US2018049877A1PendingUtilityA1

Sizing device and method of positioning a prosthetic heart valve

Assignee: ST JUDE MEDICAL CARDIOLOGY DIV INCPriority: Oct 12, 2012Filed: Oct 27, 2017Published: Feb 22, 2018
Est. expiryOct 12, 2032(~6.2 yrs left)· nominal 20-yr term from priority
A61B 5/1076A61F 2230/001A61B 5/6869A61F 2/2496A61B 5/6862A61F 2/2418A61B 5/0031
53
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

A sizing device for a collapsible prosthetic heart valve includes a collapsible and expandable stent. The stent has an annulus section at a first end with a first diameter and an aortic section at a second end with a second diameter. The second diameter is greater than the first diameter, and the first end and the second end are disposed at opposite sides of the stent. A sensor is coupled adjacent the first diameter of the stent and is capable of collecting information related to stiffness of a native valve annulus by contacting portions of the native valve annulus. A method for determining the fitment of a prosthetic heart valve within a native valve annulus is also provided.

Claims

exact text as granted — not AI-modified
1 . A method for determining the fitment of a prosthetic heart valve within a native valve annulus, comprising:
 introducing a stent having an annulus section at a first end with a first diameter and an aortic section at a second end with a second diameter, the second diameter being greater than the first diameter, and the first end and the second end being disposed at opposite sides of the stent and, a sensor coupled to the stent, the sensor being capable of collecting information related to the native valve annulus by contacting portions of the native valve annulus;   expanding the diameter of the stent within the native valve annulus; and   acquiring information related to the native valve annulus via the sensor by contacting portions of the native valve annulus with the sensor.   
     
     
         2 . The method of  claim 1 , wherein the information includes the diameter of the native valve annulus. 
     
     
         3 . The method of  claim 1 , wherein the information includes data relating to an extent of calcification of tissue of the native valve annulus. 
     
     
         4 . The method of  claim 1 , wherein the step of expanding the diameter of the stent includes rotating a first portion of a deployment device relative to a second portion of the deployment device within the native valve annulus. 
     
     
         5 . The method of  claim 1 , wherein the stent is self-expandable, and the method further includes disposing a removable cannula about the stent to maintain the stent in a collapsed configuration, and the step of expanding the diameter of the stent includes removing the cannula from around the stent. 
     
     
         6 . The method of  claim 1 , wherein the sensor comprising at least one deflectable contacting member. 
     
     
         7 . A method for determining the fitment of a prosthetic heart valve within a native valve annulus, comprising:
 introducing a stent having an annulus section and an aortic section, and a sensor coupled to the stent, the sensor being capable of collecting information related to the native valve annulus by contacting portions of the native valve annulus;   expanding the diameter of the stent within the native valve annulus by rotating a first portion of a deployment device relative to a second portion of the deployment device within the native valve annulus;   acquiring information related to the native valve annulus via the sensor by contacting portions of the native valve annulus with the sensor; and   expanding the diameter of the stent in-vitro to establish a relationship between the number of rotations of the first portion of the deployment device relative to the second portion of the deployment device and a diameter of the stent.   
     
     
         8 . The method of  claim 7 , wherein the step of acquiring information related to the native valve annulus includes comparing the number of rotations within the native valve annulus to the relationship. 
     
     
         9 . The method of  claim 7 , wherein the sensor comprising at least one deflectable contacting member. 
     
     
         10 . A method for determining the fitment of a prosthetic heart valve within a native valve annulus, comprising:
 introducing a stent having an annulus section and an aortic section and at least two diameters and, a sensor coupled to the annulus section of the stent, the sensor being capable of collecting information related to the native valve annulus by contacting portions of the native valve annulus;   acquiring information related to the native valve annulus via the sensor by contacting portions of the native valve annulus; and   expanding the diameter of the stent within the native valve annulus by rotating a first portion of a deployment device relative to a second portion of the deployment device within the native valve annulus until the sensor measures a radial force of a predetermined value.   
     
     
         11 . The method of  claim 10 , wherein the sensor comprising at least one deflectable contacting member. 
     
     
         12 . A sizing device for use in implanting a collapsible prosthetic heart valve in a native valve annulus, the sizing device comprising:
 a collapsible and expandable stent having an annulus section at a first end with a first diameter and an aortic section at a second end with a second diameter, the second diameter being greater than the first diameter, and the first end and the second end being disposed at opposite sides of the stent; and   a sensor coupled adjacent the first diameter of the stent, the sensor being capable of collecting information related to stiffness of the native valve annulus by contacting portions of the native valve annulus.   
     
     
         13 . The device of  claim 12 , wherein the stent is self-expandable. 
     
     
         14 . The device of  claim 12 , wherein the stent comprises nitinol. 
     
     
         15 . The device of  claim 12 , wherein the sensor is flexible. 
     
     
         16 . The device of  claim 12 , wherein the information includes the diameter of the native valve annulus. 
     
     
         17 . The device of  claim 12 , wherein the information includes data relating to the extent of calcification of tissue of the native valve annulus. 
     
     
         18 . The device of  claim 12 , wherein the sensor includes at least one piezoelectric material. 
     
     
         19 . The device of  claim 12 , wherein the sensor comprises a polymer.

Join the waitlist — get patent alerts

Track US2018049877A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.