MEDICAL DEVICE SUITABLE FOR LOCATION IN A BODY LUMEN
20190151123 ยท 2019-05-23
Assignee
Inventors
- Kevin Heraty (Co. Galway, IE)
- Liam MULLINS (Galway, IE)
- Paul Gilson (Co. Galway, IE)
- Martin G. Burke (West Sussex, GB)
Cpc classification
Y10S623/903
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
A61F2310/00023
HUMAN NECESSITIES
A61F2250/0096
HUMAN NECESSITIES
A61F2210/0014
HUMAN NECESSITIES
A61F2/91
HUMAN NECESSITIES
International classification
Abstract
A medical device suitable for location in a body lumen is movable between a first loaded configuration and a second loaded configuration. The device has an unloaded configuration which is intermediate the first loaded configuration and the second loaded configuration. The device can be a stent for deployment in a blood vessel.
Claims
1. A method of stenting a body lumen, comprising: deploying and expanding a stent in a body lumen, the stent having a diameter, the body lumen being deformable between an unloaded state and a loaded state; wherein the stent is one which, after deployment and expansion, is deformable between a first loaded configuration and a second loaded configuration and has an unloaded configuration intermediate the first loaded configuration and the second loaded configuration; wherein in said unloaded and second loaded configurations at least part of the longitudinal axis of the stent is substantially helically shaped and has an amplitude and wherein in the second loaded configuration the amplitude of the helical longitudinal axis divided by the diameter of the stent is greater than in the unloaded configuration; and wherein the deploying comprises deploying the stent in the body lumen so that when the body lumen is in the unloaded state the stent is in the first loaded configuration, and when the body lumen is in the loaded state the stent is in the second loaded configuration.
2. A method as claimed in claim 1, wherein the pitch of the helical longitudinal axis is less in the second loaded configuration than in the unloaded configuration.
3. A method as claimed in claim 1, wherein in the first loaded configuration at least part of the longitudinal axis of the stent is substantially helically shaped and the amplitude of the helical longitudinal axis divided by the diameter of the stent is less than in the unloaded configuration.
4. A method as claimed in claim 3, wherein the pitch of the helical longitudinal axis is greater in the first loaded configuration than in the unloaded configuration.
5. A method as claimed in claim 1, wherein in the unloaded configuration the amplitude of the helical longitudinal axis divided by the diameter of the stent is in the range of 0.3 to 0.9.
6. A method as claimed in claim 1, wherein in the first loaded configuration at least part of the longitudinal axis of the stent is helical and the amplitude of the helical longitudinal axis divided by the diameter of the stent is in the range of 0 to 0.5.
7. A method as claimed in claim 1, wherein in the second loaded configuration the amplitude of the helical longitudinal axis divided by the diameter of the stent is 0.5 or greater.
8. A method of stenting a body lumen, comprising: deploying and expanding a stent in a body lumen such that it is in a deployed, expanded configuration; and when the stent is in the deployed, expanded configuration: deforming the stent to a first loaded configuration when the body lumen bends to an unloaded state thereof; deforming the stent to a second loaded configuration when the body lumen bends to a loaded state thereof; and wherein the stent has an unloaded configuration intermediate the first and second loaded configurations and wherein in the unloaded and second loaded configurations at least part of the longitudinal axis of the stent is substantially helically shaped, wherein the amplitude of the helical longitudinal axis divided by the diameter of the stent is greater in the second loaded configuration than in the unloaded configuration.
9. A method of stenting a body lumen, comprising: deploying and expanding a stent in a body lumen, the body lumen being deformable between an unloaded state and a loaded state; wherein the stent is one which, after deployment and expansion, is deformable between a first loaded configuration and a second loaded configuration and has an unloaded configuration intermediate the first loaded configuration and the second loaded configuration; wherein in said unloaded configuration at least part of the longitudinal axis of the stent is curved; and wherein the deploying comprises deploying the stent in the body lumen so that when the stent is deformed through a curve angle of 45 degrees between the first loaded configuration and the second loaded configuration, the maximum strain in the stent, at any stage at or between the first and second loaded configurations, is less than or equal to 0.4%.
10. A method as claimed in claim 1, wherein deforming the stent comprises bending the stent between the first loaded configuration and the second loaded configuration.
11. A method as claimed in claim 1, wherein deforming the stent comprises twisting the stent between the first loaded configuration and the second loaded configuration.
12. A method as claimed in claim 1, wherein deforming the stent comprises compressing the stent between the first loaded configuration and the second loaded configuration.
13. A method as claimed in claim 1, wherein the maximum strain is less than or equal to 0.3%.
14. A method as claimed in claim 1, wherein when the stent is axially compressed by 6% from the first loaded configuration to the second loaded configuration, the maximum strain in the stent, at any stage at or between the first and second loaded configurations, is less than or equal to 0.7%.
15. A method as claimed in claim 1, wherein the unleaded configuration is approximately midway between the first loaded configuration and the second loaded configuration.
16. A method as claimed in claim 1, further comprising aligning the stent relative to a body lumen.
17. A method as claimed in claim 16, wherein aligning the stent comprises aligning a marker or the stent with the body lumen.
18. A method as claimed in claim 1, wherein the body lumen is a blood vessel.
19. A method as claimed in claim 1, wherein the stent has a longitudinal axis with a length of at least 50 mm.
20. A method as claimed in claim 1, wherein the stent is made of Nitinol.
21. A method as claimed in claim 14, wherein the maximum strain is less than or equal to 0.5%.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0034] The invention will be more clearly understood from the following description of some embodiments thereof, given by way of example only, with reference to the accompanying drawings, in which:
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DETAILED DESCRIPTION
[0048] Referring to the drawings, and initially to
[0049] In this case the medical device 1 comprises a stent suitable for deployment in a blood vessel which is movable between an unloaded straight cylindrical state (
[0050] The stent 1 is bendable through a single bend between the first loaded configuration (
[0051] The stent 1 has an unloaded configuration (
[0052] The stent 1 may be balloon expandable or self-expanding.
