Pulmonary perfusion MRI using interleaved variable density sampling and HighlY constrained cartesian reconstruction (HYCR)
Purpose: To demonstrate the feasibility of performing single breathhold, noncardiac gated, ultrafast, high spatial‐temporal resolution whole chest MR pulmonary perfusion imaging in humans. Materials and Methods: Eight subjects (five male, three female) were scanned with the proposed method on a 3 Te...
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Published in | Journal of magnetic resonance imaging Vol. 38; no. 3; pp. 751 - 756 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.09.2013
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Purpose:
To demonstrate the feasibility of performing single breathhold, noncardiac gated, ultrafast, high spatial‐temporal resolution whole chest MR pulmonary perfusion imaging in humans.
Materials and Methods:
Eight subjects (five male, three female) were scanned with the proposed method on a 3 Tesla clinical scanner using a 32‐channel phased‐array coil. Seven (88%) were healthy volunteers, and one was a patient volunteer with sarcoidosis. The peak lung enhancement phase for each subject was scored for gravitational effect, peak parenchymal enhancement and severity of artifacts by three cardiothoracic radiologists independently.
Results:
All studies were successfully performed by MR technologists without any additional training. Mean parenchymal signal was very good, measuring 0.78 ± 0.13 (continuous scale, 0 = “none” → 1 = “excellent”). Mean level of motion artifacts was low, measuring 0.13 ± 0.08 (continuous scale, 0 = “none” → 1 = “severe”).
Conclusion:
It is feasible to perform single breathhold, noncardiac gated, ultrafast, high spatial‐temporal resolution whole chest MR pulmonary perfusion imaging in humans. J. Magn. Reson. Imaging 2013;38:751–756. © 2013 Wiley Periodicals, Inc. |
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Bibliography: | ArticleID:JMRI24018 ark:/67375/WNG-RZ61SC6B-K UW Radiology R&D Committee; NIH - No. NIH-R01 EB006882 istex:610FFE6F9C440ABFD49033032E1280188B4FFD22 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1053-1807 1522-2586 1522-2586 |
DOI: | 10.1002/jmri.24018 |