Aortic pressure loss reduction apparatus and methods
Apparatus and methods are described including an aortic pressure-loss-reduction device (20) configured to be implanted inside an ascending aorta of a subject. The aortic pressure-loss-reduction device includes a frame (52) that defines an upstream anchor portion (33F), an intermediate portion (23F) configured to define a conduit (26) therethrough, and a downstream anchor portion (31F). Angled struts (150) are disposed between a downstream end of the upstream anchor portion (33F) and an upstream end of the intermediate portion (23F). The angled struts (150) are configured such that, in response to a diameter of the upstream anchor portion (33F) changing by an absolute amount, an absolute change in a diameter of the upstream end of the intermediate portion (23F) is less than the absolute amount by which the diameter of the upstream anchor portion (33F) changes. Other applications are also described.
1 . Apparatus comprising:
an aortic pressure-loss-reduction device configured to be implanted inside an ascending aorta of a subject, the aortic pressure-loss-reduction device comprising:
a frame that is configured, in a non-constrained configuration thereof, to define:
an upstream anchor portion configured to radially expand against an inner wall of the subject's ascending aorta, such as to anchor an upstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
an intermediate portion configured to define a conduit therethrough, such that blood is configured to flow through the device via the conduit, at least a portion of the conduit diverging, such that a downstream end of the diverging portion has a greater cross-sectional area than an upstream end of the diverging portion;
a downstream anchor portion configured to radially expand against the inner wall of the subject's ascending aorta, such as to anchor a downstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
a first set of angled struts disposed between a downstream end of the upstream anchor portion and an upstream end of the intermediate portion, the angled struts being shaped to form a folded portion between the downstream end of the upstream anchor portion and the upstream end of the intermediate portion;
the angled struts being configured such that, in response to a diameter of the upstream anchor portion changing by an absolute amount, an absolute change in a diameter of the upstream end of the intermediate portion is less than the absolute amount by which the diameter of the upstream anchor portion changes; and
a material layer coupled to at least a portion of the frame, the material layer configured to impede blood flow therethrough,
wherein, in the non-constrained configuration of the frame, the angled struts define a circumferential curvature with respect to a longitudinal axis of the frame.
2 . The apparatus according to claim 1 , wherein the angled struts define a sinusoidal curvature.
3 . The apparatus according to claim 1 , wherein the angled struts are configured such that a ratio of the absolute change in the diameter of the upstream end of the intermediate portion to the absolute amount by which the diameter of the upstream anchor portion changes is less than 1:2.
4 . The apparatus according to claim 1 , wherein the angled struts are configured such that in response to the diameter of the upstream anchor portion decreasing, the diameter of the upstream end of the intermediate portion increases.
5 . The apparatus according to claim 1 , wherein the material layer is coupled to an outside of at least a portion of the frame.
6 . The apparatus according to claim 1 , wherein the material layer is coupled to an inside of at least a portion of the frame.
7 . The apparatus according to claim 1 , wherein at least a portion of the frame is embedded within the material layer.
8 . The apparatus according to claim 1 , wherein the angled struts are configured such that, when the frame is in the non-radially-constrained configuration, a distance from an upstream end of the upstream anchor portion to the upstream end of the intermediate portion is less than 15 mm.
9 . The apparatus according to claim 1 , wherein the angled struts are configured such that, when the frame is in the non-radially-constrained configuration, an upstream end of the conduit extends beyond an upstream end of the upstream anchor portion in the upstream direction.
10 . The apparatus according to claim 1 , wherein the angled struts are configured such that, in response to the diameter of the upstream anchor portion decreasing, the circumferential curvature of the struts with respect to the longitudinal axis of the frame increases.
11 . The apparatus according to claim 1 , wherein the angled struts are configured such that, by virtue of an increase in the circumferential curvature of the struts with respect to longitudinal axis of the frame, the difference between the diameter of the upstream end of the intermediate portion and the diameter of the upstream anchor portion decreases.