[0053] The stent 1 is suitable for use in the blood vessel which is subject to tortuous loading, such as bending. The stent 1 has the pre-set curved geometry in the unloaded configuration, as shown in
[0054] Because of physiological movements within the body, the blood vessel may be forced to adopt tortuous configurations. Large degrees of bending may occur, for example with bends in excess of 90, for example up to 140. A bend between limb parts at a joint means the angle between the limb parts measured at the joint, for example the angle between the lower leg and the upper leg at the knee. Such a bend at the joint corresponds to a smaller curve angle of the stent as defined above, for example a bend at the joint of 90 may result in a curve angle of the stent of 45, whilst a bend at the joint of 140 may result in a curve angle of the stent of 70.
[0055] The location for the stent 1 may be in the blood vessel in the leg behind the knee which is subject to frequent bending as the patient bends the leg. Because the unloaded configuration of the stent 1 is non-straight, the degrees of deformation which the stent 1 undergoes are minimised leading to minimised strains, increased fatigue life, and reduced risk of fracture. The configuration of
[0056] Each of the angles degrees and degrees through which the device is curved is a curve angle, i.e. the angle between the longitudinal axis of the device at one end thereof and a line from a point on the longitudinal axis at that end to a point on the longitudinal axis at the other end of the device.
[0057]
[0058] Since some of the deformation of the blood vessel is already incorporated in the stent 1 in the unloaded configuration (
[0059] For example, as shown in
[0060] In use, the stent 1 is delivered into the blood vessel and deployed at a desired treatment site in the blood vessel. The stent 1 may be oriented at the desired treatment site.
[0061] As the blood vessel moves from the unloaded straight cylindrical state (
[0062] The operation of the stent of
[0063]
[0064] The leg is substantially straight in position A and at this time the stent is in a first loaded configuration corresponding to
[0065] Finite element analysis was used to evaluate the strains which occur during bending of the leg from the straight condition shown as position A to the sitting condition shown as position C. The results are shown in the graph of
[0066] By way of comparison,
[0067] During bending of the leg, the popliteal artery, which is the artery behind the knee, exhibits large degrees of bending, as seen in
[0068] The strains calculated and shown in
[0069] In
[0070] In the unloaded configuration the longitudinal axis of the stent 10 is curved through two bends in a two-dimensional plane (
[0071]
[0072] The curve embodied represents a configuration between the two opposing extremes of deformation of the blood vessel, such as those shown in
[0073]
[0074] In this case the stent 20 is bendable and twistable through multiple bends between the first loaded configuration (
[0075] In the unloaded configuration the longitudinal axis of the stent 20 is curved through multiple bends in three-dimensional space (
[0076] When the stent 20 is deployed in the blood vessel, the stent 20 exerts force on the blood vessel causing the blood vessel to adopt a helical configuration. In this manner the stent 20 acts to support at least part of the internal wall of the blood vessel in the helical configuration. Blood flowing through the helically shaped blood vessel then undergoes a swirling action. The swirling flow of blood has been found to minimise thrombosis and platelet adhesion, and to minimise or prevent coverage of the stent 20 by ingrowth of intima. The flow pattern in the blood vessel including the swirling pattern induced by the non-planar geometry of the blood vessel operates to inhibit the development of vascular diseases such as thrombosis/atherosclerosis and intimal hyperplasia.
[0077]
[0078]
[0079] When the stent is in position B, in its unloaded configuration, it has a certain relative amplitude and helical pitch. In position A5 when the stent is in its elongated first loaded configuration, the relative amplitude is decreased and the pitch is increased. In position C, when the stent is axially compressed, the relative amplitude is increased and the pitch is decreased.
[0080] The strains which are induced in stent 30 were investigated using finite element analysis and the results are shown in the graph of
[0081]
[0082] Thus for the same loading, the straight stent will exhibit higher strains than the stent with geometry which is intermediate the loaded and unloaded configurations.
[0083] The strains calculated and shown in
[0084] The helical longitudinal axis of a helical stent may follow a circular path when viewed from an end of the stent. The longitudinal axis may rotate around a central axis which is at the geometrical centre of an envelope in which the helical stent is contained. The central axis may be straight or may itself be curved, for example curved in a two-dimensional plane. The helical longitudinal axis of the stent may not necessarily be circular when viewed along the central axis, i.e. from an end of the stent. For example, the longitudinal axis could be elliptical to form an elliptical helix, or other curve in three-dimensional space. If the longitudinal axis is elliptical, then preferably the major axis of the ellipse is aligned with the plane in which the body part, such as a knee or elbow, bends.
[0085]
[0086] The geometries described, which are intermediate to the loaded and unloaded configurations, could also be manifested in a piecewise fashion, i.e. a series of straight sections along the stent, whose orientation varies with respect to one another, to achieve an overall curvature or series of bends along the stent. Thus the longitudinal axis of the stent overall could have a zig-zag shape or a saw tooth shape.
[0087]
[0088] The stent shown in
[0089] It will be appreciated that the stent may be moved between the first loaded configuration and the second loaded configuration under the action of any loading mode. For example the device may be deformed between the first loaded configuration and the second loaded configuration, and/or the device may be compressed between the first loaded configuration and the second loaded configuration.
[0090] The invention is not limited to the embodiments hereinbefore described, with reference to the accompanying drawings, which may be varied in construction and detail.