The present invention relates to apparatus and methods for deploying a tubular medical device, and in particular an implantable stent graft.
An endovascular stent-graft is designed is exclude the flow of blood to an aneurysm that has been formed within the wall of the lumen (for example the aorta). This is achieved by accessing the aneurysm via an artery, usually within the patient's leg, with a system designed to deliver, position and deploy the stent graft so that it bridges and seals off the aneurysm.
A stent graft is a (usually) tubular device with walls made from a flexible sheet material, supported by a rigidising frame (the stent) which may be formed from a super-elastic metal such as a shape memory alloy (commonly nitinol). In some designs, such as the Ovation (Trivascular Inc), the rigidising frame is added after the flexible tubular sheet component has been put in position by, for example, filling channels formed in the tubular sheet with a fluid which becomes rigid. Some stent graft designs are fixed to the aorta wall by means of barbs or hooks. The rigidising frame maintains the tubular shape of the stent graft, while providing a radial sealing force to create a proximal and distal seal with the aortic wall.
In order to deliver a stent graft to the locus of the aneurysm, it is conventionally collapsed (that is, reduced in diameter), loaded on a delivery catheter and delivered to the aneurysm where it is positioned and deployed by expanding its diameter, or otherwise dilating, to seal off the aneurysm as described above.
The stent frame can be manufactured from a multiply perforated tube of rigid material with a first narrow diameter. Upon dilation of the frame by external means, such as an endoluminal balloon, the perforations allow significant plastic deformation of the material to take place, causing the stent to adopt and maintain a second, wider, diameter. In a second method of making a stent frame, the frame may be formed of a plurality of resilient struts made from, for example, stainless steel or from Elgiloy, which are connected at their ends to provide a self-expandable frame (for example the Gianturco “Z-stent” marketed by Cook, Inc). Alternatively, the stent frame may use a shape-memory alloy, such as Nitinol, to provide a resilient or thermally initiated expansion of the stent. Examples of Nitinol stents are found in the Anaconda™ device marketed by Terumo and the Aorfix™ device marketed by the present applicant and disclosed in WO 99/37242, the contents of which are incorporated herein by reference. Self-expanding stents have one stable shape when unconstrained which is their maximum diameter. They are deformed under compression and then expand automatically when the compression is removed.
Although self-expanding stents expand within the aorta automatically when compression is removed (for example when they are ejected from a delivery sheath), it is necessary to control the deployment carefully to ensure that the stent graft is accurately positioned relative to the aneurysm. For example, the Anaconda™ device is deployed by means of a complicated system of threads and wires which are used to manipulate the mouth of the stent graft from the side stent graft proximate the heart and which then must be removed from the stent graft after deployment in order that the deployment system can be removed from the patient's body.
U.S. Pat. No. 5,713,907 (Endotex Interventional Systems, Inc.) discloses a device having an expandable frame for deploying an expandable stent graft. The frame can be advanced and retracted (and thereby expanded and contracted) by the surgeon pushing or pulling on a deployment shaft. The stent graft may be deployed incrementally. However, the disclosed device does not allow a stent graft easily to be repositioned in the body lumen.
US 2008/0300667 (Hebert) discloses a delivery system for an expandable stent which employs a flexible arm which is resiliently biased outwardly in order to pin the proximal end of the stent against the internal surface of the delivery catheter and prevent it from deploying while the distal end of the stent is being deployed.
There is a need for a deployment system which is capable of accurate deployment and positioning of a stent graft but which can easily be detached from the stent graft and removed from the patient's body without the risk of snagging.
In accordance with a first aspect of the invention, there is provided apparatus for deploying a tubular medical device in vivo, comprising an elongate element for passing into the bore of the medical device, a deployment device having at least one arm for engaging with the medical device, the arm being moveable in a radial direction relative to the longitudinal axis of the elongate element from a first position to a second position, the second position being spaced radially further from the elongate element than the first position, and a flexible element for the arm, said flexible element being associated with said arm such that pulling on the flexible element moves said arm from the second position towards the first position, whereby in use movement of the arm from the first position to the second position enables radial deployment of the medical device.
