IP Library Granted Patent US 9,295,448
Granted Patent B2
US 9,295,448 · App. 14/209,864 · Granted Mar 29, 2016

Methods for diagnosing vitreo-retinal disease

Inventors: Jeffrey A. Ketterling (New York, NY); Jonathan Mamou (New York, NY); Ronald H. Silverman (New York, NY); Jerry Sebag (Laguna Beach, CA)
Assignees: Riverside Research Institute; The Trustees of Columbia University in the City of New York
A61B8/10A61B8/5223
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Quick Facts
Patent No.
US 9,295,448
App. No.
14/209,864
Granted
Mar 29, 2016
Kind
B2
Abstract

A quantitative method to analyze phase-resolved, raw backscatter echo data or the envelope of phase-resolved, raw backscatter echo data to characterize vitreous inhomogeneities as they relate to normal aging and vitreo-retinal disease. The technique can be applied to 2D or 3D data acquired from the vitreous. The approach provides an objective end value to characterize the vitreous and provide a tool for early diagnosis, monitoring and planning treatment of vitreo-retinal diseases.

Claims (34)

1. A method to acquire and process vitreous image data to characterize vitreous inhomogeneities comprising the steps of:

creating a unit, said creating a unit comprising transmitting at least one ultrasound signal, acquiring phase-resolved, raw backscatter echo data of said transmitted signal, and normalizing said acquired data, wherein said normalized acquired data forms said unit; the method further comprising:

extracting local level estimates from said normalized data; and

processing said extracted local level estimates, said processing producing at least one global parameter, said at least one global parameter being used to objectively characterize one or more vitreous inhomogeneities.

2. The method of claim 1 , wherein said global parameter is produced from one local-level estimate from within a vitreous of an eye.

3. The method of claim 1 , wherein said global parameter is produced from a plurality of local level estimates from within a vitreous of an eye.

4. The method of claim 1 , further comprising repeating the step of creating a unit until 2D single cross-sectional image-plane data of an entire vitreous is obtained.

5. The method of claim 4 , further comprising preparing an image volume by compiling a plurality of said 2D single cross-sectional image plane data.

6. The method of claim 1 , wherein said ultrasound signal is transmitted from an annular array.

7. The method of claim 6 , further comprising applying a synthetic focusing approach to said acquired data.

8. The method of claim 1 , further comprising calculating an envelope of said phase-resolved, raw backscatter echo data.

9. The method of claim 1 , wherein said ultrasound signal is transmitted from a single-element.

10. The method of claim 1 , further comprising a step of segmenting the vitreous out from surrounding tissue prior to extracting local-level estimates.

11. A method to quantify vitreous image data to characterize inhomogeneities of a vitreous comprising the steps of:

transmitting at least one ultrasound signal;

acquiring an envelope of phase-resolved, raw backscatter echo data of said transmitted signal;

normalizing said acquired data;

extracting local level estimates from said normalized data; and

combining said local level estimates producing at least one global parameter used to characterize vitreous inhomogeneities, said at least one global parameter being incorporated into a classifier to yield at least one optimal global index or end value indicative of an overall vitreous pathology.

12. The method of claim 11 , further comprising creating a normal database, wherein said normal database is a compilation of first extracted global parameters being vitreous parameter data representing a normal vitreous.

13. The method of claim 12 , further comprising creating a disease database, wherein said disease database is a compilation of second extracted global parameters being vitreous parameter data representing diseased vitreous conditions at various stages of disease.

14. The method of claim 13 , wherein said at least one global parameter is compared with said normal database and said disease database, said comparison identifying a correlation between said global parameter and information in one of two said databases, said correlation being used to diagnose one or more vitreous conditions ranging from age-normal to various stages of diseased states, said diagnosis being further comparable with said optimal global index or end value.

15. A method to quantify vitreous image data to characterize vitreous inhomogeneities comprising the steps of:

creating a unit, said creating a unit comprising transmitting at least one ultrasound signal, acquiring phase-resolved, raw backscatter echo data of said transmitted signal, and normalizing said acquired data;

extracting local-level estimates from said normalized data;

combining said extracted local-level estimates producing at least one global parameter, said at least one global parameter being incorporated into a classifier to yield an end value indicative of an overall vitreous pathology;

creating a normal database, wherein said normal database is a compilation of first extracted global parameters being vitreous parameter data representing normal vitreous;

creating a disease database, wherein said disease database is a compilation of second extracted global parameters being vitreous parameter data representing diseased vitreous conditions at various stages of disease; and

diagnosing a vitreous condition based on comparison of said normal database with said disease database.

16. The method of claim 15 , further comprising repeating the step of creating a unit until 2D single cross-sectional image plane data of an entire vitreous is obtained.

17. The method of claim 16 , further comprising preparing an image volume by compiling a plurality of said 2D single cross-sectional image plane data.

18. The method of claim 15 , wherein said at least one transmitted ultrasound signal is transmitted from an annular array.

19. The method of claim 18 , further comprising applying a synthetic focusing approach to said acquired backscatter signal.

20. The method of claim 18 , further comprising calculating an envelope of said phase-resolved, raw backscatter echo data.

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 12, 2017
From: COLUMBIA UNIV NEW YORK MORNINGSIDE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044836/0469 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2016
From: KETTERLING, JEFFREY A.; MAMOU, JONATHAN; SEBAG, JERRY
To: RIVERSIDE RESEARCH INSTITUTE
Reel/Frame 037762/0067 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2016
From: SILVERMAN, RONALD H.
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 037762/0144 →
Continuity (2)
Provisional Application 61779484 · Mar 13, 2013
Related Publication 20140268036A1 · Sep 18, 2014