12 . Apparatus comprising:
an aortic pressure-loss-reduction device configured to be implanted inside an ascending aorta of a subject, the aortic pressure-loss-reduction device comprising:
a frame that is configured, in a non-constrained configuration thereof, to define:
an upstream anchor portion configured to radially expand against an inner wall of the subject's ascending aorta, such as to anchor an upstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
an intermediate portion configured to define a conduit therethrough, such that blood is configured to flow through the device via the conduit, at least a portion of the conduit diverging, such that a downstream end of the diverging portion has a greater cross-sectional area than an upstream end of the diverging portion;
a downstream anchor portion configured to radially expand against the inner wall of the subject's ascending aorta, such as to anchor a downstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
a first set of angled struts disposed between a downstream end of the upstream anchor portion and an upstream end of the intermediate portion, the angled struts being shaped to form a folded portion between the downstream end of the upstream anchor portion and the upstream end of the intermediate portion;
the angled struts being configured such that, in response to a diameter of the upstream anchor portion changing by an absolute amount, an absolute change in a diameter of the upstream end of the intermediate portion is less than the absolute amount by which the diameter of the upstream anchor portion changes; and
a material layer coupled to at least a portion of the frame, the material layer configured to impede blood flow therethrough,
wherein the upstream end of the intermediate portion is reinforced with respect to at least a longitudinally-central portion of the intermediate portion.
13 . The apparatus according to claim 12 , wherein the upstream end of the intermediate portion and the longitudinally-central portion of the intermediate portion comprise a first set of struts, and wherein the upstream end of the intermediate portion is reinforced with respect to at least the longitudinally-central portion of the intermediate portion by the first set of struts of the upstream end of the intermediate portion being reinforced with supporting struts that face in an opposite direction from the first set of struts of the upstream end of the intermediate portion.
14 . The apparatus according to claim 12 , wherein the upstream end of the intermediate portion and the longitudinally-central portion of the intermediate portion comprise struts, and wherein the upstream end of the intermediate portion is reinforced with respect to at least the longitudinally-central portion of the intermediate portion by the struts of the upstream end of the intermediate portion forming closed cells.
15 . The apparatus according to claim 12 , wherein the upstream end of the intermediate portion and the longitudinally-central portion of the intermediate portion comprise struts, and wherein the upstream end of the intermediate portion is reinforced with respect to at least the longitudinally-central portion of the intermediate portion by the struts of the upstream end of the intermediate portion being shorter than the struts of the longitudinally-central portion of the intermediate portion.
16 . The apparatus according to claim 12 , wherein the upstream end of the intermediate portion and the longitudinally-central portion of the intermediate portion comprise struts, and wherein the upstream end of the intermediate portion is reinforced with respect to at least the longitudinally-central portion of the intermediate portion by the struts of the upstream end of the intermediate portion being wider than the struts of the longitudinally-central portion of the intermediate portion.
17 . Apparatus comprising:
an aortic pressure-loss-reduction device configured to be implanted inside an ascending aorta of a subject, the aortic pressure-loss-reduction device comprising:
a frame that is configured, in a non-constrained configuration thereof, to define:
an upstream anchor portion configured to radially expand against an inner wall of the subject's ascending aorta, such as to anchor an upstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
an intermediate portion configured to define a conduit therethrough, such that blood is configured to flow through the device via the conduit, at least a portion of the conduit diverging, such that a downstream end of the diverging portion has a greater cross-sectional area than an upstream end of the diverging portion;
a downstream anchor portion configured to radially expand against the inner wall of the subject's ascending aorta, such as to anchor a downstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
a first set of angled struts disposed between a downstream end of the upstream anchor portion and an upstream end of the intermediate portion, the angled struts being shaped to form a folded portion between the downstream end of the upstream anchor portion and the upstream end of the intermediate portion;
the angled struts being configured such that, in response to a diameter of the upstream anchor portion changing by an absolute amount, an absolute change in a diameter of the upstream end of the intermediate portion is less than the absolute amount by which the diameter of the upstream anchor portion changes;
a material layer coupled to at least a portion of the frame, the material layer configured to impede blood flow therethrough; and
a second set of angled struts disposed between an upstream end of the downstream anchor portion and a downstream end of the intermediate portion, the second set of angled struts being shaped to form a folded portion between the upstream end of the downstream anchor portion and the downstream end of the intermediate portion.
18 . The apparatus according to claim 17 , wherein, in the non-constrained configuration of the frame, the first set of angled struts define a circumferential curvature with respect to a longitudinal axis of the frame in a given circumferential direction, and the second set of angled struts define a circumferential curvature with respect to the longitudinal axis of the frame in the given circumferential direction.
