Baroreceptor testing prior to implantation methods and apparatus
Systems and methods for screening a subject for a therapy are described. A mechanical stimulation device positioned near at target location of a blood vessel to provide a mechanical stimulus to the blood vessel. The mechanical stimulus increases strain in one or more regions of the blood vessel, such as by modifying the cross-sectional geometry and/or area of the blood vessel to have different regions of different curvature A baroreflex or related physiological response in response to the mechanical stimulation is detected. In response to the detected response, it is determined whether the subject is appropriate for the therapy and/or which of a plurality of implants with different geometries and/or cross-sectional areas is most optimally suited for deployment in the subject.
1. A method of screening a subject for a therapy, the method comprising:
providing at least one mechanical stimulus to a blood vessel, the at least one mechanical stimulus generating at least a first region of the blood vessel having increased radius of curvature and at least a second region of the blood vessel having decreased radius of curvature, wherein the at least one mechanical stimulus is provided intra-vascularly, and wherein providing the at least one mechanical stimulus comprises advancing a mechanical stimulus device through vasculature of the subject to a target location;
detecting at least one change in at least one physiological parameter in response to the provided at least one mechanical stimulus; and
selecting an implant to provide the therapy to the subject based on the detected at least one change in the at least one physiological parameter, wherein at least the first region of the blood vessel having increased curvature comprises a plurality of first regions having increased radius of curvature, wherein at least the second region of the blood vessel having decreased curvature comprises a plurality of second regions having decreased radius of curvature, and wherein the first and second regions alternate with one another around a circumference of the blood vessel.
2. The method of claim 1 , wherein the target location is located in a carotid artery, carotid sinus, aorta, aortic arch, subclavian artery, cranial artery, heart, or common artery of the subject.
3. The method of claim 1 , wherein the at least the first region of the blood vessel having increased radius of curvature comprises at least one region of the blood vessel with increased strain.
4. The method of claim 1 , wherein the at least the second region of the blood vessel having decreased radius of curvature comprises at least one region of the blood vessel with increased strain.
5. The method of claim 1 , wherein providing the at least one mechanical stimulus comprises deploying a first implant from the mechanical stimulus device to the target location, the implant increasing the curvature of at least the first region of the blood vessel and decreasing curvature of at least the second region of the blood vessel.
6. The method of claim 5 , wherein providing the at least one mechanical stimulus further comprises retracting the first implant from the target location.
7. The method of claim 6 , wherein the first implant is retracted from the target location after a time period of between 0 minutes and 1 minute, from 1 minute to 2 minute, from 2 minutes to 3 minutes, from 3 minutes to 4 minutes, from 4 minutes to 5 minutes, from 5 minutes to 10 minutes, from 10 minutes to 20 minutes, from 20 minutes to 30 minutes, from 30 minutes to 1 hour, or from 1 hour to 2 hours.
8. The method of claim 6 , wherein providing the at least one mechanical stimulus further comprises deploying a second implant from the mechanical stimulus device to the target location after the retracting the first implant, the second implant increasing the curvature of at least the first region of the blood vessel and decreasing curvature of at least the second region of the blood vessel differently than the first implant.
9. The method of claim 1 , wherein the plurality of first regions having increased radius of curvature comprises at least three regions having increased radius of curvature, and wherein the plurality of second regions having decreased radius of curvature comprises at least three regions having decreased radius of curvature.
10. The method of claim 1 , wherein the at least one physiological parameter comprises one or more of a baroreflex response, blood pressure, heart rate, blood vessel impedance, a sympathetic nerve activity, or a nerve activity.
11. The method of claim 1 , wherein selecting the implant to provide the therapy based on the detected at least one change in the at least one physiological parameter comprises selecting one implant of a plurality of implants, the selected one implant being suited to affect an optimal therapeutic response.
12. The method of claim 11 , wherein the optimal therapeutic response comprises an optimal baroreflex response modification.
13. The method of claim 1 , wherein selecting the implant to provide the therapy based on the detected at least one change in the at least one physiological parameter comprises selecting one or more of a size or geometry of the implant.
14. The method of claim 13 , wherein the geometry of the implant comprises one or more of a number of vertices or corners of a cross-section of the implant, an orientation of the vertices or corners, or a number of vessel wall contacting struts of the implant.
15. The method of claim 1 , wherein the implant comprises an expandable scaffold, the expandable scaffold being configured to alter one or more of a geometry or cross-sectional area of the target region.
