power shaver guide, the first opening configured to receive a portion of the power shaver therein, the power shaver guide having a given width from the first opening to an outer surface in a direction perpendicular to the first axis, the given width of the power shaver guide configured to prevent the wall of a cardiovascular structure from being cut by the power shaver disposed within the first opening and to permit the power shaver to be placed within the diseased valve;
positioning the power shaver within the power shaving guide;
positioning the power shaver and power shaving guide through a cardiovascular structure to the diseased heart valve; and
cutting the diseased valve with the cutting element of the power shaver so as to resect the diseased heart valve.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a set of at least three expandable arms having a proximal end and a distal end in opposition to one another, the set of expandable arms defining a longitudinal axis from the proximal end to the distal end;
a first restraining element and a second restraining element configured at the proximal end of the set of expandable arms and the distal end of the set of at least three expandable arms, respectively, the first restraining element and the second restraining element configured to selectively position the set of at least three expandable arms between a first position and a second position, the set of at least three expandable arms having a given width in a perpendicular direction to the longitudinal axis at the first position and having a larger width in the perpendicular direction to the longitudinal axis at the second position; and
a cutting device disposed on at least one of the at least three expandable arms, the cutting device configured to cut through the diseased heart valve.
In another form of the present invention, there is provided a method for resecting a diseased heart valve, the apparatus comprising:
providing apparatus for resecting the diseased heart valve, the apparatus comprising:
a set of at least three expandable arms having a proximal end and a distal end in opposition to one another, the set of expandable arms defining a longitudinal axis from the proximal end to the distal end;
a first restraining element and a second restraining element configured at the proximal end of the set of expandable arms and the distal end of the set of at least three expandable arms, respectively, the first restraining element and the second restraining element configured to selectively position the set of at least three expandable arms between a first position and a second position, the set of at least three expandable arms having a given, width in the perpendicular direction to the longitudinal axis at the first position and having a larger width in the perpendicular direction to the longitudinal axis at the second position; and
a cutting device disposed on at least one of the at least three expandable arms, the cutting device configured to cut through the diseased heart valve;
positioning the set of at least three expandable arms adjacent to the diseased heart valve;
expanding the set of at least three expandable arms from the first position to the second position; and
cutting the diseased heart valve with the cutting device disposed on the at least one of the at least three expandable arms.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising;
a first frame member and a second frame member configured in opposition to one another;
a cutting edge configured on the first frame member;
an adjustable connector positionably joining the first frame member to the second frame member, the adjustable connector configured to selectively position the first frame member and the second frame member between a first position and a second position, wherein the first frame member and the second frame member are positioned apart from one another in the first position so as to allow at least a portion of the diseased heart valve therebetween, and the first frame member and the second frame member are positioned together in the second position so as to cut the at least a portion of the diseased heart valve therebetween with the cutting blade so as to resect the diseased heart valve;
an actuator configured in operable connection to the adjustable connector, the actuator configurable to selectively position the adjustable connector between the first position and the second position; and
at least two spikes extending from the first frame member toward the second frame member, the at least two spikes being configured to pierce and secure leaflets of the diseased heart valve as the first frame member and the second frame member are positioned toward one another.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a catheter having a proximal end and a distal end, the catheter defining a longitudinal axis from the proximal end to the distal end; and
a set of blades positionably configurable at the distal end of the catheter, a hinge mechanism holding the distal end of the set of blades together, and a control rod extending from the proximal end of the blades into the catheter, the control rod being configured to selectively position the set of blades from a first position within the catheter to a second position outside of the distal end of the catheter, to selectively expand the set of blades from a narrow width for disposition within the catheter to a wide width for cutting portions of the diseased heart valve with the set of blades, and to rotate the set of blades with respect to the longitudinal axis of the catheter.
