Devices with dimensions that can be reduced and increased in vivo, and methods of making and using the same
Devices are provided with an internal dimension that can be reduced and increased in vivo. In one example, an interatrial shunt for placement at an atrial septum of a patient's heart includes a body. The body includes first and second regions coupled in fluid communication by a neck region. The body includes a shape-memory material. The body defines a passageway through the neck region for blood to flow between a first atrium and a second atrium. The first and second regions are superelastic at body temperature, and the neck region is malleable at body temperature. A flow area of the passageway through the neck region may be adjusted in vivo.
1. An interatrial shunt for placement at an atrial septum of a patient's heart, the interatrial shunt comprising:
a body comprising first and second regions coupled in fluid communication by a neck region, the body comprising a shape-memory material, the body defining a passageway through the neck region for blood to flow between a first atrium and a second atrium,
wherein the first and second regions are superelastic at body temperature, and the neck region is malleable at body temperature and comprises NITINOL having an austenitic finish temperature (Af) between 45-60° C., and
wherein a flow area of the passageway through the neck region may be adjusted in vivo.
2. The interatrial shunt of claim 1 , wherein the first and second regions that are superelastic comprise NITINOL having an austenitic finish temperature (Af) between 5-20° C.
3. The interatrial shunt of claim 1 , wherein the neck region is mechanically expandable.
4. The interatrial shunt of claim 1 , wherein the neck region is thermally contractible.
5. An interatrial shunt for placement at an atrial septum of a patient's heart for adjustably regulating fluid flow therethrough, the interatrial shunt comprising:
a first expandable end region configured to be placed in a first atrium of the heart;
a second expandable end region configured to be placed in a second atrium of the heart, the first and second expandable end regions comprising self-expanding superelastic material; and
a neck region between the first and second expandable end regions configured for placement at the atrial septum, the neck region comprising malleable shape-memory material, the interatrial shunt defining a passageway through the neck region for blood to flow between the first atrium and the second atrium,
wherein the neck region is heat treated to exhibit different shape memory properties than the first and second expandable end regions such that a cross-sectional area of the passageway is adjustable in vivo.
6. The interatrial shunt of claim 5 , wherein the malleable shape-memory material is configured to be expanded in vivo such that the passageway expands from the cross-sectional area to a second cross-sectional area larger than the cross-sectional area.
7. The interatrial shunt of claim 6 , wherein the malleable shape-memory material is configured to be contracted in vivo such that the passageway contracts from the second cross-sectional area to a third cross-sectional area smaller than the second cross-sectional area.
8. The interatrial shunt of claim 7 , wherein the cross-sectional area is between 4.9 to 28.3 mm 2 and the second cross-sectional area and the third cross-sectional area are between 15.9 to 78.6 mm 2 .
9. The interatrial shunt of claim 5 , wherein the malleable shape-memory material comprises NITINOL having an austenitic finish temperature (Af) between 45-60° C.
10. The interatrial shunt of claim 5 , wherein the self-expanding superelastic material comprises NITINOL having an austenitic finish temperature (Af) between 5-20° C.
11. The interatrial shunt of claim 5 , wherein the malleable shape-memory material is mechanically expandable.
12. The interatrial shunt of claim 5 , wherein the malleable shape-memory material is thermally contractible.
13. The interatrial shunt of claim 5 , wherein the cross-sectional area of the neck region is smaller than respective cross-sectional areas of at least one of the first and second expandable end regions.
14. The interatrial shunt of claim 5 , wherein the first and second expandable end regions extend into the first and second atria, respectively, such that respective ends of the first and second expandable end regions do not contact the atrial septum.
15. The interatrial shunt of claim 5 , wherein the first and second expandable end regions and the neck region comprise a diabolo-shaped shunt.
16. The interatrial shunt of claim 15 , wherein the neck region comprises a cylindrical shunt.
17. The interatrial shunt of claim 16 , wherein the cylindrical shunt is outside of the diabolo-shaped shunt.
18. The interatrial shunt of claim 17 , wherein the cylindrical shunt is formed of the malleable shape-memory material such that the cylindrical shunt radially constrains a dimension of the diabolo-shaped shunt at the neck region, and wherein the diabolo-shaped shunt self-expands at the neck region responsive to the malleable shape memory material expanding to a second cross-sectional area.
19. The interatrial shunt of claim 16 , wherein the cylindrical shunt is inside of the diabolo-shaped shunt.
20. The interatrial shunt of claim 16 , wherein the cylindrical shunt is not directly coupled to the diabolo-shaped shunt and the neck region,
further comprising an encapsulant indirectly and elastically coupling the cylindrical shunt to the diabolo-shaped shunt.
21. The interatrial shunt of claim 16 , wherein contraction of the cylindrical shunt does not cause contraction of the diabolo-shaped shunt at the neck region.
22. The interatrial shunt of claim 16 , wherein the diabolo-shaped shunt and the cylindrical shunt are integrally formed from a common frame.
23. The interatrial shunt of claim 5 , wherein the first and second expandable end regions and the neck region are integrally formed from a common frame.
24. The interatrial shunt of claim 5 , wherein the first and second expandable end regions and the neck region are at least partially encapsulated with a biocompatible material.
25. An interatrial shunt for adjustably regulating fluid flow in a heart having a first atrium, a second atrium, and an atrial septum, the interatrial shunt comprising:
a first region comprising a self-expanding superelastic material configured to be placed in the first atrium, the first region being superelastic at body temperature; and
a second region comprising a malleable shape-memory material configured to be placed through an opening in the atrial septum so as to provide fluid flow from the first atrium to the second atrium, the second region being malleable at body temperature,
the malleable shape-memory material having a first cross-sectional area,
the malleable shape-memory material being expandable from the first cross-sectional area to a second cross-sectional area, and
the malleable shape-memory material being contractible from the second cross-sectional area to a third cross-sectional area.
26. The interatrial shunt of claim 25 , wherein the self-expanding superelastic material comprises NITINOL having an austenitic finish temperature (Af) between 5-20° C. and the malleable shape-memory material comprises NITINOL having an austenitic finish temperature (Af) between 45-60° C.
27. The interatrial shunt of claim 25 , wherein the malleable shape-memory material is mechanically expandable and thermally contractible.
28. The interatrial shunt of claim 25 , further comprising a third region comprising a second self-expanding superelastic material, configured to be placed in the second atrium, and coupled to the second region.