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Parallel Imaging in Clinical MR Applications

E-BookPDF1 - PDF WatermarkE-Book
564 Seiten
Englisch
Springer Berlin Heidelbergerschienen am11.01.20072007
This book presents the first in-depth introduction to parallel imaging techniques and, in particular, to the application of parallel imaging in clinical MRI. It will provide readers with a broader understanding of the fundamental principles of parallel imaging and of the advantages and disadvantages of specific MR protocols in clinical applications in all parts of the body at 1.5 and 3 Tesla.mehr
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EUR320,99
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Produkt

KlappentextThis book presents the first in-depth introduction to parallel imaging techniques and, in particular, to the application of parallel imaging in clinical MRI. It will provide readers with a broader understanding of the fundamental principles of parallel imaging and of the advantages and disadvantages of specific MR protocols in clinical applications in all parts of the body at 1.5 and 3 Tesla.
Details
Weitere ISBN/GTIN9783540688792
ProduktartE-Book
EinbandartE-Book
FormatPDF
Format Hinweis1 - PDF Watermark
FormatE107
Erscheinungsjahr2007
Erscheinungsdatum11.01.2007
Auflage2007
ReiheMedical Radiology
Seiten564 Seiten
SpracheEnglisch
IllustrationenXII, 564 p.
Artikel-Nr.1429133
Rubriken
Genre9200

Inhalt/Kritik

Inhaltsverzeichnis
1;Foreword;6
2;Part I: Basic Principles of Parallel-Imaging Techniques;15
2.1;MRI from k-Space to Parallel Imaging;16
2.2;Basic Reconstruction Algorithms for Parallel Imaging;32
2.3;The g-Factor and Coil Design;50
2.4;Measurement of Signal-to-Noise Ratio and Parallel Imaging;62
2.5;Special Applications of Parallel Imaging;76
2.6;Parallel-Imaging Reconstruction of Arbitrary-k-Space-Sampling Data;84
2.7;Complementary Techniques for Accelerated Imaging;104
3;Part II: Sequence Design for (Auto-Calibrated) Parallel Imaging;118
3.1;Measurement of Coil Sensitivity Pro.les;120
3.2;Conventional Spin-Echo and Gradient-Echo Pulse Sequences;126
3.3;Single-Shot Pulse Sequences;132
3.4;Fast Sequences for Dynamic and Time-Resolved Imaging;140
3.5;The Development of TSENSE;154
3.6;Design of Dedicated MRI Systems for Parallel Imaging;168
3.7;Dedicated Coil Systems from Head to Toe;174
3.8;Design of Parallel-Imaging Protocols;182
3.9;General Advantages of Parallel Imaging;186
3.10;Limitations of Parallel Imaging;190
4;Part IV: Clinical Applications: Imaging of Morphology;194
4.1;High-Resolution Imaging of the Brain;196
4.2;High-Resolution Imaging of the Skull Base and Larynx;212
4.3;Lung Imaging;222
4.4;Liver Imaging;232
4.5;High-Resolution Imaging of the Biliary Tree and the Pancreas;246
4.6;Parallel Imaging in Inflammatory Bowel Disease;260
4.7;Musculoskeletal Imaging: Knee and Shoulder;268
4.8;Advanced Methods of Fat Suppression and Parallel Imaging;282
5;Part V: Clinical Applications: Angiography;297
5.1;MRA of Brain Vessels;298
5.2;MRA of the Carotid Arteries;304
5.3;MRA of the Pulmonary Circulation;320
5.4;MRA of the Renal Arteries;332
5.5;Peripheral MR Angiography;342
5.6;Pediatric Congenital Cardiovascular Disease;362
5.7;High-Resolution Whole-Body MRA;368
6;Part VI: Clinical Applications: Function;382
6.1;Imaging of CNS Diffusion and Perfusion;384
6.2;Diffusion Tensor Imaging of the Brain;392
6.3;Imaging of Cardiac Function;406
6.4;Imaging of Cardiac Perfusion;420
6.5;Imaging of Pulmonary Perfusion;430
6.6;Oxygen-Enhanced Imaging of the Lung;442
6.7;Imaging of Renal Perfusion;454
7;Part VII:Comprehensive Protocols;463
7.1;Cardiovascular Screening;464
7.2;Tumor Staging;474
7.3;Imaging of Bronchial Carcinoma;484
7.4;Imaging of Pulmonary Hypertension;494
8;Part VIII: Future Developments;509
8.1;New Coil Systems for;510
8.2;Highly Parallel MR Acquisition Strategies;510
8.3;Parallel-Excitation Techniques for;524
8.4;Ultra-High-Field MRI;524
8.5;Future Software Developments;536
8.6;Future Imaging Protocols;546
9;Subject Index;556mehr
Leseprobe
18 High-Resolution Imaging of the Brain (p. 183-184)