In another form of the present invention, there is provided a method of resecting diseased heart valve, the method comprising:
providing apparatus for resecting the diseased heart valve, the apparatus comprising:
a catheter having a proximal end and a distal end, the catheter defining a longitudinal axis from the proximal end to the distal end; and
a set of blades positionably configurable at the distal end of the catheter, a hinge mechanism holding the distal end of the set of blades together, and a control rod extending from the proximal end of the blades into the catheter, the control rod being configured to selectively position the set of blades from a first position within the catheter to a second position outside of the distal end of the catheter, to selectively expand the set of blades from a narrow width for disposition within the catheter to a wide width for cutting portions of the diseased heart valve with the set of blades, and to rotate the set of blades with respect to the longitudinal axis of the catheter;
placing distal end of the catheter adjacent to the diseased heart valve;
positioning the set of blades from the first position within the catheter to the second position outside of the distal end of the catheter;
expanding the set of blades from the narrow width for disposition within the catheter to the wide width for cutting portions of the diseased heart valve with the set of blades; and
rotating the set of blades with respect to the longitudinal axis of the catheter so as to cut through the diseased heart valve.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a catheter having a proximal end and a distal end, and the catheter defining a longitudinal axis from the proximal end to the distal end;
a control rod having a proximal end and a distal end, the control rod being selectively positionable through the catheter and being selectively rotatable with respect to the longitudinal axis of the catheter;
an outer shell portion having a first edge and a second edge in opposition to one another, the outer shell portion having an inwardly facing side and an outwardly facing side in opposition to one another, the first edge of the outer shell portion being attached to the control rod along a surface thereof parallel to the longitudinal axis of the catheter, and the outer shell portion adapted to be wound around the control rod; and
a spring having a first end and a second end, the first end of the spring being attached to the inwardly facing side of the outer shell portion adjacent to the second edge thereof, and the spring being disposed against the inwardly facing side of the outer shell portion;
wherein rotation of the control rod in a first direction in combination with a force applied by the spring contracts the outer shell portion toward the control rod so as to reduce a maximum outer diameter of the outer shell in a given direction perpendicular to the longitudinal axis of the catheter, and rotation of the control rod in a second direction in combination with the force applied by the spring rolls the outer shell portion away from the control rod so as to expand the maximum outer diameter of the outer shell portion in the given direction perpendicular to the longitudinal axis of the catheter.
In another form of the present invention, there is provided a method for resecting a diseased heart valve, the method comprising:
providing apparatus for resecting a diseased heart valve, the apparatus comprising:
a catheter having a proximal end and a distal end, and the catheter defining a longitudinal axis from the proximal end to the distal end;
a control rod having a proximal end and a distal end, the control rod being selectively positionable through the catheter and being selectively rotatable with respect to the longitudinal axis of the catheter;
an outer shell portion having a first edge and a second edge in opposition to one another, the outer shell portion having an inwardly facing side and an outwardly facing side in opposition to one another, the first edge of the outer shell portion being attached to the control rod along a surface thereof parallel to the longitudinal axis of the catheter, and the outer shell portion adapted to be wound around the control rod; and
a spring having a first end and a second end, the first end of the spring being attached to the inwardly facing side of the outer shell portion adjacent to the second edge thereof, and the spring being disposed against the inwardly facing side of the outer shell portion;
positioning the distal end of the catheter adjacent to the diseased heart valve;
rotating the control rod in the second direction so as to expand the outer shell portion; and
withdrawing the apparatus from the human body.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a tubular body having a proximal end and a distal end, the tubular body defining a longitudinal axis from the proximal end to the distal end; and
an auger blade disposed within the tubular body and configured to selectively rotate with respect to the longitudinal axis of the tubular body;
the tubular body defining an opening configured therein so as to allow portions of the diseased heart valve therein, and the opening defining a junction region at a location where the auger blade contacts the tubular body and cuts the portions carried by the auger blade thereto.
In another form of the present invention, there is provided a method for resecting a diseased heart valve, the method comprising:
positioning an opening of a tubular body adjacent to the diseased heart valve; and
cutting the diseased heart valve with an auger blade rotating within the tubular body.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
an inner rod having a proximal end and a distal end, the inner rod defining a longitudinal axis from the proximal end to the distal end, and the inner rod defining a first opening and a second opening in a lateral side thereof between the proximal end and the distal end;
a first outer shell and a second outer shell each having a selectively configurable length through the first opening and the second opening of the inner rod, respectively, the first outer shell and the second outer shell configured to be radially expandable depending on the length of the first outer shell and the second outer shell configured through the first opening and the second opening, respectively; and
a blade extending between the first outer shell and the second outer shell, the blade being radially expandable away from the inner rod together with the first outer shell.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
an inner cylinder having an outer tube rotatably disposed thereto, the inner cylinder and outer tube having a distal end and a proximal end, and the inner cylinder defining a longitudinal axis from the distal end to the proximal end;
at least one barb extending away from the distal end of the inner cylinder; and
three blades pivotally attached to the distal end of the outer tube, the three blades being selectively configurable in a first position and a second position, the first position configured with the blades closed toward one another so as to cover the at least one barb and provide a narrow cross-section therethrough in a perpendicular direction to the longitudinal axis, and a second position configured with the blades opened away from one another so as to expose the at least one barb and provide a cutting diameter having a greater cross-section therethrough than the narrow cross-section in the perpendicular direction to the longitudinal axis;
wherein the three blades are positioned closed toward one another through a body to a location adjacent to a diseased heart valve, the three blades are opened away from one another so as to expose the at least one barb extending away from the distal end of the inner cylinder, the inner cylinder is positioned toward the diseased heart valve so as to spear the at least one barb therethrough, and the outer tube is rotated around the inner cylinder so as to rotate the three blades to cut the diseased valve.