16. A method of screening a subject for a therapy, the method comprising:
providing at least one mechanical stimulus to a blood vessel, the at least one mechanical stimulus generating at least a first region of the blood vessel having increased radius of curvature and at least a second region of the blood vessel having decreased radius of curvature, wherein the at least one mechanical stimulus is provided intra-vascularly and wherein providing the at least one mechanical stimulus comprises advancing a mechanical stimulus device through vasculature of the subject to a target location;
detecting at least one change in at least one physiological parameter in response to the provided at least one mechanical stimulus; and
selecting an implant to provide the therapy to the subject based on the detected at least one change in the at least one physiological parameter,
wherein selecting the implant to provide the therapy based on the detected at least one change in the at least one physiological parameter comprises selecting one or more of a size or geometry of the implant, and
wherein the size of the implant comprises a cross-sectional area of the implant and the cross-sectional area of the implant is in a range of 50.0 mm 2 to 60.0 mm 2 , 60.0 mm 2 to 70.0 mm 2 , 70.0 mm 2 to 80.0 mm 2 , 80.0 mm 2 to 90.0 mm 2 , 90.0 mm 2 to 100.0 mm 2 , 100.0 mm 2 to 110.0 mm 2 , 110.0 mm 2 to 120.0 mm 2 , or 120.0 mm 2 to 130.0 mm 2 .
17. The method of claim 16 , wherein the target location is located in a carotid artery, carotid sinus, aorta, aortic arch, subclavian artery, cranial artery, heart, or common artery of the subject.
18. The method of claim 16 , wherein the at least the first region of the blood vessel having increased radius of curvature comprises at least one region of the blood vessel with increased strain.
19. The method of claim 16 , wherein the at least the second region of the blood vessel having decreased radius of curvature comprises at least one region of the blood vessel with increased strain.
20. The method of claim 16 , wherein providing the at least one mechanical stimulus comprises deploying a first implant from the mechanical stimulus device to the target location, the implant increasing the curvature of at least the first region of the blood vessel and decreasing curvature of at least the second region of the blood vessel.
21. The method of claim 20 , wherein providing the at least one mechanical stimulus further comprises retracting the first implant from the target location.
22. The method of claim 21 , wherein the first implant is retracted from the target location after a time period of between 0 minutes and 1 minute, from 1 minute to 2 minute, from 2 minutes to 3 minutes, from 3 minutes to 4 minutes, from 4 minutes to 5 minutes, from 5 minutes to 10 minutes, from 10 minutes to 20 minutes, from 20 minutes to 30 minutes, from 30 minutes to 1 hour, or from 1 hour to 2 hours.
23. The method of claim 21 , wherein providing the at least one mechanical stimulus further comprises deploying a second implant from the mechanical stimulus device to the target location after the retracting the first implant, the second implant increasing the curvature of at least the first region of the blood vessel and decreasing curvature of at least the second region of the blood vessel differently than the first implant.
24. The method of claim 16 , wherein at least the first region of the blood vessel having increased curvature comprises a plurality of first regions having increased radius of curvature, wherein at least the second region of the blood vessel having decreased curvature comprises a plurality of second regions having decreased radius of curvature, and wherein the first and second regions alternate with one another around a circumference of the blood vessel.
25. The method of claim 24 , wherein the plurality of first regions having increased radius of curvature comprises at least three regions having increased radius of curvature, and wherein the plurality of second regions having decreased radius of curvature comprises at least three regions having decreased radius of curvature.
26. The method of claim 16 , wherein the at least one physiological parameter comprises one or more of a baroreflex response, blood pressure, heart rate, blood vessel impedance, a sympathetic nerve activity, or a nerve activity.
27. The method of claim 16 , wherein selecting the implant to provide the therapy based on the detected at least one change in the at least one physiological parameter comprises selecting one implant of a plurality of implants, the selected one implant being suited to affect an optimal therapeutic response.
28. The method of claim 27 , wherein the optimal therapeutic response comprises an optimal baroreflex response modification.
29. The method of claim 16 , wherein the geometry of the implant comprises one or more of a number of vertices or corners of a cross-section of the implant, an orientation of the vertices or corners, or a number of vessel wall contacting struts of the implant.
30. The method of claim 16 , wherein the implant comprises an expandable scaffold, the expandable scaffold being configured to alter one or more of a geometry or cross-sectional area of the target region.