The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 04, 2019

Filed:

Jul. 14, 2016
Applicant:

Heartflow, Inc., Redwood City, CA (US);

Inventors:

Charles A. Taylor, Menlo Park, CA (US);

Leo Grady, Millbrae, CA (US);

Sethuraman Sankaran, Palo Alto, CA (US);

Souma Sengupta, Cupertino, CA (US);

Hyun Jin Kim, San Mateo, CA (US);

Nan Xiao, Redwood City, CA (US);

Assignee:

HeartFlow, Inc., Redwood City, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G06T 7/00 (2006.01); A61B 5/026 (2006.01); A61B 6/00 (2006.01); A61B 6/03 (2006.01); A61B 8/06 (2006.01); A61B 8/08 (2006.01); G16H 50/50 (2018.01); G06F 19/00 (2018.01);
U.S. Cl.
CPC ...
A61B 6/563 (2013.01); A61B 5/026 (2013.01); A61B 6/032 (2013.01); A61B 6/504 (2013.01); A61B 6/507 (2013.01); A61B 6/5217 (2013.01); A61B 8/06 (2013.01); A61B 8/481 (2013.01); G06F 19/00 (2013.01); G06T 7/0012 (2013.01); G16H 50/50 (2018.01); G06T 2207/10081 (2013.01); G06T 2207/30101 (2013.01); G06T 2207/30104 (2013.01);
Abstract

Systems and methods are disclosed for assessing the severity of plaque and/or stenotic lesions using contrast distribution predictions and measurements. One method includes: receiving patient-specific images of a patient's vasculature and a measured distribution of a contrast agent delivered through the patient's vasculature; associating the measured distribution of the contrast agent with a patient-specific anatomic model of the patient's vasculature; defining physiological and boundary conditions of a blood flow model of the patient's blood flow and pressure; simulating the distribution of the contrast agent through the patient-specific anatomic model; comparing the measured distribution of the contrast agent and the simulated distribution of the contrast agent through the patient-specific anatomic model to determine whether a similarity condition is satisfied; and updating the defined physiological and boundary conditions and re-simulating distribution of the contrast agent through the one or more points of the patient-specific anatomic model until the similarity condition is satisfied.


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