In another form of the present invention, there is provided a method for resecting a diseased heart valve, the method comprising:
providing apparatus for resecting a diseased heart valve, the apparatus comprising:
an inner cylinder having an outer tube rotatably disposed thereto, the inner cylinder and outer tube having a distal end and a proximal end, and the inner cylinder defining a longitudinal axis from the distal end to the proximal end;
at least one barb extending away from the distal end of the inner cylinder; and
three blades pivotally attached to the distal end of the outer tube, the three blades being selectively configurable in a first position and a second position, the first position configured with the blades closed toward one another so as to cover the at least one barb and provide a narrow cross-section thereto in a perpendicular direction to the longitudinal axis, and a second position configured with the blades opened away from one another so as to expose the at least one barb and provide a cutting diameter having a greater cross-section therethrough than the narrow cross-section in the perpendicular direction to the longitudinal axis;
wherein the three blades closed toward one another through a body to a location are positioned adjacent to a diseased heart valve, the three blades are opened away from one another so as to expose the at least one barb extending away from the distal end of the inner cylinder, the inner cylinder is positioned toward the diseased heart valve so as to spear the at least one barb therethrough, and the outer tube is rotated around the inner cylinder so as to rotate the three blades to cut the diseased valve;
positioning the three blades toward the diseased heart valve;
opening the three blades away from one another so as to expose the at least one barb; spearing the at least one barb through the diseased heart valve; and
rotating the three blades so as to cut the diseased valve.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a chamber having a proximal end and a distal end, and a sidewall extending between the proximal end and the distal end;
a retractable barb selectively positionable between a first position and a second position, the retractable bar being configured within the distal end of chamber in the first position, and the retractable bar being configured to extend beyond the distal end of the chamber in the second position; and
a set of blades surrounding the distal end of the chamber;
wherein the retractable barb extends from the chamber, pierces a portion of the diseased heart valve, and retracts into the chamber; and
wherein the set of blades cuts through the portion of the diseased heart valve pierced by the retractable barb as the retractable barb retracts into the chamber.
In another form of the present invention, there is provided a method for resecting a diseased heart valve, the method comprising:
providing apparatus for resecting the diseased heart valve, the apparatus comprising:
a chamber having a proximal end and a distal end, and a sidewall extending between the proximal end and the distal end;
a retractable barb selectively positionable between a first position and a second position, the retractable bar being configured within the distal end of chamber in the first position, and the retractable bar being, configured to extend beyond the distal end of the chamber in the second position; and
a set of blades surrounding the distal end of the chamber;
wherein the retractable barb extends from the chamber, pierces a portion of the diseased heart valve, and retracts into the chamber; and
wherein the set of blades cuts through the portion of the diseased heart valve pierced by the retractable barb as the retractable barb retracts into the chamber;
positioning the distal end of the chamber adjacent to the diseased heart valve;
extending the retractable barb from the chamber;
piercing the portion of the diseased heart valve with the retractable barb;
retracting the retractable barb into the chamber; and
cutting through the portion of the diseased heart valve pierced by the retractable barb with the set of blades.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a body portion having a proximal end and a distal end, the body portion defining a longitudinal axis from the proximal end to the distal end, and the body portion defining an opening at the distal end thereof;
a grasping tool being selectively positionable within the body portion along the longitudinal axis from a first position to a second position, the grasping tool being configured within the body portion in the first position, the grasping tool extending through the opening at the distal end of the body portion in the second position, and the grasping tool being configured to selectively close together a first portion and a second portion so as to selectively grip the diseased heart valve therebetween; and
a cutting element disposed within the body portion at a given distance from the opening, the cutting element configured to close together to cut the diseased heart valve therebetween at the given distance from the opening after the grasping tool is withdrawn to a given location between the cutting element and the proximal end of the body portion;
wherein a portion of the diseased heart valve portion cut away from an intact portion of the diseased heart valve is contained within the body portion.
