NON-INVASIVE EVALUATION OF FIT AND SIZING OF DEVICE PRIOR TO IMPLANT

• US 20150119692A1
• Filed: 10/21/2014
• Published: 04/30/2015
• Est. Priority Date: 10/25/2013
• Status: Abandoned Application

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: McHenry, Brian, Hill, Alexander, Okali, Victor
• Application Number:
  US14/519,891
• Publication Number:
  US 20150119692A1
• Time in Patent Office: Days
• US Class Current: 600/411
• CPC Class Codes: A61B 2034/105 Modelling of the patient, e.g. for ligaments or bones
• CPC Class Codes: A61B 2034/108 Computer aided selection or customisation of medical implants or cutting guides
• CPC Class Codes: A61B 2560/066 catheters therefor
• CPC Class Codes: A61B 2576/023 for the heart
• CPC Class Codes: A61B 5/0037 Performing a preliminary scan, e.g. a prescan for identifying a region of interest
• CPC Class Codes: A61B 5/0044 for the heart
• CPC Class Codes: A61B 5/055 involving electronic [EMR] or nuclear [NMR] magnetic resonance, e.g. magnetic resonance imaging
• CPC Class Codes: A61B 5/4851 Prosthesis assessment or monitoring
• CPC Class Codes: A61B 5/7292 Prospective gating, i.e. predicting the occurrence of a physiological event for use as a synchronisation signal
• CPC Class Codes: A61F 2/2496 Devices for determining the dimensions of the prosthetic valve to be implanted, e.g. templates, sizers
• CPC Class Codes: G16H 30/40 for processing medical images, e.g. editing

Abstract

Maximum and minimum dimensional characteristics of a conduit are determined by imaging a portion of the conduit into which an expandable medical device is to be implanted at appropriate points in the cardiac cycle (or other suitable cycle, such as the respiratory cycle, or at other suitable times). The dimensional characteristics of the conduits within the portion of interest may be evaluated and compared to the maximum and minimum dimensional characteristics of the medical device to be implanted in the conduit to determine whether the medical device is of an appropriate size for properly fitting in the conduit.

Claims

1. A non-invasive method for determining whether an expandable medical device is appropriate for implanting in a conduit of patient, comprising:

imaging a portion of the conduit of the patient into which the medical device is to be implanted, wherein the imaging is performed during a plurality of portions of the cardiac cycle including (i) a portion of the cardiac cycle at which one or more dimensional characteristics of the conduit are at or near minimums and (ii) a portion of the cardiac cycle at which the one or more dimensional characteristics of the conduit are at or near maximums;

deriving, from the imaging, minimum and maximum dimensional characteristics of the conduit at a plurality of locations along a length of the portion of the conduit; and

determining that the medical device is appropriate for implantation if the maximum and minimum dimensional characteristics of the conduit at the predetermined locations along the length of the conduit are within predetermined ranges of maximum, expanded and minimum, contracted dimensional characteristics of the medical device at predetermined locations along the length of the medical device.

2. A method according to claim 1, wherein the medical device is a transcatheter medical device.

3. A method according to claim 1, wherein the medical device comprises a prosthetic heart valve device having a proximal inflow region and a distal outflow region.

4. A method according to claim 3, wherein the conduit comprises a heart valve.

5. A method according to claim 4, wherein imaging comprises capturing image data at or near 30% phase and at or near 90% phase of a cardiac cycle of the patient.

6. A method according to claim 4, wherein the medical device is determined to be appropriate for implantation if the maximum dimensional characteristic of the conduit at a predetermined location along the length of the conduit is 60% to 95% of the maximum dimensional characteristic of the medical device at a location along a distal outflow portion of the medical device having the largest dimensional characteristic of the distal outflow portion of the medical device.

7. A method according to claim 4, wherein the medical device is determined to be appropriate for implantation if the maximum dimensional characteristic of the conduit at a predetermined location along the length of the conduit is 85% or less than the maximum dimensional characteristic of the medical device at a location along a distal outflow portion of the medical device having the largest dimensional characteristic of the distal outflow portion of the medical device.

8. A method according to claim 4, wherein the medical device is determined to be appropriate for implantation if the maximum dimensional characteristic of the conduit at a predetermined location along the length of the conduit is 60% to 90% of the maximum dimensional characteristic of the medical device at a location along a proximal inflow portion of the medical device having the largest dimensional characteristic of the proximal inflow portion of the medical device.

9. A method according to claim 4, wherein the conduit is a pulmonary artery.

10. A method according to claim 1, wherein the imaging comprises magnetic resonance imaging, ultrasound imaging, computed tomography imaging, or x-ray imaging.

11. A method according to claim 1, wherein the method is a computer-implemented method.

12. A computer implemented method for determining whether an expandable medical device is appropriate for implanting in a conduit of patient, comprising:

receiving input of imaging data regarding a portion of the conduit of the patient into which the medical device is to be implanted, wherein the imaging data comprises data obtained during a plurality of portions of the cardiac cycle, including (i) a portion of the cardiac cycle at which dimensional characteristics of the conduit are at or near minimums and (ii) a portion of the cardiac cycle at which the dimensional characteristics of the conduit are at or near maximums;

calculating minimum and maximum dimensional characteristics of the conduit at a plurality of locations along a length of the portion of the conduit based on the imaging data; and

determining whether the maximum and minimum dimensional characteristics of the conduit at the predetermined locations along the length of the conduit are within predetermined ranges of maximum, expanded and minimum, contracted dimensional characteristics of the medical at predetermined locations along the length of the medical.

13. A method according to claim 12, wherein the medical device is a transcatheter medical device.

14. A method according to claim 12, wherein the medical device comprises a prosthetic heart valve.

15. A method according to claim 12, further comprising receiving input regarding the length and maximum, expanded and minimum, contracted dimensional characteristics of the medical device at predetermined locations along the length of the medical device.

16. A method according to claim 15, further comprising displaying data indicative of whether the medical device is appropriate for implanting in the conduit of the patient.

17. A non-transitory computer-readable medium that when executed by a device causes the device to carry out a method according to claim 12.

18. A device for determining whether an expandable medical device is appropriate for implanting in a conduit of patient, the device comprising:

input apparatus configured to receive input of imaging data regarding a portion of the conduit of the patient into which the medical device is to be implanted, wherein the imaging data comprises data obtained during a plurality of portions of the cardiac cycle, including (i) a portion of the cardiac cycle at which dimensional characteristics of the conduit are at or near minimums and (ii) a portion of the cardiac cycle at which the dimensional characteristics of the conduit are at or near maximums; and

computing apparatus configured to;

calculate minimum and maximum dimensional characteristics of the conduit at a plurality of locations along a length of the portion of the conduit based on the imaging data; and

determining whether the maximum and minimum dimensional characteristics of the conduit at the predetermined locations along the length of the conduit are within predetermined ranges of maximum, expanded and minimum, contracted dimensional characteristics of the medical device at predetermined locations along the length of the medical device.

19. A device according to claim 18, wherein the medical device is a transcatheter medical device comprising a prosthetic heart valve.

20. A device according to any one of claims 18, wherein the input apparatus is further configured to receive input regarding the length and maximum, expanded and minimum, contracted dimensional characteristics of the medical at predetermined locations along the length of the medical device.