In accordance with a second aspect of the invention, there is provided apparatus for deploying a tubular medical device in vivo, comprising an elongate element for passing into the bore of the medical device, and a deployment device having at least one arm for engaging with the medical device, the arm being moveable in a radial direction relative to the longitudinal axis of the elongate element from a first position to a second position, the second position being spaced radially further from the elongate element than the first position, whereby in use movement of the arm from the first position to the second position enables radial deployment of the medical device, and wherein the arm has means for removably attaching the arm to the wall of the medical device.
In accordance with a third aspect of the invention, there is provided apparatus for deploying a tubular medical device in vivo, comprising an elongate element for passing into the bore of the medical device, and a deployment device having two arms for engaging with the medical device, the arms being moveable independently in a radial direction relative to the longitudinal axis of the elongate element from a first position to a second position, the second position being spaced radially further from the elongate element than the first position, whereby in use movement of at least one of the arms from the first position to the second position enables radial deployment of the medical device.
The provision of an elongate element and a deployment arm enables the apparatus to be centred in the body lumen (for example by mounting the elongate element on a guide wire) whilst deploying a tubular medical implant.
In a preferred embodiment, the deployment device has at least two arms which may be operated independently to enable a stent graft (for example) to be deployed within an artery. Alternatively, the elongate element may take the function of one of the arms.
The arm or arms are preferably resiliently biased into the second (open) position which enables the apparatus to be used to deploy stents or stent grafts which are not self-expanding (that is, which require some assistance to be expanded) for instance where a tubular sheet component is to be placed before placing or creating the rigidising element. However, in an alternative embodiment the arm(s) could be unbiased either way or even biased radially inwardly (although this is not preferred).
In a preferred embodiment, the apparatus comprises a flexible element (such as a thread) for each arm, said flexible element being associated with said arm (for example looped around said arm) such that pulling on the flexible element moves said arm from the second position to the first position.
The apparatus may also comprise means for redirecting each flexible element from a radial direction relative to the elongate element to a longitudinal direction relative to the elongate element. The means for redirecting is preferably generally toroidal in shape and is mounted on the elongate element; it may have at least one channel therein for accepting at least one flexible element.
Accordingly, in a preferred embodiment, each flexible element passes from the associated arm, around the means for redirecting and towards the end of the elongate element distal to the deployment device. However, in an alternative embodiment each flexible element passes from its arm, around the means for redirecting and towards the end of the elongate element proximate the deployment device, before turning 180 degrees and then being directed towards the end of the elongate element distal to the deployment device. In either embodiment the flexible element(s) may pass at some point through the wall of centre catheter 10 and into bore 15.
In a fourth aspect of the invention, there is provided a method of deploying a tubular medical device comprising the steps of:
Thus, the apparatus of the present invention can be employed to test, control and perfect accurate placement and deployment of medical devices in the lumen of a vessel, more particularly endovascular stent grafts. The apparatus is of particular value in situations requiring particularly exact placement and control of the implant, examples of which include:
A number of preferred embodiments of the present invention will now be illustrated by way of example, with reference to the drawings, in which:
Turning to
Centre catheter 10 (see
As mentioned above, Y-piece 20 is formed from nitinol and this is preferably shape set such that arms 30 are biased into the open configuration as shown in
The mechanism for moving Y-piece 20 between an open and collapsed configuration is shown in the perspective views of
It will be appreciated that when the user pulls on the ends of deployment thread 60 this serves to pull the associated arm 30 against its bias and to move it into the collapsed configuration. It will further be appreciated that each of the two arms 30 may be operated independently, which can be useful when deploying, for example, a stent graft within the thoracic arch.
Is use, stent graft 200 is mounted on the deployment apparatus as shown in
When stent graft 200 is in place (which may involve barbs—not shown—being implanted into the artery wall) then the deployment apparatus can be detached from stent graft 200 by pulling on release wires 50 to unthread them from the walls of stent graft 200 so as to detach arms 30. Arms 30 can then be moved into the collapsed configuration by pulling on threads 60 and Y-piece 20 and centre catheter 10 can be removed from the bore of stent graft 200.
Turning finally to
Number | Date | Country | Kind |
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1106017.5 | Apr 2011 | GB | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/GB2012/050724 | 3/30/2012 | WO | 00 | 4/3/2014 |