19 . The apparatus according to claim 17 , wherein the second set of angled struts are configured such that, in response to a diameter of the downstream anchor portion changing by an absolute amount, an absolute change in a diameter of the downstream end of the intermediate portion is less than the absolute amount by which the diameter of the downstream anchor portion changes.
20 . The apparatus according to claim 17 , wherein the second set of angled struts are configured such that, in response to diameters of both the upstream and the downstream anchor portions decreasing, torque that is generated at the upstream end of the intermediate portion, by the first set of angled struts, is at least partially cancelled by torque generated at the downstream end of the intermediate portion, by the second set of angled struts.
21 . The apparatus according to claim 17 , wherein the aortic pressure-loss-reduction device is configured, such that the intermediate portion of the device is (a) longitudinally fixed with respect to the ascending aorta by the upstream anchor portion and the downstream anchor portion exerting radial force against the inner wall of the aorta and (b) able to adjust the angle that a longitudinal axis of the intermediate portion makes with longitudinal axes of the upstream and downstream anchor portions, by the first and second sets of angled struts acting as hinges about which the intermediate portion can flex.
22 . The apparatus according to claim 17 , wherein the aortic pressure-loss-reduction device is configured such that, by virtue of flexibility of first and second sets of angled struts, a length of the intermediate portion does not change even if a distance between the upstream and downstream anchor portions changes.
23 . The apparatus according to claim 17 , wherein the struts belonging to the first set of angled struts are longer than the struts belonging to the second set of angled struts.
24 . Apparatus comprising:
an aortic pressure-loss-reduction device configured to be implanted inside an ascending aorta of a subject, the aortic pressure-loss-reduction device comprising:
a frame that is configured, in a non-constrained configuration thereof, to define:
an upstream anchor portion configured to radially expand against an inner wall of the subject's ascending aorta, such as to anchor an upstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
an intermediate portion configured to define a conduit therethrough, such that blood is configured to flow through the device via the conduit, at least a portion of the conduit diverging, such that a downstream end of the diverging portion has a greater cross-sectional area than an upstream end of the diverging portion;
a downstream anchor portion configured to radially expand against the inner wall of the subject's ascending aorta, such as to anchor a downstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
a first set of angled struts disposed between a downstream end of the upstream anchor portion and an upstream end of the intermediate portion, the angled struts being shaped to form a folded portion between the downstream end of the upstream anchor portion and the upstream end of the intermediate portion;
the angled struts being configured such that, in response to a diameter of the upstream anchor portion changing by an absolute amount, an absolute change in a diameter of the upstream end of the intermediate portion is less than the absolute amount by which the diameter of the upstream anchor portion changes; and
a material layer coupled to at least a portion of the frame, the material layer configured to impede blood flow therethrough,
wherein the intermediate portion of the frame is configured to be flexible, by the intermediate portion of the frame including struts that form a spiral, such that at least upon the aortic pressure-loss-reduction device being implanted inside the subject's ascending aorta, the intermediate portion of the frame curves such as to conform with a curvature of the ascending aorta.
25 . Apparatus comprising:
an aortic pressure-loss-reduction device configured to be implanted inside an ascending aorta of a subject, the aortic pressure-loss-reduction device comprising:
a frame that is configured, in a non-constrained configuration thereof, to define:
an upstream anchor portion configured to radially expand against an inner wall of the subject's ascending aorta, such as to anchor an upstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
an intermediate portion configured to define a conduit therethrough, such that blood is configured to flow through the device via the conduit, at least a portion of the conduit diverging, such that a downstream end of the diverging portion has a greater cross-sectional area than an upstream end of the diverging portion;
a downstream anchor portion configured to radially expand against the inner wall of the subject's ascending aorta, such as to anchor a downstream end of the aortic pressure-loss-reduction device to the subject's ascending aorta;
a first piece of material coupled to the frame, the first piece of material configured to impede blood flow therethrough; and
a second piece of material coupled to the frame, the second piece of material configured to impede blood flow therethrough,
the second piece of material being stitched to the first piece of material at a longitudinal location that varies around a circumference of the device when the device is disposed in a radially-constrained configuration.