In another form of the present invention, there is provided a method of resecting a diseased heart valve, the method comprising:
providing apparatus for resecting the diseased heart valve, the apparatus comprising:
a body portion having a proximal end and a distal end, the body portion defining a longitudinal axis from the proximal end to the distal end thereof, and the body portion defining an opening at the distal end;
a grasping tool being selectively positionable within the body portion along the longitudinal axis from a first position to a second position, the grasping tool being configured within the body portion in the first position, the grasping tool extending through the opening at the distal end of the body portion, and the grasping tool being configured to selectively close together a first portion and a second portion so as to selectively grip the diseased heart valve therebetween; and
a cutting element disposed within the body portion at a given distance from the opening, the cutting element configured to close together to cut the diseased heart valve therebetween at the given distance from the opening after the grasping tool is withdrawn to a given location between the cutting element and the proximal end of the body portion;
wherein a portion of the diseased heart valve portion cut away from an intact portion of the diseased heart valve is contained within the body portion;
positioning the distal end of the body portion adjacent to the diseased heart valve;
extending the grasping tool through the opening in the body portion to the diseased heart valve portion;
closing the first portion and the second portion of the grasping tool toward one another so as to secure a portion of the diseased heart valve therebetween;
retracting the grasping tool into the body element past the cutting element to the given location between the cutting element and the proximal end of the body portion so as to allow the cutting element to close and cut the portion of the diseased heart valve at the given distance from the opening.
In another form of the present invention, there is provided an apparatus for resetting a diseased heart valve, the apparatus comprising;
a body portion having a first end and a second end in opposition to one another, a lateral wall extending from the first end to the second end, the lateral wall defining an inner surface and an outer surface in opposition to one another, the inner surface and the outer surface defining arcuate surfaces, respectively, and the body portion defining a longitudinal axis from the first end to the second end;
a first handle and a second handle attached to the body portion to extend from the first end thereof and the second end thereof, respectively;
a cutting blade selectively rotatable about the longitudinal axis and disposed adjacent to the inner surface of the body portion;
a set of retaining arms positionably mounted between the second handle and the second end of the body portion, the set of retaining arms being selectively positionable from a contracted state to an expanded state, the contracted state forming a first diameter having a first width in a direction perpendicular to the longitudinal axis of the body portion, the expanded state forming a second diameter having a second width in a direction perpendicular to the longitudinal axis of the body portion, the second width being larger than a first width of the first diameter in the direction perpendicular to the longitudinal axis of the body portion;
a pass-off tool having a proximal end and a distal end, a first attachment device at the distal end thereof, the first attachment device configured to selectively engage the first handle attached to the body portion so as to allow placement of the second handle of the body portion adjacent to the diseased heart valve; and
a controller tool having a proximal end and a distal end, a second attachment device at the distal end thereof, the second attachment device configured to selectively engage the second handle attached to the body portion so as to allow positioning of the second end of the body portion adjacent to the diseased heart valve, a cutting blade actuator configured to cause the cutting blade to selectively rotate relative to the longitudinal axis of the body portion, and a retaining arm actuator configured to selectively position the set of retaining arms from the contracted state to the expanded state.
In another form of the present invention, there is provided a method for resecting a diseased heart valve, the method comprising;
providing apparatus for resecting a diseased heart valve, the apparatus comprising:
a body portion having a first end and a second end in opposition to one another, a lateral wall extending from the first end to the second end, the lateral wall defining an inner surface and an outer surface in opposition to one another, the inner surface and the outer surface defining arcuate surfaces, respectively, and the body portion defining a longitudinal axis from the first end to the second end thereof;
a first handle and a second handle attached to the body portion to extend from the first end thereof and the second end, respectively;
a cutting blade selectively rotatable about the longitudinal axis and disposed adjacent to the inner surface of the body portion;
a set of retaining arms positionably mounted between the second handle and the second end of the body portion, the set of retaining arms being selectively positionable from a contracted state to an expanded state, the contracted state forming a first diameter having a first width in a direction perpendicular to the longitudinal axis of the body portion, the expanded state forming a second diameter having a second width in a direction perpendicular to the longitudinal axis of the body portion, the second width being larger than a first width of the first diameter in the direction perpendicular to the longitudinal axis of the body portion;
a pass-off tool having a proximal end and a distal end, a first attachment device at the distal end thereof, the first attachment device configured to selectively engage the first handle attached to the body portion so as to allow placement of the second handle of the body portion adjacent to the diseased heart valve; and
a controller tool having a proximal end and a distal end, a second attachment device at the distal end thereof, the second attachment device configured to selectively engage the second handle attached to the body portion so as to allow positioning of the second end of the body portion adjacent to the diseased heart valve, a cutting blade actuator configured to cause the cutting blade to selectively rotate relative to the longitudinal axis of the body portion, and a retaining arm actuator configured to selectively position the set of retaining arms from the contracted state to the expanded state;
engaging the first handle attached to the body portion with the pass-off tool;
positioning the second handle of the body portion adjacent to the diseased heart valve;
engaging the second handle attached to the body portion with the controller tool;
disengaging the pass-off tool and the first handle from one another;
positioning the second end of the body portion adjacent to the diseased heart valve;
expanding the set of retaining arms with the retaining arm actuator so as to hold the cut portion of the diseased heart valve within the body portion;
rotating the cutting blade relative to the longitudinal axis of the body portion with the cutting blade actuator;
positioning the body portion toward the diseased heart valve with the controller tool so as to cut the diseased heart valve.