Roland Bammer and Scott Nagle

CONTENTS
18.1 Introduction 183
18.2 Structural MRI 185
18.3 MR Angiography 190
18.4 Quantitative/Functional MRI 193
18.5 Pediatric MRI 196
18.6 Conclusion 196
References 197

18.1 Introduction

Resolution enhancement in MRI is of great potential for increased diagnostic accuracy in brain and spine imaging. With the advent of high-. eld systems increased signal-to-noise ratio (SNR) affords smaller voxel sizes, but overall scan time is still a limiting factor for high-resolution brain imaging in a clinical setting. Parallel imaging is of great bene. t since it allows us to achieve high-resolution 2D and 3D acquisitions in clinically acceptable time frames. In addition, parallel imaging can also diminish the amount of image blurring and geometric distortions leading to obvious resolution and quality improvements without altering the acquisition matrix size.

This chapter critically addresses the general advantages and limitations of high-resolution neuroimaging in concert with the additional capacity provided by parallel imaging. Specifically, the role of parallel imaging in high-resolution structural MRI, magnetic resonance angiography, and functional MRI in the broader sense (i.e., diffusion and perfusion MRI as well as classical functional MRI) are discussed. The improved scanning efficiency of parallel imaging methods can be applied in a number of fruitful ways in the . eld of brain MR imaging. As described in the . rst part this book, these parallel-imaging strategies cleverly incorporate the spatially varying sensitivity pro. les of multiple-channel receive coils in order to reduce the number of k-space measurements necessary to reconstruct an image (Hutchinson and Raff 1988, Kwiat et al. 1991, Sodickson and Manning 1977, Pruessmann et al. 1999). In conventional Cartesian k-space sampling schemes, this is typically realized by decreasing the number of phaseencoded steps. In cases of high SNR, the reduction of phase-encoded steps by a factor R (accompanied by its obligatory R decrease in SNR Pruessman et al. 1999) can be used to increase either spatial resolution or temporal resolution. These advantages are not mutually exclusive and it depends on the specific scan protocol whether one favors more rapid scanning or higher resolution. In addition, the artefact and blurring associated with several multiple-echo or long-readout sequences can be mitigated by parallel- imaging techniques (cf. Chap. 10).

Increasing the spatial resolution may allow the detection of smaller lesions, may better characterize the internal structure of larger lesions (e.g., calcification, blood products, demyelination, cystic components, etc.), and may better delineate the lesion boundaries with respect to normal anatomy, improving the accurate localization of a lesion (especially important in the prepontine, suprasellar, cerebellopontine angle, cavernous sinus, orbital, and Meckel's cave regions). The imaging of white matter disease, stroke, neoplasm, and vascular disease could all ben e. t from these advantages. Pediatric and neonatal brain imaging also demands fast, high-resolution imaging because of the relatively small brain size and the dif. culties in keeping a child still throughout the scan. Similar considerations apply also for imaging the spinal cord. Three-dimensional spoiled gradient- echo sequences, used in the evaluation of mesial temporal sclerosis in the work-up of seizures, tumor treatment planning, and voxel-based morphometry in neurodegenerative disorders, could benefit from the use of parallel imaging in both phase-encoded directions to further increase resolution without increasing scan time (Weiger et al. 2002a).

Conversely, shortened scan times alone can increase patient throughput, resulting in obvious operational and patient comfort improvements. Simply decreasing scan time reduces the risk of patient motion degrading a study. A number of other creative methods for further reducing motion artefacts through the use of parallel imaging have been proposed and demonstrated (Bammer et al. 2004, Kuhara and Ishihara 2000, Bydder et al. 2002, 2003, Atkinson et al. 2004).mehr

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