IP Library Granted Patent US 9,846,211
Granted Patent B2
US 9,846,211 · App. 14/589,888 · Granted Dec 19, 2017

Optimised pulse sequences for evaluating spatial frequency content of a selectively excited internal volume

Inventors: Timothy W. James (Santa Barbara, CA); Lance W. Farr (Swansea, GB); James Rafferty (Godrergraig, GB); David Chase (Santa Barbara, CA)
Assignee: Osteotronix Medical PTE Limited
G01R33/4818G01R33/4833G01R33/5659G01R33/5616G01R33/5617
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Quick Facts
Patent No.
US 9,846,211
App. No.
14/589,888
Granted
Dec 19, 2017
Kind
B2
Abstract

In a structural analysis using NMR techniques, a method for gathering k-value data from frequency encoded spin echoes generated from internal volumes selectively excited by intersecting 90° and 180° slice selective and refocusing RF pulses and subjected to a read gradient for the purpose of quantifying the spatial frequency content of the selected internal volume without contamination by a FID signal, comprising: acquiring spin echo data such that the FID signal generated by imperfections in the 180° slice selective refocusing RF pulse is attenuated by the read gradient such that any remaining FID signal is spatially encoded with higher k-values than the frequency encoded k-values being recorded for subsequent structural analysis while simultaneously providing for t2 t2* and t1 contrast. Other aspects of the invention are disclosed.

Claims (16)

1. In a structural analysis using NMR techniques, a method for gathering k-value data from frequency encoded spin echoes generated from internal volumes selectively excited by intersecting 90° and 180° slice selective and refocusing RF pulses and subjected to a read gradient for the purpose of quantifying the spatial frequency content of the selected internal volume without contamination by a FID signal, comprising: acquiring spin echo data such that the FID signal generated by imperfections in the 180° slice selective refocusing RF pulse is attenuated by the read gradient such that any remaining FID signal is spatially encoded with higher k-values than the frequency encoded k-values being recorded for subsequent structural analysis while simultaneously providing for t2 t2* and t1 contrast.

2. The method of claim 1 wherein the frequency encoded spin echoes are Fourier symmetric spin echoes with T1 contrast further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

3. The method of claim 2 wherein the Fourier symmetric spin echoes are refocused using a refocusing gradient and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the gradient refocused echo, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

4. The method of claim 2 wherein the Fourier symmetric spin echoes are refocused using a 180° slice selective and refocusing RF pulse and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the echo generated, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

5. The method of claim 1 wherein the frequency encoded spin echoes are partial Fourier symmetric spin echoes with T 1 contrast further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 and further permitting shortening the spin echo time by as much as two times the time difference between a leading portion of a full Fourier symmetric echo acquisition and a leading portion of the partial Fourier echo acquisition.

6. The method of claim 5 wherein the partial Fourier symmetric spin echoes are refocused using a refocusing gradient and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the gradient refocused echo, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

7. The method of claim 5 wherein the partial Fourier symmetric spin echoes are refocused using a 180° slice selective and refocusing RF pulse and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the echo generated, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

8. The method of claim 1 wherein the frequency encoded spin echoes are Fourier symmetric spin echoes with T 2 contrast further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

9. The method of claim 8 wherein the Fourier symmetric spin echoes are refocused using a refocusing gradient and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the gradient refocused echo, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

10. The method of claim 8 wherein the Fourier symmetric spin echoes are refocused using a 180° slice selective and refocusing RF pulse and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the echo generated, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

11. The method of claim 1 wherein the frequency encoded spin echoes are Fourier asymmetric spin echoes with T 2 * contrast further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

12. The method of claim 11 wherein the Fourier asymmetric spin echoes are refocused using a refocusing gradient and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the gradient refocused echo, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

13. The method of claim 11 wherein the Fourier asymmetric spin echoes are refocused using a 180° slice selective and refocusing RF pulse and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the echo generated, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

14. The method of claim 1 wherein the frequency encoded spin echoes are partial Fourier asymmetric spin echoes with T 2 * contrast further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 and further permitting shortening the spin echo time by as much as two times the time difference between a leading portion of a full Fourier symmetric echo acquisition and a leading portion of the partial Fourier echo acquisition.

15. The method of claim 14 wherein the partial Fourier asymmetric spin echoes are refocused using a refocusing gradient and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the gradient refocused echo, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

16. The method of claim 14 wherein the partial Fourier asymmetric spin echoes are refocused using a 180° slice selective and refocusing RF pulse and further comprising gathering k-value data for subsequent structural analysis of a portion of the k-value data acquired from k 0 to k-max in the echo generated, thereby avoiding the potentially FID contaminated portion of the spin echo prior to k 0 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2017
From: ACUITAS MEDICAL LIMITED
To: OSTEOTRONIX MEDICAL PTE LIMITED
Reel/Frame 042384/0129 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 18, 2015
From: JAMES, TIMOTHY W.; FARR, LANCE W.; RAFFERTY, JAMES; CHASE, DAVID
To: ACUITAS MEDICAL LIMITED
Reel/Frame 035943/0602 →
Continuity (3)
Continuation PCTUS2013049167 · Jul 2, 2013
Provisional Application 61668472 · Jul 6, 2012
Related Publication 20150153432A1 · Jun 4, 2015