In another form of the present invention, there is provided an apparatus for resecting a diseased heart valve, the apparatus comprising:
a cylindrical body portion having a first end and a second end;
a first handle and a second handle attached to the body portion to extend from the first end thereof and the second end thereof, respectively;
a cylindrical cutting blade selectively rotatable about the longitudinal axis and disposed within the body portion;
a set of retaining arms positionably mounted therebetween the second handle and the second end of the body portion, the set of retaining arms being selectively positionable from a contracted state to an expanded state, the contracted state forming a first diameter having a first width in a direction perpendicular to the longitudinal axis of the body portion, the expanded state forming a second diameter having a second width in a direction perpendicular to the longitudinal axis of the body portion, the second width being larger than a first width of the first diameter in the direction perpendicular to the longitudinal axis of the body portion.
These and other objects and features of the present invention will be more fully disclosed or rendered obvious by the following detailed description of the preferred embodiments of the invention, which is to be considered together with the accompanying drawings wherein like numbers refer to like elements and further wherein:
The present invention can be used to implant a variety of prostheses into the arterial system or left side of the heart. The prosthesis used in the preferred embodiment is an aortic valve prosthesis. Alternatively, the prosthesis may comprise, but is not limited to, a cylindrical arterial stent, an arterial prosthesis or graft, a ventricular assist device, a device for the treatment of heart failure such as an intraventricular counterpulsation balloon, chordae tendinae prostheses, arterial filters suitable for acute or chronic filtration of emboli from the blood stream, arterial occlusion devices and the like.
For clarity of illustration, the present invention will hereinafter be discussed in the context of implanting an aortic valve prosthesis.
It should also be appreciated that the present invention may be practiced either “on-pump” or “off-pump”. In other words, the present invention may be performed either with or without the support of cardiopulmonary bypass. The present invention also may be performed either with or without cardiac arrest.
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Prosthetic valve 200 is preferably a conventional mechanical aortic valve of the sort well known in the art, although other forms of valve prostheses may also be used.
In one preferred form of the invention, first manipulation instrument 400 functions by virtue of the relative motion of an outer cannula 405 relative to an inner grasper 410. More particularly, inner grasper 410 has an elastically deformable distal gripper 415 which is open when the gripper is outside of outer cannula 405. However, when deformable gripper 415 is pulled at least partially into or against outer cannula 405, gripper 415 is elastically deformed into a closed position, whereby it may grip an object, first manipulation mount 105 formed on prosthesis holding apparatus 100. First manipulation instrument 400 is shown in
The specific embodiment of first manipulation instrument 400 shown in
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First manipulation instrument 400 is also shown as having a relatively small dimension perpendicular to its long axis. This configuration allows atriotomy 10 to be reduced in size after the passage of temporary prosthetic assembly 300 into left atrium 5. This perpendicular dimension may be constant or varied along the long axis of first manipulation instrument 400.
The specific embodiment of the prosthesis holding apparatus 100 shown in
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When the methods and devices of the present invention are employed during an off-pump valve replacement procedure, it may be beneficial to provide temporary valves and/or filters in the arterial system, downstream of the site of the native aortic valve. Thus, for example, in
Bleeding through incision 35 may be readily controlled through a variety of means. These include, but are not limited to, employing a valved or un-valved arterial cannula, a purse-string suture placed around incision 35 and then pulled tight about second manipulation instrument 500, a side-arm graft sewn to aorta 20 that may be constricted about a region of second manipulation instrument 500, the use of a tight fit between a portion of second manipulation instrument 500 and aortic incision 35, etc.
