IP Library Granted Patent US 12,682,451
Granted Patent B2
US 12,682,451 · App. 18/035,492 · Granted Jul 14, 2026

Quality maps for optical coherence tomography angiography

Inventor: Luis De Sisternes (San Franciso, CA)
Assignees: CARL ZEISS MEDITEC, INC.; CARL ZEISS MEDITEC AG
G06T7/0012G06T7/40G06T2207/10101G06T2207/20081G06T2207/20084G06T2207/30041G06T2207/30101G06T2207/30168
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Quick Facts
Patent No.
US 12,682,451
App. No.
18/035,492
Granted
Jul 14, 2026
Kind
B2
Abstract

A system, method, and/or device for determinizing a quality measure of OCT structural data and/or OCTA functional data uses a machine learning model trained to provide a single overall quality measure, or a quality map distribution for the OCT/OCTA data based on the generation of multiple features maps extracted from one or more slab views of the OCT/OCTA data. The extracted feature maps may be different texture-type maps, and the machine model is trained to determine the quality measure based on the texture maps.

Claims (36)

1 . A method for generating a quality measure of optical coherence tomography (OCT) data, comprising:

acquiring a volume of OCT data;

defining one or more slab views from the volume OCT data, wherein each slab view is a frontal, planar view of a sub-volume of the volume of OCT data;

generating a plurality of feature maps from each slab view;

determining the quality measure based on image properties of the plurality of feature maps; and

displaying the quality measure or storing the quality measure for further processing,

wherein the image properties of the feature maps include image texture features Haralick features.

2 . The method of claim 1 , wherein a plurality of said slab views are defined.

3 . The method of claim 1 , wherein determining the quality measure includes submitting the plurality of feature maps to a machine model trained using a plurality of pre-graded OCT data volume samples, one or more training slab view defined per OCT data volume sample, and a plurality of training feature maps generated from each training slab view.

4 . The method of claim 3 , wherein the machine model is a deep learning model.

5 . The method of claim 3 , wherein the machine model is a neural network model.

6 . The method of claim 1 , wherein the OCT data is OCT angiography data.

7 . The method of claim 1 , wherein the quality measure is a two-dimensional (2D) quality map identifying a quality measure for different regions of its corresponding slab view.

8 . The method of claim 7 , wherein:

determining the quality measure includes submitting the plurality of feature maps to a machine model trained to determine the quality maps based on the plurality of feature maps; and

the machine model is further trained to identify one or more causes of a quality region within the quality map having a lower quality measure than a predefined threshold, and identifying one or more corrective actions to improve the lower quality measure in a subsequent OCT acquisition.

9 . The method of claim 8 wherein the one or more causes are selected from a predefined list of error-sources including one or more of incorrect focusing, opacities, illumination below a predefined threshold, light penetration less than a predefined threshold, tracking or motion artifacts, and noise above a predefined threshold.

10 . The method of claim 8 , wherein the one or more corrective actions include a focus adjustment, a recommendation for pupil dilation, identifying an alternate imaging angle, or identifying possible cause of loss of eye tracking.

11 . The method of claim 8 , wherein the corrective action is output to an electronic display.

12 . The method of claim 8 , wherein the corrective action is transferred to an automated sub-system that automatically implements the corrective action prior to the subsequent acquisition.

13 . The method of claim 7 , further including defining an overall quality score for the acquisition based at least in part on the average of the individual quality measure distribution of the quality map.

14 . The method of claim 7 , wherein the acquisition is an OCTA acquisition defined from a plurality of OCT scans of the same region of the retina, and the method further includes defining an overall quality score for the OCTA acquisition based at least in part on the average of the individual quality measure distribution of the quality maps of the plurality of OCT scans from which the OCTA acquisition is defined.

15 . The method of claim 7 , further including, identifying a target region within the acquisition, and designating the entire acquisition as good or bad based on the quality map measures corresponding to the target region.

16 . A method for generating a quality measure of optical coherence tomography (OCT) data, comprising:

acquiring a volume of OCT data;

defining one or more slab views from the volume OCT data;

generating a plurality of feature maps from each slab view;

determining the quality measure based on image properties of the plurality of feature maps;

displaying the quality measure or storing the quality measure for further processing,

wherein the quality measure is a two-dimensional (2D) quality map identifying a quality measure for different regions of its corresponding slab view; and

wherein acquiring a volume of OCT data includes:

a) collecting a plurality of different OCT volume samples of the same retinal tissue region;

b) applying to each of the OCT volume samples the steps of defining one or more slab views, generating the plurality of feature maps, and determining the quality measure based on the plurality of feature maps, whereby a plurality of 2D quality map samples corresponding to the plurality of different OCT volume samples are defined; and

the method further comprises:

comparing the plurality of 2D quality map samples; and

defining composite OCT data based on the highest or higher quality regions of the plurality of different OCT volume samples based on their respective 2D quality map samples.