Second manipulation instrument 500 is shown in
It should be appreciated that the orientation of second manipulation mount 110 is preferably such as to enable the long axis of second manipulation instrument 500 to be substantially perpendicular to the flow area of prosthetic valve 200. This arrangement is particularly helpful when guiding prosthetic valve 200 into its final position within aorta 20 as shown hereafter in
The use of two separate manipulation instruments, and the method of passing valve prosthesis 200 from one to the other, avoids the complex manipulations of valve prosthesis 200 that would be required to position valve 200 within aorta 20 using only a single manipulation instrument introduced through the left atrium. In this respect it should be appreciated that such a “single manipulation instrument” technique has been found to be possible, however, and is best facilitated by using a manipulation instrument capable of bending or articulating at or near the site of its attachment to valve holding apparatus 100. In this respect it has been found that it can be particularly advantageous to provide a manipulation instrument capable of bending or articulating within about 4 cm or so of the point of attachment to valve holding apparatus 100. It has also been found that it can be particularly advantageous for such an articulating instrument to be able to deflect its distal tip by an angle of between about 90 to 180 degrees from the long axis of the first manipulation instrument 400 shown in
The angular offset of first manipulation mount 105 and second manipulation mount 110 is preferably set to facilitate passage of temporary prosthetic assembly 300 from left atrium 5 to aorta 20 using two substantially straight manipulation instruments, e.g., first manipulation instrument 400 and second manipulation instrument 500. This angle is preferably approximately 45 degrees. However, this angle may also be varied so as to optimize passage of different valve designs or other prostheses using curved, straight or articulating manipulation instruments from various access sites into the left atrium and arterial system. This angle may be fixed or variable on a given prosthesis holding apparatus 100.
Once second manipulation instrument 500 is safely secured to second manipulation mount 110, first manipulation instrument 400 may be released from first manipulation mount 105 and removed from left ventricle 5, as shown in
In
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In use, prosthesis holding apparatus 100 is fit about valve prosthesis 200 so that wire fingers 140 hold valve cuff 205 to struts 115. Prosthesis holding apparatus 100 is then engaged by first manipulation instrument 400, using first manipulation mount 105, and moved into and through right atrium 5, through mitral valve 30 and into left ventricle 25. Then second manipulation tool 500, comprising outer cannula 505 and inner grasper 510 having the deformable gripper 515, engages second manipulation mount 110. The distal tip 520 of outer cannula 505 is placed against edge 150 of base 120 and gripper 515 is drawn proximally-within outer cannula 505 until deformable gripper 515 engages shoulder 525, whereupon prosthesis holding apparatus 100 (and hence prosthetic valve 200) will be mounted to second manipulation tool 500. Second manipulation tool 500 is then used to maneuver temporary prosthetic assembly 300 into position, whereupon the valve's cuff 205 is secured to the side wall of the aorta, e.g., with barbs, staples, suture, etc. Then prosthesis holding apparatus 100 is detached from prosthetic valve 200 by pulling inner grasper 510 proximally relative to outer cannula 505 so that wire fingers 140 are pulled free from valve cuff 205 (
In practice, it has been found that it can sometimes be difficult to locate second manipulation mount 110 with second manipulation instrument 500 so as to “hand off” temporary prosthesis assembly 300 from first manipulation instrument 400 to second manipulation instrument 500. This can be particularly true where the procedure is to be conducted “off-pump”, i.e., without stopping the heart. To this end, and looking now at
In accordance with the present invention, it is also possible to enter the left atrium other than through an exterior wall of the left atrium. Thus, for example, it is possible to introduce the prosthetic valve through an opening in an exterior waft of the right atrium, pass the prosthetic valve through an incision in the interatrial septum and across to the left atrium, and then advance the prosthetic valve to its implantation site via the mitral valve and the left ventricle.
As noted above, the manipulation instrument(s) do not need to take the form of the installation instrument 400 or 500. It is also possible to deliver the prosthetic valve to its implant site using a guidewire and a pusher tool riding on the guidewire.
Thus, for example, in an alternative preferred embodiment, a wire, a catheter, a tube or any other filament can be placed from the left atrium, through the ventricle and into the arterial system, over (or through) which a prosthesis or device can be advanced (pushed or pulled). As an example, a catheter with a balloon can be placed through an incision in the left atrial wall. The balloon can be inflated and this catheter can then be “floated” along the flow of blood across the mitral valve, into the left ventricle, and out into the arterial system. At that point the catheter can be grasped by an instrument placed through a small incision in the aorta or passed into the aorta by means of a remote vessel such as the femoral artery. At this point, the prosthesis or device can be mounted onto the catheter and either be pushed (or pulled) over the catheter into position. This procedure can be similarly performed by the use of a wire or other filament structure. Also, a tube could be employed, with the prosthesis or device being advanced within the tube.
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In use, punch 900 is positioned at a diseased valve (not shown) with adjustable connector 915 operated to space first frame member 905 and second frame member 910 apart from one another so as to receive at least a portion of the diseased valve (not shown) therebetween. Next, adjustable connector 915 is operated so as to close first frame member 905 and second frame member 910 toward one another. This action causes blade 920 to move past cutting surface 925 so as to sever the portion of the diseased valve (not shown) therebetween. Punch 900 may be removed with the resected valve contained between first frame member 905 and second frame member 910. Punch 900 may be configured for either an approach to the valve through the aorta, referred to as an aortic approach, or an approach to the valve through the left ventricle of the heart, referred to as a left ventrical approach.
In a preferred embodiment of the present invention, and still referring to
Adjustable connector 915 of punch 900 is preferably configured with a handle 935 for opening and closing first frame portion 905 and second frame portion 910 relative to one another. A spring 940 is also provided to bias first frame portion 905 and second frame portion. 910 closed relative to one another. This configuration of punch 900 may be used in connection with the left ventrical approach with handle 935 being operable with a two tube controller (not shown). Alternatively, the shaft of adjustable connector 915 may be threadably connected to either first frame member 905 or second frame member 910 so as to allow adjustable connector 915 to open or close punch 900 with a twisting motion.
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In a preferred embodiment of the present invention, first frame member 950 and second frame member 955 each contain a mesh filter 980. Each mesh filter 980 allows blood flow through punch 945 and prevents portions of the resected valve larger than openings in mesh filter 980 from passing through punch 945.
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Wire 1040 may include a rough, abrasive surface for rotary driven or reciprocally driven cutting. Alternatively, wire 1040 may include an electrocautery element for cutting. A power shaver may also be used in place of wire 1040. The rough or abrasive embodiment of wire 1040 may include recesses formed in the wire 1040 or an abrasive metal dust coating added to it.
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In an alternative preferred embodiment of the present invention, trisector 1210 is provided with a filtering mechanism 1220 (
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The debridement tool is passed across the mitral valve on the beating heart. A catheter or controller tool 1285 based across the stenotic aortic valve (transvalvular catheter) is advanced into the left ventricular chamber, to effect an intra cardiac hand-off, as described previously. In one possible construction, the hand-off catheter 1285 is passed percutaneously, perhaps down the central lumen of a valve/filter assembly, also passed percutaneously.
Ideally, the snout 1280 of the debridement tool and the tip of the transvalvular catheter 1285 are both fitted with rare earth magnets or other appropriate structures so as to facilitate rapid reproducible alignment. Once aligned, the transvalvular catheter 1285 is actuated to achieve a mechanical coupling to allow the debridement tool to be pulled forcibly into position. The tool 1275 which was initially used to pass the debridement tool across the mitral valve is then released and removed after mechanical coupling is accomplished, but before pulling the debridement tool into position across the stenotic valve.
Attached to the aforementioned snout 1280 is an umbrella 1300 comprised of rays (or struts of nitinol or other superelastic material) or other satisfactory material supporting a disk of filter material 1340 similar to that attached to the back of the debridement tool. The umbrella 1300 is designed so that it can be milled across the stenotic valve in a closed configuration, from the ventricular side of the valve to the aortic side of the valve, and subsequently opened. The umbrella struts form a skeleton with a radius equal to that of the thin-walled cylinder 1290, and slightly greater than the cylindrical razor 1295. The disk of filter material has a radius that is somewhat greater than that of the thin-walled cylinder 1290. The umbrella struts may be attached to a ring that slides longitudinally with respect to the snout. The transvalvular catheter, when actuated, causes both delivery of the umbrella to the aortic side of the valve as well as a configuration change from closed to open. The result is that the stenotic valve is impaled on the snout and wedged between the thin-walled cylinder on the ventricular side and the open umbrella on the aortic side.
In one embodiment, the umbrella 1300 is inverted. That is to say, when it is pulled across the stenotic valve, the apex of the umbrella is the first to pass, and the outer circumference of the umbrella tines and filter disk is last to pass. In this construction, the device is preferably spring-loaded so that when the tips of the tines clear the valve orifice and tension is released, the umbrella forms as a result of its own recoil against the aortic surface of the valve.
The geometry and construction of the debridement tool is such that it will orient coaxially with respect to the left ventricular outflow tract and the valve orifice. Once the umbrella 1300 is deployed, the position is carefully inspected by echo and/or fluoroscopy. When correctly deployed, only a small gap exists between the disk and the thin-walled cylinder. It is therefore impossible to position and deploy the device with anything other than valvular tissue within this narrow gap. Only if the debridement tool was deployed at a significant angle, or was markedly undersized, could aortic or left ventricular tissue become pinched in this gap. Once it is confirmed that the debridement tool's position is correct, and the umbrella 1300 is deployed, the cylindrical razor 1295 is manually advanced and rotated, again under echo and/or fluoroscopic guidance, while maintaining tactile feedback by way of a rotating central element of the transvalvular catheter. It is not imperative that the valve be debrided in its entirety; rather, that a hole result that has edges suitable for the fixation mechanism, and that is large enough to allow fixation of the prosthesis, and that will relieve the outflow tract gradient. As the fixation mechanism and the orifice of the prosthesis may not be co-planer in this application, the demands on debridement and orifice size may be considerably less than with a conventional prosthetic valve implantation.
As soon as the cylindrical serrated razor 1295 cuts through the last of the valvular tissue, there will be no tissue remaining to prevent the spring-loaded umbrella 1300 from retracting toward the thin-walled cylinder 1290, in effect snapping a lid on the cylinder with the valve remnants inside. Inasmuch as the umbrella 1300 and the cage 1330 at the back of the thin-walled cylinder are covered with filter material, the valve tissue cannot escape. Because the filter material is fairly transparent to blood, resistance to flow and cardiac emptying should not be significantly impacted by its presence in the left ventricular outflow tract. A single-use serrated cylindrical razor 1295, with teeth of an appropriately small size, when used in a proper fashion (multiple small amplitude rotations while applying minimal force) will be able to cut a smooth round hole out of even the most calcified and thickened valve.
Once the umbrella is seen (by echo and/or fluoro) to have snapped down on the cylinder, the inference is made that the valve has been completely excised. Valvular competence at this point is provided entirely by the down-stream valve, an embodiment of which is described as the valved arch filter (see U.S. Provisional Patent Application Ser. No. 60/425,877, filed Nov. 13, 2002 by William E. Cohn for CARDIAC VALVE PROCEDURE METHODS AND DEVICES, Attorney's Docket No. VIA-41 PROV, which patent application is hereby incorporated herein by reference). Any particulate material that escapes the debridement tool is prevented from embolizing by this down-stream filter.
The closed debridement tool, with the valve remnants inside, is then passed back across the mitral valve and removed through the left atrial blood-lock.
It should also be appreciated that a valve debridement tool may also comprise a laser, an ultrasonic device, a rotary drill bit, an auger, or any other mechanism that appropriately disrupts tissue.
Furthermore, the valve debridement tool can be passed down the aorta, through the valve and across to the ventricular side for deployment and retrograde cutting.
Preferably the valve debridement tool is formed so as to be selectively collapsible, whereby it may be advanced to the surgical site through a catheter, e.g., by a catheter introduced through a peripheral artery.
Claims
1. A method for implanting a transcatheter heart valve comprising:
- introducing a catheter into a valve region located about a native deficient valve via an incision on the aorta;
- advancing a portion of the catheter past the native deficient valve;
- positioning a replacement heart valve in a position corresponding to the native deficient valve using the catheter;
- securing the replacement heart valve at the position corresponding to the native deficient valve; and
- withdrawing the catheter through the incision on the aorta.
2. The method of claim 1, wherein the native deficient valve is the aortic valve.
3. The method of claim 1, wherein the securing step includes deploying the valve.
4. The method of claim 3, wherein deploying the valve causes the valve to expand.
5. The method claim 3, wherein deploying the valve causes at least a portion of the valve to contact the region corresponding to the native deficient valve.
6. The method of claim 3, wherein the valve self deploys.
7. The method of claim 1, wherein the method is preformed while the heart is beating.
8. The method of claim 1, wherein the method is performed while the heart is arrested.
9. The method of claim 1, wherein the portion of the catheter is advanced past the native deficient valve and into the left ventricle.
Type: Application
Filed: May 21, 2014
Publication Date: Sep 11, 2014
Applicant: Medtronic, Inc. (Santa Rose, CA)
Inventors: Steven B. WOOLFSON (Boston, MA), Richard B. STREETER (Winchester, MA), Daniel C. TAYLOR (Brighton, MA), William E. COHN (Chestnut Hill, MA)
Application Number: 14/284,244
International Classification: A61F 2/24 (20060101);